Chemistry:Methylcyclopentadienyl manganese tricarbonyl

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Methylcyclopentadienyl manganese tricarbonyl
Methylcyclopentadienyl-Manganese-Tricarbonyl Skeletal.svg
MMT-3D-balls.png
Names
IUPAC name
tricarbonyl(methyl-η5-cyclopentadienyl)manganese
Other names
MMT, CI-2, Combustion Improver-2, Manganese tricarbonylmethylcyclopentadienyl, 2-Methylcyclopentadienyl manganese tricarbonyl
Identifiers
3D model (JSmol)
ChemSpider
EC Number
  • 235-166-5
RTECS number
  • OP1450000
UNII
UN number 3281
Properties
C9H7MnO3
Molar mass 218.09 g/mol
Appearance pale yellow to dark orange liquid[1]
Odor faint, pleasant[1]
Density 1.38 g/cm3
Melting point −1 °C (30 °F; 272 K)
Boiling point 232 to 233 °C (450 to 451 °F; 505 to 506 K)
Solubility Hydrocarbons (petrol), ether, alcohol, THF
Vapor pressure 7 mmHg (100°C)[1]
Structure
Tetrahedral at Mn
Hazards
Main hazards Flammable, toxic
GHS pictograms GHS06: ToxicGHS09: Environmental hazard
GHS Signal word Danger
H301, H310, H330, H315, H372, H410
P260, P273, P280, P284, P301+310, P302+350
Flash point 110 °C; 230 °F; 383 K[1]
NIOSH (US health exposure limits):
PEL (Permissible)
 C 5 mg/m3[1]
REL (Recommended)
 TWA 0.2 mg/m3 [skin][1]
IDLH (Immediate danger)
 N.D.[1]
Related compounds
Related compounds
 ferrocene
Mn2(CO)10
dicyclopentadiene
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references
Tracking categories (test):

Methylcyclopentadienyl manganese tricarbonyl (MMT or MCMT) is an organomanganese compound with the formula (C5H4CH3)Mn(CO)3. Initially marketed as a supplement for use in leaded gasoline, MMT was later used in unleaded gasoline to increase the octane rating. Following the implementation of the Clean Air Act (United States) (CAA) in 1970, MMT continued to be used alongside tetraethyl lead (TEL) in the US as leaded gasoline was phased out (prior to TEL finally being banned from US gasoline in 1995), and was also used in unleaded gasoline until 1977. Ethyl Corporation obtained a waiver from the U.S. EPA (Environmental Protection Agency) in 1995, which allows the use of MMT in US unleaded gasoline (not including reformulated gasoline) at a treat rate equivalent to 8.3 mg Mn/L (manganese per liter).[2]

MMT has been used in Canadian gasoline since 1976 (and in numerous other countries for many years) at a concentration up to 8.3 mg Mn/L (though the importation and interprovincial trade of gasoline containing MMT was restricted briefly during the period 1997–1998)[3][4] and was introduced into Australia in 2000. It has been sold under the tradenames HiTEC 3000, Cestoburn and Ecotane.[5][6] MMT is also used in China .[7]

History of usage in the United States

Although initially marketed in 1958 as a smoke suppressant for gas turbines, MMT was further developed as an octane enhancer in 1974. When the United States Environmental Protection Agency (EPA) ordered the phase out of TEL in gasoline in 1973, new fuel additives were sought. TEL has been used in certain countries as an additive to increase the octane rating of automotive gasoline but has been phased out in all countries since July 2021.[8]

In 1977, the US Congress amended the CAA to require advance approval by the EPA for the continued use of fuel additives such as MMT, ethanol, ethyl tert-butyl ether (ETBE), etc.[9] The new CAA amendment required a "waiver" to allow use of fuel additives made of any elements other than carbon, hydrogen, oxygen (within certain limits) and nitrogen.[10] To obtain a waiver, the applicant was required to demonstrate that the fuel additive would not lead to a failure of vehicle emission control systems.

