The Ba3InGa2O7.5 complex oxide, possessing the perovskite-related structure with structural oxygen vacancies, was first synthesized by the solid state method. The phase was found to be characterized by monoclinic symmetry (sp. gr. P2/c) with the following unit cell parameters: a = 7.942(1) Å, b = 5.868(5) Å, c = 18.201(6) Å, b = 91.52(9). Comprehensive investigations of electrical properties were carried out; ceramic material based on the complex oxide was shown to be a predominantly ionic conductor in the temperature range 450–900 oC. The conductivity is due to oxygen-ion transfer in dry conditions and oxygen-ion and proton transfer in wet atmosphere. The proton conductivity value is 4.5·10–5 S/cm, and the proton transport number is ~50% at 700 oC in wet air; at lower temperatures, proton transport becomes dominant. Prolonged treatment of the sample in water vapors below 450 oC leads to hydrolysis decomposition.
{"title":"Oxygen-ion and proton conductivity in the Ba3InGa2O7.5 complex oxide with incomplete oxygen sublattice","authors":"Nadezhda Kochetova, Veronika Cherepanova, Alyona Pikalova, Artem Gilev","doi":"10.15826/chimtech.2024.11.1.02","DOIUrl":"https://doi.org/10.15826/chimtech.2024.11.1.02","url":null,"abstract":"The Ba3InGa2O7.5 complex oxide, possessing the perovskite-related structure with structural oxygen vacancies, was first synthesized by the solid state method. The phase was found to be characterized by monoclinic symmetry (sp. gr. P2/c) with the following unit cell parameters: a = 7.942(1) Å, b = 5.868(5) Å, c = 18.201(6) Å, b = 91.52(9). Comprehensive investigations of electrical properties were carried out; ceramic material based on the complex oxide was shown to be a predominantly ionic conductor in the temperature range 450–900 oC. The conductivity is due to oxygen-ion transfer in dry conditions and oxygen-ion and proton transfer in wet atmosphere. The proton conductivity value is 4.5·10–5 S/cm, and the proton transport number is ~50% at 700 oC in wet air; at lower temperatures, proton transport becomes dominant. Prolonged treatment of the sample in water vapors below 450 oC leads to hydrolysis decomposition.","PeriodicalId":9964,"journal":{"name":"Chimica Techno Acta","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139617186","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 : 2024-01-16DOI: 10.15826/chimtech.2024.11.1.01
Anatoly Boyandin, L. M. Dvoinina, A. Sukovatyi, A. A. Sukhanova, N. Ertiletskaya
Oligomers of poly-3-hydroxybutyrate (PHB) were prepared by aminolysis of high molecular weight PHB with ethylenediamine and 1,4-diaminobutane. Polymer-oligomer blends (10, 30, and 50% content of the oligomers) were prepared as films by solution casting. As the content of oligomers increased, a gradual increase in the hydrophilicity of the polymer surface was observed, resulting reflected in the water contact angle decrease from 84° to 72–76°. In addition, a moderate decrease in elongation at break, Young's modulus, and tensile strength for the blends were observed as more oligomer was added to the film. Finally, the viability of NIH-3T3 mouse fibroblasts was higher compared to intact PHB when growing in non-prepared polymer/oligomer mixtures. These findings confirm the benefits of the introduction of a hydrophilic functionalized oligomer into the PHB matrix in terms of improving the biocompatibility of the resulting polymer/oligomer blends.
