Adsorption Of Heavy Metals Research Articles

Lightweight aggregates produced from low-temperature sintering of multiple solid wastes for heavy metals removal: Adsorption kinetics and stabilization

Solid wastes, including incinerated sewage sludge ash (ISSA), waste bentonite, and waste glass powder (WGP), were recycled and sintered at a low temperature (680°C) to produce lightweight aggregates (WSA). WGP acted as a fluxing agent to significantly lower sintering temperature of 1000-1200°C in other studies. WSA demonstrated an excellent mechanical strength of 3.76 MPa. The adsorbent dosage, initial pH, kinetics and isotherm on heavy metals adsorption were evaluated in batch adsorption experiments. The isothermal data exhibited a good correlation with the Langmuir model, and the maximum adsorption capacity was approximately 9.26 mg/g at 296 K. Pb(II) removal was dominated by precipitation and cation exchange. Breakthrough curves were determined for fixed-bed adsorption. At 50% breakthrough, the maximum adsorption capacity was 1.82 mg/g. The WSA after heavy metals adsorption were then reused to replace river sand (10-50%) in producing lightweight mortars. The solidification of spent WSA in the lightweight mortars could significantly reduce the leaching of Pb(II) by 98.5%. Moreover, the reuse of spent WSA resulted in low density and low thermal conductivity of cement mortars. This study demonstrates total waste management for municipal solid wastes: upcycling of waste–utilization–permanently stored as construction materials.

Adsorption of heavy metals with hyper crosslinked polymers: Progress, challenges and perspectives

Adsorption of heavy metals with hyper crosslinked polymers: Progress, challenges and perspectives

PE/PP fibrous adsorbents with bifunctional groups of tertiary amine and phosphate prepared by electron beam induced co-grafting for heavy metal adsorption of both cationic and anionic forms in acidic conditions.

PE/PP fibrous adsorbents with bifunctional groups of tertiary amine and phosphate prepared by electron beam induced co-grafting for heavy metal adsorption of both cationic and anionic forms in acidic conditions.

Comparative Study of Biosorption and Traditional Methods for Heavy Metal Removal from Industrial Wastewater in Panipat

In this research paper, I have thoroughy described about the topic Comparative Study of Biosorption and Traditional Methods for Heavy Metal Removal from Industrial Wastewater in Panipat.” Industrial wastewater contamination by toxic heavy metals poses a significant environmental threat globally, especially in rapidly industrializing regions like Panipat District in Haryana, India. Panipat, renowned for its extensive textile and chemical industries, generates substantial volumes of wastewater laden with heavy metals such as lead (Pb), cadmium (Cd), and mercury (Hg). Recent studies have revealed that the concentrations of these metals in Panipat's industrial effluents frequently surpass the permissible limits set by environmental regulations. Traditional methods for heavy metal removal, including chemical precipitation and ion exchange, are widely utilized but often entail high operational costs and the generation of secondary pollutants like sludge. Biosorption, an emerging and sustainable technology, offers a promising alternative by utilizing biological materials such as algae, bacteria, and agricultural waste to adsorb heavy metals from wastewater. This study aims to investigate the effectiveness, cost-effectiveness, and environmental impact of biosorption compared to traditional methods in Panipat District. By examining heavy metal removal efficiencies, conducting cost analysis, and assessing environmental implications, this research seeks to provide valuable insights into sustainable wastewater treatment practices.

Integration of Metal‐Organic Frameworks into Hydrogels: Optimizing Their Properties and Applications

In recent years, MOFs hydrogels have attracted extensive attention due to their unique structure and excellent performance. MOF‐based hydrogels combine the highly ordered pore structure and tunability of MOF with the biocompatibility and flexibility of hydrogels, and are widely used in environmental governance, sensors, and biomedicine. In this review, we mainly summarize the synthesis methods, structural characteristics and mechanical properties of MOF‐based hydrogels, and the specific applications of MOF‐based hydrogels in different fields including adsorption of heavy metal ions and pollutant gases stress strain sensor and drug delivery. Finally, we analyze the existing problems, and provide suggestions for the development direction of MOF‐based hydrogels in the future. This paper aims to help readers quickly understand the current development of MOF‐based hydrogels.

