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991.
The 13C n.m.r. spectra of chicle polyisoprene and cis-trans isomerized 1, 4-polyisoprenes were studied. The splittings of signals were observed in the C1, C2, and C4 carbon signals of the isomerized polyisoprenes. The newly appearing signals were assigned to the carbon atoms in cis-trans linkages. The fractions of the diad sequences (trans-trans, trans-cis, cis-trans, and cis-cis) were determined by using the four signals of C1 carbon. It was found that the cis-1, 4- and trans-1, 4-units were randomly distributed in the isomerized polyisoprenes and it was confirmed that the chicle polyisoprene was a mixture of cis-1, 4- and trans-1, 4-polyisoprenes. 相似文献
992.
A doped poly(methyl methacrylate) (PMMA)–based graded‐index plastic optical fiber (GI POF) with high mechanical strength is reported for the first time. Although the POF is generally believed to have a good mechanical flexibility even if it has a large‐core diameter, such a high mechanical strength has been provided by making the polymer chains in the POF highly oriented in its axial direction. If such an orientation of polymer chains is eliminated, the POF becomes brittle, which is similar to silica‐based fibers. On the other hand, too high an orientation of the polymer chains induces fiber deformation in a high‐temperature atmosphere resulting from orientation relaxation. This study reports how high mechanical strengths such as the tensile strength and the large elongation are provided to the GI POF. By selecting the optimum heat‐drawing conditions, the GI POF has a mechanical strength comparable to that of the commercially available step index (SI) POF. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 404–409, 2004 相似文献
993.
Radical polymerization of N-isopropylacrylamide (NIPAAm) in CHCl3 at low temperatures in the presence of pyridine N-oxide (PNO) was investigated. An isotactic poly(NIPAAm) with meso diad content of 61% was successfully prepared at −60 °C in the presence of a two-fold amount of PNO. Thermodynamic analysis suggested that the isotactic-specificity was entropically induced, probably due to conformational fixation near the propagating chain-end through coordination by PNO. 相似文献
994.
Shuichi Akasaka Taiki Tobusawa Yoichi Tominaga Shigeo Asai Masao Sumita 《应用聚合物科学杂志》2006,99(6):2878-2884
We investigated the sound absorption characteristics of an organic hybrid material comprised of chlorinated polyethylene (CPE) as the matrix polymer and N,N′‐dicyclohexyl‐2‐benzothiazolyl sulfenamide (DBS) as the second component of an organic low‐molecular‐weight compound. We found specific crystallites, obtained by annealing, that generated new absorption for a low‐frequency sound in a CPE/DBS blend. We observed two sound absorption peaks, around 300 and 1000 Hz, in the annealed CPE/DBS (50 : 50 w/w) blends, whereas those peaks were not observed in the untreated sample. There were two kinds of crystals with different melting points in the annealed samples. It was confirmed that the crystals with the lower melting point brought about sound absorption at a low frequency. The crystals that had the lower melting point were smaller and/or more disordered than the crystals that had the higher melting point. We calculated the fraction of these two types of crystals from differential scanning calorimetry and wide‐angle X‐ray diffraction measurements. The annealing or reannealing temperature specified the fraction of the crystal with the lower melting point, and the obtained crystal fraction characterized sound absorption frequency. Therefore, it is possible to control the sound absorption frequency of an organic hybrid by heat treatment such as annealing. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci, 2006 相似文献
995.
Harumi Sato Masahiko Shimoyama Taeko Kamiya Toru Amari Slobodan aic Toshio Ninomiya Heinz W. Siesler Yukihiro Ozaki 《应用聚合物科学杂志》2002,86(2):443-448
Raman spectra have been measured for pellets of five samples of high‐density polyethylene (HDPE), seven samples of low‐density polyethylene (LDPE), and six samples of linear low‐density polyethylene (LLDPE). The obtained Raman spectra have been compared to find out characteristic Raman bands of HDPE, LDPE, and LLDPE. Principal component analysis (PCA) was applied to the Raman spectra in the 1600–650 cm?1 region after multiplicative scatter correction (MSC) to discriminate the Raman spectra of the three different PE species. They are classified into three groups by a score plot of PCA factor 1 vs. 2. HDPE with high density and high crystallinity gives high scores on the factor 1 axis, while LDPE with low density and low crystallinity yields negative scores on the same axis. It seems that factor 1 reflects the density or crystallinity. A PC weight loadings plot for factor 1 shows six upward peaks corresponding to the bands arising from the crystalline parts or all‐trans ? (CH2)n? groups and seven downward peaks ascribed to the bands of the amorphous or anisotropic regions and those arising from the short branches. Partial least‐squares (PLS‐1) regression was applied to the Raman spectra after MSC to propose calibration models that predict the density, crystallinity, and melting points of the polyethylenes. The correlation coefficient was calculated to be 0.9941, 0.9800, and 0.9709 for the density, crystallinity, and melting point, respectively, and their root‐mean‐square error of cross validation (RMSECV) was found to be 0.0015, 3.3707, and 2.3745, respectively. The loadings plot of factor 2 for the prediction of melting point is largely different from those for the prediction of density and crystallinity. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 443–448, 2002 相似文献
996.
