Abstract: The present invention relates to a super absorbent polymer and a preparation method thereof, the super absorbent polymer including: surface cross-linked polymer particles prepared by surface cross-linking particles of a base resin, the base resin polymerized from a monomer composition including water-soluble ethylene-based unsaturated monomers having at least partially neutralized acidic groups; and a water-soluble component, wherein the water-soluble component has a weight average molecular weight of 150,000 to 300,000 g/mol. The super absorbent polymer may have high centrifuge retention capacity and excellent permeability at the same time, while having low content of the water-soluble component.

Abstract: The present invention relates to a method of preparing grafted copolymers of lignin and/or cellulose, comprising the generation of macroradicals in situ by mechanical impact on the backbone of said lignin and/or cellulose of said lignin and/or cellulose containing material and grafting monomers and/or polymers to said backbone. Furthermore, the present invention relates to the grafted copolymers obtainable by said method, composite materials comprising said copolymers as well as to uses thereof.

Abstract: A polymer resin comprising: (a) quantum dots, (b) a compound of formula (I) (I) wherein R1 is hydrogen or methyl and R2 is a C6-C20 aliphatic polycyclic substituent, and (c) a block or graft copolymer having Mn from 50,000 to 400,000 and comprising from 10 to 100 wt % polymerized units of styrene and from 0 to 90 wt % of a non-styrene block; wherein the non-styrene block has a van Krevelen solubility parameter from 15.0 to 17.5 (J/cm3)1/2.

Abstract: A method for synthesizing a thermoplastic elastomer comprising at least one polydiene block and at least one other poly(?-methylstyrene) block comprises: polymerizing at least one diene monomer in a starting reaction medium comprising an anionic polymerization initiator and an aprotic non-polar solvent; polymerizing ?-methylstyrene to the living polydiene chain obtained in the preceding step comprising: maintaining the reaction medium containing the living diene elastomer obtained previously and ?-methylstyrene at a positive temperature, below the ceiling temperature for the polymerization of ?-methylstyrene; cooling the reaction medium obtained at the end of step a., to a temperature below 0° C.; simultaneously, successively or prior to the cooling step, adding a purified aprotic polar solvent to the reaction medium with a volume ratio of the polar solvent to the non-polar solvent of less than 1; and propagating the polymerization of ?-methylstyrene to the living polydiene chain.

Abstract: This invention relates to compositions and a process for stabilizing or solubilize a phenolic resin containing a mixture of linear phenolic resins and calixarenes. The process comprises contacting the phenolic resin with an epoxide, to at least partially alkoxylate the phenolic hydroxyl groups of the calixarenes. This process forms a stabilized or solubilized phenolic resin with an increased solubility in a hydrocarbon solvent.

Abstract: An amine-functionalized, crosslinked porous copolymer can be synthesized by linking 1,4-benzenediamine and pyrrole with p-formaldehyde in the presence of concentrated hydrochloric acid catalyst. The polymer is permanently microporous, with a BET surface area of 250 to 350 m2/g. Due to the high concentration of polar amines within its backbone, the polymer exhibits a CO2 uptake of 17.5 to 30 cm3/g at 298 K and 1 bar, but demonstrated a remarkably high selectivity for CO2 over N2 at 298 K. Dynamic breakthrough experiments indicate that this material is an effective adsorbent for selectively separating CO2 from a dry and wet gas mixture containing N2 for over 45 cycles without significant loss of performance. Furthermore, the polymer can be regenerated at room temperature after each cycle by a simple N2 flow.

Abstract: The present invention relates to polyurethane hybrid polymers and to a process for producing same.

