Abstract: In this disclosure, we describe a new chemical treatment that can be performed on lithium metal and lithium alloy surfaces to selectively remove LiH defects. This treatment utilizes an exclusive reaction between LiH and trialkyl borane to form lithium borohydride complexes, which can be easily washed away from surface using an inert organic solvent. This treatment can be useful for lithium metal and lithium alloy anodes for high energy batteries.

Abstract: Disclosed herein is a method for producing silica gel-immobilized phosphonium salt catalysts including the steps of (a) reacting a silane compound with a silica gel in the presence of xylene, to obtain a catalyst precursor having a haloalkyl group or a haloaryl group, wherein the silane compound has a haloalkyl group or a haloaryl group, and a proportion of the silane compound is from 0.001 to 0.

Abstract: Low-copper click chemistry, 1.3-dipolar cycloadditions, and Staudinger ligations for modifying biomolecules is provided. Compositions, methods, and kits relating to low-copper click chemistry, 1.3-dipolar cycloadditions, and Staudinger ligations are also provided.

Abstract: An antifoul composition especially for use in vinyl chloride polymerisation comprising a) at least one poly acrylate (co) polymer binder and b) at least one of (i) a cross-linked product formed by reacting formaldehyde and a phenol, (ii) a phenol/formaldehyde condensate, (iii) a condensation product formed by reaction of an effective 1-naphthol and formaldehyde, and (iv) a product based on napthenic molecules substituted with sulfur compounds at at least one position on the aromatic structure and (v) the composition optionally comprising less than 2 wt %, preferably less than 1 wt % 0.5 wt % polyvinyl acetate or partially hydrolysed polyvinyl acetate.

Abstract: The invention provides methods for stably binding and immobilizing deoxyribonucleic acid onto objects and substrates. The method includes exposing the deoxyribonucleic acid to alkaline conditions, and contacting the deoxyribonucleic acid to the object or substrate. The alkaline conditions are produced by mixing the deoxyribonucleic acid with an alkaline solution having a pH of about 9.0 or higher, and contacting the deoxyribonucleic acid to the substrate. The immobilized DNA can be used as a taggant and can be used in combination with other detectable taggants, such as optical reporters. Methods for authentication of a DNA marked object are also provided.

Abstract: A synthetic bead for use in mineral separation is described. The synthetic bead has a surface made of a synthetic material such as polymer and the synthetic material is functionalized with molecules having a functional group for attracting mineral particles to the surface in a separation process. The synthetic beads can be placed in flotation cell containing a mixture of water, valuable material and unwanted material or in a pipeline where the mixture is transported from one location to another. The enriched synthetic beads carrying the mineral particles are separated from the unwanted materials in the mixture. The mineral particles are then released from the synthetic beads by means of low pH treatment, ultrasonic agitation, thermal or electromagnetic treatment.

Abstract: An architectural paint is disclosed which comprises a film-forming binder polymer, cotton fibers, and glass bubbles. The paint, in some embodiments, is capable of covering defects in a wall surface.

Abstract: A polyvinyl chloride-type covering material for electric wire that has an excellent damage-resistance property, cold-resistance property and low-temperature property after aging. The covering material containing a polyvinyl chloride comprises, with respect to 100 parts by mass of the polyvinyl chloride, (A) 15 to 30 parts by mass of a plasticizer comprising 15 parts by mass or more of one or more plasticizers selected from trimellitate plasticizers and pyromellitate plasticizers, (B) 2 to 10 parts by mass of a chlorinated polyolefin, and (C) 1 to 6 parts by mass of a methyl methacrylate-butadiene-styrene copolymer.

