<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd">
<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article">
 <front>
  <journal-meta>
   <journal-id journal-id-type="publisher-id">
    anp
   </journal-id>
   <journal-title-group>
    <journal-title>
     Advances in Nanoparticles
    </journal-title>
   </journal-title-group>
   <issn pub-type="epub">
    2169-0510
   </issn>
   <issn publication-format="print">
    2169-0529
   </issn>
   <publisher>
    <publisher-name>
     Scientific Research Publishing
    </publisher-name>
   </publisher>
  </journal-meta>
  <article-meta>
   <article-id pub-id-type="doi">
    10.4236/anp.2025.144009
   </article-id>
   <article-id pub-id-type="publisher-id">
    anp-146872
   </article-id>
   <article-categories>
    <subj-group subj-group-type="heading">
     <subject>
      Articles
     </subject>
    </subj-group>
    <subj-group subj-group-type="Discipline-v2">
     <subject>
      Biomedical 
     </subject>
     <subject>
       Life Sciences, Chemistry 
     </subject>
     <subject>
       Materials Science, Engineering
     </subject>
    </subj-group>
   </article-categories>
   <title-group>
    Adsorption of Methylene Blue from Water Solution on Mesoporous Pseudoboehmite (γ-AlOOH) Synthesized Via a Mineral Route
   </title-group>
   <contrib-group>
    <contrib contrib-type="author" xlink:type="simple">
     <name name-style="western">
      <surname>
       Idriss Mahamat
      </surname>
      <given-names>
       Yaya
      </given-names>
     </name> 
     <xref ref-type="aff" rid="aff1"> 
      <sup>1</sup>
     </xref>
    </contrib>
    <contrib contrib-type="author" xlink:type="simple">
     <name name-style="western">
      <surname>
       Djonbe Tchonnon
      </surname>
      <given-names>
       Valery
      </given-names>
     </name> 
     <xref ref-type="aff" rid="aff1"> 
      <sup>1</sup>
     </xref>
    </contrib>
    <contrib contrib-type="author" xlink:type="simple">
     <name name-style="western">
      <surname>
       Ech-chahad
      </surname>
      <given-names>
       Abdellah
      </given-names>
     </name> 
     <xref ref-type="aff" rid="aff2"> 
      <sup>2</sup>
     </xref>
    </contrib>
   </contrib-group> 
   <aff id="aff1">
    <addr-line>
     aDépartement de Chimie, University of N’Djamena—Laboratoire de l’Eau et de l’Environnement, N’Djamena, Chad
    </addr-line> 
   </aff> 
   <aff id="aff2">
    <addr-line>
     aLaboratory of Applied Chemistry and Environment, Faculty of Science and Technology, University Hassan I, Settat, Morocco
    </addr-line> 
   </aff> 
   <pub-date pub-type="epub">
    <day>
     27
    </day> 
    <month>
     10
    </month>
    <year>
     2025
    </year>
   </pub-date> 
   <volume>
    14
   </volume> 
   <issue>
    04
   </issue>
   <fpage>
    142
   </fpage>
   <lpage>
    157
   </lpage>
   <history>
    <date date-type="received">
     <day>
      1,
     </day>
     <month>
      September
     </month>
     <year>
      2025
     </year>
    </date>
    <date date-type="published">
     <day>
      28,
     </day>
     <month>
      September
     </month>
     <year>
      2025
     </year> 
    </date> 
    <date date-type="accepted">
     <day>
      28,
     </day>
     <month>
      October
     </month>
     <year>
      2025
     </year> 
    </date>
   </history>
   <permissions>
    <copyright-statement>
     © Copyright 2014 by authors and Scientific Research Publishing Inc. 
    </copyright-statement>
    <copyright-year>
     2014
    </copyright-year>
    <license>
     <license-p>
      This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/
     </license-p>
    </license>
   </permissions>
   <abstract>
    In this study, pseudoboehmite (nano-boehmite) synthesized by A Route Mineral used to adsorb of methylene blue dye solution. The effect of experimental parameters pH, contact time, temperature and initial concentration were studied on adsorption. Results indicated that the optimal pH for adsorption is 10, with the experiments conducted at a temperature of 25˚C and adsorption reaches equilibrium after 30 minutes. The optimum adsorbent amount is 0.03 g. The equilibrium data were perfectly represented by the Freundlich isotherm and the adsorption behavior can be better described by pseudo-second-order model.
   </abstract>
   <kwd-group> 
    <kwd>
     Pseudoboehmite
    </kwd> 
    <kwd>
      Adsorption
    </kwd> 
    <kwd>
      Methylene Blue
    </kwd>
   </kwd-group>
  </article-meta>
 </front>
 <body>
  <sec id="s1">
   <title>1. Introduction</title>
   <p>
    <xref ref-type="bibr" rid="scirp.146872-"></xref>Water, the source of all life, is extensively used in various industries such as textiles, dyeing, paper manufacturing, beverages, food processing, cosmetics, leather tanning, plastics, detergents, and others. These industries, which rely on synthetic dyes, generate wastewater of varying volumes and chemical compositions due to the diversity of dyes used and production methods employed <xref ref-type="bibr" rid="scirp.146872-1">
     [1]
    </xref>. This wastewater is generally toxic, resistant to biodegradation, and persistent in the environment, contaminating not only surface waters but also underground water reservoirs <xref ref-type="bibr" rid="scirp.146872-2">
     [2]
    </xref> <xref ref-type="bibr" rid="scirp.146872-3">
     [3]
    </xref>. The pretreatment of industrial wastewater is a critical concern that must be addressed before it can be safely discharged from industrial sites. It is also important to note that the presence of these dyes, even at very low concentrations in drinking water, can cause adverse health effects in both humans and animals <xref ref-type="bibr" rid="scirp.146872-4">
     [4]
    </xref> <xref ref-type="bibr" rid="scirp.146872-5">
     [5]
    </xref>. Moreover, the discharge of colored wastewater produced by these industries into aquatic environments reduces sunlight penetration and visibility, leading to eutrophication and disturbances in aquatic ecology. This phenomenon not only impairs the intensity of photosynthesis in aquatic plants and algae but also contributes to environmental degradation <xref ref-type="bibr" rid="scirp.146872-1">
     [1]
    </xref> <xref ref-type="bibr" rid="scirp.146872-6">
     [6]
    </xref>-<xref ref-type="bibr" rid="scirp.146872-8">
     [8]
    </xref>. Various techniques have been employed to remove dyes from industrial effluents, including chemical oxidation, membrane separation, coagulation/flocculation, and ion exchange <xref ref-type="bibr" rid="scirp.146872-9">
     [9]
    </xref>-<xref ref-type="bibr" rid="scirp.146872-11">
     [11]
    </xref>. Unfortunately, most of these methods are expensive, require large quantities of materials, and are not environmentally sustainable. Biological treatment, which utilizes both living and non-living biomass for dye decolorization, offers a cost-effective and eco-friendly alternative <xref ref-type="bibr" rid="scirp.146872-12">
