杭州某高校室内空气质量状况调查分析

为了解高校室内污染状况,调查选取杭州市某高校75间教室按照装修完成后时间长短分成5组,分别于2011年3、6月进行氡、氨、甲醛和苯系物(苯、甲苯和二甲苯),浓度的检测.结果显示,甲醛和苯系物浓度与装修完成后时间长短、通风情况、温度、湿度密切相关,装修完成后1.0年内的教室浓度显著高于其余组(P＜0.05).除装修完成后5.0年以上组外,各组甲醛和苯系物含量6月都呈现极显著增高趋势(p＜0.01).所有室内氡和氨浓度均未超标.总体来说,该校室内空气质量状况总体良好,但新建建筑物的室内空气污染存在一定的安全隐患.     

汽车内微环境空气污染的初步探究

为了研究车内的污染水平,在2004-04-10至2004-06-20对车内空气进行了采样和分析.对车龄在2年内的91种型号轿车的车内微环境进行了静态检测,有效检测车辆共计802辆,同时对比检测20辆2002年以前出厂的旧车.检测项目包括甲醛、苯、甲苯、二甲苯和CO等.参照国家室内空气质量标准,新车中甲苯浓度超标率达82%,苯和甲醛浓度的超标率分别为75%和24%.在被检测车辆中,甲醛、苯、甲苯和二甲苯浓度均是新车比旧车高,只有CO浓度是旧车比新车高.初步分析判断苯系物主要来源于车内的胶粘剂,甲醛来自于车椅座套和座垫等,CO来源于发动机排放残留.     

污泥含炭吸附剂对挥发性有机废气吸附实验研究

研究了污泥含炭吸附剂对挥发性有机污染物的吸附特性。结果表明,污泥含炭吸附剂对苯系物的吸附为典型的物理吸附,其吸附甲苯等温线的类型系优惠型吸附等温线,表明具有良好的吸附能力;在吸附反应温度为20℃,气体流量为500 mL/m in(停留时间为0.424 s),甲苯浓度为2 700 mg/m3时,甲苯的饱和吸附容量为150.0 mg/g;同时,研究表明污泥含炭吸附剂对苯系物的饱和吸附容量和吸附强弱次序为二甲苯甲苯苯。结果表明污泥含炭吸附剂适合对中低浓度有机废气的吸附净化。     

乙酰丙酮分光光度法测定新装修住宅室内空气中的甲醛

对乙酰丙酮分光光度法测定室内空气中甲醛的方法进行了优化,同时对北京市11户部分新装修居室室内空气中的甲醛含量进行了测定.结果表明,有8户住宅超过了我国室内空气质量标准GB/T18883-2002规定的甲醛最高容许质量浓度0.10 mg/m3.     

乙酰丙酮分光光度法测定新装修住宅室内空气中的甲醛

对乙酰丙酮分光光度法测定室内空气中甲醛的方法进行了优化,同时对北京市11户部分新装修居室室内空气中的甲醛含量进行了测定.结果表明,有8户住宅超过了我国室内空气质量标准GB/T18883-2002规定的甲醛最高容许质量浓度0.10 mg/m3.     

垃圾焚烧飞灰添加对沥青铺路烟气苯系物释放的影响

为探究垃圾焚烧飞灰(以下简称飞灰)添加对沥青铺路烟气中苯系物的影响,实验室模拟研究了不同的温度区间(50～80、80～145、145～165、165～200、200℃恒温)及飞灰添加量(质量分数分别为0、3.0%、4.0%、5.0%)条件下,沥青烟气中苯系物的释放规律。结果表明:温度对苯系物的释放有显著的影响,苯系物释放浓度随着温度的增加而增加,在50～80、80～145、145～165、165～200℃及200℃恒温5个温度区间内苯系物的平均浓度较上一区间分别增加了1.02、2.22、0.50、1.08倍。实验中飞灰的添加对沥青烟气中苯系物的释放浓度无显著影响,但对各单体影响不同。当飞灰添加量为3.0%时,苯、乙苯、二甲苯(间二甲苯、对二甲苯、邻二甲苯)、三甲苯(1,3,5-三甲苯、1,2,4-三甲苯、1,2,3-三甲苯)释放浓度增加了16.78%、20.65%、37.69%、9.72%,随着飞灰添加量的继续增加其浓度增幅逐渐减少。     

