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Effect of Lithium Chloride on the Fibre Length Distribution, Processing Temperature and the Rheological Properties of High-Yield-Pulp-Fibre-Reinforced Modified Bio-Based Polyamide 11 Composite 氯化锂对高产浆纤维增强改性生物基聚酰胺11复合材料纤维长度分布、加工温度及流变性能的影响
Pub Date : 2017-03-21 DOI: 10.4236/ANP.2017.62005
Robenson Cherizol, M. Sain, J. Tjong
The aim of this work was to investigate the effect of lithium chloride (LiCl) on the fibre length distribution, melting temperature and the rheological characteristics of high yield pulp fibre reinforced polyamide biocomposite. The inorganic salt lithium chloride (LiCl) was used to decrease the melting and processing temperature of bio-based polyamide 11. The extrusion method and Brabender mixer approaches were used to carry out the compounding process. The densities and fibre content were found to be increased after processing using both compounding methods. The HYP fibre length distribution analysis realized using the FQA equipment showed an important fibre-length reduction after processing by both techniques. The rheological properties of HYP-reinforced net and modified bio-based polyamide 11 “PA11” (HYP/PA11) composite were investigated using a capillary rheometer. The rheological tests were performed in function of the shear rate for different temperature conditions. The low-temperature process compounding had higher shear viscosity; this was because during the process the temperature was low and the mixing and melting were induced by the high shear rate created during compounding process. Experimental test results using the extrusion process showed a steep decrease in shear viscosity with increasing shear rate, and this melt-flow characteristic corresponds to shear-thinning behavior in HYP/PA11, and this steep decrease in the melt viscosity can be associated to the hydrolyse reaction of nylon for high pulp fibre moisture content at high temperature. In addition to the low processing temperature, the melt viscosity of the biocomposite using the Brabender mixer approach increases with increasing shear rate, and this stability in the increase even at high shear rate for high pulp moisture content is associated to the presence of inorganic salt lithium chloride which creates the hydrogen bonds with pulp during the compounding process.
本工作的目的是研究氯化锂(LiCl)对高产浆纤维增强聚酰胺生物复合材料的纤维长度分布、熔融温度和流变特性的影响。采用无机盐氯化锂(LiCl)降低了生物基聚酰胺11的熔融和加工温度。采用挤压法和Brabender混合器法进行了复合工艺。使用两种复合方法加工后,密度和纤维含量都有所增加。使用FQA设备实现的HYP纤维长度分布分析显示,在使用这两种技术处理后,纤维长度显著减少。用毛细管流变仪研究了HYP增强网和改性生物基聚酰胺11“PA11”(HYP/PA11)复合材料的流变性能。流变试验是在不同温度条件下根据剪切速率进行的。低温工艺配合物具有较高的剪切粘度;这是因为在该过程中温度较低,混合和熔融是由复合过程中产生的高剪切速率引起的。使用挤出工艺的实验测试结果显示,剪切粘度随着剪切速率的增加而急剧下降,这种熔体流动特性对应于HYP/PA11中的剪切稀化行为,并且这种熔体粘度的急剧下降可能与尼龙在高温下对高纸浆纤维含水量的水解反应有关。除了低加工温度外,使用Brabender混合器方法的生物复合材料的熔体粘度随着剪切速率的增加而增加,并且即使在高剪切速率下对于高纸浆水分含量,这种增加的稳定性也与无机盐氯化锂的存在有关,其在复合过程中与纸浆形成氢键。
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引用次数: 0
A Facile Synthesis and Photoluminescence Properties of SiO 2 :Tb 3+ Spherical Nanoparticles 二氧化钛:铽+球形纳米颗粒的快速合成及其光致发光性能
Pub Date : 2017-03-21 DOI: 10.4236/ANP.2017.62002
Murad M. A. Abualrejal, H. Zou, Jie Chen, Yanhua Song, Ye Sheng
Controlled synthesis of functional photoluminescent materials are of particular interest due to their fascinating optical properties. Herein, highly uniform SiO2:xTb3+spherical nanoparticles are fabricated by a facile sol-gel method. The structure, morphology, compositions, and luminescence properties of As-prepared samples were well investigated using TEM, SEM, EDX, XRD, XPS and luminescence spectroscopy. The PL intensity of SiO2:xTb3+spherical nanoparticles is Tb3+ ions concentration dependent achieved a maximum at 3 mol % of Tb3+. Particularly, SiO2:xTb3+spherical nanoparticles exhibit a green emission corresponding to 5D4→7Fj transition (541 nm) of Tb3+. These results show that As-prepared phosphors may find potential application in solid-state lighting fields.
