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1.
相邻工作面开采会导致复杂的漏风情况,浮煤易自燃,增大防火工作的难度。为明确相邻采空区自燃“三带”分布特征及确定最佳注氮防灭火参数,以贵州某矿4244工作面为背景,结合现场实测,应用Fluent流场分析软件,模拟研究不同注氮方案下采空区氧气浓度场分布规律。结果表明,实测结果与模拟相吻合,验证了模拟的可靠性;当注氮位置为X=50 m,注氮流量为100 m3/h时,采空区进、回风巷侧氧化带宽度分别为7 m和38 m,能明显减少本采空区氧化带面积,且能防止氧化带距工作面太近;此工作面进风侧注氮对相邻采空区氧化带影响范围较小,这要求在回采过程中需要对煤柱进行加固,降低孔隙率,控制漏风,减少氧气进入相邻采空区,降低煤自燃风险。模拟结果为相邻采空区灾害防治工作提供了的理论指导。 相似文献
2.
《International Journal of Hydrogen Energy》2022,47(95):40407-40414
The present work addresses the potentialities of Pt–Ru nanoparticles deposited on a graphene oxide (RGO) and TiO2 composite support towards electrochemical oxidation of ethanol in acidic media relevant for fuel cell applications. To immobilize platinum–ruthenium bimetallic nanoparticles on to an RGO-TiO2 nanohybrid support a simple solution-phase chemical reduction method is utilized. An examination using electron microscopy and energy dispersive X-ray spectroscopy (EDS) indicated that Pt–Ru particles of 4–8 nm in diameter are dispersed on RGO-TiO2 composite support. The corresponding Pt–Ru/RGO-TiO2 nanocomposite electrocatalyst was studied for the electrochemical oxidation of ethanol in acidic media. Compared to the commercial Pt–Ru/C and Pt/C catalysts, Pt–Ru/RGO-TiO2 nanocomposite yields higher mass-specific activity of about 1.4 and 3.2 times, respectively towards ethanol oxidation reaction (EOR). The synergistic boosting provided by RGO-TiO2 composite support and Pt–Ru ensemble together contributed to the observed higher EOR activity and stability to Pt–Ru/RGO-TiO2 nanocomposite compared with other in-house synthesized Pt–Ru/RGO, Pt/RGO and commercial Pt–Ru/C and Pt/C electrocatalysts. Further optimization of RGO-TiO2 composite support provides opportunity to deposit many other types of metallic nanoparticles onto it for fuel cell electrocatalysis applications. 相似文献
3.
《International Journal of Hydrogen Energy》2022,47(87):36926-36952
The ohmic resistance in solid oxide fuel cells (SOFCs) mainly comes from the electrolyte, which can be reduced by developing novel electrolyte materials with higher ionic conductivity and/or fabricating thin-film electrolytes. Among various kinds of thin-film fabrication technology, the physical vapor deposition (PVD) method can reduce the electrolyte thickness to a few micrometers and mitigate the issues associated with high-temperature sintering, which is necessary for wet ceramic methods. This review summarizes recent development progress in thin-film electrolytes fabricated by the PVD method, especially pulsed laser deposition (PLD) and magnetron sputtering. At first, the importance of the substrate surface morphology for the quality of the film is emphasized. After that, the fabrication of thin-film doped-zirconia and doped-ceria electrolytes is presented, then we provide a brief summary of the works on other types of electrolytes prepared by PVD. Finally, we have come to the summary and made perspectives. 相似文献
4.
《International Journal of Hydrogen Energy》2022,47(63):27279-27292
This study assesses a sustainable solution to greenhouse gases (GHGs) mitigation using constructed wetland-microbial fuel cells (CW-MFC). Roots of wetland plant Acorus Calamus L. are placed in biological anode to better enable anode microorganisms to obtain rhizosphere secretion for power improvement. Three selected cathode materials have a large difference in GHG emissions, and among them, carbon fiber felt (CFF) shows the lowest emissions of methane and nitrous oxide, which are 0.77 ± 0.04 mg/(m2·h) and 130.78 ± 13.08 μg/(m2·h), respectively. The CFF CW-MFC achieves the maximum power density of 2.99 W/m3. As the influent pH value is adjusted from acidic to alkaline, the GHGs emissions are reduced. The addition of Ni inhibits GHGs emission but decreases the electricity, the power density is reduced to 1.09 W/m3, and the methane and nitrous oxide emission fluxes decline to 0.20 ± 0.04 mg/(m2·h) and 15.49 ± 1.86 μg/(m2·h), respectively. Low C/N ratio reduces methane emission, while high C/N ratio effectively inhibits nitrous oxide emission. At the influent pH 8 and C/N = 5:1, the methane emission flux is approximately 10.60 ± 0.27 mg/(m2·h), and the nitrous oxide emission flux is only 10.90 ± 1.10 μg/(m2·h). Based on the above experimental results by controlling variable factors, it is proposed that CW-MFC offers an environment-friendly solution to regulate GHG emissions. 相似文献
5.
