Removal of direct Red‐31 and direct Orange‐26 by low cost rice husk: Influence of immobilisation and pretreatments

The aim of the present study is to investigate the influence of free, carboxymethyl cellulose (CMC) immobilised, PVA–alginate immobilised, and HCl treated rice husk on the removal of Direct Red‐31 and Direct Orange‐26 dyes. The biosorption capacity of the rice husk increased with HCl treatment (67.39 and 45.34 mg/g) and decreased with PVA–alginate immobilisation (9.73 and 10.03 mg/g) as compared to the free biomass (65.56 and 45.58 mg/g) at 200 mg/L dye concentration for Direct Red‐31 and Direct Orange‐26, respectively. Equilibrium data were best described by Langmuir Type 1 for Direct Red‐31 and Direct Orange‐26 (free, CMC immobilised, PVA–alginate immobilised, and HCl treated). Best correlation coefficients for Direct Red‐31 and Direct Orange‐26 using free, CMC immobilised, PVA–alginate immobilised, and HCl treated rice husk were obtained for pseudo‐second order and Elovich kinetic models. Values of Gibbs free energy (ΔG°) and enthalpy change (ΔH°) indicated that reaction was spontaneous and endothermic in nature at the studied temperatures. FT‐IR studies showed the involvement of carbonyl, carboxyl, and amide groups in the biosorption process. SEM exhibited the morphological changes on the biosorbent surface and BET analysis to determine the surface area is also carried out.     

Adsorption of anionic dyes on a reversibly swelling cationic superabsorbent polymer

A cationic monomer [2‐(methacryloyloxy)ethyl]trimethylammonium chloride was polymerized using N,N′‐methylenebisacrylamide as the crosslinker to obtain a cationic superabsorbent polymer (SAP). This SAP was characterized by Fourier transform‐infrared spectroscopy, and the equilibrium swelling capacity was determined by swelling in water. The SAP was subjected to cyclic swelling/deswelling in water and NaCl solution. The conductivity of the swelling medium was monitored during the swelling/deswelling and was related to the swelling/deswelling characteristics of the SAP. The adsorption of five anionic dyes of different classes on the SAP was carried out and was found to follow the first‐order kinetics. The Langmuir adsorption isotherms were found to fit the equilibrium adsorption data. The dye adsorption capacity of the SAP synthesized in this study was higher than that obtained for other hydrogels reported in the literature. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Enhanced selective adsorption of cation organic dyes on polyvinyl alcohol/agar/maltodextrin water-resistance biomembrane

In this study, we designed a novel hydrogel composite membrane based on the combination of polyvinyl alcohol (PVA), agar, and maltodextrin through a facile solution-casting router. From Fourier-transform infrared spectroscopy, contact angle, scanning electron microscopy, and swelling analyses, the formation of hydrogen bonds between surface functional groups of PVA, agar, and maltodextrin was confirmed. As a result, the PVA/agar/maltodextrin membranes exhibited a more hydrophobic nature compared with pure PVA. The thermal stability and integrity of such obtained composite membranes were also elucidated by the evaluation of thermogravimetric analysis and mechanical behavior. Besides, the composite membrane exhibited high selective adsorption for cationic dyes, namely 20.2 mg g⁻¹ for methylene blue and 19.17 mg g⁻¹ for crystal violet at initial dye concentration of 100 mg/L, an adsorbent dosage of 0.1 g, contact time of 180 min, and solution pH 7, while anionic dyes such as congo red and methyl orange are approximately zero. The adsorption kinetics and isotherm of the as-prepared composite membranes were well fitted to the pseudo-second-order and Temkin model. The effect of factors, including contact time, solution pH, PVA content, and initial dye concentration on the adsorption capacity of the as-prepared composite membrane was also investigated in detail. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 137, 48904.     