{"title":"Improvement of biocompatibility of high molecular weight poly-3-hydroxybutyrate by blending with its functionalized oligomers","authors":"Anatoly Boyandin, L. M. Dvoinina, A. Sukovatyi, A. A. Sukhanova, N. Ertiletskaya","doi":"10.15826/chimtech.2024.11.1.01","DOIUrl":"https://doi.org/10.15826/chimtech.2024.11.1.01","url":null,"abstract":"Oligomers of poly-3-hydroxybutyrate (PHB) were prepared by aminolysis of high molecular weight PHB with ethylenediamine and 1,4-diaminobutane. Polymer-oligomer blends (10, 30, and 50% content of the oligomers) were prepared as films by solution casting. As the content of oligomers increased, a gradual increase in the hydrophilicity of the polymer surface was observed, resulting reflected in the water contact angle decrease from 84° to 72–76°. In addition, a moderate decrease in elongation at break, Young's modulus, and tensile strength for the blends were observed as more oligomer was added to the film. Finally, the viability of NIH-3T3 mouse fibroblasts was higher compared to intact PHB when growing in non-prepared polymer/oligomer mixtures. These findings confirm the benefits of the introduction of a hydrophilic functionalized oligomer into the PHB matrix in terms of improving the biocompatibility of the resulting polymer/oligomer blends.","PeriodicalId":9964,"journal":{"name":"Chimica Techno Acta","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-01-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139618400","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 : 2023-12-28DOI: 10.15826/chimtech.2023.10.4.17
A. Sharapov, R. Fatykhov, I. Khalymbadzha, D. Kopchuk, I. Nikonov, Anastasiya P. Potapova, Y. Shtaitz, Pavel A. Slepukhin
In this work, we report the synthesis of novel coumarin-bipyridine conjugates using a sequence of C–C coupling reaction between 5,7-dimethoxycoumarins and 3-pyridyl-6-aryl-1,2,4-triazines followed by the Boger reaction with norbornandiene to obtain 8-[2,2'-bipyridyl]-5,7-dimethoxycoumarins. Photophysical properties were investigated for the obtained series of 8-[2,2'-bipyridyl]-5,7-dimethoxycoumarins: absorption and emission wavelength maxima are in the region of 212–296 and 401–410 nm, respectively; Stokes shifts are up to 116 nm, and fluorescence quantum yields are up to 15.0%. It was found that titrating the conjugates with Al3+, Zn2+, and Cd2+ ions results in an increase in the intensity of the emission maxima of the complexes, while the opposite effect was observed in the case of titration with Cu2+ ions. These findings suggest that the studied compounds may be considered as promising chemosensing materials. Finally, a positive solvatochromism of 8-[2,2'-bipyridyl]coumarins and their metal complexes was established. The experimental data are supported by mathematical calculations according to the Lippert-Mataga equation and Kosower diagram.
{"title":"Conjugates of 8-[2,2’-bipyridinyl]coumarins as potential chemosensors for Al3+, Cu2+, Cd2+, Zn2+ ions: synthesis and photophysical properties","authors":"A. Sharapov, R. Fatykhov, I. Khalymbadzha, D. Kopchuk, I. Nikonov, Anastasiya P. Potapova, Y. Shtaitz, Pavel A. Slepukhin","doi":"10.15826/chimtech.2023.10.4.17","DOIUrl":"https://doi.org/10.15826/chimtech.2023.10.4.17","url":null,"abstract":"In this work, we report the synthesis of novel coumarin-bipyridine conjugates using a sequence of C–C coupling reaction between 5,7-dimethoxycoumarins and 3-pyridyl-6-aryl-1,2,4-triazines followed by the Boger reaction with norbornandiene to obtain 8-[2,2'-bipyridyl]-5,7-dimethoxycoumarins. Photophysical properties were investigated for the obtained series of 8-[2,2'-bipyridyl]-5,7-dimethoxycoumarins: absorption and emission wavelength maxima are in the region of 212–296 and 401–410 nm, respectively; Stokes shifts are up to 116 nm, and fluorescence quantum yields are up to 15.0%. It was found that titrating the conjugates with Al3+, Zn2+, and Cd2+ ions results in an increase in the intensity of the emission maxima of the complexes, while the opposite effect was observed in the case of titration with Cu2+ ions. These findings suggest that the studied compounds may be considered as promising chemosensing materials. Finally, a positive solvatochromism of 8-[2,2'-bipyridyl]coumarins and their metal complexes was established. The experimental data are supported by mathematical calculations according to the Lippert-Mataga equation and Kosower diagram.","PeriodicalId":9964,"journal":{"name":"Chimica Techno Acta","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-12-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139152429","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 : 2023-12-28DOI: 10.15826/chimtech.2023.10.4.16
O. Tokarev, V. Volkovich
Gallium and gallium based alloys can be potentially used in pyrochemical and pyroelectrochemical reprocessing of spent nuclear fuels, particularly for separating actinides and rare earth fission products. However, the electrochemical behavior of gallium in high temperature molten salt electrolytes is very little studied. The present work was aimed at investigating the processes taking place during anodic dissolution of gallium in fused alkali chlorides (the ternary 6NaCl–9KCl–5CsCl eutectic mixture) and determining the ratio of gallium chloro-species in different oxidation states formed and remained in the melt. The experiments were performed between 550 and 750 °C, and the anodic current density varied from 0.024 to 0.094 A/cm2. Anodic polarization and coulometry were used, and the results obtained demonstrated that two gallium species, Ga(I) and Ga(III), were formed as a result of gallium anodic dissolution. The ratio between these two oxidation states depended on temperature and anodic current density. The method of processing the experimental data and the calculated values of the ratio of gallium ionic forms in the system under various conditions are presented.
