M. Nazhipkyzy, P. Harris, A. Nurgain, R. Nemkayeva
{"title":"Carbon Nanotubes Synthesized by CCVD Method using Diatomite and Shungite Minerals","authors":"M. Nazhipkyzy, P. Harris, A. Nurgain, R. Nemkayeva","doi":"10.18321/ectj1143","DOIUrl":"https://doi.org/10.18321/ectj1143","url":null,"abstract":"In this work, carbon nanotubes were prepared using catalysts consisting of nickel particles supported on the naturally occurring minerals diatomite and shungite. The carbon source for the chemical catalytic vapour deposition (CCVD) synthesis was a propane-butane gas mixture. The synthesized multiwall carbon nanotubes (MWCNT) were characterized using Raman spectroscopy, transmission and scanning electron microscopy, and the effect of temperature on their structure was investigated. The carbon content was determined by thermogravimetric analysis. In Raman spectra of CNTs the intensity ratio I(G)/I(D) for 650 °C is higher than that for 700 °C and then it begins to increase with increasing temperature. The results show that the diameter of CNTs which were synthesized on the surface of diatomite/shungite samples were in the range of 33–100.3 nm. The development of new methods for creating catalytic systems that allow controlling the structure of carbon particles is an important task leading to the improvement of existing approaches to the synthesis of CNTs with certain functional properties.","PeriodicalId":11795,"journal":{"name":"Eurasian Chemico-Technological Journal","volume":" ","pages":""},"PeriodicalIF":0.5,"publicationDate":"2022-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46848685","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Zh. Koshetova, V. Yu, T. K. Iskakova, N. Zhumanova, K. Beketov, A. Malmakova., K. Praliyev, T. Seilkhanov, K. Berlin
{"title":"Novel 7-Aryliden-3,3a,4,5,6,7-(hexahydro-5-(2-ethoxyethyl)-2-phenyl-3-aryl-2H-pyrazolo[4,3-c]pyridine Hydrochloride: \u0000Synthesis and Structure","authors":"Zh. Koshetova, V. Yu, T. K. Iskakova, N. Zhumanova, K. Beketov, A. Malmakova., K. Praliyev, T. Seilkhanov, K. Berlin","doi":"10.18321/ectj1147","DOIUrl":"https://doi.org/10.18321/ectj1147","url":null,"abstract":"A Claisen-Schmidt type reaction of 1-(2-ethoxyethyl)piperidin-4-one with differ¬ent aromatic aldehydes led to corresponding dienones with a yield of 65‒71%. 7-Arylidene-3,3a,4,5,6,7-(hexahydro-5-(2-ethoxyethyl)-2-phenyl-3-aryl-2H-pyrazolo[4,3-c]pyridines were synthesized by heterocyclization of 3,5-dia¬rylidene-piperidin-4-ones with phenylhydrazine hydrochloride in methanol at 70 °C over 4‒6 h. The X-ray crystal structure determination of 7-(p-methoxy¬benzyliden)-3,3a,4,5,6,7-(hexahydro-5-(2-ethoxyethyl)-2-phenyl-3-(p-methoxy¬phenyl)-2H-pyrazolo[4,3-c]pyridine hydrochloride (the deposition number is CCDC 862410) was completed. The piperidine and pyrazoline rings are close to a chair and envelope conformations, respectively.","PeriodicalId":11795,"journal":{"name":"Eurasian Chemico-Technological Journal","volume":" ","pages":""},"PeriodicalIF":0.5,"publicationDate":"2022-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48616087","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}