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Konstantinos Spyrou Matteo Calvaresi Evmorfia K. Diamanti Theodoros Tsoufis Dimitrios Gournis Petra Rudolf Francesco Zerbetto 《Advanced functional materials》2015,25(2):263-269
Experimental and theoretical studies are performed in order to illuminate, for first time, the intercalation mechanism of polycyclic aromatic molecules into graphite oxide. Two representative molecules of this family, aniline and naphthalene amine are investigated. After intercalation, aniline molecules prefer to covalently connect to the graphene oxide matrix via chemical grafting, while napthalene amine molecules bind with the graphene oxide surface through π–π interactions. The presence of intercalated aromatic molecules between the graphene oxide layers is demonstrated by X‐ray diffraction, while the type of interaction between graphene oxide and polycyclic organic molecules is elucidated by X‐ray photoelectron spectroscopy. Combined quantum mechanical and molecular mechanical calculations describe the intercalation mechanism and the aniline grafting, rationalizing the experimental data. The present work opens new perspectives for the interaction of various aromatic molecules with graphite oxide and the so‐called “intercalation chemistry”. 相似文献
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Herein, the assessment of commercial beef and chicken bouillons in terms of heterocyclic aromatic amines (HAAs) and some of their precursors was evaluated. Creatine and creatinine levels were ranged between 0.57–0.80 and 0.28–0.94 mg g−1, respectively. Glutamic acid was found to be the most abundant amino acid in both bouillons. 2-amino-3,7,8-trimethylimidazo[4,5-ƒ]quinoxaline (7,8-DiMeIQx, up to 0.03 ng g−1) was the only quantified analyte in beef bouillons, whereas it (up to 0.08 ng g−1) was determined in addition to 2-amino-3-methylimidazo[4,5-ƒ]quinoxaline (IQx, up to 0.08 ng g−1) in chicken bouillons. Creatine, creatinine and free amino acid composition did not have the capacity to initiate the formation of HAAs. Therefore, bouillons do not pose risk in terms of HAAs. However, it should be noted that multiple factors, such as the substrate amount and production conditions, may affect the results. Glutamic acid content is remarkable in commercial bouillons sold in Turkey. 相似文献
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游世文 《食品安全质量检测学报》2019,10(3):761-764
目的探讨水﹑气﹑土壤中多环芳烃检测标准(HJ 478-2009﹑HJ 647-2013、HJ 784-2016)的正确出峰时间和顺序。方法用高效液相色谱来对苊烯、芴、苊、?、苯并(a)蒽进行定性分析,并与3个标准中的出峰顺序进行比较。结果苊烯、苊、芴、苯并(a)蒽、?的出峰时间分别为6.450、7.923、8.233、17.760、18.740min,与标准HJ478-2009﹑HJ647-2013的出峰顺序存在差异。结论在使用标准HJ478-2009﹑HJ647-2013、HJ 784-2016同时测定16种多环芳烃时,多环芳烃的出峰顺序及时间应以HJ 784-2016为准。 相似文献
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The smoke suppression of rigid polyurethane foam (RPUF) modified by melamine was investigated based on three sections: the condensed phase, the carbon layer, and the gas phase. In the condensed phase, the results of thermogravimetry, X‐ray photoelectron spectroscopy (XPS) N1S spectrum, and Fourier transform infrared spectroscopy indicated that melamine could suppress the degradation of RPUF by reacting with the aromatic hydrocarbons. It also reduced the smoke generation because the volatilizable aromatic hydrocarbons were the principal smoke precursors in a fire. In the carbon layer, the decrease from 38.50% to 24.76% of the inner layer oxygen content identified by XPS full‐spectrum and C1S spectrum indicated that melamine could prevent oxygen from transferring into the inner foam by the formation of an enhanced surface carbon layer, and the enhanced carbon layer could also block the release of smoke precursors. In the gas phase, the content of total aromatic hydrocarbons declined to 59.12% according to pyrolysis gaseous chromatography mass spectroscopy and indicated that melamine could reduce the smoke precursors. The results of smoke density chamber and cone calorimeter tests revealed that the addition of the melamine could decrease the smoke density of burning RPUF. Copyright © 2014 John Wiley & Sons, Ltd. 相似文献
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The NW‐SE trending Cantarell structure in the Gulf of Campeche hosts the largest oilfield in Mexico. The oil occurs predominantly in latest Cretaceous – earliest Tertiary breccias with subsidiary reserves in Upper Jurassic (Oxfordian and Kimmeridgian) and Lower Cretaceous oolitic and partially dolomitized limestones, dolomites and shaly limestones. Cantarell has been interpreted both as a fold‐and‐thrust zone and as a dextral transpressional structure. Analysis of structure contours at 100m intervals, on the tops of the Tertiary breccia and the Kimmeridgian (Upper Jurassic) dolomite, indicates that the structure is an upright cylindrical fold with gently plunging conical terminations; there is also a conical portion in the central part of the structure. The axes of the central, NW and SE cones are subvertical. This geometry indicates that the two fold terminations and the central cone are aprons rather than points, with the NW and central cone axes intersecting the cylindrical fold axis at the point where the geometry switches from conical to cylindrical. The apical angle (i.e. the angle between the fold and cone axes) varies as follows: (i) in the NW cone, it is ~70° in the breccia and ~76° in the Kimmeridgian dolomite; (ii) in the central cone, it is ~77° in the breccia and ~73° in the Kimmeridgian dolomite; and (iii) in the SE cone, it is ~64° in the breccia and ~57° in the Kimmeridgian dolomite. This indicates that whereas the fold opens with depth in the NW cone, it tightens with depth in the central and SE cones. Assuming a parallel fold geometry, these apical angles indicate an increase in volume in the NW cone (i.e. larger hydrocarbon reservoirs), compared to the central and SE cones. Theoretical considerations indicate that the curvature increases dramatically towards the point of the cone. In the case of the Cantarell structure, the apices of the cones are located at the conical‐cylindrical fold junctions, where the highest curvature may have resulted in a higher degree of fracturing. The coincidence of maximum curvature and the intersection of the conical and cylindrical fold axes in the fold culminations with porous and permeable reservoir rocks may have made these locations favourable for the accumulation of hydrocarbons. 相似文献
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结合芳烃联合装置的发展形势,通过对国内某4套典型芳烃联合装置运行能耗的构成进行分析,确定该类装置的主要能耗在于燃料、电和蒸汽的消耗。总结了目前国内外常用的芳烃联合装置节能降耗方法,利用实际经验和调研结果,从采用新型吸附剂、采用单台吸附塔新工艺、采用轻质解吸剂替代对二乙苯(PDEB)、优化吸附塔运行参数、加热炉节能优化和选用高效节能设备等角度探讨芳烃联合装置的节能降耗方法。芳烃联合装置节能降耗应该由设计单位和生产单位紧密结合,在设计阶段就应充分考虑生产过程面临的问题,充分优化工艺路线、方案和设备设计,尽可能降低装置的能耗。同样,装置运行过程中,生产部门应标准化、精细化管理,优化日常操作,从而进一步降低装置的操作能耗。 相似文献