Absorption Of Metal Ions Research Articles

Enhancing wound healing with zinc and silver nanocomposites synthesized with β-lactoglobulin: antimicrobial properties, collagen deposition, and systemic effects in a C57BL/6J mouse model

This study explores the potential of zinc and silver nanocomposites, synthesized with β-lactoglobulin, a whey protein, in promoting wound healing, using the C57BL/6J mouse model. Our research is distinct in its dual focus: assessing the antimicrobial efficacy of these nanocomposites and their impact on wound healing processes. The antimicrobial properties were investigated through minimum inhibitory concentration (MIC) assessments and colony-forming unit (CFU) tests, providing insights into their effectiveness against wound-associated microorganisms. Notably, the formulation's effective antibacterial concentration did not exhibit toxicity to mouse fibroblasts. A key aspect of our methodology involved the use of a stereoscopic microscope for detailed monitoring of the wound closure process. Additionally, the distribution and potential systemic effects of the zinc and silver ions were analyzed using Inductively Coupled Plasma-Mass Spectrometry (ICP-MS). This analysis was crucial in evaluating metal ion absorption through the wound site and estimating any toxic effects on the body. Our findings are particularly significant in the field of regenerative medicine. Transmission electron microscopy (TEM) revealed that the tested nanocomposites notably enhanced collagen deposition, a vital component in the wound healing process. Furthermore, a reduction in glycogen levels in hepatocytes was observed following treatment with these metal-protein dressings. This novel finding warrants further investigation. Overall, our findings highlight the diverse roles of zinc and silver nanocomposites in wound healing. This study not only contributes to our understanding of metal-protein complexes in tissue regeneration but also opens new avenues for research into the delivery mechanisms of such treatments for hard-to-heal wounds.

Anchoring Metal-Nitrogen Sites on Porous Carbon Polyhedra with Highly Accessible Multichannels for Efficient Oxygen Reduction.

Transition metal-nitrogen-carbon complexes, featuring single metal atoms embedded in a nitrogen-doped carbon matrix, emerge as promising alternatives to traditional platinum-based catalysts, offering cost-effectiveness, abundance, and enhanced catalytic performance. This work introduces a novel method for the etching and doping of zeolitic imidazolate frameworks (ZIFs) with transition metals, creating a uniform distribution of secondary metal centers on ZIF surfaces. By disrupting the crystalline symmetry of ZIFs through synthetic defect engineering, we gain access to their entire internal volume, creating multichannel pathways. The absorption of metal ions is theoretically simulated, demonstrating their thermodynamically spontaneous nature. The selective removal of defect channels under Lewis acidic conditions, induced by metal ion alcoholysis/hydrolysis, facilitates the introduction of metal atoms into ZIF cavities. The resulting single-atom catalyst, after pyrolysis, features a three-dimensional (3D) multichannel structure, high surface area, and uniformly dispersed metal atoms within the N-doped carbon matrix, establishing it as an exceptional catalyst for the oxygen reduction reaction (ORR). Our findings highlight the potential of using metal etching in defect-engineered metal-organic frameworks (MOFs) for single-atom catalyst preparation, paving the way for the next generation of high-performance, cost-effective ORR catalysts in sustainable energy systems.

Chromium adsorption efficiency by functional polymeric nanocomposite membrane: A case study for environmental sustainability

