The present invention relates to novel color drift-stable compositions of polyisocyanates of (cyclo)aliphatic diisocyanates.

A biodegradable film is prepared from a composition that includes a copolyester obtained by extrusion reaction of a branched aliphatic-aromatic copolyester derived from monomer a, monomer b, monomer c and monomer d with an organic peroxide. The film can be completely degraded into small molecular products such as carbon dioxide, water and the like under natural or composting conditions. Moreover, the film can be prepared having a thickness of 4-50 μm as required, and its mechanical properties can reach the same level as or even better than those of LDPE film.

A resin composition, a light conversion layer and a light emitting device are provided. The resin composition includes a quantum dot (A), an alkali-soluble resin (B), an ethylenically unsaturated monomer (C), a photoinitiator (D), a solvent (E) and a phenyl-based compound (F). The phenyl-based compound (F) includes at least one of a compound represented by following Formula (F-1) and a compound represented by following Formula (F-2). Based on a total usage amount of the resin composition as 100 parts by weight, a usage amount of the phenyl-based compound (F) is 0.05 to 5 parts by weight. ##STR00001##
In Formula (F-1) and Formula (F-2), the definition of R.sup.1, R.sup.3, R.sup.4, Y, Z, m, n and p are the same as defined in the detailed description.

The invention relates to a composite based on at least one, preferably metallic, reinforcing element and on a rubber composition based on at least a. an epoxidized diene elastomer, b. a reinforcing filler, and c. a system for crosslinking the epoxidized diene elastomer comprising at least:
a polyacid compound selected from organopolyphosphorus compounds of general formula (I) and polysulfonic acids of general formula (II), and a polyphenol compound comprising at least two hydroxyl —OH functions on the same aromatic ring,

##STR00001##

in which A represents a covalent bond or a hydrocarbon group comprising at least 1 carbon atom, which is optionally substituted and optionally interrupted by one or more heteroatoms, and the R symbols represent, independently of one another, a hydrocarbon group comprising at least 1 carbon atom or a hydrogen atom;

##STR00002##

in which A′ represents a covalent bond or a hydrocarbon group comprising at least 1 carbon atom, which is optionally substituted and optionally interrupted by one or more heteroatoms.

The present invention relates to a plasticizer composition, a resin composition and a method for preparing thereof. The present invention can provide a plasticizer composition, which can improve properties required to the plasticizer composition contained in a vinyl chloride-based resin composition, such as plasticizing efficiency, volatile loss, and migration resistance, to a level equal to or better than the existing plasticizer composition, and a resin composition comprising thereof.

The present invention relates to a plasticizer composition, a resin composition and a method for preparing thereof. The present invention can provide a plasticizer composition, which can improve properties required to the plasticizer composition contained in a vinyl chloride-based resin composition, such as plasticizing efficiency, volatile loss, and migration resistance, to a level equal to or better than the existing plasticizer composition, and a resin composition comprising thereof.

The present invention is directed to a process for preparing epoxidized polymers. The process comprises reacting an unsaturated polymer with hydrogen peroxide in the presence of a polymer support having a sulfonic acid group. The present invention is also directed to an epoxidized halogenated-polymer which comprises repeating units derived from at least one isoolefin monomer and repeating units derived from at least one diolefinic monomer, and one or more allylic halide groups and one or more oxirane functional groups in the polymer backbone.

The present invention is directed to a process for preparing epoxidized polymers. The process comprises reacting an unsaturated polymer with hydrogen peroxide in the presence of a polymer support having a sulfonic acid group. The present invention is also directed to an epoxidized halogenated-polymer which comprises repeating units derived from at least one isoolefin monomer and repeating units derived from at least one diolefinic monomer, and one or more allylic halide groups and one or more oxirane functional groups in the polymer backbone.

A composite hot-melt adhesive mesh film and preparation process thereof, in particular, a composite hot-melt adhesive mesh film and preparation process thereof for bonding metal and non-polar material are disclosed. The mesh film is compounded of a polar polyamide hot-melt adhesive and a non-polar polyolefin hot-melt adhesive mesh film containing a compatibilizer. The mesh film has a high adhesive strength and a durable and stable adhesion, and is especially suitable for bonding stainless steel, aluminum, copper or other metal materials and polyethylene, polypropylene or other non-polar polymers. Additionally, the preparation process is completed in one set of production process from raw material pretreatment to the final preparation of the hot melt adhesive mesh film product, thereby greatly reducing production failures, and providing high production efficiency and low costs.

A thermoplastic polymer composition (A) leads to reduced migration of stabilisers or other ingredients (I), if it contains e.g. 50 to 90 wt. %, relative to the polymer composition (A), of a thermoplastic polymer (P), which has migration barrier properties, as well as at least one stabiliser component (S) and/or a further ingredient (I), wherein the following is true for the polymer composition (A): a) the glass transition temperature T.sub.g of the thermoplastic polymer (P) is greater than the use temperature; and b) the polymer-specific constant for polymers (Ap) of the thermoplastic polymer (P) is less than I; and c) the derived diffusion coefficient (Dp) of the thermoplastic polymer (P) for mineral oil is less than 10.sup.−12 cm.sup.2/s at 20° C.; and d) the morphology of the thermoplastic polymer (P) is either single-phase homogeneous, or two-phase heterogeneous.