粉末凹凸棒石对水溶性阳离子染料废水的脱色研究

本文研究了凹凸棒石粘土处理阳离子染料废水的吸附脱色规律。结果表明，粉末凹凸棒石对水溶性阳离子染料具有优良的脱色效果。例如，染料初始浓度１００ｍｇ·ｌ＾－１（色度相当于２２００￣４０００倍），粘土投加量０．５％，七种被研究的阳离子染料废水平均脱色率近９９％，吸附机理主要是离子交换。     

Decolourization and removal of some organic compounds from olive mill wastewater by advanced oxidation processes and lime treatment

Background Olive mill wastewater (OMW) generated by the olive oil extracting industry is a major pollutant, because of its high organic load and phytotoxic and antibacterial phenolic compounds which resist biological degradation. Mediterranean countries are mostly affected by this serious environmental problem since they are responsible for 95% of the worldwide oliveoil production. There are many methods used for OMW treatment, such as adsorption, electro coagulation, electro-oxidation, biological degradation, advanced oxidation processes (AOPs), chemical coagulation, flocculation, filtration, lagoons of evaporation and burning systems, etc. Currently, there is no such economical and easy solution. The aim of this study was to evaluate the feasibility of decolourization and removal of phenol, lignin, TOC and TIC in OMW by UV/H₂O₂ (AOPs). The operating parameters, such as hydrogen peroxide dosage, times, pH, effect of UV and natural sunlight were determined to find the suitable operating conditions for the best removal. Moreover, there is no study reported in the literature related to the use of UV/H₂O₂ and lime together in OMW treatment. Methods OMW was obtained from an olive-oil producing plant (Muğla area of Turkey) which uses a modern production process. No chemical additives are used during olive oil production. This study was realised by using two different UV sources, while taking the time and energy consumption into consideration. These two sources were mercury lamps and natural sunlight. Before starting AOPs experiments, one litre of OMW was treated by adding lime until a pH of 7.00. Then, 100 ml was taken from each sample, and 1 to 10 ml of a 30% H₂O₂ (Riedel-deHaen) solution was added. These solutions in closed vessels were laid in the natural sunlight for a week and their compositions and colour changes were analysed daily by UV-Vis spectrophotometer. At the end of the one-week period, they were treated with lime. In this study, the effect of changes in the initial pH, times and H₂O₂ concentrations on removal was investigated. At the end of all experiments, changes in colour, phenol, lignin, TOC and TIC concentrations were analysed according to standard methods. Results and Discussion In the samples exposed to natural sunlight and having an H₂O₂/OMW ratio of 3 ml/100 ml, a significant colour removal was achieved approximately 90% of the time at the end of 7 days. When the same samples were treated with lime (pH: up to 7), 99% efficiency was achieved. When phenol and lignin removals were examined in the same concentration, phenol and lignin removal were found 99.5%, 35%, respectively. However, for maximum lignin removal, more use of H₂O₂ (10 ml H₂O₂/100 ml OMW) was found to be necessary. Under these conditions, it was found that lignin can be removed by 70%, but to 90% with lime, at the end of a seven-day period. Rate constants obtained in the experiments performed with direct UV were found to be much higher than those of the samples exposed to natural sunlight (k^a _lignin = 0.3883 ≫ k^b _lignin = 0.0078; k^a _phenol = 0.5187 ≫ k^b _phenol = 0.0146). Moreover, it should be remembered in this process that energy consumption may induce extra financial burden for organisations. Conclusions It was found, in general, that colour, lignin, total organic carbon and phenol were removed more efficiently from OMW by using H₂O₂ UV and lime OMW. Moreover, in the study, lime was found to contribute, both initially and after radical reactions, to the efficiency to a great extent. Recommendations and Perspectives Another result obtained from the study is that pre-purification carried out with hydrogen peroxide and lime may constitute an important step for further purification processes such as adsorption, membrane processes, etc.     

