Biocomposite based electrode for effective removal of Cr (VI) heavy metal via capacitive deionization

Abstract

This study focuses on the fabrication of biocomposite electrode and removal of Cr (VI) ions from wastewater using a capacitive deionization (CDI) method. The activated carbon (AC) was synthesized from Bael fruit shell (BS). The synthesized AC surface has a macroporous and mesoporous structure with the large specific surface area (617.72?m² g^?1) and high adsorption capacity. The cyclic voltammetry and CDI were performed for the detection and for the removal of chromium (VI) ions, respectively. The lower level of detection of Cr (VI) by a modified electrode was found to be 10 ppt. SEM, BET, and FTIR analyses were performed to explore the surface properties of electrode materials. The removal efficiency was achieved 100% by using biocomposite electrode with an applied potential of 15?V. The highest percent removal mechanism consists of electrosorption and electroreduction due to the affinity between polyvinyl alcohol modified electrode and Cr (VI) ions, under electrochemically faradic process.     

Improvement of tea leaves fermentation with Aspergillus spp. pectinase

The pectinase enzymes isolated from Aspergillus spp., A. indicus, A. flavus and A. niveus were used for fermentation of tea leaves. The enzymes were purified and characterized. The effect of both crude enzyme preparation and purified pectinase enzymes on the improvement of tea leaf fermentation were determined in terms of theaflavin, thearubigin, high polymerized substances, total liquor colour, dry matter content and total soluble solids of the tea produced. The crude enzyme preparations obtained from ethanol precipitation were found to be more effective in improving tea leaf fermentation than the purified pectinase enzymes.     

Long‐term impact of nitrogen and potassium fertilizers on yield,soil nutrients and biochemical parameters of tea

A field experiment was conducted with tea cultivar UPASI‐9 over a period of 9 years to evaluate the long‐term effects of nitrogen (N) and potassium (K) fertilizers on yield, biochemical parameters, soil and leaf nutrient status. The yield increase was as high as 66% over the control for N application of 450 kg ha^?1 year^?1. Polyphenol and amino acid contents increased with increase in K application rate. Positive and significant correlation was found between nitrate reductase activity and the amino acid content of the tea shoots. While ammoniacal nitrogen in the soil was not affected by the application of fertilizer, ammonium acetate extractable K increased. The failure to apply fertilizer resulted in depletion of the organic matter status of the soil. Although increased rate of nitrogen application increased the overall yield of made tea (kg ha^?1 year^?1), the specific yield (kg kg^?1 N) declined. The soil tended to become acidic from frequent application of high doses of nitrogenous fertilizer. The leaf NK status was significantly influenced by the various treatments. Copyright © 2004 Society of Chemical Industry     

The experimental study on the performance,combustion and emission characteristics of a diesel engine using diesel – biodiesel – diethyl ether blends

ABSTRACT

In the present research work, the experimental analysis has been executed to investigate the influence of diethyl ether as an oxygenated additive to the diesel-biodiesel blend on the performance, combustion and emission characteristics of a diesel engine. The biodiesel (Frying oil methyl ester) was prepared by the transesterification process, and the biodiesel was added (40% by volume) to the diesel fuel to prepare the diesel-biodiesel blend (D60FME40). The diethyl ether was added to the diesel-biodiesel blends D60FM35 (diesel 60% + biodiesel 35% by volume) and D60FM30 (diesel 60% + biodiesel 30% by volume) with suitable volume proportions of 5% and 10% respectively to form diesel-biodiesel-diethyl ether blends ((D60FM35DEE5) & (D60FM30DEE10)). Initially, the test was conducted with diesel fuel to obtain the baseline reference reading. Then, the reading was compared with results taken from the engine using a diesel-biodiesel blend (D60FME40) and diethyl ether blends (D60FM35DEE5) & (D60FM30DEE10). The results reveal that the maximum brake thermal efficiency was obtained with diesel fuel and it was higher than the diesel-biodiesel blend and diethyl ether blends. The peak in-cylinder gas pressure and heat release rate in the premixed stage was less for the diesel-biodiesel blend, but it was increased with the addition of diethyl ether to the blend. The diesel-biodiesel-diethyl ether blends show less carbon monoxide and hydrocarbon emissions except for NO_X emission as compared to the diesel and diesel-biodiesel blend, especially at the engine rated power.     

Superhigh selective capture of volatile organic compounds exploiting cigarette butts-derived engineering carbonaceous adsorbent

Herein, we develop cost-efficient superhigh-performance of engineering carbonaceous adsorbent from cigarette butts using combined wet-impregnated and re-dispersed method of KOH, which optimizes the implant approach of activator, breaking the restriction of selective capture of toluene using traditional activated carbon. The Brunauer-Emmett-Teller (BET) surface area and pore volume of targeted adsorbent can attain 3088 m²·g^-1 and 1.61 cm³·g^-1, respectively, by optimizing the temperature-dependent synthetic factor effect of the adsorbent. The adsorption capacity of resultant adsorbent for presenting volatile benzene and toluene shows a positive correlation with increasing carbonization temperature of carbon precursor. Besides, we demonstrated the unsmoked and smoked butts derived adsorbents afford feeble difference in saturated adsorbed capacity of volatile organic compounds (VOCs). The highest adsorption capacity of sample CF-800 for benzene and toluene in CF group is as high as 1268.1 and 1181.6 mg·g^-1 respectively, slightly higher than that of sample UF-800, but far outperforming reported other adsorbents. The predicted adsorption selectivity of CF-800 and UF-800 for C₇H₈/H₂O (g) using the DIH (difference of isosteric heats) equation reach up to ca. 3800 and 7500 respectively, indicating the weak adsorbability of water vapor on the developed adsorbent and greater superiority of the smoked butts derived adsorbents in selective capture of VOCs at low relative humidity in the competitive adsorption process for practical mixed VOCs.     

