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亚甲基蓝在云母表面吸附状态的研究 被引量:12
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作者 赵立艳 王学恺 +2 位作者 郭玉国 吴念祖 谢有畅 《物理化学学报》 SCIE CAS CSCD 北大核心 2003年第10期896-901,共6页
利用XPS测定吸附前后亚甲基蓝(MB)各原子的电子结合能的变化,以判断原子化学环境的改变,从而确定MB在云母表面的吸附位点是二甲胺基上的氮原子.通过AFM测量得到吸附于云母表面的MB分子的平均高度为0.820nm,这证实了Hhner吸附模型的正确... 利用XPS测定吸附前后亚甲基蓝(MB)各原子的电子结合能的变化,以判断原子化学环境的改变,从而确定MB在云母表面的吸附位点是二甲胺基上的氮原子.通过AFM测量得到吸附于云母表面的MB分子的平均高度为0.820nm,这证实了Hhner吸附模型的正确性,即MB分子的最大横截面以65~70°倾斜在云母的(001)表面上. 展开更多
关键词 亚甲基蓝 云母 表面吸附状态 光电子能谱 原子力显微镜 阳离子染料 粘土矿物
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State of Pepsin and Acidic Protease in Solid Phase System and the Factors Increasing Their Destabilization
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作者 H. T. Hasanov A. H. Boboev +1 位作者 A. H. Hasanov M. M. Rahimov 《Journal of Food Science and Engineering》 2011年第4期303-312,共10页
The adsorption state and catalytic properties of pepsin and acidic protease from microorganisms Asp. awamori and Asp. oryzae were studied in solid phase system (in presence of sorsilen, DEAE- and CM-cellulose). Acco... The adsorption state and catalytic properties of pepsin and acidic protease from microorganisms Asp. awamori and Asp. oryzae were studied in solid phase system (in presence of sorsilen, DEAE- and CM-cellulose). According to the results, adsorption capacity and catalytic activity of enzymes depend on the physical nature of surface groups of the solid phase. Changing the stability of enzymes in the system with solid phase is observed even the adsorption bond is less stable (in the case of DEAE- and CM-cellulose in acidic media). Injection to the medium ethanol, surfactants, sodium chloride and changing the temperature of the incubation medium could prevent the negative effects of the solid phases. When sorsilen is used as solid phase, pepsin and acidic protease from Asp. awamori suffer from high surface inactivation. Various surfactants influence adsorption state of enzymes differently. Non-ionic surfactants (Triton X-100) prevent adsorption and restore catalytic properties of enzymes. 展开更多
关键词 PEPSIN acid proteinase Asp. awamori Asp. oryzae sorsilen adsorption state inactivation regulation.
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Gas adsorbate-induced Au atomic segregation and clustering from Cu(Au)
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作者 Lifeng Zhang Zejian Dong +1 位作者 Shuangbao Wang Langli Luo 《Science China Materials》 SCIE EI CAS CSCD 2021年第5期1256-1266,共11页
Surface compositional and phase segregation in an alloy can change its functionality, especially for applications where surface structure and chemistry play a vital role.For instance, the surface status of alloy catal... Surface compositional and phase segregation in an alloy can change its functionality, especially for applications where surface structure and chemistry play a vital role.For instance, the surface status of alloy catalysts significantly affects their catalytic performance for both heterogeneous and electrochemical processes. Surface segregation is believed to be driven by the difference in surface energy to reduce the total free energy of the alloy. However, the atomistic processes during the segregation process remain elusive, especially for gas molecule-induced segregation, where both structural and chemical reordering may occur. Herein, we achieved in-situ atomic-scale visualization of the surface segregation behaviors of a solid solution Cu(Au) alloy under the CO gas by an aberration-corrected environmental transmission electron microscope. CO-induced Cu(Au) surface ordering structures largely change the surface chemistry of the alloy. Further gas exposure at elevated temperature could facilitate Au atom diffusion through a specific "atomic channel" structure for dealloying and clustering on the surface. The segregated Au nanoparticles show rich phase and morphological dynamics interacting with the alloy surface, where the gas adsorption also plays an important role. These atomic insights provide direct evidence for the surface segregation and dealloying mechanisms of bimetallic alloys, and highlight the role of gas adsorbate in these surface processes. 展开更多
关键词 surface segregation CLUSTERING Cu(Au)alloy environmental TEM CO
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