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Fe/g-C_(3)N_(4)表面改性及其对CO加氢产物分布的影响 被引量:1
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作者 孙禹 高新华 +3 位作者 马清祥 范素兵 赵天生 张建利 《燃料化学学报(中英文)》 EI CAS CSCD 北大核心 2024年第1期19-28,共10页
采用尿素热缩合法制备了氮化碳(g-C_(3)N_(4)),经H_(2)O_(2)、NH_(3)·H_(2)O处理、浸渍法负载Fe制得改性Fe/g-C_(3)N_(4),对比研究了改性前后催化剂的CO加氢性能。结合XRD、SEM、FT-IR、CO_(2)-TPD、CO-TPD、H_(2)-TPR、接触角测试... 采用尿素热缩合法制备了氮化碳(g-C_(3)N_(4)),经H_(2)O_(2)、NH_(3)·H_(2)O处理、浸渍法负载Fe制得改性Fe/g-C_(3)N_(4),对比研究了改性前后催化剂的CO加氢性能。结合XRD、SEM、FT-IR、CO_(2)-TPD、CO-TPD、H_(2)-TPR、接触角测试和N_(2)物理吸附-脱附等系列表征,探究了表面预处理对Fe/g-C3N4催化剂织构性质以及CO加氢产物分布的影响。结果表明,不同改性方法对催化剂的织构性质和CO加氢性能影响显著。尿素热缩合法制备的g-C_(3)N_(4)具有典型蜂窝状结构,Fe与g-C_(3)N_(4)相互作用较强,且高度分散;改性前后样品均呈亲水性,且H_(2)O_(2)、 NH_(3)·H_(2)O处理后亲水性增强,H_(2)O_(2)处理增强了表面羟基,NH_(3)·H_(2)O处理增加了表面氨基,促进了CO吸附,促使Fe(NCN)物相生成;预处理后的催化剂表面碱性增强。在CO加氢反应中,两步改性后的Fe/AM-g-C3N4催化剂,CO_(2)选择性降至11.61%;Fe/AM-g-C_(3)N_(4)表面碱性增强,抑制了烯烃二次加氢,烯烃选择性较高,C_(2)^(=)-C_(4)^(=)达32.37%,O/P值3.23。 展开更多
关键词 Co加氢 表面改性 fe/g-C_(3)N_(4)催化剂 产物分布
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Fe掺杂Sn_(3)O_(4)纳米片的制备及其光催化性能
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作者 主欢 闵威 +2 位作者 邹倩 徐冰霜 谢辉 《化学研究与应用》 CAS 北大核心 2024年第10期179-184,共6页
本文采用水热法,将非贵金属Fe掺杂到Sn_(3)O_(4)纳米片晶格中制备了铁掺杂的Fe-Sn_(3)O_(4)复合光催化材料。通过X射线多晶衍射(XRD)、扫描电镜(SEM)、X射线光电子能谱(XPS)对合成的材料进行形貌、结构表征;以罗丹明B(RhB)为模拟污染物... 本文采用水热法,将非贵金属Fe掺杂到Sn_(3)O_(4)纳米片晶格中制备了铁掺杂的Fe-Sn_(3)O_(4)复合光催化材料。通过X射线多晶衍射(XRD)、扫描电镜(SEM)、X射线光电子能谱(XPS)对合成的材料进行形貌、结构表征;以罗丹明B(RhB)为模拟污染物,评价材料的光催化性能。实验结果表明,制备的Fe-Sn_(3)O_(4)为纳米片状,Fe成功掺杂入Sn_(3)O_(4)晶格中,Fe的掺杂提供了更多的活性位点,促进光生电荷分离和传输,材料的光催化性能由此得到了提高。当n(Sn)∶n(Fe)为100∶1时,材料的光催化性能最好,300 W氙灯照射120 min,降解率为87.77%,是纯Sn_(3)O_(4)(40.35%)的2.2倍。循环利用多次,材料仍有较好的光催化效果。 展开更多
关键词 四氧化三锡 水热法 铁掺杂 光催化降解
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BiOI/g-C_(3)N_(4)/NH_(2)-MIL-53(Fe)三元异质结光催化剂的合成与性能研究
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作者 何林 吴敏 《化工时刊》 CAS 2024年第3期15-22,共8页
半导体光催化技术是解决能源危机和环境污染的有效手段。作者采用一步溶剂热法制备了Bi OI/g-C_(3)N_(4)/NH_(2)-MIL-53(Fe)三元异质结催化剂。以X射线衍射、扫描电子显微镜等表征方法对样品进行分析,以双酚S为目标污染物考察了催化剂... 半导体光催化技术是解决能源危机和环境污染的有效手段。作者采用一步溶剂热法制备了Bi OI/g-C_(3)N_(4)/NH_(2)-MIL-53(Fe)三元异质结催化剂。以X射线衍射、扫描电子显微镜等表征方法对样品进行分析,以双酚S为目标污染物考察了催化剂的光催化性能,以自由基捕获实验得出·OH、h^(+)和·O_(2)^(-)在降解过程中均发挥强氧化作用,并基于催化剂光芬顿性能研究以及半导体能带结构,提出其催化光芬顿反应的可能的机理。 展开更多
关键词 Bi oI g-C_(3)N_(4) NH_(2)-MIL-53(fe) 光芬顿法
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Cathode nanoarchitectonics with Na_(3)VFe_(0.5)Ti_(0.5)(PO_(4))_(3): Overcoming the energy barriers of multielectron reactions for sodium-ion batteries
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作者 Vaiyapuri Soundharrajan Sungjin Kim +7 位作者 Subramanian Nithiananth Muhammad H.Alfaruqi JunJi Piao Duong Tung Pham Vinod Mathew Sang A.Han Jung Ho Kim Jaekook Kim 《Carbon Energy》 SCIE EI CAS CSCD 2024年第9期1-14,共14页