Covalent crosslinked assembly of tubular ceramic‐based multilayer nanofiltration membranes for dye desalination

A tubular ceramic‐based multilayer composite nanofiltration membrane has been developed for dye desalination. Poly(acrylic acid)(PAA)/poly(vinyl alcohol)(PVA)/glutaraldehyde(GA) was dynamically assembled on to the inner surfaces of tubular ceramic microporous substrates which had been pretreated using dynasylan ameo silane coupling agents. Subsequently, the composite membranes were thermally crosslinked to form covalent ester bonds. Experimental results proved that the composite membrane had good nanofiltration performance for dye desalination. The (GA/PVA/PAA)₃/ceramic multilayer membrane shows over 96% retention of Congo red and less than 3% NaCl retention using a permeate flux of about 25 L/(m²·h). An investigation of membrane performance as a function of operating conditions suggested that the covalent crosslinking multilayer membrane possessed much higher stability compared to other, electrostatically assembled, multilayer membranes. © 2013 American Institute of Chemical Engineers AIChE J, 59: 3834–3842, 2013     

Removal of dyes by poly(p-phenylene terephthamide)/polyvinylidene fluoride hollow fiber in-situ blend membranes

In order to obtain the compatible poly(p-phenylene terephthalamide) (PPTA)/polyvinylidene fluoride (PVDF) blend membranes, the casting solution was synthesized via the in situ polycondensation process and flat sheet blend membranes were successfully prepared through the immersion precipitation phase inversion method in our previous study. In this study, the polycondensation solution was directly used as the spinning dope to fabricate PPTA/PVDF hollow fiber in-situ blend membrane by the dry-wet spinning technique. Hollow fiber membranes were employed to remove the dyes including Congo red (CR) and methylene blue (MB) from the dyeing liquor. Effects of operation conditions on dye rejection and membrane water flux were investigated. With the increase of operation pressure, feed concentration and feed temperature, dye rejection rates gradually decreased, but the rejection value of CR and MB still remained above 99.5%. On the contrary, the permeation water flux basically increased. During the continuous dye filtration of 300 min, hollow fiber membrane can maintain high dye rejection rates and stable water flux. The combination method of physical backwashing and chemical cleaning can effectively alleviate membrane fouling and recover membrane water flux. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48569.     

Solubility of Two Disperse Dyes Derived from <Emphasis Type="Italic">N</Emphasis>-Alkyl and <Emphasis Type="Italic">N</Emphasis>-Carboxylic Acid Naphthalimides in the Presence of Gemini Cationic Surfactants

The solubility of naphthalimide-based monoazo dyes containing N-ethyl and N-ethanoic acid groups was investigated in the presence of a conventional monomeric counterpart (DTAB) and two cationic gemini surfactants (12-4-12 or 14-4-14) individually. The effective parameters on dye solubility such as temperature, time and concentration of surfactants were investigated by UV–Visible spectrophotometry. The results demonstrate that the solubility of both dyes was considerably increased at concentrations above the surfactant CMC. The wavelength for the maximum absorbance of dyes in the aqueous solution shifts toward longer wavelengths with changes in the concentration of the cationic surfactants. A kinetic study of solubilization of dyes in cationic surfactants solution showed that the rate of solubilization follows the pseudo-first-order reactions. Rates of solubilization were in the range of 0.5 × 10⁻³ to 6.8 × 10⁻³ min⁻¹ for both dyes. The disperse dye containing a carboxylic acid group (dye 2) has a higher solubility rate than the dye containing an alkyl group (dye 1). The type of surfactant has a very low effect on adsorption of dye 1 onto the polyester fibers, whereas changing the surfactant type from DTAB to 12-4-12 or 14-4-14 causes adsorption of dye 2 on polyester to decrease.     

Study on the dyeing properties of hemicyanine dyes. II. Cationic dyeable polyester

The absorption spectra of two hemicyanine fluorescent dyes, namely, trans‐4‐[p‐(N,N‐di(2‐hydroxyethyl))‐amino‐styryl]‐N‐ethyl pyridinium bromide (DHEASPBr‐C₂) and trans‐4‐[p‐(N,N‐di(2‐hydroxyethyl))‐amino‐styryl]‐N‐octyl pyridinium bromide (DHEASPBr‐C₈), were studied at various levels of pH and high temperatures, and were then employed to dye cationic dyeable polyester. Their dyeing properties, fluorescent reflectance and colorimetric properties were explored. The novel fluorescent dyes existed in two forms of monocation and dication in solutions at low pH and high temperature. Overall, the influence of pH on colour depth and the maximum reflectance of dyed cationic dyeable polyester was extremely small. The adsorption mechanism of DHEASPBr‐C₂ and DHEASPBr‐C₈ on cationic dyeable polyester fibres was in good accord with the Langmuir type. Compared with DHEASPBr‐C₂, DHEASPBr‐C₈ exhibited comparatively faster adsorption rate, higher affinity and dye uptake, while its fluorescence shown by cationic dyeable polyester was slightly weak.     

