1997
DOI: 10.1002/(sici)1097-4660(199709)70:1<106::aid-jctb689>3.0.co;2-l
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On the nature of transformation reactions of unsaturated glycols on the nickel cathode

Abstract: : The catalytic nature of the process of cathodic hydrogenation of the unsaturated bond has been determined by evaluating radiometrically the inÑu-ence of addition of di †erent quantities of 63Ni to the supporting solution free from nickel ions on the unsaturated bond hydrogenation rate. The catalytic activity of a nickel cathode used to hydrogenate 2-butynediol-1,4 labelled by a 14C isotope is approximately four times higher in a nickel-plating electrolyte than that in an electrolyte free from nickel ions. El… Show more

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Cited by 3 publications
(5 citation statements)
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“…The plasticity of a lustrous nickel coating formed under the same conditions reaches a value of 9% (Fig. 1b), which is very high, compared with that obtained previously (up to 6%) for the technological solutions suggested in [9]. It should be noted that sufficiently plastic deposits (6%) are also obtained from dilute nickel-plating electrolyte nos.…”
Section: ³ ääääääáääääääáäääääääääääääääääääáääääääsupporting
confidence: 66%
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“…The plasticity of a lustrous nickel coating formed under the same conditions reaches a value of 9% (Fig. 1b), which is very high, compared with that obtained previously (up to 6%) for the technological solutions suggested in [9]. It should be noted that sufficiently plastic deposits (6%) are also obtained from dilute nickel-plating electrolyte nos.…”
Section: ³ ääääääáääääääáäääääääääääääääääääáääääääsupporting
confidence: 66%
“…The table lists the electrolyte formulations and estimates of the nickel-plating rates, found by the fast method [5] with a Hull cell. The formulation suggested is similar to the technological solution of [9], which consists in that small concentrations of YN are used in combination with an ethylene compound, EN, with the key role played by the competition of acetylene and ethylene groups in hydrogenation. b-Oxyethyl cinnamide is described by the formula C 6 H 5 CH=CH3CONHCH 2 CH 2 OH and, unlike EN, contains a phenyl radical and nitrogen.…”
Section: ³ ääääääáääääääáäääääääääääääääääääáäääääämentioning
confidence: 99%
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