Transpiration in Black Willow Phytoremediation Plots as Determined by the Tree‐Trunk Heat Balance Method

Plant transpiration is a critical process that affects the water balance in phytoremediation plots. The desired effect is to remove contaminated water from the soils through the plant metabolism. Thus, the transpiration rate can be a major component in modeling the groundwater flow and solute transport for a phytoremediation project and ultimately can determine the time expected to achieve remedial goals. Two phytoremediation plots of black willows (Salix nigra) were planted during October 1996 over separate,shallow groundwater plumes at a site in southeastern Louisiana. Concentrations of less than 10 mg/l of the herbicide bentazon were present in the shallow groundwater. Field experiments were developed and performed during the 1998 and 1999 growing seasons to measure sap flow as an indicator of plant transpiration. The tree‐trunk heat balance method was used to measure sap flow. Sap flow was indexed to the cross‐sectional area of the stem, and the sum of the available stem area for each plot was used to calculate the monthly water use in each plot. Daily water use in the plots averaged between 6 to 13 l/day/m² during the periods tested in 1998 and 1999. By applying growth‐rate observations with the daily water use, annual water use at tree plot maturity was estimated to be 3.6×10⁶ l/year in Plot 1 and 11.39×10⁶ l/year in Plot 2. Application of these data will allow groundwater modeling to be performed to measure the effectiveness of phytoremediation and to predict closure of remediation at the test site. © 2001 John Wiley & Sons, Inc.     

Before‐after control‐impact paired modeling of groundwater bentazon treatment at a phytoremediation site

A Before‐ After Control‐ Impact Paired (BACIP) model was used to evaluate the effectiveness of phytoremediation treatment on reduction of bentazon concentrations in shallow groundwater at a study site in Louisiana. Two different statistical approaches were made to evaluate the impact to this test site from the remediation program through time. Data were evaluated by Bayesian analysis of variance test methods. Data sets were unique in that the control data used for impact evaluation, as compared to before and after data, were compiled from groundwater upgradient monitoring wells existing prior to remediation. The statistical model supports the hypothesis that the phytoremediation program has positively impacted groundwater at the study site. © 2006 Wiley Periodicals, Inc.     

苯达松生产高浓度含磷废水的镁盐-钙盐协同沉淀处理及资源化研究

采用鸟粪石结晶协同钙盐沉淀法从苯达松生产高浓度含磷废水中回收磷酸盐沉淀物,探讨了磷回收效果的影响因素,并对所得磷酸盐沉淀物进行了定量分析和盆栽对照实验。实验结果表明：在pH为9~10、n（Mg²⁺）∶n（NH₄⁺）∶n（PO₄^3-）为1.2∶1∶1的最佳条件下加入氯化镁和氯化铵,磷回收率（以磷计）可达95.7%;再按照n（Ca²⁺）∶n（Mg²⁺）为0.10加入氯化钙,磷总回收率达到99.1%,上清液中磷质量浓度降至8.7 mg/L;每盆施用3 g磷酸盐沉淀物,对开豆41^#具有显著的增效作用,对杂草猪殃殃也有较好的除草效果。     

Natural and Artificial Functionalized Biopolyesters. II. Medium-Chain Length Polyhydroxyoctanoates from Pseudomonas Strains

Sixteen Pseudomonas strains have been tested with a view to developing medium-chain length polyhydroxyalkanoates. Four strains were selected and it is shown that their ability for producing three different polyesters with variable properties was dependent on the strains and substrates. Otherwise, Pseudomonas oleovorans was grown on a mixture of sodium octanoate and undecenoate salts at a 90/10 mol/mol ratio. The corresponding copolymer, bearing lateral double bonds, was chemically modified in the carboxy group. Finally, the ability to tailor-make functional bacterial polyesters aimed at temporary therapeutic applications is demonstrated.     

