Mitsui Toatsu Chemicals

Mitsui Toatsu Chemical, Inc. disclosed a similar process usiag Raney copper (74) shortiy after the discovery at Dow, and BASF came out with a variation of the copper catalyst ia 1974 (75). Siace 1971 several hundred patents have shown modifications and improvements to this technology, both homogeneous and heterogeneous, and reviews of these processes have been pubHshed (76). Nalco Chemical Company has patented a process based essentially on Raney copper catalyst (77) ia both slurry and fixed-bed reactors and produces acrylamide monomer mainly for internal uses. Other producers ia Europe, besides Dow and American Cyanamid, iaclude AUied CoUoids and Stockhausen, who are beheved to use processes similar to the Raney copper technology of Mitsui Toatsu, and all have captive uses. Acrylamide is also produced ia large quantities ia Japan. Mitsui Toatsu and Mitsubishi are the largest producers, and both are beheved to use Raney copper catalysts ia a fixed bed reactor and to sell iato the merchant market. 

Jpn. Kokai 75 82008 (July 3,1975), K. Yamamoto and co-workers (to Mitsui Toatsu Chemicals, Inc.). 

LARC-TPI is a linear thermoplastic PI which can be processed ia the imide form to produce large-area, void-free adhesive bonds. Mitsui Toatsu Chemicals, Inc., has obtained Hcense to produce this product commercially for appHcations such as adhesives, films, mol ding compounds, etc. These are thermooxidatively stable and show essentially no loss ia weight at 300°C ia air. Weight loss does not exceed 2—3% after isothermal aging ia air at 300°C for 550 h. 

Jptt Kokai 1133909 (May 26, 1989), T. Kyora (to Mitsui Toatsu Chemicals). 

The first-stage catalysts for the oxidation to methacrolein are based on complex mixed metal oxides of molybdenum, bismuth, and iron, often with the addition of cobalt, nickel, antimony, tungsten, and an alkaU metal. Process optimization continues to be in the form of incremental improvements in catalyst yield and lifetime. Typically, a dilute stream, 5—10% of isobutylene tert-huty alcohol) in steam (10%) and air, is passed over the catalyst at 300—420°C. Conversion is often nearly quantitative, with selectivities to methacrolein ranging from 85% to better than 95% (114—118). Often there is accompanying selectivity to methacrylic acid of an additional 2—5%. A patent by Mitsui Toatsu Chemicals reports selectivity to methacrolein of better than 97% at conversions of 98.7% for a yield of methacrolein of nearly 96% (119). 

Jptt Kokai Tokkyo Koho 59 08,710 (fan. 18, 1984) (to Mitsui Toatsu Chemical Company). 

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