Acid Solvent Research Articles

One‐step Synthesis of Organic Terminal 2D Ti3C2Tx MXene Nanosheets by Etching of Ti3AlC2 in an Organic Lewis Acid Solvent

AbstractThe surface and interface chemistry are critical for controlling the properties of two‐dimensional transition metal carbides and nitrides (MXenes). Numerous efforts have been devoted to the functionalization of MXenes with small inorganic ligands; however, few etching methods have been reported on the direct bonding of organic groups to MXene surfaces. In this work, we demonstrated an efficient and rapid strategy for the direct synthesis of 2D Ti3C2Tx MXene nanosheets with organic terminal groups in an organic Lewis acid (trifluoromethanesulfonic acid) solvent, without introducing additional intercalations. The dissolution of aluminum and the subsequent in situ introduction of trifluoromethanesulfonic acid resulted in the extraction of Ti3C2Tx MXene (T=CF3SO3−) (denoted as CF3SO3H−Ti3C2Tx) flakes with sizes reaching 15 μm and high productivity (over 70 %) of monolayers or few layers. More importantly, the large CF3SO3H−Ti3C2Tx MXene nanosheets had high colloidal stability, making them promising as efficient electrocatalysts for the hydrogen evolution reaction.

One-step Synthesis of Organic Terminal 2D Ti3C2Tx MXene Nanosheets by Etching of Ti3AlC2 in an Organic Lewis Acid Solvent.

The surface and interface chemistry are critical for controlling the properties of two-dimensional transition metal carbides and nitrides (MXenes). Numerous efforts have been devoted to the functionalization of MXenes with small inorganic ligands; however, few etching methods have been reported on the direct bonding of organic groups to MXene surfaces. In this work, we demonstrated an efficient and rapid strategy for the direct synthesis of 2D Ti3C2Tx MXene nanosheets with organic terminal groups in an organic Lewis acid (trifluoromethanesulfonic acid) solvent, without introducing additional intercalations. The dissolution of aluminum and the subsequent in situ introduction of trifluoromethanesulfonic acid resulted in the extraction of Ti3C2Tx MXene (T=CF3SO3 -) (denoted as CF3SO3H-Ti3C2Tx) flakes with sizes reaching 15 μm and high productivity (over 70 %) of monolayers or few layers. More importantly, the large CF3SO3H-Ti3C2Tx MXene nanosheets had high colloidal stability, making them promising as efficient electrocatalysts for the hydrogen evolution reaction.

Pectin extraction from banana pere peel at various extraction times

For many years, West Sulawesi's signature plant, banana pere, has only been eaten as fruit, while its peel is often discarded as waste or used as animal feed. This study provides information on the utilization of banana pere peel in order to increase its economic value through the utilization of pectin content contained in banana pere peel. This study aims to extract pectin from banana pere peel (Loka Pere) by using the citric acid solvent extraction method. The extraction process was carried out using 5 variations of time, namely 30, 60, 90, 120 and 150 minutes. The results showed that the use of extraction time for 90 minutes resulted in a yield value of 53.11%, moisture content of 1.15%, ash content of 1.56%, methoxyl content of 2.66% and galacturonic content of 30.88%.

Anthelmintic Effects of Betel Nut to Free-Range Chicken

The study aims to evaluate the efficacy of Processed Betel Nut as an anthelmintic to Free-Range Chickens. The research employed a Completely Randomized Design (CRD) and utilized 90 heads of uniformed experimental free–range chickens. The experimental birds were divided into 5 treatment combinations replicated thrice as follows: C- (pure water), C+ (commercial anthelmintic), S1L1 (Betel nut extract (10ml), S1L2 (Betel nut extract (20ml), S1L3 – Betel nut extract (30ml). The anthelmintic effect was observed during days 1,2,3,7,14,21, and 28 of the study. Prior to the allotment of the birds, fecal samples were collected after 21 days of rearing for pre-fecalysis to ensure that all of these were infected with internal parasites. After this, administration of the different treatments was done. This was followed by the collection of fecal samples on days 1, 2, 3, 7, 14, 21, and 28 after the administration of the different treatments. The fecal samples collected were given a drop of lactic acid solvent and placed in properly labeled plastic bags. Direct Fecal Smear (DFS) was used in examining the fecal samples collected Results revealed that betel nuts at 20ml level were the best on the growth performance. Betel nut at 30ml level was comparable to that of the experimental birds in commercial anthelmintic. It is then recommended the utilization of betel nut at 20 ml in terms of growth performance and betel nut at 30 ml as herbal anthelmintic to free-range chickens.

