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1.
The effect of humidity during storage on the crosslinking reactions of isocyanate groups was investigated with attenuated total reflectance Fourier transform infrared spectroscopy with pressure‐sensitive adhesives composed of poly[ethyl acrylate‐co‐(2‐ethylhexyl acrylate)‐co‐(2‐hydroxyethyl methacrylate)] as a base resin and polyisocyanate as a crosslinker. A peak‐resolving analysis of the amide II region revealed four bands. According to an analysis of the Fourier transform infrared spectra of the model compounds, these four bands were assigned to free urethane linkages, hydrogen‐bonded urethane linkages, free urea linkages, and hydrogen‐bonded urea linkages. As expected, storage under humid conditions led to the formation of free and hydrogen‐bonded urea linkages corresponding to the promotion of isocyanate consumption. Peak resolution of the amide II region was found to be a reasonable way of monitoring urethane and urea linkages during crosslinking reactions. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 3039–3045, 2003 相似文献
2.
Tetsuya Nanba Shouichi Masukawa Atsushi Ogata Junko Uchisawa Akira Obuchi 《Applied catalysis. B, Environmental》2005,61(3-4):288-296
The catalytic decomposition of acrylonitrile (AN) over Cu-ZSM-5 prepared with various Cu loadings was investigated. AN conversion, during which the nitrogen atoms in AN were mainly converted to N2, increased as Cu loading increased. N2 selectivities as high as 90–95% were attained. X-ray diffraction measurements (XRD) and temperature-programmed reduction by H2 (H2-TPR) showed the existence of bulk CuO in Cu-ZSM-5 with a Cu loading of 6.4 wt% and the existence of highly dispersed CuO in Cu-ZSM-5 with a Cu loading of 3.3 wt%. Electron spin resonance measurements revealed that Cu-ZSM-5 contains three forms of isolated Cu2+ ions (square-planar, square-pyramidal, and distorted square-pyramidal). The H2-TPR results suggested that in Cu-ZSM-5 with a Cu loading of 2.9 wt% and below, Cu+ existed even after oxidizing pretreatment. The activity of AN decomposition over Cu/SiO2 suggested that CuO could form N2, but, independent of the CuO dispersion, nitrogen oxides (NOx) were formed above 350 °C. Cu+ and the square-pyramidal and distorted square-pyramidal forms of Cu2+ showed low activity for AN decomposition. Temperature-programmed desorption of NH3 suggested that N2 formation from NH3 proceeded on Cu2+, resulting in the formation of Cu+. The Cu+ ions were oxidized to Cu2+ at around 300 °C. Thus, high N2 selectivity over Cu-ZSM-5 with a wide range of temperature was probably attained by the reaction over the square-planar Cu2+, which can be reversibly reduced and oxidized. 相似文献
3.
On the basis of new concept using a solid disperse phase we have developed an efficient catalytic solid-phase-system for epoxidations of alkenes using urea–hydrogen peroxide (urea–H2O2) complex and cetylpyridinium dodecatungstate ((CetylPy)10[H2W12O42]) catalyst on fluorapatite (FAp). The recovered solid catalyst phase was reused to keep the catalytic activity after several times. In the conceptual idea it is a key point that in situ solid-phase-activation of the catalyst with urea–H2O2 proceeds to form microcrystals of the active species dispersed on the solid phase. The dispersion of the catalyst on FAp in the case of tungstic acid (H2WO4) was suggested by EPMA analysis. We proposed the peroxo type of species keeping the parent polyoxometalate framework as novel active species from FT-IR spectroscopic studies. FAp phase plays important roles of dispersing the active species on its surface to have high catalytic activity and of stabilizing the active species to lead to high reusability. 相似文献
4.
Hirokazu Ikeda Chikara Fukunaga Yutaka Saitoh Masahiro Inoue Junko Yamanaka 《Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment》1996,380(3):618-622
The radiation tolerance for prototype front-end chips designed for a silicon micro-strip detector was examined with a 60Co irradiation source to establish an allowable range of the radiation dose. The irradiated front-end chips were SMA2SH-64A, a 64-channel preamplifier array; SMA2SH-1, a single-channel preamplifier circuit with a comparator; and Control-C, a digital-control chip for the preamplifiers. 相似文献
5.
The reaction of isocyanate in pressure sensitive adhesive (PSA) films adhered on to various adherends having different surface tensions was monitored by depth profiling using attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy.In the latter stages of crosslinking reaction, unreacted isocyanate and its derivatives exist more in the bulk of the PSA than in the interfaces between PSA and adherends which are Teflon sheet and PE film having relatively lower surface tensions. In the case of using stainless steel having relatively higher surface tension as adherend, opposite segregation was observed compared to Teflon and PE.From X-ray photoelectron spectroscopy (XPS), it was revealed that N atoms exist more in surface than in bulk when stainless steel is used as adherend. We conclude that polyisocyanates migrate in the PSA film in order to minimize the magnitude of interfacial free energy between the PSA and the adherend, which leads to the change of surface tension of PSA film. 相似文献
6.
