Phosphoric Acid Activation Research Articles

Influence of Phosphoric Acid Activation on Physiochemical Characteristics of Activated Carbons and Their Performance as Supercapacitor

ABSTRACTWe investigate the influence of phosphoric acid (H3PO4) activation on physiochemical characteristics of activated carbons (ACs) as a function of number of activation steps such as two‐step and three‐step and impregnation ratio (IR). Scanning electron microscopy observations identified that different morphologies in the forms of graphene sheet‐like, nano‐granular, and flake‐like carbon structure in the cases of ACs. FTIR spectroscopy confirmed that successful incorporation of phosphorous group in the ACs by H3PO4 activation. X‐ray diffraction (XRD) profile exposed that irrespective of the activation method and IR, all AC samples showed narrow and sharp XRD crystalline peak along with the amorphous signals. Raman scattering analysis suggested that three‐step activation create more defective structure as compared to two‐step activation route. Nitrogen adsorption–desorption isotherm measurements indicated that upon fabricating ACs via three‐step and two‐step activation approach, around 6.5 times and 3‐fold enhancement in the value of surface area of ACs as compared to that of carbon before activation. In addition, higher the IR value, lower the textural properties of ACs. This study demonstrated that three‐step activation methodology is capable of generating highly porous AC when compared to two‐step activation route. Cyclic voltammetry analysis showed that for the electrode developed from AC that fabricated via three‐step activation, capacitance retention of 50% is achieved upon tuning the scan rate by 10 times. The same electrode exhibited the capacitance retention of 45% upon increasing the current density by 10 times. We have also compared the electrochemical performance of symmetric and asymmetric supercapacitors. Electrochemical capacitance retention of symmetric and asymmetric supercapacitors is determined to be 100% and 92% respectively after 1000 cycles at the current density of 1 A g−1. Based on the Ragone plot study, it is observed that the maximum energy density of 5 W h kg−1 and the maximum power density of 943 W kg−1 are attained for the case of symmetric supercapacitors. Asymmetric supercapacitor displayed improved energy density of 7.15 W h kg−1 and modest power density of 432 W kg−1.

Enhanced electrolytic production of hypochlorous acid using phosphorus-modified carbon felt electrodes: A study in disinfectant synthesis

In this study, we fabricated phosphorus-modified carbon felt electrode anodes for chloride oxidation in saline solutions to produce HClO via electrocatalysis, forming a compound fungicide saline applicable for debridement and disinfection. A low-cost phosphorus-modified carbon felt electrode (P@CF) with high chlorine evolution reaction activity was synthesized to address the reduced efficiency of CER and the solution's pH increase. Heteroatoms P and O were introduced into the carbon felt by phosphoric acid activation followed by heat treatment. The maximum active chlorine concentration on the P@CF electrode could reach 616.8 mg/L in 60 min under the optimal synthesis conditions of a phosphoric acid mass fraction of 30%, a phosphoric acid impregnation time of 3 h, and a heat treatment temperature of 300 °C. The active chlorine concentration was 1.8 times higher on the P@CF electrode compared to the original carbon felt electrode. The optimal reaction conditions for the generation of active chlorine were as follows: salt concentration of 9 g/L, voltage of 7 V, and electrode spacing of 2 cm as verified by response surfaces. This electrolysis reaction follows one-stage reaction kinetics. Subsequently, the disinfection efficacy of the produced disinfectants was examined. The prepared disinfectant was also compared to a commercially available hypochlorite disinfectant, showing similar disinfection effects on E. coli for both.

Coconut shell carbon via phosphoric acid activation for rhodamine B, malachite green, and methylene blue adsorption – equilibrium and kinetics

This study was aimed at evaluating the removal of different cationic dyes onto phosphoric acid-activated coconut shell carbon. The activated carbon was characterized for surface functional groups, thermal decomposition profiles, surface morphology, and textural properties. The specific area was recorded as 1,221 m2/g with 100% mesoporosity. On molecular basis, the activated carbon adsorbs malachite green, methylene blue, and rhodamine B at maximum capacities of 1.52 mmol/g, 0.80 mmol/g, and 0.58 mmol/g, respectively. It indirectly implies the selectivity of activated carbon toward malachite green, and behaves differently due to steric hindrance of dye molecules. All equilibrium data obeyed Langmuir model, while the kinetic data are closely fitted to pseudo-second order model as concentration increases. To conclude, coconut shell activated carbon is more effective to remove malachite green compared to methylene blue and rhodamine B.

