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Investigations on foamability of surface-chemically pure aqueous solutions of functionalized alkylaldonamides
The foamability of the aqueous solutions of functionalized, surface-chemically pure surfactants of the nonionic saccharide-type: N , N -di- n-alkylaldonamides, N-alkyl- N-(2-hydroxyethyl)aldonamides, and N-cycloalkylaldonamides, derivatives of D-glucono-1,5-lactone and/or D-glucoheptono-1,4-lactone,...
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Published in: | Journal of colloid and interface science 2006-02, Vol.294 (2), p.423-428 |
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container_title | Journal of colloid and interface science |
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creator | Piłakowska-Pietras, Dorota Lunkenheimer, Klaus Piasecki, Andrzej |
description | The foamability of the aqueous solutions of functionalized, surface-chemically pure surfactants of the nonionic saccharide-type:
N
,
N
-di-
n-alkylaldonamides,
N-alkyl-
N-(2-hydroxyethyl)aldonamides, and
N-cycloalkylaldonamides, derivatives of D-glucono-1,5-lactone and/or D-glucoheptono-1,4-lactone, were investigated. The approach of Lunkenheimer and Małysa for the characterization of the foamability and foam stability of these surfactant solutions was applied for these investigations. Using standard parameters related to the different physical stages of the foaming process, foam stability can be described in a simple and easy manner. In general, the investigated alkylaldonamides form foams of medium stability. However, for some homologues a transition from unstable to stable foam systems is observed with increasing concentration. Modifications of the molecular structure of the alkylaldonamides are distinctly reflected in their foam properties. This fact concerns not only changes of the hydrophobic moiety and its functionalization but also slight variations of the saccharide residue. Each homologous series reveals an exceptional foam behavior. In the case of the
N
,
N
-di-
n-alkylaldonamides the increase of the
n-alkyl chain length is accompanied by an increase of the foam stability. The aqueous solutions of the
N-alkyl-
N-(2-hydroxyethyl)aldonamides reveal most favorable foaming properties for homologues with average alkyl chain lengths. Moreover, it was found that the occurrence of a phase transition in the adsorption layers of the
N-cyclooctylgluconamides previously observed by surface tension and surface potential measurements is also remarkably reflected in their foam stability. |
doi_str_mv | 10.1016/j.jcis.2005.07.053 |
format | article |
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N
,
N
-di-
n-alkylaldonamides,
N-alkyl-
N-(2-hydroxyethyl)aldonamides, and
N-cycloalkylaldonamides, derivatives of D-glucono-1,5-lactone and/or D-glucoheptono-1,4-lactone, were investigated. The approach of Lunkenheimer and Małysa for the characterization of the foamability and foam stability of these surfactant solutions was applied for these investigations. Using standard parameters related to the different physical stages of the foaming process, foam stability can be described in a simple and easy manner. In general, the investigated alkylaldonamides form foams of medium stability. However, for some homologues a transition from unstable to stable foam systems is observed with increasing concentration. Modifications of the molecular structure of the alkylaldonamides are distinctly reflected in their foam properties. This fact concerns not only changes of the hydrophobic moiety and its functionalization but also slight variations of the saccharide residue. Each homologous series reveals an exceptional foam behavior. In the case of the
N
,
N
-di-
n-alkylaldonamides the increase of the
n-alkyl chain length is accompanied by an increase of the foam stability. The aqueous solutions of the
N-alkyl-
N-(2-hydroxyethyl)aldonamides reveal most favorable foaming properties for homologues with average alkyl chain lengths. Moreover, it was found that the occurrence of a phase transition in the adsorption layers of the
N-cyclooctylgluconamides previously observed by surface tension and surface potential measurements is also remarkably reflected in their foam stability.</description><identifier>ISSN: 0021-9797</identifier><identifier>EISSN: 1095-7103</identifier><identifier>DOI: 10.1016/j.jcis.2005.07.053</identifier><identifier>PMID: 16154577</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Aldonamides ; Foamability ; Sugar surfactants</subject><ispartof>Journal of colloid and interface science, 2006-02, Vol.294 (2), p.423-428</ispartof><rights>2005 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c354t-717a5557c0f6b487069d7bc78e0671db3962c04bc7d9b242726925ea6fe5a3153</citedby><cites>FETCH-LOGICAL-c354t-717a5557c0f6b487069d7bc78e0671db3962c04bc7d9b242726925ea6fe5a3153</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16154577$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Piłakowska-Pietras, Dorota</creatorcontrib><creatorcontrib>Lunkenheimer, Klaus</creatorcontrib><creatorcontrib>Piasecki, Andrzej</creatorcontrib><title>Investigations on foamability of surface-chemically pure aqueous solutions of functionalized alkylaldonamides</title><title>Journal of colloid and interface science</title><addtitle>J Colloid Interface Sci</addtitle><description>The foamability of the aqueous solutions of functionalized, surface-chemically pure surfactants of the nonionic saccharide-type:
N
,
N
-di-
n-alkylaldonamides,
N-alkyl-
N-(2-hydroxyethyl)aldonamides, and
