Production of 2-Pyrrolidone from Biobased Glutamate by Using Escherichia coli

We have developed a simple and highly efficient process for the production of 2-pyrrolidone (2-PRN) from biobased l-glutamic acid (Glu). First, we produced γ-aminobutyric acid (GABA) from Glu obtained by fermentation of biomass using Escherichia coli, which is known to possess GABA producing activity. The reaction solution contained only the substrate Glu, bacterial cells, and water, and did not require buffers or coenzymes, pyridoxal-5′-phosphate (PLP). Every 24 h, cells were removed by centrifugation, and GABA containing supernatant was obtained. This reaction can be repeated 14 times by adding water and Glu, without any decrease in activity. Finally, 303.7 g of GABA was produced from 560 g (40 g × 14 times) of Glu with a yield of 77.4 %. The concentration of this solution was almost 40 %. The GABA was then converted to biobased 2-PRN by heating and distillation under reduced pressure without pretreatment. The yield obtained with this chemical process was 95.8 %. These results showed that biobased 2-PRN could be produced from biomass-derived Glu. Biobased 2-PRN has great potential as a raw material to change other petroleum-based materials to biobased materials.     

Mechanism and Characterization of Polyamide 4 Degradation by <Emphasis Type="Italic">Pseudomonas</Emphasis> sp.

We identified a biodegrading microorganism of polyamide (nylon) 4, a linear polymer of γ-aminobutyric acid (GABA). From activated sludge, the biodegrading bacteria strains of Pseudomonas sp. were isolated and identified by their taxonomic characteristics and nucleotide sequences of 16S rDNA. One strain, ND-11, was grown on a minimal medium containing polyamide 4 (PA4) as the sole carbon source. The strain produced GABA as a degradation intermediate, as identified by analyzing the NMR spectra of degraded products. The culture supernatant of strain ND-11 degraded the emulsified PA4 completely within one day. These results suggest that the ND-11 strain degraded PA4 using its extracellular enzymes to hydrolyze amide bonds.     

Removal of bisphenol a in soil by cyclodextrin derivatives

The apparent aqueous solubility of the endocrine disruptor in hydroxypropyl‐cyclodextrin (HP‐CD) solutions was investigated for evaluating the remediation of soil contamination and ground water pollution. The apparent solubility of bisphenol A (BPA) in water was significantly increased in HP‐CD solutions. The solubilization effect of HP‐CD's is caused by the formation of inclusion complexes of BPA and cyclodextrin. The relative aqueous‐phase concentration of BPA linearly increased with increasing HP‐CD concentration. The solubility of BPA increased in the order of the addition of HP‐a‐CD, HP‐7‐CD, and HP‐ß‐CD. However, it did not depend upon the degree of hydroxypropylation substitution. It is concluded that HP‐CD may be utilized for the remediation of soil contamination.     

Recent trends in the decomposition of chlorinated aromatic hydrocarbons by ultrasound irradiation and Fenton's reagent

Over the past few years, a large number of studies have been conducted on the use of ultrasound for decomposition of harmful organic pollutants, particularly chlorinated aromatic hydrocarbons (CAH) in wastewater. The published reports cover a variety of applications, including both ultrasonic treatment alone and in combination with other methods, e.g., advanced chemical oxidation processes. This article presents a review of recent work on ultrasonic-based methods of CAH decomposition, with emphasis on the applications of ultrasound alone and in combination with Fenton's reagent, as attractive advanced oxidation systems. In the first part of this review, the basic principles of sonochemical treatment are presented, followed by a review of the applications of ultrasound alone for CAH degradation. In the second part, the mechanisms of CAH degradation with Fenton's reagent and its application for CAH degradation are summarized. In the final part, studies on the applications of ultrasound together with Fenton's reagent are reviewed. The reported results suggest that a combination of ultrasound and Fenton's reagent is more attractive for practical application than the use of either method separately. Further studies, however, are required in this area because the reaction mechanism and the relationship between the reaction rates and process parameters for such a combined process are not yet well established.     

Hydrogen sulfide removal by iron containing activated carbon

Activated carbon modified by impregnation with iron (III) chloride solution (Fe‐ACs) were studied to try to raise their adsorption capacity for hydrogen sulfide, a malodorous substance.

The surface area and pore volume of activated carbon were decreased by impregnation, but the amount of hydrogen sulfide adsorbed onto Fe‐AC was larger than that onto raw activated carbon (R‐AC). In particular, a large increase of the amount adsorbed onto Fe‐AC was noted at low equilibrium pressure. It was assumed that the increase of amount of hydrogen sulfide adsorbed onto Fe‐AC was due to the chemical interaction between iron (III) chloride on the pores in addition to the physical adsorption onto pores of activated carbon. Fe‐AC shows a high selectivity for hydrogen sulfide.     

