Acid insoluble lignin material production by chemical activation of olive endocarps for an efficient furfural adsorption-removal from aqueous solutions.

The present work describes a protocol of chemical activation, with acid catalyst, of olive endocarps to obtain acid insoluble lignin-rich materials with high capacities for the adsorption of furfural present in aqueous media. During biomass activation, factors such as acid concentration, reaction time and temperature, solid/liquid ratio and the presence of water extractives strongly affected both the surface characteristics of the treated bioadsorbents and their capacities for furfural retention (percentage increase close to 600% with respect to the crude biomass). Once a treated solid with good adsorbent properties was obtained, the optimal conditions for adsorption were found: stirring speed 80 rpm, temperature 303 K and adsorbent load 7.5 g solid/50 cm3. Kinetic study indicated the pseudo-second order model provided the best fit of the experimental data. At 303 K, the equilibrium adsorption capacities values ranged from 2.27 mg g-1 to 29.29 mg g-1, for initial furfural concentrations between 0.49 g dm-3 and 12.88 g dm-3. Freundlich model presented the best isotherm (R2 = 0.996 and SE = 4.7%) providing KF and n values of 0.115 (mg g-1) (mg dm-3)-n and 0.610, respectively. Since physical interactions predominate in the adsorption of furfural on chemically activated olive endocarps, the furfural removal process could have occurred reversibly on the heterogeneous surface of the bioadsorbents.

Tetracycline adsorption/desorption by raw and activated Tunisian clays.

Clay-based adsorbents have applications in environmental remediation, particularly in the removal of emerging pollutants such as antibiotics. Taking that into account, we studied the adsorption/desorption process of tetracycline (TC) using three raw and acid- or base-activated clays (AM, HJ1 and HJ2) collected, respectively, from Aleg (Mazzouna), El Haria (Jebess, Maknessy), and Chouabine (Jebess, Maknessy) formations, located in the Maknessy-Mazzouna basin, center-western of Tunisia. The main physicochemical properties of the clays were determined using standard procedures, where the studied clays presented a basic pH (8.39-9.08) and a high electrical conductivity (446-495 dS m-1). Their organic matter contents were also high (14-20%), as well as the values of the effective cation exchange capacity (80.65-97.45 cmolckg-1). In the exchange complex, the predominant cations were Na and Ca, in the case of clays HJ1 and AM, while Mg and Ca were dominant in the HJ2 clay. The sorption experimental setup consisted in performing batch tests, using 0.5 g of each clay sample, adding the selected TC concentrations, then carrying out quantification of the antibiotic by means of HPL-UV equipment. Raw clays showed high adsorption potential for TC (close to 100%) and very low desorption (generally less than 5%). This high adsorption capacity was also present in the clays after being activated with acid or base, allowing them to adsorb TC in a rather irreversible way for a wide range of pH (3.3-10) and electrical conductivity values (3.03-495 dS m-1). Adsorption experimental data were studied as regards their fitting to the Freundlich, Langmuir, Linear and Sips isotherms, being the Sips model the most appropriate to explain the adsorption of TC in these clays (natural or activated). These results could help to improve the overall knowledge on the application of new low-cost methods, using clay based adsorbents, to reduce risks due to emerging pollutants (and specifically TC) affecting the environment.

Highly sensitive detection of environmental toxic fenitrothion in fruits and water using a porous graphene oxide nanosheets based disposable sensor.

Monitoring fenitrothion (FNT) residues in food and the environment is crucial due to its high environmental toxicity. In this study, we developed a sensitive, reliable electrochemical method for detecting FNT by using screen-printed carbon electrodes (SPCE) modified with porous graphene oxide (PGO) nanosheets. PGO surface properties have been meticulously characterized using advanced spectroscopic techniques. Electrochemical impedance spectroscopy and cyclic voltammetry were used to test the electrochemical properties of the PGO-modified sensor. The PGO-modified sensor exhibited remarkable sensitivity, achieving a detection limit as low as 0.061 µM and a broad linear range of 0.02-250 µM. Enhanced performance is due to PGO's high surface area and excellent electrocatalytic properties, which greatly improved electron transfer. Square wave voltammetry was used to demonstrate the sensor's efficacy as a real-time, on-site monitoring tool for FNT residues in fruit and water. The outstanding performance of the PGO/SPCE sensor underscores its applicability in ensuring food safety and environmental protection.

