A dual-cure method for forming a solid polymeric structure is provided. An end-capped, imide-terminated prepolymer is combined with at least one photopolymerisable olefinic monomer, at least one photoinitiator, and a diamine, to form a curable resin composition, which, in a first step, is irradiated under conditions effective to polymerize the at least one olefinic monomer, thus forming a scaffold composed of the prepolymer and the polyolefin with the diamine trapped therein. The irradiated composition is then thermally treated at a temperature effective to cause a transimidization reaction to occur between the prepolymer and the diamine, thereby releasing the end caps of the prepolymer and providing the solid polymeric structure. A curable resin composition comprising an end-capped, imide-terminated prepolymer, at least one photopolymerisable olefinic monomer, at least one photoinitiator, and a diamine, is also provided, as are related methods of use.

Disclosed are single step and multi-step methods of making functional polyisobutylene (PIB)-containing oligomers and polymers and the materials made thereby. In the single step method a functional group containing PIB oligomer or polymer is made under cationic polymerization conditions in a direct, one step reaction. In the multi-step method a functional group containing PIB oligomer or polymer is made in a two-step process. The first step is performed under cationic polymerization conditions. The second step is performed under non-cationic polymerization conditions.

The present invention was made in view of the foregoing problem and has an object to provide a photocurable resin composition which can be quickly cured by irradiation with active energy rays such as ultraviolet rays and achieves excellent adhesion to polyolefin such as PP having properties difficult to bond. Specifically, provided is a photocurable resin composition containing the following (A) and (B) ingredients: (A) ingredient: a polymer having a polyisobutylene backbone mainly containing a —[CH.sub.2C(CH.sub.3).sub.2]— unit, the polymer having one or more (meth)acryloyl groups per molecule; and (B) ingredient: a photo-radical initiator of hydrogen abstraction type.

The present disclosure provides a modified polyvinyl alcohol-based polymer, which comprises a modifying monomer unit represented by Formula ##STR00001## wherein, X is a moiety comprising an alkenyl group, and the modified polyvinyl alcohol-based polymer has a saponification degree of 67 mol % to 78 mol % and a modification rate of 0.02 mol % to 1.5 mol %. The modified polyvinyl alcohol-based polymer is suitable to be used as a dispersant for suspension polymerization, to make the obtained polyvinyl chloride-based resin have reduced particle diameter and few coarse particles.

The present application relates to an encapsulant for a PV module, a method of manufacturing the same and a PV module. The encapsulant according to an embodiment of the present application has excellent heat resistance or the like and improved creep physical properties, and thus even when the encapsulant is used under conditions of a high temperature and/or high humidity for a long time, deformation is small and the encapsulant can exhibit excellent adhesive strength. Accordingly, when the encapsulant is applied to a PV module, durability or the like may be improved.

The present disclosure relates to a method for producing polymer microparticles, this method including a step for polymerizing vinyl monomers in a hydrophilic solvent, which dissolves the vinyl monomers and a dispersion stabilizer but does not dissolve a polymer formed, in the presence of the dispersion stabilizer. The present disclosure is a method for producing these polymer microparticles, wherein the dispersion stabilizer contains a macromonomer having carboxyl groups and ethylenically unsaturated groups at an intermediate location in a molecular chain thereof, the macromonomer has, on average, 1.4 to 2.5 ethylenically unsaturated groups per molecule, and an average value of a carboxyl group content in the macromonomer is 0.5 meq/g to 2.5 meq/g.

A curable composition may include 100 parts by weight of a polyisobutylene-based polymer (A) having 1.2 or more (meth)acryloyl groups per molecule, 15 to 900 parts by weight of a polyisobutylene-based polymer (B) having 0.5 to 1.0 (meth)acryloyl group per molecule, and 0.001 to 50 parts by weight, per 100 parts by weight of the total weight of the polymer (A) and the polymer (B), of a polymerization initiator (C). Each of the polymer (A) and the polymer (B) may have a number average molecular weight of 500 to 500,000 as measured by size exclusion chromatography based on polystyrene standards, and a molecular weight distribution (weight-average molecular weight Mw)/(number-average molecular weight Mn) of 1.0 to 2.0.

Low molecular weight, highly branched polyolefins are provided. Also provided are catalyst-mediated methods of making the low molecular weight, highly branched polyolefins and a catalyst system for carrying out the methods. The catalyst system is a homogeneous catalytic system that includes a single-site organozirconium complex and hydrocarbon-soluble perfluoroarylborate co-catalyst that is highly active for the oligomerization of olefin monomers in non-polar media.

The present invention relates to a solid catalyst for propylene polymerization and a method of producing a propylene polymer or copolymer using the solid catalyst for propylene polymerization, and provides a solid catalyst which prepares a dialkoxymagnesium carrier and is formed of a carrier produced through a reaction of the carrier with a metal halide, a titanium halide, an organic electron donor, etc., and a method of producing a propylene polymer or copolymer through copolymerization of propylene-alpha olefin using the solid catalyst, wherein the dialkoxymagnesium carrier has an uniform particle size range of 10 to 100 μm and a spherical particle shape by adjusting injection amounts, injection numbers, and reaction temperatures of metal magnesium, alcohol and a reaction initiator during a reaction process of metal magnesium and alcohol.

The present invention relates to a fluorine-containing alternating copolymer macromonomer and a synthesis method thereof. The synthesis method comprises steps of: subjecting a fluorine-containing alternating copolymer to a reduction reaction at 60-100° C. in an organic solvent in the presence of a reducing agent and a first catalyst to obtain a reduction product; in the presence of a second catalyst, reacting the reduction product with a mercapto-monohydric alcohol in an organic solvent at 60-100° C., to obtain a hydroxyl-terminated fluorine-containing alternating copolymer; and in the presence of a third catalyst, reacting the hydroxyl-terminated fluorine-containing alternating copolymer with an acrylic monomer or acryloyl chloride monomer at 0-30° C., to obtain the fluorine-containing alternating copolymer macromonomer. In the present invention, a fluorine-containing alternating copolymer macromonomer is initially synthesized from a fluorine-containing alternating copolymer through polymer modification.