全文获取类型
收费全文 | 736篇 |
免费 | 122篇 |
国内免费 | 18篇 |
专业分类
电工技术 | 3篇 |
综合类 | 18篇 |
化学工业 | 493篇 |
金属工艺 | 5篇 |
机械仪表 | 9篇 |
建筑科学 | 1篇 |
矿业工程 | 5篇 |
能源动力 | 2篇 |
轻工业 | 131篇 |
水利工程 | 1篇 |
石油天然气 | 11篇 |
无线电 | 38篇 |
一般工业技术 | 151篇 |
冶金工业 | 2篇 |
原子能技术 | 1篇 |
自动化技术 | 5篇 |
出版年
2024年 | 3篇 |
2023年 | 13篇 |
2022年 | 16篇 |
2021年 | 30篇 |
2020年 | 27篇 |
2019年 | 28篇 |
2018年 | 26篇 |
2017年 | 42篇 |
2016年 | 35篇 |
2015年 | 46篇 |
2014年 | 58篇 |
2013年 | 43篇 |
2012年 | 62篇 |
2011年 | 38篇 |
2010年 | 49篇 |
2009年 | 36篇 |
2008年 | 33篇 |
2007年 | 39篇 |
2006年 | 29篇 |
2005年 | 29篇 |
2004年 | 21篇 |
2003年 | 19篇 |
2002年 | 16篇 |
2001年 | 30篇 |
2000年 | 18篇 |
1999年 | 16篇 |
1998年 | 12篇 |
1997年 | 5篇 |
1996年 | 11篇 |
1995年 | 5篇 |
1994年 | 6篇 |
1993年 | 5篇 |
1992年 | 14篇 |
1991年 | 3篇 |
1990年 | 3篇 |
1989年 | 3篇 |
1987年 | 1篇 |
1986年 | 1篇 |
1985年 | 1篇 |
1984年 | 2篇 |
1983年 | 1篇 |
1982年 | 1篇 |
排序方式: 共有876条查询结果,搜索用时 9 毫秒
1.
2.
The micellar polymerisation of ionic surfactants such as allyldodecyl-dimethylammonium bromide and 3-dodecyl-1-vinyl imidazolium iodide has been studied by conductimetry in aqueous solution. The polymerisation was carried out using two different sources of γ rays directed into solutions of surfactant above the critical micellar concentration. Conductimetry is shown to be a very good physicochemical method for analysis of these solutions. The results showed different behaviour for the two surfactants, which has highlighted a change in the structure of their aggregates which led to the assumption of an interaction between the polymers of high mass and different products of the polymerisation (oligomers, products of degradation, monomers etc.). Ultrafiltration experiments coupled with 1H-NMR and conductivity analysis confirm these assumptions. 相似文献
3.
Mario J. Pires Joaquim M. S. Cabral 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》1994,61(3):219-224
Recombinant cytochrome b5 was extracted into the reversed micelle phase of an anionic surfactant (AOT) in octane and back-extracted to a final aqueous phase. The extraction of the protein was controlled by an electrostatic mechanism, since it was dependent on the global charge of the protein. This was directly demonstrated by experiments with native and mutant cytochromes obtained by site directed mutagenesis. The back-extraction of cytochrome b5 to a fresh aqueous phase was decreased by factors that reduced the size of the water pool of the organic phase, such as high salt concentrations (1–2 mol dm?3 NaCl) and low temperatures (4°C), probably because of an increase in a favourable interaction of this protein with the surfactant at closer distances. 相似文献
4.
Separations through reactions can provide reliable and economically viable alternatives to established methods of separation,
particularly for close boiling substances. New strategies in ‘Dissociation Extraction’ and ‘Dissociation Extractive Crystallization’
for separation of close boiling acidic/basic mixtures have been highlighted. Separations with aqueous solutions of hydrotrope
and aqueous micellar solutions have been brought out. Separations by membranes with facilitated transport is potentially attractive.
This paper is dedicated to Dr L K Doraiswamy on his sixtieth birthday. 相似文献
5.
Nicholas P. Petropolis Harrison M. Petropolis Nicole E. MacNeil Taylor M. Doucet D. Gerrard Marangoni 《Journal of surfactants and detergents》2021,24(1):51-66
The critical micelle concentrations (CMC) values and counterion dissociation (α values) have been determined for a number of mixed micellar systems consisting of two typical ionic surfactants and glycol ethers (glymes) as cosurfactants, namely diethylene glycol dimethyl ether, diethylene glycol diethyl ether, triethylene glycol dimethyl ether, and tetraethylene glycol dimethyl ether. Conductance experiments were used to determine the CMC and α values of the mixed micelles as a function of glyme concentration in the aqueous mixed solvent. Favorable interactions between sodium dodecyl sulfate micelles and glyme cosurfactants were deduced from the decreases in the CMC values and the large increase in the α values of these systems as a function of increasing glyme concentration in the mixed solvents. In contrast to the anionic surfactant/glyme systems, in general, there appeared to be little favorable interactions between the surfactant and glymes when micelles of the cationic surfactant dodecyltrimethylammonium bromide were formed in water/glyme solvent systems containing an increasing amount of the glymes. The interaction of glymes with the surfactant micelles was examined closely via 13C nuclear magnetic resonance (NMR) chemical shifts for both surfactant and glyme carbons; these chemical shifts changes were interpreted in terms of the distribution and the localization of the glymes in the aggregates. Finally, partition constants, determined from two-dimensional diffusion-oriented spectroscopy (2D-DOSY) experiments, were used to calculate thermodynamic quantities of transfer of the glymes between the bulk phase and the self-assembled aggregates. All these results are interpreted in terms of the key contributions that both the glyme ethoxylated groups and alkyl endgroups make to the hydrophobic interactions. 相似文献
6.
