Compatibility of NAPLs and Other Organic Compounds with Materials Used in Well Construction, Sampling, and Remediation

Structural integrity of well construction, sampling, and remediation materials may be compromised at many hazardous sites by nonaqueous phase liquids (NAPLs) and their dissolved constituents. A literature review of compatibility theory and qualitative field experiences are provided regarding the degradation and corrosion of materials in contact with NAPLs and organic compounds. A chemical compatibility table, compiled from several sources of compatibility testing results, is presented for 73 chemicals and 28 commonly used materials. Field experiences illustrate the compatibility problems of some of the common wastes and materials found at hazardous waste sites.     

An Analysis of Reducing Perchloroethylene Emissions in the Urban Environment: A Case Study of Taiwan

Selected volatile organic compounds (VOCs) emitted from commercial activities and industrial processes have been classified as hazardous air pollutants, posing a potential health risk in the urban environment. In this respect, perchloroethylene (PCE), a suspected human carcinogen, is the most noticeable compound because it is widely used in laundries and hotels as a dry‐cleaning solvent. The objective of this paper was to quantify the emissions of PCE and other petroleum‐based solvents from dry cleaning business in illustration of the regulatory infrastructure of reducing PCE exposure in the environment of Taiwan. Based on the Emission Factors (AP‐42) method, the emissions of the non‐methane hydrocarbons (NMHCs) from dry cleaning business had decreased from 5100 metric tons in 1997 to 2800 metric tons in 2007. The success of significant reduction of NMHCs in Taiwan has been ascribed to the fact that Taiwan established the relevant regulations at the end of the 1990s. From the data on the industrial/commercial demand for PCE and the emission inventories of NMHCs from dry cleaning business, the reduction of PCE emissions will show a declining trend in the near future.     

Degradation of Adsorbed Sarin on Activated Carbons: A 31P‐MAS‐NMR Study

The fate of the OP nerve agent isopropyl methylphosphonofluoridate (sarin) on granular activated and metal‐impregnated activated carbons that are used in gas‐mask filters was investigated by means of ³¹P magic‐angle‐spinning (MAS) NMR spectroscopy. The results show that most of the adsorbed sarin on extensively dried carbons decomposes with a half‐life of 5–12 days. A MAS‐NMR signal of the degradation product isopropyl methylphosphonic acid (IMPA) appears in the spectra of sarin on non‐impregnated carbons. The IMPA signal is not visible in the spectra from metal‐impregnated carbons, probably due to strong binding of the acid molecule to paramagnetic Cr³⁺ and Cu²⁺ ions. Exposure of BPL and ASC carbons to air of 53% relative humidity shortens the degradation time by approximately an order of magnitude. Wetting shortens the half‐life of sarin on BPL carbon to approximately 2 hours.     

Sediments,porewaters and diagenesis in an urban water body,Salford, UK: impacts of remediation

Contaminated sediments deposited within urban water bodies commonly exert a significant negative effect on overlying water quality. However, our understanding of the processes operating within such anthropogenic sediments is currently poor. This paper describes the nature of the sediment and early diagenetic reactions in a highly polluted major urban water body (the Salford Quays of the Manchester Ship Canal) that has undergone remediation focused on the water column. The style of sedimentation within Salford Quays has been significantly changed as a result of remediation of the water column. Pre‐remediation sediments are composed of a range of natural detrital grains, predominantly quartz and clay, and anthropogenic detrital material dominated by industrial furnace‐derived metal‐rich slag grains. Post‐remediation sediments are composed of predominantly autochthonous material, including siliceous algal remains and clays. At the top of the pre‐remediation sediments and immediately beneath the post‐remediation sediments is a layer significantly enriched in furnace‐derived slag grains, input into the basin as a result of site clearance prior to water‐column remediation. These grains contain a high level of metals, resulting in a significantly enhanced metal concentration in the sediments at this depth. Porewater analysis reveals the importance of both bacterial organic matter oxidation reactions and the dissolution of industrial grains upon the mobility of nutrient and chemical species within Salford Quays. Minor release of iron and manganese at shallow depths is likely to be taking place as a result of bacterial Fe(III) and Mn(IV) reduction. Petrographic analysis reveals that the abundant authigenic mineral within the sediment is manganese‐rich vivianite, and thus Fe(II) and Mn(II) released by bacterial reactions may be being taken up through the precipitation of this mineral. Significant porewater peaks in iron, manganese and silicon deeper in the sediment column are most probably the result of dissolution of furnace‐derived grains in the sediments. These species have subsequently diffused into porewater above and below the metal‐enriched layer. This study illustrates that the remediation of water quality in anthropogenic water bodies can significantly impact upon the physical and chemical nature of sedimentation. Additionally, it also highlights how diagenetic processes in sediments derived from anthropogenic grains can be markedly different from those in sediments derived from natural detrital material. Copyright © 2003 John Wiley & Sons, Ltd.     

