The Conductivity of Concentrated Mixtures of Alkali Chlorides

Soc. , 1934, 56 (7), pp 1435–1437. DOI: 10.1021/ja01322a002. Publication Date: July 1934. ACS Legacy Archive. Note: In lieu of an abstract, this is ...
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July, 1934

THE CONDUCTIVITY OF CONCENTRATED MIXTURFS

OF

ALKALICHLORIDES

1435

[CONTRIBUTION FROM THE DEPARTMENT OF CHEMISTRY,STANFORD UNIVERSITY ]

The Conductivity of Concentrated Mixtures of Alkali Chlorides BY PIERREVANRYSSELBERGHE AND LEE NUTTING Introduction In two recent papers’ we have interpreted migration data obtained with concentrated mixtures of alkali chlorides by means of a hypothesis which, when generalized, is of the same nature as that proposed by Guggenheim and Unmack:2 “The ratio of the mobility of a given ion in one solution to its mobility in another solution is the same for all ions.” As shown by Guggenheim and Unmack2 this same hypothesis is involved in Longsworth’s computation of moving boundary mea~urements.~It is however clear that the strict application of this assumption would lead, in the case of solutions of pure salts, to transport numbers independent of concentration. Therefore, as in our previous work,l we shall restrict the assumption of proportionality to solutions of the same total concentration and, for the time being a t least, to mixtures of alkali chlorides. In a certain mixture of the chlorides AC1 and BCl (concentration of ACl = xC moles per liter, concentration of HC1 = (1 - x)C moles per liter) the mobilities of the various ions are uA, uB,uti. I n a solution of pure ACI of concentration C the mobilities are u;, &,,A; in a solution of pure BCl Comof concentration C they are ui, u&. paring the mobilities in the mixture with those in pure ACI we have, according to the hypothesis 1LAIu.i

UCI/U8I,A

or UA/UCI

=~ / u & ,= A

W%,A

(1.1) (1.2)

Ti and T& A being the transport numbers in pure ACI at the concentration C. In the same way, comparing the mobilities in the mixture with those in pure BCI , we have UBI%;

=

UCl/u&,B

(2.1)

which is a generalization for all concentrations of the formula established by MacInnes4 for concentrations lower than 0.1 mole per liter. The derivation of (3) implies that the degrees of dissociation of ACI and BCl are the same in all mixtures and in solutions of the pure salts of the same total concentration. Equivalent Conductivity of a Mixture of Alkali Chlorides.-Calling A the equivalent conductivity of the mixture, we have

+ (1 -

= crF[xU~

X)uB

+

UCll

(4)

CY being the degree of dissociation, F one faraday of electricity. Using the formulas (1.2) and ( 2 . 2 ) we have

This equation enables us to calculate the quantity aFuCl = Acl when the total equivalent conductivity A is known. It was found, on the basis of the experimental values of h obtained by Stearns and by Ruby and KawaiJ6that the quantity Acl deduced from equation (5) is, within the limits of experimental error, a linear function of the mixing ratio x given by ACI = ~ A & A-k (1 - ~ ) A ~ I , B

(6)

and being the equivalent conductivities of the chloride ion in solutions of pure ACI and BCI of the same concentration as the total concentration of the mixture. (6) could also be written in terms of the transport numbers in solutions of the pure salts AC1,A

Aci =

&ci

T&A

+ (1 - %)A T%,B

(7)

( 5 ) becomes then

or

uBO/UEI,B = TB”/TCOI,B (2.2) T i and T&Bbeing the transport numbers in pure BCl a t the concentration C. We have previously shown’ that (1.2) and (2.2) lead to the following formula for the transport number of the ion A+ in the mixture UB/UCI

=

(1) Van Rysselberghe, Trns JOURNAL, 65, 990 (1933); Van Rysselherghe and Nutting, ibid., 66, 996 (1933). (2) Guggenheim and Unmack, Del. Kgl. Danske Videnskab. Selskab. X,14, 16 (1931). (31 Longsworth, THISJOURNAL, 62, 1897 (1930).

