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Cannabinoids represent a highly researched group of plant-derived ingredients. The substantial investment of funds from state and commercial sources has facilitated a significant increase in knowledge about these ingredients. Cannabinoids can be classified into three principal categories: plant-derived phytocannabinoids, synthetic cannabinoids and endogenous cannabinoids, along with the enzymes responsible for their synthesis and degradation. All of these compounds interact biologically with type 1 (CB1) and/or type 2 (CB2) cannabinoid receptors. A substantial body of evidence from in vitro and in vivo studies has demonstrated that cannabinoids and inhibitors of endocannabinoid degradation possess anti-inflammatory, antioxidant, antitumour and antifibrotic properties with beneficial effects. This review, which spans the period from 1940 to 2024, offers an overview of the potential therapeutic applications of natural and synthetic cannabinoids. The development of these substances is essential for the global market of do-it-yourself drugs to fully exploit the promising therapeutic properties of cannabinoids.

In this study, biochars were produced from by-products of the herbal industry, specifically fennel seeds (Foeniculum vulgare), through direct activation by carbon dioxide at two different temperatures. The biochar samples were comprehensively analysed. Additionally, adsorption studies were conducted for methylene blue. The resulting adsorbents exhibited a specific surface area ranging from 2.29 to 14.60 m2/g. The resulting materials displayed a basic character on their surface. The constants for adsorption models were determined for each dye as well as thermodynamic parameters and the kinetics of the process. The sorption capacities of methylene blue for the samples exhibited a range of 22 to 43 mg/g. The adsorption kinetics of the dye on the biochar materials were found to follow a pseudo-second-order model, with the adsorption process best described by the Langmuir isotherm for the DA-800 sample and the Freundlich isotherm for the DA-750 sample. This indicates the development of a monolayer adsorbate on the biochar surfaces. The efficacy of the adsorption process in aqueous solutions of methylene blue was found to increase with rising temperature. Furthermore, based on thermodynamic studies, the adsorption process was found to be spontaneous and endothermic.

The preparation of biocarbons from cellulose fibres utilised in the production of baby nappy mats (sourced from Feniks Recycling company, Poland) for the removal of methylene blue and rhodamine B dyes has been documented. A Brunauer, Emmett and Teller analysis revealed a surface area within the range of 384 to 450 m2/g. The objective of this study was to investigate the removal efficiency of dyes from aqueous solutions by biocarbons, with a particular focus on the influence of various parameters, including pH, dye concentration, adsorbent dosage, shaking speed, contact time, and temperature. The maximum adsorption capacity of the dyes onto the biocarbons was found to be 85 mg/g for methylene blue and 48 mg/g for rhodamine B, respectively. The Langmuir equation proved to be the most suitable for interpreting the sorption of organic dyes. The adsorption process was found to exhibit a chemisorption mechanism, effectively mirroring the pseudo-second-order kinetics. Furthermore, the adsorption of dyes was observed to be endothermic (the enthalpy change was positive, 9.1–62.6 kJ/mol) and spontaneous under the tested operating conditions. The findings of this study indicate that biocarbons represent a cost-effective option for the removal of methylene blue and rhodamine B. The adsorption method was observed to be an effective and straightforward approach for the removal of these dyes. The results of the Boehm titration analysis and zero charge point value indicated that the synthesised biomaterials exhibited a slightly basic surface character.

The present work reports an effective method for the removal of inorganic and organic pollutants using membranes based on different carbonaceous materials. The membranes were prepared based on cellulose acetate (18 wt. %), polyvinylpyrrolidone as a pore-generating agent (2 wt. %) and activated carbon (1 wt. %). Activated carbons were developed from residues after extraction of the mushroom Inonotus obliguus using microwave radiation. It has been demonstrated that the addition of activated carbon to the membranes resulted in alterations to their physical properties, including porosity, equilibrium water content and permeability. Furthermore, the chemical properties of the membranes were also affected, with changes observed in the content of the surface oxygen group. The addition of carbon material had a positive effect on the removal of copper ions from their aqueous solutions by the cellulose–carbon composites obtained. Moreover, the membranes proved to be more effective in the removal of copper ions than iron ones and phenol. The membranes were found to show higher effectiveness in copper removal from a solution of the initial concentration of 800 mg/L. The most efficient in copper ions removal was the membrane containing urea-enriched activated carbon.

