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281.
吴炎 《数学物理学报(A辑)》2004,4(6):772-785
设R=Z/2\+kZ(k>1)是\{2\}[TX-]为非单位的有限局部环. 该文首先确定了R上斜对称矩阵标准形. 设G\+m\-p(R,H)={P∈GL\-m(R)|PHP′=H}是由矩阵H确定的伪辛群,其中H=[JB((][HL(2]0[]I\+\{(v)\}\=-I\+\{(v)\}[]0[HL)][JB))]Δ,Δ=[JB((][HL(2]\{2\}[TX-]\+\{k-1\}[]\{1\}[TX-]\=-\{1\}[TX-][]0[HL)][JB))]. 其次,计算了伪辛群G\+m\-P(R,H)的阶|G\+m\-P(R,H)|. 相似文献
282.
The melting behaviour, some phase boundaries and the lattice parameters in the region of the NiAs-type phase in the ternary system cobalt-antimony-tellurium have been determined by differential thermal analysis and X-ray diffraction. A projection of the liquidus surface and the phase relationships in different sections with constant antimony/tellurium ratios are presented. The peculiar variation of the lattice parameters with the composition of the nonstoichiometric NiAs-type phase is discussed in terms of the defect structure.Dedicated to Prof. K. L. Komarek on the occasion of his 65th birthday 相似文献
283.
低功率泵浦Ti:Al2O3自锁模激光器 总被引:2,自引:0,他引:2
本文报道了低功率泵浦的Ti:Al2O3激光器实现了稳定的自锁模运转,锁模脉冲宽度为180fs。分析了激光器的结构及工作特性。 相似文献
284.
Thermal diffusivity, heat capacity, and density of polyvinyl chloride/polycaprolactone (PVC/PCL) blends were measured by the laser flash method, DSC, and pycnometry, respectively. The thermal conductivity of the PVC/PCL blends was determined from the results. The miscibility of the blend and crystallinity of PCL were determined by DSC. The effect of blend structure on thermal conductivity is discussed. The phase compositions of the PVC/PCL blends are of three types depending on PCL content: i.e., up to 33%, from 33 to 70%, and above 70% PCL by weight. Thermal conductivity, thermal diffusivity, and heat capacity of the PVC/PCL blends are strongly affected by the phase composition of the blend, which changes in a complicated way with PCL content. © 1994 John Wiley & Sons, Inc. 相似文献
285.
Sam Lohse 《Microchemical Journal》2006,82(1):66-72
Although photooxidation has previously been shown to be successful in removing organic contaminants from water, methods combining the rapid photooxidation of the desired contaminant with easy catalyst manipulation and removal are few and far between. In the absence of an easy means of catalyst removal, the photooxidation process becomes more costly and time consuming, and photocatalysis cannot be employed as an in situ method for the remediation of aqueous organic contaminants. In this study, the photocatalyst was added to an aqueous trichloroethylene (TCE) solution in the form of TiO2-coated buoyant microspheres. The solution, placed in a flow-cell photoreactor along with the buoyant catalyst, was irradiated with a UV-filtered Xenon light source. Limited sample sizes necessitated the development of a low-cost headspace GC/MS analysis method, utilizing a standard direct-injection autosampler. This analytical technique aptly monitored reaction progress and indicated that aqueous TCE concentration decreases by nearly 90% in the first hour of irradiation. Subsequent solvent extraction GC/MS analysis indicated that the TCE is initially sorbed by the photocatalyst spheres, but as irradiation continued, TCE is removed from the catalyst spheres surfaces. During the course of irradiation, the expected TCE mineralization product hydrochloric acid appeared, as indicated by a decrease in pH and ion chromatography analysis. The microsphere-born catalyst was easily removed from the treated solution by filtration. Thus, it is possible that a method for effective, low-cost in situ photooxidation of aqueous organic contaminants will be realized in the near future. 相似文献
286.
鲤鱼体中鱼腥味物质的提取和鉴定 总被引:2,自引:0,他引:2
采用同时蒸馏萃取法提取鲤鱼鱼体中的挥发和半挥发性有机物,用GC/MS从提取物中分析鉴定出鱼腥味和疑是鱼腥味物质16种。包括醛、烯醛、酮和呋喃4类化合物。其中己醛、庚醛和2,4-二烯癸醛被确认为鱼腥味的化合物。研究发现,这些物质总量在鲤鱼体的鱼鳞、鱼鳃和鱼肉的分布呈现下降趋势,且其总量与鱼腥味强度之间具有可比较的对应关系。 相似文献
287.
Summary Samples of synthetic leucite and boron-substituted leucite are investigated by infrared spectroscopy and spectrally resolved
thermoluminescence. Evidence is obtained in favour of the assumption that point defects in aluminosilicate lattices are originated
by exchanges of Si+4 and Al+3 ions lying in different cells. 相似文献
288.
讨论了结构与饱和土壤相互作用的固结分析问题.对于结构利用多重子结构分析技术实现向饱和土交界面上的凝聚.从而建立了结构与饱和土壤相互作用的固结控制方程.文中给出了问题求解的一次性算法方案,采取压力主从关系的手段处理边界上的不排水条件.文末给出数值算例.本文工作为大型结构与土体相互作用固结分析研究工作的深入创造了条件. 相似文献
289.
一个反应扩散方程的门槛结果 总被引:4,自引:0,他引:4
本文讨论反应扩散方程Cauchy问题解的整体存在性,渐近性质和Blowup问题.其中或者1<q<p<+∞,n=2.得到门槛结果. 相似文献
290.
Boena N. Kolarz Maria Wojaczyska Jan Kaczmarczyk Teresa Siemieniewska Kazimierz Tomkw 《Journal of Polymer Science.Polymer Physics》1994,32(12):1977-1990
Sulfonic cation exchangers with two ion exchange group concentrations (0.5 and 2.4 mmol/g, samples A and B, respectively) were obtained by sulfonation of a porous styrene (S) and divinylbenzene (DVB) copolymer with chlorosulfonic acid. Strong thermal decomposition of the sulfonated copolymer A, accompanied by significant changes in its porous structure, starts at ca. 400°C. The char has no sulfonic groups. After heat treatment at 400°C in steam, a sorbent was obtained (yield 65%) that shows higher phenol sorption than the untreated sample when related to the bed volume. The chlorosulfonic derivatives of the initial copolymer were less thermally resistant than the sulfonic ones obtained by hydrolysis. Pyrolysis of the cation exchanger B, in its H+ and Ca2+ forms, was carried out at 900°C (yield of both chars close to 30%). By subsequent steam activation at 800°C to a 50% burn-off of the char, sorbents with well-developed, but distinctly different, porous structures were obtained. The activated char from the sulfonated copolymer in its hydrogen form was highly microporous and indicated an effective surface area of 1180 m2/g. However, because of a low contribution of mesopores, its ability to adsorb phenol from the liquid phase was not very high. The activated char from the calcium-doped copolymer, indicating a smaller surface area (580 m2/g) but characterized by a well-developed mesoporosity, was a better sorbent for phenol. © 1994 John Wiley & Sons, Inc. 相似文献