Abstract: The present invention relates to a method for preparing a macromolecular composition comprising indene-derivatives. The invention also relates to the macromolecular compositions per se, and to methods of using the macromolecular compositions. The macromolecular compositions are useful for undergoing subsequent reactions with small molecules.

Abstract: A process for preparing a functionalized polybutadiene is provided. The process comprises the following steps: a) homopolymerising butadiene with a catalytic system based on at least one preforming conjugated diene, a salt of one or more rare earth metals of an organic phosphoric acid, an aluminium-containing alkylating agent, an alkylaluminium halide; b) adding a polyfunctional compound to the pseudo-living elastomer formed in step (a); and c) adding a functionalizing agent to the mixture formed in step (b). The total molar amount of aluminium in the polymerization medium is such that the (aluminium/rare earth salt) molar ratio has a value between 1 and 5 and the polymerization is carried out at a temperature between 40° C. and 90° C. A functionalized polybutadiene that can be obtained by the process, and a rubber composition containing the functionalized polybutadiene is also provided.

Abstract: An acrylated and/or methacrylated urethane oligomer obtained by reaction of a specific polyamine with a cyclic carbonate compound carrying m cyclic carbonate groups, giving an intermediate product carrying m formed urethane groups which carry residual reactive amine —NH— groups, and subsequently an addition reaction of each of the residual reactive amine groups of the intermediate product with an acrylate group of a compound carrying, in addition to the acrylate group, p additional acrylate and/or methacrylate groups, with each residual reactive amine —NH— group of the intermediate product being thus converted into a carbon-nitrogen bond carrying the acrylate and/or methacrylate groups, and thus production of the urethane oligomer, with the urethane oligomer carrying m urethane groups and m hydroxyl groups and having a functionality in acrylates and/or methacrylates ranging from m*p(n?1) to m*p(2n?2).

Abstract: The present invention provides a fluorescent molecular probe for efficient fluorescent detection (visualization) of tumors or for implementing fluorescent detection and photodynamic treatment, more specifically, the present invention provides a macromolecular fluorescent molecular probe for fluorescent detection of tumor, comprising a complex comprising a fluorescent molecule and a biocompatible macromolecule.

Abstract: A three-dimension forming support material for ink jet includes a warm water-soluble radiation curable compound that exhibits solubility in warm water of at least 40° C. to 90° C. after the compound is cured; and at least one polyglycerin compound selected from the group consisting of fatty acid esters of polyglycerin, ethylene oxide adducts of polyglycerin, and propylene oxide adducts of polyglycerin.

Abstract: Polyarylene sulfide compositions are described that exhibit high strength and flexibility. Methods for forming the polyarylene sulfide compositions are also described. Formation methods include dynamic vulcanization of a polyarylene sulfide composition that includes an impact modifier dispersed throughout the polyarylene sulfide. A crosslinking agent is combined with the other components of the composition following dispersal of the impact modifier throughout the composition. The crosslinking agent reacts with the impact modifier to form crosslinks within and among the polymer chains of the impact modifier. The compositions can exhibit excellent physical characteristics at extreme temperatures and can be used to form, e.g., tubular member such as pipes and hoses and fibers.

Abstract: The invention relates to a method for reacting polymers (A) comprising hydroxyl groups and which have repetitive structural units of general formula (I), wherein D represents a direct bond between the polymer backbone and a hydroxyl group, a C1- to C6-alkene group, a C5- to C12-arylene group, an oxyalkylene group of formula —O—R2—, an ester group of formula —C(O)—O—R2— or an amide group of formula —C(O)—N(R8)R2—, R2 represents a C2- to C10-alkene group, R8 represents hydrogen or an optionally substituted C2- to C10-alkyl group and n represents a number between 3 and 5000, with carboxylic acids B1) of formula (II) or carboxylic acid esters B2) of formula (III) R1—COOH (II) R1—COOR7 (III), wherein R1 represents a hydrocarbon group having 2 to 50 C atoms, and R7 represents a C1C4-alkyl group, in which the polymers (A); comprising the hydroxyl groups are exposed to microwaves in the presence of carboxylic acids of formula (II) or carboxylic acid esters of formula (III) and in the presence of water.

