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Scale formation on polypropylene and copper tubes.

机译:在聚丙烯和铜管上结垢。

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摘要

The scaling behaviors of polypropylene and copper were compared quantitatively under accelerated conditions (distilled water or high supersaturation) and more realistic conditions (potable water and low supersaturation). In addition, the effect of surface roughness on scaling on polypropylene surfaces was studied.; Polypropylene tubes, with different degrees of root mean square roughness on the inner surfaces created by machining with abrasives, were exposed to a laminar flow of distilled water supersaturated with respect to CaCO 3. Nucleation site density, i.e. the number of crystals per unit surface area, on the machined surfaces was two to ten times that on the native surfaces. However, the nucleation site density was not correlated to the roughness of the samples. These results suggest that nanometer-sized surface imperfections (e.g. steps and grooves) formed during the roughening process, rather than roughness, are responsible for the enhanced nucleation on the machined PP surfaces.; Scaling behaviors on polypropylene and copper were compared by exposing the surfaces to laminar flows of distilled water and potable water highly supersaturated with respect to CaCO3 (supersaturation, S > 9) for 0.5 to 4 hours, and distilled water mildly supersaturated (S = 4.8) for 1.5 to 15 hours. The scaling rate of polypropylene was at least 40 higher than that of copper after exposure to the distilled water at S ¿ 9. The scaling rates of polypropylene and copper were not statistically different after exposure to either mildly supersaturated distilled water (S = 4.8) or highly supersaturated potable water.; Polypropylene and copper tubes were also exposed to a laminar flow of mildly supersaturated potable water at 40°C (S = 5 with respect to CaCO3) for 1 to 8 weeks. Calcium phosphate was a major component of the calcium-rich scale deposit, a result that is linked to the presence of trace amount of phosphate ions in the water and the inhibiting effect (for CaCO3 formation) of other ions present. Under these conditions, Cu oxidizes and scales at a higher rate than PP.
机译:在加速条件下(蒸馏水或高过饱和度)和更实际的条件下(饮用水和低过饱和度)定量比较了聚丙烯和铜的结垢行为。另外,研究了表面粗糙度对聚丙烯表面结垢的影响。聚丙烯管的内表面具有不同程度的均方根粗糙度,这些内表面是通过用磨料进行机械加工制成的,将其暴露于相对于CaCO 3过饱和的蒸馏水的层流中。成核位点密度,即每单位表面积的晶体数量,在加工表面上,是原始表面上的2至10倍。但是,成核位点密度与样品的粗糙度无关。这些结果表明在粗糙化过程中形成的纳米级表面缺陷(例如台阶和凹槽),而不是粗糙度,是导致加工后的PP表面上形核增强的原因。通过将表面暴露于层流的蒸馏水和相对于CaCO3高过饱和度的饮用水(过饱和度,S> 9)0.5至4小时,以及轻度过饱和度的蒸馏水(S = 4.8),比较聚丙烯和铜的结垢行为持续1.5到15个小时。暴露于S≥9的蒸馏水中后,聚丙烯的结垢率至少比铜的结垢率高40。暴露于轻度过饱和的蒸馏水(S = 4.8)或之后,聚丙烯和铜的结垢率无统计学差异。高度过饱和的饮用水。聚丙烯管和铜管还暴露于40°C(相对于CaCO3的S = 5)的层流中的轻度过饱和饮用水中1到8周。磷酸钙是富含钙的水垢沉积物中的主要成分,其结果与水中痕量磷酸根离子的存在以及存在的其他离子的抑制作用(对于形成CaCO3)有关。在这些条件下,Cu的氧化和结垢速率比PP高。

著录项

  • 作者

    Wu, Zhen.;

  • 作者单位

    University of Minnesota.$bMaterial Science and Engineering.;

  • 授予单位 University of Minnesota.$bMaterial Science and Engineering.;
  • 学科 Engineering Materials Science.
  • 学位 Ph.D.
  • 年度 2008
  • 页码 208 p.
  • 总页数 208
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 工程材料学;
  • 关键词

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