功能性光致发光材料的可控合成由于其迷人的光学性质而引起特别的兴趣。本文采用简单的溶胶-凝胶法制备了高度均匀的SiO2:xTb3+球形纳米颗粒。利用TEM、SEM、EDX、XRD、XPS和发光光谱对As制备的样品的结构、形貌、组成和发光性能进行了研究。SiO2:xTb3+球形纳米颗粒的PL强度是Tb3+离子浓度依赖性的,在Tb3+为3mol%时达到最大值。特别地,SiO2:xTb3+球形纳米颗粒表现出对应于5D4的绿色发射→Tb3+的7Fj跃迁(541nm)。这些结果表明,As制备的磷光体可能在固态照明领域找到潜在的应用。
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引用次数: 1
Preparation Nano-Diamond Film by Sol-Gelled Coating Method for Field Emission Display 溶胶-凝胶涂覆法制备场发射显示用纳米金刚石薄膜
Pub Date : 2017-02-10 DOI: 10.4236/ANP.2017.61001
Xiuxia Zhang, Shuyi Wei, Qianyu Ji
The mixture of Nano-graphite and organic vehicles doped to Nano-diamond paste. The suitable paste proportion was found. Nano-diamond film (NDF) was prepared by sol-gel coating method on ITO glass at 3000/min. The field emission characteristics of luminance-current, luminance-voltage and luminance-power of Nano-diamond film were analyzed and tested. Comparing these tested curves, the luminance was well proportional to current was got. Theoretic, the inner resistance of NDF field emission display (FED) consumes electric energy and real voltage change between the cathode and the anode of NDF-FED was very small after electrons emit. So the characteristic of NDF-FED was preferable to describe by luminance-current linear relationship, which was advantageous to device tested and designed.
纳米石墨和有机载体的混合物掺杂到纳米金刚石糊剂中。找到了合适的浆料配比。采用溶胶-凝胶法在ITO玻璃上以3000/min的速度制备了纳米金刚石薄膜。分析并测试了纳米金刚石薄膜的发光电流、发光电压和发光功率的场发射特性。对比这些测试曲线,得到了亮度与电流成正比的结果。理论上,NDF场发射显示器(FED)的内阻消耗电能,电子发射后,NDF FED阴极和阳极之间的实际电压变化很小。因此,NDF-FED的特性最好用亮度-电流的线性关系来描述,这有利于器件的测试和设计。
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引用次数: 0
Simulation of Natural Convection Heat Transfer Enhancement by Nanoparticles in an Open-Enclosure Using Lattice Boltzmann Method 利用晶格玻尔兹曼方法模拟开壳中纳米颗粒增强自然对流换热
Pub Date : 2016-09-07 DOI: 10.4236/ANP.2016.54020
M. Keshtkar
A numerical analysis is performed to investigate the laminar, free convection flow in an Open Enclosure Using Lattice Boltzmann Method (LBM) in the presence of Carbon nanotube and Cu nanoparticles. The problem is studied for different volume fractions of nanoparticles, and aspect ratio of the cavity for various Rayligh numbers. The volume fraction of added nanoparticles to water (as base fluid) is lower than 1% to make dilute suspensions. The study presents a numerical treatment based on LBM to model convection heat transfer of Carbon nanotube based nanofluids. Results show that adding a low value of Carbon nanotube to the base fluid led to significant enhancement of convection rate. Results show that adding nanoparticles to the base fluid enhances the rate of natural convection in a cavity. Make a comparison between Carbon nanotube and Cu-nanoparticles shows that the Carbon nanotube-nano- particle has better performance to enhance convection rate at comparison with Cu- nanoparticles.
