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121.
Takahiro Matsumoto Tetsuro Nose Yasuaki Nagata Katsuhiro Kawashima Tastuya Yamada Hidetoshi Nakano Satoshi Nagai 《Journal of the American Ceramic Society》2001,84(7):1521-1525
Young's modulus and Poisson's ratio of SiC ceramics at temperatures >1400°C were obtained using a laser ultrasonics method that included a Fabry-Pérot interferometer (LUFP). At temperatures <1000°C, Young's modulus and Poisson's ratio measured using the LUFP method agreed well with those measured using standard contact methods, such as the resonance method and the ultrasonic pulse method. These results showed that the LUFP method is a powerful tool for measuring high-temperature elastic properties of advanced ceramics in a noncontact manner. 相似文献
122.
123.
Photoelectric properties of ABA‐type triblock copolymers designed using fluorine‐containing polyimide macroinitiators with polyhedral oligomeric silsesquioxane 下载免费PDF全文
Shuichi Sato Masato Ichikawa Erika Suzuki Hironaga Matsumoto Kazukiyo Nagai 《Polymer Engineering and Science》2017,57(11):1207-1213
4,4′‐(Hexafluoro‐isopropylidene) diphthalic anhydride‐2,3,5,6‐tetramethyl‐1,4‐phenylenediamine (6FDA‐TeMPD) was synthesized and reacted with polyhedral oligomeric silsesquioxane (POSS) to form an ABA‐type triblock copolymer by atom transfer radical polymerization. The solid‐state and optical properties of the resulting copolymers were systematically investigated, and their electronic states were analyzed. As the POSS concentration increased, the transparency across the entire wavelength range increased. In the ABA‐type triblock copolymers, a new transition was observed between the highest occupied molecular orbital in POSS and the lowest unoccupied molecular orbital in 6FDA‐TeMPD because of their high molecular size dispersion. Since the refractive index of 6FDA‐TeMPD decreased linearly as the POSS concentration increased, the refractive index of the ABA‐type triblock copolymers of 6FDA‐TeMPD with POSS could be easily controlled. POLYM. ENG. SCI., 57:1207–1213, 2017. © 2017 Society of Plastics Engineers 相似文献
124.
Crosslinking of poly(vinyl alcohol) and poly(vinyl acetate) using poly(maleic anhydride‐alt−2,4‐dimethyl‐1,3‐pentadiene) as polyfunctional crosslinker and decrosslinking by ozone degradation 下载免费PDF全文
Crosslinking and decrosslinking reactions of poly(vinyl alcohol) (PVA) and poly(vinyl acetate) (PVAc) using an alternating copolymer of maleic anhydride and 2,4‐dimethyl‐1,3‐pentadiene (PMAD) as the polyfunctional crosslinker and subsequent ozone degradation are reported. PVA and PVAc are heated at 200 °C for 0.5 to 3 h in the presence of 5 to 30 wt % of PMAD in the solid state to obtain the corresponding crosslinked polymers. The reactions of a hydroxy group of PVA and an acetate group of PVAc with an anhydride group of PMAD slowly proceed to give insoluble polymers with a loose crosslinking structure. Almost no change in the thermal decomposition temperatures and the IR spectra is observed during the crosslinking reactions. The crosslinked PVA produces hydrogels with a high swelling ratio of 500 to 1700%, which are readily degradable during a reaction with ozone in water at 0 °C. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44229. 相似文献
125.
Poly(N‐isopropylacrylamide) gel‐based macroporous monolith for continuous‐flow recovery of palladium(II) ions 下载免费PDF全文
Hirokazu Seto Hikaru Matsumoto Makoto Shibuya Takanori Akiyoshi Yu Hoshino Yoshiko Miura 《应用聚合物科学杂志》2017,134(4)
Macroporous monoliths, composed of thermoresponsive, tertiary‐aminated, and crosslinking monomers, were prepared for continuous‐flow separation of palladium(II) ions. N ‐Isopropylacrylamide was required to form the porous structure in the monoliths, indicating that the mechanism of porous structure formation involved polymerization‐induced phase separation of the poly(N ‐isopropylacrylamide) gel. Tertiary‐aminated monoliths showed adsorption selectivity for palladium(II) ions in hydrochloric media, compared with copper(II) ions. The maximum capacities of the monoliths with tertiary amine contents of 10, 20, 30, and 70 mol % for palladium(II) ions were 0.6, 1.1, 1.3, and 2.3 mmol/g, respectively. Darcy's permeabilities of water through the macroporous monolith were 10?14 to 10?13 m2, and those were comparable to that through a commercially available membrane filter with a pore size of several micrometers. In the continuous‐flow process, the macroporous monolith with tertiary amine selectively adsorbed palladium(II) ions in the coexistence of copper(II) ions with 10 times higher concentration than the palladium(II) ions. The palladium(II) ions were eluted from the macroporous monolith, and the concentration of palladium(II) ions in the eluate was up to 45 times of that in the feed solution. The average enrichment factor and total recovery percentage of palladium(II) ions were 8.7 times and 95%, respectively. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 44385. 相似文献
126.
