Mitsui Chemicals, Inc.

Mitsui Toatsu Chemicals, Incorporated

Masayuki Furuya

Takeshi Nishimura

Teruyuki Nagata

Shigetoshi Kuma

Masaru Wada

Tohru Miura

Mamoru Tanaka

Naoyuki Kakinuma

Shinsuke Ito

Michiharu Sakata

Koju Okazaki

Kouji Suesugi

Koichi Tokunaga

Tatsuya Ogawa

Emiko Nishida

Akinori Nagatomo

Yoshimitsu Tanabe

Masakatsu Nakatsuka

Kiyoharu Hasegawa

Tsuneji Suzuki

Hidetoshi Hayashi

Chitoshi Shimakawa

Tadashi Araki

Hiroshi Suizu

Yoshihiro Irizato

Hidetoshi Tsunoda

Chiyuki Kusuda

Yusuke Matsui

Hiroshi Naruse

Hitoshi Nakayama

Koji Suesugi

Jotaro Kida

Kouichi Tokunaga

Katsuju Watanabe

Junya Tanaka

Mihaya Matsukawa

A polymerizable composition for an optical material includes: an allyl carbonate compound (A) including two or more allyloxycarbonyl groups at a terminal which is represented by General Formula (1); and a radical polymerization initiator (B). The radical polymerization initiator (B) includes at least one kind of radical polymerization initiator (B1) which is a peroxyester-based radical polymerization initiator, and a radical polymerization initiator (B2).

Polymerizable composition for optical material, molded product, optical material, and plastic lens and method for manufacturing same

A method for setting polymerization condition includes a physical property acquiring step of, when heating a composition including a polymerization-reactive compound and a polymerization catalyst and/or a polymerization initiator and retaining heat at a predetermined temperature, acquiring a physical property value a derived from a functional group before heating of the polymerization-reactive compound and a physical property value b derived from a remaining functional group after maintaining a temperature for a predetermined time; a remaining functional group ratio calculating step of calculating a remaining functional group ratio from the physical property value a and the physical property value b; a reaction rate coefficient calculating step of calculating a reaction rate coefficient from the remaining functional group ratio on the basis of a reaction rate equation; and a polymerization temperature calculating step of calculating a polymerization temperature on the basis of the reaction rate coefficient and conditions below.

Method for setting polymerization condition and method for manufacturing optical material

The method for setting polymerization conditions includes a physical property acquiring step, in which, when a composition which includes a polymerizable reactive compound including an episulfide compound, and a polymerization catalyst is heated and maintained at a predetermined temperature, a physical property value a derived from a functional group of the polymerizable reactive compound before heating and a physical property value b derived from a remaining functional group after maintaining heat for a predetermined time, are acquired; a remaining functional group ratio calculating step of calculating a remaining functional group ratio; a reaction rate coefficient calculating step for calculating a reaction rate coefficient; and a polymerization temperature calculating step of back-calculating each polymerization temperature every predetermined time in a polymerization time.

A polythiol composition includes a polythiol compound (A) including at least one of 4,8-dimercaptomethyl-1,11-dimercapto-3,6,9-trithiaundecane, 4,7-dimercaptomethyl-1,11-dimercapto-3,6,9-trithiaundecane, or 5,7-dimercaptomethyl-1,11-dimercapto-3,6,9-trithiaundecane, and a polythiol compound (B) that is 4-mercaptomethyl-1,8-dimercapto-3,6-dithiaoctane.

Polythiol composition and applications thereof

A method for setting conditions for use of a polymerization catalyst includes a step of acquiring a physical property value derived from remaining functional groups after maintaining a temperature of a composition including a polymerization-reactive compound and a predetermined amount of a polymerization catalyst, a step of calculating a remaining functional group ratio from the physical property value, a step of calculating a reaction rate constant based on a reaction rate equation from the remaining functional group ratio, a step of calculating an activation energy and a frequency factor from the reaction rate constant using an Arrhenius plot, a step of determining whether or not the activation energy satisfies a predetermined condition for the polymerization catalyst, an step of setting an approximation equation from the frequency factor, and a step of setting an addition range with respect to the polymerization-reactive compound.

Method for setting conditions for use of polymerization catalyst, polymerization condition setting method, and method for manufacturing optical material

A molded product of the present invention includes a polythiourethane, in which an SH group concentration according to an IR analysis method is 0.30 wt % to 3.0 wt %.

Molded product and uses thereof

A polymerizable composition for an optical material of the present invention includes (A) a compound of which pKa value is 1 to 9, (B) a di- or higher functional iso(thio)cyanate compound, and (C) a di- or higher functional active hydrogen compound.

