Application of zeolite-activated carbon macrocomposite for the adsorption of Acid Orange 7: isotherm, kinetic and thermodynamic studies

In this study, the adsorption behavior of azo dye Acid Orange 7 (AO7) from aqueous solution onto macrocomposite (MC) was investigated under various experimental conditions. The adsorbent, MC, which consists of a mixture of zeolite and activated carbon, was found to be effective in removing AO7. The MC were characterized by scanning electron microscopy (SEM), energy dispersive X-ray, point of zero charge, and Brunauer–Emmett–Teller surface area analysis. A series of experiments were performed via batch adsorption technique to examine the effect of the process variables, namely, contact time, initial dye concentration, and solution pH. The dye equilibrium adsorption was investigated, and the equilibrium data were fitted to Langmuir, Freundlich, and Tempkin isotherm models. The Langmuir isotherm model fits the equilibrium data better than the Freundlich isotherm model. For the kinetic study, pseudo-first-order, pseudo-second-order, and intraparticle diffusion model were used to fit the experimental data. The adsorption kinetic was found to be well described by the pseudo-second-order model. Thermodynamic analysis indicated that the adsorption process is a spontaneous and endothermic process. The SEM, Fourier transform infrared spectroscopy, ultraviolet–visible spectral and high performance liquid chromatography analysis were carried out before and after the adsorption process. For the phytotoxicity test, treated AO7 was found to be less toxic. Thus, the study indicated that MC has good potential use as an adsorbent for the removal of azo dye from aqueous solution.     

Estimating the Lower Heating Values of Hazardous and Solid Wastes

ABSTRACT

A new equation is proposed to predict the lower heating value of hazardous and non-hazardous materials. The equation was developed by a statistical correlation of heating value and composition data for a variety of materials as reported in a number of sources. The model takes into account the carbon, hydrogen, oxygen, chlorine, and sulfur content of the material being combusted.     

Estimation of Organic Carbon Blank Values and Error Structures of the Speciation Trends Network Data for Source Apportionment

Abstract

Because the particulate organic carbon (OC) concentrations reported in U.S. Environment Protection Agency Speciation Trends Network (STN) data were not blank corrected, the OC blank concentrations were estimated using the intercept in particulate matter ≤2.5 µm in aerodynamic diameter (PM_2.5) regression against OC concentrations. The estimated OC blank concentrations ranged from 1 to 2.4 μg/m³ showing higher values in urban areas for the 13 monitoring sites in the northeastern United States. In the STN data, several different samplers and analyzers are used, and various instruments show different method detection limit (MDL) values, as well as errors. A comprehensive set of error structures that would be used for numerous source apportionment studies of STN data was estimated by comparing a limited set of measured concentrations and their associated uncertainties. To examine the estimated error structures and investigate the appropriate MDL values, PM_2.5 samples collected at a STN site in Burlington, VT, were analyzed through the application of the positive matrix factorization. A total of 323 samples that were collected between December 2000 and December 2003 and 49 species based on several variable selection criteria were used, and eight sources were successfully identi?ed in this study with the estimated error structures and min values among different MDL values from the ?ve instruments: secondary sulfate aerosol (41%), secondary nitrate aerosol (20%), airborne soil (15%), gasoline vehicle emissions (7%), diesel emissions (7%), aged sea salt (4%), copper smelting (3%), and ferrous smelting (2%). Time series plots of contributions from airborne soil indicate that the highly elevated impacts from this source were likely caused primarily by dust storms.     

Naval derusting wastewater containing high concentration of iron, treated in UV photo-Fenton-like oxidation

The UV photooxidation with Fe(III) and H2O2 was employed to treat a naval derusting wastewater, which contains the high COD (chemical oxygen demand) and various metal concentrations exceptionally with high concentrations of citric acid and iron. Because of its iron containment, the Fenton-like reaction automatically took place with the added amount of H2O2. The decomposition rate was found in a sequence of: UV/H2O2/Fe(III) > UV/H2O2 > Fe(II)/H2O2. Two H2O2 injection methods, single and multiple points, were evaluated. The multiple-point H2O2 injection was more e cient to decompose the citric acid. The decomposition of the synthetic citric acid and the real derusting citric acid wastewater was also compared. The 93% COD reduction of the derusting wastewater was achieved using the UV/H2O2/Fe(III) treatment.     

