汽油车技术发展对尾气排放影响研究进展

近年来,汽油车尾气排放已成为城市大气污染的主要来源之一.为减少油耗、温室气体和大气污染物的排放,汽油直喷技术(GDI)、醇类燃料替代以及混合动力系统等新兴技术被应用到汽车产品中,该研究对GDI发动机汽车、醇类燃料车和混合动力车的颗粒物(PM)、氮氧化物(NO_x)、总碳氢化合物(THC)的排放研究进行梳理和总结,综合评估先进动力技术和醇类燃料的环境影响.结果表明:GDI汽油车的PM排放因子为进气道喷射(PFI)汽油车的1.2~5倍,加装汽油颗粒物捕集器(GPF)后GDI汽油车的PM排放大幅下降,同时具备催化能力的GPF可减少NO_x和THC排放.与汽油车相比,乙醇燃料车PM排放量减少了35%~56%,尾气THC排放减少了10%~44%,但挥发性有机物(VOCs)蒸发排放增加了20%~41%,其主要来自于日呼吸损失.各类型车辆的NO_x排放差异较小,比较结果存在一定的不确定性.混合动力车相比传统内燃机汽车污染物减排优势明显,可积极推广其在公共交通和私家车队中的应用.建议今后研究应着重关注以下几个方面:①GDI和混合动力车在实际条件下排放污染物的环境影响;②醇类燃料车VOCs蒸发排放控制技术及相关法规标准的完善;③新兴技术汽油车排放污染物的生成机理及其影响因素.      

汽油车非常规污染物排放特性研究

选择3种不同排量的典型汽油车,基于国Ⅲ标准的轻型车排放测试循环,用SKC采样泵和2, 4-DNPH、Tenax TA采样管采集尾气中的非常规污染物,利用高效液相色谱仪和热脱附气相色谱质谱联用仪分析汽油车排放中醛酮类化合物和挥发性有机物的组成及含量,同时利用电子低压冲击仪研究了其颗粒物排放的粒径和质量浓度分布特征.结果表明,不同汽油车之间非常规污染物的比排放值有较大差异,3辆汽油车总醛酮比排放量分别为36.44、 16.71、 10.43 mg/km,TVOC分别为155.39、 103.75、 42.29 mg/km.排放的醛酮化合物中甲醛、乙醛、丙烯醛、丙酮和环己酮的检出含量较高,占总醛酮量的77.9%～89.7%,且绝大部分为有毒有害物质;废气中挥发性有机物绝大部分为芳香烃和烷烃,分别占总数的31.6%～39.2%和23.1%～27.9%,其中又以芳香烃类化合物甲苯、二甲苯和苯的检出含量最高,平均占TVOC的16.68%、 16.87%和5.23%;其颗粒物排放以超细颗粒物（<100nm）为主,高速工况下排放的颗粒物明显多于低速和中速工况.     

汽油在西北黄土上吸附特性的研究

通过动力学和热力学吸附实验,研究了汽油在西北地区黄土上的吸附行为,同时研究了提取的天然腐植酸对汽油在黄土上吸附行为的影响.结果表明,汽油在黄土上的吸附在6 h内达到平衡.无论是否加入腐植酸,汽油在黄土上的吸附动力学过程均符合Elovich方程,其热力学吸附符合Freundlich方程.腐植酸的存在使汽油在黄土上的吸附能力减小.反应温度从25℃升高到45℃,汽油在土壤上的饱和吸附量从6.300 mg·g-1减小到1.365 mg·g-1,表明汽油在黄土上的吸附属于放热反应.溶液pH和土壤粒径的增大,均不利于汽油在黄土上的吸附,溶液pH和土壤粒径越大,其在黄土上的吸附量越小.另外,在室温下对吸附了汽油的土壤样品和纯汽油挥发行为的研究表明,吸附了汽油的土壤样品的汽油挥发比纯汽油慢,其挥发率与时间成对数关系.     

乙醇对含水层中燃油芳香烃内在生物修复的潜在风险

内在生物修复,是在没有工程措施促进的情况下利用土著微生物降解含水层内灾害性物质的一种修复技术,在燃油烃污染管理方面具有显著的成本效益。该技术需要确定自然衰减过程,并能够继续提供有效的风险保护。针对燃油污染含水层,北美与欧洲认为内在生物修复是值得优先考虑的应用技术。然而,随着乙醇燃油的推广使用,我国在应用这样的经验时需要考虑乙醇的潜在影响。现有的文献研究表明乙醇存在能够阻止燃油主要污染物芳香烃(BTEX)的生物降解,降低水环境的pH值,并可能增强BTEX在水中的溶解性,或存在对生物的毒性,或因为乙醇降解降低介质的渗透性能。因此,需要更好地认识乙醇的潜在风险,为发展乙醇燃油污染含水层修复策略提供科学依据。     

废塑料处理技术进展与展望

文章介绍了解决废塑料污染的几种方法,分析了目前我国废塑料回收利用技术的现状,并介绍作者在这方面进行的一些新的研究工作：（1）使用自制的催化剂完成了聚烯烃类塑料催化热解回收燃料油的小试,获得了较好的效果;（2）通过实验对发泡聚苯乙烯热解回收苯乙烯单体的工艺流程提出了优化操作条件。根据国内外实际,文章最后对废塑料回收利用提出了几点建议。     

Comprehensive Environmental Investigation at Former Industrial/Petroleum Underground Storage Tank Sites in Long Beach,CA: A Forensic Perspective

