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A. Lappas, . Antonakou
Laboratory of Environmental Fuels and Hydrocarbons
Chemical Process Engineering Research Institute, 570 01 Thermi, Thessaloniki
E-mail: angel@cperi.certh.gr
ABSTRACT
The recycling of polystyrene is examined using the dissolution/reprecipitation method, as well as
pyrolysis. In the first technique, different solvents/non-solvents were examined at different weight
percent amounts and temperatures. The recovery of polymer in every case was greater than 90%.
Pyrolysis was carried out either conventional (non-catalytic) or catalytic in a laboratory fixed bed
reactor, using a model polymer as raw material or commercial products (food retail outlets). The
liquid fraction constituted mainly of the styrene monomer, together with a number of secondary
materials (aromatic compounds). The potential use of this product as a raw material for the
reproduction of polystyrene by polymerization was investigated using DSC and the results
compared with that from virgin monomer.
1. INTRODUCTION
Recycling of waste polymers has been a topic of interest in the fields of environmental science and
technology for some time. The produced amounts of plastic solid wastes in Greece, as well as in
most countries, continue to increase despite some increasing attempts to reduce, reuse, recycle and
recover. This is mainly due to their wide application in the manufacture of packaging for the food
industry as well as in other goods of daily life, since they do not have any side effects on the human
organism. However, due to the nature of much contaminated plastic waste it can only be partly
recycled into new products. The presently most used way of handling these waste streams is to
incinerate them with energy recovery or to use them for land-filling. In the last decade, many
environmental regulations have been implemented for a more sustainable recycling oriented society.
The approaches that have been proposed for recycling of waste polymers include [1,2]: Primary
recycling referring to the in-plant recycle of the scrap material of controlled history. Mechanical
Recycling, where the polymer is separated from its associated contaminants and it is reprocessed by
melt extrusion. Chemical recycling leading in total depolymerization to the monomers, or partial
degradation to other secondary valuable materials. Energy recovery as an effective way to reduce
the volume of organic materials by incineration. Although polymers are actually high-yielding
energy sources, this method has been widely accused as ecologically unacceptable owing to the
health risk from air born toxic substances e.g. dioxins (in the case of chlorine containing polymers).
The objective of a plastic management policy, in accordance with the principles of sustainable
development, should be not only the reuse of polymeric materials but also the production of raw
materials (monomers), from which they could be reproduced, or other secondary valuable products.
In this sense, among the techniques proposed for recycling of waste polymers the most challenging
method is chemical or feedstock recycling and various technologies have been successfully
demonstrated and continue to be developed. The recycling of plastic waste by such higher
technological routes has the potential to recover higher value end products like the hydrocarbons of
the polymer in the form of gas or oil.
Polystyrene (PSt) is a major type of thermoplastic used throughout the world in such
applications as electrical appliances, thermal insulation, tape cassettes, cups and plates. In Western
Europe alone approximately 3.14 million tones of polystyrene are consumed each year (data of
2003) [3]. Polystyrene comprises 12.3% of the plastic content of municipal solid wastes. In addition
polystyrene represents a plastic, which may be collected as a single source, for example from food
retail outlets and from commercial and industrial premises. In contrast with condensation polymers
(i.e. poly(ethylene terephthalate) (PET)), PSt can not be easily recycled to monomer by simple
chemical methods. Instead, thermochemical recycling techniques like pyrolysis are usually applied.
Thus several authors in literature have reported either thermal or catalytic cracking of PSt to obtain
the monomer styrene and a gasoline fraction [4-7]. Either acid-type [8] or solid bases [9] were used.
In the present investigation the chemical recycling of polystyrene was examined using two
different methods: the traditional method of dissolution/reprecipitation and the more challenging
technique of pyrolysis. The first belongs to the mechanical recycling techniques while the second to
chemical/feedstock recycling. During the first technique the polymer can be separated and recycled
using a solvent/non-solvent system. For this purpose different systems were examined at different
weight percent amounts and temperatures. Furthermore, conventional (non-catalytic) and catalytic
pyrolysis was carried out using either model polymer as raw material or commercial products
(mainly food retail outlets). The experiments were carried out in a laboratory fixed bed reactor. The
potential use of the oil produced as a raw material for the reproduction of PSt by polymerization
was investigated using DSC and the results compared with that from virgin monomer. Conclusions
are very encouraging concerning alternative techniques of waste polystyrene recycling.
