全文获取类型
收费全文 | 8250篇 |
免费 | 822篇 |
国内免费 | 1388篇 |
专业分类
化学 | 7233篇 |
晶体学 | 135篇 |
力学 | 1152篇 |
综合类 | 56篇 |
数学 | 265篇 |
物理学 | 1619篇 |
出版年
2024年 | 14篇 |
2023年 | 71篇 |
2022年 | 154篇 |
2021年 | 218篇 |
2020年 | 357篇 |
2019年 | 287篇 |
2018年 | 271篇 |
2017年 | 370篇 |
2016年 | 431篇 |
2015年 | 423篇 |
2014年 | 450篇 |
2013年 | 683篇 |
2012年 | 516篇 |
2011年 | 531篇 |
2010年 | 402篇 |
2009年 | 523篇 |
2008年 | 479篇 |
2007年 | 569篇 |
2006年 | 531篇 |
2005年 | 446篇 |
2004年 | 417篇 |
2003年 | 420篇 |
2002年 | 323篇 |
2001年 | 249篇 |
2000年 | 266篇 |
1999年 | 186篇 |
1998年 | 132篇 |
1997年 | 137篇 |
1996年 | 118篇 |
1995年 | 91篇 |
1994年 | 94篇 |
1993年 | 59篇 |
1992年 | 61篇 |
1991年 | 35篇 |
1990年 | 32篇 |
1989年 | 29篇 |
1988年 | 20篇 |
1987年 | 12篇 |
1986年 | 8篇 |
1985年 | 11篇 |
1984年 | 10篇 |
1983年 | 3篇 |
1982年 | 4篇 |
1981年 | 3篇 |
1980年 | 4篇 |
1979年 | 2篇 |
1976年 | 2篇 |
1974年 | 1篇 |
1971年 | 3篇 |
1959年 | 1篇 |
排序方式: 共有10000条查询结果,搜索用时 31 毫秒
131.
132.
固体超强酸催化剂SO_4~(2-)/TiO_2-WO_3的制备及其催化性能研究 总被引:1,自引:0,他引:1
制备了固体超强酸催化剂SO2 -4/TiO2 WO3 ,并以丁酸丁酯的合成作为探针反应 ,系统考察了WO3 的含量、硫酸浸渍浓度、焙烧温度等制备条件对SO2 -4/TiO2 WO3 催化活性的影响 .实验表明 :制备催化剂的适宜条件为m(H2 WO4) =12 5 % ,硫酸浸渍浓度为 1 0mol·L-1,焙烧温度为 5 80℃ ,活化时间 3h .利用优化条件下制备的催化剂SO2 -4/TiO2 WO3 催化合成缩醛 (酮 ) ,在醛 /酮与二元醇 (乙二醇 ,1,2 丙二醇 )的投料摩尔比为 1∶1 5 ,催化剂的用量占反应物总投料质量的 0 5 % ,反应时间为 1h条件下 ,2 甲基 2 乙氧羰甲基 1,3 二氧环戊烷的收率为 78 7% ,2 ,4 二甲基 2 乙氧羰甲基 1,3 二氧环戊烷的收率为 83 0 % ,环己酮 -乙二醇缩酮的收率为 85 9% ,环己酮 1,2 丙二醇缩酮的收率为 84 6% ,丁酮 -乙二醇缩酮的收率为70 7% ,丁酮 1,2 丙二醇缩酮的收率为 88 3 % ,2 丙基 1,3 二氧环戊烷的收率为 80 6% ,4 甲基 2 丙基 1,3 二氧环戊烷的收率为 79 6% ,2 异丙基 1,3 二氧环戊烷的收率为 64 2 % ,4 甲基 2 异丙基 1,3 二氧环戊烷的收率为 83 3 % ,2 苯基 1,3 二氧环戊烷的收率为 75 3 % ,4 甲基 2 苯基 1,3 二氧环戊烷的收率为 95 1% . 相似文献
133.
固相萃取柱上衍生气相色谱-质谱法测定水中烷基酚 总被引:7,自引:0,他引:7
以烷基酚(APs)主要降解产物辛基酚(4-t-OP)、壬基酚(4-n-NP)为研究对象,建立了固相萃取(SPE)柱上衍生化、气相色谱-质谱(GC-MS)法测定水中APs的分析方法。以C18柱为固相萃取柱、N,O-(三甲基硅)三氟乙酰胺(BSTFA)为硅烷化试剂,设计五因素四水平正交实验L16(45),对衍生化影响因素、衍生化溶剂、衍生化时间以及SPE主要影响因素pH值、盐度和洗脱剂进行优化;在优化条件下,方法的回收率(高于80%)和重现性(RSD低于10%)结果令人满意,4-t-OP和4-n-NP的仪器检出限分别为3.35ng/L和6.38ng/L。采用建立的方法,回收率略高于传统的SPE萃取衍生法,具有有机溶剂用量少,方法简单快速、灵敏度高的特点,适用于河水和海水中痕量烷基酚的快速测定。 相似文献
134.
