Functional Hydrogels Promote Vegetable Growth in Cadmium-Contaminated Soil.

Over the years, the concentration of cadmium in soil has increased due to industrialization. Cadmium in the soil enters the human body through plant accumulation, seriously endangering human health. In the current study, two types of hydrogels were successfully synthesized using a free radical polymerization method: an ion-type hydrogel referred to as DMAPAA (N-(3-(Dimethyl amino) propyl) acrylamide)/DMAPAAQ (N,N-Dimethyl amino propyl acrylamide, methyl chloride quaternary) and a non-ion-type hydrogel known as DMAA (N,N-Dimethylacrylamide). In the experiment carried out in this study, the ion-type hydrogel DMAPAA/DMAPAAQ was introduced to cadmium-contaminated soil for vegetable cultivation. The study found that at cadmium levels of 0 and 2 mg/kg in soil, when exposed to a pH 2 solution, cadmium wasn't detected in the filtrate using ICP. As the amount of cadmium increased to 500 mg/kg, hydrogel addition gradually reduced the filtrate cadmium concentration. Notably, the use of the 4% hydrogel resulted in 0 mg/L of cadmium. For the 0% hydrogel, vegetable cadmium absorption was determined to be 0.07 mg/g, contrasting with 0.03 mg/g for the 4% hydrogel. The DMAPAA/DMAPAAQ hydrogel significantly boosts vegetable growth by efficiently absorbing nitrate ions through ion exchange, releasing them for plant uptake. In contrast, the DMAA hydrogel, used as a control, does not enhance plant growth despite its water absorption properties. In summary, the composite hydrogel shows great potential for enhancing vegetable yield and immobilizing heavy metals in soil.

Controlling organic carbon increase in oxygenated marine sediment by using decarburization slag.

The chemical oxygen demand (COD) in the Seto Inland Sea, Japan has increased in the recent decades due to the increase of bottom dissolved oxygen (DO) concentration which stimulated several autotrophic microorganisms, specially sulfur oxidizing bacteria (SOB). This increased SOB activity due to the oxygenation of the bottom sediment synthesized new organic matter (OM) which contributed dissolved organic carbon to the overlying seawater. This phenomenon further led to hypoxia in some subareas in the Seto Inland Sea. Higher pH or alkaline environment has been found to be an unfavorable condition for SOB. In this research, we used decarburization slag to elevate the pH of sediment to control the SOB activity and consequently reduce OM production in the sediment. Ignition loss of the surface sediment increased from 5.14% 6.38% after 21 days of incubation with aeration; whereas the sediment showed the less ignition loss of 5.71% after 21 days when the slag was incubated in the same experimental setup. Microbial community analysis showed less SOB activity in the slag added aerated sediment which accounts for the controlled increase of OM in the sediment. An additional experiment was conducted with magnesium oxide to confirm whether elevated pH can control the OM increase in sediment due to rising DO. All these results showed that decarburization slag can elevate the pH of the sediment to a certain level which can control the SOB activity followed by controlled increase of OM in the sediment. The findings may be beneficial to control accumulation of sedimentary OM which can act as a source of organic carbon in the overlying seawater.

Dual Benefits of Hydrogel Remediation of Cadmium-Contaminated Water or Soil and Promotion of Vegetable Growth under Cadmium Stress.

This study aims to solve the problem of cadmium heavy metal ion pollution caused by the abuse of chemical fertilizers and activities such as mining, which pose a serious threat to the plant growth environment. We successfully synthesized DMAPAA (N-(3-(Dimethyl amino) propyl) acrylamide)/DMAPAAQ (N, N-Dimethyl amino propyl acrylamide, methyl chloride quaternary) hydrogels via free radical polymerization. Subsequently, we conducted experiments on this hydrogel for growing vegetables under cadmium stress conditions in aqueous solutions and soil. The cadmium capture capacity of DMAPAA/DMAPAAQ hydrogels under different cadmium ion concentrations and pH values was evaluated by using inductively coupled plasma optical emission spectrometry (ICP). The research results show that under the condition of pH = 7.3, the cadmium capture capacity of DMAPAA/DMAPAAQ hydrogels is the greatest. We used the Langmuir model to fit the adsorption data, and the correlation coefficient was as high as 0.96, indicating that the model fits well. The application of the hydrogels promoted the growth of vegetables in soil under cadmium stress conditions. The results showed that when the added amount of hydrogel was 4%, the dry weight of the vegetables was the largest. In addition, when the added amount of cadmium was 500 mg/kg and the added amount of hydrogel was 4%, the absorption of cadmium by the vegetables decreased to an undetectable level. In summary, the hydrogel successfully synthesized in this study can be effectively used to immobilize cadmium ions in soil while positively promoting the growth and yield of vegetables. This achievement has practical significance for solving the problem of heavy metal ion pollution.