High electrochemical stability and safety make Na+superionic conductor(NASICON)-class cathodes highly desirable for Na-ion batteries(SIBs).However,their practical capacity is limited,leading to low specific energy.Fur... High electrochemical stability and safety make Na+superionic conductor(NASICON)-class cathodes highly desirable for Na-ion batteries(SIBs).However,their practical capacity is limited,leading to low specific energy.Furthermore,the low electrical conductivity combined with a decline in capacity upon prolonged cycling(>1000 cycles)related to the loss of active material-carbon conducting contact regions contributes to moderate rate performance and cycling stability.The need for high specific energy cathodes that meet practical electrochemical requirements has prompted a search for new materials.Herein,we introduce a new carbon-coated Na_(3)VFe_(0.5)Ti_(0.5)(PO_(4))_(3)(NVFTP/C)material as a promising candidate in the NASICON family of cathodes for SIBs.With a high specific energy of∼457 Wh kg^(-1) and a high Na+insertion voltage of 3.0 V versus Na^(+)/Na,this cathode can undergo a reversible single-phase solid-solution and two-phase(de)sodiation evolution at 28 C(1 C=174.7 mAh g^(-1))for up to 10,000 cycles.This study highlights the potential of utilizing low-cost and highly efficient cathodes made from Earth-abundant and harmless materials(Fe and Ti)with enriched Na^(+)-storage properties in practical SIBs. 展开更多
关键词 fe and Ti swapping Na_(3)Vfe_(0.5)Ti_(0.5)(Po_(4))_(3) prolonged cycle life structural stabilit
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柑橘皮提取液绿色合成纳米Fe3O4及其吸附水中孔雀石绿的性能研究
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作者 张梦凡 李春光 +5 位作者 王聪 王强 杜晨阳 柳雨晴 杨洁 王寒蕊 《郑州航空工业管理学院学报》 2024年第3期81-87,共7页
以柑橘皮提取液为还原剂和稳定剂,绿色合成Fe3O4纳米材料,利用扫描电子显微镜(SEM)、X射线衍射图谱(XRD)、傅立叶变换红外光谱(FT-IR)等手段对材料进行表征,并考察了其对孔雀石绿(MG)的吸附性能。结果表明:绿色合成纳米Fe3O4呈不规则圆... 以柑橘皮提取液为还原剂和稳定剂,绿色合成Fe3O4纳米材料,利用扫描电子显微镜(SEM)、X射线衍射图谱(XRD)、傅立叶变换红外光谱(FT-IR)等手段对材料进行表征,并考察了其对孔雀石绿(MG)的吸附性能。结果表明:绿色合成纳米Fe3O4呈不规则圆球体,分散性和结晶度较好。在投加量为1.0 g/L、初始pH为4、温度为25℃、初始浓度为20 mg/L时,对孔雀石绿的吸附率达到95.33%。纳米Fe3O4对MG的吸附过程分别符合准二级动力学方程和Langmuir等温方程。热力学研究表明,纳米Fe3O4吸附MG是自发吸热过程。绿色合成纳米Fe3O4重复利用4次吸附率仍在70%以上。 展开更多
关键词 柑橘皮 绿色合成 纳米fe3o4 孔雀石绿 吸附
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Fe2O3含量对青花色料呈色的影响
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作者 李小龙 马岚 +3 位作者 李勋 胡其国 邱辉辉 包启富 《佛山陶瓷》 CAS 2024年第7期36-39,共4页
实验以二氧化三铁、氧化钴、氧化锰、釉果为主要原料,采用单因素实验法,探究了青花色料中Fe2O3/CoO对青花瓷色度值、微观结构、晶相组成的影响。实验结果表明,随着青花色料配方中Fe2O3/CoO比值增大,青花瓷着色区域表面析出大量的1~3μm... 实验以二氧化三铁、氧化钴、氧化锰、釉果为主要原料,采用单因素实验法,探究了青花色料中Fe2O3/CoO对青花瓷色度值、微观结构、晶相组成的影响。实验结果表明,随着青花色料配方中Fe2O3/CoO比值增大,青花瓷着色区域表面析出大量的1~3μm磁铁矿晶体并且发育越来越好,使得青花瓷呈现黑色调增强蓝色调减弱的现象。 展开更多
关键词 fe2o3/Coo 青花色料 磁铁矿
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Fe、La掺杂和氧缺陷对CeO_(2)表面吸附As_(2)O_(3)的密度泛函理论研究