Abstract: A method of making flexible polyurethane foams mixes a polyol (a hydroxyl group containing compound) with a cesium and/or rubidium fluoride catalyst, and reacts such mixture with at least one isocyanate. The cesium and/or rubidium fluoride may be used as the sole catalyst, replacing the blowing and gelling catalysts, such as amines, and metallic catalysts, such as a tin catalyst. Or, the cesium and/or rubidium fluoride may be used as a catalyst promoter in combination with traditional amine blowing and gelling catalysts and tin catalysts. The resulting flexible polyurethane foams exhibit increased thermal conductivity and lower levels of volatile organic compound emissions.

Abstract: A polyurethane catalyst comprises a sodium compound, the sodium compound being 1 to 60 wt % of the polyurethane catalyst by the mass percent, and further comprises a tertiary amine and/or pyridine compound. The sodium compound and the tertiary amine and/or pyridine compound achieve a synergistic effect; during the catalysis of the polymerization of isocyanate and polyalcohol, the speed of the polymerization reaction is increased; and the prepared polyurethane material has excellent physical properties, does not contain any heavy metal element at all, is an environment-friendly catalyst, solves the technical problem of ensuring environmental protection, safety and the catalytic efficiency of the polyurethane catalyst, and is particularly applicable to the preparation of polyurethane synthetic leather resin slurry, a polyurethane elastomer (prepolymer), a polyurethane coating, a polyurethane adhesive, a polyurethane composite material, flexible polyurethane foam, and a rigid polyurethane material.

Abstract: The present invention discloses silylated polyurethanes obtainable by reacting at least one polyols, at least one polyisocyanates, at least one silicon-containing heterocycle of the general formula (I): wherein R1 is hydrogen; R2 and R3 are same or different and are, independently from one another, selected from a linear or branched, substituted or unsubstituted C1-C20 alkyl or C6-C18 aryl residue which may be interrupted by at least one heteroatom; R4 is selected from a linear or branched, substituted or unsubstituted C1-C20 alkylene residue which may be interrupted by at least one heteroatom; R5 and R6 are same or different and are, independently from one another, selected from the group consisting of hydrogen, a linear or branched, substituted or unsubstituted C1-C20 alkyl or C6-C18 aryl which may be interrupted by at least one heteroatom, and a C4-C8 cycloalkyl, or R5 and R6 may form a ring, preferably a 4- to 8-membered alkyl ring; and n is 0, 1 or 2, their preparation methods, curable composition

Abstract: The present invention relates to the polyamines N,N?-diaminopropyl-2-methyl-cyclohexane-1,3-diamine and N,N?-diaminopropyl-4-methyl-cyclohexane-1,3-diamine and mixtures thereof, to the use thereof as curing agents for epoxy resin and to a curable composition comprising epoxy resin and these polyamines. Even at low temperatures this curing agent/the corresponding curable composition cures rapidly and is early-stage water resistant and is thus especially suitable for floor coatings. The invention further relates to the curing of this composition and the cured epoxy resin obtained by curing of this composition.

Abstract: A polyester resin having a diol constitutional unit and a dicarboxylic acid constitutional unit, wherein 20 to 100 mol % of the diol constitutional unit is a constitutional unit derived from a diol having a dinorbornane ring; a glass transition temperature of the polyester resin is 90° C. or higher; an amount of heat of a crystallization exothermic peak in temperature drop of the polyester resin is 5 J/g or less; and a yellow index (YI) value as measured by a reflection method according to JIS K 7103 is 10 or less.

Abstract: Cyclic imino ether polymers, such as polyoxazolines or polyoxazines, having a low polydispersity index can be obtained in a tubular flow reactor by applying a sufficiently high linear flow velocity of the reaction mixture in the tubular flow reactor, such as a flow velocity of least 100 cm/min or at least 120 cm/min. Also, methods to control the polydispersity of a cyclic imino ether polymer during polymerization are provided.

Abstract: A curable system containing a benzoxazine and a benzothiazole sulfenamide. The curable system may be catalyzed at temperatures generally used to cure multifunctional epoxy resins yet exhibits improved pot-life and processing times and provides a cured article that exhibits acceptable thermo mechanical properties.

