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1.
以硝酸铟(In(NO3)3·xH2O)、对苯二甲酸(H2BDC)、六水合硝酸钴(Co(NO3)· 6H2O) 为原料, 首先采用一锅油浴法合成了含有Co2+ 的铟基金属有机框架材料(MOFs) Co2+/CPP-3(In) 材料, 然后在450 ℃ 下焙烧制备Co3O4/In2O3 复合物气敏材料, 将Co3O4/In2O3 复合物的粉体制作成传感器, 并对其气敏性能进行研究。利用扫描电子显微镜和X 射线衍射仪(XRD) 对双金属MOFs Co2+/CPP-3(In) 材料和Co3O4/In2O3 复合物进行表征, 采用静态配气法测试其气敏性能。结果表明, Co3O4/In2O3(nCo : nIn = 0.4 : 1) 样品的形貌保留了其MOFs 前驱体的棒状结构, 棱柱形框架更为突出, 表面呈凹陷状, 棒体中间粗两边细, 六角截面和棒体均布满了孔洞。结合EDX 和XRD 表征结果, Co2+/CPP-3(In) MOFs 前驱体完全转化成Co3O4/In2O3 复合物; Co3O4/In2O3(nCo : nIn = 0.4 : 1) 复合物在 70 ℃ 下对5×10-6 H2S 的气敏性能最优, 响应值达到153, 是同条件下纯备In2O3对H2S 响应值的5 倍, 并且有较好的重复性、选择性和稳定性。  相似文献   

2.
为了解Fe2(SO4)3作为絮凝剂对活性污泥中微生物活性的影响,向活性污泥系统中投加质量浓度为20、40、60、80,100 mg·L-1的Fe2(SO4)3,反应4 h后测定活性污泥的脱氢酶活性、比耗氧速率(RSOU)、胞外聚合物(EPS)及各组分含量,同时测定系统出水的COD等各项指标.结果表明:Fe2(SO4)3质量浓度在20~60 mg·L-1时对活性污泥的脱氢酶活性、RSOUEPS及各组分含量影响均不大,此时污水中COD、TP、UV254等污染物随Fe2(SO4)3质量浓度增加而有较大幅度去除.Fe2(SO4)3质量浓度为80 mg·L-1时,污泥的脱氢酶活性、RSOU、总EPS含量均明显下降.当Fe2(SO4)3质量浓度增加到100 mg·L-1时,污泥的脱氢酶活性、RSOU进一步受到抑制,而总EPS含量则大幅度提升.此时污水中COD、TP、UV254等污染物去除率增加幅度变缓,SCOD及NH3-N去除作用有所下降.  相似文献   

3.
磁性Fe3O4微球的溶剂热法合成及光芬顿性能优化   总被引:1,自引:0,他引:1  
为探究Fe_3O_4微球的光芬顿性能,在200℃条件下,利用溶剂热法成功制备出具有较好分散性、平均粒径(200±0.5)nm的Fe_3O_4微球,并通过对其原料配比的探究进行样品优化.该合成方法所制备出的Fe_3O_4微球在Photo-Fenton降解亚甲基蓝方面有优秀的性能,降解率达95%甚至以上.此外,Fe_3O_4微球具有易回收的优点,仅利用磁场即可将其分离,且回收率超过85%甚至90%.利用回收后的Fe_3O_4微球探究其重复利用率,结果表明,重复利用过程中样品催化降解效率与第一次使用时几乎相同.本研究探究了该样品降解亚甲基蓝的最佳反应条件,其中当反应体系中加入15 mL过氧化氢且为酸性环境下降解效率达到最大.  相似文献   

4.
为开发具有优良循环性能和安全性能的大型锂离子电池的正极材料,将不同比例的LiNi_(0.4)Co_(0.2)Mn_(0.4)O_2和Li Mn2O4材料进行共混,研究了LiNi_(0.4)Co_(0.2)Mn_(0.4)O_2和Li Mn2O4共混以及共混比例(10∶0、8∶2、7∶3、6∶4、5∶5、0∶10)对锂离子电池的首次放电性能、循环性能和倍率性能以及交流阻抗和循环伏安曲线的影响,并采用扫描电镜对电极材料进行了表征.研究结果表明,共混比例会影响材料的电化学性能,8∶2,7∶3和6∶4配比的混合材料的体积比容量、循环性能和倍率性能要好于纯LiNi_(0.4)Co_(0.2)Mn_(0.4)O_2和Li Mn2O4材料.其中,8∶2配比的材料性能最好.  相似文献   

