Monomer and amino resin modified tall oil fatty acid alkyds
Summary Monomer modified tall oil fatty acid trimethylolethane medium type of phthalic alkyds made by the High Polymer Alkyd Technique show improved properties in dry time, mar resistance, and flexibility as compared with monomer modified conventional prepared systems. Greater hardness, less color d...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Kraft, William M. [verfasserIn] |
|---|
| Format: |
Artikel |
|---|---|
| Sprache: |
Englisch |
| Erschienen: |
1959 |
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| Schlagwörter: |
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| Anmerkung: |
© The American Oil Chemists' Society 1959 |
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| Übergeordnetes Werk: |
Enthalten in: Journal of the American Oil Chemists Society - Springer-Verlag, 1947, 36(1959), 4 vom: Apr., Seite 164-166 |
|---|---|
| Übergeordnetes Werk: |
volume:36 ; year:1959 ; number:4 ; month:04 ; pages:164-166 |
| Links: |
|---|
| DOI / URN: |
10.1007/BF02636967 |
|---|
| Katalog-ID: |
OLC2067998684 |
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| 520 | |a Summary Monomer modified tall oil fatty acid trimethylolethane medium type of phthalic alkyds made by the High Polymer Alkyd Technique show improved properties in dry time, mar resistance, and flexibility as compared with monomer modified conventional prepared systems. Greater hardness, less color degradation, greater resistance to extended periods at high temperature, and alkali and detergent resistances result from the urea and melamine resin modifications of tall oil fatty acid High Polymer alkyds than is obtained with similarly modified conventional alkyds. | ||
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10.1007/BF02636967 doi (DE-627)OLC2067998684 (DE-He213)BF02636967-p DE-627 ger DE-627 rakwb eng 660 VZ Kraft, William M. verfasserin aut Monomer and amino resin modified tall oil fatty acid alkyds 1959 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © The American Oil Chemists' Society 1959 Summary Monomer modified tall oil fatty acid trimethylolethane medium type of phthalic alkyds made by the High Polymer Alkyd Technique show improved properties in dry time, mar resistance, and flexibility as compared with monomer modified conventional prepared systems. Greater hardness, less color degradation, greater resistance to extended periods at high temperature, and alkali and detergent resistances result from the urea and melamine resin modifications of tall oil fatty acid High Polymer alkyds than is obtained with similarly modified conventional alkyds. Alkyd Resin Urea Formaldehyde Resin Enoic Acid Initial Esterification Amino Resin Forschirm, Alex aut Enthalten in Journal of the American Oil Chemists Society Springer-Verlag, 1947 36(1959), 4 vom: Apr., Seite 164-166 (DE-627)129595691 (DE-600)240684-6 (DE-576)015088715 0003-021X nnns volume:36 year:1959 number:4 month:04 pages:164-166 https://doi.org/10.1007/BF02636967 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_11 GBV_ILN_70 GBV_ILN_74 GBV_ILN_4012 GBV_ILN_4036 GBV_ILN_4046 GBV_ILN_4082 GBV_ILN_4315 AR 36 1959 4 04 164-166 |
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10.1007/BF02636967 doi (DE-627)OLC2067998684 (DE-He213)BF02636967-p DE-627 ger DE-627 rakwb eng 660 VZ Kraft, William M. verfasserin aut Monomer and amino resin modified tall oil fatty acid alkyds 1959 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © The American Oil Chemists' Society 1959 Summary Monomer modified tall oil fatty acid trimethylolethane medium type of phthalic alkyds made by the High Polymer Alkyd Technique show improved properties in dry time, mar resistance, and flexibility as compared with monomer modified conventional prepared systems. Greater hardness, less color degradation, greater resistance to extended periods at high temperature, and alkali and detergent resistances result from the urea and melamine resin modifications of tall oil fatty acid High Polymer alkyds than is obtained with similarly modified conventional alkyds. Alkyd Resin Urea Formaldehyde Resin Enoic Acid Initial Esterification Amino Resin Forschirm, Alex aut Enthalten in Journal of the American Oil Chemists Society Springer-Verlag, 1947 36(1959), 4 vom: Apr., Seite 164-166 (DE-627)129595691 (DE-600)240684-6 (DE-576)015088715 0003-021X nnns volume:36 year:1959 number:4 month:04 pages:164-166 https://doi.org/10.1007/BF02636967 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_11 GBV_ILN_70 GBV_ILN_74 GBV_ILN_4012 GBV_ILN_4036 GBV_ILN_4046 GBV_ILN_4082 GBV_ILN_4315 AR 36 1959 4 04 164-166 |