AbstractWe have designed and developed nonwoven fabric supported electrospun polymeric nanofibrous‐based membrane for robust filtration system for ecological sustainability of clean water. The fabricated nanocomposites filters were tested for the removal of chromium (VI) toxic heavy metal ions from contaminated feedstock water. The interpenetrating network like morphological structure obtained from pure and composite nanofibers‐based membranes have been thoroughly investigated to understand the structure–properties of highly entangled system. It has been found that incorporating functional moieties onto nanocomposite membranes significantly impacts the absorption efficiency of toxic metals. The pore sizes of the hierarchical geometries have been varied to insight into its impact on flow rate and efficiency of filtration. The strategy of interfacing the multifunctional composite polyethylene terephthalate nanofiber membrane supported on nonwoven fabric to generate heterostructures has found to provide mechanically stable platform for efficient metal ion removal. It has been found by BET surface area analysis that the nanofibers reinforced with functional nanomaterials has controlled pore geometry compared to pristine PET electrospun nanofibers which lead to higher absorption of metal ions. We have highlighted the importance of mechanically stable electrospun polymeric nanofibers membrane‐based mitigation strategies to meet the huge demand of potable water for long‐term environmental sustainability.Highlights Mechanically toughened freestanding nanofibers mat supported on nonwoven fabric. Functionally upgrade nanofibers by incorporation of carbon based nanofillers. Controlled porosity by morphological optimization for removal of contaminates.

Reduction of Metal Density of Iron (Fe) and Natrium Minerals (Na) in Boring Water Using Rubber Fruit Sheets Active Archoic

Activated carbon is a highly popular adsorbent for the absorption of metal ions. Lignocellulosic materials can be used to produce activated carbon, which is both renewable and abundant, as well as being cost-effective. The objective of this research is to investigate the reduction of iron (Fe) and sodium (Na) levels in the artesian well by utilizing activated carbon made from rubber shells. The materials utilized include rubber shells, a solution containing 10% H3PO4 (phosphoric acid), water from an artesian well, and distilled water (aquadest). The carbonization process was conducted at 300º C for 1 h, using an adsorbent size of 120 mesh. In addition, chemical activation was performed using a 10% H3PO4 solution for 24 h, followed by physical activation through heating in a furnace at a temperature of 500ºC for 1 hour. The acquired activated carbon is utilized for the absorption of Fe and Na. The activated carbon was characterized using X-ray diffraction (XRD), and the concentration of Fe and Na minerals was determined using an Atomic Adsorption Spectrophotometer (AAS). The results indicated a reduction of 97.9% in the concentration of iron (Fe) and a decrease of 90.01% in sodium (Na) levels.

Biologically templated formation of Cobalt-Phosphide-Graphene hybrids with charge redistribution for efficient hydrogen evolution

Developing highly efficient and sustainable hydrogen evolution reaction (HER) electrocatalysts is important for the practical application of emerging energy technologies. The spherical structure and phosphorus-rich properties of Chlorella can facilitate the construction of comparable transition metal phosphide electrocatalysts. Here, a microorganism template strategy is proposed to construct a cobalt-phosphide-graphene hybrid. Chlorella can absorb metal ions, and the generated rough spherical nanoparticles are uniformly distributed around the reduced graphene oxide nanosheets. This designed catalyst has comparable HER performance in acidic electrolytes and needs an overpotential of only 153 mV at a current density of 10 mA cm−2. The experimental and density functional theory results imply that the charge redistribution between Co2P and pyrrole-N is the key factor in enhancing the HER activity. The induced electron aggregation at the N and P sites can serve as a key active site for absorbing the adsorbed hydrogen atom intermediate to accelerate the HER process, contributing to the active sites of Co2P- and pyrrole-N-doped carbon with 0 eV hydrogen adsorption free energy. This work provides a broad idea for synthesizing advanced catalysts by a biological template approach, facilitating the innovative integration of biology and emerging electrochemical energy technologies.

Conductive and Enhanced Mechanical Strength of Mo2Ti2C3 MXene-Based Hydrogel Promotes Neurogenesis and Bone Regeneration in Bone Defect Repair.