Yuki Wada Hiroshi Mitomo Ken‐Ichi Kasuya Naotsugu Nagasawa Noriaki Seko Akio Katakai Masao Tamada 《应用聚合物科学杂志》2006,101(6):3856-3861
Radiation‐induced graft polymerization of acrylic acid (AAc) on poly(3‐hydroxybutyric acid) (PHB) film was carried out and the resulting film was thermally‐remolded. The PHB films grafted with AAc (PHB‐g‐AAc) having a degree of grafting higher than 5% completely lost the enzymatic degradability. The enzymatic degradability of the grafted film was recovered by thermal remolding. The highest enzymatic degradation rate was observed at degree of grafting of 10% after thermal remolding. The PHB‐g‐AAc films and thermally‐remolded PHB‐g‐AAc films were characterized by contact angle and differential scanning calorimetry. The enzymatic degradability of PHB‐g‐AAc films was lost by the grafted AAc, which covered the surface of PHB film. The acceleration of enzymatic degradation in the remolded PHB‐g‐AAc films was mainly caused by decrease of crystallinity of PHB by dispread of grafted AAc during thermal remolding. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 3856–3861, 2006 相似文献
997.
Tsuyoshi Honma Yasuhiko Benino Takumi Fujiwara Takayuki Komatsu Ryuji Sato 《Journal of the American Ceramic Society》2005,88(4):989-992
The glass formation region, crystalline phases, second harmonic (SH) generation, and Nd:yttrium aluminum garnet (YAG) laser-induced crystallization in the Sm2 O3 –Bi2 O3 –B2 O3 system were clarified. The crystalline phases of Bi4 B2 O9 , Bi3 B5 O12 , BiBO3 , Sm x Bi1− x BO3 , and SmB3 O6 were formed through the usual crystallization in an electric furnace. The crystallized glasses consisting of BiBO3 and Sm x Bi1− x BO3 showed SH generations. The formation of the nonlinear optical BiB3 O6 phase was not confirmed. The formation (writing) region of crystal lines consisting of Sm x Bi1− x BO3 by YAG laser irradiation was determined, in which Sm2 O3 contents were∼10 mol%. The present study demonstrates that Sm2 O3 –Bi2 O3 –B2 O3 glasses are promising materials for optical functional applications. 相似文献
998.
Fabrication process for picoliter volume SiO2 glass tube array partially embedded in Si wafer was developed. As a template for the glass tubes, macropore array was formed at the surface of n-Si(1 0 0) wafer by photo-assisted electrochemical etching process. The area-selective formation of the array was achieved by applying Au/Cr micropatterns formed at the back-side surface of the substrate as the shade mask, which controls the illumination condition to optimize the etching reaction conditions. Subsequently, surface of the macropores was wet-thermally oxidized to form glass layer, and the bulk Si region was removed by alkaline etching, remaining the “glass tubes”. As a result of complete removal of the bulk Si, released glass tubes were obtained. By partial removal of the bulk Si part, the glass tubes were exposed, fixed in the remaining Si substrate in the form of well-ordered array. It was confirmed that the depth, the exposed region and the wall thickness of each glass tube were controllable by adjusting the parameters such as the duration of the Si electrochemical etching, the alkaline etching and the wet-thermal oxidation, respectively. In order to demonstrate microreaction in the glass tube, aqueous rhodamine B solution was injected into the tubes and excitation light was irradiated to them. As a result, the fluorescence of rhodamine B was clearly detected, confirming the applicability of the glass tubes for various kinds of devices and systems such as microreactors. 相似文献
999.
Masao Morishita Alexandra Navrotsky Martin C. Wilding 《Journal of the American Ceramic Society》2004,87(8):1550-1555
The relative partial molar enthalpies, Δ SiO2 , of SiO2 in SiO2 –M2 O (M = Li, Na, K and Cs) binary and SiO2 –CaO–Al2 O3 ternary melts were directly measured by drop-solution calorimetry at 1465 K and 1663 K. Δ SiO2 changes from exothermic to endothermic as silica content increases, confirming the tendency toward immisciblity seen from activity measurements. It is concluded that Δ SiO2 is negative due to acid-base reactions and charge-coupled substitutions when the melt is composed of fewer Q 4 and more Q 3 and Q 2 species, but positive due to structural strain when the melt is composed of mostly Q 4 species. The Δ SiO2 obtained by calorimetry is a useful measure of basicity, when comparing different alkali and alkaline earth oxides. 相似文献
1000.
The reforming of CH4 with CO2 over supported Rh catalysts has been studied over a range of temperatures (550–1000 K). A significant effect of the support on the catalytic activity was observed, where the order was Rh/Al2O3>Rh/TiO2>Rh/SiO2. The catalytic activity of Rh/SiO2 was promoted markedly by physical mixing of Rh/SiO2 with metal oxides such as Al2O3, TiO2, and MgO, indicating a synergetic effect. The role of the metal oxides used as the support and the physical mixture may be ascribed to the promotion in dissociation of CO2 on the surface of Rh, since the CH4 + CO2 reaction is first order in the pressure of CO2, suggesting that CO2 dissociation is the rate-determining step. The possible model of the synergetic effect was proposed. 相似文献