Iodine value

From Wikipedia, the free encyclopedia
  (Redirected from Iodine number)
Jump to: navigation, search

The iodine value (or "iodine adsorption value" or "iodine number" or "iodine index") in chemistry is the mass of iodine in grams that is consumed by 100 grams of a chemical substance. Iodine numbers are often used to determine the amount of unsaturation in fatty acids. This unsaturation is in the form of double bonds, which react with iodine compounds. The higher the iodine number, the more C=C bonds are present in the fat.[1] It can be seen from the table that coconut oil is very saturated, which means it is good for making soap. On the other hand, linseed oil is highly unsaturated, which makes it a drying oil, well suited for making oil paints.

Table of iodine values[edit]

Fat Iodine number[1]
Tung oil 163 – 173
Grape seed oil 124 – 143
Palm oil 44 – 51
Olive oil 80 – 88
Coconut oil 7 – 10
Palm kernel oil 16 – 19
Cocoa butter 35 – 40
Jojoba oil ~80
Poppyseed oil ~133
Cottonseed oil 100 – 117
Corn oil 109 – 133
Wheat germ oil[2] 115 – 134
Sunflower oil 125 – 144
Linseed oil 136 – 178
Soybean oil 120 – 136
Peanut oil 84 – 105
Rice bran oil 99 – 108

Methodology[edit]

This particular analysis is an example of iodometry. A solution of iodine ions is yellow/brown in color. When added to a complex solution however, any chemical group (usually C=C double bonds) in solution that react with iodine effectively reduce the strength, or magnitude of the colour (by taking iodine ions out of solution). Thus the amount of iodine required to make a solution retain the characteristic yellow/brown colour can effectively be used to determine the amount of iodine sensitive groups present in the solution.

In a typical procedure, the fatty acid is treated with an excess of the Hanuš or Wijs solutions, which are, respectively, solutions of iodine monobromide (IBr) and iodine monochloride (ICl) in glacial acetic acid. Unreacted iodine monobromide (or monochloride) is then allowed to react with potassium iodide, converting it to iodine, whose concentration can be determined by titration with sodium thiosulfate.[3]

The chemical reaction associated with this method of analysis involves formation of the diiodo alkane (R and R' symbolize alkyl or other organic groups):

\mathrm{R{-}CH{=}CH{-}R' + I_2 \longrightarrow R{-}CHI{-}CHI{-}R'}

The precursor alkene (RCH=CHR') is colourless and so is the organoidine product (RCHI-CHIR').


Related methods of analysis[edit]

References[edit]

  1. ^ a b Thomas, Alfred (2002). "Fats and Fatty Oils". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a10_173. 
  2. ^ http://online.personalcarecouncil.org/ctfa-static/online/lists/cir-pdfs/pr248.pdf
  3. ^ Firestone D (May–Jun 1994). "Determination of the iodine value of oils and fats: summary of collaborative study". J AOAC Int. 77 (3): 674–6. PMID 8012219.