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61.
选用硬脂酸钠对ZnO进行表面湿法改性,以环十五硅氧烷硅油为溶剂,PEG-10聚二甲基硅氧烷为分散剂,通过机械球磨法制备了纳米ZnO分散浆。利用水接触角、热重、TEM和FTIR对纳米ZnO粉体进行表征。结果表明,硬脂酸钠改性后,粉体具有疏水性,且硬脂酸钠最佳包覆量为6%(以ZnO的质量计,下同)。硬脂酸钠包覆量为6%的疏水性纳米ZnO粉体,包覆层厚度约为2 nm,此时水接触角最大为145.4°。模拟防晒乳液的防晒性能测试中,纳米氧化锌分散浆的紫外屏蔽性能显著优于粉体。流变特性测试表明,分散浆为假塑性流体,流动曲线符合Ostwald-de Wale幂律方程,具有剪切稀化特性;分散浆的黏度低,触变性小,储存稳定性高;温度升高,黏度降低,配方生产中对温度的敏感程度较小 。 相似文献
62.
表面活性剂聚集体的流变性质 总被引:6,自引:2,他引:6
以流变学基础知识为出发点,系统综述了胶束、微乳液,溶致液晶(层状、六角状、立方状),囊泡、虫状胶束等表面活性剂聚集体的流变性质及其剪切诱导结构转变现象的研究现状,总结了自流变性质的特点和理论模型,对具有黏弹性的表面活性剂活性剂聚集体进行了较为详细的论述,胶束稀溶液和微乳液多为牛顿流体;溶致液晶为非牛顿流体,有应力服价值和较高的黏弹性,囊泡的弹性性质比较突出,;虫状胶束体系具有非线性黏弹性,易形成网络结构;层状液晶、囊泡和虫状胶束等结构在剪切作用下能发生变化。这些结论对指导表面活性剂的研究和应用有重要意义。 相似文献
63.
The rheological behaviors of high‐impact polystyrene (HIPS) and HIPS/TiO2 composites were investigated by use of a rheometer in the present article. HIPS exhibited a constant critical stress of the sharkskin in various temperatures, and the analysis indicated that the mechanism of sharkskin of HIPS was wall–slip and its special temperature dependency was determined by weak wall–melt adsorption. The experimental results also showed that the introduction of TiO2 into HIPS only slightly influenced the apparent viscosity (ηa) of the composites. Moreover, TiO2 exhibited an unusual effect on the non‐Newtonian index of the composites at high shear rate. Both phenomena indicated the increase of inner free volume induced by TiO2 in molecularly rigid HIPS. Moreover, it was noteworthy that a featured stress could be used to label the dispersion of TiO2 in the HIPS matrix, and the numeric affinity of this featured stress and the critical stress of sharkskin revealed that both processes were relevant to the same molecular relaxation. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 802–807, 2005 相似文献
64.
65.
Polycaproamide (PCA) and cationic dyeable poly(ethylene terephthalate) (CDP) polymers were blended mechanically (in ratios of 75/25, 50/50, and 25/75) in a melt twin‐screw extruder to prepare three PCA/CDP polyblended materials. The blends of PCA and CDP were spun into fibers. The molar ratio of dimethyl 5‐sulfoisophthalate sodium salt for CDP was 2%. This study investigated the physical properties of PCA/CDP polyblended fibers with nuclear magnetic resonance, gel permeation chromatography, gas chromatography, potentiometer, differential scanning calorimetry (DSC), thermogravimetric analysis, scanning electron microscopy (SEM), extension stress–strain measurements, density gradient analysis, and rheometry. The experimental results of DSC proved that PCA and CDP formed an immiscible system. In an SEM image of a 50/50 PCA/CDP blend, the morphological aggregation of a larger size, from 3 to 5 μm in diameter, was observed. The rheological behavior of the PCA/CDP polyblended materials exhibited negative‐deviation blends, and the 50/50 blend of the PCA/CDP polyblended fibers showed a minimum tenacity value. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 1710–1715, 2004 相似文献
66.
Good correspondence of the gel‐time values obtained by two different methods, G′ = G″ and 1/η0→0, was observed for different types of natural and modified tannin extracts. The pH presents the predominant effect on both the activation energies and the gel times observed, while the proportion of a paraformaldehyde hardener has a much lesser effect on these parameters. The rate constants of the different phases of the reaction of polycondensation with formaldehyde, both before and after the gel point, were obtained for the six commercial tannin extracts tested. The viscoelastic properties of the different tannins/formaldehyde gels were measured. The gel stiffness S, relaxation coefficient n, and relaxation time λ were determined and their dependence on the proportion of the formaldehyde hardener, on the temperature, and on the type of tannin was determined. The gel stiffness S appears to be influenced considerably by the proportion of the formaldehyde hardener. Its value decreased as the percentage of the hardener increased: This was due to early network immobilization and the resulting lower level of crosslinking resulting from it. The influence on S of the temperature is not very pronounced. The relaxation coefficient n appears to depend mainly on the reactivity of the tannin used: The faster the reactivity, the higher was the value of n. This appears to be valid exclusively in tannin extracts where the colloidal state is still present, while it is not valid in extracts where the colloidal state was eliminated by, for example, solvent extraction. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 864–871, 2002 相似文献
67.
