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101.
二价金属离子对UASB颗粒污泥的影响   总被引:16,自引:0,他引:16  
分析了Mg^2 、Ca^2 、Fe^2 等二价金属离子对UASB反应器中厌氧颗粒污泥的影响。  相似文献   
102.
Ca对原位自生Mg2Si/ZM5复合材料组织与性能的影响   总被引:10,自引:3,他引:10  
通过真空感应炉中氩气保护,在ZM5熔体中加入Si获得原位反应自生Mg2Si/ZM5复合材料.采用金相显微镜、环境扫描电镜、拉伸实验等研究了Ca对该材料组织与性能的影响规律.结果表明:Ca的加入改变了Mg2Si/ZM5复合材料中Mg2Si相的形貌,使其从不规则的汉字状变成较细小的多角形,从而改善了材料的力学性能;当加入0.05?(质量分数)时,复合材料的室温力学性能最好,屈服强度提高了10.4%,延伸率提高了52.4%;在200℃高温下,当含Ca0.05%~0.10%(质量分数)时其屈服强度和延伸率最好,分别提高了30.1%和92.3%.  相似文献   
103.
为了探究稀土离子掺杂铝硅酸盐的光温特性,本文采用燃烧合成法制备了系列荧光粉材料Ca1-3x/2Al2Si2O8:xEu3+。X射线衍射结果表明掺杂Eu3+离子不会改变基质CaAl2Si2O8的晶体结构。荧光光谱结果表明该荧光粉在近紫外光区域具有较强吸收,当被波长为393 nm的近紫外光激发后,其最大特征发射峰为611 nm,且Eu3+离子的最佳掺杂浓度为0.05。利用上升时间测温法研究了CaAl2Si2O8:Eu3+荧光粉的光温传感特性,结果表明:随着Eu3+掺杂浓度的增加,上升时间单调递减,但当掺杂掺杂超过0.100时就会发生淬灭。Ca0.985Al2Si2O8:0.01Eu3+的相对灵敏度随温度的升高先增大后减小,并在520 K时达到最大值(0.024 K-1)。上述研究表明该荧光粉具备优异的温度传感性能,在测温领域具有广泛的应用前景。  相似文献   
104.
Six phosphate rocks (PRs) of varying reactivities were compared with monocalcium phosphate (MCP) in a glasshouse experiment growing perennial ryegrass (Lolium perenne cv. Nui) as the test plant on four soils of contrasting P sorption capacity and exchangeable Ca. The cumulative dry matter yield over 10 harvests showed a significant response to P application in all soils. Based on relative yield and P uptake, MCP was the most effective P fertilizer followed by the reactive phosphate rocks, which were superior to the unreactive rocks in all soils. The relative agronomic effectiveness (RAE) and substitution ratio (SR) of individual PR fertilizers, calculated with respect to MCP using the methods of vertical and horizontal comparison, respectively, were similar over a range of fertilizer rate. There was a decline or slight increase in the performance of PRs with time in the low P sorption soils but a consistent increase in the high P sorption soils. Some initial influence of exchangeable Ca content of the soils on the relative performance of PRs was also observed. Generally the PRs performed better in high P sorption soils than low P sorption soils and in low exchangeable Ca soils than high exchangeable Ca soils.  相似文献   
105.