酸析—微电解—Fenton试剂氧化联合工艺预处理苯达松废水

采用酸析—微电解—Fenton试剂氧化联合工艺预处理苯达松废水。考察了酸析pH、铸铁粉加入量、微电解时间、双氧水加入量、Fenton试剂氧化时间等因素对废水处理效果的影响。实验结果表明：最佳工艺条件为酸析pH 3.0,铸铁粉加入量1.0 g/L,微电解时间2 h,Fenton试剂氧化时间4 h,双氧水加入量25 mL/L;在最佳工艺条件下处理初始COD为22 500 mg/L、BOD₅/COD为0.08、色度为2 500倍的苯达松废水,总COD去除率为96.2%,出水COD为858 mg/L,出水色度为150倍,BOD₅/COD为0.38;采用微电解—Fenton试剂氧化联合工艺预处理酸析后的苯达松废水,处理效果远高于单独微电解和单独Fenton试剂氧化工艺。     

Comprehensive temperature monitoring in an in-vessel forced-aeration static-bed composting process

Comprehensive temperature monitoring was done in an in-vessel forced-aeration static-bed composting process using sewage sludge. The three layers that divided the compost pile horizontally showed different temperature distributions. The temperature of the top layer appeared not to be influenced by the ambient temperature. The temperature of the center area of the top layer was taken to be the representative temperature for evaluating composting start-up performance. The temperature of the bottom layer was strongly influenced by the ambient temperature, and the temperature of the center area of the bottom layer was taken to be the representative temperature for pathogen control as it was the minimum temperature in the reactor. Composting start-up performance was influenced by several factors when the ambient temperature was either below or above 20°C. When the ambient temperature was below 20°C, the time taken to reach 65°C (T ₆₅) was influenced by the temperature of inflowing air, but when the temperature was higher than 20°C, it was influenced by the ratio of sewage sludge to seed compost (F/S). T ₆₅ was least when F/S was 1–2. Received: January 9, 2001 / Accepted: October 10, 2001     

Biochemical and Genetic Characterization of an Extracellular Poly(3-Hydroxybutyrate) Depolymerase from Acidovorax Sp. Strain TP4

To determine the properties of enzymes from bacteria that degrade polypropiolactone (PPL), we isolated 13 PPL-degrading bacteria from pond water, river water, and soil. Nine of these strains were identified as Acidovorax sp., three as Variovorax paradoxus, and one as Sphingomonas paucimobilis. All the isolates also degraded poly(3-hydroxybutyrate) (PHB). A PPL-degrading enzyme was purified to electrophoretical homogeneity from one of these bacteria, designated Acidovorax sp. TP4. The purified enzyme also degraded PHB. The molecular weight of the enzyme was estimated as about 50,000. The enzyme activity was inhibited by diisopropylfluorophosphate, dithiothreitol, and Triton X-100. The structural gene of the depolymerase was cloned in Escherichia coli. The nucleotide sequence of the cloned DNA fragment contained an open reading frame (1476 bp) specifying a protein with a deduced molecular weight of 50,961 (491 amino acids). The deduced overall sequence was very similar to that of a PHB depolymerase of Comamonas acidovorans YM1609. From these results it was concluded that the isolated PPL-degrading enzyme belongs to the class of PHB depolymerases. A conserved amino acid sequence, Gly-X₁-Ser-X₂-Gly (lipase box), was found at the N-terminal side of the amino acid sequence. Site-directed mutagenesis of the TP4 enzyme confirmed that ²⁰Ser in the lipase box was essential for the enzyme activity. This is the first report of the isolation a PHB depolymerase from Acidovorax.     

Arsenic,manganese, and cyanide removal in a tailing storage facility for a gold mine using phytoremediation

In this study, six selected plants (Acacia mangium, A. auriculiformis, Leucaena leucocepphala, bamboo, Pennisetum purpureum, and Vetiveria zizanioides) were cultivated in a mine tailing storage facility in a gold mine area. P. purpureum, a monocot species, provided the highest phytoremediation efficiency. Therefore, it is a potentially appropriate plant for site remediation. It is interesting that P. purpureum is perennial, meaning it can be easily planted and requires less effort and input for care with the ability to flourish year round. Thus, this study recommends using P. purpureum for phytoremediation of heavy metals and cyanide in gold mine areas.     

Supervisory control of a selective catalytic reactor for NOx removal in incineration plants

The purpose of this work is to present an industrial application of an optimization tool for the supervisory control of the NO_x reduction section. This work does not pretend to address any new technique of NO_x reduction but rather to show the results obtained when a comprehensive on-line optimization tool has been successfully applied. The optimization procedure consists of the search of the best working conditions that satisfy the operating and legal constraints, in terms of emission amounts and combustion quality. This procedure adopts a simulation algorithm and data reconciliation tool to verify and improve the consistency of the calculated values by experimental data. Using such algorithm it is possible to identify all the updated data necessary to optimize the plant's performance. Specifically, the DeNO_x section optimization, both from an economical and environmental point of view, is strongly related to the estimation of the nitrogen waste mass fraction together with the catalytic reactor efficiency. The results obtained in many case studies show that it is possible to achieve the desired performance and to reduce the operating costs by defining the optimal operating temperature and the corresponding amount of ammonia required for the catalytic reduction of NO_x subject to the emission limits. These tools were successfully tested on a municipal waste incineration plant.     

