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41.
以β分子筛为载体,在保持金属总负载量不变的情况下,采用等体积浸渍法制备了4种不同n(Ni)/n(Ni+Mo)的催化剂。分别采用X射线衍射(XRD)、比表面积测试(BET)、氨程序升温脱附(NH3-TPD)、氢程序升温还原(H2-TPR)、氢程序升温脱附(H2-TPD)和热重-差热分析(TG-DTG)等方法对催化剂进行了表征。结果表明,4种催化剂的酸量和酸强度相近,在n(Ni)/n(Ni+Mo)等于基准+0.2时,Mo与载体之间的相互作用最弱,其氢气吸附量最多且积炭量最少;采用某炼厂重整C10+ 重芳烃对4种催化剂进行评价,结果表明n(Ni)/n(Ni+Mo)等于基准+0.2催化剂具有最优的催化活性和稳定性。上述结果表明,影响重芳烃轻质化催化剂活性和稳定性的关键因素是催化剂氢气吸附量的多少,氢气吸附量越多金属表面的溢流氢效应越明显,积炭前驱体被溢流氢及时消除,从而保护了催化剂的加氢活性中心不被积炭覆盖,有助于催化剂在较高活性下保持稳定。 相似文献
42.
贵金属Cu、Ag、Au的电子结构和物理性质 总被引:1,自引:0,他引:1
由纯金属单原子理论(OA)确定了面心立方结构(FCC)贵金属Cu、Ag、Au的电子结构依次为[Ar](3dn)5.58(3dc)4.21(4sc)0.23(4sf)0.98、[Kr](4dn)4.87(4dc)4.56(5sc)0.66(5sf)0.91、[Xe](5dn)4.20(5dc)4.90(6sc)1.57(6sf)0.33,并确定了Cu、Ag、Au的密排六方结构(HCP)和体心立方结构(BCC)两种初态特征晶体和初态液体的电子结构。根据自然态的电子结构定性解释了熔点、拉伸强度、维氏硬度、体弹性模量、电导和热导率物理性质差异与电子结构的关系,定量计算了晶格常数、结合能、势能曲线及线热膨胀系数随温度的变化。根据非自然态的电子结构,定性解释了晶体结构BCC和HCP的关系。 相似文献
43.
Au-based catalysts, known for ambient temperature CO oxidation, have to provide stable performance of up to 5000 h in order to be commercially applicable in automotive fuel cells. In this report, the on-line deactivation characteristics of Au/TiO2 in unconventional PROX conditions are discussed. As opposed to CO removal from air, results in this report suggests that carbonates have a minor effect on deactivation of Au/TiO2 in dry H2-rich conditions. Also, no conclusive correlation between surface hydration and deactivation was observed. Rather, deactivation appeared to have occurred as a result of an intrinsic transformation in the oxidation state of the active species in the reducing operating conditions; a process which was reversible in an oxidizing atmosphere. 相似文献
44.
以定量分析钢筋与混凝土粘结滑移关系为目标,利用RCXFEHohai-P扩展有限元程序,计算采用不同粘结滑移公式时钢筋混凝土简支梁的最大裂缝宽度。结果表明,计算所得最大裂缝宽度各不相同,且都与《混凝土结构设计规范》(GB 50010—2010)所列最大裂缝宽度公式计算值存在差别。为此,基于GA-BP神经遗传网络,以规范最大裂缝宽度公式计算值为预测目标,反演得到适用于扩展有限元裂缝计算的粘结滑移公式,算例表明该公式能满足扩展有限元裂缝宽度计算要求。研究成果对提高扩展有限元裂缝分析的准确性具有一定的参考价值。 相似文献
45.
北方渠道大多使用保温板防止混凝土衬砌受冻胀破坏。在计算保温板厚度时为了降低成本,容易忽略保温板使用过程中受各种因素的影响导致保温效果变差的情况,使混凝土衬砌达不到设计使用年限便提前被破坏。内蒙古河套灌区试验结果表明,由于受酸雨、冻融作用、含水量等因素的影响,保温板保温效果平均每年降低0.9℃,其中受含水量变化的影响最大。经试验测得:聚苯乙烯保温板(EPS)含水量每增加1%,会导致导热系数增大5%。基于多层材料串联热阻叠加原理和热阻等效原理,对保温板厚度计算公式进行完善,并提出相应的铺设方法和施工技术要求。该设计对保温板在季节性冻土区的推广应用具有一定参考价值。 相似文献
46.
