Thiosulfate impregnated spent tea leaves for the remarkable uptake of malachite green.

Herein we demonstrate an enhanced performance of acid-assisted thiosulfate-impregnated spent/waste tea leaves (TWTL) for the removal of malachite green (MG) from water by batch mode. The material was characterized by pHZPC, FTIR, powder XRD, SEM, and proximate analysis. FTIR suggests the presence of polyphenolic moieties whereas a lignocellulosic peak was observed in powder XRD. SEM image shows a grafted surface texture with intermittent blocks, which upon dye uptake becomes somewhat condensed. Under optimized conditions, the highest removal efficiency of 126.8 mg/g was achieved at pH 7. A fast adsorption process was noticed with >97% removal within the first 10 min. Adsorption follows pseudo-second-order kinetics (R2 = 0.999) and the Langmuir model (R2 = 0.999). The material can be regenerated by dilute hydrochloric acid and can be reused for up to four cycles. Treatment of industrial effluent was successful in up to 47.56%. Our results highlight the potential of thiosulfate-treated spent tea leaves as a choice for the efficient removal of malachite green from water.

Tea, being one of the most popular beverages produces huge waste which requires proper management. With this aim; the thiosulfate-impregnated spent tea leaves have been exercised for effective separation of malachite green from contaminated water. Thiosulfate impregnation under mildly acidic conditions activates the tea leaves and makes the material robust with enhanced water stability than its untreated variety. With a remarkable maximum adsorption capacity of 126.8 mg/g under ambient conditions, the present methodology enjoys the edge over related phytosorbents. The protocol is techno-economic, environment friendly, and could be extended to possible field applications.

Alkali treated water chestnut (Trapa natans L.) shells as a promising phytosorbent for malachite green removal from water.

Search for eco-friendly adsorbents for sustainable dye treatment is on the rise. The present study demonstrated the enhanced removal of malachite green (MG) with alkali-modified shells of water chestnut (AWCN) under optimized physio-chemical parameters. Alkali treatment significantly reduces the lignocellulosic components which in turn increased the water stability. The material was been characterized by pHzpc, FTIR, FESEM-EDAX, and BET surface area analysis. pH-dependent adsorption was noticed and the maximum adsorption capacity was determined as 136.46 mg/g. Adsorption followed pseudo-second-order kinetics (R2=0.99) and Langmuir isotherm model (R2=0.99). Thermodynamic parameters suggested that the adsorption process is spontaneous (ΔG°= -2.99 kJ/mol), favorable and endothermic (ΔH°=34.72 kJ/mol). Simple regeneration allows multi-cycle use with minimal loss of activity. The mechanism has been proposed to be a combination of electrostatic interaction, H-bonding, and π-π stacking between AWCN and MG. In conclusion, alkali modification of Trapa natans L. shells provides excellent removal of MG from water.

Waste shells of water chestnut (Trapa natans L.), a waterborne fruit have been modified using sodium hydroxide solution and tested for removal of malachite green by batch method. Excellent adsorption capacity (136.46 mg/g) was obtained under ambient conditions. As of now, very little work has been reported on water chestnut shells for the removal of dyes from wastewater. The present work shows an excellent adsorption capacity among all the previous work on water chestnut for dye remediation. Alkali activation significantly reduces hydrophilic/lignocellulosic components within the shells, which in turn makes the material more water stable and sustainable.

Alkali assisted hydrophobic reinforcement of coconut fiber for enhanced removal of cationic dyes: equilibrium, kinetics, and thermodynamic insight.

