RESUMEN
The frequent use of an industrial dye such as malachite green (MG) has caused major water body deterioration and is one of the most pressing global challenges, demanding effective treatment techniques. To solve these issues, a simplistic method was developed to synthesize zinc-tungstate (ZnWO4) nanoparticles and also dope the surface matrix of the ZnWO4 nanoparticles using nonmetals of boron (B), carbon (C), and nitrogen (N) at different ratios for enhanced MG removal from wastewater. The prepared nanomaterials were characterized by different methods for crystal structure composition, surface properties, surface morphology, microstructures, functional groups, and elemental oxidation states. The BET analysis revealed a mesoporous structure with surface areas of 30.740 m2/g for ZnWO4, 38.513 m2/g for ZnWO4@BCN, 37.368 m2/g for ZnWO4@BCN/B, 39.325 m2/g for ZnWO4@BCN/C, and 45.436 m2/g for ZnWO4@BCN/N nanocomposites. The best removal of MG was accomplished at pH (8), contact period (50 min), nanoadsorbent dose (0.8 g/L), initial MG concentration (20 mg/L), and temperature (303 K). The maximum adsorption capacities of ZnWO4 and ZnWO4@BCN/N towards MG were 218.645 and 251.758 mg/g, respectively. At equilibrium, the Freundlich isotherm and pseudo-second-order kinetic models were the best fits for the experimental data of MG adsorption on both nanoadsorbents. After eight cycles of adsorption and desorption, both ZnWO4 and ZnWO4@BCN/N were found to be good at removing MG, with efficiencies of 71.00 and 74.20%, respectively. Thermodynamic investigations further validated the spontaneity and endothermic nature of the adsorption process. All study findings confirm the nanoadsorbents exceptional capability and economic feasibility for removing MG dye.
RESUMEN
Herein, magnetite nanoparticles (NPs), zeolite A and magnetite-zeolite A (MAGZA) composite was developed by green methods. The produced nanomaterials were characterized and the effect of process parameters such as flow rate, adsorbent bed height and adsorbate inlet concentration was evaluated for the removal of biological oxygen demand (BOD), chemical oxygen demand (COD) and total organic carbon (TOC) in a column. The characterization results demonstrated the successful synthesis of magnetite NPs, zeolite A and MAGZA composite. The performance of the MAGZA composite in the fixed-bed column was superior to zeolite A and magnetite NPs. The parametric influence indicates that an increase in bed height and a decrease in the flow rate and inlet adsorbate concentration improved the performance of the adsorption column. The adsorption column demonstrated maximum performance at a flow rate (4 mL/min), bed height (5 cm) and inlet adsorbate concentration (10 mg/L). Under these conditions, the highest percent removal of BOD, COD and TOC were 99.96, 99.88 and 99.87%. Thomas and Yoon-Nelson's model suitably fitted the breakthrough curves. After five reusability cycles, the MAGZA composite demonstrated removal percent of BOD (76.5%), COD (55.5%) and TOC (64.2%). The produced MAGZA composite effectively removed BOD, COD and TOC from textile wastewater in a continuous operating mode.
RESUMEN
Nickel nanoparticles (NiNPs) supported on activated multi-walled carbon nanotubes (MWCNTs) were used as an adsorbent applied towards Pb(II), As(V) and Cd(II) remediation from industrial wastewater. The result revealed the hydrophilic surface of MWCNTs-KOH was enhanced with the incorporation of NiNPs enabling higher surface area, functional groups and pore distribution. Comparatively, the removal of Pb(II), As(V) and Cd(II) on the various adsorbents was reported as NiNPs (58.6 ± 4.1, 46.8 ± 3.7 and 40.5 ± 2.5%), MWCNTs-KOH (68.4 ± 5.0, 65.5 ± 4.2 and 50.7 ± 3.4%) and MWCNTs-KOH@NiNPs (91.2 ± 8.7, 88.5 ± 6.5 and 80.6 ± 5.8%). Using MWCNTs-KOH@NiNPs, the maximum adsorption capacities of 481.0, 440.9 and 415.8 mg/g were obtained for Pb(II), As(V) and Cd(II), respectively. The experimental data were best suited to the Langmuir isotherm and pseudo-second order kinetic model. The fitness of experimental data to the kinetic models in a fixed-bed showed better fitness to Thomas model. The mechanism of metal ion adsorption onto MWCNTs-KOH@NiNPs show a proposed electrostatic attraction, surface adsorption, ion exchange, and pore diffusion due to the incorporated NiNPs. The nanocomposite was highly efficient for 8 adsorption cycles. The results of this study indicate that the synthesized nanocomposite is highly active with capacity for extended use in wastewater treatment.