以缅甸DAPEIN(Ⅰ)水电站工程为例,论述了将WES实用堰的闸墩墩头向上游超长延伸之后,对泄洪安全所造成的影响。针对WES实用堰流量系数、堰面动水压力容易受边界因子影响的特点,对设计断面的堰顶布置和墩头形状进行了优化。根据堰面空化数计算公式及水流特性推导出计算的关键部位,对空化数进行计算。采用几何比尺为1∶60的物理模型对溢流堰的泄流能力和堰面动水压力进行了试验测试。试验结果表明:溢流堰的模型试验泄流能力和设计泄流能力非常相近。堰面动水压力除工况2的B4测点出现了-1.2 k Pa的微小负压值外,其余堰面时均压强值均大于0。从而,在泄流能力和堰面动水压力两方面都验证了这种设计方案的合理性。该工程所遇到的结构布置问题在中低溢流坝工程中属常见问题,解决思路可为今后类似工程建设借鉴参考。 相似文献
47.
Ceria-supported Au catalyst has been synthesized by the solution combustion method for the first time and characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). Au is dispersed as Au0 as well as Au3+ states on CeO2 surface of 20-30 nm crystallites. On heating the as-prepared 1% Au/CeO2 in air, the concentration of Au3+ ions on CeO2 increases at the expense of Au0. Catalytic activities for CO and hydrocarbon oxidation and NO reduction over the as-prepared and the heat-treated 1% Au/CeO2 have been carried out using a temperature-programmed reaction technique in a packed bed tubular reactor. The results are compared with nano-sized Au metal particles dispersed on -Al2O2 substrate prepared by the same method. All the reactions over heat-treated Au/CeO2 occur at lower temperature in comparison with the as-prepared Au/CeO2 and Au/Al2O2. The rate of NO + CO reaction over as-prepared and heat-treated 1% Au/CeO2 are 28.3 and 54.0 mol g-1 s-1 at 250 and 300 °C respectively. Activation energy (E
a) values are 106 and 90 kJ mol-1 for CO + O2 reaction respectively over as-prepared and heat-treated 1% Au/CeO2 respectively. 相似文献
48.
Hydrogen evolution during formaldehyde oxidation in alkaline solution has been monitored by Differential Electrochemical Mass Spectrometry on Au(111) and polycrystalline gold. The current efficiency for hydrogen evolution increases with higher concentration and is in the same range on both, polycrystalline Au and Au(111) electrode. The onset potentials and half-wave potentials are higher on Au(111). Reaction orders for the faradaic current on the bare gold electrodes have been determined as 0.21 for higher and 0.76 for lower concentrations. Reaction orders for hydrogen evolution during formaldehyde oxidation are 1.4 times higher in each case. Tafel slopes in the range of 140-160 mV are found. This signifies that the first reaction step involving the formation of adsorbed hydrogen is largely determining the overall reaction rate. In the presence of thallium adlayers hydrogen evolution from formaldehyde oxidation is largely suppressed. On the thallium modified polycrystalline Au, formaldehyde oxidation is shifted for 100 mV to higher potentials where Tl is partially desorbed and hydroxide is coadsorbed on the modified surface. On thallium modified Au(111), a similar process takes place, but in the same potential region as the onset of formaldehyde oxidation on the bare surface and therefore the formaldehyde oxidation is only slightly shifted. Tafel slopes are decreased to 80 mV/dec in the presence of thallium. In the presence of adsorbed thallium, the first reaction step is in equilibrium, the coverage with adsorbed hydrogen is smaller and its recombination to H2 is largely suppressed. 相似文献
49.
K. Juodkazis J. Juodkazyt? T. Juodien? V. Šukien? I. Savickaja 《Electrochimica acta》2006,51(27):6159-6164
The idea of underpotential oxidation of water, taking place on the surface of noble metals in the range of potentials preceding molecular oxygen evolution, is more than 40-years old. Chemisorbed oxygen atom—Ochem is considered to be the main intermediate in the underpotential oxidation of H2O, leading eventually to chemical oxidation of noble metals and formation of anhydrous surface oxides of MeO type. This concept is still used for the evaluation of the real surface area of the noble metal electrodes and also for the interpretation of new experimental results.The existence of reversible metal-oxide electrodes demonstrated experimentally for Pt, Pd, Rh, Ir and Au electrodes, oxidized anodically in the range of potentials preceding O2 evolution, shows that noble metals do have electrochemistry of their own. Nanometric layers of amorphous, slightly soluble hydroxides, hydrous oxides or oxides can form electrochemically on the electrode surface during the anodic process and be reduced during the cathodic one. Such alternative concept admits the reversibility of anodic and cathodic processes and changes essentially the understanding and interpretation of the phenomena of anodic oxidation of noble metals. 相似文献
50.