Microbial fuel cells a state-of-the-art technology for wastewater treatment and bioelectricity generation.

Wastewater treatment and electricity generation have been the major concerns for the last few years. The scarcity of fossil fuels has led to the development of unconventional energy resources that are pollution-free. Microbial fuel cell (MFC) is an environmental and eco-friendly technology that harvests energy through the oxidation of organic substrates and transform into the electric current with the aid of microorganisms as catalysts. This review presents power output and colour removal values by designing various configurations of MFCs and highlights the importance of materials for the fabrication of anode and cathode electrodes playing vital roles in the formation of biofilm and redox reactions taking place in both chambers. The electron transfer mechanism from microbes towards the electrode surface and the generation of electric current are also highlighted. The effect of various parameters affecting the cell performance such as type and amount of substrate, pH and temperature maintained within the chambers have also been discussed. Although this technology presents many advantages, it still needs to be used in combination with other processes to enhance power output.

Polyhydroxyalkanoates: Next generation natural biomolecules and a solution for the world's future economy.

Petrochemical plastics have become a cause of pollution for decades and finding alternative plastics that are environmental friendly. Polyhydroxyalkanoate (PHA), a biopolyester produced by microbial cells, has characteristics (biocompatible, biodegradable, non-toxic) that make it appropriate as a biodegradable plastic substance. The different forms of PHA make it suitable to a wide choice of products, from packaging materials to biomedical applications. The major challenge in commercialization of PHA is the cost of manufacturing. There are a lot of factors that could affect the efficiency of a development method. The development of new strategic parameters for better synthesis, including consumption of low cost carbon substrates, genetic modification of PHA-producing strains, and fermentational strategies are discussed. Recently, many efforts have been made to develop a method for the cost-effective production of PHAs. The isolation, analysis as well as characterization of PHAs are significant factors for any developmental process. Due to the biodegradable and biocompatible properties of PHAs, they are majorly used in biomedical applications such as vascular grafting, heart tissue engineering, skin tissue repairing, liver tissue engineering, nerve tissue engineering, bone tissue engineering, cartilage tissue engineering and therapeutic carrier. The emerging and interesting area of research is the development of self-healing biopolymer that could significantly broaden the operational life and protection of the polymeric materials for a broad range of uses. Biodegradable and biocompatible polymers are considered as the green materials in place of petroleum-based plastics in the future.

Application of novel bacterial consortium for biodegradation of aromatic amine 2-ABS using response surface methodology.

There is a strong need to develop purification methods for textile industrial wastewater containing toxic azo dyes. The reductive cleavage of azo dyes can be made by anaerobic bacteria, but the products of aromatic amines require an aerobic process. In this study a novel bacterial dye degrading consortium (DDC) of five isolated strains identified with 16S rRNA sequence: Proteus mirabilis (KR732288), Bacillus anthracis (KR732289), Enterobacter hormaechei (KR732290), Pseudomonas aeruginosa (KR732293) and Serratia rubidaea (KR732296) were used to aerobically decompose metabolite 2-aminobenxenesulfonic acid (2-ABS), as a model compound. The effect of three variables: temperature (28-42 °C), pH (5.0-8.0) and initial concentration of 2-ABS (5-40 ppm) was investigated in terms of degradation and chemical oxygen demand (COD) removal. Central composite design matrixand response surface methodology (RSM) were used for experimental design to evaluate theinteraction of the three process variables. The results show that up to 95% degradation and COD 90% removal are possible at optimal values of 32.4 ppm 2-ABS, pH 6.6 and a temperature of 35.7 °C. The theoretical response variables predicted by the developed RSM model was supported the experimental results. The optimized degradation of 2-ABS and COD removal were further confirmed by UV-HPLC analysis.

Changes in bacterial community structure and humic acid composition in response to enhanced extracellular electron transfer process in coastal sediment.

Humic acids are one of the main organic matters in sediments and contribute importantly to the marine biogeochemical cycles. Extracellular electron transfer is a ubiquitous natural process and has potentials to change the macrostructure of humic acids which can act as an electron shuttle. By setting up marine sediment microbial fuel cells, the present study revealed that enhanced extracellular electron transfer process could increase the content of C and H, but decrease the O content in humic acids, which could result in an increased aromaticity and decreased polarity of humic acids, whereas no significant changes occurred to the humification degree of the humic acids. Specific bacterial groups as potential exoelectrogens including Proteobacteria (especially Pseudomonas strains) and Firmicutes were enriched under enhanced extracellular electron transfer process, indicating that they were active to exchange electrons and might play important roles during the changes of humic acids, while the relative abundance of Verrucomicrobia and Bacteroidetes was reduced during these processes. The results of the present research shed lights on the relation between exoelectrogens and the transformation of humic acids in coastal sediment, while the microbial process and mechanisms behind it require further study.

