Methyl tert-butyl ether explained

Methyl tert-butyl ether (MTBE), also known as tert-butyl methyl ether, is an organic compound with a structural formula (CH3)3COCH3. MTBE is a volatile, flammable, and colorless liquid that is sparingly soluble in water. Primarily used as a fuel additive, MTBE is blended into gasoline to increase its octane rating and knock resistance, and reduce unwanted emissions.[1] [2]

Production and properties

MTBE is manufactured via the chemical reaction of methanol and isobutylene. Methanol is primarily derived from natural gas,[3] where steam reforming converts the various light hydrocarbons in natural gas (primarily methane) into carbon monoxide and hydrogen.[4] The resulting gases then further react in the presence of a catalyst to form methanol.[5] Isobutylene can be produced through a variety of methods. n-butane can be isomerized into isobutane which can be dehydrogenated to isobutylene.[6] In the Halcon process, t-Butyl hydroperoxide derived from isobutane oxygenation is treated with propylene to produce propylene oxide and t-butanol. The t-butanol can be dehydrated to isobutylene.

MTBE production in the U.S. peaked in 1999 at 260,000 barrels per day[7] before dropping down to about 50,000 barrels per day and holding steady,[8] mostly for the export market. After the purchase of SABIC,[9] [10] oil giant Saudi Aramco is now considered to be the world's largest producer[11] with an estimated production capacity of 2.37 million metric tons per year (mt/yr).[12] Worldwide production capacity of MTBE in 2018 was estimated to be 35 million metric tons.[13]

Uses

MTBE is used as a fuel component in fuel for gasoline engines. It is one of a group of chemicals commonly known as oxygenates because they raise the oxygen content of gasoline.

As anti-knocking agent

In the U.S. MTBE has been used in gasoline at low levels since 1979, replacing tetraethyllead (TEL) as an antiknock (octane rating) additive to prevent engine knocking.[14] Oxygenates also help gasoline burn more completely, reducing tailpipe emissions. Oxygenates also dilute or displace gasoline components such as aromatics (e.g., benzene). Before the introduction of other oxygenates and octane enhancers, refiners chose MTBE for its blending characteristics and low cost.

Alternatives to MTBE as an anti-knock agent

Other oxygenates are available as additives for gasoline including ethanol and other ethers such as ETBE.

Ethanol has been advertised as a safe alternative by agricultural and other interest groups in the U.S. and Europe. In 2003, California was the first U.S. state to start replacing MTBE with ethanol.

An alternative to ethanol is ETBE, which is manufactured from ethanol and isobutene. Its performance as an additive is similar to MTBE, but due to the higher price of ethanol compared to methanol, it is more expensive.

Higher quality gasoline is also an alternative, so that additives such as MTBE are unnecessary. Iso-octane itself is used. MTBE plants can be retrofitted to produce iso-octane from isobutylene.[15] [16]

As a solvent

MTBE is sometimes used as a solvent,[17] [18] [19] although it is used less commonly than diethyl ether. Although an ether, MTBE is a poor Lewis base and does not support formation of Grignard reagents. It is also unstable toward strong acids. It reacts dangerously with bromine.[20]

MTBE forms azeotropes with water (52.6 °C; 96.5% MTBE)[21] and methanol (51.3 °C; 68.6% MTBE).[22] The solubility of water in MTBE is reported to be 1.5 g/100g at 23 °C.

In an investigational medical procedure called contact dissolution therapy, MTBE is injected directly into the gallbladder to dissolve cholesterol gallstones. Due to concerns of MTBE toxicity and potentially serious side effects in the event of solvent draining into the duodenum, and the advent of laparoscopic surgery techniques, this procedure is considered obsolete. [23] [24] [25]

MTBE is used in organic chemistry as a relatively inexpensive solvent with properties comparable to diethyl ether, but with a higher boiling point and less solubility in water. As a solvent, MTBE has one distinct advantage over most ethers - it has a much lower tendency to form explosive organic peroxides. It is widely used as a solvent in industry where, for safety and regulatory reasons, handling diethyl ether or other ethers is much more difficult and expensive. MTBE as a solvent is used in the oil refining industry as a method for dewaxing waxy petroleum fractions.

Persistence and pervasiveness in the environment

MTBE gives water an unpleasant taste at very low concentrations. MTBE often is introduced into water-supply aquifers by leaking underground storage tanks (USTs) at gasoline stations or spills of gasoline. The higher water solubility and persistence of MTBE cause it to travel faster and farther than many other components of gasoline when released into an aquifer.[26]

MTBE is biodegraded by the action of bacteria. In the proper type of bioreactor, such as a fluidized bed bioreactor, MTBE may be removed rapidly and economically from water to undetectable levels. Activated carbon produced from coconut shells and optimized for MTBE adsorption may reduce MTBE to undetectable levels,[27] although this level of reduction is likely to occur only in the most ideal circumstances. There are currently no known published cases of any in-situ treatment method that has been capable of reducing contaminant concentrations to baseline (pre-development) conditions within the aquifer soil matrix.