Abstract: A carbon nanostructure that is free of a growth substrate can include a plurality of carbon nanotubes that are branched, crosslinked, and share common walls with one another. The carbon nanostructure can be released from a growth substrate in the form of a flake material. Optionally, the carbon nanotubes of the carbon nanostructure can be coated, such as with a polymer, or a filler material can be present within the porosity of the carbon nanostructure. Methods for forming a carbon nanostructure that is free of a growth substrate can include providing a carbon nanostructure adhered to a growth substrate, and removing the carbon nanostructure from the growth substrate to form a carbon nanostructure that is free of the growth substrate. Various techniques can be used to affect removal of the carbon nanostructure from the growth substrate. Isolation of the carbon nanostructure can further employ various wet and/or dry separation techniques.

Abstract: Intermediate products (compounds, semi-finished goods) for polymer materials having coupled components, to the polymer materials based on the intermediate products, and to the components to be manufactured therefrom. A method for producing intermediate products, polymer materials and components, and to the use thereof.

Abstract: This invention relates to a supported quaternary phosphonium catalyst, preparation thereof and use thereof in producing dialkyl carbonates. The supported quaternary phosphonium catalyst of this invention has the following average molecular structure (I), and is characterized by a relatively high and stable catalyst activity. wherein, each of X, L, n, R1, R2, R3 and is the same as that in the specification.

Abstract: The invention provides articles obtained from curing a composition consisting of a polymercapto crosslinking agent, a vulcanization accelerator, an inorganic base, a nitrogen containing chelating agent, wherein the nitrogen containing chelating agent is selected from the group consisting of 1,10-phenanthroline and 2,2-bipyridyl, and polyethylenimine; and a halogenated elastomer; wherein said nitrogen containing chelating agent is soluble in said halogenated elastomer.

Abstract: Vinylidene chloride copolymer composition characterized in that it comprises: (A) at least one vinylidene chloride copolymer which is a copolymer composed of vinylidene chloride in an amount of at least 50 wt % and of at least one comonomer at least one of which is chosen from (meth)acrylic monomers corresponding to the general formula: CH2?CR1R2, in which R1 is chosen from hydrogen and the methyl radical and R2 is the —CO—R3 radical in which R3 is the —O—R4 radical with R4 chosen from the linear or branched alkyl radicals containing from 1 to 18 carbon atoms optionally bearing one or more —OH radicals, the epoxyalkyl radicals containing from 2 to 10 carbon atoms and the alkoxyalkyl radicals containing a total of 2 to 10 carbon atoms; (B) from 0.5 to 4 parts by weight, per 100 parts by weight of (A), of epoxidized soybean oil; (C) from 0.

Abstract: Heavy metal-free compostable polymers, composites and articles anaerobically biodegrade in landfills in a relatively short time. Heavy metal-free composite polymeric articles and sheets such as indoor or outdoor signs, billboards, banners, images, protective barriers, backdrops and wall coverings have very useful service durations and yet are landfill biodegradable.

Abstract: Biocidal compositions containing organoselenium compounds are disclosed, as well as methods of producing and using same.

Abstract: The invention concerns a method of polymerizing an alkene monomer to produce a polymer using a catalyst that is Cu(O), Cu2Te, CuSe, Cu2S, Cu2O, or a combination thereof, an initiator, and a component comprising a solvent and optional nitrogen-containing ligand, where the combination of the component and monomer is capable of diproportionating Cu(I)X into Cu(O) and Cu(II)X2 where X is Cl, Br, or I.

Abstract: The invention provides compositions comprising nitrogen containing chelating agents, which can be used to reduce the effects of zinc contamination on the vulcanization rates of polymercapto based cure systems for halogenated elastomers. Such chelating agents are effective at eliminating vulcanization rate inconsistencies due to zinc contamination, without inducing negative changes to the vulcanization reaction or the subsequent physical properties of the halogenated elastomer vulcanizate. The invention also provides methods of curing a halogenated elastomer using the inventive compositions, and for articles prepared from the same.