Optimizing filters of activated carbons obtained from biomass residues for ethylene removal in agro-food industry devices.

A series of adsorbents (activated carbons, ACs) were synthesized by physical and chemical activation of olive stones (OS) and their textural and chemical characteristics determined by complementary techniques such as N2 and CO2 physisorption, pH of the point zero of charge (pHPZC), HRSEM or XPS. Samples with a wide range of physicochemical properties were obtained by fitting the activation procedure. The performance of these adsorbents in filters working under dynamic conditions was studied by determining the corresponding breakthrough curves for the ethylene removal. The physicochemical transformations of OS during activation were related with the adsorptive performance of derivative ACs. Results were compared to those obtained using commercial carbons, in particular ACs, carbon black or carbon fibers, in order to identify the properties of these materials on influencing the adsorptive performance. In general, ACs from OS perform better than the commercial samples, being also easily regenerated and properly used during consecutive adsorption cycles. CO2-activation showed to be the best synthesis option, leading to granular ACs with a suitable microporosity and surface chemistry. These results could favour the integration of this type of inexpensive materials on devices for the preservation of climacteric fruits, in a clear example of circular economy by reusing the agricultural residues.

Adsorption of 2,4-dichlorophenoxyacetic acid on activated carbons from macadamia nut shells.

This study reports on the application of activated carbons from macadamia nut shells as adsorbents for the removal of 2,4-dichlorophenoxyacetic acid, a commonly used pesticide, from water. Different activating agents (FeCl3, ZnCl2, KOH and H3PO4) were used to obtain adsorbents within a wide range of porous texture and surface properties. The characterization of the resulting activated carbons was performed by N2 adsorption-desorption, elemental analysis, TG and pHPZC. The adsorption experiments were conducted in batch at 25, 45 and 65 °C. The adsorption kinetics on activated carbons obtained with FeCl3 H3PO4 or KOH was well described by the pseudo-second order model, whereas for the resulting from ZnCl2 activation the experimental data fit better the pseudo-first order model. The equilibrium studies were performed with the KOH- and ZnCl2-activated carbons, the two showing higher surface area values. In both cases, high adsorption capacities were obtained (c.a. 600 mg g-1) and the experimental data were better described by the Langmuir and Toth models. The thermodynamic study allows concluding the spontaneous and endothermic character of the adsorption process, as well as an increase of randomness at the solid/liquid interface. Breakthrough curves were also obtained and fitted to the logistic model.

Biosorption of a common micropollutant (methylene blue) from a water environment by chemically activated biomass of a widely available plant species (Pyracantha coccinea M. J. Roemer).

Recently, to protect the health of aquatic life and, indirectly, all living things, biomass-based substances have been increasingly applied as biosorbent materials to remove micropollutant agents from an aquatic environment. However, these studies are under development, and the search for more successful materials continues. Here, the biosorption of a common micropollutant, methylene blue, from an aquatic environment was investigated using the chemically activated biomass of a widely available plant species, Pyracantha coccinea M. J. Roemer. The biosorption efficiency of the biosorbent material was improved by optimizing the experimental conditions, including the contact time, micropollutant load, pH, and biosorbent material amount, and the highest performance was observed at t = 360 mins, C0 = 15 mg L-1, pH = 8 and m = 10 mg. The pseudo-second-order kinetics model and Freundlich isotherm model were in good agreement with the experimentally obtained results. The thermodynamic study suggested that the micropollutant biosorption was a favorable, spontaneous, and physical process. The micropollutant-biosorbent interaction mechanism was presented using SEM and FTIR studies. The maximum Langmuir biosorption capacity of the biosorbent was determined to be 156.674 mg g-1. The activation operation more than doubled the biosorption potential of the biosorbent material. Thus, the present study showed that the chemically activated plant biomass-based material could be a promising biosorbent for the effective removal of the micropollutant from water environment.

