L. Grishchenko, T. Bezugla, A. Vakaliuk, A. Zaderko, Оleksandr Mischanchuk, T. Zakharova, O. Boldyrieva, V. Diyuk
We proposed the brominated carbon cloth that made of polyacrylonitrile-based activated carbon fibers (PAN-ACFs) as a precursor to chemically and uniformly graft SO3H groups to prepare the solid acid catalyst. The thermal and catalytic properties of the sulfonated PAN-ACFs were examined by IR controlled catalytic measurements and thermal analysis. The catalytic test results showed that the sulfonated surface remarkably improved the operating efficiency in isopropanol dehydration by decreasing the reaction temperature. All PAN-ACFs with grafted SO3H groups prepared through brominated precursors can converse 100% of isopropanol into propylene at moderate temperature. They showed the highest catalytic activity compared to PAN-ACFs sulfonated with oleum and chlorosulfonic acid, which conversed only 40% and 70% of isopropanol into propylene and deactivated at the higher temperatures in the reaction medium.
{"title":"Chemical grafting of sulfo groups onto carbon fibers","authors":"L. Grishchenko, T. Bezugla, A. Vakaliuk, A. Zaderko, Оleksandr Mischanchuk, T. Zakharova, O. Boldyrieva, V. Diyuk","doi":"10.17721/fujcv7i2p40-51","DOIUrl":"https://doi.org/10.17721/fujcv7i2p40-51","url":null,"abstract":"We proposed the brominated carbon cloth that made of polyacrylonitrile-based activated carbon fibers (PAN-ACFs) as a precursor to chemically and uniformly graft SO3H groups to prepare the solid acid catalyst. The thermal and catalytic properties of the sulfonated PAN-ACFs were examined by IR controlled catalytic measurements and thermal analysis. The catalytic test results showed that the sulfonated surface remarkably improved the operating efficiency in isopropanol dehydration by decreasing the reaction temperature. All PAN-ACFs with grafted SO3H groups prepared through brominated precursors can converse 100% of isopropanol into propylene at moderate temperature. They showed the highest catalytic activity compared to PAN-ACFs sulfonated with oleum and chlorosulfonic acid, which conversed only 40% and 70% of isopropanol into propylene and deactivated at the higher temperatures in the reaction medium.","PeriodicalId":42056,"journal":{"name":"French-Ukrainian Journal of Chemistry","volume":" ","pages":""},"PeriodicalIF":0.2,"publicationDate":"2019-12-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47159156","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}
Information on the thermochemical properties may be useful for predicting of the concentration regions of easy glass formation in multicomponent alloys. In present investigation the integral enthalpies of mixing for the Ge–Mn–Gd melts were determined for the entire concentration interval at 1830 K using the Redlich-Kister-Muggianu method. GFT values for binary and ternary alloys of this system were calculated. Size mismatch entropy was estimated within the frameworks of hard spheres model. On the basis of performed calculations the concentration regions in which the melts of the Ge–Mn–Gd system can demonstrate considerable tendency to easy glass formation were suggested.
{"title":"Thermochemical properties and glass forming tendency modeling for the ternary Ge–Mn–Gd melts","authors":"N. Kotova, Natalia Usenko, N. Golovata","doi":"10.17721/fujcv7i2p68-79","DOIUrl":"https://doi.org/10.17721/fujcv7i2p68-79","url":null,"abstract":"Information on the thermochemical properties may be useful for predicting of the concentration regions of easy glass formation in multicomponent alloys. In present investigation the integral enthalpies of mixing for the Ge–Mn–Gd melts were determined for the entire concentration interval at 1830 K using the Redlich-Kister-Muggianu method. GFT values for binary and ternary alloys of this system were calculated. Size mismatch entropy was estimated within the frameworks of hard spheres model. On the basis of performed calculations the concentration regions in which the melts of the Ge–Mn–Gd system can demonstrate considerable tendency to easy glass formation were suggested.","PeriodicalId":42056,"journal":{"name":"French-Ukrainian Journal of Chemistry","volume":" ","pages":""},"PeriodicalIF":0.2,"publicationDate":"2019-12-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48432705","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}
S. Shapovalov, V. Ponomariov, Oryna V. Mosharenkova, Sophia V. Butenko
The association of cationic dye (pinacyanol, PC) with anionic dyes (ethyleosin, EE, or rhodamine 200 C, R200C), and also the interaction “dye+surfactant” has been investigated in aqueous solutions by visible spectroscopy and computer simulation. Cetylpyridinium bromide (CPB), sodium dodecylsulfate (SDS) and triton X-100 (TX) were used as cationic, anionic and non-ionic surfactants respectively. The formation of “dye+surfactant” associates takes place at low dye concentrations (≥10‑6 M) and concentrations of surfactant, which are much smaller than the critical micelle concentrations (CMC). In contrast, similar concentrations (10‑6 – 10‑4 M) of small cations of tetramethylammonium or tetraethylammonium have no noticeable effect on the absorption spectra of the dye in the “dye+tetraalkylammonium salt” systems; it indicates the absence of formation of new compound between the dye and salt. The standard enthalpy of formation of “dye+dye” or “dye+surfactant” associates has been determined by AM1 and PM3 semiempirical methods. The computer simulation confirms that the formation of these associates is energetically beneficial.