Validation of the UV Spectrophotometric Method for Determining the Content of Ranitidine HCl Tablets in HCl

Introduction: Ranitidine HCl tablets are widely available in the market. Ensuring the proper levels of active ingredients is crucial for ensuring the quality of medications. Objective: To find a reliable method for measuring the levels of Ranitidine HCl tablets in acidic solvents that meet validation standards, and to explore valid methods using ultraviolet spectrophotometry in acidic solvents. Methods: UV spectrophotometry with a UV detector at maximum wavelength was used. Two solvents were employed: 0.10 N HCl and 0.15 N HCl. Method validation included tests for linearity, accuracy, repeatability, precision, and selectivity. Results: The maximum wavelengths detected for each solvent were 225 nm and 226 nm, respectively. Validation results indicate excellent linearity, accuracy, and precision within the ranges of 0.9984 - 0.9998; 99.6% - 100.7%; 0.427% - 0.861%; 0.518% - 0.952%. The selectivity test yielded positive outcomes. The average Ranitidine HCl tablet levels were 98.2% for PT. Hexpharm Jaya and 98.4% for PT. Mutifa Medan, meeting the standards of the Indonesian Pharmacopoeia Edition VI. Conclusion: The method using a 0.10 N solvent for determining Ranitidine HCl tablet levels meets validation requirements and is suitable for practical application.

Magnetic transition of 1D ferromagnetic catalysts during the NO electroreduction

Exploration of magnetic phase transitions during electrochemical processes is of great importance for rational design of supported magnetic-metal electrocatalysts. Herein, we systematically investigated the magnetic transition between ferromagnetism (FM) and anti-ferromagnetism (AFM) in one-dimensional ferromagnetic Co chain supported on graphene (Co4N8-gra) during NO electroreduction (NORR) process, focusing on the impact of potential and acidity on the catalytic property and magnetic transition. A combination of catalytic kinetics calculations and microkinetic simulations reveals that the Co4N8-gra exhibits excellent NH3 selectivity and thermal stability. In the implicit solvent model, the general reaction follows optimal pathway: * + NO(g) → *NO → *HNO → *H2NO → *H2NOH → *NH2 → *NH3 → * + NH3, with the potential-determining step (PDS) identified as *NO → *HNO. In acidic solvent, the magnetic transitions follow the pathway (FM → AFM2 → AFM2 → AFM2 → AFM1 → AFM1 → AFM1 → FM) under an applied potential of −0.20 V/RHE. In neutral solvent, the magnetic transitions occur according to this pathway (FM → AFM2 → AFM2 → FM → AFM1 → AFM1 → AFM1 → FM) under an applied potential of −0.14 V/RHE. In an alkaline solvent, the magnetic transitions proceed along this sequence (FM → AFM1 → AFM2 → FM → AFM1 → AFM1 → AFM1 → FM) under an ultralow potential of −0.08 V/RHE. Essentially, the improvement of catalytic property is attributed to the synergistic influence of external potential and magnetic-state transition on the adsorption of reaction species (e.g., NO and NH3). Magnetic transitions are closely associated with ligand field effect of metal site with variable valence electron induced by applied potential. In general, this study provides valuable insights for the controllable design of magnetic metal catalysts.

Optimization of Chitosan-Carboxymethyl Chitosan Membrane Modification with PVA to Increase Creatinine and Urea Permeation Efficiency

Polyvinyl alcohol (PVA) modified chitosan-carboxymethyl chitosan (CMC) membrane has been successfully fabricated and used as a dialysis membrane. This research aims to examine the manufacturing process, characterization, and dialysis performance of CMC and PVA-modified chitosan membranes. The membrane used the phase inversion method in acetic acid solvent with 5 CS:CMC: PVA dope compositions. Based on FTIR data, the modification process did not produce new spectra. Furthermore, the interaction produces a membrane with higher physical characteristics in terms of porosity, swelling, water uptake, hydrophilicity, and pH resistance values, which increase by 1.5–115%. Meanwhile, chitosan modification makes the membrane structure different from the original, requiring a longer degradation time. The modification also increased the permeation ability of urea by 17–65% and creatinine permeation by 20–62%. Membranes have the ability to be used more than once.

