Cyclohexanedimethanol Explained

Cyclohexanedimethanol (CHDM) is a mixture of isomeric organic compounds with formula C6H10(CH2OH)2. It is a colorless low-melting solid used in the production of polyester resins. Commercial samples consist of a mixture of cis and trans isomers. It is a di-substituted derivative of cyclohexane and is classified as a diol, meaning that it has two OH functional groups. Commercial CHDM typically has a cis/trans ratio of 30:70.

Production

CHDM is produced by catalytic hydrogenation of dimethyl terephthalate (DMT). The reaction conducted in two steps beginning with the conversion of DMT to the diester dimethyl 1,4-cyclohexanedicarboxylate (DMCD):

C6H4(CO2CH3)2 + 3 H2 → C6H10(CO2CH3)2

In the second step DMCD is further hydrogenated to CHDM:

C6H10(CO2CH3)2 + 4 H2 → C6H10(CH2OH)2 + 2 CH3OHA copper chromite catalyst is usually used industrially.[1] The cis/trans ratio of the CHDM is affected by the catalyst.[2]

Byproduct of this process are 4-methylcyclohexanemethanol (CH3C6H10CH2OH) and the monoester methyl4-methyl-4-cyclohexanecarboxylate (CH3C6H10CO2CH3, CAS registry number 51181-40-9).[3] The leading producers in CHDM are Eastman Chemical in US and SK Chemicals in South Korea.

Applications

Via the process called polycondensation, CHDM is a precursor to polyesters. It is one of the most important comonomers for production of polyethylene terephthalate (PET), or polyethylene terephthalic ester (PETE), from which plastic bottles are made.[4] [5] In addition it maybe spun to form carpet fibers.[6]

Thermoplastic polyesters containing CHDM exhibit enhanced strength, clarity, and solvent resistance. The properties of the polyesters vary from the high melting crystalline poly(1,4-cyclohexylenedimethylene terephthalate), PCT, to the non-crystalline copolyesters derived from both ethylene glycol and CHDM. The properties of these polyesters also is affected by the cis/trans ratio of the CHDM monomer.[7] CHDM reduces the degree of crystallinity of PET homopolymer, improving its processability. The copolymer tends to resist degradation, e.g. to acetaldehyde. The copolymer with PET is known as glycol-modified polyethylene terephthalate, PETG. PETG is used in many fields, including electronics, automobiles, barrier, and medical, etc.

CHDM is a raw material for the production of 1,4-cyclohexanedimethanol diglycidyl ether, an epoxy diluent.[8] The key use for this diglycidyl ether is to reduce the viscosity of epoxy resins.

External links

Notes and References

  1. Synthesis and Properties of Cyclic Diester Based Aliphatic Copolyesters . S.R. Turner . Y. Li . Journal of Polymer Science Part A: Polymer Chemistry . 48 . 2162–2169 . 2010 . 10 . 10.1002/pola.23985.
  2. The materials Chemistry of Inorganic Catalyst . J. M. Thomas . R. Raja . Australian Journal of Chemistry . 54 . 551–560 . 2002 . 10.1071/CH01150.
  3. Peter Werle, Marcus Morawietz, Stefan Lundmark, Kent Sörensen, Esko Karvinen and Juha Lehtonen "Alcohols, Polyhydric" Ullmann's Encyclopedia of Industrial Chemistry, 2008, Wiley-VCH, Weinheim.
  4. Development of amorphous copolyesters based on 1,4- cyclohexane-dimethanol . S.R. Turner . Journal of Polymer Science Part A: Polymer Chemistry . 42 . 5847–5852 . 2004 . 23 . 10.1002/pola.20460. free .
  5. Mini-review The Polyoxaesters . S. Andjelic . D.D. Jamiolkowski . R. Bezwada . Polymer International . 56 . 1063–1077 . 2007 . 10.1002/pi.2257.
  6. Web site: Hatton . Nylon vs. Polyester Carpet Fibers: Comparison Guide . 2023-08-17 . Homedit . en-US.
  7. Cyclohexanedimethanol Polyesters . S. R. Turner . R.W. Seymour . T.W. Smith . Encyclopedia of Polymer Science and Technology . 2001 . 10.1002/0471440264.pst257. 0471440264 .
  8. Crivello . James V. . 2006 . Design and synthesis of multifunctional glycidyl ethers that undergo frontal polymerization . Journal of Polymer Science Part A: Polymer Chemistry . 44 . 21 . 6435–6448 . 10.1002/pola.21761 . 2006JPoSA..44.6435C . 0887-624X.