The following work presents a method for obtaining PLA composites with activated carbon modified using the liquid for fused deposition modeling (L-FDM) method in which two different compounds, i.e., rhodamine and antipyrine, are introduced. Tablets saturated with substances were obtained. Microscopic tests were carried out, and these confirmed the presence of substances that had been introduced into the polymer structure. UV-Vis spectra and observation of the active substance release process confirmed the relationship between the printing speed and the amounts of the compounds liberated from the tablets. Additionally, the contact angle of the PLA with activated carbon composites was characterized. The hydrophilic nature of the obtained composites favors an increase in the amounts of compounds released during the release process, which is a desirable effect. The surfaces and pores of the obtained materials were also analyzed. The incorporation of activated carbon into PLA results in a significant increase in its surface area. Investigations indicate that a novel approach for introducing chemicals into polymer matrices through the L-FDM method holds promise for the prospective fabrication of tablets capable of a controlled and customized release of substances tailored to individual requirements.

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.

The aim of the current study was to produce biocarbons through the activation of carbon dioxide with the extraction residues of the fungus Inonotus obliquus. To achieve this goal, a microwave oven was used to apply three different activation temperatures: 500, 600, and 700 °C. Low-temperature nitrogen adsorption/desorption was employed to determine the elemental composition, acid-base properties, and textural parameters of the resulting carbon adsorbents. Subsequently, the produced biocarbons were evaluated for their efficiency in removing malachite green and NO2. The adsorbent obtained by activation of the precursor in 700 °C had a specific surface area of 743 m2/g. In the aqueous malachite green solution, the highest measured sorption capacity was 176 mg/g. Conversely, under dry conditions, the sorption capacity for NO2 on this biocarbon was 21.4 mg/g, and under wet conditions, it was 40.9 mg/g. According to the experimental findings, surface biocarbons had equal-energy active sites that interacted with the dye molecules. A pseudo-second-order kinetics model yielded the most accurate results, indicating that the adsorption of malachite green was driven by chemisorption. Additionally, the study demonstrates a clear correlation between the adsorption capacity of the biocarbons and the pH level of the solution, as it increases proportionately.

In this study, fennel (Foeniculum vulgare) seeds were used as a precursor to obtain carbon adsorbents through physical activation with carbon dioxide and chemical activation by impregnating the precursor with sodium carbonate. The physical activation involved the carbonization of the precursor at a temperature of 600 °C for 60 min and activation at a temperature of 800 °C for 30 min with carbon dioxide. Chemical activation included impregnation of the precursor with sodium carbonate at a mass ratio of a precursor to activator of 1:2. The mixture was activated in a nitrogen atmosphere with a flow rate at a temperature of 700 °C for 45 min. The resulting biochar samples were washed with 5% hydrochloric acid and subsequently rinsed with boiling distilled water. The biochar adsorbents were characterized using low-temperature nitrogen adsorption–desorption isotherms, Boehm titration, and pH measurements of their aqueous extracts. The specific surface area of the obtained adsorbents ranged from 89 to 345 m2/g. Biochar adsorbents exhibit a predominance of acidic groups over basic groups on their surfaces. The sorption capacities of the obtained samples towards an aqueous solution of methyl red range from 26 to 135 mg/g. Based on adsorption studies, it was found that the adsorption of the dye on the obtained biochar materials follows a pseudo-second-order model. The Freundlich isotherm best describes the studied process, indicating the formation of a multilayer of adsorbate on the adsorbent surface. The efficacy of adsorption in aqueous solutions of methyl red was found to increase with the elevation of the process temperature. Moreover, thermodynamic studies have shown that the adsorption process is spontaneous and endothermic. Consequently, this work provides a description of the physicochemical parameters of two biochars obtained by physical and chemical activation of a little-studied precursor—fennel seeds—and studies on their potential use as adsorbents for contaminants from the aqueous phase.