     [12]
    </xref>-<xref ref-type="bibr" rid="scirp.146872-14">
     [14]
    </xref>. A wide range of materials—such as zeolites, clays, activated carbon, polymers, eggshell particles, etc. have been reported to exhibit dye adsorption capabilities <xref ref-type="bibr" rid="scirp.146872-15">
     [15]
    </xref>-<xref ref-type="bibr" rid="scirp.146872-20">
     [20]
    </xref>. However, these materials have limitations, including low dye removal efficiency <xref ref-type="bibr" rid="scirp.146872-21">
     [21]
    </xref> and the transfer of dyes from the liquid to the solid phase. Despite these drawbacks, adsorption remains the most promising decolorization technique due to its simple implementation, high efficiency with appropriate adsorbents, and economic viability <xref ref-type="bibr" rid="scirp.146872-22">
     [22]
    </xref>. Nanometer- and micrometer-sized materials present interesting opportunities for the complete removal of organic dyes such as methylene blue (MB) from wastewater. Their small size and high specific surface area enables them to function effectively as filtration supports and catalysts <xref ref-type="bibr" rid="scirp.146872-23">
     [23]
    </xref>-<xref ref-type="bibr" rid="scirp.146872-25">
     [25]
    </xref>. To date, extensive research has focused on these materials in various morphologies particles, spheres, sheets, rods, tubes, and spikes—each offering potential for diverse applications <xref ref-type="bibr" rid="scirp.146872-26">
     [26]
    </xref>-<xref ref-type="bibr" rid="scirp.146872-28">
     [28]
    </xref>. Precipitation is an easy, straightforward, and cost-effective method for synthesizing nanoparticles and their composites, particularly when the solvent used can be recycled. Boehmite (γ-AlOOH) and its oxide derivatives, such as α-Al<sub>2</sub>O<sub>3</sub> and γ-Al<sub>2</sub>O<sub>3</sub>, are among the nanostructures receiving considerable attention. These materials have been extensively studied for applications in catalysis, adsorption, flame retardancy, and optics <xref ref-type="bibr" rid="scirp.146872-29">
     [29]
    </xref>. To date, several types of boehmite nanostructures—such as nanorods, nanotubes <xref ref-type="bibr" rid="scirp.146872-30">
     [30]
    </xref>, nanofibers <xref ref-type="bibr" rid="scirp.146872-31">
     [31]
    </xref>, and nanowires <xref ref-type="bibr" rid="scirp.146872-32">
     [32]
    </xref> have been identified, each possessing unique physical and chemical properties. The aim of this study is to evaluate the dye removal efficiency of pseudoboehmite (γ-AlOOH), synthesized through an inorganic route, for the adsorption of cationic dyes under varying conditions, including contact time, pH, initial dye concentration, and temperature. Adsorption kinetics, isotherm models, and thermodynamic parameters were considered to describe the dye adsorption processes.</p>
  </sec><sec id="s2">
   <title>2. Materials and Methods</title>
   <sec id="s2_1">
    <title>2.1. Materials</title>
    <p>The products and materials used in this study include:</p>
    <fig id="fig1" position="float">
     <label>Figure 1</label>
     <caption>
      <title>
       <xref ref-type="bibr" rid="scirp.146872-"></xref>Figure 1. Diffractogramme DRX of pseudoboehmite.</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/2610525-rId15.jpeg?20251031113933" />
    </fig>
   </sec>
   <sec id="s2_2">
    <title>2.2. Method</title>
    <p>Batch Studies on the Adsorption of MB onto γ-AlOOH:</p>
    <p>
     <xref ref-type="bibr" rid="scirp.146872-"></xref>Adsorption tests were carried out in batch mode under varying initial conditions of pH, temperature, and dye concentration. In the experiment, beakers containing a fixed mass of adsorbent (30 mg) were filled with 50 mL of the dye solution (30 mg·L<sup>−</sup><sup>1</sup>). The beakers, adjusted to the required pH, were subjected to continuous stirring for 180 min at 25˚C using a multi-station shaker. The absorbance of the filtrates was measured using a UV-visible spectrophotometer at the wavelength corresponding to the maximum absorbance of the sample (λ = 664 nm). The adsorption capacity of methylene blue and the removal efficiency, which indicates the exact rate of MB elimination by boehmite, were calculated using Equation (1) and Equation (2), respectively:</p>
    <p>
     <math display="inline" xmlns="http://www.w3.org/1998/Math/MathML"> <mrow> 
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     </math> (1)</p>
    <p>
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     </math> (2)</p>
    <p>q<sub>e</sub>: Equilibrium adsorption capacity (mg·g<sup>−</sup><sup>1</sup>).</p>
    <p>C<sub>o</sub>: Dye’s initial concentration (mg·L<sup>−</sup><sup>1</sup>).</p>
    <p>C<sub>e</sub>: Dye’s equilibrium concentration (mg·L<sup>−</sup><sup>1</sup>).</p>
    <p>m: Adsorbant mass (g).</p>
    <p>
     <xref ref-type="bibr" rid="scirp.146872-"></xref>V: Dye’s solution volume (L).</p>
    <p>To determine the adsorption isotherms at 25˚C, we used the batch equilibration method. Then, 30 mg of adsorbent was added to 50 mL of dye solution, at concentrations ranging from 50 to 500 mg·L<sup>−</sup><sup>1</sup>; the system was allowed to reach equilibrium by maintaining a contact time of 24 h. The resulting experimental data were fitted to Langmuir (Equation (3)) and Freundlich (Equation (4)) isotherm models. The parameters obtained from isotherm modeling provide important insights into the adsorption mechanism, surface properties, and adsorbent-adsorbate affinities. Among the various models, we selected the two most significant: the Langmuir model and the Freundlich model. The Langmuir model is particularly useful for describing the monomolecular adsorption of a solute, forming a monolayer on the surface of an adsorbent. This model applies when the adsorbed species are fixed to well-defined, homogeneous sites, with each site capable of binding only one molecule. The adsorption energy is assumed to be identical for all sites and independent of the presence of other adsorbed species on neighboring sites. The empirical Freundlich model is based on adsorption onto heterogeneous surfaces, where the adsorption sites possess varying affinities and energies. Unlike the Langmuir model, which assumes uniform surface and monolayer adsorption, the Freundlich model accounts for multilayer adsorption and is particularly suitable for describing non-ideal and reversible adsorption processes on heterogeneous surfaces. It is commonly used to represent systems where the surface of the adsorbent is energetically non-uniform.</p>
    <p>
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     </math> (3)</p>
    <p>K<sub>L</sub> is the Langmuir equilibrium constant (L·mg<sup>−</sup><sup>1</sup>), q<sub>m</sub> represents the maximum adsorption capacity of the adsorbent to form a monolayer (mg·g<sup>−</sup><sup>1</sup>), while q<sub>e</sub> (mg·g<sup>−</sup><sup>1</sup>) denotes the amount of dye adsorbed at equilibrium.</p>