Ultrasound-assisted adsorption of phenol from aqueous solution by using spent black tea leaves.

This study is conducted to examine the removal of phenol using spent black tea leaves (SBTL) by the process of ultrasound-assisted adsorption. The effect of different treatment processes, i.e., sonolysis, adsorption, and ultrasound-assisted adsorption, was investigated. The morphology of SBTL was studied using a scanning electron microscope (SEM), and the porous structure of the SBTL was identified before phenol was adsorbed onto the adsorbent. FTIR analysis of SBTL after adsorption showed the presence of an aliphatic band of carboxylic acids which depict degradation of the phenol molecule due to ultrasound-assisted adsorption. The experimental results showed that the hybrid process was found more effective for phenol removal (85%) as determined by a spectrophotometer. The optimum conditions of the reaction parameters were found as: phenol conc. = 25 mg L-1, pH = 3.5, time = 60 min, adsorbent dosage = 800 mg L-1, ultrasound power = 80 W, and operating temperature = 30 ± 2 °C. Chemical oxygen demand (COD) and total organic carbon (TOC) were found to be 78 and 39%, respectively. HPLC studies suggest nonselective oxidation of phenol resulting in by-products such as catechol and hydroquinone and finally carboxylic acids and CO2. In order to find reaction kinetics, different kinetic models, viz. pseudo-first- and pseudo-second-order models, were studied. The best fit to the isotherm models, i.e., Langmuir and Freundlich, was determined. It is concluded that phenol removal by the hybrid process follows the pseudo-second-order reaction kinetics and Langmuir isotherm model. In addition, thermodynamic studies revealed the nonspontaneous and exothermic nature of the phenol adsorption process.

Optimization of HNO3 leaching of copper from old AMD Athlon processors using response surface methodology.

The present study investigates the optimization of HNO3 leaching of Cu from old AMD Athlon processors under the effect of nitric acid concentration (%), temperature (°C) and ultrasonic power (W). The optimization study is carried out using response surface methodology with central composite rotatable design (CCRD). The ANOVA study concludes that the second degree polynomial model is fitted well to the fifteen experimental runs based on p-value (0.003), R2 (0.97) and Adj-R2 (0.914). The study shows that the temperature is the most significant process variable to the leaching concentration of Cu followed by nitric acid concentration. However, ultrasound power shows no significant impact on the leaching concentration. The optimum conditions were found to be 20% nitric acid concentration, 48.89 °C temperature and 5.52 W ultrasound power for attaining maximum concentration of 97.916 mg/l for Cu leaching in solution.

Bio-electrochemical synthesis of commodity chemicals by autotrophic acetogens utilizing CO2 for environmental remediation.

Bio-electrochemical synthesis (BES) is a technique in which electro-autotrophic bacteria such as Clostridium ljungdahlii utilize electric currents as an electron source from the cathode to reduce CO2 to extracellular, multicarbon, exquisite products through autotrophic conversion. The BES of volatile fatty acids and alcohols directly from CO2 is a sustainable alternative for non-renewable, petroleum-based polymer production. This conversion of CO2 implies reduction of greenhouse gas emissions. The synthesis of heptanoic acid, heptanol, hexanoic acid and hexanol, for the first time, by Clostridium ljungdahlii was a remarkable achievement of BES. In our study, these microorganisms were cultivated on the cathode of a bio-electrochemical cell at -400 mV by a DC power supply at 37 degree Centrigrade, pH 6.8, and was studied for both batch and continuous systems. Pre-enrichment of bio-cathode enhanced the electroactivity of cells and resulted in maximizing extracellular products in less time. The main aim of the research was to investigate the impact of low-cost substrate CO2, and the longer cathode recovery range was due to bacterial reduction of CO2 to multicarbon chemical commodities with electrons driven from the cathode. Reactor design was simplified for cost-effectiveness and to enhance energy efficiencies. The Columbic recovery of ethanoic acid, ethanol, ethyl butyrate, hexanoic acid, heptanoic acid and hexanol being in excess of 80 percent proved that BES was a remarkable technology.

Synergistic effects of combining ultrasound with the Fenton process in the degradation of Reactive Blue 19.