The residues obtained from the extraction of Inonotus obliquus fungus were used to produce carbonaceous adsorbents. The initial material was subjected to pyrolysis in a microwave oven. The adsorbents were characterized through elemental analysis, low-temperature nitrogen adsorption/desorption isotherms, and Boehm titration. The carbonaceous adsorbents were tested for the removal of NO2, methylene blue, and malachite green. The results indicated that the obtained carbonaceous adsorbents exhibited basic characteristics and possessed specific surface areas of 372 and 502 m2/g. The adsorption process of liquid contaminants was modeled using the single-layer Langmuir model. The maximum adsorption capacities were found to be 101 and 109 mg/g for methylene blue, and 75 and 77 mg/g for malachite green. The kinetic study demonstrated that the adsorption of methylene blue and malachite green was better described by a pseudo-second order model. The study affirmed that the adsorption of organic dyes onto the resultant carbonaceous adsorbents was both spontaneous and endothermic. The study also demonstrated that the presence of an air stream during the NO2 adsorption process and prehumidization of the adsorbent with humid air had a beneficial effect on the obtained sorption capacities. In conclusion, the study demonstrated that pyrolysis of the extraction residues from the fungus Inonotus obliquus yields highly effective, environmentally friendly, and cost-efficient carbonaceous adsorbents for the removal of both gaseous and liquid pollutants.

In this study, biocarbon was obtained from the waste material corn digest. Carbon adsorbents were obtained by physical activation of the precursor with CO2. Detailed physicochemical characterization of the biocarbon was carried out using low-temperature nitrogen adsorption/desorption, Boehm titration, zero-charge point (pHpzc) and iodine number. In addition, the sorption capacity of the biocarbon agents towards an aqueous solution of methylene blue and methyl red was determined, and the kinetics of the adsorption process were determined. The biocarbon adsorbents were characterized by an average developed specific surface area covering the range from 320 to 616 m2/g. The sorption capacity of the biocarbon adsorbents against methylene blue ranged from 40 mg/g to 146 mg/g, and for methyl red it covered the range from 31 mg/g to 113 mg/g. It was shown that the efficiency of organic dye removal by the obtained biocarbons depends on the initial concentration of the adsorbate solution, its mass, shaking rate, adsorbent–adsorbate contact time and temperature. The results obtained from the Langmuir and Freundlich kinetic models showed that the Langmuir model is the most suitable model for describing the adsorption of the studied pollutants on biocarbon. In turn, the adsorption kinetics of dyes is described according to the pseudo-second-order model. Adsorption studies also showed that as the process temperature increases, the removal efficiency of methylene blue and methyl red increases.

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.

Poor bioavailability hampers the use of curcumin and piperine as biologically active agents. It can be improved by enhancing the solubility as well as by using bioenhancers to inhibit metabolic transformation processes. Obtaining an amorphous system of curcumin and piperine can lead to the overcoming of these limitations. Hot-melt extrusion successfully produced their amorphous systems, as shown by XRPD and DSC analyses. Additionally, the presence of intermolecular interactions between the components of the systems was investigated using the FT-IR/ATR technique. The systems were able to produce a supersaturation state as well as improve the apparent solubilities of curcumin and piperine by 9496- and 161-fold, respectively. The permeabilities of curcumin in the GIT and BBB PAMPA models increased by 12578- and 3069-fold, respectively, whereas piperine’s were raised by 343- and 164-fold, respectively. Improved solubility had a positive effect on both antioxidant and anti-butyrylcholinesterase activities. The best system suppressed 96.97 ± 1.32% of DPPH radicals, and butyrylcholinesterase activity was inhibited by 98.52 ± 0.87%. In conclusion, amorphization remarkably increased the dissolution rate, apparent solubility, permeability, and biological activities of curcumin and piperine.

The results of kinetic measurements revealed an accelerating effect of acetazolamide (ACT) on the multistep In(III) ions electroreduction in chlorates(VII) on a novel, cyclically renewable liquid silver amalgam film electrode (R–AgLAFE). The kinetic and thermodynamic parameters were determined by applying the DC polarography, square-wave (SWV) and cyclic voltammetry (CV), as well as electrochemical impedance spectroscopy (EIS). It was shown that ACT catalyzed the electrode reaction (“cap-pair” effect) by adsorbing on the surface of the R–AgLAFE electrode. The catalytic activity of ACT was explained as related to its ability to form active In(III)- acetazolamide complexes on the electrode surface, facilitating the electron transfer process. The active complexes constitute a substrate in the electroreduction process and their different structures and properties are responsible for differences in the catalytic activity. The determined values of the activation energy ΔH≠ point to the catalytic activity of ACT in the In(III) ions electroreduction process in chlorates(VII). Analysis of the standard entropy values ΔS0 confirm changes in the dynamics of the electrode process.

