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排序方式: 共有7568条查询结果,搜索用时 31 毫秒
1.
Jieyun Tu Xinghui Shi Yuanrong Jing Huimin Zou Jakub Kadlcak Zhanfu Yong Susu Liu Guangyong Liu 《Polymer Engineering and Science》2021,61(8):2213-2221
Equilibrium swelling and rheological tests were adopted to systematically investigate the effects of softener type and dosage on the crosslink densities. The results turned out that the chemical crosslink density could be distinguished from the physical crosslink density by comparing the results of equilibrium swelling and rheological tests. The liquid butadiene (LB) as a softener leads to the greatest reduction in crosslink density, followed by polyethylene wax (PW) and paraffinic oil (PO). The tensile strength decreases with increasing PO content while shows peak values with increase of LB and PW contents. The dependencies of chemical crosslink density on the aging time under 150°C are quite different for the three softeners, which can be expected from the double crosslinking networks consisting of small softener and large main crosslinking networks. Further investigation has been performed to correlate the tensile strength with chemical crosslink density of ethylene propylene diene monomer elastomer vulcanizates. Three different linear relationships can be obtained for the softeners independent of the aging time. It can now be expected from this study that the role of some new softeners in rubber compounds is not only confined to plasticization but also forms crosslinking networks in the peroxide-cured rubbers. 相似文献
2.
采用等温溶解平衡法对两个三元体系NaBr-CaBr2-H2O和KBr-CaBr2-H2O在273.15 K下的固液相平衡关系进行了研究,测定了相关盐在水溶液中的溶解度,绘制其等温相图。结果表明,两个三元体系均为水合物型,即平衡固相中未发现任何复盐及固溶体。两个三元体系在273.15 K下的等温相图均由一个共饱点、两条等温溶解度曲线、两个平衡固相结晶区组成。三元体系NaBr-CaBr2-H2O在273.15 K的两个结晶区的平衡固相分别为NaBr·2H2O和CaBr2·6H2O,NaBr·2H2O的结晶区远大于CaBr2·6H2O。三元体系KBr-CaBr2-H2O在273.15 K的两个结晶区的平衡固相分别为KBr和CaBr2·6H2O,KBr的结晶区远大于CaBr2·6H2O。基于Pitzer模型,运用已报道的Pitzer参数对所研究的两个三元体系在273.15 K下的等温溶解度进行模拟计算,其计算结果与实验结果基本吻合。 相似文献
3.
Geetanjali Yadav Leonard A. Fabiano Lindsay Soh Julie Zimmerman Ramkrishna Sen Warren D. Seider 《American Institute of Chemical Engineers》2021,67(1):e16992
Algae-to-biodiesel processes are hindered by high costs and low energy return on investment.1,2. Herein, three foci in research improve algae-to-biodiesel processes by: (1) reducing high installation and energy costs in the CO2 sequestration, cultivation, and harvesting stages; (2) improving oil extraction and biodiesel generation; and (3) increasing utilization of the proteins in lipid-extracted biomass (e.g., for animal feed), as well as the omega-3 fatty acids for nutraceuticals and food supplements. A process is introduced that uses carbon dioxide to aid in all three of these foci. CO2 is used first in the form of microbubbles to lyse algae cell walls, releasing triglyceride oils. CO2 also aids with transesterification of these triglycerides using methanol. At low temperatures (353.15–368.15 K) and intermediate pressures (5–10 MMPa), carbon dioxide causes methanol to dissolve partially in the triglyceride phase and triglyceride to dissolve partially in the methanol phase, increasing the transesterification reaction rate. Due to the nondestructive nature of these processes, other metabolites can also be harvested providing improvements in both mass and economic efficiency with an overall sharp reduction in the modeled price of biodiesel. 相似文献
4.
探究聚合物辅料对难溶性药物结晶的影响机制,是指导无定形固体分散体制剂设计和制备中辅料筛选的关键。研究了不同因素(温度、搅拌速率、聚合物浓度、聚合物分子量和聚合物种类等)对阿司匹林晶体生长动力学的影响。首先,采用基于三种不同晶体生长机制的化学势梯度模型结合UNIQUAC活度系数模型,描述和预测了阿司匹林在不同条件下的结晶动力学。进一步分析了不同因素对晶体生长速率常数 和结晶热力学推动力 的影响以及对阿司匹林结晶动力学的影响机制。结果表明,阿司匹林晶体生长速率随着结晶温度、聚合物浓度的增加而降低,随搅拌速率的增加而升高;聚乙烯吡咯烷酮(PVP K25)和羟丙基甲基纤维素(HPMC E3)显著抑制了阿司匹林的晶体生长,在PVP K25和HPMC E3水溶液体系下阿司匹林的晶体生长属于二维成核机制,在纯水和PEGs水溶液体系下晶体生长属于粗糙生长机制。所采用的化学势梯度模型能很好预测不同温度和搅拌速率下阿司匹林的结晶动力学,可有效减少实验所需的人力、物力和财力。研究可为固体分散体制剂制备中聚合物的筛选提供理论研究基础。 相似文献
5.
