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dc.contributor.authorBastug, AS
dc.contributor.authorSeyrek, N
dc.contributor.authorTuncay, M
dc.date.accessioned2021-03-06T07:54:12Z
dc.date.available2021-03-06T07:54:12Z
dc.date.issued1995
dc.identifier.citationBastug A., Tuncay M., Seyrek N., "Effects of cosolvents cetyltrimethylammonium bromide on the thresholds for nucleation of nitrogen in aqueous solutions", JOURNAL OF SOLUTION CHEMISTRY, cilt.24, ss.1059-1073, 1995
dc.identifier.issn0095-9782
dc.identifier.otherav_de6a6fa9-81c2-4642-bd5c-0463c0600467
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/146544
dc.identifier.urihttps://doi.org/10.1007/bf00973522
dc.description.abstractThe decomposition of ammonium nitrite in water creates a supersaturated solution of nitrogen. The some process occurs in water-organic solvent mixtures. Acetone, dioxane, dimethylsulfoxide (DMSO) and dimethylformamide (DMF) are the cosolvents wed in this study. The limits of supersaturation of nitrogen (C-SL/mol L(-1)) were determined in all of these solvent mixtures by releasing the dissolved gas sonicationally and measuring the volume of released gas. C-SL was generally increased in the presence of cosolvents. The effectiveness sequence of organic solvents was found to be as DMF<DMSO<Dioxanet congruent to Acetone. Transportation period of small bubbles formed during sonication is changed by compositions of solvent mixtures. These periods may depend on the viscosity of the solution. Effects of the presence of cetyltrimethylammonium bromide were also studied It was concluded that there may be a relation between the strength of the water-cosolvent H-bonds and C-SL, and all of the measured quantities of this study were generally affected by micelle formation.
dc.language.isoeng
dc.subjectTemel Bilimler (SCI)
dc.subjectTemel Bilimler
dc.subjectKİMYA, FİZİKSEL
dc.subjectKimya
dc.subjectFizikokimya
dc.titleEffects of cosolvents cetyltrimethylammonium bromide on the thresholds for nucleation of nitrogen in aqueous solutions
dc.typeMakale
dc.relation.journalJOURNAL OF SOLUTION CHEMISTRY
dc.contributor.department, ,
dc.identifier.volume24
dc.identifier.issue10
dc.identifier.startpage1059
dc.identifier.endpage1073
dc.contributor.firstauthorID116621


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