A Triton X-100-4.0G-D (4.0G-D refers to a 4.0-generation dendrimer) was brought forward as a new phosphorescence labeling reagent. Two types of specific affinity adsorption (AA) reactions (direct method and sandwich method) were carried out between the labeling product of Triton X-100-4:0G-D-Wheat germ agglutinin (WGA) and alkaline phosphatase (ALP), the product of AA reaction preserved the good characteristics of room temperature phosphorescence (RTP) of 4.0G-D and △Ip of the product was proportional to the content of ALP. According to the fact stated above, a new method for the determination of trace ALP by affinity adsorption solid substrate-room temperature phosphorimetry (AA-SS-RTP) was established on the basis of WGA labeled with the Triton X-100-4.0G-D. The detection limits were 0.20 ag·spot^-1 (corresponding concentration: 5.0×10^-16 g·mL^-1, namely 5.0×10^-18 mol·L^-1) for a direct method and 0.14 ag·spot^-1 (corresponding concentration: 3.5×10^-16 g·mL^-1, namely 3.5×10^-18 mol·L^-1) for a sandwich method, respectively. For their high sensitivity, good repeatability and high accuracy, the direct method and sandwich method have been successfully appfied to determine the content of ALP in human serum, and the results were coincided with the clinical detection results of the enzyme-linked immunosorbent assay method by the Zhangzhou Hospital of Traditional Chinese Medicine. Meanwhile, the mechanism for the determination of trace ALP by AA-SS-RTP was discussed. 相似文献
135.
Ca2-xSrxZn4Ti15O36∶Pr red long decay phosphor was synthesized by high temperature solid state reaction. Photoluminescence property and crystalline and unit cell parameters of the orthorhombic were investigated by fluorescence spectrophotometer and by powder X-ray diffraction, respectively. The emission intensity at 618 nm changes sharply when the concentration of
Sr2+ (x) is less than 0.1 and the emission intensity reaches the maximum when x is equal to 0.007. There is an obviously broad excitation band at 270 nm when x is equal to 0.003 and it disappears gradually when x is over 0.01. The unit cell a parameter of
Ca2-xSrxZn4Ti15O36∶Pr decreases while c parameter increases with the increases of the concentration of the doped
Sr2+. When x is over 0.1 the value of the unit cell parameters a and c become stable. TL peaks of
Ca2Zn4Ti15O36∶Pr, Ca1.993Sr0.007Zn4Ti15O36∶0.002Pr3+,
0.002Na+, are located at 62 ℃, 88 ℃, respectively, which indicates that there are deeper traps in
Ca1.993Sr0.007Zn4Ti15O36∶0.002Pr3+,
0.002Na+. 相似文献
136.
Effect of multi-walled carbon nanotubes on non-isothermal crystallization kinetics of polyamide 6 总被引:2,自引:0,他引:2
The non-isothermal crystallization behaviors of multi-walled carbon nanotubes (MWNTs)/polyamide 6 (PA6) composites were investigated by differential scanning calorimetry (DSC). Three methods, namely, Avrami, Ozawa and Mo, were carried out to analyze the non-isothermal crystallization data. The results showed that the MWNTs in PA6 acted as effective nucleation agents. However the crystallization rate of composites obtained was lower than that of the neat PA6. It is indicated that the presence of MWNTs influenced the mechanism of nucleation and the growth of PA6 crystallites. 相似文献
137.
A. Fendler M. P. Villanueva E. Gimenez J. M. Lagarón 《Cellulose (London, England)》2007,14(5):427-438
The present work presents and discusses the interrelation between composition, morphology, thermal history, mechanical and
barrier properties to oxygen and limonene of composites of HDPE/MA-PE/cellulose fibers of significant interest in, among others,
food packaging applications. From the overall results, it was observed that increasing the loading of purified alpha-cellulose
fibers in the polyethylene matrix beyond 10 wt.% led to a decrease in the permeability coefficient of d-limonene, effect which was found to be primarily related to a decrease in the overall solubility of this strongly plasticizing
aroma component. On the other hand, the oxygen permeability was found to decrease to a significant extend with increasing
fiber content beyond 5 wt.%, but this effect was more strongly ascribed to a significant decrease in the diffusion coefficient.
Therefore, the fibers are thought to generate a more tortuous path for the non-interacting gas molecules to travel across
the composites thickness, even when tested at high relative humidity conditions. Optimum fiber loading levels in terms of
overall property balance were found to be around 20 wt.%. 相似文献
138.
J. Rodriguez-Añón J. Prouupin M. González-Añón L. Núñez-Regueira 《Journal of Thermal Analysis and Calorimetry》1998,52(3):1005-1012
The heating values of municipal solid waste generated in three towns with a population of less than 50 000, situated in Galicia
(Spain), were measured with a static bomb calorimeter. Samples of raw refuse were burnt either as received or after sorting
of the different combustible components. A study was made of samples from controlled and uncontrolled landfills.
The calorific values were compared with those corresponding to a commercial residual derived fuel in order to study the possibility
of using municipal solid waste as a source of recovered energy.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
139.
Methane reforming by carbon dioxide has been studied over ultra-stable Ni catalysts. The catalyst was characterized by XRD, IR and TEM and temperature programmed hydrogenation. The nickel–magnesia solid solution catalyst containing low nickel has shown excellent stability (>3000 h) and no carbon deposition in the methane reforming by carbon dioxide. It was also found that the small nickel metal particle interaction with support surface is effective for the inhibition of carbon formation. 相似文献
140.
A generalization of the kinetic equation for the isotope exchange at solid—liquid interface is presented. The generalized equation may be used to describe kinetics of the isotope exchange process limited by surface reactions and diffusion without assumption of spherical symmetry of solid particles.
Eine generalisierte Gleichung für die Kinetik des Isotopenaustausches an Fest-Flüssig-Phasengrenzen
Zusammenfassung Es wird eine generalisierte kinetische Gleichung angegeben, die die Kinetik des Isotopenaustausches an Fest-Flüssig-Phasengrenzen beschreibt, wobei der Austauschprozeß durch Oberflächenreaktionen und Diffusion ohne der Annahme sphärischer Symmetrie für die festen Partikel begrenzt ist.相似文献