{"title":"Studies of the Association of Dyes with Surfactants in Aqueous Solutions: Spectrophotometry and Computer Simulation","authors":"S. Shapovalov, V. Ponomariov, Oryna V. Mosharenkova, Sophia V. Butenko","doi":"10.17721/FUJCV7I2P9-19","DOIUrl":"https://doi.org/10.17721/FUJCV7I2P9-19","url":null,"abstract":"The association of cationic dye (pinacyanol, PC) with anionic dyes (ethyleosin, EE, or rhodamine 200 C, R200C), and also the interaction “dye+surfactant” has been investigated in aqueous solutions by visible spectroscopy and computer simulation. Cetylpyridinium bromide (CPB), sodium dodecylsulfate (SDS) and triton X-100 (TX) were used as cationic, anionic and non-ionic surfactants respectively. The formation of “dye+surfactant” associates takes place at low dye concentrations (≥10‑6 M) and concentrations of surfactant, which are much smaller than the critical micelle concentrations (CMC). In contrast, similar concentrations (10‑6 – 10‑4 M) of small cations of tetramethylammonium or tetraethylammonium have no noticeable effect on the absorption spectra of the dye in the “dye+tetraalkylammonium salt” systems; it indicates the absence of formation of new compound between the dye and salt. The standard enthalpy of formation of “dye+dye” or “dye+surfactant” associates has been determined by AM1 and PM3 semiempirical methods. The computer simulation confirms that the formation of these associates is energetically beneficial.","PeriodicalId":42056,"journal":{"name":"French-Ukrainian Journal of Chemistry","volume":" ","pages":""},"PeriodicalIF":0.2,"publicationDate":"2019-12-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43406372","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}
Pub Date : 2019-12-24DOI: 10.17721/fujcv7i2p96-103
M. Blazheyevskiy, Myhailo Kucher, O. Shpychak
The oxidative derivatization method using diperoxyazelaic acid for the indirect spectrophotometric determination of Perphenazine dihydrochloride is presented. Diperoxyazelaic acid is introduced as a derivatizing agent for Perphenazine, yielding sulfoxides. This reaction product was successfully employed for the spectrophotometric determination of Perphenazine dihydrochloride. The UV spectroscopic detection of sulfoxide has been proven to be the more robust and selective. The method developed allowed determination of Perphenazine dihydrochloride in the concentration range of 1–40 µg/mL. The limits of quantification (LOQ=10S) is 3.3 µg·ml-1. A new spectrophotometric method has been developed, and the possibility of the quantitative determination of Perphenazine dihydrochloride in Perphenazine Tablets has been demonstrated. The present method is precise, accurate and other inactive excipients of the drug do not interfere. RSD = 2.00%; δ=( -µ) 100%/µ = – 0.85 %).
