Cobalt(iii) acetylacetonate initiated RAFT polymerization of acrylonitrile and its application in removal of methyl orange after electrospinning

RSC Advances ◽  
2015 ◽  
Vol 5 (72) ◽  
pp. 58393-58402 ◽  
Author(s):  
Yuanyuan Xu ◽  
Jinming Sun ◽  
Hou Chen ◽  
Liangjiu Bai

Electrostatic repulsion (ER) played a key role at low solution pH. Enhancement of hydrophobic attraction (HA) and hydrogen bond (HB) increased the adsorption capacity at higher solution pH.

2015 ◽  
Vol 11 (9) ◽  
pp. 3959-3972
Author(s):  
Misael Silas Nadiye-Tabbiruka ◽  
Foertunate Phenyo Sejie ◽  
Estella Judith Salamula

The adsorption of methyl orange (MO) from its solution by steam activated coal from Morupule colliery was investigated spectrophotometrically using the batch technique, through kinetics and thermodynamics’ study, and found to be reversible at all temperatures used. This was to check whether the coal could be used to purify dye-polluted water from dying and printing textile industry. The effects of varying methyl orange concentration, solution pH and temperature were investigated. The adsorption rate and the adsorption capacity increased with increasing initial concentration, with decreasing solution pH and with increasing temperature. The adsorption capacity was generally low probably due to the low coal surface area (10 m2g-1). The increase in rate and capacity with increasing temperature is believed to be increased surface area due to the swelling of coal which accompanies its heating.  The adsorption kinetics fitted the Lagergren pseudo second order model best indicating overall third order or dual simultaneous pseudo first order processes. Results from the thermodynamic study fitted  Freundlich model best indicating heterogeneity of the surface of the coal sample. 


Author(s):  
Shuhui Wang ◽  
Yu Huang ◽  
Yiting Wu ◽  
Xinyu Zhang ◽  
Liu Wan ◽  
...  

Abstract A cost-effective approach was applied to prepare porous carbon samples by the simple carbonization of wormwood rod followed by salt activator (NaCl) activation. The effect of preparation parameters on the characteristics of the wormwood rod based porous carbons (WWRs) were studied. The properties of these samples were investigated by SEM, BET surface area, X-ray diffraction, FT-IR spectra and X-ray photoelectron spectrometer. The prepared WWRs were applied as new adsorbent materials to remove methyl orange (MO). The experimental results indicated that WWR-800 activated at 800 °C possesses the best adsorption performance. Several factors that affected the adsorption property of the system such as the solution pH, dosing of adsorbent, initial dye concentration and ionic strength were examined. In addition, the thermodynamic parameters and kinetic parameters of MO with WWR-800 were studied. The results indicated that the adsorption of MO on WWR-800 was an endothermic process and non-spontaneity under standard conditions. The maximum equilibrium adsorption capacity of MO on WWR-800 was 454.55 mg/g. After five adsorption/desorption cycles, the adsorption capacity of MO on WWR-800 remained at 94%, which indicated that wormwood rod based porous carbon possessed good reusability.


2019 ◽  
Author(s):  
Chem Int

The kinetics of oxidation of methyl orange by vanadium(V) {V(V)} has been investigated in the pH range 2.3-3.79. In this pH range V(V) exists both in the form of decavanadates and VO2+. The kinetic results are distinctly different from the results obtained for the same reaction in highly acidic solution (pH < 1) where V(V) exists only in the form of VO2+. The reaction obeys first order kinetics with respect to methyl orange but the rate has very little dependence on total vanadium concentration. The reaction is accelerated by H+ ion but the dependence of rate on [H+] is less than that corresponding to first order dependence. The equilibrium between decavanadates and VO2+ explains the different kinetic pattern observed in this pH range. The reaction is markedly accelerated by Triton X-100 micelles. The rate-[surfactant] profile shows a limiting behavior indicative of a unimolecular pathway in the micellar pseudophase.