{"title":"Anodic dissolution of gallium in alkali metal chloride melts","authors":"O. Tokarev, V. Volkovich","doi":"10.15826/chimtech.2023.10.4.16","DOIUrl":"https://doi.org/10.15826/chimtech.2023.10.4.16","url":null,"abstract":"Gallium and gallium based alloys can be potentially used in pyrochemical and pyroelectrochemical reprocessing of spent nuclear fuels, particularly for separating actinides and rare earth fission products. However, the electrochemical behavior of gallium in high temperature molten salt electrolytes is very little studied. The present work was aimed at investigating the processes taking place during anodic dissolution of gallium in fused alkali chlorides (the ternary 6NaCl–9KCl–5CsCl eutectic mixture) and determining the ratio of gallium chloro-species in different oxidation states formed and remained in the melt. The experiments were performed between 550 and 750 °C, and the anodic current density varied from 0.024 to 0.094 A/cm2. Anodic polarization and coulometry were used, and the results obtained demonstrated that two gallium species, Ga(I) and Ga(III), were formed as a result of gallium anodic dissolution. The ratio between these two oxidation states depended on temperature and anodic current density. The method of processing the experimental data and the calculated values of the ratio of gallium ionic forms in the system under various conditions are presented.","PeriodicalId":9964,"journal":{"name":"Chimica Techno Acta","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-12-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139152047","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 : 2023-12-15DOI: 10.15826/chimtech.2023.10.4.15
Rita S. Alqubelat, Alena D. Kuznetsova, Denis O. Antonov, Maxim A. Mironov
A new method for assessing the quality of fibre coating based on a combination of fluorescence microscopy and electron paramagnetic resonance is presented in this work. An influence of the carboxymethylcellulose/polyvinylamine gel preparation method on the mobility of the spin label was established. The mobility of the spin label changes from 3.5 ns in the case of a polyvinylamine solution to 12.8 ns in the case of a cross-linked gel on the surface of the glass fibre. A qualitative relationship was found between the mobility of the spin label in the gel applied to the glass fibre and the rate of spreading of crude oil over its surface. This method can be used to make membranes for the separation of water-in-oil emulsions.