采用点阵玻尔兹曼方法(Lattice Boltzmann Method, LBM)研究了碳纳米管和铜纳米粒子存在时开放封闭室内的层流自由对流流动。研究了不同体积分数的纳米颗粒,以及不同瑞利数下的空腔长径比。加入纳米颗粒的水(作为基液)的体积分数低于1%,以形成稀释悬浮液。研究了基于LBM的碳纳米管基纳米流体对流换热数值模拟方法。结果表明,在基液中加入低碳纳米管,对流速率显著增强。结果表明,在基液中加入纳米粒子可以提高空腔内自然对流速率。碳纳米管与Cu纳米粒子的对比表明,碳纳米管-纳米粒子比Cu纳米粒子具有更好的增强对流速率的性能。
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引用次数: 3
The Interesting of Antifungal Effects of Novel In Vitro Fabrics of Stabilized ZnO Nanofluids 新型稳定ZnO纳米流体体外织物抗真菌作用的研究
Pub Date : 2016-09-07 DOI: 10.4236/ANP.2016.54022
F. Katouzian, Z. Fakhroueian, S. M. Bidhendi
According to the extent of fungal infections, to be chronic these such diseases and recently the emerging issue of increased antibiotic resistance in fungal infections, most of scientists are going to find a proper way to replace antibacterial agent by significant semiconductor ZnO nanoparticles (NPs). They are well known to be one of the most important and special metal oxide nanoparticles in pharmaceutical against the most common fungi. ZnO nanoparticles were synthesized using sol-gel, hydrothermal and functionalized surface methods and formulated in water solutions as nanofluids. XRD, FTIR and SEM techniques and UV-Vis absorbance spectroscopy characterized their ZnO modified nanostructures. Also antimycotic potential according to generally tests such as: (MIC) minimum inhibitory concentration, (MFC) minimum fungicidal concentration and normally well diffusion method with standard strains fungi were performed. Among five common fungi strains using in this research, new various ZnO nanofluids showed noticeable results for dermatophyte fungi like Trichophyton mentagrophytes, Microsporum gypseum, Microsporum canis, Candida albicans and Candid tropicalis which had un growth zones in order 70, 40, 35, 30 and 30 mm in comparing with Clotrimazole reference reagent: 30, 25, 25, 18 and 20 mm by well method. The performance of MIC for ZnO nanofluids on fungi was determined to be equal to 0.35, 3.12, 6.25, 6.25 and 6.25 μgr/ml and MFC of nanoproducts showed the 1.5, 12.5, 25, 25 and 25 μgr/ml. Therefore, the designed ZnO nanofluids could reveal the most effect on fungi which cause dermal (ringworm), mucosal (thrush) and vaginal infections, so we are able to apply these surface high energetic ZnO water-based nanofluid formulations as in vitro nanomedicine and nanohygiene for the first time.
根据真菌感染的程度、慢性以及近年来出现的真菌感染中抗生素耐药性增加的问题,大多数科学家都在寻找一种合适的方法来替代抗菌剂,用半导体ZnO纳米颗粒(NPs)代替抗菌剂。它们是抗真菌药物中最重要和最特殊的金属氧化物纳米颗粒之一。采用溶胶-凝胶法、水热法和功能化表面法合成了ZnO纳米颗粒,并在水溶液中配制成纳米流体。采用XRD、FTIR、SEM等技术和UV-Vis吸收光谱对ZnO修饰的纳米结构进行了表征。并对标准菌种进行了最低抑菌浓度(MIC)、最低杀真菌浓度(MFC)和常压扩散法等常规抑菌潜能测试。在本研究使用的5种常见真菌菌株中,新型氧化锌纳米流体对毛癣菌(Trichophyton mentagrophytes)、gypseum Microsporum、canis Microsporum、白色念珠菌(Candida albicans)和热带直孢子菌(Candid tropicalis)等皮肤真菌的生长区分别为70、40、35、30和30 mm,与孔法测定的Clotrimazole参比试剂30、25、25、18和20 mm相比效果显著。ZnO纳米流体对真菌的MIC分别为0.35、3.12、6.25、6.25和6.25 μgr/ml,纳米产物的MFC分别为1.5、12.5、25、25和25 μgr/ml。因此,所设计的氧化锌纳米流体对引起皮肤(癣),粘膜(鹅口疮)和阴道感染的真菌的作用最大,因此我们能够首次将这些表面高能氧化锌纳米流体应用于体外纳米医学和纳米卫生。
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引用次数: 6
Enhanced Thermal Stability of Promising Nano-Porous Silicon Powder 增强纳米多孔硅粉的热稳定性
Pub Date : 2016-09-07 DOI: 10.4236/ANP.2016.54021
M. Nabil, H. Motaweh
A direct synthesis method is introduced to prepare nano-porous silicon-nickel nanocomposite (nPS/Ni) powder for thermal isolation applications. In this paper, we study the thermal stability of nanocomposites consisting of nanoparticles metal incorporated into the pores of a porous silicon by a very simple method. The nickel element is chemically deposited whereas the nanoparticles are precipitated on the pore surfaces. The (nPS) and (nPS/Ni) nano-materials are thermally measured under nitrogen at temperatures of 40℃ - 1000℃, noticeable, demonstrating better thermal stability of (nPS/Ni) until 900℃ than in the case of (nPS) at 600℃. Then, the improving of the thermal stability of the nPS powder is facilitated using it in many applications of the thermal insulation process.