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10.1007/BF02636967 doi (DE-627)OLC2067998684 (DE-He213)BF02636967-p DE-627 ger DE-627 rakwb eng 660 VZ Kraft, William M. verfasserin aut Monomer and amino resin modified tall oil fatty acid alkyds 1959 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © The American Oil Chemists' Society 1959 Summary Monomer modified tall oil fatty acid trimethylolethane medium type of phthalic alkyds made by the High Polymer Alkyd Technique show improved properties in dry time, mar resistance, and flexibility as compared with monomer modified conventional prepared systems. Greater hardness, less color degradation, greater resistance to extended periods at high temperature, and alkali and detergent resistances result from the urea and melamine resin modifications of tall oil fatty acid High Polymer alkyds than is obtained with similarly modified conventional alkyds. Alkyd Resin Urea Formaldehyde Resin Enoic Acid Initial Esterification Amino Resin Forschirm, Alex aut Enthalten in Journal of the American Oil Chemists Society Springer-Verlag, 1947 36(1959), 4 vom: Apr., Seite 164-166 (DE-627)129595691 (DE-600)240684-6 (DE-576)015088715 0003-021X nnns volume:36 year:1959 number:4 month:04 pages:164-166 https://doi.org/10.1007/BF02636967 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_11 GBV_ILN_70 GBV_ILN_74 GBV_ILN_4012 GBV_ILN_4036 GBV_ILN_4046 GBV_ILN_4082 GBV_ILN_4315 AR 36 1959 4 04 164-166 |
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10.1007/BF02636967 doi (DE-627)OLC2067998684 (DE-He213)BF02636967-p DE-627 ger DE-627 rakwb eng 660 VZ Kraft, William M. verfasserin aut Monomer and amino resin modified tall oil fatty acid alkyds 1959 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © The American Oil Chemists' Society 1959 Summary Monomer modified tall oil fatty acid trimethylolethane medium type of phthalic alkyds made by the High Polymer Alkyd Technique show improved properties in dry time, mar resistance, and flexibility as compared with monomer modified conventional prepared systems. Greater hardness, less color degradation, greater resistance to extended periods at high temperature, and alkali and detergent resistances result from the urea and melamine resin modifications of tall oil fatty acid High Polymer alkyds than is obtained with similarly modified conventional alkyds. Alkyd Resin Urea Formaldehyde Resin Enoic Acid Initial Esterification Amino Resin Forschirm, Alex aut Enthalten in Journal of the American Oil Chemists Society Springer-Verlag, 1947 36(1959), 4 vom: Apr., Seite 164-166 (DE-627)129595691 (DE-600)240684-6 (DE-576)015088715 0003-021X nnns volume:36 year:1959 number:4 month:04 pages:164-166 https://doi.org/10.1007/BF02636967 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_11 GBV_ILN_70 GBV_ILN_74 GBV_ILN_4012 GBV_ILN_4036 GBV_ILN_4046 GBV_ILN_4082 GBV_ILN_4315 AR 36 1959 4 04 164-166 |
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10.1007/BF02636967 doi (DE-627)OLC2067998684 (DE-He213)BF02636967-p DE-627 ger DE-627 rakwb eng 660 VZ Kraft, William M. verfasserin aut Monomer and amino resin modified tall oil fatty acid alkyds 1959 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © The American Oil Chemists' Society 1959 Summary Monomer modified tall oil fatty acid trimethylolethane medium type of phthalic alkyds made by the High Polymer Alkyd Technique show improved properties in dry time, mar resistance, and flexibility as compared with monomer modified conventional prepared systems. Greater hardness, less color degradation, greater resistance to extended periods at high temperature, and alkali and detergent resistances result from the urea and melamine resin modifications of tall oil fatty acid High Polymer alkyds than is obtained with similarly modified conventional alkyds. Alkyd Resin Urea Formaldehyde Resin Enoic Acid Initial Esterification Amino Resin Forschirm, Alex aut Enthalten in Journal of the American Oil Chemists Society Springer-Verlag, 1947 36(1959), 4 vom: Apr., Seite 164-166 (DE-627)129595691 (DE-600)240684-6 (DE-576)015088715 0003-021X nnns volume:36 year:1959 number:4 month:04 pages:164-166 https://doi.org/10.1007/BF02636967 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE SSG-OLC-PHA SSG-OLC-DE-84 GBV_ILN_11 GBV_ILN_70 GBV_ILN_74 GBV_ILN_4012 GBV_ILN_4036 GBV_ILN_4046 GBV_ILN_4082 GBV_ILN_4315 AR 36 1959 4 04 164-166 |
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Kraft, William M. |
