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31.
十四醇聚氧化烯烃醚琥珀酸单酯磺酸盐的表面活性研究   总被引:6,自引:0,他引:6  
合成了一系列十四醇聚氧乙烯醚和聚氧丙烯醚琥珀酸单酯磺酸盐,比较了其临界胶束浓度、润湿力、起泡力等表面活性  相似文献   
32.
Ramie yarns were treated with various concentrations of NaOH at room temperature and subsequently crosslinked with 1,2,3,4‐butanetetracarboxylic acid (BTCA). The microstructure and tensile properties of the treated yarns were characterized. X‐ray diffraction (XRD) and FTIR were used to study the crystalline structure of the resultant ramie yarns. The results showed that the maximum change in the structure of the alkali‐modified ramie took place at 16% NaOH, which would completely transform cellulose I to cellulose II. At the same time, the crystallinity index and fiber orientation decreased to the minimum value while the absorption properties were enhanced. The average degree of polymerization (DP ) of the treated ramie yarns slightly decreased after NaOH treatment. Tensile properties including tenacity, breaking elongation, and modulus of the treated yarns were also investigated. Scanning electron microscopy (SEM) was used to investigate the breakage of the treated yarns. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 1857–1864, 2004  相似文献   
33.
Choo YM  Ng MH  Ma AN  Chuah CH  Hashim MA 《Lipids》2005,40(4):429-432
The application of supercritical fluid chromatography (SFC) coupled with a UV variable-wavelength detector to isolate the minor components (carotenes, vitamin E, sterols, and squalene) in crude palm oil (CPO) and the residual oil from palm-pressed fiber is reported. SFC is a good technique for the isolation and analysis of these compounds from the sources mentioned. The carotenes, vitamin E, sterols, and squalene were isolated in less than 20 min. The individual vitamin E isomers present in palm oil were also isolated into their respective components, α-tocopherol, α-tocotrienol, γ-tocopherol, γ-tocotrienol, and δ-tocotrienol. Calibration of all the minor components of palm as well as the individual components of palm vitamin E was carried out and was found to be comparable to those analyzed by other established analytical methods.  相似文献   
34.
Low temperature plasma (LTP) treatment was applied to wool fabric with the use of a nonpolymerizing gas, namely oxygen. Properties of the LTP‐treated samples including low stress mechanical behavior, air permeability, and thermal characteristics were evaluated in this study. Kawabata evaluation system fabric (KES‐F) was employed to determine the tensile, shearing, bending, and compression strength properties and surface roughness of the specimens. The changes in these properties are believed to be closely related to the interfiber and interyarn frictional force induced by the LTP. The decrease in the air permeability of the LTP‐treated wool fabric was found to be probably because of the plasma action effect on increasing the fabric thickness and a change in fabric surface morphology, which was confirmed by scanning electron microscopy micrographs. The change in the thermal properties of the LTP‐treated wool fabric was in good agreement with the earlier findings and can be attributed to the amount of air trapped between the yarns and fibers. This study suggested that the LTP treatment can influence the final properties of the wool fabric, and also provide information for developing LTP‐treated wool fabric for industrial use. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 5958–5964, 2006  相似文献   
35.
Abstract. Recently, there has been a lot of interest in modelling real data with a heavy‐tailed distribution. A popular candidate is the so‐called generalized autoregressive conditional heteroscedastic (GARCH) model. Unfortunately, the tails of GARCH models are not thick enough in some applications. In this paper, we propose a mixture generalized autoregressive conditional heteroscedastic (MGARCH) model. The stationarity conditions and the tail behaviour of the MGARCH model are studied. It is shown that MGARCH models have tails thicker than those of the associated GARCH models. Therefore, the MGARCH models are more capable of capturing the heavy‐tailed features in real data. Some real examples illustrate the results.  相似文献   
36.
