IUPAC-NIST Solubilities Database (2024)

IUPAC-NIST Solubility Database
NIST Standard Reference Database 106

IUPAC-NIST Solubilities Database (1)Solubility System: m-Xylene with Water

Components:
(1) Water; H2O; [7732-18-5]NIST Chemistry WebBook for detail
(2) m-Xylene; C8H10; [108-38-3]NIST Chemistry WebBook for detail

Evaluator:
G.T. Hefter, School of Mathematical and Physical Sciences, Murdoch University, Perth, W.A., Australia. January 1986.
Critical Evaluation:
Quantitative solubility data for the m-xylene (1) – water (2) system have been reported in the publications listed in Table 1.

The original data in all these publications are compiled in the Data Sheets immediately following this Critical Evaluation. For convenience, further discussion of this system will be divided into three parts.

1. SOLUBILITY OF M-XYLENE (1) IN WATER (2)

All the available data for the solubility of m-xylene in water at low temperatures (T ≤ 343K) are summarized in Table 2 with the exception of the datum of Krzyzanowska and Szeliga (ref 11) which does not appear to be independent of that of Price (ref 10) and has therefore been excluded from consideration.

The data are in general in reasonable agreement although with a few exceptions the agreement is insufficient for the average values to be Recommended. Selected data from Table 2 are plotted in Figure 1.

Table 3 summarizes thermodynamic functions calculated by application of the van’t Hoff equation to the solubility data obtained over various temperature ranges. At low temperatures (T < 343K) the values of ΔHs1n and ΔCp,s1n from the data of Bohon and Claussen (ref 2) and Sanemasa et al. (ref 12) are in good agreement (Table 3) and are close to calorimetric values reported for similar systems (e.g. benzene in water, ref 13). However, the ΔH s1n derived from the data of Chernoglazova and Simulin (ref 9) is much too positive.

2. SOLUBILITY of M-XYLENE (1) IN WATER (2) AT ELEVATED TEMPERATURES

Solubility data for m-xylene in water at elevated temperatures (ca. 340-550K) and system pressure in sealed tubes have been reported by Pryor and Jentoft (ref 3) and Guseva and Parnov (ref 14). The results are plotted in Figure 2 and are clearly in poor agreement. In the absence of confirmatory studies it is difficult to know which values are more reasonable. However, it may be noted that the thermodynamic functions derived from the data of Pryor and Jentoft are more reasonable than those obtained from Guseva and Parnov’s work (Table 3). The interested user is referred to the relevant Data Sheets for the experimental values.

3. SOLUBILITY OF WATER (2) IN M-XYLENE (1)

All the reported data for the solubility of water in m-xylene are collected in Table 4. The data from independent studies over a range of temperatures are in excellent agreement, enabling a number of values to be Recommended (σn~5% relative).

Selected data from Table 4 are also plotted in Figure 3, which emphasizes the general agreement.

Application of the van’t Hoff equation to the data of Englin et al. (ref 6) and Cherbigkaziva and Sunykub (ref 9) gives values for ΔHs1n of 21.3 and 24.9 kJ mo1-1 and for ΔCp,s1n of –152 and 208 J K -1 mo1-1 respectively. Comparison with related systems (e.g. water in benzene) suggests the data of Chernoglazova and Simulin (ref 9) may be more reliable.