    <p>
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    <p>The Freundlich constants, K<sub>F</sub> (mg·g<sup>−</sup><sup>1</sup>) and n, are associated with the adsorption capacity and intensity of the adsorbent, respectively. Slope 1/n is a measure of the surface heterogeneity.</p>
    <p>Kinetic modeling is essential to understand the rate-controlling steps and mechanisms involved in the adsorption process. Three commonly applied models are the pseudo-first-order and pseudo-second-order, models <xref ref-type="bibr" rid="scirp.146872-34">
      [34]
     </xref>.</p>
    <p>This model assumes that the rate of occupation of adsorption sites is proportional to the number of unoccupied sites.</p>
    <p>
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    <p>This model assumes that adsorption follows second-order kinetics and may involve chemisorption as the rate-limiting step.</p>
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    <p>q<sub>t</sub>: Adsorbed dye at time t (mg·g<sup>−</sup><sup>1</sup>); q<sub>e</sub>: Equilibrium adsorbed dye (mg·g<sup>−</sup><sup>1</sup>); k<sub>1</sub> (min<sup>−</sup><sup>1</sup>) and k<sub>2</sub> (g·mg<sup>−</sup><sup>1</sup>·min<sup>−</sup><sup>1</sup>): Equilibrium rate constant characteristics of the pseudo-first-order and pseudo-second-order models, respectively.</p>
   </sec>
  </sec><sec id="s3">
   <title>3. Results and Discussions</title>
   <sec id="s3_1">
    <title>3.1. Effect of pH</title>
    <p>
     <xref ref-type="bibr" rid="scirp.146872-"></xref>To investigate the effect of pH on the adsorption effeiciency of the dye, 0.03 g of the adsorbent was introduced into 50 mL of methylene blue (MB) solution at a concentration of 30 mg·L<sup>−</sup><sup>1</sup>. The influence of pH variation on the amount adsorbed was studied over a pH range from 3 to 12. The pH values were adjusted using acidic (HCl) or alkaline (NaOH) solutions and maintained during the equilibrium period. Pseudoboehmite contains surface functional groups (OH<sup>−</sup>) that can undergo protonation in acidic media to form 
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     </math> groups, resulting in a positively charged surface. In basic media, these hydroxyl groups can be deprotonated to form 
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       </msup> 
      </mrow> 
     </math> groups, creating a negatively charged surface. At highly acidic pH values, the large number of protons in the solution compete with MB⁺ for access to the active adsorption sites, thereby reducing the extent of MB-adsorbent complexation. Additionally, the electrostatic repulsion between MB cations and the positively charged adsorbent surface at pH &lt; pH<sub>pzc</sub> hinders effective adsorption. It should be noted that the point of zero charge (pH<sub>pzc</sub>) is defined, as the pH at which the net surface charge of an adsorbent becomes zero, is an important physico-chemical parameter providing information on the phenomena occurring at the surface of adsorbents. At a pH below pHpzc, protonated adsorbent surface functional groups attract negatively charged adsorbates due to an excess H<sup>+</sup>. At a pH above pH<sub>pzc</sub>, the positively charged adsorbates are adsorbed onto the negatively charged adsorbent surface. Therefore, strongly acidic conditions are not favorable for the removal of MB using the proposed adsorbent. As the pH increases, these effects are mitigated, leading to improved dye removal efficiency. At higher pH values (pH ≥ pH<sub>pzc</sub>), the adsorbent surface becomes negatively charged, promoting stronger electrostatic attraction with the positively charged MB⁺ molecules and resulting in enhanced adsorption <xref ref-type="bibr" rid="scirp.146872-11">
      [11]
     </xref> <xref ref-type="bibr" rid="scirp.146872-35">
      [35]
     </xref> <xref ref-type="bibr" rid="scirp.146872-36">
      [36]
     </xref>. Based on this, we focused on pH values equal to or above 7, particularly since methylene blue (MB⁺) remains positively charged (cationic) in basic media. The optimal pH was determined to be 10, at which the maximum removal efficiency of MB reached 89.07%, <xref ref-type="fig" rid="fig2">
      Figure 2
     </xref>.</p>
    <fig id="fig2" position="float">
     <label>Figure 2</label>
     <caption>
      <title>
       <xref ref-type="bibr" rid="scirp.146872-"></xref>Figure 2. Effect of pH on the efficiency of removing MB by γ-AlOOH.</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/2610525-rId32.jpeg?20251031113937" />
    </fig>
   </sec>
   <sec id="s3_2">
    <title>3.2. The Effect of Adsorbent Amount</title>
    <p>
     <xref ref-type="bibr" rid="scirp.146872-"></xref>To investigate the effect of adsorbent dosage on dye removal, varying masses of adsorbent ranging from 10 mg to 80 mg were each added to 50 mL of methylene blue (MB) solution at a concentration of 30 mg·L<sup>−</sup><sup>1</sup>. As shown in <xref ref-type="fig" rid="fig3">
      Figure 3
     </xref>, the percentage of MB removal increased with increasing adsorbent mass. This behavior is attributed to the greater number of available adsorption sites provided by the increased quantity of adsorbent, thereby enhancing the amount of dye adsorbed. Above 30 mg, the system reached equilibrium, and no significant increase in removal efficiency was observed with further increases in adsorbent mass. Therefore, subsequent experiments were conducted using this optimal dosage of 30 mg, <xref ref-type="fig" rid="fig3">
      Figure 3
     </xref>.</p>
   </sec>
   <sec id="s3_3">
    <title>3.3. The Effect of MB Dye</title>
    <p>At various initial concentrations of methylene blue (ranging from 10 to 80 mg·L<sup>−</sup><sup>1</sup>), the optimal adsorbent dosage and pH were maintained. As shown by the adsorption curve, a significant removal efficiency of MB was observed at concentrations between 10 and 30 mg·L<sup>−</sup><sup>1</sup>, reaching up to 90%. Beyond this range, the curve tends to stabilize. This phenomenon can be explained as follows: at lower dye concentrations, a large number of available pores and active sites on the surface of the adsorbent facilitate efficient adsorption. However, as the initial concentration of MB increases, these sites gradually become saturated due to the accumulation of dye molecules, leading to a decrease in removal efficiency. At a concentration of 90 mg·L<sup>−</sup><sup>1</sup>, the removal efficiency dropped to 53.073%, indicating that the adsorption capacity of the boehmite had reached near saturation, <xref ref-type="fig" rid="fig4">
      Figure 4
     </xref>.</p>
    <fig id="fig3" position="float">
     <label>Figure 3</label>
     <caption>
      <title>
       <xref ref-type="bibr" rid="scirp.146872-"></xref>Figure 3. Effect of adsorbent initial mass (γ-AlOOH) on the efficiency of removing MB.</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/2610525-rId33.jpeg?20251031113938" />
