Linseed oil

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Linseed oil

Linseed oil, is a colourless to yellowish oil obtained from the dried, ripened seeds of the flax plant (Linum usitatissimum, Linaceae). The oil is obtained by pressing, sometimes followed by solvent extraction. Boiled linseed oil is heated and treated with chemicals that make it unfit for human consumption. Linseed oil and flaxseed oil are both derived from the same plant, but oils may differ because of the way they are processed. Flax-based oils are sought after as food because of their high levels of α-Linolenic acid (a particular form of omega-3 fatty acid), but it is important that only food-grade oil be used for food.

Linseed oil is a drying oil, meaning it can polymerize into a solid form. Due to its polymer-forming properties, linseed oil is used on its own or blended with other oils, resins, and solvents as an impregnator and varnish in wood finishing, as a pigment binder in oil paints, as a plasticizer and hardener in putty, and in the manufacture of linoleum. Linseed oil use has declined over the past several decades with increased availability of synthetic alkyd resins—which function similarly but resist yellowing.[1]

Linseed oil is an edible oil marketed as a nutritional supplement. In parts of Europe, it is traditionally eaten with potatoes and quark (cheese). It is regarded as a delicacy due to its hearty taste, which enhances the flavour of quark, which is otherwise bland.[2]

Chemical aspects[edit]

Linseed oil is a triglyceride, like other fats. Linseed oil is distinctive in terms of fatty acid constituents of the triglyceride, which contain an unusually large amount of α-linolenic acid, which has a distinctive reaction toward oxygen in air. Specifically, the constituent fatty acids in a typical linseed oil are of the following types:[3]

Having a high content of di- and triunsaturated esters, linseed oil is particularly susceptible to polymerization reactions upon exposure to oxygen in air. This polymerization, which is called drying, results in the rigidification of the material. The drying process can be so exothermic as to pose a fire hazard under certain circumstances. To prevent premature drying, linseed oil-based products (oil paints, putty) should be stored in air-tight containers.

Like some other drying oils, linseed oil exhibits fluorescence under UV light after degradation.[4]

Representative triglyceride found in a linseed oil, a triester (triglyceride) derived of linoleic acid, alpha-linolenic acid, and oleic acid.

Uses[edit]

Most applications of linseed oil exploit its drying properties, i.e., the initial material is liquid or at least pliable and the aged material is rigid but not brittle. The water-repelling (hydrophobic) nature of the resulting hydrocarbon-based material is advantageous.

Paint binder[edit]

"Your country needs flax .." U.S. WWII poster soliciting linseed oil for use in paint.

Linseed oil is a common carrier used in oil paint. It can also be used as a painting medium, making oil paints more fluid, transparent and glossy. It is available in varieties such as cold pressed, alkali refined, sun bleached, sun thickened, and polymerised (stand oil). The introduction of linseed oil was a significant advance in the technology of oil painting.

Putty[edit]

Traditional glazing putty, consisting of a paste of chalk powder and linseed oil, is a sealant for glass windows that hardens within a few weeks of application and can then be painted over. The utility of putty is owed to the drying properties of linseed oil.

Wood finish[edit]

When used as a wood finish, linseed oil dries slowly and shrinks little upon hardening. Linseed oil does not cover the surface as varnish does, but soaks into the (visible and microscopic) pores, leaving a shiny but not glossy surface that shows off the grain of the wood. A linseed oil finish is easily repaired, but it provides no significant barrier against scratching. Only wax finishes are less protective. Liquid water penetrates a linseed oil finish in mere minutes, and water vapour bypasses it almost completely.[5] Garden furniture treated with linseed oil may develop mildew. Oiled wood may be yellowish and is likely to darken with age. Because it fills the pores, linseed oil partially protects wood from denting by compression.

Linseed oil is a traditional finish for gun stocks, though very fine finish may require months to obtain. Several coats of linseed oil is the traditional protective coating for the raw willow wood of cricket bats. Linseed oil is also often used by billiards or pool cue-makers for cue shafts, as a lubricant/protectant for wooden recorders, and used in place of epoxy to seal modern wooden surfboards. It is used to coat cricket bats so that the wood retains some moisture. New cricket bats are coated with linseed oil and knocked to perfection so they last longer.[6]

Additionally, a luthier may use linseed oil when reconditioning a guitar, mandolin, or other stringed instrument's fret board; lemon-scented mineral oil is commonly used for cleaning, then a light amount of linseed oil (or other drying oil) is applied to protect it from grime that might otherwise result in accelerated deterioration of the wood.

