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101.
Eisner Salamanca Yu-Hwa Pan Ying-Sui Sun Hao-Wen Hsueh Odontuya Dorj Wan-Ling Yao Jerry Chin-Yi Lin Nai-Chia Teng Ikki Watanabe Shinichi Abe Yi-Fan Wu Wei-Jen Chang 《International journal of molecular sciences》2022,23(3)
In vitro, in vivo, and clinical studies have shown how the physicochemical and biological properties of β-tricalcium phosphate (β-TCP) work in bone regeneration. This study aimed to improve the properties of β-TCP by achieving optimum surface and bulk β-TCP chemical/physical properties through the hydrothermal addition of magnesium (Mg) and to later establish the biocompatibility of β-TCP/Mg for bone grafting and tissue engineering treatments. Multiple in vitro and in vivo analyses were used to complete β-TCP/Mg physicochemical and biological characterization. The addition of MgO brought about a modest rise in the number of β-TCP surface particles, indicating improvements in alkaline phosphatase (ALP) activity on day 21 (p < 0.05) and in the WST-1assay on all days (p < 0.05), with a corresponding increase in the upregulation of ALP and bone sialoprotein. SEM analyses stated that the surfaces of the β-TCP particles were not altered after the addition of Mg. Micro-CT and histomorphometric analysis from rabbit calvaria critical defects resulted in β-TCP/Mg managing to reform more new bone than the control defects and β-TCP control at 2, 6, and 8 weeks (* p ≤ 0.05, ** p ≤ 0.01, *** p ≤ 0.001, and **** p ≤ 0.0001). The hydrothermal addition of MgO to the β-TCP surfaces ameliorated its biocompatibility without altering its surface roughness resulting from the elemental composition while enhancing cell viability and proliferation, inducing more bone regeneration by osteoconduction in vivo and osteoblastic differentiation in vitro. 相似文献
102.
Maria Maldonado Kaitlyn Madison Abe James Anthony Letts 《International journal of molecular sciences》2022,23(2)
The last steps of respiration, a core energy-harvesting process, are carried out by a chain of multi-subunit complexes in the inner mitochondrial membrane. Several essential subunits of the respiratory complexes are RNA-edited in plants, frequently leading to changes in the encoded amino acids. While the impact of RNA editing is clear at the sequence and phenotypic levels, the underlying biochemical explanations for these effects have remained obscure. Here, we used the structures of plant respiratory complex I, complex III2 and complex IV to analyze the impact of the amino acid changes of RNA editing in terms of their location and biochemical features. Through specific examples, we demonstrate how the structural information can explain the phenotypes of RNA-editing mutants. This work shows how the structural perspective can bridge the gap between sequence and phenotype and provides a framework for the continued analysis of RNA-editing mutants in plant mitochondria and, by extension, in chloroplasts. 相似文献
103.
Mina Han Ikue Abe Jihun Oh Jaehoon Jung Young Ji Son Jaegeun Noh Mitsuo Hara Takahiro Seki 《International journal of molecular sciences》2022,23(2)
Fluorescent molecular assembly systems provide an exciting platform for creating stimuli-responsive nano- and microstructured materials with optical, electronic, and sensing functions. To understand the relationship between (i) the plausible molecular structures preferentially adopted depending on the solvent polarity (such as N,N-dimethylformamide [DMF], tetrahydrofuran [THF], and toluene), (ii) the resulting spectroscopic features, and (iii) self-assembled nano-, micro-, and macrostructures, we chose a sterically crowded triangular azo dye (3Bu) composed of a polar molecular core and three peripheral biphenyl wings. The chromophore changed the solution color from yellow to pink-red depending on the solvent polarity. In a yellow DMF solution, a considerable amount of the twisted azo form could be kept stable with the help of favorable intermolecular interactions with the solvent molecules. By varying the concentration of the DMF solution, the morphology of self-assembled structures was transformed from nanoparticles to micrometer-sized one-dimensional (1D) structures such as sticks and fibers. In a pink-red toluene solution, the periphery of the central ring became more planar. The resulting significant amount of the keto-hydrazone tautomer grew into micro- and millimeter-sized 1D structures. Interestingly, when THF-H2O (1:1) mixtures were stored at a low temperature, elongated fibers were stacked sideways and eventually developed into anisotropic two-dimensional (2D) sheets. Notably, subsequent exposure of visible-light-irradiated sphere samples to solvent vapor resulted in reversible fluorescence off↔on switching accompanied by morphological restoration. These findings suggest that rational selection of organic dyes, solvents, and light is important for developing reusable fluorescent materials. 相似文献
104.
Sho Kano Huilong Yang John McGrady Tomonori Ihara Hazuku Tatsuya Hiroaki Abe 《Journal of Nuclear Science and Technology》2019,56(3):300-309
The radiation-induced surface activation (RISA) effect will be applied to the core design in supercritical light water reactor (SCWR) in order to achieve a high performance with excellent economy and safety. The purpose of the present study is to investigate the RISA effect in the candidate fuel cladding materials in SCWR such as PNC1520. The change of weldability due to RISA effect and the related microstructure analysis were performed in oxidized PNC1520 and 304 stainless steel with various oxidization periods. The phases contained in the surface oxide layer of the present specimen were identified as Fe2CrO4, γ-Fe2O3, and Fe2O3. The lifetime of 13.8 days for wettability improving factor was confirmed in the ultraviolet (UV) irradiation. Meanwhile, the long life of 13.8 days and short life of 0.8 days for wettability improving factors were identified in the γ-ray irradiation. Based on the fact that the band gap energies of Fe2CrO4, γ-Fe2O3, and Fe2O3 were, respectively, 2.1, 2.0, and 2.2 eV, and the photo energies of UV and γ-ray irradiation were 4.48 eV and 13.3 MeV, it is therefore clarified that the hydrophilization on the oxide layer is ascribed to the RISA effect. 相似文献
105.