Polymerizable composition for optical material, optical material, and producing method thereof

The thiol-containing composition for an optical material of the present invention includes a compound (A) represented by General Formula (a), and a compound (B) composed of at least one selected from a compound (b2-1) represented by General Formula (b2-1), a compound (b3-1) represented by General Formula (b3-1), a compound (b3-2) represented by General Formula (b3-2), and a compound (b4-2) represented by General Formula (b4-2), in which, in high-performance liquid chromatography measurement, the total peak area ratio of the compound included in the compound (B) is 0.1% to 60.0% with respect to the peak area 100 of the compound (A).

Thiol-containing composition for optical material and polymerizable composition for optical material

The polymerizable composition for an optical material of the present invention includes a compound (A) represented by General Formula (a) and including two or more allyloxycarbonyl groups, at least one kind of radical polymerization initiator (B) selected from the group consisting of a peroxyketal-based radical polymerization initiator, a peroxymonocarbonate-based radical polymerization initiator, and a peroxyester-based radical polymerization initiator, and a modifier (C) selected from a polyether modified siloxane compound represented by General Formula (c1) or a polyol compound represented by General Formula (c2). 

Polymerizable composition for optical material and optical material and plastic lens obtained from same composition

A polymerizable composition for an optical material according to the present invention includes one or two or more compounds selected from the group consisting of component (A): an ester compound having a specific structure and component (B): an ether compound having a specific structure, and a polymerizable compound.

Polymerizable composition for optical material and optical material and plastic lens obtainable from same composition

A process for producing a plastic lens includes a step of stirring and mixing a solution including a polymerization reactive compound in a preparation tank; a step of transferring the polymerizable composition obtained in the step from the preparation tank to a lens casting mold; a step of curing the polymerizable composition; and a step of obtaining a plastic lens molded product by separating the obtained resin from the lens casting mold. The step of transferring the polymerizable composition includes a step of re-mixing the polymerizable composition discharged from the preparation tank and injecting the polymerizable composition into the lens casting mold.

Process for producing plastic lens and apparatus for producing plastic lens

A process for producing a pentaerythritol mercaptocarboxylic acid ester of the present invention includes: a step of reacting pentaerythritol with a mercaptocarboxylic acid, in which an absorbance of a 5 wt % aqueous solution of the pentaerythritol at a wavelength of 270 nm, which is measured using a quartz cell having an optical path length of 50 mm, is 0.07 or less.

Process for producing pentaerythritol mercaptocarboxylic acid ester, polymerizable composition, resin, optical material, and lens

A manufacturing method of an amine compound including obtaining a reaction solution containing an aldehyde compound by reacting a compound represented by Formula (a1) or (a2) with hydrogen and carbon monoxide in the presence of a metal compound of groups 8 to 10 and a phosphorus compound, neutralizing the reaction, purifying an aldehyde compound by distilling the neutralized reaction solution, and reacting the aldehyde compound with ammonia and with hydrogen in the presence of a catalyst to obtain an amine compound, wherein the phosphorus compound is represented by the Formula (RO)P, and the base compound is at least one selected from carbonate and hydrogen carbonate of metals of group I and carbonate and hydrogen carbonate of metals of group II, and wherein the neutralizing the reaction solution is performed within a temperature range of 40&#xb0; C. to 50&#xb0; C.

Purification method of aldehyde compound

A manufacturing method of an isocyanate compound including obtaining a reaction solution containing an aldehyde compound by reacting a compound represented by Formula (a1) or (a2) with hydrogen and carbon monoxide in the presence of a metal compound of groups 8 to 10 and a phosphorus compound, neutralizing the reaction solution, purifying an aldehyde compound by distilling the neutralized reaction solution, reacting the aldehyde compound with ammonia and with hydrogen in the presence of a catalyst to obtain an amine compound; and reacting the amine compound with a carbonylating agent to obtain an isocyanate compound, wherein the phosphorus compound is represented by the Formula (RO)P, and the base compound is at least one selected from carbonate and hydrogen carbonate of metals of group I and carbonate and hydrogen carbonate of metals of group II, wherein the neutralizing the reaction solution is performed within a temperature range of 40&#xb0; C. to 50&#xb0; C.

The purification method of an aldehyde compound of the present invention includes a step of neutralizing a reaction solution containing an aldehyde compound by adding water and a base compound to the reaction solution, and a step of distilling the neutralized reaction solution, in which the reaction solution is obtained by reacting a compound represented by the following Formula (a1) or (a2) with hydrogen and carbon monoxide in the presence of a metal compound of groups 8 to 10 and a phosphorus compound, the phosphorus compound is represented by Formula (RO)P, and the base compound is at least one kind selected from among carbonate and hydrogen carbonate of metals of group I on the periodic table and carbonate and hydrogen carbonate of metals of group II on the periodic table. 

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Arao, Japan

Masayuki Furuya