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101.
102.
Zr对Cu—Zn—Al形状记忆合金相变的影响 总被引:2,自引:0,他引:2
采用示差扫描热分析(DSC)、X射线衍射及透射电镜,研究了Zr对Cu-Zn-Al合金高温相变、马氏体正逆转变以及形状记忆效应的影响。结果表明,添加Zr0.35wt-%时,能有效地抑制α,γ相析出,促进β_2→DO_3→18RM转变。(M_s-M_f)及(A_s-A_f)温度区间较窄,马氏体相变激活能最低,马氏体变体间界面的可动性好,形状记忆效应最佳。 相似文献
103.
A new electron beam control system was developed in a general vacuum electron beam machine by assembling with industrial control computer, programmable logic control (PLC), deflection coil, data acquisition card, power amplifier, etc. In this control system, scanning track and energy distribution of electron beam could be edited off-line, real-time adjusted and controlled on-line. Ti-Mo gradient material (GM) with high temperature resistant was fabricated using the technology of electron beam melting. The melting processes include three steps, such as preheating, melting, and homogenizing. The results show that the GM prepared by melting technology has fine appearance, and it has good integrated interface with the Ti alloy. Mo and Ti elements are gradually distributed in the inter.face of the gradient material. The microstructure close to the Ti alloy base metal is α + β basket-waver grain, and the microstructure close to the GM is a single phase of β solid solution. 相似文献
104.
Adya P. Singh Anni Ratz Bernard S. W. Dawson 《Journal of Coatings Technology and Research》2007,4(2):207-210
A new method was developed which enabled us to obtain high-resolution images of the distribution of an oil-borne stain in
a saw-textured plywood surface. The method involved treating 90 μm thick plywood sections, which had been cut transversely
through the wood-coating interface using a sliding microtome, with osmium tetroxide (OsO4) prior to examination with a field-emission scanning electron microscope (FE-SEM) operating in backscattered electron imaging
(BEI) mode. The combination of OsO4 staining and use of FE-SEM-BEI afforded excellent contrast differentiation between the coating and wood cell walls, revealing
coating penetration into even nano-size cell wall cracks and delaminations formed during band-sawing of the plywood. The novel
technique described adds a new dimension to probing wood–coating interface. 相似文献
105.
A series of binary blends of poly(ethylene oxide) (PEO), poly(propylene oxide) (PPO), and polytetrahydrofuran (PTHF), characterized by similar average molecular weights, with selected fatty acids (capric acid, lauric acid, myristic acid, palmitic acid, and stearic acid) were prepared by melt mixing. Differential scanning calorimetry was applied to characterize the phase transitions of melting and crystallization, and a synergistic effect was found to occur for PEO/fatty acid blends, as evidenced by the values of the enthalpy of the phase transition. This effect was probably due to hydrogen bonding between PEO and the fatty (carboxylic) acids, which facilitated the formation of crystalline structures; an analysis of IR spectroscopy data showed a shift in the absorption bands of OH groups. The morphology development of the PEO/carboxylic acid blends, as observed with polarizing light microscopy, could be described as spherulitic growth with spontaneous selection of the lamellar thickness. The textures of the individual fibrils, consisting of stacks of several tens of lamellae corresponding to PPO and PTHF, were less regular than the texture of PEO and showed large macroscopic heterogeneity. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 861–870, 2003 相似文献
106.
Lignin‐based chemicals, starch, and urea were used as modifiers for phenol–formaldehyde resol resins. The effects of the addition stage of the modifiers used in the synthesis of the resins and the type of modification reagent on the structures of the resins and their molar masses and reactivities were investigated. The modifications with corn starch and lignin promoted condensation; this was verified by increased molar masses and high ratios of methylene bridges to the sum of free ortho and para aromatic groups with respect to the corresponding reference resin without a modification reagent. The later the modifier was added to the resin condensation mixture, the more methylene bridges were formed with respect to the amounts of free ortho and para aromatic groups. In addition, when urea or wheat starch was added in the later condensation stage, the final condensation also reached high stages. The modifications with lignosulfonate and starch, as well as the early addition of urea, enhanced p–p′ bridge structures. The lowest condensation stage and, therefore, the highest reactivity were found when wheat starch was added with the starting reagents. The curing heat of the wheat‐starch‐modified resins decreased according to the deferred addition point of starch. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 582–588, 2003 相似文献
107.