Abstract: A polymerizable composition includes an organoborane-base complex that is a complex of an organoborane and a base, a decomplexing agent that at least partially liberates the organoborane from the organoborane-base complex, a polymerizable thiol-containing component comprising at least one polymerizable thiol-containing compound having a plurality of thiol groups in which the sulfur atom of the thiol group is covalently bonded to carbon, a hydroperoxide, and a polymerizable ethylenically-unsaturated component comprising at least one polymerizable ethylenically-unsaturated compound having a plurality of ethylenically-unsaturated groups. The combined amounts of the thiol-containing and ethylenically-unsaturated compounds total at least 50 percent by weight of all polymerizable material in the polymerizable composition. The composition may be provide as a two-part composition. Polymerized reaction product of the composition and methods of making the composition are also disclosed.

Abstract: Cross-linked polymer resins and related salts, solvates, tautomers or stereoisomers are described herein. The cross-linked polymer resins may comprise monomer units of N,N-diallyl aminoalkylphosphonate, a hydrophobic pendant, a tetraallylpiperazinium cross-linker, and sulfur dioxide. A method for producing the cross-linked polymer resins is described. The cross-linked polymer resins may be used as adsorbent materials for the removal of heavy metal ions and contaminant dyes from aqueous solutions. Used cross-linked polymer resins may be removed from solution, cleaned, and reused while maintaining adsorption capacity.

Abstract: The present invention relates to a process for preparing a polyaryl ether by reacting components (a1) and (a2) in the presence of a carbonate compound (C) to obtain a salt-containing polymer (SP) comprising the polyaryl ether and a salt (S). After the reaction, the salt (S) is extracted from the salt-containing polymer (SP) to obtain a desalinated polymer (DP) comprising the polyaryl ether.

Abstract: Phenoxyphenylsilane monomers were synthesized and polymerized. The polymers have high refractive indices and excellent UV and thermal stability. Their water and oxygen permeability is lower than commercial phenyl silicone elastomers. They show good compatibility with metal oxide nanoparticles. The polymers of the invention are suitable as LED encapsulant, as light guide material in CMOS image sensors, in OLED devices, lasers and in other optical applications.

Abstract: A silsesquioxane polymer, composition, method, and article including such polymer, wherein the polymer includes a three-dimensional network of Formula (I): wherein: each R1 and R2 is independently a (C1-C4)alkyl; each L1 and L2 is independently in a single bond, an alkylene, or an alkylene bonded to a group selected from oxy, thio, carbonyl, —NH—, and combinations thereof; each R3 is independently a linear (C14-C100)alkyl; each R4 is independently a (C1-C30)alkyl, (C2-C30)heteroalkyl having at least one oxygen, sulfur, or —NH— group, or a (C1-C30)alkyl substituted with a fluoro, thiol, isocyanato, cyanato, hydroxyl, glycidoxy, or epoxy group; with the proviso that L1, L2, and R4 are selected such that each Si atom is directly bonded to an alkylene or an alkyl; m is an integer of at least 3; n is an integer of 0 or above; m+n is an integer of at least 3; each oxygen atom at an asterisk (*) is bonded to another Si atom within the three-dimensional network; and the silsesquioxane polymer is a solid at 25° C.

Abstract: Described is a triblock copolymer of the formula ABC wherein B is a hydrogenated vinyl aromatic block having a Tg of ?110° C. and comprising 30-90 wt. % of the copolymer; C is a rubbery block having a Tg?25° C. and comprising 10-70 wt. % of the copolymer; and A is an block derived from ring-opening polymerization, substantially incompatible with both B and C blocks.

