Abstract: An organic anti-reflective material, in particular one which prevents back reflection from the surface of or lower layers in the semiconductor device and eliminates the standing waves and reflective notching due to the optical properties of lower layers on the wafer, and due to the changes in the thickness of the photosensitive film applied thereon. The organic anti-reflective polymer is useful for forming ultrafine patterns of 64M, 256M, 1G, and 4G DRAM semiconductor devices. A composition containing such an organic anti-reflective polymer, and an anti-reflective coating formed therefrom and a preparation method thereof are also disclosed.

Abstract: The invention relates to a new process for the preparation of functionalized telechelics based on vinyl polymers, the telechelics prepared in this way and their use in the plastics, fibers or coating sector.

Abstract: Provided are a fluorine-containing photosensitive polymer having a hydrate structure and a resist composition including the photosensitive polymer.

Abstract: The present invention provides a method for manufacturing a styrene-based polymer comprising the steps of continuously feeding raw materials into one end of two or more polymerization vessels connected in series; polymerizing a styrenic monomer in the coexistence of a (meth)acrylate ester monomer by using an organic radical generating agent as an initiator by a mass or solution polymerization method of continuous process; and continuously taking out a product from another end of said polymerization vessels, wherein polymerization conditions are controlled in ranges specified by the following items (a) and (b):

Abstract: The present invention relates to a polyvalent imprinted polymer useful in medicine and biotechnology and to a process for the preparation thereof More particularly it relates to the said polymer of formula (1) herein below 1

Abstract: Disclosed is a method of producing a polyolefin composition comprising contacting a metallocene pre-catalyst with a substoichiometric amount of a co-catalyst; adding a first olefin monomer; and polymerizing the first monomer for a time sufficient to form the polyolefin. The method allows for the use of a minimum amount of activating co-catalyst, and allows for the production of stereoregular and non-stereoregular polyolefins. The use of configurationally stable metallocene pre-catalysts allows for the production of monomodal isotactic polyolefins having narrow polydispersity. The use of configurationally unstable metallocene pre-catalysts allows for the production of monomodal atactic polyolefins having narrow polydispersity. The method of the present invention optionally further comprises contacting the polyolefin with a second amount of said co-catalyst; adding a second olefin monomer; polymerizing said second olefin monomer to form a block-polyolefin composition.

Abstract: A crush stop comprising a thermoplastic elastomer composition which has a hardness as measured with a hardness tester type A in accordance with JIS-K-6253 being at least 50 degrees and which has dependence of elastic modulus upon temperature being at most 3 times between 0° C. and 60° C. The crush stop is minimized in the displacement due to impact of a stopper arm, and is excellent in impact absorbing properties over a wide range of temperatures.

Abstract: The present invention is a method of preparing an acrylic copolymer using as a raw material a monomer mixture comprising 50 mole % or more of a monomer having a polymerizable double bond formed by a carbon atom to which no hydrogen atom is bonded and a carbon atom to which a hydrogen atom is bonded, wherein after the polymerization is carried out at a polymerization temperature of 150° C. or higher, further heating at 80-130° C. is done. The present invention can provide a method of preparing an acrylic copolymer with a low amount of unreacted monomers using high temperature polymerization at 150° C. or higher.

Abstract: Further improvements have been made in processes for controlled polymerization of free radically (co)polymerizable monomers mediated by a transition metal complex participating in a redox reaction which involves transfer of a radically transferable atom or group to and from an initiator or dormant polymer and the growing active polymer chain ends. Two improvements involve the choice of counterion in the transition metal complex. In one improvement the transition metal is held in close conjunction with a solid support through interaction with a counterion directly attached to the support. This cognition also allows for improvements in catalyst utilization including catalyst recovery and recycle. In another improvement, particularly suitable for controlled polymerization of certain monomers with an expanded range of transition metals, the function of counterion and ligand in the development of the transition metal based catalyst is superseded by use of salt containing a soluble organic counterion.

Abstract: Low color, aromatic modified C5 hydrocarbon resins are disclosed. The resins are predominantly an aromatic modified piperylene resin. The resins are useful as tackifies in hot melt adhesives and hot melt pressure sensitive adhesives.

