Phosphate adsorption on dried alum sludge: Modeling and application to treatment of dairy effluents.

This study evaluates Alum sludge from drinking water treatment plants for the efficient and cost-effective removal of phosphates from aqueous solutions. Extensive characterization and batch experiments have established that optimal phosphate removal was achieved with a sludge dosage of 20 g L-1 (at an initial phosphate concentration of 100 mg L-1), a pH of 5, a temperature of 23 °C, and a stirring speed of 200 rpm. These conditions significantly reduced phosphate levels, ensuring compliance with legal discharge limits. The Langmuir isotherm, pseudo-second-order kinetic and intraparticle diffusion models best described the adsorption process, highlighting the spontaneous and endothermic nature of the phenomenon. The sludge effectively reduced phosphate concentrations to acceptable levels when applied to dairy effluents. This study underscores the potential of Alum sludge as a viable solution for phosphate management in environmental cleanup efforts.

An overview on the key advantages and limitations of batch and dynamic modes of biosorption of metal ions.

Water purification using adsorption is a crucial process for maintaining human life and preserving the environment. Batch and dynamic adsorption modes are two types of water purification processes that are commonly used in various countries due to their simplicity and feasibility on an industrial scale. However, it is important to understand the advantages and limitations of these two adsorption modes in industrial applications. Also, the possibility of using batch mode in industrial scale was scrutinized, along with the necessity of using dynamic mode in such applications. In addition, the reasons for the necessity of performing batch adsorption studies before starting the treatment on an industrial scale were mentioned and discussed. In fact, this review article attempts to throw light on these subjects by comparing the biosorption efficiency of some metals on utilized biosorbents, using both batch and fixed-bed (column) adsorption modes. The comparison is based on the effectiveness of the two processes and the mechanisms involved in the treatment. Parameters such as biosorption capacity, percentage removal, and isotherm models for both batch and column (fixed bed) studies are compared. The article also explains thermodynamic and kinetic models for batch adsorption and discusses breakthrough evaluations in adsorptive column systems. The review highlights the benefits of using convenient batch-wise biosorption in lab-scale studies and the key advantages of column biosorption in industrial applications.

Production of biochar from Melia azedarach seeds for the crystal violet dye removal from water: combining of hydrothermal carbonization and pyrolysis.

Biochar has shown large potential in water treatment because of its low cost, good textural properties, and high reusability. In this study, two porous biochars were developed from the Melia azedarach seeds via direct pyrolysis process (B-700) and through hydrothermal carbonization followed with pyrolysis (HB-700). They were characterized by morphology, structural characteristics, and surface features and used to adsorb the crystal violet (CV) dye in water environment. Results of the isotherm approaches demonstrated that the removal capacity of these biochars reached 119.4 mg/g for B-700, and 209 mg/g for HB-700 (at 45°C). Also, the Avrami model best fitted the kinetic data. The electrostatic attraction was regarded as one of the adsorptions mechanisms of CV dye. The regeneration tests reveal that both B-700 and HB-700 are good reusable adsorbents. Finally, findings of the study showed that the hydrothermal carbonization method that precede the pyrolysis process can improve significantly the adsorption capacity of the produced biochar.

Use of Chrysosporium/carbon nanotubes for preconcentration of ultra-trace cadmium levels from various samples after extensive studies on its adsorption properties.

Carbon nanotubes were used to immobilize Chrysosporium fungus for building an adequate adsorbent to be used as an desirable sorbent for preconcentration and measurement of cadmium ultra-trace levels in various samples. After characterization, the potential of Chrysosporium/carbon nanotubes for the sorption of Cd(II) ions was scrutinized by the aid of central composite design, and comprehensive studies of sorption equilibrium, kinetics and thermodynamic aspects were accomplished. Then, the composite was utilized for preconcentration of ultra-trace cadmium levels, by a mini-column packed with Chrysosporium/carbon nanotubes, before its determination with ICP-OES. The outcomes vouchsafed that (i) Chrysosporium/carbon nanotube has a high tendency for selective and rapid sorption of cadmium ion, at pH 6.1, and (ii) kinetic, equilibrium, and thermodynamic studies showed a high affinity of the Chrysosporium/carbon nanotubes for cadmium ion. Also, the outcomes displayed that cadmium can quantitatively be sorbed at a flow speed lesser than 7.0 mL/min and a 1.0 M HCl solution (3.0 mL) was sufficient to desorbe the analyte. Eventually, preconcentration and measurement of Cd(II) in different foods and waters were successfully accomplished with good accuracy, high precision (RSDs ≤5.65%), and low limit of detection (0.015 µg/L).