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Summary Monomer modified tall oil fatty acid trimethylolethane medium type of phthalic alkyds made by the High Polymer Alkyd Technique show improved properties in dry time, mar resistance, and flexibility as compared with monomer modified conventional prepared systems. Greater hardness, less color degradation, greater resistance to extended periods at high temperature, and alkali and detergent resistances result from the urea and melamine resin modifications of tall oil fatty acid High Polymer alkyds than is obtained with similarly modified conventional alkyds. © The American Oil Chemists' Society 1959 |
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Summary Monomer modified tall oil fatty acid trimethylolethane medium type of phthalic alkyds made by the High Polymer Alkyd Technique show improved properties in dry time, mar resistance, and flexibility as compared with monomer modified conventional prepared systems. Greater hardness, less color degradation, greater resistance to extended periods at high temperature, and alkali and detergent resistances result from the urea and melamine resin modifications of tall oil fatty acid High Polymer alkyds than is obtained with similarly modified conventional alkyds. © The American Oil Chemists' Society 1959 |
| abstract_unstemmed |
Summary Monomer modified tall oil fatty acid trimethylolethane medium type of phthalic alkyds made by the High Polymer Alkyd Technique show improved properties in dry time, mar resistance, and flexibility as compared with monomer modified conventional prepared systems. Greater hardness, less color degradation, greater resistance to extended periods at high temperature, and alkali and detergent resistances result from the urea and melamine resin modifications of tall oil fatty acid High Polymer alkyds than is obtained with similarly modified conventional alkyds. © The American Oil Chemists' Society 1959 |
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Greater hardness, less color degradation, greater resistance to extended periods at high temperature, and alkali and detergent resistances result from the urea and melamine resin modifications of tall oil fatty acid High Polymer alkyds than is obtained with similarly modified conventional alkyds.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Alkyd Resin</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Urea Formaldehyde Resin</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Enoic Acid</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Initial Esterification</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Amino Resin</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Forschirm, Alex</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">Journal of the American Oil Chemists Society</subfield><subfield code="d">Springer-Verlag, 1947</subfield><subfield code="g">36(1959), 4 vom: Apr., Seite 164-166</subfield><subfield code="w">(DE-627)129595691</subfield><subfield code="w">(DE-600)240684-6</subfield><subfield code="w">(DE-576)015088715</subfield><subfield code="x">0003-021X</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:36</subfield><subfield code="g">year:1959</subfield><subfield code="g">number:4</subfield><subfield code="g">month:04</subfield><subfield code="g">pages:164-166</subfield></datafield><datafield tag="856" ind1="4" ind2="1"><subfield code="u">https://doi.org/10.1007/BF02636967</subfield><subfield code="z">lizenzpflichtig</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_OLC</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-TEC</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-CHE</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-PHA</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-DE-84</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_11</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_70</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_74</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4012</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4036</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4046</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4082</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4315</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">36</subfield><subfield code="j">1959</subfield><subfield code="e">4</subfield><subfield code="c">04</subfield><subfield code="h">164-166</subfield></datafield></record></collection>
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