We examined which isomer, the erythro or threo, of non-phenolic β-O-4-type lignin model compounds is stereo-preferentially attacked by hydroxyl radical and its conjugate base, oxyl anion radical, generated by the decomposition of hydrogen peroxide in the presence of ferric ion and its precipitates under hydrogen peroxide bleaching conditions. The intrinsic stereo-preference of oxyl anion radical was slightly toward the erythro isomer, while hydroxyl radical had a further smaller stereo-preference. These stereo-preferences can be explained by our prior knowledge that oxyl anion radical preferentially attacks the side-chain of the lignin model compounds rather than the aromatic nucleus. The amount of the degraded lignin model compounds became less great with decreasing pH, but reversely and intensively greater in the pH range below 10. This phenomenon can be attributed to the change in the decomposition mechanism of hydrogen peroxide accompanying the pH variation. 相似文献
127.
Microwave dielectric properties and crystal structures of Mg0.7Al2.2O4 and Mg0.4Al2.4O4 ceramics with defect structures 下载免费PDF全文
Susumu Takahashi Akinori Kan Hirotaka Ogawa 《Journal of the American Ceramic Society》2017,100(8):3497-3504
Mg0.7Al2.2O4 and Mg0.4Al2.4O4 ceramics with cation vacancies were synthesized using the molten salt method, and the relationships between the microwave dielectric properties and crystal structures of these materials were investigated. The 27Al NMR spectra of these ceramics indicate that the preferential occupation of tetrahedral sites by Al3+ cations was enhanced by the introduction of cation vacancies. The λ values of Mg0.7Al2.2O4 and Mg0.4Al2.4O4 ceramics fired at 1600°C, which correspond to the fraction of Al3+ cations in tetrahedral sites, were 0.37 and 0.60, respectively. Crystal structure refinements using the Rietveld method suggest that cation vacancies are preferentially located at octahedral sites in both ceramics. The εr and Q·f values of a Mg0.7Al2.2O4 ceramic fired at 1600°C were 7.7 and 201 111 GHz, respectively, while those of a Mg0.4Al2.4O4 ceramic fired at 1600°C were 7.5 and 232 301 GHz, respectively. These data demonstrate that the preferential occupation of tetrahedral sites by Al3+ cations following the introduction of cation vacancies enhances the Q·f value. 相似文献
128.
Suguru?MotokuchoEmail author Takeshi?Matsumoto Yu?Nakayama Ryohei?Horiuchi Hiroshi?Morikawa Hisayuki?Nakatani 《Polymer Bulletin》2017,74(3):615-623
A chemical decomposition of polyurea (PUA) by hydrolysis under high pressure of carbon dioxide (CO2) was proposed. The hydrolysis of PUA was carried out at 190 °C for 2 h under 7.0 MPa of CO2 in the presence of water. The hydrolysis reaction gave white residual solid and water soluble compound. The white residual solid was characterized to be degraded PUA by FT-IR spectrum and elemental analysis. 1H-NMR spectra of the water soluble compound revealed that the hydrolysis of PUA produced diamine only from repeating unit of PUA, which was a component of PUA. This hydrolysis gave the corresponding diamine for quantitative yields. 相似文献
129.
Yong Chen Tianmo Liu Chunlin Chen Weiwei Guo Rong Sun Shuhui Lv Mitsuhiro Saito Susumu Tsukimoto Zhongchang Wang 《Ceramics International》2013
We report a synthesis of two types of CeO2 nano-rods via the facile and efficient hydrothermal process free from any surfactant and template. The synthesized nano-rods are chemically identified as CeO2 with the standard fluorite structure but their morphologies are different. The nano-rods prepared with cerium nitrate hexahydrate and sodium phosphate are thicker and shorter with diameter of ∼30 nm and length of ∼100 nm, and those prepared with cerium acetate hydrate and dibasic sodium phosphate are thinner and longer with ∼10 nm in diameter and ∼400 nm in length. Microstructural analyses reveal that the two species of nano-rods have low-energy {111} surfaces and grow along the 〈112〉 direction. As a consequence of their morphologies, the two types of synthesized nano-rods exhibit excellent UV-absorption ability in comparison to the irregular CeO2 nanoparticles. 相似文献
130.
Nusrat J. M. Sanghamitra Hiroshi Inaba Susumu Kitagawa Takafumi Ueno 《Journal of Inorganic and Organometallic Polymers and Materials》2013,23(1):50-60
In the last decade, there has been great deal of progress in the study of self-assembly processes of protein assemblies as biotemplates to create and construct one-dimensional arrays of nanocrystalline metals and semiconductors. Successful attempts in fabricating the protein-based bioelectronics could serve as a promising alternative to synthetic template based nanomaterials. Another perspective of protein assemblies is its use in the field of tissue engineering either as scaffold for cell adhesion and proliferation or as a foreign (bio)nanofunctionality to communicate with the macromolecules present in the extracellular or intracellular milieu and participate in the precise control of vital cell functions. Three-dimensionally arranged protein monomers to form bionanotubes are promising in terms of innate biocompatibility, easy bio-conjugation to incorporate multiple functionalities and well-defined nano-scale lengths. Such unique chemical properties of protein assemblies are described in this review. 相似文献