{"title":"Combination of fluorescent and spin labels: a powerful method for the optimization of hydrophilic membranes for the separation of oil-in-water emulsions","authors":"Rita S. Alqubelat, Alena D. Kuznetsova, Denis O. Antonov, Maxim A. Mironov","doi":"10.15826/chimtech.2023.10.4.15","DOIUrl":"https://doi.org/10.15826/chimtech.2023.10.4.15","url":null,"abstract":"A new method for assessing the quality of fibre coating based on a combination of fluorescence microscopy and electron paramagnetic resonance is presented in this work. An influence of the carboxymethylcellulose/polyvinylamine gel preparation method on the mobility of the spin label was established. The mobility of the spin label changes from 3.5 ns in the case of a polyvinylamine solution to 12.8 ns in the case of a cross-linked gel on the surface of the glass fibre. A qualitative relationship was found between the mobility of the spin label in the gel applied to the glass fibre and the rate of spreading of crude oil over its surface. This method can be used to make membranes for the separation of water-in-oil emulsions.","PeriodicalId":9964,"journal":{"name":"Chimica Techno Acta","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-12-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139178404","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 : 2023-12-08DOI: 10.15826/chimtech.2023.10.4.14
L. Tarutina, Inna A. Starostina, Gennady Vdovin, Svetlana Pershina, Emma Vovkotrub, Anna Murashkina
Mixed ion-electron conductors (MIECs) are promising materials for air electrodes for protonic ceramic fuel cells (PCFCs) or oxygen permeation membranes. In this work, various aspects of the chemical stability of Co-free MIEC materials, BaCe0.7–xFexZr0.2Y0.1O3–δ, were studied, including their interaction with another functional material (BaCe0.5Zr0.3Y0.1Yb0.1O3–δ-based proton-conducting electrolyte) and gas components (H2O, CO2, and H2). Chemical compatibility studies indicate no visible chemical interaction between the electrode and electrolyte materials even at 1200 °C, which is significantly higher than the operating temperatures (600–800 °C) of PCFCs. The treatments of BaCe0.7–xFexZr0.2Y0.1O3–δ in different atmospheres at 1100 °C, according to the XRD, SEM, IR and Raman spectroscopy data, resulted in the formation of impurity phases. However, their extremely small amounts suggest that they may not form at the operating temperatures. Thus, it can be assumed that the studied materials can be good candidates for various electrochemical applications.
混合离子-电子导体(MIECs)是质子陶瓷燃料电池(pcfc)空气电极或透氧膜的理想材料。在这项工作中，研究了无co MIEC材料BaCe0.7-xFexZr0.2Y0.1O3 -δ的化学稳定性，包括它们与另一种功能材料(BaCe0.5Zr0.3Y0.1Yb0.1O3 -δ基质子导电电解质)和气体组分(H2O, CO2和H2)的相互作用。化学相容性研究表明，即使在1200℃，电极和电解质材料之间也没有明显的化学相互作用，这明显高于pcfc的工作温度(600-800℃)。根据XRD, SEM, IR和Raman光谱数据，在1100℃下不同气氛下处理BaCe0.7-xFexZr0.2Y0.1O3 -δ，导致杂质相的形成。然而，它们的极少量表明它们可能不会在工作温度下形成。因此，可以假设所研究的材料可以成为各种电化学应用的良好候选者。
{"title":"Chemical stability aspects of BaCe0.7–xFexZr0.2Y0.1O3–δ mixed ionic-electronic conductors as promising electrodes for protonic ceramic fuel cells","authors":"L. Tarutina, Inna A. Starostina, Gennady Vdovin, Svetlana Pershina, Emma Vovkotrub, Anna Murashkina","doi":"10.15826/chimtech.2023.10.4.14","DOIUrl":"https://doi.org/10.15826/chimtech.2023.10.4.14","url":null,"abstract":"Mixed ion-electron conductors (MIECs) are promising materials for air electrodes for protonic ceramic fuel cells (PCFCs) or oxygen permeation membranes. In this work, various aspects of the chemical stability of Co-free MIEC materials, BaCe0.7–xFexZr0.2Y0.1O3–δ, were studied, including their interaction with another functional material (BaCe0.5Zr0.3Y0.1Yb0.1O3–δ-based proton-conducting electrolyte) and gas components (H2O, CO2, and H2). Chemical compatibility studies indicate no visible chemical interaction between the electrode and electrolyte materials even at 1200 °C, which is significantly higher than the operating temperatures (600–800 °C) of PCFCs. The treatments of BaCe0.7–xFexZr0.2Y0.1O3–δ in different atmospheres at 1100 °C, according to the XRD, SEM, IR and Raman spectroscopy data, resulted in the formation of impurity phases. However, their extremely small amounts suggest that they may not form at the operating temperatures. Thus, it can be assumed that the studied materials can be good candidates for various electrochemical applications.","PeriodicalId":9964,"journal":{"name":"Chimica Techno Acta","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138588228","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 : 2023-12-07DOI: 10.15826/chimtech.2023.10.4.13