Abstract: Initiators for nitroxide-mediated radical polymerizations are described. The initiators have an azlactone or ring-opened azlactone moiety to provide telechelic (co)polymers.

Abstract: This invention relates to a process for the synthesis of addition polymers containing branches upon branches and having a polymerizable olefin end group by a convenient one-pot polymerization of selected vinyl monomers with chain polymerization initiators and a method to provide olefinic end groups by chain termination agents; and polymers produced thereby characterized by branch-on-branch structure and lower inherent viscosity than heretofore possible.

Abstract: The instant invention relates to multifunctional alkoxyamines based on polyalkylpiperidines, polyalkylpiperazinones and polyalkylmorpholinones and their use as polymerization regulatros/initiators. Further subjects of the invention are a polymerizable composition comprising an ethylenically unsaturated monomer or oligomer and the alkoxyamine compound as well as a process for polymerization and a process for preparation of the compounds.

Abstract: Process for manufacturing temperature-sensitive polymers utilizing a heat transfer fluid comprising a hydrocarbon fluid selected from aliphatic hydrocarbons, alicyclic hydrocarbons, aliphatic- or alicyclic-substituted aromatic hydrocarbons, or mixtures thereof, the hydrocarbon fluid having a boiling point from 220° C. to 250° C. and a melting point less than 40° C., and temperature-sensitive polymer articles produced therefrom.

Abstract: A curable casemaking adhesive, books and related articles bound thereby. In one embodiment, a UV curable hot melt adhesive is used to form the case, which is preferably also embossed. In another embodiment, a moisture curable hot melt adhesive is used to form the case, which is preferably also embossed.

Abstract: Copolymerization of Fe(II) or Co(II) pyridine diimine complexes containing olefinic substituents on aryl groups with styrene in the presence of a radical initiator results in polymerized late transition metal catalysts which can be used for olefin polymerization or oligomerization. These catalysts have high catalyst activity for olefin polymerization or oligomerization.

Abstract: An olefin polymerization catalyst system, comprising a catalyst represented by the general formula CrR4, wherein each R is independently a hydrocarbyl or substituted hydrocarbyl, with the proviso that R may not be a cyclopentadienyl group, an activator represented by the general formula, MQ2, where M is a Group II metal, where each Q is independently an alkyl, or substituted alkyl; and a support. The support may be organic or inorganic. Ethylene and one or more olefins may be polymerized by the catalyst system.

Abstract: Free-radical-initiated copolymerization of metallocene complexes containing olefinic substituents on aryl groups with styrene results in polymerized late transition metal catalysts that can be used for olefin polymerization or oligomerization. These catalysts have high catalyst activity for olefin polymerization or oligomerization.

Abstract: Initiators for nitroxide-mediated radical polymerizations are described. The initiators have an azlactone or ring-opened azlactone moiety to provide telechelic (co)polymers.

Abstract: It has been discovered that certain compounds serve as polymerization accelerators when employed together with peroxide initiators for the polymerization of vinylaromatic monomers. Suitable accelerators that increase the rate of decomposition of the peroxide initiator include, but are not necessarily limited to, hydroperoxides and/or metallic salts. Representative examples of suitable hydroperoxide accelerators include t-butyl hydroperoxide (TBH), cumyl hydroperoxide, and p-isopropyl cumyl hydroperoxide, whereas suitable metallic salt accelerators include cobalt naphthenate and cobalt acetoacetonate. Use of these accelerators when vinylaromatic monomers are polymerized in the presence of polybutadienes and peroxide initiators results in an increase in grafting as compared with similar copolymers made without the accelerator.

Abstract: Copolymerization of Ni(II) phenol imine complexes containing olefinic substituents on aryl groups with styrene in the presence of a radical initiator results in polymerized late transition metal catalysts which can be used for olefin polymerization or oligomerization. These catalysts have high catalyst activity for olefin polymerization or oligomerization.

Abstract: A complex of transition metal Ti, Fe, Co, Ni, Cr, Mn, Ta, Rh, Y, Sc, Ru, Pd, Zr, Hf, V or Nb and a mono-, bi-, tri-, or tetra-dentate ligand, wherein at least one of the donor atoms of the ligand is a nitrogen atom N with a 5-membered heterocyclic substituent joined to the N by a carbon atom. The complex is preferably formula (I) wherein R5—N-G-X1 is a bi-, tri.

