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Wettability and Surface Free Energy of Granodiorite, Dolomite and Recycled Ceramic Aggregate

机译:Granodiorite,白云石和再生陶瓷聚集体的润湿性和表面自由能

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The study of wetting properties and surface free energy (SFE) of granodiorite, dolomite and recycled ceramic aggregate was presented in the paper. Every tested aggregate had different wetting properties. Based on the SEM study, the micro structure was shown. Wetting properties of various aggregates were determined by measuring the contact angle of their surface using water as measuring liquid. Many factors influence the contact angle, including physical and chemical homogeneity, roughness and surface contamination, type of measuring liquid, drop size of measuring liquid, humidity, ambient temperature, etc. Measurements were carried out 0 minutes after the time of application of the drops. The total SFE was determined using the Neumann method. Analyzing examination results it can be noticed that the values of contact angles depends on the absorbability of aggregate and smoothness of its surface. The results of contact angle measurements proved that all contact angles for ceramic aggregate were lower than contact angles for dolomite and granodiorite. That causes the total SFE for ceramic aggregate was higher than SFE for dolomite and granodiorite aggregate. The highest contact angle was noticed for granodiorite. The smallest contact angle with water was obtained by ceramic aggregate. This is due to physical characteristics of this aggregate. Ceramic aggregate is characteristic of the high absorbability. This indicates an increased wettability and increased adhesion properties.
机译:本文介绍了对麦替菌,白云岩和再循环陶瓷聚集体的润湿性能和表面自由能(SFE)的研究。每个测试的聚集体具有不同的润湿性能。基于SEM研究,显示了微结构。通过用水测量其表面作为测量液体的水面的接触角来测定各种聚集体的润湿性能。许多因素会影响接触角,包括物理和化学均匀性,粗糙度和表面污染,测量液的类型,测量液体的液滴尺寸,湿度,环境温度等。在施加液滴的时间后进行0分钟进行测量。测量。使用Neumann方法确定总SFE。分析检查结果可以注意到接触角的值取决于其表面聚集体和平滑度的吸收性。接触角测量结果证明,陶瓷聚集体的所有接触角度低于白云石和Granodiorite的接触角。导致陶瓷聚集体的总SFE高于白细胞和Granodiorite骨料的SFE。对于Granodiorite,注意到最高的接触角。通过陶瓷聚集体获得与水的最小接触角。这是由于这种聚集体的物理特征。陶瓷聚集体是高吸收性的特征。这表明润湿性和粘合性质增加​​增加。

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