995 resultados para 225
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以辽阳市沙岭镇大闯屯村为例,对北方平原地区农村水塘系统污染现状、非点源污染物的迁移途径、控制方法进行了初步研究,研究结果表明,农田径流与村落生活污水的排放方式对农村地表水环境质量具有重要影响,进行合理的生态设计,充分利用自然净化单元,对改善地表水环境质量将会起到积极的作用。
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对早柳和小青杨的年轮宽度、年轮密度、木材纤维长度和干缩率及其径向变异进行了研究.结果表明,木材物理特性受年轮年龄的影响显著,而纤维长度不受年轮宽度影响.综合材质物理特性的径向变异规律,可将旱柳和小青杨整个生长期划分为4个时期:幼林期、速生期、成熟期和更新期,确定了各生长期的年龄值.
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以Tenax-TA、Carboxen 1000和Carbosieve SⅢ为采样管填充料,将植物源挥发性有机物吸附于采样管内,样品通过二次热解吸仪解吸后,随载气进入气相色谱仪,采用氢火焰离子化检测器(FID)测定,建立了利用二次热解吸仪与气相色谱联用技术测定植物挥发性有机物的分析方法。载气N2流速为30 mL/min,60℃下吹扫吸附管2 min,然后在250℃下解吸吸附管5 min,冷却1 min后,在275℃下解吸聚焦管3 min,样品经传输线进入气相色谱。气相色谱载气N2压力为190 kPa,FID检测器温度280℃;进样口温度225℃;初始柱温40℃,停留5 min,以2℃/min升温至120℃,保留1 min,然后以20℃/min升温至200℃,保留10 min。方法重现性好,精密度高,线性相关系数大于0.99;检出限均低于9×10-9g/L;解吸效率大于96%,适用于植物源挥发性有机物的测定。
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对中巴资源一号卫星 CCD传感器接收的辽宁省营口幅数据 ,从几何精度、空间分辨率、数据噪声等方面 ,进行了图像数据质量评价 ,认为从总体上讲 ,达到了设计要求 ,具有广阔的应用前景 ,同时指出 ,CCD传感器在稳定性和同一性方面尚需改进
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By using ethylenediamine as both an alkali and ligand, quantum size SnO2, nanocrystallites were synthesized with a solvothermal route. The transmission electron micrographs (TEM) were employed to characterize the morphologies of the products. The crystal sizes of the as-synthesized SnO2 were ranged form 2.5 to 3.6 nm. The crystal structure and optical properties of the products were investigated by X-ray diffraction, Fourier transform infrared spectroscopy, optical absorption spectra, photoluminescence and Raman spectra.
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The structural, mechanical and electronic properties Of OsC2 were investigated by use of the density functional theory. Seven structures were considered, i.e., orthorhombic Cmca (No. 12, OsSi2), Pmmn (No. 59, 002) and Pnnm (No. 58, OsN2); tetragonal P4(2)/mnm (No. 136, OsO2) and 14/mmm (No. 139, CaC2); cubic Fm-3m (No. 225, CaF2) and Pa-3 (No. 205, PtN2). The results indicate that Cmca in OsSi2 type structure is energetically the most stable phase among the considered structures. It is also stable mechanically. OsC2 in Pmmn phase has the largest bulk modulus 319 GPa and shear modulus 194 GPa. The elastic anisotropy is discussed. (C) 2009 Elsevier B.V. All rights reserved.
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Chitosan(chitin)/cellulose composites as biodegradable biosorbents were prepared under an environment-friendly preparation processes using ionic liquids. Infrared and X-ray photoelectron spectra indicated the stronger intermolecular hydrogen bond between chitosan and cellulose, and the hydroxyl and amine groups were believed to be the metal ion binding sites. Among the prepared biosorbents, freeze-dried composite had higher adsorption capacity and better stability. The capacity of adsorption was found to be Cu(II) (0.417 mmol/g) > Zn(II) (0.303 mmol/g) > Cr(VI) (0.251 mmol/g) > Ni(II) (0.225 mmol/g) > Ph(II) (0.127 mmol/g) at the same initial concentration 5 mmol L-1. In contrast to some other chitosan-type biosorbents, preparation and component of the biosorbent were obviously more environment friendly. Moreover, adsorption capacity of chitosan in the blending biosorbent could be fully shown.