Bone defects are common with increasing high-energy fractures, tumor bone invasion, and implantation revision surgery. Bone is an electroactive tissue that has electromechanical interaction with collogen, osteoblasts, and osteoclasts. Hydrogel provides morphological plasticity and extracellular matrix (ECM) 3D structures for cell survival, and is widely used as a bone engineering material. However, the hydrogels have poor mechanical intensity and lack of cell adhesion, slow gelation time, and limited conductivity. MXenes are novel nanomaterials with hydrophilic groups that sense cell electrophysiology and improve hydrogel electric conductivity. Herein, gelatin had multiple active groups (NH2, OH, and COOH) and an accelerated gelation time. Acrylamide has Schiff base bonds to cross-link with gelatin and absorb metal ions. Deacetylated chitosan improved cell adhesion and active groups to connect MXene and acrylamide. We constructed Mo2Ti2C3 MXene hydrogel with improved elastic modulus and viscosity, chemical cross-linking structure, electric conductivity, and good compatibility. Mo2Ti2C3 MXene hydrogel exhibits outstanding osteogenesis in vitro. Mo2Ti2C3 MXene hydrogel promotes osteogenesis via alkaline phosphatase (ALP) and alizarin red S (ARS) staining, improving osteogenic marker genes and protein expressions in vitro. Mo2Ti2C3 MXene hydrogel aids new bone formation in the in vivo calvarial bone defect model via micro-CT and histology. Mo2Ti2C3 MXene hydrogel facilitates neurogenesis factors nerve growth factor (NGF) and brain-derived neurotrophic factor (BDNF) expression, and aids newly born neuron marker Tuj-1 and sensory neuron marker serotonin (5-HT) and osteogenesis pathway proteins, runt-related transcription factor 2 (Runx2), osteocalcin (OCN), SMAD family member 4 (SMAD4), and bone morphogenetic protein-2 (BMP2) in the bone defect repair process. Mo2Ti2C3 MXene hydrogel promotes osteogenesis and neurogenesis, which extends its biomedical application in bone defect reconstruction.

Adsorption of Hg2+/Cr6+ by metal-binding proteins heterologously expressed in Escherichia coli

BackgroundRemoval of heavy metals from water and soil is a pressing challenge in environmental engineering, and biosorption by microorganisms is considered as one of the most cost-effective methods. In this study, the metal-binding proteins MerR and ChrB derived from Cupriavidus metallidurans were separately expressed in Escherichia coli BL21 to construct adsorption strains. To improve the adsorption performance, surface display and codon optimization were carried out.ResultsIn this study, we constructed 24 adsorption engineering strains for Hg2+ and Cr6+, utilizing different strategies. Among these engineering strains, the M’-002 and B-008 had the strongest heavy metal ion absorption ability. The M’-002 used the flexible linker and INPN to display the merRopt at the surface of the E. coli BL21, whose maximal adsorption capacity reached 658.40 μmol/g cell dry weight under concentrations of 300 μM Hg2+. And the B-008 overexpressed the chrB in the intracellular, its maximal capacity was 46.84 μmol/g cell dry weight under concentrations 500 μM Cr6+. While in the case of mixed ions solution (including Pb2+, Cd2+, Cr6+ and Hg2+), the total amount of ions adsorbed by M’-002 and B-008 showed an increase of up to 1.14- and 4.09-folds, compared to the capacities in the single ion solution.ConclusionThe construction and optimization of heavy metal adsorption strains were carried out in this work. A comparison of the adsorption behavior between single bacteria and mixed bacteria systems was investigated in both a single ion and a mixed ion environment. The Hg2+ absorption capacity is reached the highest reported to date with the engineered strain M’-002, which displayed the merRopt at the surface of chassis cell, indicating the strain’s potential for its application in practical environments.

Structural characterization and calcium absorption-promoting effect of sucrose-calcium chelate in Caco-2 monolayer cells and mice.