Asunto(s)
Arsénico , Nanopartículas , Nanotubos de Carbono , Contaminantes Químicos del Agua , Adsorción , Cadmio , Cinética , Plomo , Níquel , Aguas Residuales , Contaminantes Químicos del Agua/análisisRESUMEN
The efficient removal of toxic metals ions from chemical industry wastewater is considered problematic due to the existence of pollutants as mixtures in the aqueous matrix, thus development of advanced and effective treatment method has been identified as a panacea to the lingering problems of heavy metal pollution. In this study, KIAgNPs decorated MWCNTs nano adsorbent was developed using combination of green chemistry protocol and chemical vapor deposition techniques and subsequently characterized using UV-Vis, HRTEM, HRSEM, XRD, FTIR and XPS. The adsorptive efficiency of MWCNTs-KIAgNPs for the removal of Cr(VI), Ni(II), Fe(II), Cd(II) and physico-chemical parameters like pH, TDS, COD, BOD, nitrates, sulphates, chlorides and phosphates from chemical industrial wastewater was examined in both batch and fixed bed systems. The result exhibited successful deposition of KIAgNPs on the surface of MWCNTs as confirmed by the microstructures, morphology, crystalline nature, functional groups and elemental characteristics of the MWCNTs-KIAgNPs. Optimum batch adsorption parameters include; pH (3 for Cr(VI) and 6 for Ni(II), Fe(II) and Cd(II) ions), contact time (60 min), adsorbent dosage (40 mg) and temperature (318 K). The binding capacities were obtained as follows; Cr6+ (229.540 mg/g), Ni2+ (174.784 mg/g), Fe2+ (149.552) and Cd2+ (121.026 mg/g), respectively. Langmuir isotherm and pseudo-second order kinetic model best described the experimental data in batch adsorption, while the thermodynamic parameters validated the chemisorption and endothermic nature of the adsorption process. In continuous adsorption, the metal ions were effectively removed at low metal influent concentration, low flow rate and high bed depth, whereby the experimental data were designated by Thomas model. The high physico-chemical parameters in the wastewater were successfully treated in both batch and fixed bed systems to fall within WHO permissible concentrations. The adsorption/desorption study illustrated over 80% metal removal by MWCNTs-KIAgNPs even after 8th adsorption cycle. This study demonstrated excellent performance of MWCNTs-KIAgNPs for chemical industry wastewater treatment.
RESUMEN
Herein, Taguchi L9 orthogonal array was used for the first time to optimize synthesis of diameter-controlled multi walled carbon nanotubes (MWCNTs). The nanoadsorbents, MWCNTs5-15 nm and MWCNTs16-25 nm were applied for Pb(II) and Ni(II) ion removal from paint, battery and electroplating wastewater. The results indicated successful synthesis of MWCNTs with diameter distribution ranges of 5-15 nm and 16-25 nm. The synthetized smaller diameter MWCNTs5-15 nm revealed higher Brunauer-Emett-Teller (BET) surface area of 1306 ± 5 m2/g compared to larger diameter MWCNTs16-25 nmwith the surface area of 1245 ± 4 m2/g. They demonstrated excellent adsorption of Pb(II) and Ni(II) ions within the permissible concentration proposed by WHO at pH, contact time, adsorbent dosage and temperature of 5, 60 min, 30 mg/L and 50 °C, respectively. Particularly, MWCNTs5-15 nm possessed high adsorption capacity of 215.38 ± 0.03 mg/g for Pb(II) and 230.78 ± 0.01 mg/g for Ni(II). Again, the maximum adsorption capacity of 201.35 ± 0.02 and 206.40 ± 0.02 mg/g was achieved for Pb(II) and Ni(II) using MWCNTs16-25 nm. All in all, the adsorption capacity of the nanoadsorbents at the investigated diameter range showed higher efficiency compared to other materials for heavy metals elimination from chemical industrial wastewater.
