膜法海水淡化过程中抗泥沙剂缓解石膏结垢的机理:对农业排水回用的影响

Xinyu Tang, Haizhou Liu
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引用次数: 0

摘要

通过反渗透(RO)膜淡化,农业排水作为淡水供应具有巨大潜力。然而,在反渗透过程中,排水中的高浓度钙和硫酸盐会导致石膏(CaSO4(s))结垢。本研究调查了三种防垢剂(即两种膦酸盐型(DTPMP 和 NTMP)和一种聚合物型(PAA))以及 pH 值和天然有机物(NOM)对减轻反渗透海水淡化过程中石膏结垢的影响,并说明了三种防垢剂的石膏抑制机理。结果表明,在反渗透海水淡化的 24 小时内,1 μM 的 DTPMP 就足以防止石膏结垢,而 NTMP 和 PAA 都需要 5 μM 的剂量。在 pH 值为 3 的酸性条件下,使用 5 μM DTPMP 的渗透通量保持相对稳定,而使用 NTMP 和 PAA 的渗透通量则分别下降了 35% 和 80%。此外,NOM 的存在并没有明显影响抗垢剂的抑制能力。DTPMP 和 NTMP 的石膏抑制机理主要是由负电荷斥力造成的,pH 值越高,拮抗剂水体物种的总电荷越多,从而加强了钙、硫酸盐和石膏核之间的斥力。相比之下,PAA 的石膏抑制机制涉及负电荷斥力和晶格畸变,这使得石膏晶体扭曲成不规则形状,尺寸变小,在中性和碱性条件下阻止了大尺寸石膏沉淀的形成,但在酸性条件下却恶化了膜的缩放性。最终,在对农业排水进行反渗透脱盐时,防止石膏结垢的理想防垢剂应在不改变沉淀形态的情况下保持较高的负电荷。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Mechanisms of Alleviating Gypsum Scaling by Antiscalants during Membrane Desalination: Implications on Agricultural Drainage Water Reuse

Mechanisms of Alleviating Gypsum Scaling by Antiscalants during Membrane Desalination: Implications on Agricultural Drainage Water Reuse
Agricultural drainage water has great potential as a freshwater supply via reverse osmosis (RO) membrane desalination. However, high calcium and sulfate concentrations in the drainage water lead to gypsum (CaSO4(s)) scaling during the RO process. This study investigated the effects of three antiscalants, i.e., two phosphonate-based (DTPMP and NTMP) and one polymer-based (PAA), as well as pH and natural organic matter (NOM) on alleviating gypsum scaling during RO desalination of drainage water, and illustrated the gypsum inhibition mechanism of three antiscalants. Results showed that 1 μM of DTPMP was sufficient to prevent gypsum scaling within 24 h of RO desalination, while both NTMP and PAA required 5 μM of dosage. At acidic pH 3, the permeate flux with 5 μM of DTPMP remained relatively stable, whereas the flux with NTMP and PAA decreased by 35 and 80%, respectively. Furthermore, the presence of NOM did not significantly affect the antiscalant inhibitive capacity. The gypsum inhibition mechanism of DTPMP and NTMP was primarily contributed by negative charge repulsion, with higher pH increasing the total charge of antiscalant aqueous species, thereby strengthening the repulsive forces among calcium, sulfate, and gypsum nuclei. In contrast, PAA’s gypsum inhibition mechanism involved both negative charge repulsion and crystal lattice distortion, which distorted gypsum crystals into irregular shapes and smaller sizes, preventing the formation of large-size gypsum precipitates under neutral and alkaline conditions, but deteriorating membrane scaling under acidic conditions. Ultimately, an ideal antiscalant for preventing gypsum scaling during RO desalination of agricultural drainage water would preserve higher negative charges without changing the precipitate morphology.
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