Composite nanoparticles, nanoparticles and methods for producing same

- Vive Crop Protection Inc.

In various aspects provided are methods for producing a nanoparticle within a cross-linked, collapsed polymeric material, said method including (a) providing a polymeric solution comprising a polymeric material; (b) collapsing at least a portion of the polymeric material about one or more precursor moieties; (c) cross-linking the polymeric material; (d) modifying at least a portion of said precursor moieties to form one or more nanoparticles and thereby forming a composite nanoparticle. In various embodiments, a non-confined nanoparticle can be produced by complete pyrolysis of the confined nanoparticle, and a carbon-coated nanoparticle by incomplete pyrolysis of the confined nanoparticle.

Skip to: Description  ·  Claims  ·  References Cited  · Patent History  ·  Patent History
Description
CROSS-REFERENCE TO RELATED APPLICATIONS

The present application is a broadening reissue application of U.S. application Ser. No. 11/745,377, filed May 7, 2007, now U.S. Pat. No. 7,964,277, issued Jun. 21, 2011, which claims the benefit of and priority to International Patent Application No. PCT/CA2006/001686 filed Oct. 13, 2006, which claims the benefit of and priority to U.S. Provisional Patent Application No. 60/726,184 filed Oct. 14, 2005, the entire contents of both of which are herein incorporated by reference.

BACKGROUND OF THE INVENTION

Nanoparticles are nanometer-sized materials e.g., metals, semiconductors, polymers, and the like, possessing unique characteristics because of their small size. Nanoparticles in both aqueous and non-aqueous solvents can be synthesized using a variety of methods.

The conformation of a polymer in solution is dictated by various conditions of the solution, including its interaction with the solvent, its concentration, and the concentration of other species that may be present. The polymer can undergo conformational changes depending on the pH, ionic strength, cross-linking agents, temperature and concentration. For polyelectrolytes, at high charge density, e.g., when “monomer” units of the polymer are fully charged, an extended conformation is adopted due to electrostatic repulsion between similarly charged monomer units. Decreasing the charge density of the polymer, either through addition of salts or a change of pH, can result in a transition of extended polymer chains to a more tightly-packed globular i.e. collapsed conformation. The collapse transition is driven by attractive interactions between the polymer segments that override the electrostatic repulsion forces at sufficiently small charge densities. A similar transition can be induced by changing the solvent environment of the polymer. This collapsed polymer is itself of nanoscale dimensions and is, itself, a nanoparticle. In this specification and claims the term “collapsed polymer” refers to an approximately globular form, generally as a spheroid, but also as an elongate or multi-lobed conformation collapsed polymer having nanometer dimensions. This collapsed conformation can be rendered irreversible by the formation of intramolecular chemical bonds between segments of the collapsed polymer, i.e. by cross-linking.

Macromolecules, i.e. polymers with the appropriate functional groups can undergo inter- or intra-molecular cross-linking reactions to produce new materials or new molecules with distinct properties, such as for example, shape, solubility, thermal stability, and density. These reactions are important in making new materials and various schemes for chemical reactions leading to cross-linking are described in the literature. For example, U.S. Pat. No. 5,783,626—Taylor et al, issued Jul. 21, 1998, describes a chemical method to cross-link allyl-functional polymers in the form of latexes, containing enamine moieties and pendant methacrylate groups via a free-radical cross-linking reaction during film formation producing coatings with superior solvent resistance and increased thermal stability. Polymer cross-linking has also been used to stabilize semiconductor and metal nanoparticles. U.S. Pat. No. 6,872,450—Liu et al, issued Mar. 29, 2005, teaches a method for stabilizing surface-coated semiconductor nanoparticles by self assembling diblock polymers on the surface coating and cross-linking the functional groups on the diblock polymer. Similarly, U.S. Pat. No. 6,649,138—Adams et al, issued Nov. 18, 2003, describes how branched amphipathic dispersants coated onto hydrophobic nanoparticles can also be cross-linked to form a permanent cohesive over coating around the nanoparticle.

Chemical means of cross-linking can be through radical reactions of pendant groups containing unsaturated bonds as described in aforesaid U.S. Pat. No. 5,783,626. Another method is through the use of molecules having multifunctional groups than can react with the functional groups of the polymer as described in aforesaid U.S. Pat. Nos. 6,649,138 and 6,872,450. Alternatively, cross-linking can be achieved though high energy radiation, such as gamma radiation.

The most common method of preparing chalcogenide semiconductor nanocrystals is the TOP/TOPO synthesis (C. B. Murray, D. J. Norris, and M. G. Bawendi, “Synthesis and Characterization of Nearly Monodisperse CdE (E=S, Se, Te) Semiconductor Nanocrystallites,” J. Am. Chem. Soc., 115:8706-8715, 1993). However, this method again involves multiple chemical steps and large volumes of expensive and toxic organometallic metal precursors and organic solvents. Furthermore, such nanoparticles need to be chemically modified in order to render them soluble in aqueous solution, which is important for a number of applications. Chalcogenide nanoparticles have also been synthesized in aqueous solution at low temperature using water-soluble thiols as stabilizing agents ((a) Rajh, O. L. Mićić, and A. J. Nozik, “Synthesis and Characterization of Surface-Modified Colloidal CdTe Quantum Dots,” J. Phys. Chem., 97: 11999-12003, 1993. (b) A. L. Rogach, L. Ktsikas, A. Kornowski, D. Su. A. Eychmüller, and H. Weller, “Synthesis and Characterization of Thiol-Stabilized CdTe Nanocrystals,” Ber. Bunsenges. Phys. Chem., 100(11): 1772-1778, 1996. (c) A. Rogach, S. Kershaw, M. Burt, M. Harrison, A. Komowski, A. Eychmüller, and H. Weller, “Colloidally Prepared HgTe Nanocrystals with Strong Room-Temperature Infrared Luminescence,” Adv. Mater. 11:552-555, 1999. (d) Gaponik, N., D. V. Talapin, A. L. Rogach, K. Hoppe, E. V. Shevchencko, A. Kornowski, A. Eychmuller, H. Weller, “Thiol-capping of CdTe nanocrystals: an alternative to organometallic synthetic routes,” Journal of Physical Chemistry B, 2002, vol. 106, iss. 39, p. 7177-7185. (e) A. L. Rogach, A. Kornowski, M. Gao, A. Eychmüller, and H. Weller, “Synthesis and Characterization of a Size Series of Extremely Small Thiol-Stabilized CdSe Nanocrystals,” J. Phys. Chem. B. 103:3065-3069, 1999). However, this method generally requires the use of an inert atmosphere with multiple processing steps and production of precursor gases. Another water-based synthesis involves the formation of undesirable by-products that must first be removed before semiconductor particles can be obtained (H. Zhnag, Z. Hou, B. Yang, and M. Gao, “The Influence of Carboxyl Groups on the Photoluminescence of Mercaptocarboxylic Acid-Stabilized Nanoparticles,” J. Phys. Chem. B, 107:8-13, 2003).

CdTe nanocrystals are known to have tunable luminescence from green to red and have shown tremendous potential in light-emitting thin films (A. A. Mamedov, A. Belov, M. Giersig, N. N. Mamedova, and N. A. Kotov, “Nanorainbows: Graded Semiconductor Films from Quantum Dots,” J. Am. Chem. Soc., 123: 7738-7739, 2001), photonic crystals (A. Rogach, A. Susha, F. Caruso, G. Sukhoukov, A. Kornowski, S. Kershaw, H. Mohwald, A. Eychmüller, and H. Weller, “Nano- and Microengineering: Three-Dimensional Colloidal Photonic Crystals Prepared from Submicrometer-Sized Polystyrene Latex Spheres Pre-Coated with Luminescent Polyelectrolyte/Nanocrystal Shells,” Adv. Mater. 12:333-337, 2000), and biological applications (N. N. Memedova and N. A. Kotov, “Albumin-CdTe Nanoparticle Bioconjugates: Preparation, Structure, and Interunit Energy Transfer with Antenna Effect,” Nano Lett., 1(6):281-286, 2001). PbTe and HgTe materials exhibit tunable emission in the infrared and look promising in the telecommunications industry. HgTe nanoparticles have been incorporated into more sophisticated assemblies, particularly as components in thin-film electroluminescent devices ((a) A. L. Rogach, D. S. Koktysh, M. Harrison, and N. A. Kotov, “Layer-by-Layer Assembled Films of HgTe Nanocrystals with Strong Infrared Emission,” Chem. Mater., 12:1526-1528, 2000. (b) É. O'Conno, A. O'Riordan, H. Doyle, S. Moynihan, a. Cuddihy, and G. Redmond, “Near-Infrared Electroluminescent Devices Based on Colloidal HgTe Quantum Dot Arrays,” Appl. Phys. Lett., 86: 201114-1-20114-3, 2005. (c) M. V. Kovalenko, E. Kaufmann, D. Pachinger, J. Roither, M. Huber, J. Stang, G. Hesser, F. Schäffler, and W. Heiss, “Colloidal HgTe Nanocrystals with Widely Tunable Narrow Band Gap Energies: From Telecommunications to Molecular Vibrations,” J. Am. Chem. Soc., 128:3516-3517, 2006) or solar cells (S. Günes, H. Neugebauer, N. S. Sariiciftci, J. Roither, M. Kovalenko, G. Pillwein, and W. Heiss, “Hybrid Solar Cells Using HgTe Nanocrystals and Nanoporous TiO2 Electrodes,” Adv. Funct. Mater. 16:1095-1099, 2006). PbTe, on the other hand, can be grown in a variety of glasses at high temperatures to produce composite materials for applications in optoelectronic devices ((a) A. F. Craievich, O. L. Alves, and L. C. Barbosa, “Formation and Growth of Semiconductor PbTe Nanocrystals in a Borosilicate Glass Matrix,” J. Appl. Cryst., 30:623-627, 1997. (b) V. C. S. Reynoso, A. M. de Paula, R. F. Cuevas, J. A. Medeiros Neto, O. L. Alves, C. L. Cesar, and L. C. Barbosa, “PbTe Quantum Dot Doped Glasses with Absorption Edge in the 1.5 μm Wavelength Region,”Electron. Lett., 31(12):1013-1015, 1995).

Doping of CdTe with Hg results in the formation of CdHgTe composite nanocrystals. Red shifts in absorbance/photoluminescence spectra and enhanced PL are observed with increasing Hg content (A. L. Rogach, M. T. Harrison, S. V. Kershaw, A. Kornowski, M. G. Burt, A. Eychmüller, and H. Weller, “Colloidally Prepared CdHgTe and HgTe Quantum Dots with Strong Near-Infrared Luminescence,” phys. stat. sol., 224(1):153-158, 2001). Cd1-xHgxTe alloys are popular components in devices used for near-IR detector technology. A variety of methods have been developed to create these materials. U.S. Pat. No. 7,026,228—Hails et al, issued Apr. 11, 2006, describes an approach to fabricating devices and semiconductor layers of HgCdTe in a metal organic vapour phase epitaxy (MOVPE) process with mercury vapor and volatile organotelluride and organocadmium compounds. In a different approach, U.S. Pat. No. 7,060,243—Bawendi et al, issued Jun. 13, 2006, describes the synthesis of tellurium-containing nanocrystals (CdTe, ZnTe, MgTe, HgTe and their alloys) by the injection of organometallic precursor materials into organic solvents (TOP/TOPO) at high temperatures. U.S. Pat. No. 6,126,740—Schulz, issued Oct. 3, 2000, discloses another non-aqueous method of preparing mixed-semiconductor nanoparticles from the reaction between a metal salt and chalcogenide salt in an organic solvent in the presence of a volatile capping agent.

