Preparation and characterization of green bricks using pharmaceutical industrial wastes

This paper reports on recycling of industrial wastes (three pharmaceutical industrial sludges) into environmental friendly value-added materials. Stabilization/Solidification (S/S or bricks) process was applied to make a safer way for the utilization of pharmaceutical waste. The additives in this study include binders (cement, lime and bentonite) and strengthening material (pulverized fuel ash (PFA), silica fume and quarry dust) was used at different compositions. Bricks were cured for 28 days, and the following analysis-like compressive strength, leachability of heavy metals, mineralogical phase identity by X-ray diffraction (XRD) spectroscopy, Fourier transform infrared spectroscopy (FTIR) and thermal behaviour by thermogravimetric-differential thermal analysis (TG-DTA) had done. All the bricks were observed to achieve the standard compressive strength as required for construction according to BIS standards. Metal concentration in the leachate has reached the dischargeable limits according to Brazilian standards. Results of this study demonstrate that production of bricks is a promising and achievable productive use of pharmaceutical sludge.     

Bacopa phospholipid complex retrieves aluminum maltolate complex–induced oxidative stress and apoptotic alterations in the brain regions of albino rat

Environmental Science and Pollution Research - Highly bioavailable plant phospholipid complex that can reverse aluminum maltolate (AlM)–induced toxicity is not yet reported. Hence, the...     

Effect of operational parameters on heavy metal removal by electrocoagulation

In the present paper, the performance of electrocoagulation (EC) for the treatability of mixed metals (chromium (Cr), copper (Cu), lead (Pb), nickel (Ni), and zinc (Zn)) from metal plating industrial wastewater (EPW) has been investigated. The study mainly focused on the affecting parameters of EC process, such as electrode material, initial pH, distance between electrodes, electrode size, and applied voltage. The pH 8 is observed to be the best for metal removal. Fe–Fe electrode pair with 1-cm inter-electrode distance and electrode surface area of 40 cm² at an applied voltage of 8 V is observed to more efficient in the metal removal. Experiments have shown that the maximum removal percentage of the metals like Cr, Ni, Zn, Cu, and Pb are reported to be 96.2, 96.4, 99.9, 98, and 99.5 %, respectively, at a reaction time of 30 min. Under optimum conditions, the energy consumption is observed to be 51.40 kWh/m³. The method is observed to be very effective in the removal of metals from electroplating effluent.     

Techniques for the evaluation of maturity for composts of industrially contaminated lake sediments

Composting was applied as a bioremediation methodology for the reclamation of dredged sediments of Isnapur, Khazipally and Gandigudem lakes polluted with industrial wastes. The present study is an attempt to elaborate upon organic matter transformations and define the parameters for product maturity adapting chemical and spectroscopic methods during composting. The stability and maturity of sediments were evaluated by assessing parameters like C/N ratio, nitrification index (NH(4)-N/NO(3)-N), water-soluble organic carbon concentration, CO(2) evolution rate, cation exchange capacity and indices such as humification index, E4/E6 ratio, compost mineralization index (ash content/oxidizable carbon), germination index, dehydrogenase, polyphenoloxidase activities and FTIR spectroscopy. The results showed that the changes in the above chemical and biological parameters can be employed as reliable indicators of stability and maturity. The FTIR spectra revealed enrichment in the aromatic groups and a degradation of the aliphatic groups indicating stabilization of the final compost.     

Analysis of trace elements and ions in ambient fine particulate matter at three elementary schools in Ohio

The results from a chemical characterization study of fine particulate matter (PM2.5) measured at three elementary schools in Central and Southeast Ohio is presented here. PM2.5 aerosol samples were collected from outdoor monitors and indoor samplers at each monitoring location during the period of February 1, 1999, through August 31, 2000. The locations included a rural elementary school in Athens, OH, and two urban schools within Columbus, OH. The trace metal and ionic concentrations in the collected samples were analyzed using an X-ray fluorescence spectrophotometer and ion chromatography unit, respectively. Sulfate ion was found to be the largest component present in the samples at all three of the sites. Other abundant components included nitrate, chloride, ammonium, and sodium ions, as well as calcium, silicon, and iron. The average PM2.5 concentrations showed similar temporal variations among the three sites within the study region. PM2.5 and its major component, sulfate ion, showed strong seasonal variations with maximum concentrations observed during the summer at all three of the sites. The indoor environment was found to be more contaminated during the spring months (March through May) at New Albany (a suburb of Columbus, OH) and East Athens (rural Ohio area). Potential source contribution function analysis showed that particulate matter levels at the monitoring sites were affected by transport from adjoining urban areas and industrial complexes located along the Ohio River Valley. A preliminary outdoor source apportionment using the principal component analysis (PCA) technique was performed. The results from the PCA suggest that the study region was primarily impacted by industrial, fossil fuel combustion, and geological sources. The 2002 emissions inventory data for PM2.5 compiled by Ohio Environmental Protection Agency also showed impacts of similar source types, and this was used to validate the PCA analysis.