太湖流域太浦河周边区域突发水污染潜在风险评估

太浦河是太湖流域重要跨省界河流,沿岸区域污染源众多,下游分布重要水源地,存在突发水污染潜在风险,迫切需要开展区域污染源潜在风险评估,为突发水污染事件的风险防控提供科学依据.本研究通过太浦河周边区域的污染源调研,明确污染源的空间分布与污染源强,确定评估区域的主要污染物（化学需氧量、氨氮、锑、重金属铬、油品、危险化学品）,综合考虑污染源、河流水文、沿岸社会经济等因素,筛选突发水污染潜在风险评估指标,构建评估指标体系,评估突发水污染事件的综合风险,识别太浦河周边区域的主要突发水污染潜在风险源.研究结果表明：太浦河周边区域的高突发水污染风险区呈现片状或斑块状分布,主要包括大型污水处理厂区域、大型工业企业区域、加油站和危险化学品仓库集中分布区、太浦河沿岸工业企业区域、水源地周边工业企业区域,总面积为22 km²,占太浦河污染源风险评估范围总面积的1.4%,是突发水污染事件防控的重点区域.     

Production of Drinking Water from Highly Contaminated Surface Waters: Removal of Organic,Inorganic, and Microbial Contaminants Applying Mobile Membrane Filtration Units

In military out of area missions of the Bundeswehr, it can be necessary to produce drinking water even from highly polluted surface waters containing a variety of organic, inorganic, and microbiological contaminants. Thus, mobile drinking water purification systems must be able to remove such contaminants as far as possible to meet the requirements of the German and European drinking water regulation/directive. Presently, two novel drinking water purification units applying membrane filtration undergo intensive long‐term trials carried out by the Bundeswehr. If these trials positively proof the functionality of these units and their ability to remove all possible contaminants they shall substitute so far available devices which use large amounts of chemicals and charcoal filtration for water purification.In the course of a research project, the functionality of the new devices and their efficacy to remove high amounts of algae, microbes, and organic and inorganic pollutants are additionally tested in “worst‐case” field studies. In September 2000, the first mobile drinking water purification unit was tested at the Teltowkanal in Berlin, Germany.This canal was chosen because it carries high burdens of municipal sewage effluents. The results from the fatigue test confirmed the ability of the water purification unit to reduce the concentrations of all contaminants meeting the maximum tolerance levels set by the German/European drinking water regulation.The pre‐filtration device was very effective in removing algae and solid particles to protect the membranes from clogging and to enable an almost maintenance‐free operation. Residues of pharmaceuticals and some other organic contaminants have almost totally been removed from the surface water where they were detected at individual concentrations up to the μg/L‐level.     

Improved Removal of Indoor Volatile Organic Compounds by Activated Carbon Fiber Filters Calcined with Copper Oxide Catalyst

Heating, ventilating, and air‐conditioning (HVAC) systems ensure indoor air quality and provide a comfortable environment. However, the conventional HVAC systems only provide indoor ventilation and adjust temperature and humidity. This work removes indoor volatile organic compounds (VOCs) using a feasible and novel air‐cleaning for an HVAC system, to remove indoor VOCs. An activated carbon‐fiber (ACF) filter calcined with copper oxide (CuO) catalyst, called a CuO/ACF catalyst filter, was the developed kit. Formaldehyde, a major VOC, was chosen as the target pollutant. Experiments were performed to confirm the filtration ability of the CuO/ACF catalyst filter in removing formaldehyde in a stainless‐steel chamber equipped with a simplified HVAC system. Total air exchange rate (ACH) was controlled at 0.5 and 1.0 h⁻¹, the fresh ACH was 0.15 and 0.30 h⁻¹, and relative humidity (RH) was set at 30 and 70%. A first‐order decay of formaldehyde existed in the controlled chamber when the two pretreated CuO/ACF catalyst filters were employed. Experimental results demonstrate that the CuO/ACF catalyst filters removed formaldehyde effectively. The decay constant was 0.425 and 0.618 h⁻¹ for 0.5 and 2.0 ppm formaldehyde, respectively. Moreover, the formaldehyde decay rate increased as total ACH, fresh ACH, RH, and the Cu(NO₃)₂ concentration for calcination of CuO/ACF catalyst filter increased.     