Abstract: Emulsions for treating shingles, concrete, metallic substrates, mammalian skins, human hair or agricultural plants are described. The emulsions include soy alkyl and/or aryl ester; water; and a cationic surfactant to form the emulsion. Methods of using the emulsions are also described. Compositions including a modified oil alkyl and/or aryl ester comprising the transesterification reaction product of an oil and a surfactant having a hydroxyl group are described. Methods of using the compositions are also described. Methods of making a modified oil alkyl or aryl ester are described. The methods include transesterifying an oil with a surfactant having a hydroxyl group.

Abstract: A method of preparing polyamide (PA) powders includes the steps of: heating a composition including PA granules, a nucleating agent and an organic solvent under normal pressure to T1 not lower than melting point (Tm) of PA granules and maintaining at T1 to dissolve PA granules; cooling the heated composition to T2 to nucleate the dissolved PA granules and maintaining at T2 to crystallize, where 15° C.?Tm?T2?33° C.; cooling the crystallization product to precipitate PA; and washing the precipitated product to remove the organic solvent. The weight ratio of PA granules to the nucleating agent is 100:1, and the weight ratio of PA granules to the organic solvent ranges from 0.11 to saturation solubility of PA granules in the organic solvent.

Abstract: Provided are a tow prepreg comprising a reinforcing fiber bundle impregnated with a matrix resin composition, wherein the matrix resin composition contains a component (A) (an epoxy resin), a component (B) (dicyandiamide), a component (C) (a curing accelerator), and a component (D) (a core-shell type rubber particle), and a content of the component (D) with respect to 100 parts by mass of the component (A) is from 20 to 70 parts by mass, a viscosity is from 3 Pa·s to 80 Pa·s at 30° C., and a minimum viscosity to be obtained when a viscosity is measured by raising a temperature from room temperature to 130° C. at a rate of temperature rise of 2.0° C./min is from 0.04 Pa·s to 1 Pa·s, which exhibits excellent drape property and tackiness and less stickiness and can be unwound at a high speed; and a composite material-reinforced pressure vessel having fewer voids in a reinforcing layer which is obtainable by using the tow prepreg, a high burst pressure, and an excellent appearance due to appropriate resin flow.

Abstract: Microparticles that have a multimodal pore size distribution are provided, Notably, the pore structure of the present invention can be formed without the need for complex techniques and solvent chemistries traditionally employed to form porous microparticles. Instead, the microparticles contain a polymeric material that is formed from a thermoplastic composition, which is simply strained to a certain degree to achieve the desired porous network structure.

Abstract: The present invention relates to a polyethylene composition comprising, a base resin (A) comprising a copolymer of ethylene and at least one comonomer selected from alpha-olefins having from three to twelve carbon atoms, wherein the ethylene copolymer comprises a low molecular weight component (A-1) and a high molecular weight component (A-2) with the low molecular weight component (A-1) having a lower weight average molecular weight than the high molecular weight component (A-2), (B) carbon black in an amount of 1.0 to 10 wt % based on the total amount of the polyethylene composition, and (C) optional further additives other than carbon black; wherein the low molecular weight component (A-1) has a melt flow rate MFR2 (190° C., 2.

Abstract: A method for making water-absorbing polymer particles is provided and includes providing crosslinkers, polymerizable monomers and inorganic solid particles. The average closest distance between two neighboring crosslinkers (RXL) in a water-absorbing polymer particle for a specific X-load of the water-absorbing polymer particle is calculated via the formula below: Rxl = ( ( 1 rho_dry + x_L rho_liq ) N A · ? i ? ? w_xl i Mr_CXL i ) 1 3 ( I ) with x_L being the amount of liquid absorbed in the water-absorbing polymer particle in g liq/g water-absorbing polymer particle, rho_liq being the density at room temperature of the fluid that swells the water-absorbing polymer particle (generally saline of 0.

Abstract: The invention pertains to a tetrafluoroethylene (TFE) copolymer comprising recurring units derived from at least one per(halo)fluoroolefin different from TFE [monomer (F)] [monomer (F)], in an amount of 0.005 to 0.250% moles, with respect to the total moles of the copolymer, wherein a particular relation between monomer content and amorphous index is satisfied, and to a process for its manufacture by emulsion polymerization in the presence of certain cyclic surfactants.

