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排序方式: 共有852条查询结果,搜索用时 15 毫秒
1.
Milad Abdalrhman Hussein Sadaam Hadee Khekan Ahlam R. Rashid Mohammed Al-Msari Haitham Tran Tan Huy 《Engineering with Computers》2022,38(4):3625-3637
Engineering with Computers - Over the past few decades, it has been observed a remarkable progression in the development of computer aid models in the field of civil engineering. Machine learning... 相似文献
2.
Dr. Aline D. de Araujo Huy T. Nguyen Prof. David P. Fairlie 《Chembiochem : a European journal of chemical biology》2021,22(10):1784-1789
The conventional S-alkylation of cysteine relies upon using activated electrophiles. Here we demonstrate high-yielding and selective S-alkylation and S-lipidation of cysteines in unprotected synthetic peptides and proteins by using weak electrophiles and a Zn2+ promoter. Linear or branched iodoalkanes can S-alkylate cysteine in an unprotected 38-residue Myc peptide fragment and in a 91-residue miniprotein Omomyc, thus highlighting selective late-stage synthetic modifications. Metal-assisted cysteine alkylation is also effective for incorporating dehydroalanine into unprotected peptides and for peptide cyclisation via aliphatic thioether crosslinks, including customising macrocycles to stabilise helical peptides for enhanced uptake and delivery to proteins inside cells. Chemoselective and efficient late-stage Zn2+-promoted cysteine alkylation in unprotected peptides and proteins promises many useful applications. 相似文献
3.
Xiaoqin Yang Huy Q. Ta Huimin Hu Shuyuan Liu Yu Liu Alicja Bachmatiuk Jinping Luo Lijun Liu Jin-Ho Choi Mark H. Rummeli 《Advanced functional materials》2021,31(38):2104340
In this study, in situ transmission electron microscopy is performed to study the interaction between single (monomer) and paired (dimer) Sn atoms at graphene edges. The results reveal that a single Sn atom can catalyze both the growth and etching of graphene by the addition and removal of C atoms respectively. Additionally, the frequencies of the energetically favorable configurations of an Sn atom at a graphene edge, calculated using density functional theory calculations, are compared with experimental observations and are found to be in good agreement. The remarkable dynamic processes of binary atoms (dimers) are also investigated and is the first such study to the best of the knowledge. Dimer diffusion along the graphene edges depends on the graphene edge termination. Atom pairs (dimers) involving an armchair configuration tend to diffuse with a synchronized shuffling (step-wise shift) action, while dimer diffusion at zigzag edge terminations show a strong propensity to collapse the dimer with each atom diffusing in opposite directions (monomer formation). Moreover, the data reveals the role of C feedstock availability on the choice a single Sn atom makes in terms of graphene growth or etching. This study advances the understanding single atom catalytic activity at graphene edges. 相似文献
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5.
Phan Huy Hoang Anh Tuan Hoang Nguyen Hoang Chung Le Quang Dien Xuan Phuong Nguyen Xuan Duong Pham 《Energy Sources, Part A: Recovery, Utilization, and Environmental Effects》2018,40(3):312-319
In this study, new and efficient sorbent with density 0.2 g/cm3 was fabricated by incorporating rice straw into polyurethane matrix to get an open cell structure material with high oil uptake capacity. The influences of various important factors such as amount of adding rice straw, size of rice straw particles, and adsorption time on oil adsorption capacity of new sorbent material were investigated. The results showed that the oil absorption rate occurred fast in first 15–30 min, then slowed down and reached saturation level after about 2 h of treatment. Oil adsorption capacity of the new sorbent material was relatively high, up to 12.0 g/g. In comparison with pristine polyurethane or lignocellulosic materials, the new sorbents had higher oil adsorption capacity. Some characteristics of the as-obtained sorbent, such as surface shapes and porosity, were also studied by SEM analysis. 相似文献
6.
