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Preparation and Characterization of Fe^(3+)-doped Nanometer TiO_2 Photocatalysts 被引量:3
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作者 刘君武 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS 2006年第3期57-60,共4页
Fe^3+ -doped nanometer TiO2 photocatalysts were prepared by sol-gel technique. TiO2 powders with different Fe^3+ / Ti^4 + molar ratios ranging from 0. 05% to 25% were synthesized by calcinating the gels in the temp... Fe^3+ -doped nanometer TiO2 photocatalysts were prepared by sol-gel technique. TiO2 powders with different Fe^3+ / Ti^4 + molar ratios ranging from 0. 05% to 25% were synthesized by calcinating the gels in the temperature range of 200-600 ℃ . The effects of the content of iron ions and calcination temperature on the physical properties of the powders and their photocatalytic activities were examined by the photodecorapositon of methyl orange in sunlight. The results show that Fe dopant can decrease the temperature of nanatase-ratile transformation. The ideal photocatalytic property was achieved when the sample with an Fe^3+ / Ti^4+ ratio of 20 at% was calcined at about 300 ℃ for an hour, which is superior to that of commercial Degussa P-25. The optimum microstructure of the Fe-doped TiO2 for a high photocatalytic activity in sunlight is consisted of nanatase and ratile. 展开更多
关键词 TITANIA Fe^3 - doping SUNLIGHT methyl orange photocatalytic degradation
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Fe^(3+)-N改性二氧化钛光催化剂的研制 被引量:9
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作者 翦立新 殷小秋 +1 位作者 向建南 尹霞 《湖南大学学报(自然科学版)》 EI CAS CSCD 北大核心 2006年第1期79-82,共4页
利用微波等离子体沉膜技术和溶胶-凝胶法在载玻片上制备同时掺Fe3+和N的TiO2膜,经500℃焙烧后所得光催化剂性能较好.分别以紫外和可见光为光源,光催化降解茜素红,结果发现:掺铁量均为0.1%的Fe-N/TiO2较Fe/TiO2的光催化活性好,而且可见... 利用微波等离子体沉膜技术和溶胶-凝胶法在载玻片上制备同时掺Fe3+和N的TiO2膜,经500℃焙烧后所得光催化剂性能较好.分别以紫外和可见光为光源,光催化降解茜素红,结果发现:掺铁量均为0.1%的Fe-N/TiO2较Fe/TiO2的光催化活性好,而且可见光的利用率明显增强;UV-Vis扫描显示掺铁0.1%的Fe-N/TiO2紫外吸收峰较其他TiO2光催化剂强且明显红移.XRD谱图结果表明,分别在500℃和550℃焙烧后的0.1%Fe-N/TiO2,均为锐钛矿型,晶体粒度分别为15.3 nm和20.6 nm,XPS谱图显示Fe-N/TiO2有N1s谱峰. 展开更多
关键词 二氧化钛 等离子体 Fe^3+-n掺杂
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罗丹明B试法鉴定UO_2^(2+)用N-烯丙基-N′-(对苯磺钠)硫脲掩蔽Fe^(3+)的干扰 被引量:2
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作者 马万山 许春萱 +1 位作者 钟瑞琴 张秀兰 《信阳师范学院学报(自然科学版)》 CAS 2002年第2期188-189,共2页
以实验为基础 ,提出了用罗丹明 B试法鉴定 UO2 +2 时 ,用 N-烯丙基 - N′- (对苯磺酸钠 )硫脲掩蔽Fe3 +离子的干扰 .与传统的消除干扰的方法相比 ,具有条件容易控制 ,操作简便等优点 .
