共查询到18条相似文献,搜索用时 91 毫秒
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研究了用以脱除高浓度 CH4 和 CO的贵金属体系催化氧化燃烧剂 ,筛选出的 S3催化剂在氧过量 ,空速 15 0 0h- 1 条件下 ,可将 CH4 和 C2 H6 脱除至 0 .1× 10 - 6 的最低温度分别为 30 0℃和 180℃。在 330℃、 15 0 0 h- 1 条件下长期考察催化剂的活性 ,CH4 <0 .1× 10 - 6的时间长达 2 0 0 0 h。催化剂的最高使用温度不宜超过 6 0 0℃。 相似文献
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工业生活中苯酚及其衍生物废水的排放已经对水资源造成了严重的污染。为解决问题,以实验室自制的SiO2粒子作为催化剂载体,负载活性中心Cu(Ⅱ),通过浸渍、煅烧等处理手段分别制备了SiO2-Cu2+和SiO2-CuO催化剂,并将其应用于苯酚的CWPO中。以苯酚在水溶液中被降解后的苯酚转化率和样品COD去除率作为依据,系统地研究了反应温度、反应时间、氧化剂浓度、催化剂浓度以及介质初始pH值等反应条件对两种催化剂催化性能的影响。实验结果表明,SiO2-Cu2+和SiO2-CuO催化剂均在较宽的pH值范围内表现了优异的催化活性,在苯酚浓度1.0g/L,催化剂浓度0.23g/L,反应温度70℃,反应时间20h,过氧化氢浓度5.0g/L的条件下,可达到100%的苯酚转化率和约90%的COD去除率。 相似文献
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孟根图雅曹星辉贾美林照日格图 《材料工程》2008,(10):356-357
用沉积-沉淀法制备了纳米Au/Fe2O3-MOx(M=La和Ce)系列催化剂,考察了催化剂对于CO的低温催化氧化性能,并通过XRD,BET和AAS等表征手段对催化剂进行了表征,分析了稀土氧化物的掺杂对Au/Fe2O3催化剂性能的影响。结果表明:CeO2的加入能够有效提高Au/Fe2O3催化剂的催化活性,而La2O3的加入对催化剂性能没有明显的影响。 相似文献
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采用微沸回流体系处理制备非均相负载型Cu/Al2O3催化剂。采用XRD、BET和SEM技术分析了该材料的结构、织构参数和表观形貌。选择以H2O2为氧化剂,甲基橙催化氧化降解反应为模型反应评价催化剂的催化性能。表征分析结果表明采用微沸回流体系处理的催化剂比常规过量浸渍的催化剂的形貌颗粒直径更小,其比表面积更大,活性组分的分散度更高。反应后催化剂易分离回收,解决了Fenton反应中催化剂难回收的问题。优化后最佳工艺为:m(H2O2)/m(Cu/Al2O3)=2/1,反应温度70℃,催化剂颗粒粒度0.3~0.4mm,搅拌速度900r/min,Cu/Al2O3(N)催化剂对甲基橙的去除率达到90%以上,比传统催化剂对甲基橙的去除率提高20%。通过Arrhenius方程计算,得到该反应的表观活化能为40.7kJ/mol。 相似文献
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为了更好地理解抗硫油管钢在含硫气田中的腐蚀行为和机理,利用高温高压反应釜装置,结合SEM和XRD分析方法,对N80S和P110S抗硫油钢管在模拟下古气藏环境中CO_2,H_2S共存时的腐蚀行为进行了研究,计算了不同CO_2和H_2S分压比时的腐蚀速率,分析了腐蚀产物特征和成分,探讨了其腐蚀机理。结果表明:2种抗硫油管钢随H_2S含量的增大,腐蚀速率先增大后减小;H_2S微量时抗硫油管钢表面形成了Fe CO3和Fe S等腐蚀物,未见明显的腐蚀坑,随H_2S含量的增大,表面的腐蚀产物为铁的硫化物且存在明显的局部腐蚀。 相似文献
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Yuanyuan Liu Yanmei Zheng Weijie Zhang Zhengbin Peng Hang Xie YiXuan Wang Xinli Guo Ming Zhang Rui Li Ying Huang 《材料科学技术学报》2021,95(36):127-135
Developing environmentally friendly methods to produce hydrogen peroxide (H2O2) has received increas-ing attention.Photocatalysis has been proved to be a sustainable technology for H2O2 production.Herein,the novel non-metal elements (B,P,and S) doped g-C3N4 tubes (B-CNT,P-CNT,and S-CNT) photocata-lysts were obtained via a hydrothermal synthesis followed by thermal polymerization.By adjusting the precursor,the yield of g-C3N4 tubes (CNT) materials has been greatly improved.The as-prepared B-CNT,P-CNT,and S-CNT photocatalysts show an enhanced photocatalytic H2O2 production with the formation rate constants values of 42.31 μM min-1,24.95μM min-1,and 24.22μM min-1,respectively,which is higher than that of bulk CN (16.40 μM min-1).The doped B,P,S elements significantly enhanced the photocatalytic activity by adjusting their electronic structures and promoting the separation of electron-hole carriers.The results have shown great potential for the practical application of CNT photocatalysts. 相似文献
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Dan He Yuxuan Ma Xiaoxue Yang Huiqin Li Xiaojing Wang 《Small (Weinheim an der Bergstrasse, Germany)》2023,19(29):2207114
