Adsorption behavior of Azo Dye C. I. Acid Red 14 in aqueous solution on surface soils

Azo dyes have received considerable attention because of their association with various human health problems. The aim of the investigation is to determine the adsorption behavior ofazo dyes in aqueous solution on DG06, GSE17200, and GSE17201 soils using C. I. Acid Red 14 （AR14） as example. The experimental results indicate that the Freundlich model expresses the adsorption isotherm better than the Langmuir model and the pseudo-second-order model achieves adsorption of AR14 on the three soils well. Based on the pseudo-second-order model, the adsorption thermodynamic of AR14 on DG06 soil have been studied and the thermodynamics parameter of AGO is determined and AGO value shows the adsorption process of AR14 on DG06 is mainly physical in nature. Furthermore, the effects of temperature, pH and salinity （NaC1） on adsorption have been investigated. The decrease in pH or the increase in salinity enhances the adsorption of AR14 by DG06, GSE17200, and GSE17201.

Thermodynamic study of adsorption of phenolic compounds onto Amberlite XAD-4 polymeric adsorbents and its acetylized derivative MX-4

Adsorption equilibrium isotherms of phenolic compounds, phenol, p cresol, p chlorophenol and p nitrophenol, from aqueous solutions by Amberlite XAD 4 polymeric adsorbent and its acetylized derivative MX 4 within temperature range of 283 323K were obtained and fitted to the Freundlich isotherms. The capacities of equilibrium adsorption for all four phenolic compounds from their aqueous solutions increased around 20% on the acetylized resin, which may be contributed to the specific surface area and the partial polarity on the network. Estimations of the isosteric enthalpy, free energy, and entropy for the adsorption process were reported.

THERMODYNAMIC STUDY OF ADSORPTION OF PHENOLIC COMPOUNDS FROM AQUEOUS SOLUTION BY A WATER-COMPATIBLE HYPERCROSSLINKED POLYMERIC ADSORBENT

Equilibrium data for the adsorption of phenolic compounds, i.e., phenol, p-cresol, p-chlorophenol and p- nitrophenol from aqueous solutions by a water-compatible hypercrosslinked polymeric adsorbent (NJ-8) within temperature range of 283-323 K were obtained and correlated with a Freundlich-type of isotherm equation, so that equilibrium constants KF and n were obtained. The capacities of equilibrium adsorption for all the four phenolic compounds on the NJ-8 from aqueous solutions are around 2 times as high as those of Amberlite XAD-4, which may be attributed to the unusual micropore structure and the partial polarity on the network. The values of the enthalpy (always negative) are indicative of an exothermic process, which manifests the adsorption of all the four phenolic compounds on the two polymeric adsorbents to be a process of physical adsorption. The negative values of free energy change show that the solute is more concentrated on the adsorbent than in the bulk solution. The absolute free energy values of adsorption for NJ-8 are always higher than those for Amberlite XAD-4, which indicates that phenolic compounds are preferentially adsorbed on NJ-8. The negative values of the adsorption entropy are consistent with the restricted mobilities of adsorbed molecules of phenolic compounds as compared with the molecules in solution. The adsorption entropy values of phenolic compounds for NJ-8 are lower than those for Amberlite XAD-4, which means the micropores of NJ-8 require more orderly arranged adsorbate.

Kinetic and Thermodynamic Studies on Raney Ni/Al2O3 Adsorption for Deep Desulfurization of Benzene Stream

How to remove trace amount of sulfur in benzene is of significance,and deep desulfurization by Ni-containing absorbents is an efficient and promising method.In this paper,The Raney Ni/Al2 O3 adsorbent was prepared and its kinetic and thermodynamic characteristics on adsorptive desulfurization of benzene were studied.The results showed that Raney Ni/Al2 O3 adsorbent exhibited good adsorption performance.The equilibrium isotherms indicated that the adsorption of thiophene over the Raney Ni/Al2 O3 adsorbent complied with the Freundlich model.The results of adsorption kinetics studies showed that the pseudo-second-order kinetics equation was more advantageous than the pseudo-first-order kinetics equation in describing the adsorption kinetics of thiophene on Raney Ni/Al2 O3.The rate constant value(kp)was positively correlated with the temperature whereas the adsorption mass transfer process was mainly determined by the intraparticle and film diffusion.The adsorption thermodynamic analysis proved that△G^0<0,△H^0>0,and△S^0>0,implying that the adsorption was a spontaneous,entropy-increasing and endothermic process.

