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Title: Acid-catalyzed time-efficient synthesis of resorcinol-formaldehyde aerogels and crosslinking with isocyanates
Author (s): Leventis, Nicholas
Sotiriou-Leventis, Lia
Mulik, Sudhir
Department/Lab Affiliations: Chemistry
Keywords: Na2CO3
base-catalyzed RF aerogels
poly-condensation
supercritical fluid
Issue Date: 2006
Publisher: American Chemical Society PREPRINTS
Citation: Leventis, Nicholas; Sotiriou-Leventis, Chariklia Sudhir Mulik Acid-Catalyzed Time-Efficient Synthesis of Resorcinol-Formaldehyde Aerogels and Crosslinking with Isocyanates, Polymer Preprints , Vol. 47(2), 2006, pp. 364-365, 2006.
Abstract: Aerogels are open-cell foams derived from supercritical fluid (SCF) drying of wet gels. Their large internal void space is responsible for low thermal conductivity, high surface area and high acoustic impedance. Most aerogels are based on inorganic metal or semimetal oxide frameworks. Pekala and co-workers1-4 synthesized resorcinol-formaldehyde (RF) organic aerogels by poly-condensation of resorcinol with formaldehyde in the presence of Na2CO3 as base catalyst, followed by drying with SCF CO2. Low-density RF aerogels prepared by this method exhibit high porosities (>80%), high surface areas (400-900 m2g-1), ultrafine cell-size (<500 Å) and densities as low as 0.03 g cm-3. The major drawback though, has been the length of the preparation procedure that typically spans several days. Looking at the mechanism of the process, the RF gel formation has been associated with two major reactions: (1) formation of hydroxymethyl derivatives of resorcinol; and, (2) condensation of those derivatives to methylene (-CH2-) and methylene ether (-CH2-O-CH2-) bridges. The effect of the resorcinol to catalyst (R/C) ratio on the final aerogel structure has been studied extensively. That ratio was typically varied in the range between 50- 300. Formation of particles connected with large necks was reported for low and for very high (~1500) R/C ratios.5-7 The final pore structure and the gelation time depend strongly on the sol pH;8 at low pHs, precipitation rather than gelation was reported. The extensive literature on base-catalyzed RF aerogels has obscured attempts towards acid-catalyzed processing.9-13 Recently, Brandt and Fricke reported an aqueous acetic acid catalyzed route for RF gel synthesis, where they still allowed a two-day period for gelation and aging.10 Reasoning that not only hydroxy methylation of resorcinol, but also subsequent condensation to methylene and methylene ether bridges should be all acid-catalyzed processes, we undertook a systematic look at the reaction of resorcinol with formaldehyde in CH3CN, developing a time-efficient method that yields within a few hours (as opposed to weeks) gels indistinguishable from those reported in the literature. The -OH groups of resorcinol in the resulting gels are reactive with di- and tri-isocyanate crosslinkers in analogy to silica, leading to isocyanate-derived polymer crosslinked RF aerogels, which are more robust, and more resistive to shrinkage than their native (noncrosslinked) counterparts.
Type: Article - Journal
text
In Title: Polymer Preprints
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titleAcid-catalyzed time-efficient synthesis of resorcinol-formaldehyde aerogels and crosslinking with isocyanates
contributor.authorLeventis, Nicholas
contributor.authorSotiriou-Leventis, Lia
contributor.authorMulik, Sudhir
contributor.deptlabChemistry
subjectNa2CO3
subjectbase-catalyzed RF aerogels
subjectpoly-condensation
subjectsupercritical fluid
date.issued2006
publisherAmerican Chemical Society PREPRINTS
identifier.citationLeventis, Nicholas; Sotiriou-Leventis, Chariklia Sudhir Mulik Acid-Catalyzed Time-Efficient Synthesis of Resorcinol-Formaldehyde Aerogels and Crosslinking with Isocyanates, Polymer Preprints , Vol. 47(2), 2006, pp. 364-365, 2006.
identifier.pub.URI
http://www.polyacs.org/main/preprintsonline.shtml
description.abstractAerogels are open-cell foams derived from supercritical fluid (SCF) drying of wet gels. Their large internal void space is responsible for low thermal conductivity, high surface area and high acoustic impedance. Most aerogels are based on inorganic metal or semimetal oxide frameworks. Pekala and co-workers1-4 synthesized resorcinol-formaldehyde (RF) organic aerogels by poly-condensation of resorcinol with formaldehyde in the presence of Na2CO3 as base catalyst, followed by drying with SCF CO2. Low-density RF aerogels prepared by this method exhibit high porosities (>80%), high surface areas (400-900 m2g-1), ultrafine cell-size (<500 Å) and densities as low as 0.03 g cm-3. The major drawback though, has been the length of the preparation procedure that typically spans several days. Looking at the mechanism of the process, the RF gel formation has been associated with two major reactions: (1) formation of hydroxymethyl derivatives of resorcinol; and, (2) condensation of those derivatives to methylene (-CH2-) and methylene ether (-CH2-O-CH2-) bridges. The effect of the resorcinol to catalyst (R/C) ratio on the final aerogel structure has been studied extensively. That ratio was typically varied in the range between 50- 300. Formation of particles connected with large necks was reported for low and for very high (~1500) R/C ratios.5-7 The final pore structure and the gelation time depend strongly on the sol pH;8 at low pHs, precipitation rather than gelation was reported. The extensive literature on base-catalyzed RF aerogels has obscured attempts towards acid-catalyzed processing.9-13 Recently, Brandt and Fricke reported an aqueous acetic acid catalyzed route for RF gel synthesis, where they still allowed a two-day period for gelation and aging.10 Reasoning that not only hydroxy methylation of resorcinol, but also subsequent condensation to methylene and methylene ether bridges should be all acid-catalyzed processes, we undertook a systematic look at the reaction of resorcinol with formaldehyde in CH3CN, developing a time-efficient method that yields within a few hours (as opposed to weeks) gels indistinguishable from those reported in the literature. The -OH groups of resorcinol in the resulting gels are reactive with di- and tri-isocyanate crosslinkers in analogy to silica, leading to isocyanate-derived polymer crosslinked RF aerogels, which are more robust, and more resistive to shrinkage than their native (noncrosslinked) counterparts.
typeArticle - Journal
type.DCMITypetext
rightsThis material is presented to ensure timely dissemination of scholarly and technical work. Copyright and all rights therein are retained by authors or by other copyright holders. All persons copying this information are expected to adhere to the terms and constraints invoked by each author's copyright. In most cases, these works may not be reposted without the explicit permission of the copyright holder.
rightsAuthor(s) retain copyright. With author permission, full text may be uploaded
rights.URI
http://polyacs.org/
relation.isPartOfPolymer Preprints
date.accessioned2008-08-13T18:48:23Z
date.available2008-06-20T16:50:05Z
identifier.persist.URI
http://scholarsmine.mst.edu/post_prints/Acid-CatalyzedTime-EfficientSynthesisOfResorcin_09007dcc805225a8.html
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AcidCatalyzedTimeEfficientSynthesis_09007dcc80556c54.pdf