Asunto(s)
Nanotubos de Carbono , Contaminantes Químicos del Agua , Adsorción , Industria Química , Concentración de Iones de Hidrógeno , Cinética , Plomo , Aguas Residuales , Contaminantes Químicos del Agua/análisisRESUMEN
This research is motivated by the desire to restore the quality of life to amputees. The study uses multi-walled carbon nanotube (WMCNT) reinforced natural rubber (NR) polymer nanocomposite (PNC) for prosthetic foot application. The compound formulation was carried out in accordance to a modified procedure described by Hemkaew et al. Mixing of the ingredients during vulcanisation was performed according to ASTM D-3182 standard on an open two-roll mill. The various compositions of the nanocomposites (NCs) were cured at a temperature of 150 ± 2 °C and a pressure of 0.2 MPa for 10 minutes in an electrically heated hydraulic press. Mechanical investigation revealed that NR/MWCNT-3 exhibited the highest capacity to withstand tensile and dynamic loading (449.79 MPa). It also showed superior filler distribution and hence improved crystallinity and cross-link. Water absorption test indicated that NR/MWCNT-3 offers optimum dimensional stability at ambient conditions. Moreover, thermogravimetric analysis/differential thermogravimetry (TGA/DTG) showed degradation peaks at 305 °C and 290 °C respectively with temperature range within which the NCs degraded lying between 250 °C and 600 °C. Dynamic mechanical analysis (DMA) revealed that filler incorporation results in higher storage and loss moduli (2000-7500 MPa and 500-1413 MPa respectively). Tan δ curves proved that NR/MWCNT-3 has the highest capacity to dissipate energy through segmental motion. Furthermore, microstructure examination confirmed good filler/matrix adhesion as NR/MWCNT-3 indicated improved interaction; hence higher strength (6.02 MPa) of the NC. Better wear resistance ability can also be reported of the newly developed than existing prosthetic material. It can be deduced that the formulated nanocomposite from MWCNTs for reinforced natural rubber is suitable for the development of the anthropomorphic prosthetic foot.
RESUMEN
In this work, Ag2O/B2O3/TiO2 ternary nanocomposite was synthesized by a combination of green and precipitation method involving mixing of different concentrations of silver nitrate, boric acid, and titanium (IV) isopropoxide precursor with Plumeria acuminate leaf extract. The extract was obtained by boiling the mixture of distilled water and the powdered leaves in a beaker for few minutes followed by filtration. The microstructure, morphology, chemical composition, surface area, phase structure, and optical properties of the various prepared nanomaterials were determined by HRTEM, HRSEM, UV-Vis/DRS, BET, XRD, and XPS. The photocatalytic potential of TiO2 nanoparticles and Ag2O/B2O3/TiO2 nanocomposites to degrade local dyeing wastewater under artificial and natural sunlight irradiation was investigated. The extent of degradation of the organic pollutants was measured using chemical oxygen demand (COD) and total organic carbon (TOC) as indicator parameters. The XRD pattern of Ag2O/B2O3/TiO2 nanocomposites revealed that the formation of pure anatase TiO2 phase and the addition of both silver and boron precursors did not influenced the phase structure of the nanocomposites. The oxidation states of +1 and +3 for both Ag and B on the surface of Ag2O/B2O3/TiO2 nanocomposites were confirmed by XPS. Optical characterization of the sample revealed reduction of band gap energy from 2.6 to 2.0 eV for TiO2 and Ag2O/B2O3/TiO2, respectively. The Ag2O/B2O3/TiO2 nanocomposites demonstrated excellent photocatalytic activity under natural sunlight and artificial light than mono and binary oxide systems with TOC and COD degradation efficiencies of 86.11% and 75.69%, respectively. The kinetics of degradation of organic dyes in the wastewater followed the order of Langmuir-Hinshelwood pseudo-first-order > Freundlich > Zero > Parabolic diffusion model. The coupling effect of Ag2O and B2O3 onto TiO2 framework was responsible for the enhanced photochemical stability of the nanocomposites even after five repeated cycles.
Asunto(s)
Nanocompuestos/química , Fotólisis , Luz Solar , Aguas Residuales/química , Contaminación Química del Agua/prevención & control , Colorantes/análisis , Cinética , Contaminantes Químicos del Agua/análisisRESUMEN
This research investigated the removal of heavy metals (As, Pb, Cr, Cd, Ni, Cu, Fe, and Zn) via batch adsorption process from industrial electroplating wastewater using two different nano-adsorbents; purified carbon nanotubes (P-CNTs) and polyhydroxylbutyrate functionalized carbon nanotubes (PHB-CNTs), both produced through catalytic chemical vapour deposition (CCVD) method. HRSEM, HRTEM, XRD, DLS, BET, FTIR, XPS, TGA, pH drift and Raman spectroscopy were used to characterize the developed nano-adsorbents. In the batch adsorption process, the effects of contact time, dosage, temperature and pH were studied. Both nano-adsorbents gave optimum contact time, equilibrium time, optimum dosage, and pH of 10 minutes, 70 minutes, 20 mg, and 5.63-5.65 respectively. The heavy metals removal efficiencies by the nano-adsorbents followed the order of PHB-CNTs > P-CNTs based on ion exchange and electrostatic forces mechanism. For P-CNTs and PHB-CNTs, the equilibrium sorption isotherm suits temkin model, kinetic data fitted to pseudo-second order based on the linear regression correlation coefficient, and the thermodynamic study established spontaneity and endothermic nature of the adsorption process. The findings in this research conclude that both nano-adsorbents have exceptional capacity to remove heavy metals from the adsorbate, with PHB-CNTs possessing better quality. The treated adsorbate meets the standard for industrial or irrigation re-use.