人工湿地对模拟煤矿废水铁、锰的去除效果研究

针对贵州省煤矿酸性废水的危害日益加剧的现状,通过建立人工湿地系统对模拟煤矿废水中铁、锰的去除效果研究,结果表明在进水浓度总铁:200 mg/L,总锰:12 mg/L,停留时间为24 h的条件下,对Fe的去除率达99.7%,对Mn的去除率达88.5%,均远低于煤炭工业污染物排放标准,为进行人工湿地系统处理煤矿酸性废水的可行性提供理论依据。     

Bio-F生物吸附剂对水中铁锰的去除与特性

以Bio-F（Bio-F生物吸附剂）为材料,研究其对水中Fe2+和Mn2+的去除能力与特性. 结果表明,Bio-F可同时去除水中Fe2+和Mn2+且吸附过程符合Lagergren一级动力学模型. Langmuir吸附等温线能较好地描述Bio-F吸附Fe2+和Mn2+的过程,表现为单分子层化学优惠吸附,其对Fe2+和Mn2+的最大饱和吸附量分别达491和380 mgg. Bio-F对Fe2+和Mn2+的吸附为吸热反应且在pH 6~7范围内可保持86％以上吸附能力(P>005). 较高的c(Ca2+)和c(Mg2+)可明显抑制Bio-F去除Fe2+和Mn2+的能力（P<005),但高c(PO₄3-)则可促进该吸附过程（P>005). Bio-F经10次再生后对Fe2+和Mn2+的去除率分别达9727%和9467%. Bio-F无毒安全,采用Bio-F处理高铁锰饮用水具有应用潜力.      

Toxic elements in well water from Malaysia

Toxic elements present in well water that is used for drinking pose a threat to the human health in many countries. However, there are few reports on the toxic elements in well water in Malaysia. Since a native doctor informed us about the increasing number of patients with depigmented skin (vitiligo) in Rosob Village, Sabah State, Malaysia, the origin of diseases associated with well water was suspected. Thus, the concentrations of 15 toxic elements in 52 well water samples from Rosob (n = 21), and the control areas of Pitas (n = 8) and Telaga (n = 23) within the same state were measured. No toxic elements with levels exceeding that of the WHO health-based guidelines were detected in the well water samples from Pitas and Telaga. On the other hand, the concentration levels of arsenic (As), uranium (U), and manganese (Mn), independently found in 19% (4/21), 4.8% (1/21), and 19% (4/21), respectively, of the well water samples from Rosob, exceeded the levels given in the WHO health-based guidelines. In the well water samples from Rosob, the average concentration of Mn was found to be higher and its maximum value with levels up to 10-fold higher, respectively, than the value in the WHO health-based guidelines. Significant correlations between Mn and As and between Mn and U were noted. Thus, for the first time, the results of this pilot study showed that the levels of the toxic elements in 42.9% (9/21) of well water samples from Rosob in Malaysia were higher than the values in WHO health-based guidelines indicating the need for further studies.     

Speciation study of lead and manganese in roadside dusts from major roads in Ile-Ife,South Western Nigeria

A speciation study of Pb and Mn in roadside dust along major roads in Ile-Ife, South Western Nigeria, was investigated. Pb and Mn values obtained by total digestion ranged from 22.23 ± 3.52 to 43.48 ± 3.05 μg/g and 35.93±0.15 to 83.76 ± 0.06 μg/g, respectively. The results of speciation analysis of Pb and Mn in the samples showed that the mean levels of these metals in the various fractions followed the order: organic matter>residual>Fe-Mn>carbonate>exchangeable and organic matter-bound>exchangeable>carbonate-bound>residual>Fe-Mn oxide-bound respectively. The speciation study therefore revealed that most of the Pb and Mn were associated with the organic matter fraction and that they were least available in the exchangeable and Fe-Mn oxide fractions, respectively. The apparent mobility and potential bioavailability for these metals in the road dust was Mn>Pb. There is a significant difference between the means of Pb and Mn in the road dust of the study area at p≤0.05, which strongly suggests that they may not have come from the same source; different sources may be responsible, which may be anthropogenic, such as tyre wear, vehicular emission, brake linings and natural.     

分光光度法测定环境样品中锰的研究

研究了2-(2-喹啉偶氮)-4-甲基-1,3-二羟基苯(QAMDHB)与锰的显色反应,在pH为10的氯化铵—氨水缓冲介质中,O/W微乳液存在下,QAMDHB与锰反应生成3∶1稳定络合物,λmax=560nm,ε=8.22×104L.mol-1.cm-1。锰含量在40~800μg/L内符合比耳定律,方法用于环境样品中锰含量的测定,结果令人满意。     

生物滤池净化含铁锰高氨氮地下水试验研究

以中试有机玻璃滤柱反应器进行伴生高浓度氨氮含铁锰地下水生物同步净化试验研究,结果表明,进水氨氮浓度高于2.0mg/L时,溶解氧浓度是限制锰与氨氮去除的主要原因.下向流底部曝气过滤运行(气水逆向)可解决溶解氧不足的问题,但滤柱滤水能力有限;上向流底部曝气过滤(气水同向)同样可以满足铁锰氨氮氧化需氧量,然而曝气扰动作用削弱了滤池过滤截留能力造成铁锰氧化物穿透滤层,致使滤层出水铁锰浓度无法满足标准要求,曝气量越大,其滤池截留能力越弱.     

