Brominated vinylaromatic-diene block copolymers (Br-SBC) comprising a vinylaromatic polymer block S and a brominated diene polymer block BB, wherein before bromination the weight-average molar mass M.sub.w of the block S is greater than or equal to M.sub.w of the block BB, use thereof as flame retardants, and also polymer compositions comprising these for unfoamed and foamed thermoplastic polymers, for example EPS and XPS.

Brominated vinylaromatic-diene block copolymers (Br-SBC) comprising a vinylaromatic polymer block S and a brominated diene polymer block BB, wherein before bromination the weight-average molar mass M.sub.w of the block S is greater than or equal to M.sub.w of the block BB, use thereof as flame retardants, and also polymer compositions comprising these for unfoamed and foamed thermoplastic polymers, for example EPS and XPS.

The present invention is directed to the functionalization of butyl rubber ionomer and optionally the grafting of polyamide to halobutyl rubber ionomers. Specifically, disclosed are methods and products resulting therefrom for creating functionalized ionomers and grafting polyamide to halobutyl ionomers via reactive extrusion. The process comprises reacting a halobutyl polymer with at least one nitrogen and/or phosphorous based nucleophile to provide a halobutyl ionomer comprising conjugated diene units; grafting of an amine-reactive dienophile to said ionomer to form a functionalized ionomer; and optionally blending the resulting functionalized ionomer with polyamide.

The present invention is directed to the functionalization of butyl rubber ionomer and optionally the grafting of polyamide to halobutyl rubber ionomers. Specifically, disclosed are methods and products resulting therefrom for creating functionalized ionomers and grafting polyamide to halobutyl ionomers via reactive extrusion. The process comprises reacting a halobutyl polymer with at least one nitrogen and/or phosphorous based nucleophile to provide a halobutyl ionomer comprising conjugated diene units; grafting of an amine-reactive dienophile to said ionomer to form a functionalized ionomer; and optionally blending the resulting functionalized ionomer with polyamide.

Provided are a block copolymer having a narrow molecular weight distribution such that the copolymer can be used in a DSA technique, a block copolymer intermediate thereof, and methods for producing the same. A block copolymer intermediate represented by the general formula (1) or (2):

##STR00001##

wherein, in the formulae (1) and (2), each of R.sup.1 and R.sup.3 independently represents a polymerization initiator residue, each of R.sup.2 and R.sup.4 independently represents an aromatic group or an alkyl group, Y.sup.1 represents a polymer block of (a)an (meth)acrylic acid ester, Y.sup.2 represents a polymer block of styrene or a derivative thereof, L represents an alkylene group or a phenylene group, X represents a halogen group, and each of m and n independently represents an integer of 1 to 5.

Provided are a block copolymer having a narrow molecular weight distribution such that the copolymer can be used in a DSA technique, a block copolymer intermediate thereof, and methods for producing the same. A block copolymer intermediate represented by the general formula (1) or (2):

##STR00001##

wherein, in the formulae (1) and (2), each of R.sup.1 and R.sup.3 independently represents a polymerization initiator residue, each of R.sup.2 and R.sup.4 independently represents an aromatic group or an alkyl group, Y.sup.1 represents a polymer block of (a)an (meth)acrylic acid ester, Y.sup.2 represents a polymer block of styrene or a derivative thereof, L represents an alkylene group or a phenylene group, X represents a halogen group, and each of m and n independently represents an integer of 1 to 5.

Provided are a block copolymer having a narrow molecular weight distribution such that the copolymer can be used in a DSA technique, a block copolymer intermediate thereof, and methods for producing the same. A block copolymer intermediate represented by the general formula (1) or (2):

##STR00001##

wherein, in the formulae (1) and (2), each of R.sup.1 and R.sup.3 independently represents a polymerization initiator residue, each of R.sup.2 and R.sup.4 independently represents an aromatic group or an alkyl group, Y.sup.1 represents a polymer block of (a)an (meth)acrylic acid ester, Y.sup.2 represents a polymer block of styrene or a derivative thereof, L represents an alkylene group or a phenylene group, X represents a halogen group, and each of m and n independently represents an integer of 1 to 5.

Provided is a method for preparing a chlorinated polyvinyl chloride resin, and more particularly, a method for preparing a chlorinated polyvinyl chloride resin including a neutralization process for neutralizing to pH of 2 to 5 using metal hydroxide as a first neutralizing agent a), and completing neutralization using a carbonate-based compound as a second neutralizing agent b), wherein residual hydrochloric acid in pores of the chlorinated polyvinyl chloride resin obtained by chlorination of a polyvinyl chloride or a vinyl chloride-based copolymer may be efficiently removed, and thermal stability and extrusion appearance of processed articles may be improved.

A biomimetic ice growth inhibition material is prepared. by constructing a library for structures of compound molecules, with the compound molecules comprising a hydrophilic group and an ice-philic group, by evaluating the spreading performance of each compound molecule at an ice-water interface by adopting molecular dynamics simulation (MD simulation), and by screening the compound molecules with the desired affinities for ice and water. The present invention firstly provides the mechanism of the affinities of the ice growth inhibition material for ice and water, introduces MD simulation into the molecular structure design of the ice growth inhibition material, evaluates the affinities of the designed ice growth inhibition material for ice and water through MD simulation, predicts the ice growth inhibition performance of the ice growth inhibition material, and can realize the optimization of the structure.

A biomimetic ice growth inhibition material is prepared. by constructing a library for structures of compound molecules, with the compound molecules comprising a hydrophilic group and an ice-philic group, by evaluating the spreading performance of each compound molecule at an ice-water interface by adopting molecular dynamics simulation (MD simulation), and by screening the compound molecules with the desired affinities for ice and water. The present invention firstly provides the mechanism of the affinities of the ice growth inhibition material for ice and water, introduces MD simulation into the molecular structure design of the ice growth inhibition material, evaluates the affinities of the designed ice growth inhibition material for ice and water through MD simulation, predicts the ice growth inhibition performance of the ice growth inhibition material, and can realize the optimization of the structure.