Analysis of the effects of in-situ chemical oxidation on microbial activity using Pseudomonas putida F1.

In-situ chemical oxidation is an effective groundwater remediation approach for delivering oxidants to the subsurface environment where various contaminants of concern, natural organic matter, and other reduced species within the soil consume the oxidants. The addition of these oxidants alters microbial activity changing the physical and chemical structure of the soil. This paper studied the effects of chemical oxidation on microbial activity with and without toluene. Several oxidants were used as part of the study: sodium percarbonate, hydrogen peroxide, potassium permanganate, and sodium persulfate evaluated at low, medium, and high concentrations. A series of biometer experiments seeded with microbe Pseudomonas putida F1 and soil sample and aqueous toluene solution for each oxidant was monitored by CO2 production as a function of incubation days to evaluate the effects of oxidation on the microbial activity. Of the oxidants tested, permanganate oxidation resulted in the highest increase in microbial activity post oxidation based on CO2 production both with and without the addition of toluene. The other oxidants exhibited a direct correlation between oxidant concentration and the change in permanganate chemical oxidant demand of the soil. However, there was no correlation between oxidant concentration and microbial activity. Each of the oxidants was shown to increase CO2 yield except for sodium percarbonate, which had an adverse effect on microbial activity. It is likely that the increased microbial activity associated with permanganate oxidation was the result of chemical reactions between the oxidant and natural organic matter in the soil.

The effect of NaOH pretreatment on coal structure and biomethane production.

Biogenic CBM is an important component of detected CBM, which is formed by coal biodegradation and can be regenerated by anaerobic microorganisms. One of the rate-limiting factors for microbial degradation is the bioavailability of coal molecules, especially for anthracite which is more condense and has higher aromaticity compared with low-rank coal. In this paper, NaOH solution with different concentrations and treating time was employed to pretreat anthracite from Qinshui Basin to alter the coal structure and facilitate the biodegradation. The results showed that the optimal pretreatment conditions were 1.5 M NaOH treating for 12 h, under which the biomethane production was increased by 17.65% compared with untreated coal. The results of FTIR and XRD showed that NaOH pretreatment mainly reduced the multi-substituted aromatics, increased the C-O in alcohols and aromatic ethers and the branching degree of aliphatic chain, and decreased the aromatic ring structure, resulting in the improvement of coal bioavailability and enhancement of biomethane yield. And some organics with potential to generate methane were released to filtrate as revealed by GC-MS. Our results suggested that NaOH was an effective solution for pretreating coal to enhance biogenic methane production, and anthracite after treating with NaOH could be the better substrate for methanogenesis.

Coal-derived compounds and their potential impact on groundwater quality during coalbed methane production.

Coalbed methane (CBM) is an important unconventional energy source and accounts for a substantial portion of the overall natural gas production in the USA. The extraction of CBM generates significant amounts of produced water, where the withdrawal of groundwater may disturb the subsurface environment and aquifers. The release of toxic recalcitrant compounds from the coal seam is of great concern for those who use groundwater for irrigation and potable water sources. Experiments were conducted that determined a small fraction of coal carbon can be extracted and solubilized in water during the CBM formation and production. These soluble components included long-chain alkanes, aromatic hydrocarbons, and humic compounds. Biometer flask assays demonstrated that these compounds are bioamenable and can be potentially degraded by microorganisms to produce methane and carbon dioxide, where these biodegradation processes may further impact groundwater quality in the coal seam.

Low carbon renewable natural gas production from coalbeds and implications for carbon capture and storage.

Isotopic studies have shown that many of the world's coalbed natural gas plays are secondary biogenic in origin, suggesting a potential for gas regeneration through enhanced microbial activities. The generation of biogas through biostimulation and bioaugmentation is limited to the bioavailability of coal-derived compounds and is considered carbon positive. Here we show that plant-derived carbohydrates can be used as alternative substrates for gas generation by the indigenous coal seam microorganisms. The results suggest that coalbeds can act as natural geobioreactors to produce low carbon renewable natural gas, which can be considered carbon neutral, or perhaps even carbon negative depending on the amount of carbon sequestered within the coal. In addition, coal bioavailability is no longer a limiting factor. This approach has the potential of bridging the gap between fossil fuels and renewable energy by utilizing existing coalbed natural gas infrastructure to produce low carbon renewable natural gas and reducing global warming.Coalbeds produce natural gas, which has been observed to be enhanced by in situ microbes. Here, the authors add plant-derived carbohydrates (monosaccharides) to coal seams to be converted by indigenous microbes into natural gas, thus demonstrating a potential low carbon renewable natural gas resource.

Passive remediation of coalbed natural gas co-produced water using zeolite.

