TY - JOUR
T1 - An assessment of how distance and diesel oxidation catalyst will impact thermal decomposition behaviors of particles
AU - Zhang, Mengzhu
AU - Ge, Yunshan
AU - Zhang, Chuanzhen
AU - Wang, Xin
N1 - Publisher Copyright:
© 2019
PY - 2020/4
Y1 - 2020/4
N2 - Decomposition mass loss and pyrolysis products analyses of particles sampled at various locations along the tailpipe of a Euro-IV diesel engine were performed using a thermogravimetry in conjunction with Fourier transformation infrared spectrometry-mass spectrum. Diesel particles were collected at the same location with and without diesel oxidation catalyst (DOC) mounted on the test engine separately. The three poles in thermal gravity-differential thermal gravity images suggested that the decomposition process of diesel particles could be divided into three stages which correspond to the decompositions of lower boiling substances, higher boiling substances and soot respectively. It is noticed that no matter whether DOC was mounted or not, the further the particles were sampled away from the engine block, the lower the peak temperatures and the heavier the mass losses within the first two stages, which indicated that the soluble organic fraction in the particle samples increased and therefore lowering the activation energy of thermal decomposition. Hydroxyl, ammonia, CxHy fragments, benzene, toluene, and phenol were found to be the primary products of particle decomposition, which didn't change with the location of particle sample point. The employment of DOC increased the activation energy for particle oxidation and resulted in a higher peak temperature and lower mass loss within the first-stage. Moreover, the C[dbnd]O stretching bands of aldehyde and ketone at 1771 cm−1 was only detected without a DOC, while the NO2 peak at 1634 cm−1 was solely noticed with the presence of DOC. Compared to the first-stage pyrolysis products, more polycyclic aromatic hydrocarbons and less CxHy fragments were seen in the second-stage.
AB - Decomposition mass loss and pyrolysis products analyses of particles sampled at various locations along the tailpipe of a Euro-IV diesel engine were performed using a thermogravimetry in conjunction with Fourier transformation infrared spectrometry-mass spectrum. Diesel particles were collected at the same location with and without diesel oxidation catalyst (DOC) mounted on the test engine separately. The three poles in thermal gravity-differential thermal gravity images suggested that the decomposition process of diesel particles could be divided into three stages which correspond to the decompositions of lower boiling substances, higher boiling substances and soot respectively. It is noticed that no matter whether DOC was mounted or not, the further the particles were sampled away from the engine block, the lower the peak temperatures and the heavier the mass losses within the first two stages, which indicated that the soluble organic fraction in the particle samples increased and therefore lowering the activation energy of thermal decomposition. Hydroxyl, ammonia, CxHy fragments, benzene, toluene, and phenol were found to be the primary products of particle decomposition, which didn't change with the location of particle sample point. The employment of DOC increased the activation energy for particle oxidation and resulted in a higher peak temperature and lower mass loss within the first-stage. Moreover, the C[dbnd]O stretching bands of aldehyde and ketone at 1771 cm−1 was only detected without a DOC, while the NO2 peak at 1634 cm−1 was solely noticed with the presence of DOC. Compared to the first-stage pyrolysis products, more polycyclic aromatic hydrocarbons and less CxHy fragments were seen in the second-stage.
KW - Diesel oxidation catalyst
KW - Particle
KW - Pyrolysis products
KW - Thermal decomposition
KW - Transport distance
UR - http://www.scopus.com/inward/record.url?scp=85076929281&partnerID=8YFLogxK
U2 - 10.1016/j.jes.2019.11.001
DO - 10.1016/j.jes.2019.11.001
M3 - Article
C2 - 32081312
AN - SCOPUS:85076929281
SN - 1001-0742
VL - 90
SP - 157
EP - 169
JO - Journal of Environmental Sciences (China)
JF - Journal of Environmental Sciences (China)
ER -