介绍了一种直接合成纳米多孔硅-镍纳米复合材料(nPS/Ni)粉体的方法。本文采用一种非常简单的方法,研究了将纳米金属颗粒掺入多孔硅孔中的纳米复合材料的热稳定性。镍元素化学沉积,而纳米颗粒沉淀在孔表面。(nPS)和(nPS/Ni)纳米材料在40℃~ 1000℃的氮气温度下进行了热测量,结果表明(nPS/Ni)在900℃前的热稳定性优于(nPS)在600℃下的热稳定性。从而提高了nPS粉体的热稳定性,有利于其在保温工艺中的广泛应用。
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引用次数: 10
Green nanotechnology from plant extracts: synthesis and characterization of gold nanoparticles 植物提取物的绿色纳米技术:金纳米颗粒的合成和表征
Pub Date : 2016-07-26 DOI: 10.4236/ANP.2016.53019
A. N. Geraldes, A. A. A. Silva, Jessica Leal, G. M. Estrada-Villegas, N. Lincopán, K. Katti, Ademar Benévolo Lug atildeo
The advantage of using plants in nanoparticles synthesis is that they are easily available, safe to handle and possess a broad variability of metabolites such as antioxidants, nucleotides and vitamins. The aim of this study was to investigate the effects of Green and Zimbro tea and also Green coconut water as a reducing and stabilizer agent in gold nanoparticle synthesis. The gold nanoparticles were characterized by UV-Vis absorption spectroscopy, X-ray diffraction (XRD), Dynamic light scattering (DLS) and Transmission electron microscopy (TEM) analysis. Their physical stability was determined using a UV-Vis spectrophotometer over several days during storage at room temperature. We observed that green chemical process to obtain gold nanoparticles did not require any external chemicals reagent for stabilization of nanoparticulate. Absorption measurements indicated that the plasmon resonance wavelength appears around 530 nm. X-ray diffracto-grams of gold nanoparticles evidenced the presence of Au-rich (fcc) phases. TEM analysis showed a homogeneous dispersion of nanoparticles and some agglomerates. Differences in size and shape of the nanoparticles were observed. Zeta potential of AuNPs synthetized in presence of Green tea was -33 mV indicating stability of the synthesized nanoparticles.
在纳米颗粒合成中使用植物的优点是它们容易获得、处理安全并且具有广泛的代谢物可变性,如抗氧化剂、核苷酸和维生素。这项研究的目的是研究格林茶和辛布罗茶以及绿椰子水作为还原和稳定剂在金纳米颗粒合成中的作用。采用紫外可见吸收光谱、x射线衍射(XRD)、动态光散射(DLS)和透射电子显微镜(TEM)对纳米金进行了表征。用紫外-可见分光光度计测定其在室温下贮存数天的物理稳定性。我们观察到绿色化学过程获得金纳米颗粒不需要任何外部化学试剂来稳定纳米颗粒。吸收测量表明,等离子体共振波长出现在530 nm左右。金纳米颗粒的x射线衍射图证明了富金(fcc)相的存在。透射电镜分析显示纳米颗粒均匀分散,并有一些团聚体。观察到纳米颗粒的大小和形状的差异。在绿茶存在下合成的AuNPs的Zeta电位为-33 mV,表明合成的纳米颗粒具有稳定性。
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引用次数: 53
PtAg Nanoparticle Electrocatalysts for the Glycerol Oxidation Reaction in Alkaline Medium 碱性介质中甘油氧化反应的PtAg纳米粒子电催化剂
Pub Date : 2016-07-26 DOI: 10.4236/ANP.2016.53018
B. Lam, Masanobu Chiku, E. Higuchi, H. Inoue
To improve the activity for glycerol oxidation reaction (GOR) of Pt, PtAg (mole ratio of Pt/Ag = 3 and 1) alloy nanoparticle-loaded carbon black (Pt/CB, PtAg(3:1)/CB, PtAg(1:1)/CB) catalysts were prepared by a wet method. The resultant catalysts, moreover, were heat-treated in a N2 atmosphere at 200°C. The alloying of Pt with Ag for each PtAg/CB was confirmed by X-ray diffractometry and electron dispersive X-ray spectrometry. The heat-treatment did not change the crystal structure of the PtAg alloys and increased their particle size. X-ray photoelectron spectroscopy exhibited that stabilizers were completely removed from the PtAg alloy surface, and the Pt4f and Ag3d doublets due to metallic Pt and Ag, respectively, shifted to lower binding energies, supporting the alloying of Pt with Ag. Both PtAg/CB electrodes had two oxidation waves of glycerol irrespective of heat-treatment, which was different from the Pt/CB electrode. The onset potential of the first oxidation wave was -0.60 V, which was 0.20 V less positive than that for the Pt/CB electrode, indicating the alloying of Pt with Ag greatly improved the GOR activity of Pt. The heat-treated PtAg(3:1)/ CB electrode improved the GOR current density of the second oxidation peak. In the potentiostatic electrolysis at -0.1 and 0 V for both PtAg/CB electrodes, the ratio of oxidation current density at 60 min to that at 5 min (j60/j5), an indicator of the catalyst deterioration, at 0 V was higher than that at -0.1 V, because the adsorbed oxidation intermediates were greatly consumed at the larger overpotential. The heat-treatment of the PtAg(3:1)/CB electrode increased the j60/j5 value at -0.1 V but decreased that at 0 V. This could be attributed to the formation of high-order oxidation intermediates which might have stronger poisoning effect.
