C07C265/14

Sizing agent composition, method for producing carbon fibers, and carbon fibers each having sizing agent applied thereonto

An object of the present invention is to provide a sizing agent composition that gives a carbon fiber from which a carbon fiber-reinforced composite material having excellent adhesion between a resin and the carbon fiber and having excellent mechanical properties can be formed. The sizing agent composition of the invention is a sizing agent composition comprising (A) a blocked isocyanate, and (B) a compound containing at least one polar group and at least one unsaturated group per molecule. In the invention, the mixing ratio (mass ratio) of the blocked isocyanate (A) and the compound (B) containing at least one polar group and at least one unsaturated group per molecule (A/B) is preferably 95/5 to 5/95. In the invention, the blocked isocyanate (A) is preferably a compound having an aliphatic skeleton.

1,3-BISISOCYANATOMETHYLCYCLOHEXANE COMPOSITION AND OPTICAL RESIN PREPARED THEREFROM

Disclosed is a 1,3-bisisocyanatomethylcyclohexane composition and an optical resin prepared therefrom. The composition comprises, based on the weight of 1,3-bisisocyanatomethylcyclohexane, a) 65%-95 wt % of trans-1,3-bisisocyanatomethylcyclohexane; b) greater than 0 and less than or equal to 0.5 wt %, preferably 0.02-0.5 wt % of 1,4-bisisocyanatomethylcyclohexane. Preferably, the 1,3-bisisocyanatomethylcyclohexane composition contains greater than 0 and less than or equal to 600 ppm of 1-isocyanatomethyl-3-methylcyclohexane, based on the weight of 1,3-bisisocyanatomethylcyclohexane. The 1,3-bisisocyanatomethylcyclohexane composition is used for preparing an optical resin, which can be applied to produce an optical lens with a better performance in preventing opacification and optical distortion.

1,3-BISISOCYANATOMETHYLCYCLOHEXANE COMPOSITION AND OPTICAL RESIN PREPARED THEREFROM

Disclosed is a 1,3-bisisocyanatomethylcyclohexane composition and an optical resin prepared therefrom. The composition comprises, based on the weight of 1,3-bisisocyanatomethylcyclohexane, a) 65%-95 wt % of trans-1,3-bisisocyanatomethylcyclohexane; b) greater than 0 and less than or equal to 0.5 wt %, preferably 0.02-0.5 wt % of 1,4-bisisocyanatomethylcyclohexane. Preferably, the 1,3-bisisocyanatomethylcyclohexane composition contains greater than 0 and less than or equal to 600 ppm of 1-isocyanatomethyl-3-methylcyclohexane, based on the weight of 1,3-bisisocyanatomethylcyclohexane. The 1,3-bisisocyanatomethylcyclohexane composition is used for preparing an optical resin, which can be applied to produce an optical lens with a better performance in preventing opacification and optical distortion.

METHOD FOR ISOCYANATE AND POLYURETHANE PRODUCTION WITH IMPROVED SUSTAINABILITY
20220389150 · 2022-12-08 ·

The invention relates to a method for producing isocyanates and optionally polyurethanes by at least: synthesising (1) phosgene (20) from carbon monoxide (21) and chlorine (22); reacting (2) phosgene (20) with diamines (23) to form diisocyanates (24) and hydrogen chloride (25); providing a carbon dioxide gas flow (31); and cleaning (4) the carbon dioxide gas flow (31) of additional components, wherein the carbon dioxide is converted by means of an RWGS reaction (6) to form carbon monoxide (21) and hydrogen (29), which are used as raw materials for the polyurethane production, as well as optionally reacting (3) the diisocyanates (24) with polyether polyol (35a) and/or polyester polyol (35b) to form polyurethanes (37).