Abstract: Disclosed are an inorganic nanofiber characterized in that the average fiber diameter is 2 ?m or less, the average fiber length is 200 ?m or less, and the CV value of the fiber length is 0.7 or less; and a method of manufacturing the same. In the manufacturing method, an inorganic nanofiber sheet consisting of inorganic nanofibers having an average fiber diameter of 2 ?m or less is formed by electrospinning, and then, the inorganic nanofiber sheet is pressed using a press machine and crushed so that the average fiber length becomes 200 ?m or less, and the CV value of the fiber length becomes 0.7 or less.

Abstract: Provided is a resin composition containing: a resin (A) having a biomass-derived carbon atom; a resin (B) incompatible with the resin (A); and a plasticizer (C), in which a content of the resin (A) is larger than a content of the resin (B), and a glass transition temperature Tg(A) of the resin (A) is higher than a glass transition temperature Tg(B) of the resin (B).

Abstract: The present disclosure relates to a reinforcing material for rubber including aluminosilicate particles and a rubber composition for tires including the same. The aluminosilicate particles included in the reinforcing material for rubber according to the present disclosure exhibit an enhanced reinforcing effect due to excellent dispersibility in the rubber composition, but do not hinder processability of the rubber composition. Therefore, the aluminosilicate particles can be suitably applied as a reinforcing material in a rubber composition for tires.

Abstract: Methods of improving Mooney stability of a brominated elastomer comprising: neutralizing a brominated elastomer effluent with a neutralizing agent and water to form a neutralized effluent comprising a hydrocarbon solvent; removing the solvent from the neutralized effluent to form a brominated elastomer slurry; and separating a brominated elastomer from the brominated elastomer slurry, wherein a Mooney stabilizer package comprising an amine-functional hindered amine stabilizer (HAS) and an acid scavenger can be added, together or separately, before the removing step are provided herein. The acid scavenger can comprise a protonatable atom with a pKa greater than the pKa of the HAS nitrogen atom. The separated brominated elastomer can have a delta Mooney of not more than about 10 Mooney units after ˜7 days at ˜80° C. Stabilized brominated elastomer compositions can be made using this method, and articles can be made from those compositions.

Abstract: A crosslinked polymer composition based on a plastomer, which is suitable for producing at least one layer of cable accessories like cable joints, bushings or terminations; its use for preparing such a layer and the cable accessory comprising the composition.

Abstract: A polypropylene resin composition contains components (A), (B) and (C). A content of (A) is from 70 to 90 parts by weight, a content of (B) is from 10 to 30 parts by weight, and a content of (C) is from 1 to 5 parts by weight, when the total of the content of (A) and (B) is taken as 100 parts by weight. (A) polypropylene, (B) talc having an average particle diameter of 1 ?m to 8 ?m, (C) polyethylene glycol, wherein a molecular weight at the maximum point of refractive index intensity in a chromatogram obtained by gel permeation chromatography using a differential refractometer is from 2,000 to 4,000, and S2/S1 is from 1.3 to 2.0, where peak areas S2 and S1 are as defined herein.

Abstract: Disclosed is a glass fiber composite material composition having further improved compatibility between glass fibers and polypropylene and thus maximized interfacial adhesion between the resin and the glass fibers in a glass fiber composite material. The present invention provides a glass fiber composite material composition comprising: (A) 60-93% by weight of polypropylene; (B) 1-30% by weight of glass fiber sized with a silane-based compound; and (C) 1-10% by weight of a polypropylene resin modified with maleic anhydride and a methacryloxysilane-based compound.

