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1.
Summary If hydrogen is diffused electrolytically in a metal, it subsequently escapes out if the metal is left to itself. However this
hydrogen-treated metal does not totally regain the original magnitudes of its various physical properties,e. g., thermo e.m.f., electrical resistivity, elastic modulii etc. This effect has also been observed in the second-order elastic
effect (the Poynting effect) in nickel and two varieties of steel. Measurements were carried out first before hydrogen diffusion.
The samples were electrolytically diffused with hydrogen and the left to themselves for a few days and the measurements were
repeated. The changed values of the coefficient of Poynting effect are discussed in terms of the dislocations created by in-and
out-going hydrogen.
Now retired 相似文献
2.
Cerium(IV) ammonium nitrate in substoichiometric amounts, promotes the intramolecular cyclization of epoxypropyl cinnamyl ethers to the corresponding 3,4,5-trisubstituted tetrahydropyran derivatives in moderate to good yields. 相似文献
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R. K. Nigam B. P. Hajela S. Sengupta B. C. Srivastava K. M. Gupta 《Hyperfine Interactions》1986,28(1-4):935-939
The effect of pigments on the development of corrosion products between the painting system and metal surface when exposed to marine environments has been discussed. The pigments studied were; Red Mud Zinc chromate, Zinc chromate, Red oxide Zinc Phosphate, Manganese Phosphate Barium chromate and Basic Lead Silico Chromate. Mossbauer Spectroscopy revealed that the upper rust layer in all the cases consisted of-Fe203,-FeOOH and-FeOOH. The lower rust layer immediately in contact with the metal surface consisted of an asymmetrical doublet due to -FeOOH. 相似文献
8.
Oxidative demetalation of cyclohexadienyl ruthenium(II) complexes: a net Ru-mediated dearomatization
[reaction: see text] An experimentally simple method for the demetalation of spirocyclic cyclohexadienylruthenium(II) complexes has been developed. Treatment of an alkoxy-substituted cyclohexadienyl complex with CuCl(2) affords either azaspiro[4.5]decane derivatives or heavily functionalized tetrahydroisoquinolines. The former reaction manifold completes a net Ru-mediated dearomatization as the organometallic starting materials are prepared from (eta(6)-arene)Ru(II) precursors. Both of these heterocyclic products are well suited for further synthetic elaboration. 相似文献
9.
Some sulphur-containing ligands have been shown to inhibit the Hg(II)-catalysed substitution of p-nitrosodiphenylamine (p-NDA) for cyanide in hexacyanoferrate(II), by binding the mercury(II). This effect is used for determination of microamounts of cysteine, thioglycollic acid and thiosulphate. The reactions are followed spectrophotometrically at 640 nm (lambda(max) of [Fe(CN)(5).p-NDA](3-)). The determination range depends on the amount of mercury(II) added and the stability of the Hg(II)-ligand complex. Under specified conditions, the detection limits are: thioglycollic acid 1 x 10(-7)M, cysteine 1 x 10(-6)M and thiosulphate 4 x 10(-7)M. 相似文献
10.
Molar excess volumes, VE, for pyridine (A) + α-picoline (B), + β-picoline (B) and + γ-picoline (B) and benzene (A) + toluene (B), + o-xylene (B) and + p-xylene (B) and carbon tetrachloride (A) + n-heptane (B) have been measured dilatometrically as a function of temperature and composition and have been utilized to study B—B and B—B—B interactions in the presence of A via the Mayer—McMillan approach. A model has also been presented to account for these B—B and B—B—B interactions. The VE data at 308.15 K have also been analysed in terms of the “graph theoretical” approach which describes the VE data well for all these mixtures at 308.15 K. The “graph theoretical” approach has further been extended to successfully evaluate VE data for a mixture at any temperature, T2, when the VE data at T1 are known. 相似文献