scholarly journals Dual Functional Composite of Montmorillonite-Rich/Chitosan (MCC) for Decolorizing the Water Used in Joss Paper Process: Thermodynamic, Isotherm, and Kinetic Studies

2020 ◽  
Vol 10 (21) ◽  
pp. 7493
Author(s):  
Witsarut Muangrak ◽  
Nutthavich Thouchprasitchai ◽  
Yuththaphan Phongboonchoo ◽  
Sangobtip Pongstabodee

A hybrid montmorillonite (Mt)-rich/chitosan composite (MCC) with high adsorption performance was synthesized for the decolorization of water used in the joss paper process. The performance was reported in terms of the dye removal. The composite expressed higher performance than chitosan or Mt-rich clay, respectively. The optimum condition for complete dye removal was achieved when using at least 0.6 g of the composite over a wide pH range (3–10) and initial dye concentration (10–100 mg L−1). The composite showed good reusability without the requirement of regeneration, adsorbing the dye completely for up to eight successive cycles of adsorption (>1.33 gdye gMCC−1). Thermodynamic analyses revealed the degree of spontaneity and the endothermic adsorption process. From the isotherm studies, the Koble–Corrigan isotherm model fitted very well to the experimental data, revealing that the composite had a heterogeneous surface with various active sites to adsorb the dye molecules. This also evidenced the synergistic electrostatic attraction and hydrophobic interaction between the dye and the composite. The pseudo-second-order model best explained the kinetic rate of adsorption. From evaluation of the adsorption process using the Webber and Morris equation and Boyd model, the rate-limiting step consisted of film diffusion and intra-particle diffusion.

Clay Minerals ◽  
2012 ◽  
Vol 47 (1) ◽  
pp. 81-92 ◽  
Author(s):  
S. Tomić ◽  
N. Rajić ◽  
J. Hrenović ◽  
D. Povrenović

AbstractNatural zeolitic tuff from Brus (Serbia) consisting mostly of clinoptilolite (about 90%) has been investigated for the reduction of the Mg concentration in spring water. The sorption capacity of the zeolite is relatively low (about 2.5 mg Mg g-1for the initial concentration of 100 mg Mg dm-3). The zeolitic tuff removes Mg from water solutions by ion exchange, which has been demonstrated by energy dispersive X-ray analysis (EDS). The extent of ion exchange was influenced by the pH and the initial Mg concentration. Kinetic studies revealed that Lagergen's pseudo-second order model was followed. Intra-particle diffusion of Mg2+influenced the ion exchange, but it is not the rate-limiting step. Rather than having to dispose of the Mg-loaded (waste) zeolite, a possible application was tested. Addition to a wastewater with a low concentration of Mg showed that it could successfully make up for the lack of Mg micronutrient and, accordingly, enabled the growth of phosphate-accumulating bacteriaA. Junii, increasing the amount of phosphate removed from the wastewater.


Author(s):  
Ying Liu ◽  
Fei Liu ◽  
Rijie Wang ◽  
Xiaoxia Yang

Abstract This work investigates the adsorption of sulfur compounds in model fuel (benzothiophene dissolved in n-octane) on NaY and NiY zeolites from the points of adsorption equilibrium and kinetics. The crystal structures, textural properties and chemical compositions of zeolites were characterized by XRD, N2 physisorption and ICP-AES, respectively. The adsorption of sulfur from model diesel was processed in a batch experiment on NaY and NiY zeolites, and the effects of adsorption temperature and adsorption time on adsorption capacity were investigated. The experimental isotherm data were fitted using Langmuir, Freundlich and Toth models. The pseudo-first order, pseudo-second order, pseudo-n order and intra-particle diffusion models were applied to fit the kinetic data and determine the adsorption mechanism. It is observed from the correlation coefficient (R2) that Toth model is more appropriate to depict the isotherm equilibrium adsorption process and the sulfur uptake process follows the pseudo-n order rate expression on NaY and NiY zeolites. The diffusion study indicated that the adsorption of benzothiophene is controlled by two steps. Moreover, the results of the relative error (RE) analysis further confirm the conclusion of the kinetic study. Thermodynamic studies demonstrated that the adsorption process is exothermal and spontaneous. The equilibrium adsorption sulfur capacities are 20.66 and 28.21 mgS˙g−1 on NaY and NiY zeolites at 50 °C, respectively.


