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Composite fouling of calcium sulfate and calcium carbonate in a dynamic seawater reverse osmosis unit

机译:动态海水反渗透装置中硫酸钙和碳酸钙的复合污染

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摘要

Deposition of calcium carbonate (CaCO3) and calcium sulfate (CaSO4) causes serious processing problems and limits theproductivity of seawater reverse osmosis (RO) desalination. The interactions between CaSO4 and CaCO3 in the dynamicseawater RO systems have been neglected previously because conventional studies mainly focused on individual compounds ormixed compounds in batch systems. The present work evaluates composite fouling behavior of CaSO4 and CaCO3 in a dynamicRO unit. The fouling experiments were performed at constant pressure and velocity by a partial recycling mode which permeatewas withdrawn from the system during the recirculation of retentate to simulate the increasing of water recovery level. Thefouling phenomena were monitored by the decline of flux. Scanning electron microscopy (SEM) with a combination ofelemental dispersive x-ray microanalysis (EDS), and x-ray powder diffraction (XRD) was used to identify the morphologicalfeatures, chemical compositions and crystalline phases of foulants.The interactions of CaSO4 and CaCO3 were investigated by the comparison between individual CaSO4 or CaCO3 fouling andcomposite fouling, and by varying SO42-/HCO3- molar ratio of the feed. A recently developed approach, Scaling PotentialIndex (SPI) incorporated with measured concentration polarization modulus (CP), for assessing the fouling tendency ofinorganic salts on the membrane surface was validated in the dynamic tests. In addition, the effectiveness of two generic scaleinhibitors, polyacrylic acid (molecular weight =2100, PA) and sodium hexametaphosphate (SHMP) were evaluated. Some of thehighlights of the obtained results are as follows:••The precipitation kinetics, morphology and adhesive strength of composite scales were different from pure precipitates••CaSO4 precipitated as gypsum while CaCO3 precipitated as two crystalline phases: calcite and aragonite••The crystalline phases as well as precipitation kinetics were affected by SO42-/HCO3- ratio••Scaling Potential Index was able to predict the fouling tendency of CaSO4 and CaCO3 accurately••The dosage of PA and SHMP was effective to mitigate foulingResults of this work are significant, not only because they have made contribution to the fundamental understanding ofcomposite inorganic fouling in RO membrane systems which was ignored previously, but also because they may play a key rolein the development of scale control.
机译:碳酸钙(CaCO3)和硫酸钙(CaSO4)的沉积会导致严重的加工问题,并限制海水反渗透(RO)脱盐的生产率。以前已经忽略了动态海水反渗透系统中CaSO4和CaCO3之间的相互作用,因为常规研究主要集中在间歇系统中的单个化合物或混合化合物上。本工作评估了dynamicRO装置中CaSO4和CaCO3的复合污染行为。结垢实验通过部分再循环模式在恒定压力和速度下进行,该部分再循环模式在渗余物再循环过程中将渗透物从系统中抽出,以模拟水回收水平的提高。通过通量的下降来监测结垢现象。结合元素色散X射线显微分析(EDS)和X射线粉末衍射(XRD)的扫描电子显微镜(SEM)来鉴定污垢物的形态特征,化学组成和晶相.CaSO4和CaCO3的相互作用为通过比较单个CaSO4或CaCO3结垢与复合结垢之间的比较,以及通过改变进料的SO42- / HCO3-摩尔比来进行研究。在动态测试中验证了最近开发的一种方法,与测量的浓度极化模量(CP)结合使用的Scaling PotentialIndex(SPI),用于评估膜表面无机盐的结垢趋势。此外,评估了两种通用的阻垢剂聚丙烯酸(分子量= 2100,PA)和六偏磷酸钠(SHMP)的有效性。所得结果的一些亮点如下:•复合鳞片的沉淀动力学,形态和粘附强度与纯沉淀物不同••CaSO4以石膏形式沉淀,而CaCO3以方解石和文石两个结晶相沉淀••结晶SO42- / HCO3-比对相和沉淀动力学的影响••垢势指数能够准确预测CaSO4和CaCO3的结垢趋势••PA和SHMP的用量有效减轻结垢这项工作的结果是有意义的这不仅是因为它们为反渗透膜系统中复合无机污垢的基本理解做出了贡献,而这在以前是被忽略的,而且还因为它们可能在水垢控制的发展中发挥关键作用。

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