Sucrose emerges as a chelating agent to form a stable sucrose-metal-ion chelate that can potentially improve metal-ion absorption. This study aimed to analyze the structure of sucrose-calcium chelate and its potential to promote calcium absorption in both Caco-2 monolayer cells and mice. The characterization results showed that calcium ions mainly chelated with hydroxyl groups in sucrose to produce sucrose-calcium chelate, altering the crystal structure of sucrose (forming polymer particles) and improving its thermal stability. Sucrose-calcium chelate dose dependently increased the amount of calcium uptake, retention, and transport in the Caco-2 monolayer cell model. Compared to CaCl2 , there was a significant improvement in the proportion of absorbed calcium utilized for transport but not retention (93.13±1.75% vs. 67.67±7.55%). Further treatment of calcium channel inhibitors demonstrated the active transport of sucrose-calcium chelate through Cav1.3. Cellular thermal shift assay and quantitative reverse transcription-polymerase chain reaction (qRT-PCR) assays indicated that the ability of sucrose-calcium chelate to promote calcium transport was attributed to its superior ability to bind with PMCA1b, a calcium transporter located on the basement membrane, and stimulate its gene expression compared to CaCl2 . Pharmacokinetic analysis of mice confirmed the calcium absorption-promoting effect of sucrose-calcium chelate, as evident by the higher serum calcium level (44.12±1.90mg/L vs. 37.42±1.88mmol/L) and intestinal PMCA1b gene expression than CaCl2 . These findings offer a new understanding of how sucrose-calcium chelate enhances intestinal calcium absorption and could be used as an ingredient in functional foods to treat calcium deficiency. PRACTICAL APPLICATION: The development of high-quality calcium supplements is crucial for addressing the various adverse symptoms associated with calcium deficiency. This study aimed to prepare a sucrose-calcium chelate and analyze its structure, as well as its potential to enhance calcium absorption in Caco-2 monolayer cells and mice. The results demonstrated that the sucrose-calcium chelate effectively promoted calcium absorption. Notably, its ability to enhance calcium transport was linked to its strong binding with PMCA1b, a calcium transporter located on the basement membrane, and its capacity to stimulate PMCA1b gene expression. These findings contribute to a deeper understanding of how the sucrose-calcium chelate enhances intestinal calcium absorption and suggest its potential use as an ingredient in functional foods for treating calcium deficiency.

Removal of Ca(II) and Mg(II) ions from solutions to sulfonic cation exchanger based on plasticized polyvinylchloride

The ion-exchange material was obtained by oxidation of the product of the interaction of polyvinyl chloride with an aqueous solution of calcium polysulfide. The structure of the resulting cation exchanger and metal-containing hybrid material was identified by IR spectroscopy and elemental analysis. The kinetics of absorption of metal ions in cation exchange resin was analyzed by using pseudo-first and pseudo-second order models. The rate constants in the adsorption process were calculated. According to the correlation coefficient, it was determined that the sorption process proceeds according to the laws of a pseudo-second order reaction. Based on the equilibrium sorption it was evaluated according to the isotherm models of Langmuir, Freundlich, Temkin, and Dubinin-Radushkevich (D-R). The results showed that the absorption of Ca2+ and Mg2+ ions from aqueous solutions in cation exchange resin displays the best accordance with the Langmuir monomolecular theory. In addition, the results showed that the cation exchanger (PVC-SO3H) effectively cleans river water from Ca2+ and Mg2+ ions for industrial enterprises.

Design of Novel Poly(Propranolol) Acrylate and Methacrylate Polymers through Radical Polymerization for Antibacterial Activity and Metal Ion Absorption

The monomer 1-(isopropylamino)-3-(1-naphthyloxy)-2-propanoacrylate (IANOPA) and monomer 1-(isopropylamino)-3-(1-naphthyloxy)-2-propanomethacrylate (IANOPMA) were synthesized by treating 1-(isopropylamino)-3-(1-naphthyloxy)-2-propanol with acryloylchloride/methacryloyl chloride. The above esterification reactions were carried out in the presence of triethylamine. By employing the free radical polymerization method, the synthesized monomers were converted into polymers by using an initiator 2, 2′-azobisisobutyronitrile in the presence of nitrogen environment at 70±2°C. The monomers and polymers were characterized by various techniques such as FT-IR, UV, 1H NMR, and 13C NMR spectroscopic analyses. Further, differential scanning calorimetry (DSC) was used to estimate the glass transition temperature (Tg). Gel permeation chromatography (GPC) was used to estimate the molecular weight of the polymers. In addition, monomer and polymer surfaces’ morphology was analyzed using SEM analysis. As a primary application, the effectiveness of synthesized monomers and polymers was explored as antibacterial agents against gram-positive bacteria (Staphylococcus aureus) and gram-negative bacteria (Pseudomonas aeruginosa) which were measured from their inhibitory zone diameters. Further, the synthesized polymers, poly-IANOPA and poly-IANOPMA, were utilized for the uptake ability study of heavy metal ions such as Zn2+, Cu2+, Ni2+, and Pb2+ present in water sources by equilibrium method.

