Thermal, spectral, and diffraction properties of Co-exchanged montmorillonite with 2-, 3-, and 4-hydroxyphenol
Abstract The influence of the 2-, 3-, and 4-OH phenols on the type of interaction with Co-exchanged montmorillonite and thermal properties of these materials were studied. The results of XRD, IR, and thermal (TG, DTG) analysis show that organic species are intercalated into the interlayer space of m...
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Gespeichert in:
| Autor*in: |
Janík, R. [verfasserIn] |
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| Format: |
Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2012 |
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| Schlagwörter: |
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| Anmerkung: |
© Akadémiai Kiadó, Budapest, Hungary 2012 |
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| Übergeordnetes Werk: |
Enthalten in: Journal of thermal analysis and calorimetry - Springer Netherlands, 1998, 108(2012), 3 vom: 27. März, Seite 915-919 |
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| Übergeordnetes Werk: |
volume:108 ; year:2012 ; number:3 ; day:27 ; month:03 ; pages:915-919 |
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| DOI / URN: |
10.1007/s10973-012-2364-9 |
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OLC2049811802 |
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| 520 | |a Abstract The influence of the 2-, 3-, and 4-OH phenols on the type of interaction with Co-exchanged montmorillonite and thermal properties of these materials were studied. The results of XRD, IR, and thermal (TG, DTG) analysis show that organic species are intercalated into the interlayer space of montmorillonite. Thermal decomposition in the temperature interval 20–700 °C of studied samples with 2- and 3-hydroxyphenol proceeds in three steps (the release of adsorbed $ H_{2} $O molecules, combustion/desorption of protonated hydroxy phenols and dehydroxylation), while the sample with 4-hydroxyphenol decompose in four steps (the new peak at ~222 °C corresponds to directly coordinated organic species). The effect of different position of the hydroxyl groups on the phenol ring on the thermal decomposition is evident. | ||
| 650 | 4 | |a Co-exchanged montmorillonite | |
| 650 | 4 | |a 2-, 3-, and 4-hydroxyphenols | |
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| 700 | 1 | |a Lizák, P. |4 aut | |
| 700 | 1 | |a Pavlík, V. |4 aut | |
| 700 | 1 | |a Durný, R. |4 aut | |
| 700 | 1 | |a Mojumdar, S. C. |4 aut | |
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10.1007/s10973-012-2364-9 doi (DE-627)OLC2049811802 (DE-He213)s10973-012-2364-9-p DE-627 ger DE-627 rakwb eng 660 VZ Janík, R. verfasserin aut Thermal, spectral, and diffraction properties of Co-exchanged montmorillonite with 2-, 3-, and 4-hydroxyphenol 2012 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Akadémiai Kiadó, Budapest, Hungary 2012 Abstract The influence of the 2-, 3-, and 4-OH phenols on the type of interaction with Co-exchanged montmorillonite and thermal properties of these materials were studied. The results of XRD, IR, and thermal (TG, DTG) analysis show that organic species are intercalated into the interlayer space of montmorillonite. Thermal decomposition in the temperature interval 20–700 °C of studied samples with 2- and 3-hydroxyphenol proceeds in three steps (the release of adsorbed $ H_{2} $O molecules, combustion/desorption of protonated hydroxy phenols and dehydroxylation), while the sample with 4-hydroxyphenol decompose in four steps (the new peak at ~222 °C corresponds to directly coordinated organic species). The effect of different position of the hydroxyl groups on the phenol ring on the thermal decomposition is evident. Co-exchanged montmorillonite 2-, 3-, and 4-hydroxyphenols TG DTG IR-spectroscopy X-ray diffraction Jóna, E. aut Pajtášová, M. aut Ondrušová, D. aut Lizák, P. aut Pavlík, V. aut Durný, R. aut Mojumdar, S. C. aut Enthalten in Journal of thermal analysis and calorimetry Springer Netherlands, 1998 108(2012), 3 vom: 27. März, Seite 915-919 (DE-627)244148767 (DE-600)1429493-X (DE-576)066397693 1388-6150 nnns volume:108 year:2012 number:3 day:27 month:03 pages:915-919 https://doi.org/10.1007/s10973-012-2364-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 AR 108 2012 3 27 03 915-919 |
