甲醛等室内主要污染物分布特征与影响评价

现代人80%以上的时间是在室内度过的,室内实际上已成为越来越多的人最直接、最经常的生活环境。与此同时,室内空气质量的优劣也越来越受到人们的关注。本文在呼和浩特市选择不同时间装修的居室,对其室内空气中甲醛、氨、一氧化碳、氡的含量进行了实测,分析了居室装修后室内主要空气污染物的污染水平以及各污染物的分布特征。数据表明,目前新近装修的居室内存在严重的甲醛污染,其超标率达到55.81%,随装修后时间的推移室内甲醛含量逐渐减少,其超标率逐渐降低,说明室内甲醛含量与室内通风状况有明显的正相关性;在所测定的居室中,一氧化碳及氨均未超标,氡的超标率为20%。     

Evaluation of mercury speciation and removal through air pollution control devices of a 190 MW boiler

Air pollution control devices (APCDs) are installed at coal-fired power plants for air pollutant regulation. Selective catalytic reduction (SCR) and wet flue gas desulfurization (FGD) systems have the co-benefits of air pollutant and mercury removal. Configuration and operational conditions of APCDs and mercury speciation a ect mercury removal e ciently at coal-fired utilities. The Ontario Hydro Method (OHM) recommended by the U.S. Environmental Protection Agency (EPA) was used to determine mercury speciation simultaneously at five sampling locations through SCR-ESP-FGD at a 190 MW unit. Chlorine in coal had been suggested as a factor a ecting the mercury speciation in flue gas; and low-chlorine coal was purported to produce less oxidized mercury (Hg2+) and more elemental mercury (Hg0) at the SCR inlet compared to higher chlorine coal. SCR could oxidize elemental mercury into oxidized mercury when SCR was in service, and oxidation e ciency reached 71.0%. Therefore, oxidized mercury removal e ciency was enhanced through a wet FGD system. In the non-ozone season, about 89.5%–96.8% of oxidized mercury was controlled, but only 54.9%–68.8% of the total mercury was captured through wet FGD. Oxidized mercury removal e ciency was 95.9%–98.0%, and there was a big di erence in the total mercury removal e ciencies from 78.0% to 90.2% in the ozone season. Mercury mass balance was evaluated to validate reliability of OHM testing data, and the ratio of mercury input in the coal to mercury output at the stack was from 0.84 to 1.08.     

低温时污泥膨胀对MBR中膜污染的影响

通过一体式膜生物反应装置考察了在低温条件下发生污泥膨胀过程中反应器的运行效果和膜污染的情况,并从微生物角度分析了引起膜污染的因素.结果表明,低温时COD上清液和出水平均去除率分别为85%和92%,发生丝状菌污泥膨胀后去除率变化不大.MBR中丝状菌污泥膨胀形成的过程中,污泥沉降性变差,丝状菌丰度（FI）由2增加到5,丝状菌伸出絮体形成网状结构.低温时膜操作压力随时间呈直线变化,膜组件的水力清洗周期为15 d.在丝状菌大量繁殖时缩短到7 d,膜污染严重.通过测定活性污泥的特性,发现膨胀污泥的胞外聚合物（EPS）总量是正常污泥的3倍,污泥絮体相对疏水性（RH）随FI的提高而增大.EPS和RH增大后会引起更多物质沉积到膜表面,使膜污染速率提高,膜的运行周期变短.进一步的分析表明,混合液粘度、Zeta电位、污泥絮体形态也是影响膜污染的因素.     

温度对好氧颗粒污泥吸附铅离子的影响

由活性污泥培养得到好氧颗粒污泥,研究了温度对好氧颗粒污泥吸附Pb²⁺的影响.结果表明,好氧颗粒污泥主要含有C、H、N、O、P等元素,其经验结构式为C_5.7H_10.9O3.9NS_0.04.好氧颗粒污泥表面主要由球状细菌组成,具有明显的孔隙结构.在20～40℃时,Pb²⁺在好氧颗粒污泥上的吸附过程可以由Langmuir和Freundlich等温方程进行拟合（R²>0.914）.Pb2+最大吸附量Qmax由80.65 mg·g-1（20℃）增至97.09　mg·g-1（40℃）.吸附过程的表观自由能变ΔG<0、 ΔH>0、 ΔS>0,表明Pb2+在好氧颗粒污泥表面的吸附为吸热、熵增的自发过程.红外扫描分析(FTIR)结果表明,吸附过程Pb2+主要与—OH、蛋白质中的—COOH以及PO发生作用,与含氮官能团无关.     

水温和pH对饮用水中铝形态分布的影响

铝对输配水系统及人体健康的影响主要与其存在形态有关.本研究采用硫酸铝模拟配水考察了水温和pH对溶液中铝形态分布的影响情况.考察的主要铝形态包括单核铝、溶解铝、悬浮铝和多核铝;采用的形态分析方法为荧光分光光度法.结果表明:当pH=6.5时,悬浮铝为饮用水中铝的主要存在形态,在总铝中的质量分数为62.2%;而当pH>7.0时,单核铝为主要形态,且随反应时间的增加变化不大.各水质条件下的多核铝浓度均较低,且随反应时间的变化也不大.水温对铝形态的影响与pH是一致的,由pOH可将二者统一起来.通过调节pOH可以实现饮用水中铝形态的控制,这将对输配水系统的运行管理及铝毒性控制提供理论依据.     