Biomass-Derived Carbons as Friction Reducing Additives for Lubricants: Tribological Properties of Biochars and Activated Carbons Obtained from Sugar Cane Bagasse

Activated carbons are commonly used for adsorption/depollution applications, but only a few studies are related to their lubricating properties. In order to investigate a new family of friction reducers, the tribological properties of biochars and derived activated carbons obtained from sugar cane bagasse are investigated. Activated carbons are obtained from either a physical (steam water) or chemical (with phosphoric acid) activation process. The tribological tests show that the activated carbons present very low friction coefficients, close to 0.08. The correlation of textural and tribological investigations shows that the specific surface area of the compounds as well as the microporous and mesoporous domain extensions are key parameters to optimize the friction reduction properties of activated carbons. The friction properties of the compounds are improved if the mesoporous domain extension is above 40% of the total porous volume. This study shows that local biomass waste valorization is possible and that sugar cane bagasse-derived activated carbons appear as interesting new friction reduction additives for lubricants.

Characteristics and adsorption of methylene blue on activated carbon derived from enzyme-pretreated Camellia oleifera shells

Activated carbon is a porous material extensively utilized in water treatment field. In this study, an efficient activated carbon (E-AC) adsorbent was prepared from agricultural by-product Camellia oleifera shells (COS) by enzymatic pretreatment combined with phosphoric acid activation. The enzymatic pretreatment was beneficial for increasing the volume of mesopores and loosening the structure of the synthesized activated carbon, which ultimately led to an increased adsorption capacity of E-AC. The characteristics and adsorption performances of E-AC were thoroughly investigated. The results showed that E-AC exhibited a high adsorption capacity of 1249.01 mg/g on methylene blue (MB), and the adsorption process was a spontaneous endothermic process. The adsorption kinetics aligned closely with the pseudo-second-order kinetic model (R2 > 0.99), and the adsorption mechanisms could be a combination of hydrogen bonding, π-π conjugation, electrostatic attraction, and physical adsorption. Additionally, E-AC exhibited good reusability, with a consistent MB removal rate of 91.14 % even after five cycles. This study offered an approach for obtaining high-quality activated carbon from COS and contributed to sustainable development strategies.

Modeling 2,4-dichlorophenoxyacetic acid adsorption on candle bush pod-derived activated carbon: Insights from advanced statistical physics models

The widespread usage of 2,4-Dichlorophenoxyacetic acid (2,4-D) as an herbicide has led to alarming levels of environmental pollution, presenting severe risks to ecosystems and human health. This study aimed to synthesize a new adsorbent, activated carbon from candle bush pods (CBAC) via low-temperature phosphoric acid activation and investigate its ability for adsorptive elimination of 2,4-D. The setup of a new adsorption system requires the experimental determination of adsorption isotherms and their thorough modeling, which is achieved through advanced statistical physics models (ASPMs). The characterization of CBAC revealed a porous morphology with a remarkable specific surface area (415.31 m2/g). XRD revealed graphitic carbon structures, while XPS detected phosphate groups, graphitic structures, and oxygen-containing functional groups. Double layer with single energy (DLSE) model – one of the ASPMs revealed both non-parallel and parallel orientation of 2,4-D molecules on CBAC, with saturation adsorption capacity values increasing with temperature (up to 252.35 mg/g) at pH 2. The adsorption was physisorption (ΔE = 12.62–16.26 kJ/mol) and spontaneous and endothermic. Hence, the findings herein demonstrate the potential of CBAC as a sustainable and effective adsorbent for mitigating environmental pollution caused by 2,4-D.

Enhanced Adsorption of Aqueous Pb(II) by Acidic Group-Modified Biochar Derived from Peanut Shells

Using peanut shells, a sustainable agricultural waste product, as its raw material, the acid group-modified biochar (AMBC) was prepared through phosphoric acid activation, partial carbonization, and concentrated sulfuric acid sulfonation for efficient removal of lead ion from aqueous solutions. Characterization techniques such as N2 isothermal adsorption–desorption, SEM, XRD, FT-IR, TG-DTA, and acid–base titration were utilized to fully understand the properties of the AMBC. It was found that there were high densities of acidic oxygen-containing functional groups (-SO3H, -COOH, Ph-OH) on the surface of the AMBC. The optimal adsorption performance of the AMBC for Pb(II) in water occurred when the initial concentration of Pb(II) was 100 mg/L, the pH was 5, the dosage of the adsorbent was 0.5 g/L, and the contact time was 120 min. Under the optimal conditions, the removal ratio of Pb(II) was 76.0%, with an adsorption capacity of 148.6 mg/g. This performance far surpassed that of its activated carbon precursor, which achieved a removal ratio of 39.7% and an adsorption capacity of 83.1 mg/g. The superior adsorption performance of AMBC can be caused by the high content of acidic oxygen-containing functional groups on its surface. These functional groups facilitate the strong binding between AMBC and Pb(II), enabling effective removal from water solutions.

