Removal of basic dyes from aqueous solutions with sulfonated phenol–formaldehyde resin

In this study, we aimed to investigate the removal of basic dyes, including Safranin T (ST), Nile Blue A (NBA), and Brilliant Cresyl Blue (BCB), from aqueous solution with a sulfonated phenol–formaldehyde resin. This sulfonated resin was characterized by Fourier transform infrared spectroscopy and scanning electron microscopy. The adsorption properties of this resin were investigated under different adsorption conditions with different initial dye concentrations, contact times, and pH values. The adsorption equilibrium data were analyzed with Langmuir and Freundlich models. The adsorption behaviors of ST, NBA, and BCB onto the sulfonated resol‐type phenol–formaldehyde resin were better described by the Freundlich model. The adsorption capacities of the sulfonated resol resin for ST, NBA, and BCB decreased in the following order: NBA > BCB > ST. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Simultaneous adsorptive removal of methylene blue and copper ions from aqueous solution by ferrocene‐modified cation exchange resin

Resin was modified with ferrocene (Fc) to enhance removal of Methylene Blue (MB) and Cu²⁺ from simulated wastewater. The FTIR, N₂‐BET, and X‐ray fluorescence analysis confirmed that Fc was successfully grafted onto the surface of resin. The adsorption capacity of Fc modified cation exchange resin (FMCER) was calculated to be 392.16 mg/g Cu²⁺ and 10.01 mg/g MB. Both processes were spontaneous and exothermic, best described by Langmuir equation. Pseudo‐first‐order kinetic model satisfied the adsorption of MB, while the intraparticle‐diffusion model fitted the kinetics of Cu²⁺ adsorption best. The result revealed a multilayer adsorption of Cu²⁺ on FMCER, and the kinetics maybe controlled by intraparticle diffusion, film diffusion, and competition force. The adsorption of MB and Cu²⁺ on FMCER were physicosorptive, with activation energies of 2.09 and 1.27 kJ/mol. pH 2–7 and 4–5 are optimum for the removal of MB and Cu²⁺, and pH 4 is optimal for the simultaneous removal of MB and Cu²⁺. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 41029.     

Pseudo‐first‐order kinetic studies of the sorption of acid dyes onto chitosan

The adsorption of five acid dyes onto chitosan, derived through the deacetylation of crab‐shell chitin, from aqueous solutions was studied. The equilibrium isotherms were measured and analyzed with the Langmuir, Freundlich, and Redlich–Peterson equations; the results correlated well with the Langmuir equation. Kinetic studies were also performed in an agitated batch adsorber to study the effect of the initial dye concentration and the mass of chitosan. The kinetics were analyzed with the pseudo‐first‐order rate equation, and the rate constants were determined. The first‐order kinetic model correlated the experimental concentration and time data at short times and even up to 60% of the total adsorption period in a number of systems. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 1633–1645, 2004     

Preparation and properties of Styrene-Butyl Acrylate resin co-encapsulated Pigment Red 48:2 and Oxidized Polyethylene wax composite nanoparticles

In this study, the Pigment Red 48:2 (PR48:2) and oxidized polyethylene (OPE) wax were evenly dispersed in the aqueous phase by ball-milling method, and then the composite nanoparticles of styrene-butyl acrylate (P(St/BA)) resin co-encapsulated PR48:2 and OPE wax were prepared via in-situ emulsion polymerization. The morphology, size distribution, composition, thermal properties, colorimetric performance, acid–alkaline resistance, and anti UV-aging ability of the encapsulated nanoparticles were characterized by different analytical techniques. When the sodium dodecyl sulfate (SDS) concentration was 0.01 mol/L, the average size of encapsulated nanoparticles was about 120 nm, the particle dispersion index (PDI) was 0.132, and composite nanoparticles owned narrow size distribution and clear core–shell structure. Compared with original pigment, the encapsulated nanoparticles have better anti UV-aging property and acid–alkaline resistance. When the PR48:2 content was 0.5 g, the color changes of the encapsulated nanoparticles after soaking in alkaline solution for 30 days and UV light exposure for 60 days were only 1.70 and 6.59, respectively, indicating that the encapsulated nanoparticles have excellent color stability.     

