长期施肥下浙江稻田不同颗粒组分有机碳的稳定特征

依托浙江水网地区稻田长期定位施肥试验(1996~2013年),利用固态13C核磁共振波谱技术,研究长期不同施肥措施下土壤各颗粒组分有机碳含量及其化学结构特征.结果表明,与不施肥对照(CK)相比,秸秆与化肥配施(NPKRS)、栏肥与化肥配施(NPKOM)、单施化肥(NPK)和单施栏肥(OM)处理均显著(P0.05)增加了砂粒(2~0.02 mm)、粉粒(0.02~0.002mm)和黏粒(0.002 mm)组分中有机碳含量;而单施秸秆(RS)处理仅显著增加砂粒组分有机碳含量.此外,与单施化肥处理相比,有机肥和化肥配施促进了新增有机碳在粉粒和黏粒组分的分配,更有利于新增有机碳的稳定.应用13C-NMR波谱技术进行结构表征,结果表明粉粒和黏粒组分有机碳的化学结构存在明显差异,粉粒组分烷氧碳、芳香碳的相对含量高于黏粒,而烷基碳、羰基碳的相对含量低于黏粒.长期有机肥与化肥配施下粉粒和黏粒烷基碳相对含量较单施有机肥处理分别降低9.1%~11.9%和13.7%~19.9%,烷氧碳的相对含量则分别增加2.9%~6.3%和13.4%~22.1%,表明有机肥与化肥配施处理降低了粉粒和黏粒组分有机碳的分解程度.长期单施化肥处理下粉粒和黏粒组分有机质的芳化度和疏水性低于单施有机肥处理和不施肥处理,有机质的矿化稳定性较低.长期有机肥与化肥配施,尤其是NPKOM处理,通过增加化学抗性化合物和碳水化合物的积累,并且减缓活性组分的分解提高粉粒和黏粒组分有机碳含量,是促进稻田土壤有机碳可持续积累的有效措施.     

黄浦江流域典型污水中不同粒径胶体的三维荧光光谱特征

基于切向流超滤系统及三维荧光光谱技术,对黄浦江流域典型污水(即生活污水及农业污水)中的胶体进行粒径分级及三维荧光光谱特性分析.结果表明,所选水样的胶体质量浓度及胶体态有机碳质量浓度分别为9.60~32.50 mg·L~(-1)和0.03~6.25 mg·L~(-1),二者均随粒径的增加而呈递增趋势.不同粒径分级胶体的三维荧光图谱表现为类蛋白荧光峰(峰D和峰T)及类腐殖质荧光峰(峰C和峰A)这4个荧光峰,其中类蛋白荧光峰主要存在于M_r1×10~3~5×10~3分级胶体中,类腐殖质荧光峰主要存在于M_r10×10~3~300×10~3分级胶体中.同时,通过表征胶体荧光光谱特性的荧光指数,包括FI值、腐殖化指数HIX及生源指数BIX,分析了所选胶体的来源及光谱特性.结果表明,小粒径胶体主要为陆源来源,芳香性及腐殖化程度较高;而大粒径胶体自生源比重大,类蛋白物质是其主要成分.     

ASM1耦合曝气模型对污水处理厂的模拟研究

为了更好地模拟污水处理厂实际的曝气方式及溶解氧浓度,采用更加精确的曝气模型对某污水处理厂进行了模拟研究.该模型考虑了污泥浓度、堵塞及温度等因素对氧传质的影响,并将该曝气模型与ASM1相耦合.首先,通过灵敏度分析确定了对该污水处理厂出水指标影响较大的参数,分别为异养菌产率系数YH、异养菌最大比增长速率μH、自养菌最大比增长速率μA及自养菌氧利用半饱和系数KOA.然后,测定部分灵敏度较高的参数并使用测量结果对模型进行校正,校正结果使用希尔系数表征.最后,使用另一批数据对校正参数进行验证.模拟的COD、氨氮、总氮和好氧池末端溶解氧的希尔不等系数分别是0.13、0.23、0.20和0.15,而通过控制溶解氧浓度或理论氧转移效率模型模拟则出现氨氮、溶解氧、总氮及COD的希尔不等系数不同程度上升的结果.校验后的ASM1/曝气耦合模型参数可以很好地应用于污水处理厂的模拟当中,对于优化污水厂曝气控制具有重要意义.     