Metals ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 1777
Author(s):  
Ljiljana Suručić ◽  
Tamara Tadić ◽  
Goran Janjić ◽  
Bojana Marković ◽  
Aleksandra Nastasović ◽  
...  

An amino-functionalized magnetic macroporous copolymer of glycidyl methacrylate (GM) and ethylene glycol (E) dimethacrylate (m-poly(GME)-deta) was synthesized, fully characterized, and used to investigate the adsorption of vanadium (V) oxyanions from aqueous solutions (Ci = 0.5 mM) in a batch system at room temperature (298 K). Pseudo-first-order (PFO), pseudo-second-order (PSO), Elovich, and intra-particle diffusion (IPD) models were used to analyze the kinetic data. The study showed that sorption is rapid, i.e., the sorption half-time is approximately one minute. Initially, the sorption process primarily involved surface sorbent particles, and it was best described by the PSO model. However, after saturation of the surface active sites is attained, the sorption rate decreases significantly because of limitations of the diffusion rate, which is then primarily controlled by the IPD process. The sorption process is favorable in the pH range of 3–6 due to the strong electrostatic interactions between the absorption centers of copolymer and vanadium (V) oxyanions. In the stated pH range, deta absorption centers with two and three protonated N atoms are in equilibrium as studied by quantum chemical modeling. Among V(V) species present in diluted aqueous media, the adsorption of H2VO4− ions dominates.


Nanomaterials ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 662 ◽  
Author(s):  
Guangsheng Liu ◽  
Kunyapat Thummavichai ◽  
Xuefeng Lv ◽  
Wenting Chen ◽  
Tingjun Lin ◽  
...  

Molybdenum disulfide (MoS2) has been universally demonstrated to be an effective electrocatalytic catalyst for hydrogen evolution reaction (HER). However, the low conductivity, few active sites and poor stability of MoS2-based electrocatalysts hinder its hydrogen evolution performance in a wide pH range. The introduction of other metal phases and carbon materials can create rich interfaces and defects to enhance the activity and stability of the catalyst. Herein, a new defect-rich heterogeneous ternary nanocomposite consisted of MoS2, NiS and reduced graphene oxide (rGO) are synthesized using ultrathin αNi(OH)2 nanowires as the nickel source. The MoS2/rGO/NiS-5 of optimal formulation in 0.5 M H2SO4, 1.0 M KOH and 1.0 M PBS only requires 152, 169 and 209 mV of overpotential to achieve a current density of 10 mA cm−2 (denoted as η10), respectively. The excellent HER performance of the MoS2/rGO/NiS-5 electrocatalyst can be ascribed to the synergistic effect of abundant heterogeneous interfaces in MoS2/rGO/NiS, expanded interlayer spacings, and the addition of high conductivity graphene oxide. The method reported here can provide a new idea for catalyst with Ni-Mo heterojunction, pH-universal and inexpensive hydrogen evolution reaction electrocatalyst.


Author(s):  
Mohamed Nasser Sahmoune ◽  
Krim Louhab ◽  
Aissa Boukhiar

Dead streptomyces rimosus was found to be an effective biosorbent for the removal of chromium from industrial tanning effluents. A sorption level of 65 mg/g was observed at pH 4.8 while the precipitation effect augmented this value at a higher pH range. Chromium desorption increased with decreasing desorption agents pH (including HCl and H2SO4) to a maximum value of 95% at approximately zero pH. The biosorption data of trivalent chromium by streptomyces rimosus has been used for kinetic studies based on fractional power, Elovich, pseudo-first order and pseudo-second order rate expressions. The time-dependent Cr (III) biosorption data were well-described by a pseudo-second-order kinetic model. The intraparticle diffusion is not the rate-limiting step for the whole reaction. It was found that the biosorption equilibrium data fit well with the Langmuir model.


2018 ◽  
Vol 156 ◽  
pp. 02012 ◽  
Author(s):  
Mardiah ◽  
Rif’an Fathoni ◽  
Pratiwi Pudyaningtyas ◽  
Hamdania Gamu ◽  
Rinaldy

High Consumption of paper, bring the impact of the waste paper itself. And the utilization of the paper is limited to recycled products and crafts, whereas paper such as newspaper still contains cellulose that can be potential to be used as a heavy metal adsorbent. In this study, newspaper was dissolved in sodium bicarbonate to reduce various impurities and then was reacted with citric acid (CA). The modified adsorbent was characterized by FTIR and was tested for adsorb Cu(II) in artificial solution. After adsorption process, the solution was filtered and analysed using Atomic Absorption Spectrophotometer (AAS). The adsorption experimental data was fitted to Langmuir, Freundlich, Tempkin, and Dubinin-Radushkevich for equilibrium model and was fitted to pseudo first order reaction and pseudo second order reaction for kinetic studies. The result showed that CA-modification newspaper able to remove heavy metals Cu(II) in solution.


