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101.
Partitioning of organic substrates by thermoresponsive polymer having N‐acryloylaminoalcohol moieties in aqueous phase has been studied. Thermoresponsive polymers, such as poly(N‐isopropylacrylamide) (PNIPAAm) and poly(NIPAAm‐co‐N‐acryloyl‐(±)‐alaninol) (poly(NIPAAm‐co‐HIPAAm)), were found to concentrate several organic substrates into the hydrophobic field generated during their phase transition. The amount of the substrates recoverd from the polymer phase mainly depended on the hydrophobicity of the substrates. Aqueous solutions of PNIPAAm (lower critical solution temperature, LCST = 33°C) and poly(NIPAAm‐co‐HIPAAm) (LSCT = 41°C) containing 1‐phenylethanol showed LCSTs at 22°C and 33°C, respectively. The changes of LCSTs indicate that specific interactions such as hydrogen bonding between the side chain functionalities of the polymers and the substrates influence the phase transition behavior. Moreover, new optically active polymers having chiral aminoalcohol moieties have been synthesized by copolymerizations of NIPAAm with N‐acryloylaminoalcohols such as N‐acryloyl‐(S)‐alaninol and N‐acryloyl‐(S)‐prolinol. The (R)/(S) ratio of 1‐phenylethanol recovered from poly(NIPAAm‐co‐N‐acryloyl‐(S)‐alaninol) and poly(NIPAAm‐co‐N‐acryloyl‐(S)‐prolinol) were determined to be 75/25 and 68/32, respectively. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 3458–3464, 2013 相似文献
102.
Polymer electrolyte blend membranes composed of sulfonated block‐graft polyimide (S‐bg‐PI) and sulfonated polybenzimidazole (sPBI) were prepared and characterized. The proton conductivity and oxygen permeability coefficient of the novel blend membrane S‐bg‐PI/sPBI (7 wt%) were 0.38 S cm?1 at 90 °C and 98% relative humidity and 7.2 × 10?13 cm3(STP) cm (cm2 s cmHg)?1 at 35 °C and 76 cmHg, respectively, while those of Nafion® were 0.15 S cm?1 and 1.1 × 10?10 cm3(STP) cm (cm2 s cmHg)?1 under the same conditions. The apparent (proton/oxygen transport) selectivity calculated from the proton conductivity and the oxygen permeability coefficient in the S‐bg‐PI/sPBI (7 wt%) membrane was 300 times larger than that determined in the Nafion membrane. Besides, the excellent gas barrier properties based on an acid ? base interaction in the blend membranes are expected to suppress the generation of hydrogen peroxide and reactive oxygen species, which will degrade fuel cells during operation. The excellent proton conductivity and gas barrier properties of the novel membranes promise their application for future fuel cell membranes. © 2015 Society of Chemical Industry 相似文献
103.
The electroreductive polymerization of dichloromethylphenylsilane in the presence of triphenylsilyl group‐containing disilanes such as hexaphenyldisilane followed by the electroreductive termination with chlorotriphenylsilane afforded triphenylsilyl group‐terminated polymethylphenylsilane in 15–32% yield. The isolated polymethylphenylsilane (Mn = 3350 g mol?1, Mw/Mn = 1.4) was found to react as a macroinitiator to copolymerize with dibutyldichlorosilane under electroreductive conditions producing the corresponding block copolymer (Mn = 4730 g mol?1, Mw/Mn = 1.2) in 38% yield. The ratio of monomer units (? MeSiPh? to? BuSiBu? ) of the copolymer was determined to be 75:25 using 1H NMR analysis, which was in good agreement with the calculated ratio (74:26) on the assumption that molecular weight of the macroinitiator was not changed. The block structure of the resulting copolymer, poly(methylphenylsilane)‐block‐poly(dibutylsilane), was also confirmed by comparing its 1H NMR and UV absorption spectra with those of polymethylphenylsilane, polydibutylsilane and a statistical copolymer prepared by electroreductive polymerization of dichloromethylphenylsilane with dibutyldichlorosilane. This method is applicable to the preparation of other types of macroinitiator such as triphenylsilyl group‐terminated polydibutylsilane, and polydibutylsilane‐block‐polymethylphenylsilane was also obtained using this macroinitiator. Copyright © 2011 Society of Chemical Industry 相似文献
104.
