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61.
62.
为了明确Cr的质量分数高低对埋地用输油输气管线钢性能的影响,设计了4种Cr的质量分数的X70管线钢,研究了不同Cr的质量分数下管线钢组织及其力学性能,并采用高温高压反应釜进行了实验钢的CO2腐蚀试验.结果表明:钢中加入0.1%~0.8%的Cr后,其组织均由针状铁素体和准多边形铁素体构成,Cr元素均呈现明显的沿晶界分布状态;随着Cr的质量分数的增加,钢板强度随之升高,晶界中Cr分布密度随之增大,Cr(OH)3在腐蚀产物膜中的富集量增加,促使钢板的平均腐蚀速率降低;同时由于Cr(OH)3可以有效阻碍阴离子穿透腐蚀产物膜,因而大大减少了Cl-的催化作用导致的点蚀,使得钢板点蚀速率明显降低. 相似文献
63.
通过建立摩擦材料的传热学模型,研究摩擦材料在使用时的温度分布,克服了摩擦材料实际使用时温度分布难以实测的矛盾,并用该传热学模型分析了所研制的摩擦材料实例。 相似文献
64.
在不同直径的垂直玻璃管中盛装着不同物性(粘度与表面张力)的液体,空气经分配器注入静止的液体中,对两相流型的变化进行了观察研究。流型的确定采用了高速录相机系统,也同时进行肉眼观察,并测量了不同流型的空隙度。实验表明:空气-高粘性液体和空气-起泡液体的气、液两相流型与通常的空气-水系统的流型极不相同。其空隙度也在较广泛范围内变化。 相似文献
65.
Ten trace elements (Cr, Zn, Fe, Mn, Cu, Co, Ni, Mo, V and Sr) and sulfur were determined in the saturate, aromatic and resin fractions of 15 crude oils from Mara (DM) and Mara Oeste (DMO) fields of the Maracaibo Basin, Venezuela. The oils studied are classified as unaltered or altered by biodegradation. In the altered oil, the depletion of n-alkanes, the absence of isoprenoids and the presence of steranes and hopanes unaltered by biodegradation are indicative of moderate biodegradation. The elements Zn, Fe, Mn, Cu, Ni, and Sr were detected in the saturated hydrocarbon fraction; Cr and V were detected in the aromatic fraction in addition to the above elements; whereas the elements detected for the resin fraction were Cr, Zn, Fe, Cu, Ni, Mo, V, and Sr. Co was not detected in any fractions of the oils analyzed. Sulfur was found in all fractions of the oils studied. It was proposed that Fe, Zn, Sr, and Mn could have entered the oil during migration or Fe, Zn and Mn as pollutants during oil extraction. Cr and Cu may be of biological origin and Mo could be incorporated into the reservoir through bacteria. Only S, V, and Ni in the resin fractions can be used as indicators of the origin and correlation of Mara and Mara Oeste oils. Based on the results obtained in this work, it can be established that the V/(V+Ni) ratio in the resin fraction can be used as a correlation parameter, for these oils. 相似文献
66.
The prediction of minimum fluidization velocity for vibrated fluidized bed was performed. The Geldart group A and C particles were used as the fluidizing particles. The method based on Ergun equation was used to predict the minimum fluidization velocity. The calculated results were compared with the experimental data.The calculated results of minimum fluidization velocity are in good agreement with experimental data for Geldart group A particles. For group C particles, the difference between the calculated results and experimental data is large because of the formation of agglomerates. In this case, the determination of agglomerate diameter is considered to be necessary to predict the minimum fluidization velocity. 相似文献
67.