Research on Adsorption of Heavy Metal Ions by Polysaccharide Hydrogels

AbstractIn recent years, various industrial and agricultural problems have been highlighted, and the pollution of heavy metal ions to water bodies has become a considerable serious phenomenon. Adsorption method is an efficient, low‐cost, and easy to implement method for removing heavy metal ions, which does not produce secondary pollution, and has been widely used in water treatment. Polysaccharides are natural polymers, and their hydroxyl, carboxyl, and amine groups provide feasibility for the synthesis of hydrogels with various structures. The synthesized polysaccharide hydrogel has the characteristics of high adsorption capacity, specific adsorption, nontoxic, and so on. In this review, the kinds of polysaccharide hydrogels and different synthesis methods were discussed first. Then, the adsorption mechanism and different adsorption modes of polysaccharide hydrogels were reviewed. Finally, the effects of different environmental factors on the adsorption capacity of polysaccharide hydrogel were studied. The future research on the adsorption of heavy metal ions by polysaccharide hydrogels was proposed.

A Facile Two-Step Utilization of Sorghum Waste Derived Activated Carbon

Sorghum (Sorghum bicolor (L.) Moench) is an agricultural commodity that produces waste, including stems, during its cultivation. Sorghum stems can be used as an alternative precursor for forming activated carbon (AC) with a high surface area by utilizing ZnCl2 as an activator and followed by a pyrolysis process at 750 °C under N2 gas. In this study, AC from sorghum stems was sequentially used as an adsorbent for heavy metals in wastewater, as well as applied as an anode material for lithium-ion batteries. From the characterization analysis, the synthesized AC has an amorphous structure, a high carbon content of > 90%, and a surface area of 1189 m2/g. AC was applied to adsorb 10, 50, and 100 ppm of metal cobalt (Co) at 30 °C. The adsorption isotherm and kinetics of metal Co showed an adsorption capacity of around 28.2 mg/g. The Langmuir isotherm model also describes Co adsorption and follows the pseudo-first-order equation. As for the Li-ion anode material, the ACs material is fabricated on a cylindrical battery with LiNi0.8Co0.1Mn0.1O2 as the counter cathode material. The specific discharge capacity results are 104 mAh/g at the voltage window of 2.7-4.3 V. The sequential utilization of sorghum stem-derived activated carbon can improve the product’s sustainability, and such an approach is promising to be applied in other biomass-based waste treatments.Keywords: Activated carbon, adsorption, battery, biomass, sorghum

Current Progress on Antibiotic Resistance Genes Removal by Composting in Sewage Sludge: Influencing Factors and Possible Mechanisms

Antibiotic resistance genes (ARGs) present in sewage sludge pose significant environmental and public health challenges. Composting has emerged as a promising method to mitigate these risks by reducing ARGs. This review paper evaluated the current progress in the removal of ARGs through composting, incorporating a bibliometric analysis of 228 publications from January 2010 to January 2024. This review highlights the increasing scholarly interest in this field, with a notable rise in publications since 2010. Key mechanisms identified include the denaturation of proteins and DNA at high temperatures, the adsorption of antibiotics and heavy metals by additives like biochar, and shifts in microbial communities, all contributing to the reduction of ARGs during composting. Despite these findings, challenges remain in achieving consistent ARG removal rates, addressing the potential for ARG regrowth, and understanding horizontal gene transfer post-composting. This review suggests further research into optimizing composting conditions and integrating additional treatment methods to enhance ARG removal and minimize associated risks.

Structural Characterization and Antioxidant Activity of Exopolysaccharide Produced from Beet Waste Residue by Leuconostoc pseudomesenteroides

Lactic acid bacteria exopolysaccharide (EPS) is a large molecular polymer produced during the growth and metabolism of lactic acid bacteria. EPS has multiple biological functions and is widely used in fields such as food and medicine. However, the low yield and high production cost of EPS derived from lactic acid bacteria limit its widespread application. In this study, we used beet waste residue as a substrate to produce EPS by fermentation with Leuconostoc pseudomesenteroides to improve the utilization rate of agricultural waste and reduce the production cost of lactic acid bacterial EPS. After purification, the molecular weight (Mw) of EPS was determined to be 417 kDa using high-performance size exclusion chromatography (HPSEC). High-performance liquid chromatography (HPLC), Fourier transform infrared (FTIR) spectroscopy, and nuclear magnetic resonance (NMR) spectroscopy revealed that the EPS was composed of glucose subunits with α-1,6 glycosidic linkages. The thermal analysis and heavy metal adsorption capacity revealed a relatively high degradation temperature of 315.54 °C and that the material could effectively adsorb Cu2+. Additionally, the findings indicated that the EPS exhibited a significant ability to neutralize free radicals, a property that was found to be concentration dependent. Furthermore, the results of the intracellular study showed the protective effect of freshly isolated EPS on tBHP-induced cellular oxidative stress at a concentration of 50 µg/mL. These results suggest that the EPS from L. pseudomesenteroides may be developed as antioxidant agents for functional food products and pharmaceutical applications due to its capacity to scavenge free radicals.

