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1.
With the increase of industrialization and urbanization, humankind faces massive oil-based pollution due to tanker accidents, human error, and natural disasters. For this, hydrophobic sorbents are fabricated and their applications for the removal of oil from polluted water sources are investigated. These hydrophobic sorbents are prepared by the condensation reaction of poly(dimethylsiloxane) and tris[3-(trimethoxysilyl)propyl]isocyanurate cross-linker via bulk polymerization. The obtained sorbents exhibit high oil sorption capacity, fast absorption–desorption kinetics, and great reusability. Moreover, they can selectively absorb oil from the water surface, thus making them practical for water clean-up applications. 相似文献
2.
Junyu Chen Yuze Li Yuming Jiang Liucheng Mao Mi Lai Lixia Jiang Huihui Liu Zongxiu Nie 《Advanced functional materials》2021,31(52):2106743
Cancer remains an intractable medical problem. Rapid diagnosis and identification of cancer are critical to differentiate it from nonmalignant diseases. High-throughput biofluid metabolic analysis has potential for cancer diagnosis. Nevertheless, the present metabolite analysis method does not meet the demand for high-throughput screening of diseases. Herein, a high-throughput, cost-effective, and noninvasive urine metabolic profiling method based on TiO2/MXene-assisted laser desorption/ionization mass spectrometry (LDI-MS) is presented for the efficient screening of bladder cancer (BC) and nonmalignant urinary disease. Combined with machine learning, TiO2/MXene-assisted LDI-MS enables high diagnostic accuracy (96.8%) for the classification of patient groups (including 47 BC and 46 ureteral calculus (UC) patients) from healthy controls (113 cases). In addition, BC patients can also be identified from noncancerous UC individuals with an accuracy of 88.3% in the independent test cohort. Furthermore, metabolite variations between BC and UC individuals are investigated based on relative quantification, and related pathways are also discussed. These results suggest that this method, based on urine metabolic patterns, provides a potential tool for rapidly distinguishing urinary diseases and it may pave the way for precision medicine. 相似文献
3.
《International Journal of Hydrogen Energy》2019,44(34):18903-18914
Hydrogen adsorption and desorption over Ru/SiO2 and Ru/Vulcan are investigated in terms of hydrogen storage and release characteristics by both dynamic and static experiments. Ru particle dispersions as a function of metal loading were determined by HR-TEM and volumetric chemisorption experiments. Vulcan was more accommodating for spillover hydrogen than SiO2. High Ru dispersions, i.e., small particle sizes, favored the amount of hydrogen spillover to Vulcan, as revealed by temperature programmed desorption (TPD) of hydrogen. TPD of hydrogen under He flow experiments over Ru/SiO2 and Ru/Vulcan materials revealed a low temperature process (up to 200 °C) attributed to desorption of weakly bound hydrogen from Ru metal surface. A high temperature process (above 450 °C) was attributed to diffusion of hydrogen from the support to the Ru particle and desorption at the Ru sites. Hydrogen adsorbs strongly on Ru metal, as indicated by the initial heats of H2 adsorption measured as 100 kJ/mol over 1 wt% Ru/Vulcan by adsorption calorimetry. At higher coverages, heat of adsorption of hydrogen was measured as 10 kJ/mol. Low heat of adsorption of hydrogen at high coverages indicate multilayer weak adsorption of hydrogen over the storage material, which can desorb at lower temperatures. 相似文献
4.
羟乙基乙二胺(AEE)水溶液的CO2循环吸收量高(1.2molCO2/molAEE),吸收速度快,稳定性好,但解吸速度慢、解吸量少(0.8mol CO2/mol AEE)是限制该技术广泛应用的主要原因。本文通过向AEE水溶液中添加质量分数为0.05%~0.20%的改性氧化钛(TiO2-MWCNT和TiO2-OH)强化AEE的解吸能力。CO2循环吸收(40℃)-解吸(120℃)实验结果表明改性氧化钛的添加比氧化钛强化CO2解吸效果更好,强化顺序为TiO2-MWCNT>TiO2-OH;其对应的最大解吸速率分别为0.093L/min(质量分数0.15%)和0.083L/min(质量分数0.20%),相对于AEE水溶液,分别提高了32.9%和18.6%;其对应的最大解吸量分别为0.92molCO2/molAEE(质量分数0.15%)和0.88molCO2/molAEE(质量分数0.20%),分别提高了12.2%和9.7%;其对应的CO2循环吸收量分别是0.95molCO2/molAEE(质量分数0.15%)和0.89molCO2/molAEE(质量分数0.15%),分别提高了18.75%和11.25%;5次循环吸收解吸实验结果表明改性氧化钛强化CO2解吸效果稳定,具有较强的化学稳定性。对反应后的改性氧化钛进行XRD、BET、FTIR和SEM表征,结果表明改性氧化钛具有较强的结构稳定性。TiO2-MWCNT和TiO2-OH在促进有机胺溶液解吸CO2方面具有一定的工业应用潜力。 相似文献
5.
