An assessment of how distance and diesel oxidation catalyst will impact thermal decomposition behaviors of particles

Decomposition mass loss and pyrolysis products analyses of particles sampled at various locations along the tailpipe of a Euro-IV diesel engine were performed using a thermogravimetry in conjunction with Fourier transformation infrared spectrometry-mass spectrum. Diesel particles were collected at the same location with and without diesel oxidation catalyst (DOC) mounted on the test engine separately. The three poles in thermal gravity-differential thermal gravity images suggested that the decomposition process of diesel particles could be divided into three stages which correspond to the decompositions of lower boiling substances, higher boiling substances and soot respectively. It is noticed that no matter whether DOC was mounted or not, the further the particles were sampled away from the engine block, the lower the peak temperatures and the heavier the mass losses within the first two stages, which indicated that the soluble organic fraction in the particle samples increased and therefore lowering the activation energy of thermal decomposition. Hydroxyl, ammonia, C_xH_y fragments, benzene, toluene, and phenol were found to be the primary products of particle decomposition, which didn't change with the location of particle sample point. The employment of DOC increased the activation energy for particle oxidation and resulted in a higher peak temperature and lower mass loss within the first-stage. Moreover, the CO stretching bands of aldehyde and ketone at 1771 cm^?1 was only detected without a DOC, while the NO₂ peak at 1634 cm^?1 was solely noticed with the presence of DOC. Compared to the first-stage pyrolysis products, more polycyclic aromatic hydrocarbons and less C_xH_y fragments were seen in the second-stage.     

Treatment of 2-phenylamino-3-methyl-6-di-n-butylaminofluoran production effluent by combination of biological treatments and Fenton＇s oxidation

High strength refractory organic stream is produced during the production of 2-phenylamino-3-methyl-6-di-n-butylaminofluoran （One Dye Black 2, abbr. ODB 2）, a novel heat-sensitive material with a promising market. In this study, a combination of acidificationprecipitation, primary biological treatment, Fenton＇s oxidation and another biological treatment was successfully used for the removal of COD from 18000-25000 mg/L to below 200 mg/L from the ODB 2 production wastewater in a pilot experiment. A COD removal of 70%-80% was achieved by acidification-precipitation under a pH of 2.5-3.0. The first step biodegradafion permitted an average COD removal of 70% under an hydraulic residence time （HRT） of 30 h. By batch tests, the optimum conditions of Fenton＇s oxidation were acquired as： Fe^2＋ dose 6.0 mmol/L; H2O2 dose 3000 mg/L; and reaction time 6 h. The second step biological treatment could ensure an effluent COD below 200 mg/L under an HRT of 10 h following the Fenton＇s treatment.     

废弃电子产品的处理与回收技术

现代电子产品更新换代速度很快，废旧电脑、电池、家电等电子垃圾的数量急剧增加，由于对环境会造成严重污染，电子垃圾作为一种特殊垃圾急待处理与回收。对几种废弃电子产品的处理与回收技术进行了综合论述，并结合我国实际，提出一些建议。     

水体中的微生物对壬基酚聚氧乙烯醚的生物降解

为有效控制水体中壬基酚聚氧乙烯醚的污染 ,以芽孢杆菌、假单胞菌、诺卡氏菌和假丝酵母为试验菌株 ,研究了其对壬基酚聚氧乙烯醚的生物降解特性。试验结果表明 ,4菌株在一定的条件下对水体中的壬基酚聚氧乙烯醚均有一定的降解率。若按体积比 1∶ 2∶ 1∶ 1的比例将四菌株组合成复合菌群 ,可大幅度提高处理效率 ,降解率可达 61 %。应用该复合菌对影响壬基酚聚氧乙烯醚降解的各种主要因素进行了研究 ,发现降解菌在θ为 2 5～ 30℃ ,p H值为 5.5～ 8.5及壬基酚聚氧乙烯醚初始质量浓度ρ(NP1 0 EO)为 0～ 1 0 0 mg/ L范围内保持高活性 ;当底物质量浓度大于 1 0 0 mg/ L 时 ,平均降解速率线性下降 ;当接种量标准为 1× 1 0 8CFU/ m L (即菌悬液 /反应液为1 0 % )时壬基酚聚氧乙烯醚的降解是高效与经济的     

Evidence for biodegradation and volatilisation of dissolved petroleum hydrocarbons during in situ air sparging in large laboratory columns

Laboratory column experiments run for up to 13 days compared air sparging of groundwater contaminated by dissolved petroleum hydrocarbons in sterile and non-sterile aquifer sediments as well as uncontaminated sediments and groundwater. Loss of dissolved BTEX compounds in the contaminated columns was very rapid, occurring through volatilisation. The majority of the dissolved total organic carbon (TOC) persisted for much longer periods however. A direct comparison between losses from sterile and non-sterile columns suggested a negligible contribution of biodegradation to the removal of TOC. This was difficult to confirm through examination of O₂ utilisation because oxidation of a small amount of reduced sulphur in the aquifer materials was the dominant sink for O₂. Despite this, it was possible to conclude that less than 22% of the removal of TOC was through biodegradation during the first three days of air sparging.     