Comparison of Fiberglass and Other Polymeric Well Casings, Part I: Susceptibility to Degradation by Chemicals

Previous research has shown that the most commonly used well casing materials-stainless steel. polyvinyl chloride (PVC). and polytetra-fluoroethylene (PTFE)-are not suited for all monitoring environments and applications. This study is part of a series of experiments that were conducted to determine the suitability of four other polymeric well casing materials-acrylonitrile butadiene styrene (ABS), fluorinalcd ethylene propylene (FHP), fiberglass-reinlorced epoxy (FRE), and fiberglass-reinforced plastic (FRP)- for use in ground water monitoring wells. In these studies, these four materials were compared with two other commonly used polymeric well casings, PVC and PTFE. Part I of these studies examines the resistance of these materials to degradation by chemicals. Future reports will consider sorption and leaching of organic and metal contaminants.
In this study, the six materials were exposed to 28 neat organic compounds (including one acid) and to extremely acidic and alkaline aqueous solutions for up to 112 days. This was done to simulate the most aggressive environments to which monitoring well casings may be exposed. The casings were observed for changes in weight and signs of physical degradation (swelling, softening, deterioration, or dissolution).
The two fluorinated polymers (FEP and PTFE) were not degraded by any of the lest chemicals. Among the nonfluorinated products tested. FRE was the most inert. Three organic chemicals caused the glass fibers to separate. and two organic solvents caused weight gains exceeding 10 percent. ABS was the most readily degraded material tested. By the end of the study, only the acid and alkaline solutions had little effect on ABS. FRP was more severely degraded by the organic chemicals than FRH but was less affected than PVC. FRP and FRE. lost weight when exposed to the highly acidic conditions.     

Toxicity identification in metal plating effluent: implications in establishing effluent discharge limits using bioassays in Korea

Because of complexity and diversity of toxicants in effluent, chemical analysis alone gives very limited information on identifying toxic chemicals to test organisms. Toxicity identification evaluation (TIE) techniques have been widely used to identify toxicants in various samples including industrial wastewater as well as natural waters. In response to new regulation for effluent discharge in Korea, which will be effective from 2011, a necessity of studies emerges that investigates toxicity levels in industrial effluents. This work was a preliminary study examining toxicity levels in effluent from one metal plating factory using Daphnia magna (48 h immobility) and identifying toxicity-causing substances. Toxicity tests showed variability on different sampling occasions and the results of TIE methods indicated that both organic compounds and metals contributed to the observed toxicity in metal plating effluent. Further studies are necessary to help reduce effluent toxicity especially from direct dischargers, who will have to comply with the new regulation.     

Characterization of Estuarine and Fluvial Dissolved Organic Matter by Thermochemolysis using Tetramethylammonium Hydroxide

Selected samples of dissolved organic matter (DOM) isolated by ultrafiltration (UDOM) have been analyzed by thermochemolysis in the presence of tetramethylammonium hydroxide (TMAH). This technique cleaves ester and ether bonds of bio‐ and geological macromolecules and releases monomer subunits and methylates them in situ as their methyl ethers and methyl esters. Compared with conventional pyrolysis, TMAH thermochemolysis avoids decarboxylation of preexisting carboxylic moieties and produces aromatic acids as their methyl esters. Various phenolic derivatives, which might originate from incorporated lignin‐derived structures, from the highly aliphatic and resistant biopolymer cutan and also from proteinaceous materials, were identified among the products produced from UDOM upon thermochemolysis. The presence of lignin derivatives in UDOM indicates input of organic matter derived from terrestrial sources. Various aromatic acids, perhaps representing the final steps in the oxidation of the side‐chain during microbial oxidation of lignin, were released upon TMAH thermochemolysis, suggesting they are structural constituents of the UDOM. Different ratios of lignin‐derived materials, commonly determined using the CuO oxidation method, such as the Δ value, indicative of the amount of lignin present, the acid/aldehyde ratio (Ad/Al)_G, indicative of the extent of oxidative degradation of the lignin component, and the syringyl/guaiacyl (S/G) and p‐hydroxyphenyl/guaiacyl (P/G) ratios, indicative of the contribution for the different types of lignin, were determined.     