Mixtures of CdTe and PbTe have also been investigated for IR detection in the spectral range of 3 to 5 μm. However, because these materials have such fundamentally different structures and properties (S. Movchan, F. Sizov, V. Tetyorkin. “Photosensitive Heterostructures CdTe—PbTe Prepared by Hot-Wall Technique,” Semiconductor Physics, Quantum Electronics & Optoelectronics. 2:84-87, 1999. V), the preparation of the alloy is extremely difficult. U.S. Pat. No. 5,448,098—Shinohara et al, issued Sep. 5, 1995, describes a super-conductive device based on photo-conductive ternary semiconductors such as PbCdTe or PbSnTe. Doping of telluride quantum dots, e.g. CdTe, with transition metals, e.g. Mn offers the possibility of combining optical and magnetic properties in one single nanoparticle ((a) S. Mackowski, T. Gurung, H. E. Jackson, L. M. Smith, G. Karczewski, and J. Kossut, “Exciton-Controlled Magnetization in Single Magnetic Quantum Dots,” Appl. Phys. Lett. 87: 072502-1-072502-3, 2005. (b) T. Kümmel, G. Bacher, M. K. Welsch, D. Eisert, A. Forchel, B. König, Ch. Becker, W. Ossau, and G. Landwehr, “Semimagnetic (Cd,Mn)Te Single Quantum Dots—Technological Access and Optical Spectroscopy,” J. Cryst. Growth, 214/215:150-153, 2000). Unfortunately, these materials are mostly fabricated using thin-film technologies such as molecular beam epitaxy or chemical vapour deposition and the necessity for a very controlled environment during growth makes these materials inaccessible. Some mixed-metal tellurides such as CdHgTe (S. V. Kershaw, M. Burt, M. Harrison, A. Rogach, H. Weller, and A. Eychmüller, “Colloidal CdTe/HgTe Quantum Dots with High Photoluminescnece quantum Efficiency at Room Temperature,” Appl. Phys. Lett., 75: 1694-1696, 1999); and CdMnTe (N. Y. Morgan, S. English, W. Chen, V. Chemornordik, A. Russ, P. D. Smith, A. Gandjbakhche, “Real Time In Vivo Non-Invasive Optical Imaging Using Near-Infrared Fluorescent Quantum Dots,” Acad. Radiol, 12(3): 313-323, 2005) quantum dots have been prepared in aqueous solution which is an adaptation of the synthetic technique outlined in supra Rajh, O. L. et al. However, all of the aforementioned methods involve many processing steps, sophisticated equipment or large volumes of expensive and toxic organometallic metal precursors and organic solvents.

A simple tellurite reduction method to prepare cadmium telluride materials has been used using sodium tellurite (Na2TEO3) as a tellurium precursor salt with a suitable reducing agent, such as NaBH4 with My+ cations (H. Bao, E. Wang, and S. Dong, “One-Pot Synthesis of CdTe Nanocrytals and Shape Control of Luminescent CdTe-Cystine Nanocomposites,” small, 2(4):476-480, 2006).

Accordingly, there is a need in the art for an environmentally friendly, “one-pot”, cost-effective, and generalizable method of directly producing metallic, metallic alloyed, semiconductor, oxide, and other forms of nanocomposite particles having effective functionality in a multitude of scientific disciplines.

SUMMARY OF THE INVENTION

In various aspects, the present invention provides methods of producing a composite nanoparticle comprising a nanoparticle confined within a cross-linked collapsed polymeric material, which is itself a nanoparticle.

The term “composite nanoparticle” in this specification, means a nanoparticle substantially confined within a cross-linked, polymeric material.

In various aspects, the present invention provides said composite nanoparticles when made by the methods of the present inventions.

In various aspects, the present invention provides methods for providing non-encapsulated nanoparticles from the aforesaid composite nanoparticles.

In various aspects, the present invention provides methods for producing wholly or partially carbon-coated nanoparticles from said composite nanoparticles.

In various embodiments, the present inventions teach the ability to make a wider variety of composite nanoparticles, including oxide, semiconductor, and more complex composite nanoparticles.

In various aspects, the present inventions provide methods for producing a composite nanoparticle comprising the steps of:

a) providing a polymeric solution comprising a polymeric material and a solvent;

b) collapsing at least a portion of the polymeric material about one or more precursor moieties to form a composite precursor moiety having a mean diameter in the range between about 1 nm and about 100 nm;

c) cross-linking the polymeric material of said composite precursor moiety; and

d) modifying at least a portion of said precursor moieties of said composite precursor moiety to form one or more nanoparticles and thereby forming a composite nanoparticle.

“Confined” in this specification means that the nanoparticle is substantially within the limits of the collapsed polymer's dimensions and includes, but is not limited to, the situation wherein portions of the polymer may be strongly interacting with the nanoparticle within the polymer dimensions.

As used herein, the term “precursor moiety” refers to a compound or entity at least a portion of which is a component of the eventual nanoparticle formed and includes nanoparticle precursors.

A polymeric material of use in the practice of the present inventions can be any molecule capable of collapse that contains units of monomers, that can be synthetic or naturally occurring and can be linear, branched, hyperbranched, or dendrimeric. Non-limiting examples of suitable polymeric materials are discussed in the various examples, which include, but are not limited to, poly(diallyldimethylammonium chloride) (PDDA), and polyacrylic acid (PAA), poly(styrene sulfonic acid) (PSS),

It also can be any polymer containing ionized or ionizable moieties along its length and is of sufficient length such that the collapsed form has nanometer dimensions. The collapsed form can be of different morphologies, such as, for example, spherical, elongated, or multi-lobed. The dimensions in any direction are anywhere from 0.1 to 100 nm, and preferably 1-50 nm.

A wide variety of solvents can be used to form a polymeric solution of use in the present inventions. In various embodiments, the polymeric solution is preferably an aqueous solution.

In preferred embodiments of the present inventions, a chosen polymer is dissolved in a suitable solvent to form a solution of the polymer. The solvent can be water, an organic solvent or a mixture of two or more such solvents. The addition to the solution of the collapsing agent induces a collapse of the polymer which substantially surrounds, e.g., confines, a precursor moiety. The collapsing agent can itself be the precursor moiety. The chosen confined agent, for example a precursor moiety, can be, e.g., an organic or inorganic charged ion or a combination thereof. For example, the confined agent can be an ion from an organic salt, an inorganic salt, or an inorganic salt that is water soluble where the water soluble inorganic salt is of the form MxAy where M is a metal cation belonging to Groups I to IV of the Periodic Table possessing a charge +y and A is the counter ion to M with a charge −x or a combination thereof. The confined agent could further comprise a mixture of ions from at least two inorganic salts.

Collapsing agents are usually water-soluble inorganic salts, most preferably, those that contain metal cations and their corresponding anions, both of which are known to induce a collapse-transition for certain polymeric materials. Non-limiting examples are Cd(NO3)2, Zn(NO3)2, Cu(SO4), Pb(NO3)2, Pb(CH3COO)2, Ag(NO3), Mn(SO4), Ni(NO3)2.

A variety of techniques can be used to collapse the polymeric material around a precursor moiety. For example, in various embodiments a collapsing agent such as a different solvent, an ionic species (e.g., a salt); or combinations thereof can be used. In various embodiments, it is preferred that the precursor moiety itself serve as a collapsing agent. Multiple collapsing agents can be used.

In various embodiments the at least one collapsing agent preferably comprises at least one ionic species. Preferably, in various embodiments, the at least one ionic species is a precursor moiety.

In various embodiments, the precursor moiety comprises at least one metal cation, complexed metal cation, or complexed metal anion. In various embodiments where the precursor moiety comprises a metal cation, complexed metal cation, or complexed metal anion, the modifying step (production means) comprises treating the cation, complexed cation, or complexed anion with γ-radiation or an agent selected from a reducing agent or an oxidizing agent to effect production of the nanoparticle comprising elemental metal confined within the cross-linked, collapsed polymeric material.

In various embodiments, the precursor moiety comprises two or more different metals. In various embodiments where the precursor moiety comprises two or more different metals, the modifying step comprises forming an alloy of two or more of the two or more metals.

In various embodiments, the precursor moiety comprises ions selected from a cation, complexed cations, or complexed metal anions of a plurality of metals and the modifying step comprises treating the cations or complexed anions with radiation, for example, γ-radiation, or an agent selected from a reducing agent or an oxidizing agent to effect production of the nanoparticle comprising an alloy of said metals, confined within the cross-linked collapsed polymeric material.

In various embodiments, the precursor moiety comprises a metal species-containing compound.

By the term “metal species-containing compound” is meant a compound containing a metal or metalloid in any valence state.

In various embodiments of the present inventions having an elemental metal, alloy comprising a metal, or a metal species-containing compound, the metal is preferably Cd, Zn, Cu, Pb, Ag, Mn, Ni, Au, Mg, Fe, Hg, Pt or a combination thereof.

In various embodiments of the present inventions having a metal species-containing compound, said compound containing said metal species preferably comprises one or more of a sulphide, selenide, telluride, chloride, bromide, iodide, oxide, hydroxide, phosphate, carbonate, sulphate, chromate and a combination thereof.

In various embodiments, a composite precursor moiety formed by a method of the present inventions has a mean diameter in the range between about 1 nanometer (nm) to about 100 nm. In various embodiments, the composite precursor moiety has a mean diameter in one or more of the ranges between: (a) about 1 nm to about 10 nm; (b) about 10 nm to about 30 nm; (c) about 15 nm to about 50 nm; and (d) about 50 nm to about 100 nm). It is to be understood that the term “mean diameter” is not meant to imply any sort of specific symmetry (e.g., spherical, ellipsoidal, etc.) of a composite precursor moiety. Rather, the composite precursor moiety could be highly irregular and asymmetric.

The formation of intra-molecular covalent bonds that effects the cross-linking of the polymeric material can be induced either by chemical means or by irradiation. Chemical means of cross-linking can also be achieved through the use of multi-dentate molecules as cross-linkers. These molecules contain multiple functional groups that are complementary to, and, therefore, can form covalent bonds with the functional groups on the polyelectrolyte polymeric material. These molecules can be linear, branched, or dendrimeric. For example, a molecule containing multiple amine groups, such as 2,2′-ethylenedioxydiethylamine can effect the intramolecular cross-linking of collapsed poly(acrylic acid). The cross-linking reaction in this case is promoted by the addition of an activating agent, typically used for amide bond formation, such as a carbodiimide.

The chemical cross-linking can be carried out to derivatize the polymer, such that a fraction of the ionizable groups are converted to groups that can be cross-linked through free-radical reactions. An example is to convert some of the carboxylic acid groups of poly(acrylic acid) to allyl esters. The allyl groups can then be reacted to form intramolecular bonds through radical chemistry.

Cross-linking by irradiation can be effected by exposing a solution of the collapsed polymer to an electromagnetic radiation source. The radiation source can be, for example, an excimer laser, a mercury arc lamp, a light emitting diode, UV germicidal lamp radiation or gamma rays.

A variety of techniques can be used in the present inventions to modify at least a portion of said precursor moieties of said composite precursor moiety to form one or more nanoparticles and thereby form a composite nanoparticle. These techniques are also referred to as “production means” herein since they are used in the production of the nanoparticle.

Suitable techniques for modifying a precursor moiety to form the desired nanoparticle include, but are not limited to, exposure to electromagnetic radiation, chemical treatment, and combinations thereof. Examples of suitable electromagnetic radiation exposure, include, for example γ-radiation, ultraviolet radiation, infrared radiation, etc. In various embodiments, the electromagnetic radiation is coherent radiation, such as provided, e.g., by a laser, in others it is incoherent, such as provided, e.g., by a lamp. Examples of chemical treatments include, but are not limited to, contacting with an oxidizing agent, contacting with a reducing agent, addition of at least one counter ion, a compound containing the counter ion, or a precursor to the counter ion, where the counter ion is a counter ion with respect to the precursor moiety or a portion thereof. Generally, modification of the precursor moiety results in the formation of a nanoparticle that is no longer soluble within the solvent of the polymeric solution.

Reaction either by reduction or oxidation of the ions, ionic precursor moieties, within the cross-linked polymeric material to form the composite nanoparticles can be effected through chemical, electrochemical, or photochemical means.

The resultant nanoparticles can be, for example, semiconductor crystals, including, but not limited, to CdS, CdSe, CdTe, ZnS, ZnSe, ZnTe, PbS, PbSe, PbTe, CuI, HgS, HgSe, and HgTe. The nanoparticles can also be metal alloys.

In various embodiments, a composite nanoparticle formed by a method of the present inventions has a mean diameter in the range between about 1 nanometer (nm) to about 100 nm. In various embodiments, the composite nanoparticle has a mean diameter in one or more of the ranges between: (a) about 1 nm to about 10 nm; (b) about 10 nm to about 30 nm; (c) about 15 nm to about 50 nm; and (d) about 50 nm to about 100 nm). It is to be understood that the term “mean diameter” is not meant to imply any sort of specific symmetry (e.g., spherical, ellipsoidal, etc.) of a composite nanoparticle. Rather, the composite nanoparticle could be highly irregular and asymmetric.

In various embodiments, the nanoparticle, formed from a precursor moiety, comprises an alloy of two or more different metals. In various embodiments where the precursor moiety comprises two or more different metals, the modifying step comprises forming an alloy of two or more of the two or more metals.

In various embodiments, the nanoparticle, formed from a precursor moiety, comprises a metal species-containing compound. By the term “metal species-containing compound” is meant a compound containing a metal or metalloid in any valence state.

In various embodiments of the present inventions having an elemental metal, alloy comprising a metal, or a metal species-containing compound, the metal is preferably Cd, Zn, Cu, Pb, Ag, Mn, Ni, Au, Mg, Fe, Hg, Pt or a combination thereof.

In various embodiments of the present inventions having a metal species-containing compound, said compound containing said metal species preferably comprises one or more of a sulphide, selenide, telluride, chloride, bromide, iodide, oxide, hydroxide, phosphate, carbonate, sulphate, chromate and a combination thereof.

