Method for the manufacture of cyclododecasulfur
US-2020207621-A1 · Jul 2, 2020 · US
US11059722B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11059722-B2 |
| Application number | US-202016807671-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 3, 2020 |
| Priority date | Mar 2, 2016 |
| Publication date | Jul 13, 2021 |
| Grant date | Jul 13, 2021 |
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The present invention relates to a method for the manufacture of cyclododecasulfur, a cyclic sulfur allotrope wherein the number of sulfur (S) atoms in the allotrope's homocyclic ring is 12. The method includes reacting a metallasulfur derivative with an oxidizing agent in a reaction zone to form a cyclododecasulfur-containing reaction mixture.
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The invention claimed is: 1. A method for the manufacture of cyclododecasulfur, comprising reacting a metallasulfur derivative with an oxidizing agent in a reaction zone to form a cyclododecasulfur-containing reaction mixture containing cyclododecasulfur, wherein the metallasulfur derivative comprises (PMDETA)Zn(S 4 ). 2. The method of claim 1 wherein the oxidizing agent is characterized by the formula: X-X′ wherein X and X′ are the same or different and are selected from the group consisting of halogens and pseudohalogens. 3. The method of claim 1 , wherein the oxidizing agent comprises one or more of SO 2 Cl 2 and SO 2 Br 2 . 4. The method of claim 1 wherein the oxidizing agent comprises one or more of O 2 , H 2 O 2 , an alkyl peroxide, and an acyl peroxide. 5. The method of claim 1 , wherein the stoichiometric ratio of the oxidizing agent to the metallasulfur derivative is less than one equivalent of the oxidizing agent present for every two M-S bonds in the metallasulfur derivative. 6. The method of claim 2 , wherein X and X′ are one or more of chlorine and bromine. 7. The method of claim 1 , further comprising a step of reacting elemental sulfur with a sulfur templating agent to form the metallasulfur derivative prior to the step of reacting the metallasulfur derivative with the oxidizing agent. 8. The method of claim 7 , wherein the reacting the elemental sulfur with a sulfur templating agent to form the metallasulfur derivative is carried out in the presence of water. 9. The method of claim 1 , further comprising a step of isolating the cyclododecasulfur from the cyclododecasulfur-containing reaction mixture. 10. The method of claim 9 , wherein the step of isolating the cyclododecasulfur from the cyclododecasulfur-containing reaction mixture comprises one or more steps chosen from dissolving, heat treating, drying, acid treating, solvent washing, crystallizing, and sedimentation. 11. The method of claim 9 , wherein the step of isolating the cyclododecasulfur comprises treating the cyclododecasulfur with a solvent for the cyclododecasulfur to form a dissolution liquor. 12. The method of claim 9 , further comprising removing metal and metal-containing compounds from the cyclododecasulfur by sedimentation of the metal and the metal-containing compounds. 13. The method of claim 1 , further comprising isolating cyclododecasulfur by heating a cyclododecasulfur-containing mixture in the presence of a solvent to decompose and dissolve in the solvent impurities that are present. 14. The method of claim 1 , further comprising isolating cyclododecasulfur by treating a cyclododecasulfur-containing mixture with an acid to remove any metal or metal-containing compounds that are present. 15. The method of claim 11 , further comprising crystallizing cyclododecasulfur from the dissolution liquor.
from non-gaseous sulfur compounds other than sulfides or materials containing such sulfides · CPC title
Heterocyclic compounds containing rings having three or more sulfur atoms as the only ring hetero atoms · CPC title
Insoluble sulfur (mu-sulfur) · CPC title
Other after-treatment of sulfur · CPC title
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