The effect of degree of polymerization (DP) on the gelation and flow processability of poly(vinyl chloride) (PVC) was studied. Sheets with adjusted degree of gelation were prepared by rolling rigid pipe formulation suspension PVC compounds with DPs of 800, 1050 and 1300 by changing the milling temperature. Their degrees of gelation were measured with DSC and their capillary flow properties were measured with a capillary rheometer at 150, 170 and 190°C and the effect of DP on the relation between gelation and flow processabilities was studied. Because of the higher shearing heat during milling, the sample with the higher DP had a higher history temperature and thus tended to show a higher degree of gelation. The viscosity increased as the gelation increased. The dependency of viscosity on DP was higher at higher milling and extrusion temperatures and thus at a higher degree of gelation and a lower shear rate. This was assumed to be attributed to the more prominent uniform molecular flow as against the particle flow. The die swell increased with increasing the milling and extrusion temperatures and hence with increasing the gelation. A sample with a lower DP tended to show a larger die swell and this tendency was even more pronounced at the higher extrusion temperature. The melt fracture easily occurred when a sample with advanced gelation was extruded at low temperature. Whereas at low milling temperatures a sample with the lower DP showed a lower critical shear rate at onset of melt fracture, and thus easily generating melt fracture, at high milling temperatures it showed a higher critical shear rate and hence scarcely generated melt fracture. These experimental results were explained by the fact and concept that a sample with a lower DP shows a higher increase in the gelation during extrusion and/or the slighter feature of particle flow as against the uniform molecular flow at the same gelation level. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 1915–1938, 2004 相似文献
105.
Noritada Kaji Akio Oki Ryo Ogawa Yuzuru Takamura Takahiro Nishimoto Hiroaki Nakanishi Yasuhiro Horiike Manabu Tokeshi Yoshinobu Baba 《Israel journal of chemistry》2007,47(2):161-169
The various potential factors affecting the performance of nanopillar chips on DNA separation were investigated from the viewpoints of both numerical calculations and actual experiments. To yield higher performance and replace the conventional DNA separation techniques such as microchip electrophoresis, the phenomenon specific to the nanopillar chips should be deeply understood. In this paper, although various factors affecting the performance of the nanopillar chips are considered, we focused on the effect of electroosmotic flow, which is particularly noticeable in quartz-made nanopillar chips. High-resolution separation of DNA was realized when an electroosmotic flow was suppressed by simply using a higher concentration of buffer, but DNA separation failed in the presence of an electroosmotic flow. It was confirmed from the numerical simulations and the direct observations that the deformation of DNA band during the injection process was induced by electroosmotic flow and consequently led to a poor resolution. 相似文献
106.
Two human-machine interface configurations for safety monitoring systems are discussed: (1) A conventional fault-warning configuration, which gives an alarm message on detecting plant failure and (2) a safety-presentation configuration introduced here, which can give a safety message as well as an alarm message. It is proved mathematically that the safety-presentation configuration is superior to the fault-warning configuration in the well-defined sense of avoiding catastrophic accidents 相似文献
107.
The monthly variation in HCH (1,2,3,4,5,6-hexachlorocyclohexane) residue levels in surface waters was investigated. The logarithms of monthly HCH concentrations described the wave, and the equation of the wave was calculated by the least squares method. The waves indicated maximum concentrations in summer and minimum concentrations in winter at each sampling site. The maximum concentration of HCH in each year decreased gradually. The amplitude of the wave at the reservoir was the smallest among sampling sites. The slope of the wave at the downstream sampling site was smaller than that at the upper stream. Maximum concentration of total HCH at each sampling site in 1985 is estimated from the equations; the concentrations at the upper streams will be about a thousandth or a hundredth of that at the downstreams. Also, the equations for β-and γ-HCH were calculated, and indicated that β-HCH was more persistent than γ-HCH in surface water. The ratio of β-HCH to total HCH in surface water is estimated to be about 60% in 1985. 相似文献
108.