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作者 卢鲲鹏 张凯华 张锴 《燃料化学学报(中英文)》 EI CAS CSCD 北大核心 2024年第8期1149-1161,共13页
采用密度泛函理论研究了As_(2)O_(3)(g)在Fe、La掺杂CeO_(2)(110)表面及氧缺陷LaCeO(110)表面的吸附行为,探索了LaCeO表面砷吸附能力显著高于FeCeO表面的主要原因。结果表明,As_(2)O_(3)(g)的吸附效果与吸附位点数量、吸附能、键长和电... 采用密度泛函理论研究了As_(2)O_(3)(g)在Fe、La掺杂CeO_(2)(110)表面及氧缺陷LaCeO(110)表面的吸附行为,探索了LaCeO表面砷吸附能力显著高于FeCeO表面的主要原因。结果表明,As_(2)O_(3)(g)的吸附效果与吸附位点数量、吸附能、键长和电荷转移密切相关。纯CeO_(2)表面的吸附主要为化学吸附,吸附能绝对值大于−4.22 eV,电荷转移量为(−0.19)−(−0.31)e,As_(2)O_(3)得到电荷带负电,起表面受主作用,因此吸附量较小。FeCeO(110)表面新增Fe顶位和Bridge-2桥位两个吸附位,其中,Fe顶位为化学吸附,Fe掺杂改变了FeCeO表面电子分布和晶格结构,但并未改变As_(2)O_(3)与FeCeO之间的电荷转移方向,因此,As_(2)O_(3)仍呈负离子形式吸附。LaCeO(110)表面新增了三个吸附位:La顶位、Bridge-3桥位和Hollow-2空位,La掺杂改变了As_(2)O_(3)与LaCeO之间的电荷转移方向,使得As_(2)O_(3)失电子呈正离子吸附,起表面施主作用,因此,吸附能力增强。无O_(2)环境下,单一O缺陷LaCeO(110)表面吸附能力低于完整LaCeO表面;有O_(2)环境下,O缺陷有利于As_(2)O_(3)的吸附。 展开更多
关键词 密度泛函理论 二氧化铈 fe、La掺杂 As_(2)o_(3)吸附 o缺陷
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Ti-Si-Fe合金添加量对Si_(3)N_(4)结合SiC材料结构与性能的影响
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作者 姚路炎 韩兵强 +1 位作者 张锦化 柯昌明 《耐火材料》 CAS 北大核心 2024年第4期277-283,共7页
为促进Si_(3)N_(4)结合SiC耐火材料的致密化,降低Si粉氮化温度,以SiC颗粒和细粉、Si粉为主要原料,利用从高钛型高炉渣提取的Ti-Si-Fe合金部分取代Si粉,在埋碳气氛下于1350℃反应烧结5 h,制备了Si_(3)N_(4)结合SiC耐火材料。研究了Ti-Si... 为促进Si_(3)N_(4)结合SiC耐火材料的致密化,降低Si粉氮化温度,以SiC颗粒和细粉、Si粉为主要原料,利用从高钛型高炉渣提取的Ti-Si-Fe合金部分取代Si粉,在埋碳气氛下于1350℃反应烧结5 h,制备了Si_(3)N_(4)结合SiC耐火材料。研究了Ti-Si-Fe合金添加量(加入质量分数分别为0、1.8%、3.6%、5.4%、7.2%)对Si粉的氮化行为、材料力学性能和显微结构的影响,并探讨了氮化反应烧结机制。结果表明:1)随着Ti-Si-Fe合金添加量的增加,材料的常温力学性能和高温抗折强度明显改善,荷重软化温度均超过1700℃,Ti-Si-Fe合金添加量超过3.6%(w)后材料性能的增幅变缓;2)Ti-Si-Fe合金促进了Si粉在较低温度下的完全氮化和材料的反应烧结,Ti-Si-Fe合金中各物相及Si粉氮化反应的体积增加能够充填气孔,氮化产物改善骨料与基质、基质内部的结合状态,从而提高材料的致密化程度,改善力学性能;3)引入Ti-Si-Fe合金后,反应体系中形成了富含Ti、Si、N、Fe成分的液相,氮化物的形成除传统的VS、VLS机制外,溶解-沉淀机制在短柱状β-Si_(3)N_(4)、粒状TiN的形成中起到主导作用,交错连结的α-Si_(3)N_(4)晶须、短柱状β-Si_(3)N_(4)、粒状TiN对材料的力学性能起到增强作用。 展开更多
关键词 Ti-Si-fe合金 反应烧结 Si_(3)N_(4)结合SiC耐火材料 致密化 溶解-沉淀
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Fe改性分子筛催化剂CH_(4)选择性催化还原N_(2)O
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作者 温鹏 刘宁 +1 位作者 陈标华 代成娜 《化工环保》 CAS CSCD 北大核心 2024年第3期398-404,共7页
针对N_(2)O的CH_(4)选择性催化还原(CH_(4)-SCR),采用浸渍法制备了系列Fe改性分子筛(BEA、ZSM-5、SSZ-13)催化剂。实验结果表明:2%Fe-BEA(负载量2%(w))具有较高的催化活性,在进气(N_(2)O 40%(φ,下同),CH_(4)10%,N250%)总流量为50 mL/mi... 针对N_(2)O的CH_(4)选择性催化还原(CH_(4)-SCR),采用浸渍法制备了系列Fe改性分子筛(BEA、ZSM-5、SSZ-13)催化剂。实验结果表明:2%Fe-BEA(负载量2%(w))具有较高的催化活性,在进气(N_(2)O 40%(φ,下同),CH_(4)10%,N250%)总流量为50 mL/min、反应器气时空速为12000 h^(–1)的条件下,250℃时的N_(2)O转化率达99.5%,CH_(4)转化率达94.6%;反应器连续运行20 h,N_(2)O转化率基本保持不变,CH_(4)转化率仅略有下降。表征结果显示,2%Fe-BEA较高的催化活性与其易形成大量离子态Fe^(3+)活性物种密切相关,而2%Fe-SSZ-13更易形成大量FeOx物种,故在3种分子筛催化剂中催化活性最低。2%Fe-BEA上N_(2)O的CH_(4)-SCR遵循自由基反应机理,形成羟基自由基和甲氧基自由基,并可经进一步氧化,通过甲酸盐路径生成CO_(2)和H2O。 展开更多
关键词 N_(2)o CH_(4)选择性催化还原(CH_(4)-SCR) fe-BEA分子筛 反应机理
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MoS_(2)@2Br-MIL-53(Fe)@g-C_(3)N_(4)三元复合物的制备及光芬顿降解RhB 被引量:1