A. Burmatova, A. Khannanov, Liana Zubaidullina, Dmitry Emelianov, Olga Mostovaya, Ivan I. Stoikov, Nikolay Ulakhovich, Marianna Kutyreva
The polyol process is one of the simple, efficient and productive methods for the synthesis of metal loaded polymer composites. Functional properties of metal-polymer nanocomposites are determined by chemical composition, size and morphology of their particles. Finding effective ways to control the nanoparticle's properties during the polyol process is a crucial task. The effect of molar ratio Mn+/OHPEG on the formation of cobalt loaded metal-polymer nanocomposites during a one-pot two-component polyol process by polyethylene glycol with Mr = 4000 g·mol–1 (PEG) was studied. The PEG-based polyol process and the formation of cobalt nanophase were studied at molar ratios νCo2+/νOH(PEG) = 1:1, 1:10, 1:100 and 1:500 using UV-Vis, diffuse reflectance IR and ATR FT-IR spectroscopy, nanoparticle tracking analysis (NTA), dynamic light scattering (DLS). It was found that PEG can act as a reducing agent and stabilizing matrix for the cobalt nanophase at a ratio higher than Mn+/OHPEG= 1:10. The composition and morphology of Co/PEG nanocomposites were determined by XRD and TEM methods. Two types of spheroid particles with average diameters of 88±55 nm / 8±4 nm and 12±3 nm / 3±1 nm, respectively, represent Co/PEG nanocomposites 1:500 and 1:100. Scaly structures with a diameter of 15±5 nm are formed at a molar ratio of νCo2+/νOH(PEG) = 1:10. An increase in the Co2+ content in the PEG-based polyol process leads to the immobilized cobalt nanophase Co3O4 (1:500), Co0/CoO (1:100), CoO (1:10) in PEG. Co/PEG nanocomposites are hemocompatible. The HC50value depends on the composition and morphology of the nanoparticles.
{"title":"Towards controlling the morphology of cobalt loaded nanocomposites in polyol process with polyethylene glycol","authors":"A. Burmatova, A. Khannanov, Liana Zubaidullina, Dmitry Emelianov, Olga Mostovaya, Ivan I. Stoikov, Nikolay Ulakhovich, Marianna Kutyreva","doi":"10.15826/chimtech.2023.10.4.13","DOIUrl":"https://doi.org/10.15826/chimtech.2023.10.4.13","url":null,"abstract":"The polyol process is one of the simple, efficient and productive methods for the synthesis of metal loaded polymer composites. Functional properties of metal-polymer nanocomposites are determined by chemical composition, size and morphology of their particles. Finding effective ways to control the nanoparticle's properties during the polyol process is a crucial task. The effect of molar ratio Mn+/OHPEG on the formation of cobalt loaded metal-polymer nanocomposites during a one-pot two-component polyol process by polyethylene glycol with Mr = 4000 g·mol–1 (PEG) was studied. The PEG-based polyol process and the formation of cobalt nanophase were studied at molar ratios νCo2+/νOH(PEG) = 1:1, 1:10, 1:100 and 1:500 using UV-Vis, diffuse reflectance IR and ATR FT-IR spectroscopy, nanoparticle tracking analysis (NTA), dynamic light scattering (DLS). It was found that PEG can act as a reducing agent and stabilizing matrix for the cobalt nanophase at a ratio higher than Mn+/OHPEG= 1:10. The composition and morphology of Co/PEG nanocomposites were determined by XRD and TEM methods. Two types of spheroid particles with average diameters of 88±55 nm / 8±4 nm and 12±3 nm / 3±1 nm, respectively, represent Co/PEG nanocomposites 1:500 and 1:100. Scaly structures with a diameter of 15±5 nm are formed at a molar ratio of νCo2+/νOH(PEG) = 1:10. An increase in the Co2+ content in the PEG-based polyol process leads to the immobilized cobalt nanophase Co3O4 (1:500), Co0/CoO (1:100), CoO (1:10) in PEG. Co/PEG nanocomposites are hemocompatible. The HC50value depends on the composition and morphology of the nanoparticles.","PeriodicalId":9964,"journal":{"name":"Chimica Techno Acta","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-12-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138592805","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 : 2023-12-06DOI: 10.15826/chimtech.2023.10.4.11