Gilding[edit]

Boiled linseed oil is used as sizing in traditional oil gilding to adhere sheets of gold leaf to a substrate (parchment, canvas, Armenian bole, etc.) It has a much longer working time than water-based size and gives a firm smooth surface which is adhesive enough in the first 12–24 hours after application to cause the gold to attach firmly to the intended surface.

Linoleum[edit]

Linseed oil is used to bind wood dust, cork particles, and related materials in the manufacture of the floor covering linoleum. After its invention in 1860 by Frederick Walton, linoleum, or "lino"[citation needed] for short, was a common form of domestic and industrial floor covering from the 1870s until the 1970s when it was largely replaced by PVC ('vinyl') floor coverings.[7] However, since the 1990s, linoleum is on the rise again, being considered more environmentally sound than PVC.[8] Linoleum has given its name to the printmaking technique linocut, in which a relief design is cut into the smooth surface and then inked and used to print an image. The results are similar to those obtained by woodcut printing.

Nutritional supplement and food[edit]

Flax seeds contain lignans, a class of phytoestrogens considered to have antioxidant and cancer-preventing properties,[9][10][11] although the extracted linseed oil, according to some, does not contain lignans found in flax seed,[9] and allegedly does not have the same antioxidant properties.[citation needed] Some brands of supplement have lignans added during production. Flax seed oil is easily oxidized, and rapidly becomes rancid, with an unpleasant odour, unless refrigerated. Even when kept under cool conditions, it has a shelf life of only a few weeks.[12][13][14] Oil with an unpleasant or rancid odor should be discarded. Oxidation of flax seed oil is a major commercial concern, and antioxidants may be added to prevent rancidification.[15] Linseed oil is not generally recommended for use in cooking, yet one study does show that the alpha linolenic acid (ALA) while bound in flaxseed was found to be stable for cooking. When bound to flaxseed ALA can withstand temperatures up to 350 degrees F (176.67 C) for two hours.[16][unreliable medical source?][17]

Food-grade flaxseed oil is cold-pressed, obtained without solvent extraction, in the absence of oxygen, and marketed as edible flaxseed oil. Fresh, refrigerated and unprocessed, linseed oil is used as a nutritional supplement and is a traditional European ethnic food, highly regarded for its hearty taste. It contains the highest level of the omega-3 fatty acid ALA among vegetable oils.[18] Regular flaxseed oil contains between 52% and 63% ALA (C18:3 n-3). Plant breeders have developed flaxseed with both higher ALA (70%) and very low ALA content (< 3%).[19] The USFDA granted generally recognized as safe (GRAS) status for high alpha linolenic flaxseed oil.[20]

According to the Flax Council of Canada, ALA is required for normal infant development[21] and may be beneficial for reducing inflammation leading to atherosclerosis,[22] and for preventing heart disease and arrhythmia.[23] However, recent well-controlled placebo studies suggest the regular consumption of flaxseed oil may not reduce the risk of stroke, heart disease, or cancer.[24]

Studies[25][26] have shown a relationship between ALA and an increased risk of prostate cancer. This risk is irrespective of source (e.g., meat, vegetable oil).[27] Alternatively, at least one meta analysis has found a weak protective association between dietary ALA intake and prostate cancer risk.[28]

Nutrient content[edit]

Typical fatty acid content % [29] % European[30]
Palmitic acid6.04.0–6.0
Stearic acid2.52.0–3.0
Arachidic acid0.50–0.5
Palmitoleic acid-0–0.5
Oleic acid19.010.0–22.0
Eicosenoic acid-0–0.6
Linoleic acid24.112.0–18.0
Alpha-linolenic acid47.456.0–71.0
Other0.5-

Nutrition information from the Flax Council of Canada.[9]

Per 1 tbsp (14 g)

Flax seed oil contains no significant amounts of protein, carbohydrates or fibre.

