Viscosities of binary and ternary mixtures of polyaromatic hydrocarbons
Experimental measurements of the viscosities of the three binary-mixture combinations of the toluene/tetralin/1-methylnaphthalene system were performed over the entire concentration range for various temperatures ranging from 298 to 498 K. Viscosities were also determined for an equimolar mixture of...
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| Veröffentlicht in: | J. Chem. Eng. Data; (United States) 1987-07, Vol.32 (3), p.349-354 |
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| container_title | J. Chem. Eng. Data; (United States) |
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| creator | Byers, Charles H Williams, David F |
| description | Experimental measurements of the viscosities of the three binary-mixture combinations of the toluene/tetralin/1-methylnaphthalene system were performed over the entire concentration range for various temperatures ranging from 298 to 498 K. Viscosities were also determined for an equimolar mixture of the three components and for the binary naphthalene/tetralin system. Finally, the polar phenol/picoline mixture was found to have interesting associative properties. The viscosity data determined have an experimental uncertainty of 1.1%. The viscosity correlation of Mc Allister gave excellent representations of both binary and ternary data. |
| doi_str_mv | 10.1021/je00049a019 |
| format | Article |
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Viscosities were also determined for an equimolar mixture of the three components and for the binary naphthalene/tetralin system. Finally, the polar phenol/picoline mixture was found to have interesting associative properties. The viscosity data determined have an experimental uncertainty of 1.1%. The viscosity correlation of Mc Allister gave excellent representations of both binary and ternary data.</description><identifier>ISSN: 0021-9568</identifier><identifier>EISSN: 1520-5134</identifier><identifier>DOI: 10.1021/je00049a019</identifier><identifier>CODEN: JCEAAX</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>400201 - Chemical & Physicochemical Properties ; ALKYL RADICALS ; ALKYLATED AROMATICS ; AROMATICS ; AZINES ; BINARY MIXTURES ; CALCULATION METHODS ; Catalysis ; Catalysts: preparations and properties ; Catalytic reactions ; Chemistry ; CONDENSED AROMATICS ; DISPERSIONS ; Exact sciences and technology ; General and physical chemistry ; General. Nomenclature, chemical documentation, computer chemistry ; HETEROCYCLIC COMPOUNDS ; HIGH TEMPERATURE ; HYDROCARBONS ; HYDROXY COMPOUNDS ; INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY ; METHYL RADICALS ; MIXTURES ; NAPHTHALENE ; ORGANIC COMPOUNDS ; ORGANIC NITROGEN COMPOUNDS ; PHENOLS ; PICOLINES ; POLYCYCLIC AROMATIC HYDROCARBONS ; PYRIDINES ; RADICALS ; TETRALIN ; Theory of reactions, general kinetics ; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry ; TOLUENE ; VISCOSITY</subject><ispartof>J. Chem. Eng. Data; (United States), 1987-07, Vol.32 (3), p.349-354</ispartof><rights>1988 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a393t-7034d878005d07737b22bf0cb1c398fd8f76da121f3f325830041cf8a7cebfca3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/je00049a019$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/je00049a019$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,885,2765,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7538265$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/5680511$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Byers, Charles H</creatorcontrib><creatorcontrib>Williams, David F</creatorcontrib><creatorcontrib>Chemical Technology Div., Oak Ridge National Lab., Oak Ridge, TN 37831</creatorcontrib><title>Viscosities of binary and ternary mixtures of polyaromatic hydrocarbons</title><title>J. Chem. Eng. Data; (United States)</title><addtitle>J. Chem. Eng. Data</addtitle><description>Experimental measurements of the viscosities of the three binary-mixture combinations of the toluene/tetralin/1-methylnaphthalene system were performed over the entire concentration range for various temperatures ranging from 298 to 498 K. Viscosities were also determined for an equimolar mixture of the three components and for the binary naphthalene/tetralin system. Finally, the polar phenol/picoline mixture was found to have interesting associative properties. The viscosity data determined have an experimental uncertainty of 1.1%. The viscosity correlation of Mc Allister gave excellent representations of both binary and ternary data.</description><subject>400201 - Chemical & Physicochemical Properties</subject><subject>ALKYL RADICALS</subject><subject>ALKYLATED AROMATICS</subject><subject>AROMATICS</subject><subject>AZINES</subject><subject>BINARY MIXTURES</subject><subject>CALCULATION METHODS</subject><subject>Catalysis</subject><subject>Catalysts: preparations and properties</subject><subject>Catalytic reactions</subject><subject>Chemistry</subject><subject>CONDENSED AROMATICS</subject><subject>DISPERSIONS</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>General. Nomenclature, chemical documentation, computer chemistry</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>HIGH TEMPERATURE</subject><subject>HYDROCARBONS</subject><subject>HYDROXY COMPOUNDS</subject><subject>INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY</subject><subject>METHYL RADICALS</subject><subject>MIXTURES</subject><subject>NAPHTHALENE</subject><subject>ORGANIC COMPOUNDS</subject><subject>ORGANIC NITROGEN COMPOUNDS</subject><subject>PHENOLS</subject><subject>PICOLINES</subject><subject>POLYCYCLIC