Abstract: The new metallocene catalysts according to the present invention are prepared by reacting a metallocene compound with a compound having at least two functional groups. The metallocene compound is a transition metal compound which a transition metal is coordinated with a main ligand such as cycloalkanedienyl group and an ancillary ligand. The functional groups of the compound having at least two functional groups are selected from the group consisting of a hydroxy group, a thiol group, a primary amine group, a secondary amine group, etc. The metallocene catalysts according to the present invention have a structure which an ancillary ligand of a metallocene compound is bonded with functional groups. A structure of the metallocene catalysts can be varied according to the metallocene compounds, the compound having at least two functional groups, and the molar ratio of each reactant. The metallocene catalyst is employed with a co-catalyst for styrene and olefin polymerization.

Abstract: The present invention is directed to, in part, polymer clay nanocomposites having an acid containing monomer and clay. In one embodiment, there is provided a process for preparing an aqueous polymer clay nanocomposite dispersion, wherein the process comprises: providing an aqueous dispersion comprising at least one clay, optionally at least one ethylenically unsaturated monomer, and optionally at least one surfactant; providing a monomer mixture comprising at least 10% by weight of an acid containing monomer within the monomer mixture and optionally a surfactant; mixing the aqueous dispersion and the monomer mixture; and polymerizing the monomer to form the nanocomposite dispersion wherein the clay is at least partially exfoliated within the nanocomposite dispersion. The present invention also relates to the use of these compositions such as thickeners, dispersants, plastics additives, adhesives, coatings, flexographic inks, overprint varnishes, and dry cement powder modifiers.

Abstract: The present invention pertains to a process for controlled free radical polymerization or copolymerization of vinyl chloride at a temperature between 40° C. and 95° C., at a pressure between 5 and 30 bar in the presence of a stable free nitroxyl radical.

Abstract: The present invention is relates to a process for the preparation of an isoolefin polymer containing repeating units derived from at least one isoolefin, at least one divinyl aromatic monomer and, optionally, additional copolymerizable monomers, wherein the content of unreacted vinyl groups from the aromatic monomer is predicted by means of FTIR measurements.

Abstract: A process for producing a styrenic resin with a small content of low molecular weight components, comprising a continuous anionic polymerization process wherein a raw material system having the following composition (A) is continuously fed, either collectively or in a divided manner, from one end of a reactor tank R1 having a back mixing flow and the product system is continuously discharged from the other end of the reactor tank R1, the internal temperature of the reactor tank R1 being controlled to a range of 40-120° C., the average proportion of styrene monomers to the sum total of the styrene monomers, hydrocarbon solvent and styrenic polymers present in the reactor tank R1 being controlled to less than 10 wt. %, and the resulting styrenic polymer solution being devolatilized and dried: (A) Styrene monomer 1.0 kg Hydrocarbon solvent 0.1-3 kg Organolithium compound 0.5-200 mmoles.

Abstract: A novel one-pot cost efficient process for the preparation of homo-, co- and terpolymers of p-hydroxystyrene or substituted p-hydroxystyrene and alkyl acrylates. The process involves polymerization of esters of p-hydroxystyrene (or its substituted analogs), alkyl acrylate monomers and/or one or more of ethylenically unsaturated monomers in an alcohol solvent in the presence of a free radical initiator. The reaction mixture containing the so formed polymer is subjected to transesterification conditions using a catalytic amount of catalyst to result in co- and/or terpolymers of p-hydroxystyrene without cleavage of the alkyl ester in the acrylate repeat unit, and then removing the catalyst from the system. Preferred embodiments include homopolymers of p-hydroxystyrene, copolymer of p-hydroxystyrene and tert-butyl acrylate and terpolymer of p-hydroxystyrene, tert-butyl acrylate and styrene. These polymers have a wide variety of applications including as photoresists in microelectronics industry.