Abstract: A durable, injection moldable, thermoplastic elastomer that has the favorable resilience, feel, spin, barrier, and UV stability performance attributes is disclosed herein. An OBC grafted with silane provides a good cover shear durability (cut/tear/abrasion resistance). This invention combines the benefits of OBCs and silane crosslinking technology to yield a golf ball cover with a desirable combination of properties.

Abstract: The present invention provides novel, modified polydicyclopentadienes and methods to prepare modified polydicyclopentadienes. The modified polydicyclopentadienes prepared by the methods of the invention are useful in many applications including new and useful solid phases for chromatography.

Abstract: Metallated aminosilane compounds for use as functional initiators in anionic polymerizations and processes for producing an aminosilane-functionalized polymer using the metallated aminosilane compounds to initiate anionic polymerization of at least one type of anionically polymerizable monomer. Preferred use of the metallated aminosilane compounds results in rubber compositions for use in tires comprising an aminosilane functionalized polymer. A telechelic polymer may result from use of the metallated aminosilane compound as a functional terminator.

Abstract: A quaternized copolymer obtainable by: (A) copolymerization of straight-chain, branched or cyclic, ethylenically unsaturated C2 to C100 hydrocarbons, which may bear oxygen- or nitrogen-functional substituents which cannot be reacted with amines to give amides or imides or with alcohols to give esters, with ethylenically unsaturated C3- to C12-mono- or dicarboxylic acids or acid derivatives, which can be reacted with amines to give amides or imides or with alcohols to give esters, to give a copolymer with a number-average molecular weight of 500 to 20 000; (B) partial or full amidation or imidation or esterification of the carboxylic acid functions by reacting them with oligoamines having 2 to 6 nitrogen atoms or alcoholamines, each of which comprises primary or secondary nitrogen atom or a hydroxyl group and a quaternizable tertiary nitrogen atom; (C) partial or full quaternization of the tertiary nitrogen atom with a quaternizing agent.

Abstract: The retardation film of the present invention contains a thermoplastic polymer having at least a side chain component (A) oriented in a direction substantially orthogonal to a slow axis, and the absorption edge wavelength (?cut-off) of the side chain component (A) is 330 nm or more, and an in-plane retardation value (Re[450]) at a wavelength of 450 nm is smaller than that (Re[650]) at a wavelength of 650 nm. In the above-mentioned retardation film, the difference (?Re650-450=Re[650]?Re[450]) between the in-plane retardation value (Re[650]) at a wavelength of 650 nm and the in-plane retardation value (Re[450]) at a wavelength of 450 nm is preferably 10 nm or more. The retardation film of the present invention exhibits optical characteristics in which the in-plane birefringence is large and the difference between a retardation value on the short wavelength side and a retardation value on the long wavelength side is large.

Abstract: A polymer having a carbon-carbon double bond in a main chain is decomposed by subjecting the carbon-carbon double bond to oxidative cleavage using an oxidizing agent such as periodic acid to decrease the molecular weight, polymer chains of the decomposed polymer are combined by changing acido-basic properties such that a system containing the decomposed polymer becomes basic when acidic and becomes acidic when basic, and a modified polymer in which the structure has been changed is obtained. By this, a functional group can be incorporated in the main chain structure of a polymer. A rubber composition comprising a rubber component containing the modified polymer, and a filler compounded therewith, and a pneumatic tire comprising the rubber composition are provided.

Abstract: A method of decomposing an organic compound includes decomposing an organic compound by alkyl carbonate at 250° C. or more. The organic compound includes a cross-linked polymer. The cross-linked polymer includes a polymer cross-linked by organic peroxide cross-linking, radiation cross-linking, or silane cross-linking The alkyl carbonate includes dimethyl carbonate or diethyl carbonate.