A Novel Composite Hydrogel Material for Sodium Removal and Potassium Provision.

Sodium ions are commonly found in natural water sources, and their high concentrations can potentially lead to adverse effects on both the water sources and soil quality. In this study, we successfully synthesized potassium polyacrylate (KMAA) hydrogel through free radical polymerization and evaluated its capability to remove sodium ions from and supply potassium ions to aqueous solutions. To assess its performance, inductively coupled plasma emission spectroscopy (ICP) was employed to analyze the sodium ion removal capacity and potassium ion exchange capability of the KMAA hydrogel at various initial sodium ion concentrations and pH values. The results demonstrated that the KMAA hydrogel exhibited remarkable efficiency in removing sodium ions and providing potassium ions. At pH 7, the maximum adsorption capacity for sodium ions was measured at 70.7 mg·g-1. The Langmuir model, with a correlation coefficient of 0.98, was found to be more suitable for describing the adsorption process of sodium ions. Moreover, at pH 4, the maximum exchange capacity for potassium ions reached 243.7 mg·g-1. The Freundlich model, with a correlation coefficient of 0.99, was deemed more appropriate for characterizing the ion exchange behavior of potassium ions. In conclusion, the successfully synthesized KMAA hydrogel demonstrates superior performance in removing sodium ions and supplying potassium ions, providing valuable insights for addressing high sodium ion concentrations in water sources and facilitating potassium fertilizer supply.

Effect of Heating Temperature on Ammonia Emission in the Mainstream Aerosols from Heated Tobacco Products.

Heated tobacco products are devices that deliver nicotine into the body via inhalation of the mainstream aerosols generated during direct and/or indirect heating of tobacco leaf material. Ammonia in aerosols potentially increases the alkalinity and, therefore, the proportion of free nicotine for easy absorption. Meanwhile, ammonia can be a cause of adverse health effects when involved in the aerosols. This study aimed to grasp the emission behaviour of ammonia in the mainstream aerosols generated from four kinds of devices that employ different heating temperatures from 40 to 350 °C. The aerosols were generated by a vaping machine following the CRM 81 puffing protocol. Ammonia in the forms of gas and particles was trapped in 5 mM oxalic acid and subsequently determined by ion chromatography. The results showed that the total emission amount of ammonia increased with an increase in the heating temperature regardless of the device used. The gas-particle distribution of ammonia also depended on the heating temperature; gaseous ammonia was only found in the device with 40 °C of the heating temperature. These results show that ammonia in the mainstream aerosols was emitted from a common thermal process, probably thermal extraction in water vapour from a tobacco leaf.

Usage patterns of aromatherapy essential oil among Chinese consumers.

Given the concern over contact allergy risk associated with aromatherapy, information regarding the use of essential oils (EOs) is crucial for consumer dermal exposure assessment. In this study we mainly aim to describe the usage patterns of EOs among Chinese consumers to provide important data for exposure assessment to fragrance allergens in EOs. A web survey was conducted in April 2020 among 1,518 potential Chinese EO consumers to assess consumer usage patterns. The usage patterns of 11 types of EOs were collected among female consumers (N = 457; ages 0-70). For females aged 0-14, they used Lavanda (42.9%) and Tea tree (57.1%) oils only. Among the senior age groups (15-70), Lavanda oil was the most used EO with 46.7%, 51%, 68.1%, and 50% for females aged 15-24, 25-39, 40-59 and 60-70, respectively. The majority of females aged 25-59 used Rose, Lavanda, Sandalwood, Frankincense and Jasmine oil on their whole face more than three times a week at diverse dilution rates. Usage patterns are described for all age groups. In consideration of usage pattern of females aged 25-59, co-exposure to fragrance allergens contained in EOs and cosmetics could make them vulnerable to contact allergy. This study provides valuable information for dermal exposure assessment.

Children's exposures to boron and biocides from slime products in Asian regions.