Coalbed natural gas (CBNG) co-produced waters can contain sodium (Na(+)) concentrations that may be environmentally detrimental if discharged to receiving bodies of water or applied to land surfaces. A field demonstration and companion laboratory studies were conducted to evaluate the use of a Bear River zeolite (BR-zeolite) for mitigating impacts associated with Na(+) in CBNG waters. Bench-scale kinetic and adsorption isotherm studies were performed to determine both the rate and extent of sodium Na(+) adsorption and assess the effects of bicarbonate (HCO3(-)) and chloride (Cl(-)) anions. Results of these studies showed that the adsorption of Na(+) on BR-zeolite followed the Langmuir adsorption model with maximum adsorption equal to 21 and 18 g Na(+)/kg zeolite with 0.0012 and 0.0006 L/mg Langmuir coefficients (KL) for sodium bicarbonate and sodium chloride, respectively. The kinetics study indicated that the sorption of Na(+) was inversely related to the size of the zeolite particles with significantly greater adsorption for smaller particles. The field demonstration evaluated the effectiveness of BR-zeolite for mitigating infiltration losses from Na(+) in CBNG waters. The field site utilized 12 open boreholes, each installed to a depth of approximately 1.8 m. Each borehole was lined with a 3.0 m long, 15 cm diameter schedule 40 PVC pipe and fitted with an automatic data logging pressure transducer for measuring water levels over time. The BR-zeolite was found to mitigate much of the deleterious effect that high sodium adsorption ratio (SAR = 27 (mol/m(3))(1/2)) CBNG co-produced water had on soil permeabilities.

Improving saline-sodic coalbed natural gas water quality using natural zeolites.

Management of saline-sodic water from the coalbed natural gas (CBNG) industry in the Powder River Basin (PRB) of Wyoming and Montana is a major environmental challenge. Clinoptilolie zeolites mined in Nevada, California, and New Mexico were evaluated for their potential to remove sodium (Na+) from CBNG waters. Based on the exchangeable cation composition, naturally occurring calcium (Ca2+)-rich zeolites from New Mexico were selected for further evaluation. Batch adsorption experiments were conducted to evaluate the potential of the Ca(2+)-rich natural clinoptilolites to remove Na+ from saline-sodic CBNG waters. Batch adsorption experiments indicated that Na+ adsorption capacity ofclinoptilolite ranged from 4.3 (4 x 6 mesh) to 7.98 g kg(-1) (14 x 40 mesh). Among the different adsorption isotherms investigated, the Freundlich Model fitted the data best for smaller-sized (6 x 8, 6 x 14, and 14 x 40 mesh) zeolites. Passing the CBNG water through Ca(2+)-rich zeolite columns reduced the salt content (electrical conductivity [EC]) by 72% with a concurrent reduction in sodium adsorption 10 mmol 1/2 L(-1/2). Zeolite technology appears to be an effective water treatment alternative to industrial membrane treatment for removing Na+ from poor-quality CBNG waters.

Municipal solid waste generation in Kathmandu, Nepal.

Waste stream characteristics must be understood to tackle waste management problems in Kathmandu Metropolitan City (KMC), Nepal. Three-stage stratified cluster sampling was used to evaluate solid waste data collected from 336 households in KMC. This information was combined with data collected regarding waste from restaurants, hotels, schools and streets. The study found that 497.3 g capita(-1) day(-1) of solid waste was generated from households and 48.5, 113.3 and 26.1 kg facility(-1) day(-1) of waste was generated from restaurants, hotels and schools, respectively. Street litter measured 69.3 metric tons day(-1). The average municipal solid waste generation rate was 523.8 metric tons day(-1) or 0.66 kg capita(-1) day(-1) as compared to the 320 metric tons day(-1) reported by the city. The coefficient of correlation between the number of people and the amount of waste produced was 0.94. Key household waste constituents included 71% organic wastes, 12% plastics, 7.5% paper and paper products, 5% dirt and construction debris and 1% hazardous wastes. Although the waste composition varied depending on the source, the composition analysis of waste from restaurants, hotels, schools and streets showed a high percentage of organic wastes. These numbers suggest a greater potential for recovery of organic wastes via composting and there is an opportunity for recycling. Because there is no previous inquiry of this scale in reporting comprehensive municipal solid waste generation in Nepal, this study can be treated as a baseline for other Nepalese municipalities.

Removal of guar and humus from water by layered double hydroxides.