Abstract: The present invention is concerned with an emulsion copolymer latex comprising an acrylic/methacrylic copolymer obtainable by the emulsion copolymerisation of the following monomer components: A: from 75% weight to 97.5% by weight, based on the total weight of monomer components A+B+C+D, of methyl acrylate; B: from 0.1% to 15% by weight, based on the total weight of monomer components A+B+C+D, of at least one ethylenically unsaturated carboxylic acid monomer containing one C?C double bond capable of free radical copolymerisation with component A and at least one carboxylic acid (CO2H) group; C: from 1% to 20% by weight based on the total weight of monomer components A+B+C+D of at least one associative monomer being a (meth)acrylate ester of an alkoxylated alcohol; and D: from 0% to 15% by weight of one or more non-ionic ethylenically unsaturated monomers other than those defined above as A, B or C; wherein the total monomer components A+B+C+D together add up to 100%.

Abstract: Vulcanizates with desirable properties can be obtained from compounds incorporating polymers that include hydroxyl group-containing aryl functionalities. The functionalities can be incorporated by using any or all of appropriate initiators, monomers and optional terminating compounds. Such polymers exhibit excellent interactivity with both conventional and non-conventional fillers.

Abstract: The invention relates to a process and an apparatus for the preparation of a crosslinkable rubber mixture for vehicle tires, lines, drive belts and other industrial rubber articles, which can be carried out at least semicontinuously. The present invention is based on the discovery that the experiments known from the prior art to carry out the batchwise process usually used at least partly continuously have failed in particular because of the problem that the crosslinking agents have to be mixed rapidly and homogeneously with the base mixture, also referred to as rubber base mixture, without the mixture consisting of the base mixture and the crosslinking agents heating up too strongly. According to the invention, attention was therefore focussed on reliably mixing the base mixture homogeneously with the crosslinking agents and minimizing the mixing time. A first measure for achieving the desired aim consists in first mixing the crosslinking agents with one another before they are mixed with the base mixture.

Abstract: The present invention relates to resin pellets which comprises a thermoplastic resin (A) and an oxidation catalyst (B) which is not supported by any carrier, wherein if the peak area in the vicinity of 1715 cm?1 is defined to be Ic and the peak area observed in the vicinity of 1470 cm?1 is defined to be Im in the IR spectroscopic measurement of the pellets, the ratio: Ic/Im observed for the surface of the pellet is greater than that observed for the interior thereof. The pellets are thermoplastic resin pellets excellent in the oxygen-absorbing capacity and accordingly, they can suitably used as pellets for molding an oxygen absorptive resin article.

Abstract: A durable, injection moldable, thermoplastic elastomer that has the favorable resilience, feel, spin, barrier, and UV stability performance attributes is disclosed herein. An OBC grafted with silane provides a good cover shear durability (cut/tear/abrasion resistance). This invention combines the benefits of OBCs and silane crosslinking technology to yield a golf ball cover with a desirable combination of properties.

Abstract: This invention relates to resins useful for drainage in papermaking and the process of making paper using the resins. In particular the invention relates to glyoxalated copolymers of acrylamide containing significant amounts of cationic comonomer.

Abstract: The invention generally relates to chain shuttling agents (CSAs), a process of preparing the CSAs, a composition comprising a CSA and a catalyst, a process of preparing the composition, a processes of preparing polyolefins, end functional polyolefins, and telechelic polyolefins with the composition, and the polyolefins, end functional polyolefins, and telechelic polyolefins prepared by the processes.

Abstract: The invention generally relates to chain shuttling agents (CSAs), a process of preparing the CSAs, a composition comprising a CSA and a catalyst, a process of preparing the composition, a processes of preparing polyolefins, end functional polyolefins, and telechelic polyolefins with the composition, and the polyolefins, end functional polyolefins, and telechelic polyolefins prepared by the processes.