AROMATIC HYDROCARBONS</subject><subject>PYRIDINES</subject><subject>RADICALS</subject><subject>TETRALIN</subject><subject>Theory of reactions, general kinetics</subject><subject>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</subject><subject>TOLUENE</subject><subject>VISCOSITY</subject><issn>0021-9568</issn><issn>1520-5134</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1987</creationdate><recordtype>article</recordtype><recordid>eNptkM1KAzEUhYMoWKsrX2AQwYWM5qeZZJZStSqlCtYibkImk9DU6aQkKbRvb-qIuHB1L5zvXs45AJwieIUgRtcLDSEclBKicg_0EMUwp4gM9kEPJjkvacEPwVEIix3GMOqB0cwG5YKNVofMmayyrfTbTLZ1FrX_3pd2E9e-k1eu2UrvljJalc23tXdK-sq14RgcGNkEffIz--Dt_m46fMjHz6PH4c04l6QkMWeQDGrOOIS0howRVmFcGagqpEjJTc0NK2qJMDLEEEw5ST6RMlwypSujJOmDs-6vC9GKoGzUaq5c22oVRYoHKUIJuuwg5V0IXhux8naZsggExa4o8aeoRJ939EoGJRvjZats-D1hlHBc0ITlHWZD1JtfWfpPUaQgVExfXsVoMp08fbzPxG3iLzpeqiAWbp3KbMK_Br4A3eiD4g</recordid><startdate>19870701</startdate><enddate>19870701</enddate><creator>Byers, Charles H</creator><creator>Williams, David F</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>OTOTI</scope></search><sort><creationdate>19870701</creationdate><title>Viscosities of binary and ternary mixtures of polyaromatic hydrocarbons</title><author>Byers, Charles H ; Williams, David F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a393t-7034d878005d07737b22bf0cb1c398fd8f76da121f3f325830041cf8a7cebfca3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1987</creationdate><topic>400201 - Chemical & Physicochemical Properties</topic><topic>ALKYL RADICALS</topic><topic>ALKYLATED AROMATICS</topic><topic>AROMATICS</topic><topic>AZINES</topic><topic>BINARY MIXTURES</topic><topic>CALCULATION METHODS</topic><topic>Catalysis</topic><topic>Catalysts: preparations and properties</topic><topic>Catalytic reactions</topic><topic>Chemistry</topic><topic>CONDENSED AROMATICS</topic><topic>DISPERSIONS</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>General. Nomenclature, chemical documentation, computer chemistry</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>HIGH TEMPERATURE</topic><topic>HYDROCARBONS</topic><topic>HYDROXY COMPOUNDS</topic><topic>INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY</topic><topic>METHYL RADICALS</topic><topic>MIXTURES</topic><topic>NAPHTHALENE</topic><topic>ORGANIC COMPOUNDS</topic><topic>ORGANIC NITROGEN COMPOUNDS</topic><topic>PHENOLS</topic><topic>PICOLINES</topic><topic>POLYCYCLIC AROMATIC HYDROCARBONS</topic><topic>PYRIDINES</topic><topic>RADICALS</topic><topic>TETRALIN</topic><topic>Theory of reactions, general kinetics</topic><topic>Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry</topic><topic>TOLUENE</topic><topic>VISCOSITY</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Byers, Charles H</creatorcontrib><creatorcontrib>Williams, David F</creatorcontrib><creatorcontrib>Chemical Technology Div., Oak Ridge National Lab., Oak Ridge, TN 37831</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>OSTI.GOV</collection><jtitle>J. Chem. Eng. Data; (United States)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Byers, Charles H</au><au>Williams, David F</au><aucorp>Chemical Technology Div., Oak Ridge National Lab., Oak Ridge, TN 37831</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Viscosities of binary and ternary mixtures of polyaromatic hydrocarbons</atitle><jtitle>J. Chem. Eng. Data; (United States)</jtitle><addtitle>J. Chem. Eng. Data</addtitle><date>1987-07-01</date><risdate>1987</risdate><volume>32</volume><issue>3</issue><spage>349</spage><epage>354</epage><pages>349-354</pages><issn>0021-9568</issn><eissn>1520-5134</eissn><coden>JCEAAX</coden><abstract>Experimental measurements of the viscosities of the three binary-mixture combinations of the toluene/tetralin/1-methylnaphthalene system were performed over the entire concentration range for various temperatures ranging from 298 to 498 K. Viscosities were also determined for an equimolar mixture of the three components and for the binary naphthalene/tetralin system. Finally, the polar phenol/picoline mixture was found to have interesting associative properties. The viscosity data determined have an experimental uncertainty of 1.1%. The viscosity correlation of Mc Allister gave excellent representations of both binary and ternary data.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/je00049a019</doi><tpages>6</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0021-9568 |
| ispartof | J. Chem. Eng. Data; (United States), 1987-07, Vol.32 (3), p.349-354 |
| issn | 0021-9568 1520-5134 |
| language | eng |
| recordid | cdi_crossref_primary_10_1021_je00049a019 |
| source | American Chemical Society Journals |
| subjects | 400201 - Chemical & Physicochemical Properties ALKYL RADICALS ALKYLATED AROMATICS AROMATICS AZINES BINARY MIXTURES CALCULATION METHODS Catalysis Catalysts: preparations and properties Catalytic reactions Chemistry CONDENSED AROMATICS DISPERSIONS Exact sciences and technology General and physical chemistry General. Nomenclature, chemical documentation, computer chemistry HETEROCYCLIC COMPOUNDS HIGH TEMPERATURE HYDROCARBONS HYDROXY COMPOUNDS INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY METHYL RADICALS MIXTURES NAPHTHALENE ORGANIC COMPOUNDS ORGANIC NITROGEN COMPOUNDS PHENOLS PICOLINES POLYCYCLIC AROMATIC HYDROCARBONS PYRIDINES RADICALS TETRALIN Theory of reactions, general kinetics Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry TOLUENE VISCOSITY |
| title | Viscosities of binary and ternary mixtures of polyaromatic hydrocarbons |
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