超临界机组高温合金管氧化膜剥落问题是困扰机组安全与经济运行的难题,严重制约了机组蒸汽参数和效率的提高。特别是,在超临界机组采用给水加氧处理方式(OT)后,奥氏体不锈钢管内壁氧化膜大面积剥落事故屡见不鲜,尤以TP347H合金管为甚。本文总结了近年来国内外针对超临界机组合金管氧化膜研究的进展及相关成果,首先介绍了超临界蒸汽环境中合金管氧化机理和原子迁移机制,综述了铁素体和奥氏体合金表面氧化膜的形貌特征,分析了蒸汽溶氧对氧化膜生长速率、形貌和缺陷的影响。氧化膜完整性是决定合金抗腐蚀性能的重要因素,但在机组运行过程中氧化膜应力破坏了氧化膜完整性。进一步总结了国内外氧化膜应力和剥落研究的数值分析及实验研究情况,为我国超临界机组氧化膜剥落故障诊断研究提供参考。 相似文献
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7.
Sorption selective catalytic reduction of nitrogen oxides (NOx) (sorption-SCR) has ever been proposed for replacing commercial urea selective catalytic reduction of NOx (urea-SCR), while only the single-stage sorption cycle is hitherto adopted for sorption-SCR. Herein, various multi-stage ammonia production cycles is built to solve the problem of relative high starting temperature with ammonia transfer (AT) unit and help detect the remaining ammonia in ammonia storage and delivery system (ASDS) with ammonia warning (AW) unit. Except for the single-stage ammonia production cycle with MnCl2, other sorption-SCR strategies all present overwhelming advantages over urea-SCR considering the much higher NOx conversion driven by the heat source lower than 100°C and better matching characteristics with low-temperature catalysts. Furthermore, the required mass of sorbent for each type of sorption-SCR is less than half of the mass of AdBlue for urea-SCR. Therefore, the multifunctional multi-stage sorption-SCR can realize compact and renewable ammonia storage and delivery with low thermal energy consumption and high NOx conversion, which brings a bright potential for efficient commercial de-NOx technology. 相似文献
8.
采用Gleeble-2000热模拟试验机对Mn18Cr18N高氮奥氏体不锈钢进行高温拉伸试验,利用扫描电镜-能谱仪对拉伸试样断口形貌及断口附近的显微组织进行观察,用Thermo-Calc软件计算试验钢的相变及析出相,研究了Mn18Cr18N高氮奥氏体不锈钢的高温力学性能。结果表明,试验钢的第Ⅰ脆性区>1200 ℃,第Ⅲ脆性区为850~950 ℃,未出现第Ⅱ脆性区,第Ⅰ脆性区的出现主要是在加热过程中试验钢由γ奥氏体向δ铁素体转变引起的,第Ⅲ脆性区的出现是因为沿晶析出M23C6、M2(C, N)等硬脆相引起的;试验钢的抗拉强度随着拉伸温度升高而降低,断面收缩率在1000~1200 ℃温度范围内逐渐增大并表现出极佳的热塑性,断面收缩率均在70%以上,温度超过1200 ℃后断面收缩率急剧下降;Mn18Cr18N高氮奥氏体不锈钢的热锻温度应选择在1000~1150 ℃之间,在此温度范围内试验钢的断面收缩率均在70%以上,并且可以避开第Ⅰ与第Ⅲ脆性区。 相似文献
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10.
针对低温液氮冷却下淬硬钢高速车削过程中切屑形成及刀具磨损机理尚缺乏相关研究的问题,开展了液氮冷却下的淬硬钢高速切削研究,并与干切进行了对比。分析了切削力、切削温度、切屑特征以及刀具磨损特征,讨论了冷却润滑、切屑形成及刀具磨损机理。结果表明: 与干切相比,各组实验中低温液氮冷却切削的切削温度降低了6.9%~9.9%,因材料硬化使得切削力增大了10.1%~12.8%;低温液氮冷却下,切屑锯齿化程度相比干切明显增大,这与第一变形区应力应变更大、切屑形成存在从热塑性剪切失稳到周期性脆性断裂的过渡有关;低温液氮对切削界面的润滑降低了切削热,液氮强射流吹离了高热切屑,强传热换热能力可迅速置换切削区热量;与干切相比,低温液氮明显减小了黏结磨损,通过冷却增强刀体减缓了刀具微剥落,刀具寿命延长了28.6%~47.1%;低温液氮冷却下,黏结不再是主要磨损机理之一,磨粒磨损、冲击磨损为主要磨损机理,后刀面片状剥落和微崩刃为主要刀具破损形式。 相似文献