Abstract: The present invention generally relates to processes for converting an ester group to an acid group for polymers having a pendant ester of an acid group. This process is generally performed using an aqueous strong base.

Abstract: The method for manufacturing a polymer of the present invention is a method for manufacturing a polymer where a hydroxy group is added to a terminal of either one of a homopolymer of a non-conjugated olefin, a homopolymer of a conjugated diene compound, and a copolymer of a conjugated diene compound and a non-conjugated olefin, the method comprising: a first reaction step of reacting a hydrocarbon containing at least either one of the non-conjugated olefin and the conjugated diene compound with an organic aluminum compound, using a rare earth element compound-containing catalyst; a second reaction step of reacting a first reactant obtained from the first reaction step with oxygen; and a third reaction step of reacting a second reactant obtained from the second reaction step with at least either one of water and alcohol.

Abstract: The present invention provides a solid support for Fmoc-solid phase synthesis of peptides. In particular, the solid supports of the invention may be utilized to produce peptide acids.

Abstract: This invention relates to a functionalized co-oligomer having an Mn of 300 to 30,000 g/mol comprising 10 to 90 mol % propylene and 10 to 90 mol % of ethylene, wherein the oligomer has at least X % allyl chain ends, where: 1) X=(?0.94 (mole % ethylene incorporated)+100), when 10 to 60 mole % ethylene is present in the co-oligomer, and 2) X=45, when greater than 60 and less than 70 mole % ethylene is present in the co-oligomer, and 3) X=(1.83*(mole % ethylene incorporated)?83), when 70 to 90 mole % ethylene is present in the co-oligomer. This invention also relates to a functionalized homo-oligomer, comprising propylene, wherein the oligomer has: at least 93% allyl chain ends, an Mn of about 500 to about 20,000 g/mol, an isobutyl chain end to allylic vinyl group ratio of 0.8:1 to 1.2:1.0, and less than 100 ppm aluminum. This invention also relates to a process of making functionalized homo- or co-oligomer, comprising propylene, wherein the productivity is greater than 4500 g/mmol Hf (or Zr)/hour.

Abstract: Provided is a treatment method for fluororesin pellets to remove hydrofluoric acid released from fluororesin pellets obtained by melt-molding a melt-moldable fluororesin. The treatment method comprises bringing a hydrofluoric acid-removing medium selected from warm water of from 30 to 200° C., steam of from 100 to 200° C. and warm wind of from 40 to 200° C. into contact with fluororesin pellets obtained by melt-molding a melt-moldable fluororesin, and thereby treating the fluororesin pellets so that the amount of hydrofluoric acid released per kg of the resulting fluororesin pellets would be at most 5 ?g as determined after the storage of the resulting fluororesin pellets at 35° C. for 15 days.

Abstract: This invention provides a polyfunctional polymer having high stereoregularity, in particular, isotacticity, and provides a production process thereof. The present invention relates to a polymer having, in a molecule, a repeating unit represented by General Formula (2): wherein R1 and R2 are different, and each represents a hydrogen atom, an alkyl group and an aryl group; * represents an asymmetrical carbon, the polymer containing meso diad (m) and racemo diad (r) at a proportion of 60:40 to 100:0 (m:r). The invention also relates to chemical modifications and a production process of the polymer.

Abstract: The instant invention pertains to the preparation of polymers or copolymers wherein in a first step a controlled free radical polymerization process is carried out and in a second step the resulting polymer is modified by transesterification reactions. The final modified polymer or copolymer is useful as a dispersant for pigments. Further aspects of the invention are the thus prepared polymers or copolymers, a pigment concentrate containing the polymer or copolymer and a coating material containing the pigment concentrate.