Macroporous polymeric ion exchangers as adsorbents for the removal of cationic dye basic blue 9 from aqueous solutions

Two macroporous cation‐exchange resins, Purolite C145, a strongly acidic cation macroporous resin, and Purolite C107E, a weakly acidic cation‐exchange resin, were used to remove the dye Basic Blue 9 (BB9) from an aqueous medium. Batch adsorption experiments were carried out to analyze the effect of various parameters, such as the phase contact time, initial dye concentration, initial solution pH, resin dose, and temperature. The experimental equilibrium data were evaluated by the Langmuir, Freundlich, and Dubinin–Radushkevich (DR) adsorption models. The Freundlich model better described the adsorption processes of the BB9 dye onto both cation exchangers, and the monolayer adsorption capacities were established as 31.9846 mg/g (C145) and 27.77 mg/g (C107E) at 20°C. The values of the mean free adsorption energy (E) obtained from the DR model suggested a porous structure of the adsorbents and proposed ion exchange at the main mechanism of the adsorption process. The values of the thermodynamic parameters showed that the retention of the cationic dye was a spontaneous and endothermic process. Environmental scanning electron microscopy and Fourier transform infrared spectroscopy were used to characterize the sorbent and also to validate the adsorption mechanism as ion‐exchange ones. The desorption experiments by a batch method were performed with different solutions: 0.1 and 1 mol/L HCl, 2.5 mol/L H₂SO₄, CH₃OH, and a mixture between 1 mol/L HCl and CH₃OH. Desorption performed with sulfuric acid was shown to be most effective because more than 85% of the adsorbed dye was removed. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 39620.     

Preparation and sorption studies of β‐cyclodextrin/epichlorohydrin copolymers

β‐Cyclodextrin (β‐CD) copolymer materials were synthesized by reacting different mole ratios (1 : 15, 1 : 25 and 1 : 35) of β‐CD with epichlorohydrin (EP). The products were characterized using N₂ porosimetry, Fourier Transform Infrared spectroscopy, ¹³C CP‐MAS NMR spectroscopy, thermogravimetry analysis, elemental (C and H) analysis, and scanning electron microscopy. The sorption properties in aqueous solution were studied using p‐nitrophenol (PNP) with UV–Vis spectrophotometry. Sorption isotherms were obtained at pH 4.6 and three temperatures (22, 35, and 45°C) and at pH 10.3 at 22°C. The isotherms were analyzed using the BET isotherm model and the sorption parameters provided estimates of the surface area, sorption capacity, and isosteric heats of sorption for each polymeric material. The estimated surface areas are as follows: 58.2, 52.1, and 90.1 m²/g at pH 4.6. At pH 10.3, the estimated surface areas are 44.2, 40.5, and 58.5 m²/g, respectively. The removal efficiency of PNP by the polymeric materials ranged between 4.5 and 58% for the conditions investigated whereas the isosteric heats ranged between ?24.5 and ?13.6 kJ/mol. Removal efficiencies were concluded to strongly depend on the sorption conditions such as pH, temperature, and the relative amounts of sorbent and dye in aqueous solution. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Adsorption of methylene blue onto powdered activated carbon immobilized in a carboxymethyl sago pulp hydrogel

The potential of crosslinked carboxymethyl sago pulp (CMSP) beads immobilized with powdered activated carbon (PAC) as an adsorbent for methylene blue (MB) adsorption was investigated. The finely powdered PAC had an excellent adsorption capacity for MB but was disadvantageous for the separation process from treated effluents. To ease the separation process, the CMSP medium could be advantageous for the process by acting an immobilizing medium for PAC. The MB adsorption reached equilibrium at the 14th hour, and further adsorption was studied to determine the effects of the CMSP concentration, PAC dosage, and pH. Different CMSP concentrations in the preparation of CMSP–PAC beads showed no significant differences; this proved that CMSP–PAC adsorbed more MB than CMSP did. The MB adsorption increased with increasing PAC concentration, whereas the CMSP–PAC beads disintegrated at pH 11.5. In the equilibrium study, the Langmuir isotherm fit well into the experimental data with a linear correlation coefficient (R ²) of 0.9837 and a maximum adsorption capacity of 250 mg/g. The kinetic study showed that pseudo‐second‐order kinetics accommodated the experimental data well with an R ² value of 0.9512 and a pseudo‐second‐order rate constant value of 3.61 × 10^?3 min^?1. The crosslinked CMSP–PAC beads have the potential to remove MB dye, and this could be exploited as an alternative to treating colored dye effluents produced by industries such as the textile, printing, and cosmetics industries. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 44271.     

