The quality of materials used in nuclear-related facilities is critical, especially the ease of decontamination of different paints and coatings. Standards describe different testing methods for classification. Nevertheless, compliance with these standards cannot be carried out negligibly from a safety point of view. In this study, a withdrawn Hungarian , an international ISO (ISO 8690:1988), and Russian (GOST 25146-82) decontamination standard were compared. Four different paints were tested as part of this survey. The ease of decontamination varied mainly from poor to fair levels in the case of the Hungarian standard, while the ISO standard exhibited very good level. In the case of the Russian standard, only a theoretical comparison was carried out. Based on the results, it was found that a special epoxy-based coating can be recommended for isotope laboratories due to being the best material from an ease of decontamination point of view. From comparison of the standards considered here, it was found that the application of ISO standard is significantly faster and simpler than the withdrawn Hungarian standard. However, in the case of the Hungarian standard the data described the ease of decontamination in more details. The use of water or some other cleaning agents can be effective to remove 137 Cs and 60 Co contamination right after early identification. Isotope 137 Cs and 60 Co contamination of a surface can be cleaned quickly and effectively using distilled water for the 137 Cs isotope removal from the surfaces being several times easier than that of 60 Co.
Natural zeolite clinoptilolite CLIN with a framework ratio of Si/Al ≥ 4 containing mainly potassium and calcium ions in its internal channel system was used as a starting material. The acidic HCLIN catalysts were prepared under soft conditions avoiding the use of environmental less-benign mineral acids. The starting material was ion exchanged using a 0.2 M aqueous ammonium nitrate solution at a temperature 80 °C for 2 h. The obtained NH4CLIN was converted into the acid HCLIN catalyst by calcination at 300–600 °C. The obtained samples were characterized by XRD, FTIR, SEM/TEM, AAS, and EDX element mapping. The state of aluminium and silicon was studied by 27Al- and 29SiMAS NMR spectroscopy. The textural properties of the catalysts were investigated by nitrogen adsorption and desorption measurements. The Brønsted acidity of the HCLIN catalysts was studied by temperature-programmed decomposition of the exchanged ammonium ions releasing ammonia as well as 1H MAS NMR, {1H–27Al} Trapdor, and {1H–27Al} Redor experiments. The strongly agglomerated samples were crystalline and thermally stable up to >500 °C. Although a part of the clinoptilolite framework is maintained up to 600 °C, a loss of crystallinity is already observed starting from 450 °C. The specific surface areas of the starting CLIN and ammonium exchanged NH4CLIN are low with ca. 26 m2/g. The pores are nearly blocked by the exchangeable cations located in the zeolite pores. The thermal decomposition of the ammonium ions by calcination at 400 °C causes an opening of the pore entrances and a markable increase in the specific micropore area and micropore volume to ca. 163 m2/g and 0.07 cm3/g, respectively. It decreases with further rising calcination temperature indicating some structural loss. The catalysts show a broad distribution of Brønsted acid sites (BS) ranging from weak to strong sites as indicated the thermal decomposition of exchanged ammonium ions (TPDA). The ammonium ion decomposition leaving BS, i.e., H+ located at Al–O–Si framework bridges, starts at ≥250 °C. A part of the Brønsted sites is lost after calcination specifically at 500 °C. It is related to the formation of penta-coordinated aluminium at the expense of tetrahedral framework aluminium. The Brønsted sites are partially recreated after repeated ammonium ion exchange. The catalytic performance of the acidic HCLIN catalysts was tested in the etherification of glycerol as a green renewable resource with different C1-C4 alcohols. The catalysts are highly active in the etherification of glycerol, especially with alcohols containing the branched, tertiary alkyl groups. Highest activity is observed with the soft activated catalyst HCLIN300 (300 °C, temperature holding time: 1 min). A total of 78% conversion of glycerol to mono and di ether were achieved with tert-butanol at 140 °C after 4 h of reaction. The mono- and di-ether selectivity were 75% and 25%, respectively. The catalyst can be reused.
Cenozoic basalt regions contain various natural resources that can be used for socio-economic development. Different quantitative and qualitative methods have been applied to understand the geological and geomorphological characteristics of basalt formations. Nowadays the integration of remote sensing and geographic information systems (GIS) has become a powerful method to distinguish geological formations. In this paper, authors combined satellite and fieldwork data to analyze the structure and morphology of highland geological formations in order to distinguish two main volcanic eruption episodes. Based on remote sensing analysis in this study, different spectral band ratios were generated to select the best one for basalt classification. Lastly, two spectral combinations (including band ratios 4/3, 6/2, 7/4 in Landsat 8 and 3/2, 5/1, 7/3 in Landsat 7) were chosen for the Maximum Likelihood classification. The final geological map based on the integration of Landsat 7 and 8 outcomes shows precisely the boundary of the basalt formations with the accuracy up to 93.7%. This outcome contributed significantly to the correction of geological maps. In further studies, authors suggest the integration of Landsat 7 and 8 data in geological studies and natural resource and environmental management at both local and regional scales.
ZSM-5/SBA-15 composite materials with different acidities and mesoporous system formations were successfully synthesized by three-step method. The catalysts were characterized by XRD, HR-TEM, BET, EDX and TPD-NH3 methods. It showed that the Si/Al molar ratio had effect on the formation and property of materials. Among synthesized catalysts with the different Si/Al molar ratios of 30 (HZSC-30), 50 (HZSC-50), 70 (HZSC-70), HZSC-50 catalyst had better mesoporous system formation and acidity. These properties helped this catalyst to have higher catalytic activity in 1,3,5-triisopropylbenzene cracking reaction than other studied catalysts in term of higher benzene product yield. In comparison to HZSM-5 microporous material that had the similar Si/Al molar ratio of 50, it showed that the formation of mesopore system of HZSC-50 catalyst had a major improvement on the cracking catalytic activity.
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