Abstract: From a viewpoint of reduction in an out of spec product after surface crosslinking, particularly, when an alkylene carbonate compound is used as a surface crosslinking agent, influence by an air temperature is great, and it is necessary to reduce ethylene glycol which is produced as a byproduct, and there is provided a process for producing a polyacrylic acid (salt)-based water absorbent resin powder, comprising a step of polymerizing an aqueous acrylic acid (salt)-based monomer solution, a step of drying the resulting polymer, an optional grinding•classifying step, and a surface crosslinking step, wherein in the surface crosslinking step, (1) a surface crosslinking agent containing an alkylene carbonate compound and a polyhydric alcohol compound is mixed into a water absorbent resin powder, the mixture is heat-reacted and, further, simultaneously with, or separately from the mixing, an ion reactive surface crosslinking agent is mixed, and/or (2) mixing treatment of mixing a surface crosslinking agent solu

Abstract: A method for extracting nucleic acids from a biological material such as blood comprises contacting the mixture with a material at a pH such that the material is positively charged and will bind negatively charged nucleic acids and then eluting the nucleic acids at a pH when the said materials possess a neutral or negative charge to release the nucleic acids. The nucleic acids can be removed under mildly alkaline conditions to the maintain integrity of the nucleic acids and to allow retrieval of the nucleic acids in reagents that are immediately compatible with either storage or analytical testing.

Abstract: A method for preparing a functionalized polymer, the method comprising the steps of (i) polymerizing conjugated diene monomer by employing a lanthanide-based catalyst to form a reactive polymer, and (ii) reacting the reactive polymer with a protected oxime compound.

Abstract: A homogeneously surface cross-linked water absorbent resin and a method for the production thereof are provided. The water absorbent material is formed of a surface cross-linked water absorbent resin resulting from granular irregularly pulverized shaped surface cross-linking the product of partial neutralization or whole neutralization of a water absorbent resin having acrylic acid or a metal salt thereof as a main component, which water absorbent material shows a metal atom concentration on the surface of the water absorbent material in the range of 0-10% within 0 second of polishing and 2-35% at 10 seconds value of polishing as determined by subjecting the water absorbent material to Ar ion discharge polishing under a voltage of 500 ?. The surface cross-linked water absorbent resin to be used herein can be produced by surface cross-linking a water absorbent resin having a specific particle diameter with a surface cross-linking agent having a water concentration in a specific range.

Abstract: There is provided an adhesive composition comprising (i) at least one film forming polymer, (ii) at least one crosslinker selected from the group consisting of polynitroso compounds, polynitroso precursors, and mixtures thereof, and (iii) at least one oxidizer, wherein the molar ratio of oxidizer to crosslinker is from 0.3 to 2.0. Also provided is a method of bonding substrates together using such a composition, and an article made using such a method.

Abstract: The present disclosure is directed to a continuous process for preparing cellulose reactive adducts of polyvinylamide.

Abstract: Storage-stable glyoxalated polyacrylamide polymers and high solids aqueous compositions formulated with them are described. These glyoxalated polyacrylamide compositions can be used as additives for papermaking, providing paper with good dry and temporary wet strength, and increasing papermaking de-watering rates.

Abstract: The invention relates to a composition that can be thermally cured, containing relative to the total composition, a) 5 to 90% by weight of a diene-based polymer or copolymer containing an olefinic double bond and/or an aromatically substituted olefin, wherein the polymer or copolymer is liquid, or paste-like, at 22° C. and has a glass transition temperature between ?30° C. and +15° C., measured according to a DSC method; b) a vulcanization system selected from the group consisting of: b1) sulfur, and one or more accelerator(s), b2) peroxidic or disulfidic vulcanization systems, b3) quinones, quinone dioximes, or dinitrosobenzene.

