[go: up one dir, main page]

AT50327B - Process for the preparation of formaldehyde sulfoxylates. - Google Patents

Process for the preparation of formaldehyde sulfoxylates.

Info

Publication number
AT50327B
AT50327B AT50327DA AT50327B AT 50327 B AT50327 B AT 50327B AT 50327D A AT50327D A AT 50327DA AT 50327 B AT50327 B AT 50327B
Authority
AT
Austria
Prior art keywords
alkali
formaldehyde
parts
zinc
preparation
Prior art date
Application number
Other languages
German (de)
Original Assignee
Englert & Dr F Becker Fa R
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
Priority claimed from DE1905222195D external-priority patent/DE222195C/de
Application filed by Englert & Dr F Becker Fa R filed Critical Englert & Dr F Becker Fa R
Application granted granted Critical
Publication of AT50327B publication Critical patent/AT50327B/en

Links

Landscapes

  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

  

   <Desc/Clms Page number 1> 
 
 EMI1.1 
 
 EMI1.2 
 
 EMI1.3 
 
 EMI1.4 
 

 <Desc/Clms Page number 2> 

 
Die Umsetzung wird in der Warme oder in* der Siedehitze ausgeführt. Soweit hiebei schwerlösliches bzw. unlösliches Zinksalz der   Formaldehydsulfoxylsäurc   entsteht, kann man zum Zwecke der Überführung desselben in lösliches Sulfoxylat von vornherein Alkalisuifitc oder nachträglich diese bzw. andere Zink ausfällende Alkalisalze bzw. Alkalihydrat   hinzufügen.   
 EMI2.1 
 zeitigem Rühren 1/2 bis 3/4 Stunde gekocht, wobei das verdampfende Wasser immer wieder ersetzt wird. 
 EMI2.2 
 Niederschlag und kann durch Kochen mit Natriumsulfit usw. in Natrollsalz umgewandelt werden, ein anderer Teil ist der Hauptsache nach als Natronsalz in Lösung. 



   Beispiel II : 252 Teile Natriumsulfit, 180 Teile Zinksulfit, 30 Teile Formaldehyd (in   30% iger   Lösung), 100 Teile Zinkstaub werden gemäss Beispiel I einige Zeit gekocht. 



   Im Filtrat befindet sich das Natriumsalz der   Formaldehydsulfoxylsäure.   



   Beispiel   III :   300 Teile   Formaldehydhydrosulfit,   180 Teile Zinksuiit, 200 Teile Zinkstaub und etwa 1500 bis 2000 Teile Wasser werden einige Zeit zum Sieden erhitzt. Um das im Nieder- 
 EMI2.3 
 kann man Natriumsulfit hinzufügen und einige Zeit kochen. 



   Beispiel IV : 300 Teile   Formaldehydhydrosulfit,   180 Teile Zinksulfit, 252 Teile Natrium-   suint, 300   Teile Zinkstaub und etwa 2000 Teile Wasser werden einige Zeit zum Sieden erhitzt. 



    Das Filtrat enthält   das Natriumsalz der Formaldehydsulfoyxlsäure, welches z. B. durch Eindampfes   im Vakuum gewonnen werden   kann. 
 EMI2.4 
 vorhandenen Zinkes   ausgefällt   und das   Filtrat wie üblich   weiter verarbeitet. Man erhält in diesem Fall ein   Gemisch   des Natrium-und Ammoniumsalzes der Formaldehydsulfoxylsäure. 



   In obigen Beispielen kann man statt zu kochen auch unter Rühren solange auf 90 bis   100"C   erhitzen,   n. IR   noch eine Zunahme an Reduktionsvermögen nahcweisbar ist. Arbeitet man bei niedrigerer Temperature, so dauert die Reaktion entspreched länger.



   <Desc / Clms Page number 1>
 
 EMI1.1
 
 EMI1.2
 
 EMI1.3
 
 EMI1.4
 

 <Desc / Clms Page number 2>

 
The reaction is carried out in the warm or in the boiling heat. Insofar as sparingly soluble or insoluble zinc salt of formaldehyde sulfoxylic acid is formed, alkali metal can be added from the start or this or other zinc precipitating alkali metal salts or alkali hydrate can be added to convert it into soluble sulfoxylate.
 EMI2.1
 Stirring early for 1/2 to 3/4 hour, replacing the evaporating water again and again.
 EMI2.2
 Precipitate and can be converted into sodium salt by boiling with sodium sulfite, etc., another part is mainly in solution as sodium salt.