According to the International Agency for Research on Cancer (IARC), a branch of the World Health Organization, MTBE is not classified as a human carcinogen. MTBE may be tasted in water at concentrations of 5–15 μg/L (5-15ppb).[28]

Regulation and litigation in the U.S.

See main article: article and MTBE controversy.

Restrictions on MTBE manufacturing and use

The Energy Policy Act of 2005, as approved by the U.S. House of Representatives, did not include a provision for shielding MTBE manufacturers from water contamination lawsuits. This provision was first proposed in 2003 and had been thought by some to be a priority of Tom DeLay and Rep. Joe Barton, then chairman of the Energy and Commerce Committee.[29] This bill did include a provision that gave MTBE makers, including some major oil companies, $2 billion in transition assistance while MTBE was phased out over the following nine years.[30] Due to opposition in the Senate,[31] the conference report dropped all MTBE provisions. The final bill was signed into law by President George W. Bush.[32] The lack of MTBE liability protection is resulting in a switchover to the use of ethanol as a gasoline additive.

Cleanup costs and litigation

MTBE removal from groundwater and soil contamination in the U.S. was estimated to cost from $1 billion[33] to US$30 billion,[34] including removing the compound from aquifers and municipal water supplies and replacing leaky underground oil tanks. In one case, the cost to oil companies to clean up the MTBE in wells belonging to the city of Santa Monica, California was estimated to exceed $200 million.[35] In another case, New York City estimated a $250 million cost for cleanup of a single wellfield in the borough of Queens in 2009.[36] In 2013 a jury awarded the State of New Hampshire $236 million in damages in order to treat groundwater contaminated by MTBE.[37]

Many lawsuits are still pending regarding MTBE contamination of public and private drinking water supplies.

Drinking water regulations

EPA first listed MTBE in 1998 as a candidate for development of a national Maximum Contaminant Level (MCL) standard in drinking water.[38] The agency listed MTBE on its Contaminant Candidate List in 2022 but has not announced whether it will develop an MCL.[39] EPA uses toxicity data in developing MCLs for public water systems.[40]

California established a state-level MCL for MTBE, 13 micrograms per liter, in 2000.[41]

