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1)  reduced viscosity
还原粘度
2)  reduction temperature
还原温度
1.
Effect of reduction temperature on activities of alumina-supported tungsten phosphide in carbazole hydrodenitrogenation;
还原温度对氧化铝负载的磷化钨催化剂咔唑加氢脱氮活性影响(英文)
2.
The influence of reduction temperature and the pretreatment of reduction-reoxided on the hydrodesulfurization performance of Pd/Al2O3 and Pd-CeO2/Al2O3 catalysts have been investigated.
采用浸渍法制备CeO2改性的Pd/Al2O3加氢脱硫催化剂,考察了还原温度和还原-氧化预处理对Pd/Al2O3和Pd-CeO2/Al2O3催化剂加氢脱硫性能的影响。
3.
High-quality Mg-Zr intermediate alloy is produced through control of furnace charge proportion,reduction temperature and time,and by forward and backward mechanical agitation.
以KCl、NaCl为熔剂,用液态Mg还原K2ZrF6,通过控制炉料配比、还原温度、还原时间,并用机械正反向交替搅拌,成功地解决了传统生产工艺中渣相与Mg-Zr中间合金难以分离、合金杂质含量偏高、合金成分偏析的难题,获得了高质量的Mg-Zr中间合金。
3)  reducibility [ri,dju:sə'biliti]
还原度
1.
The effects of noble metal promoters on the structure of Co active species are reviewed and discussed in this paper,as well as the reducibility,dispersion,the formation of bimetallic particles or alloy,the behavior of deactivation and the influences on their catalytic performances.
本文重点讨论了贵金属助剂对活性钴物种的结构(还原度、分散度、双金属颗粒或合金的构成),钴基催化剂稳定性以及其对费-托合成的反应速率和产物选择性的影响规律。
4)  reductivity
还原程度
1.
For revealing the influence of the reductivity on macerals stacking structure,X-ray diffraction(XRD)was carried out to study the stacking structure characteristics of the vitrinite and inertinite from Pingshuo and Shendong coals with similar coal rank and petrographical composition but different reductivity.
采用X射线衍射法(XRD)对变质程度、煤岩组分相近但还原程度不同的平朔煤(较强还原性)、神东煤(较弱还原性)的镜质组和惰质组的堆垛结构特征进行表征,试图揭示还原程度对煤中不同显微组分堆垛结构的影响。
5)  Reduction degree
还原度
1.
Measuring basis for the characterization of reduction degree of methanation catalyst is suggested, and it is proposed that the catalyst not completely reduced should be reduced on-line once more.
分析新鲜甲烷化催化剂刚投用时,出口碳氧化合物偏高的原因,说明是催化剂未还原彻底造成,提出甲烷化催化剂表征还原度的衡量依据,建议在线对还原不彻底的催化剂进行重新还原。
6)  cobalt reducibility
Co还原度
1.
The FTS activity order was found to be: Co 1 5Th/HMS>Co/HMS>Co 1 5Zr/HMS>Co 1 5Mn/HMS>Co 1 5Ce/HMS under the conditions of H 2/CO=2 0, T =463~523 K, p =2 0 MPa, GHSV=500 h -1 , which was owing to the lower cobalt reducibility for Mn promoted Co/HMS and the cobalt oxidation at the beginning of FTS for Zr and Ce promoted Co/HMS despite t.
详细研究了钍、锆、锰及铈助剂对钴质量分数为 15 %的Co/HMS催化剂结构、F T合成CO转化率、CO2 选择性及烃分布的影响 ,结果表明 :钍能适当提高F T合成活性 ,且低温下具有较强的链增长能力 ;锆、锰、铈降低了催化剂CO转化率 ,催化剂加氢能力变强 ,导致低碳烃增加较快 ,汽柴油馏分段减低 ,相应的链增长能力降低 ,并以锰和铈较为明显 ;XRD ,TPR及TG表征表明 :锆和铈可提高催化剂Co还原度 ,但F T合成反应时金属Co易被氧化 ,反应中金属Co量明显减少 ,CO转化率降低 ,并以铈最为显著 ;Th助催化剂Co还原度稍有减低 ,Co分散度高于Co/HMS ,且反应中金属Co较为稳定 ,CO转化率得以提高 ;添加Mn助剂后 ,催化剂难以还原 ,反应中活性相金属Co量较小 ,CO转化率较低 。
补充资料:还原的
CAS:90218-40-9
中文名称:还原的;氧化的2,2'-(1,2-联二亚甲基)二[5-硝基]苯磺酸与4-[(4-氨基苯基)偶氮]苯磺酸的反应产物的钠盐
英文名称:Benzenesulfonic acid, 2,2'-(1,2-ethenediyl)bis[5-nitro-, reaction products with 4-[(4-aminophenyl)azo]benzenesulfonic acid,reduced, oxidized, sodium salts
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