In various aspects, the present inventions provide methods for producing a nanoparticle material, comprising the steps of: (a) providing a polymeric solution comprising a polymeric material and a solvent; (b) collapsing at least a portion of the polymeric material about one or more precursor moieties to form a composite precursor moiety; (c) cross-linking the polymeric material of said composite precursor moiety; and (d) modifying at least a portion of said precursor moieties of said composite precursor moiety to form one or more nanoparticles having a mean diameter in the range between about 1 nm and about 100 nm and thereby forming a composite nanoparticle; and (e) pyrolysing said composite nanoparticle to form a nanoparticle material. In various embodiments, the pyrolysis conditions are controlled such that the nanoparticle material formed comprises at least a partially carbon-coated nanoparticle

In various embodiments, the present inventions provide methods for producing a metal nanoparticle, comprising pyrolysing the composite nanoparticle prepared by a method of the present inventions described herein, wherein the metal nanoparticle is an elemental metal, an alloy comprising the metal with at least one other metal, or a metal species-containing compound, at a temperature to effective to substantially remove the polymeric material.

In various embodiments, the present inventions provide methods for producing a carbon-coated metal nanoparticle comprising incompletely pyrolysing the composite nanoparticle prepared by a method of the present inventions described herein, wherein the metal nanoparticle is selected from an elemental metal, an alloy comprising the metal with at least one other metal, and a metal species-containing compound, at a temperature to effect production of the carbon-coated metal nanoparticle.

In various aspects, the present inventions provide composite nanoparticles when made by a method or process of one of the inventions described herein.

In various aspects, the present inventions provide non-confined and wholly or partially carbon-coated metal nanoparticles when made by methods of the present inventions described herein.

Various embodiments of the present inventions can be of value in the production of semiconductor nanoparticles, including, for example, quantum dots such as CdSe, CdS, CdTe, and others. Various embodiments of the present inventions can be of value in the production of complex salts, such as LiFePO4, and oxide particles, such as Fe2O3.

Accordingly, in an various embodiments, the precursor moiety comprises at least one metal cation, complexed metal cation, or complexed metal anion, and the production means (modifying step) comprises treating the metal cation, complexed cation, or complexed anion with a suitable counterion or precursor thereof to effect production of the composite nanoparticle comprising a metal species-containing compound.

In various embodiments, the precursor moeity comprises an anion, and the modifying step (production means) comprises treating the anion with a suitable metal counterion or precursor thereof to effect production of the composite nanoparticle comprising a metal species-containing compound.

In various aspects, the modifying step comprises use of a suitable counterion or precursor thereof to effect production of a semiconductor nanoparticle or composite nanoparticle.

In a various aspects, the modifying step comprises use of a suitable counterion or precursor thereof to effect production of a composite nanoparticle comprising a complex salt.

In a various aspects, modifying step comprises use of a suitable counterion or precursor thereof to effect production of a nanoparticle comprising a hydroxide. In a preferred aspect, the hydroxide may be subsequently heated to convert the hydroxide to an oxide.

The aforesaid composite nanoparticles comprising a metal species-containing compound, a complex salt, hydroxide, or oxide, a semiconductor entity, can be, in various embodiments, effectively pyrolysed to substantially remove the polymeric material, or to only partially remove the polymeric material to produce, for example, a wholly or partially carbon-coated nanoparticle.

Thus, various embodiments of the present inventions relate to methods of making composite nanoparticles and nanoparticles that may have a wide variety of applications in a variety of sectors, including, but not limited to, biology, analytical and combinatorial chemistry, catalysis, energy and diagnostics. By utilizing starting materials that are readily soluble in water, the present inventions, in various embodiments, can provide nanoparticles and composite nanoparticles having unique characteristics applicable in the aforesaid sectors, which nanoparticles may be water soluble.

The synthesis routes of various embodiments of the present inventions, include, but are not limited to, synthesis in a “one pot” system in an aqueous medium. The particle size can be controlled, for example, by varying the molecular weight of the polymer, the degree of internal cross-linking, solution conditions and the amount of collapsing agent added. The polymer coat can be chosen to have desirable functional groups that can impart desirable properties, for example, having the capability for attachment to molecules, such as proteins or to enhance or decrease the sticking to substrates.

In various embodiments, the present inventions provide methods for making water-dispersable composite nanoparticles with inherent chemical functional groups that can be reacted with complementary functional groups on other molecules. Water-dispersable, in this context, refers to the formation of composite nanoparticles that can be prevented from aggregation in aqueous solution through adjustment of solution conditions.

In various embodiments, the methods of the present inventions provide a composite nanoparticle having at least one confined agent substantially surrounded by a polymeric material which polymer can be either a linear or branched polyanion or polycation or a combination thereof.

In preferred embodiments of the present inventions, a chosen polymer is dissolved in a suitable solvent to form a solution of the polymer. The solvent can be water, an organic solvent or a mixture of two or more such solvents. The addition to the solution of the collapsing agent induces a collapse of the polymer which substantially surrounds, e.g., confines the agent therein. The chosen confined agent can be an organic or inorganic charged ion or a combination thereof. For example, the confined agent can be an ion from an organic salt, an inorganic salt, or an inorganic salt that is water soluble where the water soluble inorganic salt is of the form MxAy where M is a metal cation belonging to Groups I to IV of the Periodic Table possessing a charge +y and A is the counter ion to M with a charge −x or a combination thereof. The confined agent could further comprise a mixture of ions from at least two inorganic salts.

In various embodiments, to retain the conformation of the collapsed polymer, cross-linking of the collapsed polymer is achieved by exposing the polymer to γ-radiation or UV radiation. Preferably, the UV radiation is UV laser radiation or UV arc lamp radiation. In various embodiments, the intra-molecular cross-links of the intra-molecular cross-linking process are chemically produced, for example, with carbodiimide chemistry with a multifunctional cross-linker.

One preferred embodiment of the present inventions involves the formation of composite nanoparticles by the addition of ions that induce precipitate formation of the confined agent within the collapsed polymeric material, wherein the collapsed polymer is intra-molecularly cross-linked. As used herein, “precipitation” of a confined ion refers to modification of the ion to a compound that is substantially insoluble in the solvent of the polymeric solution.

Various preferred embodiments of the aspects of the present inventions include, but are not limited to, using polymers dissolved in a solvent, usually water, so as to make a dilute solution. Polymers with ionizable groups, for example, NH2, RNH, and COOH can be chosen because of their water-solubility under appropriate solution conditions and their ability to undergo a collapse transition when exposed to certain concentrations of ions in solution, usually through addition of an inorganic salt. The collapse of the polymer brings about the confinement of some of the ions within a collapsed polymeric structure. In order to make the collapsed conformation of the polymers permanent, intra-macromolecular bond formation is facilitated either through radiation exposure, through the use of chemical cross-linkers, or both. In various embodiments, the collapsed intra-molecular, cross-linked polymer have some of the ions from an inorganic salt confined within the collapsed structure as the basis for the formation of the composite nanoparticle. The confined ions, for example, can be reduced, oxidized, and/or reacted (e.g. by precipitation with an external agent), which results in the formation of the composite nanoparticle of the inner nanoparticle confined within the collapsed intra-molecular cross-linked polymeric material. Un-reacted ionizable groups, for example, can serve as future sites for further chemical modification, dictate the particles solubility in different media, or both.

An ionizable moiety or group is any chemical functional group that can be rendered charged by adjusting solution conditions, while ionized moieties refers to chemical functional groups that are charged regardless of solution conditions. The ionized or ionizable moiety or group can be either cationic or anionic, and can be continuous along an entire chain as in the case of regular polymers, or can be interrupted by blocks containing different functional groups, as in the case of block polymers.

In various embodiments, a preferred cationic group is the amino group and preferred anionic groups are carboxylic acid, sulfonic acid, phosphates, and the like. For cationic polymers, examples are poly(allylamine), poly(ethyleneimine) poly(diallyldimethylammonium chloride, and poly(lysine). For anionic polymers, examples are poly(acrylic acid), poly(styrene sulfonic acid), poly(glutamic acid), etc. Block polymers are made up of blocks of polymers having different functional groups. The block polymers can be made up of blocks of any of the mentioned anionic and cationic polymers and another polymer that imparts a specific desirable property to the block polymer.

In various embodiments, functional groups of the polymeric material can be used for conjugating the composite nanoparticles to other molecules containing complementary functional groups. These molecules can be any member of affinity-binding pairs such as antigen-antibody, DNA-protein, DNA-DNA, DNA-RNA, biotin-avidin, hapten-antihapten, protein-protein, enzyme-substrate and combinations thereof. These molecules can also be protein, ligand, oligonucleotide, aptamer, carbohydrate, lipid, or other nanoparticles. An example is the conjugation of poly(acrylic acid)-encased nanoparticles to proteins through amide bond formation between amine groups on proteins and the carboxylic acid groups on poly acrylic acid (PAA).

A fraction of the functional groups of the polyelectrolyte polymer can also be modified to convert them to other functional groups that can be used for conjugation. For example, a hetero bi-functional molecule containing an amine group and a latent thiol group can be reacted with poly(acrylic acid)-encased nanoparticles through amide bond formation thereby converting the carboxylic acid to a thiol group. The thiol group can be used for conjugation to other molecules containing thiol-reactive groups.

The wide variety of potential applications for the composite nanoparticles and nanoparticles, produced by the methods of the present invention include, but are not limited to, the absorption of light energy selected from the group consisting of UV, visible, and IR light, wherein the composite nanoparticle or nanoparticle are used as pigments or are incorporated into an optical device. In various embodiments, after absorbing light energy the composite nanoparticle may be capable of emitting light.

In various embodiments of the present inventions, provided are methods wherein the polymeric material is conjugated to molecules containing functional groups for binding to complementary binding partners to form an affinity-binding pair selected from the group having an enzyme-substrate, antigen-antibody, DNA-DNA, DNA-RNA, biotin-avidin, hapten-antihapten and combinations thereof. Preferably, the molecules are selected from the group consisting of protein, ligand, oligonucleotide, aptamer, and other nanoparticles.

In various embodiments, a composite nanoparticle of the present inventions may be used, e.g., to enhance spectroscopic techniques, including vibrational spectroscopy.

In various embodiments, provided are methods wherein the composite nanoparticles are further assembled on a surface of a substrate using layer-by-layer assembly or further aggregated into three-dimensional systems of composite nanoparticles, whereby the three-dimensional systems are created on a surface. In various embodiments this substrate is a film.

Accordingly, in various aspects the present inventions provide a coated substrate having a plurality of layers of composite nanoparticles as herein a described interspersed between adjacent layers of oppositely charged compounds.

In various embodiments, a coated substrate as herein described is preferably coated, with a composite nanoparticle of CdS/PAA and the oppositely charged compound is poly(allylamine) hydrochloride (PAH).

In various embodiments, the present inventions provide use of a composite nanoparticle as herein described in the production of a multi-layered coated substrate. This substrate could be of value, for example, as one or more of: (a) a solid substrate comprising catalytic or otherwise reactive nanoparticles; and (b) an optical filter or as an element in an optical device where the incorporated composite nanoparticles have useful properties.

In various embodiments, the compounds according to the present inventions could be of value as semiconductor materials, for example, as quantum dots.

BRIEF DESCRIPTION OF THE DRAWINGS

The foregoing and other aspects, embodiments, objects, features and advantages of the present inventions can be more fully understood from the following description in conjunction with the accompanying drawings. In the drawings, like reference characters generally refer to like features and structural elements throughout the various figures. The drawings are not necessarily to scale, emphasis instead being placed upon illustrating the principles of the present inventions, wherein.