Experimental study on enrichment of heavy metals by modified mullite during co-combustion of lignite with eucalyptus wood

ABSTRACT Modifying the content of oxygen vacancies (OVs) has emerged as a crucial approach to tailoring silicate's adsorption properties, microstructure, conductivity, and catalytic performance. Some studies have reported the formation of OVs during ammonia treatment. However, there are limited studies on the production of OV-enriched mullite by treating it with N-containing compounds at low temperatures. In this work, formamide, urea, and ammonium acetate were used as ammonia-assisted reduction modifiers to induce oxygen vacancies in mullite at 30 ℃, 60 ℃, and 90 °C. The aim was to enhance the enrichment effect of heavy metals (Cr, Cu, Mn, Ni, Pb, Zn) during the co-combustion of coal and biomass. The modified mullite was analyzed by using X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET) surface area analysis, scanning electron microscopy (SEM), and Fourier transform infrared spectroscopy (FTIR). The results indicated that the particle size of mullite decreased, and the concentration of internal Al3+ ions and oxygen vacancies was enhanced. Coal-biomass-mullite combustion experiments were conducted in a tubular furnace at 900 °C, revealing a significant enhancement in the enrichment of heavy metals during the combustion process, particularly when the modification temperature was 60 °C using ammonium acetate as the modifier. This work holds significant importance for developing novel heavy metal adsorbents and the reduction of pollutant emissions from coal-biomass co-combustion in industrial applications.

Titanium Dioxide Nanoparticle: A Comprehensive Review on Synthesis, Applications and Toxicity

Nanotechnology has garnered significant interest worldwide due to its wide-ranging applications across various industries. Titanium dioxide nanoparticles are one type of nanoparticle that is commonly utilised in everyday use and can be synthesized by different techniques using physical, chemical and biological extracts. Green synthesis is an economical, environmentally benign and non-toxic method of synthesising nanoparticles. Titanium dioxide nanoparticles have a positive impact on plant physiology, particularly in response to biotic and abiotic stresses, depending on various factors like size, concentration, exposure of the nanoparticles and other variables. Further, titanium dioxide nanoparticles have many applications, such as being used as nano-fertilizers, adsorption of heavy metal from industrial wastewater and antimicrobial activity, as discussed in this review paper. Previous studies investigated whether titanium dioxide nanoparticles also induce genotoxicity may be due to mishandling procedure, exposure time, size, concentration and other variables. This is still contradictory and requires more research. The present review is a pragmatic approach to summarize the synthesis, application, nanotoxicity, genotoxicity and eco-friendly method of nanoparticle synthesis and disposable.

Recent Developments in the Adsorption of Heavy Metal Ions from Aqueous Solutions Using Various Nanomaterials

Water pollution is caused by heavy metals, minerals, and dyes. It has become a global environmental problem. There are numerous methods for removing different types of pollutants from wastewater. Adsorption is viewed as the most promising and financially viable option. Nanostructured materials are used as effective materials for adsorption techniques to extract metal ions from wastewater. Many types of nanomaterials, such as zero-valent metals, metal oxides, carbon nanomaterials, and magnetic nanocomposites, are used as adsorbents. Magnetic nanocomposites as adsorbents have magnetic properties and abundant active functional groups, and unique nanomaterials endow them with better properties than nonmagnetic materials (classic adsorbents). Nonmagnetic materials (classic adsorbents) typically have limitations such as limited adsorption capacity, adsorbent recovery, poor selective adsorption, and secondary treatment. Magnetic nanocomposites are easy to recover, have strong selectivity and high adsorption capacity, are safe and economical, and have always been a hotspot for research. A large amount of data has been collected in this review, which is based on an extensive study of the synthesis, characterization, and adsorption capacity for the elimination of ions from wastewater and their separation from water. The effects of several experimental parameters on metal ion removal, including contact duration, temperature, adsorbent dose, pH, starting ion concentration, and ionic strength, have also been investigated. In addition, a variety of illustrations are used to describe the various adsorption kinetics and adsorption isotherm models, providing insight into the adsorption process.

