共查询到19条相似文献,搜索用时 125 毫秒
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腐植酸溶液在煤表面接触角的实验研究 总被引:2,自引:1,他引:2
测定了不同浓度及不同PH值下黄腐酸溶液的表面张力及其在煤表面的接触角。结果表明:随浓度的增大,黄腐酸溶液的表面张力减小,而在煤表面的接触角增大;在酸性条件下随PH值的增大黄酸溶液在煤表面的接触角减小且变化明显,在碱性条件下,接触角变化不明显。 相似文献
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接触角测量方法及其对纤维/树脂体系的适应性研究 总被引:1,自引:0,他引:1
接触角是衡量材料表面润湿性能的重要参数。接触角测试是材料表面探测的重要技术手段,通过接触角测试可得到固液、气液、气固界面相互作用的许多重要信息,诸如表面湿润性能、固液界面张力、表面粗糙度、化学多相性等。本文介绍了常见的接触角的测量方法,并针对玻璃纤维/树脂体系的特点,详细分析了常用接触角测量方法对玻璃纤维/树脂体系的适应性,以此探讨新的实验技术。 相似文献
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表面张力对传质过程的影响 总被引:4,自引:1,他引:4
表面张力对传质过程的影响主要是影响传质界面积,当物系为正物系时,对板式塔有较小较稳定的汽泡,对填料塔和湿壁塔,有较稳定的液膜,结果使二者均有较大的传质界面积,传质效果较好;负物系的情况相反。当液体混合物的平均表面张力较小时,也有利于形成较小较稳定的汽泡,从而有利于传质。表面张力对传质过程的影响机理相当复杂,这方面的研究工作有待深入开展。 相似文献
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用接触角法测量聚合物共混体系的表面性能 总被引:11,自引:0,他引:11
利用接触角的方法研究了聚合物HDPF、PET及其共混物HDPE/PET的表面自由能、极化度以及与不同液体一水和甘油间界面张力的大小。 相似文献
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《Journal of Adhesion Science and Technology》2013,27(9):1037-1051
Contact angle, surface tension and wetting properties are of fundamental importance in many industrial processes, e.g. coating of television screens and fluorescent lights. In addition, different stages of many processes may involve immersion cleansing and subsequent drying. We consider two different problems: one being very practical and involving cleansing and drying of silicon substrates in the semiconductor industry, and the other being theoretical whereby the problem of the shape of scssile and pendant drops is addressed with a possible practical application for making contact angle and surface tension measurements. In the case of cleansing of silicon substrates, we model a process whereby dirt particles are removed as a result of the surface tension forces exerted on a particle passing through a water/air interface and give a possible explanation as to why the efficiency of the process is vclocity dependent. For the case of small liquid drops, a new formulation of the governing equation yields solutions for multiple pendant and extended sessile drops. 相似文献
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Surface tension is a parameter of decisive importance for characterizing painted and unpainted surfaces related to wetting and adhesion phenomena. Measurements of the surface tension of solids by means of an automatic contact angle measurement device are presented. The theoretical evaluations provide for a separation of the surface tension into polar and disperse components. In addition, this paper briefly touches on other more far-reaching approaches (acid/base) and discusses a method for the determination of the dynamic surface tension of liquids. 相似文献
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Young-Wun Kim Keunwo Chung Eun-A. Lee Yong-Geol Seo 《Journal of Industrial and Engineering Chemistry》2008,14(6):752-758
A series of alcohols containing perfluorinated segments F(CF2)m(CH2)n–OH (m = 8, 10 and n = 10) were synthesized. First, the alcohols were reacted with fatty acid to produce several esters (i.e. F(CF2)m(CH2)n–OOC–R (m = 8, 10 and n = 10)) containing perfluoro group by a condensation reaction, and characterized by FT-IR, GC, and surface tension. The esters were found to be soluble in ethyl ether, toluene, hexane, ethyl acetate, chloroform, and acetone, but insoluble in methyl alcohol, ethyl alcohol and isopropyl alcohol. Preliminary experiments on 1,2-dichloroethane solutions showed a remarkable decrease of surface tension upon the addition of the esters. In addition, the esters using urethane resin were coated onto a glass substrate using a spin-coating method. It was found that the contact angle of coated films ranged from 100° to 120°, depending on the structure of fatty acid esters. As a part of experiments, the water-repellency of coated paper and cotton was evaluated, and it was observed that the water droplet on the film surface was not permeated for 2 weeks. 相似文献
