载镁活化天然沸石处理高氟水实验研究

为了提高沸石对氟的吸附能力,采用氯化镁对活化天然沸石进行改性,分析了除氟剂的性能,确定了除氟剂改性的最佳条件:10%氯化镁溶液,固液比1∶4,pH=7.0,室温以300 r/min的速度振荡改性3h。最佳除氟条件:pH=7.0,室温以300 r/min的速度搅拌反应1.5 h。吸附剂对F-的吸附过程符合Langmuir及Freundlich等温线方程,由D-R模型拟合可知,除氟剂对氟的吸附为物理吸附过程。在最佳反应条件下,水样中氟浓度由2 mg/L降低到0.78 mg/L,符合GB5949-2006《生活饮用水卫生标准》(≤1 mg/L)。     

晶种法处理含氟废水与氟化钙沉淀砂状化研究

采用晶种法对含氟废水进行了处理,考察了pH和Ca/F对出水F-浓度和CaF2沉降性能的影响,得到了含水率低、沉降性能好的砂状化CaF2颗粒.实验结果表明,晶种的加入对提高除氟效果、促进CaF2的砂状化有重要作用.当pH为中性偏酸性且0.5＜Ca/F＜1时,除氟效果较好且所得到的CaF2具有较好的沉降性能;当pH=5.5...     

蓄电池生产废水处理技术研究

针对蓄电池生产废水的特点,主要是含有浓度较高的氟化物和重金属铅类,同时含有一定量的有机物质和悬浮物,主要处理方法为物理化学方法。粉煤灰处理含氟水、石灰-硫酸-铁盐法、聚合硫酸铁和氢氧化钙以及聚丙烯酰胺联合处理含氟废水等处理方法都具有较高的除氟率。处理废水中重金属铅离子,目前工业中一般采用化学沉淀法和离子交换法。采用pH调节-石灰-铝盐反应沉淀工艺去除废水中的氟、铅及部分磷酸盐,采用生化处理去除有机物。     

颗粒海藻酸镧对饮用水中氟的吸附去除

以氯化镧与海藻酸钠为原料,采用滴球法制备了粒径为1～1.5mm的海藻酸镧小球,经过水洗、干燥后得到镧负载量25%(质量分数)的海藻酸镧颗粒吸附剂,应用该吸附剂进行饮用水除氟研究.通过间歇吸附实验,分别进行了吸附速率、pH值影响、吸附等温线、共存离子影响等吸附性能评价,并对吸附前后吸附剂表面与溶液组成变化进行研究.结果表明,该颗粒的吸附速率很快,反应2h后出水氟浓度即逐渐趋于稳定,吸附速率曲线符合拟二级反应速率方程;吸附效果受pH影响显著,在pH=4附近吸附量最大;吸附等温线数据对Langmuir方程拟合较好,其最大吸附量高达197.2mg·g-1;在常见无机干扰离子中,磷酸根与碳酸根对吸附有较大负面影响.SEM照片显示吸附前、后颗粒表面形态差异明显;吸附前、后颗粒表面EDX成分分析及溶液中离子浓度测量结果显示,吸附过程中溶液中F-同时与颗粒表面Cl-及OH-发生离子交换作用.     

茶园土壤水溶性氟含量的模拟调控

以湖北英山、大悟、竹山、赤壁和浙江杭州茶园土壤为研究对象,通过施加一定量的CaCO3、CaO、Ca3(PO4)2、CaCl2和CaSO4来调控土壤中水溶性氟含量,结果表明：英山、大悟和竹山茶园土壤中施加一定量的CaCl2或CaSO4均可降低土壤中水溶性氟含量,英山和大悟茶园土壤中可施加1～2 g·kg-1的CaCl2或...     

废旧锂电池电极活性材料真空热解固氟研究

以废旧锂离子电池电极活性材料为研究对象,在真空热解过程中加入CaO作为固氟剂,用以吸收电极活性材料在真空热解的回收工艺中产生的氟磷化合物,能有效减轻二次污染。研究了温度、CaO添加量、停留时间等热解条件对真空热解固氟效果的影响。结果表明固氟效果随温度的增加而增加,在温度500℃以上变化不大,并略有下降;CaO添加量对固氟效果有促进作用,30%可达到很高的固氟效果;30 min的停留时间对于含氟化合物的分解已经足够。得到CaO固氟工序的最佳操作参数:CaO添加量30%左右,温度500~600℃,停留时间30 min。     