不同锰处理对镉胁迫下2种油菜重金属累积和根系形态的影响

采用水培试验,研究Cd胁迫(10μmol·L~(-1))条件下,不同浓度Mn(0,0.1,1,10,100μmol·L~(-1))处理对2种镉累积能力不同的油菜生物量、Cd和Mn含量以及根系形态参数的影响。结果表明,与正常营养处理Mn1相比,缺Mn和Mn过量处理显著降低2种油菜的地上部和镉低积累油菜"华骏"的根部生物量,而对普通油菜"寒绿"的根部生物量没有显著影响。与Mn1处理相比,缺Mn处理下2种油菜的Cd累积总量和"华骏"地上部Cd含量显著降低;Mn过量处理下2种油菜根部和地上部Cd含量均呈升高趋势,2种油菜的Cd累积总量无显著变化或显著降低。随Mn处理浓度升高,2种油菜地上部和根部Mn含量显著升高,缺Mn处理下2种油菜根部的Mn含量低于Mn缺乏的临界值。与Mn1处理相比,缺Mn处理下"华骏"的根长、表面积、体积、平均直径和根尖数显著降低;Mn过量处理下"寒绿"的根长以及"华骏"的根系表面积、体积显著降低;缺Mn处理下2种油菜细根表面积所占的比例增加,粗根表面积比例降低;Mn过量时,"寒绿"的粗根表面积比例增加,细根比例降低,而"华骏"则相反。总的来看,缺Mn处理影响油菜根系和地上部生长,减少地上部Cd含量和植株Cd累积总量;Mn过量处理下油菜生长也受到抑制,但是油菜地上部和根部Cd含量有所升高;2种油菜的根系形态学参数在不同Mn处理下变化规律不同,表现出不同的响应策略。     

锰-稀土/Y分子筛复合电催化处理含酚模拟废水

采用浸渍焙烧法制备了以Y分子筛为载体的Mn-RE复合催化剂,置于电解槽内形成反应床体,构建Mn-RE多相催化电解氧化体系处理人工模拟苯酚废水.考察了浸渍液中锰的质量分数、稀土元素组成和质量分数、焙烧温度、焙烧时间对电催化活性的影响,用SEM和XRD等手段对催化剂的微观结构、表面形貌进行了表征,探讨了Mn-RE/Y分子筛催化剂对含酚废水降解的电催化效果.研究表明, Mn-RE/Y分子筛催化剂的最佳制备条件是浸渍液中锰质量分数6%,铈质量分数为3%,焙烧温度为550℃,焙烧时间为5h.Y分子筛中引入Mn、Ce后没有破坏Y分子筛的晶体结构, Mn-RE/Y分子筛催化剂的表面并没有检测到稀土氧化物和锰氧化物的物相.反应过程中, Mn-RE/Y分子筛在阴极和阳极的同时催化氧化作用强化了含酚废水的降解效果.     

Occurance and control of manganese in a large scale water treatment plant

The continuous variations of dissolved oxygen (DO), manganese (Mn), pH, and their effect on manganese removal by different water treatment processes are investigated. The results show that the declined DO concentration and pH value in the bottom of reservoir results in the increasing release of Mn from sediment to source water. Manganese concentration increased from 0.1 to 0.4 mg·L^-1 under the condition that DO concentration decreased from 12.0 to 2.0 mg·L^-1 in raw water. The different water treatment processes exhibited different efficiency on manganese removal. The processes with recycling of the suspended sludge, low elevation velocity in settling tank and slow filter rate, will benefit the manganese removal. During a high release of manganese in raw water, traditional coagulation-sedimentation and filtration could not completely remove Mn, although granular activated carbon filtration (GAC) had been applied. At that case, preoxidation with chlorine or potassium permanganate (KMnO₄) was necessary to address the high manganese concentration.     

Effects of humic acid and surfactants on the aggregation kinetics of manganese dioxide colloids

The aggregation of common manganese dioxide (MnO₂) colloids has great impact on their surface reactivity and therefore on their fates as well as associated natural and synthetic contaminants in engineered (e.g. water treatment) and natural aquatic environments. Nevertheless, little is known about the aggregation kinetics of MnO₂ colloids and the effect of humic acid (HA) and surfactants on these. In this study, the early stage aggregation kinetics of MnO₂ nanoparticles in NaNO₃ and Ca(NO₃)₂ solutions in the presence of HA and surfactants (i.e., sodium dodecyl sulfate (SDS), and polyvinylpyrrolidone (PVP)) were modeled through time-resolved dynamic light scattering. In the presence of HA, MnO₂ colloids were significantly stabilized with a critical coagulation concentration (CCC) of ~300 mmol·L^-1 NaNO₃ and 4 mmol·L^-1 Ca(NO₃)₂. Electrophoretic mobility (EPM) measurements confirmed that steric hindrance may be primarily responsible for increasing colloidal stability in the presence of HA. Moreover, the molecular and/or chemical properties of HA might impact its stabilizing efficiency. In the case of PVP, only a slight increase of aggregation kinetics was observed, due to steric reactions originating from adsorbed layers of PVP on the MnO₂ surface. Consequently, higher CCC values were obtained in the presence of PVP. However, there was a negligible reduction in MnO₂ colloidal stability in the presence of 20 mg·L^-1SDS.