为提高Pt的甘油氧化反应(GOR)活性,采用湿法制备了PtAg(Pt/Ag摩尔比为3和1)合金纳米粒子负载炭黑(Pt/CB、PtAg(3:1)/CB、PtAg(1:1)/CB)催化剂。所得催化剂在200℃的N2气氛中进行热处理。通过x射线衍射和电子色散x射线光谱法证实了各PtAg/CB中Pt与Ag的合金化。热处理没有改变PtAg合金的晶体结构,但增大了合金的晶粒尺寸。x射线光电子能谱分析表明,稳定剂被完全从PtAg合金表面去除,金属Pt和Ag分别使Pt4f和Ag3d重态向较低结合能转移,支持Pt与Ag的合金化。PtAg/CB电极与Pt/CB电极不同的是,无论热处理与否,PtAg/CB电极都有两个甘油氧化波。第一个氧化波的起始电位为-0.60 V,比Pt/CB电极的起始电位低0.20 V,表明Pt与Ag的合金化大大提高了Pt的GOR活性。经过热处理的PtAg(3:1)/ CB电极提高了第二个氧化峰的GOR电流密度。PtAg/CB电极在-0.1和0 V的恒电位电解中,60min氧化电流密度与5min氧化电流密度之比(j60/j5)(催化剂劣化指标)在0 V时高于-0.1 V,这是因为在较大的过电位下吸附的氧化中间体被大量消耗。PtAg(3:1)/CB电极在-0.1 V时的j60/j5值升高,在0 V时的j60/j5值降低。这可能是由于形成了高阶氧化中间体,可能具有更强的中毒作用。
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引用次数: 5
Preparation, Characterization and in Vitro Evaluation of the Antitumor Activity of the Biologically Synthesized Silver Nanoparticles 生物合成纳米银的制备、表征及体外抗肿瘤活性评价
Pub Date : 2016-05-19 DOI: 10.4236/ANP.2016.52017
Omama E. Elshawy, E. Helmy, L. Rashed
This study was concentrated on the biosynthesis of silver nanoparticles from Penicillium aurantiogresium (IMI 89372) with a focus on its cytotoxicity in MCF-7 and MCT cancer cell lines as well as Vero (normal) cell line that was assessed by crystal violet assay after treatment with various concentrations (0.44 – 145 μg/ml) for 24 h. The cell morphology was examined by inverted light microscopy. Further, the radiosensitizing effect of silver nanoparticles (AgNPs) on MCF-7 was also demonstrated by assessing cell morphology, cell proliferation of MTT assay, LDH activity and induction of apoptosis through checking of some apoptotic genes that altered during carcinogenesis, including caspase-3, Bax and Bcl-2. Caspase-3 activity was also estimated. Synthesis of AgNPs was determined by UV-Visible spectrum and it was further characterized by TEM, FT-IR and X-Ray analysis (EDX, XRD). The biosynthesized AgNPs were spherical and of 12.7 nm in size as recorded by direct electron microscopy visualization. The biosynthesized AgNPs showed variation in cytotoxicity against MCF-7, MCT and Vero cell lines in a concentration dependant response with a varied degree of alteration in cell morphology. The result showed that AgNPs were highly toxic towards MCF-7 with IC50 value of 10.5 μg/ml. Treatment of MCF-7 (10.5 μg/ml) prior to irradiation improved the effect of irradiation dose (6 Gy) via increasing alteration of cell morphology, inhibition of cell proliferation, activation of the lactate dehydrogenase (LDH) and caspase-3 leading to induction of apoptosis which was further confirmed through increasing nuclear DNA damage and up regulation of caspase 3 and Bax genes and downrgulation of Bcl-2 genes. In conclusion, the present findings clearly indicated that AgNPs showed dose dependant cytotoxicity and verified that AgNPs acted as a potent radiosensitizer and could enhance gamma irradiation induced killing of MCF-7 breast cancer cells.