{"title":"The quantitative determination of Perphenazine in tablets by the spectrophotometric method as its sulfoxide obtained with diperoxyazelaic acid","authors":"M. Blazheyevskiy, Myhailo Kucher, O. Shpychak","doi":"10.17721/fujcv7i2p96-103","DOIUrl":"https://doi.org/10.17721/fujcv7i2p96-103","url":null,"abstract":"The oxidative derivatization method using diperoxyazelaic acid for the indirect spectrophotometric determination of Perphenazine dihydrochloride is presented. Diperoxyazelaic acid is introduced as a derivatizing agent for Perphenazine, yielding sulfoxides. This reaction product was successfully employed for the spectrophotometric determination of Perphenazine dihydrochloride. The UV spectroscopic detection of sulfoxide has been proven to be the more robust and selective. The method developed allowed determination of Perphenazine dihydrochloride in the concentration range of 1–40 µg/mL. The limits of quantification (LOQ=10S) is 3.3 µg·ml-1. A new spectrophotometric method has been developed, and the possibility of the quantitative determination of Perphenazine dihydrochloride in Perphenazine Tablets has been demonstrated. The present method is precise, accurate and other inactive excipients of the drug do not interfere. RSD = 2.00%; δ=( -µ) 100%/µ = – 0.85 %).","PeriodicalId":42056,"journal":{"name":"French-Ukrainian Journal of Chemistry","volume":" ","pages":""},"PeriodicalIF":0.2,"publicationDate":"2019-12-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47872120","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}
Pub Date : 2019-12-24DOI: 10.17721/fujcv7i2p145-152
E. Yanovska, O. Nikolaeva, O. Kondratenko, L. Vretik
In situ modification with copolymer of 4-vinylpyridine and styrene (molar ratio 3:1) of natural mineral saponite from deposit Tashkivske(Ukraine) by radical polymerization was carried out. Anchorage of organic polymer 4-vinylpyridine-co- styrene on the mineral surface was proved by IR spectroscopy, mass spectrometry and scanning electron microscopy. The amount of immobilized copolymer in the synthesized composite material according to the thermogravimetric analysis is 8.5 wt.%. The recorded adsorption capacity of the composite with respect to Cu(II), Pb(II) and Fe(III) ions was increased in comparison with native mineral saponite.
{"title":"Sorption properties of saponite clay, in situ modified by poly(4-vinylpyridine-co-styrene), towards Cu(II), Cd(II), Pb(II), Mn(ІІ) and Fe(III) ions","authors":"E. Yanovska, O. Nikolaeva, O. Kondratenko, L. Vretik","doi":"10.17721/fujcv7i2p145-152","DOIUrl":"https://doi.org/10.17721/fujcv7i2p145-152","url":null,"abstract":"In situ modification with copolymer of 4-vinylpyridine and styrene (molar ratio 3:1) of natural mineral saponite from deposit Tashkivske(Ukraine) by radical polymerization was carried out. Anchorage of organic polymer 4-vinylpyridine-co- styrene on the mineral surface was proved by IR spectroscopy, mass spectrometry and scanning electron microscopy. The amount of immobilized copolymer in the synthesized composite material according to the thermogravimetric analysis is 8.5 wt.%. The recorded adsorption capacity of the composite with respect to Cu(II), Pb(II) and Fe(III) ions was increased in comparison with native mineral saponite.","PeriodicalId":42056,"journal":{"name":"French-Ukrainian Journal of Chemistry","volume":" ","pages":""},"PeriodicalIF":0.2,"publicationDate":"2019-12-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48029960","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}
Host-Guest complexation of 5,17-bis-(N-tolyliminomethyl)-25,27-dipropoxycalix[4]arenewithaliphatic dicarboxylicacidsC4 – C10 hasbeenstudiedin water-organic solution by the RP HPLC and molecular modeling methods. The stability constants (log KA =2.56– 3.05) of the supramolecular complexes are depended on structure, pKa and log Pvalues of the acids. The complexation is determined by the hydrogen bonds of the COOH group of the dicarboxylic acids with nitrogen atoms at the upper rim or oxygen atoms at the lower rim of the calixarene.
采用反相高效液相色谱和分子模拟方法研究了5,17-二-(n -聚氨基甲基)-25,27-二丙氧基杯[4]芳烃与脂肪族二羧酸sc4 - C10在水-有机溶液中的主-客络合作用。超分子配合物的稳定性常数(log KA =2.56 ~ 3.05)取决于酸的结构、pKa和log p值。二羧酸的COOH基团的氢键与杯芳烃的上缘氮原子或下缘氧原子的配合作用是决定的。
{"title":"Recognition and Binding of Aliphatic Dicarboxylic Acids C4 – C10 by Diiminocalix[4]arene","authors":"O. Kalchenko, A. Solovyov, V. Kalchenko","doi":"10.17721/fujcv7i2p61-67","DOIUrl":"https://doi.org/10.17721/fujcv7i2p61-67","url":null,"abstract":"Host-Guest complexation of 5,17-bis-(N-tolyliminomethyl)-25,27-dipropoxycalix[4]arenewithaliphatic dicarboxylicacidsC4 – C10 hasbeenstudiedin water-organic solution by the RP HPLC and molecular modeling methods. The stability constants (log KA =2.56– 3.05) of the supramolecular complexes are depended on structure, pKa and log Pvalues of the acids. The complexation is determined by the hydrogen bonds of the COOH group of the dicarboxylic acids with nitrogen atoms at the upper rim or oxygen atoms at the lower rim of the calixarene.","PeriodicalId":42056,"journal":{"name":"French-Ukrainian Journal of Chemistry","volume":" ","pages":""},"PeriodicalIF":0.2,"publicationDate":"2019-12-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43805045","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}