J. A. Segura M. L. Herrera M. C. Añón 《Journal of the American Oil Chemists' Society》1995,72(3):375-378
Time-dependent flow properties of both commercial and pilot plant-made margarines were characterized under steady shear. Flow
curves were fitted to the kinetic expression τ = τ
i
+a e
−k1t
+b e
−k2t
. A first-order kinetic model did not describe the observed destruction process of the margarine structure in an adequate
manner. In the proposed model, two structures with different destruction rates are postulated. Each structure contributes
to a part of the shear stress necessary to deform the margarine sample. The parameters τ
i
a andb are temperature-dependent. Decreasing temperatures produce an exponential increase of τ
i
, a linear increase ofb and an increase ofa up to a point beyond which it remains constant. A physical interpretation of the model is proposed. The role of the aqueous
phase was also studied. Greater hardness was detected at higher water content. Parameter τ
i
increased, at any selected temperature, with increasing aqueous phase content of the sample. Parametera increased with decreasing temperatures and higher water content. On the other hand, parameterb was not affected by the amount of aqueous phase. This kinetic model could be employed to perform studies on the influence
of different parameters of margarine formulation on its rheologic behavior. 相似文献
68.
An O?carboxymethylated chitosan (O? CMCh) water solution (I) and N,N‐dimethylacetamide (DMAc) emulsion (II) were blended with a cellulose LiCl/DMAc solution, and corresponding polyblends (Polyblends I and II) were obtained. The rheology of the three fluids, that is, the cellulose solution and Polyblends I and II, was investigated. The cellulose solution was characterized by a power‐law fluid. When an O‐CMCh water solution or DMAc emulsion was added to the cellulose solution, the power‐law curve was preserved. The power‐law indexes (n) of all three fluids increased along with the temperature. Polyblend I displays an n close to but a little higher than that of the cellulose solution, while Polyblend II shows a much higher power index than those of the other two fluids. The values of the apparent viscosity (ηa) for all the three fluids are close and decrease along with an increase in the temperature. Adding O‐CMCh microparticles into Polyblends I and II results in a decrease in the structural viscosity index (Δη) in comparison to that of the cellulose solution, and this effect is very obvious for Polyblend I. A cellulose solution's Δη declines with the augmentation of temperature, while the Δη's of both Polyblends I and II show minimum values at about 323 K. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 1719–1725, 2003 相似文献
69.
The effect of ultrasonic vibration and binary processing aid in improving the processability of metallocene linear low‐density polyethylene (mLLDPE) was investigated. During extrusion, ultrasonic vibration clearly reduced the die pressure and apparent viscosity of mLLDPE but had only a slight effect on its melt fracture. The effect of diatomite/PEG binary processing aid (BPA) was excellent in reducing the viscosity and eliminating the sharkskin fracture of mLLDPE. The effect of ultrasonic vibration and binary processing aid in improving the processability of mLLDPE was synergetic. With a combination of ultrasonic vibration and a small amount of processing aid, the flowability of mLLDPE was further improved, and the critical shear rate for the onset of sharkskin fracture was increased. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 1927–1935, 2007 相似文献
70.
Effect of DAG on milk fat TAG crystallization 总被引:1,自引:0,他引:1
Amanda J. Wright Alejandro G. Marangoni 《Journal of the American Oil Chemists' Society》2002,79(4):395-402
The effect of milk fat and standard DAG on the crystallization behavior of milk fat TAG (MF-TAG) was investigated. When milk
fat DAG were added to MF-TAG at the 0.1 wt% level, crystallization was delayed. Racemic purity was shown to be an important
factor in the ability of DAG to influence TAG crystallization. Only sn-1,2 isomers of blends of MF-TAG with 0.1 wt% of the racemic mixtures of dipalmitin and diolein increased the activation free
energy barrier to MF-TAG nucleation (ΔG
c
) and delayed the subsequent crystallization process by increasing the crystallization induction time (τSFC) determined from solid fat content-time measurements. Although crystallization kinetics were affected, the properties of
the resulting network structures remained unchanged upon addition of milk fat minor components at the 0.1 wt% level 相似文献