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Decaffeination

From Wikipedia, the free encyclopedia
"Decaf" redirects here. For the computer software program, see DECAF.

Decaffeination is the removal of caffeine from coffee beans, cocoa, tea leaves, and other caffeine-containing materials. Decaffeinated products are commonly termed by the abbreviation decaf. Decaffeinated drinks contain typically 1–2% of the original caffeine content, but sometimes as much as 20%.[1]

Decaffeination of coffee

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Friedlieb Ferdinand Runge performed the first isolation of caffeine from coffee beans in 1820, after the German poet Goethe heard about his work on belladonna extract, and requested he perform an analysis on coffee beans.[2] Though Runge was able to isolate the compound, he did not learn much about the chemistry of caffeine itself, nor did he seek to use the process commercially to produce decaffeinated coffee.[citation needed]

Decaffeination processes

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Various methods can be used for decaffeination of coffee. These methods take place prior to roasting and may use organic solvents such as dichloromethane or ethyl acetate, supercritical CO2, or water to extract caffeine from the beans, while leaving flavour precursors in as close to their original state as possible.[3]

Organic solvent processes

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Direct method
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The first commercially successful decaffeination process was invented by German merchant Ludwig Roselius and co-workers in 1903, after Roselius observed that a consignment of coffee beans accidentally soaked in sea water had lost most of their caffeine content while losing little of their flavour.[4][5] The process was patented in 1906, and involved steaming coffee beans with various acids or bases, then using benzene as a solvent to remove the caffeine.[6][7] Coffee decaffeinated this way was sold as Kaffee HAG after the company name Kaffee Handels-Aktien-Gesellschaft (Coffee Trading Company) in most of Europe, as Café Sanka in France and later as Sanka brand coffee in the United States. Café HAG and Sanka are now worldwide brands of Kraft Foods.[citation needed]

1914 American newspaper advert for Kaffee HAG decaffeinated coffee

Methods similar to those first developed by Roselius have continued to dominate, and are sometimes known as the direct organic solvent method. However, because of health concerns regarding benzene (which is recognized today as a carcinogen),[8] other solvents, such as dichloromethane or ethyl acetate, are now used.[9] The unroasted (green) beans are first steamed and then rinsed with the solvent which extracts the caffeine, while leaving other constituents largely unaffected. The process is repeated between 8 and 12 times until the caffeine content meets the required standard (97% of caffeine removed according to the US standard, or 99.9% caffeine-free by mass per the EU standard).[3]

Indirect method
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Another variation of Roselius' method is the indirect organic solvent method. In this method, instead of treating the beans directly, they are first soaked in hot water for several hours, then removed. The remaining water is treated with solvents (e.g. dichloromethane or ethyl acetate) to extract the caffeine from the water. As in other methods, the caffeine can then be separated from the organic solvent by simple evaporation. The same water is recycled through this two-step process with new batches of beans. An equilibrium is reached after several cycles, wherein the water and the beans have a similar composition except for the caffeine. After this point, the caffeine is the only material removed from the beans, so no coffee strength or other flavorings are lost.[10] Because water is used in the initial phase of this process, indirect method decaffeination is sometimes referred to as "water-processed". This method was first mentioned in 1941, and people have made significant efforts to make the process more "natural" and a true water-based process by finding ways to process the caffeine out of the water in ways that circumvent the use of organic solvents.[11]

Swiss Water process

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Sack of green coffee beans decaffeinated by the Swiss Water process

An alternative method for removal of caffeine from coffee is the Swiss Water process. This process uses no organic solvents, and instead only water is used to decaffeinate beans. It is a technique first developed in Switzerland in 1933, and commercialized by Coffex S.A. in 1980.[5] The Swiss Water process was then introduced by The Swiss Water Decaffeinated Coffee Company of Burnaby, British Columbia, in 1988.[12]

The process uses green coffee extract (GCE) for the caffeine extraction mechanism. Green coffee extract is a solution containing the water-soluble components of green coffee except for the caffeine, obtained by soaking green coffee beans in hot water, then filtering through an activated charcoal filter to remove the caffeine molecules.[5] Fresh beans containing both caffeine and the other components are added to the GCE solution, where the gradient pressure difference between the GCE (which is caffeine-lean) and the green coffee (which is caffeine-rich) causes the caffeine molecules to migrate from the green coffee into the GCE.[13] Because GCE is saturated with the other water-soluble components of green coffee, only the caffeine molecules migrate to the GCE; the other water-soluble coffee elements are retained in the green coffee. The newly caffeine-rich GCE solution is then passed through the activated carbon filters to remove the caffeine again, and the process is repeated. The continuous batch process takes 8–10 hours to meet the final residual decaffeinated target.[14]

Food engineer Torunn Atteraas Garin also developed a process to remove caffeine from coffee.[15][16]

Triglyceride process

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In this process, green coffee beans are soaked in a hot water and coffee solution to draw the caffeine to the surface of the beans. Next, the beans are transferred to another container and immersed in coffee oils that were obtained from spent coffee grounds and left to soak.