Durable, multifunctional cotton fabrics with in situ deposited micro/nanomaterials for effective self–cleaning, oil–water separation and antibacterial activity

The facile modification of cotton fabrics for excellent self–cleaning, oil–water separation, and antibacterial activity is of great interest for multifunctional requirements. Herein, a durable, robust, fluorine–free multifunctional cotton fabric was fabricated via in-situ growing zeolitic imidazolate framework-67 (ZIF-67) on the cotton surface, followed by depositing hydrophobic SiO2 (H-SiO2) nanoparticles synthesized via an improved Stöber reaction. Meanwhile, the abundant hydroxyls of the cotton fabrics provided the necessary ion interaction sites for the uniform deposition of micro/nanomaterials, confirmed by the visualized Raman imaging technology. The resultant H-SiO2/ZIF-67@cotton fabric exhibited superhydrophobicity with a water contact angle of 159° and versatile self–cleaning, antifouling, oil–water separation, as well as prominent antibacterial activity against S. aureus and E. coli. At the same time, the superhydrophobic cotton fabric possessed excellent durability and stability against harsh environments, including abrasion, washing, acid, base, salt, and organic solvents. This facile technique can be applied for large-scale production of multifunctional superhydrophobic cotton fabrics due to its easy operation, low cost, and environmental friendliness.

Model-based process intensification of deep eutectic solvent treatment of eucalyptus slabs for lignin extraction and pulp production

This work revealed the reaction characteristics in the delignification process of eucalyptus slabs catalyzed by acidic deep eutectic solvent (benzyltriethylammonium chloride/formic acid) from the perspective of heterogeneous reactions. The limitation of internal diffusion on delignification process cannot be ignored. Afterwards, a kinetic model based on cell wall structure was proposed to describe the relationship between the delignification degree and reaction conditions, and it also hold excellent predictive ability for lignin removal, carbohydrate retention and solid residue yield. Compared with other reported kinetic models, this novel model not only took into account all operational parameters of reaction process, but also can be applied to the entire reaction process without the need for segmentation. Besides, an essential requirement based on the developed model was a 44.40 wt% formic acid concentration and a temperature of 130 °C, when the purpose of DES treatment was pulping. Generally, this work could provide guidance on process adjustments and product quality control during the DES processing.

An efficient and mild fractionation of corn stover via 2-phenoxyethanol and silicotungstic acid biphasic pretreatment for biomass valorization

Developing an efficient and facile pretreatment is of great importance to comprehensive utilization of lignocellulosic biomass. Herein, a biphasic system of 2-phenoxylethanol (EPH) and silicotungstic acid (STA) was employed for fractionation of corn stover. The EPH/STA biphasic system demonstrated remarkable fractionation efficiency to remove 90.23 % of xylan and 88.54 % of lignin, while retaining 85.60 % of cellulose under the mild pretreatment conditions of 130 °C for 90 min with 7/3 of EPH/STA and 40 mM of STA. The xylose of 52.93 % and lignin of 88.01 % were recovered in aqueous phase and organic phase by EPH/STA biphasic pretreatment, respectively. In the further process, 94.27 % of saccharification was achieved by enzymatic hydrolysis of cellulose-rich solid residue, and 106.17 mg/g of xylonic acid was obtained by oxidation of xylose in aqueous phase. Additionally, the recovered lignin in organic phase could be fabricated to lignin-based films with good mechanical properties. Notably, acid solvent in biphasic system had an important role in fractionation efficiency of corn stover. The STA had the best effect among the different acid solvents. This work provided a promising route to full components utilization of corn stover for biomass valorization.

High-Temperature Hydrothermal Extraction of Phenolic Compounds from Brewer's Spent Grain and Malt Dust Biomass Using Natural Deep Eutectic Solvents.

