A pilot-scale study of cryolite precipitation from high fluoride-containing wastewater in a reaction-separation integrated reactor

Fluoride removal by traditional precipitation generates huge amounts of a water-rich sludge with low quality, which has no commercial or industrial value. The present study evaluated the feasibility of recovering fluoride as low water content cryolite from industrial fluoride-containing wastewater. A novel pilot-scale reaction-separation integrated reactor was designed. The results showed that the seed retention time in the reactor was prolonged to strengthen the induced crystallization process. The particle size of cryolite increased with increasing seed retention time, which decreased the water content. The recovery rate of cryolite was above 75% under an influent fluoride concentration of 3500 mg/L, a reaction temperature of 50℃, and an influent flow of 40 L/hr. The cryolite products that precipitated from the reactor were small in volume, large in particle size, low in water content, high in crystal purity, and recyclable.     

Synthesis and characterization of agricultural controllable humic acid superabsorbent

Humic acid superabsorbent polymer (P(AA/AM-HA)) and superabsorbent polymer (P(AA/AM)) were synthesized by aqueous solution polymerization method using acrylic acid (AA), acrylamide (AM) and humic acid (HA) as raw material. The effects of N,N'-methylenebisacrylamide (MBA) crosslinking agent, potassium peroxydisulfate (KPS) initiator, reaction temperature, HA content, ratio of AA to AM, concentration of monomer and neutralization of AA on water absorption were investigated. Absorption and desorption ratios of nitrogen fertilizer and phosphate fertilizer were also investigated by determination of absorption and desorption ratio of NH₄⁺, PO₄^3- on P(AA/AM-HA) and P(AA/AM). The P(AA/AM-HA) and P(AA/AM) were characterized by Fourier translation infrared spectroscopy, biological photomicroscope and scanning electron microscopy (SEM). The optimal conditions obtained were as follows: the weight ratio of MBA to AA and AM was 0.003; the weight ratio of KPS to AA and AM was 0.008; the weight ratio of HA to AA was 0.1; the mole ratio of AM to AA is 0.1; the mole ratio of NaOH to AA is 0.9; the reaction temperature was 60℃. P(AA/AMHA) synthesized under optimal conditions, has a good saline tolerance, its water absorbency in distilled water and 0.9 wt.% saline solution is 1180 g/g and 110 g/g, respectively. P(AA/AM-HA) achieves half saturation in 6.5 min. P(AA/AM-HA) is superior to P(AA/AM) on absorption of NH₄⁺, PO₄^3-. The SEM micrograph of P(AA/AM-HA) shows a fine alveolate structure. The biological optical microscope micrograph of P(AA/AM-HA) shows a network structure. Graft polymerization between P(AA/AM) and HA was demonstrated by infrared spectrum. The P(AA/AM-HA) superabsorbent has better absorbing ability of water and fertilizer, electrolytic tolerance and fewer cost than P(AA/AM) superabsorbent.     

Supercritical water oxidation of polyvinyl alcohol and desizing wastewater：Influence of NaOH on the organic decomposition

Polyvinyl alcohol is a refractory compound widely used in industry. Here we report supercritical water oxidation of polyvinyl alcohol solution and desizing wastewater with and without sodium hydroxide addition. However, it is difficult to implement complete degradation of organics even though polyvinyl alcohol can readily crack under supercritical water treatment. Sodium hydroxide had a significant catalytic effect during the supercritical water oxidation of polyvinyl alcohol. It appears that the OH ion participated in the C-C bond cleavage of polyvinyl alcohol molecules, the CO2-capture reaction and the neutralization of intermediate organic acids, promoting the overall reactions moving in the forward direction. Acetaldehyde was a typical intermediate product during reaction. For supercritical water oxidation of desizing wastewater, a high destruction rate (98.25%) based on total organic carbon was achieved. In addition, cases where initial wastewater was alkaline were favorable for supercritical water oxidation treatment, but salt precipitation and blockage issues arising during the process need to be taken into account seriously.     

