Application of Activated Carbons Obtained from Polymer Waste for the Adsorption of Dyes from Aqueous Solutions.

Plastic waste disposal is a major environmental problem worldwide. One recycling method for polymeric materials is their conversion into carbon materials. Therefore, a process of obtaining activated carbons through the carbonization of waste CDs (as the selected carbon precursor) in an oxygen-free atmosphere, and then the physical activation of the obtained material with CO2, was developed. Dyes such as methylene blue (MB) and malachite green (MG) are commonly applied in industry, which contaminate the water environment to a large extent and have a harmful effect on living organisms; therefore, adsorption studies were carried out for these cationic dyes. The effects of the activation time on the physicochemical properties of the activated materials and the adsorption capacity of the dyes were investigated. The obtained microporous adsorbents were characterized by studying the porous structure based on low-temperature nitrogen adsorption/desorption, scanning electron microscopy (SEM-EDS), elemental analysis (CHNS), Raman spectroscopy, X-ray powder diffraction (XRD), infrared spectroscopy (ATR FT-IR), thermal analysis (TG, DTG, DTA), Boehm's titration method, and pHpzc (the point of zero charge) determination. Moreover, adsorption studies (equilibrium and kinetics) were carried out. The maximum adsorption capacities (qm exp) of MB and MG (349 mg g-1 and 274 mg g-1, respectively) were identified for the obtained material after 8 h of activation. The results show that the use of waste CDs as a carbon precursor facilitates the production of low-cost and effective adsorbents.

Preparation of Activated Biocarbons from Cones and their Potential Application for Adsorption of Antibiotics (Tetracycline).

The pine cones (PC), spruce cones (SC) and fir cones (FC) were used for biocarbons preparation. Chemical activation with sodium hydroxide was applied to prepare activated biocarbons. All the materials under investigation were characterized by the N2 adsorption, scanning electron microscopy (SEM), elemental analysis (CHNS), infrared spectroscopy (ATR FT-IR), and the Boehm's titration method. Moreover, pHpzc (the point of zero charge) was determined. It was shown that cones are a good, cheap precursor from which biocarbons with a developed porous structure, characterized by good adsorption properties, can be obtained. All the obtained adsorbents are characterized mainly by a microporous structure. Moreover, they contain both acidic and basic surface functional groups (acidic ones prevail over basic ones). The tested activated biocarbons have large specific surface area values ranging from 578 to 1182 m2 g-1. The efficacy of selected materials in the adsorption of an essential contaminant of increasing concern, tetracycline (TC), was investigated. The experimental data were described using the Langmuir and Freundlich adsorption isotherm models. The maximum adsorption capacity of the tested biocarbons ranges from 200 to 392 mg g-1. Thermodynamic studies proved that adsorption is a spontaneous and endothermic process. In summary, economical and environmentally friendly adsorbents were obtained.

Effect of pyrolysis temperature and hydrothermal activation on structure, physicochemical, thermal and dye adsorption characteristics of the biocarbons.

In this study, the possibility of using sawdust from mixed woods to obtain biocarbons in the pyrolysis and steam activation using microwave radiation as an energy source was investigated. Biocarbons were characterized based on the results of N2 adsorption, thermogravimetric analysis (TGA), Fourier spectroscopy (ATR-FTIR), and Raman spectroscopy. Surface characterization was performed by Boehm titration and pHpzc determination. The adsorption capacity of methylene blue (MB) and methyl orange (MO) was studied. It was proved that the pyrolysis temperature and hydrothermal activation increased the biocarbons structural, surface and adsorption parameters of the obtained biocarbons. The amorphous materials of small specific surface area with a significant share of micropores were obtained. The steam activation resulted in significant development of the porous structure (to SBET =729.2 m2 /g and Vp =0.36 cm3 /g). The presence of functional groups, mainly phenolic ones, and pHpzc values indicating a potential for adsorption applications regarding MO and MB were found. The highest sorption capacity concerning MB (qe =122.8 mg/g) and MO (qe =99.1 mg/g) was observed for the steam-activated biocarbon BC-800MW . Using microwave energy hydrothermal activation proved very efficient, resulting in significant surface area and porosity development with a small loss of carbon matter.

Assessment of the Porous Structure and Surface Chemistry of Activated Biocarbons Used for Methylene Blue Adsorption.

In the presented research, activated carbons from wheat bran were obtained as a result of pyrolysis and physical activation (CO2 or/and steam). In addition, the obtained materials were subjected to additional modification with superheated steam using the microwave radiation as an energy source. The detailed materials characterization was performed using low-temperature nitrogen adsorption/desorption, Raman spectroscopy, X-ray diffraction, thermal analysis (TG), Boehm's titration, point of zero charge (pHpzc), scanning electron microscopy (SEM) and FT-IR/ATR methods. Moreover, the sorption capacity towards methylene blue (MB) was determined. The activated carbons were characterized with a well-developed surface and pore structure (SBET = 339.6-594.0 m2/g; Vp = 0.157-0.356 cm3/g). Activation in the presence of steam and additional modification with microwave radiation resulted in much better development of the porous structure (SBET = 600.4 m2/g; Vp = 0.380 cm3/g). The materials were shown to possess amorphous structure and thermal stability up to the temperatures of ~450-500 °C. They have good adsorption capacity towards MB varying from 150 mg/g to 241 mg/g depending on activation manner. The adsorption can be described by the pseudo-second order model (R2 = 0.99) and fitted to the Langmuir isotherm.

