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A Comprehensive Treatise on Inorganic and Theoretical Chemistry

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56 INOKGANIC AND THEORETICAL CHEMISTRY<br />

B. Delachanal <strong>and</strong> A. Mermet found that the red colour—red colloidal platinum—<br />

produced when soln. of platinum salts are treated with stannous chloride is due<br />

to the presence of colloidal metallic platinum in a very fine state of subdivisi<strong>on</strong>,<br />

<strong>and</strong> that the formati<strong>on</strong> of this in place of the more usual brown colloidal metal<br />

is due to the acti<strong>on</strong> of stannic chloride <strong>and</strong> its products of hydrolysis as protective<br />

colloids. The red colloid is also formed when the reducti<strong>on</strong> of platinum salts is<br />

effected by means of a soln. of phosphorus in ether, if gelatin is added as a protective<br />

colloid. The identity of the two red substances has been established by spectroscopic<br />

observati<strong>on</strong>s. If the colloidal soln. obtained by reducti<strong>on</strong> with stannous<br />

chloride is shaken up -with ethyl ether or ethyl acetate, the organic solvents take<br />

up the red colour, <strong>and</strong> this is found to be c<strong>on</strong>nected -with the solubility of stannic<br />

chloride in these media, in which it plays the part of protective colloid. When the<br />

aq. soln. is diluted with a large volume of water, or when the ethyl acetate soln.<br />

is poured into water, a chocolate-brown precipitate is obtained. According to<br />

K. A. Schneider, the precipitate has the compositi<strong>on</strong> PtSn3O5, but actually no<br />

definite compound is formed because the compositi<strong>on</strong> of the precipitate varies<br />

c<strong>on</strong>siderably with the c<strong>on</strong>diti<strong>on</strong>s under which it is produced. It is probable that<br />

it is analogous -with purple of Cassius, <strong>and</strong> is a mixture of colloidal platinum <strong>and</strong><br />

colloidal stannic acid. The properties of the purple of Cassius, <strong>and</strong> red colloidal<br />

platinum are similar.<br />

J. Duclaux found that the osmotic press, of the soln. is less than 2 cm. of water.<br />

C. Thomas said that the change to white of the colour of the ultramicroscopic<br />

particles marks the beginning of coagulati<strong>on</strong>. P. LaI <strong>and</strong> P. B. Ganguly observed<br />

that the colloid is coagulated by exposure to ultra-violet light. E. Miiller studied<br />

the polarizati<strong>on</strong>, <strong>and</strong> extinctive coeff. of the colloidal soln. ; A. T. Williams, <strong>and</strong><br />

O. Scarpa, the spectra of colloidal soln. of platinum ; E. B. Spear <strong>and</strong> co-workers,<br />

the coagulati<strong>on</strong> of the sol in ultra-violet light ; <strong>and</strong> E. B. Spear <strong>and</strong> K. D. Kahn,<br />

the precipitati<strong>on</strong> of the colloid <strong>on</strong> metallic surfaces. H. Freundlich observed that<br />

the hydrosol of platinum shows anodic c<strong>on</strong>vecti<strong>on</strong> like arsenic sulphide sol.<br />

S. W. Pennycuick studied the cataphoretic velocity. L. Holla found that the<br />

velocity of migrati<strong>on</strong> of the colloidal particles in an electric field with a drop of<br />

potential of 1 volt per cm. is 24 O X 1O -5 cm. per sec<strong>on</strong>d ; T. Svedberg gave for the<br />

lower limit 7*6 x K) -3 cm. per sec<strong>on</strong>d; <strong>and</strong> E. F. Burt<strong>on</strong>, 2-3xl0 -5 cm. per sec<strong>on</strong>d<br />

for the speed of colloidal soln. in ethyl mal<strong>on</strong>ate. The subject was discussed by<br />

A. Einstein, F. Evers, J. J. Bikermann, N. Bach <strong>and</strong> N. Balaschowa, W. Biltz,<br />

<strong>and</strong> W. R. Whitney <strong>and</strong> J. C. Blake.<br />

According to L. Liebermann, reddish-brown, colloidal soln. of platinum become<br />

dark brown when hydrogen is passed through the liquid. The colloidal soln. of<br />

platinum dissolves hydrogen gas roughly in proporti<strong>on</strong> to the c<strong>on</strong>centrati<strong>on</strong>.<br />

E. O. Auerswald studied the subject. G. Kernot <strong>and</strong> F. de S. Niquessa found that<br />

some protective colloids—e.g. gum arabic, dextrin, <strong>and</strong> albumen—reduce the proporti<strong>on</strong><br />

of gas absorbed, but sucrose has a negligibly small effect. In virtue of the<br />

absorbed hydrogen, colloidal platinum favours many reducti<strong>on</strong>s catalytieally<br />

though the activity of the colloid decreases with use, <strong>and</strong> the chemical work d<strong>on</strong>e<br />

increases, but not proporti<strong>on</strong>ally, with the c<strong>on</strong>e, of the colloidal soln. Thus,<br />

C. Paal <strong>and</strong> A. Schwarz found that acetylene is reduced to ethylene <strong>and</strong> ethane ;<br />

<strong>and</strong> ethylene to ethane. C. Paal <strong>and</strong> J. Gerum observed that many organic<br />

substances such as unsaturated oils are hydrogenized—e.g. linseed oil is hardened<br />

to a white fat. J. D<strong>on</strong>au found that a borax bead is coloured reddish-brown by<br />

colloidal platinum. J. Eggert found that ferric salts are reduced to the ferrous<br />

state ; <strong>and</strong> C. Paal <strong>and</strong> H. Biittner, that amm<strong>on</strong>ium molybdate is reduced.<br />

E. C. Auerswald studied the pois<strong>on</strong>ing of the catalytic activity of platinum hydrosol<br />

by mercury.<br />

Li. Liebermann observed that the colloidal soln. of platinum c<strong>on</strong>tains activated<br />

oxygen. C. Paal observed that carb<strong>on</strong> m<strong>on</strong>oxide is oxidized by oxygen to carb<strong>on</strong><br />

dioxide in the presence of colloidal platinum ; <strong>and</strong> C. Paal <strong>and</strong> A. Schwarz, that

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