    </fig>
    <fig id="fig4" position="float">
     <label>Figure 4</label>
     <caption>
      <title>
       <xref ref-type="bibr" rid="scirp.146872-"></xref>Figure 4. Effect of initial dye concentration on adsorption of MB.</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/2610525-rId34.jpeg?20251031113938" />
    </fig>
   </sec>
   <sec id="s3_4">
    <title>3.4. The Effect of Adsorption Time</title>
    <p>Kinetic studies aim to determine the sufficient and necessary time required to reach adsorption equilibrium or maximum adsorption capacity. In the case of methylene blue (MB), the adsorption process was found to be rapid and increased progressively with contact time. In our study, equilibrium was reached after 30 minutes of contact. The high availability of active sites on the surface of the adsorbent is responsible for this rapid initial adsorption of MB from the aqueous solution during the first few minutes. Beyond this point, the amount of dye adsorbed remained nearly constant, even with extended contact time up to 180 minutes, indicating that equilibrium had been attained. The effect of contact time on MB adsorption by pseudoboehmite (γ-AlOOH). MB adsorption follows rapid kinetics, reaching a near-equilibrium state after 30 min, <xref ref-type="fig" rid="fig5">
      Figure 5
     </xref>. This could be justified by the availability of active sites.</p>
    <fig id="fig5" position="float">
     <label>Figure 5</label>
     <caption>
      <title>
       <xref ref-type="bibr" rid="scirp.146872-"></xref>Figure 5. Effect of contact time on the adsorption of MB onto boehmite (γ-AlOOH).</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/2610525-rId35.jpeg?20251031113939" />
    </fig>
   </sec>
   <sec id="s3_5">
    <title>3.5. The Effect Temperature</title>
    <p>
     <xref ref-type="bibr" rid="scirp.146872-"></xref>Similarly, the effect of temperature was studied using a thermostatic system at different temperatures (25˚C, 30˚C, 35˚C, and 60˚C), with absorbance readings taken at each condition. It was observed that increasing the temperature led to a decrease in removal efficiency, indicating a reversal of the adsorption process—desorption. This behavior suggests that the adsorption of methylene blue onto pseudoboehmite is an exothermic process. The observed desorption at higher temperatures is also advantageous for the regeneration of the adsorbent, allowing reuse in subsequent cycles. The optimal temperature for this experiment was found to be 25˚C, as the highest amount of MB was adsorbed at this ambient condition, <xref ref-type="fig" rid="fig6">
      Figure 6
     </xref>.</p>
    <fig id="fig6" position="float">
     <label>Figure 6</label>
     <caption>
      <title>
       <xref ref-type="bibr" rid="scirp.146872-"></xref>Figure 6. Effect of temperature on the adsorption of MB onto boehmite (γ-AlOOH).</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/2610525-rId36.jpeg?20251031113940" />
    </fig>
   </sec>
   <sec id="s3_6">
    <title>3.6. Kinetic Studies</title>
    <p>Two models, including the pseudo-first-order and the pseudo-second-order (<xref ref-type="fig" rid="fig7">
      Figure 7
     </xref> and <xref ref-type="fig" rid="fig8">
      Figure 8
     </xref>), were used to adjust the experimental data. The pseudo-second-order model has a correlation coefficient (R<sup>2</sup> = 0.997) higher than the value obtained for the pseudo-first-order model (R<sup>2</sup> = 0.791). This indicates that the pseudo-second-order model best describes the adsorption data. The pseudo-second-order kinetic model fitted well with all experimental data, meaning that the adsorption rate was mainly determined by the chemical adsorption process. This fitting result indicated that the electron transfer, exchange, or sharing was generated, and chemical bond was formed in the adsorption process. The k<sub>1</sub> and k<sub>2</sub> are presented in <xref ref-type="table" rid="table1">
      Table 1
     </xref> <xref ref-type="bibr" rid="scirp.146872-11">
      [11]
     </xref> <xref ref-type="bibr" rid="scirp.146872-37">
      [37]
     </xref>-<xref ref-type="bibr" rid="scirp.146872-40">
      [40]
     </xref>.</p>
   </sec>
   <sec id="s3_7">
    <title>3.7. The Equilibrium Studies</title>
    <p>The adjustment of the experimental data to the Langmuir and Freundlich models is shown in <xref ref-type="fig" rid="fig9">
      Figure 9
     </xref> and <xref ref-type="fig" rid="fig10">
      Figure 10
     </xref>. The Freundlich model is considered most appropriate because it provides a better fit with the highest (R<sup>2</sup> = 0.85) compared to the Langmuir isotherm, which had a correlation coefficient of about 0.81 (<xref ref-type="table" rid="table2">
      Table 2
     </xref>). However, the intrinsic parameters of Langmuir isotherm have a negative value. These negative values of Q<sub>max</sub> and K<sub>L</sub> are attributed more to the properties of the adsorbent than to the experimental conditions. Specific characteristics of the adsorbent, such as the presence of heterogeneous surface sites or complex interactions between adsorbed molecules, can render the Langmuir model unsuitable. Perwitasari et al. reported that, for the Langmuir equation, all linearized plots yield negative values of K<sub>L</sub> and Q<sub>max</sub>; consequently, the adsorption process is better suited to a heterogeneous surface <xref ref-type="bibr" rid="scirp.146872-41">
      [41]
     </xref>. Indeed, our adsorbent is a material with a heterogeneous surface <xref ref-type="bibr" rid="scirp.146872-33">
      [33]
     </xref>. The Freundlich isotherm was all better than the Langmuir isotherm, implying that the adsorption process involved multimolecular layers of coverage, and heterogeneous nature of adsorptive sites on the surface of adsorbent <xref ref-type="bibr" rid="scirp.146872-1">
      [1]
     </xref> <xref ref-type="bibr" rid="scirp.146872-42">
      [42]
     </xref>. The Langmuir and Freundlich constants for the adsorption isotherm models and statistical are summarized in <xref ref-type="table" rid="table2">
      Table 2
     </xref>. The intensity factor was found higher to unity (1/n = 1.39) which corresponded to a favourable adsorption <xref ref-type="bibr" rid="scirp.146872-43">
      [43]
     </xref>.</p>
    <fig id="fig7" position="float">
     <label>Figure 7</label>
     <caption>
      <title>
       <xref ref-type="bibr" rid="scirp.146872-"></xref>Figure 7. Plots of the pseudo-first-order.</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/2610525-rId37.jpeg?20251031113942" />
    </fig>
    <fig id="fig8" position="float">
     <label>Figure 8</label>
     <caption>
      <title>
       <xref ref-type="bibr" rid="scirp.146872-"></xref>Figure 8. Plot of the pseudo-second order.</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/2610525-rId38.jpeg?20251031113942" />