Novel synthesis blends between bacterial polyesters and acrylic rubber: A study on enzymatic biodegradation

The biodegradability of a multicomponent system based on biotechnological occurring polyester (poly(-hydroxybutyrate-co--hydroxyvalerate) (PHBV)) with inclusion of acrylate elastomer (polybutylacrylate) (PBA) was investigated. A bacterium which produced extracellular enzymes that degrades PHBV even when blended with PBA was isolated and tentatively designated asAureobacterium saperdae. It was observed, by morphological investigation, that, while the bacterial degradation was permitted for PBA content of 20% by weight, it was inhibited for PBA content of 30%, owing to the occurrence of a rubbery layer that prevents to the bacteria an easy accessibility in the PHBV-rich regions. In fact, owing the bacterial growth, only PHBV was metabolized, whereas no degradation of PBA was detected for blend samples. It was confirmed that the degradation proceeded via surface erosion of PHBV also in the blends. Finally, mechanical tests on PHBV/PBA specimens as a function of degradation extent have shown different behavior of the blends at different the PBA content. Thermal analysis of blends and PHBV has been reported, too     

Anammox: an option for ammonium removal in bioreactor landfills

Experiments carried out in bioreactor landfill simulators demonstrated that more than 40% of the total N was transferred into the liquid and gas phases during the incubation period of 380 days. Ammonium, an end product of protein degradation and important parameter to consider during landfill closure, tends to accumulate up to inhibitory levels in the leachate of landfills especially in landfills with leachate recirculation. Most efforts to remove ammonium from leachate have been focused on ex situ and partial in situ methods such as nitrification, denitrification and chemical precipitation. Besides minimal contributions from other N-removal processes, Anammox (Anaerobic Ammonium Oxidation) bacteria were found to be active within the simulators. Anammox is considered to be an important contributor to remove N from the solid matrix. However, it was unclear how the necessary nitrite for Anammox metabolism was produced. Moreover, little is known about the nature of residual nitrogen in the waste mass and possible mechanisms to remove it. Intrusion of small quantities of O₂ is not only beneficial for the degradation process of municipal solid waste (MSW) in bioreactor landfills but also significant for the development of the Anammox bacteria that contributed to the removal of ammonium. Volatilisation and Anammox activity were the main N removal mechanisms in these pilot-scale simulators. The results of these experiments bring new insights on the behaviour, evolution and fate of nitrogen from solid waste and present the first evidence of the existence of Anammox activity in bioreactor landfill simulators.     

Occurrence of Sediment-Bound Pyrethroids in Danish Streams and their Impact on Ecosystem Function

In a total of 189 water samples collected from Danish streams no traces of the pyrethroid esfenvalerate were detected. However, pyrethroids have previously been found in sediments in 9 out of 30 streams investigated. We found that the shredding activity of the Trichopteran Sericostoma personatum and the amphipod Gammarus pulex was significantly reduced with increased concentration of the pyrethroid lambda-cyhalohtrin adsorbed to the leaves on which they fed. Predation rate on the Plecopteran Leuctra nigra by the leech Erpobdella octoculata increased significantly with increasing concentration of lambda-cyhalothrin on the leaves on which L. nigra was fed. Our results clearly indicate that the ongoing monitoring of pesticides is likely to underestimate pyrethroid occurrence and that sediment-bound pyrethroids have a potential negative impact on ecosystem function and biotic interactions in streams.     

Gene Cloning and Characterization of a Poly(<Emphasis Type="SmallCaps">l</Emphasis>-Lactic Acid) Depolymerase from <Emphasis Type="Italic">Pseudomonas</Emphasis> sp. Strain DS04-T

A gene encoding a poly(l-lactic acid) (PLA) depolymerase from Pseudomonas sp. strain DS04-T was cloned and overexpressed in Escherichia coli. The recombinant PLA depolymerase with a molecular weight of 19.2 kDa was purified to homogeneity. The optimum pH and temperature of the PLA depolymerase are 8.5 and 60 °C, respectively. K⁺, Ca²⁺ and Ni²⁺ enhance the enzyme activity, while Na⁺, Zn²⁺, Mg²⁺, Cu²⁺, Fe²⁺, Mn²⁺ and Co²⁺ inhibit it. The inhibition of different chemicals on the PLA depolymerase activity were examined, in which EDTA was found to have a significantly inhibitory effect. The main degradation product of the depolymerase is identified as lactic acid monomer by mass spectrometric analysis. Physicochemical properties, substrate specificity and sequence analysis indicated that PME is a new type of PLA depolymerase.     

