Humic acid

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Humic acid is a principal component of humic substances, which are the major organic constituents of soil (humus), peat, coal, many upland streams, dystrophic lakes, and ocean water.[1] It is produced by biodegradation of dead organic matter. It is not a single acid; rather, it is a complex mixture of many different acids containing carboxyl and phenolate groups so that the mixture behaves functionally as a dibasic acid or, occasionally, as a tribasic acid. Humic acids can form complexes with ions that are commonly found in the environment creating humic colloids. Humic and fulvic acids (fulvic acids are humic acids of lower molecular weight and higher oxygen content than other humic acids) are commonly used as a soil supplement in agriculture, and less commonly as a human nutritional supplement. As a nutrition supplement, fulvic acid can be found in a liquid form as a component of mineral colloids. Fulvic acids are poly-electrolytes and are unique colloids that diffuse easily through membranes whereas all other colloids do not[citation needed]. "Synthesis of fulvic acid (1a) was accomplished by a route involving selective ozonization of 9-propenylpyranobenzopyran (1c), obtained by a regioselective cyclization of the 2-methylsulphinylmethyl 1,3-dione(3c)."[2]

Formation and description[edit source | edit]

Humic substances are formed by the microbial degradation of dead plant matter, such as lignin. They are very resistant to further biodegradation. The precise properties and structure of a given sample depend on the water or soil source and the specific conditions of extraction. Nevertheless, the average properties of humic substances from different sources are remarkably similar.

Humic substances in soils and sediments can be divided into three main fractions: humic acids, fulvic acids, and humin. The humic and fulvic acids are extracted as a colloidal sol from soil and other solid phase sources into a strongly basic aqueous solution of sodium hydroxide or potassium hydroxide. Humic acids are precipitated from this solution by adjusting the pH to 1 with hydrochloric acid, leaving the fulvic acids in solution. This is the operational distinction between humic and fulvic acids. Humin is insoluble in dilute alkali. The alcohol-soluble portion of the humic fraction is, in general, named ulmic acid. So-called "gray humic acids" (GHA) are soluble in low-ionic-strength alkaline media; "brown humic acids" (BHA) are soluble in alkaline conditions independent of ionic strength; and fulvic acids (FA) are soluble independent of pH and ionic strength.[3]

Liquid chromatography and liquid-liquid extraction can be used to separate the components that make up a humic substance. Substances identified include mono-, di-, and tri-hydroxy acids, fatty acids, dicarboxylic acids, linear alcohols, phenolic acids, and terpenoids.[4]

Chemical characteristics of humic substances[edit source | edit]

Example of a typical humic acid, having a variety of components including quinone, phenol, catechol and sugar moieties[1]

A typical humic substance is a mixture of many molecules, some of which are based on a motif of aromatic nuclei with phenolic and carboxylic substituents, linked together; the illustration shows a typical structure. The functional groups that contribute most to surface charge and reactivity of humic substances are phenolic and carboxylic groups.[1] Humic acids behave as mixtures of dibasic acids, with a pK1 value around 4 for protonation of carboxyl groups and around 8 for protonation of phenolate groups. There is considerable overall similarity among individual humic acids.[5] For this reason, measured pK values for a given sample are average values relating to the constituent species. The other important characteristic is charge density. The molecules may form a supramolecular structure held together by non-covalent forces, such as Van der Waals force, π-π, and CH-π bonds.[6]

The presence of carboxylate and phenolate groups gives the humic acids the ability to form complexes with ions such as Mg2+, Ca2+, Fe2+ and Fe3+. Many humic acids have two or more of these groups arranged so as to enable the formation of chelate complexes.[7] The formation of (chelate) complexes is an important aspect of the biological role of humic acids in regulating bioavailability of metal ions.[5]

Determination of humic acids in water samples[edit source | edit]

The presence of humic acid in water intended for potable or industrial use can have a significant impact on the treatability of that water and the success of chemical disinfection processes. Accurate methods of establishing humic acid concentrations are therefore essential in maintaining water supplies, especially from upland peaty catchments in temperate climates.

As a lot of different bio-organic molecules in very diverse physical associations are mixed together in natural environments, it is cumbersome to measure their exact concentrations in the humic superstructure. For this reason, concentrations of humic acid are traditionally estimated out of concentrations of organic matter (typically from concentrations of total organic carbon (TOC) or dissolved organic carbon (DOC).

