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21.
Jingcheng Hao Hanqing Wang Shuo Shi Runhua Lu Taotao Wang Ganzuo Li Haiying Sun 《中国科学B辑(英文版)》1997,40(3):225-235
By the orthogonal design, the optimal formation conditions for the middle-phase microemulsions in the system dioctadecyldimethylammonium
chloride (DODMAC)/ sodium dodecyl sulfate (SDS)/n-butanol/n-hep-tane/brine were obtained as follows: WDODMAC: WSDS = 1:4-1:5,C
π-butanol (%) = 11.0-12.0, andC
NaCl (%) = 3.25
Investigations have been made on the effects of the concentrations of NaCl and n-butanol (l.0%-14.0%), the ratios ofWDODMAC: to WSDS, and the kinds of alcohols (n-propanol, n-butanol, and n-pentanol) on the formation, the phase behaviour, the ultralow interfacial
tensions, the optimal salinity (S*), and the length of salinity (δS). Some rules and data were worked out about the formation and characteristics of the middle-phase
microemulsions. The mi-crostructures of the middle-phase microemulsions were also studied by using FT-IR, ESR, and freeze
fracture electron microscopy techniques. The results from the three methods show that the microstructures of the middlephase
mi-croemulsions undergo the change from O/W to bicontinuous (B.C.) and to W/O. The distribution rule of the orga-nized molecule
assemblies in the middle-phase microemulsions is conducible to constructing the model of microemulsion systems, to recognizing
the microstructures of the middle-phase microemulsions, and to setting forth the relationship between the microstructures
and macro-properties of rnicroemulsions.
Project supported by the Niltional Natural Science Foundation of China and the Chinese Postdoctoral Science Foundation. 相似文献
22.
在室温下,于pH 2.5的Britton-Robinson缓冲溶液中及非离子表面活性剂OP存在下,牛血清白蛋白(BSA)与偶氮胂-DBS的复合物的最大吸收在514 nm波长处,但显色复合物与试剂空白吸光度之差在370 nm处最大,选择在370 nm处测定,反应迅速完成。非离子表面活性剂OP可提高反应灵敏度及复合物稳定性。乙醇可提高体系灵敏度。BSA的质量范围在0~60.0 mg.L-1范围内符合比耳定律,方法表观摩尔吸光率3ε70 nm=8.58×105L.mol-1.cm-1。方法用于测定血清样品中蛋白质的总量,5次测定值的RSD为0.60%,回收率为98.0%。 相似文献
23.
R. A. Shagidullina E. P. Zhil'tsova L. A. Kudryavtseva 《Russian Chemical Bulletin》1998,47(9):1686-1689
The reaction ofn-hexylamine withO-alkylO-4-nitrophenyl chloromethylphosphonates in toluene solutions of poly(ethylene glycol)-600 monolaurate (PM) has been studied
by spectrophotometry. The reverse micelles of the nonionic surfactant increase more than tenfold the observed rate constant
of aminolysis. The catalytic activity of the surfactant is practically independent of the alkyl radical length of phosphonate.
An increase in the concentration of amine results in a decrease in the catalytic efficiency. The character of the dependence
of the rate constant on the concentration of PM is affected by the alkyl chain length of the substrate.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 1735–1738, September, 1998. 相似文献
24.
消除夹带溶胀的新液膜操作法曹汉瑾,褚莹,何彦涛,吴子生,严忠(东北师范大学化学系长春130024)关键词液膜,油/水乳液,溶胀,夹带,包裹消除液膜操作中的夹带溶胀对液膜的工业化具有重要意义,夹带溶胀分为包裹溶胀和再液化溶胀。前者是乳状液滴上浮时将水相... 相似文献
25.
羧甲基纤维素系列高分子表面活性剂超声合成的研究 总被引:27,自引:2,他引:27
研究了在超声波作用下羧甲基纤维素的降解反应及CMC与具有不同亲水亲油比值的活性大单体「烷基醇(酚)聚氧乙烯醚丙烯酸酯及第三单体」的超声共聚反应。经萃取提纯的共聚产物用IR,^13C NMR和UV等方法进行表证,证实通过超声反应制得了二元和三元共聚物。 相似文献
26.
本文报道了一种光敏型的阳离子表面活性剂(AZO),其分子结构中含有偶氮苯基团,并研究了光照对表面活性和泡沫性能的影响。经紫外光照射后,表面活性剂的饱和吸附量(Гmax)减小,临界胶束浓度(cmc)、最低表面张力(γcmc)和分子极限占有面积(Amin)增大;气泡数目增多,直径变小,发泡能力和泡沫稳定性降低。实验结果证实,该表面活性剂的表面活性和泡沫稳定性可以用光照进行调控。 相似文献
27.