Ethyl Corporation applied to the US EPA for a waiver for MMT in both 1978 and 1981; in both cases the applications were denied because of stated concerns that MMT might damage catalytic converters and increase hydrocarbon emissions. In 1988, Ethyl began a new series of discussions with the EPA to determine a program for developing the necessary data to support a waiver application. In 1990, Ethyl filed its third waiver application prompting an extensive four-year review process. In 1993, the U.S. EPA determined that use of MMT at 8.3 mg Mn/L would not cause, or contribute to, vehicle emission control system failures.[11]

Despite that finding, the EPA ultimately denied the waiver request in 1994 due to uncertainty related to health concerns regarding manganese emissions from the use of MMT.[12]

As a result of this ruling, Ethyl initiated a legal action claiming that the EPA had exceeded its authority by denying the waiver on these grounds. This was upheld by the US Court of Appeals[13] and EPA subsequently granted a waiver which allows the use of MMT in US unleaded gasoline (not including reformulated gasoline) at a treat rate equivalent to 8.3 mg Mn/L.

Implementation of this less-toxic alternative to TEL has been controversial. Opposition from automobile manufacturers and some areas of the scientific community has reportedly prompted oil companies to stop voluntarily the usage of MMT in some of their countries of operation.[14]

MMT is currently manufactured in the U.S. by the Afton Chemical Corporation, a subsidiary of New Market Corporation.[15] It is also produced and marketed as Cestoburn by Cestoil Chemical Inc. in Canada.

Structure and synthesis

MMT is manufactured by reduction of bis(methylcyclopentadienyl) manganese using triethylaluminium. The reduction is conducted under an atmosphere of carbon monoxide. The reaction is exothermic, and without proper cooling, can lead to catastrophic thermal runaway.[16]

MMT is a so-called half-sandwich complex, or more specifically a "piano-stool" complex (since the three CO ligands are like the legs of a stool). The manganese atom in MMT is coordinated with three carbonyl groups as well as to all five main carbon atoms of the methylcyclopentadienyl ring. These hydrophobic organic ligands make MMT highly lipophilic.

A variety of related complexes are known, including ferrocene, which has also been used as an additive to gasoline. Many derivatives of MMT are known.[17]

Safety

The human and environmental health impacts that may result from the use of MMT will be a function of exposure to either: (1) MMT in its original, unchanged, chemical form and/or (2) manganese combustion products emitted from vehicles operating on gasoline containing MMT as an octane improver.

Pre-combustion storage and handling

The general public has minimal direct exposure to MMT. As stated by the US EPA in their risk assessment on MMT, "except for accidental or occupational contacts, exposure to MMT itself was not thought likely to pose a significant risk to the general population."[18] Similarly, the Australian National Industrial Chemicals Notification and Assessment Scheme (NICNAS) stated that "[m]inimal public exposure to MMT is likely as a result of spills and splashes of LRP [lead replacement petrol] and aftermarket additives".[19]

The MMT dossier registered in the European Chemical Agency's webpage indicates that before combustion in gasoline, MMT is classified as an acute toxicant by the oral, dermal, and inhalation routes of exposure under the European Union's Classification, Labeling and Packaging Regulation (EC/1272/2008), implementing the Global Harmonized System (GHS) of Classification and Labeling. The US ATSDR (Agency for Toxic Substances and Disease Registry) notes that MMT is very unstable in light and degrades to a mixture of less harmful substances and inorganic manganese in less than 2 minutes.[20][21] Therefore, human exposure to MMT prior to combustion in gasoline would not likely occur at significant levels.

The US OSHA (Occupational Health and Safety Administration) has not established a permissible exposure limit specifically for MMT. However, OSHA has set a permissible exposure limit at a ceiling of 5 mg/m3 for manganese and its compounds, while the National Institute for Occupational Safety and Health recommends workers not be exposed to more than 0.2 mg/m3, over an eight-hour time-weighted average.[22] In Europe, the MMT DNELs (Derived No Effect Level) for workers by the inhalation and dermal routes of exposure are 0.6 mg/m3 and 0.11 mg/kg-day, respectively. The MMT DNELs for the general population by the inhalation and dermal routes of exposure are 0.11 mg/m3 and 0.062 mg/kg-day, respectively.

Combustion products

In 1994 (reaffirmed in 1998, 2001 and 2010), Health Canada concluded that "airborne manganese resulting from the combustion of MMT in gasoline powered vehicles is not entering the Canadian environment in quantities or under conditions that may constitute a health risk"[23] and confirmed they were taking no action with respect to MMT. Similarly, the 2003 NICNAS report states that the airborne concentrations of manganese as a result of car emissions from vehicles using fuel containing MMT poses no health hazard.[citation needed]

The assessment conducted by NICNAS asserts that "[m]anganese, the principle degradation by-product from combustion of MMT, is naturally occurring and ubiquitous in the environment. It is an essential nutrient of plants and animals. Environmental exposure to Mn compounds will mostly arise through the gaseous phase. Eventually, these will deposit to land and waters. The emission of Mn into the environment from use of fuels containing MMT is unlikely to develop to levels of concern and therefore poses a low risk for terrestrial or aquatic environments."