5.
采用牺牲模板法合成N掺杂Co3O4纳米片(N-Co NS),通过透射电子显微镜(TEM)、原子力显微镜(AFM)和光电子能谱(XPS)对制备材料的形貌结构、化学组成进行分析,并通过催化活化过一硫酸盐(PMS)降解水中双酚A (BPA)来探究催化剂的催化性能.实验结果表明与Co3O4纳米颗粒(Co NP)、Co3O4纳米片(Co NS)相比,N-Co NS表现出了较高的催化性能.在PMS浓度为2 mmol·L-1、BPA初始质量浓度为50 mg·L-1的反应条件下,N-Co NS在10 min内完全降解水中的BPA,表明N掺杂和二维纳米片结构有利于催化剂性能的提升.通过pH及离子影响实验证实N-Co NS在复杂水化学环境中仍具有较高的活性.此外结合自由基捕获实验和电子顺磁共振(EPR)测试证实反应体系中产生了高氧化活性的羟基自由基和硫酸根自由基.  相似文献   

6.
为高效地去除水中环境激素类污染物,采用共沉淀法合成了氧化石墨烯负载钴尖晶石铁氧体(GO/CoFe_2O_4)催化剂,催化过硫酸盐(PMS)去除水中邻苯二甲酸二丁酯(DBP).采用SEM、TEM、XPS、XRD对催化剂进行表征,研究不同条件下催化PMS去除水中DBP的效果,提出催化PMS反应机理.结果表明,GO/CoFe_2O_4为颗粒状尖晶石结构,室温下,DBP初始浓度为2μmol/L、催化剂投量为0.1 g/L、PMS浓度为20μmol/L、pH为7时,GO/CoFe_2O_4催化PMS体系对DBP的去除率可达89%,使用5次后催化效果仅降低5%.该新型复合催化剂高效、具有磁性、方便回收,具有良好的工程应用前景.  相似文献   

7.
通过水热技术在二维(2D)多层材料Ti_3C_2 (multi-layer Ti_3C_2, ML-Ti_3C_2)的表面及层间原位晶化和生长锐钛矿相TiO_2纳米球,制备出TiO_2/ML-Ti_3C_2复合纳米材料。采用XRD、SEM、氮吸附等表征技术对TiO_2/ML-Ti_3C_2纳米复合材料进行分析表征,并以亚甲基蓝(MB)为模拟污染物,对纯TiO_2和TiO_2/ML-Ti_3C_2复合纳米材料的光催化性能进行了评价。实验结果表明,两种材料的耦合抑制了Ti O_2中光生电子-空穴对的湮灭,延长了复合光催化剂中载流子寿命,拓宽了复合材料的光谱响应范围。在紫外光照射下,以TiO_2/ML-Ti_3C_2复合纳米材料为光催化剂,200 mg/L的MB溶液在20 min内几乎完全脱色,降解率为98.98%。TiO_2/ML-Ti_3C_2纳米复合材料的光催化性能优于纯TiO_2和Ti_3C_2, Ti_3C_2优异的电子传输能力和超强的吸附性能优化了TiO_2的光催化性能。本研究为使用光催化技术处理废水提供了一种新的思路,具有一定的实际应用前景。  相似文献   

