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91.
交联聚丙烯酰胺吸水凝胶的强度 总被引:1,自引:0,他引:1
高吸水材料是一类新型的功能高分子材料,已有广泛开发和应用。本文讨论了含大量无机填料膨润土的阴离子型交联聚丙烯酰胺(JSWAM)吸水凝胶的强度及其形态结构。 吸水材料JSWAM的制备:将填料搅拌分散于丙烯酰胺水溶液中,同时加入规定量的甲叉基双丙烯酰胺、过硫酸铵、碱,而后聚合并水解。将聚合物胶块造粒、烘干、粉碎。凝胶强度 相似文献
92.
93.
An investigation of heparinase immobilization 总被引:1,自引:0,他引:1
Bernstein Howard Yang Victor C. Langer Robert 《Applied biochemistry and biotechnology》1987,16(1):129-143
A systematic investigation of the parameters that affect the efficiency of immobilizing heparinase onto cyanogen bromide activated
crosslinked 8% agarose beads was conducted. Two experimental measures, the “fraction bound” and the “fraction retained,” were
used to monitor the coupling efficiency. The fraction bound is the portion of the total initial enzyme that is bound to the
agarose gel. The fraction retained is the fraction of bound enzyme that is active. The product of the two measures indicates
the coupling efficiency. The activity of the immobilized heparinase was measured under conditions free of both internal and
external mass transfer limitations, and thus, the fraction retained represents the true immobilized enzyme activity.
Increasing the degree of activation of the beads results in an increase in the fraction bound, the fraction retained, and
consequently, the coupling efficiency. As the ratio of enzyme solution to gel volume increases from 1.5 to 2.2, the fraction
bound remains constant but the fraction retained decreases (heparinase concentration; 0.15 mg/mL and degree of activation;
9.5 μmol of cyanate esters/g of gel). At volume ratios greater than 2.2, both the fraction bound and the fraction retained
decline continuously. Changing the heparinase concentration in the coupling solution changes the coupling efficiency in a
manner similar to that of the volume ratio change.
When heparin is added during the coupling process, the fraction bound declines as the heparin concentration increases, whereas
the fraction retained increases up to a heparin concentration of 12 mg/mL and decreases thereafter. When arginine, lysine,
and glycine are used to block the unreacted cyanate ester groups after the coupling process, the immobilized heparinase shows
different pH optima of 6.5, 6.9, and 7.2, respectively. Based upon these findings, a protocol to optimize heparinase immobilization
is developed. 相似文献
94.
95.
程序涂渍柱“柱效能程序效应”的研究 总被引:1,自引:0,他引:1
本文从理论上给出程序柱“柱效能程序效应”的概念并导出了函数关系式,通过计算机可计算柱效能程序效应与柱内各变量之间的关系,实践证明实验数据的变化趋势与理论数据相符。 相似文献
96.
Mohammad M. Fares Adeeb S. El-Faqeeh 《Journal of Thermal Analysis and Calorimetry》2005,82(1):161-166
Summary Thermal degradation under N2atmosphere and thermoxidative degradation under air atmosphere of increasingly grafting efficiency values (i.e. GE%=0.0 to 35.5) for starch and starch grafted with N-tert-butylacrylamide thermosensitive copolymers (starch-g-BAM) by Ozawa and Kissinger methods using thermogravimetric analysis
(TG) and differential scanning calorimetry techniques (DSC) at 10, 30 and 50% mass losses respectively have been studied.
Influence of physical inter and intra molecular interactions on grafting and consequently on activation energy of degradation
(Ea,d) was investigated using Ozawa's method, whereas linear dependence of Ea,don GE% by scaling relations using Kissinger's method was determined. Furthermore, the thermoxidative degradation induces the possibility
of molecular rearrangement, cyclization and partial crosslinking that is deduced from the activation energy of degradation
(Ea,d) and residual mass of TG profile. Thermal stability of starch does not alter as a result of different grafting efficiency
percentages. 相似文献
97.
We present a microstructural model of aerogels that includes the effect of particle necks, tortuosity and dangling ends on the scaling of elastic moduli with density. Relative neck radii can be determined for sintering series of silica aerogels and for Resorcinol Formaldehyde (RF) aerogels produced with different catalyst concentrations. The density of elastically ineffective dangling ends and the tortuosity can be estimated using information from thermal conductivity and elastic modulus measurements in silica aerogels. Typical values for the load bearing mass range from >50% for high density and heat treated aerogels to <10% of the total mass for low density wet-gels. 相似文献
98.
G. Schomburg 《Journal of separation science》1979,2(7):461-474
Glass capillary gas chromatography is a high resolution separation method which allows the qualitative and quantitative analysis of even complex mixtures, which may contain many components–also isomeric–in a wide range of volatilities, polarities and concentrations. The principal limitation of gas chromatographic application is given by an insufficient volatility of the species to be separated. Elevated temperatures have to be applied if the application range is to be extended and to achieve steep peak profiles, i.e. low detection limits at high resolution. The use of elevated temperatures is limited, of course, by the temperature stability of both the solvent (stationary liquid and support) and the solutes. The problems of trace analysis for low volatility compounds at high resolution and its limitational parameters regarding sampling, separation and detection are discussed. The applicability of glass capillary columns in this field is influenced by the following parameters: tailing behaviour; irreversible adsorption of polar and decomposition of unstable solutes; thermal stability of stationary liquid (including the support deactivation); separation efficiency and sample capacity (film thickness). Multidimensional gas chromatography using capillary columns coupled either with a packed or another capilllary column for preseparations may be applied with advantage in the analysis of complex mixtures. 相似文献
99.
咪唑类化合物-CuCl络合催化剂在甲醇氧化羰基化反应中的催化性能 总被引:21,自引:0,他引:21
研究了咪唑及其衍生物配合CuCl对甲醇液相氧化羰化合成碳酸二甲酯的催化性能。筛选出溶解性好、腐蚀性小且催化活性高的多功能助催剂。实验结果表明,反应体系中加入N-甲基咪唑后,CuCl可以完全溶解。当催化剂的浓度为0.2 mol/L, N-甲基咪唑与CuCl的量为4∶1,反应温度为120 ℃,反应压力为2.40 MPa,CO与O2的进气比2∶1,反应3 h的条件下甲醇的摩尔转化率为15.4%,选择性为98%以上。从腐蚀性试验结果看,50 ℃时,加入N-甲基咪唑化合物后,Q235钢在CuCl/CH3OH/H2O/CO/O2体系中的腐蚀速率为0.22mm/a,缓蚀效率为94.5%。动力学研究表明,反应近似为一级,加入N-甲基咪唑后,反应速率常数为0.15 min-1。 相似文献
100.
Summary The efficiency of packed columns was measured as a function of flow rate, temperature, outlet density, and the density differential across the column, unsing pure carbon dioxide as the mobile phase. Although density differentials are often blamed for a serious loss in efficiency in packed column supercritical fluid chromatography, the results show that efficiency was not a function of the density differential. Peak shapes suggest that apparent loss in efficiency is actually due to inadequate solubility of the solute in carbon dioxide. 相似文献