半导体硫化银纳米管的制备与光学性能 总被引:1,自引:0,他引:1
在以Triton X-100为表面活性剂形成的反相胶束体系中,成功地制备了半导体硫化银纳米管,管径88 nm~120nm、长度大于2.6 μm.X射线衍射测定表明,产物为纯单斜结构.紫外-可见光谱在275 nm处发现新的吸收峰,最大发射波长与体相材料相比,蓝移了38 nm. 相似文献
7.
Markus Nuopponen 《Polymer》2004,45(11):3643-3650
Series of amphiphilic diblock copolymers with poly(N-isopropylacrylamide) as a hydrophilic block and a hydrophobic block consisting of either polystyrene or poly(tert-butyl methacrylate) were synthesised using RAFT polymerisations. Differential scanning calorimetry showed the chemically different blocks being phase separated in dry polymers. Light scattering and microcalorimetry studies were performed on aqueous solutions to investigate the phase behavior of the diblock copolymers. By carefully transferring the polymers from an organic solvent to water, either micellar particles or large aggregates were obtained depending on the relative lengths of the blocks. Large aggregates collapsed upon heating, whereas collapse occurred slowly within a broad temperature range in the case of micelle like structures. However, microcalorimetrically the collapse of the PNIPAM chains was observed to take place in all samples, suggesting that the shells of the micellar particles are crowded in a way which hinders the compression of the poly(N-isopropylacrylamide) chains. 相似文献
8.
Xuezhi Tang 《Polymer》2007,48(21):6354-6365
Novel amphiphilic block copolymers, poly(ethylene oxide)-b-poly(p-nitrophenyl methacrylate) (PEO-b-PNPMA) with controlled molecular weights and narrow molecular weight distribution were successively synthesized by ATRP of NPMA using PEO-Br as initiator. Self-assembling of the diblock copolymer PEO113-b-PNPMA28 in the different solvent mixtures yielded various morphologies of star micelle-like aggregates, such as spheres, vesicles, cauliflower-like aggregates and rod-like aggregates, which are determined by the nature of the common solvents and the selective solvents. Thus the critical selective solvent contents and the solvent contents in PNPMA-rich phase were measured, and they have the following order: ethanol > methanol > water, and THF > CH3NO2 > DMSO. The probable self-assembling mechanism is discussed. This method is convenient for preparation of multiple morphological star micelle-like aggregates in solution, especially from the amphiphilic block copolymers with relatively longer block shell. 相似文献
9.
Kabanov Alexander V.; Klyachko Natalya L.; Nametkin Sergei N.; Merker Steffen; Zaroza Anna V.; Bunik Vita I.; Ivanov Mikhail V.; Levashov Andrey V. 《Protein engineering, design & selection : PEDS》1991,4(8):1009-1017
The size of the inner water cavity of reversed micelles formedin a triple system water-surfactant-organic solventcan be widely varied by changing the degree of surfactant hydration.This gives grounds to use reversed micelles as matrix microreactorsfor the design of supramolecular complexes of proteins. Usingultracentrifugation analysis, it has been demonstrated thatthe oligomeric composition of various enzymes (ketoglutaratedehydrogenase, alkaline phosphatase, lactic dehydrogenase, glyceraldehyde-3-phosphatedehydrogenase) solubilized in reversed micelles of Aerosol OT[sodium bis(2-ethylehexyl)sulfosuccinate] in octane changesupon variation of the degree of hydration. An oligomeric complexforms under conditions when the radius of the micelle innercavity is big enough to incorporate this complex as a whole.At lower degrees of hydration the micelles uncouplesuch complexes to their components. The catalytic propertiesof various oligomeric complexes have been studied. Possibilitiesof using reversed micelles for the separation of subunits ofoligomeric enzymes under non-denaturating conditions have beendemonstrated. In particular, the isolated subunits of alkalinephosphatase, lactic dehydrogenase and glyceralde-hyde-3-phosphatedehydrogenase have been found to be active in Aerosol OT reversedmicelles. The dependences of the catalytic activity of oligomericenzymes represent saw-like curves. The maxima of the catalyticactivity observed at these curves relate to the functioningof various oligomeric forms of an enzyme. The radii of the micelleinner cavity under conditions when these maxima are observedcorrelate with the linear dimensions of the enzyme oligomericforms. Correlation of the position of a maximum with the shapeof an oligomeric complex is discussed. 相似文献
10.
Moritz Tebbe Elizabeth Galati Gilbert C. Walker Eugenia Kumacheva 《Small (Weinheim an der Bergstrasse, Germany)》2017,13(37)
Future progress in nanoscience and nanotechnology necessitates further development of versatile, labor‐, and cost‐efficient surface patterning strategies. A new approach to nanopatterning is reported, which utilizes surface segregation of a smooth layer of an end‐grafted homopolymer in a poor solvent. The variation in polymer grafting density yields a range of surface nanostructures, including randomly organized pinned spherical micelles, worm‐like structures, networks, and porous films. The capability to use the polymer patterns for site‐specific deposition of small molecules, polymers, or nanoparticles is shown. This versatile strategy enables patterning of curved surfaces with direct access to the substrate and no need in changing polymer composition to realize different surface patterns. 相似文献