The biosorption of a common micropollutant, methylene blue, from a water environment was studied using chemically activated biomass of Pyracantha coccinea M. J. Roemer. The activation operation more than doubled the biosorption potential of the biosorbent material. It exhibited higher micropollutant biosorption performance compared to most other biosorbents. These results indicated that the chemically activated biomaterial could be a very effective biosorbent for the micropollutant biosorption from an aqueous medium.

Adsorption of Nitrogen Dioxide on Nitrogen-Enriched Activated Carbons.

The aim of this study was to obtain nitrogen-enriched activated carbons from orthocoking coal. The initial material was subjected to a demineralisation process. The demineralised precursor was pyrolysed at 500 °C and then activated with sodium hydroxide at 800 °C. Activated carbon adsorbents were subjected to the process of ammoxidation using a mixture of ammonia and air at two different temperature variants (300 and 350 °C). Nitrogen introduction was carried out on stages of demineralised precursor, pyrolysis product, and oxidising activator. The elemental composition, acid-base properties, and textural parameters of the obtained carbon adsorbents were determined. The activated carbons were investigated for their ability to remove nitrogen dioxide. The results demonstrated that the ammoxidation process incorporates new nitrogen-based functional groups into the activated carbon structure. Simultaneously, the ammoxidation process modified the acid-base characteristics of the surface and negatively affected the textural parameters of the resulting adsorbents. Furthermore, the study showed that all of the obtained carbon adsorbents exhibited a distinct microporous texture. Adsorption tests were carried out against NO2 and showed that the carbon adsorbents obtained were highly effective in removing this gaseous pollutant. The best sorption capacity towards NO2 was 23.5 mg/g under dry conditions and 75.0 mg/g under wet conditions.

Production of activated carbon from spent coffee grounds (SCG) for removal of hexavalent chromium from synthetic wastewater solutions.

In this research, spent coffee grounds (SCG) are converted into a highly valuable porous adsorbent which removes chromium (VI) from wastewater with high efficiency. A set of nine Spent Coffee Ground Activated Carbon (SCG-AC) adsorbent samples were synthesized, by varying key parameters including pyrolysis temperature (400, 600 °C), pyrolysis duration (1 and 2 h), and the impregnation ratio of the activating agent, KOH (ranging from 0:1 to 2:1). Characterizations of these adsorbent samples were conducted by advanced analytical tools including SEM, EDX, XRD, FTIR, TGA, and BET. Furthermore, we carried out adsorption studies, exploring the effects of temperature and dosage variations. Additionally, point zero charge experiments and desorption studies were carried out to further understand the adsorption process. The outcomes of our investigation demonstrate the successful synthesis of these spent coffee ground-derived adsorbents, with a yield of up to 34%. Notably, these adsorbents exhibited high efficiency in extracting chromium (VI) from water, with removal efficiencies ranging from 75% to 100%. The adsorption isotherms revealed the Langmuir model to be the most fitting descriptor of the adsorption behavior. Moreover, a thermodynamics study revealed the process to be endothermic in nature which furthers our understanding of the underlying mechanisms. Importantly, our cost assessment shows the economic advantage of the synthesized adsorbent over commercial counterparts such as zeolite, making it a competitive choice for real-world applications. In summation, the study not only introduces an innovative and sustainable utilization of spent coffee grounds but also delivers an in-depth exploration of the synthesized adsorbent's ability in chromium (VI) removal. Our holistic approach, encompassing thorough experimentation, characterization, and economic evaluation, solidifies the significance of this research in tackling environmental concerns and propelling advancements in wastewater treatment methodologies.

Surface modification of toner-based recyclable iron oxide self-doped graphite nanocomposite to enhance methylene blue and tetracycline adsorption.

