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运用沉积学理论,通过对铁法煤田大兴井田4#煤层中发育的砂岩、砾岩体的研究,指出它们均为河道沉积产物,并从中识别出了聚煤早期河道正常沉积、聚煤期后河道水携物与坍塌物混积和河道泥石流沉积三种成因类型,论述了它们各自的岩相和空间发育特征,这将有益于揭示其平面分布规律,为进一步指导采场的科学设计和修订提供了基础. 相似文献
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Charlotte Doussier Philippe Léone Alain Meerschaut 《Journal of solid state chemistry》2007,180(8):2323-2334
The new oxy-chloro-sulfide (Mn1−xPbx)Pb10+ySb12−yS26−yCl4+yO (x ∈ [0.2-0.3]; y ∈ [0.3-1.6]) was synthesized by dry way at 500-600 °C. A single crystal ∼Mn0.7Pb11.0Sb11.3S25.3Cl4.7O indicates a monoclinic symmetry, space group C2/m, with a = 37.480(8), b = 4.1178(8), c = 18.167(4) Å, β = 106.37(3)°, V = 2690.2(9) Å3, Z = 2. Its crystal structure was determined by X-ray single crystal diffraction, with a final R = 5.11%. Modular analysis of the crystal structure reveals a “waffle” architecture, where complex rods with lozenge section delimitate an internal channel filled by a single chain of (Mn0.7Pb0.3)Cl6 octahedra connected by opposite edges. Minimal inter-chain distances are close to 18 Å. The rod wall, two-atom thick, presents, in alternation with S atoms, Pb or (Pb,Sb) cations with prismatic coordination in the internal atom layer, while the external atom layer is constituted exclusively by Sb cations with dissymmetric square pyramidal coordination. A (Pb,Sb)2S2 fragment connects two successive rods along (2 0 1) to form a waffle-type palissadic layer. The unique O position, half filled, presents the same environment than the isolated O positions in the oxy-sulfide Pb14Sb30S54O5, or oxy-chloro-sulfides Pb18Sb20S46Cl2O and (Cu,Ag)2Pb21Sb23S55ClO. This compound belongs to a pseudo-homologous series of chalcogenides with waffle structure, ordered according to the size of their lozenge shape channel. Such a complex senary compound of the oxy-chloro-sulfide type illustrates the structural competition between three cations, on one hand, and, on the other hand, three anions. This compound is of special interest regarding the 1D distribution of magnetic Mn2+ atoms at the ∼2 nm scale. 相似文献
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SbPO4, a phosphate with a layered structure, was tested as an electrode material for lithium cells spanning the 3.0-0.0 V range. Two main electrochemical processes were detected as extensive plateaus at ca. 1.6 and 0.7 V in galvanostatic measurements. The first process was found to be irreversible, thus excluding a potential intercalation-like mechanism for the reaction and being better interpreted as a decomposition reaction leading to the formation of elemental Sb. This precludes the use of this compound as a cathodic material for lithium cells. By contrast, the process at 0.7 V is reversible and can be ascribed to the formation of lithium-antimony alloys. The best electrochemical response was obtained by cycling the cell at a C/20 discharge rate over the voltage range 1.25-0.25 V. Under these conditions, the cell delivers an average capacity of 165 Ah/kg—a value greater than those reported for other phosphates—upon successive cycling. 相似文献
5.
Dmitry V. Moiseev Vera A. Morugova Andrey S. Shavirin Victor A. Dodonov 《Journal of organometallic chemistry》2004,689(4):731-737
Tetraphenylantimony(V) carboxylates have been used in the palladium-catalyzed C-phenylation reaction of methyl acrylate in the presence of (PhCO2)2 or t-BuOOH under mild conditions (50 °C). The peroxides promote a cascade participation of the organoantimony compound and result in the transfer of three phenyl groups. Organoantimony intermediates have been isolated from the reaction. 相似文献
6.
应用控制理论与方法分析消费、储蓄、工资收入与利率之间的关系,建立相应的数学模型。利用此模型,可以确定合理的消费与储蓄的比例关系,为制定相应的宏观经济政策提供依据。 相似文献
7.
陈启光 《河北理工学院学报》1995,(4)
经对采自砂金矿床,金矿床氧化带和块金(狗头金)样品的观察研究,特别是采用电子显微镜进行精细矿物学研究后发现,所研究的样品无一例外地均具有代表性,它是表生电流动溶液中生成的表面生长结构图象,证明它们均是在天然水系和开放式物化环境中白含金溶液不断的淀积作用生成的。因而砂金颗粒均属表生条件下形成的溶液沉积矿物,砂金矿床从成因上说应属表生化学沉积矿床。砂金颗粒是在原地生成的。金粒表面生长结构应作为标型特征。 相似文献
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A systematic study of antimony reduction prior to its determination by hydride generation atomic fluorescence spectrometry (HG-AFS) was carried out. The efficiency of l-cysteine, potassium iodide and potassium iodide/ascorbic acid was studied for this purpose. The hydride generation step was optimised in the presence of those pre-reductors. From the results, l-cysteine was found to be the most suitable pre-reducing agent. Methodology was validated, obtaining detection limits lower than 90 ng l−1 and repeatability and reproducibility better than 3% R.S.D. and 5% R.S.D., respectively, in all cases. In order to evaluate the methodology developed and the influence of the matrix, recovery from waters from different sources was tested by HG-AFS and also by inductively coupled plasma mass spectrometry (ICP-MS). Accuracy was assessed by analysing three water reference materials at different antimony concentration levels. The high sensitivity of the developed methodology enables it to be applied for monitoring drinking waters according to the maximum admissible concentration of antimony established by the EU Directives. 相似文献
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