DE672121C - Process for the production of stable metal brines - Google Patents

Process for the production of stable metal brines

Info

Publication number
DE672121C
DE672121C DEI53920D DEI0053920D DE672121C DE 672121 C DE672121 C DE 672121C DE I53920 D DEI53920 D DE I53920D DE I0053920 D DEI0053920 D DE I0053920D DE 672121 C DE672121 C DE 672121C
Authority
DE
Germany
Prior art keywords
production
stable metal
brines
water
solution
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
DEI53920D
Other languages
German (de)
Inventor
Dr Max Bockmuehl
Eugen Doerzbach
Dr Walther Persch
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Priority to DEI53920D priority Critical patent/DE672121C/en
Application granted granted Critical
Publication of DE672121C publication Critical patent/DE672121C/en
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J13/00Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
    • B01J13/0004Preparation of sols
    • B01J13/0034Additives, e.g. in view of promoting stabilisation or peptisation

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Dispersion Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

Verfahren zur Herstellung von stabilen Metallsolen Es hat sich gezeigt, daß bei der Herstellung von Metallsolen erst durch die kambinierte Verwendung von lysalbin- oder protalbinsauren Salzen einerseits und wasserlöslichen Oxaikylcellulosen oder ihren Derivaten andererseits ein Optimum an Haltbarkeit der Metallsole zu erzielen ist, während die Oxalkylcellulosen oder die lysalbin- bzw. protalbinsauren Salze für sich allein keine über lange Zeiträume hin anhaltende Stbilisie-. rungswirkung zeigen. Es gelingt hierdurch, zu Metallslen zu gelangen, welche noch nach 1 Jahr und länger haltbar sind Selbstverständlich müssen bei der Herstellung und Aufbewahrung dieser Metallsole die für diese Klasse erforderlichen Vorsichtsmaßregeln beachtet werden.Process for the production of stable metal brines It has been shown that in the production of metal brines only through the use of kambiniert lysalbinic or protalbinic acid salts on the one hand and water-soluble oxaikylcelluloses or their derivatives, on the other hand, to achieve optimum durability of the metal brine is, while the oxalkylcelluloses or the lysalbinic or protalbinic acid salts in and of itself no long-term stbilisia. effect demonstrate. This makes it possible to get metal beads that are still available after 1 year and have a longer shelf life, of course, during manufacture and storage of this metal brine, the precautionary measures required for this class are observed will.

Beispiele I. 2,75 ccm einer von freiem Ammoniak weitgehendst befreiten Wismut-Ammon- Citrat-Lösung mit einem Gehalt von 6 % Wismut werden unter Umriihren langsam in ein Gemisch von 25 ccm einer Lösung vcan 0,1% lysalbin- und 0,1% protalbinsaurem Natrium und 25 ccm einer Oxäthylmethylcelluloselösung von der Viscosität 3 eingetragen. Die Lösung wird bei 500 c in stickstoffatmosphäre und unter durchperlendem Stickstoff mit Glucose oder Natriumhydrosulfit oder Formaldehyd reduziert. Das entstandene Sol wird mit Alkohol-Äther gefällt und die Fällung in Wasser gelöst. Examples I. 2.75 cc of a freed ammonia as far as possible Bismuth-ammon-citrate solution with a content of 6% bismuth are stirred with stirring slowly into a mixture of 25 cc of a solution of 0.1% lysalbic acid and 0.1% protalbic acid Sodium and 25 cc of an oxethylmethylcellulose solution of viscosity 3 were entered. The solution is at 500 c in a nitrogen atmosphere and under nitrogen bubbling reduced with glucose or sodium hydrosulfite or formaldehyde. The resulting Sol is precipitated with alcohol-ether and the precipitate is dissolved in water.

