全文获取类型
收费全文 | 10849篇 |
免费 | 1712篇 |
国内免费 | 668篇 |
专业分类
化学 | 922篇 |
晶体学 | 18篇 |
力学 | 690篇 |
综合类 | 47篇 |
数学 | 256篇 |
物理学 | 5480篇 |
无线电 | 5816篇 |
出版年
2024年 | 20篇 |
2023年 | 93篇 |
2022年 | 181篇 |
2021年 | 208篇 |
2020年 | 245篇 |
2019年 | 183篇 |
2018年 | 196篇 |
2017年 | 400篇 |
2016年 | 464篇 |
2015年 | 492篇 |
2014年 | 779篇 |
2013年 | 677篇 |
2012年 | 848篇 |
2011年 | 860篇 |
2010年 | 601篇 |
2009年 | 610篇 |
2008年 | 741篇 |
2007年 | 785篇 |
2006年 | 686篇 |
2005年 | 559篇 |
2004年 | 507篇 |
2003年 | 465篇 |
2002年 | 357篇 |
2001年 | 401篇 |
2000年 | 320篇 |
1999年 | 253篇 |
1998年 | 207篇 |
1997年 | 207篇 |
1996年 | 165篇 |
1995年 | 124篇 |
1994年 | 98篇 |
1993年 | 100篇 |
1992年 | 79篇 |
1991年 | 75篇 |
1990年 | 48篇 |
1989年 | 34篇 |
1988年 | 35篇 |
1987年 | 24篇 |
1986年 | 13篇 |
1985年 | 24篇 |
1984年 | 18篇 |
1983年 | 13篇 |
1982年 | 16篇 |
1981年 | 5篇 |
1980年 | 2篇 |
1979年 | 3篇 |
1976年 | 2篇 |
1974年 | 1篇 |
1973年 | 2篇 |
1957年 | 2篇 |
排序方式: 共有10000条查询结果,搜索用时 15 毫秒
181.
分光光度计测铁矿石中钛的测量不确定度评定 总被引:1,自引:0,他引:1
紫外-可见分光光度计在化学分析中应用较为广泛。对于借助其进行化学分析测量不确定度的评定,目前较多见于溶液测定。实际应用中,测试样品多为固体,涉及到称样、溶解、稀释、定容等步骤。此文试从随机效应和系统效应的角度考虑,对紫外-可见分光光度计应用ISO4691:1985铁矿石中钛含量的测定——二安替比林甲烷分光光度法对铁矿石中钛的测量过程中的不确定度来源进行了较为全面的分析,并最终给出评定结果。 相似文献
182.
针对计量人员在贯彻《测量不确定表示指南》,尤其是在撰写“建标技术报告”时遇到的一些体问题,进行了探讨。 相似文献
183.
E.?DesimoniEmail author B.?Brunetti R.?Cattaneo 《Accreditation and quality assurance》2004,9(8):445-449
Considering the uncertainty of measurement when assessing compliance with reference values given in compositional specifications and statutory limits is still a controversial matter. In theory, assessing compliance requires considering both type I (false positive) and type II (false negative) errors. The more the concentration of the analyte in the sample under investigation is close to the allowed concentration limit, the more critical it is to consider both types of errors. This paper describes how this could be done. The matter is discussed in the light of the most recent literature information. 相似文献
184.
Ion association in the system Ca(OH)2–H3PO4–KCl–H2O at 37°C has been studied potentiometrically over a range of pH from 3 to 9. The experimental conditions were optimized for the accurate determination of the association constants for the formation of the ion pairs CaH2PO
4
+
, CaHPO4 and CaPO
4
–
which were found to be 27.9±0.1, 591±2, and (1.35±0.02)×106 L-mol–1, respectively. 相似文献
185.
Otto Vogl Jan Bartus Joseph R. Murdoch 《Monatshefte für Chemie / Chemical Monthly》1990,121(4):311-316
Summary We report techniques for measuring optical rotation of suspended solids, including dissymmetric molecular crystals (e.g. sodium chlorate and bromate), synthetic polymers, polypeptides and biopolymers. Examples include poly(triphenylmethyl methacrylate), poly-S-lactide, poly-L-hydroxyproline, hemocyanine, cellulose acetate andRNA. The results indicate that optical rotation measurements are sensitive to differences in secondary structure and can serve as a probe for structural differences between solid-state and solution.
Messung der optischen Rotation von Makromolekülen im Festzustand unter Verwendung von Pulversuspensionen
Zusammenfassung Es wird über eine Methode zur Messung der optischen Rotation von Festkörpern in Suspensionen berichtet, wobei dissymetrische Kristalle (z. B. Natriumchlorat und -bromat), synthetische Polymere, Polypeptide und Biopolymere behandelt werden. Die Beispiele umfassen Poly(triphenylmethylmethacrylat), Poly-S-lactid, Poly-L-hydroxyprolin, Hemocyanin, Celluloseacetat undRNA. Die Ergebnisse zeigen, daß die optischen Rotationen bezüglich Unterschiede in der Sekundärstruktur empfindlich sind und daß diese Messungen als ein Maß für Strukturunterschiede zwischen Festzustand und Lösung herangezogen werden können.相似文献
186.