改善微电网电能质量的分层控制策略研究

微电网技术具有许多优点,但分布式电源的不稳定性将导致微电网不易运行控制,对微电网的电能质量产生不利影响。针对此问题,提出了分层控制策略,以改善和提高微电网的电能质量。分层控制包含上下 2 层,通过上层将控制信息发送到下层实现。其中,初级控制采用下垂控制方法,提出了基于电压外环、电流内环和功率环的反馈控制器。二级控制(secondarycontrol)通过向初级控制(primary control)反馈二级控制后控制逆变器的输出电压幅值和频率,使之重新达到平衡,实现系统运行的稳定性。利用 Matlab/simulink 仿真结果表明:该分层控制策略对改善微电网电能质量是有效的。     

Single and mixture effects of pesticides and a degradation product on fluvial biofilms

The Morcille River located in the Beaujolais vineyard area (Eastern France) is subjected to strong vine-growing pressure leading to the contamination by a range of herbicides and fungicides of the surrounding freshwater environment. Particularly high concentrations of norflurazon, desmethyl norflurazon and tebuconazole were recorded in spring 2010 at the downstream site of the river. Despite their occurrence in rivers, scarce toxicity data are available for these products, in particular in the case of desmethyl norflurazon (main norflurazon degradation product). Furthermore, the toxicity data are generally available only for single compounds and are issued from single species toxicity tests, leading to a lack of ecological relevance. Consequently, this study was undertaken to evaluate the toxic effects of norflurazon, desmethyl norflurazon and tebuconazole singly and in a ternary mixture on fluvial biofilm. Toxicity tests were performed in microplates for 48 h. Photosynthetic endpoints were measured using pulse amplitude-modulated fluorometry; diatom densities and taxonomic composition were determined. After 48 h of exposure, significant effects on optimal quantum yield (F _v/F _m) for desmethyl norflurazon and mixture were observed.     

Diurnal vertical migration of Cochlodinium polykrikoides during the red tide in Korean coastal sea waters

The diurnal vertical migration of Cochlodinium polykrikoides (C. polykrikoides), which caused a red tide in the Korean coastal waters of the East Sea/Sea of Japan in September 2003, was examined by determining the time-dependent changes in the density of living cells in relation to the depth of the water column. The ascent of this species into the surface layer (depth of water 2 m) occurred during 1400-1500. The descent started at 1600 and a high distribution rate (86%) at 15-20 m was observed at 0300. During the ascent, the cells were widely distributed at each depth level from 0600 hr and at 0800-1100, the cells were primarily distributed in the middle layer (0-6 m). The concentration of dissolved inorganic nitrogen was generally < or = 2.86 micromol l(-1), but at 1400-1500, the concentration in the surface layer reduced to < or = 0.14 micromol l(-1). Moreover, the concentration gradually increased as the depth increased to > or = 5 m. These results showed that the nutrient-consumption rate associated with the proliferation of C. polykrikoides during a red tide is more influenced by the inorganic-nitrogen resources ratherthan the inorganic-phosphorus compounds.     

Synthesis and characterization of Fe-MCM-41 from rice husk silica by hydrothermal technique for arsenate adsorption

Rice husk (RH) agro-waste was used as a raw material for synthesizing mesoporous molecular sieves, MCM-41. The Fe-MCM-41 was prepared by the hydrothermal technique (HT), resulting in a higher surface area and crystallinity than when prepared under ambient conditions. In addition, a hexagonal structure was clearly seen with hydrothermal technique (HT) preparation. The adsorption of arsenate by HT-Fe-MCM-41 was investigated. The factors studied affecting arsenate adsorption capacity were ferric content in MCM-41, contact time, pH of solution, and initial arsenate concentration. It was found that HT-Fe-MCM-41 at the Si/Fe mole ratio of 10 gave the highest adsorption capacity. Arsenate adsorption reached equilibrium within 4 h. The adsorption capacity of HT-Fe-MCM-41 (Si/Fe = 10) was affected by the initial pH value and the initial arsenate concentration. The adsorption capacity was highest at pH 3 and decreased thereafter with increases in the pH of solution value. The Langmuir model fit the arsenate adsorption isotherm well. The maximum adsorption capacity for arsenate was 1,111 μg g⁻¹.     

The role of Acidithiobacillus ferrooxidans and Acidithiobacillus thiooxidans in arsenic bioleaching from soil

Bioleaching of As from the soil in an abandoned Ag–Au mine was carried out using Acidithiobacillus ferrooxidans and Acidithiobacillus thiooxidans. A. ferrooxidans is an iron oxidizer and A. thiooxidans is a sulfur oxidizer. These two microbes are acidophilic and chemoautotrophic microbes. Soil samples were collected from the Myoungbong and Songcheon mines. The main contaminant of the soil was As, with an average concentration of 4,624 mg/kg at Myoungbong and 5,590 mg/kg at Songcheon. A. ferrooxidans and A. thiooxidans generated lower pH conditions during their metabolism process. The bioleaching of As from soil has a higher removal efficiency than chemical leaching. A. ferrooxidans could remove 70 % of the As from the Myoungbong and Songcheon soils; however, A. thiooxidans extracted only 40 % of the As from the Myoungbong soil. This study shows that bioleaching is an effective process for As removal from soil.