Adsorptive removal of dichlorophenoxyacetic acid (2,4-D) using novel nanoparticles based on cationic surfactant-coated titania nanoparticles.

A novel nanomaterial based on cationic surfactant-coated TiO2 nanoparticle (CCTN) was systematically fabricated in this work. Synthesized titania nanoparticles were thoroughly characterized by XRD, FT-IR, HR-TEM, TEM-EDX, SEM with EDX mapping, BET, and ζ potential measurements. The adsorption of cationic surfactant, cetyltrimethylammonium bromide (CTAB), on TiO2 was studied under various pH and ionic strength conditions. Adsorption of CTAB on TiO2 increased with ionic strength increment in the presence of hemimicelle monolayer structure, indicating that nonelectrostatic and electrostatic forces control CTAB uptake. CTAB adsorption isotherms on TiO2 were according to a two-step model. Potential application in pesticide removal of 2,4-dichorophenoxy acetic acid (2,4-D) using CCTN was also studied. Optimum parameters for 2,4-D treatment through adsorption technique were pH 5, adsorption time of 120 min, and CCTN dosage of 10 mg·mL-1. Very low 2,4-D removal efficiency using TiO2 without CTAB coating was found to be approximately 28.5% whereas the removal efficiency was up to about 90% by using CCTN under optimum conditions, and the maximum adsorption capacity of 12.79 mg·g-1 was found. Adsorption isotherms of 2,4-D on CCTN were more suitable with the Langmuir model than Freundlich. Adsorption mechanisms of 2,4-D on CCTN were mainly governed by Columbic attraction based on isotherms and surface charge changes.

Adsorptive Removal of Azo Dye New Coccine Using High-Performance Adsorbent-Based Polycation-Modified Nano-Alpha Alumina Particles.

The azo dyes new coccine (NCC) were successfully removed through the adsorption onto PVBTAC-modified α-Al2O3 particles. The optimal conditions of both the surface modification by PVBTAC adsorption and the NCC adsorption were thoroughly investigated. Formerly, polycations PVBTAC were adsorbed onto the nanosized α-Al2O3 particles at pH 8, NaCl 100 mM, with a contact time of 2 h, and initial concentration of 1000 ppm to modify the α-Al2O3 surface. Latterly, the NCC adsorptive removal was conducted at pH 8, NaCl 10 mM, α-Al2O3 adsorbent dosage of 3 mg mL-1, and a contact time of 45 min. Interestingly, the optimal pH of 8 potentially applies to treat real wastewater as the environmental pH range is often about 7-8. High removal efficiency and adsorption capacity of the NCC azo dyes were, respectively, found to be approximately 95% and 3.17 mg g-1 with an initial NCC concentration of 10 ppm. The NCC adsorption on the modified α-Al2O3 particles was well fitted with a Freundlich model isotherm. A pseudo-second kinetic was more suitable for the NCC adsorption on the PVBTAC-modified α-Al2O3 surface than a pseudo-first kinetic. The NCC adsorptive removal kinetic was also affirmed by the FT-IR spectra, based especially on the changes of functional group stretch vibrations of -SO3 - group in the NCC molecules and -N+(CH3)3 group in the PVBTAC molecules. The high reusability of the α-Al2O3 particles was proved to be higher than 50% after four generation times.

Adsorption of Binary Mixture of Highly Positively Charged PTMA5M and Partially Negatively Charged PAA onto PSL Particles Studied by Means of Brownian Motion Particle Tracking and Electrophoresis.

Effects of ionic strength on the adsorption of highly charged polycationic ((2-dimethylamino)ethyl methacrylate) methyl chloride quaternary salt (PTMA5M) individually as well as in a binary mixture with polyanionic acrylic acid (PAA) onto polystyrene sulfate latex (PSL) particles with negative charges were investigated by means of Brownian movement particle tracking and measurement of electrophoretic mobility. In addition, the adsorption mechanism was confirmed by Fourier transform infrared (FT-IR) and energy-dispersive X-ray (EDX) spectroscopic methods. The hydrodynamic thickness of the adsorbed polyelectrolyte layer (δH) and electrophoretic mobility (EPM) of particles as a function of concentration ratios of the two polyelectrolytes were measured to clarify the effect of negatively charged molecules on the structure of the positively charged adsorbed layer at various ionic strengths. Extremely thick δH was confirmed for the case of excess dosage of polycations. The δH decreased more significantly with the addition of PAA than increasing ionic strength. Interestingly, in the presence of PAA, the adsorbed layer thickness increased more at lower ionic strength than at higher ionic strength. In addition, the initial δH decreases remarkably after a time lapse of 1 h. Contrary to the decrease of the δH, almost all EPM either remained unchanged or increased over time depending on the concentration ratio of the two polyelectrolytes. Constant charge density, desorption of polyanions, and then reconformation of the adsorbed polycationic layer are proposed model components.

Temporal Changes of Adsorbed Layer Thickness and Electrophoresis of Polystyrene Sulfate Latex Particles after Long Incubation of Oppositely Charged Polyelectrolytes with Different Charge Densities.

The different desorption concepts of the two polyelectrolytes PTMA5M and PTMC5M, which have similar molecular weights and differ in the charge density on the polystyrene sulfate latex (PSL) particles by 25 times, and with various charge densities in a long incubation, were systematically investigated based on hydrodynamic adsorbed layer thickness (δH) and electrophoretic mobility (EPM) under two ionic strengths in the present study. Herein, in the case of highly charged polyelectrolyte PTMA5M, desorption continued for 4 h and re-adsorbing proceeded after a longer incubation time higher than 4 h. Meanwhile, in the case of lowly charged polyelectrolyte PTMC5M, an adsorption-desorption equilibrium was suggested to take into account the unchanging of both δH and EPM.