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作者 郑佳红 郑馨 +1 位作者 蔺小朋 马嘉祺 《中国陶瓷》 CSCD 北大核心 2023年第12期24-36,共13页
采用简单的水热法制备了光芬顿催化剂MoS_(2)@2Br-MIL-53(Fe)@g-C_(3)N_(4)。通过XRD、SEM、FT-IR、XPS、EIS、UV-Vis等对其进行表征,研究了MoS_(2)和g-C_(3)N_(4)的引入对2Br-MIL-53(Fe)的晶体结构、形貌、组成及催化活性的影响。探究... 采用简单的水热法制备了光芬顿催化剂MoS_(2)@2Br-MIL-53(Fe)@g-C_(3)N_(4)。通过XRD、SEM、FT-IR、XPS、EIS、UV-Vis等对其进行表征,研究了MoS_(2)和g-C_(3)N_(4)的引入对2Br-MIL-53(Fe)的晶体结构、形貌、组成及催化活性的影响。探究了H_(2)O_(2)用量、RhB初始浓度、催化剂用量和初始RhB溶液pH对催化性能的影响。结果表明,在H_(2)O_(2)浓度为5 m M,RhB溶液浓度为10 mg/L,催化剂浓度为0.1 g/L以及pH=4的最佳反应条件下,MoS_(2)@2Br-MIL-53(Fe)@g-C_(3)N_(4)在40 min对RhB的降解效率为93.7%。自由基捕获实验表明,RhB降解体系中e-起主要作用,并给出了可能的光芬顿降解RhB的反应机理。 展开更多
关键词 g-C_(3)N_(4) MIL-53(fe) MoS_(2) 光芬顿
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Folate-conjugated Fe_3O_4 nanoparticles for in vivo tumor labeling
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作者 周春姣 王少华 +4 位作者 周宇 容鹏飞 陈孜孜 刘进言 周建大 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2013年第7期2079-2084,共6页
Highly biocompatible superparamagnetic Fe3O4 nanoparticles were synthesized by amide of folic acid (FA) ligands and the NH2-group onto the surface of Fe3O4 nanoparticles. The as-synthesized folate-conjugated Fe3O4 n... Highly biocompatible superparamagnetic Fe3O4 nanoparticles were synthesized by amide of folic acid (FA) ligands and the NH2-group onto the surface of Fe3O4 nanoparticles. The as-synthesized folate-conjugated Fe3O4 nanoparticles were characterized by X-ray diffraction diffractometer, transmission electron microscope, FT-IR spectrometer, vibrating sample magnetometer, and dynamic light scattering instrument. The in vivo labeling effect of folate-conjugated Fe3O4 nanoparticles on the hepatoma cells was investigated in tumor-bearing rat. The results demonstrate that the as-prepared nanoparticles have cubic structure of Fe3O4 with a particle size of about 8 nm and hydrated diameter of 25.7 nm at a saturation magnetization of 51 A·m2/kg. These nanoparticles possess good physiological stability, low cytotoxicity on human skin fibroblasts and negligible effect on Wistar rats at the concentration as high as 3 mg/kg body mass. The folate-conjugated Fe3O4 nanoparticles could be effectively mediated into the human hepatoma Bel 7402 cells through the binding of folate and folic acid receptor, enhancing the signal contrast of tumor tissue and surrounding normal tissue in MRI imaging. It is in favor of the tumor cells labeling, tracing, magnetic resonance imaging (MRI) target detection and magnetic hyperthermia. 展开更多
关键词 fe3o4 nanoparticles superparamagnetic property folic acid TUMoR CoNJUGATIoN magnetic resonance imaging (MRI) cell labeling
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Fe^(0)@Fe_(3)O_(4)/火山岩催化H_(2)O_(2)氧化亚甲基蓝脱色研究