Air-mediated phosphoric acid activation strategy for preparation of oxygenated functional groups rich activated carbon for capacitive deionization

Atmosphere during H3PO4 activation is vital to the texture structure and surface-interface properties of activated carbon (AC), but the researches are way out of sufficiency. In this work, it is found that the air in the H3PO4 activation process is not only conducive to the introduction of more-oxidized oxygenated functional groups on ACs, but also beneficial to the formation of micropores rather than mesopores. Besides, as the air content increases in H3PO4 activation, the ACs’ ash, phosphorous content and conductivity reduce, but their wettability, disorder degree and defect number increase. In addition, the potential of zero charge of the as-prepared ACs is positively correlated with the O-CO content, which show a pattern of first increasing and then decreasing with the increase of air content. Benefit from the improved hydrophilicity, electrolyte-affinity, additional adsorption sites for sodium ions, the optimal AC exhibits excellent salt adsorption capacity of 12.08 mg g−1 and good cycling stability at 1.0 V in single-pass capacitive deionization. This work not only establishes a novel and effective method for regulating the texture structure and surface properties of ACs, but also provides promising cathode candidates for capacitive deionization application.

Adsorption Study of Methylene Blue and Methyl Red on Activated Carbon from Silver Composite Using the Extract of Spent Coffee Grounds

The activated carbon was prepared from silver composite via an extract of spent coffee grounds with phosphoric acid activation. The activated carbon was used to study the removal of methylene blue and methyl red from an aqueous medium. Fourier-transform infrared spectroscopy (FTIR) spectra confirmed the functional group of O–P–O that can interact with dye molecules and the reduction process of Ag+ to Ag0. Field Emission Scanning Electron Microscopy (FESEM) morphology suggests a porous and irregular polygonal shape. The efficiency removal and adsorption capacity of methylene blue reached 98.73% and 9.87 mg/g at pH 9, while methyl red reached 98.55% and 9.86 mg/g at pH 4. The kinetics adsorption study followed the pseudo-first order. The isotherm adsorption study followed the Langmuir model. Based on the kinetics and isotherm study, the adsorption study of methylene blue and methyl red is chemical sorption.

Robust and efficient hydrogen production performance using nitrogen- and phosphorus-doped microalgal carbon-based metal-free carbon composite

Carbon-based metal-free catalysts are attracting attention in different applications. However, these metal-free carbon materials do not have sufficient active sites, resulting in low catalytic activity. Therefore, modification of metal-free carbon materials with appropriate approaches is important. The simultaneous doping of different electronegative heteroatoms has a positive effect on catalytic performance due to the synergistic effect caused by the electronic interactions between different atoms compared to mono-doping. In this study, Spirulina platensis, a microalgae species that is easy to culture, was used as the carbon source. First, ammonia (NH3) and phosphoric acid (H3PO4) activation were used to modify the surface of activated carbon obtained from Spirulina platensis by KOH activation (SPAC). Thus, the SPAC surface is enriched with N(SPAC-N) and P atoms whose electronegativity is different from carbon. These modified carbon particles (SPAC-N-P) were used as a metal-free catalyst to increase the H2 production rate from NaBH4 methanolysis. XRD, TEM, TG/DTG, FTIR and XPS analyses were used for the characterization of the obtained catalysts. FTIR and XPS analyses showed successful incorporation of N, P and O atoms. HGR values of 5737, 6104 and 13,052 mL min−1gcat−1 by SPAC, SPAC-N and SPAC-N-P catalysts were obtained, respectively. There is a significant increase in the catalytic performance of the catalysts obtained with both NH3 and H3PO4 activations.

