C08G2261/60

RESIN COMPOSITION

Provided is a resin composition that is highly fluid and has good moldability, and that has excellent optical properties. More specifically, provided is a resin composition that contains a thermoplastic resin and a specific compounding agent containing a naphthalene structure and/or a fluorene structure.

MICHAEL-ADDITION-HARDENING SYNTHETIC RESIN FOR CHEMICAL FIXING TECHNOLOGY

Use of a synthetic resin system as an adhesive for chemical fixing technology, especially for fixing anchoring means in drilled holes, which synthetic resin system includes a) a reaction resin based on α, β-unsaturated compounds, b) a reaction resin based on compounds that include CH-acidic methylene groups, and c) a catalyst, and to related subject matter.

Production of ketone-based biopolymers from catalytic fast pyrolysis of biomass

The present disclosure relates to a composition that includes ##STR00001##
where R.sub.1 and R.sub.2 include at least one of a hydrogen, a hydroxyl group, and/or an alkyl group, R.sub.3 and R.sub.4 include at least one of hydrogen, a hydroxyl group, an alkyl group, and/or a ketone, and 1≤n≤2000.

PHOTOCURABLE COMPOSITION AND SHAPED PRODUCT FORMED FROM THE SAME

An object of the present disclosure is to provide a photocurable composition from which a molded product having excellent mechanical properties is obtained. The present disclosure provides a photocurable composition containing a urethane (meth)acrylate oligomer and a vinyl monomer, wherein the vinyl monomer includes a first monomer having a glass transition temperature (Tg) of −100° C. or more and 20° C. or less, and a second monomer having a glass transition temperature (Tg) of more than 20° C. and 150° C. or less, an amount of the urethane (meth)acrylate oligomer ranges from 20 mass % to 80 mass %, an amount of the first monomer ranges from 15 mass % to 75 mass %, an amount of the second monomer ranges from 5 mass % to 65 mass %, and a total amount of the urethane (meth)acrylate oligomer and the vinyl monomer is 100 mass %.

RUBBER COMPOUNDS FOR PASSENGER TIRE TREADS AND METHODS RELATING THERETO

A rubber compound suitable for passenger tires may comprise: 40 to 70 parts by weight per hundred parts by weight rubber (phr) of a long chain branched cyclopentene ring-opening rubber (LCB-CPR) having a glass transition temperature (Tg) of −120° C. to −80° C., a g′.sub.vis of 0.50 to 0.91, and a ratio of cis to trans of 40:60 to 5:95, 30 phr to 60 phr of a styrene-butadiene rubber (SBR), wherein the SBR has a glass transition temperature (Tg) of −60° C. to −5° C., 50 phr to 110 phr of a reinforcing filler, and 20 phr to 50 phr of a process oil.

Resin material for forming underlayer film, resist underlayer film, method of producing resist underlayer film, and laminate

Provided is a resin material for forming an underlayer film which is used to form a resist underlayer film used in a multi-layer resist process, the resin material including a cyclic olefin polymer (I), in which a temperature at an intersection between a storage modulus (G′) curve and a loss modulus (G″) curve in a solid viscoelasticity of the resin material for forming an underlayer film which is as measured under conditions of a measurement temperature range of 30° C. to 300° C., a heating rate of 3° C./min, and a frequency of 1 Hz in a nitrogen atmosphere in a shear mode using a rheometer is higher than or equal to 40° C. and lower than or equal to 200°.

Enhanced yield, structural control, and transport properties of polynorbornenes for natural gas upgrading through Mizoroki-Heck cross-couplings

Gas separation membranes are provided and more particularly, a series of addition-type and ROMP type polynorbornenes with substituents derived from Mizoroki-Heck reactions are provided and have particular utility as gas separation membranes for natural gas upgrading.

RUBBER COMPOUNDS FOR HEAVY-DUTY TRUCK AND BUS TIRE TREADS AND METHODS RELATING THERETO

A rubber compound for heavy-duty truck or bus tire treads may comprise: 5 to 100 parts by weight per hundred parts by weight rubber (phr) of a long chain branched cyclopentene ring opening rubber (LCB-CPR) having a glass transition temperature (Tg) of −120° C. to −80° C., a g′vis of 0.50 to 0.91, and a ratio of cis-to-trans of 40:60 to 5:95; 0 phr to 95 phr of a rubber selected from a group consisting of a natural rubber (NR), a polybutadiene rubber (BR), and a combination thereof; 30 phr to 90 phr of a reinforcing filler; and 0.5 phr to 20 phr of a process oil.

POLYBENZOXAZINE PRECURSOR AND METHOD FOR PREPARING SAME

This invention relates to a polybenzoxazine precursor and a method of preparing the same, and more particularly, to a polybenzoxazine precursor which includes benzoxazine obtained by reacting a phenol novolak resin with an aldehyde compound and allylamine and diaminodiphenylmethane as an amine compound, and to a method of preparing the same. The polybenzoxazine precursor may serve to prepare a hardened material having excellent thermal and electrical characteristics and dimensional stability. Accordingly, the polybenzoxazine precursor may be available for use in a copper clad laminate, a semiconductor encapsulant, a printed circuit board, an adhesive, a paint, and a mold.

WHITE-LIGHT HYPERBRANCHED CONJUGATED POLYMER, METHOD FOR PREPARING THE SAME AND IT'S USE

This application discloses a white-light hyperbranched conjugated polymer, a method for preparing the same and its use. The polymer uses a red phosphorescent Ir(III) complex as a core and polyfluorene derivative blue fluorescent materials as a framework which either contains or does not contain carbazole derivatives, and the white light hyperbranched polymers realize white-light emission by adjusting the content of the red phosphorescent Ir(III) complex connected using the complementation of blue and red color. The electroluminescent spectrum of the conjugated polymer in the present application covers the whole visible light emission area and is close to the pure white light emission, by which the conjugated polymer could be used as a material used in light-emitting layer to prepare the organic electroluminescent devices.