传统北京烤鸭烤制过程中大气污染物的排放特征

烤鸭是具有北京特色的传统美食之一,制作过程采用果木炭火烤制方式,与其它食物烹饪过程存在明显的差异,国内还未对这类餐饮源的排放特征进行过系统研究,为掌握这类餐饮源排放特征,从而为污染控制提供技术依据,选取北京市具有代表性的烤鸭店,研究了其烤鸭烤制过程中大气污染物的排放特征.结果表明,传统烤鸭烤制过程中排放的油烟、颗粒物、挥发性有机物(VOCs)和醛酮类化合物的基准排放浓度分别为(0.74±0.45)、(15.32±7.93)、(7.60±3.41)和(1.22±0.59)mg·m~(-3);颗粒物排放浓度要远高于油烟排放浓度,VOCs组分构成相对复杂,既包括烷烃、烯烃、芳香烃等VOCs也包括醛酮类、醇类、酯类等含氧VOCs和卤代烃,其中3-甲基呋喃、乙醇和乙酸甲酯的浓度最高;醛酮类化合物的主要组分有乙醛、甲醛和丙烯醛等,其中C1~C3物质占72.27%.     

Quantum chemical investigation on photodegradation mechanisms of sulfamethoxypyridazine with dissolved inorganic matter and hydroxyl radical

Sulfamethoxypyridazine(SMP) is one of the commonly used sulfonamide antibiotics(SAs).SAs are mainly studied to undergo triplet-sensitized photodegradation in water under natural sunlight with other coexisting aquatic environmental organic pollutants.In this work,SMP was selected as a representative of SAs.We studied the mechanisms of triplet-sensitized photodegradation of SMP and the influence of selected dissolved inorganic matter,i.e.,anions(Br~-,Cl~-,and NO~-_3) and cations ions(Ca~(2+),Mg~(2+),and Zn~(2+)) on SMP photodegradation mechanism by quantum chemical methods.In addition,the degradation mechanisms of SMP by hydroxyl radical(OH·) were also investigated.The creation of SO_2 extrusion product was accessed with two different energy pathways(pathway-1 and pathway-2) by following two steps(step-I and step-II) in the tripletsensitized photodegradation of SMP.Due to low activation energy,the pathway-1 was considered as the main pathway to obtain SO_2 extrusion product.Step-II of pathway-1 was measured to be the rate-limiting step(RLS) of SMP photodegradation mechanism and the effect of the selected anions and cations was estimated for this step.All selected anions and cations promoted photodegradation of SMP by dropping the activation energy of pathway-1.The estimated low activation energies of different degradation pathways of SMP with OH·radical indicate that OH·radical is a very powerful oxidizing agent for SMP degradation via attack through benzene derivative and pyridazine derivative ring.     

Simulated reaction of formaldehyde and ambient atmospheric particulate matter using a chamber

The reaction of HCHO with Beijing winter's real ambient particulate matter(PM) inside a 3.3 m~3 Teflon Chamber was conducted in this study. NO_2, O_3 and H_2O gases were removed from the ambient aerosol before entering into the chamber. The decays of HCHO were monitored(acetylacetone spectrophotometry method) during the reactions at different PM number concentrations(N_a) and relative humidities(RHs), and the formed particulate formate was detected by IC and XPS techniques. The results showed that when RH was10%–15%, the decay rate of HCHO in the chamber was higher with the existence of PM from relatively clean days(with number concentration(N_a) 200,000 particle/L, 0.35–22.5 μm)compared to dirty days(N_a 200,000 particle/L, 0.35–22.5 μm). When RH increased to 30%–45%, PM can hardly have significant influences on the decay of HCHO. The formations of formate on the reacted PM were consistent with the HCHO decay rates at different ambient PM N_aand RH conditions. This is a first study related to the "real" ambient PM reacted with HCHO and suggested that in the clean and low RH days, PM could be an effective medium for the conversion of HCHO to formate.     

覆盖金属氧化物对湖泊沉积物溶解性有机质特征的影响

为揭示不同金属氧化物对湖泊沉积物DOM（溶解性有机质）影响机制,通过室内模拟试验,在沉积物表层分别覆盖Fe、Al、Mn氧化物及湖沙后培养1 a,并利用三维荧光和紫外光谱方法进行表征.结果表明:① 覆盖Al、Fe、Mn氧化物和湖沙主要降低了0~3 cm沉积物的w（DOC）,降幅分别为8.61%、6.27%、22.38%和0.44%. ② 沉积物中DOM的类络氨酸峰（peak B₁）和类色氨酸峰（peak T₂）均产生较大变化.其中三种氧化物均显著降低了上层沉积物中DOM的peak T₂,使底层DOM的peakT₂显著增加. Mn氧化物使DOM的peak B₁降低,Fe和Al氧化物使DOM的peak B₁增加,湖沙则使两类峰均降低. ③ 覆盖金属氧化物改变了沉积物DOM结构特征,其中覆盖Fe氧化物增强了其芳香性,而覆盖Mn氧化物和Al氧化却降低其芳香性,但三者均使DOM腐质化程度及官能团数量增加,并使FI（Fluorescence Index,荧光指数）增大,表明DOM向生物源转化.研究显示,沉积物表层覆盖金属氧化物影响了沉积物中DOM迁移和转化,并促进了其降解,导致其分子量和腐殖化程度增加.      