“Chacco” clay from the Peruvian highlands as a potential adsorbent of heavy metals in water

This research aimed to remove Cd (II), Cr (VI), Ni (II), Pb (II), and V (V) from aqueous solutions prepared in distilled water using “Chacco” clay from the Peruvian highlands as adsorbent. The adsorption process was carried out in Batch type systems for 120 min using solutions of each metal at a concentration of 5 mg/L in aqueous systems of a single metal or monometallic (MAS) and solutions of the five metals simultaneously or multimetallic (MMAS). For this purpose, the “Chacco” clay was first characterized by SEM-EDS analysis, finding a laminated clay structure with an elemental composition of C, Al, Fe, Na, Mg, Ca, K, As, Cu, Pd, O, and Ta. The results using 10 g/L of “Chacco” clay showed that the best adsorption efficiency in both MAS and MMAS aqueous systems is achieved at pH = 4 achieving in MAS aqueous systems the removal of 64.16 ± 0.98 % of Cd (II), 95.70 ± 0.81 % of Cr (VI), 97.20 ± 0.89 % of Ni (II), 92. 78 ± 0.79 % of Pb (II), and 95.80 ± 0.67 % of V (V), on the other hand, in aqueous MMAS systems a decrease in adsorption efficiency was observed, managing to remove 6.88 ± 0.53 % of Cd (II), 63.04 ± 0.94 of Cr (VI), 7.81 ± 0.43 % of Ni (II), 62.34 ± 0.77 % Pb (II), and 14.33 ± 0.56 % of V (V). The kinetic study showed that the adsorption mechanism would correspond to chemisorption since the process fitted best to the pseudo-second order model and Elovich. SEM-EDS analysis after adsorption confirmed the presence of the heavy metals under study in the “Chacco” clay. Metal adsorption is evidenced at 1418 cm−1 by -CH2-metal deformation vibrations according to FTIR analysis. In conclusion, the “Chacco” clay would be a promising adsorbent of heavy metals in polluted waters so that scaling up to real environments could be feasible. On the other hand, the “Chacco” clay is consumed by the population of Puno, Peru, therefore its potential impact on health should be evaluated due to its capacity to accumulate metals and the presence of Al in this clay.

Manganese-modified biochar for sediment remediation: Effect, microbial community response, and mechanism

Heavy metal sediment pollution has become an increasingly serious problem associated with industrial development, so extensive studies have been conducted concerning their removal. Biochar has recently shown good potential for in-situ remediation of heavy metal-contaminated sediments. The heavy metal adsorption capacity of inexpensive biochar can be improved by loading it with metal oxides. In this study, manganese-modified biochar (MBC) was prepared by KMnO4-modified waste-activated sludge biochar and applied to immobilize Pb and Cd in sediments. Its effects on the sediment microbial community were also investigated. The Results showed that manganese modification of the biochar made it more conducive to the adsorption of heavy metals, owing to its higher specific surface area and graphitization structure, more active sites and oxygen-containing groups, and the presence of Mn2O3 crystal structure on the surface. The maximum adsorption capacities of this material for Pb2+ and Cd2+ in solution were 176.9 mg/g and 44.0 mg/g, respectively. The application of MBC to the remediation of heavy metal-contaminated sediments transformed Pb and Cd in the sediments from exchangeable to residual state. The F4 content of Pb in the sediments increased from 40.52%-42.36% to 49.11%–51.14% after application of 1% MBC, and to 63.94%–64.49% after application of 5% MBC. Correspondingly, the F1 content of Pb in the sediments decreased from 29.09%-30.68% to 17.43%–17.69% after the application of 5% MBC. Furthermore, MBC efficiently enriched the microbial biodiversity and affected the microbial population structure within 60 days. The relative abundance of uncultured f Symbiobacteraceae and Fonticella communities significantly increased after incubation. The results may provide empirical support for the combination of metal oxides and biochar for the remediation of heavy metal-contaminated sediments.

Sustainable polyelectrolyte complexes of pectin and chitosan as adsorbents for heavy metal ions from surface water

Sustainable polyelectrolyte complexes of pectin and chitosan as adsorbents for heavy metal ions from surface water

Agro-waste based biomass residues valorization for effective adsorption of heavy metal.