Watanabe Masahito Sato Fumiya Abe Raiki Ueda Kyosuke Matsuwaka Daisuke Kudo Fumiaki Narushima Takayuki 《Metallurgical and Materials Transactions B》2019,50(4):1553-1558
Metallurgical and Materials Transactions B - A two-step plasma arc melting process, comprising a first step under Ar-30 pct H2 gas flow and the second step under Ar gas flow, has been... 相似文献
106.
Plasma osmolality estimated from plasma concentrations of Na+, Cl-, K+, glucose, and urea was compared with measured osmolality in preweaned Holstein calves. When calves (n = 5) were fed only milk replacer after fasting for 24 h, measured osmolality fluctuated almost in parallel with estimated osmolality during the 8-h period after feeding, although estimated values were about 90% of measured values. When calves (n = 5) were fed only calf starter after fasting for more than 16 h, measured osmolality did not parallel the estimated osmolality during the 8-h period after feeding. Some factors depressed measured osmolality in the first 2 h. 相似文献
107.
Electron beam sterilization of cyclo olefin polymer leads to polymer degradation and production of alkyl radicals
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Hideaki Kiminami Yasufumi Imae Eiji Takahashi Hong Wei Satoshi Oomura Yoshihiko Abe 《应用聚合物科学杂志》2016,133(23)
We investigated the effects of electron‐beam (EB) sterilization on syringe barrels manufactured from cyclo olefin polymer (COP). The chemical structure of the polymer was determined by interpreting the 13C NMR and DEPT‐135 spectra of the COP resin. The antioxidants in the resin were identified by analyzing the liquid chromatography‐photo diode array‐mass spectrometry (LC‐PDA‐MS) data for the methanol extract of the resin and the gas chromatography‐mass spectrometry (GC‐MS) data for the supercritical methanol degradation products of the extract. NMR and LC‐PDA‐MS analyses revealed that EB sterilization produces degradation products in the COP main chain and reduces the quantity of the antioxidants in the COP resin. ESR spectra of the EB‐sterilized syringe barrels indicated the presence and location of alkyl radicals, which were generated in the COP main chain by EB sterilization. ESR analyses also indicated that the quantity of alkyl radicals decreased over time. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43498. 相似文献
108.
Infrared study of catalytic reduction of lean NOx with alcohols over alumina-supported silver catalyst 总被引:3,自引:0,他引:3
Two intense IR absorption bands due to surface isocyanate (-NCO) species have been observed at 2262 and 2232 cm–1 when an alumina-supported silver catalyst is exposed to a mixture of NO, O2 and ethanol at 150°C and subsequently heated to > 300°C in vacuum. The intensity of the isocyanate band is hardly affected by the water existing in the mixture. Methanol is less reactive than ethanol for the formation of isocyanate species. The reaction mechanism of catalytic reduction of lean NOx with alcohols is discussed based on these IR spectroscopic findings. 相似文献
109.
Masayuki Nogami Naoya Hayakawa Naoya Sugioka Yoshihiro Abe 《Journal of the American Ceramic Society》1996,79(5):1257-1261
Samarium ions (Sm2+ ) incorporated into aluminosilicate glasses by a sol-gel process showed persistent spectral hole burning at room temperature. Gels of the system Na2 O-Al2 O3 SiO2 synthesized by the hydrolysis of Si(OC2 H5 )4 , Al(OC4 H9 )3 , CH3 COONa, and SmCl3 ·6H2 O were heated in air at 500°C, then reacted with H2 gas to form Sm2+ ions. Whereas Al3+ ions effectively dispersed the Sm3+ ions in the glass structure, Na+ ions were not effective. The Al2 O3 -SiO2 glasses proved appropriate for reacting the Sm3+ ions with H2 gas and exhibited the intense photoluminescence of Sm2+ ions. The reaction of Sm3+ ions with H2 in the Al2 O2 -SiO2 glasses was determined by first-order kinetics, and the activation energy equaled 95 kJ/mol. At 800°C, the maximum photoluminescence of the Sm2+ ions was achieved within 20 min. 相似文献
110.
Porous glass-ceramics with a skeleton of the fast-lithium-conducting crystal Li1+ x Ti2− x Al x (PO4 )3 (where x = 0.3–0.5) were prepared by crystallization of glasses in the Li2 O─CaO─TiO2 ─Al2 O3 –P2 O5 system and subsequent acid leaching of the resulting dense glass-ceramics composed of the interlocking of Li1+ x Ti2− x Al x (PO4 )3 and β-Ca3 (PO4 )2 phases. The median pore diameter and surface area of the resulting porous Li1+ x Ti2− x Al x (PO4 )3 glass-ceramics were approximately 0.2 μm and 50 m2 /g, respectively. The electrical conductivity of the porous glass-ceramics after heating in LiNO3 aqueous solution was 8 × 10−5 S/cm at 300 K or 2 × 10−2 S/cm at 600 K. 相似文献