JPS5581866A - Production of cyanuric chloride - Google Patents
Production of cyanuric chlorideInfo
- Publication number
- JPS5581866A JPS5581866A JP15496578A JP15496578A JPS5581866A JP S5581866 A JPS5581866 A JP S5581866A JP 15496578 A JP15496578 A JP 15496578A JP 15496578 A JP15496578 A JP 15496578A JP S5581866 A JPS5581866 A JP S5581866A
- Authority
- JP
- Japan
- Prior art keywords
- dicyan
- chlorine
- reaction
- catalyst
- mey
- 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.)
- Granted
Links
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
PURPOSE: The reaction between dicyan and chlorine is effected in the presence of a specific catalyst at relatively mild temperatures lower than 500°C, thus reducing the amount of the catalyst used and energy consumed and producing title compound that is used as a synthetic intermediate of agricultural chemicals and dyes in high yield.
CONSTITUTION: The reaction between dicyan and chlorine is effected using two kinds of catalysts in two stages, of which the first is activated carbon supporting at least 13% of an aluminum salt and a compound of MeY (MeY is at least one salt selected from salts of Mg, Ca, Cr, Mn, Fe, Co, Ni, Cu, and Zn) and the second is activated carbon. The reaction temperature at both stages is commonly 350W500, preferably 380W460°C and the space velocity of the gas mix of dicyan and chlorine is 100W10,000hr-1 based on the metal-supporting catalyst.
EFFECT: The running operation can be conducted advantageously with high space velocity.
COPYRIGHT: (C)1980,JPO&Japio
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15496578A JPS5581866A (en) | 1978-12-18 | 1978-12-18 | Production of cyanuric chloride |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15496578A JPS5581866A (en) | 1978-12-18 | 1978-12-18 | Production of cyanuric chloride |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5581866A true JPS5581866A (en) | 1980-06-20 |
| JPS6343392B2 JPS6343392B2 (en) | 1988-08-30 |
Family
ID=15595765
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP15496578A Granted JPS5581866A (en) | 1978-12-18 | 1978-12-18 | Production of cyanuric chloride |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5581866A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111533632A (en) * | 2020-06-02 | 2020-08-14 | 新乡市瑞丰新材料股份有限公司 | Preparation method of high-content monoalkylbenzene |
-
1978
- 1978-12-18 JP JP15496578A patent/JPS5581866A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111533632A (en) * | 2020-06-02 | 2020-08-14 | 新乡市瑞丰新材料股份有限公司 | Preparation method of high-content monoalkylbenzene |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6343392B2 (en) | 1988-08-30 |
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