Removal and transformation of organic matters in domestic wastewater during lab-scale chemically enhanced primary treatment and a trickling filter treatment

To find a simple and economical way for treating the domestic wastewater in small counties and towns, a process combining chemically enhanced primary treatment and a trickling filter (CEPT-TF, representing the physical and biological effects) was constructed and operated in laboratory conditions. The characteristic behaviors of dissolved organic matter in raw wastewater and effluents were examined during steady-state operation. Experimental results showed that the process of CEPT and TF in series was beneficial for the removal of hydrophobic and hydrophilic organics. Specially, the hydrophobic and aromatic materials could be preferentially removed in the CEPT unit, and the hydrophilic fraction in the TF. Structural changes of the organic fractions during the operation of the different units were also characterized via spectrum analysis.     

干热河谷林地燥红土固碳特征及"新固定"碳表观稳定性

全球气候变化背景下,森林土壤固碳能力及所固定碳的稳定性受到极大关注.基于土壤密度分组和酸水解技术,对比研究了1991年营造的大叶相思(Acacia auriculiformis)林不同阶段(1991、1997、2003和2010年)土壤及其物理和生化组分中有机碳密度.结果表明,造林19 a后林地表层(0～15 cm)和亚表层(15～30 cm)土壤有机碳密度分别为1.40 kg.m-2和0.99kg.m-2.研究期内(1991～2010年)表层和亚表层土壤平均固碳速率分别为37.89 g.(m2.a)-1和16.84 g.(m2.a)-1,且土壤呈现加速固碳特征.2003年林地表层重组有机碳分配比例为71.44%,显著高于2010年(67.99%).2003年林地表层或亚表层轻组顽固性碳指数显著高于重组,但均随林龄的增加而降低,尤其是轻组顽固性碳指数.2003～2010年间燥红土"新固定"碳中57%～70%受物理保护,33%～49%为生化稳定性碳.研究揭示出干热河谷人工林燥红土具备较大的固碳能力.受物理保护碳的生化稳定性低于非保护碳,其稳定性均随林龄的增加而降低.     

膜生物反应器中进水组成对膜污染的影响

研究了膜生物反应器中进水组成对膜污染的影响. 结果表明, 相对于正常组成来说进水中限氮或限磷引起的膜污染程度更重, 尤以进水中限氮时更为严重. 系统缺氮或缺磷时, 污泥絮体的相对憎水性和膜的憎水性增加, 使得膜和污泥之间的憎水相互作用增强, 加速了污染物在膜表面的沉积和/或吸附. 另外, 进水中限氮或限磷时, 污泥中丝状菌的数量增加, 把颗粒污泥捆扎、束缚在其立体网状结构中, 滤层结构更加致密, 孔隙度减小, 增加了膜污染阻力; 丝状菌的作用还在于它们能够将污染物牢牢地缠绕、固定在膜表面, 加强了膜表面污染物抵御曝气的水力冲刷作用的能力, 从而也加速了膜污染.     

Transformations of particles, metal elements and natural organic matter in different water treatment processes