N-cycloalkylaldonamides, derivatives of D-glucono-1,5-lactone and/or D-glucoheptono-1,4-lactone, were investigated. The approach of Lunkenheimer and Małysa for the characterization of the foamability and foam stability of these surfactant solutions was applied for these investigations. Using standard parameters related to the different physical stages of the foaming process, foam stability can be described in a simple and easy manner. In general, the investigated alkylaldonamides form foams of medium stability. However, for some homologues a transition from unstable to stable foam systems is observed with increasing concentration. Modifications of the molecular structure of the alkylaldonamides are distinctly reflected in their foam properties. This fact concerns not only changes of the hydrophobic moiety and its functionalization but also slight variations of the saccharide residue. Each homologous series reveals an exceptional foam behavior. In the case of the
N
,
N
-di-
n-alkylaldonamides the increase of the
n-alkyl chain length is accompanied by an increase of the foam stability. The aqueous solutions of the
N-alkyl-
N-(2-hydroxyethyl)aldonamides reveal most favorable foaming properties for homologues with average alkyl chain lengths. Moreover, it was found that the occurrence of a phase transition in the adsorption layers of the
N-cyclooctylgluconamides previously observed by surface tension and surface potential measurements is also remarkably reflected in their foam stability.</description><subject>Aldonamides</subject><subject>Foamability</subject><subject>Sugar surfactants</subject><issn>0021-9797</issn><issn>1095-7103</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNp9kE9r3DAQxUVpaTabfIEcik692R3ZlrWGXEJo_sBCL-1ZyNKo1Ua2tpIdcD99ZXYht5yGGd57vPkRcsOgZMDab4fyoF0qKwBegiiB1x_IhkHHC8Gg_kg2ABUrOtGJC3KZ0gGAMc67z-SCtYw3XIgNGZ7HV0yT-60mF8ZEw0htUIPqnXfTQoOlaY5WaSz0HxycVt4v9DhHpOrvjGFONAU_n72W2nnU66K8-4eGKv-yeOVNPgzOYLoin6zyCa_Pc0t-PXz_ef9U7H88Pt_f7Qtd82bK9YXinAsNtu2bnYC2M6LXYofQCmb6umsrDU2-mK6vmkpUbVdxVK1FrmrG6y35eso9xpBrpkkOLmn0Xo1rZymA7WAHTRZWJ6GOIaWIVh6jG1RcJAO5QpYHuUKWK2QJQmbI2fTlnD73A5o3y5lqFtyeBJh_fHUYZdIOR43GRdSTNMG9l_8fnoiQRA</recordid><startdate>20060215</startdate><enddate>20060215</enddate><creator>Piłakowska-Pietras, Dorota</creator><creator>Lunkenheimer, Klaus</creator><creator>Piasecki, Andrzej</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20060215</creationdate><title>Investigations on foamability of surface-chemically pure aqueous solutions of functionalized alkylaldonamides</title><author>Piłakowska-Pietras, Dorota ; Lunkenheimer, Klaus ; Piasecki, Andrzej</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c354t-717a5557c0f6b487069d7bc78e0671db3962c04bc7d9b242726925ea6fe5a3153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Aldonamides</topic><topic>Foamability</topic><topic>Sugar surfactants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Piłakowska-Pietras, Dorota</creatorcontrib><creatorcontrib>Lunkenheimer, Klaus</creatorcontrib><creatorcontrib>Piasecki, Andrzej</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of colloid and interface science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Piłakowska-Pietras, Dorota</au><au>Lunkenheimer, Klaus</au><au>Piasecki, Andrzej</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Investigations on foamability of surface-chemically pure aqueous solutions of functionalized alkylaldonamides</atitle><jtitle>Journal of colloid and interface science</jtitle><addtitle>J Colloid Interface Sci</addtitle><date>2006-02-15</date><risdate>2006</risdate><volume>294</volume><issue>2</issue><spage>423</spage><epage>428</epage><pages>423-428</pages><issn>0021-9797</issn><eissn>1095-7103</eissn><abstract>The foamability of the aqueous solutions of functionalized, surface-chemically pure surfactants of the nonionic saccharide-type:
N
,
N
-di-
n-alkylaldonamides,
N-alkyl-
N-(2-hydroxyethyl)aldonamides, and
N-cycloalkylaldonamides, derivatives of D-glucono-1,5-lactone and/or D-glucoheptono-1,4-lactone, were investigated. The approach of Lunkenheimer and Małysa for the characterization of the foamability and foam stability of these surfactant solutions was applied for these investigations. Using standard parameters related to the different physical stages of the foaming process, foam stability can be described in a simple and easy manner. In general, the investigated alkylaldonamides form foams of medium stability. However, for some homologues a transition from unstable to stable foam systems is observed with increasing concentration. Modifications of the molecular structure of the alkylaldonamides are distinctly reflected in their foam properties. This fact concerns not only changes of the hydrophobic moiety and its functionalization but also slight variations of the saccharide residue. Each homologous series reveals an exceptional foam behavior. In the case of the
N
,
N
-di-
n-alkylaldonamides the increase of the
n-alkyl chain length is accompanied by an increase of the foam stability. The aqueous solutions of the
N-alkyl-
N-(2-hydroxyethyl)aldonamides reveal most favorable foaming properties for homologues with average alkyl chain lengths. Moreover, it was found that the occurrence of a phase transition in the adsorption layers of the
N-cyclooctylgluconamides previously observed by surface tension and surface potential measurements is also remarkably reflected in their foam stability.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>16154577</pmid><doi>10.1016/j.jcis.2005.07.053</doi><tpages>6</tpages></addata></record> |
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issn | 0021-9797 1095-7103 |
language | eng |
recordid | cdi_proquest_miscellaneous_70180804 |
source | Elsevier:Jisc Collections:Elsevier Read and Publish Agreement 2022-2024:Freedom Collection (Reading list) |
subjects | Aldonamides Foamability Sugar surfactants |
title | Investigations on foamability of surface-chemically pure aqueous solutions of functionalized alkylaldonamides |
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