Abstract: The invention provides new polymeric or oligomeric active agents with a biocidal effect. Such particularly advantageous polymeric or oligomeric active agents with a biocidal effect are obtainable via polycondensation of a guanidine acid addition salt with an amine mixture comprising at least one diamine and/or one triamine, wherein at least one amine is selected from the group comprising i) diamine, comprising at least one cycloaliphatic residue, and ii) dialkylenetriamine. At least one amine is hereby preferably selected from 4,4?-methylenebis(cyclohexylamine) and diethylenetriamine. Furthermore, it is favorable if the guanidine acid addition salt is guanidinehydrochloride.

Abstract: The present invention provides a compound represented by the Formula I: Wherein substituents R16, R17 and R17? are each independently selected from an electron withdrawing group having a Hammett ?p value of from 0.05 to 0.85, provided that one of R16 and R17 is hydrogen.

Abstract: Disclosed is a method for preparing a hydroxyl functionalized polymer from a Lewis acid promoted carbonyl-ene reaction comprising: selecting a vinylidene terminated polyolefin having a number average molecular weight from about 950 to about 5000 and having a terminal vinylidene content greater than 50 mole percent; selecting a carbonyl enophile; selecting a Lewis acid; and contacting the components in step a), b) and c) under reactive conditions to form the hydroxyl functionalized polymer.

Abstract: Disclosed is a method of preparing a modified halogenated polymer surface, comprising the steps of (a) activating the surface by modification with a polymerisation initiator by (a1) reacting the halogenated polymer surface with sodium azide and subsequent (a2) 1,3 dipolar cycloaddition with an alkine-functionalized initiator; or (a3) reacting the halogenated polymer surface with mercapto-functionalized initiators; and (b) reacting the activated surface obtained in steps (a1)/(a2) or (a3) with polymerizable monomeric units A and/or B. The modified halogenated polymer substrates according to the invention exhibit outstanding properties.

Abstract: Compositions of vinyl halide polymers such as PVC are rendered compostable by a prodegradant system of a monomeric adduct of an organotitanate or zirconate and an organotin. PVC sheets and composites are compostable in landfills.

Abstract: The present invention provides a process for producing a treated or modified polymer, which process comprises the steps of: (I) providing a mixture comprising a liquid, an additive and a polymer, wherein the additive is dispersed in the liquid; and (II) heating the mixture obtained in step (I) to soften the surface of the polymer so that the additive attaches to the polymer.

Abstract: A copolymer of (i) an alkyl acrylate or alkyl methacrylate and (ii) a hydroxyalkyl acrylate or hydroxyalkyl methacrylate is used as a secondary protective colloid in the suspension polymerization of vinyl chloride monomer. The alkyl group of the alkyl acrylate or alkyl methacrylate is preferably a 2-ethylhexyl group. The hydroxyalkyl group of the hydroxyalkyl acrylate or hydroxyalkyl methacrylate is preferably a hydroxyethyl group.

Abstract: According to the present invention, during or after the process of separating an aqueous solution of hydrochloric acid by-produced from a chlorinated vinyl chloride resin slurry obtained by chlorinating vinyl chloride resin or a copolymer of vinyl chloride and another copolymerizable monomer, hypochlorite is added to the chlorinated vinyl chloride slurry or water-containing resin. Due to this, the concentration of hydrochloric acid in the chlorinated vinyl chloride resin or chlorinated vinyl chloride copolymer resin before drying is reduced, and the problem of removing hydrochloric acid in the subsequent drying treatment is reduced, whereby the problem of corrosion of a drier can be reduced.

Abstract: Methods are described for preparing graft copolymers from poly(vinyl chloride) or vinyl chloride copolymers comprising reacting these materials with sources of selected metal-centered free radicals in the presence of one or more monomers that can undergo free-radical addition polymerization. The metal-centered free radicals used are capable of abstracting chlorine atoms from the starting polymer to form C-centered radicals that add to the monomer(s) in order to start the growth of branches via a free-radical route. This method is an effective method for producing PVC graft copolymers, and can be used to produce PVC graft copolymers having novel compositions. The methods of the invention are particularly useful for providing highly branched PVC graft copolymers.

