流化床焚烧含盐苯胺废液的NOx排放特性

在流化床焚烧实验装置上进行含盐苯胺(C6H5NH2)废液的焚烧实验研究,用IMR-IMR2800P废气分析仪对焚烧尾气成分进行了在线监测,考察了焚烧工艺条件对NOx排放浓度的影响规律.结果显示:采用分级燃烧工艺和提高焚烧温度,可以降低NOx浓度;增大进料速率却导致NOx排放浓度的增加.当过剩空气系数(α)低于1.0时,NOx排放浓度随着α的增大急剧上升;大于1.1时,NOx排放浓度随α增加而减小.苯胺废液高温焚烧时添加氯化钠能降低NOx排放.     

剩余污泥中木质纤维素稳定并转化能源可行性分析

剩余污泥中往往含有大量木质纤维素物质,在厌氧消化过程中难以降解,最终被浓缩于熟污泥中,这就是导致污泥有机物稳定并转化能源效率低下的主要原因之一.本文分析了剩余污泥中木质纤维素的含量与来源;阐述了木质纤维素的结构特点以及对其生物降解的关键技术所在;揭示了污泥常规预处理与木质纤维素预处理存在工艺条件不同的相似技术.文章结合两种预处理技术的特点和工艺条件,从原理、技术等角度分析了通过强化剩余污泥预处理而同时达到破解木质纤维素的技术思路.为此,提出了将污泥细胞破碎与木质纤维素破解耦合的观点,以期将污泥中木质纤维素的稳定与能源转化合二为一,从而构建木质纤维素稳定化、能源化与碳减排三位一体的技术策略     

复合生物絮凝剂CBF-1的絮凝作用机理研究

采取PAC+絮凝剂的复配方式开展高岭土悬浊液烧杯实验,考察了复合生物絮凝剂CBF-1、CBF-1溶解物及微生物絮凝剂MBF8的絮凝特性,并借助iPDA仪分析和扫描电镜、光学显微镜观察等手段,比较分析了絮凝过程及絮体特性的差异.结果表明,各复配絮凝的浊度去除效果排序为CBF-1＞ CBF-1溶解物＞MBF8,CBF-1投加量1 mg·L-1时,浊度去除率可达到97.5％;絮体强度排序为CBF-1＞ CBF-1溶解物＞MBF8,絮体恢复因子排序为MBF8＞CBF-1溶解物＞CBF-1,絮体大小排序为CBF-1＞ CBF-1溶解物＞MBF8.单独投加PAC或投加PAC+MBF8的情况下,形成的絮体形态相对规整、密实;投加PAC+ CBF-1溶解物或投加PAC+ CBF-1形成的絮体则相对无序、疏松,CBF-1作用下絮体大、沉降快.CBF-1中高电荷MBF8组分及大分子羧甲基纤维素、羧甲基多聚糖等组分具有强的电荷中和与桥联协同增效作用;CBF-1还含有纤维素、木质素等大分子量且带多种官能团的不溶性组分,在桥联和吸附过程中也起着重要作用.     

改性壳聚糖CAD与微生物絮凝剂MBF8复配絮凝研究

采用水溶液自由基聚合反应,将丙烯酰胺(AM)、二甲基二烯丙基氯化铵(DMDAAC)接枝到壳聚糖分子上制成了阳离子改性壳聚糖(CAD).经FT-IR、XRD、zeta(ξ)电位、凝胶色谱等分析确定,CAD为淡黄色透明液体,pH值为3.7,相对分子质量为2.88×10⁶,阳离子度为16.7,等电点(0.1%溶液)约为pH值10.5,有效成分2.6%,主要特征官能团有羟基、氨基、季铵基和酰胺基, 呈不规则晶体结构.将CAD与相对分子质量3.67×10⁵的多糖类电负性微生物絮凝剂MBF8复配,对浊度12~460 NTU、离子强度3.0 mmol·L^-1的高岭土悬浊液进行烧杯实验.结果表明,MBF8与CAD的最佳使用方式为先投加MBF8后投加CAD,复配比5:3时效果最好,适用的pH范围为6.0~10.0.采用PAC(3.0 mg·L^-1)+MBF8+CAD(1.0 mg·L^-1)复配絮凝,pH=8.0下,对浊度为110 NTU的高岭土悬浊液,浊度去除率>97%,残余铝<0.08 mg·L^-1,絮体大、沉降快,絮凝效果优于PAC+分子量800万、1200万的阴离子PAM及分子量1500万的阳离子PAM.     