光催化与生物技术联用工艺处理油漆废气中试研究

光催化与生物技术联用工艺用于油漆生产、加工过程有机废气的现场处理,中试实验结果表明:油漆生产、加工过程现场的主要污染物是甲苯、乙苯、间/对二甲苯和邻二甲苯等苯系物,浓度在27～55 mg/m3之间。单独使用光催化和微生物技术现场处理这些苯系物,其去除效率都不很高。虽然在中试开始阶段光催化对苯系物的平均去除效率达到了86.2%,在中试稳定期,光催化技术对苯系物的平均去除效率却只有67.6%,而生物滴滤床在成功挂膜之后对现场有机废气的平均去除效率也仅为67.5%。但是将这两种工艺联合使用之后,在中试稳定期该组合工艺对苯系物的平均去除效率可以达到99.2%。     

西安市冬夏季交通主干道环境空气中苯系物的污染特征

利用活性炭吸附/二硫化碳解吸—气相色谱法对西安市具有代表性的大庆路和长安路两处交通主干道进行环境空气监测,分析了冬季和夏季的苯、甲苯、乙苯、二甲苯(BTEX)等苯系物的浓度水平和日变化特征。结果表明,大庆路和长安路环境空气中总BTEX平均质量浓度冬季分别为55.27、46.01μg/m3,夏季分别为32.54、20.32μg/m3。两路段最主要的BTEX均为苯和甲苯。BTEX日变化趋势研究显示,冬季呈现早中晚3个高峰,而夏季只有早晚两个高峰;长安路由于地处西安市繁华的商业区,晚高峰出现的比大庆路晚。     

顶空气相色谱测试水中苯系混合物在不同材料上的吸附行为

设计了正交实验对5种材料吸附模拟废水中苯系混合物(苯、甲苯、二甲苯)的条件进行优化,CD02硅藻土与X型纳米分子筛以2∶1(质量比)进行复合后,对苯系混合物去除效果最好.采用顶空气相色谱法测定8种不同材料对水中苯系混合物的去除情况,结果表明复合材料对苯系混合物具有良好的去除效果,仅次于活性炭.复合材料在pH为7、搅拌时间为25 min、用量为1.8g/L时,对苯系混合物质量浓度为4.0 mg/L模拟废水的平均去除率为87.56％.经过4次再生后,复合材料的再生率仍高达84.90％,对苯系混合物的平均去除率为91.49％.     

室内空气中挥发性有机物的释放特征分析

房屋装修后1周、1个月、3个月、6个月、12个月采集其室内空气样品进行甲醛、苯系物浓度的测定,分析释放规律;另选某处新居于装修后24 h、1周、1个月且密闭状态下采集室内空气中总挥发性有机化合物(TVOC)样品分析研究.结果表明,房屋装修后12个月内甲醛浓度随时间呈非线性递减,多项式回归方程为:y=0.277 13-0.199 72x+0.079 74x2-0.011 67x3+0.000 525 61x4,其中y为甲醛质量浓度,mg/m3;x为时间,月;各苯系物浓度也随时间呈逐渐下降趋势,且通过SPSS13.0软件进行Spearman相关性分析,发现各苯系物间显著相关;装修后不同时间段室内空气中TVOC组分发生变化,随着房屋封闭时间延长,TVOC浓度超标严重;TVOC组分的增多或减少是由于室内装修材料TVOC释放的增强或减弱,以及门窗缝隙所带来的微弱通风造成,无二次污染物的生成.     