Abstract: The present invention relates to aqueous compositions comprising component (A) which comprises at least one water-soluble component comprising at least one functional group that undergoes a crosslinking reaction, preferably upon drying and/or heating; component (B) which comprises at least one film-forming material, preferably a latex material; and component (C) which comprises at least one component that provides at least one of moisture and/or water barrier properties and/or vapor barrier properties greater than that provided by the combination of components (A) and (B) alone.

Abstract: According to the present invention, during or after the process of separating an aqueous solution of hydrochloric acid by-produced from a chlorinated vinyl chloride resin slurry obtained by chlorinating vinyl chloride resin or a copolymer of vinyl chloride and another copolymerizable monomer, hypochlorite is added to the chlorinated vinyl chloride slurry or water-containing resin. Due to this, the concentration of hydrochloric acid in the chlorinated vinyl chloride resin or chlorinated vinyl chloride copolymer resin before drying is reduced, and the problem of removing hydrochloric acid in the subsequent drying treatment is reduced, whereby the problem of corrosion of a drier can be reduced.

Abstract: A molding material for use with carbon dioxde, which comprises chlorinated polyethylene having a chlorine content of 25–47% by weight or a blend of chlorinated polyethylene with vinyl chloride-based resin, can be used as a suitable material for sealing materials in carbon dioxide-contacting apparatuses using carbon dioxide as a refrigerant. Addition of a specific silane coupling agent to the molding material can effectively prevent vulcanization moldings from blister generation.

Abstract: The present invention provides a vinyl chloride polymer composition which comprises (i) a vinyl chloride polymer (a) and (ii) a block copolymer (b) having a polymer block (I) comprising of a block copolymer, which may be hydrogenated, of an aromatic vinyl compound polymer block and a conjugated diene polymer block, and a polymer block (II) of a polyurethane, in a specific weight ratio. The vinyl chloride polymer composition of the present invention has non-tackiness, excellent handling properties, favorable flexibility and mechanical properties, and favorable melt-adhesiveness to other materials, and shows no migration of the component serving as a plasticizer. The vinyl chloride polymer composition of the present invention can be applied for various uses such as a production of various molded articles and a production of a laminated structure with other materials.

Abstract: An electron beam curing resin for a magnetic recording medium is provided, wherein a known thermosetting vinyl chloride resin or polyurethane resin is modified to become sensitive to an electron beam, and the resulting resin has a high cross-linking property. A method for readily manufacturing the above-described electron beam curing resin from a known thermosetting resin is provided. Furthermore, a high-performance magnetic recording medium including the above-described electron beam curing resin is provided. The electron beam curing resin is produced through a reaction between active hydrogen groups of a vinyl chloride resin or polyurethane resin having the active hydrogen groups in a molecule and a compound having an isocyanate group and a radical-polymerizing unsaturated double bond in a molecule, wherein the amount of water in the reaction system is controlled at 0.05 to 0.5 percent by mass relative to the resin when the reaction is effected.

Abstract: The present invention provides a vinyl polymer with an epoxy group terminally introduced therein and an epoxy resin composition comprising (A) an epoxy resin and (B) a vinyl polymer which has a main chain produced by living radical polymerization and has a reactive functional group at a main chain terminus. A flexible epoxy resin composition can be obtained using these compounds. The invention further provides an epoxy resin composition having an epoxy group at a main chain terminus thereof.

Abstract: A molding material for use with carbon dioxide, which comprises chlorinated polyethylene having a chlorine content of 25-47% by weight or a blend of chlorinated polyethylene with vinyl chloride-based resin, can be used as a suitable material for sealing materials in carbon dioxide-contacting apparatuses using carbon dioxide as a refrigerant. Addition of a specific silane coupling agent to the molding material can effectively prevent vulcanization moldings from blister generation.

Abstract: Chlorinated olefin polymers prepared from olefin polymer base resins having I10 values of 0.05-0.8 dg/minute act as impact modifiers for vinyl chloride polymers under low to ambient temperature conditions. When vinyl chloride polymers are mixed with a preferred class of the chlorinated polymers, having chlorine contents of 20-30 percent by weight, compositions that exhibit short fusion times and low fusion temperatures are produced.