Brownfields Update: The Reform of the Brownfields Economic Redevelopment Initiative

This journal first reported on the U.S. EPA's Brownfields Initiative in the summer 1995 edition of Remediation. At that time, the initiative was only about 15 months old, most of the state programs were in proposal stages, and little federal legislation addressing brownfields had been proposed. Today, brownfields has become such a common term that almost every environmental professional is familiar with it. The EPA has placed extremely high priority on the Brownfields Initiative and it has become a politically hot issue. This article provides an update on the current status of EPA's Brownfields program and also discusses recent legislation proposed by Congress to promote brownfields redevelopment. © 2001 John Wiley & Sons, Inc.     

A Review of the Fate and Effects of Silicones in the Environment

Silicones are well-known useful materials varying in structure, reactivity, and chemical and physical properties, but they all contain a covalent bond between the silicon atom and an organic group. Most common of these polymers are those based on polydimethylsiloxane (PDMS) having a siloxane (Si–O–Si) repeat unit and two methyl groups on each silicon atom. All these polymers are manmade, and the organosilicon linkage is not found in nature. It was therefore erroneously assumed that these polymers do not degrade naturally in the environment. It is the purpose of this review to refute this myth and to describe the degradation processes of PDMS in the environment and any potential ecological impact on the terrestrial, aquatic, and atmospheric compartments. Although it was found that minor degradation takes place by hydrolysis of PDMS to dimethylsilandiol followed by oxidation of the methyl group to aldehyde and ultimately to CO₂ by Arthobacter and Fusarium oxysporium schlechtendahl, the major degradation processes are abiotic. High molecular weight PDMS are initially depolymerized by soil hydrolysis of the siloxane bonds to yield organosilanol terminated oligomers. These organosilanols and low molecular weight linear PDMS and cyclics are evaporated into the atmosphere and are oxidized there by hydroxyl radicals to benign silica, water, and CO₂.     

Miscibility and Biodegradability of Poly(Butylene Succinate)/Poly(Butylene Terephthalate) Blends

As one of the biodegradable polymers, the blend of poly(butylene succinate) and poly(butylene terephthalate) is dealt with in this study. In our previous work, it was demonstrated that PBS and PBT are immiscible not only from the changes of T _g but also from logG–log G plots. It is expected that the biodegradability of the blends could be improved by enhancing the miscibility. We tried to induce the transesterification reaction between two polyesters with various time intervals to enhance the miscibility of the blends. The extent of transesterification reaction was examined by ¹H-NMR. We utilized a dynamic mechanical thermal analyzer and a rotational rheometer to investigate the changes in miscibility. We also verified the biodegradability of PBS/PBT blends after the transesterification reaction by the composting method.     

The toxicity of composts from sewage sludges evaluated by the direct contact tests phytotoxkit and ostracodtoxkit

Limitations relating to permissible standards of undesirable substances in sewage sludges make it necessary to optimize sludge properties. One of the methods to achieve the above goal is the use of a composting process. The aim of this study was to determine the toxicity of composts obtained from sewage sludges composted for 76 days. Dewatered sewage sludges were collected from the four wastewater treatment plants located in the south-eastern part of Poland (Kraśnik, Lublin, Biłgoraj and Zamość). The sludges were mixed with standard OECD soil at doses of 6% and 24%. Phytotoxkit (with Lepidium sativum) and ostracodtoxkit (with Heterocypris incongruens) tests were used to evaluate toxicity. The results obtained showed different toxicity of sewage sludge depending on the sludge dose and bioassay used. H. incongruens mortality ranged from 0% to 90% and depended on the sewage sludge. The greatest inhibition of test organism growth was noted at a level of 55%. In the case of the Phytotoxkit test, a clearly negative influence of the sewage sludges on seed germination was observed at a dose of 24%. Root growth inhibition was noted in the case of most sewage sludges and was at a level of 20–100%. The influence of the composting on the toxicity of biosolids also showed various trends depending on the sludge type. Sludge composting often resulted in a toxicity increase in relation to H. incongruens. In the case of plants (Phytotoxkit test) and most sewage sludges, however, the composting process influenced both the seed germination and root growth in a positive way.     

