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Improving plasma sterilization by constructing a plasma photocatalytic system with a needle array corona discharge and Au plasmonic nanocatalyst
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作者 朱斌 李其玮 +3 位作者 高亚楠 闫妍 朱益民 徐力 《Plasma Science and Technology》 SCIE EI CAS CSCD 2023年第1期111-119,共9页
Efficient sterilization by a plasma photocatalytic system(PPS)requires strong synergy between plasma and photocatalyst to inactivate microorganisms while suppressing the formation of secondary pollutants.Here,we repor... Efficient sterilization by a plasma photocatalytic system(PPS)requires strong synergy between plasma and photocatalyst to inactivate microorganisms while suppressing the formation of secondary pollutants.Here,we report that a PPS constructed from a needle array corona discharge and Au/TiO2plasmonic nanocatalyst could remarkably improve the sterilization of Escherichia coli(E.coli)and alleviate formation of the discharge pollutant O3.At 6 kV,the combination of corona discharge and Au/TiO2achieves sterilization efficiency of 100%within an exposure time of 5 min.At 5 kV and an exposure time of 8 min,the presence of Au/TiO2improves sterilization efficiency of the corona discharge from 73%to 91%and reduces the O3concentration from 0.38 to 0.04 ppm,whereas the presence of TiO2reduces the sterilization efficiency and O3concentration to 66%and 0.17 ppm,respectively.The Au/TiO2in the PPS enables a uniform corona discharge,enhances the interaction between plasma,E.coli and nanocatalysts,and suppresses the formation of O3.Further,the Au/TiO2can be excited by ultraviolet-visible light emitted from the plasma to generate electron-hole pairs,and thus contributes to the formation of reactive radicals and the oxidative inactivation of E.coli.The PPS constructed from a needle array corona discharge and Au-based plasmonic nanocatalyst provides a promising approach for developing high-efficiency sterilization techniques. 展开更多
关键词 plasma photocatalysis STERILIZATION corona discharge au/TiO2 nanocatalyst synergetic effect
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HNTs@CeO_(2)-Au@Co_(3)O_(4)催化还原对硝基苯酚和染料污染物
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作者 方嘉声 陈铭 +4 位作者 刁琪琪 赵硕 黄振庭 卫昆 卓琼芳 《中国环境科学》 EI CAS CSCD 北大核心 2024年第1期193-201,共9页
制备了HNTs@CeO_(2)-Au@Co_(3)O_(4)核壳中空管状复合催化剂,用于还原降解水体中对硝基苯酚(4-NP)和染料(MB,MO)污染物.采用TEM,SEM,EDS,XRD,N_(2)吸脱附,XPS等方法对催化剂微观结构和物化特征进行表征.结果表明,CeO_(2)和Co_(3)O_(4)... 制备了HNTs@CeO_(2)-Au@Co_(3)O_(4)核壳中空管状复合催化剂,用于还原降解水体中对硝基苯酚(4-NP)和染料(MB,MO)污染物.采用TEM,SEM,EDS,XRD,N_(2)吸脱附,XPS等方法对催化剂微观结构和物化特征进行表征.结果表明,CeO_(2)和Co_(3)O_(4)作为内外活性层较好地分散固载Au纳米颗粒,通过界面反应构筑于埃洛石纳米管中,形成CeO_(2)/Co_(3)O_(4)叠层结构封装埃洛石载金核壳复合催化剂(HNTs@CeO_(2)-Au@Co_(3)O_(4)).该催化剂分别在3.5,8和3min内可还原去除96%以上的4-NP,MB和MO污染物,其相应的一级反应动力学速率常数(0.856,0.370,1.337min^(-1))和转换频率(10.99,1.90,2.80min^(-1))均明显优于HNTs-Au@Co_(3)O_(4),HNTs@CeO_(2)-Au和HNTs@CeO_(2)@Co_(3)O_(4)对照材料.HNTs@CeO_(2)-Au@Co_(3)O_(4)催化剂连续进行6次使用后,仍保持较高的4-NP,MB和MO污染物还原转化率(91.2%,87.3%,89.5%)和结构稳定性.独特的CeO_(2)/Co_(3)O_(4)叠层结构特征和复合组分协同增强效应有效促进了高性能催化体系的构建,极大提升了Au颗粒的催化活性和稳定性,使HNTs@CeO_(2)-Au@Co_(3)O_(4)催化剂呈现较为优异的催化效能和循环使用性能. 展开更多
关键词 纳米金催化剂 埃洛石 核壳结构 对硝基苯酚 染料污染物 催化还原
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负载型Au纳米催化剂的制备及稳定性研究
