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111.
利用硫酸羟胺(HAS)催化臭氧(O3)降解含有邻苯二甲酸二甲酯(DMP)的模拟废水,比较O3/HAS体系和O3体系中DMP的降解情况,研究了叔丁醇(TBA)和pH值对O3/HAS体系中O3分解的影响。结果表明:当pH=3.0且HAS初始浓度为20μmol/L时,反应5min后O3/HAS体系中DMP的降解率比O3体系中提高了82.58%,表明O3/HAS体系降解DMP的效率优于单独O3体系;加入TBA后O3/HAS体系对DMP的降解率显著下降,证明在O3/HAS体系中产生了羟基自由基;在pH值为3.0、7.0和9.2的条件下,O3的降解率均随着HAS浓度的升高而升高,说明HAS促进了O3的分解。此外,选择盐酸羟胺(HAC)、磷酸羟胺(HAP)催化O3降解DMP,将O3/HAS体系、O3/HAC体系、O3/HAP体系中DMP的去除效果进行对比,结果显示三种体系均可促进DMP的降解。 相似文献
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8-Hydroxyqunioline end-capped polystyrene was prepared through atom transfer free radical polymerization (ATRP) with 8-(5-chloromethyl) quinolyl acetate as initiator. The results indicated that this polymerization is a first order reaction with respect to monomer conversion. The molecular weight increased linearly with monomer consumption and very narrow distribution of molecular weight was obtained (polydispersity index less than 1.2). The FT-IR and NMR results show that the 8-hydroxyquinloine group was chemically bonded to the polymer end and there is nearly one 8-hydroxyquinoline group in per polymer chain. All those data show that polymerization of styrene at such conditions displayed living characters. The polymer with 8-hydroxyqquinoline end group reacted with triethylaluminum to form polymeric light-emitting complex and single layer LED was prepared by common spin-coating method. The peak wavelength of LED based on synthesized polymeric complex was around 570 nm. 相似文献
115.
John F. Quinn Author Vitae Author Vitae Leonie Barner Author Vitae Author Vitae 《Polymer》2007,48(22):6467-6480
Ionizing radiation, such as γ, ultraviolet, microwave and X-ray radiation, has long been used in polymer chemistry as a means of initiating polymerization, crosslinking gels and decomposing particular polymer components. More recently, ionizing radiation has found application in tandem with living radical polymerization to form novel polymeric materials with defined molecular weight and narrow molecular weight distribution. In particular, γ-rays and ultraviolet light both have shown promise as sources of initiation in reversible addition-fragmentation chain transfer (RAFT) polymerization. The ability to apply these sources of initiation at low temperatures is useful in applications where elevated temperature is likely to be detrimental to the system, for instance, in preparing protein-polymer conjugates. Similarly, the use of these initiating sources at low temperature is particularly suitable for some monomers, such as allyl compounds, which have not been synthesized using any other living radical approach. The current review examines the development of ionizing radiation as a tool in RAFT polymerization, with particular reference to the elucidation of the polymerization mechanism, the synthesis of high functionality polymers and probing the kinetic parameters of the RAFT process. 相似文献
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M.?NaczkEmail author R.?B.?Pegg R.?Zadernowski F.?Shahidi 《Journal of the American Oil Chemists' Society》2005,82(4):255-260
Possible use of canola hulls as a source of natural anti-oxidants was explored. Cyclone canola hulls were extracted with methanol
(30 to 80%, vol/vol) and acetone (30 to 80%, vol/vol). The free radical-scavenging activity of phenolic extracts so prepared
was evaluated using the 2,2′-azinobis-(3-ethylbenzothiazoline-6-sulfonate) (ABTS) radical ion (ABTSo−), 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical, and chemiluminescence assays. The total content of phenolics in prepared
extracts from canola hulls ranged from 15 to 136 mg sinapic acid equivalents per gram of extract. Higher levels of condensed
tannins were detected in the acetone extracts than in the corresponding methanolic counterparts. Seventy and 80% (vol/vol)
acetone extracts displayed markedly stronger antioxidant activity than any of the other extracts investigated. Statistically
significant linear correlations were found between TEAC (Trolox equivalent antioxidant capacity) values (expressed in mM of
Trolox equivalents per gram of extract) and total pehnolics, TEAC and total condensed tannins (i.e., determined using the
modified vanillin and pronthocyanidin assays), as well as TEAC and protein precipitation activity of phenolic extracts (i.e.,
measured using the dye-labeled assay). The antioxidant activities of extracts as determined by the ABTSo− radical ion assay correlated highly with those of the chemiluminescence and DPPH radical assays. 相似文献
118.
A series of monomers were prepared by reacting (meth)acryloyl chloride with 2,4‐dihydroxybenzophenone, 2,4‐dihydroxybenzaldehyde, and 2,4‐dihydroxyacetophenone, respectively. The monomers were polymerized in dimethylformamide (DMF) at 70°C using benzoyl peroxide as an initiator. Polymer–metal complexes were obtained from DMF solutions of polymers with an aqueous solution of metal ions. The polymers and polymer–metal complexes were characterized by elemental analysis and spectral studies. The IR spectra of these complexes suggest that the metals are coordinated through the oxygen of the carbonyl group and the oxygen of the phenolic–OH group. The electronic spectra, electron paramagnetic resonance (EPR) spectra, and magnetic moments of polychelates showed an octahedral and square planar structure for Ni(II) and Cu(II) complexes, respectively. X‐ray diffraction studies revealed that polychelates are highly crystalline. The thermal and electrical properties, catalytic activity, and structure–property relationships are discussed. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 2083–2090, 2003 相似文献
119.
p-(Iodomethyl)styrene was polymerized under the action of a radical initiator (AIBN). The polymerization proceeds with degenerative chain transfer and leads to well defined branched polymers with functional primary and secondary iodomethyl groups as revealed by NMR studies. The obtained polymer can be further used as macroinitiator for radical polymerization of styrene. This polymerization proceeds in controlled way to polystyrene star polymers with reactive groups at the end of their arms. The characterization of branched and star structures was performed by NMR and GPC with absolute molar mass detection (MALLS). 相似文献
120.