Abstract: Caps and closures comprising high density polyethylene, polyolefin elastomer and polypropylene wherein the amount of high density polyethylene is more than 50% by weight of the total amount of high density polyethylene, polyolefin elastomer and polypropylene and wherein the total amount of high density polyethylene, polyolefin elastomer and polypropylene is 100% by weight.

Abstract: Provided is a thermoplastic resin composition which enables the production of an inner liner for pneumatic tires, said inner liner having excellent durability and being suppressed in deterioration of air permeation prevention properties due to repeated deformation. A thermoplastic resin composition which is composed of a continuous phase containing an ethylene/vinyl alcohol copolymer and a polyamide and a dispersed phase containing a halogenated isomonoolefin/para-alkyl styrene copolymer, and which is characterized in that an acyl glycerol that is composed of glycerol and a fatty acid having 8 or less carbon atoms is contained in an amount of 0.5-20 parts by mass per 100 parts by mass of the ethylene/vinyl alcohol copolymer.

Abstract: An object of the present invention is to provide a resin composition for reducing an acetic acid odor that is generated during melt molding of a polyvinyl alcohol (PVA)-based resin and may remain in a molded product. The resin composition of the present invention contains: a PVA-based resin (A); and a multimeric aldehyde compound (B), wherein a content of the multimeric aldehyde compound (B) is 0.5×10?4 to 100×10?4 parts by weight with respect to 100 parts by weight of the PVA-based resin (A).

Abstract: A composition comprising; a) at least one homopolymer or copolymer of vinyl acetate; and b) at least one softener.

Abstract: A thermoplastic elastomeric network is taught. The thermoplastic elastomer network includes hyperbranched styrenic block copolymers and styrenic block copolymers physically crosslinked though aggregation. Additionally, the hyperbranched styrenic block copolymers of the thermoplastic elastomeric network are a plurality of styrenic block copolymers chemically crosslinked.

Abstract: Disclosed is a polyamide moulding compound formed from a mixture of partially crystalline, aliphatic polyamides and partially crystalline, partially aromatic polyamides and also fibrous reinforcing materials. The partially crystalline, partially aromatic polyamides are thereby formed from a diamine component, a dicarboxylic acid component and possibly a lactam- and/or ?-amino acid component. The mixture and/or the moulding compound can include further components. Moulded articles produced from these moulding compounds are used, for example, in the automobile sphere, in the household sphere, in measuring, regulating and control technology or in mechanical engineering.

Abstract: A polyphenylene sulfide resin composition is obtained by mixing a polyphenylene sulfide resin (a), a fluororesin (b) and an organosilane compound (c). When a resin phase-separated structure of a molded product formed from the polyphenylene sulfide resin composition is observed by an electron microscope, the component (a) forms a continuous phase, the component (b) forms a primary dispersed phase having a number-average dispersion diameter of not greater than 1 ?m, and a secondary dispersed phase of the component (a) is included in the primary dispersed phase of the component (b).

Abstract: The invention relates to a silicone composition comprising (a) crosslinked polymers comprising consecutive —Si—O— units containing exchangeable pendant bonds and exchangeable crosslinking points, that are exchangeable by aldehyde-imine exchange reactions and/or by imine-imine exchange reactions and/or by imine-primary amine exchange reactions, obtained by crosslinking linear or branched polymers comprising consecutive —Si—O— units and (b) monofunctional free aldehydes and/or monofunctional free imines and/or monofunctional free primary amines.

Abstract: Binders, resinated furnishes, and methods for making composite lignocellulose products therefrom. The binder can include about 70 wt % to about 99.7 wt % of an aldehyde-based resin, about 0.3 wt % to about 30 wt % of an isocyanate-based resin, about 10 wt % to about 63 wt % of an extender, and about 145 wt % to about 230 wt % of water, where all weight percent values are based on a combined solids weight of the aldehyde-based resin and the isocyanate-based resin. The binder has a long pot life and can be used with lignocellulose substrates having a water content of 10 wt % or more.

