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排序方式: 共有376条查询结果,搜索用时 31 毫秒
1.
2.
Tushar S. Deore Amid L. Sadgar Radha V. Jayaram 《Journal of surfactants and detergents》2021,24(1):185-190
Ionic liquids have been found to be suitable alternatives to volatile organic solvents in chemical transformation. Through a proper choice of cations and anions, the properties of an ionic liquid can be tuned so that it resembles an amphiphile. Such specially designed molecules are known as surface-active ionic liquids (SAIL). Like conventional surfactants, SAIL also form aggregates in an aqueous medium. Studies show that the mixing of SAIL with conventional surfactants leads to synergistic micellization. However, very few reports are available on the application of such systems as reaction media. Present study focuses on the application of mixed micelles of 1-tetradecyl-3-methylimidazol-1-ium bromide, ([C14mim]Br) with nonionic surfactant, Octylphenol ethoxylate with 10 moles of ethylene oxide (OPE-10). Enhanced solubilization and selective catalytic oxidation of toluene using hydrogen peroxide as an oxidant and tungstic acid as a catalyst have been studied in detail using this system. 相似文献
3.
Viscosity measurements under Newtonian flow conditions had been performed on cetyltrimethylammonium bromide (CTAB) aqueous
solutions in the combined presence of sodium salts of aromatic acids (sodium salicylate, NaSal; sodium benzoate, NaBen; sodium
anthranilate, NaAn) and organic additives (1-hexanol, C6OH; n-hexylamine, C6NH2) at 30°C. On addition of C6OH or C6NH2, the viscosity of 25 mM CTAB solution remained nearly constant without salt as well as with a lower salt concentration. This
is due to low CTAB concentration which is not sufficient to produce structural changes in this concentration range of salts.
However, as the salt concentration was increased further, the effect of C6OH/C6NH2 addition was different with different salts: The viscosity first increased; then a decrease was observed with the former
while with C6NH2 a decrease followed by constancy appeared in plots of relative viscosities (η
r
) vs. organic additive concentrations. At further higher salt concentration, the magnitude of η
r
was much higher. The viscosity increase is explained in terms of micellar growth and the decrease in terms of swollen micelle
formation (due to interior solubilization of organic additive) or micellar disintegration (due to formation of water + additive
pseudophase). 相似文献
4.
NanoSolve--一种包裹亲油性活性物的新技术 总被引:1,自引:0,他引:1
说明厂磷脂是天然化妆品成分,指出传统加溶方式的缺点,介绍了一种用磷脂包裹亲油性活性物的新技术、NanoSolve的原理和优点及其在护肤品等领域的应用。 相似文献
5.
E. D. Goddard 《Journal of the American Oil Chemists' Society》1994,71(1):1-16
The field of polymer/surfactant interaction is reviewed in this work. Results from two investigative methods,viz., dialysis and surface tension, are discussed, illustrating the main behavioral patterns and outlining the principles of the
interactions. Next, aspects of the interaction phenomena that appear to have relevance to detergent formulation are presented.
These include solution rheology, solubility control and surface conditioning. Lastly, the importance of surface activity of
the polymer itself is stressed, culminating in a discussion of the properties of hydrophobically modified water-soluble polymers
(“polymeric surfactants”), both alone and in the presence of conventional surfactants.
Based on the Samuel Rosen Memorial Award lecture, given at the AOCS Annual Meeting, Anaheim, CA, April 1993. 相似文献
6.
Functional polyurethane surfactants (di‐block and tri‐block) were synthesized by addition polymerization of 2,4‐toluenediisocyanate with poly(propylene oxide) and monoallyl‐end‐capped poly(ethylene oxide). The chemical structure of the polyurethane surfactants was confirmed by Fourier transform infrared and 1H NMR spectroscopy. These polymeric surfactants were found to have excellent surface activity. The lowest surface tension of polyurethane surfactant aqueous solutions could be reduced to 37.6 mN m?1. All the polyurethane surfactants synthesized had low critical micelle concentrations and could reduce the surface tension even at very low concentration levels (10?6–10?5 mol L?1). The solubilization of toluene in micelles of the synthesized polyurethane surfactants was studied using UV‐visible spectroscopy, and the results showed that they all exhibited good solubilization capacity. Possible solubilization positions of toluene in the micelles are conjectured. Copyright © 2006 Society of Chemical Industry 相似文献
7.
