Adsorptive features of banana (Musa paradisiaca) stalk-based activated carbon for malachite green dye removal

Chemically prepared activated carbon derived from banana stalk (BSAC) was used as an adsorbent to remove malachite green (MG) dye from aqueous solution. BSAC was characterised using thermogravimetric analyser, Brunauer Emmett Teller, Fourier transform infrared spectrometry, scanning electron microscopy, pH_pzc, elemental analysis and Boehm titration. The effectiveness of BSAC in adsorbing MG dye was studied as a function of pH, contact time, temperature, initial dye concentration and repeated desorption–adsorption processes. pH_pzc of BSAC was 4.5 and maximum dye adsorption occurred at pH 8.0. The rate of dye adsorption by BSAC was very fast initially, attaining equilibrium within 120 min following a pseudo-second-order kinetic model. Experimental data were analysed by Langmuir, Freundlich and Dubinin–Raduschevich isotherms. Equilibrium data fitted best into the Langmuir model, with a maximum adsorption capacity of 141.76 mg·g^?1. Δ G ⁰ values were negative, indicating that the process of MG dye adsorption onto BSAC was spontaneous. The positive values of Δ H ⁰ and Δ S ⁰ suggests that the process of dye adsorption was endothermic. The regeneration efficiency of spent BSAC was studied using 0.5 M HCl, and was found to be in the range of 90.22–95.16% after four cycles. This adsorbent was found to be both effective and viable for the removal of MG dye from aqueous solution.     

Accumulation and elimination of cadmium and lead in juvenile milkfish during sublethal exposure

Pollution of aquatic environments by trace metals is a worldwide environmental problem. Metal pollutants are increasingly being released into the environment as a result of industrialization. In this study, the bioaccumulation of cadmium and lead in young juvenile milkfish liver (Chanos chanos) was investigated after exposure to three sublethal concentration of each pollutants (1/20, 1/10, and 1/5 LC₅₀ of 96-h LC₅₀) for acute time 12, 24, and 96 h and subchronically for 7, 14, and 21 days. Cadmium and lead accumulation in liver increased with the exposure period and concentrations of pollutant. Compared to controls, the uptake of cadmium is much higher than that of lead. Accumulation factors showed an increase with exposure time and for lead an inverse relationship between accumulation factor and exposure concentration. The elimination of the two pollutants during the 30 days depuration was investigated after 30 days depuration time. During this phase, cadmium and lead concentrations decreased.     

Clean electrochemical deposition of calcium carbonate to prevent scale formation in cooling water systems

Calcium carbonate (CaCO₃) deposited in water systems leads to scale formation, decreases flow rate, reduces heat transfer and favors microbial proliferation of toxic bacteria such as Legionella. This issue may be solved by electrochemical deposition, without adding toxic chemicals. Therefore, we studied here the deposition of CaCO₃ by electrochemical reduction of oxygen into hydroxide ions with stainless steel and titanium (Ti) working electrodes. Analysis was done using cyclic voltammetry, chronoamperometry, dynamic impedance spectroscopy, scanning electron microscopy, and energy-dispersive X-ray spectroscopy (EDX) coupled with X-ray diffraction (XRD). Results show that optimal formation of CaCO₃ is done at ?1.2 V with the stainless steel electrode and at ?1.4 V for the Ti electrode. More negative potentials induce the formation of calcite. Using the Ti electrode, we found that aragonite is the major form (82 %), with only one capacitive loop. Using the stainless steel electrode at 1.2 V, we found 47 % of aragonite and 38 % of calcite. Overall, our findings demonstrate the feasibility of the electrochemical deposition of CaCO₃ in cooling water systems, without the addition of any chemical.     

Remediation rates and translocation of heavy metals from contaminated soil through Parthenium hysterophorus

The potential translocation of heavy metals by Parthenium hysterophorus over 30 and 90 days and its effect on biomass, chlorophyll content and photosynthetic activity were studied on 0, 10, 25, 50 and 100% fly-ash-amended soil (FAS). The results showed a decrease in chlorophyll content and photosynthetic area on exposure to 50–100% FAS. Heavy metal reduction was in the order Pb>Cd>Zn>Fe>according to accumulation trends. The plant exhibited good biomass growth on exposure to 25–50% FAS, but this decreased at>100% FAS. Heavy metal concentrations in P. hysterophorus after 90 days of the experiment were in the order Fe>Zn>Cu>Pb>Cd>Ni. Parthenium hysterophorus was suitable for translocating Fe, Zn and Cu based on translocation factors (TF=1.5, 1.3 and 1.05), but was more efficient for Pb, Ni and Cd (TF=8.5, 4.3 and 3.3). Plant uptake of Pb, Ni and Cd was high, whereas translocation of Fe, Zn and Cu was poor. These results indicated that P. hysterophorus can efficiently reduce heavy metal pollution in soil.     