    </fig>
    <table-wrap id="table1">
     <label>
      <xref ref-type="table" rid="table1">
       Table 1
      </xref></label>
     <caption>
      <title>
       <xref ref-type="bibr" rid="scirp.146872-"></xref>Table 1. Chemical bond formed in the adsorption process.</title>
     </caption>
     <table class="MsoTableGrid custom-table" border="0" cellspacing="0" cellpadding="0"> 
      <tr> 
       <td class="custom-bottom-td acenter" width="34.44%"><p style="text-align:center">Order</p></td> 
       <td class="custom-bottom-td acenter" width="34.44%"><p style="text-align:center">Pseudo-first order</p></td> 
       <td class="custom-bottom-td acenter" width="38.82%"><p style="text-align:center">Pseudo-second order</p></td> 
      </tr> 
      <tr> 
       <td class="custom-top-td acenter" width="34.44%"><p style="text-align:center">R<sup>2</sup></p></td> 
       <td class="custom-top-td acenter" width="34.44%"><p style="text-align:center">0.79</p></td> 
       <td class="custom-top-td acenter" width="38.82%"><p style="text-align:center">0.99783</p></td> 
      </tr> 
      <tr> 
       <td class="acenter" width="34.44%"><p style="text-align:center">K</p></td> 
       <td class="acenter" width="34.44%"><p style="text-align:center">0.00014</p></td> 
       <td class="acenter" width="38.82%"><p style="text-align:center">0.0043</p></td> 
      </tr> 
      <tr> 
       <td class="acenter" width="34.44%"><p style="text-align:center">q<sub>e</sub></p></td> 
       <td class="acenter" width="34.44%"><p style="text-align:center">3.40</p></td> 
       <td class="acenter" width="38.82%"><p style="text-align:center">46.75</p></td> 
      </tr> 
     </table>
    </table-wrap>
    <fig id="fig9" position="float">
     <label>Figure 9</label>
     <caption>
      <title>
       <xref ref-type="bibr" rid="scirp.146872-"></xref>Figure 9. Langmuir model.</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/2610525-rId39.jpeg?20251031113942" />
    </fig>
    <fig id="fig10" position="float">
     <label>Figure 10</label>
     <caption>
      <title>
       <xref ref-type="bibr" rid="scirp.146872-"></xref>Figure 10. Freundlich model.</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/2610525-rId40.jpeg?20251031113942" />
    </fig>
    <table-wrap id="table2">
     <label>
      <xref ref-type="table" rid="table2">
       Table 2
      </xref></label>
     <caption>
      <title>
       <xref ref-type="bibr" rid="scirp.146872-"></xref>Table 2. The Langmuir and Freundlich constants for the adsorption isotherm models.</title>
     </caption>
     <table class="MsoTableGrid custom-table" border="0" cellspacing="0" cellpadding="0"> 
      <tr> 
       <td class="custom-bottom-td acenter" width="53.88%" colspan="4"><p style="text-align:center">Langmuir isotherm</p></td> 
       <td class="custom-bottom-td acenter" width="46.12%" colspan="4"><p style="text-align:center">Freundlich isotherm</p></td> 
      </tr> 
      <tr> 
       <td class="custom-top-td acenter" width="12.10%"><p style="text-align:center">R<sup>2</sup></p></td> 
       <td class="custom-top-td acenter" width="12.09%"><p style="text-align:center">K<sub>L</sub> (l/mg)</p></td> 
       <td class="custom-top-td acenter" width="16.77%"><p style="text-align:center">Q<sub>max</sub> (mg/g)</p></td> 
       <td class="custom-top-td acenter" width="12.92%"><p style="text-align:center">R<sub>L</sub></p></td> 
       <td class="custom-top-td acenter" width="12.94%"><p style="text-align:center">R<sup>2</sup></p></td> 
       <td class="custom-top-td acenter" width="8.21%"><p style="text-align:center">1/n</p></td> 
       <td class="custom-top-td acenter" width="12.48%"><p style="text-align:center">n</p></td> 
       <td class="custom-top-td acenter" width="12.48%"><p style="text-align:center">K<sub>f</sub></p></td> 
      </tr> 
      <tr> 
       <td class="acenter" width="12.10%"><p style="text-align:center">0.81</p></td> 
       <td class="acenter" width="12.09%"><p style="text-align:center">−0.036</p></td> 
       <td class="acenter" width="16.77%"><p style="text-align:center">−91.99</p></td> 
       <td class="acenter" width="12.92%"><p style="text-align:center">1.00</p></td> 
       <td class="acenter" width="12.94%"><p style="text-align:center">0.85</p></td> 
       <td class="acenter" width="8.21%"><p style="text-align:center">1.39</p></td> 
       <td class="acenter" width="12.48%"><p style="text-align:center">0.72</p></td> 
       <td class="acenter" width="12.48%"><p style="text-align:center">7.26</p></td> 
      </tr> 
     </table>
    </table-wrap>
   </sec>
   <sec id="s3_8">
    <title>3.8. Thermodynamic Studies</title>
    <p>The Gibb’s free energy (ΔG<sup>0</sup>), entropy (ΔS<sup>0</sup>), and enthalpy (ΔH<sup>0</sup>) changes for the adsorption were determined by:</p>
    <p>
     <math xmlns="http://www.w3.org/1998/Math/MathML"> <mrow> 
       <mi>
         ln 
       </mi> 
       <msub> 
        <mi>
          k 
        </mi> 
        <mi>
          l 
        </mi> 
       </msub> 
       <mo>
         = 
       </mo> 
       <mrow> 
        <mrow> 
         <mrow> 
          <mo>
            ( 
          </mo> 
          <mrow> 
           <mi>
             Δ 
           </mi> 
           <msup> 
            <mi>
              S 
            </mi> 
            <mn>
              0 
            </mn> 
           </msup> 
          </mrow> 
          <mo>
            ) 
          </mo> 
         </mrow> 
        </mrow> 
        <mo>
          / 
        </mo> 
        <mi>
          R 
        </mi> 
       </mrow> 
       <mo>
         − 
       </mo> 
       <mrow> 
        <mrow> 
         <mrow> 
          <mo>
            ( 
          </mo> 
          <mrow> 
           <mi>
             Δ 
           </mi> 
           <msup> 
            <mi>
              H 
            </mi> 
            <mn>
              0 
            </mn> 
           </msup> 
          </mrow> 
          <mo>
            ) 
          </mo> 
         </mrow> 
        </mrow> 
        <mo>
          / 
        </mo> 
        <mrow> 
         <mi>
           R 
         </mi> 
         <mi>
           T 
         </mi> 
        </mrow> 
       </mrow> 
      </mrow> 
     </math> (7)</p>
    <p>
     <math xmlns="http://www.w3.org/1998/Math/MathML"> <mrow> 
       <mi>
         Δ 
       </mi> 
       <msup> 
        <mi>
          G 
        </mi> 
        <mn>
          0 
        </mn> 
       </msup> 
       <mo>
         = 
       </mo> 
       <mi>
         Δ 
       </mi> 
       <msup> 
        <mi>
          H 
        </mi> 
        <mn>
          0 
        </mn> 
       </msup> 
       <mo>
         − 
       </mo> 
       <mi>
         T 
       </mi> 
       <mi>
         Δ 
       </mi> 
       <msup> 
        <mi>
          S 
        </mi> 
        <mn>
          0 
        </mn> 
       </msup> 
      </mrow> 
     </math> (8)</p>