Abstract: Disclosed is a selected type of copolymer composition comprising copolymers having units derived from ethylene and dicyclopentadiene (DCPD) co-monomers. Such copolymer compositions: a) have a DCPD-derived comonomer unit content of from about 25 mole % to about 45 mole %; b) have a Weight Average Molecular Weight, Mw, of greater than about 170,000; c) comprise amorphous material and have glass transition temperatures, Tg, of from about 8° C. to about 129° C., which also fit the equation Tg (in ° C.)?[(mole % DCPD×3.142)?4.67]; and d) comprise no significant amount of crystalline polyethylene homopolymer or crystallizable polyethylene segments within the ethylene-dicyclopentadiene copolymers. Such copolymers can be readily derivatized by hydrogenation and/or epoxidation to provide polymeric materials suitable for use as engineering thermoplastics.

Abstract: The invention provides a method for producing a polymeric photoinitiator, of the general formula I: Polymer-[CR2-CHR-Spacer(PI)n]m (I) wherein m is an integer from 1-5000; n is a real number above 0 and below 5; R is as defined herein, and PI is a photoinitiator moiety. The method comprises grafting one or more photoinitiator moieties (PI), each of which comprises at least one activated alkene functional group, onto the polymer. Polymeric photoinitiators are also provided.

Abstract: This invention relates to a functionalized co-oligomer having an Mn of 300 to 30,000 g/mol comprising 10 to 90 mol % propylene and 10 to 90 mol % of ethylene, wherein the oligomer has at least X % allyl chain ends, where: 1) X=(?0.94(mole % ethylene incorporated)+100), when 10 to 60 mole % ethylene is present in the co-oligomer, and 2) X=45, when greater than 60 and less than 70 mole % ethylene is present in the co-oligomer, and 3) X=(1.83*(mole % ethylene incorporated)?83), when 70 to 90 mole % ethylene is present in the co-oligomer. This invention also relates to a functionalized homo-oligomer, comprising propylene, wherein the oligomer has: at least 93% allyl chain ends, an Mn of about 500 to about 20,000 g/mol, an isobutyl chain end to allylic vinyl group ratio of 0.8:1 to 1.2:1.0, and less than 100 ppm aluminum. This invention also relates to a process of making functionalized homo- or co-oligomer, comprising propylene, wherein the productivity is greater than 4500 g/mmol Hf (or Zr)/hour.

Abstract: The present invention relates to a novel multi functional additive grafted rubber. More particularly the present invention relates to novel grades of rubber and in particular to chemically grafted with cardanol (meta-penta decenyl phenol) and/or its derivatives. Importantly the rubber grades of the invention involve chemically anchored/grafted selective meta alkenyl phenol and/or its derivatives in the backbone of natural or synthetic rubber. Importantly, such rubber variant of the invention have high plasticity, lower Mooney and melt viscosities, better cure properties as compared to conventional virgin natural rubber or natural rubber plasticized with aromatic process oils.

Abstract: [Problem] To provide a conjugated diene polymer cyclized product free from coloring, a conjugated diene polymer cyclized product that has a narrow molecular weight distribution and is free from coloring, and a method for producing these conjugated diene polymer cyclized products. [Means for Resolution] A conjugated diene polymer cyclized product having a Gardner color scale of not more than 3.0. A conjugated diene polymer cyclized product having a Gardner color scale of not more than 3.0 and a ratio of weight average molecular weight/number average molecular weight of not more than 1.5. A method for producing a conjugated diene polymer cyclized product includes adding water to a conjugated diene polymer solution obtained by polymerizing a conjugated diene in a solvent by using an organoalkali metal compound as an initiator, thereby terminating the polymerization and then subjecting the subject conjugated diene polymer to a cyclization reaction.

Abstract: A polymer formed by controlled radical polymerization includes groups that can be modified after controlled radical polymerization to form a radical. The polymer can be the reaction product of a controlled radical polymerization of radically polymerizable monomers, wherein at least one of the radically polymerizable monomers includes at least one group that can be modified after the controlled radical polymerization to form a radical. A compound includes a first group that is stimulated upon application of energy to the molecule to tether the molecule to a surface or to another polymer chain and a second group comprising a controlled radical polymerization initiator functionality. A block copolymer includes at least a first segment to impart a predetermined functionality to a target surface and at least a second segment including functional groups to interact with the targeted surface to attach the block copolymer to the surface.

