Ontology type: schema:ScholarlyArticle
1989-12
AUTHORSP. Douša, Č. Koňák, V. Fidler, K. Dušek
ABSTRACTThe effect of curing on the fluorescence intensity of 1,6-diphenyl-1,3,5-hexatriene (DPH) and 9,10-dimethylanthracene (DMA) was studied using two epoxide/amine systems. In the system diglycidyl ether of Bisphenol A (DGEBA)/1,3-diaminopropane the fluorescence intensity of DMA, If, increases with increasing conversion of epoxy groups; this is explained by means of a dynamic model of fluorescence quenching by dissolved molecular oxygen. Contrariwise, in the other system under study, DGEBA/poly (oxypropylene) diamine (JeffamineR D-400), If of the DPH probe decreases, which is interpreted by using the model of static fluorescence quenching. Both effects are suggested for use in the cure monitoring of epoxy resins. More... »
PAGES585-592
http://scigraph.springernature.com/pub.10.1007/bf00718938
DOIhttp://dx.doi.org/10.1007/bf00718938
DIMENSIONShttps://app.dimensions.ai/details/publication/pub.1030432058
JSON-LD is the canonical representation for SciGraph data.
TIP: You can open this SciGraph record using an external JSON-LD service: JSON-LD Playground Google SDTT
[
{
"@context": "https://springernature.github.io/scigraph/jsonld/sgcontext.json",
"about": [
{
"id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/0299",
"inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/",
"name": "Other Physical Sciences",
"type": "DefinedTerm"
},
{
"id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/02",
"inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/",
"name": "Physical Sciences",
"type": "DefinedTerm"
}
],
"author": [
{
"affiliation": {
"alternateName": "Institute of Macromolecular Chemistry",
"id": "https://www.grid.ac/institutes/grid.424999.b",
"name": [
"Institute of Macromolecular Chemistry, Czechoslovak Academy of Sciences, CS-162 06, Prague 6, Czechoslovakia"
],
"type": "Organization"
},
"familyName": "Dou\u0161a",
"givenName": "P.",
"type": "Person"
},
{
"affiliation": {
"alternateName": "Institute of Macromolecular Chemistry",
"id": "https://www.grid.ac/institutes/grid.424999.b",
"name": [
"Institute of Macromolecular Chemistry, Czechoslovak Academy of Sciences, CS-162 06, Prague 6, Czechoslovakia"
],
"type": "Organization"
},
"familyName": "Ko\u0148\u00e1k",
"givenName": "\u010c.",
"id": "sg:person.015103777355.10",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.015103777355.10"
],
"type": "Person"
},
{
"affiliation": {
"alternateName": "Charles University",
"id": "https://www.grid.ac/institutes/grid.4491.8",
"name": [
"Department of Physical Chemistry, Charles University, Albertov 2030, CS-128 40, Prague 2, Czechoslovakia"
],
"type": "Organization"
},
"familyName": "Fidler",
"givenName": "V.",
"type": "Person"
},
{
"affiliation": {
"alternateName": "Institute of Macromolecular Chemistry",
"id": "https://www.grid.ac/institutes/grid.424999.b",
"name": [
"Institute of Macromolecular Chemistry, Czechoslovak Academy of Sciences, CS-162 06, Prague 6, Czechoslovakia"
],
"type": "Organization"
},
"familyName": "Du\u0161ek",
"givenName": "K.",
"id": "sg:person.01151570140.64",
"sameAs": [
"https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01151570140.64"
],
"type": "Person"
}
],
"citation": [
{
"id": "https://doi.org/10.1351/pac198658091239",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1002427498"
],
"type": "CreativeWork"
},
{
"id": "https://doi.org/10.1016/0032-3861(86)90099-6",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1005916595"
],
"type": "CreativeWork"
},
{
"id": "https://doi.org/10.1016/0032-3861(86)90099-6",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1005916595"
],
"type": "CreativeWork"
},
{
"id": "https://doi.org/10.1016/0144-2880(84)90032-0",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1024999791"
],