This paper deals with the adsorption of organic and inorganic pollutants on the surface of carbonaceous adsorbents prepared via the chemical activation of expired or broken food products—the solid residue of the “cola-type” drink as well as spoilt grains of white rice and buckwheat groats. The activation process was conducted in the microwave furnace with the use of two activating agents of different chemical nature—potassium carbonate and orthophosphoric acid. The activated carbons were characterized based on the results of elemental analysis, low-temperature nitrogen adsorption/desorption, Boehm titration, thermal analysis, and scanning electron microscopy. Additionally, the suitability of the materials prepared as the adsorbents of methylene blue and iodine from the aqueous solutions was estimated. The materials obtained via chemical activation with H3PO4 turned out to be much more effective in terms of both model pollutant adsorptions. The maximum sorption capacity toward iodine (1180 mg/g) was found for the white-rice-based activated carbon, whereas the most effective in the methylene blue removal (221.3 mg/g) was the sample obtained from the solid residue of the expired “cola-type” drink. For all carbonaceous materials, a better fit for the experimental adsorption data was obtained with the Langmuir isotherm model than the Freundlich one.

The main objective of this study was to prepare a series of biochars and activated biocarbons via conventional pyrolysis as well as chemical or physical activation of solid residue after solvent extraction of wild growing plant (popular weed)–mugwort. The influence of the variant of the thermochemical treatment of the precursor on such parameters as elemental composition, textural parameters, acidic-basic character of the surface as well as adsorption abilities of the prepared carbonaceous materials was checked. Moreover, the suitability of the biochars prepared as renewable fuels was also investigated. It has been shown that the products obtained from the mugwort stems differ in many respects from the analogous materials obtained from mugwort leaves. The products were micro/mesoporous materials with surface area reaching 974.4 m2/g and total pore volume–1.190 cm3/g. Surface characterization showed that chemical activation with H3PO4 results in the acidic character of the adsorbents surface, whereas products of pyrolysis and especially physical activation show strongly alkaline surface properties. All the adsorbents were used for methylene blue and iodine adsorption from the aquatic environment. To understand the nature of the sorption process, the Langmuir, Freundlich and Temkin isotherm models were employed. The Langmuir model best described the experimental results, and the maximum sorption capacity calculated for this model reached 164.14 mg of methylene blue per gram of adsorbent. In case of iodine removal, the maximum capacity reached 948.00 mg/g. The research carried out for the biochars prepared via conventional pyrolysis showed that the value of their heat of combustion varies in the range from 21.74 to 30.27 MJ/kg, so they can be applied as the renewable fuels.

The aim of this study was to prepare biocarbons by biomass activation with carbon(IV) oxide. Fennel and caraway fruits were used as the precursors of bioadsorbents. The impact of the precursor type and temperature of activation on the physicochemical properties of the obtained biocarbons and their interaction with methyl red sodium salt upon adsorption process have been checked. The obtained bioadsorbents were characterized by determination of-low temperature nitrogen adsorption/desorption, elemental analysis, ash content, Boehm titration, and pH of water extracts. The biocarbons have surface area varying from 233–371 m2/g and basic in nature with acidic/basic oxygen-containing functional groups (3.23–5.08 mmol/g). The adsorption capacity varied from 63 to 141 mg/g. The influence of different parameters, such as the effectiveness of methyl red sodium salt adsorption, was evaluated. The adsorption kinetics was well fitted using a pseudo-second-order model. The Freundlich model best represented the equilibrium data. The amount of adsorbed dye was also found to increase with the increasing temperature of the process.

Biochars that are the subjects of this report have been obtained from the residue of supercritical extraction of common nettle seeds with CO2. The residue was subjected to direct activation with carbon(IV) oxide as an activator. The obtained biochars were found to have a specific surface area inthe range of 888–1024 m2/g and a basic surface. They were used for the adsorption of a liquid organic pollutant (methylene blue) and a gas inorganic pollutant (NO2). As follows from the test results, the biochars were able to adsorb 150–239 mg of the dye. The Langmuir model was found to better describe the adsorption experimental data, while the kinetics of the process was better described by the pseudo-second-order model. From the thermodynamic analysis, it was inferred that the adsorption of methylene blue from a water solution was an endothermic and spontaneous reaction. It was established that elevated temperature of activation and the presence of air stream during adsorption had a positive impact on the adsorption of NO2 by the biochars studied. The greatest sorption capacity of the biochars towards NO2 was 59.1 mg/g.