A new the oxidative derivatization method by means of peroxoacid for the indirect spectrophotometric determination of Periciazine is presented. A potassium hydrogenperoxymonosulfateas a derivatizing agent for Periciazine, yielding the absorbative Periciazine sulfoxide at λmaх=362 nm is proposed. This reaction product was successfully employed for spectrophotometric determination of the Periciazine. The UV spectrophotometric determination of the Periciazine as its sulfoxide proved to be the more simple and selective method. Limit of quantification (LOQ=10S) is 2.8 µg·mL-1. The common excipients employed do not interfere in the determination of phenothiazine drug. Results of analysis of the drug dosage forms by the proposed method are in good agreement with those of the official method. RSD=1.76 % (δ
提出了一种新的过氧化物酸氧化衍生法间接光度法测定哌嗪的方法。提出了一种以过氧单硫酸氢钾为衍生剂，在λ max =362 nm处制得吸收性Periciazine亚砜。该反应产物成功地用于分光光度法测定哌嗪。紫外分光光度法测定哌嗪亚砜是一种简便、选择性好的方法。定量限(LOQ=10S)为2.8µg·mL-1。常用赋形剂对吩噻嗪类药物的测定无干扰。该方法与官方方法的分析结果吻合较好。Rsd = 1.76% (δ
{"title":"A new oxidative derivatization method for spectrophotometric determination of Periciazine in pharmaceutical preparations","authors":"M. Blazheyevskiy, V. Moroz","doi":"10.17721/fujcv7i2p52-60","DOIUrl":"https://doi.org/10.17721/fujcv7i2p52-60","url":null,"abstract":"A new the oxidative derivatization method by means of peroxoacid for the indirect spectrophotometric determination of Periciazine is presented. A potassium hydrogenperoxymonosulfateas a derivatizing agent for Periciazine, yielding the absorbative Periciazine sulfoxide at λmaх=362 nm is proposed. This reaction product was successfully employed for spectrophotometric determination of the Periciazine. The UV spectrophotometric determination of the Periciazine as its sulfoxide proved to be the more simple and selective method. Limit of quantification (LOQ=10S) is 2.8 µg·mL-1. The common excipients employed do not interfere in the determination of phenothiazine drug. Results of analysis of the drug dosage forms by the proposed method are in good agreement with those of the official method. RSD=1.76 % (δ","PeriodicalId":42056,"journal":{"name":"French-Ukrainian Journal of Chemistry","volume":"1 1","pages":""},"PeriodicalIF":0.2,"publicationDate":"2019-12-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"67433634","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}
The results of a comparative numerical simulation of combustion and formation of toxic substances in a diesel engine combustion chamber are given. Experimental findings were used to identify the mathematical models. The impact of the standard, RNG and realizable k-ε turbulence models on the accuracy of numerical simulation of combustion and the formation of toxic substances was studied. The realizable k-ε turbulence model was shown to provide a closer agreement of computational and experimental data during simulation of the diesel engine process when turbulent flows are described.
{"title":"Selecting a k-ε turbulence model for investigating n-decane combustion in a diesel engine combustion chamber","authors":"A. Avramenko","doi":"10.17721/fujcv7i2p80-87","DOIUrl":"https://doi.org/10.17721/fujcv7i2p80-87","url":null,"abstract":"The results of a comparative numerical simulation of combustion and formation of toxic substances in a diesel engine combustion chamber are given. Experimental findings were used to identify the mathematical models. The impact of the standard, RNG and realizable k-ε turbulence models on the accuracy of numerical simulation of combustion and the formation of toxic substances was studied. The realizable k-ε turbulence model was shown to provide a closer agreement of computational and experimental data during simulation of the diesel engine process when turbulent flows are described.","PeriodicalId":42056,"journal":{"name":"French-Ukrainian Journal of Chemistry","volume":" ","pages":""},"PeriodicalIF":0.2,"publicationDate":"2019-12-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46869688","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}
Pub Date : 2019-12-24DOI: 10.17721/fujcv7i2p120-137
I. Sokolovskaya, A. Kutsak, V. Zarytska, Valentina Nechiporenko, Natalia Gordiyenko, Yuliia Siliavina, K. Horash, Oleg Plakhotnik
For the first time on the basis of clinical and laboratory researches were revealed the correlation of indicators of lipid metabolism, platelet level of hemostasis and general reactivity in patients with chronic inflammatory processes of the genital system. The new pathogenetic aspects of the course of inflammatory diseases have been established. It has been shown that chronic inflammatory process is accompanied by disorders of lipid metabolism. The degree of severity of these changes depends on the severity of the inflammatory process, the reduction of phagocytic activity of polymorphonuclear leukocytes and the activation of macrophage and specific cellular mechanisms, accompanied by auto-intoxication. It is established that the frequency of atherogenic dyslipoproteinemias, as well as the intensity of lipid peroxidation increases in accordance with the increase age of the examined patients. Most atherogenic dyslipoproteinemias are found in patients with viral and chlamydial infections. The summarized data of the correlation analysis allow us to establish that the growth of atherogenic properties of blood plasma of patients with chronic inflammatory processes of the reproductive system occurs in accordance with the increase of adhesive-aggregation properties of platelets and damage of the vascular endothelium. These shifts occur in parallel with the predominance of the monocyte-macrophage linkage of phagocytosis against the background of reduced activity of neutrophils and cellular mechanisms of development of immunopathological reactions.
