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排序方式: 共有291条查询结果,搜索用时 15 毫秒
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基于在硫酸介质中,铼催化溴酸钠氧化铬黑T的褪色反应,建立了测定铼的光度分析新方法。确定了催化体系的动力学条件,计算得出催化反应的表观活化能Ea=39.12KJ/mol,反应速率常数为K=1.248×10-3/s。在选定的试验优条件下,铼的浓度在0~10.02mg/L范围内与相对吸光度呈良好的线性关系,检出限为2.7675mg/L。方法所用仪器简单,操作简便。 相似文献
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研究了一种化学气相沉积(CVD)制备超细铼粉的新方法,即以NH4ReO7为原料,通过将其分解为Re2O7后气相输运至还原区,经氢气还原生成超细铼粉。对不同还原温度下制备的超细铼粉样品,采用XRD、SEM、激光粒度分析进行表征,实验揭示了烧结作用对晶粒尺寸、形貌、表面状态及粒度等粉末性能的影响规律。结果表明,随还原温度升高,烧结作用增强,制备的超细铼粉晶粒尺寸增大,具有更好的球形度,表面趋于光洁,平均粒径增大。 相似文献
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Min Jia Hongmin Cui Weiqun Jin Lili Zhu Yu Liu Ji Chen 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》2013,88(3):437-443
BACKGROUND: Rhenium is a rare and valuable metal coexisting with molybdenum in molybdenite and sulfide copper ores and is hard to separate. Methods such as solvent extraction, ion exchange, adsorption, precipitation, etc. have been used to separate and purify Re(VII), and resin ion exchange has been widely investigated and used owing to its convenient operation and relatively low‐cost. The main challenge comes from the preparation of resins having high performance and stability. In an earlier study, an N‐methylimidazolium functionalized strong basic anion exchange resin was successfully synthesized and used for Cr(IV) extraction. This paper, reports on further synthesis and application of this resin for adsorption and separation of Re(VII) and Mo(VI), especially from copper arsenic filter cake. RESULTS: At pH 6.25, Re(VII) and Mo(VI) can be effectively separated with the N‐methylimidazolium functionalized strong basic anion exchange resin, giving a Re(VII) recovery of up to 93.3%, but only 5.1% for Mo(VI). When using the copper arsenic filter cake sample 89.1% Re(VII) recovery was achieved. CONCLUSION: The N‐methylimidazolium functionalized strong basic anion exchange resin exhibited high selectivity and recovery for Re(VII) in a mixed system. © 2012 Society of Chemical Industry 相似文献
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Dehydrogenation of Light Alkanes Over Rhenium Catalysts on Conventional and Mesoporous MFI Supports 总被引:1,自引:0,他引:1
Anne Krogh Rovik Anke Hagen Iver Schmidt Søren Dahl Ib Chorkendorff Claus Hviid Christensen 《Catalysis Letters》2006,109(3-4):153-156
Recently, Re/HZSM-5 (Si/Al = 15) was shown to be an efficient catalyst for ethane dehydrogenation and aromatization at 823 K
and atmospheric pressure. In this reaction, the major initial products were benzene, toluene and xylene (BTX), but increasing
amounts of ethene were produced with time on stream due to deactivation of the catalyst. We show that by use of rhenium impregnated
MFI supports with very few or no acidic sites (Si/Al > 500), highly selective ethane dehydrogenation catalysts are obtained
with ethene selectivities of 98%. By use of mesoporous MFI supports (Si/Al >500) the lifetime of the catalyst appears to be
slightly improved compared to conventional MFI crystals. The beneficial effect of a mesoporous MFI support is convincingly
demonstrated in propane dehydrogenation, where both conversion and selectivities on the mesoporous MFI (Si/Al > 500) impregnated
with Re are significantly higher than on Re supported on a comparable conventional MFI support. 相似文献
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Øyvind Borg Sølvi Storsæter Sigrid Eri Hanne Wigum Erling Rytter Anders Holmen 《Catalysis Letters》2006,107(1-2):95-102
The effect of water on the activity and selectivity for a series of γ-Al2O3 supported cobalt Fischer–Tropsch catalysts has been studied in an isothermal fixed-bed reactor at T = 483 K, P = 20 bar, and H2/CO = 2.1. The catalysts were produced applying incipient wetness impregnation and consisted of 20 wt.% cobalt and 0.5 wt.%
rhenium deposited on γ-Al2O3 supports with different pore characteristics. For the narrow-pore catalysts, addition of water corresponding to an inlet
partial pressure ratio of PH2O/PH2 = 0.4 reduced the reaction rates. In contrast, for a catalyst with larger pores the same water pressure increased the reaction
rates. For all catalysts, water amounts equal to PH2O/PH2 = 0.7 at the reactor inlet suppressed the reaction rates and led to permanent deactivation. The addition of water increased
the C5+ selectivity and decreased the CH4 selectivity for all catalysts. The pore characteristics seem to determine the effect of water on the rates. 相似文献
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