Preparation of PFS coagulant by sectionalized reactor

The oxidation rate of ferrous sulfate is investigated for the preparation of polyferric sulfate(PFS)coagulant.In is proved that this reaction is zero order with respect to Fe^2 ,first order with respect to NO2(g),and first order with respect to the interface area between gas phase and liquid phase.According to this mechanism,sectionalized reactor(SR) is used in place of traditional reactor(TR),and the liquid of reaction mixture is recycled by pump.As a result,not only the flow path of reaction liquid is prolonged,but also gas-liquid contact area enlarged,and the reaction distinctly accelerated,compared with traditional reactor.The effects of parameters including temperature,acidity and others on the reaction rate are also discussed.     

陶瓷印花废水处理的混凝剂及工艺条件

采用混凝剂聚合氯化铝（PAC）、聚丙烯酰胺（PAM）、聚合硫酸铁（PFS）对陶瓷印花废水进行混凝沉降处理,监测水样的吸光度、浊度、悬浮物,以脱色率、浊度去除率、悬浮物去除率评价混凝处理的效果。结果表明：PAC是陶瓷印花废水沉降处理的理想混凝剂;水样的吸光度、浊度、悬浮物随混凝剂用量增大和沉降时间延长而呈降低趋势,而脱色率、浊度去除率、悬浮物去除率随混凝剂和沉降时间的增大呈增大的趋势;PAC投加量为20mg／L,沉降时间约为24h,水样脱色率达到90．0％,而当PAC投加量达到100mg／L,沉降时间约为4h,陶瓷印花水的脱色率可达到96．0％。证明了药剂用量的增加与沉降时间的延长对混凝过程具有增效作用。     

聚合硫酸铁对污泥脱水性能研究

采用聚合硫酸铁作为化学调理剂,对浓缩池污泥进行调理.以污泥比阻为主要指标考察了投药量、调理剂浓度、pH值和搅拌强度对污泥过滤脱水性能的影响;同时,考察了污泥经过沉降后上清液的浊度变化.调理实验结果表明,PFS的适宜调理参数为:投加量1mL,浓度6％,pH为7(未调节),快速搅拌速度120 rpm,慢速搅拌速度50 rpm.污泥经PFS调理后,比阻降低到1.56×10-14 m/kg,显然,调理剂影响污泥调理脱水效果和它们的种类、浓度和投加量等条件相关.     

铁聚合反应速率研究

研究了聚合硫酸铁絮凝剂制备中亚铁的氧化反应速率，证明该速率对Ｆｅ＾２＋为零级，对ＮＯ２（ｇ）为一级，因此提高气相中ＮＯ２的分压可大大缩短制备时间。     

硫铁矿烧渣制备PFS、PFPS及其除浊效果比较

以硫铁矿烧渣为原料，采用胶体分散法新工艺制备得到聚合硫酸铁（PFS），然后在PFS溶液中加入磷酸钠得到聚磷硫酸铁（PFPS）。研究了影响PFPS盐基度的因素，以及PFS、PFPS的除浊效果。结果表明，采用胶体分散法制备PFS的工艺独特，无污染物氮氧化物的产生。实验还表明，PFPS的絮凝效果明显好于PFS。PFPS投放量以及盐基度适宜时可达到最佳除浊效果。     

混凝沉淀工艺处理餐厨废水的研究

通过单因素试验考察了聚合氯化铝(PAC)、聚合硫酸铁(PFS)、聚合氯化铝铁(PAFC)对餐厨废水生化处理出水中COD、TP的去除效果,并确定了絮凝沉淀最佳工艺条件:最优絮凝剂为PFS,最佳投加量为450 mg/L,絮凝反应时间为30 min,PAM投加量为0.6 mg/L,PAM投加时间为距离PFS投加后至少l min.在最佳工艺条件下,COD、TP平均去除率可分别达36％、83％,此时絮体体积比为13％.     