The objective of this work was to develop and evaluate a soil test suitable for estimating the phosphorus status of soils whether they were fertilized with soluble or sparingly soluble P fertilizers or both. Four New Zealand soils of contrasting P sorption capacity and exchangeable Ca content were incubated alone or with monocalcium phosphate (MCP), reactive North Carolina (NC) phosphate rock or unreactive Florida (FRD) rock, at 240 mg P kg–1 soil, to allow the P sources of different solubilities to react with each soil and provide soil samples containing different amounts of extractable P, Ca and residual phosphate rock. The phosphorus in the incubated soils was fractionated into alkali soluble and acid soluble P fractions using a sequential extraction procedure to assess the extent of phosphate rock dissolution. Eight soil P tests [three moderately alkaline — Olsen (0.5M NaHCO3) modified Olsen (pretreatment with 1M NaCl) and Colwell; three acid tests — Bray 1, modified Bray 1 and Truog; and two resin tests — bicarbonate anion exchange resin (AER) and combined AER plus sodium cation exchange resin (CER)] were assessed in their ability to extract P from the incubated soils.The 0.5M NaHCO3 based alkaline tests could not differentiate between the Control and FRD treatments in any soil nor between the Control, NC and FRD treatments in the high P sorption soils. The acid extractants appeared to be affected by the P sorption capacity of the soil probably because of reabsorption of dissolved P in the acid medium. The AER test gave results similar to Olsen. Only the combined AER + CER test extracted P in amounts related to the solubility of the P sources incubated with each soil. Furthermore, when soil samples were spiked with FRD and NC and extracted immediately, the P extracted by the AER + CER test, over and above the control soils, increased with the amount and chemical reactivity of the rocks. There was no extraction of rock P by any of the alkaline extractions.Increases in the amounts of P extracted (P) by each soil test from the fertilized soils, over and above the control soils were compared with the amounts ofP dissolved from the fertilizers during incubation (measured by P fractionation). Soil P sorption capacity had least influence on the amounts of P extracted by the AER + CER and Colwell tests. However, the Colwell test was unable to differentiate between all P sources in all four soils and suffered from the disadvantage of producing coloured extracts. The AER + CER test appeared to have the potential to assess the available P status of soils better than the other tests used because of its ability to extract a representative portion of residual PR (in accordance with the amount and reactivity) and dissolved P, and thus to differentiate between fertilizer treatments in all four soils.  相似文献   
106.
Three types of anode, Pb–Sb, Pb–Ca–Sn and Pb–Co3O4, for copper electrowinning were investigated. The corrosion resistance, as evaluated by cyclic voltammetric (CV) measurements was higher for Pb–Co3O4 than for Pb–Sb and Pb–Ca–Sn. During prolonged electrowinning under galvanostatic conditions, the anodic reaction on the Pb–Co3O4 anode was depolarized by 0.053 V as compared to Pb–Sb, and by 0.106 V with respect to Pb–Ca–Sn. The composition and structure of the anodic layer were determined by XPS, X-ray and SEM analyses. The surface layer on the three anodes examined was composed mainly of PbSO4, -PbO2 and -PbO2. Different structure of the surface layer was observed: loose and highly spread coral-like structure in the case of Pb–Sb; fibrous structure in the case of Pb–Ca–Sn and dense, fine-grained structure in the case of Pb–Co3O4.  相似文献   
107.
Phosphate application changes chemical properties of surface soils, consequently influencing crop nutrient availability and pedological process. Sodium ortho- (OP) or pyrophosphate (PP) was equilibrated with three Quebec soils: an Uplands sand (Orthic-Podzol), a St. Bernard loam (Eutric-Cambisol), and a Dalhousie clay (Humic Gleysol) in 0.03 M KClO4 solution at an initial pH 6.0. Both autoclaved and nonautoclaved soils were used, and dissolution of Fe, Al, Si, Ca and organic C was studied.Concentrations of Fe and Al in OP equilibrated solutions were not detectable. Ca solubility was reduced while dissolution of Si and organic C was increased in the presence of OP. These changes were possibly due to P—Ca precipitates or increased Ca sorption by P, and competition between OP and Si or organic materials for sorption sites. PP enhanced dissolution of Fe, Al, Si and organic C but reduced solubility of Ca. Comparisons showed that PP added to autoclaved soils had greater effects on increasing dissolutions of Fe, Al, Si and organic C and on reducing Ca solubility than OP in both autoclaved and nonautoclaved soils. Autoclaving resulted in greater dissolution of organic C. Dissolved Si with added OP was greater with nonautoclaved soils probably due to more P sorption in the nonautoclaved system, compared with autoclaved soil. Added PP dissolved Fe and Al ions which may ultimately enhance P precipitation by forming less soluble compounds upon hydrolysis of PP to OP.  相似文献   
108.
