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排序方式: 共有98条查询结果,搜索用时 15 毫秒
1.
对测试用例的可复用性度量进行研究,构建测试用例可复用性评估模型,通过分析转化得到易于度量的层次分析模型。通过层次分析模型构建权重比较矩阵,再进行相关属性的度量,并可进一步开展自动的测试用例可复用性度量。 相似文献
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Glucose isomerase (GI) from Streptomycesrubiginosus was immobilized covalently onto Eupergit C 250 L made by copolymerization of N,N-methylene-bis-methacrylamide, glycidyl methacrylate, allyl glycidyl ether and methacrylamide. The catalytic efficiency of immobilized GI in isomerization of glucose to fructose was found as three fold higher than that of free GI. The residual activity of immobilized GI after 18 reuses in a batch type stirred reactor was about 85% of its initial activity. The thermal stability of immobilized GI was almost same with that of the free GI at 60 °C for 18 h preincubation time. The residual activities of immobilized GI when stored at 5 °C and 25 °C for four weeks were 72% and 69% of the initial activity, respectively. However, free GI retained 88% and 78% of its initial activity at 5 °C and 25 °C upon four weeks storage, respectively. Thus, the use of Eupergit C 250 L immobilized GI instead of free GI is suggested in enzymatic isomerization of glucose to fructose. 相似文献
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Mineralization of Para-Chlorobenzoic Acid in Water by Cobalt-Incorporated MCM-41 Catalyzed Ozonation
Cobalt-incorporated MCM-41(Co-MCM-41) was used as a heterogeneous catalyst for the ozonation of para-chlorobenzoic acid (p-CBA) in aqueous solution. Cobalt oxide supported on MCM-41(Co/MCM-41) was synthesized for comparison. Their textural properties were elucidated by various characterization techniques to understand the relationship between surface texture and catalytic activity. TOC removal at 60 min reached 91% with Co-MCM-41, 83% with Co/MCM-41 and only 52% with ozone alone, respectively. Observations from diffuse reflection spectroscopy demonstrated that different metal phases were formed in these cobalt-modified molecular sieves samples. Radical scavenger experiments indicated the formation of hydroxyl radicals that were responsible for the effective degradation of p-CBA. An integrated approach to the catalytic mechanism was proposed by considering the variation of pH in the course of ozonation as well as its subsequent influence on the dissociation of targeted compounds and surface charge of the catalyst. In the reusability experiments, the reused Co-MCM-41 was able to regain the same catalytic capability as the fresh one within 5 cycles. X-ray photoelectron spectroscopy results indicated that a part of Co2+ was oxidized to Co3+ after oxidation reaction. 相似文献
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Heterostructured dysprosium vanadate – ZnO for photo-electrocatalytic and self-cleaning applications
In this article, we report fabrication of 5 wt% of Dy as DyVO4 supported ZnO by template-free hydrothermal-thermal decomposition method and its photocatalytic activity towards degradation of azo dyes Rhodamine-B (Rh-B) and Trypan Blue (TB) in solar light, Electrocatalytic activity in methanol oxidation and Self-cleaning properties. The as prepared DyVO4-ZnO was characterized by surface analytical and spectroscopic techniques. The results suggested that Dysprosium vanadate doping on ZnO has increased its photocatalytic efficiency with high reusability. DyVO4-ZnO exhibits higher electrocatalytic activity than prepared ZnO for methanol electrooxidation in alkaline medium, revealing its promising potential as the anode in direct methanol fuel cells. Hydrophobicity of ZnO increases by doping of DyVO4. 相似文献
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Catalytic selective oxidation of benzyl alcohol with molecular oxygen under mild conditions was carried out over novel crystalline Mo-V-O oxide. The present research is focused on investigation of recycling, reusability and stability of the crystalline oxide in the liquid-phase reaction. The Mo-V-O oxide catalyst was used at least four times with comparable activities to that of fresh catalyst. The separation of the catalyst from reaction medium can stop the conversion of benzyl alcohol, and the addition of the catalyst to the reaction medium can trigger the reaction immediately. The catalytic oxidation of 2,3,6-trimethylphenol as a reference reaction suggested that there were no leached active species in the reaction mixture. The results of the ICP–MS analysis, XRD, and SEM characterization confirmed that the structure and composition of the catalyst were stable. Besides, the Mo-V-O oxide can catalyze the oxidation of a series of alcohols with high selectivities for corresponding carbonyl compounds. 相似文献
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本文研究了复杂系统建模的方法,并由此开发出一个复杂系统的建模工具。文中最后通过一个具体实例的演示验证了该工具的简捷性和有效性。 相似文献