After several hours of high temperatures, the triglycerides in the oils remove the caffeine, but not the flavor elements, from the beans. The beans are separated from the oils and dried. The caffeine is removed from the oils, which are reused to decaffeinate another batch of beans. This is a direct-contact method of decaffeination.

Supercritical CO2 process

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Food scientists have also turned to supercritical carbon dioxide (sCO2) as a means of decaffeination. Developed by Kurt Zosel, a scientist of the Max Planck Institute, it uses CO2 (carbon dioxide), heated and pressurised above its critical point, to extract caffeine.[5] Green coffee beans are steamed and then added to a high pressure vessel. A mixture of water and CO2 is circulated through the vessel at 300 atm and 65 °C (149 °F). At this pressure and temperature CO2 is a supercritical fluid, with properties midway between a gas and a liquid. Caffeine dissolves into the CO2; but compounds contributing to the flavour of the brewed coffee are largely insoluble in CO2 and remain in the bean. In a separate vessel, caffeine is scrubbed from the CO2 with additional water. The CO2 is then recirculated to the pressure vessel.[3][17]

Caffeine content of coffee

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Main article: Coffee § Caffeine content

Caffeine content of decaffeinated coffee

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To ensure product quality, manufacturers are required to test the newly decaffeinated coffee beans to make sure that caffeine concentration is relatively low. A caffeine content reduction of at least 97% is required under United States standards.[18] There is less than 0.1% caffeine in decaffeinated coffee and less than 0.3% in decaffeinated instant coffee in Canada.[19] Many coffee companies use high-performance liquid chromatography (HPLC) to measure how much caffeine remains in the coffee beans. However, since HPLC can be quite costly, some coffee companies are beginning to use other methods such as near-infrared (NIR) spectroscopy.[20] Although HPLC is highly accurate, NIR spectroscopy is much faster, cheaper and overall easier to use. Lastly, another method typically used to measure the remaining caffeine includes ultraviolet–visible spectroscopy: useful for decaffeination processes that include supercritical CO2, as CO2 does not absorb in the UV-Vis range.[21]

A controlled study in 2006 at Florida State University of ten samples of prepared decaffeinated coffee from coffee shops showed that some caffeine remained.[1] Fourteen to twenty cups of such decaffeinated coffee would contain as much caffeine as one cup of regular coffee.[1] The 473 ml (16 ounce) cups of coffee samples contained caffeine in the range of 8.6 mg to 13.9 mg. In another study of popular brands of decaf coffees, the caffeine content varied from 3 mg to 32 mg.[22] In contrast, a 237 ml (8 ounce) cup of regular coffee contains 95–200 mg of caffeine,[23] and a 355 ml (12 ounce) serving of Coca-Cola contains 36 mg.[24]

Decaffito

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As of 2009, progress toward growing coffee beans that do not contain caffeine was still continuing. The term "Decaffito" has been coined to describe this type of coffee, and trademarked in Brazil.[25]

The prospect for Decaffito-type coffees was shown by the discovery of the naturally caffeine-free Coffea charrieriana variety, reported in 2004. It has a deficient caffeine synthase gene, leading it to accumulate theobromine instead of converting it to caffeine.[26] Either this trait could be bred into other coffee plants by crossing them with C. charrieriana, or an equivalent effect could be achieved by knocking out the gene for caffeine synthase in normal coffee plants.[27]

Decaffeinated tea

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Further information: Health effects of tea

Tea may also be decaffeinated, usually by using processes analogous to the direct method or the CO2 process, as described above. Oxidizing tea leaves to create black tea ("red" in Chinese tea culture) or oolong tea leaves from green leaves does not affect the amount of caffeine in the tea, though tea-plant subspecies (i.e. Camellia sinensis sinensis vs. Camellia sinensis assamica) may differ in natural caffeine content. Younger leaves and buds contain more caffeine by weight than older leaves and stems.[citation needed] Although the CO2 process is favorable because it is convenient, nonexplosive, and nontoxic,[28] a comparison between regular and decaffeinated green teas using supercritical carbon dioxide showed that most volatile, nonpolar compounds (such as linalool and phenylacetaldehyde), green and floral flavor compounds (such as hexanal and (E)-2-hexenal), and some unknown compounds disappeared or decreased after decaffeination.[29]

