Other

Tdk Corporation

Ueda Textile Science Foundation

Mutsumi Kimura

Hirofusa Shirai

Yuichi Kubota

Kenji Hanabusa

Toshiki Koyama

Toshihiro Hirai

Kunihiro Hamada

Methods and equipment are provided for making polybichlorophenyl non-toxic. Methods include a first oxidation step, in which polybichlorophenyl is burned, and a second oxidation step, in which exhaust gas from the first oxidation step is oxidized by contact with metallic phthalocyanines or metallic phthalocyanine derivatives and with an oxygen supply compound. Equipment includes a first furnace for burning a polybichlorophenyl-containing oil with an auxiliary fuel and a second oxidation reaction unit. The second oxidation reaction unit connects to the first furnace under seal, and includes metallic phthalocyanine or metallic phthalocyanine derivative solution supply source and an oxygen supply compound supply source.

Method and equipment for making polychlorobiphenyl nontoxic

A novel phthalocyanine compound having improved solubility and high purity and containing a polymerizable vinyl group within its molecule is provided. Intermediates to this phthalocyanine compound also have improved solubility and high purity. Further, with the novel phthalocyanine compound used as a starting monomer, a novel polymer is obtained which has a high content of (metal) phthalocyanine and is easy to control the orientation of phthalocyanine rings. The polymer having improved solubility and high purity is expected of use as functional material such as catalysts and recording material.

Phthalaocyanine compound as a layer in optical recording medium

Novel naphthalocyanine compounds are provided including nitro- and amino-substituted naphthalocyanine compounds, and vinyl-containing naphthalocyanine compounds. The compounds have improved solubility and high purity and are expected to find use as photo-functional materials such as dyes. Polymers are obtained using the vinyl-containing naphthalocyanine compounds. The polymers also have improved solubility, high purity, a high naphthalocyanine content and ease of control of the orientation of naphthalocyanine rings and are expected of use as various functional materials.

Naphthalocyanine compounds, naphthalocyanine polymers and method for

Novel naphthalocyanine compounds are provided including nitro- and amino-substituted naphthalocyanine compounds, and vinyl-containing naphthalocyanine compounds. The compounds have improved solubility and high purity and are expected to find use as photo-functional materials such as dyes. Polymers are obtained using the vinyl-containing naphthalocyanine compounds- The polymers also have improved solubility, high purity, a high naphthalocyanine content and ease of control of the orientation of naphthalocyanine rings and are expected of use as various functional materials.

Growing community of inventors

Ueda, Japan

Mutsumi Kimura