Identification of key factors governing chemistry in groundwater near the water course recharged by reclaimed water at Miyun County, Northern China

Reclaimed water was successfully used to recover the dry Chaobai River in Northern China, but groundwater may be polluted. To ensure groundwater protection, it is therefore critical to identify the governing factors of groundwater chemistry. Samples of reclaimed water, river and groundwater were collected monthly at Chaobai River from January to September in 2010. Fifteen water parameters were analyzed. Two kinds of reclaimed water were different in type (Na-Ca-Mg-Cl-HCO3 or Na-Ca-Cl-HCO3 ) and concentration of nitrogen. The ionic concentration and type in river were similar to reclaimed water. Some shallow wells near the river bed had the same type (Na-Ca-Mg-Cl-HCO3 ) and high concentration as reclaimed water, but others were consistent with the deep wells (Ca-Mg-HCO3 ). Using cluster analysis, the 9 months were divided into two periods (dry and wet seasons), and all samples were grouped into several spatial clusters, indicating different controlling mechanisms. Principal component analysis and conventional ionic plots showed that calcium, magnesium and bicarbonate were controlled by water-rock interaction in all deep and some shallow wells. This included the dissolution of calcite and carbonate weathering. Sodium, potassium, chloride and sulfate in river and some shallow wells recharged by river were governed by evaporation crystallization and mixing of reclaimed water. But groundwater chemistry was not controlled by precipitation. During the infiltration of reclaimed water, cation exchange took place between (sodium, potassium) and (calcium, magnesium). Nitrification and denitrification both happened in most shallow groundwater, but only denitrification in deep groundwater.     

湄公河下游国家水质管理状况与区域合作前景

本文分析了老挝、缅甸、泰国、柬埔寨和越南等湄公河下游五国的水质状况及原因,通过汇总湄公河五国的水质管理法律法规及水质标准和介绍各国的水质管理措施,阐述了湄公河国家在水质管理方面做出的努力以及水质管理中存在的问题,并对湄公河国家在流域水质区域合作方面进行了展望。     

基于生命周期评价的城市固体废弃物处理模式研究进展

通过回顾2003-2010年国内外不同城市固体废弃物管理体系生命周期评价结果,列举比较了不同固体废弃物处理模式下的全球变暖潜力、酸化潜力和净能源效用等影响评价因子的大小,得出城市固体废弃物处理模式环境影响等级:填埋的环境影响潜值最大,焚烧的环境影响潜值小于填埋,而结合堆肥后环境影响潜值降低;此外,将固体废弃物资源化引入到处理模式后,特别是垃圾源头分类回收后,环境影响潜值大大降低。结合我国城市固体废弃物处理现状,提出单一的处理模式应转变为综合处理模式,多种生活垃圾处理方式适当的有机结合,因地制宜地开展固体废弃物资源化管理,以及餐厨垃圾源头分类收集处理等建议,为政府能有效利用城市固体废弃物处理设施的能力提供参考。     

纳米Fe_3O_4/膨润土的制备、表征及光催化降解焦化废水

以铝柱撑膨润土负载纳米Fe_3O_4制备出性能良好的复合型催化剂。结合X射线粉末衍射(XRD)、扫描电镜(SEM)和比表面孔隙分析(BET)对催化剂的晶相、比表面积和粒度进行表征。负载的纳米Fe_3O_4粒径约为20～30nm,均匀分散到膨润土表面,未发生明显的团聚。在紫外光作用下用该催化剂对焦化厂二沉池出水进行深度处理。结果表明,在催化剂投加量为0.7 g/L,pH为2.5,温度40℃,H_2O_2初始浓度为17.6mmol/L的反应条件下,二沉池出水(化学需氧量COD=140mg/L,色度=400度)经催化氧化降解后,COD和色度可分别降低到54.44 mg/L和10度,达到国家工业再生用水水质标准GB/T 19923-2005(COD≤60 mg/L,色度≤30度)。催化剂重复使用4次时,废水COD和色度去除率保持稳定。     

高校校园景观水体浮游植物调查与水质评价

对华侨大学厦门校区景观水体浮游植物群落结构和水质的理化指标进行了调查研究,结合生物监测和理化监测手段,基于浮游植物优势度、丰度和多样性指数的评价标准,对水体进行了生态评价。评价结果表明,水体受到一定程度的污染并出现富营养化现象。     

中国煤炭资源不同区带的生态环境特征

中国煤炭的“井”字型分布格局除了是对煤炭资源地质的、地理的、社会经济的区域分异现象,同时也基本是对不同煤炭资源发展区的生态环境特征进行区域上的归结。论文总结了不同煤炭资源发展区的生态环境特征和存在的主要生态环境问题。     

关于不锈钢酸洗废水处理的技术分析

随着社会经济的快速发展,不锈钢酸洗废水处理技术成为了当前的一项重要技术参数。本文旨在分析当前不锈钢酸洗废水的相关处理技术,从多种技术综合的应用出发,围绕当前工业发展的实际需要,多角度的分析不锈钢酸洗废水的技术,实现整体技术的全面运用。