    <p>where T is the solution temperature (K), R is the universal gas constant (8.314 J·K<sup>−</sup><sup>1</sup>·mol<sup>−</sup><sup>1</sup>) and K<sub>l</sub> is the equilibrium constant. The calculated thermodynamic parameters are demonstrated in <xref ref-type="table" rid="table3">
      Table 3
     </xref>. The values of Gibbs free energy ΔG<sup>0</sup> had been calculated by knowing the ΔH<sup>0</sup> and the ΔS<sup>0</sup> and ΔH<sup>0</sup> were obtained from a plot of lnK<sub>l</sub> versus 1/T, from Equation (7). Once these two parameters were obtained, ΔG<sup>0</sup> is determined from Equation (8). The respective values of thermodynamic parameters for adsorption of methylene blue using pseudoboehmite are given in <xref ref-type="table" rid="table3">
      Table 3
     </xref>. The negative values of the free energy change (ΔG<sup>0</sup>) indicate that the adsorption of methylene blue is favorable and spontaneous process. The negative value of change in enthalpy (ΔH<sup>0</sup>) indicates the exothermic nature of adsorption process. The negative entropy (ΔS<sup>0</sup>) value of entropy change indicated a more ordered distribution of Methylene Blue solution in solid phase rather than in liquid phase <xref ref-type="bibr" rid="scirp.146872-1">
      [1]
     </xref> (<xref ref-type="fig" rid="fig11">
      Figure 11
     </xref>).</p>
    <fig id="fig11" position="float">
     <label>Figure 11</label>
     <caption>
      <title>
       <xref ref-type="bibr" rid="scirp.146872-"></xref>Figure 11. Plot of lnkd vs. 1/T for the adsorption of BM onto Pseudoboehmite.</title>
     </caption>
     <graphic mimetype="image" position="float" xlink:type="simple" xlink:href="https://html.scirp.org/file/2610525-rId45.jpeg?20251031113943" />
    </fig>
    <table-wrap id="table3">
     <label>
      <xref ref-type="table" rid="table3">
       Table 3
      </xref></label>
     <caption>
      <title>
       <xref ref-type="bibr" rid="scirp.146872-"></xref>Table 3. Thermodynamic parameters.</title>
     </caption>
     <table class="MsoTableGrid custom-table" border="0" cellspacing="0" cellpadding="0"> 
      <tr> 
       <td class="custom-bottom-td acenter" width="19.32%"><p style="text-align:center">Adsorbant</p></td> 
       <td class="custom-bottom-td acenter" width="19.32%"><p style="text-align:center">T (K)</p></td> 
       <td class="custom-bottom-td acenter" width="20.69%"><p style="text-align:center">ΔG<sup>0</sup> (KJ/mol)</p></td> 
       <td class="custom-bottom-td acenter" width="20.69%"><p style="text-align:center">ΔH<sup>0</sup> (KJ/mol)</p></td> 
       <td class="custom-bottom-td acenter" width="19.96%"><p style="text-align:center">ΔS<sup>0</sup> (KJ/mol)</p></td> 
      </tr> 
      <tr> 
       <td class="custom-top-td acenter" width="19.32%"><p style="text-align:center"></p></td> 
       <td class="custom-top-td acenter" width="19.32%"><p style="text-align:center">298</p></td> 
       <td class="custom-top-td acenter" width="20.69%"><p style="text-align:center">–7.05709549</p></td> 
       <td class="custom-top-td acenter" width="20.69%"><p style="text-align:center">–86.6984793</p></td> 
       <td class="custom-top-td acenter" width="19.96%"><p style="text-align:center">−0.26854062</p></td> 
      </tr> 
      <tr> 
       <td class="acenter" width="19.32%"><p style="text-align:center"></p></td> 
       <td class="acenter" width="19.32%"><p style="text-align:center">303</p></td> 
       <td class="acenter" width="20.69%"><p style="text-align:center">–4.53876283</p></td> 
       <td class="acenter" width="20.69%"><p style="text-align:center"></p></td> 
       <td class="acenter" width="19.96%"><p style="text-align:center"></p></td> 
      </tr> 
      <tr> 
       <td class="acenter" width="19.32%"><p style="text-align:center"></p></td> 
       <td class="acenter" width="19.32%"><p style="text-align:center">308</p></td> 
       <td class="acenter" width="20.69%"><p style="text-align:center">–4.39775412</p></td> 
       <td class="acenter" width="20.69%"><p style="text-align:center"></p></td> 
       <td class="acenter" width="19.96%"><p style="text-align:center"></p></td> 
      </tr> 
     </table>
    </table-wrap>
   </sec>
  </sec><sec id="s4">
   <title>4. Conclusion</title>
   <p>The adsorption capacity of γ-AlOOH particles was evaluated for MB dye removal. Adsorbent shows promising adsorption capacitie for MB. Investigation of the isotherms revealed a close correlation with the Freundlich isotherm model. However, both models can also be applied under specific conditions. The kinetic data are in good agreement with the pseudo-second-order kinetic model. The efficiency of methylene blue removal increases as the temperature decreases. The negative enthalpy change (ΔH<sup>0</sup>) further corroborates the exothermic nature of the adsorption process. Hence, pseudoboehmite can be regarded as a highly promising material for wastewater remediation.</p>
  </sec><sec id="s5">
   <title>Acknowledgements</title>
   <p>Authors acknowledge the Universities Université de Ndjamena (Tchad) et Université Hassan 1<sup>er</sup> de Settat (Maroc).</p>
  </sec>
 </body><back>
  <ref-list>
   <title>References</title>
   <ref id="scirp.146872-ref1">
    <label>1</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Salimi, F., Emami, S.S. and Karami, C. (2017) Removal of Methylene Blue from Water Solution by Modified Nano-Boehmite with Bismuth. Inorganic and Nano-Metal Chemistry, 48, 31-40. &gt;https://doi.org/10.1080/24701556.2017.1357628 
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref2">
    <label>2</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Rane, N.R., Chandanshive, V.V., Khandare, R.V., Gholave, A.R., Yadav, S.R. and Govindwar, S.P. (2014) Green Remediation of Textile Dyes Containing Wastewater by Ipomoea hederifolia L. RSC Advances, 4, 36623-36632. &gt;https://doi.org/10.1039/c4ra06840h 
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref3">
    <label>3</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Wu, Y., Chen, L., Long, X., Zhang, X., Pan, B. and Qian, J. (2018) Multi-Functional Magnetic Water Purifier for Disinfection and Removal of Dyes and Metal Ions with Superior Reusability. Journal of Hazardous Materials, 347, 160-167. &gt;https://doi.org/10.1016/j.jhazmat.2017.12.037
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref4">
    <label>4</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Ai, L., Zhang, C., Liao, F., Wang, Y., Li, M., Meng, L., et al. (2011) Removal of Methylene Blue from Aqueous Solution with Magnetite Loaded Multi-Wall Carbon Nanotube: Kinetic, Isotherm and Mechanism Analysis. Journal of Hazardous Materials, 198, 282-290. &gt;https://doi.org/10.1016/j.jhazmat.2011.10.041
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref5">
    <label>5</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Kamaria, M., Shafieea, S., Salimia, F. and Karami, C. (2019) Comparison of Modified Boehmite Nanoplatelets and Nanowires for Dye Removal from Aqueous Solution. Desalination and Water Treatment, 161, 304-314. 