Preparation and Characterization of Physicochemical Properties of Spruce Cone Biochars Activated by CO2.

In this study the pyrolysis of Norway spruce cones, a lignocellulosic biomass was made. The biochar product was obtained by means of the physical activation method. CO2 was used as the activating gas. The surface properties of biochars were characterized by the nitrogen adsorption/desorption isotherms, scanning electron microscopy (SEM/EDS), X-ray fluorescence energy dispersion spectroscopy (ED-XRF), thermal analysis (TGA/DTA), infrared spectroscopy (ATR FT-IR), Raman spectroscopy and the Boehm's titration method as well as the point of zero charge (pHpzc). The adsorption capacity and the possibility of ammonia desorption (TPD) were also examined. It has been shown that spruce cones can be successfully used as a cheap precursor of well-developed surface biochars, characterized by a large pore volume and good sorption properties. All obtained activated biochars exhibit a largely microporous structure and an acidic character surface. The investigated activated materials have the specific surface areas from 112 to 1181 m2 g-1. The maximum NH3 adsorption capacity of the activated biochar was determined to be 5.18 mg g-1 (88.22 mmol g-1) at 0 °C. These results indicate the applicability of spruce cones as a cheap precursor for the sustainable production of the cost-effective and environmentally friendly biochar adsorbent.

Multiple phosphorylation sites on γ-tubulin are essential and contribute to the biogenesis of basal bodies in Tetrahymena.

The mechanisms that regulate γ-tubulin, including its post-translational modifications, are poorly understood. γ-Tubulin is important for the duplication of centrioles and structurally similar basal bodies (BBs), organelles which contain a ring of nine triplet microtubules. The ciliate Tetrahymena thermophila carries hundreds of cilia in a single cell and provides an excellent model to specifically address the role of γ-tubulin in the BBs assembly and maintenance. The genome of Tetrahymena contains a single γ-tubulin gene. We show here that there are multiple isoforms of γ-tubulin that are likely generated by post-translational modifications. We identified evolutionarily conserved serine and threonine residues as potential phosphosites of γ-tubulin, including S80, S129, S131, T283, and S360. Several mutations that either prevent (S80A, S131A, T283A, S360A) or mimic (T283D) phosphorylation were conditionally lethal and at a higher temperature phenocopied a loss of γ-tubulin. Cells that overproduced S360D γ-tubulin displayed phenotypes consistent with defects in the microtubule-dependent functions, including an asymmetric division of the macronucleus and abnormalities in the pattern of BB rows, including gaps, fragmentation, and misalignment. In contrast, overexpression of S129D γ-tubulin affected the orientation, docking, and structure of the BBs, including a loss of either the B- or C-subfibers or the entire triplets. We conclude that conserved potentially phosphorylated amino acids of γ-tubulin are important for either the assembly or stability of BBs.

Modelling and Microstructural Characterization of Sintered Metallic Porous Materials.

This paper presents selected characteristics of the metallic porous materials produced by the sintering of metal powders. The authors focus on materials produced from the iron powder (Fe) of ASC 100.29 and Distaloy SE. ASC 100.29 is formed by atomization and has a characteristic morphology. It consists of spherical particles of different sizes forming agglomerates. Distaloy SE is also based on the sponge-iron. The porous material is prepared using the patented method of sintering the mixture of iron powder ASC 100.29, Fe(III) oxide, Distaloy SE and Fe(III) oxide in the reducing atmosphere of dissociated ammonia. As a result, the materials with open pores of micrometer sizes are obtained. The pores are formed between iron particles bonded by diffusion bridges. The modelling of porous materials containing diffusion bridges that allows for three-dimensional (3D) imaging is presented.

Cell cycle-dependent modulations of fenestrin expression in Tetrahymena pyriformis.

In Tetrahymena, besides apparent cell polarity generated by specialized cortical structures, several proteins display a specific asymmetric distribution suggesting their involvement in the generation and the maintenance of cell polarization. One of these proteins, a membrane skeleton protein called fenestrin, forms an antero-posterior gradient, and is accepted as a marker of cell polarity during different cellular processes, such as cell division or oral replacement. In conjugating cells, fenestrin forms an intracytoplasmic net which participates in pronuclear exchange. The function of fenestrin is still unknown. To better understand the role of fenestrin we characterized this protein in an amicronuclear Tetrahymena pyriformis. We show that in this ciliate not only does fenestrin localization change in a cell division-dependent manner, but its mRNA and protein level is also cell cycle-regulated. We determine that the two available anti-fenestrin antibodies, 3A7 and 9A7, recognize different pools of fenestrin isoforms, and that 9A7 is the more general. In addition, our results indicate that fenestrin is a phosphoprotein. We also show that the level of fenestrin in the amicronuclear T. pyriformis and the amicronuclear BI3840 strain of T. thermophila is several times lower than in micronuclear T. thermophila.