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)。     

恶臭假单胞菌降解苯酚的动力学研究

研究了恶臭假单胞菌（Pseudomonas putida LY1）利用苯酚作为唯一碳源和能源时的生长动力学特性。通过对该菌株在不同温度、pH和初始苯酚浓度下的生长和降解情况的研究,可知该菌株在温度为25℃左右、pH为中性和偏碱性的条件下具有更高的降解活性。细菌的生长动力学过程符合基质抑制型的Haldane方程,可利用该...     

Enhanced biodegradation of endosulfan and its major metabolite endosulfate by a biosurfactant producing bacterium

The present study was carried out to isolate bacteria capable of producing biosurfactant that solublize endosulfan (6,7,8,9,10,10-Hexachloro-1,5,5a,6,9,9a-hexahydro- 6,9-methano-2,4,3-benzodioxathiepine-3-oxide) and for enhanced degradation of endosulfan and its major metabolite endosulfate. The significance of the study is to enhance the bioavailability of soil-bound endosulfan residues as its degradation is limited due to its low solubility. A mixed bacterial culture capable of degrading endosulfan was enriched from pesticide-contaminated soil and was able to degrade about 80% of α-endosulfan and 75% of β-endosulfan in five days. Bacterial isolates were screened for biosurfactant production and endosulfan degradation. Among the isolates screened, four strains produced biosurfactant on endosulfan. ES-47 showed better emulsification of endosulfan and degraded 99% of endosulfan and 94% of endosulfate formed during endosulfan degradation. The strain reduced the surface tension up to 37 dynes/cm. The study reveals that the strain was capable of degrading endosulfan and endosulfate with simultaneous biosurfactant production.     

Pseudomonas sp. ZXY-1, a newly isolated and highly efficient atrazine-degrading bacterium, and optimization of biodegradation using response surface methodology

Atrazine, a widely used herbicide, is increasing the agricultural production effectively, while also causing great environmental concern. Efficient atrazine-degrading bacterium is necessary to removal atrazine rapidly to keep a safe environment. In the present study, a new atrazine-degrading strain ZXY-1, identified as Pseudomonas, was isolated. This new isolated strain has a strong ability to biodegrade atrazine with a high efficiency of 9.09 mg/L/hr.Temperature, p H, inoculum size and initial atrazine concentration were examined to further optimize the degradation of atrazine, and the synthetic effect of these factors were investigated by the response surface methodology. With a high quadratic polynomial mathematical model(R~2= 0.9821) being obtained, the highest biodegradation efficiency of 19.03 mg/L/hr was reached compared to previous reports under the optimal conditions(30.71°C, pH 7.14, 4.23%(V/V) inoculum size and 157.1 mg/L initial atrazine concentration).Overall, this study provided an efficient bacterium and approach that could be potentially useful for the bioremediation of wastewater containing atrazine.     

EDTA增强Cr(VI)共存时Burkholderia cepacia降解孔雀绿的效率

重金属共存严重抑制了微生物降解染料的效率,本研究拟采用EDTA螯合Cr提高Burkholderia cepacia C09G降解复合污染中孔雀绿的效率.实验结果表明,0.1 mmol·L~(-1)孔雀绿单独存在条件下,24 h的生物降解率达到96.2%;然而,在0.5 mmol·L~(-1)Cr(VI)共存条件下,60 h的降解率仅为6.7%.当加入0.5 mmol·L~(-1)EDTA螯合剂后,60 h时孔雀绿的降解率提高到18.8%.当EDTA浓度为0.5 mmol·L~(-1)时,最佳螯合Cr(VI)的浓度为0.7 mmol·L~(-1),此时,60 h后孔雀绿的降解率达到35.3%,对Cr(VI)的吸附率为24.6%.此外,通过EDS、SEM、XPS分析证明,EDTA可以减小Cr(VI)的毒性,Burkholderia cepacia C09G可将吸附的Cr(VI)还原为Cr(III).