a formula giving the equivalent conductivity of the mixture in terms of the conductivities and transport numbers of the pure salts a t a concentration equal to the total concentration of the mixture. In order to show the high degree of (4) MacInnes, ibid., 47, 1922 (1925). ( 5 ) Stearn, ibid., 44,670 (1922). (6) Ruby and Rawai, ibid.. 48, 1119 (1926)

PIERREVAN RYSSELBERGHE AND LEE NUTTING

1436

accuracy of this formula and to compare it to the old mixture rule

+ (1 -

A = ~Aici

X)

A&I

(9)

we have presented in Table I for the various mixtures studied by Stearns and by Ruby and Kawai,6 respectively : the total concentration, the ratio x of the concentration of potassium chloride to the total concentration, the measured equivalent conductivity and the values calculated according to formulas (8) and (9). The conductivities for the pure salts used in the calculations are those of Stearn and of Ruby and Kawai. The transport numbers used at 0.1 and 0.25 are those of Long~worth.~At higher concentrations the transport numbers of potassium chloride were obtained from the data of MacInnes and Dole.* The transport numbers of sodium chloride were obtained by drawing the best possible curve through all the available data.s 70

60

2 50

concentrations. It is to be noted that the mixture law (9) is never strictly valid except at zero total concentration. It happens to be sufficiently accurate at concentrations lower than 0.1 for which ACI = A 8 i . ~= A ~ L B

TABLE I CONDUCTIVITIES OF MIXTURES OF POTASSIUM CHLORIDE AND SODIUM CHLORIDE AT 25' Data of Stearn Total concn. moles per 1000 g. of water

A

measured

calcd. form. (9)

114.12 117.46 120.97 107.02 110.69 114.58 101.51 105.16 109.10 94.14 98.75 102.82 85.17 90.12 95.20 71.21 77.06 83.31

114.01 117.60 121.18 107.38 111.02 114.65 101.49 105.32 109.25 94.58 98.74 102.95 85.43 90.26 95.47 71.20 77.13 83.29

113.99 117.58 121.16 107.40 111.05 114.69 101.63 105.50 109.35 94.77 98.98 103.19 85.83 90.80 95.77 72.16 78.18 84.20

Data of Ruby and Kawai 103.08 103.24 107.80 107.93 '/5 91.14 91.14 96.24 96.29 '/s 101.54 101.50 "/r 106.88 106.84 '/b 81.25 81.19 2/5 87.02 87.05 3/6 93.05 93.12 '/6 99.45 99.36 '/6 66.30 66.33 2/6 73.22 73.27 '/s 80.52 80.55 4/6 88.13 58.17

103.37 108.09 91.31 96.56 101.80 107.05 81.53 87.60 93.66 99.73 67.03 74.30 81.58 88.85

0.10 .10 .10 .25 .25 .25 .50 .50 .50 1.00 1.00 1.00 2.00 2.00 2.00

0.4 X

0.8

= cKCl/CiotJ.

Fig. 1.-Conductivity of the chloride ion in mixtures of potassium and sodium chlorides at 25': 0, Stearn; A, Ruby and Kawai.

The values calculated according to formula (8) agree remarkably well with the measured conductivities throughout the whole range of concentrations. Those calculated according to formula (S), satisfactory at low concentrations, exhibit large departures from the measured ones at higher (7) Longsworth, THISJOURNAL, 64, 2741 (1932). (8) MacInnes and Dole, ibid., 113, 1357 (1931). (9) "International Critical Tables;" Landolt-B6rnstein-Roth, Tables: McBain, Proc. Washington Acod. Sci., 9, 1-78 (1907).

0.50 .50 1.00 1.00 1.00 1.00 2.00 2.00 2.00 2.00 4.00 4.00 4.00 4.00

A

calcd. form. (8)

A

4.00 4.00

0

(10)

It is easy to see that (8) and (9) become mathematically equivalent when (10) holds. On Fig. 1 are plotted against the mixing ratio x the values of Acl deduced from the measurements of Stearn and of Ruby and Kawai by means of formula (5). This diagram justifies equation (6).