Groundwater arsenic removal by coagulation using ferric(III) sulfate and polyferric sulfate: A comparative and mechanistic study

Elevated arsenic (As) in groundwater poses a great threat to human health. Coagulation using mono-and poly-Fe salts is becoming one of the most cost-effective processes for groundwater As removal. However, a limitation comes from insufficient understanding of the As removal mechanism from groundwater matrices in the coagulation process, which is critical for groundwater treatment and residual solid disposal. Here, we overcame this hurdle by utilizing microscopic techniques to explore molecular As surface complexes on the freshly formed Fe flocs and compared ferric(III) sulfate (FS) and polyferric sulfate (PFS) performance, and finally provided a practical solution in As-geogenic areas. FS and PFS exhibited a similar As removal efficiency in coagulation and coagulation/filtration in a two-bucket system using 5 mg/L Ca(ClO)₂. By using the two-bucket system combining coagulation and sand filtration, 500 L of As-safe water (<10 μg/L) was achieved during five treatment cycles by washing the sand layer after each cycle. Fe k-edge X-ray absorption near-edge structure (XANES) and As k-edge extended X-ray absorption fine structure (EXAFS) analysis of the solid residue indicated that As formed a bidentate binuclear complex on ferrihydrite, with no observation of scorodite or poorly-crystalline ferric arsenate. Such a stable surface complex is beneficial for As immobilization in the solid residue, as confirmed by the achievement of much lower leachate As (0.9 μg/L-0.487 mg/L) than the US EPA regulatory limit (5 mg/L). Finally, PFS is superior to FS because of its lower dose, much lower solid residue, and lower cost for As-safe drinking water.     

Groundwater arsenic removal by coagulation using ferric(Ⅲ)sulfate and polyferric sulfate: A comparative and mechanistic study

Elevated arsenic(As) in groundwater poses a great threat to human health. Coagulation using mono- and poly-Fe salts is becoming one of the most cost-effective processes for groundwater As removal. However, a limitation comes from insufficient understanding of the As removal mechanism from groundwater matrices in the coagulation process, which is critical for groundwater treatment and residual solid disposal. Here, we overcame this hurdle by utilizing microscopic techniques to explore molecular As surface complexes on the freshly formed Fe flocs and compared ferric(III) sulfate(FS) and polyferric sulfate(PFS)performance, and finally provided a practical solution in As-geogenic areas. FS and PFS exhibited a similar As removal efficiency in coagulation and coagulation/filtration in a two-bucket system using 5 mg/L Ca(ClO)_2. By using the two-bucket system combining coagulation and sand filtration, 500 L of As-safe water( 10 μg/L) was achieved during five treatment cycles by washing the sand layer after each cycle. Fe k-edge X-ray absorption near-edge structure(XANES) and As k-edge extended X-ray absorption fine structure(EXAFS) analysis of the solid residue indicated that As formed a bidentate binuclear complex on ferrihydrite, with no observation of scorodite or poorly-crystalline ferric arsenate. Such a stable surface complex is beneficial for As immobilization in the solid residue, as confirmed by the achievement of much lower leachate As(0.9 μg/L–0.487 mg/L)than the US EPA regulatory limit(5 mg/L). Finally, PFS is superior to FS because of its lower dose, much lower solid residue, and lower cost for As-safe drinking water.     

聚合硫酸铁处理终端焦化废水的研究

确定了聚合硫酸铁处理终端焦化废水的最佳投药量和 p H值 ,讨论了影响其混凝效果的主要因素。实验结果表明 ,处理后出水 COD、浊度的去除率达 80 %以上 ,对酚、氰的去除率可达到 40 %、5 0 %。     

混凝法去除城市生活污水中抗性基因

采用聚合氯化铝(PACl)和聚合硫酸铁(PFS)混凝处理城市生活污水(格栅出水和二级出水),考察混凝剂投加量、pH值对污水中抗生素抗性基因(ARGs)的去除率影响。结果表明,随着PACl和PFS投加量的增加,污水中目标基因的去除率先升高后降低;在pH 3~10的范围内,PACl对目标基因的去除效果随pH值的增加而降低,PFS对目标基因的去除随着pH值的增加先升高后降低。对于格栅出水,PACl和PFS的最佳投加量为400 mg/L,基因的去除率分别达到2.33~2.97 log和0.98~2.11 log,对于二级出水,PACl和PFS的最佳投加量分别为200 mg/L和150 mg/L,基因的去除率分别为1.85~2.64 log、1.81~2.46 log;混凝去除最优pH条件分别为pH=3(投加PACl)及pH=5~6(投加PFS)。PACl的处理效果优于PFS。