Aligned with the EU Sustainable Development Goals 2030 (EU SDG2030), extensive research is dedicated to enhancing the sustainable use of biomass waste for the extraction of pharmaceutical and nutritional compounds, such as (poly-)phenolic compounds (PC). This study proposes an innovative one-step hydrothermal extraction (HTE) at a high temperature (120 °C), utilizing environmentally friendly acidic natural deep eutectic solvents (NADESs) to replace conventional harmful pre-treatment chemicals and organic solvents. Brewer's spent grain (BSG) and novel malt dust (MD) biomass sources, both obtained from beer production, were characterized and studied for their potential as PC sources. HTE, paired with mild acidic malic acid/choline chloride (MA) NADES, was compared against conventional (heated and stirred maceration) and modern (microwave-assisted extraction; MAE) state-of-the-art extraction methods. The quantification of key PC in BSG and MD using liquid chromatography (HPLC) indicated that the combination of elevated temperatures and acidic NADES could provide significant improvements in PC extraction yields ranging from 251% (MD-MAC-MA: 29.3 µg/g; MD-HTE-MA: 103 µg/g) to 381% (BSG-MAC-MA: 78 µg/g; BSG-HTE-MA: 375 µg/g). The superior extraction capacity of MA NADES over non-acidic NADES (glycerol/choline chloride) and a traditional organic solvent mixture (acetone/H2O) could be attributed to in situ acid-catalysed pre-treatment facilitating the release of bound PC from lignin-hemicellulose structures. Qualitative 13C-NMR and pyro-GC-MS analysis was used to verify lignin-hemicellulose breakdown during extraction and the impact of high-temperature MA NADES extraction on the lignin-hemicellulose structure. This in situ acid NADES-catalysed high-temperature pre-treatment during PC extraction offers a potential green pre-treatment for use in cascade valorisation strategies (e.g., lignin valorisation), enabling more intensive usage of available biomass waste stream resources.

Dispersive liquid–liquid microextraction based on deep eutectic solvent followed by high-performance liquid chromatography-ultraviolet for imidacloprid, hexythiazox, and fenpyroximate determination: Experimental design approach

Dispersive liquid–liquid microextraction (DLLME) of three insecticides, including imidacloprid (I), hexythiazox (H), and fenpyroximate (F), was performed as an efficient method for separation and preconcentration using a deep eutectic choline chloride-acetic acid solvent (DES) followed by determination by high-performance liquid chromatography-ultraviolet (HPLC-UV). The experimental design approach (central composite design) was used to optimize the effective parameters. According to the results, the addition of salt had no significant effect on extraction among the four parameters studied, including pH, DES volume (dispersive solvent), salt concentration, and chloroform volume. The optimized conditions in the DES-DLLME-HPLC-UV method were pH = 6.00, 100 µL DES, and 138 µL chloroform. Under optimized conditions, a wide linear range of 1.00 × 10−3-20.00 µg mL−1 was obtained for three insecticides. The enhancement factors were 11.22, 58.04, and 39.65 and the limit of detection of 3.00 × 10−4, 2.00 × 10−4, and 2.00 × 10−4 µg mL−1, and the limit of quantification of 9.00 × 10−4, 8.00 × 10−4, and 6.00 × 10−4 µg mL−1 were also determined for imidacloprid, hexythiazox, and fenpyroximate, respectively. The presence of other components including benomyl, dimethoate, mancozeb, captan, thiodicarb, carbendazim, and oxyfluorfen, showed no significant interference effect on the determination of three insecticides up to 50-fold. The method is eco-friendly benign, sensitive, precise, and straightforward as shown by the results.

Unveiling the Potential of Highly Porous Covalent Organic Frameworks for Water-Jet Rewritable Papers.

The massive use of paper has resulted in significant negative impacts on the environment. Fortunately, recent progress has been made in the field of rewritable paper, which has great potential in solving the increasing demand for paper while minimizing its environmental footprint. In this work, we report a green and economic strategy to develop ink-free rewritable paper by introducing hydrochromic covalent organic frameworks (COFs) in paper and using water as the sole trigger. When exposed to water or acidic solvents, two kinds of imino COFs change their colors reversibly from red to black. Additionally, a new visible absorption band appears, indicating that it can be transformed into another structure reversibly. This reversibility may be due to the isomerization from the diiminol to an iminol/cisketoenamine and its inability to doubly tautomerize to a diketoenamine. Specifically, we prepared the rewritable paper by loading these two COFs onto filter paper by using the decompression filtration method. When exposed to water, the paper undergoes a color change from red to black, which shows promising potential for applications in water-jet printing. Additionally, there is no significant performance degradation after 20 uses and 10 days between, further highlighting their potential as rewritable papers. To further improve its uniformity, we take the interface polymerization strategy to yield highly crystalline and more compact membranes, which are then transferred to paper to prepare writable papers. Our research has opened up a way for the application of COFs as a water-based printing material.