山东单县浅层高氟高碘地下水的水化学特征及成因分析

氟和碘作为人体必需的微量元素,过少或过多摄入都会影响人身健康,相较于缺氟、缺碘,高氟高碘地下水对人体的危害更加难以控制。该研究选择单县作为典型的水源型高氟高碘地区,通过对浅层高氟高碘地下水进行采样测试,采用箱线图、Piper图及双变量相关性分析等多元统计技术剖析了该区域浅层地下水的水环境特征;采用R型因子分析揭示了水化学成分之间的相互关系,探讨了该区浅层高氟高碘地下水的成因。结果表明:①单县浅层地下水中的氟化物和碘化物的质量浓度均值分别为1.2 mg/L和391 μg/L。②随着氟化物浓度的增加,水化学类型偏向于向HCO₃-Na型和HCO₃-Na·Mg型集中,而随着碘化物浓度的增加,水化学类型则倾向于以HCO₃-Na·Mg为主。③该区域强烈的蒸发浓缩作用是控制单县浅层地下水化学成分的最重要因子;萤石平衡控制作用是控制单县浅层地下水高氟背景的因子;水-有机沉积物相互作用是控制单县浅层地下水高碘背景的因子。     

季铵化纳米SiO2-N+@PCMS荷电改性正渗透复合膜及其对四环素的分离性能

通过化学法合成叔胺化纳米SiO₂（SiO₂-N）和聚对氯甲基苯乙烯（PCMS）,利用SiO₂-N中的叔胺基与PCMS中的氯甲基反应,生成大分子季铵化纳米SiO₂（SiO₂-N⁺@PCMS）,通过进一步与聚偏氟乙烯（PVDF）共混,以相转化法制备纳米荷电改性的PCMS/PVDF支撑底膜,进而采用界面聚合法制备正渗透（FO）复合膜.采用红外光谱、扫描电镜、zeta电位计和接触角测定仪等对支撑底膜和FO膜表面的化学结构、形貌、荷电性和亲水性等进行了分析,并通过正渗透装置对膜的分离性能进行了测试.结果表明该改性正渗透膜具有较好的荷正电性能,且随着SiO₂-N的加入可以有效提高正渗透膜的亲水性和分离性能,添加2 %的SiO₂-N改性正渗透膜的纯水通量最高可达到22.76 L·m^-2·h^-1,对四环素的截留率可达到98.5 %,经3次水-四环素-水循环过滤后,纯水通量恢复率仍然可达到90.1%.     

Utilization of aluminum hydroxide waste generated in fluoride adsorption and coagulation processes for adsorptive removal of cadmium ion

Although Al-based coagulation and adsorption processes have been proved highly efficient for fluoride (F) removal, the two processes both generate large amount of Al(OH)₃ solid waste containing F (Al(OH)₃-F). This study aimed to investigate the feasibility of utilizing Al(OH)₃-F generated in Al(OH)₃ adsorption (Al(OH)₃-F_ads) and coagulation (Al(OH)₃-F_coag) for the adsorption of cadmium ion (Cd(II)). The adsorption capacity of Al(OH)₃-F_ads and Al(OH)₃-F_coag for Cd(II) was similar as that of pristine aluminum hydroxide (Al(OH)₃), being of 24.39 and 19.90 mg·g^–1, respectively. The adsorption of Cd(II) onto Al(OH)₃-F_ads and Al(OH)₃-F_coag was identified to be dominated by ion-exchange with sodium ion (Na⁺) or hydrogen ion (H⁺), surface microprecitation, and electrostatic attraction. The maximum concentration of the leached fluoride from Al(OH)₃-F_ads and Al(OH)₃-F_coag is below the Chinese Class-I IndustrialWastewater Discharge Standard for fluoride (<10 mg·L^–1). This study demonstrates that the Al(OH)₃ solid wastes generated in fluoride removal process could be potentially utilized as a adsorbent for Cd(II) removal.     

Single and multiple daily dose toxicokinetics of fluoride after oral administration of sodium fluoride along with aluminum sulfate in goats

Our previous study suggested that toxicokinetic parameters of fluoride were significantly changed on the 30th day as compared with 1st day, after repeated oral administration of sodium fluoride alone for 30 days in goats. The purpose of this study was to investigate whether aluminum sulfate has ameliorative effect on the toxicokinetics of fluoride. For this, sodium fluoride (20 mg kg^?1 b. wt.) along with aluminum sulfate (150 mg kg^?1 b. wt.) was administered in goats for 30 days to investigate its effect on toxicokinetics of fluoride on days 1 and 30. The fluoride levels against time were adequately described by one compartment open model. The peak plasma level of fluoride was observed at 2 h. The toxicokinetics data revealed a nonsignificant decrease in β (elimination rate constant) and C _max (the maximum plasma concentration) and increase in t _1/2 K _a (absorption half-lives), t _1/2 β (elimination half-lives), area under the plasma (AUC) concentration versus time curve and mean residence time (MRT) was observed for the last dose from their respective first dose values. On the basis of changes in the toxicokinetic parameters, it was concluded that repeated oral administration has cumulative effect on plasma fluoride level and concurrent oral administration of aluminum sulfate has ameliorative action on the toxicokinetics of fluoride in goats.