Pan-Genome-Wide Identification and Transcriptome-Wide Analysis of ZIP Genes in Cucumber

The ZRT/IRT-like proteins (ZIPs) play critical roles in the absorption, transport, and intracellular balance of metal ions essential for various physiological processes in plants. However, little is known about the pan-genomic characteristics and properties of ZIP genes in cucumber (Cucumis sativus L.). In this study, we identified 10 CsZIP genes from the pan-genome of 13 C. sativus accessions. Among them, only CsZIP10 showed no variation in protein sequence length. We analyzed the gene structure, conserved domains, promoter cis-elements, and phylogenetic relationships of these 10 CsZIP genes derived from “9930”. Based on phylogenetic analysis, the CsZIP genes were classified into three branches. Amino acid sequence comparison revealed the presence of conserved histidine residues in the ZIP proteins. Analysis of promoter cis-elements showed that most promoters contained elements responsive to plant hormones. Expression profiling in different tissues showed that most CsZIP genes were expressed at relatively low levels in C. sativus leaves, stems, and tendrils, and CsZIP7 and CsZIP10 were specifically expressed in roots, indicating their potential involvement in the absorption and transport of metal ions. Transcriptomic data indicated that these 10 ZIP genes displayed responses to both downy mildew and powdery mildew, and CsZIP1 was significantly downregulated after both salt and heat treatments. In conclusion, this study deepens our understanding of the ZIP gene family and enhances our knowledge of the biological functions of CsZIP genes in C. sativus.

Synthesis of supramolecular polymers with calix[4]arene and β-cyclodextrin and their application in heavy metal ion absorption

Two categories of supramolecular polymer monomers were produced by introducing the ureidopyrimidone quadruple-hydrogen bonding assemblies on the calix[4]arene and the β-cyclodextrin host units, which adsorbed up to 99% of Pb2+ and Cd2+.

NA

NA

Sensor Absorbents for Heavy Metal Ions By Low-Cost Functionalization of Porous Carbons

Porous carbons are key materials in electrodes for electrochemical energy storage as well as in water purification. Methods to modify porous carbons to enhance their properties as charge storing or water purification materials have been explored during the past decades [1,2]. The main application fields if porous carbon, water purification and energy storage, are highly cost sensitive. For this reason, there is a need to develop low-cost methods to modify porous carbons. Here, the use of benzoxazine chemistry to modify porous carbons is explored. Benzoxazine chemistry can be considered a protection group strategy for phenols, where the phenols from which the benzoxazines are synthesized, are deprotected upon benzoxazine polymerization. Further, benzoxazine polymerization produces Mannich bridges located near phenol groups, motifs that can be used to capture heavy metal ions. More specifically, in the first step, the porous carbons are partially impregnated with benzoxazine monomers, from melt or solutions to afford powders impregnated far below the liquid saturation level of the particles. That is, the particles retain porosity after the impregnation but still have a dry appearance. After impregnation, the particles are heated over the polymerization temperature of the benzoxazine to afford the porous carbon with immobilized functionalities. As phenols can initiate benzoxazine polymerization and be incorporated in the polymer, this method offers a simple route to produce polymerized and immobilized structure at a carbon interface. Here, results on metal ion absorption and the electrochemical response after exposure are presented for carbons modified by impregnation-polymerization of benzoxazines with or without incorporation of phenols. Inks were manufactured from the modified carbons. The electrochemical characterizations were performed on printed arrays of electrochemical cells on a substrate having dimensions of well plates and intended for automatized testing and where the carbon inks were deposited on the working electrodes. This methodology has a potential of simplifying the development of sensor materials and absorbents and can be automatized and potentially be supported with machine learning schemes. The electrochemical responses of exposure of the modified carbon electrodes to metal salt solutions show that impregnation-polymerization of functional benzoxazine can produce absorbents responding electrochemically to metal ion absorption with a scalable process starting from low-cost materials.