An innovative task was undertaken to convert ubiquitous and toxic electronic waste, waste toner powder (WTP), into novel adsorbents. Alkaline modification with KOH, NaOH, and NH4OH was employed for the first time to synthesize a series of surface-modified WTP with enhanced dispersibility and adsorption capacity. XRD, XRF, FTIR, and BET analyses confirmed that the prepared KOH-WTP, NaOH-WTP, and NH4OH-WTP were oxygen-functionalized self-doped iron oxide-graphite nanocomposites. The prepared adsorbents were used to remove methylene blue and tetracycline from aqueous solutions. KOH-WTP (0.1 g/100 mL) adsorbed 80% of 10 mg/L methylene blue within 1 h, while 0.1 g/100 mL NH4OH-WTP removed 72% of 10 mg/L tetracycline in 3 h. Exploring surface chemistry by altering solution pH and temperature suggested that hydrogen bonding, electrostatic interactions, π-π electron stacking, and pore filling were plausible adsorption mechanisms. Scanning electron microscopy revealed a diminishing adsorbents porosity after adsorption proving the filling of pores by the adsorbates. KOH-WTP and NH4OH-WTP removed 77% and 61% of methylene blue and tetracycline respectively in the fourth reuse. The adsorption data of methylene blue and tetracycline fitted the Freundlich isotherm model. The maximum adsorption capacities of KOH-WTP and NH4OH-WTP for methylene blue and tetracycline were 59 mg/g and 43 mg/g respectively. The prepared adsorbents were also compared with other adsorbents to assess their performance. The transformation of waste toner powder into magnetically separable oxygen-functionalized WTP with outstanding recyclability and adsorption capacity showcases a significant advancement in sustainable wastewater treatment. This further aligns with the principles of the circular economy through the utilization of toxic e-waste in value-added applications. Additionally, magnetic separation of surface-modified WTP post-treatment can curtail filtration and centrifugation expenses and adsorbent loss during wastewater treatment.

Spherical Lignin-Derived Activated Carbons for the Adsorption of Phenol from Aqueous Media.

In this work, a synthesis and activation path, which enabled the preparation of spherical activated carbon from a lignin precursor, characterized by high adsorption capacity in the removal of phenolic compounds from water, was successfully developed. Two industrial by-products, i.e., Kraft lignin and sodium lignosulfonate, were used to form spherical nanometric lignin grains using pH and solvent shift methods. The obtained materials became precursors to form porous activated carbons via chemical activation (using K2CO3 or ZnCl2 as activating agents) and carbonization (in the temperature range of 600-900 °C). The thermal stabilization step at 250 °C was necessary to ensure the sphericity of the grains during high-temperature heat treatment. The study investigated the influence of the type of chemical activator used, its quantity, and the method of introduction into the lignin precursor, along with the carbonization temperature, on various characteristics including morphology (examined by scanning electron microscopy), the degree of graphitization (evaluated by powder X-ray diffraction), the porosity (assessed using low-temperature N2 adsorption), and the surface composition (analyzed with X-ray photoelectron spectroscopy) of the produced carbons. Finally, the carbon materials were tested as adsorbents for removing phenol from an aqueous solution. A conspicuous impact of microporosity and a degree of graphitization on the performance of the investigated adsorbents was found.

A Study on the Adsorption of Rhodamine B onto Adsorbents Prepared from Low-Carbon Fossils: Kinetic, Isotherm, and Thermodynamic Analyses.

The aim of this study was to obtain a series of activated carbon samples by the chemical activation of low-rank coal. The precursor was impregnated with a NaOH solution. Activated carbons were characterized by determining their textural parameters and content of surface oxygen functional groups and by using an elemental analysis. The carbons were tested as potential adsorbents for the removal of liquid pollutants represented by rhodamine B. The effectiveness of rhodamine B removal from water solutions depended on the initial concentration of the dye, the mass of rhodamine B, and the pH and temperature of the reaction. The isotherm examination followed the Langmuir isotherm model. The maximum adsorption capacity of the rhodamine B was 119 mg/g. The kinetic investigation favored the pseudo-second-order model, indicating a chemisorption mechanism. The thermodynamic assessment indicated spontaneous and endothermic adsorption, with decreased randomness at the solid-liquid interface. The experiment revealed that a 0.1 M HCl solution was the most effective regenerative agent.