The present study illustrates enhanced removal of methylene blue (MB) and malachite green (MG) from water using alkali-activated coconut fiber (ACF) as adsorbent. Alkali activation effectively reduces the lignocellulosic components present within coco-fiber which in turn reinforces the coco-fiber to become more water-stable. The material was characterized by FTIR, SEM-EDS, BET, XRD, and pHZPC. BET surface area was found to be 10.901 m2 g-1, whereas pHZPC of the material is 6.05. FESEM images reveal rod-like morphology. Batch experiments were optimized with respect to contact time (0-120 min), temperature (288-308 K), pH (3-10), dose (1-5 g) and input dye concentration (10-50 mg L-1). The maximum adsorption coefficient was found to be 133.11 and 110.74 mg g-1 for MB and MG respectively. Adsorptions are best described by pseudo-second-order kinetics (kMB = 1.712, R2 = 0.999; kMG = 1.399, R2 = 0.999) and Langmuir isotherm model (R2 = 0.999). Thermodynamic data suggests a spontaneous (ΔG, -14 kJ mol-1) and feasible process. Spent material could be regenerated by using 0.5 M HCl. Up to 50% retention of activities was seen after five cycles. It can be concluded that alkali-activated coconut fiber is an economic and sustainable choice for dye removal. Novelty statement: Spent coconut was converted into an effective biosorbent by simple alkali activation under ambient conditions to increase the hydrophobicity of the fibers by reducing the lignocellulosic components. Two cationic dyes; methylene blue and malachite green have been efficiently removed with adsorption capacities of 133.11 and 110.74 mg g-1. The operation is simple, economically viable, and partially fulfills the principles of green engineering. Comparing with contemporary adsorbents, this material offers higher adsorption capacities with multi-cycle reusability and enhanced water stability.

Dewaxed Honeycomb as an Economic and Sustainable Scavenger for Malachite Green from Water.

Dewaxed honeycomb powder (HCP) was used as a promising adsorbent for removal of malachite green (MG) from aqueous solution. Raw honeycomb was strategically dewaxed by petroleum ether, and the purified product was characterized by Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), pHzpc, and proximate analysis. A high uptake capacity (123 mg/g) was found at neutral pH. Experimental data follow pseudo-second-order kinetics (k 2 as 0.45 × 10-2 g/min/mg, R 2 = 0.986) and Langmuir isotherm with R 2 0.999. Thermodynamic parameters suggested a spontaneous (ΔG = -26.28 kJ/mol) and exothermic (ΔH = -11.61 kJ/mol) process, which suggests increased randomness (ΔS = 0.0486 kJ/mol) at the solid-liquid interface during the adsorption process. The material can be regenerated by ordinary salt solution (1 M NaCl) and efficiently reused for three cycles with a minimal loss in efficiency. Adsorption mechanism is proposed to be a combination of electrostatic interaction and π-π stacking between aromatic units of HCP and MG. Abundant availability, possibility of wax commercialization, economic sustainability, and comprehensive waste management make HCP an ideal choice for dye decolorization.

Sucrose-Triggered, Self-Sustained Combustive Synthesis of Magnetic Nickel Oxide Nanoparticles and Efficient Removal of Malachite Green from Water.

Dye-containing industrial effluents create major concern nowadays. To address the problem, magnetic nickel oxide nanoparticles (NONPs) were synthesized using the autopropagator combustion technique assisted by sucrose as fuel and used for the removal of toxic malachite green (MG) from water. The material was characterized by scanning electron microscopy (SEM-EDS), Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), vibrating sample magnetism (VSM), point of zero charge (pHZPC), and Brunauer-Emmet-Teller surface area analysis. SEM images show flowerlike texture with the presence of multiple pores. VSM reveals a well-defined hysteresis at room temperature, confirming a permanent magnetic nature of the material. pHZPC was found to be 6.63, which enables dye separation in the drinking water pH range. MG removal from water was carried out in the batch mode with optimized physicochemical parameters such as contact time, pH, temperature, and dose. Langmuir adsorption capacity was estimated to be 87.72 mg/g. Pseudo-second order kinetics (R 2 = 0.999) and Langmuir isotherm model (R 2 = 0.997) were found to best fit. The magnetic nature facilitates fast and quantitative separation of NONPs from solution using a hand-held magnet. Dye-loaded NONPs can be easily regenerated up to 89% and reused up to five cycles without significant loss of activity. The mechanism of adsorption is proposed to be a combination of electrostatic attraction and weak hydrogen bonding. Strategically designed straightforward synthetic protocol, low cost, high uptake capacity, and sustainable use render NONPs an ideal alternative for future dye treatment.