Two industrial sites were investigated based on years of available hydrogeologic information and monitoring data for soil and groundwater. Collected data were forensically evaluated using age-dating and fingerprinting methods. The previous business uses of the project sites were as a gas station, laundry/dry-cleaning service, and car wash with petroleum underground storage tanks (USTs). As a result, these sites were exposed to a number of toxic contaminants at relatively high concentrations. Source control was necessary for successful remediation and the ultimate removal of the remaining compounds from these industrial sites. Although contaminated soil around the source was excavated during the remedial action and the high concentrations of contaminants were reduced, typical groundwater contaminants such as petroleum hydrocarbons as gasoline (TPH-G), benzene, toluene, ethylbenzene, xylenes (BTEX), and oxygenates including methyl tert-butyl ether (MTBE), diisopropyl ether (DIPE), ethyl tert-butyl ether (ETBE), tert-amyl methyl ether (TAME), and tert-butyl alcohol (TBA) were persistently found at the studied sites around the source points. The plume and concentration of contaminants had changed their shapes and strength for all monitoring periods. Thus, additional source control seems to be a requirement for the complete removal of source contamination, which must be ascertained with groundwater and soil monitoring on a regular time base. For the study sites, monitored natural attenuation was relatively feasible for the long-term plan; however, it did not offer a perfect remediation solution for an ultimate goal because of residual toxic compounds that might have affected the surrounding residential areas at higher concentrations than their health limits. Therefore, as a remediation strategy, the combination of clean-up technology and natural attenuation with monitoring activities are more highly recommended than either clean-up or natural attenuation used separately.     

聚烯烃类废塑料热分解技术中催化剂的选择和机理初探

研究使用不同催化剂情况下聚烯烃类废塑料热分解回收燃油的技术,并对废塑料的热分解机理进行了探讨．结果表明,自制的含大孔径分子筛的ＮＬＧ系列催化剂具有较好的催化性能,在裂解温度４３０℃,催化温度为３６０℃情况下,热分解后油产率为８７．５％,油品中汽油馏分达４１．３％,辛烷值为８８．３,每ｔ生产成本仅１２０００元左右,循环使用２０５余次后,仍保持良好的催化性能．     

Twenty-five years of biomonitoring lead in the Frankfurt/Main area

The present study is an example of the historical monitoring of heavy metals. The specific question it aims to explore is: to what extent has the lead content of selected organisms used for biomonitoring in Frankfurt/Main—one of the cities in Germany most heavily affected by automobile traffic—changed as a result of legislation on leaded gasoline?

Data on the lead content of the moss speciesBryum argenteum Hedw. from the years 1974, 1975 and 1978 and data on the lead content of the outer bark of the ash speciesFraxinus excelsior L. from 1973 served as the basis for the repeated measurements. Remeasurement was successful in 76.5% (i.e. 124 trees at 26 growth sites). The study produced the following results:

• ? As was expected, the lead content of the short-term accumulatorBryum argenteum Hedw. was distinctly lowered with a decreasing particulate lead concentration. However, the reduction factor varied greatly between the different growth sites.
• ? On the other hand, the lead content measured in the outer bark layers ofFraxinus excelsior L. has risen markedly during the past two decades. Whereas in 1973 nearly all trees examined displayed very low concentrations of lead (< 38 ppm), only 9.5% were still in this category in 1997 and nearly 30% exhibited high or even unacceptable lead concentrations (< 150 ppm → > 225 ppm). Various factors have to be taken into account to explain this increase. First of all, bark is a long-term accumulator for heavy metals like lead and its enrichment capacity could have increased as the surface becomes rougher over time. Furthermore, lead is most probably leached out of the bark to a lesser degree now than in the 1970s, owing to the reduced concentration of sulphuric acid in the rain. The dramatic growth of automobile traffic in the Frankfurt/Main area during the period covered by the study undoubtedly plays an important role as well.

     

汽油机排气颗粒粒径分布特征试验研究

对汽油机排气中颗粒的数浓度和粒径分布特征进行了测试．在测试工况下,汽油机排气中的颗粒呈包含核模态粒子(10 nmp-3．汽油机在开环控制状态下(车速不低于 90km·h-1 时)的颗粒数量排放明显高于闭环控制状态 (车速不高于70km·h-1),总颗粒质量浓度随车速的增大显著增加．随车速增大,积聚模态粒子的平均粒径先减小后增大,核模态粒子的几何平均粒径先增大后减小,低车速时,有大量 10—20 nm的核模态粒子生成．柴油机和汽油机排气颗粒中核模态粒子通常占有大的数量百分比,为 75%—5%,而其质量百分比仅为 5%—25%．汽油机的总颗粒、核模态粒子和积聚模态粒子的数量和质量排放均远低于柴油机．     

掺甲醇汽油对国III汽油机排放性能影响

在一台整车试验满足国III排放法规要求的多点电喷汽油机上,采用甲醇掺入汽油的混合燃料(甲醇的体积分数分别为0%、15%和50%)进行台架试验,使用傅里叶变换红外光谱分析仪(FTIR)在线检测了常规车用三效催化转化器前后的常规和非常规排放.研究结果表明:怠速工况下,掺醇燃料对NOx排放基本没有影响,但CO和HC随掺醇比增加而普遍降低,非常规排放中乙醛排放有所降低,甲醇和甲醛则随掺醇比的增加有较大幅度升高,热怠速时经催化后掺醇燃料对各种排放均无影响,可被控制在极低的水平;其它工况下,随掺醇比增加,CO和HC减少,NOx在高掺醇比下低速低负荷和高速高负荷时有较为明显的改善,非常规排放甲醛和甲醇排放随掺醇比增大而急剧增加,乙醛排放则随之减少.经三效催化转化器作用,无论常规排放NOx、CO和HC,还是非常规排放甲醛、甲醇和乙醛基本上能够实现零排放.