In this experiment four agro-waste based biomass residues (soybean stover-SSb, buckwheat stover-BWb, Artemisia vulgaris- AVb and Chromolaena odorata-COb) was valorized into low cost amendment called biochar followed by compositional characterization for their application in heavy metal removal. Investigation was carried out on the removal of the most common heavy metal ions including arsenic, cadmium, lead, nickel, zinc, and copper through adsorption on four types of biomass valorised biochar. According to preliminary testing, all the biochar was effective to eliminate a mixture of six heavy metals from the aqueous phase, with the removal of arsenic being the most removed and nickel being the least. In comparison to no biochar treatment, the average removal rate of heavy metal from aqueous solution using four distinct types of biochar was 45.75-62.42% (Cd), 43.64-56.33% (Pb), 41.85-59.73% (Ni), 42.87-60.28% (Zn), 45.64-59.51% (Cu), and 49.02-60.53% (As). The percent decrease of cadmium heavy metal adsorption with increase in maximum contaminant level (MCL) from 1- to fivefold was 20.0 (SSb), 20.7 (COb), 21.6 (BWb), and 22.9 (AVb). The results of the dosage study indicated that As adsorption was the most beneficial on all four types of biochar, whereas Ni adsorption was the least effective. With increase in application rate of biochar the heavy metals adsorption (%) was also increased. Four different agro-waste valorized biochar were used to treat the wastewater, and the physical and chemical changes that occurred both before and after the biochar treatment were noted. There was a drop in the wastewater CODT, CODD, TSS, ammonia, TKN, TP and pH values of 79.7-103.5%, 57.7-81.5, 52.3-68.4%, 1.23-2.23%, 14.1-20.6%, and 1.23-3.03%, respectively. Furthermore, after being passed through a biochar, the wastewater's Zn, Pb, Cd, As, Cr and Cu levels decreased by 3.26-6.15%, 0.06-0.34%, 0.01-0.08%, 2.37-3.65%, 3.95-5.53%, and 2.24-3.34%, respectively at 2.5 and 5.0g/litre of wastewater. Thus, in order to comply with regulations for the disposal of wastewater effluent, the process of valorizing biomass into biochar offered enormous potential for the removal of heavy metals in addition to wastewater treatment.

Heavy Metal Removal from Water Using Graphene Oxide in Magnetic-Assisted Adsorption Systems: Characterization, Adsorption Properties, and Modelling

This study investigated the adsorption properties of graphene oxide in a magnetic-assisted adsorber for the depollution of water containing heavy metals. Two samples of graphene oxide with different surface chemistry were synthetized and assessed using the magnetic-assisted adsorption systems. One graphene oxide sample exhibited a dual magnetic behavior presenting both diamagnetic and ferromagnetic phases, while the other graphene oxide was diamagnetic. The adsorption properties of these graphene oxide samples for removing Pb2+ and Cu2+ were tested and compared with and without a magnetic field exposure. The results showed that the Pb2+ removal increased using both graphene oxide samples in the magnetic-assisted configuration, while Cu2+ adsorption was less sensitive to the application of the magnetic field. A monolayer model was used to simulate all the heavy metal adsorption isotherms quantified experimentally. It was concluded that the adsorption mechanism designed to remove Pb2+ and Cu2+ using tested graphene oxide samples was mainly multi-ionic where two metallic cations could interact with one active site (i.e., oxygenated functional groups) from the adsorbent surface. The oxygenated surface functionalities of graphene oxide samples played a relevant role in determining the impact of magnetic field exposure on the heavy metal removal efficacy. Magnetic-assisted adsorption using graphene oxide is an interesting alternative to reduce the concentration of Pb2+ in polluted effluents, and it can also be applied to improve the performance of adsorbents with a limited concentration of oxygenated functional groups, which usually show poor removal of challenging water pollutants such as toxic heavy metals.

