Kikuchi

Iwahashi M, Kikuchi K, Achiba Y, Ikemoto I, Araki T, Mochida T, Yokoi S-l, Tanaka A and Iriyama K 1992 Morphological study ofthin-film systems of pure fuiierene (Cgg) and some other amphiphilic compounds on the electron microscopic scale Langmuir 8 2980-4... 

Y. Sekizawa and T. Kikuchi. Meiji Seiko Kenkyu Nempo. 12, 104 (1972) Chem. Absrr.. 78. 80266. 

We would like to stress at this point that the derivation of (1.36) and (1.38)-(1.39) is connected with the simulation of contact problems and therefore contains some assumptions of a mechanical character. This remark is concerned with the sign of the function p in the problem (1.36) and with the direction of the vector pi,P2,p) in the problem (1.38), (1.39). Note that the classical approach to contact problems is characterized by a given contact set (Galin, 1980 Kikuchi, Oden, 1988 Grigolyuk, Tolkachev, 1980). In contact problems considered in the book, the contact set is unknown, and we obtain the so called free boundary problems. Other free boundary problems can be found in (Hoffmann, Sprekels, 1990 Elliot, Ock-endon, 1982 Antontsev et ah, 1990 Kinderlehrer et ah, 1979 Antontsev et ah, 1992 Plotnikov, 1995). 

The principal producers of lead chromate pigments ia North America are Cookson, DCC (owned by Kikuchi), Engelhard, and Wayne Pigment. In Europe, lead chromates are produced by Ciba ia Holland, CapeUe ia Erance, and Heubach GmGH ia Germany. 

H. Kikuchi, ed.. Dusty and Dirty Plasmas, Noise and Chaos in Space and in the Eaboratoy, Plenum Publishing Corp., New York, 1994. 

M. Kikuchi and Y. Nakao in K. Aida and co-eds.. Biotechnology of Amino Acid Production, Kodansha, Ltd., Tokyo, Japan, 1986, pp. 101—116. 

Ohashi, Sugawara, Kikuchi, and Konno,y. Chem. Engr. Japan, 14, 433... 

Cyanoanthracene (anthracene-9-carbonitrile) [1210-12-4] M 203.2, m 134-137°. Purified by crystn from EtOH or toluene, and vacuum sublimed in the dark and in an inert atmosphere [Ebied et al. 7 Chem Soc, Faraday Trans 7 76 2170 1980 Kikuchi et al. J Phys Chem 91 574 1987. ... 

Methoxynaphthalene [93-04-9] M 158.2, m 73.0-73.6°, b 273°/760mm. Fractionally distd under vacuum. Crystd from absolute EtOH, aqueous EtOH, benzene or n-heptane, and dried under vacuum in an Abderhalden pistol or distd in vacuo. [Kikuchi et al. J Phys Chem 91 574 1987.]... 

Naphthol [135-19-3] M 144.2, m 122.5-123.5°, pK 9.57. Crystd from aqueous 25% EtOH (charcoal), water, benzene, toluene or CCI4, e.g. by repeated extraction with small amounts of EtOH, followed by dissolution in a minimum amount of EtOH and pptn with distilled water, then drying over P2O5 under vacuum. Has also been dissolved in aqueous NaOH, and ppted by adding acid (repeated several times), then ppted from benzene by addition of heptane. Final purification can be by zone melting or sublimation in vacuo. [Bardez et al. J Phys Chem 89 5031 7955 Kikuchi et al. J Phys Chem 91 574 1987.]... 

M. Imamura, N. Matsubayashi.T. Kikuchi, H. IcHiMURA, A. Kawana, Surf. Interface Anal. 27 (1999) 1098-1106. 

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