4.00

40

Vol. 56

'/r '/s

Other measurements on mixtures, like those of Bray and Hunt,'O of Dewey," etc., were found to (10) Bray and Hunt, THIS JOURNAL. 33, 781 (1911) (11) Dewey, i b i d . . 47, 1927 (1926).

ACTIVITYCOEFFICIENTS OF SULFURIC ACID

July, 1934

be less suitable for our purpose (presence of hydrochloric acid as one of the constituents, total concentration too low to obtain significant departures from the old mixture rule, etc.). Remarks.-(6) could also be written in terms of mobilities UC1

=

XU81.A

+ (1 -

X)U8l,B

=

[X%&l,A

UB = (X7481,A

-k (1

- X)U&,B]

+ (1 -

X)&,B]

(T.UT&,A) (12.1) (T~/T&,B)

(12.2)

and the limiting mobilities of ion A + a t infinite dilution in BCI and of ion B + at infinite dilution in ACl (13.1)

(13.2)

Figure 2 gives the ratios uK/ug and U N ~ / Uin~ terms of x for mixtures of potassium chloride and sodium chloride of a total concentration of 2 moles per liter. We notice that in the mixture the potassium ion moves more slowly and the sodium ion more rapidly than in solutions of the pure salts. This is in qualitative agreement with the theoretical deductions of Onsager and Fuoss for very dilute solutions.l 2 (12) Onsager and Fuoss,J . Phys. Chem.. 56, 2889 (1932)

[CONTRIBUTION FROM

THE

M

(11)

From (1.2), (2.2) and (11) we deduce the interesting relations UA

1.o

1437

0.51 0

I

I

I

0.4 x =

1

I

0.8

CKCllCtQtJ.

Fig. 2.-Mobility ratios U K / U ~ ( A ) and upia/uGa (B) in 2 M mixtures of KCl and NaCI.

Summary

1. A formula is obtained giving the equivalent conductivity of a mixture of alkali chlorides in terms of the conductivities and transport numbers ~ of the pure salts at the same concentration as the total concentration of the mixture. 2. Measured and calculated conductivities of mixtures of potassium and sodium chloride agree remarkably well up to as high a total concentration as 4 moles per liter. 3. It is shown that at concentrations of the order of 0.1 mole per liter the new formula and the old mixture rule give the same results. STANFORD UNIV.,CALIF. RECEIVED DECEMBER 11, 1933

CHEMISTRY LABORATORY OF THE UNIVERSITY OF NORTH CAROLINA ]

The Activity Coefficients of Sulfuric Acid in Aqueous Solutions of Ammonium Sulfate at 25' BY H. D. CROCKFORD AND N. L. SIMMONS, JR.

In this paper are given data for the above cell with ammonium sulfate as the added salt and with ml (HzSOJ = 0.1 and 0.01 and a t a temperature of 25'. These results are directly comparable to those obtained by Harned and Sturgis wherein m2 represents potassium or sodium and ml with sodium and potassium sulfates at these acid (H2S04) = 0.1 and 0.01. Measurements were concentrations. From the results the activity also- made with magnesium sulfate. Akerlof2 coefficients of the acid have been calculated. extended the measurements to ml (H~SOI) = Experimental Procedure 0.05 and 0.005, and included lithium sulfate as an added salt. Randall and Langford3 have exAll reagents employed were purified carefully tended the data with sodium sulfate up to con- and where necessary were analyzed accordingto the centrations of 2 molal in various acid concentra- accepted methods. All electrical measuring instrutions. All the above work was carried out at 25'. ments had been calibrated by the Bureau of Stand(1) Harned and Sturgiu, THISJOURNAL, 47, 945 (1925). ards. The temperature was accurate to *0.03'. (2) Akerldf, ihid., 48, 1180 (1928); Physik. Z.,17,411 (1928). The usual experimental procedure was followed. (3) Randall and Langford, THISJOURNAL, 49, 1445 (1927). Electromotive force data on solutions of various sulfates in sulfuric acid have been obtained by Harned and Sturgis' from a study of cells of the