本研究以金黄色青霉(Penicillium aurantiogresium, IMI 89372)为主要材料合成银纳米粒子,研究其对MCF-7、MCT癌细胞和Vero(正常)细胞株在不同浓度(0.44 ~ 145 μg/ml)作用24 h后的细胞毒性。倒置光镜下观察细胞形态。此外,银纳米粒子(AgNPs)对MCF-7的放射增敏作用也通过评估细胞形态、MTT试验的细胞增殖、LDH活性和通过检查一些在癌变过程中改变的凋亡基因(包括caspase-3、Bax和Bcl-2)诱导凋亡来证明。同时估计Caspase-3活性。通过紫外可见光谱确定AgNPs的合成,并通过TEM、FT-IR和x射线分析(EDX、XRD)对其进行表征。通过直接电镜观察,生物合成的AgNPs为球形,尺寸为12.7 nm。生物合成AgNPs对MCF-7、MCT和Vero细胞系的细胞毒性表现出浓度依赖性,细胞形态发生不同程度的改变。结果表明,AgNPs对MCF-7具有高毒性,IC50值为10.5 μg/ml。辐照前处理MCF-7 (10.5 μg/ml)可通过增加细胞形态学改变、抑制细胞增殖、激活乳酸脱氢酶(LDH)和caspase-3导致细胞凋亡,从而改善辐照剂量(6 Gy)的效果,这一效应通过核DNA损伤增加、caspase 3和Bax基因上调、Bcl-2基因下调进一步得到证实。总之,本研究结果清楚地表明AgNPs具有剂量依赖性的细胞毒性,并证实AgNPs作为一种有效的放射增敏剂,可以增强γ辐射诱导的MCF-7乳腺癌细胞的杀伤。
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引用次数: 33
High Sensitivity of Porous Cu-Doped SnO2 Thin Films to Methanol 多孔cu掺杂SnO2薄膜对甲醇的高灵敏度
Pub Date : 2016-05-19 DOI: 10.4236/ANP.2016.52016
S. Benzitouni, M. Zaabat, A. Khial, D. Rechem, A. Benaboud, D. Bouras, A. Mahdjoub, M. Toubane, Raphael Coste
Porous Cu-doped SnO2 thin films were synthesized by the sol-gel dip-coating method for enhancing methanol sensing performance. The effect of Cu doping concentration on the SnO2 sensibility was investigated. XRD data confirm that the fabricated SnO2 films are polycrystalline with tetragonal rutile crystal structure. AFM and SEM micrographs confirmed the roughness and the porosity of SnO2 surface, respectively. UV-Vis spectrum shows that SnO2 thin films exhibit high transmittance in the visible region ~95%. The band gap (3.80 - 3.92 eV) and the optical thickness (893 - 131 nm) of prepared films were calculated from transmittance data. The sensing results demonstrate that SnO2 films have a high sensitivity and a fast response to methanol. In particular, 3% Cu-SnO2 films have a higher sensitivity (98%), faster response (10-2 s) and shorter recovery time (18 s) than other films.
采用溶胶-凝胶浸包法制备了多孔掺铜SnO2薄膜,提高了其甲醇传感性能。研究了Cu掺杂浓度对SnO2敏感性的影响。XRD数据证实制备的SnO2薄膜是具有四方金红石晶体结构的多晶。原子力显微镜(AFM)和扫描电镜(SEM)分别证实了SnO2表面的粗糙度和孔隙度。紫外可见光谱表明,SnO2薄膜在可见光区具有较高的透过率,达到95%。利用透射率数据计算了薄膜的带隙(3.80 ~ 3.92 eV)和光学厚度(893 ~ 131 nm)。结果表明,SnO2薄膜对甲醇的响应速度快,灵敏度高。其中,3% Cu-SnO2薄膜比其他薄膜具有更高的灵敏度(98%)、更快的响应(10-2 s)和更短的恢复时间(18 s)。
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引用次数: 19
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