The local parameters for kerosene–water upward flow are measured in a vertical pipe of 77.8 mm inner diameter at 4200 mm from the inlet (L/D = 54) using hot‐film and dual optical probes. The effect of superficial water velocity and volumetric quality on radial distribution of two‐phase flow parameters is investigated. The results show the following: (i) the profiles of volume fraction and drop frequency are very similar, and increasing superficial water velocity at low volumetric qualities (<18.6%) change the profile from a convex shape with peak at the pipe centreline to uniform then to concave shape with peak near the wall; (ii) the profiles of drop cut chord change from a parabolic shape with peak at centreline for low superficial water velocities to a flat shape at higher superficial water velocity, and the area‐averaged drop diameter decreases with higher superficial water velocities for all volumetric qualities; (iii) velocity profiles for both phases have shapes similar to single phase flow, flatter at higher values of superficial water velocity and volumetric quality and centreline peaked at low superficial water velocities and volumetric qualities; (iv) the slip velocity decreases with radial distance having a peak at centreline and zero values near the wall; (v) introducing kerosene drops into single phase water flow results in a sharp increase in turbulent intensity, particularly at low water velocity, and the difference between the single phase and two‐phase flow turbulence intensities decreases with higher superficial water velocities and (vi) the results show that interfacial area concentration increased with higher volumetric quality and higher number of bubbles thereby increases the contact area between the two phases. © 2012 Canadian Society for Chemical Engineering 相似文献
68.
Masni Mat Yusoff Chin Ping Tan Yaakob Bin Che Man Mat Sahri Miskandar Sivaruby Kanagaratnam Imededdine Arbi Nehdi 《Journal of the American Oil Chemists' Society》2013,90(1):91-101
Thirteen fat blends intended for cookie filler (CF) production that consist of 20–70 % palm mid-fraction (PMF), 20–70 % virgin coconut oil (VCO), and 0–10 % palm stearin (POs) were developed based on the solid fat contents (SFC) of the fat portions extracted from five commercial CF samples: A, B, C, D, and E. A mixture design was applied for fat blend optimization, and the combination that best approached the target SFC values was composed of 70 % PMF, 20 % VCO, and 10 % POs. The optimized coconut- and palm-based fat blend (O-CP) exhibited a steeper SFC profile, with 8.2 % (±0.2) SFC at 25 °C (room temperature) and 0.2 % (±0.2) SFC at 37 °C (body temperature); lower slip melting point of 34.0 °C (±0.0); and a lower iodine value (IV) of 40.25 g/100 g (±1.04). In addition, O-CP contained higher proportions of medium-chain fatty acids (MCFA) and lauric acid (C12:0) of 3.2 % (±0.18) and 9.7 % (±0.43), respectively. In terms of its thermal profile, O-CP showed no significant difference in terms of its crystallization range, 49.7 °C (±2.66) with the exception of sample C, but it exhibited a smaller melting range, 65.8 °C (±1.47), compared to the fat portions of the commercial samples. The ranges represented the span between the onset and offset temperatures of both crystallization and melting profiles as determined by differential scanning calorimetry. 相似文献
69.
In the present work, the silane grafting and water cross-linking of low density polyethylene (LDPE) were investigated. The grafting reaction was carried out in an internal mixer and polyethylene cross-linking was done in hot water. The effect of silane, peroxide, catalyst, carbon black, cross-linking time, and cross-linking temperature on the grafting and cross-linking processes are reported. Vinyl trimethoxy silane (VTMO) and di-cumyl peroxide (DCP) were selected as grafting agent and initiator respectively. Silane grafting on polyethylene was determined using Fourier transform infrared (FTIR) spectroscopy and torque monitoring of the mixer. Absorption peak due to –Si–OCH3 groups in FTIR and torque increasing due to silane grafting in the mixer illustrated that silane-grafting reactions occurred. The FTIR data demonstrated that the extent of silane grafting was increased as the concentration of silane and peroxide was increased. Thermogravimetry analysis (TGA) determined that the thermal stability of LDPE increased by increasing the amount of silane grafting. Gel fraction increased with silane and peroxide concentration. As the percent of of catalyst increase the time scale for specified gel content shifted to shorter times. Incorporation of carbon black into LDPE decreased the extent of silane grafting and gel fraction. Water temperature increasing in cross-linking stage reduced the time to maximum degree of cross-linking. 相似文献
70.