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作者 国洁 宋佳乐 +1 位作者 侯永江 梁茹茹 《安全与环境学报》 CAS CSCD 北大核心 2023年第12期4498-4506,共9页
以火山岩为载体,采用化学沉淀法和液相还原法制备Fe~0@Fe_(3)O_(4)/火山岩催化剂,结合X射线衍射(XRD)、透射电子显微镜(TEM)、傅里叶变换红外光谱(FT-IR)和比表面积测试(BET)进行表征,并通过亚甲基蓝(Methylene Blue,MB)模拟废水试验对... 以火山岩为载体,采用化学沉淀法和液相还原法制备Fe~0@Fe_(3)O_(4)/火山岩催化剂,结合X射线衍射(XRD)、透射电子显微镜(TEM)、傅里叶变换红外光谱(FT-IR)和比表面积测试(BET)进行表征,并通过亚甲基蓝(Methylene Blue,MB)模拟废水试验对催化剂活性进行评价。XRD结果显示,两种方法制得的催化剂中有明显的铁氧化物和零价铁衍射峰;TEM结果显示,Fe~0和Fe_(3)O_(4)以核壳结构分布在火山岩表面;BET结果显示,Fe~0@Fe_(3)O_(4)/火山岩的比表面积是火山岩的5倍,且孔容和孔径都有所增加。利用火山岩自身铁元素质量分数高的特性,对火山岩改性并制备Fe~0@Fe_(3)O_(4)/火山岩催化剂,制得的催化剂能够有效地催化废水中的MB脱色,成本低且3 h的脱色率可达98.47%。Fe~0@Fe_(3)O_(4)/火山岩催化剂提高了MB的矿化度并具有较高的可重复利用价值,催化氧化系统主要遵循羟基自由基的反应机理。 展开更多
关键词 环境工程学 催化化学 fe^(0)@fe_(3)o_(4)/火山岩 催化氧化 亚甲基蓝
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Fe改性g-C_(3)N_(4)掺杂磷钨酸/氧化铋复合光催化剂的制备及去除硫化氢性能研究
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作者 田杨懿 田丽红 +2 位作者 于连军 冉太全 张惠宁 《化学研究与应用》 CAS 北大核心 2024年第6期1277-1285,共9页
通过熳烧方法制备了Fe改性的g-C_(3)N_(4),然后利用水热法制备掺杂了磷钨酸(HPW)和氧化铋(Bi_(2)O_(3))光催化材料。通过X射线衍射(XRD)扫描电子显微镜(SEM)、X射线光电子能谱(XPS)、光致发光(PL)发射光谱、阻抗谱(EIS)和紫外-可见漫反... 通过熳烧方法制备了Fe改性的g-C_(3)N_(4),然后利用水热法制备掺杂了磷钨酸(HPW)和氧化铋(Bi_(2)O_(3))光催化材料。通过X射线衍射(XRD)扫描电子显微镜(SEM)、X射线光电子能谱(XPS)、光致发光(PL)发射光谱、阻抗谱(EIS)和紫外-可见漫反射光谱(UV-vis DRS)研究了制备的样品的结构和光电特性。考察了不同影响因素对紫外灯照射下H_(2)S去除的活性影响。结果表明:负载8g光催化材料,在30min对H_(2)S的去除率达到83%。光催化降解机理研究发现,在光催化去除H_(2)S中,·O_(2)^(-)为主要活性物种。这一工作通过简单的方法合成清洁低碳的光催化材料,去除污废水处理过程中产生的有害气体提供了新的视角和策略。 展开更多
关键词 磷钨酸 fe-C_(3)N_(4) 氧化铋 硫化氢 光催化
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基于Fe_(3)O_(4)@MIL-100(Fe)@Ag NPs的三唑磷SERS检测方法 被引量:1
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作者 阳能静 朱浩帆 +2 位作者 韦庆益 孙大文 蒲洪彬 《食品科学》 EI CAS CSCD 北大核心 2023年第12期376-384,共9页
针对在农产品中简便、快速地检测农药三唑磷残留问题,建立基于磁纳米、金属有机框架和Ag纳米颗粒(Ag NPs)的核-壳-卫星纳米结构表面增强拉曼光谱(surface-enhanced Raman scattering,SERS)基底,并应用在有机磷农药三唑磷的灵敏检测。通... 针对在农产品中简便、快速地检测农药三唑磷残留问题,建立基于磁纳米、金属有机框架和Ag纳米颗粒(Ag NPs)的核-壳-卫星纳米结构表面增强拉曼光谱(surface-enhanced Raman scattering,SERS)基底,并应用在有机磷农药三唑磷的灵敏检测。通过低温循环自组装法和银镜循环制备了由MIL-100(Fe)包覆的Fe_(3)O_(4),并在表面原位负载Ag NPs组成的核-壳-卫星纳米结构的Fe_(3)O_(4)@MIL-100(Fe)@Ag NPs基底。对苹果中的三唑磷残留进行SERS传感,三唑磷特征峰强度对数值与质量浓度对数值的线性检测范围为0.05~10 mg/L,线性方程为Y=0.573 8X+2.804(R^(2)=0.980),检出限低至11.9μg/L。在加标量为2、5、10 mg/L时,该方法的回收率为90.07%~103.27%。表明制备的SERS基底在食品农残中的检测领域具有巨大潜力。 展开更多
关键词 表面增强拉曼散射 金属有机框架 fe_(3)o_(4)@MIL-100(fe)@Ag NPs 三唑磷
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Preparation and Analysis of Fe3O4 Magnetic Nanoparticles Used as Targeted-drug Carriers 被引量:32
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作者 赵原壁 邱祖民 黄佳英 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2008年第3期451-455,共5页