单光子/光电子在线质谱实时分析聚氯乙烯热分解/燃烧产物

实验室研制了低能光电子磁场增强电离(MEPEI)和单光子电离(SPI)复合电离源,该电离源具有电离化合物范围宽、碎片离子少、质谱图简单等优点,结合飞行时间质谱(TOF-MS)实现了聚氯乙烯(PVC)热分解/燃烧产物的在线分析.针对不同的目标化合物,MEPEI/SPI复合电离源通过调节电离区电场强度,可以快速在SPI和SPI-MEPEI之间切换.PVC热分解/燃烧产物中电离能大于光子能量(10.60 eV)的HCl和CO2(12.74 eV、13.77 eV)利用MEPEI模式电离;而烯烃、二氯乙烯、苯系物、氯苯、苯乙烯、茚满及萘系物等可通过SPI-MEPEI复合模式电离.通过实时监测PVC主要燃烧产物的信号强度随温度的变化趋势可推断出,PVC燃烧产物主要是通过两种机制生成:①250～370℃时,PVC发生脱氯及分子内环化反应,产生大量的HCl、苯和萘;②380～510℃时,PVC发生分子间交联反应,生成烷基芳烃,如甲苯和二甲苯/乙苯等.实验结果表明,SPI/SPI-MEPEI复合离子源TOF-MS分析速度快,应用范围广,在在线分析中具有广泛的应用前景.     

扑草净降解菌的分离、筛选与鉴定及降解特性初步研究

从安徽农药厂废水处理系统的活性污泥中筛选扑草净(prometryne)降解菌.通过富集驯化和选择性培养筛选纯化细菌,分离到2株细菌,分别命名为P-1、P-2.根据表型特征、生理生化特性和16S rDNA序列同源性分析:P-1为G-,鉴定为苍白杆菌属(Ochrobactrum);P-2为G+,鉴定为芽胞杆菌属(Bacillus).GenBank登录号分别为HM004554和HM004555.通过12 d液体降解实验,菌株P-1、P-2对40 mg.L-1扑草净降解率分别达到46.5%和65.4%.该研究为扑草净的生物降解与污染土壤的生物修复提供了依据.     

深水型水库藻类功能组时空演替及生境变化的影响

藻类功能分组是近年来生态学藻类研究的重要理论和方法.为了探明西安某深水型水源水库藻类功能组时空演替及生境变化的影响,于2011年8月起开展实验研究.研究采用现场在线监测和实验室分析相结合的方法.结果表明,水库藻类可分为10个功能组类别:B、D、P、X1、X3、F、G、J、LM、MP.其中,功能组B、P、F、X1、MP、D、J在水库中较为常见,X3、G、LM出现几率较低,功能组B、D、P、X1、X3的藻类数量占优.通过分析环境因子的变化对功能组时空演替的影响,发现水温为最主要的影响因子.水库藻类生长策略为:春季R/CR策略藻种→春末夏初CR/C策略藻种→夏末秋初C/CR/R/CS/S策略藻种→秋末及冬季CR/R策略藻种.此研究可为深水型水库安全取水提供理论支持.     