Additional health studies, overseen by the US EPA, were conducted to explain the transport of manganese in the body. In studies published from 2007 through 2011, no significant health effects are anticipated from the use of MMT in gasoline.[24]

Overall combined risk assessment

Based on the low potential for the release of concentrated MMT (before its combustion in gasoline) under normal storage and use, as well as its rapid photo-degradation properties, it has been concluded in multiple technical and global regulatory assessments that significant impacts to human health or the environment from MMT use are not anticipated. NICNAS concluded that there is "low occupational risk associated with MMT" both "for workers involved in formulating and distributing LRP or aftermarket fuel additives and those involved in automotive maintenance". Further, they also concluded that there is a "low risk" to the public from the use of MMT.

Significant human or environmental exposures associated with manganese compounds (manganese phosphate, manganese sulfate and manganese dioxide) from the combustion of MMT are not expected. In Health Canada's risk assessment on the health implications of the manganese combustion products of MMT, it was concluded that manganese exposures from MMT use are unlikely to pose a risk to health for any sub-group of the population. NICNAS similarly concluded that chronic Mn exposures (from all sources combined) are unlikely to be significantly changed by the use of MMT as a fuel additive.

In 2013, a risk assessment on MMT was developed by ARCADIS Consulting and verified by an independent panel, according to the methodology provided by the European Commission in compliance with the requirements of the European Fuel Quality Directive (2009/30/EC). The conclusions of a risk assessment are that "for MMT and its transformation products, when MMT is used as a fuel additive in petrol, no significant human health or environmental concerns related to exposure to either MMT or its transformation [combustion] products (manganese phosphate, manganese sulfate and manganese tetroxide) were identified at use at levels up to 18 mg Mn/L. Depending on the regional needs and the vehicle emission control technology available, an MMT treat rate in the range of 8.3 mg Mn/L to 18 mg Mn/L is scientifically justified and may deliver both environmental and economic benefits without significant adverse effects."[25]

T2 Laboratories explosion and fire

On December 19, 2007 an explosion and fire occurred in the production of MMT in Florida, which killed four people and injured fourteen.[26]

