1999
DOI: 10.1006/jcht.1999.0526
|View full text |Cite
|
Sign up to set email alerts
|

Phase diagram ofn-hexacosane andn-octacosane: experimental determination and calculation

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
8
0

Year Published

2001
2001
2020
2020

Publication Types

Select...
6
1

Relationship

1
6

Authors

Journals

citations
Cited by 15 publications
(8 citation statements)
references
References 69 publications
0
8
0
Order By: Relevance
“…(ii) With the concentration increase of C 7 , the solid which crystallizes is a phase whose orthorhombic structure is different from the triclinic or monoclinic structure of pure C 26 and C 28 , respectively (Appendix 1 in the Supporting Information). This phase, observed by X-ray diffraction in equilibrium with the liquid, is isostructural to the orthorhombic intermediate solid solution β′′ 1 of the consecutive C n binary molecular alloys, especially in the (C 26 /C 28 ) system: 42 the chemical analysis shows that the concentration of this β" phase which forms the first deposits is greater in C 28 . 198 The crystallization of the β′′ intermediate solid solution explains the following notable phenomenon, observed by Ghogomu et al, 200,202 Provost et al, 199 and Flo ¨ter et al: 212 the addition of one long C n (0 < xC n < 0.1) to a short one (C n-1 or C n-2 ) increases the solubility of the latter (C n-1 or C n-2 ) in the solvents; thus, as shown by all these authors, the solubility of each binary heavy C n mixture in a light solvent is greater than the solubility of the corresponding hypothetical ideal mixtures (Figure 18).…”
Section: (D) Solubility Of Heavy Pure C N 'S and Their Binary Model M...mentioning
confidence: 89%
See 2 more Smart Citations
“…(ii) With the concentration increase of C 7 , the solid which crystallizes is a phase whose orthorhombic structure is different from the triclinic or monoclinic structure of pure C 26 and C 28 , respectively (Appendix 1 in the Supporting Information). This phase, observed by X-ray diffraction in equilibrium with the liquid, is isostructural to the orthorhombic intermediate solid solution β′′ 1 of the consecutive C n binary molecular alloys, especially in the (C 26 /C 28 ) system: 42 the chemical analysis shows that the concentration of this β" phase which forms the first deposits is greater in C 28 . 198 The crystallization of the β′′ intermediate solid solution explains the following notable phenomenon, observed by Ghogomu et al, 200,202 Provost et al, 199 and Flo ¨ter et al: 212 the addition of one long C n (0 < xC n < 0.1) to a short one (C n-1 or C n-2 ) increases the solubility of the latter (C n-1 or C n-2 ) in the solvents; thus, as shown by all these authors, the solubility of each binary heavy C n mixture in a light solvent is greater than the solubility of the corresponding hypothetical ideal mixtures (Figure 18).…”
Section: (D) Solubility Of Heavy Pure C N 'S and Their Binary Model M...mentioning
confidence: 89%
“…Since then, the crystalline structures, as well as the thermodynamic data of pure C n 's and of the synthetic model mixtures consisting of two, three, four or five C n 's, 26,41,42,44,59,66,123,133, have been the subject of numerous publications. The literature results, obtained before 1960, have been reviewed by Mnyukh, 3 an exhaustive bibliography of the papers previous to 1971 has been presented by Turner, 53 the structural parameters of pure C n 's have been given by Heyding et al, 24 and the monograph of Srivastava et al 54 concerns more particularly the C n polymorphism.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…It exists at room temperature as an orthorhombic structure and changes at 57.5 8C into a rhombohedral structure with a melting point at 60.8 8C. [23] DSC and RFM analyses resolve both transitions. The two peaks in the DSC curve are very close (Figure 3 a), at 60.4 and 62.9 8C, and must be accurately measured to avoid seeing only one broad peak.…”
Section: Melting Temperaturementioning
confidence: 99%
“…Reports on the formation of alloys, or solid solutions, of organic compounds, although still rare, have been appearing regularly in the last few years for aromatic compounds, such as substituted benzenes and naphtalenes [1][2][3], pyrene and anthracene [4][5][6], for carbohydrates [7], terpenes [8], neopentane derivatives [9][10] and fulerenes, besides solid solutions of C 60 with C 70 [11][12] solid solutions of C 60 in sulphur have been reported [13]. Nevertheless it is among the molecules with long n-alkyl chains such as n-alcohols [14], fats [15], soaps [16] and alkanes [17][18][19][20] that solid solutions appear more frequently. Although most of these alloys are still just interesting academic curiosities, these new materials seem quite promising and interesting applications for some of them have been identified.…”
Section: Introductionmentioning
confidence: 99%