猪粪堆肥与化肥配施对水稻产量和氮效率的影响

采用大田试验方法研究猪粪堆肥与化肥配施对水稻产量和氮效率的影响.结果表明:在本试验条件下,猪眄粪堆肥与化肥配施能显著提高水稻籽粒产量,增加水稻每穗实粒数.尤其是1 500 kg·hm-2猪粪堆肥 化肥配施处理,稻谷产量达8 595 kg·hm-2,比未施氮处理和化肥处理分别增产57.8%和13.6%,差异达显著水平.猪粪堆肥与化肥配施处理水稻氮素养分效率均高于化肥处理.猪粪堆肥与化肥配施的氮肥回收率为35.3%～38.6%,而化肥处理仅为27.6%.     

五氯酚对斜生栅藻的毒性效应研究

以斜生栅藻细胞的生长状况、色素(叶绿素a、叶绿素b、类胡萝卜素)及蛋白质含量的变化作为指标,研究了不同质量浓度的五氯酚(0,0.02,0.05,0.10,0.50,1.00 mg/L)对斜生栅藻(Scenedesmus obliquus)的毒性效应.24,48,72,96和120 h五氯酚对斜生栅藻的EC50分别为0.883,0.283,0.225,0.168和0.192 mg/L.斜生栅藻生长受抑制程度随五氯酚质量浓度增加而加强,当五氯酚的质量浓度超过0.50 mg/L时,斜生栅藻的生长几乎完全受到抑制.染毒96 h的斜生栅藻色素(叶绿素a、叶绿素b、类胡萝卜素)含量以及蛋白质含量随着五氯酚质量浓度的增加呈下降趋势,色素比例失调,色素对五氯酚的敏感程度为:类胡萝卜素＞叶绿素a＞叶绿素b;可溶性蛋白质含量与色素含量的减少呈明显线性相关(r=0.793,n=6).      

Radiation Crosslinking of Poly(Butylene Succinate) in the Presence of Inorganic Material and Its Biodegradability

Three kinds of poly(butylene succinate)s (PBS) with different molecular weight were irradiated with electron beams in the presence of inorganic material. Fourteen kinds of inorganic materials were used in this work. The presence of inorganic material inside cross-linked PBS samples enhances the yield of gel formation. The heat stabilities of PBS samples were checked; it was found that silicon dioxide and carbon black significantly improve these properties. Enzymatic and soil burial tests were performed; the presence of these inorganic materials in cross-linked PBS accelerates the rate of biodegradation.     

土壤重金属镉、铅及其复合污染对羊蹄(Rumex japonicus Houtt)生长及其抗性生理指标的影响

为探究重金属Cd、Pb及其复合污染对植物的生长及生理的影响,选用乐安河湿地优势乡土植物羊蹄(Rumex japonicus Houtt),采用室内土培盆栽实验,分别设置不同的Cd、Pb单因素及其双因素复合污染水平,研究羊蹄的生物量、株高等生长指标及植物组织中丙二醛(MDA)、可溶性糖等抗性生理指标的变化特性。结果表明:随着Cd、Pb污染胁迫浓度的增加以及胁迫时间的延长,羊蹄的生物量及株高均受到显著(P0.05)抑制,且Cd+Pb双因素复合污染胁迫的抑制作用大于单因素Pb或Cd的污染胁迫;羊蹄植物组织中的MDA含量及可溶性糖含量随Cd、Pb污染胁迫强度的增加及胁迫时间的延长显著增加(P0.05);在盆栽土壤中单因素Cd或Pb的高浓度胁迫下,羊蹄的自我调控能力显著增强(P0.05),MDA含量下降。不同污染水平的单因素Cd、Pb及Cd+Pb双因素复合污染胁迫对羊蹄可溶性糖含量的影响均存在显著性(P0.05)差异。     

丹江口水库表层沉积物有机/无机磷形态特征

采用连续分级提取法研究了丹江口水库表层沉积物中有机磷和无机磷的形态及其赋存特征,同时结合间隙水体中溶解性总磷(DTP)的空间分布特征,讨论了各形态磷的生物可利用性及其释放风险.结果表明,丹江口水库沉积物中各形态磷均在入库河流处高于库区.各采样点沉积物总磷在203.08~1625.61mg/kg之间,平均值为642.51mg/kg,其中以无机磷为主,占总磷的52.9%.无机磷形态中生物可利用性差的Ca-P_i占优势,平均值为196.46mg/kg,占无机磷的57.8%;沉积物有机磷形态中活性最差的NA-P_o占绝对的优势,NA-P_o平均值为180.83mg/kg,占有机磷(OP)的59.7%. WA-P_i、PA-P_i、Fe/Al-P_i、WA-P_o、PA-P_o均与间隙水体DTP呈显著正相关(P < 0.05), Ca-P_i、MA-P_o、NA-Po与间隙水DTP相关性较差.入库河流沉积物生物可利用性磷含量及释放通量均较库区高,具有较高的释磷风险.     