Fe3O4 magnetic nanoparticles were prepared by the aqueous co-precipitation of FeCl3-6H2O and FeCl2-4H2O with addition of ammonium hydroxide. The conditions for the preparation of Fe3O4 magnetic nanoparticles were opti... Fe3O4 magnetic nanoparticles were prepared by the aqueous co-precipitation of FeCl3-6H2O and FeCl2-4H2O with addition of ammonium hydroxide. The conditions for the preparation of Fe3O4 magnetic nanoparticles were optimized, and Fe3O4 magnetic nanoparticles obtained were characterized systematically by means of transmission electron microscope (TEM), dynamic laser scattering analyzer (DLS) and X-ray diffraction (XRD). The results revealed that the magnetic nanoparticles were cubic shaped and dispersive, with narrow size distribution and average diameter of 11.4 nm. It was found that the homogeneous variation of pH value in the solution via the control on the dropping rate of aqueous ammonia played a critical role in size distribution. The magnetic response of the product in the magnetic field was also analyzed and evaluated carefully. A 32.6 mT magnetic field which is produced by four ferromagnets was found to be sufficient to excite the dipole moments of 0.05 g Fe3O4 powder 2 cm far away from the ferromagnets. In conclusion, the Fe3O4 magnetic nanoparticles with excellent properties were competent for the magnetic carders of targeted-drug in future application. 展开更多
关键词 targeted--drug fe3o4 magnetic particle nanometre
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Size-dependent peroxidase-like catalytic activity of Fe_3O_4 nanoparticles 被引量:16
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作者 Fang Fang Peng YU Zhang Ning Gu 《Chinese Chemical Letters》 SCIE CAS CSCD 2008年第6期730-733,共4页
Peroxidase-like catalytic properties of Fe3O4 nanoparficles (NPs) with three different sizes, synthesized by chemical coprecipitation and sol-gel methods, were investigated by UV-vis spectrum analysis. By comparing ... Peroxidase-like catalytic properties of Fe3O4 nanoparficles (NPs) with three different sizes, synthesized by chemical coprecipitation and sol-gel methods, were investigated by UV-vis spectrum analysis. By comparing Fe3O4 NPs with average diameters of 11, 20, and 150 nm, we found that the catalytic activity increases with the reduced nanoparticle size. The electrochemical method to characterize the catalytic activity of Fe3O4 NPs using the response currents of the reaction product and substrate was also developed. 展开更多
关键词 fe3o4 nanoparticles Peroxidase-like catalytic activity ELECTRoCHEMISTRY
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Surface organic modification of Fe_3O_4 nanoparticles by silane-coupling agents 被引量:7
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作者 CUI Sheng SHEN Xiaodong LIN Benlan 《Rare Metals》 SCIE EI CAS CSCD 2006年第z1期426-430,共5页
