排水造林对小兴安岭湿地土壤溶解性有机碳生物降解和淋溶的影响

以小兴安岭湿地为研究对象,分析了不同年代排水造林的森林沼泽湿地土壤溶解性有机碳(DOC)含量变化及生物降解特征,探讨了排水造林时间对土壤DOC及无机氮(NH+4-N+NO-3-N)淋溶动态变化的影响.结果表明:1排水造林时间对土壤DOC含量变化影响显著(p0.05).2003年(PS03)、1992年(PS92)、1985年(PS85)排水造林后的人工兴安落叶松湿地土壤DOC含量均低于未排水造林的天然兴安落叶松苔草湿地(XATC),且排水造林时间越长,土壤DOC含量越少.2在生物降解过程中,土壤DOC的变化趋势表现为初期降解速率较快,而后逐渐减慢并趋于稳定.其中周转时间为1 d的易降解DOC所占比重表现为:PS92XATCPS03PS85,表明排水时间达到一定阈值后,易降解DOC部分可能会转化为难降解部分.3在淋溶过程中,随着淋溶次数的增加,淋出液中DOC含量呈现为先增加后减小的趋势,淋溶1 d后,不同年代排水造林的森林沼泽湿地土壤DOC的淋失率表现为:PS85PS92PS03XATC,表明排水造林时间越长,土壤DOC淋失率越大,因此长时间的排水造林改造可能进一步影响土壤养分的贮量及其有效性.     

鄱阳湖沉积物有机磷形态及对水位变化响应

选取鄱阳湖枯水期不同高程出露表层沉积物,通过研究有机磷含量及形态差异,试图揭示江湖关系变化引起的水位下降对鄱阳湖沉积物有机磷潜在释放风险的影响.结果表明:1鄱阳湖枯水期表层沉积物有机磷含量(115.2~448.3 mg·kg-1)占总磷的19.3%~45.1%,有机磷含量空间分布呈"五河"入湖尾闾区高于湖心区和北部湖区.2鄱阳湖表层沉积物各形态有机磷含量大小顺序为:残渣态有机磷盐酸提取有机磷胡敏酸有机磷碳酸氢钠提取有机磷富里酸有机磷.3水位下降引起的沉积物出露时间延长是引起鄱阳湖不同高程沉积物有机磷形态变化的重要原因.沉积物出露时间越长,碳酸氢钠提取有机磷、盐酸提取有机磷与富里酸有机磷的含量越低,而胡敏酸有机磷和残渣态有机磷含量越高.同时,水位下降引起的沉积物出露时间延长致使活性有机磷和中活性有机磷占总有机磷比例下降,而非活性有机磷占总有机磷比例增加,反映了沉积物出露时间延长可能会促进有机磷形态由活性向非活性转化,在一定程度上能够降低沉积物有机磷的潜在性风险.     

化学氧化耦合电动力技术修复有机污染土壤

有机污染物严重危害着我国土壤环境。探讨了电动力技术修复有机污染土壤的可行性及相关参数的变化特性,并探究了电动力修复耦合化学氧化工艺及表面活性剂辅助等多种措施对修复效果的影响。结果表明:表面活性剂辅助反应可帮助提高有机污染物溶解性与迁移性能,从而提高修复效果;采用KMn O4氧化耦合电动力工艺修复受污染高岭土时有着最佳的修复效率,污染物平均去除率可达70%。     

湖北省主要固定燃烧源大气颗粒物及VOCs排放特征研究

于2014年1月至12月对湖北省9个城市21家典型企业的固定燃烧源进行了典型大气颗粒物及挥发性有机物(VOCs)的监测工作,研究了固定燃烧源大气颗粒物及VOCs的排放特征及其物质组成。结果表明:大气颗粒物年排放总量与装机容量呈正相关关系,颗粒物粒径越细占总颗粒物的质量百分比越低;不同燃料的锅炉废气中的PM10和PM2.5质量浓度表现为:石油焦煤生活垃圾,燃气锅炉废气中只检出PM1.0;焦化厂和炼铁厂锅炉废气中的VOCs以烯(炔)烃为主,各占79.21%和81.09%,乙烯占总VOCs的百分比最高,分别为69.13%和68.88%;燃油锅炉废气中的VOCs以烯(炔)烃(91.74%)为主,燃气锅炉废气中的VOCs以烯(炔)烃(37.96%)和醛脂(38.79%)为主;锅炉废气中VOCs的组分和浓度受锅炉使用类型和燃料类型差异的影响,排放废气中的VOCs浓度水平表现为:焦化厂锅炉炼铁厂锅炉,燃油锅炉燃气锅炉,且组分更复杂。     

Bi2O3-TiO2复合光催化剂协同处理铬-邻苯二甲酸酯复合污染

以硝酸铋和钛酸丁酯为前驱体,采用水热法制备了Bi_2O_3-TiO_2复合半导体材料,并利用X射线衍射(XRD)、紫外-可见吸收光谱(UVVis)、能谱分析(EDS)、X射线光电子能谱(XPS)等手段对复合材料的结构进行了表征.同时,考察了Bi_2O_3-TiO_2复合材料对重金属Cr(Ⅵ)和难降解邻苯二甲酸二丁酯(DBP)复合污染的处理性能,并探讨了复合催化剂协同处理复合污染的作用机制.结果表明:该复合催化剂在可见光下能同时降低重金属Cr(Ⅵ)和有机物DBP的浓度,抑制电子和空穴复合,表现出比对单一Cr(Ⅵ)及DBP污染物更高的处理效率.当Bi_2O_3含量为4%时,复合催化剂表现出最佳的光催化活性.     