6.
为了确定土钉在基坑防护中合理的支护参数,以济南汉峪B9地块深基坑为例,根据基坑不同区域特点有针对性地制定了支护方案,计算验证了方案的合理性并提出可优化方案,分析了土钉的支护倾角、支护位置、土钉长度等参数变化对表征基坑稳定性的安全系数与潜在滑移面的影响。结果表明:当土钉长度小于有效支护长度时,基坑安全系数随着土钉长度的增加而逐渐增大,近似呈指数函数规律,土钉长度超出潜在滑移面1.28 m时支护效果最优;随着土钉支护位置的降低,基坑安全系数先增高后减小,安全系数在达到峰值安全系数前,安全系数与土钉位置呈一次函数规律,最优的支护位置为距基坑底部1/4坡面高度;随着土钉支护角度的增加,基坑坡面安全系数逐渐降低,呈一次函数关系,考虑施工便利性,土钉支护角度可定为5°~20°。 相似文献
7.
Yuhao Zhang Liang Zhao Feng Chen Yongtao Wang Jinsen Gao Liyuan Cao Hui Wang Chunming Xu 《American Institute of Chemical Engineers》2021,67(5):e17153
The fluid catalytic cracking (FCC) naphtha critical component-oriented separation process is an efficient method to produce ultra-low-sulfur (<10 μg/g) gasoline with minimal loss of octane number (<1 RON). However, the product quality is highly dependent on the structure of the components of FCC naphtha. Aromatics and thiophene sulfides without a methyl side chain favor the separation of olefin. The major impulse of olefin separation is the solvent-induced dipole of aromatics or thiophene sulfides, leading to a “Plane-to-Plane” combination between the solvent and aromatics or thiophene sulfides, accompanied by a steric hindrance due to their side chains. This condition resulted in 2–3 times greater θ of benzene and thiophene compared with that of toluene and 3-methylthiophene. In addition, an improved non-random two-liquid model was proposed based on the above results, and a simulation method for FCC naphtha solvent extraction process was established. The calculation results accorded well with industry data. 相似文献
8.
Katja F. Hellendahl Felix Kaspar Dr. Xinrui Zhou Zhaoyi Yang Prof. Dr. Zhen Huang Prof. Dr. Peter Neubauer Dr. Anke Kurreck 《Chembiochem : a European journal of chemical biology》2021,22(11):2002-2009
Selenium-modified nucleosides are powerful tools to study the structure and function of nucleic acids and their protein interactions. The widespread application of 2-selenopyrimidine nucleosides is currently limited by low yields in established synthetic routes. Herein, we describe the optimization of the synthesis of 2-Se-uridine and 2-Se-thymidine derivatives by thermostable nucleoside phosphorylases in transglycosylation reactions using natural uridine or thymidine as sugar donors. Reactions were performed at 60 or 80 °C and at pH 9 under hypoxic conditions to improve the solubility and stability of the 2-Se-nucleobases in aqueous media. To optimize the conversion, the reaction equilibria in analytical transglycosylation reactions were studied. The equilibrium constants of phosphorolysis of the 2-Se-pyrimidines were between 5 and 10, and therefore differ by an order of magnitude from the equilibrium constants of any other known case. Hence, the thermodynamic properties of the target nucleosides are inherently unfavorable, and this complicates their synthesis significantly. A tenfold excess of sugar donor was needed to achieve 40−48 % conversion to the target nucleoside. Scale-up of the optimized conditions provided four Se-containing nucleosides in 6–40 % isolated yield, which compares favorably to established chemical routes. 相似文献
9.
采用塔河油田缝洞型油藏稀油和常规稠油两种代表性油样,通过开展向前多次接触相平衡实验模拟蒸发气驱过程、向后多次接触相平衡实验模拟凝析气驱过程,研究了氮气与塔河油田原油在高温高压条件下的相态变化,明确了氮气与地层原油充分接触混合后地层流体的气液组分变化规律,提出了抽提指数的计算表达式,定量评价了氮气在高温高压条件下对原油轻组分的抽提效果,深化了注氮气提高采收率作用机理的认识。研究结果表明,塔河油田油藏条件(压力>65 MPa、温度>415 K)下,原油中轻质组分(C1—C5)经过5次接触后的流失率高达94%~100%,氮气对原油有较强的抽提作用;向前接触实验中,随接触次数增加,抽提作用越来越强,抽提指数越来越大,同次接触氮气对稀油的抽提指数是稠油的5倍以上;注入气中加入20%的CO2后对原油中轻质组分的抽提效果增强不显著,抽提指数仅小幅变化。两种气体与塔河油田稀油在多次向前接触后展现出了近混相的趋势;向后接触实验表明,首次接触抽提作用最大,抽提指数随着接触次数的增加逐渐减小至0,较之向前接触明显偏小。 相似文献
10.