The foam copper (FCu) has been first used as a promising supporting material to prepare a photo-activated catalyst of Co3O4/CuxO/FCu, in which the fine Co3O4 particles are inlayed on the CuxO nanowires to form a Z-type heterojunction array connected by substrate Cu. The prepared samples have been used as a photo-activated catalyst to directly decompose gaseous benzene and the optimized Co3O4/CuxO/FCu demonstrates a 99.5% removal efficiency and 100% mineralizing rate within 15 min in benzene concentration range from 350 to 4000 ppm under simulate solar light irradiation. To track the reactive mechanism, a series of MOx/CuxO/FCu (M = Mn, Fe, Co, Ni, Cu, Zn) is prepared and a novel photo-activated direct catalytic oxidation route is proposed based on the comparative investigation of material properties. Moreover, the approach grew in situ via layer upon layer oxidation on FCu dedicates to the extra lasting reusability and the easy accessibility in the diverse situations. This work provides a novel strategy for the preparation of Cu connected series multidimensional heterojunction array and a promising application for the quick abatement of the high-leveled concentration gaseous benzene and its derivatives from the industrial discharged flow or the accident scene's leakage. 相似文献
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Fengzhan Si Jianwen Liu Yan Zhang Bin Zhao Yue Liang Xuexian Wu Xiaomin Kang Xiaoqiang Yang Jiujun Zhang Xian-Zhu Fu Jing-Li Luo 《Small (Weinheim an der Bergstrasse, Germany)》2023,19(2):2205257
Nickel based materials are promising electrocatalysts to produce hydrogen from water in alkaline media. However, the stability is of great challenge, limiting its practical material functions. Herein, a new technique for electro-deposition flower-like NiCo2S4 nanosheets on carbon-cloth (CC@NiCo2S4) is proposed for energy-saving production of H2 from water/methanol coelectrolysis at high current density by constructing array architectures and regulating surface magnetism. The optimized and fine-tuned magnetism on the surface of the electrochemical in situ grown CC@NiCo2S4 nanosheet array result in (0 1 −1) surface universally exposed, high catalytic activity for methanol electrooxidation, and long-term stability at high current density. X-ray photoelectron spectroscopy in combination of density functional theory calculations confirm the valence electron states and spin of d electrons for the surface of NiCo2S4, which enhance the surface stability of catalysts. This technology may be utilized to alter the surface magnetism and increase the stability of Ni-based electrocatalytic materials in general. 相似文献
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H2C2O4稳定剂对SOl-Gel法制备LiNbO3薄膜的影响 总被引:1,自引:0,他引:1
研究了分别以H2C2O,HNO3,HCOOH和CH3COOH作稳定剂的LiNbO3薄膜先驱液的稳定性,发现H2C2O4作稳定剂的先驱液的稳定性最好,用sol-gel法在Si(110)基板上制备了以H2C2O4作稳定剂的LiNbO3薄膜,并对LiNbO3薄膜进行了IR,XRD和SEM表征,结果表明,生成的LiNbO3为多晶,与HNO3相比,以H2C2O4作稳定剂制备的LiNbO3薄膜形貌较差。 相似文献
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目的 探究热处理工艺对黏结剂喷射3D打印17?4PH不锈钢样品微观组织、力学性能及电化学腐蚀性能的影响规律,为BJ3DP技术制备综合性能良好的17?4PH不锈钢零件提供参考。方法 基于黏结剂喷射3D打印技术制备17?4PH不锈钢生坯,并将其固化、脱脂、烧结,得到烧结态样品,然后对烧结态样品进行热处理,热处理工艺为在1 040 ℃固溶热处理2 h,随后分别在410、480、550 ℃下热处理3 h后空冷至室温。对烧结态和热处理态样品进行金相试验、单向拉伸试验以及电化学腐蚀试验。 结果 经热处理后,试样在480 ℃时效热处理3 h时力学性能提升最为显著,其屈服强度由608 MPa提升至806 MPa,抗拉强度由1 159 MPa提升至1 245 MPa,伸长率由3.6%提升至13.6%。当时效热处理温度提升至550 ℃时,由于沉淀相的粗化,其力学性能有所下降;同时,电化学腐蚀性能中腐蚀电流密度(Jcorr)减小,腐蚀电位(Ecorr)增大,电荷转移电阻(Rct)增大,出现明显的钝化区。结论 黏结剂喷射3D打印17?4PH不锈钢经热处理后力学性能得到提升,试样在480 ℃时效热处理3 h时力学性能提升最为显著,优于商用热轧17?4PH不锈钢,电化学腐蚀性能与商用热轧17?4PH不锈钢电化学腐蚀性能水平相当。 相似文献
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原位无压烧结制备Si2 N2O-Si3 N4复相陶瓷 总被引:1,自引:0,他引:1
以Y2O3和Al2O3陶瓷粉体作为烧结助剂,原位无压液相烧结制备Si3N4-Si2N2O复相陶瓷,Si2N2O相通过SiO2 Si3N4 2Si2N2O反应生成.生坯采用注凝成型制备,然后在1780℃保温2h烧结,烧结体基本由板条状的Si2N2O及长柱状的β-Si3N4晶粒构成.Si2N2O陶瓷相对于Si3N4陶瓷而言,具有优异的抗氧化性能,低的弹性模量,以及低的热膨胀系数,因此,Si2N2O-Si3N4复相陶瓷结合了两者的优异性能,并大大提高了材料的热冲击性,材料的热冲击温差即使达到1200℃,其残余强度基本上没有变化. 相似文献