8.
为研究使用过一硫酸盐(PMS)的高级氧化技术去除水体中微量有机污染物的高效可行方法,通过柠檬酸辅助溶胶-凝胶法制备纳米CuFe_2O_4材料,以其为非均相催化剂,探究CuFe_2O_4/PMS体系对诺氟沙星(NFX)的降解性能.采用X射线衍射仪、电子透射显微镜、BET手段对材料进行表征,考察煅烧温度对纳米CuFe_2O_4结构及催化性能的影响,并试验纳米CuFe_2O_4的重复使用性和稳定性.探讨纳米CuFe_2O_4投加量、PMS浓度、溶液初始pH对CuFe_2O_4/PMS体系降解NFX性能的影响,并探究该体系的氧化活性物种及降解机理.结果表明:制备纳米CuFe_2O_4的最佳煅烧温度为400℃,该温度下纳米CuFe_2O_4晶型较好,比表面积较大,且表现出较高的催化活性;在纳米CuFe_2O_4/PMS体系中,控制NFX初始质量浓度为5 mg/L,最适宜的反应条件为:纳米CuFe_2O_4投加量为0.1 g/L、PMS浓度为0.5 mmol/L、初始溶液pH为9.5,该条件下反应30 min后NFX的去除率高达99%;纳米CuFe_2O_4能有效活化PMS生成·OH和SO_4~-·,SO_4~-·是实现NFX快速降解的主要活性物种.  相似文献   

9.
通过水热法制备Cu2O/Cu2S 复合材料对甲基橙(MO) 进行光催化降解实验。在Cu2O 中引入S 元素, 通过 改变Cu/S 投加摩尔比, 从而得到不同Cu/S 的复合材料。利用XRD、SEM、UV-vis、EIS 等手段对材料进行表征, 并 对MO 进行光催化降解实验。XRD 结果表明, 随着S 含量的增多, Cu2S 的衍射强度逐渐上升, Cu2O 的f111g 晶面 衍射强度逐渐降低。SEM 结果表明Cu2S 能较好地包覆在Cu2O 八面体的表面。通过UV-vis 和EIS 结果计算得知, 复合材料带隙为1.49 eV, 电荷转移电阻大幅降低。降解实验结果表明复合材料最佳Cu/S 投加摩尔比为15 : 1, 其在 100 min 时对MO (100 mL, 10 mg/L) 降解率达到91.4%, 明显高于纯Cu2O 对于MO 的降解率(60.3%)。猝灭实验表 明了?OH 和 ?O2 -在光催化过程中起到主要作用。  相似文献   

10.
通过拉拔法测定纳米Al2O3改性环氧胶黏剂和钢铁之间的附着强度,并结合环氧胶的表面能参数测定以及X射线光电子能谱(XPS)分析,对纳米Al2O3提高环氧胶和钢铁附着力的机理进行研究.表面能测定结果表明,添加纳米Al2O3使环氧胶的极性增加;XPS能谱分析结果表明,当纳米Al2O3质量分数达到2%时,环氧胶中形成新的羧基极性基团;进一步研究发现,当纳米Al2O3质量分数为1%时未形成新的羧基基团,当纳米Al2O3质量分数为8%时单位接触面积上新的羧基基团的数目较2%时少,这与附着强度的变化规律是一致的.因此,纳米Al2O3改性的环氧胶黏剂与钢铁的附着强度的增强是由于Al2O3与环氧胶的相互作用形成了新的羧基极性基团.  相似文献   

11.
The kinetics of Fe3O4 formation by air oxidation of slightly acidic suspension of Fe(OH)2 was studied. The effects of initial concentration of Fe(II), temperature, partial pressure of oxygen, air flow rate and stirring rate on the oxidation rate were investigated. The results show that Fe3O4 formation is composed of two-step reaction, the first step is the formation of Fe(OH) 2 + by oxidation of Fe(OH)+ complex ions, the second step is the formation of magnetite by dehydration and deprotonation of Fe(OH)+ and Fe(OH) 2 + . The oxidation reaction is zero-order with respect to the concentration of Fe(II) and around 0.5-order with respect to partial pressure of oxygen, and oxygen transfer process is rate-limiting step of oxidation reaction with apparent activation energy of 2.74 kJ · mol−1.  相似文献   

12.