Fe3O4 nanoparticles were prepared by chemistry co-precipitation and the mean crystal size was 17.9 nm measured by XRD. After it had been treated by silane-coupling agents KH570, magnetic micro-spheres dispersed in org... Fe3O4 nanoparticles were prepared by chemistry co-precipitation and the mean crystal size was 17.9 nm measured by XRD. After it had been treated by silane-coupling agents KH570, magnetic micro-spheres dispersed in organic medium glycol were gained and the mean size of Fe3O4 nanopowders was 33.7 nm. So it can be concluded that magnetic micro-sphere is made of a few Fe3O4 crystals. Many factors of modification were researched, such as the time of ball milling, the content of Fe3O4 and the content of KH570. The modification of Fe3O4 is relative to the time of ball milling, but the dominant function is affected by the content of Fe3O4 and KH570. When the content of Fe3O4 is known, there is a suitable content of KH570. Different content of Fe3O4 will make the different suitable content of KH570, but the range of latter is less than former, which is relative to the distribution of KH570 on Fe3O4 surface or in the solution. 展开更多
关键词 fe3o4 nanoparticles organic modification silane-coupling agents
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Fabrication of Poly(y-glutamic acid)-coated Fe3O4 Magnetic Nanoparticles and Their Application in Heavy Metal Removal 被引量:6
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作者 常菁 仲兆祥 +2 位作者 徐虹 姚忠 陈日志 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2013年第11期1244-1250,共7页
In this study, poly(y-glutamic acid)-coated Fe3O4 magnetic nanoparticles (y-PGA/Fe304 MNPs) were successfully fabricated using the co-precipitation method. Fe3O4 MNPs were also prepared for comparison. The av erag... In this study, poly(y-glutamic acid)-coated Fe3O4 magnetic nanoparticles (y-PGA/Fe304 MNPs) were successfully fabricated using the co-precipitation method. Fe3O4 MNPs were also prepared for comparison. The av erage size and specific surface area results reveal that 7-PGA/Fe304 MNPs (52.4 nm, 88.41 m2.g-1) have smaller particle size and larger specific surface area_ than Fe3O4 MNPs (62.0 nm, 76.83 mLg-1). The y-PGA/Fe3O4 MNPs 展开更多
关键词 y-PGA magnetic nanoparticles fe3fo4 heavy metal removal
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Surface Organic Modification of Fe_3O_4 Magnetic Nanoparticles 被引量:4
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作者 CUI Sheng SHEN Xiaodong LIN Benlan JIANG Guodong ZHANG Weihua 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS 2008年第4期436-439,共4页
