共查询到19条相似文献,搜索用时 62 毫秒
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应用水热法掺杂钴离子到纳米镍锌铁氧体粉末中,制备处纳米镍锌钴铁氧体,继而用钴离子代替镍离子制备钴锌铁氧体.并利用XRD、TEM、VNA对其进行表征和分析,研究了纳米镍锌钴铁氧体和纳米钴锌铁氧体的样品粒度、形貌、电磁损耗性能及吸收性能.结果表明:纳米镍锌钴铁氧体由原先纳米镍锌铁氧体的类球形转变为不规则四边形结构.掺杂钴离子后增加吸收器的带宽, 改善材料在低频率的吸波性能。钴锌铁氧体中当Co2+: Zn2+=1: 1时,对于电磁波吸收性能比镍锌钴铁氧体要好,在16.47 GHz处到达33.9 dB. 相似文献
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利用溶胶直接自蔓延反应制备了镍锌铁氧体纳米粉末,采用XRD分析了其结构。以聚乙烯醇为基体(PVA)制备了炭黑,镍锌铁氧体复合材料吸波平板;采用矢量网络分析仪测量了其在2~18GHz频带上的吸波性能。结果表明:具有双层结构的炭黑,镍锌铁氧体复合材料具有较好的吸波效果,试样厚度为3mm;当面层镍锌铁氧体的质量分数为40%,底层炭粉的质量分数为20%时,在8~18GHz的测试频段范围内,复合材料最大吸收峰值为-15.7GHz,优于-6dB的有效带宽为6.4GHz;当底层炭粉的质量分数为15%时,复合材料最大吸收峰值为-13.6GHz,优于-6dB的有效带宽为8.2GHz。 相似文献
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采用溶胶-凝胶法制备锂锌铁氧体(Li0.435Zn0.195Fe2.37O4,LZFO),界面聚合法制备纯聚苯胺(PANI)和PANI纳米纤维/LZFO复合材料。通过SEM、XRD、FTIR和矢量网络分析(PNA)等对材料的物相、结构和吸波性能进行了表征和分析。结果表明:制备出的样品分别为PANI、LZFO和不同配比的PANI纳米纤维/LZFO复合材料。在2~18 GHz范围内,PANI纳米纤维/LZFO复合材料的电磁波反射率<-10 dB的波段有2个,吸波性能较纯PANI和LZFO有了很大提高,并且拓宽了吸波频带,当PANI纳米纤维/LZFO复合材料中PANI纳米纤维的质量分数为10%,其综合吸波性能最佳,电磁波反射率<-10 dB的波段分别为2.5~5.5 GHz波段和14.5~16.5 GHz波段,最大吸收峰可达到-33.8 dB。而PANI和LZFO在电磁波反射率<-10 dB的波段只有1个。因此通过PANI纳米纤维接枝铁氧体,可调节电磁参数,提高材料的吸波性能。 相似文献
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以马尾松木材为原料,使用低温预处理、真空浸注和高温原位生长等手段制备了性能优异的木基多孔炭/铁氧体复合吸波材料(WPC/Fe3 O4),采用XRD、XPS、SEM、VNA等技术对复合材料的物相、成分、形貌和电磁特性等进行表征分析,初步阐述了其吸波机理.结果表明:制备的WPC/Fe3 O4具有优异的吸波性能,其反射损耗峰值达-35.6 dB,有效吸波频带宽超过5.6 GHz,并且在3~4.3 mm厚度范围内均可实现对全部Ku频段电磁波的有效吸收;WPC/Fe3 O4具有规则通直的孔隙结构和丰富的异质界面,高温下Fe3 O4纳米粒子均匀生长于木基多孔炭的孔隙和炭壁中;随着碳化温度的升高,WPC/Fe3 O4的介电常数显著增大而磁导率变化较小;WPC/Fe3 O4的电磁损耗机制主要为导电损耗、磁损耗和界面极化损耗.复合材料表现出对Ku频段电磁波的高效与宽频吸收,有望实现其在电子通讯或目标隐身等微波领域的应用. 相似文献
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以柠檬酸为络合剂制备镍锌铁氧体溶胶,以活性炭为基体负载Ni-Zn铁氧体,再通过焙烧制备出形态和结构理想的活性炭/镍锌铁氧体复合材料;详细地考察烧结温度、煅烧气氛及活性炭与铁氧体的配比等工艺参数对复合材料的形态和结构的影响;分别采用X射线衍射(XRD)和扫描电镜(SEM)对制备出的复合材料进行形貌、结构表征分析。采用波导法在8.2~12.4GHz波段对活性炭负载纳米镍锌铁氧体复合材料进行电磁参数测试,结果表明所制备活性炭负载镍锌铁氧体复合材料具有较高的电、磁损耗角正切值,其吸波性能较好。 相似文献
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ZnO/CNTs复合材料的制备、表征及光催化性能 总被引:1,自引:0,他引:1
采用水热法制备了一系列氧化锌和碳纳米管的复合材料(ZnO/CNTs),详细考察了碳纳米管的含量对复合材料光催化性能的影响。利用X射线衍射仪、紫外-可见漫反射吸收光谱、扫描电子显微镜、X射线能谱、透射电子显微镜、X射线光电子能谱和氮气吸附-脱附等测试手段对样品的结构、形貌和光学性质进行了表征,并用亚甲基蓝溶液模拟污染物,评价了ZnO/CNTs复合材料的光催化性能。结果表明:添加CNTs提高了ZnO的比表面积,增强了ZnO的可见光吸收。ZnO/CNTs复合材料较纯ZnO具有更高的光催化活性,并且随着CNTs含量的增加,ZnO/CNTs复合材料的光催化活性呈先增加后减小的趋势。当CNTs的含量为0.3%(质量分数)时,ZnO/CNTs复合材料的光催化活性最高,经过50 min光照后,亚甲基蓝的降解率达到了96.2%。 相似文献
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Jifen Wang ) Huaqing Xie ) Zhong Xin ) ) State Key Laboratory of Chemical Engineering East China University of Science Technology Shanghai China ) School of Urban Development Environmental Engineering Shanghai Second Polytechnic University Shanghai China 《材料科学技术学报》2011,(3):233-238