Herbal raw materials with antidiabetic activity can be a valuable support to therapy. An optimized extraction process allows for the best possible health-promoting effect. Box–Behnken design was employed to optimize the content of methanol used in the extraction mixture, its time, and temperature. The aim of this study was to enhance the efficiency of the pomegranate flowers extraction process in order to obtain extracts with the highest enzyme inhibition power (α-amylase and α-glucosidase), which is important for the antidiabetic effect and the highest antioxidant activity (DPPH assay). In the Box–Behnken design model, the content of pelargonidin-3,5-glucoside–anthocyanin compound that is associated with antidiabetic activity was also optimized as a variable associated with the action profile of pomegranate flower extracts. The process optimization carried out in this study provides a basis for further research using the pomegranate flower extract with the most potent desired properties, essential for supporting diabetes treatment based on pomegranate flowers.

Oxidized mesoporous carbon CSBA-15, obtained by the hard method, was applied to remove rhodamine B from the aqueous system. The process of carbon oxidation was performed using 0.5 and 5 M of nitric (V) acid solution at 70 and 100 °C. Functionalization of mesoporous carbon with HNO3 solutions led to reduction in the surface area, pore volume, and micropore area, however, it also led to an increased number of oxygen functional groups of acidic character. The functional groups probably are located at the entrance of micropores, in this way, reducing the values of textural parameters. Isotherms of rhodamine B adsorption indicate that the oxidation of mesoporous carbons resulted in an increase in the effectiveness of the removal of this dye from aqueous solutions. The influence of temperature, pH, and contact time of mesoporous material/rhodamine B on the effectiveness of dye removal was tested. The process of dye adsorption on the surfaces of the materials studied was established to be most effective at pH 12 and at 60 °C. Kinetic studies of the process of adsorption proved that the equilibrium state between the dye molecules and mesoporous carbon materials is reached after about 1 h. The adsorption kinetics were well fitted using a pseudo-second-order model. The most effective in rhodamine B removal was the sample CSBA-15-5-100, containing the greatest number of oxygen functional groups of acidic character. The Langmuir model best represented equilibrium data.

Activated carbons were obtained by physical and chemical activation of the residue of supercritical extraction of green tea leaves. All the adsorbents obtained were characterized by: elemental analysis, low-temperature nitrogen adsorption, and the contents of acidic and basic oxygen functional groups on the surface of activated carbons by the Boehm method. The activated carbons were micro- or micro-mesoporous with well-developed surface area ranging from 520 to 1085 m2/g and total pore volume from 0.62 to 0.64 cm3/g. The physical activation of the precursor led to the strongly basic character of the surface. Chemical activation with 50% solution of H3PO4 of the residue of supercritical extraction of green tea leaves promoted the generation of acidic functional groups. All adsorbents were used for methylene blue and methyl red adsorption from the liquid phase. The influence of the activation method, pH of the dye solution, contact time of adsorbent with adsorbate, the temperature of adsorption, and rate of sample agitation on the effectiveness of organic dyes removal was evaluated and optimized. In the process of methylene blue adsorption on adsorbents, an increase in the sorption capacity was observed with increasing pH of the adsorbate, while in the process of methyl red adsorption, the relation was quite the reverse. The adsorption data were analyzed assuming the Langmuir or Freundlich isotherm models. The Langmuir model better described the experimental results, and the maximum sorption capacity calculated for this model varied from 144.93 to 250.00 mg/g. The results of the kinetic analysis showed that the adsorption of organic dyes on activated carbon was following the pseudo-second-order model. The negative values of the Gibbs free energy indicate the spontaneous character of the process.

Carbon xerogels were obtained by polycondensation of resorcinol and formaldehyde in a water medium. Their surface was oxidized by ammonium persulfate and then modified with amine groups. Four amines were used: methylamine, ethylamine, propylamine, and ethylenediamine, differing in carbon chain length and number of amine groups. The materials were characterized by low-temperature nitrogen sorption, elemental analysis, thermal analysis, X-ray diffraction, infrared spectroscopy, and determination of the surface oxygen group content with the use of the Boehm method. The final carbon adsorbents had surface areas ranging from 172–663 m2/g and acid–base nature. They were applied for adsorption of thymol blue from water solution. The sorption capacities of the studied adsorbents ranged from 83 to 140 mg/g. The presence of amine groups on the xerogel surface was found to increase its sorption capacity towards the dye studied. The dye adsorption process is endothermic and spontaneous, as indicated by the positive values of ΔH and the negative values of ΔG, respectively. The kinetics of adsorption of thymol blue was established to be described by the pseudo-second-order model. The equilibrium data were analyzed by the Langmuir and Freundlich models. The character of thymol blue adsorption is much better described by the Langmuir isotherm.