Iodine adsorption and electrochemical double-layer capacitor characteristics of activated carbon prepared from low-cost biomass.

The efficient adsorption application and electric double-layer capacitor material with low-cost biomass-based activated carbon materials have been quite common recently. In this study, chestnut shell-based activated carbons were produced by chemical activation. ZnCl2, H3PO4, and KOH agents were used for chemical activation. The obtained activated carbon, iodine adsorption from aqueous solutions, and its use as an electro capacitor were investigated. The scanning electron microscope, nitrogen adsorption/desorption, and Fourier transform infrared spectroscopy were used for characterization. The values of surface area and iodine adsorption capacity of the chestnut shell-based activated carbon are 1544 m2 g-1 and 1525 mg g-1. As a result, a specific capacitance of 97 Fg-1 with chestnut shell-based activated carbon was obtained in a 1 M KCl electrolyte for the electrochemical double-layer capacitor. This study shows that activated carbon based on the chestnut shell can be used both as an electrochemical energy storage material and as an adsorbent in iodine adsorption.

Exploring synergistic effects in physical-chemical activation of Acorus calamus for water treatment solutions.

The research proposed a novel method of obtaining sorption material from readily available Acorus calamus biomass through a combination of physical and chemical activation processes. The material with the highest specific surface area (1652 m2 g-1) was obtained by physical activation with CO2, followed by chemical activation with KOH. Reversing the order of activation methods resulted in a lower specific surface area (1014 m2 g-1) of the carbon sample. Chemical activation produced activated carbon with a surface area of 1066 m2 g-1-, while physical activation produced 390 m2 g-1. This confirms the synergistic effect of combining the two activation methods for biocarbon. It was observed that physical activation with CO2 generates a diverse range of pores, including meso- and macropores, while chemical activation induces the formation of micropores. In contrast, reversing the order of these processes leads to the degradation of the porous structure. The application of physical-chemical activation with synergistic effects represents a significant advancement in producing high-quality activated biocarbon for various applications, such as wastewater treatment and energy storage. The combination of the two activation methods resulted in a synergistic effect, leading to the production of carbon material of higher quality. Additionally, the diversified pore sizes will enable the sorption of various pollutants in the aquatic environment and air pollutants, where gas particles are much smaller.

Tailoring the porosity of chemically activated carbons derived from the HTC treatment of sewage sludge for the removal of pollutants from gaseous and aqueous phases.

The management of sewage sludge is currently an open issue due to the large volume of waste to be treated and the necessity to avoid incineration or landfill disposal. Hydrothermal carbonization (HTC) has been recognized as a promising thermochemical technique to convert sewage sludge into value-added products. The hydrochar (HC) obtained can be suitable for environmental application as fuel, fertilizer, and sorbent. In this study, activated hydrochars (AHs) were prepared from sewage sludge through HTC followed by chemical activation with potassium hydroxide (KOH) and tested for the removal of pollutants in gaseous and aqueous environments, investigating carbon dioxide (CO2) and ciprofloxacin (CIP) adsorption capacity. The effects of activation temperature (550-750 °C) and KOH/HC impregnation ratio (1-3) on the produced AHs morphology and adsorption capacity were studied by Response Surface Methodology (RSM). The results of RSM analysis evidenced a maximum CO2 uptake of 71.47 mg/g for mild activation conditions (600-650 °C and KOH/HC = 1 ÷ 2), whereas the best CIP uptake of 628.61 mg/g was reached for the most severe conditions (750 °C, KOH/HC = 3). The prepared AHs were also applied for the removal of methylene blue (MB) from aqueous solutions, and the MB uptake results were used for estimating the specific surface area of AHs. High surface areas up to 1902.49 m2/g were obtained for the highest activation temperature and impregnation ratio investigated. Predictive models of CO2 and CIP uptake were developed by RSM analysis, and the optimum activation conditions for maximizing the adsorption performance together with high AH yield were identified: 586 °C and KOH/HC ratio = 1.34 for maximum yield (26.33 %) and CO2 uptake (67.31 mg/g); 715 °C and KOH/HC ratio = 1.78 for maximum yield (18.75 %) and CIP uptake (370.77 mg/g). The obtained results evidenced that chemical activation of previously HTC-treated sewage sludge is a promising way to convert waste into valuable low-cost adsorbents.

