TG-FTIR-MS study of synergistic effects during co-pyrolysis of corn stalk and high-density polyethylene (HDPE)
- 1. Key Laboratory of Clean Energy of Liaoning, School of Energy and Environment, Shenyang Aerospace University, Shenyang 110136, Liaoning (China)
- 2. Key Laboratory of Ocean Energy Utilization and Energy Conservation of Ministry of Education, School of Energy and Power Engineering, Dalian University of Technology, Dalian 116024 (China)
Description
Highlights: • Devolatilization behavior during co-pyrolysis of corn stalk and HDPE was studied. • Model-free methods were applied to analyze the kinetics. • The optimum ratio was given based on the thermal behavior and activation energy. • Interaction between CS and HDPE on the release of gas products was investigated. • The yields of oxygen-containing species were restrained for CS content below 60%. -- Abstract: Co-pyrolysis corn stalk (CS) and high-density polyethylene (HDPE) is an effective method to mitigate environmental pollution and reuse the problematic plastic to produce valuable energy. The devolatilization kinetics and the evolution of gaseous species during co-pyrolysis were investigated via TG-FTIR-MS. Moreover, the possible interactions of CS and HDPE were explored. The co-pyrolysis process of CS-HDPE blends was found to be divided into two decomposition stages. The first stage (150–400 °C) was mainly associated with the decomposition of CS. The second stage (400–515 °C) was the result of combinations of the thermal degradations of CS and HDPE, with the degradation of HDPE contributing the most. Co-pyrolysis CS with HDPE could delay the decomposition of HDPE. In addition, the difference between experimental and theoretical weight loss (△W) was found to be less than zero when the percentage of CS was 80%. Furthermore, the average of the experimental activation energy was lower than that of the theoretical value for 80% CS. Thus, the positive synergy was strongest when the CS content was 80%, based on the thermal decomposition behavior and the activation energy. However, the blending ratio of CS-HDPE had little effect on the major categories of gaseous products during co-pyrolysis. Moreover, the interaction between CS and HDPE in the first stage (150–400 °C) could promote the release of H2, CO/C2H4 and C3H6 in the blends with 80%, 60%, and 60% CS, respectively. Additionally, aliphatic hydrocarbons (CH4, C2H6, C3H8, C4H10, C4H8, C2H2) and oxygen-containing compounds (aldehydes, alcohols, ketones, acids) were suppressed by the interaction when the percentage of CS was less than 60%. In the second stage (400–850 °C), the yields of aliphatic hydrocarbons (CH4, C2H6, C3H8, C4H10, C4H8, C2H2, C4H6) were inhibited, independent of the content of CS in the blends. In addition, the production of H2, CO/C2H4, and C3H6 was promoted when the percentage of CS was below 80%, 80%, and 60%, respectively.
Additional details
Identifiers
- DOI
- 10.1016/j.enconman.2018.11.065;
- PII
- S0196890418313177;
Publishing Information
- Journal Title
- Energy Conversion and Management
- Journal Volume
- 181
- Journal Page Range
- p. 202-213
- ISSN
- 0196-8904
- CODEN
- ECMADL
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 55005373
- Subject category
- S46: INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND TECHNOLOGY; S36: MATERIALS SCIENCE;
- Descriptors DEI
- ACTIVATION ENERGY; ALDEHYDES; BUTADIENE; BUTANE; CARBON MONOXIDE; ETHANE; ETHYLENE; FOURIER TRANSFORM SPECTROMETERS; INFRARED SPECTRA; KETONES; METHANE; PLASTICS; POLYETHYLENES; PROPANE; PYROLYSIS; THERMAL DEGRADATION
- Descriptors DEC
- ALKANES; ALKENES; CARBON COMPOUNDS; CARBON OXIDES; CHALCOGENIDES; CHEMICAL REACTIONS; DECOMPOSITION; DIENES; ENERGY; HYDROCARBONS; MATERIALS; MEASURING INSTRUMENTS; ORGANIC COMPOUNDS; ORGANIC POLYMERS; OXIDES; OXYGEN COMPOUNDS; PETROCHEMICALS; PETROLEUM PRODUCTS; POLYENES; POLYMERS; POLYOLEFINS; SPECTRA; SPECTROMETERS; SYNTHETIC MATERIALS; THERMOCHEMICAL PROCESSES
Optional Information
- Copyright
- Copyright (c) 2018 Elsevier Ltd. All rights reserved.