Extraction procedures are bound to alter some of the chemical linkages present in the soil humic substances (mainly ester bonds in biopolyesters such as cutins and suberins). The humic extracts are composed of large numbers of different bio-organic molecules that have not yet been totally separated and identified. However, single classes of residual biomolecules have been identified by selective extractions and chemical fractionation, and are represented by alkanoic and hydroxy alkanoic acids, resins, waxes, lignin residues, sugars, and peptides.

Ecological effects[edit source | edit]

Organic matter soil amendments have been known by farmers to be beneficial to plant growth for longer than recorded history.[8] However, the chemistry and function of the organic matter have been a subject of controversy since humans began their postulating about it in the 18th century. Until the time of Liebig, it was supposed that humus was used directly by plants, but, after Liebig had shown that plant growth depends upon inorganic compounds, many soil scientists held the view that organic matter was useful for fertility only as it was broken down with the release of its constituent nutrient elements into inorganic forms. At the present time, soil scientists hold a more holistic view and at least recognize that humus influences soil fertility through its effect on the water-holding capacity of the soil. Also, since plants have been shown to absorb and translocate the complex organic molecules of systemic insecticides, they can no longer discredit the idea that plants may be able to absorb the soluble forms of humus;[9] this may in fact be an essential process for the uptake of otherwise insoluble iron oxides.

A study on the effects of Humic acid on plant growth was conducted at Ohio State University which said in part “humic acids increased plant growth” and that here were “relatively large responses at low application rates” [10]

Ancient masonry[edit source | edit]

In Ancient Egypt, according to archeology, straw was mixed with mud in order to produce building bricks. Straw produces stronger bricks that are less likely to break or lose their shape. Modern investigations have found that humic acid is released from straw when mixed with mud, basically a mixture of sand and clay. Humic acid increases clay's plasticity.[11]

See also[edit source | edit]

Further reading[edit source | edit]

References[edit source | edit]

  1. ^ a b c F.J. Stevenson (1994). Humus Chemistry: Genesis, Composition, Reactions. John Wiley & Sons, New York. 
  2. ^ "Journal of the Chemical Society, Chemical Communications". J. Chem. Soc., Chem. Commun., 1984, 1565-1566. Retrieved 2012-12-17. 
  3. ^ Baigorri R, Fuentes M, González-Gaitano G, García-Mina JM, Almendros G, González-Vila FJ. (2009). "Complementary Multianalytical Approach To Study the Distinctive Structural Features of the Main Humic Fractions in Solution: Gray Humic Acid, Brown Humic Acid, and Fulvic Acid". J Agric Food Chem. 57 (8): 3266–72. doi:10.1021/jf8035353. PMID 19281175. 
  4. ^ Fiorentino G., Spaccini R., Piccolo A (2006). "Separation of molecular constituents from a humic acid by solid-phase extraction following a transesterification reaction". Talanta 68 (4): 1135–1142. doi:10.1016/j.talanta.2005.07.037. PMID 18970442. 
  5. ^ a b Ghabbour, E.A.; Davies, G. (Editors) (2001). Humic Substances: Structures, Models and Functions. Cambridge, U.K.: RSC publishing. ISBN 978-0-85404-811-3. .
  6. ^ A. Piccolo (2002). "The Supramolecular structure of humic substances. A novel understanding of humus chemistry and implications in soil science". Advances in Agronomy. Advances in Agronomy 75: 57–134. doi:10.1016/S0065-2113(02)75003-7. ISBN 978-0-12-000793-6. 
  7. ^ Tipping, E (1994). "'WHAM - a chemical equilibrium model and computer code for waters, sediments, and soils incorporating a discrete site/electrostatic model of ion-binding by humic substances". Computers and Geosciences 20 (6): 973–1023. doi:10.1016/0098-3004(94)90038-8. 
  8. ^ McGraw-Hill (1966). "McGraw-Hill encyclopedia of science and technology: an international reference work, Volume 12". McGraw-Hill. p. 428. Retrieved 2012-01-28.  Unknown parameter |reason= ignored (help)
  9. ^ Pan American Union. Dept. of Cultural Affairs. División de Fomento Científico, Pan American Union. Dept. of Scientific Affairs, Organization of American States. Dept. of Scientific Affairs (1984). "Ciencia interamericana: Volumes 24-27". Retrieved 2012-01-28.  Unknown parameter |reason= ignored (help)
  10. ^ "Effects of humic acids from vermicomposts on plant growth". Retrieved July 31, 2013. 
  11. ^ A. Lucas; J.R. Harris (1998). Ancient Egyptian Materials and Industries. New York: Dover Publications. p. 49. ISBN 0-486-40446-3. Retrieved 2011-11-23.