Removal of Methylene Blue and Methyl Red from Aqueous Solutions Using Activated Carbons Obtained by Chemical Activation of Caraway Seed.

In this study, activated carbons were produced through the chemical activation of caraway seeds using three different activators: Na2CO3, K2CO3, and H3PO4. A 1:2 weight ratio of precursor to activator was maintained in every instance. Comprehensive analyses were conducted on the resultant activated carbons, including elemental analysis, textural parameters determination, Boehm titration for surface oxygen functional groups, pH assessment of aqueous extracts, and quantification of ash content. The produced materials were subjected to adsorption tests for methylene blue and methyl red sodium salt from the liquid phase and the effects of adsorbent dosage, pH of the aqueous dye solution, process temperature, and adsorbent-adsorbate contact time on sorption capacity obtained. To characterize the adsorption model of the examined pollutants, both the Langmuir and Freundlich equations were employed. In addition, the sorption capacity of the obtained carbon materials against an iodine aqueous solution was assessed. The specific surface area of the obtained adsorbents ranged from 269 to 926 m2/g. By employing potassium carbonate to chemically activate the starting substance, the resulting activated carbons show the highest level of specific surface area development and the greatest sorption capacity against the tested impurities-296 mg/g for methylene blue and 208 mg/g for methyl red sodium salt. The adsorption rate for both dyes was determined to align with a pseudo-second-order kinetic model. The experimental adsorption data for methylene blue were well-described by the Langmuir model, whereas the Freundlich model was found to be congruent with the data pertaining to methyl red sodium salt.

Statistical Design and Optimization of Cr (VI) Adsorption onto Native and HNO3/NaOH Activated Cedar Sawdust Using AAS and a Response Surface Methodology (RSM).

The removal of heavy metals from wastewater has become the subject of considerable interest at present. Thus, the use of novel adsorbents that are highly efficient is of critical importance for the removal of Cr (VI) ions from aqueous media. The adsorption of Cr (VI) ions from aqueous solutions by a new adsorbent, cedar wood sawdust, and the optimization of its adsorption parameters, were investigated in this study. Cedar wood sawdust was used in its native and HNO3/NaOH chemically modified forms as new low-cost sorbents to remove Cr (VI) ions from aqueous solutions in a batch system. The adsorption conditions were analyzed via response surface methodology. The RSM results showed that the optimal adsorption conditions yielding the best response were an adsorbent mass of 2 g for native Cedar and 1.125 g for its activated form, a metal concentration of 150 mg/L for native Cedar and 250 mg/L for activated, a temperature of 50 °C, a pH of 1, and a contact time of 67.5 min. At optimum adsorption conditions, the maximum adsorption capacities and the adsorption yields were 23.64 mg/g and 84% for native Cedar and 48.31 mg/g and 99% for activated Cedar, respectively.

Characterization of Activated Carbon from Rice Husk for Enhanced Energy Storage Devices.

The production of activated carbon (AC) from lignocellulosic biomass through chemical activation is gaining global attention due to its scalability, economic viability, and environmental advantages. Chemical activation offers several benefits, including energy efficiency, reduced carbonization time, and lower temperature requirements. In this study, potassium hydroxide (KOH) was employed for chemical activation, resulting in activated carbon with a high specific surface area of ~3050 m2/g. The structural analysis revealed the presence of graphitized carbon in the activated carbon matrix, accounting for over 15%. The X-ray diffraction (XRD) technique was employed to investigate the activated carbon derived from rice husk (RH). The potential applications of activated carbon obtained from rice husks through chemical activation were explored, including its use for heavy metal removal, elimination of organic pollutants, and as an active material in hybrid energy storage devices. Furthermore, a scaling methodology for the production of activated carbon was proposed, facilitating its industrial implementation.