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作者 可望 王婉人 汪杨 《化工新型材料》 CAS CSCD 北大核心 2022年第S01期390-396,400,共8页
由于负载型Au纳米催化剂容易在高温、高压的反应条件下中毒失活,因此提高催化剂的稳定性至关重要。通过双(亚乙基二氨)氯化金(Ⅲ)中间体,将Au纳米颗粒沉积在SBA-15孔道之中。使用SBA-15介孔材料作为载体,将Au纳米颗粒包裹在介孔结构之中... 由于负载型Au纳米催化剂容易在高温、高压的反应条件下中毒失活,因此提高催化剂的稳定性至关重要。通过双(亚乙基二氨)氯化金(Ⅲ)中间体,将Au纳米颗粒沉积在SBA-15孔道之中。使用SBA-15介孔材料作为载体,将Au纳米颗粒包裹在介孔结构之中,提高催化剂的稳定性;同时,使用原子层沉积技术在SBA-15载体上制备TiO薄膜,稳定Au纳米颗粒。使用苯甲醇氧化反应评估催化活性。结果表明:所制备的负载型Au纳米催化剂稳定性较好,在连续3次反应后,Au纳米颗粒仍均匀分布在SBA-15的孔径中并且催化性能没有下降。 展开更多
关键词 金纳米颗粒 原子层沉积 二氧化钛薄膜 负载型纳米催化剂 催化剂稳定性
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Stable Au nanoparticles confined in boron nitride shells for optimizing oxidative desulfurization 被引量:1
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作者 Linjie Lu Jing He +7 位作者 Peiwen Wu Yang Sun Mingqing Hua Peng Cui Wenshuai Zhu Huaming Li Zhichang Liu Chunming Xu 《Nano Research》 SCIE EI CSCD 2023年第10期12076-12083,共8页
Supported gold(Au)nanocatalysts have long played an important role in numerous heterogeneous catalysis.However,the dominant difficulty of poor thermodynamic stability hampers its practical application.Herein,a core–s... Supported gold(Au)nanocatalysts have long played an important role in numerous heterogeneous catalysis.However,the dominant difficulty of poor thermodynamic stability hampers its practical application.Herein,a core–shell structured Au nanocatalyst with Au nanoparticles(NPs)confined in boron nitride(BN)shells is proposed for enhanced thermodynamic stability.The two-dimensional porous structure of BN not only functions as a physical separator for the sintering resistance of Au NPs,but also provides a microchannel for catalytic reaction substrates.Besides,owing to the confinement effect,a strengthened interaction between well-designed Au NPs and the BN can be expected,which further boosts the stability and catalytic activity.Detailed experiments show that a proper BN shell thickness is important to maintain the balance between the sintering resistance and catalytic activity.A significantly boosted performance of 97.2%conversion in oxidative desulfurization(ODS)was obtained with a proper number of BN coating layers,outperforming the one with a thicker BN shell.Moreover,the recyclability of the prepared catalyst was investigated with no obvious decrease in catalytic performance after 10 runs,greatly higher than that without a BN shell,suggesting excellent durability. 展开更多
关键词 oxidative desulfurization core–shell boron nitride au nanocatalyst confinement effect
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HF改性的多壁碳纳米管负载Au纳米粒子对甲醇的电催化氧化 被引量:4
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作者 肖海峰 张正富 +3 位作者 徐明丽 杨喜昆 江克柱 韩亚梅 《稀有金属》 EI CAS CSCD 北大核心 2012年第6期921-925,共5页
利用HF溶液处理20~40 nm的MWCNTs后,负载光化学还原法合成的Au纳米粒子,获得了HF改性的Au/MWCNTs纳米催化剂。TEM图表明Au纳米粒子平均粒径约为4.5 nm,均匀负载在MWCNTs表面。XPS结果表明Au/MWCNTs表面可能存在Au-F配位键。另外,C,F之... 利用HF溶液处理20~40 nm的MWCNTs后,负载光化学还原法合成的Au纳米粒子,获得了HF改性的Au/MWCNTs纳米催化剂。TEM图表明Au纳米粒子平均粒径约为4.5 nm,均匀负载在MWCNTs表面。XPS结果表明Au/MWCNTs表面可能存在Au-F配位键。另外,C,F之间易形成共价键。由于这些化学键的相互作用共同导致C,F,Au三者之间的电子效应,改变了Au的电子结构,从而有利于改善Au的负载效果,提高Au/MWCNTs的电催化活性。电化学测试结果表明Au/MWCNTs纳米催化剂对甲醇具有明显的电催化氧化活性和良好的稳定性。 展开更多
关键词 HF功能化处理 多壁碳纳米管 au MWCNTs纳米催化剂 碱性介质 甲醇
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