"type": "CreativeWork"
},
{
"id": "https://doi.org/10.1016/0144-2880(84)90032-0",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1024999791"
],
"type": "CreativeWork"
},
{
"id": "https://doi.org/10.1016/0032-3861(84)90079-x",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1032884045"
],
"type": "CreativeWork"
},
{
"id": "https://doi.org/10.1016/0032-3861(84)90079-x",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1032884045"
],
"type": "CreativeWork"
},
{
"id": "sg:pub.10.1295/polymj.11.691",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1040583221",
"https://doi.org/10.1295/polymj.11.691"
],
"type": "CreativeWork"
},
{
"id": "https://doi.org/10.1021/ma00166a008",
"sameAs": [
"https://app.dimensions.ai/details/publication/pub.1056181095"
],
"type": "CreativeWork"
}
],
"datePublished": "1989-12",
"datePublishedReg": "1989-12-01",
"description": "The effect of curing on the fluorescence intensity of 1,6-diphenyl-1,3,5-hexatriene (DPH) and 9,10-dimethylanthracene (DMA) was studied using two epoxide/amine systems. In the system diglycidyl ether of Bisphenol A (DGEBA)/1,3-diaminopropane the fluorescence intensity of DMA, If, increases with increasing conversion of epoxy groups; this is explained by means of a dynamic model of fluorescence quenching by dissolved molecular oxygen. Contrariwise, in the other system under study, DGEBA/poly (oxypropylene) diamine (JeffamineR D-400), If of the DPH probe decreases, which is interpreted by using the model of static fluorescence quenching. Both effects are suggested for use in the cure monitoring of epoxy resins.",
"genre": "research_article",
"id": "sg:pub.10.1007/bf00718938",
"inLanguage": [
"en"
],
"isAccessibleForFree": false,
"isPartOf": [
{
"id": "sg:journal.1123778",
"issn": [
"0170-0839",
"1436-2449"
],
"name": "Polymer Bulletin",
"type": "Periodical"
},
{
"issueNumber": "5-6",
"type": "PublicationIssue"
},
{
"type": "PublicationVolume",
"volumeNumber": "22"
}
],
"name": "Cure monitoring of epoxy resins by fluorescence quenching",
"pagination": "585-592",
"productId": [
{
"name": "readcube_id",
"type": "PropertyValue",
"value": [
"90f9b9a2620a7acecede55383dbef6974070f96047882310ea7fb124a6098456"
]
},
{
"name": "doi",
"type": "PropertyValue",
"value": [
"10.1007/bf00718938"
]
},
{
"name": "dimensions_id",
"type": "PropertyValue",
"value": [
"pub.1030432058"
]
}
],
"sameAs": [
"https://doi.org/10.1007/bf00718938",
"https://app.dimensions.ai/details/publication/pub.1030432058"
],
"sdDataset": "articles",
"sdDatePublished": "2019-04-11T14:19",
"sdLicense": "https://scigraph.springernature.com/explorer/license/",
"sdPublisher": {
"name": "Springer Nature - SN SciGraph project",
"type": "Organization"
},
"sdSource": "s3://com-uberresearch-data-dimensions-target-20181106-alternative/cleanup/v134/2549eaecd7973599484d7c17b260dba0a4ecb94b/merge/v9/a6c9fde33151104705d4d7ff012ea9563521a3ce/jats-lookup/v90/0000000372_0000000372/records_117117_00000001.jsonl",
"type": "ScholarlyArticle",
"url": "http://link.springer.com/10.1007/BF00718938"
}
]
Download the RDF metadata as: json-ld nt turtle xml License info
JSON-LD is a popular format for linked data which is fully compatible with JSON.
curl -H 'Accept: application/ld+json' 'https://scigraph.springernature.com/pub.10.1007/bf00718938'
N-Triples is a line-based linked data format ideal for batch operations.
curl -H 'Accept: application/n-triples' 'https://scigraph.springernature.com/pub.10.1007/bf00718938'
Turtle is a human-readable linked data format.
curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/bf00718938'
RDF/XML is a standard XML format for linked data.
curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/bf00718938'
This table displays all metadata directly associated to this object as RDF triples.
102 TRIPLES
21 PREDICATES
33 URIs
19 LITERALS
7 BLANK NODES