PYROLYSIS UNIT
dt H T dt
where HT denotes the total reaction enthalpy (690 J/g for styrene).
The polymerization enthalpy was calculated by integrating the area between the DSC thermograms
and the baseline established by extrapolation from the trace produced after complete polymerization
(no change in the heat produced during the reaction).
3. RESULTS AND DISCUSSION
3.1 Recycling of polystyrene by the dissolution/reprecipitation technique
Two solvent/nonsolvent systems and three dissolution temperatures were investigated. The effect of
temperature as well as solvent/nonsolvent used on the % recovery of polystyrene from a model
polymer and several commercial products appears in Table 1. The polymer concentration was
always 20 %.-wt. It is obvious that at all different experimental conditions and for all commercial
samples examined the polymer recovery was always high. An increase in dissolution temperature
leads to increased polymer recovery values.
TABLE 1. Polystyrene recovery by the dissolution/reprecipitation technique
Model PSt
Plastic
Plastic
Packaging Plastic bowl
Solvent/Nonsolvent Temp.
(oC)
Glass
container
for foods
of yoghurt
(EPS)
(PSt)
(EPS)
(PSt)
Toluene/n-Hexane
Toluene/n-Hexane
Toluene/n-Hexane
Xylene/methanol
Xylene/methanol
Xylene/methanol
20
50
100
20
50
100
84.0
87.7
92.5
89.2
92.8
97.9
93.6
95.1
96.0
96.4
99.6
99.8
76.2
90.6
95.7
95.5
96.9
99.7
89.1
93.1
95.7
90.1
95.4
96.2
96.4
97.0
96.5
94.3
97.7
96.8
Comparing the FT-IR spectra of the solid obtained from commercial samples with that of model
polystyrene identified the polymer recovered with this technique. The interpretation of spectra
showed that in all cases the product of recycling was polystyrene. Indicative spectra of a plastic
glass and model PSt are presented in Figure 2.
100
% Transmittance
80
60
40
20
Model PSt
Commercial product
(plastic glass from PSt)
0
0
500
1000
1500
2000
2500
3000
3500
4000
-1
Wavenumber, cm
Figure 2. FT-IR spectra of model polystyrene and the polymer recovered from a commercial plastic
glass
3.2 Recycling of polystyrene by pyrolysis
Thermal cracking or pyrolysis, involves the degradation of the polymeric materials by heating in the
absence of oxygen (usually in a nitrogen atmosphere). During pyrolysis at increased temperatures,
depending on polymer type, either end-chain, or random scission of the macromolecules occurs. In
the first case (occurring in poly(methyl methacrylate)) the monomer can be produced in a large
amount, while in the second (polyethylene) the amount of monomer produced is very low.
Polystyrene degradation is in the middle, meaning that both end-chain and random scission occur
simultaneously. Thus, the amount of monomer produced depends upon the experimental conditions
and range between 40-70%.
In this investigation results are presented for the thermal and catalytic pyrolysis of model
polystyrene using an acid FCC catalyst and a base-type BaO. In addition, pyrolysis of several
commercial samples was carried out and all results on the product yield appear in Table 2.
TABLE 2. Product yield from the thermal and catalytic pyrolysis of model polystyrene and
commercial products containing polystyrene.
Pyrolytic process/
sample
Temperature
(C)
Gas (wt.%)
Liquid (wt.%)
Coke
(wt.%)
Residue
(wt.%)
Model polystyrene
Thermal
510
2.5
89.8
0.1
7.6
Catalytic, FCC
510
2.0
83.7
9.8
4.5
Catalytic, BaO
510
0.7
87.0
0.3
12.0
Commercial products
Plastic glass (EPS)
510
6.0
86.7
0.9
6.4
510
3.6
49.9
30.8
15.7
From Table 2, it is seen that the oil produced is much larger compared to gas and is in the range
84-90% in all but the plastic container samples. Commercial products leave more residue and coke.
The composition of the gaseous fraction is presented in Table 3.