BACKGROUND: Chemical exposure from slime toys can cause potential health effects. Although slime toys are popular in Asia, the regulation of boron, chloromethylisothiazolinone (CMIT), and methylisothiazolinone (MIT) in these toys has been implemented only in Korea. OBJECTIVE: In this study, we investigated boron migration levels and CMIT and MIT concentrations in 127 slime products from Asian cities and estimated children's exposure to boron and the biocides in Korea. METHODS: Slime boron migration levels were analyzed by inductively coupled plasma optical emission spectrometry (ICP-OES), according to Part 3 of the European Standard on the safety of toys (EN 71-3:2013). CMIT and MIT concentrations were analyzed using liquid chromatography tandem mass spectrometry (LC-MS/MS). Exposure doses of boron, CMIT, and MIT were calculated using the exposure pattern of children slime users in Korea. RESULTS: Average boron migration levels of the slime products in Seoul, Bangkok, Hong Kong, Taipei, and Yokohama were 691.9, 851.1, 806.6, 509.0, and 956.2 mg/kg, respectively. Of the 127 slime products tested, 70.1% exceeded the EU boron migration limit of 300 mg/kg for toys made with sticky material. Boron migration levels in slime products in Korea did not differ significantly by manufacturing date, although the Korean boron regulations were enacted in January 2019. CMIT and MIT were detected from 51.2% and 36.2% of all products, respectively, and tended to be detected simultaneously. Exposure doses of boron, CMIT, and MIT were highest among infants. SIGNIFICANCE: Oral exposure was the most important for boron exposure. It is necessary to manage boron level in slime products and minimize exposure from hand to mouth action in infants.

Responses of the benthic environment to reduction in anthropogenic nutrient loading in the Seto Inland Sea (Japan), based on M-AMBI assessment.

Deterioration of the sediment environment and benthic ecosystem is an undesirable effect of eutrophication, but little is known about the response of macrobenthic communities to eutrophication and their long-term recovery. In the present study, temporal changes in benthic ecological status, associated with reductions in anthropogenic impacts on a largest semi-enclosed sea in Japan, were determined using long-term monitoring data from water and sediment quality based on the multivariate AZTI Marine Biotic Index (M-AMBI), focusing on spatial differences in anthropogenic impacts. Several sub-areas were classified based on Chlorophyll a (Chl.a) concentrations in surface water during the 1980s. Chl.a concentrations decreased in all sub-areas except the sub-area with <2 µg Chl.a L-1 from the 1990s-2010s. On the other hand, total organic carbon contents in sediment decreased and M-AMBI values increased in all sub-areas during this period may be due to reduced lateral organic matter advection from surrounding areas.

Synthesis of Oxidant Functionalised Cationic Polymer Hydrogel for Enhanced Removal of Arsenic (III).

A cationic polymer gel (N-[3-(dimethylamino)propyl]acrylamide, methyl chloride quaternary)(DMAPAA-Q gel)-supported oxidising agent (KMnO4 or K2Cr2O7) was proposed to remove As from water. The gel could adsorb arsenite, As(III), and arsenate, As(V), through the ion exchange method, where the oxidising agent oxidised As(III) to As(V). theoretically speaking, the amount of oxidant in the gels can reach 73.7 Mol%. The maximal adsorption capacity of the D-Mn gel (DMAPAA-Q gel carrying MnO4-) and D-Cr gel (DMAPAA-Q gel carrying Cr2O72-) for As(III) could reach 200 mg g-1 and 263 mg g-1, respectively; moreover, the As(III) removal rate of the gels could still be maintained above 85% in a neutral or weak acid aquatic solution. Studies on the kinetic and adsorption isotherms indicated that the As adsorption by the D-Mn and D-Cr gels was dominated by chemisorption. The thermodynamic parameters of adsorption confirmed that the adsorption was an endothermic process. The removal of As is influenced by the co-existing high-valence anions. Based on these results, the gels were found to be efficient for the As(III) adsorption and could be employed for the As(III) removal from the industrial wastewater.

Increase in sedimentary organic carbon with a change from hypoxic to oxic conditions.

In the Seto Inland Sea, Japan, chemical oxygen demand has increased over recent decades, while average dissolved oxygen concentrations in the bottom water have increased. In this study, we investigated responses of organic carbon (OC) in hypoxic sediment to changes of redox conditions using experimental columns containing sediment and overlying water. Surface sediment showed an increase in OC along with the change to an aerobic condition. Microbial community analysis showed a predominance of sulfur-oxidizing bacteria (SOB) such as Sulfurovum sp. in the sediment. This dominance could account for the increased OC. Additionally, the dissolved organic carbon (DOC) concentration in the overlying water increased. Further experiments using sandy sediment showed that biodegradation of Sulfurimonas denitrificans was associated with DOC release. These results show that a change in the sedimentary environment (increase in dissolved oxygen) increased the sedimentary OC and DOC of overlying water by stimulating certain autotrophic bacteria, especially the SOB.

