Naphthenic acid

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Naphthenic acid
Naphthensaure.svg
Example component of naphthenic acid
Identifiers
ECHA InfoCard 100.014.239 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 215-662-8
PubChem CID
UNII
Properties
Variable
Molar mass Variable
Hazards
GHS labelling:
GHS-pictogram-exclam.svg GHS-pictogram-pollu.svg
Warning
H315, H317, H319, H335, H411
P261, P264, P271, P272, P273, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P333+P313, P337+P313, P362, P363, P391, P403+P233, P405, P501
Flash point 101 °C (214 °F; 374 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Naphthenic acids (NAs) are mixtures of several cyclopentyl and cyclohexyl carboxylic acids with molecular weights of 120 to well over 700 atomic mass units. The main fractions are carboxylic acids with a carbon backbone of 9 to 20 carbons. McKee et al. claim that "naphthenic acids (NAs) are primarily cycloaliphatic carboxylic acids with 10 to 16 carbons", [1] although acids containing up to 50 carbons have been identified in heavy petroleum. [2]

Contents

Nomenclature

Naphthenic acid can refer to derivatives and isomers of naphthalene carboxylic acids. In the petrochemical industry, NA's refer to alkyl carboxylic acids found in petroleum. [3] The term naphthenic acid has roots in the somewhat archaic term "naphthene" (cycloaliphatic but non-aromatic) used to classify hydrocarbons. It was originally used to describe the complex mixture of petroleum-based acids when the analytical methods available in the early 1900s could identify only a few naphthene-type components with accuracy. Today "naphthenic" acid is used in a more generic sense to refer to all of the carboxylic acids present in petroleum, [1] whether cyclic, acyclic, or aromatic compounds, and carboxylic acids containing heteroatoms such as N and S. Although commercial naphthenic acids often contain a majority of cycloaliphatic acids, multiple studies [4] [5] have shown they also contain straight chain and branched aliphatic acids and aromatic acids; some naphthenic acids contain >50% combined aliphatic and aromatic acids.

Salts of naphthenic acids, called naphthenates, are widely used as hydrophobic sources of metal ions in diverse applications. [6]

Classification

Naphthenic acids are represented by a general formula CnH2n-zO2, where n indicates the carbon number and z specifies a homologous series. The z is equal to 0 for saturated, acyclic acids and increases to 2 in monocyclic naphthenic acids, to 4 in bicyclic naphthenic acids, to 6 in tricyclic acids, and to 8 in tetracyclic acids. [5] Crude oils with total acid number (TAN) as little as 0.5 mg KOH/g acid or petroleum fractions greater than about 1.0 mg KOH/g oil usually qualify as a high acid crude or oil. At the 1.0 mg/g TAN level, acidic crude oils begin to be heavily discounted in value and so are referred to as opportunity crudes. [7] Commercial grades of naphthenic acid are most often recovered from kerosene/jet fuel and diesel fractions, where their corrosivity [6] and negative impact on burning qualities require their removal. Naphthenic acids are also a major contaminant in water produced during the extraction of oil from Athabasca oil sands. [8] [9]

Sources and occurrence

Naphthenic acids are extracted from petroleum distillates by extraction with aqueous base. Acidification of this extract acidic neutralization returns the acids free from hydrocarbons. Naphthenic acid is removed from petroleum fractions not only to minimize corrosion but also to recover commercially useful products. [10] Some crude oils are high in acidic compounds (up to 4%). [11]

Naphthenic acid corrosion

The composition varies with the crude oil composition and the conditions during refining and oxidation.. [3] [12] Fractions that are rich in naphthenic acids can cause corrosion damage to oil refinery equipment; the phenomenon of naphthenic acid corrosion (NAC). [13] [14] Crude oils with a high content of naphthenic acids are often referred to as high total acid number (TAN) crude oils or high acid crude oil (HAC).