FIG. 1 represents UV-Vis absorption spectra of CdS/PAA composite nanoparticles prepared according to Example 13;

FIG. 2 represents emission spectra of different CdS/PAA composite nanoparticles prepared according to Example 13;

FIG. 3 represents STEM image of CdS/PAA composite nanoparticles prepared according to Example 13;

FIG. 4 represents uv-vis absorption and emission spectra of CdSe/PAA composite nanoparticles prepared according to Example 14;

FIG. 5 represents uv-vis absorption and emission spectra of (CdSe—CdS)/PAA composite nanoparticles prepared according to Example 15;

FIG. 6 represents uv-vis absorption and emission spectra of CdTe/PAA composite nanoparticles prepared according to Example 16;

FIG. 7 represents uv-vis absorption and emission spectra of (CdTe—ZnS)/PAA composite nanoparticles produced according to Example 17;

FIGS. 8(a)-8(c) represent STEM with EDX analysis of LiFePO4/PAA composite nanoparticles produced according Example 18;

FIG. 9 represents a XRD pattern of LiFePO4/PAA composite nanoparticles produced according Example 18;

FIGS. 10(a)-10(c) represents STEM with EDX analysis of Fe2O3/PAA composite nanoparticles produced according Example 19;

FIG. 11 represents an XRD x-ray diffraction pattern of Fe2O3/PAA composite nanoparticles produced according to Example 19;

FIG. 12 represents STEM image of ZnO/PAA composite nanoparticles made according to Example 20;

FIG. 13 represents uv-vis absorbance and emission spectra of ZnO/PAA composite nanoparticles made according to Example 20;

FIG. 14 represents emission spectra of both CdS/PAA composite nanoparticles coated and non-coated polystyrene prepared according to Example 21;

FIG. 15 represents uv-vis absorption spectra of Ag/PAA composite nanoparticles produced according to Example 22;

FIG. 16 represents a STEM image of Ag/PAA composite nanoparticles produced according to Example 22;

FIG. 17 represents uv-vis absorption spectra of Au/PAA composite nanoparticles produced according to Example 23;

FIG. 18 represents STEM image of Au/PAA composite nanoparticles produced according to Example 23;

FIG. 19 represents uv-vis spectra of (Au, Ag)/PAA composite nanoparticles produced according to Example 24;

FIGS. 20(a)-20(c) represent STEM with EDX analysis image of (Au, Ag)/PAA composite nanoparticles produced according to Example 24;

FIG. 21 represents uv-vis and emission spectra of CdS/PSS composite nanoparticles produced according to Example 27;

FIG. 22 represents uv-vis and emission spectra of CdS/PDDA composite nanoparticles produced according to Example 28; and

FIG. 23 represents absorbance and emission spectra of CdPbTe/PAA composite nanoparticles produced according to Example 36 according to the present invention;

FIG. 24 absorbance and emission spectra of CdZnTe/PAA composite nanoparticles produced according to Example 37 according to the invention; and

FIG. 25 absorbance and emission spectra of CdMnTe/PAA composite nanoparticles produced according to Example 38 according to the present invention.

 DETAILED DESCRIPTION OF VARIOUS EMBODIMENTS Examples

In the following examples, the term

(a) “My+/polymer refers to the collapsed polymeric material with the metal cation My+, wherein M is the stated metal in the example; and

(b) Ax−/polymer refers to the collapsed polymeric material collapsed with the anion Ax−.

In the case of multiple cations or anions used to collapse a single polymer, the different metal cations and anions will be separated by a comma “,” as in the case (M1y1+, M2y2, etc . . . )/Polymer and (A1x1−, A2x2−, etc . . . )/Polymer (e.g. Cd2+/PAA, Cl−/PDDA, etc.). Nanoparticles formed from the metal ions will be designated as M1 x1 A1 y1/Polymer (e.g. CdS/PAA, (CdS, PbS)/PAA, etc). Nanoparticles formed from the metal ions that have been treated with another agent to form a different material will be designated by a “−” as in (M1 x1 A1 y1-M2 y2 A2 y2)/Polymer (e.g. (CdSe—CdS)/PAA, (CdTe—ZnS)/PAA, etc).

Example 1 Polycation Collapse with (−1) Anion

In a plastic 400.0 ml beaker, 3.0 ml of poly(diallyldimethylammonium chloride) (PDDA) [Sigma, Average Mw 400-500K, 20 wt % in water] was diluted to 300 ml with deionized water. The solution was stirred for 10 minutes. 5.0 ml aliquots were obtained, and placed in 20 ml scintillation vials. To each was added dropwise with vigorous stirring 5.0 ml of aqueous NaCl solutions of different concentrations (2 mM-60 mM) yielding 10 mL of Cl−/PDDA solutions with different [Cl−] between 1 and 50 mM and a final PDDA concentration of 1 mg/ml. The relative viscosity of each solution was measured with an Ostwald viscometer. The viscosity as a function of NaCl concentration changed suddenly at approximately 10 mM; this was taken as the PDDA collapse point with Cl−, such that at lower concentrations, the PDDA is primarily in an extended configuration.

Example 2 Polycation Collapse with (−2) Anion

In a plastic 400.0 ml beaker, 3.0 ml of poly(diallyldimethylammonium chloride) (PDDA) [Sigma, Average Mw 400-500K, 20 wt % in water] was diluted to 300 ml with deionized water. The solution was stirred for 10 minutes. 5.0 ml aliquots were obtained, and placed in 20 ml scintillation vials. To each was added dropwise with vigorous stirring 5.0 ml of aqueous Na2SO4 solutions of different concentrations (2 mM-20 mM) yielding 10 mL of SO42−/PDDA solutions with different [SO42−] between 1 and 10 mM and a final PDDA concentration of 1 mg/ml. The relative viscosity of each solution was measured with an Ostwald viscometer. The viscosity as a function of Na2SO4 concentration changed suddenly at approximately 3 mM; this was taken as the PDDA collapse point with SO42−, such that at lower concentrations, the PDDA is primarily in an extended configuration.

Example 3 Polycation Collapse with (−3) Anion

In a plastic 400.0 ml beaker, 15 ml of poly(diallyldimethylammonium chloride) (PDDA) [Sigma, Average Mw 400-500K, 20 wt % in water] was diluted to 300 ml with deionized water. The solution was stirred for 10 minutes. 5.0 ml aliquots were obtained, and placed in 20 ml scintillation vials. To each was added dropwise with vigorous stirring 5.0 ml of aqueous Na3PO4 solutions of different concentrations (2 mM-50 mM) yielding 10 mL of PO43−/PDDA solutions with different [PO43−] between 1 and 25 mM and a final PDDA concentration of 5 mg/ml. The relative viscosity of each solution was measured with an Ostwald viscometer. The viscosity as a function of Na2SO4 concentration changed suddenly at approximately 2 mM; this was taken as the PDDA collapse point with PO43−, such that at lower concentrations, the PDDA is primarily in an extended configuration.

Example 4 Polyanion Collapse with (+1) Cation

In a 400 ml plastic beaker, 400.0 mg of (PAA) (Sigma, Average Mv 1.2 million) was dissolved in 200 ml deionized water. The plastic beaker was immersed in a hot water bath (approximately 80-90° C.) and was stirred vigorously for at least 30 minutes or until all of the solid PAA has dissolved. Once the solution has cooled to room temperature, the pH was adjusted to 6.8 using 0.1 M NaOH. pH measurements were done using narrow range pH paper. 5 ml aliquots of the pH adjusted PAA were obtained and to each was added 5.0 ml aliquots were obtained, and placed in 20 ml scintillation vials. To each was added dropwise with vigorous stirring 5.0 ml of aqueous NaCl solutions of different concentrations (0.2 mM-10.0 mM) yielding 10 mL of Na+/PDDA solutions with different [Na+] between 0.1 mM and 5.0 mM and a final PAA concentration of 1 mg/ml. The relative viscosity of each solution was measured with an Ostwald viscometer. The viscosity as a function of NaCl concentration changed suddenly at approximately 2 mM; this was taken as the PAA collapse point with Na+, such that at lower concentrations, the PAA is primarily in an extended configuration.

Example 5 Polyanion Collapse with (+2) Cation

In a 400 ml plastic beaker, 400.0 mg of PAA (Sigma, Average Mw 1.2 million) was dissolved in 200 ml deionized water. The plastic beaker was immersed in a hot water bath (approximately 80-90° C.) and was stirred vigorously for at least 30 minutes or until all of the solid PAA has dissolved. Once the solution has cooled to room temperature, the pH was adjusted to 6.8 using 0.1 M NaOH. pH measurements were done using narrow range pH paper. 5 ml aliquots of the pH adjusted PAA were obtained and to each was added 5.0 ml aliquots were obtained, and placed in 20 ml scintillation vials. To each was added dropwise with vigorous stirring 5.0 ml of aqueous Cd(NO3)2 solutions of different concentrations (0.1 mM-6.0 mM) yielding 10 mL of Cd2+/PAA solutions with different [Cd2+] between 0.1 mM and 3.0 mM and a final PAA concentration of 1 mg/ml. The relative viscosity of each solution was measured with an Ostwald viscometer. The viscosity as a function of Cd(NO3)2 concentration changed suddenly at between 1-2 mM; this was taken as the PAA collapse point with Cd2+, such that at lower concentrations, the PAA is primarily in an extended configuration. Addition of more Cd(NO3)2 such that the final concentration >2 mM caused a white precipitate to form. Solutions with a final concentration of 1.2 mM Cd(NO3)2 and approx 0.7 mg/ml PAA were then prepared for use in subsequent examples below; this solution is referred to as Cd2+/PAA in this work.

Example 6 Polyanion Collapse with (+3) Cation

In a 400 ml plastic beaker, 400.0 mg of poly(styrene sulfonic acid) (PSS) (Alfa Aesar, Average MW 1 million) was dissolved in 200 ml deionized water. 5 ml aliquots of the PSS solution were obtained, and placed in 20 ml scintillation vials. To each was added dropwise with vigorous stirring 5.0 ml of aqueous solutions containing FeCl3 of different concentrations (0.2 mM-20.0 mM) yielding 10 mL of Fe3+/PDDA solutions with different [Fe3+] between 0.1 mM and 10.0 mM and a final PSS concentration of 1 mg/ml. The relative viscosity of each solution was measured with an Ostwald viscometer. The viscosity as a function of FeCl3 concentration changed suddenly at approximately 2 mM; this was taken as the PSS collapse point with Fe3+ such that at lower concentrations, the PSS is primarily in an extended configuration.

Example 7 Polyanion Collapse with 2 Cations

In a 400 ml plastic beaker, 400.0 mg of PAA (Sigma, Average MV 1.2 million) was dissolved in 200 ml deionized water. The plastic beaker was immersed in a hot water bath (approximately 80-90° C.) and was stirred vigorously for at least 30 minutes or until all of the solid PAA has dissolved. Once the solution had cooled to room temperature, the pH was adjusted to 6.8 using 0.1 M NaOH. pH measurements were done using narrow range pH paper. 5.0 ml aliquots were obtained, and placed in 20 ml scintillation vials. To each was added dropwise with vigorous stirring 5.0 ml of aqueous solutions containing FeCl2 and LiCl at a mole ratio of (2:1) of different concentrations* (0.2 mM-8.0 mM) yielding 10 mL of (2Fe2+, Li+)/PAA solutions with different [2Fe2+, Li2+] between 0.1 mM and 4.0 mM and a final PAA concentration of 1 mg/ml. The relative viscosity of each solution was measured with an Ostwald viscometer. The viscosity as a function of FeCl2 and LiCl concentration changed suddenly at approximately 0.3 mM; this was taken as the PAA collapse point with 2Fe2+, Li+ such that at lower concentrations, the PAA is primarily in an extended configuration. *concentrations refer to the total concentration of both metal ions combined

Example 8 Preparation of Cd2+/PAA Crosslinked Composite Nanoparticles According to the Invention Using Mercury Arc Lamp

A solution of Cd2+/PAA was prepared by dropwise addition of 10 ml of 0.005M Cd(NO3)2 solution to 10 ml of 2 mg/ml aqueous solution of PAA (Sigma, Ave Mw 1.2 million PAA, pH adjusted to 6.8 with 0.1 M NaOH). The solution was exposed to light from a 200 W mercury arc lamp for approximately 1 hour to effect collapse, while undergoing vigorous stirring. The irradiated solution was then dialyzed against deionized water for 3 hours. The dialysis is expected to substantially reduce the concentration of ions in solution, thus reversing the polymer collapse. However, it was found that the solution viscosity remains unchanged (still low), indicating that the collapsed configuration is retained, and that the collapsed polymer has been crosslinked to remain in the collapsed configuration. An aliquot of the solution was cast onto mica and allowed to air dry. Atomic force microscopy imaging indicated the presence of particles 10-25 nm in size.

Example 9 Preparation of Zn2+/PAA and Cd2+/PAA Crosslinked Composite Nanoparticles According to the Invention Using Laser Irradiation

A solution of Zn2+/PAA was prepared by dropwise addition of 10 ml of 0.005M Zn(NO3)2 solution to 10 ml of 2 mg/ml aqueous solution of PAA (Sigma, Ave Mw 1.2 million PAA, pH adjusted to 6.8 with 0.1 M NaOH) with vigorous stirring. The solution was exposed to 5000 pulses from an excimer laser source (10 mJ/cm3) while undergoing vigorous stirring. The laser irradiated solution was then dialyzed against deionized water for 3 hours, changing the deionized water reservoir every hour. The solution viscosity remained unchanged by dialysis, indicating that the collapsed configuration is retained.

A solution of Cd2+/PAA was prepared by dropwise addition of 10 ml of 0.005M Cd(NO3)2 solution to 10 ml of 2 mg/ml aqueous solution of PAA (Sigma, Ave Mw 1.2 million PAA, pH adjusted to 6.8 with 0.1 M NaOH) with vigorous stirring. The solution was exposed to 5000 pulses from an excimer laser source (10 mJ/cm3) while undergoing vigorous stirring. The laser irradiated solution was then dialyzed against deionized water for 3 hours, changing the deionized water reservoir every hour. The solution viscosity remained unchanged by dialysis, indicating that the collapsed configuration is retained.