This paper deals with the adsorption of heavy metal ions on the surface of carbonaceous materials obtained via the chemical activation of biomass. Waste plum stones, pine sawdust and horsetail herb were used as the precursors of carbonaceous adsorbents. The effect of the precursor type and preparation procedure on the physicochemical properties of activated biocarbons and their sorption abilities towards Pb(II) and Cu(II) ions have been checked. The obtained micro-mesoporous activated biocarbons were characterized by determination of elemental composition and ash content, the number of surface functional groups and pH of water extracts as well as textural study based on low temperature nitrogen adsorption/desorption and scanning electron microscopy. Additionally, the electrokinetic studies including solid surface charge density and zeta potential determination were performed. Moreover, the adsorption data modelling (equilibrium and kinetics), XPS results analysis and comparison of parameters characterizing electrical double layer formed at the solid-liquid interface enabled the specification of the mechanism of heavy metals binding with the activated biocarbons surface. The maximum adsorption capacity towards copper and lead ions (177.5 and 178.1 mg/g, respectively) was found for plum stone-based activated biocarbon. For all carbonaceous materials, better fit to the experimental data was achieved with a Langmuir isotherm than a Freundlich one. In turn, a better fit of the kinetics data was obtained using the pseudo-second order model.

In the present work, we reported on the efficiency of the removal of organic dyes by adsorption on activated carbons prepared from the residue of supercritical extraction of marigold. The performance of adsorbents prepared was tested towards methyl red, methylene blue, malachite green, and crystal violet at room temperature. The effects of carbonization (500 and 700 °C) and activation (700 and 800 °C) temperatures, textural parameters, and acid-base character of the adsorbent surface on the sorption properties of the activated carbons were established. Activated carbons are characterized by low developed specific surface area, from 2 to 206 m2/g, and have a basic character of the surface (pH of carbons water extracts ranging from 10.4 to 11.2). Equilibrium adsorption isotherms were investigated. The equilibrium data were analyzed in the Langmuir, Freundlich, and Temkin models. The adsorption capacities of activated carbons studied varied from 47.62 to 102.43 mg/g towards methyl red, 53.14 to 139.72 mg/g towards methyl red, 425.46 to 622.80 towards malachite green and 155.91 to 293.75 mg/g towards crystal violet, from their water solutions. Kinetics of the adsorption of the organic dyes studied were found to be described by the pseudo-second-order model. It was proven that through the physical activation of the residue of supercritical extraction of marigold, it is possible to obtain carbonaceous materials of very high adsorption capacity towards organic pollutants.

This paper deals with the adsorption of heavy metal ions (Cu2+ and Zn2+) on the carbonaceous materials obtained by chemical activation and ammoxidation of Polish brown coal. The effects of phase contact time, initial metal ion concentration, solution pH, and temperature, as well as the presence of competitive ions in solution, on the adsorption capacity of activated carbons were examined. It has been shown that the sample modified by introduction of nitrogen functional groups into carbon structure exhibits a greater ability to uptake heavy metals than unmodified activated carbon. It has also been found that the adsorption capacity increases with the increasing initial concentration of the solution and the phase contact time. The maximum adsorption was found at pH = 8.0 for Cu(II) and pH = 6.0 for Zn(II). For all samples, better fit to the experimental data was obtained with a Langmuir isotherm than a Freundlich one. A better fit of the kinetic data was achieved using the pseudo-second order model.

The waste materials left after supercritical extraction of hop cones and marigold flowers were tested as precursors of activated bio-carbons. Adsorbents were produced by means of the physical (also called thermal) activation method using CO2 as the gasifying agent. All the activated bio-carbons were tested for the removal of NO2 and H2S from the gas phase under dry and wet conditions. The effects of the type of precursor and the activation procedure on the porous structure development, the acid-base properties of the surface, as well as the sorption capacities of the materials produced were also checked. The final products were bio-carbons of medium developed surface area with a basic surface nature, characterized by their high effectiveness in removal of gas pollutants of acidic character, especially nitrogen dioxide (sorption capacities in the range from 12.5 to 102.6 mg/g). It was proved that the toxic gas removal efficiency depends considerably on the sorption conditions and the activation procedure. All materials showed greater effectiveness in gas removal when the process of adsorption was carried out in the presence of steam.