Effects of coralline lime on yield and nutrient uptake by sweet corn (Zea mays saccharata Sturt.) and peanut (Arachis hypogea) were studied at three locations in Western Samoa. Coarse (0-10 mm) coralline material containing 31.1% Ca and 1.67% Mg was used as lime. There were two modes of application: band and broadcast, and three rates: 6, 12 and 18 ton ha–1. In the highest rainfall location, marketable yields were increased by 250% for peanut and 160% for sweet corn by liming at 6 ton ha–1, relative to the unamended control. Peanut yield increases were associated with reduced Mn toxicity and/or with Ca and Mg deficiency. Sweet corn was less susceptible to Mn toxicity, but more responsive to exchangeable Ca. The critical level of exchangeable Ca was found to be about 2.0 cmol(+)kg–1. Applying lime to a band of 0.25-m wide did not reduce yield relative to broadcast. Soil cultivation caused the lime to spread over a wider band, diluting the applied calcium with a larger soil volume, suggesting that less than 6 ton ha–1 broadcast coarse coralline lime could still be adequate for most Samoan soils.  相似文献   
109.
Changes in soil pH, exchangeable aluminium (Al), calcium (Ca), magnesium (Mg), and potassium (K) and extractable manganese (Mn) were investigated after urea fertigation of a sandy loam soil in an apple orchard in New Zealand. Urea at three rates (0, 25, 50 kg N ha–1 yr–1 or 0, 16.9, 33.8 g N emitter–1 yr–1) was applied in 4 equal fertigations. Soil cores at 4 profile depths (0–10, 10–20, 20–40 and 40–60 cm) directly below and 20 cm from the emitter were sampled approximately 4 weeks after each fertigation and in the following winter. Results obtained showed that the largest changes in soil pH and cations occurred in soils directly below the emitter in the 50 kg N ha–1 yr–1 treatment where the soil pH decreased by 1.6 pH units at all soil depths. The lowest pH of 4.3 was observed at a depth of 27 cm. Exchangeable Al and extractable Mn levels increased to 11 meq kg–1 and 78µg g–1 respectively. Estimated losses of Ca, Mg and K from the upper soil profile depth (0–10 cm) represented 23, 63 and 27% of their respective total exchangeable levels. At lower profile depths (>20 cm), accumulation of displaced K was evident. Variable, and generally non-significant, chemical changes recorded in soils 20 cm from the emitter were attributed to restricted lateral water movement, and therefore urea movement, down the profile.The present study showed that one season of urea fertigation by trickle emitters, applied to a sandy loam, at half the rate conventionally applied to apple orchards (50 kg N ha–1 yr–1) resulted in pH and mineral element imbalances which were potentially and sufficiently severe to inhibit tree growth.  相似文献   
110.
脂肪醇制备叔胺的新型催化剂的最新进展   总被引:2,自引:0,他引:2  
对采用脂肪醇和二甲胺一步胺化制备(得率100%)相应的叔胺(烷基二甲基叔胺)的新型催化剂的最新进展进行了论述,对高活性Cu/Ni/Ca/Ba-St胶体催化剂(Cu0/Ni0/Ca0的比为5∶1∶1)和不含镍的Cu/La2O3进行了讨论。由此得出结论:要达到定量制备的关键因素是,通过结合还原钙或更活泼的促进剂,如Ce0和La0,尽可能地增加催化体系的氢解活性,由此形成金属氢化物,在铜/镍的作用下产生活性氢的“自供体系”。这一就地形成金属氢化物的基本功能将可极大地减少催化剂的用量,使铜质量分数减少到2×10-3%,从而极大地降低二甲胺的歧化,增加目的叔胺的选择性。总的来说,观察到在铜/镍固体催化剂以及胶体催化剂作用下,活性氢自供体系的基本功能使充入的大量氢一点都不被消耗掉。  相似文献   
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