   Example II: 252 parts of sodium sulfite, 180 parts of zinc sulfite, 30 parts of formaldehyde (in 30% strength solution), 100 parts of zinc dust are boiled according to Example I for some time.



   The sodium salt of formaldehyde sulfoxylic acid is in the filtrate.



   Example III: 300 parts of formaldehyde hydrosulfite, 180 parts of zinc oxide, 200 parts of zinc dust and about 1500 to 2000 parts of water are heated to the boil for some time. In order to
 EMI2.3
 you can add sodium sulfite and cook for a while.



   Example IV: 300 parts of formaldehyde hydrosulfite, 180 parts of zinc sulfite, 252 parts of sodium suint, 300 parts of zinc dust and about 2000 parts of water are heated to the boil for some time.



    The filtrate contains the sodium salt of Formaldehydsulfoyxläure, which z. B. can be obtained by evaporation in a vacuum.
 EMI2.4
 existing zinc is precipitated and the filtrate is processed further as usual. In this case, a mixture of the sodium and ammonium salts of formaldehyde sulfoxylic acid is obtained.



   In the above examples, instead of boiling, the mixture can be heated to 90 to 100 ° C. with stirring, as long as an increase in reducing power is evident. If one works at a lower temperature, the reaction takes correspondingly longer.

 

Claims (1)

PATENT-ANSPRUCH : Verfahren zur Darstellung von Formaldehydsulfoxylaten, darin bestehend, dass man Formaldehydalkalibisulfit oder Formaldchyd zugleich mit neutralem alkalisulfit ode rformaldehydalkalihydrosuiit mit Zink ohne Anwesenheit von Säuren in der Wärme behandelt, entweder EMI2.5 herein Alkalisulfite oder nachträglich diese bzw. andere Zink ausfällende Aikaiisaize bzw. Alkalihydrathinzugefügtwerden. PATENT CLAIM: Process for the preparation of formaldehyde sulfoxylates, consisting in that one treats formaldehyde alkali bisulfite or formaldehyde at the same time with neutral alkali sulfite or rformaldehyde alkali hydrosulite with zinc without the presence of acids in the heat, either EMI2.5 alkali sulphites or these or other zinc precipitating alkali metals or alkali hydrates can be added subsequently.
AT50327D 1905-05-03 1909-03-06 Process for the preparation of formaldehyde sulfoxylates. AT50327B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE1905222195D DE222195C (en) 1905-05-03

Publications (1)

Publication Number Publication Date
AT50327B true AT50327B (en) 1911-10-25

Family

ID=5844073

Family Applications (1)

Application Number Title Priority Date Filing Date
AT50327D AT50327B (en) 1905-05-03 1909-03-06 Process for the preparation of formaldehyde sulfoxylates.

Country Status (1)

Country Link
AT (1) AT50327B (en)

Similar Documents

Publication Publication Date Title
AT50327B (en) Process for the preparation of formaldehyde sulfoxylates.
AT26860B (en) Process for the preparation of aminooxy derivatives of phenylnaphtimidazole.
US5276A (en) Improvement in making sugar
CH155687A (en) Process for the preparation of a water-soluble antimony salt.
DE557449C (en) Process for the preparation of 2-methylaminobenzene-1-carboxylic acid-4-sulfonic acid
AT65225B (en) Process for the preparation of anhydrous hydrosulfites.
DE392461C (en) Process for the production of tanning substances
DE531517C (en) Process for the preparation of alkali salts of the cyano mercury phenols
DE540328C (en) Process for the preparation of easily soluble complex double salts of cyano mercuriphenols
DE1210888B (en) Process for the production of thiophene-2, 5-dicarboxylic acid
CH137466A (en) Process for converting metal salts into those with a higher oxidation state.
US1757829A (en) Pickling of metals
DE222195C (en)
AT78987B (en) Process for the preparation of water-soluble condensation products.
AT37386B (en) Process for preparing soluble starch.
DE596448C (en) Process for the production of salts from core-mercured cresols
DE491405C (en) Process for the preparation of concentrated solutions of Trimercuri-diacetone hydrate
AT88646B (en) Process for the production of tanning substances.
DE436443C (en) Process for the preparation of an oxypyridinecarboxylic acid
AT117502B (en) Process for the representation of tanning substances.
DE202242C (en)
DE675408C (en) Increase in the yield from the heat-hydrolytic precipitation of titanium compounds
CH89235A (en) Process for the representation of chrome yellow using chrome waste liquor.
CH101402A (en) Process for the preparation of an aryloxynaphthyl ketone.
Laurent On the ferric and ferri-mangani-tungstic acids