Simultaneous sorption and diffusion of a 4-aminoazobenzene derivative and its conjugate acid in cellulose membrane carrying sulfonic acid groups

An azo dye, 2-methyl-N,N-bis(2-hydroxyethyl)-4-aminoazobenzene (nonionic dye) and its conjugate acid (cationic dye) are simultaneously adsorbed by the cellulose membranes carrying sulfonic acid groups from a slightly acidic aqueous solution. Sorption equilibria of the nonionic and the cationic dye are described in terms of the Henry's partition and the ionic exchange mechanism, respectively, in the latter case, the ion exchange constants obtained for the membrane with sulfonic acid group content (SAG) = 261 meq/kg at 30°C are K = 1.43 × 10^?5 and K = 0.542, respectively, where Na, H, and DH refer to sodium, hydrogen, and cationic dye ions. The diffusion coefficients of the nonionic dye (D_N) and the cationic dye (D_C) in the membranes were estimated from the permeation data of the dyes through the membrane. Both D_N and D_C decrease with increasing SAG. The ratio D_N/D_C ranged in 2.2–10, the ratio increases with the SAG.     

Synthetic absorbent for dyestuffs based on gamma crosslinked poly(vinyl alcohol) (PVA)

This work reports on the characterization and uses of gamma radiation‐crosslinked poly(vinyl alcohol) (PVA) films as absorbents for different classes of dyestuffs normally released from textile factors. Dyestuffs were selected from different producers. These dyestuffs were Remacryl Blue (basic dye), Remazol Golden Orange (reactive dye), Solar Orange (direct dye), and Sandolan (acid dye). The percentage dye sorption by PVA was determined by spectroscopic analysis and color‐strength measurements of the PVA films after absorbing the different dyestuffs. The results showed that the concentration of dimethylbisacrylamide as a crosslinking agent has a great effect on the gel fraction and percentage swelling in water of the PVA polymer. In general, crosslinked PVA showed a low tendency to absorb the different dyestuffs under investigation at room temperature. This tendency was shown to increase with an increasing temperature of the dye solution from room temperature to 70°C. Meanwhile, the highest percentage of dye sorption was found in the case of the basic dye and the lowest one in the case of the reactive dye depending on the active groups on the dyes. Moreover, the percentage dye sorption by PVA was slightly higher in the acid medium rather than in the alkaline one. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 349–354, 2003     

Diffusion and sorption studies of dyes through PVA cryogel membranes

The capacity of poly(vinyl alcohol) (PVA) to crosslink through freeze/thaw method was used to obtain PVA hydrogel membranes (HG) that were subjected to sorption and diffusion experiments using three dyes: Congo red (CR), methylthymol blue (MTB), and crystal violet (CV). To study the sorption of dyes into the cryogenic membrane, dye solutions at different concentrations were used. After sorption, desorption of dyes from the PVA membrane was monitored to quantify the possible regeneration of the membrane (PVA HG). To have a deep insight on the mechanism behind the desorption process, dye‐release kinetics were studied. The diffusion experiments reveal the fact that CR and MTB do not permeate the PVA HG membrane making it a promising candidate in the advanced purification processes of wastewaters. The effect of the incorporation of dyes (CV, CR, and MTB) on the chemical properties of PVA cryogel matrices has been studied by using several techniques such as: differential scanning calorimetry (DSC), scanning electron microscopy (SEM), and Fourier transform infrared (FTIR) spectroscopy. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

6‐Pyridinium benzo[a]phenazine‐5‐oxide derivatives as visible photosensitisers for polymerisation