The influence of degree of substitution on blend miscibility and biodegradation of cellulose acetate blends

In this account, we report our findings on blends of cellulose acetate having a degree of substitution (DS) of 2.49 (CA2.5) with a cellulose acetate having a DS of 2.06 (CA2.0). This blend system was examined over the composition range of 0–100% CA2.0 employing both solvent casting of films (no plasticizer) and thermal processing (melt-compressed films and injection molding) using poly(ethylene glycol) as a common plasticizer. All thermally processed blends were optically clear and showed no loss in optical quality after storage for several months. Thermal analysis and measurement of physical properties indicate that blends in the middle composition range are partially miscible, while those at the ends of the composition range are miscible. We suggest that the miscibility of these cellulose acetate blends is influenced primarily by the monomer composition of the copolymers. Bench-scale simulated municipal composting confirmed the biodestructability of these blends and indicated that incorporation of a plasticizer accelerated the composting rates of the blends.In vitro aerobic biodegradation testing involving radiochemical labeling conclusively demonstrated that both the lower DS CA2.0 and the plasticizer significantly enhanced the biodegradation of the more highly substituted CA2.5.While this work was in progress, Robert Gardner was struck with cancer and died on June 6, 1995. This paper is dedicated to his memory and to his contributions as a friend and colleague.     

钻井液化学剂可生物降解性评定方法

介绍研究钻井液化学剂生物降解性的必要性及开发可生物降解钻井液的进展。阐述了常用的评定有机物生物降解性的试验方法。推荐采用BOD_5／COD_Cr比值来评定我国石油行业钻井液化学剂及油田化学剂的可生物降解性，规范石油行业生物降解研究工作，保证评定结果的可靠性和可比性。     

钻井液化学剂可生物降解性研究

实验测定了16种钻井液化学剂的BOD_5和COD_cr，并计算其BOD_5／COD_cr比值。提出了以BOD_5／COD_cr的比值划分钻井液化学剂可生物降解性的分级标准，并对16种钻井液化学剂的可生物降解性进行分级，为其应用提供依据。     

Starch- polyvinyl alcohol crosslinked film— performance and biodegradation

Starch-PVOH cast films were prepared with and without crosslinking agent (hexamethoxymethylmelamine) in the absence of plasticizer. Moisture absorption in films without crosslinking agent at a low relative humidity was similar to that of PVOH and increased as the relative humidity increased. Films with crosslinking agent showed moisture absorption linearly proportional to the relative humidity. Significant improvement in resistance to water disintegration for crosslinked starch-PVOH films was observed. While the tensile strength decreased with increased relative humidity, crosslinking significantly improved the tensile strength. Increased PVOH content improved elongation of films even when the relative humidity was 80% or higher. Biodegradation studies revealed that the degradation rate was negatively correlated with the PVOH content in films and crosslinking generated more converged degradation curves. Names are necessary to report factually on available data; however, the USDA neither guarantees nor warrants the standard of the product, and the use of the name by USDA implies no approval of the product to the exclusion of others that may also be suitable.     

高活性萘降解细菌Hydrogenophaga Palleronii LHJ38的研究

为了研究微生物对多环芳烃的降解和转化规律,以萘作为研究对象,从餐厨油烟污染土壤中筛选到一株萘降解活性较高的细菌菌株,经菌种鉴定,定名为帕氏氢噬胞菌(H ydrogenophaga Palleronii)LH J38。测定了该菌的生长曲线和萘降解曲线,建立了菌株对萘的降解活性的定量测定方法,并研究了其最适生长条件。结果表明,在28℃、初始pH6.6、碳氮摩尔比为4的最适培养条件下,LH J38对初始质量浓度为2 000m g/L的萘在96h内的降解率可达98%以上;处于对数生长期的LH J38对萘的降解活性可达47.3nm o l/(m g.m in)。