Reduction of ozone dosage by using ozone in ultrafine bubbles to reduce sludge volume.

Sludge ozonation, which promotes sludge disintegration and solubilization, is a promising technology for reducing waste sludge volume from biological wastewater treatment process. However, if this technology is to be widely adopted, reducing the energy consumption associated with ozone generation will be necessary. We used ultra-fine bubbles (UFBs) as ozone carriers to determine if their use could improve the efficiency of ozone treatment and reduce the ozone dose required. We used a spiral, liquid-type UFB generator, which can introduce UFBs directly into a sludge suspension. The death ratio of bacteria in sludge was used as an indicator of sludge reduction. The ozone requirement was reduced by UFBs. The ozone consumption required to achieve a death ratio of 80% was 15 mg-O3/g-MLSS in the sludge treated with ozone supplied by UFBs versus 25 and 45 mg-O3/g-MLSS in sludges treated with ozone supplied as a spiral, liquid-type microbubbles and by a diffuser, respectively. When mixing water ozonated with UFBs with sludge, the depth of the dead cell layer from the surface to the interior of the sludge floc was larger than that of ozonated water lacking UFBs at the same rate of ozone consumption. Ozone in UFBs kills bacteria inside the flocs. However, the fragmentation of sludge flocs by shear forces in the UFB generator made a larger contribution to the acceleration of bacterial death in sludge treated with ozone supplied by UFBs.

A quantitative analysis method to determine the amount of cellulose fibre in waste sludge.

A novel quantitative analysis method for cellulose fibre was developed to understand its behaviour in biological wastewater treatment and waste sludge processes. The method developed in this study was designed using Pseudomonas aeruginosa to remove it by dissolving all the organic components except cellulose from the sludge due to needing the solubilisation of bacteria occupied almost of sludge matrix and quantifying the amount of remaining cellulose. The results of this study indicated that a combined treatment process that employed 2,000 U/L protease, 2 M hydrogen peroxide, and 2 mM potassium hydroxide after pre-treatment for floc dispersion with an ultrasonic treatment at 26 W for 1 min resulted in a solubilisation of 96% of P. aeruginosa without losing the cellulose fibre. When it was applied to the cellulose fibre added in the sludge from a municipal wastewater treatment facility, 99.5% of the cellulose fibre was recovered by using the high-speed centrifuge.

Application of Aurantiochytrium sp. L3W for food-processing wastewater treatment in combination with polyunsaturated fatty acids production for fish aquaculture.

Thraustochytrids such as Aurantiochytrium are heterotrophic microorganisms that are known to produce valuable polyunsaturated fatty acids (PUFAs) such as docosahexaenoic acid (DHA) and eicosapentaenoic acid (EPA). In this study, Aurantiochytrium sp. strain L3W was used to remove dissolved organic carbon (DOC) and dissolved nitrogen (DN) from bean-boiling (BB) and miso-processing (MP) wastewater and to simultaneously produce PUFAs. Strain L3W removed 52% of the DOC and 37% of the DN from sterilized BB wastewater and produced biomass that contained 137 mg/g of fatty acids (FAs), including 96.2 mg/g of DHA. Growth of strain L3W in sterilized MP wastewater resulted in the production of biomass containing 147.6 mg/g of FAs, including 97.8 mg/g of DHA, and removal of 47% of the DOC and 55% of the DN from the wastewater. The biomass of strain L3W was digestible by the enzymes extracted from the stomachs of rainbow trout. These results confirmed the potential for use of strain L3W to remove DOC and DN from food processing wastewater and to produce PUFAs. This study also provided the first evidence that the raw biomass of Aurantiochytrium sp. can be used as a fish feed additive.

Synthesis, Phase-Transition Behaviour, and Oil Adsorption Performance of Porous Poly(oligo(ethylene glycol) Alkyl Ether Acrylate) Gels.