2017 ◽  
Vol 2 (1) ◽  
pp. 13-26
Author(s):  
Tengku Khamanur Azma Tg. Mohd Zamri ◽  
Mimi Sakinah Abd Munaim ◽  
Zularisam Ab Wahid

Natural dye extracted from the rhizome of Curcuma longa L. were applied to bamboo yarns using exhaustion dyeing process. This study investigates the dyeing behaviour of Curcumin; the major color component isolated from rhizomes of Curcuma longa L.on bamboo yarn. Langmuir, Freundlich, Tempkin and Dubinin-Radushkevich isotherm models were used to test the adsorption process of curcumin on bamboo yarn. Comparison of regression coefficient value indicated that the Freundlich isotherm most fitted to the adsorption of curcumin onto bamboo yarn. Furthermore, the kinetics study on this research fitted the pseudo-second order model which indicates that the basis of interaction was chemical adsorption.


Water ◽  
2020 ◽  
Vol 12 (10) ◽  
pp. 2720
Author(s):  
Ting Liang ◽  
Lianfang Li ◽  
Changxiong Zhu ◽  
Xue Liu ◽  
Hongna Li ◽  
...  

Arsenic has become a global concern in water environment, and it is essential to develop efficient remediation methods. In this study, a novel adsorbent by loading cerium and manganese oxide onto wheat straw-modified biochar (MBC) was manufactured successfully aiming to remove arsenic from polluted water. Through scanning electron microscopy and energy-dispersive spectroscopy (SEM-EDS), X-ray diffractometer (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectrometer (FT-IR), and other techniques, it was found the loading of cerium and manganese oxide on MBC played a significant role in As(V) adsorption. The results of the batch test showed that the adsorption of MBC followed the pseudo-second order kinetics and Langmuir equation. The adsorption capacity of MBC was 108.88 mg As(V)/g at pH = 5.0 (C0 = 100 mg/L, dosage = 0.5 g/L, T = 298 K) with considerable improvement compared to the original biochar. Moreover, MBC exhibited excellent performance over a wide pH range (2.0~11.0). Thermodynamics of the sorption reaction showed that the entropy (ΔS), changes of enthalpy (ΔH) and Gibbs free energy (ΔG), respectively, were 85.88 J/(moL·K), 22.54 kJ/mol and −1.33 to −5.20 kJ/mol at T = 278~323 K. During the adsorption, the formation of multiple complexes under the influence of its abundant surface M-OH (M represents the Ce/Mn) groups involving multiple mechanisms that included electrostatic interaction forces, surface adsorption, redox reaction, and surface complexation. This study indicated that MBC is a promising adsorbent to remove As(V) from polluted water and has great potential in remediating of arsenic contaminated environment.


Author(s):  
Bruna Assis Paim dos Santos ◽  
Aline Silva Cossolin ◽  
Hélen Cristina Oliveira dos Reis ◽  
Ketinny Camargo de Castro ◽  
Evanleide Rodrigues da Silva ◽  
...  

In this study, baker’s yeast-MnO2 composites, produced by direct oxidation of yeast with KMnO4 under acidic conditions, were used as biosorbent to remove the triphenylmethane dye Malachite green (MG) from an aqueous solution. Parameters that influence the adsorption process, such as pH, contact time, temperature, initial dye concentration and biosorbent dosage, were evaluated in batch experiments. The optimum removal of MG was found to be  86.7 mg g-1 at pH 10, 1.0 g L-1 of biomass dosage and 45°C. The kinetic data of dye removal was better described by the pseudo-second-order model. The adsorption process followed the Langmuir isotherm model and the maximum biosorption capacity was estimated to be  243.9 mg g-1 (at 25°C). The negative values of ∆G° and the positive value of ∆H° indicated that the MG biosorption onto yeast-MnO2 composites is spontaneous and endothermic. Fourier transform infrared spectroscopy (FTIR) indicated that the nano-MnO2 particles deposited on yeast-MnO2 composites surface facilitated the MG adsorption. It was concluded that baker’s yeast-MnO2 composites have potential for application as adsorbent for removal of MG from aqueous solution.


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