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排序方式: 共有113条查询结果,搜索用时 312 毫秒
1.
Examples are worked out using a new equation proposed in the previous paper to show that it has new physical predictions for mesoscopic systems. 相似文献
2.
We show by general considerations that it is not possible to test violation of the existing versions of Bell’s inequality
in entangled neutral kaons system using experimentally accessible thin regenerators. We point out the loophole in the recent
argument (A Bramon and M Nowakowski, Phys. Rev. Lett.
83, 1 (1999)) that claimed such a test to be possible. 相似文献
3.
Samalíková M Carey J Grandori R 《Rapid communications in mass spectrometry : RCM》2005,19(18):2549-2552
The arginine repressor (ArgR) from Escherichia coli regulates genes for L-arginine metabolism and is a required recombination factor for colE1 plasmid replication. Both functions require binding of L-arginine to the protein. In this work, nano-electrospray ionization time-of-flight mass spectrometry (nano-ESI-TOFMS) is used to study conformational and oligomeric states of intact ArgR and its isolated structural domains. In agreement with X-ray diffraction studies, it is shown that ArgR oligomerizes to form hexamers in both the presence and absence of L-arginine, and the basic unit of oligomerization appears to be the trimer. Higher-order assembly into dodecamers is also detected. The isolated C-terminal domain is found to associate into trimers and hexamers whereas the N-terminal domain is detected in its monomeric form. The observed species distributions suggest a role for the N-terminal domain in hexamer stabilization. 相似文献
4.
Rajani K. Samal R. R. Das M. C. Nayak G. V. Suryanarayana G. Panda D. P. Das 《Journal of polymer science. Part A, Polymer chemistry》1981,19(11):2751-2758
The kinetics of polymerization of acrylonitrile initiated by KHSO5 and catalyzed by Ag(I) have been investigated in an aqueous medium over the temperature range of 35–50°C. The rates of polymerization Rp have been calculated and studied with respect to monomer and initiator. The catalytic activity of various metal ions on the initiator has been determined from a comparison of Rp values. The effects of monomer, catalyst, neutral salts, various amines, and inhibitor (hydroquinone) on the initial rate as well as maximum conversion have been studied. From the kinetics results a suitable reaction scheme has been proposed. 相似文献
5.
Rajani K. Samal Padma L. Nayak Mohan C. Nayak Akshaya K. Dhal 《Journal of polymer science. Part A, Polymer chemistry》1980,18(6):2001-2010
Kinetics of the polymerization of acrylonitrile has been investigated in aqueous sulfuric acid in a temperature range of 25–45°C. The rate of polymerization (Rp) and the rate of managanic ion disappearance, etc., have been measured. The effect of the various additives, such as water-miscible organic solvents, neutral electrolytes, complexing agents, and surfactants, on the rate has been thoroughly studied. A mechanism that involves the initial complex formation between the thiol form of the thioamide and Mn3+, whose decomposition yields the initiating free radical with the polymer chain terminated by mutual combination of growing radicals, has been suggested. 相似文献
6.
Rajani K. Samal M. C. Nayak G. Panda G. V. Suryanarayana D. P. Das 《Journal of polymer science. Part A, Polymer chemistry》1982,20(1):53-62
Vinyl polymerization of acrylonitrile initiated by the Ce(IV)/thioacetamide redox system has been investigated in aqueous sulfuric acid in the temperature range of 10–20°C. The rate of polymerization (Rp) and the rate of Ce(IV) disappearance (?RCe) were measured. The effect of certain water-soluble organic solvents, added electrolytes, and aromatic and heterocyclic organic nitrogen compounds on the rate of polymerization has been investigated. Depending on the experimental results, we have suggested a suitable reaction scheme for the system which involves the production of initiating radicals from the oxidation of thioacetamide (TAm) by ceric ion and the termination of the polymer chain by metal ions. 相似文献
7.
Padma L. Nayak Rajani K. Samal Mohan C. Nayak 《Journal of polymer science. Part A, Polymer chemistry》1979,17(1):1-7
The kinetics of thermal polymerization of methyl methacrylate initiated by the redox system Mn(III)–glycerol was studied in aqueous sulfuric acid in the temperature range of 30–40°C, and the rates of polymerization, Rp, and Mn3+ disappearance, etc., were measured. The effect of certain water-miscible organic solvents and certain cationic and anionic surfactants on the rates of polymerization has been investigated. A mechanism involving the formation of a complex between Mn3+ and glycerol whose decomposition yields the initiating free radical with the polymerization being terminated by the metal ion has been suggested. 相似文献
8.
9.
Shahram Mehdipour-Ataei Samal Babanzadeh 《International Journal of Polymer Analysis and Characterization》2020,25(3):147-157
AbstractA new monomeric building block was prepared via three consecutive reactions. 4-(4-Nitrobenzyl)pyridine was catalytically reduced to 4-(4-aminobenzyl)pyridine by converting the nitro to amino group. In second step, the later compound was reacted with 3,5-dinitrobenzoyl chloride to obtain a dinitro compound which finally was converted to a new diamine by reduction of nitro groups. Polycondensation reactions of the diamine with diacidchlorides led to preparation of novel cardo polyamides with high thermal stability and flame retardancy, as well as improved solubility. The structure-property relations were studied by varying the diacidchlorides to investigate the effect of symmetry and aromaticity on the polymers. 相似文献
10.
Manjushree Senapati Narayan C. Samal Ranu Mishra Swoyam P. Rout Lalit N. Patnaik Mahendra K. Rout 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(5-6):567-575
The present investigation aims at estimating the retarding effect of acetophenone in the polymerization of methyl methacrylate initiated by α,α' -azobisisobutyronitrile in the temperature range of 50 to 80°C. The results are interpreted in terms of Tüdös kinetic parameter (β). The effects of varying concentrations of substrate, monomer, initiator, and salts have been investigated. A suitable reaction scheme and rate expression have been suggested on the basis of the experimental findings, and another kinetic parameter (K) to represent the reactivity of acetophenones toward the polymer radical has been obtained graphically. 相似文献