Abstract: Polymers derived from 4-acyloxystyrene are purified by fractionalization plus heating and cooling of the polymers in alcoholic solvents.

Abstract: The invention relates to a process for the preparation of an aqueous dispersion of halogenated vinyl polymers by polymerization, according to which, after polymerization, a basic agent is added in an amount such that the pH of the aqueous dispersion is less than approximately 5. The invention also relates to the aqueous dispersion obtained, which can be coated onto polymeric substrates made of paper or of regenerated cellulose.

Abstract: Objects of the present invention are to provide a process for easily producing an alkenyl-terminated vinyl polymer without using a metal compound requiring a complicated purification step, and to provide a curable composition containing the vinyl polymer. An alkenyl group is incorporated into an end of a vinyl polymer having a thiocarbonylthio structure at the end to produce an alkenyl-terminated vinyl polymer. Mixing this vinyl polymer with a compound having a hydrogen-silicon bond and a hydrosilylation catalyst gives the curable composition.

Abstract: The invention relates to a process for the preparation of an aqueous dispersion of halogenated vinyl polymers by polymerization, according to which, after polymerization, a basic agent is added in an amount such that the pH of the aqueous dispersion is less than approximately 5. The invention also relates to the aqueous dispersion obtained, which can be coated onto polymeric substrates made of paper or of regenerated cellulose.

Abstract: There is provided an excellent impact modifier for a vinyl chloride resin. There is used, as an excellent impact modifier, a copolymer which is prepared by polymerizing 10 to 70% by weight of a monomer or monomers containing 60 to 100% by weight of at least one vinyl monomer selected from the group consisting of a (meth)acrylate compound, an aromatic vinyl compound, a vinyl cyanide compound and vinyl chloride, and 0 to 40% by weight of the other monomer copolymerizable therewith, in the presence of 30 to 90% by weight of a hollow rubber particle of which glass transition temperature Tg is at most 0° C. and a void ratio is 3 to 90% by volume in a latex state, and which contains a cross linking agent in an amount of 0.1 to 5 parts by weight based on 100 parts by weight of the total rubber component monomer.

Abstract: Polymers derived from 4-acyloxystyrene are purified by fractionalization plus heating and cooling of the polymers in alcoholic solvents.

Abstract: A graft copolymer composition and the preparation of the composition by living radical polymerization is disclosed. The polymerization reaction can be initiated at active chlorine sites on the poly(vinyl chloride) backbone in conjunction with a transition metal catalyst and an optional ligand. The graft copolymers are useful as, among others, compatibilizers for blends and alloys, as high heat distortion temperature poly(vinyl chloride) materials, as impact modifiers, and permanently plasticized materials.

Abstract: A polymer, possibly fabricated as part of a medical device or as part of a medical prostheses (such as a contact lens) is functionalized to facilitate the introduction of functional groups, such as biomedical species including heparin. The polymer is reacted in an aqueous medium with a water soluble azo compound (such as cyanovaleric acid or 2-methylpropionamidine) to produce oxygen centered radicals responsible for introducing functional groups into the polymer.

Abstract: Block chlorinated polyolefins are disclosed as performance enhancer of high rubber graft copolymers or chlorinated polyethylenes impact modifier in PVC and/or CPVC resins. The block chlorinated polyolefins (e.g. block chlorinated polyethylene) provide good dispersion of the impact modifier particles in the matrix and better adhesion between the impact modifier and the PVC and/or CPVC interface, providing better physical properties such as impact strength as measured by Notched Izod than did the randomly chlorinated polyolefins, often used as processing aids and as impact modifiers in PVC or CPVC. The differences in properties achieved with block chlorinated polyolefins versus randomly chlorinated polyolefins are attributed to the individual blocks of the blocky polyolefin being compatible with either the impact modifier or the PVC/CPVC resulting in better adhesion between phases.