Global decrease in crude oil resources and frequent crude oil leaks cause the energy crisis and ecological pollution. The absorption and release of leaked crude oil through absorption materials are a necessary process for environmental protection and recycling. In this article, a CO2-responsive olefin copolymer was obtained by copolymerization of styrene and an amine-containing olefin monomer. The structure of resultant copolymer was characterized by FTIR; thermal properties and CO2-responsive morphology changes were determined by DSC/TGA and SEM, respectively. Copolymers had certain absorption capacity for toluene with absorption rate up to 180.0%. The absorbed toluene could be released upon CO2 stimulation with desorption rate up to 84.6%. The CO2-responsive copolymer could be regenerated through a simple heating process and showed stable absorption–desorption performance even after being recycled for 4 times. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47439. 相似文献
6.
《International Journal of Hydrogen Energy》2019,44(17):8751-8758
Understanding the influence of plastic deformation on diffusion is critical for hydrogen embrittlement (HE) study. In this work, thermal desorption spectroscope (TDS), slow strain rate test (SSRT), feritscope, transmission electron microscope (TEM) and TDS model were used to study the relation between plastic deformation and hydrogen diffusion, aiming at unambiguously elucidating the effect of plastic deformation on hydrogen diffusion of austenitic stainless steel, S30408. An effective method was developed to deduce apparent hydrogen diffusion coefficient of austenitic stainless steel in this paper. Results indicate apparent hydrogen diffusion coefficient decreases firstly and then increases with increasing plastic deformation at room temperature. Hydrogen diffusion effected by plastic deformation is a complicated process which is suggested to be divided into two processes controlled by dislocation and strain-induced martensite, respectively, and the transition point is about 20% strain demonstrated by experiments in this case. 相似文献
7.
8.
Due to the availability and timeliness of autologous cells, the in vitro cultivation and expansion of cells in large scale is very necessary before clinical treatments. However, traditional cell-harvesting methods including machinery scraper and enzymatic method would produce irreversible damage for treated cells. The appearance of intelligent temperature-responsive cell culture surfaces can solve the problem. Therefore this review focuses on the development of temperature-responsive surfaces based on poly(N-isopropylacrylamide) in recent years and the impact on cell adsorption and desorption processes. 相似文献
9.
《International Journal of Hydrogen Energy》2020,45(30):15281-15293
In this work, absorption/desorption isotherms of the LaNi3·6Mn0·3Al0·4Co0.7 alloy, have been determined from the experimental data at three temperatures (TFluid = 298 K, TFluid = 303 K, and TFluid = 313 K). However, the experimental isotherms are compared with a proposed theoretical model. The physicochemical parameters of the proposed model are determined from the experimental data. Using these parameters, the absorption and desorption processes of hydrogen by the LaNi3·6Mn0·3Al0·4Co0.7 alloy can be compared. During the absorption/desorption process, the behaviors of each parameter are studied under the effect of temperature and pressure. In addition, internal energy, entropy, and enthalpy are calculated by using the proposed model. On the other hand, the temperature and pressure effects on the variation of these functions have been studied. The calculated physicochemical parameters suggested that the hydrogen absorption/desorption process in the LaNi3·6Mn0·3Al0·4Co0.7 alloy was feasible, spontaneous and exothermic in nature. 相似文献
10.
《International Journal of Hydrogen Energy》2022,47(70):30234-30247
The dehydrogenation temperature of LiAlH4 was significantly reduced by the production of mixtures with ZrCl4. Stoichiometric 4:1, and 5 mol % mixtures of LiAlH4 and ZrCl4 were produced by ball milling at room temperature and ?196 °C, and tested for dehydrogenation at low temperature. Cryogenic ball-milling resulted in an effective way to produce reactive mixtures for hydrogen release; because of achieving small aggregates size (5–20 μm) in 10 min of cryomilling while preventing substantial decomposition during preparation. Dehydrogenation reaction in the mixtures LiAlH4/ZrCl4 started around 31–47 °C under different heating rates. Partial dehydrogenation was proved at 70 °C: 4.4 wt % for the 5 mol% ZrCl4–LiAlH4 mixture, and 3.4 wt % for the best 4:1 stoichiometric mixture. Complete dehydrogenation up to 250 °C released 6.4 wt% and 4.1 wt%, respectively. Dehydrogenation reactions are exothermic, and the LiAlH4/ZrCl4 mixtures are unstable and difficult to handle. The activation energy of the exothermic reactions was estimated as 113.5 ± 9.8 kJ/mol and 40.6 ± 6.6 kJ/mol for 4LiAlH4+ZrCl4 and 5%mol ZrCl4+LiAlH4 samples milled in cryogenic conditions, respectively. The dehydrogenation pathway was changed in the LiAlH4/ZrCl4 mixtures as compared to pure LiAlH4. Dehydrogenation reaction is proposed to form Al, LiCl, Zr, and H2 as main products. Modification of the dehydrogenation reaction of LiAlH4 was achieved at the cost of reducing the total hydrogen release capacity. 相似文献