空气分级燃烧条件下Fe2O3对玻璃微珠生成的影响

张远军,王大凯,程星星,王志强*

(山东大学能源与动力工程学院,济南 250061)

摘要:

在空气分级燃烧条件下,研究了Fe2O3对玻璃微珠(MGBs)生成的影响。实验温度为1450℃,以鹤岗烟煤作为实验对象。利用X射线衍射仪(XRD)、灰熔融测试仪、粘度公式和扫描电镜(SEM)对飞灰进行了分析。使用Nano-Measurer 1.2软件测量了玻璃微珠的直径。结果表明,随着鹤岗煤中Fe2O3含量的增加,飞灰中的玻璃相含量先增加后降低。当Fe2O3含量为15%时,玻璃相含量达到最高,为51.26%。灰熔点先降低后升高,而粘度逐渐降低,颗粒逐渐呈球形。随着Fe2O3含量的增加,粒径小于10μm的玻璃微珠比例逐渐增加。从以上结果可以得出结论,Fe2O3的加入有利于玻璃微珠的生成和粒径的减小。

关键词:玻璃微珠;飞灰;Fe2O3;空气分级燃烧

  相似文献   

13.
Luminescent properties of BaO-La2O3-B2O3 glasses with dopant   总被引:4,自引:0,他引:4  
The luminescent properties of glasses synthesized in air atmosphere by conventional high temperature process were stud{ed. The emissions spectra of Eu^2 and Eu^3 were observed in BaO-La2O3-B2O3-Eu2O3 glasses.The results show that the broad emission peaks at 430 nm correspond to 5d→4f emission transition of Eu^2 , the sharp emission peaks at 592, 616, 650 and 250 nm correspond to 5^D0→1Fj(j=1--4) emission transition of Eu^3 ,respectively, which indicates that the BaO-La2O3a-B2O3-Eu2O3 glass can convert ultraviolet and green omponents of sunlight into blue and red light so as to increase the intensity of blue and red light, respectively. The luminescent in--tensity of Eu^2 increases with increasing the molar ratio of Tb^3 in BaO-La2O3-B2O3-Eu2O3a-Tb4O3 glasses, whereas the luminescent intensity of Eua^3 decreases. So the luminescent intensity of Eu(Ⅲ,Ⅱ) is influenced by Tb^3 .These phenomena can be explained by electron transfer mechanism; Eu^3 (4f6) Tb^3 (4f^8)→Eu^2 (4f′) Tb^4 (4f′). Taking advantage of the luminescent properties of BaO-La2O3-B2O3-Eu2O3 glasses, light-conversion glass for agriculture can be produced.  相似文献   

14.
In order to obtain a new precursor for LiFePO4, Fe2P2O7 with high purity was prepared through solid phase reaction at 650 ℃ using starting materials of FeC2O4 and NH4H2PO4 in an argon atmosphere. Using the as-prepared Fe2P2O7, Li2CO3 and glucose as raw materials, pure LiFePO4 and LiFePO4/C composite materials were respectively synthesized by solid state reaction at 700 ℃ in an argon atmosphere. X-ray diffractometry and scanning electron microscopy(SEM) were employed to characterize the as-prepared Fe2P2O7, LiFePO4 and LiFePO4/C. The as-prepared Fe2P2O7 crystallizes in the Cl space group and belongs to β-Fe2P2O7 for crystal phase. The particle size distribution of Fe2P2O7 observed by SEM is 0.4-3.0 μm. During the Li^+ ion chemical intercalation, radical P2O7^4- is disrupted into two PO4^3- ions in the presence of O^2-, thus providing a feasible technique to dispose this poor dissolvable pyrophosphate. LiFePO4/C composite exhibits initial charge and discharge capacities of 154 and 132 mA·h/g, respectively.  相似文献   

15.
LiCo1/3Ni1/3Mn1/3O2 was coated by a layer of 1.0 wt% CeO2 via sol-gel method. The bared and coated LiMn1/3Co1/3Ni1/3O2 was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), cyclic voltammogram (CV) and galvanotactic charge-discharge test. The results show that the coating layer has no effect on the crystal structure, only coating on the surface; the 1.0 wt% CeO2-coated LiCo1/3Ni1/3Mn1/3O2 exhibits better discharge capacity and cycling performance than the bared LiCo1/3Ni1/3Mn1/3O2. The discharge capacity of 1.0 wt% CeO2-coated cathode is 182.5 mAh·g−1 at a current density of 20 mA·g−1, in contrast to 165.8 mAh·g−1of the bared sample. The discharge capacity retention of 1.0 wt% CeO2-coated sample after 12 cycles reaches 93.2%, in comparison with 86.6% of the bared sample. CV results show that the CeO2 coating could suppress phase transitions and prevent the surface of cathode material from direct contact with the electrolyte, thus enhance the electrochemical performance of the coated material.  相似文献   