次氯酸钠发生器的研制

介绍了电解法生产次氯酸钠的原理 ,并在原有生产工艺的基础上进行了重新设计和对设备的重新选择、改造 ,得出了各个工艺参数的最佳值 ,生产出高品质的次氯酸钠     

Estimation of uncertainty of sampling for analysis of pesticide residues

Abstract

A computer model was used to take random samples from primary sample populations obtained from field trials to simulate the uncertainty of sampling for residue analysis of plant commodities and soil. The results indicate about 40%, 30% and 20% relative uncertainty when random samples of size 5, 10 and 25 are taken respectively, from a single lot. Therefore the sample size should be the same for establishing and enforcing legal limits.     

不同泥源对厌氧氨氧化反应器启动的影响

采用2套上流式生物膜反应器,分别接种少量厌氧氨氧化污泥和大量硝化污泥,考察其对厌氧氨氧化反应器启动的影响。污泥接种入反应器后,测得接种厌氧氨氧化污泥的反应器(R1)内MLSS为0.22 g/L,另一个反应器(R2)MLSS为2.7 g/L。与直接接种厌氧氨氧化污泥相比,R1经过72 d的运行才显现出厌氧氨氧化特性。经过114 d的培养,前者氮去除速率由0.23 kg/(m3.d)提升到5.29 kg/(m3.d),总氮去除率大于89%;R2的氮去除速率由0.01 kg/(m3.d)提升到1.1 kg/(m3.d),总氮去除率大于84.6%。说明普通污泥启动需要一个较长的筛选过程,直接接种少量的厌氧氨氧化污泥比接种普通的污泥能够更快启动厌氧氨氧化反应器。     

Evaluation of the presence of drugs of abuse in tap waters

A total of seventy samples of drinking water were tested for non-controlled and illicit drugs. Of these, 43 were from Spanish cities, 15 from seven other European countries, three from Japan and nine from seven different Latin American countries. The most frequently detected compounds were caffeine, nicotine, cotinine, cocaine and its metabolite benzoylecgonine, methadone and its metabolite EDDP. The mean concentrations of non-controlled drugs were: for caffeine 50 and 19 ng L⁻¹, in Spanish and worldwide drinking water respectively and for nicotine 13 and 19 ng L⁻¹. Illicit drugs were sparsely present and usually at ultratrace level (<1 ng L⁻¹). For example, cocaine has mean values of 0.4 (Spain) and 0.3 ng L⁻¹ (worldwide), whereas for benzoylecgonine, these mean values were 0.4 and 1.8 ng L⁻¹, respectively. Higher concentrations of benzoylecgonine were found in Latin American samples (up to 15 ng L⁻¹). No opiates were identified in any sample but the presence of methadone and EDDP was frequently detected. Total mean values for EDDP were 0.4 ng L⁻¹ (Spain) and 0.3 ng L⁻¹ (worldwide). Very few samples tested positive for amphetamines, in line with the reactivity of chlorine with these compounds. No cannabinoids, LSD, ketamine, fentanyl and PCP were detected.     

Mechanisms of biodegradation of dibenzoate plasticizers

Biodegradation mechanisms were elucidated for three dibenzoate plasticizers: diethylene glycol dibenzoate (D(EG)DB), dipropylene glycol dibenzoate (D(PG)DB), both of which are commercially available, and 1,6-hexanediol dibenzoate, a potential green plasticizer. Degradation studies were done using Rhodococcus rhodochrous in the presence of pure alkanes as a co-substrate. As expected, the first degradation step for all of these systems was the hydrolysis of one ester bond with the release of benzoic acid and a monoester. Subsequent biodegradation of the monobenzoates of diethylene glycol (D(EG)MB) and dipropylene glycol (D(PG)MB) was very slow, leading to significant accumulation of these monoesters. In contrast, 1,6-hexanediol monobenzoate was quickly degraded and characterization of the metabolites indicated that the biodegradation proceeded by way of the oxidation of the alcohol group to generate 6-(benzoyloxy) hexanoic acid followed by β-oxidation steps. This pathway was blocked for D(EG)MB and D(PG)MB by the presence of an ether function.The use of a pure hydrocarbon as a co-substrate resulted in the formation of another class of metabolites; namely the esters of the alcohols formed by the oxidation of the alkanes and the benzoic acid released by hydrolysis of the original diesters. These metabolites were biodegraded without the accumulation of any intermediates.     