Synergistic microwave and acidic deep eutectic solvent-based pretreatment of Theobroma cacao pod husk biomass for xylooligosaccharides production

The bioconversion of lignocellulosic biomass into novel bioproducts is crucial for sustainable biorefineries, providing an integrated solution for circular economy objectives. The current study investigated a novel microwave-assisted acidic deep eutectic solvent (DES) pretreatment of waste cocoa pod husk (CPH) biomass to extract xylooligosaccharides (XOS). The sequential DES (choline chloride/citric acid, molar ratio 1:1) and microwave (450W) pretreatment of CPH biomass was effective in 67.3% xylan removal with a 52% XOS yield from total xylan. Among different XOS of varying degrees of polymerization, a higher xylobiose content corresponding to 69.3% of the total XOS (68.22 mg/g CPH) from liquid fraction was observed. Enzymatic hydrolysis of residual xylan from pretreated CPH biomass with low commercial xylanase (10 IU/g) concentration yielded 24.2% XOS. The MW-ChCl/citric acid synergistic pretreatment approach holds great promise for developing a cost-effective and environmentally friendly method contributing to the sustainable production of XOS from agricultural waste streams.

Improving energy storage performance of sol-gel-derived PbZrO3 thin films by adjusting the water/acetic acid solvent ratio

Improving energy storage performance of sol-gel-derived PbZrO3 thin films by adjusting the water/acetic acid solvent ratio

Iron oxide nanoparticle synthesis: Simulation-based comparison of laboratory- and pilot plant-scale spray-flame synthesis

This study analyzes burner scale-dependent effects for iron-oxide nanoparticles synthesis in spray flames through a combined experimental and numerical approach. A laboratory- and a pilot plant-scale synthesis facility generate iron oxide nanoparticles from iron nitrate dissolved in ethanol/2-ethylhexanoic acid solvents on the 0.5 and 15 g/h scale, respectively. Phase Doppler measurements supply initial conditions for spray development in the numerical approach, while in situ OH* chemiluminescence and multi-line nitric oxide laser-induced fluorescence (NO-LIF) thermometry provide experimental data for comparison with simulation results of the pilot plant burner. Ex situ particle sizing by gas adsorption according to Brunauer-Emmet-Teller (BET) and transmission electron microscopy (TEM), along with phase composition determination via X-ray diffraction (XRD), are used to compare products of both burners and the corresponding simulations. The numerical approach employs a Reynolds-averaged Eulerian–Lagrangian description of the flow in combination with a flamelet/progress variable (FPV) combustion and monodisperse particle model to reflect spray-flame synthesis. Despite similar chemiluminescence between experiment and simulation, more significant discrepancies are observed in NO-LIF thermometry and particle sizing. Nanoparticle formation and growth at both burner scales is investigated using the numerical method. Special attention is directed to the high-temperature particle residence time (HTPRT). Notably, the average temperature–time profiles particles experience are almost identical in the burners, although their geometric scales and designs differ substantially. Simulation results show that while the primary particle diameter remains mostly consistent, the pilot-scale burner produces larger particle agglomerates than the laboratory burner. The difference is attributed to an increased particle number concentration during the initial formation of soft agglomerates. The findings demonstrate that, despite retaining a similar HTPRT, the overall flow conditions and liquid spray dispersion, which impact the distribution of the particle number concentration, influence the final agglomerate size.

Ursodeoxycholic and chenodeoxycholic bile acids attenuate systemic and liver inflammation induced by lipopolysaccharide in rats.

Bacterial lipopolysaccharide (LPS) induces general inflammation, by activating pathways involving cytokine production, blood coagulation, complement system activation, and acute phase protein release. The key cellular players are leukocytes and endothelial cells, that lead to tissue injury and organ failure. The aim of this study was to explore the anti-inflammatory, antioxidant, and cytoprotective properties of two bile acids, ursodeoxycholic acid (UDCA) and chenodeoxycholic acid (CDCA) in LPS-induced endotoxemia in rats. The experiment involved six distinct groups of Wistar rats, each subjected to different pretreatment conditions: control and LPS groups were pretreated with propylene glycol, as a bile acid solvent, while the other groups were pretreated with UDCA or CDCA for 10 days followed by an LPS injection on day 10. The results showed that both UDCA and CDCA reduced the production of pro-inflammatory cytokines: TNF-α, GM-CSF, IL-2, IFNγ, IL-6, and IL-1β and expression of nuclear factor-κB (NF-κB) induced by LPS. In addition, pretreatment with these bile acids showed a positive impact on lipid profiles, a decrease in ICAM levels, an increase in antioxidant activity (SOD, |CAT, GSH), and a decrease in prooxidant markers (H2O2 and O2-). Furthermore, both bile acids alleviated LPS-induced liver injury. While UDCA and CDCA pretreatment attenuated homocysteine levels in LPS-treated rats, only UDCA pretreatment showed reductions in other serum biochemical markers, including creatine kinase, lactate dehydrogenase, and high-sensitivity troponin I. It can be concluded that both, UDCA and CDCA, although exerted slightly different effects, can prevent the inflammatory responses induced by LPS, improve oxidative stress status, and attenuate LPS-induced liver injury.