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref6">
    <label>6</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Pearce, C. (2003) The Removal of Colour from Textile Wastewater Using Whole Bacterial Cells: A Review. Dyes and Pigments, 58, 179-196. &gt;https://doi.org/10.1016/s0143-7208(03)00064-0 
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref7">
    <label>7</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Arslan, İ., Balcioǧlu, I.A. and Bahnemann, D.W. (2000) Advanced Chemical Oxidation of Reactive Dyes in Simulated Dyehouse Effluents by Ferrioxalate-Fenton/UV-A and TiO2/UV-A Processes. Dyes and Pigments, 47, 207-218. &gt;https://doi.org/10.1016/s0143-7208(00)00082-6
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref8">
    <label>8</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Sauer, T., Neto, G.C., Jose, H. and Moreira, R. (2002) Kinetics of Photocatalytic Degradation of Reactivedyes in a TiO2 Slurry Reactor. Journal of Photochemistry and Photobiology A: Chemistry, 149, 147-154. 
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref9">
    <label>9</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Srinivasan, A. and Viraraghavan, T. (2010) Decolorization of Dye Wastewaters by Biosorbents: A Review. Journal of Environmental Management, 91, 1915-1929. &gt;https://doi.org/10.1016/j.jenvman.2010.05.003
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref10">
    <label>10</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Ben Younes, S., Bouallagui, Z. and Sayadi, S. (2012) Catalytic Behavior and Detoxifying Ability of an Atypical Homotrimeric Laccase from the Thermophilic Strain Scytalidium Thermophilum on Selected Azo and Triarylmethane Dyes. Journal of Molecular Catalysis B: Enzymatic, 79, 41-48. &gt;https://doi.org/10.1016/j.molcatb.2012.03.017
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref11">
    <label>11</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Salimi, F., Rahimi, H. and Karami, C. (2019) Removal of Methylene Blue from Water Solution by Modified Nanogoethite by Cu. Desalination and Water Treatment, 137, 334-344. &gt;https://doi.org/10.5004/dwt.2019.22922 
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref12">
    <label>12</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Yagub, M.T., Sen, T.K., Afroze, S. and Ang, H.M. (2014) Dye and Its Removal from Aqueous Solution by Adsorption: A Review. Advances in Colloid and Interface Science, 209, 172-184. &gt;https://doi.org/10.1016/j.cis.2014.04.002
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref13">
    <label>13</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Park, C., Lee, M., Lee, B., Kim, S., Chase, H.A., Lee, J., et al. (2007) Biodegradation and Biosorption for Decolorization of Synthetic Dyes by Funalia Trogii. Biochemical Engineering Journal, 36, 59-65. &gt;https://doi.org/10.1016/j.bej.2006.06.007
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref14">
    <label>14</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Taha, M., Adetutu, E.M., Shahsavari, E., Smith, A.T. and Ball, A.S. (2014) Azo and Anthraquinone Dye Mixture Decolourization at Elevated Temperature and Concentration by a Newly Isolated Thermophilic Fungus, Thermomucor Indicae-Seudaticae. Journal of Environmental Chemical Engineering, 2, 415-423. &gt;https://doi.org/10.1016/j.jece.2014.01.015
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref15">
    <label>15</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Cornell, R. and Schwertmann, U. (2003) Dissolution, the Iron Oxides: Structure, Properties, Reactions, Occurrences and Uses. 2nd Edition, Wiley-VCH, 297-344. 
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref16">
    <label>16</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Senthil Kumar, P., Sivaranjanee, R., Vinothini, U., Raghavi, M., Rajasekar, K. and Ramakrishnan, K. (2014) Adsorption of Dye onto Raw and Surface Modified Tamarind Seeds: Isotherms, Process Design, Kinetics and Mechanism. Desalination and Water Treatment, 52, 2620-2633. &gt;https://doi.org/10.1080/19443994.2013.792016
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref17">
    <label>17</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Kumar, P.S., Pavithra, J., Suriya, S., Ramesh, M. and Kumar, K.A. (2015) Sargassum wightii, a Marine Alga Is the Source for the Production of Algal Oil, Bio-Oil, and Application in the Dye Wastewater Treatment. Desalination and Water Treatment, 55, 1342-1358. &gt;https://doi.org/10.1080/19443994.2014.924032
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref18">
    <label>18</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Mathivanan, V., Geetha Manjari, S., Ineya, R., Saravanathamizhan, R., Senthil Kumar, P. and Ramakrishnan, K. (2016) Enhanced Photocatalytic Decolorization of Reactive Red by Sonocatalysis Using TiO2 Catalyst: Factorial Design of Experiments. Desalination and Water Treatment, 57, 7120-7129. &gt;https://doi.org/10.1080/19443994.2014.983182
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref19">
    <label>19</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Salimi, F., Eskandari, M. and Karami, C. (2017) Investigation of Methylene Blue Adsorption in Wastewater Using Nano-Zeolite Modified with Copper. Desalination and Water Treatment, 85, 206-214. &gt;https://doi.org/10.5004/dwt.2017.21248
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref20">
    <label>20</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Salimi, F., Tahmasobi, K., Karami, C. and Jahangiri, A. (2017) Preparation of Modified Nano-SiO2 by Bismuth and Iron as a Novel Remover of Methylene Blue from Water Solution. Journal of the Mexican Chemical Society, 61, 250-259. &gt;https://doi.org/10.29356/jmcs.v61i3.351
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref21">
    <label>21</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Alvarez, M., Rueda, E.H. and Sileo, E.E. (2007) Simultaneous Incorporation of Mn and Al in the Goethite Structure. Geochimica et Cosmochimica Acta, 71, 1009-1020. &gt;https://doi.org/10.1016/j.gca.2006.11.012
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref22">
    <label>22</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Crini, G., Lichtfouse, E., Wilson, L.D. and Morin-Crini, N. (2019) Conventional and Non-Conventional Adsorbents for Wastewater Treatment. Environmental Chemistry Letters, 17, 195-213. &gt;https://doi.org/10.1007/s10311-018-0786-8
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref23">
    <label>23</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     AbdEl-Salam, A.H., Ewais, H.A. and Basaleh, A.S. (2017) Silver Nanoparticles Immobilised on the Activated Carbon as Efficient Adsorbent for Removal of Crystal Violet Dye from Aqueous Solutions. a Kinetic Study. Journal of Molecular Liquids, 248, 833-841. &gt;https://doi.org/10.1016/j.molliq.2017.10.109 
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref24">
    <label>24</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Sadegh, H., Ali, G.A.M., Gupta, V.K., Makhlouf, A.S.H., Shahryari-ghoshekandi, R., Nadagouda, M.N., et al. (2017) The Role of Nanomaterials as Effective Adsorbents and Their Applications in Wastewater Treatment. Journal of Nanostructure in Chemistry, 7, 1-14. &gt;https://doi.org/10.1007/s40097-017-0219-4
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref25">
    <label>25</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Shinde, S.G. and Shrivastava, V.S. (2016) Synthesis of γ-Alumina (Al₂O₃) Nanoparticles and their Potential for Use as an Adsorbent in the Removal of Methylene Blue Dye from Industrial Wastewater. Asian Journal of Chemical and Environmental Research, 9, 129-132.
