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Fe的原位掺杂对Pt/Silicalite-1催化丙烷脱氢反应性能的提升作用 被引量:1
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作者 沈姗姗 刘晓晖 +1 位作者 郭勇 王艳芹 《物理化学学报》 SCIE CAS CSCD 北大核心 2023年第7期79-88,共10页
利用一步水热法制备了原位掺杂Fe的Silicalite-1分子筛载体,浸渍得到相应的Pt基催化剂,用于丙烷的直接脱氢反应。作为对比,也制备了Pt/Silicalite-1和共浸渍的Pt1Fe2/Silicalite-1催化剂。研究发现较之Pt/Silicalite-1催化剂,原位掺入Fe... 利用一步水热法制备了原位掺杂Fe的Silicalite-1分子筛载体,浸渍得到相应的Pt基催化剂,用于丙烷的直接脱氢反应。作为对比,也制备了Pt/Silicalite-1和共浸渍的Pt1Fe2/Silicalite-1催化剂。研究发现较之Pt/Silicalite-1催化剂,原位掺入Fe的Pt/Fe-Silicalite-1催化剂反应性能有了很大程度地提高,而共浸渍制备的Pt1Fe2/Silicalite-1催化剂反应性能有所降低。在Pt/Fe-Silicalite-1催化剂上,尽管丙烷的初始转化率略有降低,但丙烯的选择性和催化稳定性大幅提高。反应8h后丙烷转化率稳定在43.7%、丙烯选择性达到98.0%;且在80h内基本保持不变。深入表征发现Fe的原位掺入使得Pt物种配位饱和度提高,避免了丙烷的深度脱氢使得丙烯选择性提高、结焦速率降低;且通过Fe-Pt之间电子转移,使得Pt上的电子云密度增强,增强了丙烯的脱附能力,进一步降低了结焦速率。另外载体中的Fe位点可以锚定Pt,使得Pt物种不易聚集,从而进一步提高了Pt/Fe-Silicalite-1的稳定性,使得该催化剂在反应80 h后仍保持高转化率和选择性。 展开更多
关键词 丙烷脱氢 SILICALITE-1 Pt基催化剂 Fe原位掺杂
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Analysis of the binding sites with NL-101 to amino acids and peptides by HPLC/MS/MS 被引量:4
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作者 Lingzi Dai Nian Guo +3 位作者 Yaqin Liu shanshan shen Qiufu Ge Yuanjiang Pan 《Chinese Chemical Letters》 SCIE CAS CSCD 2019年第1期103-106,共4页
The binding between NL-101, a novel nitrogen mustard anti-cancer drug, with amino acids and peptides has been investigated by high performance liquid chromatography electrospray tandem mass spectrometry(HPLC/ESI-MS/MS... The binding between NL-101, a novel nitrogen mustard anti-cancer drug, with amino acids and peptides has been investigated by high performance liquid chromatography electrospray tandem mass spectrometry(HPLC/ESI-MS/MS). This study offers supporting data of the interaction among drug and amino acids and peptides, which could potentially explain the cytotoxic and mutagenic effects of the drug. Collision-induced dissociation(CID) experiment demonstrated that under the same collision energy, the amino group combined with NL-101 adducts are sensitive and often produce more fragment ions; the carboxyl group combined with NL-101 adducts are hard to break and display fewer fragment ions. In addition, when other group(like sulfhydryl group) of amino acids binds to NL-101, CID spectra show different fragmentation pattern. These differences could display structural information about the drug adducts and be utilized as location of the authentic binding sites. 展开更多
关键词 High-performance liquid chromatography/ tandem mass SPECTROMETRY NL-101 AMINO ACIDS PEPTIDES Binding sites
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Boundary evaluation and error correction on pseudorandom spread spectrum photon counting system
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作者 shanshan shen Qian Chen +1 位作者 Weiji He Vuqiang Wang 《Chinese Optics Letters》 SCIE EI CAS CSCD 2017年第9期36-40,共5页
The Cramer–Rao lower bound on range error is modeled for pseudo-random ranging systems using Geiger-mode avalanche photodiodes. The theoretical results are shown to agree with the Monte Carlo simulation, satisfying b... The Cramer–Rao lower bound on range error is modeled for pseudo-random ranging systems using Geiger-mode avalanche photodiodes. The theoretical results are shown to agree with the Monte Carlo simulation, satisfying boundary evaluations. Experimental tests prove that range errors caused by the fluctuation of the number of photon counts in the laser echo pulse leads to the range drift of the time point spread function. The function relationship between the range error and the photon counting ratio is determined by using numerical fitting.Range errors due to a different echo energy is calibrated so that the corrected range root mean square error is improved to 1 cm. 展开更多
关键词 Boundary evaluation and error correction on pseudorandom spread spectrum photon counting system
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