Efficiency of Moso Bamboo Charcoal and Activated Carbon for Adsorbing Radioactive Iodine

Preventing radioactive pollution is a troublesome problem but an urgent concern worldwide because radioactive substances cause serious health‐related hazards to human being. The adsorption method has been used for many years to concentrate and remove radioactive pollutants; selecting an adequate adsorbent is the key to the success of an adsorption‐based pollution abatement system. In Taiwan, all nuclear power plants use activated carbon as the adsorbent to treat radiation‐contaminated air emission. The activated carbon is entirely imported; its price and manufacturing technology are entirely controlled by international companies. Taiwan is rich in bamboo, which is one of the raw materials for high‐quality activated carbon. Thus, a less costly activated carbon with the same or even better adsorptive capability as the imported adsorbent can be made from bamboo. The objective of this research is to confirm the adsorptive characteristics and efficiency of the activated carbon made of Taiwan native bamboo for removing ¹³¹I gas from air in the laboratory. The study was conducted using new activated carbon module assembled for treating ¹³¹I‐contaminated air. The laboratory results reveal that the ¹³¹I removal efficiency for a single‐pass module is as high as 70%, and the overall efficiency is 100% for four single‐pass modules operated in series. The bamboo charcoal and bamboo activated carbon have suitable functional groups for adsorbing ¹³¹I and they have greater adsorption capacities than commercial activated carbons. Main mechanism is for trapping of radioiodine on impregnated charcoal, as a result of surface oxidation. When volatile radioiodine is trapped by potassium iodide‐impregnated bamboo charcoal, the iodo‐compound is first adsorbed on the charcoal surface, and then migrates to iodide ion sites where isotope exchange occurs.     

Sources of particulate and dissolved organic carbon in the St Lawrence River: isotopic approach

We investigate sources of both dissolved and particulate organic carbon in the St Lawrence River from its source (the Great Lakes outlet) to its estuary, as well as in two of its tributaries. Special attention is given to seasonal interannual patterns by using data collected on a bi‐monthly basis from mid‐1998 to mid‐2003. δ¹³C measurements in dissolved inorganic carbon, dissolved organic carbon (DOC) and particulate organic carbon (POC), as well as molar C : N in particulate organic matter (POM), are used to bring insight into the dynamic between aquatic versus terrigenous sources. In addition, ¹⁴C activities of DOC were measured at the outlet of the St Lawrence River to its estuary to assess a mean age of the DOC exported to the estuary. In the St Lawrence River itself, aquatically produced POC dominates terrestrially derived POC and is depleted in ¹³C by approximately 12‰ versus dissolved CO₂. In the Ottawa River, the St Lawrence River's most important tributary, the present dataset did not allow for convincing deciphering of POC sources. In a small tributary of the St Lawrence River, aquatically produced POC dominates in summer and terrestrially derived POC dominates in winter. DOC seems to be dominated by terrestrially derived organic matter at all sampling sites, with some influence of DOC derived from aquatically produced POC in summer in the St Lawrence River at the outlet of the Great Lakes and in one of its small tributaries. The overall bulk DOC is relatively recent (¹⁴C generally exceeding 100% modern carbon) in the St Lawrence River at its outlet to the estuary, suggesting that it derives mainly from recent organic matter from topsoils in the watershed. Copyright © 2005 John Wiley & Sons, Ltd.     

