Integrating Human Waste with Microbial Fuel Cells to Elevate the Production of Bioelectricity.

Due to the continuous depletion of natural resources currently used for electricity generation, it is imperative to develop alternative energy sources. Human waste is nowadays being explored as an efficient source to produce bio-energy. Human waste is renewable and can be used as a source for an uninterrupted energy supply in bioelectricity or biofuel. Annually, human waste such as urine is produced in trillions of liters globally. Hence, utilizing the waste to produce bioenergy is bio-economically suitable and ecologically balanced. Microbial fuel cells (MFCs) play a crucial role in providing an effective mode of bioelectricity production by implementing the role of transducers. MFCs convert organic matter into energy using bio-electro-oxidation of material to produce electricity. Over the years, MFCs have been explored prominently in various fields to find a backup for providing bioenergy and biofuel. MFCs involve the role of exoelectrogens which work as transducers to convert the material into electricity by catalyzing redox reactions. This review paper demonstrates how human waste is useful for producing electricity and how this innovation would be beneficial in the long term, considering the current scenario of increasing demand for the supply of products and shortages of natural resources used to produce biofuel and bioelectricity.

A direct contact bioassay using sulfur-oxidizing bacteria (SOB) for toxicity assessment of contaminated field soils.

In this study, 11 low/uncontaminated (including Lufa 2.2) and 9 contaminated field soils with varying geophysical and physicochemical characteristics were evaluated for toxicities based on oxygen consumption of sulfur-oxidizing bacteria (SOB). Oxygen consumption of the low/uncontaminated soils ranged between 7.9 mL and 9.5 mL, while contaminated soils ranged between 0.4 mL and 5.4 mL. Inherent test variability (CVi), variation due to soil natural properties (CVns) and minimal detectable difference (MDD) values ranged 1.2%-3.9%, 3.5%-16.9%, and 2.1%-4.3%, respectively. The toxicity threshold of 20% was established for soil toxicity based maximal tolerable inhibition (MTI). All the contaminated soils were found to be toxic and showed inhibition between 42% and 100% above the 20% threshold value. Increased proportions of clay and slit enhanced the of inhibitory effect of contaminants on SOB by reducing the oxygen consumption. Current study provides a suitable method for the rapid toxicity assessment of contaminated field soils with the advantages of ease of handling and rapidity without employing elutriates and sophisticated equipments and tools.

Optimization of Fenton process for removing TOC and color from swine wastewater using response surface method (RSM).

The Fenton oxidation process was applied to biologically treated swine wastewater (BSWW) for the removal of TOC and color constituents after coagulation with FeCl3. Optimizing of operational variables such as FeSO4 and H2O2 doses was achieved by the response surface method (RSM). Statistical analysis led to the conclusion that FeSO4 is the more important than H2O2 in the removal of TOC. However, H2O2 plays a more significant role than FeSO4 in color removal. The optimal conditions for effective removal of TOC and color from swine wastewater were derived by using process optimization. The experimental results show that overall removal of TOC and color is 76.7% and 98%, respectively, when optimal conditions of 800 mg/L (FeSO4) and 5207 mg/L (H2O2) at 120 min were used. Furthermore, the optimization model produces a desirability value of 0.980 that verifies the optimal conditions. Finally, it is observed that removal of undesirable compounds follows a pseudo-first order and pseudo-second order kinetics model with high R2 values of 0.99 for both TOC and color removal, respectively. Statistical analysis and process optimization show that the employed model may determine conditions conducive to the effective removal of TOC and color from swine wastewater.

A Microbial Bioassay for Direct Contact Assessment of Soil Toxicity Based on Oxygen Consumption of Sulfur Oxidizing Bacteria.

A new direct contact assessment of soil toxicity using sulfur oxidizing bacteria (SOB) is proposed for analyzing the toxicity of soils. The proposed method is based on the ability of SOB to oxidize elemental sulfur to sulfuric acid in the presence of oxygen. Since sulfate ions are produced from sulfur by SOB oxidation activity, changes in electrical conductivity (EC) serve as a proxy to assess toxicity in water. However, in soil medium, EC values are not reliable due to the adsorption of SO4 2- ions by soils. Here, we suggest a new parameter which measures oxygen consumption by SOB for 6 hours to assess soil toxicity by using a lubricated glass syringe method. The proposed method is rapid, simple, cost- effective as well as sensitive and capable of assessing direct contact soil toxicity.

Effect of pH on phosphorus (P) dissolution and recovery from polyaluminum chlorides (PAC) sludge.

Phosphorus (P) dissolution from polyaluminum chlorides (PAC) sludge was investigated for sustainable P recovery. P dissolution followed 1st order kinetics with the rate constants of 3.8 × 10-2, 0.8 × 10-2, 1.3 × 10-2 and 1.9 × 10-2 min-1 at pH 1, 2.5, 10.5 and 12, respectively. Strong acidic and alkaline conditions dissolved about 82 (pH 1) and 88% (pH 12) of the total P by adding 0.214 g HCl and 0.357 g NaOH per gram P dissolved, respectively. Chemical P fractionation showed that more than 96% of the total P of the PAC sludge was AlP and it was reduced to 11.3 (pH 12) and 12.6% (pH 1.0) after the acid and alkali treatment. ATR-FTIR showed that AlPO4 in the PAC sludge was transformed to Mg3(PO4)2∙4H2O and CaHPO4∙2H2O after alkali treatment and H3PO4 and Na/MgP after acid treatment. Dissolved P can be recovered by precipitation with Ca and Mg.

Development, Validation and Application of RP-HPLC Method: Simultaneous Determination of Antihistamine and Preservatives with Paracetamol in Liquid Formulations and Human Serum.

In this article we describe development and validation of stability indicating, accurate, specific, precise and simple Ion-pairing RP-HPLC method for simultaneous determination of paracetamol and cetirizine HCl along with preservatives i.e. propylparaben, and methylparaben in pharmaceutical dosage forms of oral solution and in serum. Acetonitrile: Buffer: Sulfuric Acid (45:55:0.3 v/v/v) was the mobile phase at flow rate 1.0 mL min(-1) using a Hibar(®) Lichrosorb(®) C18 column and monitored at wavelength of 230nm. The averages of absolute and relative recoveries were found to be 99.3%, 99.5%, 99.8% and 98.7% with correlation coefficient of 0.9977, 0.9998, 0.9984, and 0.9997 for cetirizine HCl, paracetamol, methylparaben and Propylparaben respectively. The limit of quantification and limit of detection were in range of 0.3 to 2.7 ng mL(-1) and 0.1 to 0.8 ng mL(-1) respectively. Under stress conditions of acidic, basic, oxidative, and thermal degradation, maximum degradation was observed in basic and oxidative stress where a significant impact was observed while all drugs were found almost stable in the other conditions. The developed method was validated in accordance with ICH and AOAC guidelines. The proposed method was successfully applied to quantify amount of paracetamol, cetirizine HCl and two most common microbial preservatives in bulk, dosage form and physiological fluid.