Abstract: The present disclosure provides composition having at least one leuco composition conforming to Formula (I): Ar1Ar2Ar3CH??(I) wherein Ar2 and Ar3 are independently a carbocyclic aryl or heteroaryl, and Ar1 is selected from the group consisting of: unsubstituted phenyl, electron deficient carbocyclic aryl, and heteroaryl. The present disclosure also provides a method of detecting an authentic composition and test kits for detecting authentic compositions.

Abstract: The present invention relates to novel cationic azomethine direct dyes of formula (I) and the leuco forms thereof of formula (II), and also to the use thereof for dyeing keratin fibres, in particular human keratin fibres such as the hair: (I) (II) in which formula (I) or (II) X1, X2, R1, R2, R3, R4, R5, R6, n and n? are as defined in the description. The compounds of formula (I) according to the invention can give powerful, chromatic and sparingly selective colourings with good colour build-up, which are resistant to the various attacking factors to which keratin fibres may be subjected, such as inclement weather, light, washing and perspiration.

Abstract: Disclosed are a fluorescent dye, a preparation method and an application thereof. The fluorescent dye has a structure of formula (I), where X and Y are independently selected from O, S, C(CH3)2 and NR6; R2 and R3 are independently hydrogen or a functional group; R1, R4, R5 and R6 are independently selected from functional groups; and Z? is a negative ion. The fluorescent dye has an ability to permeate the living cell membrane, so that it can be used in the fluorescence imaging of living cell microstructures, and can also be used in the STED super-resolution fluorescence imaging and laser scanning confocal microscopy of live cells.

Abstract: The present invention provides a nanoparticle containing a hydrophobic fluorescent substance accumulated therein and a thermosetting resin as a matrix, which nanoparticle, when used for labeling of a biological substance such as a protein or nucleic acid, has brightness sufficient for allowing pathological diagnosis using a fluorescence image obtained thereby. The present invention is a phosphor integrated dots nanoparticles wherein a thermosetting resin contains a structural unit formed from a raw material containing a hydrophobic substituent, and wherein a fluorescent substance is accumulated in the nanoparticle at least by hydrophobic interaction, preferably further by stacking interaction, with the hydrophobic substituent of the thermosetting resin.

Abstract: Water-based coating compositions or paint having improved gloss retention, including a latex or water-dispersible polymer, a UV-VIS absorber comprising a substituted benzophenone capable of being a free radical generator, a hindered amine light stabilizer, and optionally a low-VOC coalescent provided in a preferably desired amount. A composition comprising a blend a UV-VIS absorber comprising a substituted benzophenone capable of being a free radical generator, a hindered amine light stabilizer, and a low-VOC coalescent, providing a thermally-stable coalescent that can be used in a paint formulation for gloss retention. Gloss retention of paints containing the UV-VIS absorber and hindered amine light stabilizer being markedly improved over paints that do not have both components present.

Abstract: The present invention relates to a powder coating formulation, comprising at least one partially crystalline thermoplastic unsaturated polyester (A), at least one thermoplastic allyl prepolymer (B) which is copolymerizable with said polyester, and a thermal initiation system (C), including at least one thermal initiator, wherein the allyl prepolymer (B) has a weight average molar mass greater than 5000 g/mol, preferably greater than 10000 g/mol, and particularly preferably greater than 20000 g/mol, and/or has a viscosity of 30 mPas to 200 mPas, preferably of between 40 mPas and 170 mPas, particularly preferably of between 50 mPas and 150 mPas, and wherein the unsaturated polyester (A) has a melting point of between 90 and 120° C., preferably of 90-110° C., particularly preferably of 90-105° C., and still more preferably of 90-100° C.

Abstract: The invention comprises synergistic compositions of at least one metal polycarboxylate and lithium phosphate. The synergistic compositions are designed to be added to film-forming or other compositions to reduce the corrosion of various metal surfaces or substrates on which the synergistic compositions are applied.