三维荧光光谱解析城市污水有机物的去除特征

利用荧光区域积分结合物料平衡计算及多元直接梯度分析,考察强化除磷-硫自养系统对低COD/TN比市政污水中有机物、氮和磷污染物的去除特性.结果表明,在进水COD/TN比为4.5～6.0的条件下,强化除磷-硫自养系统出水中的TN、NH₄⁺-N和TP浓度分别降至1.31、1.11和0.23mg/L,其去除率分别达到了96.3%、96.0%和86.9%.强化除磷-硫自养系统对荧光区域Ⅰ～Ⅴ标准积分体积的去除率分别为73.7%、64.3%、50.6%、61.3%和28.1%.物料平衡计算表明,非曝气区对荧光区域Ⅰ、Ⅱ和Ⅳ的物质有明显的去除效果;好氧区对荧光区域Ⅰ、Ⅱ和Ⅲ的物质有明显的去除效果.多元直接梯度分析表明,磷的释放过程可能与溶解性微生物代谢产物荧光区中的有机物相关,而自养的硝化反应、吸磷过程和有机物的去除可在好氧区达到统一.     

流溪河水库流域非点源溶解态氮磷污染负荷估算

流溪河水库作为广州市最重要的水源地之一,其水环境质量受到广泛关注. 利用基于SCS模型的污染负荷输出,对流溪河水库流域非点源溶解态氮磷污染负荷进行估算. 结果表明:流域非点源溶解态氮污染负荷为384.31 t/a,溶解态磷污染负荷为20.68 t/a.其中氮贡献最大的为林地,占50.93%;其次为园地,占18.10%.磷贡献最大的亦为林地,占49.22%;其次为旱地,占15.85%.溶解态氮单位面积污染负荷道路最高,为50.57 kg/(hm2·a);其次是水田,为33.60 kg/(hm2·a).而溶解态磷单位面积污染负荷最大是水田,为3.43 kg/(hm2·a);其次是道路,为3.19 kg/(hm2·a). 与水库流域颗粒态氮磷污染负荷比较表明,溶解态氮大于颗粒态氮,氮以溶解态迁移为主;溶解态磷则小于颗粒态磷,但由于颗粒态磷易随泥沙受阻或沉降,溶解态磷对水库水质的影响依然是总磷关注的重点.      

镉胁迫对续断菊Sonchus asper L.Hill.根系分泌物的影响

通过盆栽试验,研究了不同Cd质量分数(0、50、100、200 mg.kg-1)对续断菊Sonchus asper L.Hill.根系分泌总有机酸、游离氨基酸、可溶性糖的影响,旨在探明根系分泌物对续断菊超积累Cd的影响。结果表明:Cd胁迫下续断菊根系分泌总有机酸、游离氨基酸和可溶性糖的质量浓度显著增加,同时,总有机酸、可溶性糖和游离氨基酸又促进了植株对Cd的吸收。随着Cd处理质量分数的增加,续断菊地上部和根部镉质量分数显著增加,90 d时续断菊地上部镉质量分数与可溶性糖、游离氨基酸的质量浓度呈极显著正相关,相关系数分别为0.999(P<0.01)和0.995(P<0.01),根部镉质量分数与可溶性糖、游离氨基酸的质量浓度也呈显著正相关,相关系数分别为0.998(P<0.01)和0.987(P<0.05);Cd对续断菊根系可溶性糖的分泌、游离氨基酸的合成有刺激作用,根系分泌的可溶性糖和游离氨基酸可能在续断菊累积镉的过程中有重要作用。