Relationship of structure to properties of surfactants. 16. Linear decyldiphenylether sulfonates 总被引:1,自引:0,他引:1
Milton J. Rosen Zhen Huo Zhu Xi Yuan Hua 《Journal of the American Oil Chemists' Society》1992,69(1):30-33
The properties of some well-characterized sodium linear decyldiphenylether (C10DPE)sulfonates have been studied. Among the properties investigated are dynamic and equilibrium surface tension, critical
micelle concentration (CMC), area per molecule at the aqueous solution/air interface, wetting time by the Draves technique,
foaming by the Ross-Miles method, solubilization, and hydrotropy. The decyldiphenylether moiety appears to be equivalent to
a terminally substituted straight alkyl chain of 16 carbon atoms. The trialkyl- and dialkyl-mono-sulfonates have solubilities
of < 0.01 g/dm3 in water, but are readily soluble in hexane. The didecyldiphenyl ether disulfonate (DADS) has a very low CMC value (1.0 ×
10−5 mol dm−3) in aqueous 0.1 N Na+ solution (NaCl), characteristic of surfactants with two hydrophilic and two hydrophobic groups. It also has a much larger
area per molecule at the aqueous solution/air interface than the monodecyldiphenyl-ether monosulfonate (MAMS) and a much higher
surface tension at the CMC. MAMS has a much lower surface tension at a surface age of 1 second (γ1s) than either DADS or the monodecyldiphenylether disulfonate (MADS). In agreement with γ1s and γeq values, wetting times increase in the order: MAMS < DADS < MADS and initial foam heights decrease in the order: MAMS > DADS
> MADS. Solubilization for three water-insoluble surfactants decreases in the order: DADS > MAMS > MADS, while hydrotropy
is most pronounced with the disulfonates. 相似文献
8.
Gladys E. Granero Chandrasekharan Ramachandran Gordon L. Amidon 《Drug development and industrial pharmacy》2013,39(9):917-922
The solubility of fenofibrate in pH 6.8 McIlvaine buffers containing varying concentrations of sodium lauryl sulfate was determined. The dissolution behavior of fenofibrate was also examined in the same solutions with rotating disk experiments. It was observed that the enhancement in intrinsic dissolution rate was approximately 500-fold and the enhancement in solubility was approximately 2000-fold in a pH 6.8 buffer containing 2% (w/v) sodium lauryl sulfate compared to that in buffer alone. The micellar solubilization equilibrium coefficient (k*) was estimated from the solubility data and found to be 30884 ± 213 L/mol. The diffusivity for the free solute, 7.15 × 10? 6 cm2/s, was calculated using Schroeder's additive molal volume estimates and Hayduk-Laurie correlation. The diffusivity of the drug-loaded micelle, estimated from the experimental solubility and dissolution data and the calculated value for free solute diffusivity, was 0.86 × 10? 6 cm2/s. Thus, the much lower enhancement in dissolution of fenofibrate compared to its enhancement in solubility in surfactant solutions appears to be consistent with the contribution to the total transport due to enhanced micellar solubilization as well as a large decrease ( ~ 8-fold) in the diffusivity of the drug-loaded micelle. 相似文献
9.
探讨了几种具代表性的无机盐离子对鼠李糖脂(RL)增溶2,2’,4,4’-四氯联苯的影响。结果表明,适当增加Na+、Mg2+、Ca2+的浓度对RL增溶2,2’,4,4’CB有显著的促进作用,且Mg2+的促进作用比Na+的大,但当Mg2+浓度大于0.8 mmol/L时,促进作用减弱。当Ca2+浓度超过0.2mmol/L时,RL开始产生沉淀,导致RL对2,2’,4,4’CB的增溶作用逐渐降低。无机阴离子对RL增溶2,2’,4,4’CB的影响很小。 相似文献
10.