J ◽  
2021 ◽  
Vol 4 (2) ◽  
pp. 193-205
Author(s):  
Opeyemi A. Oyewo ◽  
Sam Ramaila ◽  
Lydia Mavuru ◽  
Taile Leswifi ◽  
Maurice S. Onyango

The presence of toxic metals in surface and natural waters, even at trace levels, poses a great danger to humans and the ecosystem. Although the combination of adsorption and coagulation techniques has the potential to eradicate this problem, the use of inappropriate media remains a major drawback. This study reports on the application of NaNO2/NaHCO3 modified sawdust-based cellulose nanocrystals (MCNC) as both coagulant and adsorbent for the removal of Cu, Fe and Pb from aqueous solution. The surface modified coagulants, prepared by electrostatic interactions, were characterized using Fourier transform infrared, X-ray diffraction (XRD), and scanning electron microscopy/energy-dispersive spectrometry (SEM/EDS). The amount of coagulated/adsorbed trace metals was then analysed using inductively coupled plasma atomic emission spectroscopy (ICP-AES). SEM analysis revealed the patchy and distributed floccules on Fe-flocs, which was an indication of multiple mechanisms responsible for Fe removal onto MCNC. A shift in the peak position attributed to C2H192N64O16 from 2θ = 30 to 24.5° occurred in the XRD pattern of both Pb- and Cu-flocs. Different process variables, including initial metal ions concentration (10–200 mg/L), solution pH (2–10), and temperature (25–45 °C) were studied in order to investigate how they affect the reaction process. Both Cu and Pb adsorption followed the Langmuir isotherm with a maximum adsorption capacity of 111.1 and 2.82 mg/g, respectively, whereas the adsorption of Fe was suggestive of a multilayer adsorption process; however, Fe Langmuir maximum adsorption capacity was found to be 81.96 mg/g. The sequence of trace metals removal followed the order: Cu > Fe > Pb. The utilization of this product in different water matrices is an effective way to establish their robustness.


Molecules ◽  
2021 ◽  
Vol 26 (12) ◽  
pp. 3718
Author(s):  
Mohammad Azam ◽  
Saikh Mohammad Wabaidur ◽  
Mohammad Rizwan Khan ◽  
Saud I. Al-Resayes ◽  
Mohammad Shahidul Islam

The aim of the research was to prepare low-cost adsorbents, including raw date pits and chemically treated date pits, and to apply these materials to investigate the adsorption behavior of Cr(III) and Cd(II) ions from wastewater. The prepared materials were characterized using SEM, FT-IR and BET surface analysis techniques for investigating the surface morphology, particle size, pore size and surface functionalities of the materials. A series of adsorption processes was conducted in a batch system and optimized by investigating various parameters such as solution pH, contact time, initial metal concentrations and adsorbent dosage. The optimum pH for achieving maximum adsorption capacity was found to be approximately 7.8. The determination of metal ions was conducted using atomic adsorption spectrometry. The experimental results were fitted using isotherm Langmuir and Freundlich equations, and maximum monolayer adsorption capacities for Cr(III) and Cd(II) at 323 K were 1428.5 and 1302.0 mg/g (treated majdool date pits adsorbent) and 1228.5 and 1182.0 mg/g (treated sagai date pits adsorbent), respectively. It was found that the adsorption capacity of H2O2-treated date pits was higher than that of untreated DP. Recovery studies showed maximal metal elution with 0.1 M HCl for all the adsorbents. An 83.3–88.2% and 81.8–86.8% drop in Cr(III) and Cd(II) adsorption, respectively, were found after the five regeneration cycles. The results showed that the Langmuir model gave slightly better results than the Freundlich model for the untreated and treated date pits. Hence, the results demonstrated that the prepared materials could be a low-cost and eco-friendly choice for the remediation of Cr(III) and Cd(II) contaminants from an aqueous solution.


2015 ◽  
Vol 713-715 ◽  
pp. 2789-2792
Author(s):  
Huan Yan Xu ◽  
Xue Li ◽  
Yan Li ◽  
Ping Li ◽  
Wei Chao Liu

An active dye, Methyl Orange (MO) was employed as the target pollutant to evaluate the photocatalytic activity of TiO2/schorl composite and the kinetics and thermodynamics of this process was emphasized in this work. Langmuir–Hinshelwood kinetic model was employed for the kinetic studies and the results revealed that the process of MO photocatalytic discoloration by TiO2/schorl composite followed one order reaction kinetic equation under different conditions. The reaction rate constant (k) increased with initial MO concentration decreasing. When the catalyst dosage or solution pH increased,kvalues increased and then decreased. The possible reasons for these phenomena were discussed. Finally, the thermodynamic parameters ΔG, ΔH, ΔSwere obtained by the classical Van't Hoff equation.


2018 ◽  
Vol 19 (4) ◽  
pp. 1066-1072
Author(s):  
Q. H. Jin ◽  
C. Y. Cui ◽  
H. Y. Chen ◽  
Y. Wang ◽  
J. F. Geng ◽  
...  