Polylactide (PLA) has been melt spun to produce multifilament continuous yarns. The thermal characteristics of PLA filaments have been investigated using modulated differential scanning calorimetry (MDSC). With MDSC, it is possible to separate the different thermal events and to analyze them more precisely. The influence of hot drawing on thermal properties of PLA filaments has been studied. Hot drawing promotes an increase of glass transition temperature (Tg) and a decrease of heat capacity. The cold crystallization spreads on a larger range of temperature and the peak occurs at a lower temperature. The initial degrees of cristallinity of PLA filaments have been calculated thanks to the reversing and non reversing curves of MDSC. Tensile properties of PLA filaments are also investigated. 相似文献
108.
The N‐[3‐(dimethoxy‐methyl‐silanyl)‐propyl]‐N′‐ (9‐methyl‐3,9‐dioxo‐2,4,8,10‐tetraoxa‐3,9‐diphospha‐spiro[5.5]undec‐3‐yl)‐ethane‐1,2‐diamine/dimethoxy dimethyl silane copolymer (PSiN II), which simultaneously contains silicon, phosphorus, and nitrogen, is synthesized and incorporated into polypropylene (PP). The flame retardancy is evaluated by the limiting oxygen index value, which is enhanced to 29.5 from 17.4 with 20% total loading of PSiN II. The thermal degradation behavior of PP/PSiN II is investigated by thermogravimetric analysis under N2 and air. The PP/PSiN II sample degrades at 400°C for different amounts of time, and the process of degradation is studied by Fourier transform IR. The morphology of the char formed at 400°C for 10 min is investigated by scanning electron microscopy. The swollen inner structure, close, and smooth outer surface provide a much better barrier for the transfer of heat and mass during fire and good flame retardancy. The thermal stability of PP is improved by incorporation of PSiN II. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 2487–2492, 2005 相似文献
109.
P. N. Mayamol C. Balachandran T. Samuel A. Sundaresan C. Arumughan 《Journal of the American Oil Chemists' Society》2007,84(6):587-596
Crude palm oil (CPO) is the richest natural source of carotenes that are destroyed in the conventional processing. There is
a growing demand for nutritional products containing bioactive constituents externally fortified or preserved through modified
process. A commercially viable process for the production of red palm olein (RPOn) rich in carotenes, tocols and sterols has
been developed at pilot scale. The process developed involved neutralization of CPO followed by crystallization at controlled
rate of cooling and deodorization of the resultant neutralized and winterized palm olein (WPOn) under controlled conditions
of temperature and high vacuum. Analytical data related to micronutrients at each process step was monitored. The RPOn thus
produced had not more than 0.25% of free fatty acids (FFA) and it retained more than 80% of the carotenes, about 85% of tocols
and 65% of sterols originally present in the CPO. The physico-chemical characteristics of RPOn revealed that it is nutritionally
of superior quality compared to that of the commercial refined bleached deodorized (RBD) palm olein currently available in
the market. The carotenes, tocols and sterols profile of RPOn by HPLC showed that they were retained in their natural forms. 相似文献
110.
A series of phosphorus‐containing, wholly aromatic thermotropic copolyesters from acetylated 2‐(6‐oxide‐6H‐dibenz〈c,e〉〈1,2〉oxa phosphorin‐6‐yl)‐1,4‐dihydroxy phenylene, p‐acetoxybenzoic acid, terephthalic acid, and isophthalic acid were prepared by melting polycondensation. The structure and basic properties of the polymers, such as the glass‐transition temperature (Tg), melting temperature (Tm), thermal stability, crystallinity, and liquid crystallinity, were investigated with Fourier transform infrared, elemental analysis, differential scanning calorimetry (DSC), thermogravimetric analysis, wide‐angle X‐ray diffraction, and hot‐stage polarizing optical microscopy. The copolyesters had relatively high Tg values ranging from 183 to 192°C. The Tm values obtained from DSC curves for samples P‐20 and P‐25 were 290 and 287°C, respectively (where the number in the sample name indicates the molar fraction of the phosphorus‐containing monomer in the reactants). The initial flow temperatures of other samples observed with hot‐stage polarizing microscopy were 271–290°C. The 5% degradation temperatures in nitrogen ranged from 431 to 462°C, and the char yields at 640°C were 41–52%. All the copolyesters, except P‐40, were thermotropic and nematic. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 1278–1284, 2002 相似文献