Enhanced transformation of triclosan by laccase in the presence of redox mediators

Triclosan (TCS), an antimicrobial agent, is an emerging and persistent environmental pollutant that is often found as a contaminant in surface waters and sediments; hence, knowledge of its degradability is important. In this study we investigated laccase-mediated TCS transformation and detoxification, using laccase (from the fungus Ganoderma lucidum) in the presence and absence of redox mediators. Transformation products were identified using HPLC, ESI-MS and GC-MS, and transformation mechanisms were proposed. In the absence of redox mediator, 56.5% TCS removal was observed within 24 h, concomitant with formation of new products with molecular weights greater than that of TCS. These products were dimers and trimers of TCS, as confirmed by ESI-MS analysis. Among the various mediators tested, 1-hydroxybenzotriazole (HBT) and syringaldehyde (SYD) significantly enhanced TCS transformation (∼90%). The presence of these mediators resulted in products with lower molecular weights than TCS, including 2,4-dichlorophenol (2,4-DCP; confirmed by GC-MS) and dechlorinated forms of 2,4-DCP. When SYD was used as the mediator, dechlorination resulted in 2-chlorohydroquinone (2-CHQ). Bacterial growth inhibition studies revealed that laccase-mediated transformation of TCS effectively decreased its toxicity, with ultimate conversion to less toxic or nontoxic products. Our results confirmed the involvement of two mechanisms of laccase-catalyzed TCS removal: (i) oligomerization in the absence of redox mediators, and (ii) ether bond cleavage followed by dechlorination in the presence of redox mediators. These results suggest that laccase in combination with natural redox mediator systems may be a useful strategy for the detoxification and elimination of TCS from aqueous systems.     

Interfacial area and mass transfer coefficients in liquid-gas ejectors

Measurements and correlations are reported for the interfacial area and mass transfer coefficients as a function of energy dissipation in a liquid-gas ejector. The correlations for interfacial area and mass transfer coefficients have been developed using Kolmogorov’s theory and Levich’s hydrodynamic derivations. The present developed correlations are validated using experimental results.     

An optimization study on microwave irradiated decomposition of phenol in the presence of H2O2

BACKGROUND Removal of phenol from industrial waste waters involves basic techniques namely extraction, biodegradation, photocatalytic degradation, etc. Among the available processes, the oxidation of phenols using H₂O₂ is a suitable alternative because of low cost and high oxidizing power. The application of an oxidation process for the decomposition of stable organic compounds in waste water leads to the total degradation of the compounds rather than transferring from one form to another. Since oxidation using Fenton's reagent is more dependent on pH, in this present work it was proposed to use H₂O₂ coupled with microwave irradiation. The effects of initial phenol concentration, microwave power and the irradiation time on the amount of decomposition were studied. RESULTS: In the present work experiments were conducted to estimate the percentage degradation of phenol for different initial concentrations of phenol (100, 200, 300, 400 and 500 mg L^?1), microwave power input (180, 360, 540, 720 and 900 W) for different irradiation times. The kinetics of the degradation process were examined through experimental data and the decomposition rate follows first‐order kinetics. Response surface methodology (RSM) was employed to optimize the design parameters for the present process. The interaction effect between the variables and the effect of interaction on to the responses (percentage decomposition of phenol) of the process was analysed and discussed in detail. The optimum values for the design parameters of the process were evaluated (initial phenol concentration 300 mg L^?1, microwave power output 668 W, and microwave irradiation time 60 s, giving phenol degradation 82.39%) through RSM by differential approximation, and were confirmed by experiment. CONCLUSION: The decomposition of phenol was carried out using H₂O₂ coupled with microwave irradiation for different initial phenol concentrations, microwave power input and irradiation times. The phenol degradation process follows first‐order kinetics. Optimization of the process was carried out through RSM by forming a design matrix using CCD. The optimized conditions were validated using experiments. The information is of value for the scale up of the oxidation process for the removal of phenol from wastewater. Copyright © 2008 Society of Chemical Industry     

Experimental study on productivity enhancement of an improvised inclined solar still

Experimental studies are carried out on the inclined solar still with baffle plates for enhancing its performance. The baffles placed in the inclined solar still act as a solar collector which helps in increasing the contact time with solar radiation thereby raising the saline water temperature. Experiments are carried out during winter and early summer climate of Chennai, India. Experimental parameters, such as ambient temperature, solar radiation, glass temperature, water temperature and distillate output are recorded. Hourly productivity is found to be higher during sunny days. The estimated production of fresh water through analytical study is 3.50?kg/m² per day for a minimum mass flow rate of 0.0833?kg/min. The actual experimental yield is 2.793?kg/m² per day. Also, the inlet saline water temperature affects the yield and the latter is found to be highest at 48.5°C.