Facile phosphorus and oxygen heteroatom functionalization of biochar based on biomass prepared by microwave pyrolysis for adsorption process of cadmium in aqueous solution

AbstractIn this study, in the first stage, biochar is produced from green pistachio hulls (PGHMAC) by microwave heating method, which saves energy, time and cost. In the second step, with the activation of phosphoric acid (H3PO4), the surface properties of the biochar were modified by phosphorus (P) and oxygen (O) doping (O- and P-doped PGHMAC). This adsorbent obtained was applied to remove cadmium (Cd(II)) from wastewater. FTIR, SEM, EDX, and ICP-OES analyses were used for the characterization of the samples. FTIR, EDX, and ICP-OES analysis results showed the presence of oxygen and phosphorus groups on the surface of the relevant adsorbent. The contents of C and O atoms for P- and O-doped PGHMAC were found to be 62.54% and 36.12%, respectively. Also, about 1.29% of P atoms were found with H3PO4 activation. The kinetic, isotherm, and thermodynamic parameters of the adsorption studies were investigated. Maximum Cd(II) adsorption capacities of P- and O-doped PGHMAC at 298 K, 308 K, and 318 K temperatures were calculated as 78.74, 109.89, and 133.33 mg/g by Langmuir model, respectively. The mechanism of Cd(II) adsorption on O- and P-doped PGHMAC has been proposed.

Dipole-induced hydrogen bonds enhanced P/O co-doped Lyocell-based porous carbon fiber cloth for hydrogen storage under ambient pressure

Currently, the hydrogen storage application of carbon-based adsorbent materials is mostly implemented under the pressure conditions of 30–300 bar, while there is few targeted studies conducted on the unsaturated adsorption under ambient pressure conditions. Therefore, based on industrialized Lyocell biopolymer fiber precursors and the enhancement effects of dipole-induced hydrogen bonds (DIHB), this work presents a facile construction strategy for P/O co-doped Lyocell-based porous carbon fiber cloth (Ly-ACF-F40). By the technical route of thermal stabilization---sonication assisted phosphoric acid activation---hydrogen bonds introduced by interfacial fluorination, the constructed Ly-ACF-F40 acquires a high specific surface area (1870 m2/g) and total pore volume (1.277 cm3/g), and an excellent hydrogen storage capacity of 3.22 wt% under ambient pressure conditions (77 K, 1 bar). The study directly demonstrated in the experiment that dipole induced hydrogen bonding H(I)-H(II)···F can effectively enhance the atmospheric hydrogen storage density on the basis of other eliminating influencing factors of specific surface area. The simple construction strategy of porous carbon-based materials can provide reference for the research of unsaturated adsorption hydrogen storage materials under ambient pressure conditions, also assist in the application and promotion of low-cost solid hydrogen storage materials.

Valorization of cardboard waste adsorbents for efficient malachite green removal – equilibrium, kinetics, and thermodynamics

ABSTRACT This work was aimed at evaluating the adsorptive properties of cardboard waste-based adsorbents for malachite green removal. The adsorbents were produced through hydrothermal carbonization and/or phosphoric acid activation and characterized for specific area, surface morphology, and functional groups. Batch adsorption was performed at varying concentrations, contact times, and temperatures. Results show that the activated carbon derived from cardboard waste with surface area of 196 m2/g exhibits a 134 mg/g (31.6%) adsorption capacity of malachite green. On the other hand, the cardboard hydrochar displays a peak capacity at 400 mg/g (94%) due to dye precipitation before the magnitude subsides to 47 mg/g (5.7%) at higher concentration of 820 mg/L. The equilibrium data of activated carbons could be well described by the Langmuir model, while the kinetics fitted well with the pseudo-second order model. The adsorption of malachite green is endothermic and spontaneous at high solution temperature.

Phosphoric Acid Activation of Titanium-Supported Lead Dioxide Electrodes for Bipolar Battery Applications

Titanium foil coated with doped tin dioxide is an attractive option for the positive current collector interface of bipolar lead batteries due its corrosion resistance and mechanical performance. The phosphoric acid and two of its derivatives, one inorganic (calcium hydrogen phosphate) and one organic (poly-vinylphosphonic acid), have been studied as additives with potential for improvement of the capacity retention of such positive electrodes. The results show that the jar-formation process of the electrodes in the sulfuric acid electrolyte containing phosphoric acid successfully overcomes the capacity retention problem at all studied cases. This leads also to considerable improvement of the lead dioxide utilization. The cycling ageing of the electrodes combined with periodic impedance spectroscopy measurements, indicate progressive capacity loss corresponding to the typical processes of degradation of the lead dioxide structure. Rather small changes in the electrode resistance prove the corrosion and the passivation resistance of the current collectors. It is concluded that the combined doping with phosphoric acid species in the electrolyte and in the positive paste offers a potential for further improvements of the electrodes cyclability.