Microbial bioavailability of dissolved organic nitrogen (DON) in the sediments of Lake Shankou, Northeastern China

Dissolved organic nitrogen(DON)extracted from Lake Shankou sediments using KCl was isolated into hydrophobic and hydrophilic fractions.The bioavailabilities of the hydrophobic and hydrophilic fractions to three types of bacterial communities collected from sediments,activated sludge and compost products were examined.The DON recoveries obtained by DAX-8 and cation exchange resins treatment were 96.17% ± 1.58% and 98.14% ±0% for the samples obtained from N4 and N14 stations,respectively.After 25 days of incubation at 25°C,most DON(59% to 96%)was degraded.Hydrophilic DON exhibited a higher reduction rate than hydrophobic DON during the growth phase.Untreated wastewater from Changshuihe town was the main degradable DON source to station N4,and 93% of hydrophilic DON and 80% of hydrophobic DON were degraded.Station N14 received a large amount of refractory DON from forest soils and exhibited DON degradation rates of 82% and 71% for the hydrophilic and hydrophobic fractions,respectively.Amino acid contents and fluorescence intensities were also analyzed.Approximately 27% to 74% of amino acids were taken up by day 5,and their concentration gradually increased in the following days due to the decomposition of dissolved proteins.Parallel factor analysis resulted in identification of tryptophan-like proteins,tyrosine-like proteins and FA-like substances.During the growth phase,40%–51% of the tryptophan-like proteins were taken up by bacteria,and the accumulation of tyrosine-like proteins was attributed to the release of biotic substances.The concentration of the FA-like substances decreased due to microbial decomposition.     

Comparison of using polyurethane foam passive samplers and tree bark samples from Western China to determine atmospheric organochlorine pesticide

Polyurethane foam(PUF)passive samplers were deployed and tree bark samples were collected at 15 sites across western China in 2013,and the organochlorine pesticide(OCP)concentrations in the samples were determined.Dichlorodiphenyltrichloroethane and its degradation products(collectively called DDTs),hexachlorocyclohexanes(HCHs),and hexachlorobenzene(HCB)were the dominant OCPs in the PUF samples and tree bark samples.The mean DDTs,HCHs and HCB concentrations were 33,22 and 18 ng/sample in the PUF samples,and 428,74,and 43 ng/(g lipid weight(lw))in the tree bark,respectively.The OCP concentrations in the air,calculated using PUF–air and tree-bark–air partitioning models,were of the same order of magnitude.Both sample types showed that relatively fresh inputs of DDT and HCHs to the environment have occurred in western China.Meanwhile,PUF passive samplers were compared with the use of tree bark samples as passive samplers.The OCP compositions in the PUF and tree bark samples were different.Only the relatively stable OCPs(such as HCB,β-HCH and p,p′-dichlorodiphenyldichloro-ethylene(DDE))were consistent in the PUF and tree bark samples.     

全自动消解测定土壤/沉积物中的有机碳

基于传统方法重铬酸钾氧化-分光光度法的原理,应用全自动消解仪测定土壤/沉积物中的有机碳。通过优化反应条件,将复杂的前处理过程自动化,可同时分析大批量样品。实验结果表明:该方法在0~24 mg线性关系良好,相关系数大于0.999。测定高、中、低3种浓度的样品,其相对标准偏差均小于4%;高浓度和低浓度的加标回收率分别为95.9%~106%和91.7%~105%。当取样量为0.5000 g时,检出限为0.0586%,方法指标满足对样品的准确分析。对比现有实验方法,该方法具有高效、节能、准确、安全等优点。     

成都市中心城区春季大气颗粒物PM_(2.5)的污染特征研究

于2012年5月11日至5月15日同时对成都中心城区及其大气环境监测对照点都江堰灵岩寺大气PM2.5进行采集,并分析其中的化学组分。研究结果表明:成都市中心城区PM2.5的总体质量浓度大于灵岩寺,且各化学组分的质量浓度也均大于灵岩寺。两站点PM2.5中OC/EC均大于2,有2次有机碳的存在;中心城区WSOC和TN日均浓度大于灵岩寺,同时发现中心城区TN日变化趋势与灵岩寺一致,WSOC变化不明显;水溶性二次离子(SO2-4、NO-3和NH+4)浓度相对较高,中心城区SO2-4/NO-3值比灵岩寺小,说明成都市机动车尾气是主要排放源。