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IUPAC-NIST Solubility Database
NIST Standard Reference Database 106
Solubility System:
Nitromethane with Cycloheptane
Components:
(1) Nitromethane; CH3NO2; [75-52-5]
NIST Chemistry WebBook
for detail
(2) Cycloheptane; C7H14; [291-64-5]
NIST Chemistry WebBook
for detail
Original Measurements:
Riccardi, R.; Franzosini, P.; Rolla, M., Z. Naturforsch. 23A, 1816-8 (1968).
Variables:
Temperature = 362 K to 375 K
Prepared By:
V. P. Sazonov
Experimental Remarks:
The numerical data were not included in the original publication but were provided by Professor R. Riccardi at the request of the compiler.
Experimental Data:
(Notes on the Nomenclature)
Mutual solubility of nitromethane and cycloheptane
t/°C
T/K
10
2
* Mass Fraction w
1
(compiler)
Mole Fraction x
1
Comment(s)
88.8
362.0
-
-
Hydrocarbon-rich phase
88.8
362.0
77.9
0.850
Nitromethane-rich phase
96.2
369.4
-
-
Hydrocarbon-rich phase
96.2
369.4
70.3
0.792
Nitromethane-rich phase
96.3
369.5
23.7
0.333
Hydrocarbon-rich phase
96.3
369.5
-
-
Nitromethane-rich phase
97.3
370.5
-
-
Hydrocarbon-rich phase
97.3
370.5
68.7
0.779
Nitromethane-rich phase
98.7
371.9
26.2
0.363
Hydrocarbon-rich phase
98.7
371.9
-
-
Nitromethane-rich phase
99.3
372.5
-
-
Hydrocarbon-rich phase
99.3
372.5
64.3
0.743
Nitromethane-rich phase
100.2
373.4
30.6
0.415
Hydrocarbon-rich phase
100.2
373.4
-
-
Nitromethane-rich phase
100.8
374.0
36.2
0.477
Hydrocarbon-rich phase
100.8
374.0
-
-
Nitromethane-rich phase
100.9
374.1
39.4
0.511
Hydrocarbon-rich phase
100.9
374.1
-
-
Nitromethane-rich phase
101.3
374.5
47.2
0.590
Hydrocarbon-rich phase
101.3
374.5
-
-
Nitromethane-rich phase
101.4
374.6
-
-
Hydrocarbon-rich phase
101.4
374.6
55.8
0.670
Nitromethane-rich phase
101.4
374.6
-
-
Hydrocarbon-rich phase
101.4
374.6
- (UCST)
-
Nitromethane-rich phase
Method/Apparatus/Procedure:
The synthetic method
1
was used. Tubes were filled under vacuum with known masses of degassed and moisture-free components, sealed, and then placed in a thermostat bath filled with paraffin oil. The mixtures in the tubes were shaken by a Chemap vibromixer type E-1. Temperatures were measured with Degussa Pt resistance thermometers, which were checked against standards. Phase changes (cloud points) were observed as mixtures were cooled.
Source and Purity of Materials:
(1) Fluka AG; purity 99 mole %; fractionally distilled, degassed and finally distilled through a P
2
O
5
filled tube.
(2) Fluka AG; purity 99 mole %; purification as above.
Estimated Errors:
Temperature: reproduced better than 0.1K.
References:
1
P. Franzosini, Z. Naturforsch. 18A, 224 (1963).