Additional uses[edit]

Modified linseed oils[edit]

Stand oil[edit]

Stand oil is generated by heating linseed oil near 300 °C for a few days in the complete absence of air. Under these conditions, the polyunsaturated fatty esters convert to conjugated dienes, which then undergo Diels-Alder reactions, leading to crosslinking. The product, which is highly viscous, gives highly uniform coatings that "dry" to more elastic coatings than linseed oil itself. Soybean oil can be treated similarly, but converts more slowly. On the other hand, tung oil converts very quickly, being complete in minutes at 260 °C. Coatings prepared from stand oils are less prone to yellowing than are coatings derived from the parent oils.[32]

Boiled linseed oil[edit]

Boiled linseed oil is used as a paint binder or as a wood finish on its own. Heating the oil causes it to polymerise and oxidise, making it thicker and shortening its drying time. Today, most products labelled as "boiled linseed oil" are a combination of raw linseed oil, petroleum-based solvent, and metallic dryers (catalysts to accelerate drying). The heating of the oil and its polymerisation as well as forming Diels-Alder products and the use of metallic dryers make boiled linseed oil inedible. Some products contain only heat-treated linseed oil, without exposure to oxygen. Heat-treated linseed oil is thicker and dries very slowly. This grade of linseed oil is usually labelled as "polymerized" or "stand" oil, though some types may still be labelled as "boiled".

Spontaneous combustion[edit]

Rags soaked with linseed oil stored in a pile are considered a fire hazard because they provide a large surface area for oxidation of the oil, and the oil oxidises quickly. The oxidation of linseed oil is an exothermic reaction, which accelerates as the temperature of the rags increases. When heat accumulation exceeds the rate of heat dissipation into the environment, the temperature increases and may eventually become hot enough to make the rags spontaneously combust.[33]

In 1991, One Meridian Plaza, a high rise in Philadelphia, was severely damaged and three firefighters perished in a fire caused by linseed oil-soaked rags.[34] In 2011, a garage in Sacramento also caught fire due to the spontaneous combustion of linseed oil-soaked rags.[35]

See also[edit]

Further reading[edit]

References[edit]