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref26">
    <label>26</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Arshadi, M., Mehravar, M., Amiri, M.J. and Faraji, A.R. (2015) Synthesis and Adsorption Characteristics of an Heterogenized Manganese Nanoadsorbent Towards Methyl Orange. Journal of Colloid and Interface Science, 440, 189-197. &gt;https://doi.org/10.1016/j.jcis.2014.10.053 
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref27">
    <label>27</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Huang, Q., Liu, M., Chen, J., Wan, Q., Tian, J., Huang, L., et al. (2017) Facile Preparation of Mos2 Based Polymer Composites via Mussel Inspired Chemistry and Their High Efficiency for Removal of Organic Dyes. Applied Surface Science, 419, 35-44. &gt;https://doi.org/10.1016/j.apsusc.2017.05.006 
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref28">
    <label>28</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Jiang, Y., Gong, J., Zeng, G., Ou, X., Chang, Y., Deng, C., et al. (2016) Magnetic Chitosan-Graphene Oxide Composite for Anti-Microbial and Dye Removal Applications. International Journal of Biological Macromolecules, 82, 702-710. &gt;https://doi.org/10.1016/j.ijbiomac.2015.11.021 
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref29">
    <label>29</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Mishra, D., Anand, S., Panda, R.K. and Das, R.P. (2000) Hydrothermal Preparation and Characterization of Boehmites. Materials Letters, 42, 38-45. &gt;https://doi.org/10.1016/s0167-577x(99)00156-1
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref30">
    <label>30</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Hou, H., Xie, Y., Yang, Q., Guo, Q. and Tan, C. (2005) Preparation and Characterization of γ-ALOOH Nanotubes and Nanorods. Nanotechnology, 16, 741-745. &gt;https://doi.org/10.1088/0957-4484/16/6/019
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref31">
    <label>31</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Wierenga, A., Philipse, A.P., Lekkerkerker, H.N.W. and Boger, D.V. (1998) Aqueous Dispersions of Colloidal Boehmite: Structure, Dynamics, and Yield Stress of Rod Gels. Langmuir, 14, 55-65. &gt;https://doi.org/10.1021/la970376z
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref32">
    <label>32</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Zhang, J., Liu, S., Lin, J., Song, H., Luo, J., Elssfah, E.M., et al. (2006) Self-Assembly of Flowerlike ALOOH (Boehmite) 3D Nanoarchitectures. The Journal of Physical Chemistry B, 110, 14249-14252. &gt;https://doi.org/10.1021/jp062105f
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref33">
    <label>33</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Yaya, I.M., Guillaume, N. and Arkhis, M. (2018) The Synthesis of Mesoporous Pseudo Boehmite by a Route Mineral and Its Transformation into Alumina-γ. Materials Science: An Indian Journal, 16, Article 140.
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref34">
    <label>34</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Revellame, E.D., Fortela, D.L., Sharp, W., Hernandez, R. and Zappi, M.E. (2020) Adsorption Kinetic Modeling Using Pseudo-First Order and Pseudo-Second Order Rate Laws: A Review. Cleaner Engineering and Technology, 1, Article 100032. &gt;https://doi.org/10.1016/j.clet.2020.100032
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref35">
    <label>35</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Kamari, M., Shafiee, S., Salimi, F. and Karami, C. (2019) Comparison of Modified Boehmite Nanoplatelets and Nanowires for Dye Removal from Aqueous Solution. Desalination and Water Treatment, 161, 304-314. &gt;https://doi.org/10.5004/dwt.2019.24295 
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref36">
    <label>36</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Wang, D., Li, Z., Lv, F., Guan, M., Chen, J., Wu, C., et al. (2023) Characterization of Microspheres γ-ALOOH and the Excellent Removal Efficiency of Congo Red. Journal of Physics and Chemistry of Solids, 174, Article 111043. &gt;https://doi.org/10.1016/j.jpcs.2022.111043
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref37">
    <label>37</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Sun, Y., Ding, C., Cheng, W. and Wang, X. (2014) Simultaneous Adsorption and Reduction of U(VI) on Reduced Graphene Oxide-Supported Nanoscale Zerovalent Iron. Journal of Hazardous Materials, 280, 399-408. &gt;https://doi.org/10.1016/j.jhazmat.2014.08.023
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref38">
    <label>38</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Khan, H., Iram, Gul, K., Ara, B., Khan, A., Ali, N., et al. (2020) Adsorptive Removal of Acrylic Acid from the Aqueous Environment Using Raw and Chemically Modified Alumina: Batch Adsorption, Kinetic, Equilibrium and Thermodynamic Studies. Journal of Environmental Chemical Engineering, 8, Article 103927. &gt;https://doi.org/10.1016/j.jece.2020.103927
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref39">
    <label>39</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Sheng, G., Li, J., Shao, D., Hu, J., Chen, C., Chen, Y., et al. (2010) Adsorption of Copper (II) on Multiwalled Carbon Nanotubes in the Absence and Presence of Humic or Fulvic Acids. Journal of Hazardous Materials, 178, 333-340. &gt;https://doi.org/10.1016/j.jhazmat.2010.01.084
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref40">
    <label>40</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Ciopec, M., Davidescu, C.M., Negrea, A., Grozav, I., Lupa, L., Negrea, P., et al. (2012) Adsorption Studies of Cr(iii) Ions from Aqueous Solutions by DEHPA Impregnated onto Amberlite XAD7—Factorial Design Analysis. Chemical Engineering Research and Design, 90, 1660-1670. &gt;https://doi.org/10.1016/j.cherd.2012.01.016
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref41">
    <label>41</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Perwitasari, D.S., Pracesa, Y.A.Y., Pangestu, M.A. and Tola, P.S. (2021) Langmuir and Freundlich Isotherm Approximation on Adsorption Mechanism of Chrome Waste by Using Tofu Dregs. 2nd International Conference Eco-Innovation in Science, Engineering, and Technology, Samara, 11 December 2021, 106-112.&gt;https://doi.org/10.11594/nstp.2021.1417 
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref42">
    <label>42</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Mve, M.Z., Mba, C.M.M., Eba, F. and Ondo, J.A. (2020) Study of the Adsorption Equilibrium of the Methylene blue from Aqueous Solution onto Activated Carbon of Coula Edulis Nut Shells. Research Journal of Chemistry and Environment, 24, 40-50. 
    </mixed-citation>
   </ref>
   <ref id="scirp.146872-ref43">
    <label>43</label>
    <mixed-citation publication-type="other" xlink:type="simple">
     Danesh, N., Hosseini, M., Ghorbani, M. and Marjani, A. (2016) Fabrication, Characterization and Physical Properties of a Novel Magnetite Graphene Oxide/Lauric Acid Nanoparticles Modified by Ethylenediaminetetraacetic Acid and Its Applications as an Adsorbent for the Removal of Pb(ii) Ions. Synthetic Metals, 220, 508-523. &gt;https://doi.org/10.1016/j.synthmet.2016.07.025
    </mixed-citation>
   </ref>
  </ref-list>
 </back>
</article>