See also

References

  1. ↑ 1.0 1.1 1.2 1.3 1.4 1.5 1.6 NIOSH Pocket Guide to Chemical Hazards. "#0409". National Institute for Occupational Safety and Health (NIOSH). https://www.cdc.gov/niosh/npg/npgd0409.html. 
  2. ↑ "60 FR 36414 - Fuels and Fuel Additives; Grant of Waiver Application". https://www.gpo.gov/fdsys/granule/FR-1995-07-17/95-17476/content-detail.html. 
  3. ↑ "Threat of NAFTA Case Kills Canada's MMT Ban: Challenge over gasoline additive could have cost Ottawa millions". The Globe and Mail. July 20, 1998. 
  4. ↑ "MMT, A Risk Management Masquerade". http://leiss.ca/wp-content/uploads/2009/12/mmt_a_risk_management_masquerade.pdf. 
  5. ↑ Frumkin, Howard (1997). "Manganese in the US Gas Supply". American Journal of Industrial Medicine 31 (1): 107–115. doi:10.1002/(SICI)1097-0274(199701)31:1<107::AID-AJIM16>3.0.CO;2-6. PMID 8986262. 
  6. ↑ Patterson, Steve (15 September 2009). "Report: Owners of Jacksonville's T2 Lab never knew risks of deadly explosion" (in en-US). The Florida Times-Union. https://www.jacksonville.com/story/news/2009/09/15/report-owners-of-jacksonvilles-t2-lab-never-knew-risks-of-deadly-explosi/15973372007/. 
  7. ↑ Geng, Peng; Zhang, Hui (2015). "Combustion and emission characteristics of a direct-injection gasoline engine using the MMT fuel additive gasoline". Fuel 144: 380–387. doi:10.1016/j.fuel.2014.12.064. 
  8. ↑ "End of leaded fuel use a 'milestone for multilateralism'" (in en). UN News. 30 August 2021. https://news.un.org/en/story/2021/08/1098792. 
  9. ↑ "42 USC § 7545 - Regulation of fuels". https://www.law.cornell.edu/uscode/text/42/7545. 
  10. ↑ Definition of Substantially Similar.[ www.epa.gov/otaq/regs/fuels/additive/jan91.pdf][ www.epa.gov/otaq/regs/fuels/additive/july81.pdf ]
  11. ↑ 58 Fed. Reg. 64,761 (December 9, 1993)
  12. ↑ "Fuels and Fuel Additives;Waiver Decision/Circuit Court Remand". https://www.gpo.gov/fdsys/pkg/FR-1994-08-17/html/94-18941.htm. 
  13. ↑ "Waiver Ruling". 13 January 1995. p. 1053. http://openjurist.org/51/f3d/1053/ethyl-corporation-v-environmental-protection-agency. 
  14. ↑ Marco Di Girolamo, Maura Brianti, Massimo Conte, Mario Marchionna "Octane Enhancers" in Ullmann's Encyclopedia of Industrial Chemistry 2002, Wiley-VCH, Weinheim.
  15. ↑ "Afton Chemical Ltd". http://www.aftonchemical.com/Solutions/FuelAdd/Octane_Improver/Pages/Octane%20Improver.aspx. 
  16. ↑ "T2 Laboratories Inc. Reactive Chemical Explosion". USCSB. http://www.csb.gov/t2-laboratories-inc-reactive-chemical-explosion/. Retrieved 29 April 2016. 
  17. ↑ Petz, W., "40 years of transition-metal thiocarbonyl chemistry and the related CSe and CTe compounds", Coordination Chemistry Reviews, 2008, volume 252, pp. 1689-1733.doi:10.1016/j.ccr.2007.12.011.
  18. ↑ Davis, J. M; Jarabek, A. M.; Mage, D. T.; Graham, J. A. (Feb 1998). "The EPA health risk assessment of methylcyclopentadienyl manganese tricarbonyl (MMT)". Risk Assessment 18 (1): 57–70. doi:10.1111/j.1539-6924.1998.tb00916.x. PMID 9523444. https://pubmed.ncbi.nlm.nih.gov/9523444/. Retrieved 25 June 2023. 
  19. ↑ "National Industrial Chemicals Notification and Assessment Scheme; Methylcyclopentadienyl Manganese Tricarbonyl June 2003". http://www.nicnas.gov.au/__data/assets/pdf_file/0020/4385/PEC_24_Methylcyclopentadienyl-Manganese-Tricarbonyl-MMT_Full_Report_PDF.pdf. 
  20. ↑ Garrison, AW (1995). "Environmental fate of methylcyclopentadienyl manganese tricarbonyl". Environmental Toxicology and Chemistry 14 (11): 1859–1864. doi:10.1002/etc.5620141107. 
  21. ↑ Wallington, TJ (1999). "Atmospheric Chemistry of Methylcyclopentadienyl Manganese Tricarbonyl: Photolysis, Reaction with Hydroxyl Radicals and Ozone". Environmental Science & Technology 33 (23): 4232–4238. doi:10.1021/es990350p. Bibcode: 1999EnST...33.4232W. 
  22. ↑ "NIOSH Pocket Guide to Chemical Hazards. Centers for Disease Control and Prevention. April 4, 2011. Retrieved November 19, 2013". https://www.cdc.gov/niosh/npg/npgd0409.html. 
  23. ↑ "Petition to the Commissioner of the Environment and Sustainable Development, under section 22 of the Auditor General Act. July 2001". http://www.oag-bvg.gc.ca/internet/English/pet_032_e_28732.html. 
  24. ↑ "Methylcyclopentadienyl Manganese Tricarbonyl (MMT) Alternative Tier 2 Health Effects Test Program, Docket EPA-HQ-OAR-2004-0074". https://www.regulations.gov/#!documentDetail;D=EPA-HQ-OAR-2004-0074-0153. 
  25. ↑ conclusions of this risk assessment
  26. ↑ "Investigation Report Report: T2 Laboratories, Inc. Runaway Reaction" (in en-US). United States Chemical Safety and Hazard Investigation Board. 15 September 2009. https://www.csb.gov/userfiles/file/t2%20final%20report.pdf. 



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