C08F2810/50

PROCESS FOR PRODUCING A POLYETHYLENE COMPOSITION USING MOLECULAR WEIGHT ENLARGEMENT

The present invention provides a process for producing a polyethylene composition by treating a cross-linkable ethylene copolymer containing monomer units with hydrolysable silane-groups and polar monomer units. The invention further provides a treated cross-linkable polyethylene composition 5 obtained by the process and a silane-crosslinked polyethylene composition obtained by the process. The invention further provides articles comprising the treated cross-linkable polyethylene composition or comprising the silane-crosslinked polyethylene composition.

UV CURABLE ADHESION PROMOTERS BASED ON FUNCTIONALISED POLYVINYL ALCOHOLS

Suggested are new adhesion promoters, which are particular suitable for use in displays. Its inclusion in the polymerisable LC mixture results in an excellent adhesion on substrate without colouration over time i.e. compared to amino siloxanes. The new additives have no effect on alignment of LC on the substrate while improving the adhesion.

MALEIMIDE COPOLYMER, METHOD FOR PRODUCING SAME, RESIN COMPOSITION AND INJECTION MOLDED BODY

A maleimide based copolymer, manufacturing method thereof, and a resin composition using the maleimide based copolymer is provided. The maleimide based copolymer includes 40 to 60 mass % of aromatic vinyl monomer unit, 5 to 20 mass % of vinyl cyanide monomer unit, 35 to 50 mass % of maleimide monomer unit, and 0 to 10 mass % of monomer copolymerizable with these monomer units. The maleimide based copolymer has a glass transition temperature of 165° C. or higher and a melt mass flow rate of 25 to 80 g/10 min measured at 265° C. with 98 N load. By using such maleimide based copolymer, flowability can be improved without decreasing heat resistance providing ability.

Single-ion conductive polymers for electrochemical devices

A solid single-ion conductive polymer comprising a repeat unit of formula (Ia): ##STR00001## wherein R.sup.1 is H, or C.sub.1 to C.sub.16 linear or branched alkyl, alkenyl, alkinyl; m is 1 to 5; each M.sup.+ is independently selected from Li.sup.+, Na.sup.+ or K.sup.+; and X is selected from CF.sub.3, CH.sub.3, or F; and the polymer has an average molecular weight of 350.000 to 1.200.000 Da.

ANTIMICROBIAL NANOWORMS
20220331262 · 2022-10-20 ·

At least one nanoworm comprises a plurality of alkene units and a plurality of macroCTA polymer units. The macroCTA polymer units include R.sup.1 groups from reversible addition-fragmentation chain-transfer agents. In certain aspects, the R.sup.1 groups of the macroCTA polymer units are functional groups, such as a carboxylic acid, an alkyne, a pyridine, a dopamine, a thiolactone, a biotin, an azide, a peptide sequence, a sugar sequence, a protease, a glycanase, a polymer, other functional groups, and combinations thereof. In certain aspects, the macroCTA polymer units comprise quaternized amines, In certain aspects, the macroCTA polymer units comprise functionalized quaternized amines, such as an alkyl group, a carboxylic acid, an alkyne, a pyridine, a dopamine, a thiolactone, a biotin, an azide, a peptide sequence, a sugar sequence, a protease, a glycanase, a polymer, other functional groups, and combinations thereof. In certain aspects, the coating comprises the at least one nanoworm.

Polymer for treating hair

The present invention relates to a polymer comprising repeating units derived from at least one first monomer (monomer A) which is a molecule comprising a thiolactone ring and an ethylenically unsaturated, polymerizable double bond, and at least one second monomer (monomer B) which is N-vinyl pyrrolidone. Furthermore the present invention relates to a modified polymer, the structure of which is identical to the structure of the said polymer apart from the only difference, which is that all or at least some of the thiolactone moieties of the said polymer are modified by opening the thiolactone ring with a substance selected from the group consisting of ammonia, a primary amine, 2-amino-1-ethanol and L-lysine, wherein the N-atom of said substance is binding to the carbonyl group of the opened thiolactone ring. Furthermore, the present invention relates to a process for making the modified polymer and to the use of the polymer or of the modified polymer for treating hair.

Post-Polymerization Functionalization of Pendant Functional Groups

Modification of functional groups along a polymer backbone to render the groups activatable upon exposure to actinic radiation is described. The polymers are typically controlled architecture polymers. Also described are adhesives containing the modified architectured polymers and related methods of use.

Porous membranes including triblock copolymers

A porous membrane includes a triblock copolymer of the formula ABC. B is a hydrogenated vinyl aromatic block present in a range from 30 to 90 weight percent, based on the total weight of the copolymer and has a T.sub.g of ≥110° C. C is a rubbery block present in a range from 10 to 70 weight percent, based on the total weight of the copolymer and has a T.sub.g≤25° C. A is substantially incompatible with both the B and C blocks and is derived from ring-opening polymerization. B+C is present in a range from 70 to 95 weight percent, based on the total weight of the copolymer.

Click-active Janus particles and methods for producing and using the same

A method for producing a click-active Janus particle includes combining seed particles with a monomer emulsion to obtain monomer-swollen seed particles; and polymerizing the monomer-swollen seed particles to obtain click-active Janus particles. A method for functionalizing a click-active Janus particle includes combining seed particles with a monomer emulsion to obtain monomer-swollen seed particles; polymerizing the monomer-swollen seed particles to obtain click-active Janus particles; and functionalizing the click-active Janus particles using one or more click chemistry reactions.

PREPARATION METHOD FOR A FLAME RETARDANT POLYSTYRENE
20230151199 · 2023-05-18 ·

The present application relates to a field of a flame retardant polystyrene, and specifically discloses a preparation method for a flame retardant polystyrene. The preparation method for a flame retardant polystyrene includes the following steps: predissolving a brominated flame retardant containing a first active functional group in a reaction system of a styrene monomer to form a homogeneous solution; then, performing an end capping reaction by an olefin monomer containing a second active functional group to introduce a double bond at an end of the brominated flame retardant, so that it can be bonded to a polystyrene molecular chain by copolymerizing; performing a prepolymerization in a reactor to obtain a prepolymer; performing a post polymerization in the reactor or by extruding, to obtain a special material or a flame retardant masterbatch of the flame retardant polystyrene.