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71.
在线(氢—钯)色谱—质谱联用法研究分散黄RGFL中的芳胺 总被引:1,自引:0,他引:1
研究了一种检测偶氮染料中芳胺的新方法,对分散黄进行了在线(氢-钯)色谱-质谱联用分析,测出了芳胺组分,并对两种催化还原装置进行了比较。 相似文献
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原位漫反射红外光谱研究氮氧化物在Ag-ZSM-5催化剂上的吸附态及选择性催化还原反应机理 总被引:3,自引:0,他引:3
利用原位分析方法对催化剂表面吸附态进行动态表征,对了解催化反应机理具有重要的意义。漫反射红外光谱是一种理想的原位方法,应用该方法在298-773K范围原位考察了以丙烯为还原剂,NO在Ag-ZSM-5催化剂上的吸附态及选择性催化还原过程。认为NO的选择性催化还原符合直接作用机理,还原的关键是形成有机-氮氧化物(R-NO2或R-ONO)中间体。O2的作用是使C3H6充分活化,并是有效产生有机-氮氧化物不可缺少的条件。 相似文献
74.
本文用^1H NMR谱研究了3-芳基丙酮酸的烯醇式结构及推测其Clemmensen还原反应机理。 相似文献
75.
Uncoupled metabolism stimulated by chemical uncoupler and oxic-settling-anaerobic combined process to reduce excess sludge production 总被引:1,自引:0,他引:1
The effects of three uncoupled metabolic systems (conventional activated sludge process with the addition of 3,3′,4′,5-tetrachlorosalicylanilide
[TCS], oxic-settling-anaerobic [OSA] process modified by insertion of a sludge-holding tank in the sludge return line, and
TCS and OSA combined process) on reducing excess sludge production were studied. Compared with the control conventional activated
sludge process, the most effective system was the combined process, which could reduce excess sludge production by 46.90%.
The 180-d operation results confirmed that TCS is an effective chemical uncoupler in reducing the sludge yield but that it
had an adverse effect on substrate removal capability, effluent nitrogen concentration, and sludge settleability. The OSA
process decreased excess sludge production by only 26% but had less adverse effect on effluent quality and could improve sludge
settleability. The effluent total phosphorous concentration of the three systems was slightly lower than of the control unit.
Microbial populations were monitored by both microscopic and molecular biologic analysis method (polymerase chain reaction
[PCR]-denaturing gradient gel electrophoresis [DGGE]). The presence of TCS caused metazoans to disappear and decreased the
number and activity of protozoa. PCR amplification of 16S rRNA and sequent DGGE analysis found a shift in the diversity of
the predominant species. The results imply that OSA combined with the chemical uncoupler process may effectively reduce excess
sludge yield and not affect process performance significantly. 相似文献
76.
N. S. Arutyunyan L. A. Akopyan G. A. Gevorgyan G. M. Snkhchyan G. A. Panosyan 《Chemistry of Heterocyclic Compounds》2005,41(4):437-441
A preparative method was developed for the synthesis of ethyl furfurylidenecyanoacetate. Its condensation with phenylmagnesium bromide gave ethyl α-cyano-β-(2-furyl)hydrocinnamate, the decarboxylation of which led to β-(2-furyl)hydrocinnamonitrile. Reduction of this nitrile with lithium aluminum hydride gave 2-(3-amino-1-phenylpropyl)furan. Some of its transformations were studied.__________Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 517–521, April, 2005. 相似文献
77.
ZheLi DangLi WeiHuang KechangXie 《天然气化学杂志》2005,14(2):115-118
The Cu-Mo/ZSM-5 catalysts with different Cu/Mo ratios were prepared by wet impregnation method, and their catalytic performance for selective catalytic reduction of NOx was studied. The results showed that Cu-Mo/ZSM-5 is a very effective catalyst for NOx catalytic reduction with ammonia, especially when Cu/Mo molar ratio is about 1.5. It not only exhibited the extremely high catalytic activity, but also showed good stability for 02. The bulk phase structure of Cu-Mo/ZSM-5 catalysts was determined by XRD technique, and the results indicated that there is a maximum dispersion for Cu species when Cu/Mo molar ratio is 1.5, and an interaction between Cu and Mo along with HZSM-5 may be present in Cu-Mo/ZSM-5, which may possibly result in a special structure favorable for the catalytic reduction of NOx over Cu-Mo/ZSM-5 catalyst. 相似文献
78.
I. E. Karpeiskaya L. F. Godunova E. S. Levitina M. R. Lyubeznova E. I. Klabunovskii E. S. Shpiro G. N. Baeva E. D. Lubuzh L. B. Krentsel' A. D. Litmanovich N. A. Plate 《Russian Chemical Bulletin》1992,41(10):1858-1867
Pd complexes have been obtained from linear and cross-linked copolymers ofR,S-, R-, andS-1-(4-vinylphenyl)ethylamine (1) with styrene and divinylbenzene. Reduction of these compounds gave catalysts which were active in the reductive solvolysis of -acetaminocinnamic acid azlactone (2) and hydrogenation of the solvolysis products -acetamidocinnamic acid (ACA), its esters, and its 1-phenylethylamide. The catalysts showed no enantioselective properties in the reductive hydrolysis, but were more active than the catalyst obtained in the absence of the polymer (the monomeric analog). The use of polymeric catalysts has shown that, in reductive aminolysis, the chiral nucleophile plays the dominant part in determining the stereoselectivity of the reaction, rather than the chiral ligand of the catalytic complex. The polymer matrix stabilizes the low-valent state of the palladium in the complex. In the hydrogenation of ACA and its esters, the catalyst on the cross-linked polymer is much more active than its monomeric analog, but showed no enantioselectivity. Hydrogenation of acetamidocinnamic acidR-andS-1-phenylethylamides on a chiral Pd-polymer catalyst occurred with double asymmetric induction.Deceased.N. D. Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, 117913 Moscow. A. V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, 117912 Moscow. Translated from Izvestiya Akademii Nauk, Seriya Khimicheskaya, No. 10, pp. 2368–2380, October, 1992. 相似文献
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