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991.
Bo Nan Susana Olhero Rui Pinho Paula M. Vilarinho Tim W. Button José M. F. Ferreira 《Journal of the American Ceramic Society》2019,102(6):3191-3203
Direct ink writing (DIW) has become a widespread additive manufacturing technique for material engineering, but its application in lead-free Ba0.85Ca0.15Zr0.1Ti0.9O3 piezoelectric ceramics from aqueous systems has not been reported so far to our knowledge. The main obstacle is the high extent of hydrolysis reactions undergone by the starting powders when dispersed in water, hindering the attainment of stable water-based colloidal suspensions. This paper reports on the preparation of stable aqueous inks from a deagglomerated and surface-treated powder synthesized by solid-state reaction and on DIW of macroporous lead-free piezoelectrics. Based on zeta potential and rheological measurements, the optimal amounts of processing additives (dispersant, binder, and coagulating agent) were selected to transform the initial fluid suspension to a viscoelastic paste with sufficient stiffness and stability for the printing process. Dielectric and piezoelectric properties of samples sintered under different temperatures were also investigated. 相似文献
992.
993.
Josiane Ferreira da Silva Débora Lemos da Silva Rui Gomes Nascimento Lizzy Ayra Alcântara Veríssimo Cristiane Martins Veloso Renata Cristina Ferreira Bonomo Rafael da Costa Ilhéu Fontan 《应用聚合物科学杂志》2019,136(37):47956
The use of macroporous monolithic matrices in the purification of biocompounds is constantly growing and developing. In this work, the objective was to optimize the quantity of N-acetyl-D-glucosamine (D-GlcNAc) immobilized on the surface of macroporous polymeric cryogels for capture of lectins from less clarified solutions. Surface response methodology was applied and it was observed that the immobilization temperature of the glutaraldehyde (GLU) and the D-GlcNAc concentration influenced the amount of sugar immobilized. The matrices produced with 1.1% of allyl glycidyl ether were functionalized by GLU. Optimal maximum condition was obtained with mean value of 160.39 ± 26.38 mg of D-GlcNAc immobilized per gram of dry cryogel. Characterization analyses of the matrices showed that the activation process was effective, maintaining the macroporous structure and physical characteristics. The adsorbents produced were tested for capture of lectins from a crude protein solution of barley. At tested conditions, adsorbent capture around 11% of protein in solution but reduce the hemaglutinating capacity in 40%, demonstrating its selectivity. The cryogels functionalized with D-GlcNAc present potential for use in capture compounds by affinity with carbohydrates, such as lectins. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47956. 相似文献
994.
André Campaniço Dr. Marta P. Carrasco Dr. Mathew Njoroge Ronnett Seldon Prof. Kelly Chibale Dr. João Perdigão Prof. Isabel Portugal Prof. Digby F. Warner Prof. Rui Moreira Prof. Francisca Lopes 《ChemMedChem》2019,14(16):1537-1546
Herein we report the screening of a small library of aurones and their isosteric counterparts, azaaurones and N-acetylazaaurones, against Mycobacterium tuberculosis. Aurones were found to be inactive at 20 μm , whereas azaaurones and N-acetylazaaurones emerged as the most potent compounds, with nine derivatives displaying MIC99 values ranging from 0.4 to 2.0 μm . In addition, several N-acetylazaaurones were found to be active against multidrug-resistant (MDR) and extensively drug-resistant (XDR) clinical M. tuberculosis isolates. The antimycobacterial mechanism of action of these compounds remains to be determined; however, a preliminary mechanistic study confirmed that they do not inhibit the mycobacterial cytochrome bc1 complex. Additionally, microsomal metabolic stability and metabolite identification studies revealed that N-acetylazaaurones are deacetylated to their azaaurone counterparts. Overall, these results demonstrate that azaaurones and their N-acetyl counterparts represent a new entry in the toolbox of chemotypes capable of inhibiting M. tuberculosis growth. 相似文献
995.
Xiaoyan Qiu Yongqiang Zhang Haitao Wu Rui Yang Jun Yang Rongjuan Liu Yong Liu Zhiping Zhou Tongfan Hao Yijing Nie 《Polymer International》2019,68(2):218-224
The crystallization of capped ultrathin polymer films is closely dependent on film thickness and interfacial interaction. Using dynamic Monte Carlo simulations, the crystallization behaviors of polymer films confined between two substrates were investigated. The crystallization rate of confined polymers is reduced with high interfacial interactions. Above a critical strength of interfacial interaction, polymer crystallization in the thin film is inhibited within the simulation time scales. An increase in film thickness leads to a rise in critical interfacial interaction. In thicker films, the chains have more space to change conformation to form crystal stems. In addition, there are fewer absorbed segments in confined chains for the thicker films, and thus the chains have stronger ability to adjust their conformation. Therefore an increase in film thickness can cause a reduction in the entropic barrier required for the formation of crystals and thus an increase in the critical interfacial interaction. © 2018 Society of Chemical Industry 相似文献
996.
