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C. DE VISSER, W. J. M. HEUVELSLAND, and G. SOMSEN. Department of Chemistry, Free University of Amsterdam,. De Boelelaan 1083, Amsterdam, The ...
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7 Enthalpies of Solution of Some Electrolytes Thermodynamic Behavior of Electrolytes in Mixed Solvents—II Downloaded from pubs.acs.org by UNIV OF MISSOURI COLUMBIA on 10/26/17. For personal use only.

with a Large Cation in Mixtures of Water with Aprotic Solvents C. DE VISSER, W. J. M. HEUVELSLAND, and G. SOMSEN Department of Chemistry, Free University of Amsterdam, De Boelelaan 1083, Amsterdam, The Netherlands

Measured enthalpies of solution of tetra-n-butylammonium bromide (Bu4NBr)in mixtures of water (W) with acetonitrile (ACN) and with ethylene carbonate (EC) are compared with those in mixtures of water with some other aprotic solvents which were reported earlier. The results can be fairly well described by an equation which can be derived either from a cooperative hydration model or from a chemical, pseudo equilibrium model. This equation is tested by varying sys­ tematically the nature of the solute and of the cosolvent. In order to describe the experimental results in W-ACN and in W - E C as such, it will be necessary to extend the equation with a term which comprises any specific (nonhydrophobic) interactions of the solute with the (inert) cosolvent.

' " p h e e n t h a l p y o f s o l u t i o n o f a solute i n v a r i o u s solvents is a n i m p o r t a n t Α

d a t u m i n s t u d y i n g the b e h a v i o r of different solutions b e c a u s e i t m i g h t

g i v e d i r e c t i n f o r m a t i o n o n t h e energetic aspects of b o t h s o l u t e - s o l u t e a n d s o l u t e - s o l v e n t interactions. D u r i n g the last d e c a d e i n o u r l a b o r a t o r y

(see

Réf. 1 a n d l i t e r a t u r e c i t e d t h e r e i n ) enthalpies o f s o l u t i o n o f a l k a l i - a n d tetraalkylammonium halides have been measured i n water a n d i n several nonaqueous

solvents

including formamide

(F),

N-methylformamide

( N M F ) , N , 2 V - d i m e t h y l f o r m a m i d e ( D M F ) , IV,2V-dimethylacetamide ( D M A ) , and dimethylsulfoxide ( D M S O ) . (AH °) tr

T h e standard

enthalpies

of

transfer

( t h e difference b e t w e e n the s t a n d a r d enthalpies of s o l u t i o n o f a

c e r t a i n solute i n t w o s o l v e n t s ) for b o t h a l k a l i b r o m i d e s a n d t e t r a a l k y l 0-8412-0428-4/79/33-177-099$05.00/l © 1979 American Chemical Society

100

T H E R M O D Y N A M I C BEHAVIOR OF E L E C T R O L Y T E S

II

a m m o n i u m b r o m i d e s b e t w e e n t w o n o n a q u e o u s solvents are a l m o s t i n d e ­ p e n d e n t of the size of t h e c a t i o n , e s p e c i a l l y i f o n l y a p r o t i c solvents are considered.

O n t h e o t h e r h a n d , i f w a t e r is one of t h e solvents, àH

0

tr

of

t h e t e t r a a l k y l a m m o n i u m b r o m i d e s d e v i a t e as c o m p a r e d w i t h t h e c o r r e ­ s p o n d i n g a l k a l i b r o m i d e s since i n w a t e r these salts s h o w a c o n s i d e r a b l e e x o t h e r m i c s h i f t of t h e e n t h a l p i e s of s o l u t i o n . B e s i d e s t h a t , e n t h a l p i e s of

Thermodynamic Behavior of Electrolytes in Mixed Solvents—II Downloaded from pubs.acs.org by UNIV OF MISSOURI COLUMBIA on 10/26/17. For personal use only.

s o l u t i o n ( Δ Η ° ) of b o t h a l k a l i b r o m i d e s a n d t e t r a a l k y l a m m o n i u m b r o ­ mides

are a l m o s t p r o p o r t i o n a l to

m i x t u r e s of t w o n o n a q u e o u s

t h e solvent

composition

solvents, w h i l e i n aqueous

i n binary

m i x t u r e s the

a l k a l i b r o m i d e s s h o w a s i m i l a r b e h a v i o r b u t t h e Δ / ί ° of the t e t r a a l k y l ­ a m m o n i u m bromides reach large endothermic m a x i m a i n the water-rich r e g i o n (see

Ref. 2 a n d literature cited therein).