  1. ^ Jones, Frank N. (2003). Alkyd Resins. doi:10.1002/14356007.a01_409. 
  2. ^ "'Rezept Kartoffeln mit Leinoel'". 
  3. ^ A. G. Vereshagin and G. V. Novitskaya (1965) The triglyceride composition of linseed oil. Journal of the American Oil Chemists' Society 42, 970-974. [1]
  4. ^ E. René de la Rie, Fluorescence of Paint and Varnish Layers (Part II), Studies in Conservation Vol. 27, No. 2 (1982), pp65-69
  5. ^ Flexner, Bob. Understanding Wood Finishing. Reader's Digest Association, Inc, 2005, p. 75.
  6. ^ James Laver, "Preparing Your Cricket Bat - Knocking In," ABC of Cricket.
  7. ^ S. Diller and J. Diller, Craftsman's Construction Installation Encyclopedia, Craftsman Book Company, 2004, p. 503
  8. ^ Julie K. Rayfield, The Office Interior Design Guide: An Introduction for Facility and Design Professionals, John Wiley & Sons, 1994, p. 209
  9. ^ a b c "Flax - A Healthy Food". Flax Council of Canada. Retrieved 2008-01-24. 
  10. ^ Diane H. Morris. "Flax - A Smart Choice" (PDF). New Flax Facts. Flax Council of Canada. 
  11. ^ "Flaxseed Oil". University of Maryland Medical Center. April 2002. Retrieved 2006-11-12. 
  12. ^ "Flax Seed Oil Capsules". Flax Seed Oil. Retrieved 2008-01-24. ]
  13. ^ "Flax Seed Oil". Busy Women's Fitness. Retrieved 2008-01-24. 
  14. ^ "A Danish Expert Finds Flaxseed and Other Plant Oils Simply Better than Fish and Krill". Fatty Acids Hub. Retrieved 2011-04-01. 
  15. ^ D. Berab, D. Lahirib and A. Naga (June 2006). "Studies on a natural antioxidant for stabilization of edible oil and comparison with synthetic antioxidants". Journal of Food Engineering 74 (4): 542–545. doi:10.1016/j.jfoodeng.2005.03.042. 
  16. ^ "Grain Information". Retrieved 2013-01-29. 
  17. ^ "Oxidative stability of flaxseed lipids during baking". Retrieved 2013-01-29. 
  18. ^ Muir, Alister D. (2003). Flax, The genus Linum, p. 298. Taylor & Francis Ltd. ISBN 0-415-30807-0.
  19. ^ Thompson, Lilian U and Cunnane, Stephen C. eds (2003). Flaxseed in human nutrition. 2nd ed. AOCS Press. pp. 8–11. ISBN 1-893997-38-3. 
  20. ^ "U.S. FDA/CFSAN Agency Response Letter GRAS Notice No. GRN 00256". U.S. FDA/CFSAN. Retrieved 2013-01-29. 
  21. ^ Diane H. Morris. "Omega-3 Fats Are Essential For Infants" (PDF). New Flax Facts. Flax Council of Canada. Retrieved 2013-01-29. 
  22. ^ Diane H. Morris. "Flax Reduces Inflammation Leading to Atherosclerosis" (PDF). New Flax Facts. Flax Council of Canada. Retrieved 2013-01-29. 
  23. ^ Diane H. Morris. "ALA and Other Omega-3 Fats May Protect Against Arrhythmia" (PDF). New Flax Facts. Flax Council of Canada. Retrieved 2013-01-29. 
  24. ^ Nigel Hawkes (March 24, 2006). "The benefits of fish and linseed oils as elixir of life are another health myth". Times Online. Archived from the original on 2007-03-31. Retrieved 2013-01-29. 
  25. ^ Ramon JM, Bou R, Romea S, et al. (September 2000). "Dietary fat intake and prostate cancer risk: a case-control study in Spain". Cancer Causes & Control 11 (8): 679–85. doi:10.1023/A:1008924116552. PMID 11065004. 
  26. ^ Brouwer IA, Katan MB, Zock PL (April 2004). "Dietary alpha-linolenic acid is associated with reduced risk of fatal coronary heart disease, but increased prostate cancer risk: a meta-analysis". The Journal of Nutrition 134 (4): 919–22. PMID 15051847. 
  27. ^ De Stéfani E, Deneo-Pellegrini H, Boffetta P, Ronco A, Mendilaharsu M (March 2000). "Alpha-linolenic acid and risk of prostate cancer: a case-control study in Uruguay". Cancer Epidemiology, Biomarkers & Prevention 9 (3): 335–8. PMID 10750674. 
  28. ^ Carayol M, Grosclaude P, Delpierre C (March 2010). "Prospective studies of dietary alpha-linolenic acid intake and prostate cancer risk: a meta-analysis". Cancer Causes & Control 21 (3): 347–55. doi:10.1007/s10552-009-9465-1. PMID 19921446. 
  29. ^ "Linseed" (PDF). Interactive European Network for Industrial Crops and their Applications. October 14, 2002. Retrieved 2008-01-24. 
  30. ^ Deutsche Gesellschaft für Fettwissenschaft (see 'Leinöl Europa': Fettsäurezusammensetzung wichtiger pflanzlicher und tierischer Speisefette und -öle (PDF)
  31. ^ Leah Goldberg (2008-10-26). "Measuring Rate Capability of a Bakelite-Trigger RPC Coated with Linseed Oil". American Physical Society. Bibcode:2008APS..DNP.DA033G. 
  32. ^ Ulrich Poth, "Drying Oils and Related Products" in Ullmann's Encyclopedia of Industrial Chemistry Wiley-VCH, Weinheim, 2002. doi:10.1002/14356007.a09_055
  33. ^ Ettling, Bruce V.; Adams, Mark F. (1971). "Spontaneous combustion of linseed oil in sawdust". Fire Technology 7 (3): 225. doi:10.1007/BF02590415. 
  34. ^ Routley, J. Gordon; Jennings, Charles; Chubb, Mark (February 1991), "Highrise Office Building Fire One Meridian Plaza Philadelphia, Pennsylvania", Report USFA-TR-049 (Federal Emergency Management Agency) 
  35. ^ http://blogs.sacbee.com/crime/archives/2011/08/two-morning-fir.html

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