Synthesis,Mechanism, and Performance Assessment of Zero‐Valent Iron for Metal‐Contaminated Water Remediation: A Review

Recently, increased industrial and agriculture activities have resulted in toxic metal ions, which has increased public concern about the quality of surface and groundwater. Various types of physical, biological, and chemical approaches have been developed to remove surface and groundwater metal ions contaminants. Among these practices, zero‐valent iron (ZVI) is the most studied reactive material for environmental clean‐up over the last two decade and so. Although ZVI can remove the contaminants even more efficiently than any other reactive materials. However, low reactivity due to its intrinsic passive layer, narrow working pH, and the loss of hydraulic conductivity due to the precipitation of metal hydroxides and metal carbonates limits its wide‐scale application. The aim of this work is to document properties, synthesis, and reaction mechanism of ZVI for the treatment of metal ions from the surface and groundwater in recent 10 years (2008–2018). So far, different modified techniques such as conjugation with support, bimetal alloying, weak magnetic field, and ZVI/oxidant coupling system have been developed to facilitate the use of ZVI in various environmental remediation scenarios. However, some challenges still remain to be addressed. Therefore, development and research in this field are needed to overcome or mitigate these limitations.     

Visibility and Incidence of Respiratory Diseases During the 1998 Haze Episode in Brunei Darussalam

— Air pollution episodes as a result of forest fires in Brunei Darussalam and neighbouring regions have reached hazardous levels in recent years. Such episodes are generally associated with poor visibility and air quality conditions. In the present study, data on PM₁₀ (particulate matter of size less than 10 microns) and CO in Brunei Darussalam have been considered to study the incidence of respiratory diseases whereas data on relative humidity (RH) in addition to PM₁₀ have been used to explain the visibility with a particular emphasis on haze episode during 1998.¶Initial exploratory analysis indicates significant correlation of visibility with PM₁₀ and RH. An attempt has been made to explain visibility on the basis of PM₁₀ and RH using multiple linear regression analysis. The regression model shows that PM₁₀ and RH are two significant factors affecting the visibility at a given site. Further, canonical correlation, a multivariate method of analysis, has been used to explain the incidence of respiratory diseases as a function of air quality during the haze period. The results indicate that PM₁₀ and CO levels during the haze period have a significant bearing on the incidence of respiratory diseases (Asthma, Acute Respiratory Infections and Influenza (ARII)).     

The Use of Waste Materials in the Passive Remediation of Mine Water Polution

The contamination and resulting degradation of water coursesby effluents from abandoned and active mines is a world-wideproblem. Traditional methods of remediating the dischargesfrom mines involve the addition of chemicals and the utilisationof artificial energy sources. Over the last 15–20 years passivetreatment systems have been developed that harness naturalchemical and biological processes to ameliorate the potentiallytoxic effects of such discharges. There are many different typesof passive system, including compost wetlands, reducing andalkalinity producing systems (RAPS), permeable reactive barriersand inorganic media passive systems. Different waste materialscan be utilised as reactive media within each of these systems,dependent upon the type of mine water and treatment technology.In many cases the reactivity of these recycled waste materialsis key to the remedial performance of these systems. The materialsused may be organic (e.g., composts) or inorganic (e.g., blast furnaceslag) and where possible are sourced locally in order to minimisetransport costs. The remediation of mine waters in itself canproduce large quantities of waste products in the form of ironoxide sludge. Potential uses of this material in the productionof pigments and in the treatment of phosphate contaminatedwaters is also currently under investigation.The exploitation of what are traditionallythought of as waste materials within treatmentsystems for polluted waters is an expandingtechnology which provides great scope for recycling.     

Removal of COD from Industrial Effluent Containing Indigo Dye Using Adsorption Method by Activated Carbon Cloth: Optimization,Kinetic, and Isotherm Studies

The pollution of underground and surface water streams is a tremendous environmental problem. Adsorption, in which activated carbon (AC) is used as an adsorbent, is one of efficient procedures to remove organic and inorganic pollutants from industrial wastewaters. Activated carbon fiber (ACF), a newly developed form of AC, has high adsorption rate and surface area and can be used for the treatment of industrial wastewaters. In this work, ACF was prepared by physicochemical activation method from kenaf and we studied its ability in the treatment of indigo‐containing wastewater produced from a dying factory. The filtered wastewater was treated via adsorption by ACF, and response surface experimental design method was used to study the effect of ACF dosage, contact time, temperature, and pH of the wastewater on the removal process. ACF dosage of 0.256 g, temperature of 12.5°C, pH 8.5, and contact time of 125 min were optimum treatment conditions. The adsorption process obeys pseudo‐second‐order kinetic and Freundlich isotherm models.     