Abstract Adsorption (ADS) and dielectrophoresis (DEP) techniques were combined (ADS/DEP) to efficiently remove As(V) in industrial wastewater. Fly ash, activated carbon, corncob and plant ash were tested to determine the best adsorbent by their adsorption capacity. Plant ash showed the highest adsorption capacity compared with the others. Different parameters such as solution pH and adsorbent dose were explored. The maximum As(V) removal efficiency was 91.4% at the optimized conditions (pH 9.0, adsorbent dose 5 g/L) when the initial concentration of As(V) was 15 mg/L. With the ADS/DEP technique, the plant ash particles with adsorbed As(V) were trapped on the electrodes in a DEP device. The ADS/DEP process could increase the removal efficiency of As(V) to 94.7% at 14 V even when the initial concentration of As(V) was 15 mg/L. And the residual concentration of As(V) decreased to 0.34 mg/L after two series of the ADS/DEP process. The adsorbents before and after DEP were examined by scanning electron microscope (SEM) and energy dispersive X-ray (EDX) analysis. After the DEP process, the weight percentage of As(V) on the adsorbent surface increased to 0.96% from 0.5%. The ADS/DEP process could be a new efficient way to remove arsenic pollutant at high concentrations.


2018 ◽  
Vol 788 ◽  
pp. 83-88
Author(s):  
Oskars Leščinskis ◽  
Ruta Švinka ◽  
Visvaldis Švinka

Clays are materials consisting of clay minerals and non-clay minerals. Clay mineral fraction is considered to be a nanofraction. Clay minerals can be used for water purification and treatment. Description and characterization of 3 different Latvian clay nanosized minerals from 3 different geological periods (clay Liepa from Devonian period, clay Vadakste from Triassic period and clay Apriki from Quaternary period) as well as their adsorption capacity concerning organic compounds such as methyl orange and rhodamine B are summarized. Nanosized clay mineral particles were obtained using sedimentation method. Particle size distribution, zeta potential and FTIR spectra is given. The adsorption tests of above mentioned organic compounds were carried out in water solutions at 3 different pH values. The adsorption values were determined by means of UV-spectrophotometric technique. Zeta potential values for clay minerals Apriki, Liepa and Vadakste are -40.9 mV, -49.6 mV and -43.0 mV, respectively. FTIR spectra show similar tendencies for all 3 clay minerals. The best adsorption capacity concerning methyl orange and rhodamine B were in solutions with a pH value of 2, whereas at neutral and alkaline pH values adsorption in 24 hours was not observed.


2015 ◽  
Vol 18 (2) ◽  
pp. 121-131
Author(s):  
Khoa Tien Le ◽  
Ngoc Chau Hoang ◽  
Tien Thuy Thai ◽  
Anh Trung Le ◽  
Thinh Nguyen Huu Pham ◽  
...  

TiO2 P25 was fluorinated by thermal shock method in order to study the influence of thermal shock fluorination on the surface properties and the photocatalytic activity for the degradation of cationic and anionic organic dyes at different pH values. The surface charge of catalysts was characterized by the pHPZC measurement. The photocatalytic activity of catalysts was evaluated via the degradation of methylene blue (cationic dye) and methyl orange (anionic dye). The results showed that the thermal shock fluorination and the rise of solution pH can increase the surface negative charge of TiO2, which enhanced the adsorption of methylene blue and then improved the photocatalytic degradation of this cationic dye under UV and visible light. On the other hand, after the fluorination, the adsorption of methyl orange on TiO2 was strongly reduced, which limited the photocatalytic oxidation of this anion dye.


Author(s):  
Lorena Alcaraz ◽  
María Esther Escudero ◽  
Francisco J. Alguacil ◽  
Irene Llorente ◽  
Ana Urbieta ◽  
...  

This paper describes the physico-chemical study of the adsorption of dysprosium (Dy3+) in aqueous solution onto two types of activated carbons synthesized from spent coffee ground. KOH activated carbon is a microporous material with a specific BET surface area of 2330 m2·g-1 and pores with a diameter of 3.2 nm. Carbon activated with water vapor and N2 is a solid mesoporous, with pores of 5.7 nm in diameter and a specific surface of 982 m2·g-1. A significant dependence of the adsorption capacity on the solution pH was found, while it does not depend significantly neither on the dysprosium concentration nor on the temperature. A maximum adsorption capacity of 31.26 mg·g-1 and 33.52 mg·g-1 for the chemically and physically activated carbons, respectively, were found. In both cases, the results obtained from adsorption isotherms and kinetic study were better fit to a Langmuir model and a pseudo-second-order kinetics. In addition, thermodynamic results indicate that dysprosium adsorption onto both activated carbons is an exothermic, spontaneous and favorable process.


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