Characterizing natural organic matter （NOM）, particles and elements in different water treatment processes can give a useful information to optimize water treatment operations. In this article, transformations of particles, metal elements and NOM in a pilot-scale water treatment plant were investigated by laser light granularity system, particle counter, glass-fiber membrane filtration, inductively coupled plasma-optical emission spectroscopy, ultra filtration and resin absorbents fractionation. The results showed that particles, NOM and trihalomethane formation precursors were removed synergistically by sequential treatment of different processes. Preozonation markedly changed the polarity and molecular weight of NOM, and it could be conducive to the following coagulation process through destabilizing particles and colloids; mid-ozonation enhanced the subsequent granular activated carbon （GAC） filtration process by decreasing molecular weight of organic matters. Coagulation-flotation and GAC were more efficient in removing fixed suspended solids and larger particles; while sand-filtration was more efficient in removing volatile suspended solids and smaller particles. Flotation performed better than sedimentation in terms of particle and NOM removal. The type of coagulant could greatly affect the performance of coagulation-flotation. Pre-hydrolyzed composite coagulant （HPAC） was superior to FeCl3 concerning the removals of hydrophobic dissolved organic carbon and volatile suspended solids. The leakages of flocs from sand-filtration and microorganisms from GAC should be mitigated to ensure the reliability of the whole treatment system.     

基于活性污泥模型的污水COD组分划分方案研究

活性污泥数学模型(ASM)在污水处理厂的成功应用与进水组分的正确划分密切相关.从标准化和定量化的角度利用3个批式试验开发了COD组分划分方案及Matlab计算程序.该方案在上海2个污水处理厂的测定结果表明,曲阳污水厂进水COD中含有8.1%±1.6%的易生物降解组分SS、6.3%±2.2%的溶解性惰性组分SI、45.5%±3.5%的慢速生物降解组分XS、31.1%±2.1%的颗粒性惰性组分XI和9.0%±1.1%的异养菌组分XH.而白龙港污水厂进水COD中含有11.1%±2.2%的SS、9.9%±2.0%的SI、38.9%±10.7%的XS、23.3%±9.8%的XI和16.9%±1.8%的XH.与曲阳污水厂相比,白龙港污水厂进水COD中XS和XI含量偏低,而XH/COD值则明显偏高,表明长距离管道输送会显著影响COD组分浓度.     

四川某中小城镇污水处理厂进水水质统计分析

生活污水水质对处理工艺的选择、设计参数的选取以及稳定运行十分重要。运用SPSS软件,对四川某中小城镇污水处理厂为期一年的进水指标(水量、COD、氨氮、总磷、pH、SS)进行方差和相关性分析。方差分析结果显示进水量、氨氮和SS在月份和季节之间存在显著性差异,而总磷和pH仅在月份之间存在显著差异,COD在季度和月份之间无显著性差异;指标相关性分析表明,进水量和氨氮之间呈负相关,氨氮和总磷、COD和总磷之间呈正相关,且相关性显著。在此分析的基础上对污水处理厂设计、工艺选择及运行管理提出了一些建议。     

Transport and fate of mercury under different hydrologic regimes in polluted stream in mining area

Seepage from Hg mine wastes and calcines contains high concentrations of mercury (Hg). Hg pollution is a major environmental problem in areas with abandoned mercury mines and retorting units. This study evaluates factors, especially the hydrological and sedimentary variables, governing temporal and spatial variation in levels and state of mercury in streams impacted by Hg contaminated runo . Samples were taken during di erent flow regimes in theWanshan Hg mining area in Guizhou Province, China. In its headwaters the sampled streams/rivers pass by several mine wastes and calcines with high concentration of Hg. Seepage causes serious Hg contamination to the downstream area. Concentrations of Hg in water samples showed significant seasonal variations. Periods of higher flow showed high concentrations of total Hg (THg) in water due to more particles being re-suspended and transported. The concentrations of major anions (e.g., Cl??, F??, NO3?? and SO4 2??) were lower during higher flow due to dilution. Due to both sedimentation of particles and dilution from tributaries the concentration of THg decreased from 2100 ng/L to background levels (< 50 ng/L) within 10 km distance downstream. Sedimentation is the main reason for the fast decrease of the concentration, it accounts for 69% and 60% for higher flow and lower flow regimes respectively in the upper part of the stream. Speciation calculation of the dissolved Hg fraction (DHg) (using Visual MINTEQ) showed that Hg(OH)2 associated with dissolved organic matter is the main form of Hg in dissolved phase in surface waters in Wanshan (over 95%).