Department of Civil and Environmental Engineering, University of Massachusetts, Amherst, MA 01003-9293, USA.
Water Res. 2011 Nov 1;45(17):5428-40. doi: 10.1016/j.watres.2011.08.014. Epub 2011 Aug 16.
The paper addresses the effects of salinity and temperature on the chemistry of important parameters affecting coagulation pretreatment including the ion product of water, acid-base chemistry, dissolved metal speciation, and precipitation reactions for aluminum and iron coagulants. The ion product of seawater is greater than for freshwaters and affects chemical hydrolysis and metal-hydroxide solubility reactions. Inorganic carbon is the main cause of seawater alkalinity and buffer intensity but borate B(OH)(4)(1-) also contributes. Buffer intensity is an important parameter in assessing coagulation pH adjustment. Mineral particles are relatively unstable in seawater from electrical double layer compression, and when present these particles are easily coagulated. Algal-particle stability is affected by steric effects and algal motility. Dissolved natural organic matter from algae and humic substances causes fouling of RO membranes and pretreatment removal is essential. Aluminum coagulants are not recommended, and not used, because they are too soluble in seawater. Ferric coagulants are preferred and used. The equilibrium solubility of Fe with amorphous ferric hydroxide in seawater is low over a wide range of pH and temperature conditions. Ferric chloride dosing guidelines are presented for various raw seawater quality characteristics. The effect of pH on coagulant dose and the role of buffer intensity are addressed. A dual coagulation strategy is recommended for treating seawater with moderate to high concentrations of algae or seawater with humic matter. This involves a low and constant dose with high charge-density cationic polymers using Fe as the main coagulant where it is varied in response to raw water quality changes.
本文探讨了盐度和温度对影响混凝预处理的重要参数化学性质的影响,这些参数包括水的离子积、酸碱化学、溶解金属形态、铝和铁混凝剂的沉淀反应。海水的离子积大于淡水,会影响化学水解和金属氢氧化物的溶解度反应。无机碳是海水碱度和缓冲强度的主要原因,但硼酸 B(OH)(4)(1-)也有贡献。缓冲强度是评估混凝 pH 调整的一个重要参数。由于电双层压缩,矿粒在海水中相对不稳定,而当这些颗粒存在时,它们很容易被凝聚。藻类颗粒的稳定性受到空间位阻效应和藻类运动的影响。来自藻类和腐殖质的溶解天然有机物会导致反渗透膜结垢,因此预处理去除是必不可少的。不推荐也不使用铝混凝剂,因为它们在海水中的溶解度太高。推荐使用铁混凝剂。在广泛的 pH 和温度条件下,海水中无定形氢氧化铁与铁的平衡溶解度很低。针对各种原海水水质特性,提出了氯化铁投加的指南。还讨论了 pH 对混凝剂剂量的影响以及缓冲强度的作用。对于高浓度藻类或富含有机物的海水,建议采用双重混凝策略。这涉及使用带高电荷密度的阳离子聚合物进行低且恒定的剂量,其中铁是主要的混凝剂,根据原水水质的变化进行调整。