{"title":"Investigation of aspects of the interaction of the indicators of lipid exchange, trombocitarian block of hemostasis, total body reactivity and their influence on the psychosomatic harmonization of the man in chronic inflammatory processes","authors":"I. Sokolovskaya, A. Kutsak, V. Zarytska, Valentina Nechiporenko, Natalia Gordiyenko, Yuliia Siliavina, K. Horash, Oleg Plakhotnik","doi":"10.17721/fujcv7i2p120-137","DOIUrl":"https://doi.org/10.17721/fujcv7i2p120-137","url":null,"abstract":"For the first time on the basis of clinical and laboratory researches were revealed the correlation of indicators of lipid metabolism, platelet level of hemostasis and general reactivity in patients with chronic inflammatory processes of the genital system. The new pathogenetic aspects of the course of inflammatory diseases have been established. It has been shown that chronic inflammatory process is accompanied by disorders of lipid metabolism. The degree of severity of these changes depends on the severity of the inflammatory process, the reduction of phagocytic activity of polymorphonuclear leukocytes and the activation of macrophage and specific cellular mechanisms, accompanied by auto-intoxication. It is established that the frequency of atherogenic dyslipoproteinemias, as well as the intensity of lipid peroxidation increases in accordance with the increase age of the examined patients. Most atherogenic dyslipoproteinemias are found in patients with viral and chlamydial infections. The summarized data of the correlation analysis allow us to establish that the growth of atherogenic properties of blood plasma of patients with chronic inflammatory processes of the reproductive system occurs in accordance with the increase of adhesive-aggregation properties of platelets and damage of the vascular endothelium. These shifts occur in parallel with the predominance of the monocyte-macrophage linkage of phagocytosis against the background of reduced activity of neutrophils and cellular mechanisms of development of immunopathological reactions.","PeriodicalId":42056,"journal":{"name":"French-Ukrainian Journal of Chemistry","volume":" ","pages":""},"PeriodicalIF":0.2,"publicationDate":"2019-12-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42686984","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}
O. Ridka, V. Matiychuk, I. Sobechko, N. Tyshchenko, M. Novyk, V. Sergeev, L. Goshko
The enthalpy and the entropy of dissolution of methyl 4-(4-methoxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate in 2-propanol, ethyl acetate, acetonitrile, 2-propanone and benzene were determined from the temperature dependence of its solubility.The enthalpies and the entropies of mixing at 298 K were calculated taking into account the enthalpy of melting of the compound, determined via differential thermal analysis.The influence of the solvent on the solubility of the compound and on the corresponding enthalpy and entropy of mixing values was shown.
{"title":"Thermodynamic properties of methyl 4-(4-methoxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate in organic solutions","authors":"O. Ridka, V. Matiychuk, I. Sobechko, N. Tyshchenko, M. Novyk, V. Sergeev, L. Goshko","doi":"10.17721/fujcv7i2p1-8","DOIUrl":"https://doi.org/10.17721/fujcv7i2p1-8","url":null,"abstract":"The enthalpy and the entropy of dissolution of methyl 4-(4-methoxyphenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate in 2-propanol, ethyl acetate, acetonitrile, 2-propanone and benzene were determined from the temperature dependence of its solubility.The enthalpies and the entropies of mixing at 298 K were calculated taking into account the enthalpy of melting of the compound, determined via differential thermal analysis.The influence of the solvent on the solubility of the compound and on the corresponding enthalpy and entropy of mixing values was shown.","PeriodicalId":42056,"journal":{"name":"French-Ukrainian Journal of Chemistry","volume":" ","pages":""},"PeriodicalIF":0.2,"publicationDate":"2019-12-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46166088","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}
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