DE243948C - - Google Patents

Info

Publication number
DE243948C
DE243948C DENDAT243948D DE243948DA DE243948C DE 243948 C DE243948 C DE 243948C DE NDAT243948 D DENDAT243948 D DE NDAT243948D DE 243948D A DE243948D A DE 243948DA DE 243948 C DE243948 C DE 243948C
Authority
DE
Germany
Prior art keywords
perborates
melt
borax
boric acid
pressure
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.)
Active
Application number
DENDAT243948D
Other languages
German (de)
Publication of DE243948C publication Critical patent/DE243948C/de
Active legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B15/00Peroxides; Peroxyhydrates; Peroxyacids or salts thereof; Superoxides; Ozonides
    • C01B15/055Peroxyhydrates; Peroxyacids or salts thereof
    • C01B15/12Peroxyhydrates; Peroxyacids or salts thereof containing boron

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Oxygen, Ozone, And Oxides In General (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

KAISERLICHESIMPERIAL

PATENTAMT.PATENT OFFICE.

PATENTSCHRIFTPATENT LETTERING

- JVl 243948 -. KLASSE 12 t. GRUPPE - JVl 243948 -. CLASS 12 t. GROUP

Dr. FRIEDRICH BERGIUS in HANNOVER. Verfahren zur Darstellung von Perboraten.Dr. FRIEDRICH BERGIUS in HANOVER. Procedure for the representation of perborates.

Zusatz zum Patent 232001 vom 19. April 1910.Addendum to patent 232001 from April 19, 1910.

Patentiert im Deutschen Reiche vom 7. Dezember 1910 ab. Längste Dauer: 18. April 1925.Patented in the German Empire on December 7, 1910. Longest duration: April 18, 1925.

Es ist gelungen, in ähnlicher Weise, wie es gemäß Patentschrift 232001 für die Herstellung von Erdalkalisuperoxyden vorgeschlagen worden, Perborate herzustellen. Es hat sich nämlich gezeigt, daß ζ. B. eine Lösung von Borax in geschmolzenem Ätznatron imstande ist, Sauerstoff aufzunehmen, wenn man diesen bei erhöhtem Druck hindurchleitet. Es ist hierbei wichtig, eine möglichst niedere Temperatur der lösenden Schmelze zu wählen, da bei hoher Temperatur die Perborate zersetzt werden.It has succeeded in a similar way as it is according to patent specification 232001 for the production of alkaline earth peroxides have been proposed to produce perborates. It has namely shown that ζ. B. a solution of borax in molten caustic soda capable is to absorb oxygen when it is passed through at increased pressure. It is It is important here to choose the lowest possible temperature for the dissolving melt, since at high temperature the perborates are decomposed.

Zur Ausführung des Verfahrens löst man z. B. Borax oder Borsäure in dem niedrigstTo carry out the method you solve z. B. Borax or boric acid in the lowest

schmelzenden Gemisch von Ätznatron und Ätzkali, und leitet bei etwa 200 ° C. in einem druckfesten Eisengefäß komprimierten Sauerstoff von etwa 50 Atm. durch die Schmelze. Nach beendeter Oxydation läßt man die Schmelze unter Aufrechterhaltung des Druckes abkühlen und wäscht mit Alkohol aus. Die Ätzalkalien werden dadurch gelöst, und das Perborat bleibt als Niederschlag zurück. Während die früheren Verfahren meist Natriumsuperoxyd zur Herstellung von Perboraten benutzten, kann man nach dem vorliegenden Verfahren den leicht zugänglichen komprimierten Sauerstoff direkt. an die Borverbindung anlagern, und man erspart die umständliche und kostspielige Herstellung des Natriumsuperoxyds. Als Katalysator werden zweckmäßig Eisen - Mangan -Vanadinverbindungen benutzt.melting mixture of caustic soda and caustic potash, and conducts at about 200 ° C. in one Pressure-tight iron vessel compressed oxygen of about 50 atm. through the melt. When the oxidation has ended, the melt is left while the pressure is maintained cool and wash off with alcohol. The caustic alkalis are thereby dissolved, and that Perborate remains as a precipitate. While the earlier procedures mostly sodium peroxide used for the production of perborates, you can use the present process the easily accessible compressed Oxygen directly. add to the boron compound, and you save the cumbersome and expensive manufacture of sodium peroxide. Suitable as a catalyst Iron-manganese-vanadium compounds used.

Claims (1)

Patent-Anspruch:Patent claim: Weitere Ausbildung des durch Patent 232001 geschützten Verfahrens zum Zweck der Herstellung von Perboraten, dadurch gekennzeichnet, daß man Borsäure, Borax oder andere Borverbindungen in einer indifferenten Schmelze, z. B. Alkali, löst und durch die Schmelze Sauerstoff unter Druck oder in Gegenwart eines Katalysators hindurchleitet. Further development of the method protected by patent 232001 for the purpose the preparation of perborates, characterized in that boric acid, borax or other boron compounds in an indifferent Melt, e.g. B. alkali, dissolves and passes oxygen through the melt under pressure or in the presence of a catalyst. 3535 4040
DENDAT243948D Active DE243948C (en)

Publications (1)

Publication Number Publication Date
DE243948C true DE243948C (en)

Family

ID=503030

Family Applications (1)

Application Number Title Priority Date Filing Date
DENDAT243948D Active DE243948C (en)

Country Status (1)

Country Link
DE (1) DE243948C (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5127558A (en) * 1989-11-03 1992-07-07 Conti P Method and device for turning out men's stockings outside the relevant operating machine

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5127558A (en) * 1989-11-03 1992-07-07 Conti P Method and device for turning out men's stockings outside the relevant operating machine

Similar Documents

Publication Publication Date Title
DE2100373B2 (en) Catalyst for the hydrogenation of nitro compounds
DE1185187B (en) Process for the production of organoaluminum compounds
DE1041960B (en) Process for the production of organic hydroperoxides
DE243948C (en)
DE2037928B2 (en) Process for the production of a nickel sponge and its use as a catalyst for the hydrogenation of organic compounds
DE2222173B2 (en) PROCESS FOR MANUFACTURING METALS OR METAL ALLOYS
DE857841C (en) Process for the preparation of 1-amino-4- (4'-oxy) -phenylaminoanthraquinones
DE237096C (en)
DE2301739B2 (en) Process for the preparation of optionally halogen-substituted m-aminobenzenesulfonic acids
DE734312C (en) Process for the preparation of 1,4-butenediols
DE1016026B (en) Process for the production of metals by reduction
DE186526C (en)
DE353948C (en) Process for the pretreatment of cellulose for the production of easily filterable viscose
DE706694C (en) Process for the preparation of salts or sulfenamides of mercaptobenzothiazoles
DE120586C (en)
DE195351C (en)
DE204279C (en)
DE672910C (en) Process for the preparation of 2-oxy-6-aminonaphthalene
DE204204C (en)
DE439511C (en) Process for the preparation of 1, 4, 5, 8-naphthalenetetracarboxylic acid
DE539891C (en) Process for the production of water gas
DE2729073A1 (en) Indigo prodn. from phenyl-glycine carboxylic acid salt - by fusion in mixed potassium hydroxide and sodium hydroxide melt, then oxidn.
DE855561C (en) Process for the production of cyclic imines or their salts
DE269852C (en)
DE263330C (en)