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981.
982.
983.
SO2气体激光诱导色散荧光时间断层扫描研究 总被引:2,自引:0,他引:2
以纳秒Nd:YAG激光器的四倍频(266 nm)为激发源,利用门选通增强光学多通道光谱分析仪 (OMA),研究了SO2分子第一激发带粒子的荧光辐射与碰撞弛豫相结合的复杂退激发过程。通过对SO2分子第一激发带的激发及碰撞弛豫过程的时间断层扫描分析,可以将激光诱导色散荧光谱中以305.6 nm、337.2 nm为中心的荧光包络和以424.7 nm为中心的规则序列分别归属于B1B1、A1A2低振动能级和a3B1基振动能级到基电子态X1A1不同振动能级的荧光跃迁,由此可以确定大气污染气体SO2的诱导荧光的灵敏检测波长为425 nm;由规则序列的实验数据可以计算出SO2分子基电子态X1A1的对称振动和弯曲振动模式的基振动角频率分别为ω1= 1151.8±0.6 cm-1和ω2= 517.8±0.6 cm-1,两振动模式的非谐性常数分别为 = 8±0.6 cm-1和 = 9.2±0.6 cm-1。 相似文献
984.
激光诱导击穿光谱实验装置的参数优化研究 总被引:1,自引:0,他引:1
Zhang L Ma WG Yan XJ Li ZX Hu ZY Zhang YZ Wang L Dong L Yin WB Jia ST 《光谱学与光谱分析》2011,31(9):2355-2360
为了使激光诱导击穿光谱(LIBS)实验装置中的多个关键参数达到最优化设置,以便更好地服务于煤质分析,实验中对这些参数与煤粉等离子体中待测元素发射谱线信噪比间的关系进行了详细研究,并根据信噪比大小来进行最优化参数的选择.实验结果表明,对于本LIBS实验装置,其最优化参数设置是将激光脉冲能量设为120 mJ·Pulse-1... 相似文献
985.
发红色荧光铽配合物的合成及荧光性能的研究 总被引:2,自引:0,他引:2
以二苯甲酰甲烷(HDBM)为第一配体,邻菲罗啉(phen)和二吡啶并[3,2-a:2',3'-c]哇喔啉(dpq)为第二配体合成两种三元铽配合物,并进行元素分析、稀土络合滴定、摩尔电导率、红外光谱、紫外光谱、荧光激发和发射光谱的测定,推测化合物的组成分别为:Tb(DBM)3phen,Tb(DBM)3dpq.DBM通过氧... 相似文献
986.
在上海光源硬X射线微聚焦光束线站(BL15U1)上, 基于EPICS软件平台, 集成运动控制, 光强探测, 荧光探测等功能, 实现了"飞行"模式 (on-the-fly) X射线扫描微束荧光成像方法. 用"飞行"扫描X射线荧光成像法获得了标准镍网, 以及微量元素Cu, Zn,K, Fe在样品老鼠脾内的分布图像, 结果显示该方法不但在速度上有了极大的提高, 而且获得的元素分布图像具有高质量.
关键词:
快速扫描X射线微束荧光成像
同步辐射
微量元素分布 相似文献
987.
Bone chemistry is an important source of biological and environmental information. Elemental compositions of archaeological and fossil bone have granted insight into the diets of ancient humans and other animals, as well as informing about the burial conditions of bone. Chemical studies of ancient bone can be performed non‐destructively with portable energy‐dispersive X‐ray fluorescence (EDXRF) spectrometers, which is particularly advantageous for on‐site analyses of museum specimens. Portable EDXRF instruments carry some analytical disadvantages, however, which may result in reduced precision or accuracy. Analytical shortfalls may be overcome by analysing inter‐sample trends in EDXRF spectral data instead of reported concentration measurements. We investigated the utility of statistically treating handheld EDXRF spectra from fossil bone and teeth, specifically the normalisation and mean centering of spectral data before principal component analysis. Fossil bone and tooth specimens were sourced from two Pleistocene localities in the Western Cape of South Africa, Swartklip 1 and Elandsfontein Main. Samples from the two localities could be distinguished using principal component score values, and coefficient loadings allowed chemical interpretation of the score clusters. Swartklip 1 samples were associated with elevated concentrations of Ca, indicating an additional Ca‐bearing mineral (i.e. calcite), whereas Elandsfontein Main samples were associated with elevated Fe and Sr concentrations. Fossil bone chemistry could be related to groundwater percolation through the sedimentary matrices of each locality. The methodology behind the case study presented here could readily be applied elsewhere and would be particularly useful to handheld EDXRF studies of museum specimens. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
988.
989.
《Analytical letters》2012,45(14):1185-1189
Abstract A specific and non-destructive test for basic esters of benzilic and α-glycolic acids in water is described. The compounds are collected on a glass fiber filter as water insoluble complexes with sodium tetraphenylboron. The filter is dried and sprayed with a 2-diphenylacetyl-l, 3-indandione-l-imine derivative. A positive test is the visual observation of fluorescence. 相似文献
990.
《Analytical letters》2012,45(11):1225-1243
Abstract The use of fluorescence difference decay curves was explored as a way to isolate the decays of components in a complex system. Time-correlated single photon methodology allows one to subtract a “reference” curve from a “sample” curve from a “sample” curve to yield a difference decay curve. To test the feasibility of this method, a model 3-component system (6-carboxyfluorescein, pyranine, and 1-dimethyl-aminoaphtalene-5-sulfonate) was examined. From its complex fluorescence decay curve, the individual decays were obtained by subtracting the appropriate binary solution decay curves. These difference curves coincided with those of the single component systems. Stringent requirements included: use of the same instrumental settings for all solutions, low counting efficiency, avoidance of inner filter effects, absence of energy transfer, and lack of chemical interaction between components. The difference decay method was applied to: 1. Sequential dansylation of serum albumin. Lifetimes of the first two dyes bound are longer than those of the third. 2. Dynamic quenching of quinine fluorescence by chloride ion. When the reference differs from the sample only by having a shorter lifetime, the difference decay curve has a characteristic shape. 3. Quenching of intrinsic protein fluorescence by acrylamide. Bovine serum albumin and liver alchol dehydrogenase were examined. Of the two tryptophans in each protein, one was preferentially quenched and its decay curve was obtained by difference. 相似文献