Polydopamine-modification of a magnetic composite constructed from citric acid-cross-linked cyclodextrin and graphene oxide for dye removal from waters.

The effect of polydopamine (PDA) modification on aminated Fe3O4 nanoparticles (Fe3O4-NH2)/graphite oxide (GO)/ß-cyclodextrin polymer cross-linked by citric acid (CDP-CA) composites were studied for the removal of a cationic dye (methylene blue, MB) and an anionic dye (Congo red, CR) from waters. The micro-structural and magnetic characterizations confirmed the successful preparation of Fe3O4-NH2/GO/CDP-CA and PDA/Fe3O4-NH2/GO/CDP-CA composites. The maximum MB and CR adsorption capacities of Fe3O4-NH2/GO/CDP-CA were 75 mg/g and 104 mg/g, respectively, while the corresponding amounts for PDA/Fe3O4-NH2/GO/CDP-CA composite were 195 mg/g and 64 mg/g, respectively. The dye sorption behaviors of these two composites were explained by their corresponding surface-charged properties according to the measured zeta potential results. Moreover, the high saturation magnetizations and the stable dye removal rate in the adsorption-desorption cycles indicated the good recyclability and reusability of the fabricated composites.

Adsorptive removal of acid blue dye 113 using three agricultural waste biomasses: The possibility of valorization by activation and carbonization - A comparative analysis.

The presence of various organic and inorganic contaminants in wastewater leads to serious health effects on humans and ecosystems. Industrial effluents have been considered as noticeable sources of contaminating water streams. These effluents directly liberate the pollutants such as dye molecules and heavy metal ions into the environment. In the present study, three biowaste materials (groundnut shell powder, coconut coir powder and activated corn leaf carbon) were utilized and compared for the removal of acid blue dye 113 from aqueous solutions. The characterization study of newly prepared sorbent material (H3PO4-activated corn leaf carbon) and the other utilized sorbents was carried out by Scanning Electron Microscope (SEM) and Fourier Transform Infrared Spectrophotometer (FTIR), along with Energy Dispersive X-Ray (EDX) Analysis. The influence of experimental conditions such as pH, initial dye concentration, temperature, contact time, and sorbent dosage on the removal efficiency of the dye were appraised. The adsorption isotherm and kinetic result of acid blue dye 113 adsorption onto the sorbents best obeyed from Sips and pseudo-second-order kinetic model. Overall, the outcomes confirmed that the newly synthesized sorbent material (carbonized H3PO4-activated corn leaf) has superior adsorption capacity, rapid adsorption, and higher suitability for the removal of toxic dyes from the contaminated waters.

Agricultural waste biomass for sustainable bioenergy production: Feedstock, characterization and pre-treatment methodologies.

The worldwide trend in energy production is moving toward circular economy systems and sustainable availability of sources. Some advanced methods support the economic development of energy production by the utilization of waste biomass, while limiting ecological effects. The use of agro waste biomass is viewed as a major alternative energy source that expressively lowers greenhouse gas emissions. Agricultural residues produced as wastes after each step of agricultural production are used as sustainable biomass assets for bioenergy production. Nevertheless, agro waste biomass needs to go through a few cyclic changes, among which biomass pre-treatment contributes to the removal of lignin and has a significant role in the efficiency and yield of bioenergy production. As a result of rapid innovation in the utilization of agro waste for biomass-derived bioenergy, a comprehensive overview of the thrilling highlights and necessary advancements, in addition to a detailed analysis of feedstock, characterization, bioconversion, and contemporary pre-treatment procedures, appear to be vital. To this end, the current status in the generation of bioenergy from agro biomass through various pre-treatment procedures was examined in this study, along with presenting relevant challenges and a perspective for future investigations.

Graphene-based materials for effective adsorption of organic and inorganic pollutants: A critical and comprehensive review.