Metal naphthenates

As the greatest current and historical usage, naphthenic acid are used to produce metal naphthenates. [10] Metal naphthenates are referred often to as "salts" of naphthenic acids, but metal naphthenates are not ionic. They are covalent, hydrophobic coordination complexes. More specifically they are metal carboxylate complexe with the formula M(naphthenate)2, or M3O(naphthenate)6 for basic oxides. Metal naphthenates are not well defined in conventional chemical sense because they are a complex mixture rather than a specific single component, structure or formula. They have diverse applications. [6] [15]

The naphthenates have industrial applications including synthetic detergents, lubricants, corrosion inhibitors, fuel and lubricating oil additives, wood preservatives, insecticides, fungicides, acaricides, wetting agents, thickening agent of napalm and oil drying agents used in painting and wood surface treatment. Industrially useful naphthenates include those of aluminium, magnesium, calcium, barium, cobalt, copper, lead, manganese, nickel, vanadium, and zinc.< [6] Illustrative is the use of cobalt naphthenate for the oxidation of tetrahydronaphthalene to the hydroperoxide. [16]

The complex mixture and hydrophobic nature of naphthenic acid allows metal naphthenates to be highly soluble in organic media such as petroleum-based hydrocarbons, oftentimes much more so than single isomer carboxylates such as metal acetates and stearates. Their industrial applications exploits this property, where they are used as oil-borne detergents, lubricants, corrosion inhibitors, fuel and lubricating oil additives, wood preservatives, insecticides, fungicides, acaricides, wetting agents, oil drying agents (driers) used in oil-based paint and wood surface treatment including varnish. Industrially useful metal naphthenates include those of aluminum, barium, calcium, cobalt, copper, iron, lead, magnesium manganese, nickel, potassium, vanadium, zinc, and zirconium. [5]

Environmental impact

Naphthenic acids are the major contaminant in water produced from the extraction of oil from Athabasca oil sands (AOS). [17]

It has been stated that "naphthenic acids are the most significant environmental contaminants resulting from petroleum extraction from oil sands deposits." Nonetheless, the same authors suggest that "under worst-case exposure conditions, acute toxicity is unlikely in wild mammals exposed to naphthenic acids in AOS tailings pond water, but repeated exposure may have adverse health effects." [18] Naphthenic acids are present in Athabasca oil sands and tailings pond water at an estimated concentration of 81 mg/L [19]

Using Organisation for Economic Co-operation and Development [OECD] protocols for testing toxicity, refined NAs are not acutely genotoxic to mammals. [20] Damage, however, induced by NAs while transient in acute or discontinuous exposure, may be cumulative in repeated exposure. [21]

Naphthenic acids have both acute and chronic toxicity to fish and other organisms. [22]

