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61.
PVA基活性碳纤维的研制 总被引:2,自引:0,他引:2
探索了由民用大丝束聚乙烯醇纤维(PVAF)试制活性碳纤维(ACF)的可能性,以开辟新的原料路线,降低产品成本。PVAF首先用脱水剂处理,脱水剂浓度为10%(质量),然后在200—300℃进行热处理,处理后的纤维再经预氧化和碳化活化转化为ACF,ACF的收率为37.7%,比表面积为1050m~2/g。此外,还探索了用O_3处理PVAF。用差热、热失重和红外等手段对产物进行了表征,推论了相应的反应机理。结果表明:经适当处理的PVAF可制得具有较好吸附性能的ACF。 相似文献
62.
The disposal and re-use of spent bleaching clay from the vegetable oil processing industry is a problem of growing importance.
Although today the only practical way of removal of the spent material is disposal, extraction with organic solvents is a
well-known method of de-oiling contaminated bleaching clay. In our investigations we compare the extractibility of two different
types of bleaching clays with CO2 as a solvent. All experiments were carried out with a high-pressure extraction plant. The extraction and separation conditions,
temperature and pressure, as well as the CO2 mass flow, were varied during experiments. The aim of our investigations was a complete separation of the oil from the adsorbent.
The latter should then be re-used as bleaching clay. The oil and the bleaching clay were analyzed and tested, respectively.
The results show that oil of good quality can be recovered and the bleaching clay still has an activity approximately 50%
of fresh clay. 相似文献
63.
64.
该文利用多壁碳纳米管(MWCNTs)和聚(2-乙酰基-5-溴噻吩)复合纳米材料修饰电极,用于同时检测对苯二酚(HQ)、邻苯二酚(CC)和对甲苯酚(PC)。通过循环伏安法(CV),示差脉冲伏安法(DPV)和透射电镜(TEM)表征了该复合纳米材料的电化学性能和表面形貌。结果表明该电极对HQ、CC和PC具有较高的灵敏度和选择性。DPV峰电流与HQ、CC和PC的浓度在1.0×10-5~8.0×10-4mol/L,5.0×10-6~5.5×10-4mol/L和5.0×10-6~7.5×10-4mol/L范围内分别呈良好的线性关系,且检测限分别为3.0×10-6 mol/L,1.7×10-6 mol/L和2.0×10-6mol/L。 相似文献
65.
Three-dimensionally ordered long-range macroporous carbon structures were prepared using commercially available phenolic resin
by utilizing sacrificial colloidal silica crystalline arrays as templates that were subsequently removed by HF etching after
pyrolysis in an argon atmosphere. SEM, TEM, and BET were employed to characterize the morphology and the surface area of the
porous carbon structures. The pore size (150–1000 nm) and BET surface area, which reflect pore volume (298.6 m2/g (1.32 cm3/g) ∼ 93.7 m2/g (0.12 cm3/g)), of the macroporous carbon structures produced were approximately proportional to the size (150–1000 nm) of the sacrificial
silica sphere templates used (annealing temp. 550°C). The achieved 550 nm porous carbon structures were examined to function
as potential catalyst carriers and were successfully impregnated with Ag or Pt-Ru on their inner walls after borohydride reduction
at room temperature. In addition, porous carbon patterns were fabricated using the ‘micromolding in capillary’ technique,
which has potential applications in the microreaction technology. 相似文献
66.
Alumina supported vanadia catalysts (V/Al) for selective oxidehydrogenation of ethylbenzene with CO2 were prepared by impregnation method. During preparation the effect of promoters and calcined temperature was investigated,
it was found these two items had a strong influence on the activity of V/Al catalysts. Dehydrogenation reaction with CO2 was happened in the fixed-bed reactor at 450 °C. Results showed that 15.2% ethylbenzene conversion and 99.2% styrene selectivity
were acquired when V2K/Al catalyst was used. 相似文献
67.
A supercritical fluid extraction method has been applied to test the feasibility of tocopherol concentration from soybean
sludge with carbon dioxide at temperatures and pressures ranging from 35 to 70°C and 200 to 400 bar, respectively. The supercritical
solubility of the esterified soybean sludge was over 4–6 times greater than that of the original soybean sludge. By a simple
batch-type one-stage method the tocopherols in the esterified soybean sludge could be concentrated up to 40 wt%. The overall
results of the present study show that soybean sludge initially containing about 13–14 wt% tocopherols may require a countercurrent
multistage column to be highly and effectively concentrated. 相似文献
68.
Noboru Hashimoto Yasushi Sawada Takashi Bando Hiroyoshi Yoden Shigehito Deki 《Journal of the American Ceramic Society》1991,74(6):1282-1286
AIN powder was synthesized from aluminum polynuclear complexes. Basic aluminum chloride and basic aluminum lactate were used as the aluminum polynuclear complexes. These starting materials and glucose were dissolved in water and mixed homogeneously. AIN powder was obtained by calcining after drying and precalcining at 800°C under nitrogen gas flow. Then excess carbon was removed by firing in air. Nitridation in the system was investigated and compared with that in the alumina–carbon black system. It was found that in our reaction system nitridation began and proceeded at lower calcination temperatures above 1200°C than in the alumina–carbon black system. Using aluminum polynuclear complexes, AIN was synthesized through the nitridation of γ-alumina and produced in a very fine and sharp particle size distribution. 相似文献
69.
《Fuel》2003,82(2):147-151
The aim of this paper is to show how a cheap carbonaceous material such as low rank coal-based carbon (or char) can be used in the combined SO2/NO removal from exhaust gas at the linear gas velocity used in commercial systems (0.12 m s−1). Char is produced from carbonization and optionally activated with steam. This char is used in a first step to abate the SO2 concentration at the following conditions: 100 °C, space velocity of 3600 h−1, 6% O2, 10% H2O, 1000 ppmv SO2, 1000 ppmv NO and N2 as remainder. In a second step, when the SO2 concentration in the flue gas is low, NO is reduced to N2 and steam at the following experimental conditions: 150 °C, space velocity of 900 h−1, 6% O2, 10% H2O, 0-500 ppmv SO2, 1000 ppmv NO, 1000 ppmv NH3 and N2 as remainder.It has been shown that the presence of NO has no effect on SO2 abatement during the first step of combined SO2/NO removal system and that low SO2 inlet concentration has a negligible effect on NO reduction in the second step. Moreover, this char can be thermally regenerated after use for various cycles without loss of activity. On the other hand, this regenerated char shows the highest NO removal activity (compared to parent chars, either carbonized or steam activated) which can be attributed to the activating effect of the sulfuric acid formed during the first step of the combined SO2/NO removal system. 相似文献
70.