Water scarcity has been felt in many countries and will become a critical issue in the coming years. The release of toxic organic and inorganic contaminants from different anthropogenic activities, like mining, agriculture, industries, and domestic households, enters the natural waterbody and pollutes them. Keeping this in view in combating the environmental crises, removing pollutants from wastewater is one of the ongoing environmental challenges. Adsorption technology is an economical, fast, and efficient physicochemical method for removing both organic and inorganic pollutants, even at low concentrations. In the last decade, graphene and its composite materials have become the center of attraction for numerous applications, including wastewater treatment, due to the large surface area, highly active surface, and exclusive physicochemical properties, which make them potential adsorbents with unique physicochemical properties, like low density, chemical strength, structural variability, and the possibility of large-scale fabrications. This review article provides a thorough summary/critical appraisal of the published literature on graphene-, GO-, and rGO-based adsorbents for the removal of organic and inorganic pollutants from wastewater. The synthesis methods, experimental parameters, adsorption behaviors, isotherms, kinetics, thermodynamics, mechanisms, and the performance of the regeneration-desorption processes of these substances are scrutinized. Finally, the research challenges, limitations, and future research studies are also discussed. Certainly, this review article will benefit the research community by getting substantial information on suitable techniques for synthesizing such adsorbents and utilizing them in water treatment and designing water treatment systems.

Recruiting chemical grafting method for surface modification of stainless steel to fabricate a selective sorbent for solid phase microextraction of mercury metal ion.

Keeping selectiveness and efficiency in view with solid-phase microextraction (SPME) of metal ions, this work was aimed at synthesis of a novel modified sorbent on a stainless-steel surface to fabricate a selective and efficient fiber for SPME of mercury ions from real food and biological samples. After the confirmation of sorbent structure grafted on the stainless-steel surface, by different techniques, the synthesized fiber was utilized for extraction and preconcentration of mercury before its measurement by an inductively coupled plasma-optical emission spectroscopy (ICP-OES). For optimizing the efficiency, the influences of various factors on the extraction of Hg (II) ion were scrutinized. The optimized values used for extraction were pH 7.0, adsorption time 8 min, desorption time 5 min, 5 mL of eluent solvent containing nitric acid with concentration of 0.5 mol L-1, and stirring rate of 300 rpm. Underneath optimum condition, the relative standard deviation for 30 extractions, done by one synthesized fiber, was calculated to be 2.89% and for five extractions, done by 5 synthesized fibers, was calculated to be 1.78%. The high performance of the synthesized fiber was checked with high recoveries obtained from 30 successive sorption-desorption cycles, using a unique synthesized fiber. Finally, the suggested procedure was triumphally exploited for extraction and pre-concentration of Hg (II) ion in real food and biological samples.

Adsorption performance of Enterobacter cloacae towards U(VI) ion and application of Enterobacter cloacae/carbon nanotubes to preconcentration and determination of low-levels of U(VI) in water samples.

Keeping the high potential of some microorganisms in adsorption of radionuclides in view, the adsorption properties of Enterobacter cloacae towards uranium were attentively scrutinized, and then it was used for preconcentration of uranium in different samples, using Enterobacter cloacae/carbon nanotube composite. First, using ultrasonic agitation, the effects of operational factors on biosorption of uranium on the inactive Enterobacter cloacae were appraised and modeled by central composite design, and a comprehensive study was performed on the equilibrium, kinetics, thermodynamic, and selectivity aspects of biosorption. The optimization studies along with the evaluations of the adsorption properties revealed that Enterobacter cloacae have a high affinity for fast and selective biosorption of uranium ions, at pH 5.1. Second, the Enterobacter cloacae/carbon nanotube was synthesized, characterized, and utilized for preconcentration of uranium in different samples, using a mini-column packed with the composite. The optimization of operational factors on recovery of uranium, using the central composite design, showed that uranium can be quantitively adsorbed at a sample flow rate lower than 4.5 mL min-1 and the desorption could be accomplished with 3.0 mL HCl 0.6 M solution. Finally, the mini-column was exploited for preconcentration and determination of uranium in different samples. The results revealed the low detection limit (0.015 µg.L-1), high precision (RSDs ≤3.92%), and good accuracy of the proposed procedure.

Ecofriendly biopolymers and composites: Preparation and their applications in water-treatment.