In addition to CO2 process extraction, tea may be also decaffeinated using a hot water treatment. Optimal conditions are met by controlling water temperature, extraction time, and ratio of leaf to water. Temperatures of 100 °C or more, moderate extraction time of 3 minutes, and a 1:20 leaf to water weight per volume[clarification needed] ratio removed 83% caffeine content and preserved 95% of total catechins.[30] Catechins, a type of flavanol, contribute to the flavor of the tea and have been shown to increase the suppression of mutagens that may lead to cancer.[31]

Both coffee and tea have tannins, which are responsible for their astringent taste, but tea has around one third of the tannin content of coffee.[32] Thus, decaffeination of tea requires more care to maintain tannin content than decaffeination of coffee in order to preserve this flavor. Preserving tannins is desirable not only because of their flavor, but also because they have been shown to have anticarcinogenic, antimutagenic, antioxidative, and antimicrobial properties. Specifically, tannins accelerate blood clotting, reduce blood pressure, decrease the serum lipid level, and modulate immunoresponses.[33]

Certain processes during normal production might help to decrease the caffeine content directly, or simply lower the rate at which it is released throughout each infusion. In China, this is evident in many cooked pu-erh teas, as well as more heavily fired Wuyi Mountain oolongs; commonly referred to as 'zhonghuo' (mid-fired) or 'zuhuo' (high-fired).[citation needed]

A generally accepted statistic is that a cup of normal black (or red) tea contains 40–50 mg of caffeine, roughly half the content of a cup of coffee.[34]

Although a common technique of discarding a short (30 to 60 seconds) steep[35] is believed to much reduce caffeine content of a subsequent brew at the cost of some loss of flavor, research suggests that a five-minute steep yields up to 70% of the caffeine, and a second steep has one-third the caffeine of the first (about 23% of the total caffeine in the leaves).[clarification needed][36]