Example 10 Preparation of Zn2+/PAA Crosslinked Composite Nanoparticles According to the Invention Using Chemical Crosslinking Agent

Zn2+/PAA solution was prepared according to example 9. 2.0 ml of Zn2+/PAA was placed in a 5 ml glass vial and 160 μl of a solution that was 26.4 mg/mL in 1-Ethyl-N′(3-dimethylaminopropyl)carbodiimide (EDC) and 33.45 mM in 2,2′-(Ethylenedioxy)bis-(ethylamine) (EDE) was added under constant stirring. The resulting solution was stirred for 12 hours and was then dialyzed against deionized water for 3 hours, changing the deionized water reservoir every hour. Zn2+/PAA that was not treated with the EDC/EDE solution was also dialyzed against deionized water for 3 hours, changing the deionized water reservoir every hour. After dialysis, the viscosity of the EDC/EDE treated Zn 2+/PAA solution was much lower than that of an untreated Zn2+/PAA solution. This indicates that the collapsed configuration is retained after Zn2+/PAA was treated with the EDC/EDE solution.

Example 11 Polyacrylic Acid Crosslinking with Gamma Radiation to Produce Cd2+/PAA Composite Nanoparticles According to the Invention

20 ml of Cd2+/PAA, prepared as described in Example 5, was placed in a 20 ml scintillation vial. To this, 200 μl of isopropanol (ACS grade) was added. The vial was sealed with a rubber septum and was vortexed for 10 seconds. The solution was exposed to a total dose of ˜15 kGy of gamma radiation at a dose rate of 3.3 kGy/hr. The irradiated solution was then dialyzed against deionized water for 3 hours, changing the deionized water reservoir every hour. Similarly, Cd2+/PAA that was not exposed to gamma radiation was also dialyzed in a similar manner. After dialysis, the viscosity of the collapsed irradiated, dialyzed solution was much lower than that of a collapsed, un-irradiated solution. Na+/PAA prepared according to example 4, [Na+]=2 mM, was also exposed to the same gamma radiation dose, and similarly the viscosity of the collapsed irradiated, dialyzed Na+/PAA solution was much lower than that of a collapsed, un-irradiated solution.

Example 12 Polyacrylic Acid Crosslinking with 4 G25T8 Germicidal Lamps to Produce Cd2+/PAA Composite Nanoparticles According to the Invention

20 ml of Cd2+/PAA was prepared according to Example 5 was placed in a 50.0 ml glass beaker. The solution was exposed to 4 G25T8 germicidal UV lamps (approximate power is 12 μW/mm2) for approximately 1.5-2 hours under vigorous stirring. The irradiated solution was then dialyzed against deionized water for 3 hours, changing the deionized water reservoir every hour. Cd2+/PAA that was not exposed to the UV lamp was also dialyzed in a similar manner. The viscosity of the irradiated, dialyzed Cd2+/PAA solution was much lower than that of a Cd2+/PAA solution that was not exposed to the UV lamp. Collapsed PAA with Zn(NO3)2, Pb(NO3)2, Cd/Pb(NO3)2, Zn/Cd(NO3)2, FeCl2, LiCl, FeCl3, Co(SO4), Cu(SO4), Mn(SO4), Ni(CH3COOH), Zn(NO3)2/MgCl2 was also UV irradiated in a similar manner and the viscosity of the collapsed irradiated, dialyzed solutions were much lower than that of a collapsed, un-irradiated solutions. These solutions were filterable using a 0.2 μm nylon syringe filter.

Example 13 CdS/PAA Composite Nanoparticles According to the Invention

20 ml of crosslinked Cd2+/PAA composite nanoparticles was prepared according to example 12 and was placed in a 50 ml glass beaker. Under vigorous stirring, 20.0 ml of 0.60 mM Na2S solution was added dropwise at a rate of 2 ml/min using a syringe pump. The resulting solution was yellow in color. Absorbance and emission spectra of the resulting solution are shown in FIG. 1. The maximum emission wavelength can be tuned to different frequencies by varying the ratio of Na2S to the amount to Cd2+ ions present in the Cd2+/PAA solution. This is shown in FIG. 2. A red shift in the Emissionmax is observed as more Na2S is added. Scanning Transmission Electron microscopy images of the CdS/PAA prepared are shown in FIG. 3.

Example 14 CdSe/PAA Composite Nanoparticles According to the Invention

300 mL of Cd2+/PAA was prepared according to Example 12. The pH of the solution adjusted to ˜8.5-9.0 with 0.1 M NaOH and was bubbled with N2(g) for 30 minutes in a 500 ml round bottom flask. 18.2 mg of 1,1′-dimethylselenourea was dissolved in 5 ml of degassed, deionized water and was sealed with a septa in a 5 ml glass vial. Using a 5 ml syringe, 4.1 ml of this dimethlyselenourea solution was added to the Cd2+/PAA under N2 atmosphere. The resulting solution was stirred for 10 minutes and then heated on a heating mantle to a temperature of approximately 80° C. for 1 hour. After one hour, the solution was allowed to cool. The resulting solution has an absorption and emission spectra shown in FIG. 4.

Example 15 (CdSe—CdS)/PAA Composite Nanoparticles According to the Invention

150 ml of CdSe/PAA nanoparticles produced according to Example 14 was placed in a 250 ml round bottom flask. 125.0 ml of 0.30 M thioacetamide in water was added to the flask containing the CdSe/PAA nanoparticles. The resulting mixture was stirred vigorously for 5 minutes, and was then heated to 80° C. on a heating mantle with very light stirring for 24 hours. The absorption and emission spectra of the resulting (CdSe—CdS)/PAA composite nanoparticles are shown in FIG. 5.

Example 16 CdTe/PAA Composite Nanoparticles According to the Invention

Under ambient conditions, 300 ml of Cd2+/PAA produced according to Example 12 was placed in a 500 ml round bottom flask. To this solution, 0.156 g of NaBH4 and 0.312 g of trisodium citrate was added while the solution was being stirred. Immediately after the addition of the borohydride and the citrate, 12.5 ml of 0.01M NaTeO3 was added. Upon addition of the NaTeO3 solution, the solution develops a yellow color. The solution was then refluxed for approximately 20 hours to allow CdTe/PAA nanoparticles to form. The absorption and emission spectra of the resulting solution after 20 hours of reflux is shown in FIG. 6.

Example 17 (CdTe—ZnS)/PAA Composite Nanoparticles According to the Invention

In 50 a ml falcon tube, 1.7 ml of 3M NaCl was added to 15 ml CdTe/PAA nanoparticles particles formed according to Example 16. The resulting mixture was vortexed for 10 seconds after which 30 ml of absolute ethanol was added and was centrifuged at 8500 rpm for 15 minutes. After centrifugation, the brown pellet formed at the bottom of the falcon tube was rinsed with 20 ml 70% ethanol. The resulting solution was centrifuged at 8500 rpm for 10 mins. The brown pellet was isolated and resuspended in 15 ml deionized water. To 10 ml of the resuspended CdTe/PAA nanoparticles, 278 μL of 24 mM Zn(NO3)2 was added. The solution was stirred for 10 minutes after which 167 μL 39.5 mM Na2S was added. After 10 minutes of stirring, a second 278 μL of 24 mM Zn(NO3)2 was added. The solution was stirred for 10 minutes after which 167 μL 39.5 mM Na2S was added. After 10 more minutes of stirring, a third 278 μL of 24 mM Zn(NO3)2 was added. The solution was stirred for 10 minutes after which 167 μL 39.5 mM Na2S was added. The solution was left in a 50 ml falcon tube for at least 3 days before taking the emission spectra. The resulting solution's absorption and emission spectra after 3 days is shown in FIG. 7.

Example 18 Formation of LiFePO4/PAA Composite Nanoparticles According to the Invention

A 20 ml solution of (Fe2+, Li+)/PAA was prepared according to Example 7 with some modifications. Briefly, in a 400 ml plastic beaker, 400.0 mg of PAA (Sigma, Average MV 1.2 million) was dissolved in 200 ml deionized water. The plastic beaker was immersed in a hot water bath (approximately 80-90° C.) and was stirred vigorously for at least 30 minutes or until all of the solid PAA has dissolved. Once the solution has cooled to room temperature, the pH was adjusted to 3.0 using 0.1 M HNO3. pH measurements were done using narrow range pH paper. 10.0 ml of this PAA solution was taken and placed in a 50 ml glass beaker to which 10.0 ml of a solution that was 6.7 mM in both FeCl2 and LiCl was added dropwise with vigorous stirring. The solution was crosslinked for 1.5 hours under 4 G25T8 Germicidal lamps. 5.0 ml of a 13 mM NH4H2PO4 was then added to the UV exposed (Fe2+, Li+)/PAA. The solvent (water) of the resulting solution was removed using a rotary evaporator. When all of the solvent was removed, a light green colored residue remained and was then dried under vacuum for 12 hours. This light green residue was placed in tube furnace and was heated under N2 atmosphere for 12 hours at 600° C. After 12 hours of heating in the furnace, the light green residue tuned black. The STEM images with EDX analysis of the LiFePO4/PAA composite nanoparticle are shown in FIG. 8. FIG. 8a is a STEM image of LiFePO4/PAA prepared according to the present invention, and wherein FIG. 8b shows the cross-sectional abundance of phosphorous along the scanned line in FIG. 8a acquired using electron dispersive x-rays; and FIG. 8c shows the cross-sectional abundance of iron along the scanned line in FIG. 8a acquired using electron dispersive x-rays. The XRD pattern for the LiFePO4/PAA composite nanoparticle is shown in FIG. 9.

Example 19 Formation of Fe2O3/PAA Composite Nanoparticles According to the Invention

Fe2O3/PAA is formed by following exactly Example 18 with only one modification. The pH of the PAA should be adjusted to pH 6.8 instead of pH 3.0 using 0.1M NaOH before adding the FeCl2 and LiCl solution. The rest of the procedure remains the same. Surprisingly, this single modification leads to the formation of Fe2O3/PAA instead of LiFePO4/PAA. The STEM images with EDX analysis of the LiFePO4/PAA nanocomposite particles are shown in FIG. 10. FIG. 10a is a STEM image Fe2O3/PAA nanocomposite prepared according to the present invention, and wherein FIG. 10b shows the cross-sectional abundance of iron along the scanned line in FIG. 10a acquired using electron dispersive x-rays; and FIG. 10c shows the cross-sectional abundance of phosphorous along the scanned line in FIG. 10a acquired using electron dispersive x-rays. The XRD pattern is shown in FIG. 11, wherein H is hematite, alpha-Fe203 and M is defect spinal structure of magnetite, gamma-Fe203, maghemite. Note that although the EDX images show the presence of phosphate, the XRD pattern suggests that Fe2O3 is present and not LiFePO4.

Example 20 Formation of ZnO/PAA Composites Nanoparticles According to the Invention

A 20 ml solution of Zn2+/PAA was prepared by dropwise addition of 10 ml of 0.005M Zn(NO3)2 solution to 10 ml of 2 mg/ml aqueous solution of PAA (Sigma, Ave Mw 1.2 million PAA, pH adjusted to 6.8 with 0.1 M NaOH) with vigorous stirring. The solution was exposed to UV radiation for 1.5 hours under 4 G25T8 Germicidal lamps as in Example 12. The pH UV exposed Zn2+/PAA was adjusted to pH 11.0 with 0.1 M NaOH, and then refluxed for 1 hour. After reflux, the solution turns slightly cloudy. The absorbance, emission spectra and STEM image are shown in FIG. 12 and the absorbance and emission spectra are shown in FIG. 13.

Example 21 Incorporation of CdS/PAA Composite Nanoparticles According to the Invention into Layer-by-Layer Thin Films

Polystyrene substrates were sonicated in 0.01M sodium dodecyl sulfate +0.1M HCl solution for 3 minutes, rinsed with distilled water, and dried with nitrogen. Layer by Layer (LbL) thin films were formed by immersing the substrate in 1 mg/ml PAH (poly(allylamine) hydrochloride) in 0.1M NaCl for 5 minutes, followed by a 5 minute rinse in 0.1M NaCl, then immersed in a solution of CdS/PAA nanoparticle solution (prepared according Example 13) for 5 minutes, then rinsed in 0.1M NaCl solution for 5 minutes. This process was repeated 100 times. Emission spectra of the polystyrene substrate coated with the LbL thin films of PAH:CdS/PAA composite nanoparticles is shown in FIG. 14.