Natural organic matter such as guar and humus are recalcitrant to conventional pretreatment technologies and can potentially foul processes such as membranes during water treatment. An innovative method of using synthetic layered double hydroxides (LDH) was investigated for removing common natural organic matter in the form of guar gum (GG) and humic acid (HA) from water. Adsorption isotherms were evaluated with Langmuir and Freundlich models. Results show the affinity of GG and HA to LDH to be 11.31 and 9.33 mg g(-1) LDH, respectively. Kinetic isotherms indicate that the sorbing rates of LDH to GG and HA increase with initial GG and HA concentrations, fitting a pseudo-second order model. This study demonstrate that LDH may be an effective material in removing GG and HA from waters and offer an alternative to conventional pretreatment technologies for the mitigation fouling of membrane and other systems in water treatment.

Report: Searching for a way to sustainability: technical and policy analyses of solid waste issues in Kathmandu.

Kathmandu Metropolitan City has attempted to reorganize its solid waste management a number of times. The German Technical and Financial Aid Organization led early efforts that were followed by a number of more recent experiments that left the city with an unsustainable solid waste management system following the termination of foreign aid. To examine this failure, the research team evaluated household surveys, field observations, interviews, and other primary and secondary information within the context of technical, social, and institutional analyses. The survey results show that the solid waste collection rates are far below the 90% claimed by the metropolis and street sweeping consumes approximately 51% of its solid waste budget. As a result of the relatively low collection rates the city residents are encouraged to dump waste into public lands. Consequently, too much of the city's resources are focused on sweeping rather than collection. Kathmandu needs to recognize informal waste picking, privatize, use local techniques, build capacity, promote bottom-up and participatory styles of management, and regulate policies to maintain solid waste management.

Use of stratified cluster sampling for efficient estimation of solid waste generation at household level.

Relatively few studies have been performed to characterize municipal solid waste (MSW) at household level. This is due in part to the difficulties involved with collecting the data and selecting an appropriate statistical sample size. The previous studies identified in this paper have used statistical tools appropriate for analysing data collected at a material recovery facility or landfill site. This study demonstrates a statistically sound and efficient approach for characterizing MSW at the household level. Moreover, a household approach also allowed for consideration of the socio-economic conditions, level of waste generation, geography, and demography. The study utilized two-stage cluster sampling within strata in Kathmandu Metropolitan City (KMC) to measure MSW for 2 weeks. In KMC, the average household solid waste generation was 161.2 g capita( -1) day(- 1)with an average generation rate between 137.7 and 184.6 g capita(-1) day(-1) for a 95% confidence interval and 14.5% relative margin of error. The results show a positive relation between income and waste production rate. Organic waste was the biggest portion of MSW, and hazardous waste was the smallest of the total. Sample size considerations suggest that 273 households are required in KMC to attain a 10% relative margin of error with a 95% confidence interval.

Kinetics of natural oxidant demand by permanganate in aquifer solids.

During in situ chemical oxidation with permanganate, natural organic matter and other reduced species in the subsurface compete with the target compounds for the available oxidant and can exert a significant natural oxidant demand. This competition between target and nontarget compounds can have a significant impact on the permeation, dispersal, and persistence of permanganate in the subsurface. The kinetics of natural oxidant demand by permanganate was investigated using a composite sample made up of aquifer material collected from three different sites. The study found that although the depletion of organic carbon increased with increased permanganate dosage and increased reaction period, the mass ratio of MnO(4)(-):OC (wt/wt) was relatively constant over time (11.4+/-0.9). The reaction order and rate with respect to permanganate were found to decrease with time suggesting a continuum of reactions with the slower reactions becoming more controlling with time. However, the data also suggests that this continuum of reactions can be simplified into short- and long-term kinetic expressions representing fast and slow reactions. An independent first-order kinetic model with separate fast and slow reaction rate constants was used to successfully describe the complete kinetic expression of natural oxidant demand. The kinetic parameters used in the model are easily determined and can be used to better understand the complex kinetics of natural oxidant demand.

Interphase mass transfer during chemical oxidation of TCE DNAPL in an aqueous system.

The chemical oxidation of trichloroethene dense non-aqueous phase liquid by permanganate was studied in an aqueous system using micro-reaction/extraction vessels in a novel approach. Experiments were conducted at ambient temperature ( approximately 20 degrees C) under static and mixed conditions to evaluate the rate of TCE(DNAPL) dissolution as a function of permanganate concentration. Chemical oxidation by permanganate was shown to increase the rate of TCE(DNAPL) dissolution under static conditions and decrease the rate of dissolution under mixed conditions. The apparent inconsistency in results appears to result from the local deposition of a film at the DNAPL interface composed of manganese oxide solids as discovered through visual observation with the aid of a Goniometer. Data from interfacial deposition experiments suggest that the film formed rapidly and reached maturation within approximately 2 h with little or no growth occurring thereafter. A conceptual model of the reaction and mass transfer processes occurring at the DNAPL interface was proposed based on the experimental results.