G e n e r a l l y these

phe­

n o m e n a are a t t r i b u t e d to the w e l l - k n o w n h y d r o p h o b i c h y d r a t i o n b e h a v i o r of the t e t r a a l k y l a m m o n i u m salts i n w a t e r (3). is absent i n n o n - h y d r o g e n - b o n d e d

Since this special behavior

solvents, m i x t u r e s of these

solvents

w i t h w a t e r c a n serve as m o d e l systems to s t u d y t h e h y d r o p h o b i c h y d r a ­ t i o n effect m o r e s y s t e m a t i c a l l y .

I t is p o s s i b l e t o d e s c r i b e t h e results

f o r b o t h the e n t h a l p i e s of d i l u t i o n (4) (2)

a n d f o r t h e e n t h a l p i e s of s o l u t i o n

i n terms of a c o o p e r a t i v e h y d r a t i o n m o d e l (2,5)

although a chemical

m o d e l ( 6 ) leads to exactly t h e same final e q u a t i o n . B o t h m o d e l s i n v o l v e (n)

surrounding

a h y d r o p h o b i c p a r t i c l e a n d the e n t h a l p i c c o n t r i b u t i o n to

o n l y t w o p a r a m e t e r s : the n u m b e r of w a t e r m o l e c u l e s

hydrophobic

hydration i n pure water, H b W . I n a n e a r l i e r p u b l i c a t i o n (6) of the m o d e l s .

w e c o n s i d e r e d t h e b a s i c assumptions

T h i s c h a p t e r b r i e f l y r e v i e w s this subject a n d extends t h e

tests b y a d d i n g n e w results of the ΔΗ°

of t e t r a b u t y l a m m o n i u m b r o m i d e

( B u N B r ) i n m i x t u r e s of w a t e r w i t h a c e t o n i t r i l e ( A C N ) a n d w i t h e t h y l ­ 4

ene c a r b o n a t e

(EC)

a n d p r e l i m i n a r y results of s o m e s u b s t i t u t e d a n d

u n s y m m e t r i c a l t e t r a a l k y l a m m o n i u m salts i n m i x t u r e s of w a t e r w i t h D M F . Experimental

and Results

T h e e n t h a l p i e s of s o l u t i o n w e r e m e a s u r e d w i t h a L K B 8700-1 p r e c i ­ s i o n c a l o r i m e t r y system. T h e e x p e r i m e n t a l p r o c e d u r e a n d test of t h e i n s t r u m e n t h a v e b e e n g i v e n b e f o r e (6,7). E C ( F l u k a , purissimum) was d i s t i l l e d u n d e r r e d u c e d pressure a n d the m i d d l e f r a c t i o n w a s s t o r e d o v e r m o l e c u l a r sieves ( 4 Â ) f o r at least 48 h r . A C N ( M e r c k , p r o a n a l y s i s ) w a s d r i e d over m o l e c u l a r sieves a n d u s e d w i t h o u t f u r t h e r p u r i f i c a t i o n . T h e p u r i t y of b o t h solvents ( d e t e r m i n e d s h o r t l y b e f o r e u s e ) , as d e d u c e d f r o m G L C , w a s a l w a y s b e t t e r t h a n 9 9 . 8 % . T h e v o l u m e f r a c t i o n of w a t e r , d e t e r m i n e d b y K . F i s c h e r t i t r a t i o n (8) w a s a l w a y s less t h a n 3.10" . T h e m i x e d solvents w e r e p r e p a r e d b y w e i g h t as s h o r t l y as p o s s i b l e b e f o r e the m e a s u r e m e n t s . Δ Η ° of B u N B r i n W - A C N m i x t u r e s h a v e b e e n m e a s u r e d at 2 5 ° C w h i l e those i n W - E C are at 4 5 ° C , w h i c h is a b o v e the m e l t i n g p o i n t of p u r e E C . 4

4

7.

D E VISSER E T A L .

T*ble I.

Enthalpies

of

Standard Δ Η of B u N B r in Mixtures of Water and A C N at 2 5 ° C and in Mixtures of Water and E C at 4 5 ° C 0

4

InW-ACN

In kj

Thermodynamic Behavior of Electrolytes in Mixed Solvents—II Downloaded from pubs.acs.org by UNIV OF MISSOURI COLUMBIA on 10/26/17. For personal use only.