Thermodynamic and Kinetic Studies of Effective Adsorption of 2,4,6-trichlorophenol onto Calcine Mg/Al-CO_3 Layered Double Hydroxide

Adsorption of 2, 4, 6-trichlorophenol（TCP） onto the calcined Mg/Al-CO_3 layered double hydroxide（CLDH） was investigated. The prepared Mg/Al-CO_3 layered double hydroxide（LDH） and CLDH were characterized by powder X-ray diffraction（XRD） and thermo gravimetric analyzer-differential scanning calorimeters（TG-DSC）. Moreover, 2,4,6-trichlorophenol（TCP） was removed effectively（94.7% of removal percentage in 9h） under the optimized experimental conditions. The adsorption kinetics data fitted the pseudosecond-order model well. The Freundlich, Langmuir, and Tempkin adsorption models were applied to the experimental equilibrium adsorption data at different temperatures of solution. The adsorption data fitted the Freundlieh adsorption isotherm with good values of the correlation coefficient. A mechanism of the adsorption process is proposed according to the intraparticle diffusion model, which indicates that the overall rate of adsorption can be described as three steps.

THERMODYNAMIC STUDY ON ADSORPTION OF AROMATIC SULFONIC ACIDS ONTO MACROPOROUS WEAK BASE ANION EXCHANGER FROM AQUEOUS SOLUTIONS

The adsorption equilibrium isotherms of three aromatic sulfonic acid compounds, 2-naphthalenesulfonic acid, p-toluenesulfonic acid and p-chlorobenzenesulfonic acid, from aqueous solutions by macroporous weak base anion exchanger within the temperature range of 293 K-313 K were obtained. Several isotherm equations were correlated with the equilibrium data, and the experimental data was found to fit the three-parameter Redlich-Peterson equation best within the entire range of concentrations. The study showed that the hydrophobicity of solute has distinct influence on adsorption capacity of the anion exchanger for the aromatic sulfonic acid. Moreover, estimations of the isosteric enthalpy, free energy, and entropy change of adsorption were also reported. The positive isosteric enthalpy and entropy change for adsorption indicate an endothermic and entropy driven process in the present study.

Preparation of Waste Coffee-grounds Carbon and Study on Phenol Adsorption Ability

The waste coffee-grounds carbon(WCGC)was prepared with H_(3)PO_(4)treated using waste coffee-grounds as precursor.Its adsorption ability was studied using phenol as test molecule.The influence of H_(3)PO_(4)treated,calcined temperature,the initial phenol concentration,the doge of carbon and original pH values on phenol adsorption ability were investigated.Characterization of WCGC was performed by N_(2)adsorption isotherms,Fourier transform infrared spectroscopy(FT-IR),scanning electron microscopy(SEM),and X-ray diffraction(XRD)techniques.First,the second order and Weber-Morris model reaction rate models were used to estimate the WCGC adsorption ability.The results show that the produced WCGC(700℃,2 h)has been graphitized and the layered structure increased BET surface to 435.98 m^(2)/g and adsorption phenol ability.The initial phenol concentration is 50 mg/L,the amount of WCGC(700℃,2 h)is 0.2 g,and the phenol adsorption rate is 97%after 270 min and no intermediate product formation.The adsorption kinetics of the selected WCGC is best fitted by the Weber-Morris model.

The Removal of Chromium(VI) from Aqueous Solution by Amine-Functionalized Zeolite: Kinetics, Thermodynamics, and Equilibrium Study

In this study, the removal of Cr(VI) from aqueous solution by modified zeolite with 3-aminopropyltriethoxysilane was investigated. The effect of various parameters such as pH, contact time, temperature, initial concentration of Cr(VI) ion, common cations, and anions on the adsorption of Cr(VI) was studied. The modified zeolite was characterized by following instrumental analysis of XRD, SEM/EDS, BET, and FT-IR. Based on calculated thermodynamic parameters values (ΔG0 < 0, ΔH0 > 0, and ΔS0 > 0) and kinetic properties of the adsorption of Cr(VI) by modified zeolite, it was concluded that the rate-limiting step of the process is a second-order chemical reaction. The results of the adsorption isotherm study confirmed that the adsorption follows the Langmuir isotherm model. The maximum adsorption capacity was 13.5 mg/g.

K^+ Adsorption Kinetics of Fluvo-Aquic and Cinnamon Soil Under Different Temperature

The K+ adsorption kinetics of fluvo-aquic soil and cinnamon soil under different temperatureswere studied. The results showed: 1) The first order equations were the most suitable forfitting the adsorption under various temperature levels with constant K+ concentration indisplacing fluid. With temperature increasing, the fitness of Elovich equation increased,while those of power equation and parabolic diffusion equation decreased; 2)the apparentadsorption rate constant ka and the product of ka multiplied by the apparent equilibriumadsorption qincreased when temperature increased, while the apparent equilibrium adsorptionqreduced; 3)temperature influenced hardly the reaction order, the order of concentrationand adsorpton site were always 1 under various temperatures, if they were taken intoaccount simultaneously, the adsorption should be a two-order reaction process; 4)theGibbs free energy change △G of potassium adsorption were negative, ranged from -4444.56to -2450.63Jmol-1,and increased with temperature increasing, while enthalpy change △H,entropy change △S, apparent adsorption activation Ea, adsorption activation energy E1and desorption activation energy E2 were temperature-independent; 5)the adsorption wasspontaneous process with heat releasing and entropy dropping, fluvo-aquic soil releasedmore heat than cinnamon soil.