16.
Nanometer 3Y-TZP/20%Al2O3 (mass fraction) composite powders prepared by the chemical coprecipitation method were pressureless sintered at 1550 °C for 2 h. Effects of calcining temperatures at 800 °C, 1 000 °C, and 1 200 °C on phase structure, relative density, and Vicker’s hardness of the sintered bodies were studied. The results show that 1 000 °C was the optimal calcining temperature, and the powder calcined was composed of tetragonal zirconia with the Scherrer crystalline size of 6.3nm. The relative density was up to 98.5% under pressureless sintering, and the sintered body was t-ZrO2 (without m-ZrO2)+α-Al2O3 with the average size of 0.4 μm. Foundation item: State Key Laboratory for Powder Metallurgy(No.9706-36) Biography of the first author: YIN Bang-yao, born in 1966, majoring in advanced ceramic materials.  相似文献   

17.
Mg3(PO4)2-coated Li1.05Ni1/3Mn1/3Co1/3O2 cathode materials were synthesized via co-precipitation method. The morphology, structure, electrochemical performance and thermal stability were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), cyclic voltammetry(CV), electrochemical impedance spectroscopy(EIS), charge/discharge cycling and differential scanning calorimeter (DSC). SEM analysis shows that Mg3(PO4)2-coating changes the morphologies of their particles and increases the grains size. XRD and CV results show that Mg3(PO4)2-coating powder is homogeneous and has better layered structure than the bare one. Mg3(PO4)2-coating improved high rate discharge capacity and cycle-life performance. The reason why the cycling performance of Mg3(PO4)2-coated sample at 55 °C was better than that of room temperature was the increasing of lithium-ion diffusion rate and charge transfer rate with temperature rising. Mg3(PO4)2-coating improved the cathode thermal stability, and the result was consistent with thermal abuse tests using Li-ion cells: the Mg3(PO4)2 coated Li1.05Ni1/3Mn1/3Co1/3O2 cathode did not exhibit thermal runaway with smoke and explosion, in contrast to the cells containing the bare Li1.05Ni1/3Mn1/3Co1/3O2. Funded by the National Natural Science Foundation of China (No. 20273047)  相似文献   

18.

Li(Ni1/3Co1/3Mn1/3)O2的(3b)位有序-无序效应研究

曹春晖1,2, 张建1, 杨传铮1, 夏保佳1

(1.上海微系统与信息技术研究所,上海 200050;

2.中国科学院大学, 北京100049)

创新点说明:

提出了有序度的概念,通过理论模拟了过渡金属在3b位不同有序度下的衍射情况。

研究目的:

借助理论衍射研究镍钴锰在三元材料中的占位情况,为实际得到的衍射数据分析起指导作用。

研究方法和结果:

借助Powercell程序模拟不同结构下的衍射情况。结果表明:对于Li(Ni1/3Co1/3Mn1/3)O2,基体衍射线的强度不随有序度而变化,有序度增加时,超点阵衍射线强度增加,但是即使对于有序度最大时,超点阵线的相对强度只有0.225%和0.043%。

结论:

3b位的有序无序很难通过常规的衍射实验观测到,必须提高X射线源的强度才可能观测到。

关键词:Li(Ni1/3Co1/3Mn1/3)O2, 有序-无序,超结构,衍射

  相似文献   

19.
We report on a GaN metal-oxide-semiconductor high electron mobility transistor (MOS-HEMT) using atomic-layer deposited (ALD) Al2O3 as the gate dielectric. Through further decreasing the thickness of the gate oxide to 3.5 nm and optimizing the device fabrication process, a device with maximum transconductance of 150 mS/mm was produced. The drain current of this 0.8 μm gate-length MOS-HEMT could reach 800 mA/mm at +3.0 V gate bias. Compared to a conventional AlGaN/GaN HEMT of similar design, better interface property, lower leakage current, and smaller capacitance-voltage (C-V) hysteresis were obtained, and the superiority of this MOS-HEMT device structure with ALD Al2O3 gate dielectric was exhibited. Supported by the National Natural Science Foundation of China (Grant No. 60736033) and the National Basic Research Program of China (“973“) (Grant No. 51327020301)  相似文献   

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