See also

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References

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  1. ^ a b c "Study: Decaf coffee is not caffeine-free". October 15, 2006. doi:10.1093/jat/30.8.611. Retrieved 2008-01-12.
  2. ^ Weinberg, Bennett Alan; Bealer, Bonnie K. (2001). The World of Caffeine: The Science and Culture of the World's Most Popular Drug. Psychology Press. ISBN 9780415927222.
  3. ^ a b c Ramalakshmi, K.; Raghavan, B. (1999). "Caffeine in Coffee: Its Removal. Why and How?". Critical Reviews in Food Science and Nutrition. 39 (5): 441–56. doi:10.1080/10408699991279231. PMID 10516914.
  4. ^ "Where Does My Decaf Come From?". Illumin. February 7, 2012. Archived from the original on 2012-02-08.
  5. ^ a b c d Emden, Lorenzo (6 July 2012). "Decaffeination 101: Four Ways to Decaffeinate Coffee". Coffee Confidential. Retrieved 29 October 2014.
  6. ^ US patent 897840, Johann Friedrich Meyer Jr., Ludwig Roselius, Karl Heinrich Wimmer, "Preparation of coffee", issued 1908-09-01 
  7. ^ "Ludwig Roselius (1874–1943)". Archived from the original on 2012-06-29. Retrieved 2012-08-20.
  8. ^ International Agency for Research on Cancer. "Chemical agents and related occupations, Volume 100F. A review of human carcinogens" (PDF). International Agency for Research on Cancer. Archived from the original (PDF) on 2014-08-21. Retrieved 2014-08-20.
  9. ^ Ronald Clarke and O.O. Vizthum Coffee: Recent Developments. Blackwell Science 2001, p. 109.
  10. ^ US Patent 4409253, Morrison, Lowen; Elder, Melisse & John, Phillips, "Recovery of noncaffeine solubles in an extract decaffeination process", published 1983-10-11 
  11. ^ Ronald Clarke and O.O. Vizthum Coffee: Recent Developments. Blackwell Science 2001, p. 111.
  12. ^ History of the SWISS WATER Decaffeination Process Archived 2006-12-30 at the Wayback Machine, Jan 04, 2007
  13. ^ Dowling, Stephen. "How do you decaffeinate coffee?". www.bbc.com. Retrieved 2020-08-07.
  14. ^ "Extraction of Caffeine from Tea: Greening the Chemistry" (PDF).
  15. ^ "Torunn A. Garin, 54, Noted Food Engineer". The New York Times. 1 May 2002.
  16. ^ US 4113887A, Kramer, Franklin; Henig, Yair Steve & Garin, Torunn Atteraas et al., "Adsorption process", issued 1977-02-24 
  17. ^ "How Do They Do It?: S7 E15 - Decaf Coffee; Smoked Salmon; Water Jets". How Do They Do It?. 1 December 2013. Archived from the original on 1 April 2019. Retrieved 1 April 2019.
  18. ^ "Decaffeinated Coffee". www.espressocoffeeguide.com. Retrieved 2015-12-08.
  19. ^ Branch, Legislative Services. "Consolidated federal laws of canada, Food and Drug Regulations". laws.justice.gc.ca. Retrieved 2018-07-19.
  20. ^ "Determination of caffeine in decaffeinated coffee by NIR spectroscopy" (PDF). The Unscrambler. Archived from the original (PDF) on 2016-03-03. Retrieved 2015-12-08.
  21. ^ "Measuring Caffeine Concentration" (PDF). Applied Analytics Application Note No. AN-019.
  22. ^ "Are You Really Getting Caffeine-Free Decaf Coffee?" Archived 2008-05-27 at the Wayback Machine Independent research on 10 popular decaffeinated coffees. Viewed Aug 05, 2008
  23. ^ "Caffeine Content for Coffee, Tea, Soda, and More" List of caffeine content in beverages known to contain caffeine. Viewed Aug 28, 2012
  24. ^ "Caffeine Amounts in Soda: Every Kind of Cola You Can Think Of" List of caffeine content in popular soft drinks. Viewed Aug 28, 2012
  25. ^ Paulo Mazzafera; Thomas W. Baumann; Milton Massao Shimizu; Maria Bernadete Silvarolla (June 2009). "Decaf and the Steeplechase Towards Decaffito—the Coffee from Caffeine-Free Arabica Plants". Tropical Plant Biology. 2 (2): 63–76. doi:10.1007/s12042-009-9032-7. S2CID 36008460.
  26. ^ Silvarolla MB, Mazzafera P, Fazuoli LC (June 2004). "Plant biochemistry: a naturally decaffeinated arabica coffee". Nature. 429 (6994): 826. Bibcode:2004Natur.429..826S. doi:10.1038/429826a. PMID 15215853. S2CID 4428420.
  27. ^ Coghlan, Andy (June 23, 2004). "Naturally decaffeinated coffee plant discovered". New Scientist.
  28. ^ Moyler, D (1993). "Extraction of flavours and fragrances with compressed CO2". In King, M; Bott, Theodore (eds.). Extraction of Natural Products Using Near-Critical Solvents (First ed.). Glasgow: Springer Netherlands. pp. 140–183. ISBN 978-94-010-4947-4.
  29. ^ Lee, S.; Park, M.K.; Kim, K.H.; Kim, Y.-S. (September 2007). "Effect of Supercritical Carbon Dioxide Decaffeination on Volatile Components of Green Tea". Journal of Food Science. 72 (7): S497–S502. doi:10.1111/j.1750-3841.2007.00446.x. PMID 17995663.
  30. ^ Liang, Huiling; Liang, Yuerong; Dong, Junjie; Lu, Jianliang; Xu, Hairong; Wang, Hui (2007). "Decaffeination of fresh green tea leaf (Camellia sinensis) by hot water treatment". Food Chemistry. 101 (4): 1451–1456. doi:10.1016/j.foodchem.2006.03.054.
  31. ^ Bu-Abbas, A; Nunez, X; Clifford, M; Walker, R; Ioannides, C (1996). "A comparison of the antimutagenic potential of green, black and decaffeinated teas: contribution of flavanols to the antimutagenic effect". Mutagenesis. 11 (6): 597–603. doi:10.1093/mutage/11.6.597. PMID 8962430.
  32. ^ Savolainen, H (1992). "Tannin content of tea and coffee". J Appl Toxicol. 12 (3): 191–192. doi:10.1002/jat.2550120307. PMID 1629514. S2CID 42678826.
  33. ^ Chung, King-Thom; Wong, Tit Yee; Wei, Cheng-I; Huang, Yao-Wen; Lin, Yuan (1998). "Tannins and Human Health: A Review". Critical Reviews in Food Science and Nutrition. 38 (6): 421–464. doi:10.1080/10408699891274273. PMID 9759559.
  34. ^ Upton Tea Imports (2003). "Tea and Caffeine". Upton Tea Imports Newsletter. 16 (1). Retrieved 2007-01-26.
  35. ^ "FAQ at imperial tea court", www.imperialtea.com, 2002
  36. ^ Monique B. Hicks; Y.-H. Peggy Hsieh & Leonard N. Bell (1996). "Tea preparation and its influence on methylxanthine concentration". Food Research International. 29 (3–4): 325–330. doi:10.1016/0963-9969(96)00038-5.
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