二次富集气相色谱法测定环境中的痕量磷化氢

本文研究了富集柱类型、富集温度和色谱操作条件等因素对二次富集气相色谱法测定环境中痕量PH3的影响,并将其应用于青岛大气和东海陆架沉积物中PH3的测定,取得了较为满意的结果.该方法具有操作简单、灵敏度高、分析速度快、干扰少等优点,其检测限为0.02 pg、精密度2.0%、线性范围为0.56 pg～5.6 ng.用此方法测定了冬季东海大陆架表层沉积物中PH3含量为(0.51～23.10)×10-9,其分布明显受到人类活动的影响,研究结果还表明东海沉积物中的PH3是海洋中磷的潜在来源之一;青岛崂山大气中PH3日变化趋势说明大气中PH3明显受光照的影响.     

粮食蔬菜与土壤和大气中苯并（a）芘含量的相关性研究

对山西省运城市盐湖区不同区域内小麦、西红柿、白菜和土壤中B（a）P含量的空间一时间分布及大气、土壤与粮食、蔬菜中B（a）P含量关系进行了调查研究,结果表明,粮食和蔬菜中的B（a）P主要来自大气污染的“贡献”,土壤中的B（a）P的含量也直接影响粮食和蔬菜中B（a）P的含量。当小麦子实中B（a）P的含量达到一定水平后,并不随土壤中B（a）P含量的增加而增加。     

生物菌剂对石油污染土壤生物修复作用的研究

在实验室条件下,研究了生物菌剂的投加量、投加方式及环境温度对石油污染土壤的修复作用 结果表明,土壤中石油烃的降解效果与生物菌剂的投加量呈正相关,当生物菌剂投加量为0.6mg·kg^-1时,修复,48 d 后,石油烃的降解率为87%.GC-MS分析结果表明,石油污染原土中烷烃的含量最高为82.1%其次为烯烃,含量为16%,还含有少量的胡萝卜烷、烷基萘、甾烷和藿烷% 添加生物菌剂修复40 d 后,峰的数量由32个减少为14个,表明异构烷烃、烯烃、胡萝卜烷全部被降解,残留的物质为较难降解的正构烷烃、藿烷和甾烷,呈现前高后低的峰形,即接种细菌优先降解高碳组分,将长链的烷烃降解为短链的烷烃,随着生物菌剂投加量的增加,土壤中残留石油烃的含量逐渐降低% 一次加入生物菌剂修复,48 d后的峰高明显低于分2 次加入的相应值,故一次性全部加入生物菌剂是最佳的投加方式% 温度是限制石油污染土壤生物修复的重要环境因素,当温度为30℃第,48 d 的降解率可达80%,当温度为20℃,第,48 d的降解率可达60%,温度高有利于土壤中石油烃的降解,加快修复     

Evaluation of multiple reactions in dilute benzoyl peroxide concentrations with additives using calorimetric technology

Benzoyl peroxide (BPO) is a typical organic peroxide widely used in food processing, particularly flour bleaching. Due to the unstable nature of the oxygen-oxygen bond in BPO, it readily reacts under even mid-low-temperature conditions. Lower concentrations of BPO are also potentially explosive, even when combined with acid or alkaline additives. Given the history of both potential and documented industrial accidents, this study investigates the thermal stability of various BPO concentrations when mixed with acid or alkaline solutions. In addition, differential and integral kinetic models were applied to verify that the apparent activation energy data from the differential scanning calorimetry experiments were valid. The results of autocatalysis reactions and nth-order reaction simulations presented characteristics consistent with the experimental findings. The findings in this paper can be used as a reference for BPO products that are mediated with either an acid or an alkaline solution during production, storage, transportation, or use.     

Inhibiting effects by Fe2O3 on combustion and explosion characteristics of ABS resin

The global increase in the use of, and reliance on, plastics has prompted the demand for acrylonitrile-butadiene-styrene (ABS) resin in various fields. With this increased requirement, numerous failures have occurred in the ABS process. Those incidents, resulting from electrostatic discharge, powder accumulation, heat accumulation, construction sparks, and plant fires, have caused dust fire and explosions.In this study, the ABS resin was gleaned from the site and tested for its explosion parameters, including minimum ignition temperature of dust cloud (MIT_C), minimum ignition energy (MIE), and minimum explosion concentration (MEC). To improve loss prevention in the manufacturing process, ferric oxide (Fe₂O₃) as an inert additive was added in the ABS powder. According to the MIE test, Fe₂O₃ has an apparent inhibiting effect on dust explosion for the ABS dust. With the proportion of Fe₂O₃ increased from 25 to 50 mass% in ABS, the MIE increased from 67 to 540 mJ. The explosion tests via 20-L apparatus indicated that Fe₂O₃ mixed with ABS could not increase the MEC significantly. However, the explosion pressure dropped by increasing in the ratio of Fe₂O₃ in ABS. This inerting strategy of ABS was deemed to substantially lessen the probability and severity of fire and explosion.