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The effect of film thickness and surface preparation techniques on contact angles of water, 1-bromonaphtalene, and n-hexadecane on Teflon® AF 1600 polymeric surfaces is studied. It was found that contact angles of water on different thicknesses of spin-coated films ranging from 27?nm to 420?nm are essentially constant. This is due to the homogeneity and smoothness of the coating layers as shown by the scanning force microscopy of the samples. Furthermore, the contact angle measurements with these three liquids on both dip-coated and spin-coated films suggested that the film preparation technique does not affect contact angles dramatically. Interestingly, slightly higher contact angles on dip-coated surfaces were measured. It is also argued that the anomaly of the water contact angle—in the sense that the measured contact angle is much higher than the expected ideal value—is due to specific interactions between water and Teflon®. 相似文献
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通过动态法研究了浸润粉层的液体质量的平方随时间的变化规律,测定了不同探测液对花生壳的接触角。采用平衡接触角仪测定了探测液对改性聚乙烯的接触角,进而根据Focks理论推导出花生壳和改性聚乙烯的表面自由能及其极性分量和非极性分量,并计算出花生壳粉/聚乙烯复合材料的界面张力和黏附功。结果表明:相容剂Bondyram 5108的加入,使聚乙烯的极性分量和非极性分量都不同程度地增加,改善了花生壳粉在聚乙烯基体中的分散性,降低了复合材料的界面张力,增大了黏附功。 相似文献
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Natthakeeraya Luangpirom Nimit Dechabumphen Chintana Saiwan John F. Scamehorn 《Journal of surfactants and detergents》2001,4(4):367-373
In this study, the contact angle of a saturated aqueous surfactant solution onto the surface of a precipitate of that surfactant
is investigated. Those precipitates include fatty acids (C10, C12, C14, C16, and C18), sodium salts of fatty acids (C14, C16, and C18), calcium salts of fatty acids (C8, C10, C12, C14, C16, and C18). On virgin surfaces, free fatty acids and calcium salts of fatty acids have advancing contact angles (θA) between 77 and 92°, with little dependence on alkyl chain length for C12 and higher alkyl chains. The sodium salt of a fatty acid has a lower θA than the free fatty or the calcium salt of the soap. The calcium salt of dodecyl sulfate has a lower θA than the calcium salt of dodecanoic acid (θA = 46 vs. 82°), but the calcium salt of the 18-carbon hydrophobes showed nearly the same contact angle for the soap and the
alkyl sulfate. Greasiness, or slipperyness, or a scummy feel of a precipitated surfactant does not necessarily correspond
to a hydrophobic surface. 相似文献
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Low-rate dynamic contact angles of 12 liquids on a poly(methyl methacrylate/n-butyl methacrylate) P(MMA/nBMA) copolymer are measured by an automated axisymmetric drop shape analysis-profile (ADSA-P). It is found that 6 liquids yield non-constant contact angles, and/or dissolve the polymer on contact. From the experimental contact angles of the remaining 6 liquids, it is found that the liquid- vapour surface tension times the cosine of the contact angle changes smoothly with the liquid-vapour surface tension, i.e., γiv cos θ depends only on γiv for a given solid surface (or solid surface tension). This contact angle pattern is in harmony with those from other inert and noninert (polar and non-polar) surfaces [34-42, 51 -53]. The solid-vapour surface tension calculated from the equation-of-state approach for solid -liquid interfacial tensions [14] is found to be 34.4 mJ/m2, with a 95% confidence limit of \pm 0.8mJ/m2, from the experimental contact angles of the 6 liquids. 相似文献