101

Solution

0 0.025 0.060 0.109 0.175 0.244 0.329 0.400 0.496 0.578 0.601 0.636 0.720 0.750 0.797 0.850 0.901 0.920 0.953 0.976 1.000

W-EC ΔΗ°

ΔΗ° mol'

kj

1

0 0.030 0.052 0.101 0.151 0.250 0.354 0.499 0.625 0.740 0.850 0.900 0.950 0.970 1.000

16.80 11.69 10.83 9.79 9.96 10.79 12.28 13.53 14.87 15.56 15.80 15.95 16.64 17.05 17.82 18.77 18.24 16.58 10.30 2.09 -8.42

moi

1

33.08 27.95 25.71 23.59 22.26 21.65 21.86 22.62 23.05 22.87 22.35 21.80 18.48 14.92 5.89

T h e c o n c e n t r a t i o n of B u N B r i n the m i x t u r e s v a r i e d b e t w e e n 0.003 a n d 0.01 m o l k g " i n w h i c h r a n g e a n y c o n c e n t r a t i o n d e p e n d e n c e a p p e a r e d t o b e m a s k e d b y t h e e x p e r i m e n t a l error. T h e r e f o r e , Δ ί ί ° w a s t a k e n t o b e t h e average of 2 - 4 i n d e p e n d e n t m e a s u r e m e n t s a g r e e i n g w i t h i n 150 J m o l " . F i n a l results i n Δ Η ° as a f u n c t i o n of t h e m o l e f r a c t i o n of w a t e r x are g i v e n i n T a b l e I . 4

1

1

w

Discussion Recently (6)

w e f o u n d t h a t the Δ ί / ° of B u N B r i n W - D M F , 4

W -

D M S O , a n d W - D M A m i x t u r e s c a n b e d e s c r i b e d f a i r l y w e l l i n terms of a c o o p e r a t i v e h y d r a t i o n m o d e l (2,5) AH°(M)

=

(1 - X )

l e a d i n g to the f o l l o w i n g e q u a t i o n :

A f f ° ( S ) +XAH°(W)

+

( X

n

- X ) H b W

(1)

w h e r e Δ / / ° ( Μ ) is t h e s t a n d a r d e n t h a l p y of s o l u t i o n i n a m i x t u r e of w a t e r w i t h a cosolvent S a n d X is t h e m o l e f r a c t i o n of w a t e r .

As mentioned

before, the same e q u a t i o n is o b t a i n e d c o n s i d e r i n g t h e h y d r a t i o n of tetraalkylammonium ion ( R N ) 4

+

a

b y η cooperatively interacting water

m o l e c u l e s as a p s e u d o c h e m i c a l e q u i l i b r i u m , w h i c h c a n b e d e s c r i b e d b y :

102

T H E R M O D Y N A M I C BEHAVIOR O F E L E C T R O L Y T E S

Κ η H 0 *± R N .

R N

+

+

I n this e q u a t i o n R N

+

. . . (H 0)

4

4

2

+

4

2

n

. . (H 0) 2

II

(2)

n

denotes t h e r e s u l t i n g h y d r o p h o b i c

e n t i t y a n d Κ is a n e q u i l i b r i u m constant.

T h e e n t h a l p i c effect of h y d r o ­

p h o b i c h y d r a t i o n t h e n c a n b e c o n s i d e r e d as t h e r e s u l t of t h e f o r m a t i o n o f this h y d r a t i o n c o m p l e x .

I n b o t h m o d e l s the c h o i c e of the

cosolvent

Thermodynamic Behavior of Electrolytes in Mixed Solvents—II Downloaded from pubs.acs.org by UNIV OF MISSOURI COLUMBIA on 10/26/17. For personal use only.

o u g h t to b e r a t h e r u n i m p o r t a n t as l o n g as this s o l v e n t does n o t specific i n t e r a c t i o n s l i k e h y d r o g e n b o n d i n g . HbW

show

A s a consequence η a n d

s h o u l d n o t v a r y w i t h t h e different cosolvents.

B e s i d e s t h a t , the

b a s i c a s s u m p t i o n i n the concepts is t h a t i n t h e absence of h y d r o p h o b i c hydration Δ / /

0

w o u l d c h a n g e p r o p o r t i o n a l l y to t h e s o l v e n t c o m p o s i t i o n .

I n t h i s c h a p t e r w e w i l l i n v e s t i g a t e m o r e s y s t e m a t i c a l l y b o t h aspects. V a r i a t i o n of t h e solute gives i n f o r ­

Influence of Different Solutes. m a t i o n o n the f o l l o w i n g q u e s t i o n s :

(1)

what happens i f hydrophobic

h y d r a t i o n c a n n o t or does not o c c u r ? I n the case of the n o n h y d r o p h o b i c

τ

I 0

• 0.1

I

1

1

I

I

0.3

1

τ



0.5 X

Γ





0.7



I

0.9

1 1

DMF

Figure I . Δ Η of various solutes in mixtures of DMF with water and with DMSO as a function of the mote fraction of DMFX at25°C 0

DMF

Thermodynamic Behavior of Electrolytes in Mixed Solvents—II Downloaded from pubs.acs.org by UNIV OF MISSOURI COLUMBIA on 10/26/17. For personal use only.