To probe the effects of pendant side-chain structures on the properties of porous thermoresponsive polymer gels, oligo(ethylene glycol) alkyl ether acrylates were polymerised in an aqueous medium under radical-mediated phase-separation conditions. The monomer structures varied according to the lengths and termini of their ethylene glycol side chains. The porous poly(oligo(ethylene glycol) alkyl ether acrylate) (POEGA) gels exhibited variable lower critical solution temperatures (LCSTs) but similar and rapid swelling-deswelling behaviours. Although the LCST of the poly(tri(ethylene glycol) monomethyl ether acrylate) (PTEGA) gel decreased with increasing aqueous NaCl or CaCl2 concentration, PTEGA showed excellent thermosensitivity in highly concentrated salt solutions, recommending its application in saline environments. Examination of PTEGA adsorption performance in an oil-water emulsion showed that n-tridecane adsorption increased with temperature. Although n-tridecane was effectively adsorbed at 70 °C, its release from the fully adsorbed PTEGA gel was difficult despite a temperature reduction from 70 to 20 °C.

Impact of eelgrass bed recovery and expansion on phytoplankton growth through nutrient competition.

Eelgrass beds are highly productive and support diverse faunal assemblages; they also take in nutrients from the water and prevent excessive phytoplankton growth in eutrophic coastal waters through the reduction of available nutrients. Despite its importance, the global distribution of eelgrass has declined worldwide. In eutrophic areas with high chlorophyll a (Chl.a) concentrations, natural recovery of eelgrass beds after eutrophication is possible. To facilitate this, sufficient water clarity can be reached after a large enough decrease in phytoplankton concentration. In this study, we proposed a novel indicator for the maximum possible Secchi depth (MPSD), defined as the Secchi depth when the Chl.a concentration is equal to a reference Chl.a concentration. We applied the MPSD to evaluate water clarity improvements through the reduction of terrigenous anthropogenic nutrient loading. We found that phytoplankton did not control water clarity in the study area, which was instead controlled by background factors. Therefore, improvements in water clarity would not be expected after reducing terrigenous anthropogenic nutrient loading. The habitat of Zostera marina is determined by light availability, so we investigated a potential area with ≥20% surface irradiance and Z. marina existed in 27% of it (100 of 373 ha). The maximum further recovery of eelgrass by Secchi depth improvements to the MPSD was estimated at 36 ha. The impact of eelgrass recovery and expansion on phytoplankton growth from May to September was evaluated by a mathematical model under two scenarios: the current eelgrass distribution (100 ha) and potential maximum eelgrass distribution (373 ha). A Chl.a decrease of 1.0-3.0 µg l-1 from 4.0 to 7.0 µg l-1 was achieved in an area from May to July, and the improvement decreased with time. These evaluation methods and findings could help us gain a better understanding of the nutrient management in seagrass-vegetated semi-enclosed seas subjected to anthropogenic nutrient input.

The effect of γ-FeOOH on enhancing arsenic adsorption from groundwater with DMAPAAQ + FeOOH gel composite.

Arsenic contamination of groundwater is a serious concern worldwide. The research gaps in removing arsenic are selectivity, regeneration and effective removal rate at neutral pH levels. In this study, we discussed the reasons of the high arsenic adsorption from groundwater of our previously developed adsorbent, a cationic polymer gel, N,N-dimethylamino propylacrylamide, methyl chloride quaternary (DMAPAAQ), loaded with iron hydroxide. We used a transmission electron microscope (TEM) and thermogravimetric analyser (TGA) to detect the iron contents in the gel and ensure its maximum impregnation. We found that the gel contains 62.05% FeOOH components. In addition, we used the Mössbauer spectroscopy to examine the type of impregnated iron in the gel composite and found that it was γ-FeOOH. Finally, we used Fourier transform infrared spectroscopy (FTIR) to examine the surface functional groups present in the gel and the differences in those groups before and after iron impregnation. Similarly, we also investigated the differences of the surface functional groups in the gel, before and after the adsorption of both forms of arsenic. To summarize, this study described the characteristics of the gel composite, which is selective in adsorption and cost effective, however further applications should be investigated.

Deterioration Mechanism of a Tertiary Polyamide Reverse Osmosis Membrane by Hypochlorite.