Several 6‐pyridinium benzo[a]phenazine‐5‐oxide derivatives have been synthesised and characterised by proton nuclear magnetic resonance spectroscopy and mass spectrometry. The spectroscopic and electrochemical properties of these dyes were examined. The dyes were used as reducible sensitisers for selected electron donors (phenylthioacetic acid, phenoxyacetic acid, N‐phenylglycine, and ethyl 4‐N,N‐dimethylaminobenzoate) and as oxidisable sensitisers for electron acceptors (onium and N‐alkoxypyridinium salts). These photoredox pairs were found to be effective visible‐wavelength photoinitiators for the free radical polymerisation of trimethylolpropane triacrylate under visible light. The cationic photopolymerisation of cyclohexene oxide by the studied dyes and the onium salt photoredox pairs was ineffective. The obtained results are discussed on the basis of both free energy change for electron transfer to or from the benzo[a]phenazine dyes and the photochemical properties of the dyes, particularly their photobleaching. The proposed mechanism of dye fading is supported by density functional theory calculations and spectroscopic characterisation of the radical cation of the dye.     

Adsorption of different dyes from aqueous solution using Si-MCM-41 having very high surface area

Adsorption characteristics of four different dyes Safranin O (cationic), Neutral Red (neutral), Congo Red (anionic) and Reactive Red 2 (anionic) on Si-MCM-41 material having very high surface area are reported. The surface morphology of Si-MCM-41 material before and after adsorbing dye molecules are characterised by FTIR, HRXRD, nitrogen adsorption–desorption isotherms, FESEM, and HRTEM. The adsorption capacities of Si-MCM-41 for the dyes followed a decreasing order of NR > SF > CR > RR2. The adsorption kinetics, isotherm and thermodynamic parameters are investigated in detail for these dyes using calcined Si-MCM-41. The kinetics and isotherm data showed that both SF and NR adsorb more rapidly than CR and RR2, in accordance with pseudo-second-order kinetics model as well as intraparticle diffusion kinetics model and Langmuir adsorption isotherm model respectively. The thermodynamic data suggest that the dye uptake process is spontaneous. The high adsorption capacities of dyes on Si-MCM-41 (q_m = 275.5 mg g^?1 for SF, q_m = 288.2 mg g^?1 for NR) is explained on the basis of electrostatic interactions as well as H-bonding interactions between adsorbent and adsorbate molecules. Good regeneration capacity is another important aspect of the material that makes it potent for the uptake of dyes from aqueous solution.     

Gellan gum‐based novel composite hydrogel: Evaluation as adsorbent for cationic dyes

A semi‐interpenetrating network system [(GG‐g‐PAAm)‐PVA] was made by microwave irradiation of aqueous mixture of gellan gum (GG), acrylamide (AAm), and poly(vinyl alcohol) (PVA) containing N,N′‐methylene‐bis‐acrylamide as crosslinking agent. The gel was characterized by Fourier transform infrared spectroscopy, thermogravimetric analysis, X‐ray diffraction, and scanning electron microscopy techniques. The swelling behavior was studied under different pH conditions. A pH‐dependent swelling with maximum swelling under neutral pH was observed. The swelling process is found to follow second‐order kinetics and the mechanism of water transport is found to be Fickian type of diffusion. The (GG‐g‐PAAm)‐PVA was evaluated for removal of dye from aqueous solution, using crystal violet, a cationic dye. The maximum adsorption capacity of the gel was found to be 45.45 mg/g. The kinetic studies revealed a second‐order adsorption process which fits well into Langmuir model. The evaluation of thermodynamic parameters indicated the adsorption process to be exothermic and spontaneous at lower temperatures. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45527.     

Interaction of dis‐azo dyes with quaternized poly(dimethylaminoethyl methacrylate) as a function of the dye structure and polycation charge density

Interactions between some dis‐azo dyes, different by either the position of their sulfonic groups or their number (Ponceau SS, Crocein Scarlet MOO, Congo Red, and Direct Blue 1), and some strong polycations (PCs), with cationic centers in their side chains and dye removal from artificial wastewaters were systematically investigated in this study. PCs with variable charge densities (CDs) were prepared from poly(dimethylaminoethyl methacrylate) by controlled quaternization with benzyl chloride. Even when the main process in the dye removal was charge neutralization (coagulation) for all of the dyes, significant effects of the CD and dis‐azo dye structure on the metachromatic behavior of the dyes in dilute aqueous solutions and on the dye removal efficiency were observed. The stability of the PC/azo dye complex and, connected with this, the flocculation window were higher when the PC with the highest CD was used. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Photocatalytic Discoloration of Dyes: Relation between Effect of Operating Parameters and Dye Structure