The decoloration of reactive dye C.I. Reactive Blue 19 (RB 19) using combined ultrasound with the Fenton process has been investigated. The effect of varying the concentrations of hydrogen peroxide and iron sulfate, initial pH, ultrasonic power, initial dye concentration and dissolved gas on the decoloration and degradation efficiencies was measured. Calibration of the ultrasound systems was performed using calorimetric measurements and oxidative species monitoring using the Fricke dosimeter and degradations were carried out with a 20 kHz probe type transducer at 2, 4, 6 and 8 W cm(-2) of acoustic intensity at 15, 25, 50 and 75 mg L(-1) initial dye concentrations. First order rate kinetics was observed. It was found that while the degradation rate due to ultrasound alone was slow, sonication significantly accelerated the Fenton reaction. While the results were similar to those reported for other dyes, the effects occurred at lower concentrations. The rate and extent of decoloration of RB 19 increased with rising hydrogen peroxide concentration, ultrasonic powers and iron sulfate concentration but decreased with increasing dye concentration. An optimum pH value of pH=3.5 was found. The rate of decoloration was higher when dissolved oxygen was present as compared with nitrogen and argon confirming the solution phase mechanism of the degradation.

Enhanced decomposition of reactive blue 19 dye in ultrasound assisted electrochemical reactor.

Textile industry effluents contain reactive dyes that may harm our receiving waters. A typical reactive blue (RB) 19 dye is frequently detected in significant concentrations in textile industry effluents. Such dyes have generally shown resistance to decomposition and tend to persist in the environment for long periods and multiply the impacts to water and environment. Therefore, the present investigation focused on high-rate decomposition of a typical reactive dye RB 19 under various ultrasound and electrochemical process conditions. The decomposition of un-hydrolyzed and hydrolyzed forms of reactive blue (RB) 19 dye by ultrasound assisted electrochemical process was investigated using various parameters including dye concentration, pH, ultrasonic frequency and reaction time. Reaction kinetics, organic carbon and mechanism for dye decomposition were determined using UV-Visible spectrophotometry, TOC (total organic carbon) analysis and gas chromatography-mass spectrometry (GC-MS). Almost complete 90% color removal and a maximum of 56% TOC removal for 50 mg L(-1) dye concentration of un-hydrolyzed RB 19 dye was achieved at an ultrasonic frequency of 80 kHz, pH of 8 after 120 min. GC-MS analysis showed that a sonoelectrochemical treatment of un-hydrolyzed RB 19 dye for 30 min resulted in the formation of products e.g. acetic acid, benzoic acid etc. with the complete removal of dye. For hydrolyzed dye, a treatment of 10 min was enough and the results were comparable with 30 min treatment of un-hydrolyzed dye. Kinetics of ultrasound assisted electrolysis showed that the dye decomposition followed 1st order. The ultrasound assisted electrolysis for dye decomposition and hence decolorization proved to be more effective and the total energy consumption reduced to half as compared with simple electrolysis/sonochemical decomposition. Therefore, ultrasound assisted electrolysis was found to be more effective technique for dye decomposition of an otherwise environmentally persistent reactive dye.

Phytoremediation potential of Arundo donax in arsenic-contaminated synthetic wastewater.

The present study reports the potential of Arundo donax for phytoextraction of arsenic from synthetic wastewater. A. donax plants were grown under greenhouse conditions in pots containing a nutrient solution amended with increasing doses of As (0, 50, 100, 300, 600 and 1000 microg L(-1)) for 21 days in a completely randomized design. Shoot and roots dry matter production, growth parameters, arsenic and nutrient tissue concentrations were measured at the end of the experiment. Increasing As concentration in nutrient solution caused an increase in shoot and root biomass without toxicity symptoms in A. donax growing under a range of As concentration from 50 to 600 microg L(-1). Elevated oxidative stress was observed at As supplied level of 1000 microg L(-1). The As doses up to 600 microg L(-1) did not affect the growth of A. donax. It is suggested that A. donax plants may be employed to treat contaminated waters containing arsenic concentrations up to 600 microg L(-1).

Thermal-pressure-mediated hydrolysis of Reactive Blue 19 dye.

