A curable composition for making polyisocyanurate comprising products obtained by combining and mixing at an isocyanate index of at least 100 at least a polyisocyanate composition, a polytetrahydrofuran polyol (P-THF) having average molecular weight in range 1000-5000 g/mol as toughening agent and diols having an average molecular weight <1000 g/mol.

Provided is a method for preparing an alkaline red mud coating for preventing marine organism attachment, including: (1) mixing stearic acid and absolute ethanol by stirring to obtain a mixed solution; (2) mixing the mixed solution and a red mud powder to obtain a mixture, and drying the mixture to obtain a modified hydrophobic red mud powder; (3) adding benzyl glycidyl ether into an epoxy resin and conducting dispersion to be uniform to obtain a mixed system, adding the modified hydrophobic red mud powder into the mixed system, continuing the dispersion to be uniform to obtain a blend, and grinding the blend to obtain an antifouling coating material; and (4) during use, mixing the antifouling coating material with a polyamide curing agent to obtain a mixture system, and applying the mixture system onto a surface of building to form the alkaline red mud coating for preventing marine organism attachment.

In a tumbler and the like, polypropylene pellets are blended with 1 to 5 wt % of carbon nanotubes, 10 to 30 wt % of fly ash, 10 to 20 wt % of talc and 0.3 to 1 wt % of a modifier, the resulting blend is extruded from a screw extruder while heating the blend to a melting temperature of about 160 to 260 C., to generate a strand. This strand is cooled and cut into pellets having a predetermined length. Owing to blending with fly ash, talc and a modifier, an inexpensive lightweight electroconductive thermoplastic resin excellent in dust-proofness, heat resistance and recyclability is obtained, even if the blending amount of carbon nanotubes is small.

In a tumbler and the like, polypropylene pellets are blended with 1 to 5 wt % of carbon nanotubes, 10 to 30 wt % of fly ash, 10 to 20 wt % of talc and 0.3 to 1 wt % of a modifier, the resulting blend is extruded from a screw extruder while heating the blend to a melting temperature of about 160 to 260 C., to generate a strand. This strand is cooled and cut into pellets having a predetermined length. Owing to blending with fly ash, talc and a modifier, an inexpensive lightweight electroconductive thermoplastic resin excellent in dust-proofness, heat resistance and recyclability is obtained, even if the blending amount of carbon nanotubes is small.

Composite materials and methods for their preparation are described herein. The composite materials can comprise (a) a polyurethane and (b) from 35% to 90% by weight, based on the total weight of the composite, of a particulate filler dispersed in the polyurethane. The polyurethane can be formed by the reaction of (i) one or more isocyanates selected from the group consisting of diisocyanates, polyisocyanates, and mixtures thereof, and (ii) one or more polyols. The one or more polyols that form the polyurethane comprise a high hydroxyl number polyol having a hydroxyl number of at least 250 mg KOH/g. In some cases, the one or more polyols that form the polyurethane can have a weight average equivalent weight of from 200 to 1100 amu. In some cases, the one or more polyols that form the polyurethane can include less than 5% by weight, based on the total weight of the one or more polyols that form the polyurethane, of one or more flexible polyols having a hydroxyl number of less than 150 mg KOH/g and a functionality of less than 3.

Composite materials and methods for their preparation are described herein. The composite materials can comprise (a) a polyurethane and (b) from 35% to 90% by weight, based on the total weight of the composite, of a particulate filler dispersed in the polyurethane. The polyurethane can be formed by the reaction of (i) one or more isocyanates selected from the group consisting of diisocyanates, polyisocyanates, and mixtures thereof, and (ii) one or more polyols. The one or more polyols that form the polyurethane comprise a high hydroxyl number polyol having a hydroxyl number of at least 250 mg KOH/g. In some cases, the one or more polyols that form the polyurethane can have a weight average equivalent weight of from 200 to 1100 amu. In some cases, the one or more polyols that form the polyurethane can include less than 5% by weight, based on the total weight of the one or more polyols that form the polyurethane, of one or more flexible polyols having a hydroxyl number of less than 150 mg KOH/g and a functionality of less than 3.

The present invention provides biodegradable compositions for making biodegradable plastic. The composition comprise about 25% to about 50% by weight starch; about 0.5% to about 10% by weight ground plant waste material; about 20% to about 50% a polymer derived from ethylene, vinyl alcohol and/or an ester of vinyl alcohol; about 10% to about 30% of a plasticizer; and about 3% to about 10% a filler and optionally a processing agent.

A method for producing a flame-retardance-imparting material comprises: a shredding step of shredding plant material containing stems and/or leaves of tomato plants and/or eggplant plants in a aqueous solvent; and an aqueous solvent removal step or removing the aqueous solvent from the plant material after shredding.

A biodegradable composite including: (a) a polymeric matrix having a biodegradable polymer; (b) a filler; and (c) an anhydride grafted compatibilizer including one or more biodegradable polymers modified with an anhydride group. The composite may also include (d) polymer additives such as polymer chain extenders or plasticizers. An in situ method of manufacturing the biodegradable composite of the present invention, including the steps of: (a) melting one or more biodegradable polymers in the presence of a functional monomer and a free radical initiator to form a mixture; and (b) adding a filler and polymer additives to the mixture thereby manufacturing the biodegradable composite. A method of manufacturing a biodegradable polymer including (a) synthesizing a compatibilizer by (i) mixing a free radical initiator and a functional monomer, (ii) melting one or more biodegradable polymers to form a melt, and (iii) combining the product of step (i) and the melt of step (ii) thereby synthesizing the compatibilizer; and (b) mixing the compatibilizer of step (a), with a matrix of one or more biodegradable polymers and a filler and polymer additives, thereby manufacturing the biodegradable or compostable composite.

A biodegradable composite including: (a) a polymeric matrix having a biodegradable polymer; (b) a filler; and (c) an anhydride grafted compatibilizer including one or more biodegradable polymers modified with an anhydride group. The composite may also include (d) polymer additives such as polymer chain extenders or plasticizers. An in situ method of manufacturing the biodegradable composite of the present invention, including the steps of: (a) melting one or more biodegradable polymers in the presence of a functional monomer and a free radical initiator to form a mixture; and (b) adding a filler and polymer additives to the mixture thereby manufacturing the biodegradable composite. A method of manufacturing a biodegradable polymer including (a) synthesizing a compatibilizer by (i) mixing a free radical initiator and a functional monomer, (ii) melting one or more biodegradable polymers to form a melt, and (iii) combining the product of step (i) and the melt of step (ii) thereby synthesizing the compatibilizer; and (b) mixing the compatibilizer of step (a), with a matrix of one or more biodegradable polymers and a filler and polymer additives, thereby manufacturing the biodegradable or compostable composite.