Flexible MOF@fabrics composites: The in-situ growth of metal-organic frameworks on cotton and selectively adsorption of gold(III) from aqueous solution

Metal-organic frameworks (MOFs) show great potential applications in dealing with heavy metal pollution due to their unique large specific surface area, tunable pore size, and diverse active groups. However, the powder form of MOFs has suffered from the disadvantages of difficult recycling and secondary contamination after adsorption of heavy metals, which seriously limits their practical application. Therefore, in this work, we prepared a series of bifunctional zirconium-based MOFs cotton fabric composites (MCFC) via in situ growth of MOFs on carboxylated cotton fabric, exhibiting large specific surface area, adjustable pore size, and effective adsorption ability. The prepared CF-UiO-66-(OH)2-FA shows an excellent adsorption efficiency of Au(III) more than 99.990 %, and the saturated adsorption amount is up to 190.98 mg·g−1 at 25 °C. Meanwhile, the kinetic experiment analysis demonstrated that the Au(III) adsorption behavior of MCFC follows pseudo-second-order (PSO) kinetic model. More importantly, it also exhibits great selectivity in adsorbing Au(III) from the mixture of multiple metal ions coexisted solution. The results of adsorption thermodynamics and adsorption isotherms indicate that adsorption is monolayer and a spontaneous, exothermic process. And the ideal adsorption and separation process could be finished by quickly filtrating with a single or multi-layer MCFC. Excellent adsorption performance even after four cycles of adsorption. Therefore, the fabricated MCFC shows great processability, flexibility, collectability and reusability in adsorbing and recycling precious metal ion from wastewater.

Sight of Aged Microplastics Adsorbing Heavy Metal Exacerbated Intestinal Injury: A Mechanistic Study of Autophagy-Mediated Toxicity Response.

Contaminant-bearing polystyrene microplastics (PSMPs) may exert significantly different toxicity profiles from their contaminant-free counterparts, with the role of PSMPs in promoting contaminant uptake being recognized. However, studies investigating the environmentally relevant exposure and toxic mechanisms of aged PSMPs binding to Cr are limited. Here, we show that loading of chromium (Cr) markedly alters the physicochemical properties and toxicological profiles of aged PSMPs. Specifically, Cr-bearing aged PSMPs induced severe body weight loss, oxidative stress (OS), autophagy, intestinal barrier injury, inflammation-pyroptosis response, and enteropathogen invasion in mice. Mechanistic investigations revealed that PSMPs@Cr exacerbated the OS, resulting in intestinal barrier damage and inflammation-pyroptosis response via overactivated Notch signaling and autophagy/cathepsin B/IL-1β pathway, respectively, which ultimately elevated mortality related to bacterial pathogen infection. In vitro experiments confirmed that autophagy-mediated reactive oxygen species (ROS) overproduction resulted in severe pyroptosis and impaired intestinal stem cells differentiation alongside the overactivation of Notch signaling in PSMPs@Cr-exposed organoids. Overall, our findings provide an insight into autophagy-modulated ROS overproduction within the acidic environment of autophagosomes, accelerating the release of free Cr from PSMPs@Cr and inducing secondary OS, revealing that PSMPs@Cr is a stable hazard material that induces intestinal injury. These findings provided a potential therapeutic target for environmental MPs pollution caused intestinal disease in patients.

ENVIRONMENTAL ASPECTS OF WASTE-DERIVED BOTTOM BLEND CLAY LINERS INCORPORATING ZEOLITE AND BENTONITE

This research investigated the effects of incorporating bentonite and zeolite into bottom blended clay liners (BBCLs) on their engineering properties and adsorption capacity. BBCLs composed of clay, water treatment residue, and calcium carbide in a 40:40:20 ratio by volume were investigated with the addition of 1, 2, and 3 wt.% bentonite or zeolite. The experimental results indicated that bentonite and zeolite had positive effects on the slake durability index and the equilibrium time for the adsorption of lead (Pb) and chromium (Cr) from the leachate, whereas the unconfined compressive strength (UCS) and coefficient of permeability were negatively affected compared to those of the samples without bentonite and zeolite. At 56 days, the UCS of BBCLs with bentonite and zeolite decreased from 3.4 to 2.2MPa, while the coefficient of permeability of all the samples met the regulatory limit of sanitary landfills, which was given at 1×10-7cm/s. The slake durability index of all samples was lower 50% but it remained higher compared to BBCLs without bentonite and zeolite (approximately doubled). Both additives enhanced the equilibrium time and percentage of Pb and Cr adsorption by about 20% and 200%, respectively. SEM-EDS results show the adsorption of Pb and Cr onto the raw materials, calcium silicate hydrate (CSH), zeolite, and bentonite. Therefore, the addition of zeolite can increase the ability to adsorb heavy metals form leachate, which is suitable for use in secured landfills.