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10.1007/s10973-012-2364-9 doi (DE-627)OLC2049811802 (DE-He213)s10973-012-2364-9-p DE-627 ger DE-627 rakwb eng 660 VZ Janík, R. verfasserin aut Thermal, spectral, and diffraction properties of Co-exchanged montmorillonite with 2-, 3-, and 4-hydroxyphenol 2012 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Akadémiai Kiadó, Budapest, Hungary 2012 Abstract The influence of the 2-, 3-, and 4-OH phenols on the type of interaction with Co-exchanged montmorillonite and thermal properties of these materials were studied. The results of XRD, IR, and thermal (TG, DTG) analysis show that organic species are intercalated into the interlayer space of montmorillonite. Thermal decomposition in the temperature interval 20–700 °C of studied samples with 2- and 3-hydroxyphenol proceeds in three steps (the release of adsorbed $ H_{2} $O molecules, combustion/desorption of protonated hydroxy phenols and dehydroxylation), while the sample with 4-hydroxyphenol decompose in four steps (the new peak at ~222 °C corresponds to directly coordinated organic species). The effect of different position of the hydroxyl groups on the phenol ring on the thermal decomposition is evident. Co-exchanged montmorillonite 2-, 3-, and 4-hydroxyphenols TG DTG IR-spectroscopy X-ray diffraction Jóna, E. aut Pajtášová, M. aut Ondrušová, D. aut Lizák, P. aut Pavlík, V. aut Durný, R. aut Mojumdar, S. C. aut Enthalten in Journal of thermal analysis and calorimetry Springer Netherlands, 1998 108(2012), 3 vom: 27. März, Seite 915-919 (DE-627)244148767 (DE-600)1429493-X (DE-576)066397693 1388-6150 nnns volume:108 year:2012 number:3 day:27 month:03 pages:915-919 https://doi.org/10.1007/s10973-012-2364-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 AR 108 2012 3 27 03 915-919 |
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10.1007/s10973-012-2364-9 doi (DE-627)OLC2049811802 (DE-He213)s10973-012-2364-9-p DE-627 ger DE-627 rakwb eng 660 VZ Janík, R. verfasserin aut Thermal, spectral, and diffraction properties of Co-exchanged montmorillonite with 2-, 3-, and 4-hydroxyphenol 2012 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Akadémiai Kiadó, Budapest, Hungary 2012 Abstract The influence of the 2-, 3-, and 4-OH phenols on the type of interaction with Co-exchanged montmorillonite and thermal properties of these materials were studied. The results of XRD, IR, and thermal (TG, DTG) analysis show that organic species are intercalated into the interlayer space of montmorillonite. Thermal decomposition in the temperature interval 20–700 °C of studied samples with 2- and 3-hydroxyphenol proceeds in three steps (the release of adsorbed $ H_{2} $O molecules, combustion/desorption of protonated hydroxy phenols and dehydroxylation), while the sample with 4-hydroxyphenol decompose in four steps (the new peak at ~222 °C corresponds to directly coordinated organic species). The effect of different position of the hydroxyl groups on the phenol ring on the thermal decomposition is evident. Co-exchanged montmorillonite 2-, 3-, and 4-hydroxyphenols TG DTG IR-spectroscopy X-ray diffraction Jóna, E. aut Pajtášová, M. aut Ondrušová, D. aut Lizák, P. aut Pavlík, V. aut Durný, R. aut Mojumdar, S. C. aut Enthalten in Journal of thermal analysis and calorimetry Springer Netherlands, 1998 108(2012), 3 vom: 27. März, Seite 915-919 (DE-627)244148767 (DE-600)1429493-X (DE-576)066397693 1388-6150 nnns volume:108 year:2012 number:3 day:27 month:03 pages:915-919 https://doi.org/10.1007/s10973-012-2364-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 AR 108 2012 3 27 03 915-919 |