Development of a land-use forecast tool for future water resources assessment: case study for the Mekong River 3S Sub-basins

Land-use change is one of the major factors that alter local and regional hydrology. For areas experiencing fast expansion of urban and agriculture areas, land-use changes often adversely affect stream flow and water resources at the local and watershed scale. The Sekong, Sesan, and Srepok (3S) Sub-basins are a part of the Lower Mekong River Basin and include land in Cambodia, Lao People’s Democratic Republic (Laos), and Viet Nam. The region is experiencing a dynamic land-use transition because of rapid changes in its economy, society, and environment. Major land-use changes include deforestation of native rain forest, expansion of agricultural and urban areas, and expansion of commercial plantation such as rubber trees. These land-use alterations have affected local and regional hydrologic processes, resulting in stream flow shortages during the dry season and flash flooding due to deforestation. In this research, deforestation in the 3S Sub-basins over the period 1993–1997 was analyzed using multi-logistic regression. The regression analysis indicated that density of agricultural cells within a 5-km radius from each forest cell and slope strongly affected the deforestation process. A land-use forecast model to simulate deforestation and urbanization sites was developed in GIS based on local land-use change trends. The model was applied to 2003 land use to forecast 2033 land use and future water demand, which was further compared with present stream flow measurements during the dry season at various places in the region. The entire approach from the land-use forecast to its impact assessment on stream flow could help local stakeholders understand watershed-wide future water resources risks and develop future water resources plans. With the 3S Sub-basins being used as a case study area, this article presents a land-use forecast tool; simulated 2033 land-use and water demand; and the estimation of the impact of the forecasted future water demand on the local stream flow.     

The Axford Debate Revisited: A Case Study Illustrating Different Approaches to the Aggregation of Benefits Data

Recent debate following the rejection of the Environment Agency case regarding an application for water abstraction at Axford on the River Kennet has focused upon the benefits procedure employed for aggregating non-user benefits which underpinned the economic case put forward by the Agency (although this was not the reason cited by the inquiry for rejection of the case). Commentators have seen this case as setting an unfortunate precedent for the use of economic assessments in such resource management issues. The paper presents a number of highly tractable alternative methods for the aggregation of benefits estimates designed to address the central problems of the definition of a relevant aggregation population and a potential decay of values with increasing distance from a given valuation site. These methods are tested using data obtained from a national survey of non-users of a specific natural area. Results from this application indicate that simpler approaches such as that used at the Axford inquiry may result in aggregate benefits estimates which are very substantially larger than those produced by our proposed alternative approaches to aggregation.     

Accelerating effect of sodium chloride on mexiletine adsorption onto activated charcoal

The effective use of activated charcoal as an oral adsorbent for primary treatment of acute poisoning was investigated in vitro by evaluating the characteristics of mexiletine, an anti-arrhythmic drug, adsorbed onto activated charcoal in the presence of sodium chloride solutions at various concentrations. The equilibrium amount of mexiletine adsorbed onto activated charcoal was increased by the addition of sodium chloride. In particular, there was a marked increase in the amount adsorbed from a solution of lower mexiletine concentration. The removal rate is another important factor in the evaluation of activated charcoal, and a rapid decrease of mexiletine concentration by the addition of sodium chloride was recognized. The acceleration of mexiletine adsorption onto activated charcoal by the addition of sodium chloride was due to the occurrence of salting-out. It could be concluded that the administration of activated charcoal suspended in saline solution was more effective in the primary treatment of acute poisoning by mexiletine overdose.     

Removal of pentachlorophenol from contaminated soil by catalytic oxidation with iron(III)-porphyrin complexes and potassium monopersulfate

Pentachlorophenol (PCP) in contaminated soil was removed by treatment with aqueous solutions of iron(III)-porphyrin complexes as catalysts and potassium monopersulfate (KHSO₅) as the oxygen donor. The contaminated soils were artificially prepared by spiking PCP to the kaolin and ando soils. Three types of iron(III)-porphyrin complexes, tetra(?p-sulfophenyl) porphineiron(III) (Fe(III)-TPPS), tetra(N-methyl-4-pyridil)porphineiron(III) (Fe(III)-TMPyP) and heme, were examined, and Fe(III)-TPPS was found to be the most effective for removing PCP. Although the sequential addition of KHSO₅ was examined, in an attempt to improve the efficiency of PCP removal, it was not effective. In a preliminary test of various aqueous solutions, the addition of humic acid (HA), with a lower degree of humification, led to a significant enhancement in PCP removal. When HA was added to the soil system, the percentages of PCP removal were increased by up to 10% compared to the absence of HA. Therefore, the addition of HA to the catalytic system was useful in enhancing PCP removal from contaminated soil.     

Recovery efficiency of the hydrofluorocarbon (HFC‐134a) by activated carbons of different physicochemical properties

The adsorption characteristics of 1,1,1,2‐tetrafluoroethane (HFC‐134a) on activated carbon were investigated to evaluate the recovery efficiency of HFC‐134a by six activated carbons (two granular activated carbons (GAC1 and GAC2), one high‐surface area activated carbon (HAC), and three activated carbon fibers (ACF10, ACF15, and ACF20)). HFC‐134a adsorption on the activated carbons increased with increase in the specific surface area and pore volume of the activated carbon. The differential heat of the HFC‐134a adsorption decreased with increase in the percentage of the micropore volume to the total pore volume. The adsorption model of HFC‐134a on the activated carbon could be based on the Langmuir model. The constant a of the Langmuir plot of HAC and ACF20 is smaller than GAC1 or GAC2 and ACF10 or ACF15, respectively. The constant W_s of HAC has the largest value. The constant a was correlated to the heat of adsorption. It is concluded that the largest amount of HFC‐134a was adsorbed on HAC, and the least amount of interaction occurred between HFC‐134a and the HAC. The amount of HFC‐134a adsorbed on the activated carbons over time was applied to the Sameshima equation. The adsorption rate constant of HFC‐134a on HAC was the largest. The HAC could be suitable for the recovery of HFC‐134a.