GB255904A - Improvements in the manufacture and production of active adsorbent and catalytic masses - Google Patents

Improvements in the manufacture and production of active adsorbent and catalytic masses

Info

Publication number
GB255904A
GB255904A GB18633/26A GB1863326A GB255904A GB 255904 A GB255904 A GB 255904A GB 18633/26 A GB18633/26 A GB 18633/26A GB 1863326 A GB1863326 A GB 1863326A GB 255904 A GB255904 A GB 255904A
Authority
GB
United Kingdom
Prior art keywords
jelly
added
sol
products
washed
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
GB18633/26A
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
Publication of GB255904A publication Critical patent/GB255904A/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
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/02Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
    • B01J20/06Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising oxides or hydroxides of metals not provided for in group B01J20/04
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J21/00Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • B01J21/06Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
    • B01J21/08Silica

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Analytical Chemistry (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)

Abstract

255,904. I. G. Farbenindustrie Akt.- Ges. July 27, 1925, [Convention date]. Grant of Patent opposed. Purifying liquids. - In preparing liquidrefining products comprising catalytic materials precipitated on a colloidal support, the support, whether in the form of sol or jelly, is intimately mixed with the catalytic materials or with substances giving rise thereto, whereafter the mixture, which may be washed at any convenient stage, is dried. Gel-forming irreversible colloids, particularly silica, alumina, and iron oxide, are used as supports, and the admixed substances, which may be added in solution or in finely divided solid, preferably colloidal, form, may comprise metal compounds decomposed at raised temperatures, such as acetates, nitrates, carbonates, or ammonium compounds. When the support is taken in the sol form, the catalytic materials may be added without first purifying the sol, and when several materials are to be added, some may be added to the components used in making the sol. The sol is allowed to set to a jelly before washing and drying, and by suitably controlling the additions, it may be made to set directly after the additions have been made or after standing, with or without heating. When the support is taken in the jelly form, it is preferably purified, it may be by pressure, and is then suspended in water or a suitable solution, whereafter the catalvtic materials are added separately or together; one or more of the materials may, however, be added to the components used in making the jelly. The jelly, whether or not containing the catalytic materials, may be pressed before drying and may be mechanically treated, as in a ball mill, with the addition, it may be, of catalytic materials. Further additions may be made to the final products, and if the products contain metal oxides, these may be reduced. The adsorbing power of the products may be increased by removing the included additions or their decomposition products, such as metal oxides, for example by treatment with nitrogen oxides and water vapour. According to one example, a silica sol prepared by treating sodium silicate with sulphuric acid is treated at once with copper sulphate solution. After standing for some time, or on heating, the mixture sets to a jelly which is partially washed, dried at 100‹ C., saturated with water vapour, and completely washed, whereafter it is dried at 150-300‹ C. The copper oxide can be removed from the product by treating it with acids, preferably after saturation with water vapour. According to another example, sodium silicate is treated with acetic acid so as to produce, after a time, a jelly, which is washed and then slightly pressed until it contains 94.5 per cent of water. To the jelly suspended in water is added a solution of uranyl nitrate, mercurous nitrate, or ammonium vanadate, and the mixture is stirred and allowed to settle. The jelly is drawn off, slightly washed, and dried slowly at 50-200‹ C. On heating to higher temperatures the added substances decompose and products containing oxide of uranium, mercury, or vanadium may be obtained, and on heating to still higher temperatures the product may contain mercury. Specifications 212,034 and 220.771, [both in Class 1 (i), Chemical processes &c.], are referred to.
GB18633/26A 1925-07-27 1926-07-26 Improvements in the manufacture and production of active adsorbent and catalytic masses Expired GB255904A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE255904X 1925-07-27

Publications (1)

Publication Number Publication Date
GB255904A true GB255904A (en) 1927-07-07

Family

ID=5965835

Family Applications (1)

Application Number Title Priority Date Filing Date
GB18633/26A Expired GB255904A (en) 1925-07-27 1926-07-26 Improvements in the manufacture and production of active adsorbent and catalytic masses

Country Status (1)

Country Link
GB (1) GB255904A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2462236A (en) * 1945-07-30 1949-02-22 Universal Oil Prod Co Manufacture of silica hydrogel and catalysts
US2754304A (en) * 1952-05-27 1956-07-10 Quaker Oats Co Catalytic production of furfuryl alcohol and catalyst therefor
CN115608320A (en) * 2022-09-19 2023-01-17 四川澳凯化工有限公司 Preparation method of mercury removal agent with desulfurization effect

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2462236A (en) * 1945-07-30 1949-02-22 Universal Oil Prod Co Manufacture of silica hydrogel and catalysts
US2754304A (en) * 1952-05-27 1956-07-10 Quaker Oats Co Catalytic production of furfuryl alcohol and catalyst therefor
CN115608320A (en) * 2022-09-19 2023-01-17 四川澳凯化工有限公司 Preparation method of mercury removal agent with desulfurization effect
CN115608320B (en) * 2022-09-19 2024-05-07 成华区雾夜话辛工程管理部 Preparation method of mercury removal agent with desulfurization effect

Similar Documents

Publication Publication Date Title
US1755496A (en) Process of preparing siliceous materials
US1976875A (en) Gel and method of making same
JPS6351732B2 (en)
ES411067A1 (en) Process for purifying metallurgical gases containing sulphurous anhydride by extracting mercury
US1964516A (en) Production of monocarboxylic acids
GB255904A (en) Improvements in the manufacture and production of active adsorbent and catalytic masses
US3186794A (en) Oxidation of sulphur dioxide to sulphur trioxide and catalysts therefor
GB816047A (en) Process for refining crude silicon
GB1512305A (en) Process for regenerating spent oxidation catalysts containing vanadium oxide
US1797804A (en) Manufacture of active masses
US2897159A (en) Catalyst manufacture
GB749645A (en) Improvements relating to the catalytic oxidation of sulphur dioxide to sulphur trioxide
US2046166A (en) Vanadium catalyst
CN114433071A (en) Denitration catalyst prepared by taking attapulgite as carrier and preparation method thereof
US1631823A (en) Purifying gases
JPS6071507A (en) Manufacture of expanded graphite
US2330553A (en) Ferric oxide and its preparation
GB1280855A (en) Process for the recovery of metallic catalysts
US2683122A (en) Process of regenerating an oxidation catalyst comprising oxides of phosphorus and molybdenum
US1455060A (en) Process of recovering iron oxide and other products from spent iron sludgf
SU432921A1 (en) Method of producing a catalyst for the oxidation of sulfur-containing anhydride
CN86100770A (en) The peroxidation method for preparing hydrogen
US2204543A (en) Process for the purification of sulphur dioxide-containing technical gases obtained from roasting
US1886023A (en) Catalytic oxidation of anthracene
US1786509A (en) Gas purification