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81.
The present paper deals with the extraction of cobalt from a solution containing cobalt and nickel in a sulphate medium similar
to the leach liquor obtained by the dilute sulphuric acid pressure leaching of the Pacific Ocean nodules matte followed by
copper extraction. The commercial extractant Cyanex 272 (bis (2, 4, 4-trimethylpentyl) phosphinic acid) is used for this purpose.
The leach liquor used for the present study contains Co =1.78 g/L and Ni=16.78 g/L. Before cobalt extraction, impurities,
such as copper and iron, are removed from the leach liquor by the precipitation method. Increasing the concentration of Cyanex
272 increased the extraction percentage of cobalt due to the increase of equilibrium pH. Cobalt extraction efficiency of >99.9
% is achieved with 0.20 M Cyanex 272 in two counter-current stages at an aqueous: organic (A:O) phase ratio of 1.5∶1. Complete
stripping of cobalt from the loaded organic containing 2.73 g/L Co was carried out at pH 1.4 by a synthetic cobalt spent electrolyte
in two stages at an A:O ratio of 1∶2. The enrichment of cobalt during extraction and stripping operations was about 3.5 times.
A complete process flowsheet for the separation and recovery of cobalt is presented. 相似文献
82.
目的 降低炼厂的柴汽比,提高企业经济效益。方法 对惠州石化4.0 Mt/a蜡油加氢裂化装置生产5号工业白油的可行性进行了分析,认为通过提高柴油馏分初馏点实现生产5号工业白油产品是可行的。前期,装置已通过主分馏塔降压调整、增设蒸汽汽提塔和原柴油汽提塔再沸器改蒸汽汽提工艺3种方式提高柴油初馏点,均未取得良好的运行效果。鉴于以上3种工艺的局限性,开发了热氮气气提工艺,工艺采用热氮气气提替代柴油汽提塔塔底再沸器,主分馏塔塔顶排出不凝气,以维持塔压稳定。结果 该工艺实施后,装置生产合格白油60 t/h,航煤产量增加14 t/h,不凝气产量增加1.3 t/h,不再产柴油产品;白油产品开口闪点由85℃提高至126℃,解决了开口闪点低和产品含水问题。结论 采用该工艺生产的5号工业白油产品性质稳定,满足行业指标的要求,装置改造工程量小,经济效益显著,对国内外同类装置的生产优化具有重要的借鉴意义。 相似文献
83.
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86.
A novel carbon paste electrode containing chitosan microspheres for the determination of Cu(II) in instant coffee by anodic stripping voltammetry was developed. Chitosan was crosslinked with the chelating agent 8-hydroxyquinoline-5-sulphonic acid and glutaraldehyde. The microspheres of the crosslinked chitosan biopolymer were obtained by the spray drying technique and employed in the construction of the sensor. In acetate buffer solution (0.1 mol L−1, pH 6.0), the calibration curve obtained was linear for concentrations of 5.0 × 10−7 to 1.4 × 10−5 mol L−1 (r = 0.9990); the detection limit was 5.5 × 10−8 mol L−1. The relative standard deviation (n = 8) was lower than 3.0% for solutions containing 6.0 × 10−6, 5.0 × 10−5 and 1.5 × 10−4 mol L−1 of Cu(II). The method was successfully employed for determination of Cu(II) in instant coffee and the results obtained showed good agreement when compared with those using electrothermal atomic absorption spectrometry. 相似文献
87.
88.
Jinhua Huang Qingji Xie Yueming Tan Yingchun Fu Zhaohong Su Yi Huang Shouzhuo Yao 《Materials Chemistry and Physics》2009,118(2-3):371-378
Pt nanoparticles well dispersed on multiwalled carbon nanotubes (MWCNTs) were prepared for high-performance electrocatalytic oxidation of methanol in both acidic and alkaline media via the co-electrodeposition/stripping (CS) protocol, namely, co-electrodeposition of Pt and Cu followed by electrochemical stripping of Cu, as examined by cyclic voltammetry (CV), electrochemical quartz crystal microbalance (EQCM), scanning electron microscopy (SEM), and X-ray diffraction (XRD). The Pt catalyst prepared by the CS protocol on MWCNTs (Ptcs/MWCNTs/Au) exhibited a specific electrocatalytic activity of 519 and 2210 A g−1 toward cyclic voltammetric electrooxidation (50 mV s−1) of methanol in 0.5 M CH3OH + 0.5 M H2SO4 and 0.5 M CH3OH + 1.0 M NaOH media, respectively, which are larger than those prepared by conventional electrodeposition from chloroplatinic acid on Au and MWCNTs/Au, as well as that by a CS protocol on Au. The Ptcs/MWCNTs/Au electrode also possessed the highest stability, which maintained 91% and 90% of its initial catalytic activity after 120-cycle CV in 0.5 M CH3OH + 0.5 M H2SO4 and 0.5 M CH3OH + 1.0 M NaOH, respectively. The electrode kinetics of methanol oxidation is also briefly discussed. The nanosubstrate-based CS protocol is simple, convenient and efficient, which is expected to find wide applications in film electrochemistry and electrocatalysis. 相似文献
89.
Determination of aflatoxins B1 and B2 by adsorptive cathodic stripping voltammetry in groundnut 总被引:1,自引:0,他引:1
In this study, adsorptive stripping voltammetry was proposed for determination of aflatoxins B1 (AFB1) and B2 (AFB2) using hanging mercury drop electrode (HMDE) as the working electrode. Both aflatoxins were found to adsorb and undergo irreversible reduction reaction at the working mercury electrode. The experimental conditions were optimised by one-at-a time and experimental design to obtain the best characterised peak in terms of peak height with analytical validation of the method for each aflatoxin. The calibration curves for aflatoxins AFB1 and AFB2 were linear in the ranges of 0.4–40 ng ml−1 and 0.2–70 ng ml−1 with the limit of detections (LOD) 0.15 and 0.10 ng ml−1, respectively. The proposed method was applied for the analysis of aflatoxins in groundnut samples and the results were compared with those obtained by the HPLC technique. 相似文献