Compositional Limitations in Poly–3–Hydroxyalkanoates Produced by Pseudomonas oleovorans

It is well known that Pseudomonas oleovorans can utilize sodium octanoate for both cell growth and the synthesis of polyhydroxyalkanoates (PHAs), but it can utilize sodium butyrate only for limited cell growth and not for the polyester formation when this substrate is the sole carbon source. Therefore, these two substrates were evaluated as cofeeds for the possible incorporation of 3-hydroxybutyryl groups in the resulting PHA. When sodium butyrate and sodium octanoate were fed to P. oleovorans as cosubstrates in various proportions, the resultant cell density and polymer content were proportional to the amount of sodium octanoate in the feed. The PHA extracted from cells grown in all combinations of these cosubstrates had similar unit compositions of approximately 8 mole % 3-hydroxyhexanoate, 91 mole % 3-hydroxyoctanoate and 1 mole % 3-hydroxydecanoate. 3-Hydroxybutyrate units were not detected in any of the PHAs isolated, indicating that these units could not be incorporated in the copolymer synthesized by P. oleovorans either because the cell did not synthesize that monomer or, if it did, the PHA synthase could not copolymerize it with the longer chain monomers.     

Detecting and quantifying reductive dechlorination under monitored natural attenuation conditions

Field sampling and testing were used to investigate the relationship between baseline geochemical and microbial community data and in situ reductive dechlorination rates at a site contaminated with trichloroethene (TCE) and carbon tetrachloride (CTET). Ten monitoring wells were selected to represent conditions along groundwater flow paths from the contaminant source zone to a wetlands groundwater discharge zone. Groundwater samples were analyzed for a suite of geochemical and microbial parameters; then push‐pull tests with fluorinated reactive tracers were conducted in each well to measure in situ reductive dechlorination rates. No exogenous electron donors were added in these tests, as the goal was to assess in situ reductive dechlorination rates under natural attenuation conditions. Geochemical data provided preliminary evidence that reductive dechlorination of TCE and CTET was occurring at the site, and microbial data confirmed the presence of known dechlorinating organisms in groundwater. Push‐pull tests were conducted using trichlorofluoroethene (TCFE) as a reactive tracer for TCE and, in one well, trichlorofluoromethane (TCFM) as a reactive tracer for CTET. Injected TCFE was transformed to cis‐ and trans‐dichlorofluoroethene and chlorofluoroethene, and, in one test, injected TCFE was completely dechlorinated to fluoroethene (FE). In situ TCFE transformation rates ranged from less than 0.005 to 0.004/day. In the single well tested, injected TCFM was transformed in situ to dichlorofluoromethane and chlorofluoromethane; the TCFM transformation rate was estimated as 0.001/day. The results indicate that it is possible to use push‐pull tests with reactive tracers to directly detect and quantify reductive dechlorination of chlorinated ethenes and ethanes under monitored natural attenuation conditions, which has not previously been demonstrated. Transformation rate estimates obtained with these techniques should improve the accuracy of contaminant transport modeling. © 2012 Wiley Periodicals, Inc.     

Biodegradable Polymers from 5-Hydroxylevulinic Acid: 1. Synthesis and Characterization of Poly(5-hydroxylevulinic acid)

As an attempt to synthesize new biodegradable polymers from renewable cellulose resources, melt polycondensation of 5-hydroxylevulinic acid (5-HLA) was reported for the first time. The resulting product, poly(5-hydroxylevulinic acid) (PHLA), was synthesized and characterized with GPC, FTIR, ¹H NMR and DSC. The in vitro degradation behaviors in phosphate-buffered saline (PBS) and in deionized water (DW) were also examined. The molecular weight of PHLA is not high (several 1,000s), but it possesses unordinary high glass transition temperature (as high as 120 °C). This is very different from existing aliphatic polyesters that usually have T _gs lower than 60 °C. The high T _g is attributed to the formation of inter- and/or intramolecular hydrogen bonds due to a characteristic keto–enol tautomerism equilibrium in the polymer structure. PHLA readily degraded hydrolytically in aqueous media.