Anionic dye adsorption characteristics of surfactant‐modified coir pith,a ‘waste’ lignocellulosic polymer

The surface of coir pith, an agricultural solid waste, was modified using a cationic surfactant hexadecyltrimethylammonium bromide. Adsorption of anionic dyes on surfactant‐modified coir pith was investigated in a series of batch adsorption experiments. Two anionic dyes, acid brilliant blue (acid dye) and procion orange (reactive dye), were used in the adsorption studies. The effect of process variables such as contact time, concentration of the dyes, adsorbent dose, temperature, and pH were studied in order to understand the kinetic and thermodynamic parameters of the process. The kinetics of adsorption obeyed the second‐order rate equation. The equilibrium adsorption data were fitted into the Langmuir and Freundlich isotherms. It was found that modified coir pith yielded adsorption capacities of 159 and 89 mg/g for acid brilliant blue and procion orange, respectively. Mechanisms involving ion exchange and chemisorption might be responsible for the uptake of dyes. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 1538–1546, 2006     

Synthesis of polypyrrole‐modified TiO2 composite adsorbent and its adsorption performance on acid Red G

The adsorption–desorption characteristics of Acid Red G (ARG) on the polypyrrole‐modified TiO₂ (PPy/TiO₂) composite as a novel adsorbent was investigated. PPy/TiO₂ was synthesized via the in‐situ polymerization of pyrrole monomer in the prepared TiO₂ sol solution. Results from X‐ray diffraction and Fourier transform infrared spectra indicated the formation of the PPy/TiO₂ composite. The adsorption experiments showed that the modification of PPy substantially improved the adsorption and regeneration abilities of PPy/TiO₂. The adsorption equilibrium was achieved in a short time of 20 min, and the adsorption kinetics followed the pseudo‐second‐order model. The Langmuir adsorption isotherm was found for PPy/TiO₂, with the maximum adsorption capacity of 179.21 mg/g. The regeneration experiments showed that PPy/TiO₂ could be successfully regenerated by simple alkali‐acid treatment. The adsorption efficiency of the regenerated PPy/TiO₂ adsorbent for ARG was still greater than 90% after regeneration for 10 times. Additionally, the adsorption efficiency of PPy/TiO₂ for the ARG effluent was still higher than 78% after adsorption–desorption for four times. It is expected that the PPy/TiO₂ composite can be considered as a stable adsorbent for the removal of dye. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

对甲基苯甲酸在大孔吸附树脂上的吸附热力学及动力学研究

研究了对甲基苯甲酸在NDA-1800和JX-101大孔吸附树脂上的静态吸附热力学和动力学行为。结果表明,在283～313 K和研究的浓度范围内,两种大孔吸附树脂吸附对甲基苯甲酸的行为符合Freundlich吸附等温方程。对甲基苯甲酸在两种大孔吸附树脂上的吸附焓变△H〈0,为放热过程;自由能变△G〈0,吸附过程能自发进行;吸附熵变△S〈0,这是因为吸附质分子从水溶液中被吸附到树脂表面后,其分子运动受到了限制,使吸附熵减少。两种大孔树脂吸附对甲基苯甲酸的速率常数都比较大,且随着温度的升高而增大。吸附活化能都比较低,吸附较容易进行。     

Superabsorbent resin of acrylic acid/ammonium acrylate copolymers synthesized by ultraviolet photopolymerization