Masato Takeuchi Junichi Deguchi Manabu Hidaka Shiro Sakai Kyoungja Woo Pyuck-Pa Choi Jong-Ku Park Masakazu Anpo 《Applied catalysis. B, Environmental》2009,89(3-4):406-410
The photocatalytic oxidation of gaseous acetaldehyde with O2 on commercial TiO2 nano-particles could be successfully enhanced by a simple mechanical blending with a high-silica mordenite (MOR) zeolite, the surface of which showed high hydrophobic properties. When the TiO2 nano-particles of ca. 5–20 wt% were mixed with the MOR zeolite powders in an agate mortar for only 5 min, the blended TiO2/MOR samples showed higher photocatalytic reactivity as compared to the pure TiO2 nano-particles. Since the high-silica zeolite powders are highly transparent in UV light regions, the incident UV light is effectively irradiated onto the whole part of the TiO2 nano-particles without any loss of light intensity. Furthermore, the siliceous MOR zeolite powders effectively adsorb the gaseous acetaldehyde molecules and supply them onto the surfaces of the blended TiO2 nano-particles, resulting in an enhancement of the photocatalytic reactivity. 相似文献
109.
Paveena Srirangsan Kiyoshi Kawai Naoko Hamada-Sato Manabu Watanabe Toru Suzuki 《Food chemistry》2010,119(1):209-213
In order to improve the remaining activity of a practically important freeze-dried enzyme, xanthine oxidase (XOD), the effects of disaccharide (sucrose and trehalose), polymer (bovine serum albumin: BSA and dextran) and a mixture of them on the loss of XOD activity during freeze-drying and subsequent storage were investigated. All samples were amorphous solids and their glass transition temperatures (Tg) were evaluated by using differential scanning calorimetry. Although dextran showed no stabilizing effect on the freeze-dried XOD, the others protected XOD from the activity loss during freeze-drying to a certain extent. It was found that the mixture of disaccharide (sucrose or trehalose) and BSA improved the XOD activity synergistically. The XOD activity of the samples decreased gradually during storage at a temperature range of between 25 and 60 °C. Samples stored at temperatures below the Tg showed a lower loss of XOD activity than those stored at just the Tg. 相似文献
110.
Akihiro Nakano Tetsuhiko Maeda Hiroshi Ito Masao Masuda Yoshiaki Kawakami Manabu Tange Toru Takahashi Keiichi Nishida 《International Journal of Hydrogen Energy》2012
We have been performing research on the Totalized Hydrogen Energy Utilization System (THEUS) which has applications to commercial buildings and a planned added function of supplying energy to stations for hydrogen and electric vehicles. In that case we will utilize liquid hydrogen transported from a hydrogen station and all Boil-Off Gas (BOG) will be recovered in THEUS’s metal hydride tanks. It is known that BOG is chiefly composed of para-hydrogen, which has different thermo-physical properties from normal hydrogen. It has been reported that some metal hydride alloys work as a catalyst to accelerate the para-ortho conversion and the conversion proceeds relatively fast in the case of La–Ni5. The conversion is considered to be an endothermic reaction. A misch metal (Mm)-Ni5 metal hydride alloy, which contained La and Ni, was used in our THEUS metal hydride tank. To examine the effect of the para-ortho conversion on the THEUS operation, we investigated the absorption/desorption characteristics of the metal hydride tank with BOG. We confirmed that the effect of the heat of conversion was very small and BOG could be treated as normal hydrogen for practical application. 相似文献