Junko Hatori Yasumitsu Matsuo Masaru Komukae Seiichiro Ikehata 《Materials Chemistry and Physics》2006,100(2-3):520-523
We have carried out the optical observation, electrical conductivity and 205Tl NMR measurements, and subsequently investigated the origin of the large conductivity above ferroelastic phase transition temperature Tc (=661 K) on the basis of the domain structure and the crystal structure. Electrical conductivity exhibits the discontinuous increase around Tc with increasing temperature and becomes approximately 5 × 10−3 S m−1 above Tc. Moreover, from the 205Tl NMR measurements, it is found that mobile Tl ions exist above Tc. Furthermore, from the analysis of the domain structure based on the crystal structure in the low-temperature ferroelastic phase, it is also found that the anomalously large fluctuations of SeO4 tetrahedrons exist above Tc. It is deduced from these results that the high electrical conductivity above Tc is caused by the mobile Tl ions closely related to the anomalously large fluctuations of SeO4 tetrahedrons accompanied by the ferroelastic phase transition. 相似文献
7.
Motonaka Kuroda Yumiko Kato Junko Yamazaki Naoko Kageyama Toshimi Mizukoshi Hiroshi Miyano Yuzuru Eto 《Food chemistry》2012
The determination of the kokumi peptide, γ-glutamyl-valyl-glycine (γ-Glu-Val-Gly) in raw scallop and processed scallop products was carried out using high pressure liquid chromatography–tandem mass spectrometry (LC/MS/MS). The detection of γ-Glu-Val-Gly was achieved using a multiple reaction monitoring (MRM) method. The optimised condition enabled the precise determination of γ-Glu-Val-Gly. Raw scallop contained 0.08 μg/g γ-Glu-Val-Gly, and the γ-Glu-Val-Gly levels in processed scallop products, such as dried-scallop and scallop extract, were measured to be 0.64 and 0.77 μg/g, respectively. This is the first report to confirm the existence of γ-Glu-Val-Gly in foodstuff. 相似文献
8.
Masatoshi Hasegawa Masahito Horiuchi Kyoko Kumakura Junko Koyama 《Polymer International》2014,63(3):486-500
Alkyl‐substituted cyclobutanetetracarboxylic dianhydrides (CBDAs) were synthesized by photo‐dimerization of alkyl‐substituted maleic anhydrides to obtain novel colorless polyimides (PIs). Dimethyl‐substituted CBDA (DM‐CBDA) showed much higher polymerizability with various diamines than conventional cycloaliphatic tetracarboxylic dianhydrides and led to high molecular weights of PI precursors. Polyaddition of non‐substituted CBDA and trans‐1,4‐cyclohexanediamine (t‐CHDA) was completely inhibited by salt formation in the initial reaction stage. The use of DM‐CBDA allowed the formation of a homogeneous/viscous PI precursor solution by overcoming the salt formation problem. The prominent substituent effect probably reflects how the methyl substituents of DM‐CBDA contributed to increasing the salt solubility. Some of the thermally imidized DM‐CBDA‐based systems simultaneously possessed non‐coloration, low coefficient of thermal expansion (CTE), very high Tg exceeding 300 °C and very low dielectric constant. Copolymerization was very effective for improving the solubility of DM‐CBDA‐based PIs. The copolyimide cast films prepared via chemical imidization displayed a further decreased CTE without sacrificing other target properties, suggesting that the present materials can be useful as plastic substrates in display devices. The mechanism of self‐chain orientation behavior during solution casting is also discussed. A potential application of the copolyimide systems as optical compensation film materials in liquid crystal displays is proposed. © 2013 Society of Chemical Industry . 相似文献
9.
Kei Noda Ko Okamura Junko Taniguchi Masaru Suzuki Mitsunori Hieda 《Journal of Low Temperature Physics》2013,171(5-6):638-643
We have carried out quartz crystal microbalance (QCM) experiments for 4He films on an exfoliated single-crystalline graphite using a 32 kHz tuning fork, and have measured the temperature dependence of the resonance frequency and the Q value for various areal densities and oscillation amplitudes. Comparing with the previous experiments for Grafoil, the decoupling of the films due to the slippage or the superfluidity was larger than that of Grafoil, and the competition between the slippage and the superfluidity was observed in three-atom thick films. Furthermore, it was found that the slippage is suppressed gradually at higher temperature than the superfluid onset T c , and that the relaxation time decreases at low temperatures while it obeys the Arrhenius law at high temperatures. These results suggest a precursor to the superfluidity of 4He films. 相似文献
10.
Junko Shindo 《Nutrient Cycling in Agroecosystems》2012,94(1):47-61
Gross and per unit agricultural land area nitrogen balance (NB G and NB A, respectively) in agricultural areas were estimated with a nitrogen-flow model for 13 Asian countries, for regions within a country, and for individual grid cells, from 1970 to 2005. Country- and regional-level estimates showed that NB A is higher in Japan and South Korea than in other Asian countries, but has recently been stable or decreasing. The contribution of inorganic fertilizer to the nitrogen input is decreasing, whereas that of livestock manure is increasing in these countries. In many other countries, the primary nitrogen source is inorganic fertilizer and its input rate and NB A have increased sharply since the 1980s. NB A of some Chinese provinces and Indian states were as high as those of Japan and South Korea. The results suggest that regional-scale estimation is necessary because of the large spatial variability in nitrogen flows within a country. Based on the NB G estimated for each 0.5°?×?0.5° grid cell, nitrogen outflow from agriculture into major river basins was evaluated. About 20?% of the nitrogen balance flowed into China??s Changjiang River basin, versus 10?% into the Ganges River basin. Uncertainties in the basic data and estimation results, and the use of an alternative measure of a country??s environmental performance were discussed. 相似文献