A series of new granular carbonaceous adsorbents was prepared via single-stage physical and chemical activation of walnut shells. Their suitability for removing various types of organic pollutants (represented by dyes, surfactants and water-soluble polymers) from the liquid phase was assessed. The activation of the precursor was carried out with CO2 and H3PO4 using conventional heating. Activated biocarbons were characterized in terms of chemical composition, acidic-basic nature of the surface, textural and electrokinetic properties as well as thermal stability. Depending on the type of activating agent used during the activation procedure, the obtained biocarbons differed in terms of specific surface area (from 401 to 1361 m2/g) and the type of porous structure produced (microporosity contribution in the range of 45-75%). Adsorption tests proved that the effectiveness of removing organic pollutants from the liquid phase depended to a large extent on the type of prepared adsorbent as well as the chemical nature and the molecular size of the adsorbate used. The chemically activated sample showed greater removal efficiency in relation to all tested pollutants. Its maximum adsorption capacity for methylene blue, poly(acrylic acid), poly(ethylene glycol) and Triton X-100 reached the levels of 247.1, 680.9, 38.5 and 61.8 mg/g, respectively.

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.

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.

Activated biocarbons were prepared using biomass wastes: sugarcane bagasse, coconut shell and endocarp of babassu coconut; as a renewable source of low-cost raw materials and without prior treatments. These activated biocarbons were characterized by textural analysis, solid-state 13C nuclear magnetic resonance spectroscopy, X-ray diffraction and scanning electronic microscopy. Textural analysis results revealed that those activated biocarbons were microporous, with specific surface area values of 547, 991 and 1,068 m2 g-1 from sugarcane bagasse, coconut shell and endocarp of babassu coconut, respectively. The innovation of this work was to evaluate which biomass residue was able to offer the best performance in removing 2,4-dichlorophenoxyacetic acid herbicide (2,4-D) from water by adsorption. Adsorption process of 2,4-D was investigated and the Langmuir and Redlich-Peterson models described best the adsorption process, with R2 values within 0.96-0.99. The 2,4-D removal performance were 97% and 99% for the coconut and babassu biocarbons, respectively. qM parameter values obtained from Langmuir model were 153.9, 233.0 and 235.5 mg g-1 using sugarcane bagasse, coconut shell and endocarp of babassu, respectively. In addition, the adsorption kinetics were described nicely by the second-order model and the Gibbs free energy parameter values were negative, pointing to a spontaneous adsorption, as well.

Activated carbons are synthesized from rice husk by one- and two-step pyrolysis. In general, two-step pyrolysis produces a higher yield of activated carbons. The yield of activated carbon decreases with the increase of mass ratio of KOH and biomass, which has a significant impact on the development of surface area and porosity. The maximum S BET (2138 m2 g-1) is achieved with micro- and mesoporous structures, which is favored for the adsorption process. The activated carbons can efficiently remove phenol from water by a few minutes. In particular, the maximum adsorption capacity (201 mg g-1) is achieved due to the excellent surface textural properties. The Langmuir model can better define the adsorption isotherm. The high correlation coefficient value (R 2 = 0.9991) indicates a monolayer adsorption behavior. The adsorption process can be well-fitted by the pseudo-second-order model. Herein, the phenol molecules pass into the internal surface via liquid-film-controlled diffusion, so the behavior of phenol adsorption onto activated carbons is mainly controlled via chemisorption. In addition, the functional groups on the outer surfaces of activated carbons can attract the phenol molecules onto their internal surface via the \"π-π dispersion interaction\" and \"donor-acceptor effect.\"