Example 22 Ag/PAA Composite Nanoparticles According to the Invention

20 ml of Ag+/PAA was made according to Example 4. Briefly, in a 400 ml plastic beaker, 400.0 mg of PAA (Sigma, Average MV 1.2 million) was dissolved in 200 ml deionized water. The plastic beaker was immersed in a hot water bath (approximately 80-90° C.) and was stirred vigorously for at least 30 minutes or until all of the solid PAA has dissolved. Once the solution has cooled to room temperature, the pH was adjusted to 6.8 using 0.1 M NaOH. pH measurements were done using narrow range pH paper. 10.0 ml of this PAA solution was placed in a 20 ml scintillation vial and to this, 10 ml of 4.0 mM AgNO3 solution was added drop wise under constant stirring. 0.5 mL of 2-propanol was added to the mixture. The final solution volume was 20 mL. The vials were sealed with rubber septa and subjected to 60Co irradiation using a gamma cell type G.C. 220 with a dose rate of 3.3 kGy/hr, at a total dose of 15 kGy. The UV-vis spectra and STEM images of the resulting Ag/PAA composite nanoparticles are shown in FIGS. 15 and 16, respectively.

Example 23 Au/PAA Composite Nanoparticles According to the Invention

20 ml of Au3+/PAA was made according to Example 4. Briefly, in a 400 ml plastic beaker, 400.0 mg of PAA (Sigma, Average MV 1.2 million) was dissolved in 200 ml deionized water. The plastic beaker was immersed in a hot water bath (approximately 80-90° C.) and was stirred vigorously for at least 30 minutes or until all of the solid PAA has dissolved. Once the solution has cooled to room temperature, the pH was adjusted to 6.8 using 0.1 M NaOH. pH measurements were done using narrow range pH paper. 10.0 ml of this PAA solution was placed in a 20 ml scintillation vial, and to this 10 ml of 4.0 mM HAuCl3 solution was added drop wise under constant stirring. 0.5 mL of 2-propanol was added to the mixture. The final solution volume was 20 mL. The vials were sealed with rubber septa and subjected to 60Co irradiation using a gamma cell type G.C. 220 with a dose rate of 3.3 kGy/hr, at a total dose of 15 kGy. The UV-vis spectra and STEM images of the resulting Au/PAA composite nanoparticles are shown in FIGS. 17 and 18, respectively.

Example 24 (Au, Ag)/PAA Composite Nanoparticles According to the Invention

20 ml of (Ag+, Au3+)/PAA was made according to Example 4. Briefly, in a 400 ml plastic beaker, 400.0 mg of PAA (Sigma, Average MV 1.2 million) was dissolved in 200 ml deionized water. The plastic beaker was immersed in a hot water bath (approximately 80-90° C.) and was stirred vigorously for at least 30 minutes or until all of the solid PAA has dissolved. Once the solution has cooled to room temperature, the pH was adjusted to 6.8 using 0.1 M NaOH. pH measurements were done using narrow range pH paper. 10.0 ml of this PAA solution was placed in a 20 ml scintillation vial, and to this 5 ml of 4.0 mM HAuCl3 solution was added drop wise under constant stirring. This was then followed by the drop wise addition of 5.0 ml 4 mM Ag(NO3), and finally the addition of 0.5 ml of 2-propanol. The final solution volume was 20 mL. The solution was exposed to 4 G25T8 germicidal UV lamps (approximate power is 12 μW/mm2) for approximately 1.5-2 hours under vigorous stirring. After irradiation, the solution changed from colorless to light purple. The UV-vis spectra and STEM images of the resulting (Au.Ag)/PAA composite nanoparticles are shown in FIGS. 19 and 20, respectively. FIG. 20a is a STEM image (Au, Ag)/PAA nanocomposite prepared according to the present invention; and wherein FIG. 20b shows the cross-sectional abundance of silver along the scanned line in FIG. 20a acquired using electron dispersive x-rays; and FIG. 20c shows the cross-sectional abundance of gold along the scanned line in FIG. 20a acquired using electron dispersive x-rays.

Example 25 Formation of CdSePAA-Fluorescein Conjugate According to the Invention

In a 1.5 mL microfuge tube, 400 μL of CdSePAA (˜0.2 mg/mL in ddH2O) was combined with 4.9 mg 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (EDC) and 6 mg N-hydroxysuccinimide (NHS) in 500 μL of ddH2O. 100 μL of 250 mM 2-morpholinoethanesulfonic acid (MES) (pH ˜6.5) was added. And finally, 20 μL of 5 mg/mL fluorescein in N,N-dimethylformamide (DMF) was also added. The tube containing this mixture was wrapped in aluminum foil and placed on a rotating table for ˜20 h at room temperature. The resulting mix was placed in a 10 kDa MWCO dialysis bag and dialyzed against ddH2O. The dialysis solution (˜200 fold dilution each time) was changed five times over a period of ˜24 h. The solution remaining in the dialysis bag was recovered and centrifuged for 10 min at 15,000 RCF. A brown pellet is found after the centrifugation. The fluorescent supernatant was transferred to a new microfuge tube and further purified by precipitation with the addition of ˜1/10 volume of 3M sodium acetate (pH ˜5.5) and 2× volume of absolute ethanol. The resulting fluorescent precipitate was then isolated by centrifugation for 10 min at 15,000 RCF and resuspended in 200 μL ddH2O.

The presence of fluorescein conjugated to CdSePAA was confirmed by gel permeation chromatography using a fluorescence detector (excitation at 480 nm and emission at 515 nm).

Example 26 Formation of CdSePAA-BSA Conjugate According to the Invention

In a 1.5 mL microfuge tube, 900 μL of CdSe/PAA (˜0.2 mg/mL in ddH2O) was combined with 5.3 mg EDC and 10.8 mg NHS in 100 μL of 250 mM MES (pH ˜6.5). And finally, 5.1 mg bovine serum albumin (BSA) was also added. The tube containing this mixture was placed on a rotating table for ˜19 h at room temperature. The resulting mix was centrifuged for 10 min at 15,000 RCF. ˜500 μL of the supernatant was transferred to a 100 kDa MWCO centrifugal filter and centrifuged for 12 min at 14,000 RCF. The resulting filtrate was discarded, and the retenate was resuspended in 500 μL of ddH2O in the same filter and centrifuged again. This was repeated three more times. The final retenate was recovered for characterization.

Removal of unconjugated BSA using the 100 kDa MWCO filter was confirmed by gel permeation chromatography. And the presence of BSA conjugated to CdSe/PAA remaining in the retenate was confirmed by assay with BioRad protein reagent.

Example 27 CdS/PSS Composite Nanoparticles According to the Invention

400 mg of Poly(styrene sulfonic acid) sodium salt (Alfa Aesar, Ave Mw 1 million) was dissolved in 200.0 ml deionized water. 20.0 ml of this solution was placed in an 80 ml vial and to this, 20.0 ml 4.8 mM Cd(NO3)2 solution was added dropwise with vigorous stirring. The solution was exposed to 4 G25T8 germicidal UV lamps (approximate UV power is 12 μW/mm2) for 1 hour under vigorous stirring. CdS was formed by adding 0.5 ml 1.4 mM Na2S to 0.5 ml of the irradiated Cd2+/PSS solution. UV-visible absorbance and emission spectra are shown in FIG. 21.

Example 28 CdS/PDDA Nanoparticles

15.0 ml of poly(diallyldimethylammonium chloride) (PDDA) [Sigma, Average Mw 400-500K, 20 wt % in water] was diluted to 300 ml with deionized water. The solution was stirred for 10 minutes. 5.0 ml of this solution was diluted to 25.0 ml with deionized water in a 80 ml glass beaker. To this solution, 25.0 ml of 4 mM Na2S was added dropwise with vigorous stirring. The solution was exposed to 4 G25T8 germicidal UV lamps (approximate UV power is 12 μW/mm2) for 1 hour under vigorous stirring. CdS/PDDA was formed by adding 0.50 ml of 2.68 mM Cd(NO3)2 to 0.50 ml of irradiated S2−/PDDA. UV-visible absorbance and emission spectra are shown in FIG. 22.

Example 29 Polyanion Collapse with Cd2+/Pb2+ Cations

In a 400 mL plastic beaker, 400.0 mg of PAA (Sigma, Average MV 1.2 million) was dissolved in 200 mL deionized water. The plastic beaker was immersed in a hot water bath (approximately 80-90° C.) and was stirred vigorously for at least 30 minutes or until all of the solid PAA had dissolved. Once the solution had cooled to room temperature, the pH was adjusted to 6.8 using 0.1 M NaOH. pH measurements were done using narrow-range pH paper. 25 mL of a CdxPb1-x(NO3)2 solution was prepared by the addition of 5 mM Cd(NO3)2 and 5 mM Pb(NO3)2 salt solutions in various proportions, where x=0.1, 0.2, 0.3, 0.4, 0.5, 0.6, . . . , 1. The total concentration of metal ions in the final solution was 5 mM. 20 mL of the pH-adjusted PAA and 25 mL of deionized water were obtained and placed in a 100 mL beaker. 15 mL of the metal solution was then added dropwise under vigorous stirring to yield 60 mL of a Cdx2+Pb1-x2+/PAA solution with a final [Cdx2+Pb1-x2+] of 1.25 mM and final PAA concentration of 0.67 mg/mL.

Example 30 Polyanion Collapse with Cd2+—Mg2+ (10%) Cations

In a 400 mL plastic beaker, 400.0 mg of PAA (Sigma, Average MV 1.2 million) was dissolved in 200 mL deionized water. The plastic beaker was immersed in a hot water bath (approximately 80-90° C.) and was stirred vigorously for at least 30 minutes or until all of the solid PAA had dissolved. Once the solution had cooled to room temperature, the pH was adjusted to 6.8 using 0.1 M NaOH. pH measurements were done using narrow-range pH paper. 25 mL of a Cd0.9Mg0.1(NO3)2 solution was prepared by mixing together of 22.5 mL and 2.5 mL of 5 mM Cd(NO3)2 and 5 mM Mg(NO3)2 solutions, respectively. The total concentration of metal ions in solution was 5 mM. 20 mL of the pH-adjusted PAA and 25 mL of deionized water were obtained and placed in a 100 mL beaker. 15 mL of the metal solution was then added dropwise under vigorous stirring to yield 60 mL of a Cd0.92+Mg2+/PAA solution with a final [Cd0.92+Mg0.12+] of 1.25 mM and final PAA concentration of 0.67 mg/mL.

Example 31 Polyanion Collapse with Cd2+—Zn2+ (90%) cations

In a 400 mL plastic beaker, 400.0 mg of PAA (Sigma, Average MV 1.2 million) was dissolved in 200 mL deionized water. The plastic beaker was immersed in a hot water bath (approximately 80-90° C.) and was stirred vigorously for at least 30 minutes or until all of the solid PAA had dissolved. Once the solution had cooled to room temperature, the pH was adjusted to 6.8 using 0.1 M NaOH. pH measurements were done using narrow-range pH paper. 10 mL of a Cd0.1Zn0.9(NO3)2 solution was prepared by mixing together of 1 mL and 9 mL of 5 mM Cd(NO3)2 and 5 mM Zn(NO3)2 solutions, respectively. The total concentration of metal ions in solution was 5 mM. 10 mL of pH-adjusted PAA was obtained and placed in a 50 mL beaker followed by the dropwise addition of 10 mL of the metal salt solution under vigorous stirring to yield 20 mL of a Cd0.12+Zn0.92+/PAA solution with a final [Cd0.12+Zn0.92+] of 2.5 mM and final PAA concentration of 1 mg/mL.

Example 32 Polyanion Collapse with Cd2+—Zn2+ (10%) Cations

In a 400 mL plastic beaker, 400.0 mg of PAA (Sigma, Average MV 1.2 million) was dissolved in 200 mL deionized water. The plastic beaker was immersed in a hot water bath (approximately 80-90° C.) and was stirred vigorously for at least 30 minutes or until all of the solid PAA had dissolved. Once the solution had cooled to room temperature, the pH was adjusted to 6.8 using 0.1 M NaOH. pH measurements were done using narrow-range pH paper. 6 mL of a Cd0.9Zn0.1(NO3)2 solution was prepared by mixing together of 5.4 mL and 0.6 mL of 5 mM Cd(NO3)2 and 5 mM Zn(NO3)2 solutions, respectively. The total concentration of metal ions in solution was 5 mM. 10 mL of pH-adjusted PAA and 4 mL of deionized water were obtained and placed in a 50 mL beaker. 6 mL of the metal salt solution was then added dropwise under vigorous stirring to yield 20 mL of a Cd0.92+Zn0.12+/PAA solution with a final [Cd0.92+Zn0.32+] of 1.5 mM and final PAA concentration of 1 mg/mL.

