Separation of linoleic acid from linolenic acid by azeotropic distillation

Information

  • Patent Grant
  • 5928478
  • Patent Number
    5,928,478
  • Date Filed
    Monday, September 14, 1998
    26 years ago
  • Date Issued
    Tuesday, July 27, 1999
    25 years ago
  • Inventors
  • Examiners
    • Manoharan; Virginia
Abstract
Linoleic acid cannot be separated from linolenic acid by distillation or rectification because of the closeness of their boiling points. Linoleic acid is readily separated from linolenic acid by azeotropic distillation. Effective agents are nonane, dimethyl formamide, 2-nitropropane and pentyl propionate.
Description

FIELD OF THE INVENTION
This invention relates to a method for separating linoleic acid from linolenic acid using certain organic liquids as the agent in azeotropic distillation.
DESCRIPTION OF PRIOR ART
Azeotropic distillation is the method of separating close boiling compounds or azeotrones from each other by carrying out the distillation in a multiplate rectification column in the presence of an added liquid,said liquid forming an azeotrope with one or more of the compounds to be separated. It presence on each plate of the rectification column alters the relative volatility in a direction to make the separation on each plate greater and thus require either fewer plates to effect the same separation or make possible a greater degree of separation with the same number of plates. The azeotrope forming agent is introduced with the feed to a continuous column. The azeotrope forming agent and the more volatile component are taken off as overhead product and the less volatile component comes off as bottoms product. The usual methods of separating the azeotrope former from the more volatile component are cooling and phase separation or solvent extraction.
The usual method of evaluating the effectiveness of azeotropic distillation agents is the change in reddjative volatility of the compounds to be separated. Table 1 shows the degree of separation or purity obtainable by theoretical plates at several relative volatilites. Table 1 shows that a relative volatility of at least 1.2 is required to get an effective separation by rectification.
TABLE 1______________________________________Effect Of Relative Volatility on Theoretical Stage Requirements.Separation Purity, Relative VolatilityBoth Products 1.02 1.1 1.2 1.3 1.4 1.5 2.0 3.0(Mole Fraction) Theoretical Stages at Total Refux______________________________________0.999 697 144 75 52 40 33 19 120.995 534 110 57 39 30 25 14 90.990 463 95 49 34 26 22 12 70.98 392 81 42 29 22 18 10 60.95 296 61 31 21 16 14 8 40.90 221 45 23 16 12 10 5 3______________________________________
Linoleic acid and linolenic acid boil only one degree apart and have a relative volatility of 1.05 which makes it impossible to separate them by conventional distillation or rectification. Table 2 shows that with an agent giving a relative volatility of 1.4, only 35 actual plates are required to get 99% purity.
TABLE 2______________________________________Theoretical And Actual Plates Required vs. RelativeVolatility For Linoleic Acid From Linolenic Acid Separation Theoretical Plates Actual PlatesRelative Required At Total Required, 75%Volatility Reflux, 99% Purity Efficiency______________________________________1.16 62 831.27 39 521.35 31 411.40 26 35______________________________________
OBJECTIVE OF THE INVENTION
The objectof this invention is to provide a process or method of azeotropic distillation that will enhance the relative volatility ot linoleic acid from linolenic acid in their separation in a rectification column. It is a further object of this invention to identify effective azeotropic distillation agents that are stable and can be recyled.
SUMMARY OF THE INVENTION
The objects of this invention are provided by a process for the separation of linoleic acid from linolenic acid which entails the use of certain organic compounds when employed as the agent in azeotropic distillation.
TABLE 3______________________________________Effective Azeotropic Distillation Agents ForSeparating Linoleic Acid From Linolenic Acid RelativeCompounds Volatility______________________________________None 1.05Dimethyl formamide 1.35Ethyl acetate 1.172-Nitropropane 1.271-Methyl-2-pyrrolidinone 1.16Nonane 1.4______________________________________
TABLE 4______________________________________Effective Azeotropic Distillation Agents ForSeparating Linolenic Acid From Linoleic Acid RelativeCompounds Volatility______________________________________None 1.05Pentyl propionate 1.27Propiophenone 1.17______________________________________
DETAILED DESCRIPTION OF THE INVENTION
I have discovered that certain organic compounds will effectively increase the relative volatility between linoleic acid and linolenic acid during rectification when employed as the agent in azeotropic distillation. They are dimethyl formamide, ethyl acetate, 2-nitro- propane, 1-methyl-2-pyrtolidinone, nonane, pddlntyl propionate, and propiophenone.
THE USEFULNESS OF THE INVENTION
The usefulness of this invention can be demonstrated by referring to the data presented in Tables 1, 2, 3 and 4. All of the successful agents show that linoleic acid can be separated from linolenic acid by means of azeotropic distillation in a rectification column and that the ease of separation as measured by relative volatility is considerable.





WORKING EXAMPLE
1. Fifty grams of linoleic--linolenic acids and fifty grams of nonane were charged to a vapor--liquid equilibrium still and refluxed for two hours. The vapor composition was64.5% linoleic acid and 35.5% linolenic acid. The liquid composition was 56.2% linoleic acid and 43.8% linolenic acid. This is a relative volatility of 1.4. 2. Fifty grams of linolenic--linoleric acids and fifty grams of pentyl propionate were charged to a vapor--liquid equilibrium still and refluxed for two hours. The vapor composition was 61.1% linolenic acid and 38.9% linolenic acid. The liquid composition was 55.2 linolenic acid and 44.9% linoleric acid. This is a relative volatility of 1.27.
Claims
  • 1. A method for recovering linoleic acid from linolenic acid which comprises distilling a mixture of linoleic acid and linolenic acid in the presence of an azeotrocde forming agent, recovering the linoleic acid and the azeotrope forming agent as overhead product and obtaining the linolenic acid as bottoms product, wherein said azeotrope forming agent consists essentially of one material selected from the group consisting of ethyl acetate and 2 -nitropropane.
  • 2. A method for recovering linolenic acid from linoleic acid which comprises distilling a mixture of linolenic acid and linoleic acid in the presence of an azeotropic forming agent, recovering the linolenic acid and the azeotrope forming agent as overhead product and obtaining the linoleic acid as bottoms product, wherein said azeotrope forming agent consists essentially of one material selected from the group consisting of pentyl propionate and propiophenone.
US Referenced Citations (5)
Number Name Date Kind
2200390 Freeman May 1940
2200391 Freeman May 1940
3892789 Parsons Jul 1975
5084142 Berg et al. Jan 1992
5085739 Berg et al. Feb 1992