Insights into nitrobenzene adsorption mechanism on apricot stone activated carbon: A study via statistical physics models and thermodynamic analysis

Statistical physics modelling was performed to analyze the adsorption forces and the thermodynamics of the removal of nitrobenzene molecules using an activated carbon obtained from apricot stones. This adsorbent was prepared using phosphoric acid activation and exhibited a surface area of 1762 m2 g−1, total pore volume of 1.09 cm3 g−1 and an experimental maximum adsorption capacity of 295.63 mg g−1 for nitrobenzene at 298 K. The removal of this organic molecule was exothermic. A double layer adsorption model with two energies was utilized to calculate the main steric parameters for the removal of this compound. This model was employed to perform a thermodynamic analysis of this adsorption system. It was concluded that 2 and 3 adsorption sites can be involved for the removal of nitrobenzene molecules on activated carbon surface. Physical interaction forces were expected to participate in the removal of this pollutant. This activated carbon can be regenerated with NaOH thus offering the alternative of its recycling to reduce the removal costs of this organic molecule from water.

Structural characterisation and reactivity measurement of chemically activated kaolinite

This study examines the structural evaluation of differently activated kaolins for potential use as supplementary cementitious materials (SCM) or as precursor for alternative cementitious materials (ACM). Chemical activation involved amorphizing the kaolinite structure using varying phosphoric acid concentrations, reaction times, and temperatures. Metakaolin obtained via thermal activation served as a comparison. Inductively Coupled Plasma – Optical Emission Spectroscopy (ICP-OES) characterization of the activating solutions revealed phosphoric acid activation leading to dealumination in kaolinite structures, with temperature emerging as the most significant parameter. X-ray diffraction (XRD) confirmed amorphization, attributed to the dealumination process causing Al loss and creating new Si–O–Si interlayered bonds, as monitored by 29Si magic-angle spinning nuclear magnetic resonance (MAS NMR) tracking the change from Q3 to Q4 environments. Furthermore, pozzolanic activity was assessed through Ca(OH)2 consumption and reaction heat release via modified Chapelle and R3 tests, respectively. Kaolinite subjected to intensive chemical activation exhibited high reactivity and increased specific surface area, indicating its potential as a pozzolanic material. Keywords: Kaolin; Chemical activation; Supplementary cementitious materials; Alternative cementitious materials; Dealumination; Pozzolanic reactivity.

Biomass-derived activated carbon catalysts for the direct dimethyl ether synthesis from syngas

The direct DME synthesis from syngas was studied by using activated carbon-based bifunctional catalytic beds. Two kinds of activated carbons, prepared by physical (by CO2 partial gasification) and chemical (with phosphoric acid) activation of olive stones, were used as supports for the preparation of the catalysts. The chemically activated carbon presented a considerable amount of thermally and chemically stable surface phosphorus complexes, which played an important role on the catalytic performance of the prepared catalysts. A Zr-loaded P-containing activated carbon presented a relatively high activity, selectivity and stability for the production of DME from methanol and was used as methanol dehydration catalyst. On the other hand, Cu-Zn was loaded on both P-containing and P-free activated carbon supports for the preparation of methanol synthesis catalysts. The presence of surface-phosphorus on the carbon support resulted in a strong metal-support interaction, hindering the catalytic activity for the hydrogenation of CO to methanol. However, the catalyst that did not contain phosphorus showed noticeable activity for this reaction. The physical mixing of the methanol synthesis and methanol dehydration catalysts resulted in the preparation of carbon-based bifunctional catalytic beds, which performed very efficiently in the direct DME synthesis from syngas in a fixed-bed reactor. Different mass ratios of the individual (metallic and acid) catalysts were studied. An acid/metallic catalyst mass ratio of 2 provided the catalytic bed with enough acid sites to promote methanol dehydration to its maximum extent and make the overall product distribution controlled by the methanol synthesis reaction on the metallic phase.