Example 33 Polyanion Collapse with Cd2/Mn2+ (1%) Cations

In a 400 mL plastic beaker, 400.0 mg of PAA (Sigma, Average MV 1.2 million) was dissolved in 200 mL deionized water. The plastic beaker was immersed in a hot water bath (approximately 80-90° C.) and was stirred vigorously for at least 30 minutes or until all of the solid PAA had dissolved. Once the solution had cooled to room temperature, the pH was adjusted to 6.8 using 0.1 M NaOH. pH measurements were done using narrow-range pH paper. 25 mL of a Cd0.99Mn0.01(NO3)2 solution was prepared by mixing together of 24.75 mL and 0.25 mL of 5 mM Cd(NO3)2 and 5 mM Mn(NO3)2 solutions, respectively. The total concentration of metal ions in solution was 5 mM. 20 mL of the pH-adjusted PAA and 25 mL of deionized water were obtained and placed in a 100 mL beaker. 15 mL of the metal solution was then added dropwise under vigorous stirring to yield 60 mL of a Cd0.992+Mn0.012+/PAA solution with a final [Cd0.992+Mn0.012+] of 1.25 mM and final PAA concentration of 0.67 mg/mL.

Example 34 Polyanion Collapse with Cd2+/Hg2+(50%) Cations

In a 400 mL plastic beaker, 400.0 mg of PAA (Sigma, Average MV 41.2 million) was dissolved in 200 mL deionized water. The plastic beaker was immersed in a hot water bath (approximately 80-90° C.) and was stirred vigorously for at least 30 minutes or until all of the solid PAA had dissolved. Once the solution had cooled to room temperature, the pH was adjusted to 6.8 using 0.1 M NaOH. pH measurements were done using narrow-range pH paper. 25 mL of a Cd0.5Hg0.5(NO3)2 solution was prepared by mixing together of 12.5 mL and 12.5 mL of 5 mM Cd(NO3)2 and 5 mM Hg(NO3)2 solutions, respectively. The total concentration of metal ions in solution was 5 mM. 20 mL of the pH-adjusted PAA and 25 mL of deionized water were obtained and placed in a 100 mL beaker. 15 mL of the metal solution was then added dropwise under vigorous stirring to yield 60 mL of a Cd0.52+Hg0.52+/PAA solution with a final [Cd0.52+Hg0.52+] of 1.25 mM and final PAA concentration of 0.67 mg/mL.

Example 35 Polyacrylic Acid Crosslinking with 4 G25T8 Germicidal Lamps

60 mL of Cdx2+Pb1-x2+/PAA was prepared according to Example 29 and was placed in a 150.0 mL glass beaker. The solution was exposed to 4 G25T8 germicidal UV lamps (approximate power is 12 μW/mm2) for approximately 30 minutes under vigorous stirring. The irradiated solution was then dialyzed against deionized water for 3 hours, changing the deionized water reservoir every hour. Collapsed PAA with CdxZn1-x(NO3)2, CdxMn1-x(NO3)2, CdxMg1-x(NO3)2 . . . was UV-irradiated in a similar manner for approximately 1 hour. The viscosity of the collapsed irradiated, dialyzed solutions was much lower than that of collapsed, un-irradiated solutions. These solutions were filterable using a 0.2 μm nylon syringe filter.

Example 36 Cd0.5Pb0.5Te/PAA Nanoparticles

Under ambient conditions, 20 ml of Cdx2+Pb1-x2+/PAA produced according to Example 35 was placed in a 100 mL round bottom flask. The pH was adjusted to 11 using 1.1 M NaOH. pH measurements were done using narrow-range pH paper. To this solution, 20.4 mg of NaBH4 and 28.3 mg of trisodium citrate were added while the solution was being stirred. Immediately after the addition of the borohydride and the citrate, 0.625 mL of 0.01 Na2TeO3 was added. The solution develops a yellow colour upon addition of the tellurium-containing salt. The solution was then refluxed for approximately one hour under N2 atmosphere to allow CdPbTe/PAA nanoparticles to form. The absorbance and emission spectra of the resulting solution after one hour of reflux is shown in FIG. 23. Unfortunately, the colloidal solutions were extremely unstable upon exposure to air and this was marked by a quick disappearance of the characteristic absorbance and emission spectra shown in FIG. 23.

Example 37 Cd0.9Zn0.1Te/PAA Nanoparticles

Under ambient conditions, 8 mL of Cd0.92+Zn0.12+/PAA produced according to Example 32 was placed in a 25 mL round bottom flask, and cross-linked using the permitted lamp as hereinabove described. To this solution, 15 mg of NaBH4 and 30 mg of trisodium citrate were added while the solution was being stirred. Immediately after the addition of the borohydride and the citrate, 0.3 mL of 0.01 Na2TeO3 was added. The solution develops a peach colour upon addition of the tellurium-containing salt. The solution was then refluxed for approximately two hours to allow CdZnTe/PAA nanoparticles to form. The absorbance and emission spectra of the resulting solution after two hours of reflux are shown in FIG. 24.

Example 38 Cd0.99Mn0.01Te/PAA Nanoparticles

Under ambient conditions, 10 mL of Cd0.992+Mn0.012+/PAA produced according to Example 33 was placed in a 25 mL round bottom flask, and cross-linked using the permitted lamp as hereinabove described. To this solution, 20 mg of NaBH4 and 37 mg of trisodium citrate were added while the solution was being stirred. Immediately after the addition of the borohydride and the citrate, 0.313 mL of 0.01 Na2TeO3 was added. The solution develops a peach colour upon addition of the tellurium-containing salt. The solution was then refluxed for approximately one hour to allow CdMnTe/PAA nanoparticles to form. The absorbance and emission spectra of the resulting solution after one hour of reflux are shown in FIG. 25.

Example 39 Cd0.5Hg0.5Te/PAA Nanoparticles

Under ambient conditions, 10 mL of Cd0.52+Hg0.52+/PAA produced according to Example 34 was placed in a 25 mL round bottom flask, and cross-linked using the permitted lamp as hereinabove described. To this solution, 16 mg of NaBH4 and 29 mg of trisodium citrate were added while the solution was being stirred. Immediately after the addition of the borohydride and the citrate, 0.313 mL of 0.01 Na2TeO3 was added. The solution remained colourless upon addition of the tellurium-containing salt. The solution was then refluxed for approximately one hour to allow CdHgTe/PAA nanoparticles to form. However, the refluxed solution was not fluorescent.

Example 40 Formation of Methylene Blue/PAA Nanoparticles

In a 400 ml plastic beaker, 400.0 mg of PAA (Sigma, Average MV 1.2 million) was dissolved in 200 ml deionized water. The plastic beaker was immersed in a hot water bath (approximately 80-90° C.) and was stirred vigorously for at least 30 minutes or until all of the solid PAA has dissolved. Once the solution has cooled to room temperature, the pH was adjusted to 6.8 using 0.1 M NaOH. pH measurements were done using narrow range pH paper. 20.0 ml of this PAA solution was placed in a glass beaker and to this, 20.0 ml of aqueous 5.0 mM Methylene Blue solution was added dropwise under vigorous stirring. After all of the Methylene Blue solution was added, the viscosity of the mixture was observed to be much less than the original PAA solution. The resulting solution was exposed to UV radiation using 4 G25T8 germicidal UV lamps for 1.5 hours. The viscosity of the UV-irradiated Methylene Blue/PAA solution was less than the viscosity of the solution not exposed to UV radiation.

All literature and similar material cited in this application, including, patents, patent applications, articles, books, treatises, dissertations and web pages, regardless of the format of such literature and similar materials, are expressly incorporated by reference in their entirety. In the event that one or more of the incorporated literature and similar materials differs from or contradicts this application, including defined terms, term usage, described techniques, or the like, this application controls.

The section headings used herein are for organizational purposes only and are not to be construed as limiting the subject matter described in any way.

While the present inventions have been described in conjunction with various embodiments and examples, it is not intended that the present inventions be limited to such embodiments or examples. On the contrary, the present inventions encompass various alternatives, modifications, and equivalents, as will be appreciated by those of skill in the art. Accordingly, the descriptions, methods and diagrams of should not be read as limited to the described order of elements unless stated to that effect.

Although this disclosure has described and illustrated certain preferred embodiments of the invention, it is to be understood that the invention is not restricted to those particular embodiments. Rather, the invention includes all embodiments which are functional or mechanical equivalence of the specific embodiments and features that have been described and illustrated.

The claims should not be read as limited to the described order or elements unless stated to that effect. It should be understood that various changes in form and detail may be made without departing from the scope of the appended claims. Therefore, all embodiments that come within the scope and spirit of the following claims and equivalents thereto are claimed.

Claims

1. A method for producing a nanoparticle material, comprising the steps of:

a) providing a polymeric solution comprising a polyelectrolyte polymer material and a solvent;
b) collapsing at least a portion of the polymeric material about one or more precursor moieties to form a composite precursor moiety;
c) cross-linking the polymeric material of said composite precursor moiety; and
d) modifying at least a portion of said precursor moieties of said composite precursor moiety to form one or more nanoparticles having a mean diameter in the range between about 1 nm and about 100 nm and thereby forming a composite nanoparticle; and
e) pyrolysing said composite nanoparticle to form a nanoparticle material.

2. The method of claim 1, wherein the pyrolysis substantially removes the polymeric material from the composite nanoparticle.

3. The method of claim 1, wherein the pyrolysis conditions are controlled such that the nanoparticle material formed comprises at least a partially carbon-coated nanoparticle, wherein the carbon is in an amorphous form.

4. A composite nanoparticle made by the method as claimed in claim 1.

5. An at least partially carbon-coated nanoparticle made by the method as claimed in claim 3.

6. A composite nanoparticle having a mean diameter in the range between about 1 nm and about 100 nm, the composite nanoparticle comprising a nanoparticle substantially confined within a collapsed, internally cross-linked polyelectrolyte polymer material wherein said nanoparticle comprises a metal alloy.

7. The composite nanoparticle of claim 6, wherein said metal alloy comprises two or more of Cd, Zn, Cu, Pb, Ag, Mn, Ni, Au, Mg, Fe, Hg, and Pt.

8. A composite nanoparticle having a mean diameter in the range between about 1 nm and about 100 nm, the composite nanoparticle comprising a nanoparticle substantially confined within a collapsed, internally cross-linked polyelectrolyte polymer material wherein said nanoparticle comprises a metal species-containing compound.

9. The composite nanoparticle of claim 8, wherein said metal species-containing compound comprises one or more of a of a sulphide, selenide, telluride, chloride, bromide, iodide, oxide, hydroxide, phosphate, carbonate, sulphate, chromate and a combination thereof.

10. The composite nanoparticle of claim 8, wherein said nanoparticle is capable of emitting electromagnetic radiation after the absorption of energy.

11. A composite nanoparticle having a mean diameter in the range between about 1 nm and about 100 nm, the composite nanoparticle comprising a nanoparticle substantially confined within an internally cross-linked polyelectrolyte polymer material wherein said nanoparticle comprises an elemental metal.

12. The composite nanoparticle of claim 11, wherein said elemental metal comprises Cd, Zn, Cu, Pb, Ag, Mn, Ni, Au, Mg, Fe, Hg, or Pt.

13. A method for producing a substrate coated with a material comprising nanoparticles, comprising the steps of:

a) i) providing a first solution comprising a first polymeric material and a first solvent; ii) collapsing at least a portion of the first polymeric material about one or more first precursor moieties to form a first composite precursor moiety having a mean diameter in the range between about 1 nm and about 100 nm; iii) cross-linking the first polymeric material of said first composite precursor moiety; iv) modifying at least a portion of said first precursor moieties of said first composite precursor moiety to form one or more first nanoparticles and thereby forming a first composite nanoparticle material in the first solution;
b) i) providing a second solution comprising a second polymeric material and a second solvent; ii) collapsing at least a portion of the second polymeric material about one or more second precursor moieties to form a second composite precursor moiety having a mean diameter in the range between about 1 nm and about 100 nm; iii) cross-linking the second polymeric material of said second composite precursor moiety; iv) modifying at least a portion of said second precursor moieties of said second composite precursor moiety to form one or more second nanoparticles and thereby forming a second composite nanoparticle material in the second solution;
c) contacting a substrate with at least a portion of the first composite nanoparticle material to form a first layer on at least a portion of the substrate;
d) contacting at least a portion of the first layer with solution containing a first charged compound to form a second layer, the charged compound having a charge substantially opposite to that of the first composite nanoparticle material; and
e) contacting a substrate with at least a portion of the second composite nanoparticle material to form a third layer on at least a portion of the second layer.

14. The method of claim 13, wherein the first solution and the second solution are the same solution.

15. The method of claim 13, wherein the substrate is a thin film.

16. The method of claim 13, wherein at least one of the composite nanoparticle materials comprises CdS/PAA and at least one of the charged compounds is poly(allylamine).

17. The method of claim 13, wherein one or more of the layers on the substrate form an optically active material.

18. A method for producing a composite nanoparticle of a nanoparticle confined within a cross-linked, collapsed polyelectrolyte polymer material, said method comprising

a) providing said polymeric material in a suitable solvent at a suitable concentration;
b) providing an entity or a precursor thereof said nanoparticle in said solvent;
c) treating said polymeric material in said solvent with at least one collapsing agent to collapse said polymeric material,
d) cross-linking said collapsed polymeric material; and
e) treating said entity or precursor thereof with suitable production means to produce said composite nanoparticle.