Occurrence and formation potential of N-nitrosodimethylamine in ground water and river water in Tokyo 总被引:1,自引:0,他引:1
N-nitrosodimethylamine (NDMA), a disinfection byproduct of water and wastewater treatment processes, is a potent carcinogen. We investigated its occurrence and the potential for its formation by chlorination (NDMA-FP2Cl) and by chloramination (NDMA-FP2NHCl) in ground water and river water in Tokyo. To characterize NDMA precursors, we revealed their molecular weight distributions in ground water and river water. We collected 23 ground water and 18 river water samples and analyzed NDMA by liquid chromatography-tandem mass spectrometry. NDMA-FP2Cl was evaluated by chlorinating water samples with free chlorine for 24 h at pH 7.0 while residual free chlorine was kept at 1.0-2.0 mgCl2/L. NDMA-FP2NHCl was evaluated by dosing water samples with monochloramine at 140 mgCl2/L for 10 days at pH 6.8. NDMA precursors and dissolved organic carbon (DOC) were fractionated by filtration through 30-, 3-, and 0.5 kDa membranes. NDMA concentrations were <0.5-5.2 ng/L (median: 0.9 ng/L) in ground water and <0.5-3.4 ng/L (2.2 ng/L) in river water. NDMA concentrations in ground water were slightly lower than or comparable to those in river water. Concentrations of NDMA-FP2Cl were not much higher than concentrations of NDMA except in samples containing high concentrations of NH3 and NDMA precursors. The increased NDMA was possibly caused by reactions between NDMA precursors and monochloramine unintentionally formed by the reaction between free chlorine and NH3 in the samples. NDMA precursors ranged from 4 to 84 ng-NDMA eq./L in ground water and from 11 to 185 ng-NDMA eq./L in river water. Those in ground water were significantly lower than those in river water, suggesting that NDMA precursors were biodegraded, adsorbed, or volatilized during infiltration. The molecular weight of NDMA precursors in river water was dominant in the <0.5 kDa fraction, followed by 0.5-3 kDa. However, their distribution was inconsistent in ground water: one was dominant in the <0.5 kDa fraction, and the other in 0.5-3 kDa. Molecular weight distributions of NDMA precursors were very different from those of DOC. This is the first study to reveal the widespread occurrence and characterization of NDMA precursors in ground water. 相似文献
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8.
Upconversion phosphors are known as a material system that can convert near-infrared light into visible/ultraviolet emissions by sequentially absorbing multiple photons. The studies on upconversion materials often use two rare earth (RE) ions as a sensitizer-activator pair. We investigated the influences on luminescence intensity depending on Cr-doping content (x) of hexagonal NaLu0.98–xCrxF4Er0.02 (x = 0–0.9) upconversion material by substituting Lu3+ ions with Cr3+in the absence of Gd3+. The change in upconversion luminescence intensity appears with saddle-like shape. We suggest that Cr3+ ions play the dual role as a constituent in host lattice and a sensitizer in the upconversion process. Optimal conditions for gaining the strongest upconversion emission correspond to x = 0.3–0.5, where there are effective energy transfers between Cr3+ and Er3+ ions and CrEr dimers. Apart from these values, the emission intensity decreases rapidly which can be ascribed to the absence of multiple-photon absorption for the case of low Cr3+ contents, and to the coupling between Cr3+ and/or Er3+ ions for the case of high Cr3+ contents. Magnetization and electron-spin-resonant measurements were performed to understand the correlation between the optical and magnetic properties. 相似文献
9.
10.
Luc Huy Hoang Pham Van Hai Pham Van Hanh Nguyen Hoang Hai Xiang-Bai Chen In-Sang Yang 《Materials Letters》2011,65(19-20):3047-3050
Ti1 ? xVxO2 (x = 0.0–0.10) nanopowders were successfully synthesized by a microwave-assisted sol–gel technique and their crystal structure and electronic structure were investigated. The products were characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), Raman and UV–Vis spectroscopy. The results revealed that TiO2 powders maintained the anatase phase for calcination temperature below 600 °C, but gradually changed to the rutile phase above 800 °C. The formation of the rutile phase was completed at 1000 °C. For Ti1 ? xVxO2 (x = 0.05) powders, the phase transformation appeared at 600 °C. The absorption edge of Ti1 ? xVxO2 (x > 0) powders broadened to the visible region with increasing V concentration and a strong visible light absorption was obtained with 10% V doping. V doping and subsequent coexistence of both anatase and rutile phases in our Ti1 ? xVxO2 nanoparticles are considered to be responsible for the enhanced absorption of visible light up to 800 nm. 相似文献