Adsorption Properties of Magnetic Phosphorous Camellia Oleifera Shells Biochar to Sulfamethoxazole in Water

Magnetic phosphorous biochar （MPBC） was prepared from Camellia oleifera shells using phosphoric acid activation and iron co-deposition. The materials were characterized and analyzed through scanning electron microscopy （SEM）， X-ray diffractometry （XRD）， specific surface area and pore size analysis （BET）， Fourier infrared spectroscopy （FT-IR）， and X-ray photoelectron spectroscopy （XPS）. MPBC had a high surface area （1 139.28 m2·g-1） and abundant surface functional groups， and it could achieve fast solid-liquid separation under the action of an external magnetic field. The adsorption behavior and influencing factors of sulfamethoxazole （SMX） in water were investigated. The adsorbent showed excellent adsorption properties for SMX under acidic and neutral conditions， and alkaline conditions and the presence of CO32- had obvious inhibition on adsorption. The adsorption process conformed to the quasi-second-order kinetics and Langmuir model. The adsorption rate was fast， and the maximum adsorption capacity reached 356.49 mg·g-1. The adsorption process was a spontaneous exothermic reaction， and low temperature was beneficial to the adsorption. The adsorption mechanism was mainly the chemisorption of pyrophosphate surface functional groups （C-O-P bond） between the SMX molecule and MPBC and also included hydrogen bonding， π-π electron donor-acceptor （π-πEDA） interaction， and a pore filling effect. The development of MPBC adsorbent provides an effective way for resource utilization of waste Camellia oleifera shells and treatment of sulfamethoxazole wastewater.

Comparing specific capacitance in rice husk-derived activated carbon through phosphoric acid and potassium hydroxide activation order variations

This manuscript investigates the influence of the chemical activation step order and process parameters on the specific capacitance of activated carbon derived from rice husk. The chemical activation was performed either before or after the carbonization step, using phosphoric acid (H3PO4) and potassium hydroxide (KOH) as activating agents. For activation before carbonization, the carbonization process was conducted at various temperatures (600, 750, 850, and 1050 °C). On the other hand, for activation after carbonization, the effect of the volume of the chemical agent solution was studied, with 0, 6, 18, 21, 24, and 30 mL/g of phosphoric acid and 0, 18, 30, 45, 60, and 90 mL/g of 3.0 M KOH solution. The results revealed that in the case of chemical activation before carbonization, the optimum temperature for maximizing specific capacitance was determined to be 900 °C. Conversely, in the case of chemical activation after carbonization, the optimal volumes of the chemical agent solutions were found to be 30 mL/g for phosphoric acid (H3PO4) and 21 mL/g for potassium hydroxide (KOH). Moreover, it was observed that utilizing phosphoric acid treatment before the carbonization step leads to an 21% increase in specific capacitance, attributed to the retention of inorganic compounds, particularly silica (SiO2). Conversely, when rice husks were treated with KOH after the carbonization step, the specific capacitance was found to be doubled compared to treatment with KOH prior to the carbonization step due to embedding of SiO2 and KHCO3 inorganic constituents. This study provides valuable insights into the optimization of the chemical activation step order and process parameters for enhanced specific capacitance in rice husk-derived activated carbon. These findings contribute to the development of high-performance supercapacitors using rice husk as a sustainable and cost-effective precursor material.

Nitrogen-doped mesoporous activated carbon from Lentinus edodes residue: an optimized adsorbent for pharmaceuticals in aqueous solutions.

In this study, phosphoric acid activation was employed to synthesize nitrogen-doped mesoporous activated carbon (designated as MR1) from Lentinus edodes (shiitake mushroom) residue, while aiming to efficiently remove acetaminophen (APAP), carbamazepine (CBZ), and metronidazole (MNZ) from aqueous solutions. We characterized the physicochemical properties of the produced adsorbents using scanning electron microscopy (SEM), nitrogen adsorption isotherms, and X-ray photoelectron spectroscopy (XPS). MR1, MR2, and MR3 were prepared using phosphoric acid impregnation ratios of 1, 2, and 3mL/g, respectively. Notably, MR1 exhibited a significant mesoporous structure with a volume of 0.825cm3/g and a quaternary nitrogen content of 2.6%. This endowed MR1 with a high adsorption capacity for APAP, CBZ, and MNZ, positioning it as a promising candidate for water purification applications. The adsorption behavior of the contaminants followed the Freundlich isotherm model, suggesting a multilayer adsorption process. Notably, MR1 showed excellent durability and recyclability, maintaining 95% of its initial adsorption efficiency after five regeneration cycles and indicating its potential for sustainable use in water treatment processes.