TABLE 3. Composition of the gaseous fraction of the thermal and catalytic pyrolysis of model
polystyrene and commercial products containing polystyrene (%)
Catalytic
FCC
Catalytic
BaO
Plastic
glass
(EPS)
Plastic
container
(PSt)
0.0
0.0
0.0
21.8
0.0
57.9
0.0
11.9
0.0
8.4
0.0
0.0
26.9
0.0
0.0
23.0
0.0
29.5
0.0
18.6
0.0
0.0
2.0
0.0
81.6
0.0
0.0
4.8
0.0
6.2
0.0
2.5
2.7
1.2
0.0
1.0
0.0
0.0
52.0
7.2
0.0
0.0
0.0
2.6
0.0
2.8
28.9
6.5
0.0
55.4
0.0
6.2
2.0
10.0
0.0
4.7
14.6
1.1
3.1
2.9
100.0
100.0
100.0
100.0
100.0
Thermal
Hydrogen, H2
Carbon dioxide, CO2
Carbon monoxide, CO
Methane, CH4
Ethane, C2H6
Ethylene, C2H4
Propane, C3H8
Propylene, C3H6
Butane-Butylene, nC4
Pentane-Pentene, nC5
Isopentane-Isopentene, iC5
C6
Total
It is observed that cracking of model polystyrene does not lead to the production of CO and CO2,
since in this polymer molecule there are not any oxygen atoms. However, in the commercial
samples either CO, or CO2 have been detected meaning the appearance of additives containing
oxygen. Furthermore, in the plastic glass which constitutes of expandable polystyrene it was evident
the existence of pentanes in a rather large amount (32%), verifying thus the introduction of mainly
isobutene as an expanding agent [1]. The gases produced from cracking of the model PSt are mainly
H2, CH4, ethylene and propylene (>90%). Hydrogen is only produced from catalytic cracking.
Moreover, the compounds identified in the liquid fraction from pyrolysis appear in Table 4. It
was observed that the largest amount of monomer was obtained during thermal pyrolysis of model
polymer and EPS as well as with the BaO catalyst. In the commercial samples the % amount of
monomer in the plastic glass was very high while much less in the other plastic container. Several
other aromatic compounds were identified differing mainly by the existence or not of catalyst.
TABLE 4. Aromatic compounds identified in the liquid fraction of the thermal and catalytic
pyrolysis of model polystyrene and commercial products containing polystyrene (%)
Compounds
Styrene (monomer)
2,4-Diphenyl-1-butene (dimer)
2,4,6-Triphenyl-1-hexene (trimer)
Benzene
Toluene
Ethylbenzene
a-Methylstyrene
Xylene
Indane, ndene, etc.
1,2-Diphenylethane
1-methyl-1,2 Diphenylethane
1,3-Diphenylpropane
1,1-Diphenylpropene
Cumene
Naphthalene and derivatives
Phenanthrene and derivatives
Other aromatic compounds
Thermal
Catalytic
FCC
63.9
14.0
2.2
2.0
0.5
2.1
0.3
2.2
1.1
0.6
0.2
10.9
45.1
1.9
0.3
1.9
3.1
6.3
16.8
4.2
0.9
0.5
0.5
1.1
1.7
0.8
2.6
12.3
70.0
9.0
5.2
0.1
2.5
1.5
2.3
0.2
0.8
0.4
0.8
0.7
0.3
0.3
6.1
53.3
13.2
3.5
5.6
1.9
5.9
2.5
2.1
1.4
2.8
0.2
0.4
7.2
correspond to final double bond conversion equal to 100, 82, 52 and 14%, respectively. Therefore,
the possibility of using directly the oil product from pyrolysis for the reproduction of polystyrene is
under question.
-1
6
pure Styrene
liquid product of thermal pyrolysis
liquid product of catalytic pyrolysis (BaO)
liquid product of catalytic pyrolysis (FCC)
5
4
3
2
1
0
0
20
40
60
80
100
120
140
Figure 3. Polymerization rate versus time of different oil fractions obtained from pyrolysis of model
polystyrene compared to polymerization of pure styrene monomer. Initiator: AIBN 0.1M, reaction
temperature 90oC.
4. CONCLUSIONS
The chemical recycling of polystyrene was examined by both a dissolution/reprecipitation
technique and pyrolysis. The first leads to high recovery of polymer with the disadvantage of using
large amounts of organic solvents. Pyrolysis seems to be the most promising technique resulting in
an oil fraction with a great percentage of styrene monomer. The possibility of using directly this
product for the reproduction of PSt is not so clear.
Aknowledgements
This work was funded by the ... / ...... in the framework of the research program
PYTHAGORAS II, Metro 2.6.
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