Enhancing textile ink-jet printing with chitosan   总被引:1,自引:0,他引:1  
Following on from previous research, the possibility of using chitosan in preparing the pretreatment print paste for textile ink-jet printing was investigated but the final colour was not as good as expected. In this study, chitosan was applied separately on cotton fabric for ink-jet printing. A two-bath method was proposed and it was confirmed that a better colour yield was achieved with this method. However, the use of chitosan reduced the tensile strength of the ink-jet printed fabric slightly.  相似文献   
37.
Qingwen Song  Jianwei Xing  Yuen Marcus 《Polymer》2007,48(11):3317-3323
This paper reports a study on the thermal stability of phase change material microcapsules that are incorporated with silver nano-particles (Ag-NPs). The novel microcapsules were fabricated by the technique of in situ polymerization, with aminoplast as the wall and phase change material bromo-hexadecane (PCM BrC16) as the core. Thermal gravimetry (TG) analysis was applied to measure the thermal stability of these microcapsules and surface morphology of the microcapsules was observed by means of scanning electron microscopy (SEM) after an application of curing treatment at 130 °C. Comparing with conventional phase change material microcapsules (PCMMs), nano-composite phase change material microcapsules (NCPCMMs) have higher thermal stability. This can be attributed to nano-composite structure of the microcapsules, in which metal Ag-NPs distributed on the surface to increase wall toughness and strength. The possible reinforcement mechanisms of the nano-composite structure are explored.  相似文献   
38.
The mechanical peel behaviour of laminates consisting of polyimide films adhered to copper foil using a modified acrylic adhesive has been studied over a wide range of test rates and temperatures. The laminates were prepared from polyimide films which had been subjected to either a “high-thermal history” or a “low-thermal history” treatment during the production of the film. The measured peel energies of the laminates could be superimposed to give a master curve of peel energy versus the reduced rate of peel test, RaT, where R is the rate of peel test and aT is the time-temperature shift factor. The appropriate shift factors were a function of the test temperature and were mainly deduced from tensile tests conducted on the bulk adhesive. The “high-thermal history” laminates gave higher peel energies and the locus of failure of the laminates was mainly by cohesive fracture through the adhesive layer. At low values of log10 RaT, i.e. Low rates of peel and high test temperatures, the “low-thermal history” laminates also failed in the adhesive layer and possessed similar peel energies to those measured for the “high-thermal history” laminates. However, at high log10 RaT values, the peel energies measured for the “low-thermal history” laminates were lower and showed a wider scatter. These arose from a different locus of failure occurring in these “low-thermal history” laminates when tested under these conditions. Namely, it was found that most of these laminates failed in a weak boundary layer in the outer regions of the “low-thermal history” polyimide film.  相似文献   
39.
Successful separation of triglycerides, diglycerides, free fatty acids, carotenes, tocopherol, and tocotrienols from crude palm oil has been achieved by supercritical fluid chromatography (SFC) with a combination of a C18 and a silica gel column. The separation was carried out by the programmed extraction elution method. Free fatty acids were separated into five components by gas-liquid chromatography; tocopherol and tocotrienols were also separated into four components by SFC analysis, and the pure fractionated carotenes were obtained by preparative SFC. Thus, by using supercritical fluid chromatography, crude palm oil components can be separated and fractionated, based on differences in their functional groups.  相似文献   
40.
Sorption isotherms for carbon dioxide in poly(ethylene terephthalate) have been measured at 35–55°C. The isotherms were measured gravimetrically on a Mettler Thermoanalyzer-1 from vacuum to 1 atmosphere. The sorption data were used to generate sorption isotherms from which the isosteric heat of sorption of CO2 in PET was determined. At 45°C the isosteric heat of sorption increases from −10 kcal/mole at a concentration of 0.5 cm3 (STP)/cm3 (polymer) to −8 kcal mole−1 at a concentration of 1.5 cm3 (STP)/cm3 (polymer). It has been reported in the literature that the isosteric heat of sorption for this system decreased through a minimum before increasing with increasing concentration. Our measurement of the low-pressure sorption isotherms shows that this is not the case.  相似文献   
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