Abstract: This invention is based upon the discovery that rubbery polymers having a high vinyl content and a low degree of branching can be synthesized with an initiator system that is comprised of (a) a lithium initiator selected from the group consisting of allylic lithium compounds and benzylic lithium compounds, (b) a Group I metal alkoxide, and (c) a polar modifier; wherein the molar ratio of the Group I metal alkoxide to the polar modifier is within the range of about 0.1:1 to about 10:1; and wherein the molar ratio of the Group I metal alkoxide to the lithium initiator is within the range of about 0.01:1 to about 20:1. These high vinyl polymers offer reduced levels of hysteresis and better functionalization efficiency.

Abstract: This invention discloses a process for synthesizing an amine functionalized monomer that comprises (1) reacting a secondary amine with a 2,3-dihalopropene to produce a vinyl halide containing secondary amine having a structural formula selected from the group consisting of 1

Abstract: A process for producing a copolymer which comprises reacting a vinyl monomer with a macromonomer composition containing a macromonomer. The macromonomer composition is obtained by polymerizing at a temperature of 160 to 350° C. a monomer mixture comprising 10 to 80 wt. % first vinyl monomer having an alkyl group in the &agr;-position, 0 to 30 wt. % styrene as an optional ingredient, and 0 to 90 wt. % one or more other vinyl monomers based on the total amount of all monomers.

Abstract: The invention relates to a method for the production of a template-textured material by synthesis of a template-textured polymer (TTP) by performing crosslinking polymerization of functional monomers on a support in the presence of a template, which method is characterized in that a support having a thin polymer layer on the surface thereof is added with a reaction mixture consisting of polymerization initiator, template, functional monomer, crosslinker, solvent and/or buffer and, following sorption of the reaction mixture in the thin polymer layer, the polymerization is initiated and continued until the absorption capacity of the thin polymer layer for the template-textured polymer (TTP) is reached, and the template is optionally removed in a final step, the support used being selected in such a way that it cannot absorb the reaction solution. The materials of the invention are remarkable for their high binding specificity and selectivity for the template.

Abstract: A polymeric reaction product is prepared by a process comprising a reaction, under free radical conditions, of a reaction mixture containing at least one monomer (a) capable of undergoing free radical reactions, in the presence of a compound (I) of the formula: 1

Abstract: Fluorine-modified comb polymers based on acryloyldimethyltaurine The invention provides water-soluble or water-swellable copolymers obtainable by free-radical copolymerization of

Abstract: An olefin polymerization pre-catalyst, an activated catalyst and a process for preparing the catalysts are described herein.

Abstract: A curable polyvinyl benzyl compound represented by the following general formula (1): 1

Abstract: Rubber-free copolymers of unsaturated monomers selected from the group comprising styrenes and vinyl cyanides containing 65 wt. % to 80 wt. %, preferably 68 wt. % to 77 wt. % of styrene and 20 wt. % to 35 wt. %, preferably 23 wt. % to 32 wt. % of acrylonitrile, and a process and a device for the preparation thereof are set out and described. As a result of a gentle, two-stage evaporative treatment, the copolymers have a low residual monomer content, namely less than 20 ppm, preferably 10 ppm of acrylonitrile and less than 200 ppm, preferably 100 ppm of styrene and less than 200 ppm, preferably 100 ppm of ethyl benzene. To this end, solutions of the product are brought to concentrations greater than/equal to 99.8% in a first step of gentle concentration by introducing energy with simultaneous evaporation, and further monomers are removed in a second step without intermediate heating.

Abstract: This invention relates to a process for the synthesis of addition polymers containing branches upon branches and having a polymerizable olefin end group by a convenient one-pot polymerization of selected vinyl monomers with chain polymerization initiators and a method to provide olefinic end groups by chain termination agents; and polymers produced thereby characterized by branch-on-branch structure and lower inherent viscosity than heretofore possible.

Abstract: Novel ethylene styrene interpolymers having atactic ES repeating units and an alternating structure substantially higher than that predicted using Bemoullian statistics may be prepared in the presence of a transition metal phosphinimine compound and an activator.