Acidic deep eutectic solvent as a novel catalyst for urea–formaldehyde resin curing

ABSTRACT The effect of a novel catalyst, acidic deep eutectic solvent, on the characteristics of urea–formaldehyde (UF) resins-bonded particleboard was studied in this research work. Methyltriphenyl-phosphonium bromide–protocatechuic acid (MTPPBr–PCAT) as a DES was added to the UF resin at different percentages (1%, 2%, and 3% by weight). Then, the prepared resin was used for manufacturing particleboards. Based on this research finding, DES appears to be an effective UF resin catalyst. Increasing the MTPPBr–PCAT–DES level from 0 to 3 wt% caused a decrease in pH but still within the limits acceptable to international standards requirements, and also it caused a shorter gel time and acceleration of resin curing. Wood particleboard prepared with only 1 wt% DES had higher mechanical strength and dimensional stability and lower formaldehyde emission compared to the controls bonded with UF resins catalyzed with 2 wt% NH4Cl. Under scanning electron microscopy, acidic deep eutectic solvent catalyzed UF resins-bonded panels presented a smooth and monotonous appearance. DESs as UF acidic catalysts present advantages, such as being non-toxic, being able to catalyze resin cure similarly or more effectively than the acid itself, and being recyclable as well.

Efficient recovery of Al foil and regeneration of cathode materials from spent lithium-ion batteries with methanol-citric acid

Efficient separation of cathode materials from current collectors is an important step to simplify the recycling process of spent lithium-ion batteries (LIBs). However, traditional methods have the shortcomings of incomplete separation, release of toxic substances and high cost. Here, the methanol-citric acid solvent (MeOH-CA), prepared from green and low-cost reagents methanol (MeOH) and citric acid (CA), can separate above 99.5 wt% of spent nickel-manganese-cobalt (NCM) cathode materials in 15 min with negligible metal loss at an ultralow temperature of 45 °C. The separated NCM has high purity and no structure changes, and the recovered Al foil is intact and non-corrosive. The mechanism analysis indicates that the reaction between MeOH-CA and Al foil and the inactivation of PVDF by the abundant hydrogen bonds in the MeOH-CA solvent cause the separation. Meanwhile, the formation of AlF3 passivation layer and the ester film on the surface of Al foil prevent further corrosion of Al foil. Through hydrothermal treatment combined with a short thermal annealing, the regenerated NCM delivers a reversible capacity of 151 mAh g−1 at 1C and 117 mAh g−1 after 100 cycles. The facile separation strategy provides a sustainable and economic solution for the recovery of spent LIBs.

Synthesis of Ion Imprinted Polymers (IIPs) Adsorbent Materials Using Fe(III) Leaching Process with Variation of Hydrochloric Acid Solvent Concentration and Heat Treatment

Fe(III)-IIPs material was prepared using a cooling-heating method with different leaching variations. The synthesis process used several chemical components, including EGDMA, MAA, and BPO as the crosslinker, functional monomer, and initiator. This study focused on the template formation process of IIPs with leaching variations, using parameters such as molarity concentration, solution mixture, and temperature to influence the amount of template formed in the polymer body. The spectra of XRD showed a widening value of FWHM as higher molarity was applied during the leaching process, with the widest one at 0.163 rad for IIPs 3 M. Fe(III) peak is located at 680-610 cm−1 or 1386-1350 cm−1 within the unleached sample, according to FTIR spectra. It also can be traced at minimum intensity in leached samples. SEM data processing showed that higher concentrations were essential in releasing Fe(III) ions from the polymer body. Meanwhile, heat treatment did not strongly impact the template formation sites of IIPs. Synthesized Fe(III)-IIPs materials had adsorption capacity, optimum time, and efficiency of 9.35 mg.g−1, 40 minutes, and 93.48%, respectively. Based on the results, Fe(III)-IIPs materials had great potential as adsorbents for removing metal pollutants from water.