Abstract: The present invention relates to a method for radically curing an unsaturated polyester resin or vinyl ester resin composition, wherein the resin composition contains at least 10 ppm radical inhibitor; the resin composition has an acid value of from 0.001 to 300 mg KOH/g resin composition and the curing is effected in the presence of at least 5 mmol Mn/kg primary resin system and at least 10 mmol of thiol/kg primary resin system. The invention also relates to cured objects or structural parts obtained from a resin composition obtained by such a process.

Abstract: A fluororubber composition according to the present invention contains 0.1 to 3 parts by weight of a polyol compound, 0.1 to 4 parts by weight of a peroxide crosslinking agent, and 1 to 9 parts by weight of a co-crosslinking agent per 100 parts by weight of a peroxide-crosslinkable fluoropolymer. A crack-resistant seal according to the present invention contains a crosslinked fluoropolymer and a polyol compound. The crack-resistant seal according to the present invention can be formed by crosslinking the fluororubber composition, and the resultant crack-resistant seal has particularly high crack resistance. With the fluororubber composition according to the present invention, a durable crack-resistant seal having high plasma resistance, crack resistance, and compression set and that produces few particles can be formed at low cost.

Abstract: Method for producing an oxidized PAN fiber (OPF) wherein a PAN fiber is subjected to an oxidation process in which reactive oxidizing species are maintained in close enough proximity to the PAN fiber during the oxidation process such that a core of the PAN fiber is converted to a crosslinked thermoset morphology before an oxidized shell of the PAN fiber becomes thick enough to substantially inhibit penetration of the reactive oxidizing species into the core. The resulting OPF possesses a density greater than 1.35 g/cm3 and a substantially homogeneous crosslinked thermoset morphology along a radial dimension of the oxidized PAN fiber. Flame-retarded materials containing the resulting OPF, as well as methods for producing such flame-retarded materials, are also described.

Abstract: The present invention relates to a process for producing an interpenetrating polymer network structure, which comprises the steps of impregnating a polymer molding with a radical polymerizable composition containing an ethylenically unsaturated compound and a radical polymerization initiator; and polymerizing the ethylenically unsaturated compound in a swollen state of the polymer molding impregnated with the radical polymerizable composition; wherein a chain transfer agent and/or a radical polymerization inhibitor are added to the radical polymerizable composition and/or the polymer molding before impregnating the polymer molding with the radical polymerizable composition. According to the present invention, a highly uniform interpenetrating polymer network structure can be obtained.

Abstract: The present invention is directed to compositions comprising a cellulose reactive functionalized polyvinylamine first adduct, compositions comprising combinations of the cellulose reactive functionalized polyvinylamine first adduct and cellulose reactive functionalized polyvinylamide second adduct, methods for preparing first adduct and second adduct blends and finally methods of increasing the wet or dry strength of paper by incorporation into the paper furnish or coating a paper or board with said adducts.

Abstract: The present invention is directed to a method for preparing a cellulose reactive adduct of polyvinylamide and a composition resulting from the method. The preparation of the cellulose reactive adduct is carried out close to a Critical Concentration defined herein. When the reaction is run close to this Critical Concentration, the risk of gelation is minimized, consumed glyoxal is maximized, and shelf live is enhanced. Additionally, the glyoxalated vinylamides of the present invention impart improved wet and dry strengthening efficiency to paper and paperboard when compared to adducts disclosed in previously described art.

Abstract: Described is a pre-adhesive, curable composition comprising an acid-functional (meth)acrylate copolymer and a novel (meth)acryloyl-aziridine crosslinking agent, which when crosslinked provides a pressure-sensitive adhesive composition.