A new method of synthesizing a superabsorbent resin (SAR) from an acrylic acid/ammonium acrylate copolymer by direct UV photopolymerization was studied. The effects of the degree of neutralization of acrylic acid, the photoinitiators, the crosslinking agents, and the UV‐light exposure time on the water absorbency (Q) were investigated. The results showed that Q of an SAR based on Irgacure 1700 or Irgacure 1800 and Irgacure 651 was high, reaching about 1200 mL/g, but under the same conditions, Q was low for an SAR based on other photoinitiators. The UV absorption spectrum proved that the photoinitiators matched the UV light source. Among the crosslinking agents, N,N′‐methylene bisacrylamide was more efficient than the others at a small concentration and a high value of Q. ¹³C‐NMR spectrometry was used to identify the mechanism of the crosslinking reaction through the esterification of hydroxyethyl acrylate (HEA) and 2‐hydroxypropyl acrylate with carboxylic acid group in acrylic acid/ammonium acrylate copolymerization, but the efficiency of the crosslinking reaction by esterification was lower than that of the copolymerization of vinyl groups in the crosslinking agent. Q of the acrylic acid/ammonium acrylate copolymer for the SAR reached 1255 mL/g under certain conditions (degree of neutralization of acrylic acid = 75%, Irgacure 651 concentration = 0.2 wt %, [HEA] = 0.2 wt %, exposure time = 10 min). © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 95: 546–555, 2005     

Synthesis of acid dyes containing polyetheramine moieties and their low‐temperature dyeing properties on wool fiber

To realize the low‐temperature dyeing of wool fibers, the use of auxiliaries and wool modification are common methods. Low‐temperature auxiliaries may cause water‐pollution problems, and wool modification is a costly and uncontrollable process. In this study, new acid dyes, named D1–D3, containing polyetheramine groups were synthesized and applied to wool fiber by conventional and low‐temperature exhaust dyeing procedures. The results indicate that the new acid dyes could interact with wool‐fiber‐like auxiliaries and render a high exhaustion rate to the wool fiber at a dyeing temperature of 80 °C. In comparison with Acid Blue 25, the D1–D3 dyes showed an increased dyeing rate, especially under a dyeing temperature of 80 °C. Despite the bigger relative molecular masses of D1–D3, the exhaustion rates of D1–D3 were still higher, and the times of half‐dyeing were shorter than that of Acid Blue 25. The color differences between the wool fabrics dyed with the four dyes at 80 and 98 °C, respectively, were compared. We found that the color differences of D1–D3 between 80 and 98 °C were smaller than that of Acid Blue 25. The interactions between the dyes and wool fiber were analyzed and manifested by the measurement of the ζ potential of the dyes and wool fiber. The leveling and transfer properties of the D1–D3 dyes were also investigated, and the color differences of the wool fabrics dyed with Acid Blue 25, D1, and D2 were very low at all measured pH values and temperatures. The fastnesses of D1–D3 on wool fabric were almost the same as that of Acid Blue 25. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45793.     

Adsorptive removal of uranium from water by sulfonated phenol–formaldehyde resin

Adsorption characteristics of a sulfonated phenol‐formaldehyde resin (SPR) have been studied for U removal from aqueous solution by means of batch method. Adsorption experiments have been carried out as a function of contact time, solution/adsorbent ratio, particle size and pH. Adsorption isotherm has been evaluated by changing adsorbent dosage in the range of 0.04–80 g/L at an initial uranyl nitrate concentration of 0.05 mol/L. The enormous adsorption capacity of 0.29 mol/g estimated from the plateau region of the S shaped isotherm is well comparable the Langmuir capacity of 0.31 mol/g. Equilibrium data are also adequately well described by the Freundlich and the Dubinin‐Radushkevich (D‐R) isotherm equations. The parameters of the isotherms and pH dependency of distribution coefficients (K_D) indicate that polymeric uranyl chains form on bidentate surface complex as a result of solute–solute interactions on the adsorbent surface. Both desorption and elution studies show that uranyl chains are irreversibly bounded on the SPR. Kinetic curves having a fast initial part followed by a slower process well fit both McKay model based on two‐resistance diffusion and Nernst‐Plank model with single diffusion coefficient. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Preparation and characterization study on maleic acid cross-linked poly(vinyl alcohol)/chitin/nanocellulose composites