A tertiary polyamide membrane was synthesized using N,N'-dimethyl-m-phenylenediamine. The durability of this membrane to chlorination by hypochlorite treatment followed by sodium hydroxide treatment was examined, and then deterioration mechanisms were proposed. The tertiary polyamide membrane demonstrated better durability to free chlorine than a conventional secondary polyamide one; however, the former was deteriorated by hypochlorite for 24 h at 2000 ppm of free chlorine below pH 7.5. The salt rejection and permeation performance of the membrane were almost unchanged, and the least chlorination of the active layer occurred during hypochlorite treatment at pH 10. These results indicated that hypochlorous acid rather than hypochlorite ion was the free chlorine species that induced membrane deterioration. The deterioration became severe as chlorination progressed, resulting in collapse of the active layer below pH 7.5. Chlorination and hydrolysis of the model tertiary amide N-methylbenzanilide and Fourier transfer infrared spectroscopy of a deteriorated membrane showed that chlorination of the tertiary polyamide occurred via direct chlorination of the benzene bound to the amidic nitrogen. Silver ion probing of the deteriorated membrane revealed that amide bond scission occurred in the active layer, which might be related to the electron deficiency of the amidic nitrogen caused by chlorination of its benzene ring.

Removal of Arsenic Using a Cationic Polymer Gel Impregnated with Iron Hydroxide.

In this work, we prepared an adsorbent composed of a cationic polymer gel containing iron hydroxide in its structure designed to adsorb arsenic from groundwater. The gel we selected was the N,N-dimethylamino propylacrylamide methyl chloride quaternary (DMAPAAQ) gel. The objective of our preparation method was to ensure the maximum content of iron hydroxide in the structure of the gel. This design approach enabled simultaneous adsorption by both the polymer structure of the gel and the iron hydroxide component, thus, enhancing the adsorption capacity of the material. To examine the performance of the gel, we measured reaction kinetics, carried out pH sensitivity and selectivity analyses, monitored arsenic adsorption performance, and conducted regeneration experiments. We determined that the gel undergoes a chemisorption process and reaches equilibrium at 10 h. Moreover, the gel adsorbed arsenic effectively at neutral pH levels and selectively in complex ion environments, achieving a maximum adsorption volume of 1.63 mM/g. The gel could be regenerated with 87.6% efficiency and NaCl could be used for desorption instead of harmful NaOH. Taken together, the presented gel-based design method is an effective approach for constructing high-performance arsenic adsorbents.

Benthic quality assessment using M-AMBI in the Seto Inland Sea, Japan.

Benthic invertebrates that inhabit the seafloor respond to anthropogenic and natural stresses, and are good indicators for assessing the benthic ecological status. We evaluated the ecosystem health of the Seto Inland Sea based on the multivariate AZTI Marine Biotic Index (M-AMBI), being its first application in a Japanese coastal sea with numerous endemic species. From the 415 locations studied, we were able to use M-AMBI in 384 sites (92.5% in all sites). The result revealed a statistically significant correlation among biotic indices including AMBI, M-AMBI, Richness, and H' (p < 0.01). Most of the physico-chemical parameters of the sediment (water content, total organic carbon (TOC) content, sulfide content, mud content, and oxidation-reduction potential (ORP)) were significantly correlated with each other excluding sediment temperature. The M-AMBI was significantly correlated with physico-chemical variables including water content, TOC content, sulfide content, and ORP. We found that the sites classified into the organically enriched cluster, and having high contents of TOC, mud, and sulfide and negative ORP, corresponded with sites that had significantly low M-AMBI values (bad-poor ecological status). Conversely, sites in the unpolluted sandy cluster were assigned high M-AMBI values (high-good ecological status). Therefore, M-AMBI would be a useful biotic index in Japanese coasts due to the representation of the comprehensive sediment quality.

Development and regeneration of composite of cationic gel and iron hydroxide for adsorbing arsenic from ground water.

Globally, arsenic contaminated groundwater is a serious concern for human health. Previous studies have developed various methods to remove arsenic. But, most of them fail to selectively adsorb arsenic and regenerate. In this study, we developed an adsorbent, a cationic polymer gel loaded with iron hydroxide, which can adsorb arsenic from groundwater more effectively than the other adsorbents. The cationic polymer gel is N,N-dimethylamino propylacrylamide, methyl chloride quaternary (DMAPAAQ). The preparation of the gel is different from the other polymer gels used for adsorption of arsenic and other metals, and it ensures that the gel contains 53.7% FeOOH particles. It should also provide good selectivity, be simple to use and be cost-effective in terms of reusability. The study showed that the gel selectively adsorbed arsenic effectively at neutral pH levels. The results demonstrate that the maximum amount of As(V) adsorption was 123.4 mg/g, which is higher than the other adsorbents. In addition, the gel adsorbed As(V) selectively in the presence of Sulphate. Also, regeneration of the gel was performed for eight consecutive days with 87.6% effectiveness. Additionally, the adsorption mechanism of this gel composite and time required for reaching the equilibrium adsorption is discussed in this paper.