Balancing Vinyl Chloride Production Process

Balancing Vinyl Chloride Production Process
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In the production of vinyl chloride, different routes are explored to address drawbacks and limitations. The acetylene process, the balance route process, and the drawbacks of each method are analyzed. The use of ethane, ethylene, and acetylene in the manufacturing process is evaluated, highlighting challenges such as HCl by-product formation and capital cost implications.

  • Vinyl chloride
  • Production process
  • Acetylene process
  • Balance route
  • Manufacturing

Uploaded on Mar 04, 2025 | 0 Views


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Presentation Transcript


  1. Diagram

  2. the acetylene process. This route has the major drawback of converting half the chlorine set to it to HCl of this severely limited use of ethane or ethylene in vinyl chloride manufacture.

  3. (3). THE BALANCE ROUTE PROCESS

  4. called balance route. In this, acetylene based of ethylene based process is reacted in parallel, the HCl produced by ethylene do chloride pyrohysis is being fed to the acetylene based process.

  5. Diagram

  6. in bp inUK. However, this solution to the problem of HCl by-product is not as attractive as it appears at first soght for two reasons.

  7. Firstly, the process requires three reaction stages, so that capitals of operating cost are increased.

  8. Secondly, half the fed is still the expensive acetylene in this form described, it is not a favoured way of making vinyl chloride.

  9. Reduction of aldehyde can also be affected by reduction with aluminium isopropoxide Al(isopropyl). It is known as meerwen pondoff reduction.

  10. Diagram

  11. DESCENT OF HOMOLOGOUS SERIES

  12. RCH2COOH RCOOH

  13. RCH2OH ROH

  14. RCH2COOt RCOO t

  15. BARBIER LORQUIN WISLAND DEGRADATION REACTION

  16. Diagram

  17. Diagram

  18. If we make use of Ba salt of the carboxylic acid with barium acetate, there will be reduction in the no of carbon atoms.

  19. Diagram

  20. GALLAHER HOLLANDER REDUCTION: -

  21. This knocks off two carbon atoms

  22. Diagram

  23. HOFFMANS DEGRADATION

  24. Diagram

  25. SCHMIDT DEGRADATION REACTION

  26. Diagram

  27. RING CONTRACTION

  28. ZELINSKYS REACTION

  29. Action of nitrons acid on cyclic amines

  30. Action of silver nitrate on cyclic halides

  31. Diagram

  32. Action of GRIGNARDS REAGENT

  33. OXIDATION OF CYCLIC KETONE

  34. The oxidants are usually KMnO4, O3, of nitric acid HNO3

  35. Diagram

  36. BY HYDROGENATION

  37. RING FUSSION BY ISOMERISATIOON (AL2O3)

  38. Preparation of 1-tetralone and tetralin

  39. Preparation of naphthalene derivative

  40. Preparation of phenanthrene

  41. Diagram

  42. Diagram

  43. It is used in the preparation of indicators e.g phenolpyhalein

  44. Preparation of osin

  45. Preparation of Quinizarrn

  46. Preparation of triphenyl methane

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