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磷酸钙沉淀法去除猪场废水中磷的实验研究
摘要点击 1625  全文点击 2275  投稿时间:2010-06-18  修订日期:2010-09-21
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中文关键词  猪场废水  磷酸钙  沉淀反应  磷去除  碳酸根  镁离子
英文关键词  swine wastewater  calcium phosphate  precipitation reaction  phosphorus removal  carbonate  magnesium
作者单位
宋永会 中国环境科学研究院城市水环境研究室北京100012 
钱锋 中国环境科学研究院城市水环境研究室北京100012 
向连城 中国环境科学研究院城市水环境研究室北京100012 
中文摘要
      以模拟猪场废水为处理对象,进行了磷酸钙沉淀除磷小试实验,考察了pH值、不同初始n(Ca)/n(P)、CO2-3、Mg2+以及CO2-3和Mg2+共存对磷酸钙沉淀反应的影响;利用X射线衍射仪(XRD)对沉淀产物进行了表征.结果表明,在溶液pH=8.0和初始n(Ca)/n(P)=3.33时,延长反应时间至360 min 后,P的去除率可达92.2%.较高的pH值和初始n(Ca)/n(P)有利于磷酸钙沉淀反应,但当pH≥10,初始n(Ca)/n(P) ≥3.33时,这2个因子对提高磷去除率的贡献不明显.当pH=9.0时,CO2-3、Mg2+单独存在对磷酸钙沉淀反应的影响很小,磷去除率均在94.1%左右;CO2-3通过与Ca2+生成CaCO3降低羟基磷酸钙(HAP)沉淀产物的纯度;Mg2+的存在使沉淀产物转化为无定形的磷酸钙(ACP),对热处理后的沉淀产物进行XRD分析发现,Mg2+掺入到磷酸钙结构中,(Ca,Mg)3(PO4)2形成改变了沉淀产物的结构.CO2-3和Mg2+共存时,控制CO2-3和Mg2+在一定范围内,提高溶液pH≥9.0,CO2-3和Mg2+的相互作用有利于磷酸钙沉淀反应.
英文摘要
      Using synthetic swine wastewater, bench-scale experiments were carried out to investigate the effects of pH, varied initial n(Ca)/n(P) molar ratio, carbonate (CO2-3), magnesium (Mg2+) as well as coexistence of CO2-3 and Mg2+ on calcium phosphate (CP) precipitation for phosphorus removal. The composition of the obtained precipitate was analyzed and characterized by X-ray diffraction (XRD). The results showed that with pH value of 8.0 and initial n(Ca)/n(P) of 3.33, through extending the reaction time to 360 min, the removal rate of phosphate could reach 92.2%. Higher pH value and initial n(Ca)/n(P) were beneficial to calcium phosphate precipitation. However, with pH ≥10.0 and the initial n(Ca)/n(P) ≥3.33, these two factors had negligible effects on the improvement of phosphate removal rate. At pH=9.0, the effects of the separately existing CO2-3 and Mg2+ on the precipitation of phosphate was very small, with the phosphate removal rate keeping stable at 94.1%, averagely. The reaction of CO2-3 and Ca2+ caused the formation of prior production of calcite (CaCO3) and reduced the purity of HAP. The coexisting of Mg2+ made the precipitate be transformed into amorphous calcium phosphate (ACP); through XRD analysis of the heat treated precipitate, it was found that Mg2+ incorporated into the calcium phosphate, forming Mg-substituted whitlockite (Ca,Mg)3(PO4)2, which changed the structure of the precipitate. When CO2-3 and Mg2+ coexisted, the interaction of CO2-3 and Mg2+ would be beneficial to calcium phosphate precipitation with controlled CO2-3 and Mg2+ concentration and elevated solution pH value (≥9.0).

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