Preparation and utilization of wheat straw anionic sorbent for the removal of nitrate from aqueous solution

In order to reduce the impact of eutrophication caused by agricultural residues （i.e., excess nitrate） in aqueous solution, economic and effective anionic sorbents are required. In this article, we prepared anionic sorbent using wheat straw. Its structural characteristics and adsorption properties for nitrate removal from aqueous solution were investigated. The results indicate that the yield of the prepared anionic sorbent, the total exchange capacity, and the maximum adsorption capacity were 350%, 2.57 mEq/g, and 2.08 mmol/g, respectively. The Freundlich isotherm mode is more suitable than the Langmuir mode and the adsorption process accords with the first order reaction kinetic rate equation. When multiple anions （SO4^2-, H2PO4^-, NO3^-, and NO2^-） were present, the isotherm mode of prepared anionic sorbent for nitrate was consistent with Freundlich mode; however, the capacity of nitrate adsorption was reduced by 50%. In alkaline solutions, about 90% of adsorbed nitrate ions could be desorbed from prepared anionic sorbent. The results of this study confirmed that the wheat straw anionic sorbent can be used as an excellent nitrate sorbent that removes nitrate from aqueous solutions.

Adsorption of herring sperm DNA onto pine sawdust biochar:Thermodynamics and site energy distribution

Environmental deoxyribonucleic acid(eDNA),which includes antibiotic resistance genes,is ubiquitous in the environment.The interactions between eDNA and biochar,a promising material widely used in soil amendment and water treatment,greatly affect the environmental behavior of eDNA.Hitherto few experimental evidences are available yet,especially on the information of thermodynamics and energy distribution to explains the interactions between biochar and eDNA.This study investigated the adsorption of herring sperm DNA(hsDNA)on pine sawdust biochar,with a specific emphasis on the adsorption thermodynamics and site energy distribution.The adsorption of hsDNA on biochar was enhanced by an increase in the pyrolysis and adsorption temperatures.The higher surface area,strongerπ−πinteraction,and weaker electrostatic repulsion between hsDNA and biochars prepared at high pyrolysis temperatures facilitated the adsorption of hsDNA.The thermodynamics indicated that the adsorption of hsDNA on biochar was spontaneous and endothermic.Therefore,higher temperature was beneficial for the adsorption of hsDNA on biochar;this was well explained by the increase in E*and F(E*)with the adsorption temperature.These results are useful for evaluating the migration and transformation of eDNA in the presence of biochar.

Mesoporous V-doped TiO_2 Nanoparticles as New Adsorbents for the Removal of Methylene Blue from Color Textile Wastewater

V-doped TiO2 nanoparticles（NPs） as dye adsorbents are synthesized by the co-precipitation method and characterized by X-ray powder diffraction, transmission electron microscope, N2 adsorption at 77 K, and X-ray photoelectron spectroscopy. The adsorption of methylene blue（MB） on the V-doped TiO2 NPs is studied in detail by varying the calcination temperature and V doping amount of the adsorbent, adsorbate concentration, adsorbent dosage, agitation rate, reaction temperature, and p H. The comparison of dye adsorption on V-doped TiO2 and parent TiO2 demonstrates that the adsorptive activity of TiO2 can be improved by V doping. The enhanced adsorptive performance can be attributed to the tremendous changes in texture, structure, and surface morphology of adsorbent. The adsorption kinetic analysis shows that the adsorption follows the pseudo-second order kinetics. The apparent activation energy for adsorption is calculated by Arrhenius formula to be 37.6 k J·mol-1, indicating that the adsorption is controlled by both of the diffusion and interfacial adsorption steps. The adsorption data are analyzed using Langmuir and Freundlich isotherms and the results indicate that the Langmuir model provides better correlation of the experimental data. The results conclusively show that the adsorption of MB is a spontaneous behavior and endothermic reaction with the ΔH value of 17.60 k J·mol-1.