Oleylamine(G18) and octanol(G8) were grafted onto the surfaces of the multi-walled carbon nanotubes(CNTs).The grafted CNTs were dispersed into palmitic acid(PA) and paraffin wax(PW) to prepare phase change composites.The heat storage/retrieval experiments showed that the composites kept stable after repeating melting and solidification for 80 times.The structure of the G18-CNT/PA and G8-CNT/PA was homogenous compared with the pristine CNT(P-CNT)/PA.The latent heat capacity(Ls) of solid liquid phase change of G18-CNT/PW was higher than that of PW while those of the G8-CNT/PW and P-CNT/PW were lower than that of PW.Compared with PA,all PA based composites with both P-CNTs and grafted CNTs decreased Ls evidently.The Ls values of G18-CNT composites in both matrices were higher than that of the counterparts of G8-CNT.The thermal conductivities of all the PA based composites in the study were higher than that of PA,as well as those of all the PW based composites.However,the thermal conductivities of the G18-CNT composites in both matrixes were lower than those of the G8-CNT composites in both matrixes at all measured temperatures. 相似文献
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采用一步水热法合成NiCo2S4和NiCo2S4/CNTs复合材料,通过进行XPS、XRD以及SEM对NiCo2S4、NiCo2S4/CNTs复合材料进行物理表征,采用三电极测试体系在电化学工作站上进行电化学测试。测试结果表明:通过掺杂CNTs改变了NiCo2S4的形貌结构,NiCo2S4在1 A/g电流密度下,比电容可以达到830 F/g,在10 A/g的大电流密度下,比电容保持率仅为78.3%;而NiCo2S4/CNTs复合材料在10 A/g下的比电容保持率可达到78.6%,并且在3 A/g电流密度下循环1000次,比电容保持率高达98.2%。 相似文献
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《Materials Letters》2007,61(4-5):934-936
A layer of manganese dioxides (γ-MnO2) was adsorbed upon carbon nanotubes (CNTs) surface by using a chemical deposit process. The morphologies of the MnO2/CNTs composite were characterized using transmission electron microscopy (TEM), energy-dispersive X-ray spectrometry (EDS), X-ray diffraction (XRD) and laser Raman spectroscopy (RS). It is found that the adsorbed layer belongs to the γ-MnO2 nanoparticles in the size of about 10 nm, and coated homogeneously around the CNTs. It is expected that this γ-MnO2/CNTs composite will be applied to make supercapacitors. 相似文献
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Ce-Ti-O_x/CNTs复合粒子的制备及其对风化煤氧解的催化性能 总被引:1,自引:0,他引:1
以柠檬酸为螯合剂,以自制碳纳米管(CNTs)为载体,采用柠檬酸螯合沉积法制备了Ce-Ti-Ox/CNTs复合粒子,考察了柠檬酸的用量和乙二醇的添加对产物形貌的影响,采用TEM、XRD和FR-IR等手段对样品的形貌和晶相结构进行表征。结果表明,乙二醇的"桥接"作用有效地改善了负载效果及被负载的粒子均匀。探讨了复合金属氧化物的负载机理,并在此基础上研究了所得样品在风化煤硝酸氧解制备腐植酸中的催化性能,催化结果表明,Ce-Ti-Ox/CNTs复合粒子的催化性能明显优于单纯的CNTs、CeO2、TiO2、CeO2/CNTs以及TiO2/CNTs的催化性能,使腐殖酸的产率达到了65.43%。 相似文献
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Ni-Cu-P/carbon nanotubes (CNTs) quaternary composite coatings were successfully obtained on low carbon steel matrix by electroless plating. The effects of CNTs concentration in the bath on the microstructure of the composite coatings, CNTs content in the composite coatings and the hardness of composite coatings before and after heat treatment at 400 °C have been studied. In addition, the corrosion resistance of Ni-Cu-P/CNTs composite coatings was evaluated by anodic polarization curves in 3.5 wt.% NaCl solution at room temperature. It was noted that the CNTs concentration remarkably influenced the surface morphology of the coatings. With increasing CNTs concentration, both the CNTs content in the composite coatings and the hardness of composite coatings increased at first and then decreased. And the composite coatings after heat treatment provided higher hardness than the as-deposited coatings. The corrosion resistance of Ni-Cu-P/CNTs composite coatings is excellent compared with that of Ni-Cu-P coatings. 相似文献
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