Yuchuan Zhang Jiasheng Qian Zhuo KeXiangcheng Zhu Hong BiKangming Nie 《European Polymer Journal》2002,38(2):333-337
The intermolecular interactions between poly(vinyl chloride) (PVC) and poly(vinyl acetate) (PVAc) in tetrahydrofuran (THF), methyl ethyl ketone (MEK) and N,N′-dimethylformamide (DMF) were thoroughly investigated by the viscosity measurement. It has been found that the solvent selected has a great influence upon the polymer-polymer interactions in solution. If using PVAc and THF, or PVAc and DMF to form polymer solvent, the intrinsic viscosity of PVC in polymer solvent of (PVAc+THF) or (PVAc+DMF) is less than in corresponding pure solvent of THF or DMF. On the contrary, if using PVAc and MEK to form polymer solvent, the intrinsic viscosity of PVC in polymer solvent of (PVAc+MEK) is larger than in pure solvent of MEK. The influence of solvent upon the polymer-polymer interactions also comes from the interaction parameter term Δb, developed from modified Krigbaum and Wall theory. If PVC/PVAc blends with the weight ratio of 1/1 was dissolved in THF or DMF, Δb<0. On the contrary, if PVC/PVAc blends with the same weight ratio was dissolved in MEK, Δb>0. These experimental results show that the compatibility of PVC/PVAc blends is greatly associated with the solvent from which polymer mixtures were cast. The agreement of these results with differential scanning calorimetry measurements of PVC/PVAc blends casting from different solvents is good. 相似文献
187.
The reaction of [ReOCl3(PPh3)2] with 5,6-diphenyl-3-(2-pyridyl)-1,2,4-trazine (dppt) has been examined and [ReCl3(OPPh3)(dppt)] has been obtained. The triphenylphosphine oxide can be easily replaced by PPh3 in the reaction of [ReCl3(OPPh3)(dppt)] with an excess of triphenylphosphine. The [ReCl3(OPPh3)(dppt)] and [ReCl3(PPh3)(dppt)] complexes have been structurally and spectroscopically characterized. Their molecular orbital diagrams have been calculated with the density functional theory (DFT) method, and their electronic spectra have been discussed on the basis of time-dependent DFT calculations. The compound [ReCl3(OPPh3)(dppt)] has been studied additionally by magnetic measurement. The magnetic behavior is characteristic of mononuclear complexes with d4 low-spin octahedral Re(III) complexes (3T1g ground state) and arise because of the large spin–orbit coupling (ζ = 2500 cm−1), which gives diamagnetic ground state. 相似文献
188.
A coalesced high-intensity dc discharge is maintained between three cathodes and a single anode, stabilized by using resistors on each cathode leg. Jets of plasma gas are produced from either the cathode area or the anode area of the device. Cathode jets are generated by the self-induced pumping at the cathode tips and augmented by central gas injection. Arc voltage-current characteristics show classical convection-stabilized arc behavior. Anode heat transfer rates may be substantially increased by central gas injection toward the anode. Temperature fields in the coalesced, axially symmetric portion of the arc are determined spectrometrically and compared to those of a classical single-cathode free-burning arc. 相似文献
189.
Hideyuki Yoshida Junichiro Sonoda Junichi Ishida Masatoshi Yamaguchi 《Analytica chimica acta》2005,534(2):177-183
A simple screening method of organic aciduria by spectrofluorometric measurement of total dicarboxylic acids in human urine is described. This method is based on an intramolecular excimer-forming fluorescence derivatization with a pyrene reagent, 4-(1-pyrene)butanoic acid hydrazide (PBH). Dicarboxylic acids in urine were converted to the corresponding dipyrene-labeled derivatives by reaction with PBH in the presence of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide and pyridine, and the derivatives afforded intramolecular excimer fluorescence (420-540 nm) which can clearly be discriminated from the normal fluorescence (360-420 nm) emitted from reagent blanks. The technique is so selective that it permits spectrofluorometric measurement of total amount of dicarboxylic acids by the direct derivatization of diluted urine samples. The same reaction mixture has also served as a liquid chromatographic (LC) sample for the separative determination of individual dicarboxylic acids. The spectrofluorometric data did not contradict with the LC data. These methods were usefully applied to preliminary screening test of glutaric aciduria. In conclusion, the present derivatization method allows rapid and direct determination of total amount of dicarboxylic acids in human urine samples. 相似文献
190.