See also

External links

Notes and References

  1. Web site: Methyl tertiary butyl ether prices, markets & analysis . 2020-06-28 . ICIS Explore . en-US.
  2. Web site: Oxygenates . 2020-06-28 . www.api.org . en.
  3. Web site: How is Methanol Produced . 2020-06-29 . METHANOL INSTITUTE . en-US.
  4. Anzelmo . Bryce . Wilcox . Jennifer . Liguori . Simona . Hydrogen production via natural gas steam reforming in a Pd-Au membrane reactor. Investigation of reaction temperature and GHSV effects and long-term stability . Journal of Membrane Science . 25–32 .
  5. Web site: methanol Properties, Production, Uses, & Poisoning . 2020-06-29 . Encyclopedia Britannica. en.
  6. Web site: Methyl Tertiary Butyl Ether (MTBE) Production and Manufacturing Process . 2020-06-29 . ICIS Explore . en-US.
  7. Web site: The United States continues to export MTBE, mainly to Mexico, Chile, and Venezuela - Today in Energy - U.S. Energy Information Administration (EIA). 2020-06-28 . www.eia.gov.
  8. Web site: United States Methyl Tertiary Butyl Ether (MTBE): Production Economic Indicators . 2020-06-28 . www.ceicdata.com.
  9. Web site: Aramco completes its acquisition of a 70% stake in SABIC from the Public Investment Fund (PIF) . 2020-06-29 . www.saudiaramco.com . 17 June 2020 . en.
  10. News: 2020-06-14 . Saudi Aramco buys SABIC shares on market as it completes acquisition . en . Reuters . 2020-06-29.
  11. Web site: Saudi Aramco to have largest MTBE capacity in Middle East and Asia . 2020-06-29 . en-US.
  12. Web site: 2019-04-09 . Saudi Aramco's MTBE trading volume likely to rise after Sabic purchase S&P Global Platts . 2020-06-29 . www.spglobal.com . en.
  13. Web site: MTBE annual production capacity globally 2023 . 2020-06-28 . Statista . en.
  14. Web site: Overview Methyl Tertiary Butyl Ether (MTBE) US EPA . 2021-04-07 . archive.epa.gov . en.
  15. Web site: NExOCTANE™ - Neste Jacobs . www.nesteengineering.com . https://web.archive.org/web/20060106041047/http://www.nesteengineering.com/default.asp?path=111%2C360%2C362%2C477 . January 6, 2006.
  16. Web site: KBR - NExOCTANE™ . 2006-01-31 . https://web.archive.org/web/20060106003915/http://www.halliburton.com/kbr/hydroChem/petroChem/nexoctane.jsp . 2006-01-06 . dead .
  17. 10.1194/jlr.D700041-JLR200 . free . 18281723 . Lipid extraction by methyl-tert-butyl ether for high-throughput lipidomics . The Journal of Lipid Research. 49 . 5 . 1137–1146 . 2008 . Matyash . V. . Liebisch . G. . Kurzchalia . T. V. . Shevchenko . A. . Schwudke . D. . 2311442.
  18. Sorption of methanol, dimethyl carbonate, methyl acetate, and acetone vapors in CTA and PTMSP: General findings from the GAB Analysis . . 2016-03-01 . 1099-0488 . 561–569 . 54 . 5 . 10.1002/polb.23945 . en . Ondřej . Vopička . Kryštof . Pilnáček . Petr . Číhal . Karel . Friess . 2016JPoSB..54..561V.
  19. Sorption of vapour mixtures of methanol and dimethyl carbonate in PTMSP: Cooperative and competitive sorption in one system . . 2016-02-01 . 243–250 . 75 . 10.1016/j.eurpolymj.2015.12.015 . Ondřej . Vopička . Daniel . Radotínský . Karel . Friess.
  20. Web site: Interaction between bromine and tert-butyl methyl ether . UK Chemical Reaction Hazards Forum . 13 May 2010 . https://web.archive.org/web/20110313064840/http://www.crhf.org.uk/incident09.html . 13 March 2011.
  21. http://www.zeon.co.jp/business_e/enterprise/spechemi/cpme_tec_sup_e_200906.pdf Zeon Corporation
  22. CRC Handbook of Chemistry and Physics, 90th edition
  23. Schoenfield LJ, Marks JW . Oral and contact dissolution of gallstones . . 165 . 4 . 427–30 . 1993 . 8480875 . 10.1016/S0002-9610(05)80934-1 .
  24. News: Health Guide: Gallstones . New York Times.
  25. https://www.aetna.com/cpb/medical/data/500_599/0509.html | access-date = June 3, 2024
  26. http://www.swrcb.ca.gov/rwqcb2/download/WMI%202004%20Executive%20Summary.pdf San Francisco Bay Area Regional Water Quality Control Board Integrated Basin Management Plan (2004)
  27. http://www.wcponline.com/pdf/spotlight.pdf link text
  28. Environ Sci Pollut Res Int . 2005 . 12 . 6 . 381–6 . Biotic and abiotic transformations of methyl tertiary butyl ether (MTBE) . Fischer A, Oehm C, Selle M, Werner P . 16305145 . 10.1065/espr2005.08.277 . 97168152.
  29. http://www.cnn.com/2005/POLITICS/04/21/energy.bill.mtbe.ap/ http://www.cnn.com/2005/POLITICS/04/21/energy.bill.mtbe.ap/
  30. Web site: House approves $12 billion energy package. NBC News. 2005-04-22.
  31. Charles Babington, House Again Passes GOP Energy Measures, Washington Post, June 16, 2004, at A4 (House passes Energy Bill, but Senate opponents of MTBE provision in House Bill have the votes to prevent its enactment).
  32. United States. Energy Policy Act of 2005. . Approved 2005-08-08.
  33. Web site: MTBE Cleanup Estimates . . 2005-05-23 . SIGMA Weekly Report . Society of Independent Gasoline Marketers of America (SIGMA) . Fairfax, VA . https://web.archive.org/web/20091009071418/http://www.sigma.org/wr/reports/05/050523.html . 2009-10-09.
  34. Web site: Long Island Utility Fighting to Defeat MTBE Safe Harbor . . 2004-03-16 . The MTBE e-Resource . Napoli Bern, LLP . New York, NY . https://web.archive.org/web/20071020072714/http://www.mtbe-eresource.com/liu.cfm . 2007-10-20.
  35. Web site: Oil Companies Pay Santa Monica MTBE Cleanup Costs . . 2005-02-17 . Environment News Service . Ecology Prime Media, Inc..
  36. News: City Awarded $105 Million in Exxon Mobil Lawsuit . The New York Times . Mireya . Navarro . 2009-10-20 . 2010-05-12.
  37. News: Exxon Mobil is Found Negligent in New Hampshire MTBE Use . Bloomberg . Sarah . Earle . 2013-04-09.
  38. EPA (1998-03-02). "Announcement of the Drinking Water Contaminant Candidate List." Federal Register,
  39. EPA (2022-11-14). "Drinking Water Contaminant Candidate List 5―Final." Federal Register,
  40. Web site: How EPA Regulates Drinking Water Contaminants . . 2017-05-03 . EPA.
  41. Web site: MTBE: Regulations and Drinking Water Monitoring Results . . 2014-08-04 . California State Water Resources Control Board . Sacramento, CA.