多相流中细长颗粒数值模拟研究综述

纤维干燥尾气中的飞灰含有大量的木质纤维、砂光粉和其他粉尘。从形状来看,木质纤维属细长颗粒,和研究较为成熟的球形颗粒在许多方面存在较多差异。目前,国内外学者们已对细长颗粒在多相流中的悬浮、沉降及流化方面开展了大量数值模拟研究,取得了一定的进展;在此基础上,继续完善木质纤维的运动特征、推导出其在换热器表面的碰撞沉积模型是下一步的主要工作。     

Effects of Cu2+ and humic acids on degradation and fate of TBBPA in pure culture of Pseudomonas sp. strain CDT

Soil contamination with tetrabromobisphenol A(TBBPA) has caused great concerns;however, the presence of heavy metals and soil organic matter on the biodegradation of TBBPA is still unclear. We isolated Pseudomonas sp. strain CDT, a TBBPA-degrading bacterium, from activated sludge and incubated it with ~(14)C-labeled TBBPA for 87 days in the absence and presence of Cu~(2+)and humic acids(HA). TBBPA was degraded to organic-solvent extractable(59.4% ± 2.2%) and non-extractable(25.1% ± 1.3%) metabolites,mineralized to CO_2(4.8% ± 0.8%), and assimilated into cells(10.6% ± 0.9%) at the end of incubation. When Cu~(2+)was present, the transformation of extractable metabolites into non-extractable metabolites and mineralization were inhibited, possibly due to the toxicity of Cu~(2+)to cells. HA significantly inhibited both dissipation and mineralization of TBBPA and altered the fate of TBBPA in the culture by formation of HA-bound residues that amounted to 22.1% ± 3.7% of the transformed TBBPA. The inhibition from HA was attributed to adsorption of TBBPA and formation of bound residues with HA via reaction of reactive metabolites with HA molecules, which decreased bioavailability of TBBPA and metabolites in the culture. When Cu~(2+)and HA were both present, Cu~(2+)significantly promoted the HA inhibition on TBBPA dissipation but not on metabolite degradation. The results provide insights into individual and interactive effects of Cu~(2+)and soil organic matter on the biotransformation of TBBPA and indicate that soil organic matter plays an essential role in determining the fate of organic pollutants in soil and mitigating heavy metal toxicity.     

滴定分析法在土壤胡敏酸研究中的应用

胡敏酸是土壤有机质的重要组成部分,是研究土壤有机质物理化学性质的重要环节之一。本文综述了国内外在土壤胡敏酸研究中所采用的各种分析方法,详细论述了滴定分析方法在土壤胡敏酸官能团测定、土壤胡敏酸带电性质测定以及胡敏酸与金属相互作用研究中的应用,并使用滴定分析法测定了贵州喀斯特地区石灰土胡敏酸中酸性官能团及其与Ca2+形成络合物的稳定系数。通过总结对比滴定分析法在研究胡敏酸方面的应用,本文认为现代滴定分析法在表征土壤胡敏酸物化特性和研究土壤胡敏酸演化规律等方面具有广泛应用前景。     

基于质谱技术的在线大气颗粒物来源与污染过程解析研究——以江苏省淮安市为例

通过大气细颗粒物实时在线源解析技术(质谱直接测量法)采集录入淮安市市区部分特征污染源排放成分谱,对淮安市大气细颗粒物进行在线源解析,获取高时间分辨的颗粒物源解析结果,分析颗粒物来源、季度变化和重污染天气的污染过程,评估形成重污染过程的污染影响因子和影响程度,为区域大气污染综合整治提供重要目标指向,同时也为淮安环境空气PM2.5重度污染实时预警与监控、大气污染源减排方案评估、污染事件监控等提供有效的在线监测技术平台.     

川东北低山丘陵区细颗粒物主要相关因素和季节变化分析——以南充主城区为例

基于中国空气质量在线监测分析平台和全球天气精准预报网的大气质量和气象数据,以四川盆地东北低山丘陵区典型城市南充市主城区为例,检验了细颗粒物(PM_(2.5))浓度的概率密度分布,发现其接近对数正态分布,由相关分析确定了PM_(2.5)浓度的主要相关因素为CO、NO_2(相关系数r分别为0.76、0.55,P0.01),再通过对2014年1月—2016年6月的日数据的逐步回归筛选出最优的回归指标和模拟方程(决定系数R_(adj)~2为0.68,P0.05),2016年7月—2017年6月的数据验证表明模拟效果较好(拟合优度为0.64,相对误差15.48%);最后根据时序插值、浓度和IAQI(PM_(2.5))的时段均值发现PM_(2.5)浓度在年际上有降低趋势;在季节上由高到低依次为冬季、春季、秋季、夏季;PM_(2.5)浓度在1月和6月分别呈现出年内的峰值和谷值,5、10月出现了阶段性峰值,尤其是5月;IAQI(PM_(2.5))的季节变化与浓度变化规律相似;且PM_(2.5)与PM_(10)比值的均值为0.67,表明现阶段南充市主城区大气污染物中细颗粒物占有较大比重。     

山西省2015年细颗粒物的污染状况和空间分布

大气污染因其对人体健康、生态环境和气候变化的影响而成为全球关注的环境问题,细颗粒物（PM_2.5）是雾霾产生的主要原因之一。为全面掌握山西省细颗粒物的污染状况与空间分布格局,本文运用统计学方法和Arc GIS技术,根据环境空气质量评价技术规范,对2015年山西省57个空气质量指数监测站提供的PM_2.5实时数据进行处理分析。结果表明：山西省PM_2.5的浓度有明显的季节性变化特征,由高到低依次为冬、春、秋、夏;PM_2.5月平均浓度最高值分别出现在1月和12月,且高值中心都位于运城;在空间分布上则表现为南部高于北部。全省11个地市级城市有9个超过国家二级标准,超标指数达到72%。聚类分析结果表明：山西省城市可以分为两大类,一类为产业结构转型良好的城市,如阳泉、朔州、吕梁、大同;另一类为第二产业发展粗放,工业污染严重的区域。