Over the past few decades, the term polymer has been repeatedly used in several industries for their immense characteristics in different applications. Polymers and their composites which were prepared from chemical monomer sources turned out to be potentially harmful to the environment due to their tedious degradation process. Biopolymers are natural substitutes for synthetic polymers which can be efficiently extricated from natural sources. They are predominantly available as polymeric units as well as monomeric units that are linked covalently. These environment-friendly biopolymers and their composites can be categorized based on their numerous sources, different methods of preparation and their potential form of usage. They were found to be biocompatible and biodegradable which make them exceptionally useful in environment based applications, mainly in the process of water treatment, both potable and wastewater. Further, the biopolymer and biopolymer composites easily fit into different parts of the treatment process by acting as filtration media, adsorbents, coagulants and as flocculants. The primary focus of this review is to provide a comprehensive information of biopolymers and biopolymer composites from synthesis to their usefulness for their productive application in water treatment processes. On the whole, it can be substantiated that the biopolymers were identified to play a notable adversary to the synthetic polymers in treating waters with an indispensable need for an elaborative study in the production of the biopolymers.

Acenaphthene adsorption onto ultrasonic assisted fatty acid mediated porous activated carbon-characterization, isotherm and kinetic studies.

Adsorbents originated from biological materials play a vital role in the remediation of diverse toxic pollutants due to their high efficacy, low cost and being environmentally friendly. The present study focusses on the palm shell activated carbon obtained from agricultural waste precursor (palm shell) with the aid of oleic acid activation along with ultrasonic assistance and its effective utilization for acenaphthene adsorption from aqueous and real effluent. The synthesized Ultrasonic assisted palm shell activated carbon (UAC) possessed high surface area of 506.84 m2/g and distinct porous structure as depicted by SEM analysis. The outcomes of zero discharge analyses and acenaphthene adsorption results vouchsafed that, using oleic acid as an effective catalyst, is explicitly advantageous to combine with ultrasonic assistance to fabricate a highly efficient adsorbent for acenaphthene removal from aqueous solution. The UAC obtained at the selected parameters levels, such as temperature of 45 °C and ultrasonic time of 40 min, has the adsorption capacity of 52.745 mg/g. Sips isotherm model computed from the experimental data gave the best fit among the examined isotherm models. To complete the study of adsorption properties of UAC towards acenaphthene, kinetic modeling and thermodynamic aspects of the adsorption process were also scrutinized. The kinetic studies proved that pseudo-second order model is compatible with the experimental data and thermodynamic results revealed that the adsorption process is of endothermic nature. Overall, ultrasonic-assisted preparation of activated carbon from palm shell actuated using Oleic acid was found to be a highly efficient adsorbent which was suitable for acenaphthene removal from aqueous solution.

Effect of Mg2+ ions on competitive metal ions adsorption/desorption on magnesium ferrite: Mechanism, reusability and stability studies.

The adsorption behavior of magnesium ferrite in single- and multicomponent metal ions solutions in the presence of Mg2+ ions were studied. A dramatic decrease in the adsorption capacity of magnesium ferrite towards Mn2+, Co2+, and Ni2+ ions for comparison study of single- and multicomponent solutions was established. The affinity of the sorbent in accordance with the maximum sorption capacities increases in the following order Cu2+ > Co2+ > Ni2+ > Mn2+. High efficiency of magnesium ferrite regeneration (~100%) with aqueous solutions of magnesium chloride in the concentration range of 0.001-0.1 M was shown. The low degree of toxic metal ions desorption combined with XRD, IR spectroscopy, and EDX analysis data indicate the key role of Mg2+ ion adsorption in the magnesium ferrite adsorbent regeneration. The positive effect of the introduction of Mg2+ ions into multicomponent solutions on metal ions adsorption was established, which is accompanied by an increase in the maximum sorption capacity for all metal ions and especially significant increase in the selectivity towards Cu2+ ions (2.41 mmol/g). The stability of the crystal structure of magnesium ferrite and a low degree of Mg2+ and Fe3+ ions leaching during multiple cycles of adsorption and regeneration of the adsorbent were observed.

Use of NH4Cl for activation of carbon xerogel to prepare a novel efficacious adsorbent for benzene removal from contaminated air streams in a fixed-bed column.

