Depolymerization (or depolymerisation) is the process of converting a polymer into a monomer or a mixture of monomers.[1] This process is driven by an increase in entropy.

Depolymerization of polystyrene via radical elimination mechanism

Ceiling temperature

edit

The tendency of polymers to depolymerize is indicated by their ceiling temperature. At this temperature, the enthalpy of polymerization matches the entropy gained by converting a large molecule into monomers. Above the ceiling temperature, the rate of depolymerization is greater than the rate of polymerization, which inhibits the formation of the given polymer.[2]

Ceiling Temperatures of Common Organic Polymers
Polymer Ceiling Temperature (°C)[3] Monomer
polyethylene 610 CH2=CH2
polyisobutylene 175 CH2=CMe2
polyisoprene (natural rubber) 466 CH2=C(Me)CH=CH2
poly(methyl methacrylate) 198 CH2=C(Me)CO2Me
polystyrene 395 PhCH=CH2
Polytetrafluoroethylene 1100 CF2=CF2

Applications

edit

Depolymerization is a very common process. Digestion of food involves depolymerization of macromolecules, such as proteins. It is relevant to polymer recycling. Sometimes the depolymerization is well behaved, and clean monomers can be reclaimed and reused for making new plastic. In other cases, such as polyethylene, depolymerization gives a mixture of products. These products are, for polyethylene, ethylene, propylene, isobutylene, 1-hexene and heptane. Out of these, only ethylene can be used for polyethylene production, so other gases must be turned into ethylene, sold, or otherwise be destroyed or be disposed of by turning them into other products.[4]

Depolymerization is also related to production of chemicals and fuels from biomass. In this case, reagents are typically required. A simple case is the hydrolysis of celluloses to glucose by the action of water. Generally this process requires an acid catalyst:

H(C6H10O5)nOH + (n − 1) H2O → n C6H12O6


See also

edit

References

edit
  1. ^ Depolymerization, IUPAC Goldbook
  2. ^ Carraher Jr; Charles E (2010). "7". Introduction of Polymer Chemistry (2nd ed.). New York: CRC Press, Taylor and Francis. p. 224. ISBN 978-1-4398-0953-2.
  3. ^ Stevens, Malcolm P. (1999). "6". Polymer Chemistry an Introduction (3rd ed.). New York: Oxford University Press. pp. 193–194. ISBN 978-0-19-512444-6.
  4. ^ Nisar, Jan; Ali, Mukhtiar; Ahmad Awan, Iftikhar (2011). "Catalytic thermal decomposition of polyethylene by pyrolysis gas chromatography". Journal of the Chilean Chemical Society. 56 (2): 653–655. doi:10.4067/S0717-97072011000200006.
edit


📚 Artikel Terkait di Wikipedia

Thermal depolymerization

most polymers, thermal depolymerization is a chaotic process, giving a mixture of volatile compounds. Materials may be depolymerized in this way during waste

Catalysis

Catalysis (/kəˈtælɪsɪs/, kə-TAL-iss-iss) is the increase in rate of a chemical reaction due to an added substance known as a catalyst (/ˈkætəlɪst/ KAT-əl-ist)

Condensed tannin

assay) is a colorimetric assay. It is based on acid catalysed oxidative depolymerization of condensed tannins into corresponding anthocyanidins. The method

Poly(phthalaldehyde)

allowing head-to-tail fluoride-triggered depolymerization. PPA is known as a self-immolative material which depolymerizes through endcap cleavage in response

Heparin

7 nm) on either side of the helical axis. Either chemical or enzymatic depolymerization techniques or a combination of the two underlie the vast majority of

Biochar

therefore defined as "hydrochar" rather than "biochar". Thermo-catalytic depolymerization is another method to produce biochar, which utilizes microwaves. It

Cytoskeletal drugs

Promotion of depolymerization Certain drugs enhance the disassembly of already formed polymers. Demecolcine acts by promoting the depolymerization of microtubules

Microtubule

different from those of GTP-tubulin, as GDP-tubulin is more prone to depolymerization. A GDP-bound tubulin subunit at the tip of a microtubule will tend