Pembuatan Karbon Aktif Dari Limbah Pelepah Kelapa Sawit (Elaies Guineesis Jacq.) Sebagai Media Peyerapan Ion Logam Fe Air Sumur Menggunakan Aktivator Asam Fosfat (H3PO4)

Oil palm (elaies) is a tropical plant that is widely found in Indonesia. The increasing production of this plant has an impact on the increasing amount of oil palm frond waste every year. During this time, the community only utilizes the fruit for the manufacture of CPO while the fronds are discarded and become waste. Palm frond waste contains constituent components in the form of cellulose and lignin so that it has the potential to be utilized as an adsorbent. The manufacture of activated carbon is carried out with the stages of carbonization and activation using H3PO4. The finished activated carbon was then tested for moisture content, ash content, and iodine absorption according to SNI 06-3730-1995, functional group analysis testing with Fourier Transform Infra Red FTIR and Fe metal ion absorption test in well water using an AAS spectrophotometer. From these tests, 7% moisture content, 4% ash content and 909.45 mg/gr iodine absorption were obtained. FT-IR testing obtained 11 fungal groups and Fe metal absorption using an AAS spectrophotometer obtained 77%, so it can be concluded that the activated carbon made is in accordance with SNI 06-3730-1995 specifications

A novel sulfhydryl-modified superparamagnetic photonic crystal sensing material for the simultaneous heavy metal ions detection and adsorption treatment

A novel superparamagnetic photonic crystal (Fe3O4@SiO2@Sulfhydryl SPC) was successfully created for simultaneous visual detection and absorption of harmful heavy metal ions. This SPC was made by combining photonic crystal and superparamagnetic nanosphere technologies. During detection, Fe3O4@SiO2@Sulfhydryl nanospheres can move in the liquid sample and fully absorb the target substances. The detection range is from 1 μg/L to 5 mg/L, which corresponds to the critical concentration range for heavy metal ions in drinking water and sewage. The detection limit is 1 μg/L. In the detection process, the signal responded rapidly and remained stable when analyzed with a fiber optic spectrometer. Notably, the signal intensity decreased significantly, with a reduction of 62.22 a.u. for Hg2+ and 124.31 a.u. for Ag+. Simultaneously, the visual results were striking. The SPC changed color from orange (PC structural color) to the original reddish-brown color of the solution with the formation of magnetic aggregates (PC structural color disappeared). This SPC exhibits excellent sensitivity, offers a clear visual display, possesses strong absorption detection capabilities, is easy to use, cost-effective, and, importantly, does not cause secondary pollution. Furthermore, the harmful heavy metal ions absorbed by the SPC can be easily removed from the water sample using an external magnetic field, overcoming challenges related to efficient separation of the adsorbent material from wastewater. As a result, this SPC holds great promise for real-time visual monitoring and practical sewage purification processes.

Pengaruh Kecepatan Pengadukan dan Waktu Kontak Ampas Kulit Durian (Durio Zibethinus L.) terhadap Penyerapan Ion Logam Tembaga (II) dengan Metode Batch

One of the effective methods in handling the impact of pollution by copper ion is the biosorption method using durian peel powder (Durio Zibethinus L.). The purpose of this research is to determine the optimum absorption conditions and the optimum capacity for absorption of copper metal ions (Cu2+) using the batch method with variations in pH, concentration, stirring speed, contact time, and mass of biosorbent. The results of the research showed that the optimum conditions for the absorption of Cu2+ metal ions were at pH 6, concentration of 220 ppm, stirring speed of 250 rpm, contact time of 90 minutes and mass of biosorbent 0,4 gram was 7,788 mg/g. The adsorption isotherm of Cu2+ metal with durian skin biosorbent (Durio Zibethinus L.) tends to follow the Langmuir isotherm equation with a determinant coefficient (R) of 0,1854. Durian peel powder was characterized by the FTIR instrument, before being activated, after being activated, and after contacting the analyte there were functional groups, namely hydroxyl (O-H), alkene (C=C), carbonyl (C-O), and ether (-COC) groups.