混凝试验搅拌器的研制

影响混凝效果的因素众多,混凝沉淀烧杯试验是进行水的混合、絮凝、沉淀工艺研究、设计和生产指导的最有效方法之一,阐述了智能型混凝试验搅拌器的设计原理和技术性能.     

生物质快速热裂解主要参数对生物油产率的影响

以松木木屑为原料,在自制的小型流化床上,开展了生物质热裂解温度、生物质粒径和进料速率对生物油产率的影响实验研究.结果表明,在热裂解温度分别为450、475、500、525和550℃条件下,当热裂解温度为500℃时,生物油产率最高,平均产率达到53.33%（质量百分比）.反应温度越高,炭产量越低,不可冷凝气体产量越高,气体发热值越高;粒径＜1 mm的生物质其粒径对生物油产率影响不大;生物质进料速率增加时,生物油产率增加.本研究为生物能的利用提供了新的途径.     

An application of the theory of kinematics of mixing to the study of tropospheric dispersion

The most common technique used for numerical simulations of tracer mixing is that of the numerical solution of the advection–diffusion equation with the unresolved fluxes parameterized using the similarity theory. Despite correct predictions of the overall directions of transport, models based on a numerical solution of the advection–diffusion equation lack sufficient accuracy to correctly reproduce the coupling of mixing with small scale processes which are sensitive to the microstructure of the tracer distribution. The objective of this paper is to revisit the basic formalism employed in numerical models used to investigate atmospheric tracers. The main mathematical method proposed here is the theory of kinematics of mixing which could be applied effectively for simulations of atmospheric transport processes. At the beginning of the paper, we introduce simple mathematical transformations in order to demonstrate how complex topological structures are created by mixing processes. These idealistic flow systems are essential to explain transport properties of much more complex three-dimensional geophysical flows. An example of the application of the kinematics of mixing to the analysis of tracer transport on a planetary scale is presented in the following sections. The complex filamentary structures simulated in the numerical experiment are evaluated using some commonly applied statistical measures in order to compare the results with the data published in the literature. The results of the experiment are also analysed with the help of simple conceptual models of fluid filaments. The microstructure of the tracer distribution introduced in the paper is essential to increase our understanding of atmospheric transport and to develop more realistic parameterizations of small-scale mixing. The presented results could also be used to improve calculations of the coupling between microphysical processes and tracer mixing.     

造纸废水混凝处理中SFT助凝替代性研究

中小造纸厂废水处理常用PAC作混凝剂 ,PAM作助凝剂。由于PAM成本很高 ,影响了处理设备的投运率。用超细滑石粉 (SFT)替代PAM助凝 ,与混凝剂PAC配合 ,其混凝处理效果基本相当 ,但是处理成本降低 0 .10元 /m3 。由于SFT属环境无害材料 ,不会给排泥带来二次污染     

产油微藻培养与回收的关键技术研究进展

寻找廉价而高效的替代原料是实现生物柴油产业化的关键所在.微藻以含油量高、生长周期短、环境适应能力强、生物产量高等优点,有望成为一种极具潜力的生物柴油生产原料.然而,目前尚存在微藻培养低效成本高和微藻回收效率低两大难题.综述了微藻培养与回收过程中的关键技术,并对存在的两大难题及其改进技术进行了详细的探讨.最后,总结并展望了微藻培养、回收技术未来的发展趋势.