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71.
以高铼酸银为起始物,合成了在空气和湿气环境中稳定的新型稀散金属铼离子液体,并对其进行了核磁氢谱、拉曼光谱及DSC的表征,验证了所合成的离子液体结构的正确性,且离子液体的含水量小于0.7%,纯度较高. 相似文献
72.
铼/铱发动机喷管研究最新进展 总被引:1,自引:0,他引:1
Re/Ir发动机是美国研制成功的应用于空间飞行器的第三代高性能发动机.作者对Re/Ir发动机的核心部件-Re/Ir喷管研究的国内外进展进行了简要的评述,内容包括:Re和Ir的性能;Re和Ir的CVD制备;Re/Ir喷管的制备;Re/Ir喷管的连接以及发动机工作寿命等. 相似文献
73.
Feili Lai Nan Chen Xiaobin Ye Guanjie He Wei Zong Katherine B. Holt Bicai Pan Ivan P. Parkin Tianxi Liu Renjie Chen 《Advanced functional materials》2020,30(11)
Electrocatalytic nitrogen reduction reaction (NRR) and hydrogen evolution reaction (HER) are intriguing approaches to nitrogen fixation and hydrogen production under ambient conditions, given the need to discover efficient and stable catalysts to light up the “green chemistry” future. However, bottlenecks are often found during N2/H2O activation, the very first step of NRR/HER, due to energetic electron injection from the surface of electrocatalysts. It is reported that the bottlenecks for both NRR and HER can be tackled by engineering the energy level via low‐valent transition‐metal doping, simultaneously, where rhenium disulfide (ReS2) is employed as a model platform to prove the concept. The doped low‐valent transition‐metal domains (e.g., Fe, Co, Ni, Cu, Zn) in ReS2 provide more active sites for N2/H2O chemisorption and electron transfer, not only weakening the N?N/O? H bonds for easier dissociation through proton coupling, but also elevating d‐band center toward the Fermi level with more electron energy for N2/H2O reduction. As a result, it is found that iron‐doped ReS2 nanosheets wrapped nitrogen‐doped carbon nanofiber (Fe‐ReS2@N‐CNF) catalyst exhibits superior electrochemical activity with eightfold higher ammonia production yield of 80.4 µg h?1 mg?1cat., and lower onset overpotential of 146 mV and Tafel slope of 63 mV dec?1, when comparing with the pristine ReS2. 相似文献
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Reactions of (CO)5Re(Br), (η5‐C5H5)Ru(Cl)(PPh3)2, and [Pt(μ‐Cl)(C6F5)(S(CH2CH2‐)2)]2 with the alkyne‐containing phosphine Ph2P(CH2)6C≡CCH3 give the bis(phosphine) complexes fac‐(CO)3Re(Br)(Ph2P(CH2)6C≡CCH3)2 ( 5 ), (η5‐C5H5)Ru(Cl)(Ph2P(CH2)6C≡CCH3)2 ( 6 ), and trans‐(Cl)(C6F5)Pt(Ph2P(CH2)6C≡CCH3)2 ( 7 ). Alkyne metatheses with the catalyst (t‐BuO)3W(≡C‐t‐Bu) (10–15 mol %, chlorobenzene, 80 °C) give the seventeen‐membered metallamacrocycles fac‐(CO)3Re(Br)(Ph2P(CH2)6CC(CH2)6P Ph2) ( 8 ), (η5‐C5H5)Ru(Cl)(Ph2P(CH2)6CC(CH2)6P Ph2) ( 9 ), and trans‐(Cl)(C6F5)Pt(PPh2(CH2)6CC(CH2)6P Ph2) ( 10 ). 31P NMR analyses show 90–75% conversions to 8 – 10 (59–47% isolated after chromatography). The identity of 8 was confirmed by a crystal structure, and 10 was hydrogenated over Pd/C to fac‐(CO)3Re(Br)(Ph2P(CH2)6CC(CH2)6P Ph2) ( 12 , 87%), which was crystallographically characterized earlier. A catalyst derived from Mo(CO)6/4‐chlorophenol effects a slower conversion of 7 to 10 at 140 °C. In the case of 5 , a mer, trans isomer of 8 is isolated ( 11 , 44%), as established by NMR and IR data. In 10 – 12 , the diphosphines span trans positions. These results, together with previous examples involving group VIII metallocenes, establish the wide viability of the title reaction. 相似文献
77.
T. Ohmori H. Yamada S. Narita T. Mizuno Y. Aoki 《Journal of Applied Electrochemistry》2003,33(7):643-646
It was found that potassium forms on rhenium electrodes during plasma electrolysis in K2CO3/H2O and K2CO3/D2O solutions, and the new potassium has unnatural isotopic ratios. The isotope 41K increases from the natural abundance, 6.7%, to as much as 32–37%. The percentage of 41K in the potassium contamination in a rhenium electrode before electrolysis was close to the natural isotopic abundance (6.7%). This result suggests that the 41K was enriched by some unknown process connected with a vigorous discharge of plasma electrolysis. 相似文献
78.
采用双氧水常压氧化浸出富铼渣,考察液固比、双氧水用量、硫酸浓度、浸出温度和时间对铼浸出率的影响。结果表明,在液固比2∶1,双氧水体积为水2倍,硫酸浓度20g/L,室温下搅拌浸出2h的最优条件下,富铼渣中铼的综合平均浸出率达到96.52%。 相似文献
79.
三道庄多金属共生矿综合利用浅析 总被引:1,自引:0,他引:1
三道庄钼钨矿床属多金属共生矿,介绍了三道庄钼钨矿床的地质构造特征,分析了资源开采的现状和存在的问题,并对资源综合利用的前景进行了展望。 相似文献
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