Pengaruh Konsentrasi Awal Larutan Ion Logam Cd2+ terhadap Penyerapan Biomassa Kulit Langsat (Lansium domesticum) yang Dimodifikasi Metanol

Industrial activities have been growing rapidly lately. Increased industrial activity can improve the quality of human life, but behind it there are adverse effects on the environment and human health. There are many harmful heavy metals found in industrial waste. One of them is cadmium metal, which is one of the dangerous heavy metals that if accumulated in the body can threaten human health. Langsat fruit peel waste can be utilized as an adsorbent. Adsorbent is an absorbent substance/material to absorb heavy metal ions. Biomass was characterized using AAS instrument to determine the concentration of Cd2+ metal ion absorption in langsat peel biomass. This study was conducted to determine the effect of the initial concentration of solution on the absorption of Cd2+ metal ions in methanol-modified langsat peel biomass. The results showed that the optimal absorption of Cd2+ metal ions in methanol-modified langsat peel biomass was at a concentration of 400 mg/L with an absorption capacity of 9.387 mg/g.

Analysis of double phytoextraction of Cadmium and microplastics by Galinsoga Quadriradiata in soil An exploration for a comprehensive treatment method for the environment

The wide usage of microplastics and heavy metals has led to the accumulation of these pollutants in our environment. Among heavy metals and microplastics, Cadmium (Cd), polyvinyl chloride (PVC), and polyethylene (PE) are the most severe and ubiquitous pollutants. With large surface areas, microplastics have the ability to absorb metal ions, potentially performing "carrier effect", by which microparticles enhance the transfer of other pollutants from soil to plants. Phytoextraction has been shown to be the most effective strategy to remediate heavy metal contamination. In this study, we selected Galinsoga quadriradiata (G. quadriradiata) as the test species to investigate the effectiveness of phytoextraction in soil contaminated with Cd, PVC and PE. According to our results, G. quadriradiata present effective phytoextraction to Cd and microplastics. However, the carrier effect between Cd and PVC or PE only exists in the value of maximal quantum efficiency of photosystem II (Fv/Fm) but has no effect on the uptake of Cd by G. quadriradiata. For future studies, we propose to investigate the carrier effect between heavy metals and microplastics in plants, test the pathway of microplastics by which they are up-taken by plants from soil, and increase the efficiency of phytoextraction by exposing plants (such as G. quadriradiata) that have been proved to absorb heavy metal to microplastics.

APPLICATION OF ULTRASONIC TECHNOLOGY ON THE ADSORPTION OF Fe (II) AND Mg (II) METAL IONS USING KAOLIN AS ADSORBENTS

Kaolin is a mineral found in sedimentary rocks known as claystone. Ultrasonic is used to accelerate the adsorption of metal ions on the adsorbent. This study aims to see the effect of the optimal temperature and time needed by the ultrasonic device to absorb metal ions in wastewater. Choline was activated using HCl, then modified with CTAB and ABS surfactants. Organokaolin modified with ABS was used to adsorb Fe (II) metal ions at 50℃, and those modified with CTAB were used to adsorb Mg (II) metal at 70℃, and each time varied 10,20,30,40,50 minutes. From this study, the highest value of efficiency in absorbing Fe metal ions was 92.97% at 50 minutes of irradiation, and for the absorption of Mg metal ions was 95.69% at 50 minutes of irradiation. This shows that the longer the irradiation time used, the better the absorption efficiency obtained. FTIR test results showed the presence of groups, O-H, C-H, and O=C=O. The results of the SEM test showed that the voids that were empty before adsorption were filled with metal ions during the conditions after adsorption