G. A. Gainanova E. P. Zhil’tsova L. A. Kudryavtseva S. V. Kharlamov Sh. K. Latypov A. P. Timosheva A. I. Konovalov 《Russian Chemical Bulletin》2006,55(8):1411-1418
Micelle formation in a cetyltrimethylammonium bromide-poly(ethylene glycol)-600 monolaurate-chloroform system in the absence
and presence of hydroxybenzylated polyethylenimines (PEI) was studied by dielcometric titration, NMR self-diffusion, light
scattering, and kinetic methods. A catalytic effect of mixed micelles on the reaction of 4-nitrophenylbis(chloromethyl)phosphinate
with PEI was shown. The catalytic effect depends on the degree of substitution of PEI and composition of a surfactant mixture.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 1359–1365, August, 2006. 相似文献
28.
The interaction of a nonionic polymeric surfactant with an anionic surfactant at the oil–water interface has been studied
by its effects on the droplet size, stability and rheology of emulsions. Oil-in-water (o/w) emulsions were prepared using
isoparaffinic oil and mixtures of a nonionic polymeric surfactant with an anionic surfactant. The macro-molecular surfactant
was a graft copolymer with a backbone of polymethyl methacrylate and grafted polyethylene oxide (a graft copolymer with PEO
chains of MW=750). The anionic surfactant was sodium dodecyl sulfate (SDS). The stabiliza-tion of the emulsion droplets was
found to be different when using one or the other surfactant. The mechanism of stabilization of emulsion droplets by the macro-molecular
surfactant is of the steric type while the stabilization by anionic surfactant is of the electrostatic repulsion type. Emulsions
stabilized with mixtures present both types of stabilization. Other effects on the preparation and stabilization of emulsions
were found to be dependent on properties associated with the surfactant molecular weight such as the Marangoni effect and
Gibbs elasticity. The initial droplet size of the emulsions showed a synergistic effect of the surfactant combination, showing
a minimum for the mixtures compared to the pure components. Emulsion stability also shows a synergistic interaction of both
surfactants. Rheological measurements allow for the estimation of the interparticle interaction when measured as a function
of volume fraction. Most of the effects observed can be attributed to the differences in interfacial tension and droplet radius
produced by both surfactants and their mixtures. The elastic moduli are well explained on the basis of droplet deformation.
Ionic versus steric stabilization produce little difference in the observed rheology, the only important differences observed
concerned the extent of the linear viscoelasticity region.
Received: 22 November 1996 Accepted: 24 March 1997 相似文献
29.
Formation at low surfactant concentrations and characterization of mesoporous MCM-41 总被引:2,自引:0,他引:2
At low concentrations of cetyltrimethylammonium bromide,all silica-based mesoporous materials with hexagonal phase have been synthesized via interactions between self-assembled surfactant molecule aggregates and aniomc silicate polymers.The resulting materials are characterized by XRD,FT-IR,solid state 29Si MAS NMR,thermal analysis and N2 adsorption-desorption measurements.After soluble ions are removed,the interactors between surfactant micelles and silicate polymers are reorganized and then form mesostructures 1 he hexagonal framework is sonsistent with amorphous silica gel.The structures of materials depend on the synthesis conditions Hydrothermal process improves the interactions between molecules and increases the degree of framework silicon atom polymerization The.surface area and the mesopore volume of the material prepared at 100℃ increase by 87% and 71 %,respectively,compared with those obtained at room temperature. 相似文献
30.
Highly hydrophobically modified (with n-dodecylamide chain) linear poly(acrylic acid)s (HHMPAAH) and poly(sodium acrylate)s (HHMPAANa) with various degrees of grafting
(τ) were synthesized and used as emulsifiers of the n-dodecane/water system. The type of emulsion, oil in water (O/W) or water in oil (W/O), was investigated as a function of
the polymer chemical structure (τ, salt or acid form of the copolymer) and aqueous phase electrolyte concentration (NaNO3). Increasing τ and/or salt concentration was found to favor the formation of inverse emulsions. Direct liquid–liquid dispersions
are more likely to form with poly(sodium acrylate)s than with poly(acrylic acid)s. Hence, field variables such as τ, pH and
ionic strength are relevant parameters to control emulsion type. Moreover, a balanced polyelectrolyte neither soluble in oil
nor in water was synthesized for the first time. With this original emulsifier, the dispersion type was found to change from
O/W to W/O with polymer salting out. The work provides convenient model system for fundamental studies of polymer conformation
at liquid–liquid interfaces.
Received: 31 March 1998 Accepted: 30 April 1998 相似文献