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排序方式: 共有171条查询结果,搜索用时 31 毫秒
1.
H Shinozuka T Ohmura SL Katyal AI Zedda GM Ledda-Columbano A Columbano 《Canadian Metallurgical Quarterly》1996,23(6):1572-1577
Several proteins from culture supernatants of Streptococcus sobrinus were able to bind avidly to Sephadex G-75. The proteins could be partially eluted from the Sephadex by low-molecular-weight alpha-1,6 glucan or fully eluted by 4 M guanidine hydrochloride. Elution profiles were complex, yielding proteins of 16, 45, 58 to 60, 90, 135, and 145 kDa, showing that the wild-type strain possessed multiple glucan-binding proteins. Two mutants of Streptococcus sobrinus incapable of aggregation by high-molecular-weight alpha-1,6 glucan were isolated. One mutant was spontaneous, from a cell suspension to which glucan had been added, whereas the other was induced by ethyl methanesulfonate. Both mutants were devoid of a 60-kDa protein, as shown by gel electrophoresis of culture supernatants and whole cells. Amino acid analysis showed that the 58- to 60-kDa protein and the 90-kDa protein were distinct, although both were N-terminally blocked. Both mutants retained their ability to adhere to glass in the presence of sucrose and to ferment mannitol and sorbitol. Both mutants retained their glucosytransferase activities, as shown by activity gels. Western blots (immunoblots), employing antibody against a glucan-binding protein of Streptococcus mutans, failed to reveal cross-reactivity with S. sobrinus proteins. The results show that even though S. sobrinus produces several proteins capable of binding alpha-1,6 glucans, the 60-kDa protein is probably the lectin needed for glucan-dependent cellular aggregation. 相似文献
2.
Interaction of cation-exchange membrane with polycation I. Poly(N-methyl-4-vinylpyridinium chloride)
We elucidated the effect of the molecular weight of poly(N-methyl-4-vinylpyridinium chloride) (PMVP) on its adsorbed or ion-exchanged amount on the cation-exchange membrane and the preferntial permselectivity of the membrane for sodium ion to calcium ion. The amount of the adsorbed or ion-exchanged PMVP increases with time and then attains to a definite value at a definite concentration. Also, the ultimate value increases with increasing the concentration of PMVP. When the molecular weight of PMVP is 3090, the ratio of the pyridinium groups of PMVP ion-exchanged with the sulfonic acid groups on the membrane surface to the total pyridinium groups of the cohered PMVP is in the range of 70–80%. The relative transport number of calcium ions to sodium ions(PNaCa) decreases with increasing the amount of adsorbed or ion-exchanged PMVP and the numbe rof non-ion-exchanged pyridinium groups of PMVP and the number of non-ion-exchanged pyridinium groups of PMVP on the membrane surface. The smaller the molecular weight of PMVP, the more the adsorbed or ion-exchanged amount and the more preferable the permselectivity for sodium ion. 相似文献
3.
D. P. Gosain T. Shimizu M. Ohmura M. Suzuki T. Bando S. Okano 《Journal of Materials Science》1991,26(12):3271-3274
Composition dependence of properties of Sb2Te3–x
Se
x
in the range 0x<3 were studied using differential thermal analysis and X-ray diffraction. Sb2Te3–x
Se
x
form solid solution for 0<x1.25 and 2.75x<3. A systematic study of crystallization temperature in Sb2Te3–x
Se
x
(0x2.75) thin films prepared by flash evaporation was carried out. In preliminary experiments for some compositions, more than 103 repetitions between amorphous and crystalline states were attained by the application of electric pulses. 相似文献
4.
The modeling of particle aggregation under a simple shear flow and the extension of the model to a stirred vessel is described. The model quantitatively demonstrates the change of the number of aggregates with time for each shear rate. This number increased with higher shear rate and, conversely, the aggregate size became small when raising the shear rate. This was because aggregates were broken by the stronger shear force. The number of aggregates for different impellers was determined. The shear rate was back‐calculated from the experimentally obtained aggregate size and the model equation. This shear rate was different from that estimated from the Metzner‐Otto method, consequently, some revisions of the Metzner‐Otto equation might be necessary for its application to particle aggregation. 相似文献
5.
6.
Thermodynamic Properties of Ionic Semiclathrate Hydrate Formed with Tetrabutylammonium Propionate
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The phase equilibrium temperature and dissociation heat of tetrabutylammonium propionate (TBAPr) hydrate are reported. TBAPr hydrate is a type of ionic semiclathrate hydrates and also could potentially be used as thermal energy storage material. The temperature‐composition phase diagram of the TBAPr hydrate was determined in a defined range of mass fractions. Considering the dissociation heat of differential scanning calorimetry (DSC) measurements, multiple peaks of heat flow were observed in the TBAPr‐water system at the TBAPr mass fraction lower than 0.35, and there was a single peak at the mass fraction higher than 0.37. 相似文献
7.
The block copolymers consisting of 2,7-dimethoxycarbazole- and oxadiazole-containing segments as hole and electron transporting units, respectively, were synthesized by NMRP manner. OLED devices were fabricated using block copolymer, random copolymer, and polymer blend for matrix of the emitting layer with Ir(ppy)3 as a phosphorescent dopant in order to investigate morphological effect on the performance. From the finding that the block copolymer system overwhelmed the others in EQE, we assumed that a morphology with dimethoxycarbazole units assembled to the surface of PEDOT:PSS played a considerable role for effective recombination of charges as well as sufficient charge injection into the emitting layer. 相似文献
8.
The asymmetric oxidation of poly(phenylvinyl sulfide) (poly-Ph VS) and poly(t-butylvinyl sulfide) (poly-t-BuVS) was carried out with optically active percamphoric acid, and the optically active polysulfoxides were obtained. The values of the specific rotation for the oxidation products of poly-PhVS and poly-t-BuVS were + 1.0 (having 56% of sulfoxide unit contents) and +9.1 (49%), respectively. The specific rotation of the product increased with increasing the contents of sulfoxide units. The optical rotatory dispersion curves of the oxidation products of poly-PhVS and poly-t-BuVS were positive curves and were found to fit the simple Drude equation. The λc values of the oxidation products (poly-PhVS, 271 mμ; poly-t-BuVS, 212 mμ) suggested that the chromophore which caused optically activity was the sulfoxide group. Similarly, the asymmetric oxidation of t-BuVS–MMA copolymer, t-BuVS–styrene copolymer, and PhVS–MMA copolymer was carried out, and the optically active copolysulfoxides were obtained. Furthermore, the biosynthetic oxidation of poly-PhVS and PhVS–maleic anhydride copolymer treated with aqueous KOH was carried out using Aspergillus niger or Penicillium notatum in Czapeck solution, and the optically active polymers were obtained. 相似文献
9.
10.
Ji?í Jeništa Hidemasa Takana Hideya Nishiyama Milada Bartlová Vladimír Aubrecht Petr K?enek Viktor Sember Alan Mašláni 《Computer Physics Communications》2011,182(9):1776-1783
The paper presents numerical simulations of the discharge and the near-outlet regions of the hybrid-stabilized argon–water electric arc. Two different numerical methods for solving the set of conservative equations for the continuity, momentum and energy have been applied. The major difference between the results using the two methods occurs in the temperature distribution in arc fringes within the discharge chamber. This fact influences the potential drop, overpressure, reabsorption of radiation and arc efficiency. It is shown that the radial profiles of temperature at the exit nozzle are less influenced by different temperature distribution within the discharge chamber. Comparison with chosen experimental temperature profiles shows very good agreement. 相似文献