Journal of Physical Chemistry

Figure 2. Δ Η ° of tetraalkylammonium bromides in mixtures of water with DMF as a function of the mole fraction of water at 25°C(6) u r e a w e h a v e f o u n d t h a t Δ / / ° i n W - D M F i n d e e d are a l m o s t p r o p o r t i o n a l to t h e solvent c o m p o s i t i o n ( 9 ) l i k e f o r s o m e a l k a l i h a l i d e s i n W - D M S O g i v e n i n the l i t e r a t u r e ( 1 0 ) . P r e l i m i n a r y results i n o u r l a b o r a t o r y o f C s B r i n W - D M F d i s p l a y t h e same b e h a v i o r ( F i g u r e 1 ). I n this context i t is also i m p o r t a n t to m e a s u r e Δ Η ° of a h y d r o p h o b i c particle i n mixtures of two

non-hydrogen-bonded

solvents. P r e l i m i n a r y results f o r B u N B r i n m i x t u r e s o f D M S O a n d D M F 4

y i e l d e d a s t r a i g h t l i n e . A l l o f these results a r e s u m m a r i z e d i n F i g u r e 2 w h i c h c l e a r l y demonstrates that o n l y i n the case o f h y d r o p h o b i c h y d r a t i o n is a l a r g e e n d o t h e r m i c m a x i m u m i n the ΔΗ° present.

( 2 ) W h a t is the

i n f l u e n c e o f the size o f t h e h y d r o p h o b i c solute? I n F i g u r e 2 Δ Η DMF

0

inW -

are given f o r M e N B r , E t ^ N B r , P r N B r , B ^ N B r , a n d P e n N B r . 4

4

4

D e t a i l s o f t h e measurements h a v e b e e n r e p o r t e d e a r l i e r ( 6 ) . A s t h i s figure s h o w s , a l l five t e t r a a l k y l a m m o n i u m salts d i s p l a y s i m i l a r profiles a l t h o u g h i n the case o f M e N B r t h e h y d r o p h o b i c c h a r a c t e r a l m o s t 4

has d i s a p p e a r e d . A c a r e f u l analysis o f these results i n terms o f E q u a t i o n 1 a n d after c o r r e c t i o n o f t h e i n f l u e n c e o f t h e B r " i o n y i e l d e d a v a l u e o f t h e p a r a m e t e r η o f a b o u t 10, r a t h e r i n d e p e n d e n t o f t h e n u m b e r o f C atoms

104

T H E R M O D Y N A M I C BEHAVIOR OF E L E C T R O L Y T E S

Π

a n d a v a l u e of H b W o f a b o u t — 4 k j m o l " p e r C H g r o u p . S i m i l a r results 1

2

h a v e b e e n f o u n d b y L i n d e n b a u m et a l . ( 5 )

i n the case of t r i a l k y l p h o s -

phates i n W - D M F . T h e r e f o r e , i n these cases, E q u a t i o n 1 p r o v i d e s a g o o d p o s s i b i l i t y to d e s c r i b e the e x p e r i m e n t a l results. ( 3 ) W h a t is t h e i n f l u e n c e of different s u b s t i t u t i o n g r o u p s o n the h y d r o p h o b i c c h a r a c t e r of a t e t r a ­ a l k y l a m m o n i u m salt? I n F i g u r e 3 p r e l i m i n a r y results of t h r e e different solutes are c o m p a r e d w i t h those of P r N B r i n W - D M F .

When in Pr NBr

Thermodynamic Behavior of Electrolytes in Mixed Solvents—II Downloaded from pubs.acs.org by UNIV OF MISSOURI COLUMBIA on 10/26/17. For personal use only.

4

the

four terminal C H

((EtOH) NBr) 4

composition

groups

3

the Δ Η °

4

OH

groups

a g a i n is a l m o s t p r o p o r t i o n a l to t h e

solvent

showing that

are s u b s t i t u t e d b y

(EtOH) NBr 4

is n o

four

longer

a

hydrophobic

solute i n w a t e r n o r i n m i x t u r e s of w a t e r w i t h D M F . T h i s c o n c l u s i o n is i n a g r e e m e n t w i t h results f r o m o t h e r m e a s u r e m e n t s f o r this salt i n w a t e r (11).

O b v i o u s l y , i n t r o d u c t i o n of t h e h y d r o p h i l i c O H g r o u p s converts this

salt to a r a t h e r n o r m a l n o n h y d r o p h o b i c one. W h e n i n P r N B r t h e a l k y l 4

τ

1— ( Et OH) NBr 4

30 h [6.6] Β Γ

ο Ε