Plastics waste management
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Contents |
Decision situation
Can commercially viable fuel be produced sustainably from plastic waste?
Plastic Waste Management
Plastic waste has a major negative impact on the environment. This impact is increasing as landfill space is depleted and pollution grows.
Types of plastic waste
74% of all plastic waste falls into the following categories:
- Polyethylene:
- Low density polyethylene (LDPE)
- Linear low density polyethylene (LLDPE)
- High density polyethylene(HDPE)
- Polypropylene (PP)
- Polyvinylchloride (PVC)
- Polystyrene (PS)
- Polyethylene - terephthalate (PET)
End-of-life treatments of plastic waste
Of the options for managing plastic waste, re-use and waste minimisation are seen to have little impact on overall reduction compared with recycling and energy recovery.
Landfill is the other option for managing plastic waste and indeed is by far the most used; for instance in Western Europe in 2005, 53% of plastic was disposed of into landfill[1]
Trends
- Landfill:
- disposal of plastic waste is dropping by 2% annually as available space is dinishing
- Recycling:
- Governments are legislating to promote it
- Civil society is co-operating in recycling
- Technological developments are facilitating new ways of recycling plastic
Energy recovery
- incineration of plastics
- emissions of toxic fumes
Recycling
Recycling a PET bottle still costs more than producing a new one, with the result that the recycling rate for PET bottles in Europe is around 25%. The situation is even worse for other plastics. Recycling rates for polystyrene are 2%[2].
Mechanical recycling
'mechanical recycling recovers the plastic material for similar or lower-quality plastics'[1]
Feedstock recycling
'feedstock recycling turns the plastic waste by means of chemical reactions into chemical raw materials or fuels'[1]
- represents only 2% of total plastics recycling in Western Europe, for instance
- recycling treatments have high investment costs
- economics more favourable with larger volumes
- requirement for plastic sorting
- liquefaction
- a type of feedstock recycling
- converts plastics into hydrocarbon mixtures that are useful as fuels via thermal and /or catalytic cracking
- commercialised by H.Smart Inc and Ozmotech
- technology being developed to solve the issue of residual PVC in the waste
- thermal processes
- Thermal cracking of these plastics can achieve a worthwhile yield of starting monomers:
- Polystyrene (PS)
- Poly(methyl) methacrylate (PMMA)
- Polytetrafluoroethylene (PTFE)
- Thermal cracking of these plastics can achieve a worthwhile yield of starting monomers:
- catalytic processes
- comparison
The table below gives some outcomes for various use of reactors, catalysts, heat etc in the cracking of these plastics.
| Process / variables | Outcome |
| Reactor: | |
| Fluidized bed | uniform temps -> narrower distribution and more valuable products |
| enhancement in polymer/catalysts mass ratio results in smaller amounts of gases and coke and larger amounts of liquid; | |
| increase of the flow of the fluidizing gas augments yield of primary cracking products (olefins) | |
| Screw kiln | recombination of gaseous hydrocarbons favoured ->less gaseous hydrocarbon content & more liquid |
| Output: | |
| Temp 500 deg C | oils with scarce amounts aromatics |
| Temp 650-700 deg C | gaseous hydrocarbons and olefins increase |
| Solvent / oils used in reaction | viscosity reduced ->heat & mass transfer rates augmented; gas yield decreased |
| Poor H donating solvents used in reaction: | increases liquid hydrocarbons C5 - C32; increases 1-olefins |
| Catalyst used: | decreases cracking temp; increases plastic conversion (vs thermal processes) |
| Zeolite (HZSM-5) - strong acid sites | C3 - C5 olefins |
| Mesoporous materials (Al-MSM-41, SiO2-Al2O3) - medium acid sites | gasolines and middle distillates |
| Catalysts with highly accessible sites: | improved performance as effect of bulk and high viscosity reduced |
| Nanocrystalline zeolites as catalyst | higher conversion than conventional zeolites |
| hierarchical mesoporous-microporous zeolites | higher conversion than conventional zeolites |
| Deactivation of Catalysts (dependent on acidity and pore structure of catalyst) | |
| HMOR and HUSY zeolites | quicker deactivation because large pore |
| HZSM-5, SIO2-Al2O3 and Al-MCM-41 | slower deactivation because smaller pores |
| Two Stage process - thermal then catalytic: | avoids catalyst deactivation |
| REY | best performing catalyst for yielding gasolines from 2 stage process |
| HZSM-5, SIO2-Al2O3 and Al-MCM-41 | best catalyst for larger share of gaseous hydrocarbons from 2 stage process |
| Two stage catalytic process i.e. >1 catalysis step: | better gasoline |
| Two catalysts in series (SiO2-Al2O3 + HZSM-5) in a fixed bed | high yields of gasoline with good octane number |
| Above series PLUS increase share of HZSM-5 | yield of aromatics and RON increases and yield of liquids decreases |
| Prepare mixtures of plastic/vacuum gas oil and crack catalytically over fluidized catalytic cracking (FCC) catalysts: | reduces viscosity |
| composition of cracking products depends on plastic share: | |
| mixture with plastic content of 5% | only gaseous products |
| mixture with plastic content of 10% | |
| Fast pyrolysis of the plastic then cracking with catalysis | Viscosity of reaction medium is decreased |
| Polyvinyl chloride (PVC) present: | serious problem because HCl released above 260deg C |
| addition of CaO / Ca(OH)2, iron oxides (FeOOH, Fe2O3, or Fe3O4) or CaCO3 | Remove released HCl from PVC degradation |
References
- ↑ 1.0 1.1 1.2 Aguado, J et alFuels from waste plastics by thermal and catalytic processes: A review, Industrial & Engineering Chemistry Research, 2008 47,7982-7992
- ↑ Bioplastics get growing: Everyone knows that we should stop depending upon petroleum