METHOD FOR ISOCYANATE AND POLYURETHANE PRODUCTION WITH IMPROVED SUSTAINABILITY
20220389150 · 2022-12-08 ·

The invention relates to a method for producing isocyanates and optionally polyurethanes by at least: synthesising (1) phosgene (20) from carbon monoxide (21) and chlorine (22); reacting (2) phosgene (20) with diamines (23) to form diisocyanates (24) and hydrogen chloride (25); providing a carbon dioxide gas flow (31); and cleaning (4) the carbon dioxide gas flow (31) of additional components, wherein the carbon dioxide is converted by means of an RWGS reaction (6) to form carbon monoxide (21) and hydrogen (29), which are used as raw materials for the polyurethane production, as well as optionally reacting (3) the diisocyanates (24) with polyether polyol (35a) and/or polyester polyol (35b) to form polyurethanes (37).

Method of preparing diisocyanate composition and optical lens

In the embodiments, an aqueous hydrochloric acid solution and an organic solvent instead of hydrogen chloride gas and solid triphosgene instead of phosgene gas may be used in the process of preparing a diisocyanate from a diamine through a diamine hydrochloride. In addition, the embodiments provide processes for preparing a diisocyanate composition and an optical lens, which are excellent in yield and quality with mitigated environmental problems by controlling the total content of metals, cations, or anions in a diamine hydrochloride composition.

Method of preparing diisocyanate composition and optical lens

In the embodiments, an aqueous hydrochloric acid solution and an organic solvent instead of hydrogen chloride gas and solid triphosgene instead of phosgene gas may be used in the process of preparing a diisocyanate from a diamine through a diamine hydrochloride. In addition, the embodiments provide processes for preparing a diisocyanate composition and an optical lens, which are excellent in yield and quality with mitigated environmental problems by controlling the total content of metals, cations, or anions in a diamine hydrochloride composition.

PROCESS FOR THE DISTILLATION OF ISOCYANATES

The present invention relates to a process for distillative purification of a crude isocyanate obtained by phosgenation of the corresponding amine in a distillation apparatus under vacuum to obtain the corresponding isocyanate, characterized in that at least one liquid ring compressor is used to generate the vacuum in the distillation apparatus, a particular operating liquid is used for the at least one liquid ring compressor, the pressure p on the suction side of the at least one liquid ring compressor is 10 to 200 mbar(a), the operating temperature of the at least one liquid ring compressor is −17° C. to +15° C. and the operating liquid at the exit from the at least one liquid ring compressor has an AC value of less than 35 000 ppm, to a corresponding use of at least one liquid ring compressor for generating a vacuum in an apparatus for distillation of a crude isocyanate and to a corresponding process for operating a liquid ring compressor for providing the vacuum for distillative purification of an isocyanate obtained by phosgenation of the corresponding amine in a distillation apparatus to obtain the corresponding isocyanate.

PROCESS FOR THE DISTILLATION OF ISOCYANATES

The present invention relates to a process for distillative purification of a crude isocyanate obtained by phosgenation of the corresponding amine in a distillation apparatus under vacuum to obtain the corresponding isocyanate, characterized in that at least one liquid ring compressor is used to generate the vacuum in the distillation apparatus, a particular operating liquid is used for the at least one liquid ring compressor, the pressure p on the suction side of the at least one liquid ring compressor is 10 to 200 mbar(a), the operating temperature of the at least one liquid ring compressor is −17° C. to +15° C. and the operating liquid at the exit from the at least one liquid ring compressor has an AC value of less than 35 000 ppm, to a corresponding use of at least one liquid ring compressor for generating a vacuum in an apparatus for distillation of a crude isocyanate and to a corresponding process for operating a liquid ring compressor for providing the vacuum for distillative purification of an isocyanate obtained by phosgenation of the corresponding amine in a distillation apparatus to obtain the corresponding isocyanate.

Heterogeneous catalysts for the direct carbonylation of nitro aromatic compounds to isocyanates

A process for preparing an aromatic isocyanate by direct carbonylation of a nitro aromatic compound by reacting the nitro aromatic compound with carbon monoxide in the presence of a catalyst, characterized in that the catalyst contains a multi metallic material comprising one or more binary intermetallic phases of the general formula A.sub.xB.sub.y wherein: A is one or more element selected from Ni, Ru, Rh, Pd, Ir, Pt and Ag, B is one or more element selected from Sn, Sb, Pb, Zn, Ga, In, Ge and As, x is in the range 0.1-10, y in is in the range 0.1-10.