Traffic ‐and Industry‐Related Air Pollution Exposure Assessment in an Asian Megacity

Like other Asian countries, Pakistan is facing the issue of air pollution due to rapid urbanization, enormous transportation increases, and other related human activities. Moreover, continuously increasing emission sources have not only raised pollutant concentrations but also their types, thus damaging both human health and the environment. Faisalabad is the third largest megacity of Pakistan and its state of air quality is getting worse due to factors such as industrialization, high traffic volumes, and extensive fossil‐fuel‐burning activities. This review article aims to highlight the present status of air pollution in this city with special reference to particulate matter, elemental profiles, gaseous pollutants, organic–inorganic particulate contents as well as their sources. The concentration levels of these entities were also compared with other national and international cities, and related environmental standards. It is found that current levels of these pollutants are beyond safety limits as specified by various environment protection agencies and organizations. Several weak aspects and gaps are also identified along with suggestions for improvements of the present situation and directions for future research.     

Chemical composition and photochemical reactivity of exhaust from aircraft turbine engines

Assessment of the environmental impact of aircraft emissions is required by planners and policy makers. Seveal areas of concern are: 1. exposure of airport workers and urban residents to toxic chemicals emitted when the engines operate at low power (idle and taxi) on the ground; 2. contributions to urban photochemical air pollution of aircraft volatile organic and nitrogen oxides emissions from operations around airports; and 3. emissions of nitrogen oxides and particles during high-altitude operation. The environmental impact of chemicals emitted from jet aircraft turbine engines has not been firmly established due to lack of data regarding emission rates and identities of the compounds emitted. This paper describes an experimental study of two different aircraft turbine engines designed to determine detailed organic emissions, as well as emissions of inorganic gases. Emissions were measured at several engine power settings. Measurements were made of detailed organic composition from C₁ through C₁₇, CO, CO₂, NO, NO _x , and polycyclic aromatic hydrocarbons. Measurements were made using a multi-port sampling pro be positioned directly behind the engine in the exhaust exit plane. The emission measurements have been used to determine the organic distribution by carbon number and the distribution by compound class at each engine power level. The sum of the organic species was compared with an independent measurement of total organic carbon to assess the carbon mass balance. A portion of the exhaust was captured and irradiated in outdoor smog chambers to assess the photochemical reactivity of the emissions with respect to ozone formation. The reactivity of emissions from the two engines was apportioned by chemical compound class.     

Toxicity identification in metal plating effluent: Implications in establishing effluent discharge limits using bioassays in Korea

Because of complexity and diversity of toxicants in effluent, chemical analysis alone gives very limited information on identifying toxic chemicals to test organisms. Toxicity identification evaluation (TIE) techniques have been widely used to identify toxicants in various samples including industrial wastewater as well as natural waters. In response to new regulation for effluent discharge in Korea, which will be effective from 2011, a necessity of studies emerges that investigates toxicity levels in industrial effluents. This work was a preliminary study examining toxicity levels in effluent from one metal plating factory using Daphnia magna (48 h immobility) and identifying toxicity-causing substances. Toxicity tests showed variability on different sampling occasions and the results of TIE methods indicated that both organic compounds and metals contributed to the observed toxicity in metal plating effluent. Further studies are necessary to help reduce effluent toxicity especially from direct dischargers, who will have to comply with the new regulation.     

Regeneration and Reuse of a Seaweed‐Based Biosorbent in Single and Multi‐Metal Systems

A seaweed‐waste material resulting from the processing of Ascophyllum nodosum was previously shown to be very efficient at removing Zn(II), Ni(II) and Al(III) both in single and multi‐metal waste streams. In this study, the regeneration of the biosorbent using an acid wash resulted in the release of high metal concentrations during multiple desorption cycles. Maximum desorption efficiencies (DE) of 183, 122 and 91% were achieved for Zn(II), Ni(II) and Al(III), respectively, for subsequent metal loading cycles, significantly exceeding the desorption rates observed for conventional sorbents. The regeneration of the sorbent was accomplished with very little loss in metal removal efficiency (RE) for both single and multi‐metal systems. Values of 92, 96 and 94% RE were achieved for Zn(II), Ni(II) and Al(III), respectively, for the 5^th sorption cycle in single metal aqueous solutions. A slight decrease was observed for the same metals in multi‐metal systems with maximum REs of 85, 82 and 82% for Zn(II), Ni(II) and Al(III), respectively. This study showed that the novel sorbent derived from a seaweed industrial waste would be suitable for multiple metal sorption cycles without any significant loss in RE.