GB473342A - Improvements in the manufacture of hydrogen peroxide - Google Patents

Improvements in the manufacture of hydrogen peroxide

Info

Publication number
GB473342A
GB473342A GB1043236A GB1043236A GB473342A GB 473342 A GB473342 A GB 473342A GB 1043236 A GB1043236 A GB 1043236A GB 1043236 A GB1043236 A GB 1043236A GB 473342 A GB473342 A GB 473342A
Authority
GB
United Kingdom
Prior art keywords
distillation
hydrogen peroxide
residue
water
sulphuric acid
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
GB1043236A
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to GB1043236A priority Critical patent/GB473342A/en
Publication of GB473342A publication Critical patent/GB473342A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25BELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B1/00Electrolytic production of inorganic compounds or non-metals
    • C25B1/01Products
    • C25B1/28Per-compounds
    • C25B1/30Peroxides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Vaporization, Distillation, Condensation, Sublimation, And Cold Traps (AREA)

Abstract

<PICT:0473342/III/1> In obtaining hydrogen peroxide by a cyclic process in which solutions comprising ammonium sulphate and sulphuric acid are electrolyzed and the resulting solution is distilled to liberate hydrogen peroxide, all or part of the residual solution from the hydrogen peroxide distillation is subjected to a separate, rapid, thin layer distillation in the presence of water or steam at a high temperature in order to evaporate ammonia and sulphuric acid which are condensed and cooled for return to the electrolysis step. Residual lye from the hydrogen peroxide distillation containing ammonium sulphate and sulphuric acid flows from a tank 1 down a quartz tube 3 which is externally heated by combustion gases to 300--400 DEG C. The vapours pass through a pipe 8 to a washing tower 9 which is irrigated by a circulation of washing liquid passing through a cooler 11, pump 12 and spray 13. The circulating liquid has the same composition as the distillate coming from the pipe 8. The undistilled residue passes through an outlet 6 to a receptacle 7 and may consist of 10 per cent of the original liquid. It contains all the catalytic impurities of the original liquid. If the residue consists of 30 per cent it may be returned continuously to the tank 1 until it has been sufficiently concentrated when it can be neutralized to precipitate catalytic impurities and evaporated. This step is preferable if non-volatile compounds such as sodium or calcium sulphates are employed during the electrolysis. The residue may be treated with water and allowed to stand in order to hydrolyze the pyrosulphates it contains prior to the neutralization step. It is preferable to maintain, by the addition of water, a water concentration of not lower than 30 per cent in the liquor proceeding to the tube 3. Alternatively, the distillation may be effected by flowing the liquors down a quartz filled tower up which passes steam, superheated to 500 DEG C., the vapours being treated as before; or the residue from the distillation set forth in the Figure, can be subjected to a steam distillation, a common condensing plant being employed. The distillation may be conducted at atmospheric or diminished pressure.
GB1043236A 1936-04-09 1936-04-09 Improvements in the manufacture of hydrogen peroxide Expired GB473342A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1043236A GB473342A (en) 1936-04-09 1936-04-09 Improvements in the manufacture of hydrogen peroxide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1043236A GB473342A (en) 1936-04-09 1936-04-09 Improvements in the manufacture of hydrogen peroxide

Publications (1)

Publication Number Publication Date
GB473342A true GB473342A (en) 1937-10-11

Family

ID=9967722

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1043236A Expired GB473342A (en) 1936-04-09 1936-04-09 Improvements in the manufacture of hydrogen peroxide

Country Status (1)

Country Link
GB (1) GB473342A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114606517A (en) * 2022-03-18 2022-06-10 化学与精细化工广东省实验室 High-quality raw material for producing ultra-pure electronic grade hydrogen peroxide and preparation method thereof
CN114737207A (en) * 2022-03-18 2022-07-12 化学与精细化工广东省实验室 Method for synthesizing and purifying electronic-grade hydrogen peroxide

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114606517A (en) * 2022-03-18 2022-06-10 化学与精细化工广东省实验室 High-quality raw material for producing ultra-pure electronic grade hydrogen peroxide and preparation method thereof
CN114737207A (en) * 2022-03-18 2022-07-12 化学与精细化工广东省实验室 Method for synthesizing and purifying electronic-grade hydrogen peroxide

Similar Documents

Publication Publication Date Title
US1906467A (en) Distilling hydrochloric acid
ES359619A1 (en) Condensing power plant system
GB473342A (en) Improvements in the manufacture of hydrogen peroxide
GB1347884A (en) Process for cracking sulphuric acid
US2141773A (en) Recovery of fluorine compounds from water vapor containing volatile fluorine compounds
GB454558A (en) Improvements in or relating to a process of and apparatus for separating water contained in a liquid
GB669928A (en) Improvements in and relating to compression distillation plant
GB889037A (en) Improvements in and relating to the treatment of sulphur
GB1389566A (en) Apparatus for and a method of purifying waste liquor
GB912772A (en) Improvements in heat exchange processes
US2222559A (en) Method of treating feed water
US1922278A (en) Process of concentrating nitric acid
GB441586A (en) Process of producing crystallized ammonium nitrate with utilization of the reaction heat for the evaporation of water
GB851935A (en) Improvements in or relating to processes and plants for treating substances by vapour injection
US1546910A (en) Process of concentrating nitric acid
CN116639657A (en) Hydrochloric acid purification treatment method containing sulfuric acid impurities
GB379319A (en) Improvements in and relating to the manufacture of ammonium carbonate and bicarbonate
GB436369A (en) Improvements in process and apparatus for the recovery of acid gases
GB811050A (en) Process for the production of highly concentrated hydrogen peroxide solutions
GB380699A (en) Process for the treatment of ammoniacal gas liquor and other liquids containing tar acids
US1816123A (en) Production of ammonium sulphate
GB770172A (en) Process and apparatus for the preparation of ammonium sulphate
GB445334A (en) An improved process for fractionally condensing hydrogen peroxide vapours from mixtures with water vapour
SU473772A1 (en) Method of removing carbon disulfide from viscose fiber
SU27049A1 (en) The method of obtaining furfural