The process of TiO₂/UV photocatalytic discoloration of wastewaters containing organic dyes is influenced by a number of variables. In this paper, the effects of some of these parameters, i.e., mass of catalyst, initial dye concentration, and pH, were related to the structural nature of the dyes investigated, azo and anthraquinone dyes, two families that are representative of about 75 % of the dyes marketed nowadays. Both bibliographical and own experimental data were used to analyze and discuss the photocatalytic discoloration in terms of dye structure and degradation pathways. It is shown that azo dyes (Methyl Orange, Metanil Yellow, Acid Orange 7, and Reactive Red 120) are more easily discolored than Reactive Blue 19 (anthraquinone dye), due to the higher molecular stability of the latter. It is also shown that azo dye discoloration is more influenced by the initial dye concentration, whereas recalcitrant anthraquinone dyes (Reactive Blue 19) mainly demand for basic pH values to generate enough OH^• radicals. Concerning TiO₂ loading, both the bibliographical and current research data showed no effect of this variable in the experimental range analyzed.     

Dye removal using hydrophobic polyvinylidene fluoride hollow fibre composite membrane by vacuum membrane distillation

Hydrophobic polyvinylidene fluoride (PVDF) hollow fibre composite membranes were prepared by the dilute solution coating process to build a special surface structure that was similar to the dual micro‐nano structure on the lotus leaf. Poly(vinylidene fluoride‐co‐hexafluoropropene) was chosen as the hydrophobic polymer candidate in dilute solution. Membrane morphology and surface hydrophobicity were evaluated by scanning electron microscopy and dynamic water contact angle measurement. The prepared PVDF hollow fibre membranes were employed to separate dyes (Congo Red and Methylene Blue) from water by vacuum membrane distillation. The effects of operational conditions (feed temperature, vacuum pressure and feed flow rate) on the vacuum membrane distillation performance of different PVDF membranes were investigated. The results indicated that the water contact angle values of PVDF composite membrane surfaces improved from 93.6° to 130.8°, which was mainly attributed to the formation of micro‐nano rods. This structure was similar to the dual micro‐nano structure on the lotus leaf. Under test feed temperature, vacuum pressure and feed flow rate conditions, the dye rejection rate of Congo Red and Methylene Blue by the hydrophobic PVDF hollow fibre membrane remained above 99.5% and 99%, which was higher than that of the pristine PVDF membrane (99% and 98%, respectively). In addition, the hydrophobic PVDF hollow fibre composite membrane showed higher permeation flux under different conditions compared with the pristine PVDF membrane, which was attributed to membrane surface hydrophobicity and the electrostatic interactions between dyes and the PVDF membrane surface.     

Green and feasible fabrication of loose nanofiltration membrane with high efficiency for fractionation of dye/NaCl mixture by taking advantage of membrane fouling

Loose nanofiltration membrane emerges as required recently, since it is hard for conventional nanofiltration membrane to fractionate mixture of dyes and salts in textile wastewater treatment. However, the polymeric membranes unavoidably suffer from membrane fouling, which was caused by the adsorption of organic pollutants (like dyes). Normally, the dye fouling layer will shrink membrane pore size, thus resulting in flux decline and rejection increase. It is thought that membrane fouling may be a double-edged sword and can be an advantage if properly utilized. Thereby, loose nanofiltration membranes were constructed here by a green yet effective method to fractionate dyes/salt mixture by taking advantage of membrane fouling without using poisonous ingredients. A commercially available polyacrylonitrile (PAN) ultrafiltration membrane with high permeability was chosen as the substrate, and dyes were used to contaminate PAN substrate and formed a stable barrier layer when adsorption of dyes reached dynamic equilibrium. The resultant PAN-direct red 80 (DR80) composite membranes displayed superior permeability (~128.4 L m⁻² h⁻¹) and high rejection (~99.9%) to DR80 solutions at 0.4 MPa. Moreover, PAN-DR80 membranes allowed fast fractionation of dyes/sodium chloride (NaCl) mixture, which maintained a negligible dye loss and a low NaCl rejection (~12.4%) with high flux of 113.6 L m⁻² h⁻¹ at 0.4 MPa. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47438.     