Adsorption of 2-mercaptobenzothiazole from aqueous solution by organo-bentonite

The adsorption behavior of 2-mercaptobenzothiazole onto organo-bentonite was investigated.Natural bentonite from Gaozhou in Guangdong Province,China was collected.Organo-bentonite was prepared by intercalation of cetyltrimethyl ammonium bromide into the natural bentonite.The physicochemical properties of the prepared organo-bentonite were characterized by X-ray diffraction,N2 adsorption-desorption isotherm and Fourier transform infrared spectroscopy.The results showed that montmorillonite is the main component of the natural bentonite.The basal spacing of the natural bentonite is 1.47 nm,which increased to 1.98 nm on intercalation with cetyltrimethyl ammonium bromide.Moreover,both the surface area and pore volume increased with intercalation.Clear CH2 stretching(3000-2800 cm-1) and scissoring(1480-1450 cm-1) modes of the intercalated surfactants were observed for organobentonite.Compared with the pseudo first-order kinetic model,the pseudo second-order kinetic model is more suitable to describe the adsorption kinetics of 2-mercaptobenzothiazole onto organo-bentonite.The adsorption capacity of 2-mercaptobenzothiazole onto organo-bentonite increased with increasing initial concentration of 2-mercaptobenzothiazole,but decreased with increasing adsorbent dosage.The adsorption isotherm of 2-mercaptobenzothiazole onto organo-bentonite fits well with the Langmuir model.The maximum adsorption capacity of organo-bentonite for 2-mercaptobenzothiazole was 33.61 mg/g,indicating that organo-bentonite is a promising adsorbent for 2-mercaptobenzothiazole.     

Decrease of NH4+-N by bacterioplankton accelerated the removal of cyanobacterial blooms in aerated aquatic ecosystem

We used aerated systems to assess the influence of the bacterioplankton community on cyanobacterial blooms in algae/post-bloom of Lake Taihu, China. Bacterioplankton community diversity was evaluated by polymerase chain reaction-denaturing gradient gel electrophoresis(PCR-DGGE) fingerprinting. Chemical analysis and nitrogen dynamic changes illustrated that NH4+-N was nitrified to NO2-N and NO3-N by bacterioplankton. Finally, NH4+-N was exhausted and NO3-N was denitrified to NO2-N, while the accumulation of NO2-N indicated that bacterioplankton with completely aerobic denitrification ability were lacking in the water samples collected from Lake Taihu. We suggested that adding completely aerobic denitrification bacteria(to denitrify NO2-N to N2)would improve the water quality. PCR-DGGE and sequencing results showed that more than 1/3 of the bacterial species were associated with the removal of nitrogen, and Acidovorax temperans was the dominant one. PCR-DGGE, variation of nitrogen, removal efciencies of chlorophyll-a and canonical correspondence analysis indicated that the bacterioplankton significantly influenced the physiological and biochemical changes of cyanobacteria. Additionally, the unweighted pair-group method with arithmetic means revealed there was no obvious harm to the microecosystem from aeration. The present study demonstrated that bacterioplankton can play crucial roles in aerated ecosystems, which could control the impact of cyanobacterial blooms in eutrophicated fresh water systems.     

日本沼虾与秀丽白虾的营养生态位

为科学评估虾类的营养关系及资源的保护,利用稳定同位素技术研究了2种淡水虾类在大型通江湖泊——洞庭湖和鄱阳湖中的营养生态位和生态宽幅大小.结果表明,日本沼虾与秀丽白虾的δ13C值呈显著差异,而δ15N值无明显差异.同时,由于营养状况及水文的差异,虾类同位素值的差异在2个湖泊中表现不同.日本沼虾的δ13C值范围比秀丽白虾大,频率分布相对集中在-25.0‰～-23.0‰区间,表明其摄食的食物来源更广,对某些饵料生物有所偏好.另外,日本沼虾与秀丽白虾的营养生态位重叠程度较大,表明二者的主要食物来源相同,在食物网中占据的营养级相近,存在着激烈的种间竞争.在鄱阳湖中,日本沼虾占有的营养生态位和生态宽幅大于秀丽白虾;而在洞庭湖的研究结果则相反,主要是由于采样区域生境的差异及人类活动干扰的程度不同所致.