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Breakup process of polyamide 6 (PA6) in polypropylene (PP) matrix under shear flow was online studied by using a Linkam CSS 450 stage equipped with optical microscopy. Both tip streaming and fracture breakup modes of PA6 droplets were observed in this study. It was reported that the droplet would break up by tip streaming model when the radio of the droplet phase viscosity to the matrix phase viscosity (n(r) = n(d)/n(m)) is smaller than 0.1 (Taylor, Proc R Soc London A 1934, 146, 501; Grace, Chem Eng Commun 1982, 14, 225; Bartok and Mason, J Colloid Sci 1959, 14, 13; Rumscheidt and Mason, J Colloid Sci 1961, 16, 238; de Bruijn, Chem Eng Sci 1993, 48, 277). However, the tip streaming model was observed even when the viscosity ratio was much greater than 0.1 (n(r) = 1.9). In this study for the tip streaming mode, small droplets were ruptured from the tip of the mother droplet. On the other hand, the mother droplet was broken into two or more daughter droplets with one or several satellite droplets between them for the fracture mode. It was found that PA6 droplet was much elongated at first, and then broke up via tip streaming or fracture to form daughter droplets or small satellite droplets with the shape of fiber or ellipse.
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A novel method to fabricate a hydrogen peroxide sensor was developed by immobilizing horseradish peroxidase (HRP) on colloidal An modified ITO conductive glass support. The cleaned glass support was modified with (3-aminopropyl)trimethoxysilane (APTMS) first to yield an interface for the assembly of colloidal An. Then 15 nm colloidal Au particles were chemisorbed onto the amine groups of the APTMS. Finally, HRP was adsorbed onto the surface of the colloidal An. The immobilized HRP displayed excellent electrocatalytical response to the reduction of hydrogen peroxide. The performance and factors influencing the resulted biosensor were studied in detail. The resulted biosensor exhibited fast amperometric response (within 5 s) to H2O2. The detection limit of the biosensor was 8.0 mumol l(-1), and linear range was from 20.0 mumol l(-1) to 8.0 mmol l(-1). Furthermore, the resulted biosensor exhibited high sensitivity, good reproducibility, and long-term stability.
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通过溶胶-凝胶法合成了Ni0.65Zn0.35Cu0.1Fe1.9O4/SiO2纳米复合材料。借助XRD、TEM和VSM对纳米复合材料进行了表征,试验表明,当热处理温度达550℃,可得到分散于SiO2中的单相纳米NiZnCu铁氧体。纳米复合材料的磁学性质呈明显的温度依赖性。饱和磁化强度随热处理温度的提高而增加。
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The effect of copper phthalocyanine (CuPc) and LiF interfacial layers on the charge-carrier injection in NN'-di(naphthalene-l-yl)N,N'-diphenyl-benzidine (NPB)/tris(8-hydroxyquinoline) aluminium (Alq(3)) organic heterojunction devices have been studied through the analysis of current-voltage characteristics. The investigation clearly demonstrated that the hole injection into NPB from anode is Fowler-Nordheim (FN) tunneling and the electron injection into Alq3 from cathode is Richardson-Schottky (RS) thermionic emission. The barrier heights obtained from the FN and RS models proved that the band alignments for charge-carrier injection are greatly improved by the CuPc and LiF interfacial layers, which should fully clarify the role of the interfacial layer on the improvement of device performance.
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Two commercial biaxially oriented polypropylene (BOPP) resins, resin A and resin B, having different processing properties, were fractionated by preparative temperature-rising elution fractionation (TREF). The TREF fractions were further characterized by gel permeation chromatography (GPC), gel permeation chromatography coupled with light scattering (GPC-LS), wide-angle X-ray diffraction (WAXD), and differential scanning calorimetry (DSC). GPC-LS did not find visible long-chain branching in either resin A or B. The results from TREF and DSC indicate that the fractional melting parameter f(T) may be used to predict the profile of the TREF cumulative weight distribution curve. GPC results show that the molecular weights of the fractions tend to increase with elution temperature. WAXD and DSC data show that the crystallinity of fractions does not increase monotonically with increase of elution temperature. There appears to be a maximum in the plot of crystallinity versus elution temperature. The high-speed BOPP resin A has a lower isotacticity but a homogeneous isotacticity distribution and a higher molecular weight but a broader molecular weight distribution than resin B.