TY - JOUR
T1 - An experimental analysis of diesel fuel produced from HDPE (high-density polyethylene) waste using thermal and catalytic pyrolysis with passive heat pipe cooling system
AU - Kurniawati, Desy
AU - Putra, Nandy
AU - Abdullah, Nasruddin
AU - Ibnu Hakim, Imansyah
AU - Nurrokhmat, Agus
N1 - Funding Information:
The authors thank the DRPM (Directorate of Research and Community Service), Universitas Indonesia for funding this research through the PUTI Q2 Program 2020.
Publisher Copyright:
© 2021 Elsevier Ltd
PY - 2021/6/1
Y1 - 2021/6/1
N2 - Diesel produced from plastic waste is an attractive alternative energy source as it offers the dual benefits of satisfying the increasing global energy demand and reducing plastic waste. Pyrolysis is considered to be one of the most reliable oil conversion methods from high-density polyethylene (HDPE) waste into diesel fuel, but it requires a large amount of energy. Therefore, we propose thermal and catalytic pyrolysis methods that require a minimal amount of cooling energy to produce diesel fuel from HDPE using a passive cooling system with heat-pipes. The specific energy consumption of 44.35 Wh/g, a heating rate of 14497.85 KJ/h, and a reactor feedstock size of 2–20 mm. The oil produced through thermal pyrolysis was 61.1 wt% liquid, 1.29 wt% wax, and 37.61 wt% gas, and its density, kinematic viscosity, high heating value, and cetane index were 0.83 g/ml, 2.045 mm2/s, 0.185 MJ/kg, and 32.6, respectively. The oil produced through catalytic pyrolysis was 85 wt% liquid and 15 wt% gas, with no wax phase. Its density, kinematic viscosity, high heating value, and cetane index were 0.827 g/ml, 1.038 mm2/s, 59.57 MJ/kg, and 90, respectively. The optimal pyrolysis operating conditions were a reactor temperature of 500 °C, and liquid collection system (LCS) cooling water temperature of 20 °C. The cetane index of the catalytic pyrolysis oil was significantly higher than the corresponding standard specification for diesel. Owing to its high cetane index, the catalytic pyrolysis diesel can be combined with conventional diesel to increase its cetane index and combustion performance.
AB - Diesel produced from plastic waste is an attractive alternative energy source as it offers the dual benefits of satisfying the increasing global energy demand and reducing plastic waste. Pyrolysis is considered to be one of the most reliable oil conversion methods from high-density polyethylene (HDPE) waste into diesel fuel, but it requires a large amount of energy. Therefore, we propose thermal and catalytic pyrolysis methods that require a minimal amount of cooling energy to produce diesel fuel from HDPE using a passive cooling system with heat-pipes. The specific energy consumption of 44.35 Wh/g, a heating rate of 14497.85 KJ/h, and a reactor feedstock size of 2–20 mm. The oil produced through thermal pyrolysis was 61.1 wt% liquid, 1.29 wt% wax, and 37.61 wt% gas, and its density, kinematic viscosity, high heating value, and cetane index were 0.83 g/ml, 2.045 mm2/s, 0.185 MJ/kg, and 32.6, respectively. The oil produced through catalytic pyrolysis was 85 wt% liquid and 15 wt% gas, with no wax phase. Its density, kinematic viscosity, high heating value, and cetane index were 0.827 g/ml, 1.038 mm2/s, 59.57 MJ/kg, and 90, respectively. The optimal pyrolysis operating conditions were a reactor temperature of 500 °C, and liquid collection system (LCS) cooling water temperature of 20 °C. The cetane index of the catalytic pyrolysis oil was significantly higher than the corresponding standard specification for diesel. Owing to its high cetane index, the catalytic pyrolysis diesel can be combined with conventional diesel to increase its cetane index and combustion performance.
KW - Catalytic pyrolysis
KW - Cetane index
KW - Diesel fuel
KW - HDPE waste
KW - Heat-pipe
KW - Passive cooling system
KW - Thermal pyrolysis
UR - http://www.scopus.com/inward/record.url?scp=85104088152&partnerID=8YFLogxK
U2 - 10.1016/j.tsep.2021.100917
DO - 10.1016/j.tsep.2021.100917
M3 - Article
AN - SCOPUS:85104088152
SN - 2451-9049
VL - 23
JO - Thermal Science and Engineering Progress
JF - Thermal Science and Engineering Progress
M1 - 100917
ER -