著者
木村 哲二
出版者
社団法人日本獣医学会
雑誌
日本獸醫學雜誌 (ISSN:00215295)
巻号頁・発行日
vol.27, no.6, pp.1-4, 1965-12-25
著者
津留 壽昭 木村 哲二 乾 忠孝
出版者
The Surface Finishing Society of Japan
雑誌
金属表面技術 (ISSN:00260614)
巻号頁・発行日
vol.27, no.3, pp.130-134, 1976

A study was made on electrodeposition of cobalt from cobalt ethylenediamine chelate solution for the purpose of investigating the stability of chelate on pH and the optimum condition in electrolysis. The results obtained were as follows: 1) Ethylenediamine (en) and cobalt ion (II) formed stable chelate compound of (Coen<sub>3</sub>)<sup>2+</sup> in a pH range 8.0-10. 2) Bright cobalt platings were obtained from chelate solutions of pH 3.0-5.0 by the addition of two addition agents, and cathodic current efficiency was found to be decreased. The optimum bath composition for bright cobalt plating was as follows: CoCl<sub>2</sub>⋅6H<sub>2</sub>O (CoSO<sub>4</sub>⋅7H<sub>2</sub>O) 0.05-0.20mol/<i>l</i> (0.1-0.3mol/<i>l</i>), en 0.15-0.60mol/<i>l</i> (0.3-0.9mol/<i>l</i>), HOCH<sub>2</sub>C: CCH<sub>2</sub>OH 0.05g/<i>l</i>, C<sub>10</sub>H<sub>6</sub> (SO<sub>3</sub>Na)<sub>2</sub>⋅2H<sub>2</sub>O 0.03g/<i>l</i>, pH 3.0-5.0, Temperature Room temperature, Cathodic current density 0.8-1.5A/dm<sup>2</sup>. The cathodic current efficiency under the above condition was about 70-80%. 3) The cobalt deposits obtained from Co-en baths were of small grains in crystal structure, and the brightness apparently increased with increasing electrolysis time.
著者
津留 壽昭 木村 哲二 乾 忠孝
出版者
The Surface Finishing Society of Japan
雑誌
金属表面技術 (ISSN:00260614)
巻号頁・発行日
vol.27, no.2, pp.80-84, 1976

The stability of electrolyte containing cadmium-ethylenediamine (en) chelate in various pH ranges has been investigated to determine the optimum condition for electrodeposition of cadmium. Cathodic polarization measurement was made in the above bath, and the cadmium deposits obtained under various conditions were examined by X-ray diffraction. The results obtained were as follows: 1) Cadmium (II) ions seemed to react with en to form a stable complex, and bright and smooth cadmium deposits on copper plates were obtained over the range of pH 9-12. 2) Complex ions were greatly affected by anion. Cadmium was not deposited from acidic baths containing a small amount of chloride ions and various precipitates such as Cd(en)<sub>m</sub>Cl<sub>2</sub>(<i>m</i>=1-3), but was deposited from neutral and weak acidic baths. Cadmium-en complex was not formed, when pH-value was in acidic or strong alkaline ranges. In this case, en seemed to act merely as an addition agent upon electrolysis. 3) By the addition of gelatine in to the cadmium-en bath, adherent cadmium deposits having a fine grain (270-290Å) structure were obtained. It was shown by X-ray diffraction analysis that the orientation of the cadmium deposits was strong in (101), but weak in (102) and (103). 4) The optimum composition and operation condition of the bath were found to be Cd (CH<sub>3</sub>COO)<sub>2</sub>⋅2H<sub>2</sub>O: 0.3-0.5mol/<i>l</i>, en: 1.2-2.0mol/<i>l</i>, gelatine: 0.5-1.0g/<i>l</i>, pH: 9-11, temperature: 20-50°C, current density: 1.0-2.5A/dm<sup>2</sup>; current efficiency was above 90%.
著者
津留 壽昭 木村 哲二 小林 繁夫 乾 忠孝
出版者
The Surface Finishing Society of Japan
雑誌
金属表面技術 (ISSN:00260614)
巻号頁・発行日
vol.27, no.5, pp.230-234, 1976
被引用文献数
3

By using N, N-dimethylformamide(DMF), an aprotic polar solvent, the electrodeposition of lead from PbCl<sub>2</sub>-DMF and Pb(NO<sub>3</sub>)<sub>2</sub>-DMF solutions was studied. The deposits of lead gave rise to the welldefined dendrites, when the electrolysis was carried out in higher concentration bath and at higher current densities, while at lower current densities (-3mA/cm<sup>2</sup>), the deposits became dark-gray and smooth. The dendrites of lead were of 2D [110], 3D [110] and 2D [100] types. The deposits from PbCl<sub>2</sub>-DMF solutions were the isolated nuclei of the layer growth (hexagonal, tetragonal and trigonal deposits), when temperature was higher than 40°C. The deposits from Pb(NO<sub>3</sub>)<sub>2</sub>-DMF solutions were white powder when temperature was higher than 50°C, while at 100°C the dendrites were not observed. The X-ray analysis of the deposits of crystalline lead had well-defined diffraction patterns. By the addition of thiourea and 2-butyne-1, 4 diol to Pb(NO<sub>3</sub>)<sub>2</sub>-H<sub>3</sub>BO<sub>3</sub>-DMF baths, semi-bright and smooth lead deposits were obtained. They had fine grains in crystal structure and were found to have the strong preferred orientation of (220). The grain size of the deposit was 150-350Å. From these results the optimum condition for the electrolysis was as follows: Pb(NO<sub>3</sub>)<sub>2</sub>: 100g/<i>l</i>, H<sub>3</sub>BO<sub>3</sub>: 10g/<i>l</i>, (NH<sub>2</sub>)<sub>2</sub>CS: 4g/<i>l</i>, HOCH<sub>2</sub>C≡CCH<sub>2</sub>OH: 3g/<i>l</i>, temperature:room temperature, current density:0.5-1.0mA/cm<sup>2</sup>, plating time: 60min, current efficiency: ca 50%.