关键词 UO2^2+ 罗丹明B试法 N-烯丙基-n′-(对苯磺钠)硫脲 掩敝Fe^3+ 掩蔽剂 分析化学 离子鉴定 干扰消除
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基于碳纤维强化的Fe^(0)混养反硝化脱氮效能与机制
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作者 王铮 贾林春 +2 位作者 史大林 何月玲 薛罡 《工业水处理》 CAS CSCD 北大核心 2024年第4期66-75,共10页
以含NO_(3)^(-)-N合成废水为处理对象,对比了单独投加Fe^(0)与碳纤维强化Fe^(0)混养反硝化连续流反应器反硝化脱氮的效能。结果表明,在COD/NO_(3)^(-)-N为2.9~3.1、水力停留时间(HRT)为24 h时,投加碳纤维强化Fe^(0)的实验组R1对TN和NO_(... 以含NO_(3)^(-)-N合成废水为处理对象,对比了单独投加Fe^(0)与碳纤维强化Fe^(0)混养反硝化连续流反应器反硝化脱氮的效能。结果表明,在COD/NO_(3)^(-)-N为2.9~3.1、水力停留时间(HRT)为24 h时,投加碳纤维强化Fe^(0)的实验组R1对TN和NO_(3)^(-)-N平均去除率分别高达89.04%和97.13%,显著高于单独投加Fe^(0)的对照组R0。胞外聚合物(EPS)及电子传递活性(ETSA)变化规律表明,碳纤维的投入可进一步促进EPS生成,且强化了微生物对电子的利用率。扫描电镜-能量色散光谱仪(SEM-EDS)和X射线衍射仪(XRD)分析结果发现R1中Fe^(0)表面有明显的微生物腐蚀现象,FeO(OH)和含铁有机复合物是主要的腐蚀产物。微生物学分析表明,有机碳源投加量的提高及碳纤维的投加有效提高铁自养反硝化菌属丰度,促进反硝化功能基因的富集。 展开更多
关键词 NO_(3)^(-)-n废水 Fe^(0) 碳纤维 混养反硝化 COD/NO_(3)^(-)-n 微生物群落
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Influence mechanism of Fe^(3+)doping on the hydrophobic regulation of kaolinite/water interface:Experiments and MD simulations
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作者 Jun Chen Huanhuan Shang +3 位作者 Yunjia Ling Feifei Jia Yali Cheng Fanfei Min 《International Journal of Mining Science and Technology》 SCIE EI CAS 2024年第11期1575-1586,共12页
The surface/interfacial reactivity of clay is a critical factor influencing the sedimentation of coal slurry water.To achieve efficient sedimentation of coal slurry water,this paper introduces a novel approach that re... The surface/interfacial reactivity of clay is a critical factor influencing the sedimentation of coal slurry water.To achieve efficient sedimentation of coal slurry water,this paper introduces a novel approach that regulates the hydrophobicity of defective active sites in clay minerals.Fe^(3+)-doped kaolinite(Fe^(3+)-Kao)was synthesized by hydrothermal methods.Subsequently,tests were conducted on the adsorption capacity,surface wettability,and agglomeration sedimentation of alkyl amine/ammonium salts(AAS)on Fe^(3+)-Kao surfaces.Fe^(3+)doping significantly enhances AAS adsorption and alters surface properties from hydrophilic to hydrophobic,promoting kaolinite particle aggregation and sedimentation,thereby improving coal slurry water treatment efficiency.Molecular dynamics(MD)simulations were performed to analyze the statistical adsorption behavior of AAS on Fe^(3+)-Kao surfaces.The simulation results indicate that the mechanism by which Fe^(3+)doping influences the hydrophobic regulation of kaolinite surfaces is due to the enhanced interfacial interactions between the kaolinite surface and AAS,where the interfacial effects are more pronounced on surfaces closer to the dopant sites.The findings of this research offer valuable insights for future studies on other types of lattice defects in clay minerals,as well as for the development of more efficient treatment chemicals for coal slurry water. 展开更多
关键词 Kaolinite Fe^(3+)doping Hydrophobic regulation Hydrothermal synthesis Molecular dynamics
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Electrochemical synthesis of Ni doped carbon quantum dots for simultaneous fluorometric determination of Fe^(3+)and Cu^(2+)ion facilely
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作者 Siyuan Sun Yang Sun +4 位作者 Fan Yang Sai Che Xiaoyun Zhang Ge Zhang Yongfeng Li 《Green Chemical Engineering》 CSCD 2023年第1期115-122,共8页
A novel Ni doped carbon quantum dots(Ni-CQDs)fluorescence probe was synthesized by facile electrolysis of monoatomic Ni dispersed porous carbon(Ni–N–C).The obtained Ni-CQDs showed a high quantum yield of 6.3%with th... A novel Ni doped carbon quantum dots(Ni-CQDs)fluorescence probe was synthesized by facile electrolysis of monoatomic Ni dispersed porous carbon(Ni–N–C).The obtained Ni-CQDs showed a high quantum yield of 6.3%with the strongest excitation and emission peaks of 360 nm and 460 nm,and maintained over 90%of the maximum fluorescence intensity in a wide p H range of 3–12.The metal ions detectability of Ni-CQDs was enhanced by Ni doping and functional groups modification,and the rapid and selective detection of Fe^(3+)and Cu^(2+)ions was achieved with Ni-CQDs through dynamic and static quenching mechanism,respectively.On one hand,the energy band gap of Ni-CQDs was regulated by Ni doping,so that excited electrons in Ni-CQDs were able to transfer to Fe^(3+)easily.On the other hand,the abundant functional groups promoted the generation of static quenching complexation between Cu^(2+)and Ni-CQDs.In metal ions detection,the linear quantitation range of Fe^(3+)and Cu^(2+)were 100–1000μM(R^(2)=0.9955)and 300–900μM(R^(2)=0.9978),respectively.The limits of detection(LOD)were calculated as 10.17 and 7.88μM,respectively.Moreover,the fluorescence quenched by Cu^(2+)could be recovered by EDTA2-due to the destruction of the static quenching complexation.In this way,NiCQDs showed the ability to identify the two metal ions to a certain degree under the condition of Fe^(3+)and Cu^(2+)coexistent.This work paves the way of facile multiple metal ion detection with high sensitivity. 展开更多
关键词 Electrolysis Ni doped CQDs Fe^(3+)detection Cu^(2+)detection Ions distinction
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