Experimental Data:(Notes on the Nomenclature)
Table 1. Quantitative Solubility Studies of the m-Xylene (1) - Water (2) System
AuthorT/KReferenceSolubilityMethodMethod Note
Andrews and Keefer274-3131(1) in (2)spectrophotometric-
Bohon and Claussen274-3132(1) in (2)spectrophotometric-
Pryor and Jentoft344-5443(1) in (2)synthetic-
Guseva and Parnov400-5124(1) in (2)unspecifieda
Hoegfeldt and Bolander2985(2) in (1)Karl Fischer-
Englin et al.283-3036(2) in (1)analytical-
Polak and Lu273, 2987mutualGLC, Karl Fischer-
Sutton and Calder2988(1) in (2)GLC-
Chernoglazova293-3439mutualsnythetic, GLC-
Price29810(1) in (2)GLC-
Krzyzanowske and Szeliga29811(1) in (2)GLC-
Sanemasa et al.288-31812(1) in (2)spectrophotometric-
Table 2. Recommended (R) and Tentative Values of the Solubility of m-Xylene (1) in Water (2)
T/KReferenceSol. PowerSolubilitySol. NoteBest Sol. PowerBest SolubilityBest Sol. Notex1 Powerx1x1 Note
2732, 722.10*, 1.96 g(1)/100g slna22.03 ± 0.07 (R) g(1)/100g slnb53.44 (R)b
283221.97* g(1)/100g slna22.0 g(1)/100g slnb53.4b
2932, 9, 1221.95*, 1.6, 1.60* g(1)/100g slna21.7 ± 0.2 g(1)/100g slnb52.9b
2981, 2, 7, 8, 9, 10, 1221.73, 1.96, 1.62, 1.46, 1.7*, 1.34, 1.62 g(1)/100g slna21.6 ± 0.2 g(1)/100g slnb52.7b
3032, 9, 1221.98*, 1.8*, 1.65* g(1)/100g slna21.8 ± 0.1 g(1)/100g slnb53.1b
3132, 922.19*, 2.2 g(1)/100g slna22.20 (R) g(1)/100g slnb53.73 (R)b
3239, 1222.6*, 2.0* g(1)/100g slna22.3 ± 0.3 g(1)/100g slnb53.9b
333923.2* g(1)/100g slna23.2 g(1)/100g slnb55.4b
343323.5* g(1)/100g slna23.5 g(1)/100g slnb55.9b
Table 3. Thermoydnamic Functions for the Dissolution of m-Xylene in Water Derived from Solubility Data
AuthorReferenceHeat CapacityEnthalpy
Bohon and Claussen2386 J K–1 mol–12.8 kJ mol–1
Pryor and Jentofy3200 J K–1 mol–18.6 kJ mol–1
Guseva and Parnov455 J K–1 mol–136.7 kJ mol–1
Chernoglazova and Simulin9167 J K–1 mol–111.4 kJ mol–1
Sanemasa12317 J K–1 mol–12.6 kJ mol–1
"Best" valuesTable 2516 J K–1 mol–12.9 kJ mol–1
Table 4. Recommended (R) and Tentative Values of the Solubility of Water (2) in m-Xylene (1)
T/KReferenceSol. PowerSolubilitySol. NoteBest Sol. PowerBest SolubilityBest Sol. Notex2 Powerx2x2 Note
273721.88 g(2)/100g slna21.9 g(2)/100g slnb31.1b
2836, 722.89, 2.8* g(2)/100g slna22.9 ± 0.1 (R) g(2)/100g slnb31.7 (R)b
2936, 7, 924.02, 3.7*, 3.4 g(2)/100g slna23.7 ± 0.3 (R) g(2)/100g slnb32.2 (R)b
2985, 6, 7, 924.4, 4.7*, 4.32, 4.0 g(2)/100g slna24.4 ± 0.3 (R) g(2)/100g slnb32.6 (R)b
3036, 925.36, 4.8 g(2)/100g slna25.1 ± 0.3 (R) g(2)/100g slnb33.0 (R)b
313926.7 g(2)/100g slna26.7 g(2)/100g slnb36.7b
3239210* g(2)/100g slna210 g(2)/100g slnb35.9b
3339214* g(2)/100g slna214 g(2)/100g slnb38.3b
3439219* g(2)/100g slna219 g(2)/100g slnb311b
View Figure 1 for this Evaluation

View Figure 2 for this Evaluation

View Figure 3 for this Evaluation

Notes:
Table 1aThe synthetic method was probably used.
Table 2aValues marked with an asterisk (*) have been obtained by the Evaluator by graphical interpolation of the authors' original data.
Table 2bObtained by averaging where appropriate; σn has no statistical significance.
Table 4aValues marked with an asterisk (*) have been obtained by the Evaluator by graphical interpolation of the authors' original data.
Table 4bCalculated by averaging where appropriate; σn has no statistical significance.
References: (Click a link to see its experimental data associated with the reference)
1Andrews, L.J.; Keefer, R.M., J. Am. Chem. Soc. 1949, 71, 3644-77.
2Bohon, R.L.; Claussen, W.F., J. Am. Chem. Soc. 1951, 73, 1571-8.
3Pryor, W.A.; Jentoft, R.E., J. Chem. Eng. Data 1961, 6, 36-7.
4Guseva, A.N.; Parnov, E.I., Vestn. Mosk. Univ. Khim. 1963, 18, 76-9.
5Hoegfeldt, E.; Bolander, B., Ark. Kemi 1964, 21, 161-86.
6Englin, B.A.; Plate, A.F.; Tugolukov, V.M. Pryanishnikova, M.A., Khim. Tekhnol. Topl. Masel 1965, 10, 42-6.
7Polak, J.; Lu, B.C.Y., Can. J. Chem. 1973, 51, 4018-23.
8Sutton, C.; Calder, J.A., J. Chem. Eng. Data 1975, 20, 320-2.
9Chernoglazova, F.S.; Simulin, Yu.N., Zh. Fiz. Khim. 1976, 50, 809. Deposited doc. 1976, VINITI 3528-75.
10Price, L.C., Am. Assoc. Petrol. Geol. Bull. 1976, 60, 213-44.
11Krzyzanowska, T.; Szeliga, J., Nafta (Katowice) 1978, 12, 413-7.
13Gill, S.J.; Nichols, N.F.; Wadso, I. J., Chem. Thermodyn. 1976, 8, 445-52.

IUPAC-NIST Solubilities Database (2024)
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