The surface organic modification of Fe3O4 nanoparticles with silane coupling reagent KH570 was studied. The modified and unmodified nanoparticles were characterized by FT-IR, XPS and TEM. The spectra of FT-IR and XPS ... The surface organic modification of Fe3O4 nanoparticles with silane coupling reagent KH570 was studied. The modified and unmodified nanoparticles were characterized by FT-IR, XPS and TEM. The spectra of FT-IR and XPS revealed that KH570 was coated onto the surface of Fe3O4 nanoparticles to get Fe-O- Si bond and an organic coating layer also was formed. Fe3O4 nanoparticles were spheres partly with mean size of 18,8 nm studied by TEM, which was consistent with the result 17.9 nm calculated by Scherrer's equation. KH570 was adsorbed on surface and formed chemistry bond to be steric hindrance repulsion which prevented nanoparticles from reuniting. Then glycol-based Fe3O4 magnetic liquids dispersed stably was gained. 展开更多
关键词 fe3o4 nanoparticles KH570 surface organic modification chemical adsorb DISPERSIVITY
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Fe3O4 nanoparticles impregnated eggshell as a novel catalyst for enhanced biodiesel production 被引量:2
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作者 Ch.Chingakham Asha David V.Sajith 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2019年第11期2835-2843,共9页
Biodiesel is a green fuel which can replace diesel while addressing various issues such as scarcity of hydrocarbon fuels and environmental pollution to an extent. The high production cost of biodiesel and the recovery... Biodiesel is a green fuel which can replace diesel while addressing various issues such as scarcity of hydrocarbon fuels and environmental pollution to an extent. The high production cost of biodiesel and the recovery of the catalyst after the transesterification process are the major challenges to be addressed in biodiesel production. In the present work, a cheap and promising solid base oxide catalyst was synthesized from chicken eggshell by calcination at 900 ℃ forming catalyst eggshells(CES) and was impregnated with the nanomagnetic material(Fe3O4) to obtain Fe3O4 loaded catalytic eggshell(CES–Fe3O4). Fe3O4 nanomaterials were synthesized by co-precipitation method and were loaded in catalytic eggshell by sonication, for better recovery of the catalyst after transesterification process. CES–Fe3O4 material was characterized by Thermogravimetric analysis, X-ray diffraction, Fourier transform infrared spectroscopy, a vibrating-sample magnetometer, Brunauer-Emmett-Teller, Dynamic light scattering, and Scanning electron microscopy. Biodiesel was synthesized by transesterification of Pongamia pinnata raw oil with 1:12 oil to methanol molar ratio and 2 wt% catalyst loading for 2 h at a temperature of 65 ℃ and yields were compared. The reusability of the catalyst was studied by the transesterification of the raw oil and its catalytic activity was found to be retained up to 7 cycles with a yield of 98%. 展开更多
关键词 CATALYST BIoDIESEL nanoparticles fe3o4 IMPREGNATIoN TRANSESTERIFICATIoN
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