BACKGROUND: Ammonium chloride as an explosive salt has proved to be a prominent activation agent for adsorbents and increase the specific surface area and volume of cavities. In this work, the ability of this substance was scrutinized for activation of carbon aerogel to prepare an efficient adsorbent for benzene removal from air streams. METHODS: A carbon xerogel was fabricated from Novallac polymer and activated by ammonium chloride.The changes in structure and morphology were considered via Brunauer-Emmett-Teller (BET), scanning electron microscopy (SEM), Fourier transform infrared (FTIR), Barrett-Joyner-Halenda (BJH), and energy dispersive X-ray (EDX) analyses. Also, comprehensive studies were conducted to vouchsafe the properties of the new adsorbent for benzene removal, using a fixed-bed column mode. RESULTS: The results showed both the successful synthesis and the suitability of the activation process. ACX possessed a higher specific surface area (1008 g/m3), compared to the parent carbon xerogel (CX; 543.7 g/m3) and organic xerogel (OX; 47 g/m3), as well as a higher adsorption capacity. CONCLUSION: NH4CL is a very beneficial for modifying the structure and morphology of carbon aerogel, and the dynamic behavior of the column with respect inlet benzene concentration can be explained by Yan-Nelson model.

Sorption and mechanism studies of Cu2+, Sr2+ and Pb2+ ions on mesoporous aluminosilicates/zeolite composite sorbents.

The research aimed to develop a novel mesoporous aluminosilicate/zeolite composite by the template co-precipitation method. The effect of aluminosilicate (AlSi) and zeolite (NaY) on the basic properties and adsorption capacity of the resultant composite was conducted at different mass ratios of AlSi/NaY (i.e., 5/90, 10/80, 15/85, 20/80, and 50/50). The adsorption characteristics of such composite and its feedstock materials (i.e., aluminosilicates and zeolite) towards radioactive Sr2+ ions and toxic metals (Cu2+ and Pb2+ ions) in aqueous solutions were investigated. Results indicated that BET surface area (SBET), total pore volume (VTotal), and mesopore volume (VMeso) of prepared materials followed the decreasing order: aluminosilicate (890 m2/g, 0.680 cm3/g, and 0.644 cm3/g) > zeolite (623 m2/g, 0.352 cm3/g, and 0.111 cm3/g) > AlSi/NaY (20/80) composite (370 m2/g, 0.254 cm3/g, and 0.154 cm3/g, respectively). The Langmuir maximum adsorption capacity (Qm) of metal ions (Sr2+, Cu2+, and Pb2+) in single-component solution was 260 mg/g, 220 mg/g, and 161 mg/g (for zeolite), 153 mg/g, 37.9 mg/g, and 66.5 mg/g (for aluminosilicate), and 186 mg/g, 140 mg/g, and 77.8 mg/g for (AlSi/NaY (20/80) composite), respectively. Ion exchange was regarded as a domain adsorption mechanism of metal ions in solution by zeolite; meanwhile, inner-surface complexation was domain one for aluminosilicate. Ion exchange and inner-surface complexation might be mainly responsible for adsorbing metal ions onto the AlSi/NaY composite. Pore-filling mechanism was a less important contributor during the adsorption process. The results of competitive adsorption under binary-components (Cu2+ and Sr2+) and ternary-components (Cu2+, Pb2+, and Sr2) demonstrated that the removal efficacy of target metals by the aluminosilicate, zeolite, and their composite remarkably decreased. The synthesized AlSi/NaY composite might serve as a promising adsorbent for real water treatment.

Effective Adsorptive Removal of Methylene Blue from Water by Didodecyldimethylammonium Bromide-Modified Brown Clay.

In the present investigation, brown clay (BC) was modified with didodecyldimethylammonium bromide (DDAB) to produce a sorbent (DDAB-BC), which was characterized and applied for sorption of methylene blue (MB) from aqueous media. BC was functionalized using DDAB by cation exchange of the DDAB moiety with positive ions existing inside the interlayer spaces of the BC. X-ray diffraction (XRD) studies confirmed that the d-spacing of DDAB-BC became wider (3.39 Å) than that of BC (3.33 Å). Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM) were exploited to explore the functional groups and morphological structure of sorbents, respectively. The Brunauer-Emmett-Teller (BET) surface area, pore volume, and pore diameter of DDAB-BC were determined as 124.6841 m2/g, 0.316780 cm3/g, and 8.75102 nm, respectively. Batch sorption investigations were carried out to determine the optimum experimental conditions, using the one-factor one-time procedure. The sorption of MB on DDAB-BC strongly obeyed the Langmuir isotherm and agreed well with pseudo-second-order kinetics. Sorption of MB onto DDAB-BC showed maximum efficiency (∼98%) and maximum sorption capacity (∼164 mg/g) at optimal values of pertinent factors: dye concentration (100 mg/L), pH (7), and temperature (55 °C). Sorption isothermal studies predicted that removal of MB on DDAB-BC follows multilayer sorption at higher MB dye concentrations and monolayer sorption at lower MB dye concentrations.

