Jiao Ruyuan, Fabris Rolando, Chow Christopher W K, Drikas Mary, van Leeuwen John, Wang Dongsheng
State Key Laboratory of Environmental Aquatic Chemistry, Research Center for Eco-Environmental Sciences, CAS, POB 2871, Beijing 100085, China.
Australian Water Quality Centre, South Australian Water Corporation, 250 Victoria Square, Adelaide, South Australia 5000, Australia.
Chemosphere. 2016 May;150:211-218. doi: 10.1016/j.chemosphere.2016.02.030. Epub 2016 Feb 20.
In full scale water treatment operation, the rapid filtration process, as the last step of solid-liquid separation, is largely influenced by floc characteristics. In this study, aluminium sulphate (alum) and nano-Al13 were investigated to understand the influence of coagulant species on the formation and filterability of flocs. At neutral pH, it was found that nano-Al13, a high MW polymer, showed better floc filterability than alum. This is because of the densely compacted and well-distributed size flocs from nano-Al13, even though floc sizes of alum were generally bigger. Al specie distributions of the two coagulants at different pH levels were compared by using electrospray ionization time-of-flight mass spectrometry (ESI-TOF-MS) to further elucidate the reasons for the superiority of nano-Al13 in floc filterability. Depolymerisation/re-polymerisation of nano-Al13 occurred as pH changed, and Al species from nano-Al13were more abundant than that from alum, especially for the high molecular weight (MW) oligomers such as Al11, Al12, Al13 and Al14. Under the charge neutralisation mechanism, higher MW Al species was found to improve coagulation performance and floc filterability. In addition, breakage resistance and regrowth ability of nano-Al13 was better than alum, at weak acid condition. Flocs formed by the charge neutralisation mechanism readily regenerated after being thoroughly broken up. The floc regrowth ability of nano-Al13 at high shear rates (200 rpm and 300 rpm) was much better than at low shear and better than any shear applied to alum., and the flocs after breakage at 200 rpm and 300 rpm also showed better filterability than other conditions.
在全规模水处理操作中,快速过滤过程作为固液分离的最后一步,在很大程度上受絮凝体特性的影响。在本研究中,对硫酸铝(明矾)和纳米Al13进行了研究,以了解混凝剂种类对絮凝体形成和过滤性的影响。发现在中性pH值下,高分子量聚合物纳米Al13表现出比明矾更好的絮凝体过滤性。这是因为纳米Al13形成的絮凝体尺寸紧密压实且分布均匀,尽管明矾形成的絮凝体尺寸通常更大。通过使用电喷雾电离飞行时间质谱(ESI-TOF-MS)比较了两种混凝剂在不同pH值水平下的铝形态分布,以进一步阐明纳米Al13在絮凝体过滤性方面具有优势的原因。随着pH值的变化,纳米Al13发生解聚/再聚合,并且纳米Al13的铝形态比明矾更丰富,特别是对于高分子量(MW)低聚物,如Al11、Al12、Al13和Al14。在电荷中和机制下,发现较高分子量的铝形态可改善混凝性能和絮凝体过滤性。此外,在弱酸条件下,纳米Al13的抗破碎性和再生长能力优于明矾。通过电荷中和机制形成的絮凝体在被彻底破碎后很容易再生。纳米Al13在高剪切速率(200 rpm和300 rpm)下的絮凝体再生长能力比低剪切时要好,且优于施加在明矾上的任何剪切,并且在200 rpm和300 rpm下破碎后的絮凝体也表现出比其他条件更好的过滤性。