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10.1007/s10973-012-2364-9 doi (DE-627)OLC2049811802 (DE-He213)s10973-012-2364-9-p DE-627 ger DE-627 rakwb eng 660 VZ Janík, R. verfasserin aut Thermal, spectral, and diffraction properties of Co-exchanged montmorillonite with 2-, 3-, and 4-hydroxyphenol 2012 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Akadémiai Kiadó, Budapest, Hungary 2012 Abstract The influence of the 2-, 3-, and 4-OH phenols on the type of interaction with Co-exchanged montmorillonite and thermal properties of these materials were studied. The results of XRD, IR, and thermal (TG, DTG) analysis show that organic species are intercalated into the interlayer space of montmorillonite. Thermal decomposition in the temperature interval 20–700 °C of studied samples with 2- and 3-hydroxyphenol proceeds in three steps (the release of adsorbed $ H_{2} $O molecules, combustion/desorption of protonated hydroxy phenols and dehydroxylation), while the sample with 4-hydroxyphenol decompose in four steps (the new peak at ~222 °C corresponds to directly coordinated organic species). The effect of different position of the hydroxyl groups on the phenol ring on the thermal decomposition is evident. Co-exchanged montmorillonite 2-, 3-, and 4-hydroxyphenols TG DTG IR-spectroscopy X-ray diffraction Jóna, E. aut Pajtášová, M. aut Ondrušová, D. aut Lizák, P. aut Pavlík, V. aut Durný, R. aut Mojumdar, S. C. aut Enthalten in Journal of thermal analysis and calorimetry Springer Netherlands, 1998 108(2012), 3 vom: 27. März, Seite 915-919 (DE-627)244148767 (DE-600)1429493-X (DE-576)066397693 1388-6150 nnns volume:108 year:2012 number:3 day:27 month:03 pages:915-919 https://doi.org/10.1007/s10973-012-2364-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 AR 108 2012 3 27 03 915-919 |
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10.1007/s10973-012-2364-9 doi (DE-627)OLC2049811802 (DE-He213)s10973-012-2364-9-p DE-627 ger DE-627 rakwb eng 660 VZ Janík, R. verfasserin aut Thermal, spectral, and diffraction properties of Co-exchanged montmorillonite with 2-, 3-, and 4-hydroxyphenol 2012 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Akadémiai Kiadó, Budapest, Hungary 2012 Abstract The influence of the 2-, 3-, and 4-OH phenols on the type of interaction with Co-exchanged montmorillonite and thermal properties of these materials were studied. The results of XRD, IR, and thermal (TG, DTG) analysis show that organic species are intercalated into the interlayer space of montmorillonite. Thermal decomposition in the temperature interval 20–700 °C of studied samples with 2- and 3-hydroxyphenol proceeds in three steps (the release of adsorbed $ H_{2} $O molecules, combustion/desorption of protonated hydroxy phenols and dehydroxylation), while the sample with 4-hydroxyphenol decompose in four steps (the new peak at ~222 °C corresponds to directly coordinated organic species). The effect of different position of the hydroxyl groups on the phenol ring on the thermal decomposition is evident. Co-exchanged montmorillonite 2-, 3-, and 4-hydroxyphenols TG DTG IR-spectroscopy X-ray diffraction Jóna, E. aut Pajtášová, M. aut Ondrušová, D. aut Lizák, P. aut Pavlík, V. aut Durný, R. aut Mojumdar, S. C. aut Enthalten in Journal of thermal analysis and calorimetry Springer Netherlands, 1998 108(2012), 3 vom: 27. März, Seite 915-919 (DE-627)244148767 (DE-600)1429493-X (DE-576)066397693 1388-6150 nnns volume:108 year:2012 number:3 day:27 month:03 pages:915-919 https://doi.org/10.1007/s10973-012-2364-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 AR 108 2012 3 27 03 915-919 |