In the quest on improving composite formulations for environmental sustainability, maleic acid (MA) cross-linked poly(vinyl alcohol) (PVA)-α-chitin composites reinforced by oil palm empty fruit bunch fibers (OPEFB)-derived nanocellulose crystals (NCC) had been successfully prepared. Based on the Fourier transform infrared (FTIR) spectroscopic analysis, it was proven that molecular interactions of the cross-linker to the polymeric networks was through conjugated ester linkage. Differential scanning calorimetry (DSC) showed that the influence of MA was minimal toward crystallization in the PVA/chitin/NCC composite. Maximum tensile strength, elongation at break and Young's modulus of the respective PVA/chitin/NCC composites were achieved at different content of MA, dependent on the PVA/chitin mass ratio. Among all compositions, a maximum Young's modulus was achieved at 30 wt% MA loading in PVA/chitin-30/NCC, amounting to 2,413.81 ± 167.36 MPa. Moreover, the mechanical properties and selected physicochemical properties (swelling, gel content, and contact angle) of the PVA/chitin/NCC composites could be tailored by varying the chitin content (10–30 wt%) and MA content (10–50 wt% based on total mass of composite). In brief, this chemically cross-linked PVA-based biocomposites formulated with sustainable resources exhibited tunable physicochemical and mechanical properties.     

Bamboo charcoal modified with Cu2+ and 3-aminopropyl trimethoxy silane for the adsorption of acid fuchsin dye: Optimization by response surface methodology and the adsorption mechanism

The bamboo charcoal modified with Cu²⁺ and 3-aminopropyl trimethoxy silane (BC-Cu/Si-NH₂) was synthesized and characterized by X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, energy dispersive spectroscopy, and surface acid–base potentiometric titration. The adsorption for acid fuchsin (AF) dyes onto BC-Cu/Si-NH₂ was investigated. Moreover, response surface methodology was performed to optimize the process parameters including pH, initial dye concentration, adsorbent dosage, and temperature. The results presented that the adsorption process was mainly influenced by initial AF concentration and adsorbent dosage. Isotherm studies revealed that the adsorption data fitted well with the Sips model and Dubinin–Radushkevich (D–R) model, which indicated the monolayer, homogeneous, and physical nature of the adsorption process. The maximum adsorption capacity calculated from D–R model could approach approximately to 14.91 mg g⁻¹ at 40 °C, and the maximum adsorption capacity of Sips reached to 10.77 mg g⁻¹ at 40 °C. The kinetic experimental data matched well with Spahn and Schlunder model as well as pseudo-second-order model. In addition, intraparticle diffusion was not the only rate-controlling step of adsorption process. Thermodynamic parameters revealed the feasibility, spontaneity, and endothermic nature of adsorption. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47728.     

Combined use of chitosan and alginate in the treatment of wastewater

This study examined the combined use of chitosan and sodium alginate in the treatment of wastewater containing heavy‐metal ions and dye. Wastewater samples were divided into two equal parts before chitosan and sodium alginate solutions were added to each part. When these two solutions were mixed together, the heavy‐metal ions and dye molecules were separated from the water as the positively charged chitosan and the negatively charged sodium alginate precipitated each other. The effects of the concentration and ratio of chitosan and sodium alginate, the treatment temperature, and the time on the efficiency of metal‐ion and dye removal were investigated. The results showed that when used in combination, sodium alginate and chitosan were effective in removing copper, cadmium, lead, and silver ions as well as acid dye molecules © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 3581–3587, 2007     

Synthesis of calix[6]arene based XAD‐4 material for the removal of reactive blue 19 from aqueous environments