Z. Mikhaylovskaya, A. V. Klimova, Sofia A. Petrova, E. Pankrushina, E. S. Buyanova
CaMoO4- and SrMoO4-based scheelite-type phases are noteworthy functional materials, whose properties strongly correlate with their structure. This work is devoted to La- or Bi-doped scheelite-type molybdates. The purpose of the present study is to quantify the effect of isolated electron pairs of bismuth on the distortion of the structure and related properties. Conventional solid-state technology was used for the synthesis of (Ca/Sr)1–3xLa2xФxMoO4 and Sr1–3xBi2xФxMoO4, (0.025≤ x ≤ 0.275). The structure was investigated by X-ray powder diffraction and Raman spectroscopy. Rates of structure distortion were characterised by the analysis of the autocorrelation function (AAF) of Raman spectra. Energy gaps were calculated by the Kubelka-Munk method. The conductivity was studied with a.c. impedance spectroscopy. For (Ca/Sr)1−3x(Bi/La)2xФxMoO4 series 0.025 ≤ x ≤ 0.15 compositions show a basic defect scheelite structure, while 0.15 x ≤ 0.225 compositions of Bi-doped samples exhibit tetragonal supercells. The chemical compression of unit cell is more evident in the case of Bi-doping, indicating the preferred orientation of the isolated electron pairs. The distortion of MoO4 polyhedra showed by AAF was more significant for Sr1−3xBi2xФxMoO4 than for Sr1−3xLa2xФxMoO4, the Δcorr parameters for Bi-doped compositions were almost double in comparison with La-doped one in the range of 50–600 cm–1 of the Raman shift. The «critical» x = 0.15 point was also clearly indicated by Δcorr parameter. The AAF of the Raman spectra of solid oxides was shown to be a good tool for prediction of properties and points of phase transitions in solid oxides.
{"title":"Comparative characteristic of Bi- and La- doped (Ca/Sr)MoO4 -based materials with a defect scheelite-type structure","authors":"Z. Mikhaylovskaya, A. V. Klimova, Sofia A. Petrova, E. Pankrushina, E. S. Buyanova","doi":"10.15826/chimtech.2023.10.4.11","DOIUrl":"https://doi.org/10.15826/chimtech.2023.10.4.11","url":null,"abstract":"CaMoO4- and SrMoO4-based scheelite-type phases are noteworthy functional materials, whose properties strongly correlate with their structure. This work is devoted to La- or Bi-doped scheelite-type molybdates. The purpose of the present study is to quantify the effect of isolated electron pairs of bismuth on the distortion of the structure and related properties. Conventional solid-state technology was used for the synthesis of (Ca/Sr)1–3xLa2xФxMoO4 and Sr1–3xBi2xФxMoO4, (0.025≤ x ≤ 0.275). The structure was investigated by X-ray powder diffraction and Raman spectroscopy. Rates of structure distortion were characterised by the analysis of the autocorrelation function (AAF) of Raman spectra. Energy gaps were calculated by the Kubelka-Munk method. The conductivity was studied with a.c. impedance spectroscopy. For (Ca/Sr)1−3x(Bi/La)2xФxMoO4 series 0.025 ≤ x ≤ 0.15 compositions show a basic defect scheelite structure, while 0.15 x ≤ 0.225 compositions of Bi-doped samples exhibit tetragonal supercells. The chemical compression of unit cell is more evident in the case of Bi-doping, indicating the preferred orientation of the isolated electron pairs. The distortion of MoO4 polyhedra showed by AAF was more significant for Sr1−3xBi2xФxMoO4 than for Sr1−3xLa2xФxMoO4, the Δcorr parameters for Bi-doped compositions were almost double in comparison with La-doped one in the range of 50–600 cm–1 of the Raman shift. The «critical» x = 0.15 point was also clearly indicated by Δcorr parameter. The AAF of the Raman spectra of solid oxides was shown to be a good tool for prediction of properties and points of phase transitions in solid oxides.","PeriodicalId":9964,"journal":{"name":"Chimica Techno Acta","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138597834","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 : 2023-12-06DOI: 10.15826/chimtech.2023.10.4.12