The thermal-pressure-mediated hydrolysis rates and the degradation kinetics of environmentally persistent Reactive Blue (RB) 19 dye were studied. The dye decomposition was studied at 40-120 degrees C, pH 2-10, and atmospheric pressure range of 1-2 atm. The intermediates and end products formed during the degradation were identified using gas chromatography/mass spectrometry and a possible degradation pathway of RB 19 was proposed. The stability of the dye in aqueous solution was influenced by changes in pH. At pH 4, half-life was 2247.5 min at 40 degrees C and it reduced to 339.4 min when the temperature was increased to 120 degrees C. Acidic conditions were more conducive to enhance hydrolysis rate than basic ones as the decomposition was optimum at pH 4. The kinetic studies indicated that the rate of hydrolysis apparently followed first order reaction. A linear relationship was observed between hydrolysis rate of RB 19 dye and increasing temperatures and pressures. Overall, 23% dye decomposition occurred in 120 minutes at pH 4, 120 degrees C and pressure of 2 atm. Along with thermal-pressure, a combination of techniques like physico-chemical, biological, enzymatic etc. may be more suitable choice for the effective treatment of RB19 dye.

Evaluation of trace metals in tobacco of local and imported cigarette brands used in Pakistan by spectrophotometer through microwave digestion.

Uncontrolled exposure of active and passive smokers to trace metals causes increase in health risks. The primary objective of this study was to determine whether local and imported cigarette brands used in Pakistan, have elevated levels of metals or not. Six metals manganese (Mn), cobalt (Co), copper (Cu), cadmium (Cd), lead (Pb) and zinc (Zn) were determined in tobacco of twenty cigarette brands (local and imported) used in Pakistan by flame atomic absorption Spectrophotometry. To overcome contamination chances and for complete digestion of analytes a microwave digester was used. The analytical results showed highest concentration of Mn (84.78 microg/g dry weight), Cd (0.525 microg/g dry weight) and Zn (14.34 microg/g dry weight) metals in imported brands in relation to counterparts from the local brands. Certain elevated levels were observed for Co (3.344 microg/g dry weight), Pb (14.16 microg/g dry weight) and Cu (7.889 microg/g dry weight) metals in local brands. The inter-metal relationships in the tobacco of local and imported cigarette brands showed some integrated variation in the selected metal levels. In view of health risk associated with the above metals, there should be a strict quality control over monitoring of heavy metals during growing, processing and smoking of tobacco. Therefore, it is prudent to minimize exposure to toxic substances whenever possible because smoking and exposure to cigarette smoke is a confounder to be taken into account when carrying out epidemiological studies on human exposure to metals.

Complete (1)H and (13)C NMR assignments of two new trans-clerodane diterpenoids from Otostegia limbata.

Two new tricyclic trans-clerodane diterpenoids trivially named as ballotenic acid A (1) and ballodiolic acid A (2) have been isolated from ethyl acetate fraction of Otostegia limbata. The structure assignments are based on (1)H and (13)C NMR spectra, 2D NMR (HMQC, HMBC, COSY, NOESY and NOE) techniques and comparison with the literature data.

Sonochemical degradation of organophosphorus pesticide in dilute aqueous solutions.

Ultrasonic irradiation was found to accelerate the rate of hydrolysis of omethoate in aqueous solution over the pH range of 2-12. Process parameters studied include pH, steady-state temperature, concentration, and the type of gases. Greater than 96% hydrolysis was observed in 30 minutes through this process and the rate of destruction increased with the help of more soluble and low thermal inert gas. So with Krypton, omethoate was found to undergo rapid destruction as compared with Argon. In the presence of ultrasound, the observed first-order rate of hydrolysis of omethoate is found to be independent of pH. The formation of transient supercritical water (SCW) appears to be an important factor in the acceleration of chemical reactions in the presence of ultrasound. A detailed chemical reaction mechanism for omethoate destruction in water was formulated. Experimental results and theoretical kinetic mechanism demonstrated that the most of the omethoate undergo destruction inside the cavitating holes. A very less effect of temperature on the degradation of omethoate within a temperature range of 20-70 degrees C proves that a small quantity of omethoate undergoes secondary destruction in the bulk liquid.

Removal of copper from a copper sulphate solution using an ultrasonic-electrolysis process.

The application of ultrasonic-electrolysis process for the removal of copper is studied. In the ultrasonic field cavitation acts as jets and agitates the solution and breaks the barrier layer between the cathode surface and the bulk of the solution. Thus increases metal deposition on the cathode surface. The results show that an ultrasonic field is successful for the removal of low copper concentrations in solution.

Effect of ultrasound on the removal of copper from the model solutions for copper electrolysis process.

A novel combination of an ultrasonic field with electrolysis for the removal of copper is studied. In the ultrasonic field, cavitation acts as jets and agitates the solution and breaks the barrier layer between the cathode surface and the bulk of the solution, thus increases the metal deposition on the cathode surface. The results show that an ultrasonic field is successful for the removal of low copper concentrations in solution.