Removal of cationic dyes from aqueous solutions with poly (<Emphasis Type="Italic">N</Emphasis>-isopropylacrylamide-<Emphasis Type="Italic">co</Emphasis>-itaconic acid) hydrogels

In this study, N-isopropylacrylamide-based temperature and pH-sensitive hydrogels were synthesized by free radical polymerization for removal of cationic dyes from aqueous solutions. For this purpose, N-isopropylacrylamide was copolymerized with various amounts of sodium salt of itaconic acid in the presence of crosslinking agent (N,N-methylene bisacrylamide). The chemical structures of hydrogels were characterized by FT-IR analysis. In order to investigate swelling properties of the hydrogels, water absorption (swelling) and shrinking (deswelling) kinetics, the equilibrium swelling ratios in water and different pH buffer solutions, and the temperature dependent swelling ratios were determined. Then, their adsorption properties such as adsorption capacities, kinetics, isotherms were investigated in case of their usage in removal of Safranine T (ST), Brilliant Green (BG), and Brilliant Cresyl Blue (BCB) aqueous solutions. According to adsorbed dye amount, the adsorption capacities are followed the order BG > ST ≅ BCB. In addition, the results indicated that the pseudo-second-order kinetic model fitted better than the data obtained from pseudo-first-order model for the adsorption of all dyes onto hydrogels. Furthermore, according to effect of the initial dye concentration findings, it is concluded that, Freundlich isotherm explains the adsorption better than Langmuir isotherm.     

Diffusion with simultaneous reaction of reactive dyes in cellulose

The theoretical equations which described the concentration profile of immobilized species of reactive dyes in the substrate were derived from the diffusion equation with the chemical reaction of first-order or pseudofirst-order. The theoretical profiles in the substrate described by the equations were discussed. The larger the diffusion coefficient D of active species and the smaller the reaction rate constant k, the deeper is the penetration of the immobilized and active species of reactive dyes into the substrate. The method of estimating D and k from the diffusion profiles of both species obtained by means of the method of the cylindrical cellophane film roll was described. The diffusion coefficients of the hydrolyzed species of C.I. Reactive Orange 1 and Red 1 were nearly constant in all the pH values examined. The concentration profiles of both the species of Orange 1 at pH 8.8 were identical with the theoretical ones; while the profiles of immobilized species of Red 1 at pH 10 and of Orange 1 at pH 12 agreed with the theoretical ones and those of active species did not because of the hydrolysis. The diffusion coefficients of active species of these dyes at these pH ranges were smaller than those of the hydrolyzed species.     

Swelling Characterization of Polyelectrolyte Poly(Hydroxamic Acid) Hydrogels in Aqueous Thiazin Dye Solutions

In this study, swelling behavior of polyelectrolyte poly(hydroxamic acid) (PHA) hydrogels have been investigated in aqueous thiazin dye solutions. PHA hydrogels were prepared by free radical polymerizations of acrylamide with some cross-linkers such as N,N′ methylenebisacrylamide (NBisA) and ethylene glycol dimethacrylate (EGDMA); then they were used in experiments on swelling and diffusion of some water-soluble cationic dyes such as methylene blue (MB), thionin (T), and toluidin blue (TB). Swelling experiments were performed in water at 25°C, gravimetrically. The equilibrium swelling percent (S%) values of PHA hydrogels were calculated as 238–2705%. Some swelling kinetic parameters such as initial swelling rate, swelling rate constant, and maximum (theoretical) swelling percent were found. Diffusional behavior of dye solutions was investigated. Dye diffusion into hydrogels was found to be non-Fickian in character. Diffusion exponent (n) is over 0.50. For sorption of thiazin cationic dyes, MB, T, and TB to PHA hydrogels were studied by batch sorption technique at 25°C. PHA hydrogels in the dye solutions showed the dark coloration. In the experiments of the adsorption, S-type adsorption in the Giles classification system was found.