D. Shurpik, Yulia I. Aleksandrova, Lyaysan I. Makhmutova, Alan Akhmedov, Ivan I. Stoikov
Recently, materials obtained using supramolecular chemistry approaches, and, in particular, spatially preorganized macrocyclic compounds, have attracted close attention of the researchers. Pillar[n]arenes are of special interest due to their tubular spatial structure and macrocyclic cavity. A similar tubular structure is retained in the supramolecular packaging of pillar[5]arene crystals, forming pores. In this study, we developed a block synthetic approach for the preparation of bis-pillar[5]arene containing amide groups. The ability of the synthesized bis-pillar[5]arene to form stable self-associates in solvents of different polarity (CHCl3 and CH3OH) was demonstrated by the DLS method. In trichloromethane at concentration of 1·10–3 M, monodisperse associates with average hydrodynamic diameter of 227 nm (PDI = 0.28) are formed; in methanol, stable associates (1·10–6 M) have an average hydrodynamic diameter of 136 nm (PDI = 0.21). The results obtained can be used to create new supramolecular systems, molecular machines, or capture and detect various organic molecules.
{"title":"Towards nanomaterials with tubular pores: synthesis and self-assembly of bis-pillar[5]arene","authors":"D. Shurpik, Yulia I. Aleksandrova, Lyaysan I. Makhmutova, Alan Akhmedov, Ivan I. Stoikov","doi":"10.15826/chimtech.2023.10.4.12","DOIUrl":"https://doi.org/10.15826/chimtech.2023.10.4.12","url":null,"abstract":"Recently, materials obtained using supramolecular chemistry approaches, and, in particular, spatially preorganized macrocyclic compounds, have attracted close attention of the researchers. Pillar[n]arenes are of special interest due to their tubular spatial structure and macrocyclic cavity. A similar tubular structure is retained in the supramolecular packaging of pillar[5]arene crystals, forming pores. In this study, we developed a block synthetic approach for the preparation of bis-pillar[5]arene containing amide groups. The ability of the synthesized bis-pillar[5]arene to form stable self-associates in solvents of different polarity (CHCl3 and CH3OH) was demonstrated by the DLS method. In trichloromethane at concentration of 1·10–3 M, monodisperse associates with average hydrodynamic diameter of 227 nm (PDI = 0.28) are formed; in methanol, stable associates (1·10–6 M) have an average hydrodynamic diameter of 136 nm (PDI = 0.21). The results obtained can be used to create new supramolecular systems, molecular machines, or capture and detect various organic molecules. ","PeriodicalId":9964,"journal":{"name":"Chimica Techno Acta","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138597561","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 : 2023-11-28DOI: 10.15826/chimtech.2023.10.4.e
Dmitry A. Medvedev
We thank the scientists and experts in various fields represented in Chimica Techno Acta (CTA) for dedicating their time and effort to review the papers that we have sent them. Their assistance ensures that the CTA journal maintains a high-quality peer-review process, which is of paramount importance for the published articles. The CTA editorial office appreciates the contributions of the following reviewers and looks forward to future collaboration.
{"title":"Acknowledgment of Chimica Techno Acta’s reviewers for 2023","authors":"Dmitry A. Medvedev","doi":"10.15826/chimtech.2023.10.4.e","DOIUrl":"https://doi.org/10.15826/chimtech.2023.10.4.e","url":null,"abstract":"We thank the scientists and experts in various fields represented in Chimica Techno Acta (CTA) for dedicating their time and effort to review the papers that we have sent them. Their assistance ensures that the CTA journal maintains a high-quality peer-review process, which is of paramount importance for the published articles. The CTA editorial office appreciates the contributions of the following reviewers and looks forward to future collaboration.","PeriodicalId":9964,"journal":{"name":"Chimica Techno Acta","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2023-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139215378","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}
京公网安备 11010802042870号
京ICP备2023020795号-1
扫码关注我们
求助内容：
应助结果提醒方式：