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961.
温小兵 《科技情报开发与经济》2009,19(29):51-53
为使高校图书馆电子阅览室更好地为教学、科研服务,提高图书馆现有资源的利用效率,结合工作实际,从图书馆电子阅览室计算机网络建设的体系结构及关键技术分析入手,总结出了高校图书馆电子阅览室计算机网络建设方案及管理策略。 相似文献
962.
为了无损、快速地识别半刚性基层沥青路面的结构非连续状态,实现病害预警和预养护,对冲击作用下路面板体强迫振动机理及其振动噪声特征进行了分析,并对单自由度路面系统的强迫振动微分方程进行求解.研究表明:因土基沉降、低温施工、压实不足等原因,沥青路面将产生结构内部及层间非连续病害;而非连续状态下的板体强迫振动噪声特征对冲击加载... 相似文献
963.
分析了网络环境下基层图书馆利用计算机网络进行图书采访的优越性,提出了网络采访的流程和对采访人员的素质要求。 相似文献
964.
叶川 《科技情报开发与经济》2011,21(18):213-214
针对王庄矿的小煤矿CO涌出情况,将罗克休E和高水速凝材料有机结合、喷浆与注浆工艺有机结合的方法应用于煤矿井下对废弃巷道进行封堵,介绍了施工方案和具体施工工艺。 相似文献
965.
The meta kaolin (MK) clay particulate filler with different weight ratios viz., 0, 5, 10, 20 and 30 wt% were incorporated into castable polyurethane (PU)/polystyrene (PS) (90/10) interpenetrating polymer network (IPN). The effects of MK particulate filler loading on the mechanical and thermal properties of PU/PS (90/10) IPN composites have been studied. From the tensile behavior, it was noticed that a significant improvement in tensile strength and tensile modulus as an increase in MK filler content. Thermogravimetric analysis (TGA) data reveals the marginal improvement in thermal stability after incorporation of MK filler. TGA studies of the IPN composites have been performed in order to establish the thermal stability and their mode of thermal degradation. It was found that degradation of all composites takes place in two steps. Degradation kinetic parameters were obtained for the composites using three mathematical models. Tensile fractured composite specimens were used to analyze the morphology of the composites by scanning electron microscopic (SEM) technique. 相似文献
966.
M. Rätzsch 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(5):517-526
The investigations presented deal with the experimental results of the copolymerization of maleic anhydride (MAn) with alkenes. The course of the reaction is explained by the overall rate of the copolymerization (v Br), which correlates with the solution viscosity of the copolymer, and the dependence of the v Br maximum on the mole ratio of the monomers at constant total monomer concentration. The use of solvents with increasing donor power leads to increased complexing of the free MAn molecules and of the MAn radical chain ends. The results demonstrate that, for low 1-alkenes, the addition of the MAn chain radical is the rate-determining step of the copolymerization. As the substituents on the olefinic double bond become larger or the double bond shifts to the 1,2-position, the addition of MAn to the hydrocarbon radical becomes more and more the rate-determining step. On the other hand, an increase of the CT complexation of the MAn polymer radical by use of donor solvents decreases the alkene addition rate. 相似文献
967.
In this paper, 1,2-bis(2-acetamido-6-pyridyl)ethane, receptor 1, having an ethylene spacer is reported to recognise dicarboxylic acids. The binding study in the solution phase is carried out using 1H NMR (1:1) and UV–vis experiments and in the solid phase by single-crystal X-ray analysis. In 1H NMR, the downfield shifts of specific amide protons of receptor 1 in 1:1 complexes of receptor and guest diacids, and in the UV–vis experiment, the appearance of an isosbestic point as well as significant binding constants are observed, which thus unambiguously support the complexation of receptor 1 with dicarboxylic acids in solution. Receptor 2, simple 2-acetamido-6-methylpyridine, has lower binding constants than receptor 1 due to cooperative binding of two pyridine amide groups with two acid groups of diacids. In the solid phase, the ditopic receptor 1 shows a grid-like polymeric hydrogen-bonded network that changes to a polymeric wave-like 1:1 anti-perpendicular network instead of the syn–syn polymeric 1:1 (Goswami, S.; Dey, S.; Fun, H.-K.; Anjum, S.; Rahman, A.-U. Tetrahedron Lett. 2005, 46, 7187–7191), anti–anti polymeric 1:1 (Goswami, S.; Jana, S.; Dey, S.; Razak, I.A.; Fun, H.-K. Supramol. Chem. 2006 , 18, 571–574; Goswami, S.; Jana, S.; Fun, H.-K. Cryst. Eng. Comm. 2008, 10, 507–517; Goswami, S.; Jana, S.; Dey, S.; Sen, D.; Fun, H.-K.; Chantrapromma, S. Tetrahedron 2008, 64, 6426–6433), syn–syn 2:2 (Karle, I.L.; Ranganathan, D.; Haridas, V. J. Am. Chem. Soc. 1997 , 119, 2777–2783) or top–bottom-bound 1:1 (Garcia-Tellado, F.; Goswami, S.; Chang, S.K.; Geib, S.J.; Hamilton, A.D. J. Am. Chem. Soc. 1990 , 112, 7393–7394) co-crystals. 相似文献
968.
J. Devillers 《SAR and QSAR in environmental research》2013,24(6):515-528
Abstract In aquatic toxicology, QSAR models are generally designed for chemicals presenting the same mode of toxic action. Their proper use provides good simulation results. Problems arise when the mechanism of toxicity of a chemical is not clearly identified. Indeed, in that case, the inappropriate application of a specific QSAR model can lead to a dramatic error in the toxicity estimation. With the advent of powerful computers and easy access to them, and the introduction of soft modeling and artificial intelligence in SAR and QSAR, radically different models, designed from large non-congeneric sets of chemicals have been proposed. Some of these new QSAR models are reviewed and their originality, advantages, and limitations are stressed. 相似文献
969.
970.