This study describes the synthesis of calix[6]arene (C6) appended Amberlite XAD‐4 resin and its application for the removal of anthraquinone‐based reactive blue 19 (RB‐19) dye from aqueous environments. The C6‐resin 5 was characterized with various analytical techniques, including Fourier transform infrared spectroscopy, scanning electron microscopy, thermogravimetric analysis, and elemental analysis. Adsorption experiments were carried out to investigate the effects of the pH, adsorbent dosage, electrolyte, contact time, and temperature on the adsorption of RB‐19 dye onto the C6‐resin 5. From the results, we observed that the percentage adsorption of the RB‐19 dye was highly dependent on the concentration of electrolyte and the pH of the solution. The maximum adsorption was achieved at pH 9. The thermal study demonstrated that the adsorption process was endothermic and spontaneous in nature. The isothermic study showed that the adsorption behavior could be better demonstrated by the Langmuir and Dubinin and Radushkevich isotherm model. From field studies, it has been concluded that C6‐resin 5 is an effective adsorbent for the removal of RB‐19 dye. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 776‐785, 2013     

Synthetic polymeric absorbent for dye based on chemically crosslinked acrylamide/mesaconic acid hydrogels

Adsorption properties of copolymers of acrylamide and mesaconic acid (CAME) in aqueous Basic Blue 12 (Nile blue chloride) solution have been investigated. Chemically crosslinked CAME hydrogels with various compositions were prepared from ternary mixtures of acrylamide (A), mesaconic(ME) acid, and water by free radical polymerization in aqueous solution, using a multifunctional crosslinker such as ethylene glycol dimethacrylate (EGDMA). Dynamic swelling tests in water was applied to the hydrogels. Weight swelling ratio (S) values have been calculated. Sorption of Basic Blue 12 (BB 12) onto CAME hydrogels was studied by batch sorption technique at 25°C. In the experiments of the sorption, L type sorption in the Giles classification system was found. Some binding parameters such as initial binding constant (K_i), equilibrium constant (K), monolayer coverage (n), site‐size (u), and maximum fractional occupancy (Ô) for CAME hydrogels‐BB 12 binding system were calculated by using Klotz, Scatchard, and Langmuir linearization methods. Finally, the amount of sorbed BB 12 per gram of dry hydrogel (q) was calculated to be 2.28 × 10^?6–7.91× 10^?6 mol BB 12 per gram for hydrogels. Sorption % was changed range 16.09–58.86%. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 405–413, 2006     

Self‐assembly of alginate/polyethyleneimine multilayer onto magnetic microspheres as an effective adsorbent for removal of anionic dyes

A novel magnetic adsorbent alginate/polyethyleneimine (ALG/PEI)_n/MN was developed for removal of anionic dyes from aqueous solution in this study. (ALG/PEI)_n/MN was prepared by depositing ALG/PEI multi‐layers onto amine‐modified Fe₃O₄ microspheres through layer‐by‐layer method. The morphologies and structures of the adsorbent were characterized by scanning electron microscopy, X‐ray diffractometer, and Fourier transform infrared spectrometer, respectively, and its performance in adsorption of anionic dye (acid orange 10, AO10) under varied experimental conditions were also investigated. The results revealed that the uptake capacity of AO10 by (ALG/PEI)_n/MN increased with the number of coated (ALG/PEI) bilayer on the adsorbents, and the maximum adsorption capacity for AO10 by (ALG/PEI)₄MN was 246.3 mg g^?1 at 25 °C. The adsorption process was exothermic and well described by the pseudo‐second order kinetic model and the Langmuir isothermal model. Moreover, (ALG/PEI)₄/MN showed good reusability and excellent magnetic separability. All the results demonstrate that (ALG/PEI)₄/MN is a potential recyclable adsorbent for removal of anionic dyes from wastewater. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45876.     

Effect of Magnesium Ions on the Adsorption of Poly(acrylic acid) onto Alumina

The adsorption isotherms of poly(acrylic acid) (PAA) onto alumina powder have been determined as a function of pH, ionic strength, and magnesium-ion concentration. The adsorption of PAA is strongly enhanced by magnesium ions in alkaline media but less affected under acidic conditions. The adsorption isotherms display a maximum when PAA is fully complexed with magnesium ions in the solution, corresponding to a ratio of 0.25 ± 0.05 [Mg²⁺]/[acrylic acid monomer]. The decrease in adsorbed amount with an increase in PAA concentration at constant magnesium-ion concentration is related to a decrease in the complexation ratio.