See also

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References

  1. 1 2 Richard H. McKee; Colin M. North; Paula Podhasky; Jeffrey H. Charlap; Adam Kuhl (February 2014). "Acute and Subchronic Mammalian Toxicity of Naphthenic Acids from Oil Sands Tailings". International Journal of Toxicology. 33 (1): 347–355. doi: 10.1177/1091581813504229 .
  2. ↑ Qian, K. and W.K. Robbins (2001). Resolution and identification of elemental compositions for more than 3000 crude acids in heavy petroleum by negative-ion microelectrospray high-field Fourier Transform ion cyclotron resonance mass spectrometry. Energy & Fuels. 15:1505-1511.
  3. 1 2 Barros, Eliane V.; Filgueiras, Paulo R.; Lacerda, Valdemar; Rodgers, Ryan P.; Romão, Wanderson (2022). "Characterization of Naphthenic Acids in Crude Oil Samples – A literature review". Fuel. 319. doi:10.1016/j.fuel.2022.123775. S2CID   247340497.
  4. ↑ Clemente, J. S.; Fedorak, P. M. (2005). "A review of the occurrence, analyses, toxicity, and biodegradation of naphthenic acids". Chemosphere. 60 (5): 585–600. Bibcode:2005Chmsp..60..585C. doi:10.1016/j.chemosphere.2005.02.065. PMID   15963797.
  5. 1 2 3 James Brient, Peter Wessner, Mary Doyle (1995). "Naphthenic Acid" in Kirk-Othmer, ed. Encyclopedia of Chemical Technology 4th ed. 16: 1017-1029.
  6. 1 2 3 4 Nora, Angelo; Koenen, Gunther (2010). "Metallic Soaps". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a16_361.pub2. ISBN   978-3-527-30385-4.
  7. ↑ Qing, W. (2010). "Processing high TAN crude: Part 1". Digital Refining.
  8. ↑ Vincent V. Rogers, Karsten Liber, and Michael D. MacKinnon (August 2002). "Isolation and characterization of naphthenic acids from Athabasca oil sands tailings pond water". Chemosphere48 (5): 519–527. doi : 10.1016/S0045-6535(02)00133-9
  9. ↑ Allen, E. W. (2008). "Process water treatment in Canada’s oil sands industry: I. Target pollutants and treatment objectives" (PDF). Journal of Environmental Engineering and Science7 (2): 123–138. doi : 10.1139/S07-038
  10. 1 2 J. A. Brient; P. J. Wessner; M. N. Doyle (1995). "Naphthenic Acids". Napthenic Acids. Kirk-Othmer Encyclopedia of Chemical Technology. Weinheim: Wiley-VCH. doi:10.1002/0471238961.1401160802180905.a01. ISBN   0-471-23896-1.
  11. ↑ Conrad Environmental Aquatics Technical Advisory Group (CEATAG ) (1998). Naphthenic Acids Background Information Discussion Report, 65 pp.
  12. ↑ Walter E. Rudzinski; Leon Oehlers & Yi Zhang (2002). "Tandem Mass Spectrometric Characterization of Commercial Naphthenic Acids and a Maya Crude Oil". Energy Fuels. 16 (5): 1178–1185. doi:10.1021/ef020013t.
  13. ↑ Slavcheva E.; Shone B.; Turnbull A. (1999). "Review of naphthenic acid corrosion in oil refining". British Corrosion Journal. 34 (2): 125–131. doi:10.1179/000705999101500761.
  14. ↑ "Article with details concerning naphthenic acid corrosion" (PDF).
  15. ↑ M. Landau. 1993. "Driers and metallic soaps", in J. Kroschwitz, ed., Kirk-Othmer Encyclopedia of Chemical Technology. New York: John Wiley & Sons. Vol. 8, pp. 432-445. doi : 10.1002/0471238961.0418090512011404.a01
  16. ↑ Knight, H. B.; Swern, Daniel (1954). "Tetralin Hydroperoxide". Organic Syntheses. 34: 90. doi:10.15227/orgsyn.034.0090.
  17. ↑ Allen, E. W. (2008). "Process water treatment in Canada's oil sands industry: I. Target pollutants and treatment objectives" (PDF). Journal of Environmental Engineering and Science. 7 (2): 123–138. doi:10.1139/S07-038.}
  18. ↑ Vincent V. Rogers; Karsten Liber & Michael D. MacKinnon (August 2002). "Isolation and characterization of naphthenic acids from Athabasca oil sands tailings pond water". Chemosphere. 48 (5): 519–527. doi:10.1016/S0045-6535(02)00133-9.
  19. ↑ Vincent V. Rogers; Mark Wickstrom; Karsten Liber; Michael D. MacKinnon (2001). "Acute and Subchronic Mammalian Toxicity of Naphthenic Acids from Oil Sands Tailings" . Toxicological Sciences. 66 (2): 347–355. doi:10.1093/toxsci/66.2.347.
  20. ↑ Richard H. McKee; Colin M. North; Paula Podhasky; Jeffrey H. Charlap; Adam Kuhl (February 2014). "Acute and Subchronic Mammalian Toxicity of Naphthenic Acids from Oil Sands Tailings". International Journal of Toxicology. 33 (1): 347–355. doi: 10.1177/1091581813504229 .
  21. ↑ Vincent V. Rogers; Karsten Liber & Michael D. MacKinnon (August 2002). "Isolation and characterization of naphthenic acids from Athabasca oil sands tailings pond water". Chemosphere. 48 (5): 519–527. doi:10.1016/S0045-6535(02)00133-9.
  22. ↑ Allen, E. W. (2008). "Process water treatment in Canada's oil sands industry: I. Target pollutants and treatment objectives" (PDF). Journal of Environmental Engineering and Science. 7 (2): 123–138. doi:10.1139/S07-038.
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