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Janík, R. Jóna, E. Pajtášová, M. Ondrušová, D. Lizák, P. Pavlík, V. Durný, R. Mojumdar, S. C. |
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Janík, R. |
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10.1007/s10973-012-2364-9 |
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thermal, spectral, and diffraction properties of co-exchanged montmorillonite with 2-, 3-, and 4-hydroxyphenol |
| title_auth |
Thermal, spectral, and diffraction properties of Co-exchanged montmorillonite with 2-, 3-, and 4-hydroxyphenol |
| abstract |
Abstract The influence of the 2-, 3-, and 4-OH phenols on the type of interaction with Co-exchanged montmorillonite and thermal properties of these materials were studied. The results of XRD, IR, and thermal (TG, DTG) analysis show that organic species are intercalated into the interlayer space of montmorillonite. Thermal decomposition in the temperature interval 20–700 °C of studied samples with 2- and 3-hydroxyphenol proceeds in three steps (the release of adsorbed $ H_{2} $O molecules, combustion/desorption of protonated hydroxy phenols and dehydroxylation), while the sample with 4-hydroxyphenol decompose in four steps (the new peak at ~222 °C corresponds to directly coordinated organic species). The effect of different position of the hydroxyl groups on the phenol ring on the thermal decomposition is evident. © Akadémiai Kiadó, Budapest, Hungary 2012 |
| abstractGer |
Abstract The influence of the 2-, 3-, and 4-OH phenols on the type of interaction with Co-exchanged montmorillonite and thermal properties of these materials were studied. The results of XRD, IR, and thermal (TG, DTG) analysis show that organic species are intercalated into the interlayer space of montmorillonite. Thermal decomposition in the temperature interval 20–700 °C of studied samples with 2- and 3-hydroxyphenol proceeds in three steps (the release of adsorbed $ H_{2} $O molecules, combustion/desorption of protonated hydroxy phenols and dehydroxylation), while the sample with 4-hydroxyphenol decompose in four steps (the new peak at ~222 °C corresponds to directly coordinated organic species). The effect of different position of the hydroxyl groups on the phenol ring on the thermal decomposition is evident. © Akadémiai Kiadó, Budapest, Hungary 2012 |
| abstract_unstemmed |
Abstract The influence of the 2-, 3-, and 4-OH phenols on the type of interaction with Co-exchanged montmorillonite and thermal properties of these materials were studied. The results of XRD, IR, and thermal (TG, DTG) analysis show that organic species are intercalated into the interlayer space of montmorillonite. Thermal decomposition in the temperature interval 20–700 °C of studied samples with 2- and 3-hydroxyphenol proceeds in three steps (the release of adsorbed $ H_{2} $O molecules, combustion/desorption of protonated hydroxy phenols and dehydroxylation), while the sample with 4-hydroxyphenol decompose in four steps (the new peak at ~222 °C corresponds to directly coordinated organic species). The effect of different position of the hydroxyl groups on the phenol ring on the thermal decomposition is evident. © Akadémiai Kiadó, Budapest, Hungary 2012 |
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Thermal, spectral, and diffraction properties of Co-exchanged montmorillonite with 2-, 3-, and 4-hydroxyphenol |
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https://doi.org/10.1007/s10973-012-2364-9 |
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Jóna, E. Pajtášová, M. Ondrušová, D. Lizák, P. Pavlík, V. Durný, R. Mojumdar, S. C. |
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Jóna, E. Pajtášová, M. Ondrušová, D. Lizák, P. Pavlík, V. Durný, R. Mojumdar, S. C. |
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