Application of Fusarium sp. immobilized on multi-walled carbon nanotubes for solid-phase extraction and trace analysis of heavy metal cations.

In the present work, for the first time, the filamentous fungus Fusarium sp. was utilized for devising a novel method for pre-concentration and determination of trace amounts of Pb(II), Cu(II), Cd(II), and Zn(II) ions, using a mini-column packed with Fusarium-coated multi-walled carbon nanotubes and inductively coupled plasma-optical emission spectrometry. Optimal analytical conditions including pH, ionic strength, elution solution, sample and eluent flow rates, and sample volume were determined. The detection limits were 0.39, 0.060, 0.021, and 0.025 ng mL-1 for Pb(II), Cu(II), Cd(II), and Zn(II) cations, respectively. This new method demonstrated a high performance for the analytes, and their adsorption was not affected by the different co-existing ions. The present procedure was validated by the analysis of standard reference materials, since the obtained data were in close agreement with reference values. Finally, this new procedure was successfully applied to analysis of heavy metal cations in natural food and water samples.

Use of chicken feather and eggshell to synthesize a novel magnetized activated carbon for sorption of heavy metal ions.

Keeping environment and sustainability concept in view with preparation of new sorbents, two waste by-products from the poultry industry, i.e. feather and eggshell, were used for synthesis of a new magnetic activated carbon for sorption of heavy metal ions. Using response surface methodology based central composite design (RSM-CCD) technique, chicken feather and acid-digested eggshell were used as precursor and activation material, respectively, for the synthesis of the herein studied activated carbon (eggshell activated chicken feather carbon; ESCFC). The prepared activated carbon was magnetized for easy separation from water media, and iron oxide magnetized ESCFC (IOM-ESCFC) was comprehensively examined for removing some heavy metallic ions (Pb2+, Cd2+, Cu2+, Zn2+, and Ni2+) from water. The maximum mono-layer sorption capacities and the highness of sorption speed, along with thermodynamic studies, demonstrated that IOM-ESCFC can be regarded as a potential adsorbent against heavy metal ions from waters and wastewaters.

Metal Organic Frameworks as Desulfurization Adsorbents of DBT and 4,6-DMDBT from Fuels.

Ultradeep desulfurization of fuels is a method of enormous demand due to the generation of harmful compounds during the burning of sulfur-containing fuels, which are a major source of environmental pollution. Among the various desulfurization methods in application, adsorptive desulfurization (ADS) has low energy demand and is feasible to be employed at ambient conditions without the addition of chemicals. The most crucial factor for ADS application is the selection of the adsorbent, and, currently, a new family of porous materials, metal organic frameworks (MOFs), has proved to be very effective towards this direction. In the current review, applications of MOFs and their functionalized composites for ADS are presented and discussed, as well as the main desulfurization mechanisms reported for the removal of thiophenic compounds by various frameworks. Prospective methods regarding the further improvement of MOF's desulfurization capability are also suggested.

A novel route for preparation of chemically activated carbon from pistachio wood for highly efficient Pb(II) sorption.

Pistachio wood-derived activated carbon prepared by a two-stage process (PWAC-2), conducting two consecutive chemical activation processes with NH4NO3 and NaOH, respectively. The results showed that explosive characteristic of NH4NO3 can primarily be employed to produce a char, with a large surface area and a highly-ordered pore structure, which can be subjected to a second activation process with NaOH to prepare a more suitable activated carbon, with a highly porous structure and useful functional groups, for removal of lead ions from aqueous media. An L25 Taguchi experimental design was used by varying impregnation ratio, activation time and temperature in both pre- and post-activation stages, and the results showed that, in both stages, a small activating agent/precursor and a proportional low activation time suffice for preparation of an advantageous activated carbon for Pb(II) adsorption. A comprehensive study was performed on the equilibrium, kinetic and thermodynamic aspects of Pb(II) adsorption by the new activated carbon. The results exhibited that, having had a high lead adsorption capacity (190.2 mg g-1), a high adsorption rapidness, and thermodynamic favorability, PWAC-2 is a beneficial alternative for utilization in full-scale plants of lead removal from waters and wastewaters.