Anti-adsorption mechanism of ion-adsorption type rare earth tailings

To investigate the process of RE^(3+)anti-adsorption on ion-adsorption type rare earth tailings,the thermodynamics,adsorption kinetics and infrared spectroscopy of these materials were investigated.The results indicate that the initial reaction rate of anti-adsorption of rare earth tailings is fast,but it reaches a balance in 6 min.The formula 1-2a/3-(1-a)2/3=k_2t(k represents rate constant of the reaction,a represents anti-adsorption rate of rare earth ore,t represents anti-adsorption time)of internal diffusion can be used to predict the kinetics of anti-adsorption in IATRE tailings.BecauseΔH<0,ΔG<0,ΔS>0(ΔH,ΔG,ΔS represent change of enthalpy,Gibbs free energy and entropy,respectively),the anti-adsorption of RE^(3+)on ion-adsorption type RE tailings is a spontaneous physical adsorption process.The effects of ligand exchange and strong chemical bond are not found in this process.Because the anti-adsorption process is exothermic,heating will inhibit the reaction and decrease the anti-adsorption performance.According to the infrared spectrum analysis,there are no significant changes in the mineral surface after anti-adsorption.Based on these findings,the anti-adsorption of rare earth tailings is physical adsorption.

Thermodynamics and Kinetics of Bacterial Cellulose Adsorbing Persistent Pollutant from Aqueous Solutions

The adsorption capability of bacterial cellulose（BC） for anionic dye acid fuchsine was studied. Meanwhile, the processes of the adsorption were investignted and fitted by adsorption isotherm models, adsorption thermodynamics and adsorption kinetics models, respectively. The changes of BC before and after adsorbing acid fuchsine were investigated via scanning electron microscopy（SEM） and Fourier transform infrared spectroscopy（FTIR） to further explain the adsorption mechanism. The results show that acid fuchsine could be effectively adsorbed by BC. The adsorption process was fitted well by Langmuir equation and the pseudo-second order kinetics, indicating that the adsorption process was monolayer molecule adsorption with the main action of chemical adsorption. The adsorption process was spontaneous and endothermic. Glucuronic acid groups and hydroxyl groups were responsible for the adsorption of acid fuchsine on BC.

Preparation and evaluation of bis(diallyl alkyl tertiary ammonium salt) polymer as a promising adsorbent for phosphorus removal

Problems associated with water eutrophication due to high phosphorus concentrations and related environmentally safe solutions have attracted wide attention.A novel bis(diallyl alkyl tertiary ammonium salt)polymer,particularly poly(N1,N1,N6,N6-tetraallylhexane-1,6-diammonium dichloride)(PTAHDADC),was synthesized and characterized by Fourier transform infrared spectroscopy,nuclear magnetic resonance,scanning electron microscopy,mercury intrusion method,and thermogravimetric analysis.The adsorption characteristics in phosphorus were evaluated in dilute solution,and the recycling properties of PTAHDADC were investigated.Results showed that PTAHDADC possessed macropores with a size distribution ranging from 30 to 130μm concentrating at 63μm in diameter and had 46.52%of porosity,excellent thermal stability below 530 K,and insolubility.PTAHDADC could effectively remove phosphorus at p H=7–11 and had a removal efficiency exceeding 98.4%at pH=10–11.The adsorption equilibrium data of PTAHDADC for phosphorus accorded well with the Langmuir and pseudo-second-order kinetic models.Maximum adsorption capacity was 52.82 mg/g at 293 K.PTAHDADC adsorbed phosphorus rapidly and reached equilibrium within 90 min.Calculated activation energy Eawas 15.18 k J/mol.PTAHDADC presented an excellent recyclability with only 8.23%loss of removal efficiency after five adsorption–desorption cycles.The morphology and structure of PTAHDADC slightly changed as evidenced by the pre-and post-adsorption of phosphorus,but the process was accompanied by the partial deprotonation of the(–CH2)3-NH+group of PTAHDADC.The adsorption was a spontaneous exothermic process driven by entropy through physisorption,electrostatic attraction,and ion exchange.Survey results showed that PTAHDADC was a highly efficient and fast-adsorbing phosphorus-removal material prospective in treating wastewater.

Corrosion Inhibition of Mild Steel in Sulphuric Acid Using Luffa Aegyptiaca Leaves Extract

The corrosion inhibition of mild steel（MS） in sulphuric acid using Luffa aegyptiaca（LA） leaves extract was investigated by weight loss studies, colorimetric measurements, potentiodynamic polarisation and electrochemical impedance spectroscopy. The adsorption of LA leaves extract was confirmed by Fourier transform infrared spectroscopy and optical profilometry. The inhibition efficiency increased with increasing concentration of the extract but decreased with rise in temperature and with the increase in acid strength. Furthermore, the inhibition efficiency synergistically increased on the addition of halide ions. Polarisation studies revealed that the LA extract acts as mixed- type inhibitor. Physical adsorption mechanism is proposed from the trend in inhibition efficiency with the change in temperature and from thermodynamic parameters. The adsorption of LA on MS surface obeys Langmuir adsorption isotherm and follows the kinetic thermodynamic model of ElAwady at all temperatures studied.