2. 1,0g Silbernitrat wird in 3 ccm Wasser gelöst und im Überschuß mit einer 30 0/0igefl Lösung von Triäthanolamin versetzt und mit 25 ccm einer Oxäthylmethylcelluloselösung von der Viscosität I,25 und 25 ccm einer Lösung, die 0,1% lysalbin- und 0,1% protalbinsaures Natrium enthält, gemischt. Man erwärmt auf etwa a 70 C. Das entstandene Sol wird entweder durch Alkohol-Äther gefällt und nachher in Wasser wieder gelöst oder durch verdünnte Salzsäure gefällt, mit Wasser gewaschen und in schwach alkalischem Wasser wieder gelöst. 2. 1.0 g of silver nitrate is dissolved in 3 cc of water and in excess mixed with a 30% solution of triethanolamine and with 25 cc of an oxethylmethylcellulose solution of viscosity I, 25 and 25 ccm of a solution containing 0.1% lysalbic acid and 0.1% protalbic acid Contains sodium, mixed. It is heated to about a 70 C. The resulting sol is either precipitated by alcohol-ether and then dissolved again in water or by diluted hydrochloric acid precipitated, washed with water and soaked in weakly alkaline water solved again.

Claims (1)

PANTENTANSPRUCH: Verfahren zur Herstellung von stabilen Metallsolen, dadurch gekennzeichnet, daß die Bildung der Metallsole in Gegenwart von wasserlöslichen Oxalkylcellulosen oder ihrer Derivate und von protalbin-und/ oder lysalbinsauren Salzen erfolgt. PANTENT CLAIM: Process for the production of stable metal brines, characterized in that the formation of the metal brine in the presence of water-soluble Oxalkylcelluloses or their derivatives and of protalbic and / or lysalbic acids Salting takes place.
DEI53920D 1935-12-19 1935-12-19 Process for the production of stable metal brines Expired DE672121C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEI53920D DE672121C (en) 1935-12-19 1935-12-19 Process for the production of stable metal brines

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEI53920D DE672121C (en) 1935-12-19 1935-12-19 Process for the production of stable metal brines

Publications (1)

Publication Number Publication Date
DE672121C true DE672121C (en) 1939-02-23

Family

ID=7193735

Family Applications (1)

Application Number Title Priority Date Filing Date
DEI53920D Expired DE672121C (en) 1935-12-19 1935-12-19 Process for the production of stable metal brines

Country Status (1)

Country Link
DE (1) DE672121C (en)

Similar Documents

Publication Publication Date Title
DE672121C (en) Process for the production of stable metal brines
DE585532C (en) Process for the preparation of aqueous solutions of 1-phenyl-2íñ3-dialkyl-4-dialkylamino-pyrazolones with 1-phenyl-2íñ3-dialkylpyrazolone-4-aminomethanesulfonic acid salts and their derivatives
DE568339C (en) Process for the production of a silver-containing preparation from ethylene diamine
DE690488C (en) Process for the production of concentrated aqueous caffeine solutions
DE565414C (en) Process for the preparation of arsenic compounds
DE463792C (en) Process for the production of a cold mixture
DE414146C (en) Process for the preparation of a red dye
DE564124C (en) Manufacture of water glass powder
AT157575B (en) Process for the production of undecomposed, sterilizable drug solutions from the double compound theophylline-piperazine.
DE425419C (en) Process for the production of aromatic stibic acids
DE545915C (en) Process for the preparation of compounds of 7-iodo-8-oxyquinoline-5-sulfonic acid which are easily soluble in water
DE526392C (en) Process for the production of metal complex compounds
AT149825B (en) Process for the production of alkali or alkaline earth double compounds of dimethylxanthines with organic acids.
DE812342C (en) Process for the preparation of water-soluble salts of sulfonamides
DE521123C (en) Process for the production of non-settling aqueous dye pastes
DE666266C (en) Process to increase the water solubility of azo compounds
DE549840C (en) Process for the preparation of 6-bromo-2-oxynaphthalene-3-carboxylic acid
DE818047C (en) Process for the preparation of concentrated neutral solutions of theophylline
DE559333C (en) Process for the preparation of 1-oxyanthracene-2-carboxylic acid
DE859344C (en) Process for the preparation of a green dye
DE525654C (en) Process for the preparation of an o-amino-p-cresol carbonic acid
DE614337C (en) Process for the preparation of a calcium salt solution suitable for injection
AT117492B (en) Process for the preparation of w-aminoalkylaminonaphthalenecarboxylic acids.
DE748824C (en) Process for the production of acidic wool dyes
AT152742B (en) Process for the preparation of 10-halo-1,5-phenanthrolines.