The Influence of Oxidation and Nitrogenation on the Physicochemical Properties and Sorption Capacity of Activated Biocarbons Prepared from the Elderberry Inflorescence.

The main objective of the study was to prepare a series of new activated biocarbons by means of physical and chemical activation of elderberry inflorescence. The influence of carbon matrix nitrogenation/oxidation on the physicochemical properties and sorption abilities of the carbonaceous materials was investigated. The impact of initial dye concentration, pH and temperature of the system on methylene blue and rhodamine B removal efficiency was checked. It was shown that activation of elderberry inflorescences with CO2 or H3PO4, and their further modification by introducing nitrogen or oxygen functional groups, allowed us obtain a wide range of materials that differ significantly in terms of the chemical nature of the surface, degree of specific surface development and the type of porous structure generated. The samples prepared by chemical activation proved to be very effective in terms of cationic dyes adsorption. The maximum sorption capacity toward methylene blue and rhodamine B reached the level of 277.8 and 98.1 mg/g, respectively. A better fit to the experimental data was achieved with a Langmuir isotherm than a Freundlich one. It was also shown that the efficiency of methylene blue and rhodamine B adsorption from aqueous solutions decreased with increasing temperature of the system.

Carbon Adsorbents Obtained from Pistachio Nut Shells Used as Potential Ingredients of Drinking Water Filters.

Water resources are increasingly degraded due to the discharge of waste generated in municipal, industrial and agricultural areas. Therefore, the search for new materials enabling the effective treatment of drinking water and sewage is currently of great interest. This paper deals with the adsorption of organic and inorganic pollutants on the surface of carbonaceous adsorbents prepared by thermochemical conversion of common pistachio nut shells. The influence of the direct physical activation with CO2 and chemical activation with H3PO4 on parameters, such as elemental composition, textural parameters, acidic-basic character of the surface as well as electrokinetic properties of the prepared carbonaceous materials was checked. The suitability of the activated biocarbons prepared as the adsorbents of iodine, methylene blue and poly(acrylic acid) from the aqueous solutions was estimated. The sample obtained via chemical activation of the precursor turned out to be much more effective in terms of all the tested pollutants adsorption. Its maximum sorption capacity toward iodine was 1059 mg/g, whereas in relation to methylene blue and poly(acrylic acid) 183.1 mg/g and 207.9 mg/g was achieved, respectively. For both carbonaceous materials, a better fit to the experimental data was achieved with a Langmuir isotherm than a Freundlich one. It has also been shown that the efficiency of organic dye, and especially anionic polymer adsorption from aqueous solutions, is significantly affected by solution pH and temperature of the adsorbate-adsorbent system.

Polyethylene-Derived Activated Carbon Materials for Commercially Available Supercapacitor in an Organic Electrolyte System.

High-performance supercapacitors based on activated carbons (AC) derived from polyethylene (PE), which is one of the most abundant plastic materials worldwide, are fabricated. First, PE carbons (PEC) are prepared via sulfonation, which is a reported solution for successful carbonization of innately non-carbonizable PE. Then, the physico-electrical changes of PECs upon a chemical activation process are explored. Interestingly, upon the chemical activation, PECs are converted ACs with a large surface area and high crystallinity at the same time. Subsequently, PE-derived ACs (PEAC) are exploited as electrode materials for supercapacitors. Resultant supercapacitors based on PEACs exhibit impressive performance. When compared to supercapacitors based on YP50f, representative commercial ACs, devices using PEACs presented considerably good capacitance, low resistance, and great rate capability. Specifically, the retention rate of devices using PEACs is significantly higher than that of YP50f-based devices. At the high rate of charge-discharge situation reaching 7 A g-1 , the capacitance of supercapacitors using PEACs is ≈70% higher than that of YP50f-based devices. It is assumed that the carbon structure accompanying both large surface area and high conductivity endows a great electrochemical performance at the high current operating conditions. Therefore, it is envisioned that PE may be a viable candidate electrode material for commercially available supercapacitors.