Abstract: An organic anti-reflective polymer which prevents back reflection of lower film layers and eliminates standing wave that is occurred by a thickness change of photoresist and light, in a process for fabricating ultrafine patterns that use photoresist for lithography by using 193 nm ArF and its preparation method. More particularly, the organic anti-reflective polymer of the present invention is useful for fabricating ultrafine patterns of 64M, 256M, 1G, and 4G DRAM semiconductor devices. A composition containing such organic anti-reflective polymer, an anti-reflective coating layer made therefrom and a preparation method thereof.

Abstract: A novel class of organic semiconductor with a high charge carrier mobility by high regio-regularity. The regio-regularity is produced by the production of the polymer, starting from an AB elimination of the monomers.

Abstract: Low molecular weight olefin polymers are prepared by a polymerization process employing titanium complexes comprising a 3-aryl-substituted cyclopentadienyl ring or substituted derivatives thereof as polymerization catalysts.

Abstract: The invention provides bonding compositions and reactive two-part bonding compositions that are useful, for example, in bonding low surface energy substrates (e.g., polyethylene, polypropylene and polytetrafluoroethylene). Bonding compositions of the invention include an organoborane, a polymerizable monomer, and a metal salt which modifies the cure kinetics of the bonding composition to provide a favorable balance of long bonding composition worklife and fast rate of strength build.

Abstract: Novel fluorine-containing paper sizes which impart oil and grease resistance to paper and soil-release properties to textile products are described which are the copolymerization products of (a) a perfluoroalkyl-substituted (meth)acrylate or (meth)acrylamide, (b) a secondary- or tertiary-amino or quaternary ammonium group-containing (meth)acrylate or (meth)acrylamide, (c) vinylidene chloride and, optionally, d) other copolymerizable nonfluorinated vinyl monomers.

Abstract: A conjugated diene rubber gel comprising 80-99 weight % of conjugated diene monomer units and 20-1 weight % of aromatic vinyl monomer units and having a swelling index of 16 to 70 as measured in toluene. A rubber vulcanizate made from a rubber composition comprising this conjugated diene rubber gel and a rubber capable of being crosslinked with sulfur exhibits good abrasion resistance and low heat-build up without deterioration of mechanical properties, and thus, is suitable for tire materials. This conjugated diene rubber gel can be produced with high efficiency by emulsion-polymerization of a monomer mixture comprising 50-99.9 weight % of a conjugated diene monomer, 0-30 weight % of an aromatic vinyl monomer, 0-20 weight % of a crosslinking monomer.

Abstract: Membranes made from amphiphilic copolymers are disclosed. The amphiphilic copolymers can be ABA copolymers, where one of A and B is hydrophilic and the other is hydrophobic. The copolymers may be crosslinked to form more stable structures. Crosslinking can be accomplished using a variety of methods, including end to end polymerization of copolymers having terminal unsaturated groups. Molecules such as membrane proteins can be incorporated into the membrane to allow the transport there through of selected components.

Abstract: Process for the preparation of polymerizable compounds, apparatus for this purpose and use of this apparatus.

Abstract: A process for production of methacrylic copolymers, characterized by charging a monomer mixture comprising from 70 to 95% by weight of methyl methacrylate, from 0 to 15% by weight of &agr;-methylstyrene, from 0 to 20% by weight of styrene and from 2 to 15% by weight of maleic anhydride at a molar ratio of the sum of &agr;-methylstyrene and styrene to maleic anhydride laying within the range of 1.0 to 2.5 into a polymerizing vessel containing at least one polymeric membrane layer having an oxygen permeability of 1.5×10−13 (mol·m−2·s−1·Pa−1) or below, sealing the polymerizing vessel, and polymerizing the monomer mixture under heating in a gas phase; a methacrylic copolymer obtained by the production process which is reduced yellowing and shows excellent transparency and heat resistance; and an optical element composed of the methacrylic copolymer.

Abstract: The present invention relates to a rubbery polymer which is comprised of repeat units that are derived from (1) at least one conjugated diolefin monomer, and (2) at least one functionalized monomer of the structural formula: 1

Abstract: An ethylene styrene copolymer having isolated styrene monomer units separated by 5 or 6 methylene groups as determined by 13C-NMR may be polymerized in the presence of an activator and a transition metal catalyst containing a phosphinimine ligand.