The adsorption process of cadmium ions (Cd), manganese ions (Mn) and lead ions (Pb) onto the spent coffee grounds (SCG) and activated spent coffee grounds (biochar, A-SCG) was investigated. The SCG activation was carried out in the pyrolysis process in a fluidized bed reactor. scanning electron microscope (SEM) with energy dispersive X-ray spectroscopy (EDX), Fourier-transform infrared spectroscopy (FTIR), Brunauer–Emmett–Teller (BET) measurements and CHN analysis were used in order to define the differences between biomaterials. In the study the different mass of materials (0.2–0.5 g) and constant heavy metal volume and concentration (20 cm3/100 ppm) were investigated on the adsorption process. In order to describe the sorption parameters the Langmuir, Freundlich and Temkin isotherms were used. The maximum adsorption for biochar reached 22.3 mg/g for Pb ions, 19.6 mg/g for Mn ions and 19.4 mg/g for Cd ions which were noticeably higher than the results obtained for spent coffee grounds which reached 13.6 mg/g for Pb ions, 13.0 mg/g for Mn ions and 11.0 mg/g for Cd ions. Metal ion adsorption on both SCG and A-SCG was best described by the Langmuir model, thus chemisorption was a dominant type of adsorption. Studying the kinetics of the sorption process, one can see that the process is of a chemical nature according to the best fit of the pseudo-second rate order model. The obtained results show that the chosen sorbents can be used for the removal of cadmium, manganese and lead compounds from aqueous solutions with high efficiency.

This article presents flame retardant compounds for silicone rubber (SR) in the form of polyhedral oligomeric silsequioxanes (POSS), containing both isobutyl groups and amino-propyl (AM-POSS) or chloro-propyl group (HA-POSS) or vinyl groups (OL-POSS). Silsequioxanes were incorporated into the silicone rubber matrix in a quantity of 3 and 6 parts by wt by the method of reactive stirring with the use of a laboratory mixing mill. Based on the analyses performed by TG (Thermogravimetry) FTIR (Fourier Transform Infrared Spectroscopy), conical calorimeter, and SEM-EDX (Scanning Electron Microscopy and Energy Dispersive X-ray Spectroscopy) methods, the thermal degradation mechanism of non-cross-linked and cross-linked silicone rubber has been elucidated. The effects of POSS, and POSS in a synergic system with melamine polyphosphate (MPP), on the thermal properties and flammability of silicone rubber composites were presented. Based on the test results obtained, a mechanism of flame retardant action POSS and POSS-MPP has been proposed. It has been shown that POSS, especially with MPP, considerably increases the thermal stability and decreases the flammability of the SR rubber composites under investigation.

The present article presents unreported yet in the subject literature examinations of the effect of a lignocellulose filler obtained from an alkalized wheat straw treated with di-potassium phosphate on the properties of natural rubber composites. The thermal and mechanical properties as well as the fire hazard of the composites obtained were tested also in the presence of an additive flame-retardant compound (poly(ammonium phosphate)), exploiting the synergism of its action with pentaerythritol, antimony trioxide, aluminum hydroxide and zinc borate. Based on the results obtained by the methods of thermal and mechanical analyses, micro-calorimetry and cone calorimetry, it has been found that the bio-filler increases, especially in the presence of additive flame-retardant, the resistance of the bio-composites tested to the action of fire, without a significant deterioration in their mechanical properties.

Aluminosilicate microspheres are a valuable fraction of coal fly ash with diverse applications due to their low density. Currently, there is no efficient and ecologically rational method of cenosphere recovery from fly ash. A combination of dry methods for the recovery of both fine ash particles and aluminosilicate microspheres from coal fly ash is presented. It is comprised of fluidised bed separation followed by screening and pneumatic separation in a free-fall air chamber. Fluidised bed separation was assisted by a mechanical activator to prevent agglomeration. This step reduced the portion of material that required further treatment by 52–55 wt.%, with the recovery of microspheres exceeding 97%. Then, the concentrates were individually subjected to pneumatic separation. The final separation product for the fly ash containing 0.64 wt.% cenospheres was a cenosphere concentrate that constituted about 17 wt.% of the initial fly ash. The recovery of cenospheres was around 81%. Usage of a combination of dry methods allowed for maintaining almost 83 wt.% of the raw material in its dry form. Furthermore, the produced fly ash grain fractions could be used for different industrial purposes.

This paper presents the results of testing the flammability of silicone rubber composites containing fillers, such as cenospheres, cenospheres covered with iron, attapulgite, wollastonite, aluminum hydroxide and silica. In order to increase the insulating character of boundary layer, boron trioxide was incorporated into the composites of silicone rubber as a ceramization additive. The flammability of the composites was tested with the use of a cone calorimeter. The composition of the gaseous products of thermal decomposition was determined quantitatively and qualitatively in the system with intensive stirring in the fluidal bed, under isothermal conditions at temperatures T = 550, 650 and 750 °C. All the test results show that the fillers used, especially with ceramization additives considerably reduce the fire hazard of silicone rubber composites containing these fillers.

The study presents the investigation results concerning the thermal properties of non-cross-linked and cross-linked silicone rubber with organic peroxide. The rubber was filled with mineral fillers such as cenospheres, including cenospheres covered with iron, attapulgite, wollastonite, aluminum hydroxide and silica. The thermal stability of the silicone rubber was considered from the point of view of the mineral fillers used, particularly taking into account the modern cenospheric filler. Thermal analysis was carried out under both air and a neutral gas at temperatures ranging from 120 to 700 °C. The activation energy value of the silicone rubber destruction was determined with the use of the non-isothermal method of Flynn–Wall–Ozawa.