Removing ammonia from air with a constant pH,slightly acidic water spray wet scrubber using recycled scrubbing solution

Slightly acidic solutions are a practical means of removing ammonia from air Scrubbed NH₃ accumulates in solution as NH₄⁺ and should be an excellent fertilizer Increased air velocity decreased NH₃ removal and increased NH₄⁺ collection Previous research on wet scrubbers has only studied highly acidic scrubbing solutions because of their high ammonia capture efficiencies; however, the high acidity created practical problems. Lower acidity solutions would reduce corrosion, maintenance, and cost; however, designers may need to use strategies for increasing scrubber effectiveness, such as using lower air velocities. The objective of this study was to determine if a spray scrubber with slightly acidic and higher pH scrubbing solution (pH from 2 to 8) could effectively remove NH₃ from NH₃ laden air (such as animal building exhaust air), and also collect this valuable resource for later use as a fertilizer. A bench-scale spray wet scrubber treated 20 ppmv NH₃/air mixture in a countercurrent contact chamber. First, the solution pH was varied from 2 to 8 while maintaining constant air velocity at 1.3 m·s⁻¹. Next, air velocity was increased (2 and 3 m·s⁻¹) while solution pH remained constant at pH6. At 1.3 m·s⁻¹, NH₃ removal efficiencies ranged between 49.0% (pH8) and 84.3% (pH2). This study has shown that slightly acidic scrubbing solutions are a practical means of removing ammonia from air especially if the scrubber is designed to increase collisions between solution droplets and NH₃ molecules. The NH₃ removed from the air was held in solution as NH₄⁺ and accumulates over time so the solution should be an excellent fertilizer.     

Enhancing transverse mixing in streams with submerged vanes

In order to maintain the water quality of moving streams, it is essential to know the process of pollutant mixing. The transverse mixing is very important which is needed to be modeled to understand mixing phenomenon. It was observed that transverse mixing is a strong function of secondary currents, thus, submerged vanes, which are aerofoil skewed at angle of 10°–40° with respect to flow, generate transverse circulations that can be utilized to induce secondary currents in the flow to enhance transverse mixing. Present study is an attempt to utilize submerged vanes as an instrument to enhance the transverse mixing by incorporating various vane configurations. In order to study the effect of vane generated circulations on transverse mixing, experimentations were conducted on three vane sizes and for various row arrangements of vanes attached to bed. An attempt is made to investigate the effect of submerged vane size and rows on transverse velocity, concentration profile and transverse mixing coefficient. It was observed by measurement of concentration profile that transverse mixing was more enhanced for submerged vanes of higher height. It was also observed that as the number of rows is proportional to the transverse mixing. By measuring the transverse velocity profile, it was observed that more and more fluid was advected in transverse direction for higher rows of vanes. By utilizing the observed transverse mixing coefficients, number of vane rows and relative height of vane, a predictor was derived to predict transverse mixing coefficient in the presence of submerged vane rows. It was observed that the derived predictor shows a fair amount of agreement in the result predicted.     

Occurrence,abundance, and distribution of microplastics pollution: an evidence in surface tropical water of Klang River estuary,Malaysia

Environmental Geochemistry and Health - Microplastics have been considered as contaminants of emerging concern due to ubiquity in the environment; however, the occurrence of microplastics in river...     

Faecal and nitrate contamination in the groundwater of Mardan district,Pakistan

Environmental Geochemistry and Health - This study aimed to determine the status of groundwater contamination with faecal coliform and nitrate in the rural areas of Mardan district, Pakistan. Both...     

Effects of methionine sulfoximine on growth and nitrogen assimilation of the marine microalga Chlorella autotrophica

Chlorella autotrophica Shihira and Krauss (clone 580), a euryhaline microalga from the marine coastal environment is subject to large fluctuations in external salinity and nitrogen supply. The alga exhibits maximum growth at salinities lower than 100% ASW (artificial seawater). Cells divide faster and show higher cell yields when the supply of either NH ₄ ⁺ or NO ₃ ^- is increased above 0.2 mM. Cells growing on NH ₄ ⁺ show high levels of NADPH-glutamate dehydrogenase (GDH) activity, and the levels of glutamine synthetase (GS) are decreased to very low levels under these conditions. Methionine sulfoximine (MSX), an inhibitor of GS, has little effect on cell division and nitrogen assimilation of cells growing on NH ₄ ⁺ . Cells growing on NO ₃ ^- , however, show marked inhibition (65%) in nitrogen assimilation in the presence of 5 mM MSX. This MSX concentration also causes growth retardation and a progressive decrease in cell protein and nitrogen content. GS is almost completely inhibited by 5 mM MSX in both NH ₄ ⁺ and NO ₃ ^- -grown cells. Cells growing on NH ₄ ⁺ maintain high levels of NADPH-GDH activity in the presence of MSX. NADPH-GDH activity in MSX-treated NO ₃ ^- -grown cells increases, and, in the presence of 5 mM MSX, reaches 40% of the level found in NH ₄ ⁺ -grown cells. These results are consistent with NADPH-GDH providing an alternate pathway for NH ₄ ⁺ assimilation by this marine Chlorella species.