19. A method as claimed in claim 18 wherein said entity or a precursor thereof said nanoparticle is said at least one collapsing agent.

20. A method as claimed in claim 18 or claim 19 wherein said at least one collapsing agent comprises at least one ionic species.

21. A method as claimed in claim 20 wherein said at least one ionic species is said entity or a precursor thereof of said nanoparticle.

22. A method as claimed in claim 20 wherein said collapsing agent comprises said ionic species that is provided by a salt selected from the group consisting of inorganic salts, organic salts, and a combination of inorganic and organic salts.

23. A method as claimed in claim 18 wherein said production means comprises a radiation step.

24. A method as claimed in claim 18 wherein said production means comprises suitable chemical treatment.

25. A method as claimed in claim 24 wherein said chemical treatment comprises a reduction or oxidation step.

26. A method as claimed in claim 24 wherein said chemical treatment comprises addition of a suitable counter ion or precursor of said counter ion to effect formation of said nanoparticle.

27. A method as claimed in claim 18 wherein said solvent is an aqueous solution.

28. A method as claimed in claim 18 or claim 19 wherein said entity or precursor is a metal cation, complexed metal cation or complexed metal anion and said production means comprises treating said cation or complexed anion with radiation or an agent selected from a reducing agent or an oxidizing agent to effect production of said nanoparticle comprising elemental said metal.

29. A method as claimed in claim 28 wherein said precursor entity comprises ions selected from a cation or complexed metal anions of a plurality of metals and said production means comprises treating said cations or complexed anions with radiation or an agent selected from a reducing agent or an oxidizing agent to effect production of said nanoparticle comprising an alloy of elemental said metals.

30. A method as claimed in claim 18 wherein said polymeric material comprises linear or branched segments comprising polyions selected from anions, cations or combinations thereof.

31. A method as claimed in claim 18 wherein said polymeric material comprises linear or branched segments comprising one or more functional groups.

32. A method as claimed in claim 18, wherein said polymeric material is conjugated to molecules capable of binding to complementary binding partners to form affinity-binding pairs.

33. A method as claimed in claim 32, wherein the affinity-binding pair is selected from the group consisting of protein-protein, protein-DNA, enzyme-substrate, antigen-antibody, DNA-DNA, DNA-RNA, biotin-avidin, hapten-antihapten and combinations thereof.

34. A method as claimed in claim 32, wherein the molecules are selected from the group consisting of protein, DNA ligand, oligonucleotide, aptamer, their nanoparticles and combinations thereof.

35. A method for producing a nanoparticle, said method comprising pyrolysing said composite nanoparticle prepared by a method as claimed in claim 18, wherein said nanoparticle is an elemental metal, alloy thereof, or a metal species-containing compound, at an effective temperature to effectively remove said polymeric material.

36. A method for producing a wholly or partially carbon-coated nanoparticle said method comprising incompletely pyrolysing said composite nanoparticle prepared by a method as claimed in claim 18, wherein said nanoparticle is selected from the group consisting of an elemental metal, alloy thereof and a metal species-containing compound, at an effective temperature to effect production of said wholly or partially carbon-coated nanoparticle.

37. A composite nanoparticle when made by a process as claimed in claim 18.

38. A nanoparticle when made by a method as claimed in claim 35.

39. A wholly or partially carbon-coated nanoparticle when made by a method as claimed in claim 36.

40. A composite nanoparticle comprising a nanoparticle confined within a cross-linked collapsed polyelectrolyte polymer material wherein said nanoparticle is selected from the group consisting of an elemental metal, an alloy comprising said a metal with at least one other metal, and a compound containing a metal or metalloid species.

41. A composite nanoparticle as claimed in claim 40 wherein said nanoparticle is selected from the group consisting of an alloy comprising said a metal with at least one other metal, and a compound containing said a metal or metalloid species.

42. A composite nanoparticle as claimed in claim 41 wherein said compound containing said metal species comprises a compound selected from the group consisting of a sulphide, selenide, telluride, chloride, bromide, iodide, oxide, hydroxide, phosphate, carbonate, sulphate, chromate and a combination thereof.

43. A composite nanoparticle as claimed in any one of claims 40 to 42 claim 40 wherein said metal is selected from Cd, Zn, Cu, Pb, Ag, Mn, Ni, Au, Mg, Fe, Hg, Pt and a combination thereof nanoparticle is a compound containing a metalloid species.

44. A composite nanoparticle as claimed in any one of claims 37 to 43, wherein said nanoparticle is capable of emitting light after the absorption of light energy.

45. A coated substrate having a plurality of layers of composite nanoparticles as claimed in claim 37 interspersed between adjacent layers of oppositely charged compounds.

46. A coated substrate as claimed in claim 45 wherein said substrate is a film.

47. A coated substrate as claimed in claim 45 wherein said composite nanoparticle is CdS/PAA and said oppositely charged compound is poly(allylamine).

48. A composite nanoparticle having a mean diameter in the range between about 1 nm and about 100 nm, the composite nanoparticle comprising a precursor moiety substantially confined within an internally cross-linked polyelectrolyte polymer material wherein said precursor moiety comprises an inorganic ion.

49. The composite nanoparticle of claim 48, wherein the inorganic ion is selected from the group consisting of copper, iron, magnesium, manganese, molybdenum, zinc, and chlorine ions and combinations thereof.

50. The composite nanoparticle of claim 48, wherein the inorganic ion is a metal ion.

51. The composite nanoparticle of claim 50 wherein the metal ion is selected from the group consisting of copper, iron, magnesium, manganese, molybdenum, and zinc ions and combinations thereof.

52. A composite nanoparticle having a mean diameter in the range between about 1 nm and about 100 nm, the composite precursor moiety comprising a precursor moiety substantially confined within an internally cross-linked polyelectrolyte polymer material wherein said precursor moiety comprises a chloride or sulphide and the polyelectrolyte polymer material comprises a cationic polymer.

53. The composite nanoparticle of claim 52 wherein the cationic polymer is selected from the group consisting of poly(allylamine), poly(ethyleneimine), poly(diallyldimethylammonium chloride), poly(lysine), co-polymers thereof and combinations thereof.

54. The method of claim 21, wherein the ionic species is an inorganic ion.

55. The method of claim 21, wherein the ionic species is selected from the group consisting of chloride, sulphate and sulphide.

56. The method of claim 21, wherein the ionic species is chloride.

57. The method of claim 54, wherein the inorganic ion is a metal ion.

58. The method of claim 57, wherein the wherein the metal ion is selected from the group consisting of copper, iron, magnesium, manganese, molybdenum, and zinc ions and combinations thereof.

59. A method for producing a cross-linked composite nanoparticle, comprising the steps of:

a) providing a polymeric solution comprising a polyelectrolyte polymer material and a solvent;
b) providing a precursor moiety in the solvent;
c) collapsing at least a portion of the polyelectrolyte polymer material about the precursor moiety to form a composite precursor moiety; and
d) cross-linking the polyelectrolyte polymeric material of said composite nanoparticle.

60. The method of claim 59, wherein the collapsing is caused by a collapsing agent.

61. The method of claim 60, wherein the collapsing agent comprises at least one ionic species.

62. The method of claim 61, wherein said at least one ionic species is the precursor moiety.

63. The method of claim 61, wherein the at least one ionic species is an inorganic ion.

64. The method of claim 61, wherein the at least one ionic species is selected from the group consisting of chloride, sulphate and sulphide.

65. The method of claim 61, wherein the at least one ionic species is chloride.

66. The method of claim 63, wherein the inorganic ion is a metal ion.

67. The method of claim 66, wherein the metal ion is selected from the group consisting of copper, iron, magnesium, manganese, molybdenum, and zinc ions and combinations thereof.

Referenced Cited
U.S. Patent Documents
5433797 July 18, 1995 Erb et al.
5807636 September 15, 1998 Sheu et al.
5874111 February 23, 1999 Maitra et al.
6090858 July 18, 2000 El-Sayed
6562403 May 13, 2003 Klabunde et al.
6607994 August 19, 2003 Soane et al.
6616869 September 9, 2003 Mathiowitz et al.
6632671 October 14, 2003 Unger et al.
6649138 November 18, 2003 Adams et al.
6680013 January 20, 2004 Stein et al.
6689338 February 10, 2004 Kotov
6721083 April 13, 2004 Jacobson et al.
6846345 January 25, 2005 Keller et al.
7022156 April 4, 2006 Hattori et al.
7108915 September 19, 2006 Adams et al.
7129293 October 31, 2006 Kataoka et al.
7147917 December 12, 2006 Adams et al.
7189279 March 13, 2007 Guillet
7217457 May 15, 2007 Elaissari et al.
7267875 September 11, 2007 Whiteford et al.
7303819 December 4, 2007 Brotzman, Jr.
7319127 January 15, 2008 Kim et al.
7501180 March 10, 2009 Anderson et al.
7534490 May 19, 2009 Goh et al.
7594949 September 29, 2009 Guillet
7666506 February 23, 2010 Rieger et al.
7964277 June 21, 2011 Goh et al.
8003166 August 23, 2011 Goh et al.
20030082237 May 1, 2003 Cha et al.
20030124194 July 3, 2003 Gaw et al.
20030129405 July 10, 2003 Zhang et al.
20030177868 September 25, 2003 Guillet
20030219384 November 27, 2003 Donath et al.
20040079195 April 29, 2004 Perry et al.
20050245658 November 3, 2005 Mehrotra et al.
20060145138 July 6, 2006 Sato et al.
20060153929 July 13, 2006 Drake
20060251896 November 9, 2006 Ferencz et al.
20070054119 March 8, 2007 Garstecki et al.
20070101825 May 10, 2007 He
20070154709 July 5, 2007 Koch et al.
20070218019 September 20, 2007 Andre et al.
20070243145 October 18, 2007 Andre et al.
20070264481 November 15, 2007 DeSimone et al.
20080020051 January 24, 2008 Dahne et al.
20080081192 April 3, 2008 Goh et al.
20100086488 April 8, 2010 Hoheisel et al.
20100119829 May 13, 2010 Karpov et al.
Foreign Patent Documents
1129044 August 1996 CN
1129044 August 1996 CN
1566381 January 2005 CN
1566381 January 2005 CN
1649922 August 2005 CN
1649922 August 2005 CN
2003519565 June 2003 JP
2005161238 June 2005 JP
2006/213592 August 2006 JP
2008/526995 July 2008 JP
WO-9501643 January 1995 WO
WO-9501643 January 1995 WO
WO-0151196 July 2001 WO
WO2006076636 July 2006 WO
WO-2006076636 July 2006 WO
WO2007038192 April 2007 WO
WO-2007038192 April 2007 WO
WO-2007041862 April 2007 WO
WO2007106771 September 2007 WO
WO-2007106771 September 2007 WO
Other references
  • Examination Report for European Patent Application No. 067908418.8.
  • Office Action for European Patent Application No. 06790841.8.
  • Office Action for Japanese Patent Application No. 2008-534839.
  • Laguecir et al., “Charge Polymer/Nanoparticles Mixtures Monte Carlo Simulations,” Chimia 56: 702-706, (2002).
  • Written Opinion for PCT/IB2008/000817 (2008).
  • Search Report for International Application No. PCT/CA2006/001686.
  • Written Opinion for International Application No. PCT/CA2006/001686.
  • International Search Report for PCT/IB2008/000817 (2008).
  • Laguecir et al., “Charge Polymer/Nanoparticles Mixtures Monte Carlo Simulations,” Chimia 56:702-706 (2002).
  • Wrriten Opinion for PCT/IB2008/000817 (2008).
  • Supplementary European Search Report for EP 06 79 08 41 (Mar. 2010).
  • Office Action for Chinese Patent Application No. 20060047088.6, date of issue Apr. 14, 2010.
Patent History
Patent number: RE45848
Type: Grant
Filed: Jun 19, 2013
Date of Patent: Jan 19, 2016
Assignee: Vive Crop Protection Inc. (Toronto)
Inventors: Cynthia M. Goh (Toronto), Jose Amado Dinglasan (Toronto), Jane B. Goh (Toronto), Richard Loo (Toronto), Emina Veletanlic (Toronto)
Primary Examiner: Norca L Torres Velazquez
Application Number: 13/922,022
Classifications
Current U.S. Class: Solid Graft Or Graft-type Copolymer Contains Backbone Derived From Ethylenic Reactants Only (525/69)
International Classification: B32B 5/16 (20060101); C08J 3/12 (20060101); C09D 7/12 (20060101); C08J 3/215 (20060101); C08J 3/24 (20060101); C08J 3/28 (20060101);