Jie Yang Sun‐Duo Zhao Rui‐Mei Jin Dong‐Hui Zhao Wei Chen Wei Hu Qiong Wang Bo Liu 《大分子材料与工程》2019,304(4)
An injectable and self‐healing multifluorescent hydrogel system based on engineered coiled‐coil polypeptide and CdSe@ZnS quantum dots (QDs) is developed. The mechanical properties of the PC10A‐QD hydrogel are able to be tuned by changing the concentrations of PC10A and QDs. The G′ of PC10A hydrogel increases from 800 to 1000 Pa by doping 6 nm oil‐soluble CdSe@ZnS QDs. The PC10A‐QD hydrogel can easily pass through a 26‐gauge needle without clogging. In addition, through interfacial assembly of PC10A polypeptide on the surface of the PC10A‐QD hydrogel, each of these hydrogel can self‐assemble into a multifluorescent hydrogel. This approach for preparation of injectable self‐healing multifluorescent hydrogels is expected to apply in biomedicine. 相似文献
997.
含氟工业废水的排放污染水源,长期饮用高氟水引起各种氟中毒疾病。通过简单高效的化学处理方法使含氟水达到国家一级排放标准(10 mg·L^(-1))。以硝酸镁、硝酸铝为原料,尿素为沉淀剂,通过水热法成功制备镁铝层状双氢氧化物(Mg-Al-LDHs)材料。该层状材料经400℃焙烧后,层板有效空间增大,离子吸附性能增强,晶化程度高,结构稳定。考察400℃焙烧后Mg-AlLDHs层状材料对高氟水中氟离子(F!)吸收的影响。实验结果表明Mg/Al物质的量比为2∶1,反应时间为2 h时,F!去除率82. 61%,实现高效除氟。 相似文献
998.
从工业废气中回收分离乙烯(C2H4)具有重要意义,选用了三种低黏度二氰胺类离子液体,分别测定了293.15~333.15 K下其密度、黏度等物化性质,研究了其对乙烯(C2H4)吸收性能。采用非随机(局部)双液体模型(NRTL)关联了三种二元体系溶解度数据,实验值与计算值的平均相对偏差均小于3%。结果表明,低黏度二氰胺类离子液体对C2H4气体吸收性能良好,其中阳离子侧链长度增加和羟基功能团引入可增强对C2H4溶解度。同时,离子液体1-丁基-3-甲基咪唑二氰胺盐([Bmim][DCN])经过3次的吸收解吸循环,仍可以保持较好的C2H4吸收性能,表明该离子液体循环稳定性好,而1-丁基-3-甲基咪唑二氰胺盐([Bmim][DCN])对乙烯吸收量较高,具有作为C2H4吸收剂的潜力。 相似文献
999.
针对硅孔雀石天然可浮性差,表面多孔和高孔隙度,性质变化不均匀,并且亲水性强,难溶解的特性,通过XRD、SEM检测硅孔雀石原矿性质和表面形态,核心地提出了硅孔雀石改性高分子聚合物吸附-中间金属铜离子联接-捕收剂吸附的试验方案.高分子活化剂通过对硅孔雀石表面有机改性,使其能够吸中间金属铜离子,在硅孔雀石浮选改性中起着至关重要的作用.通过硫酸铵、乙二胺磷酸盐、高分子药剂实际浮选试验情况分析对比,发现高分子药剂和硫酸铵共同使用时试验效果最好,最终硅孔雀石的回收率达到了86.9%的良好指标. 相似文献
1000.
硫酸化氧化锆固体酸(SO42-/ZrO2)烷烃异构化催化剂兼具高活性、可再生和环境友好的优点,具有广阔的应用前景。本文综述了SO42-/ZrO2催化剂在轻质烷烃异构化中的工业应用进展,包括市场现状、现有技术、经济性等方面,并对专利和文献中报道的催化剂制备技术进行了论述总结。重点针对催化剂的关键制备参数以及对催化剂结构和异构化性能的影响进行了深入分析和探讨,包括氢氧化物前体的沉淀和焙烧条件、助剂的添加和改性作用、催化剂预处理条件和原料水含量的影响等。最后对催化剂开发和工业化中的难点给出了分析和建议,并展望了未来的催化剂发展方向,指出拓宽催化剂的原料适应性、发展新型制备技术和助剂体系、结合催化剂再生等工艺研究是未来的发展方向。 相似文献