Emissions from a flex fuel GDI vehicle operating on ethanol fuels show marked contrasts in chemical, physical and toxicological characteristics as a function of ethanol content

2019 ◽  
Vol 683 ◽  
pp. 749-761 ◽  
Author(s):  
Jiacheng Yang ◽  
Patrick Roth ◽  
Thomas D. Durbin ◽  
Martin M. Shafer ◽  
Jocelyn Hemming ◽  
...  
Keyword(s):  
2013 ◽  
Vol 21 (3) ◽  
pp. 590-603 ◽  
Author(s):  
Kyung-ho Ahn ◽  
Anna G. Stefanopoulou ◽  
Mrdjan Jankovic

Author(s):  
Kyung-ho Ahn ◽  
Anna G. Stefanopoulou ◽  
Mrdjan Jankovic

Flexible fuel vehicles (FFVs) can operate on a blend of ethanol and gasoline in any volumetric concentration of up to 85% ethanol (93% in Brazil). Existing FFVs rely on ethanol sensor installed in the vehicle fueling system, or on the ethanol-dependent air-to-fuel ratio (AFR) estimated via an exhaust gas oxygen (EGO) or λ sensor. The EGO-based ethanol detection is desirable from cost and maintenance perspectives but has been shown to be prone to large errors during mass air flow sensor drifts [1, 2]. Ethanol content estimation can be realized by a feedback-based fuel correction of the feedforward-based fuel calculation using an exhaust gas oxygen sensor. When the fuel correction is attributed to the difference in stoichiometric air-to-fuel ratio (AFR) between ethanol and gasoline, it can be used for ethanol estimation. When the fuel correction is attributed to a mass air flow (MAF) sensor error, it can be used for sensor drift estimation and correction. Deciding under which condition to blame (and detect) ethanol and when to switch to sensor correction burdens the calibration of FFV engine controllers. Moreover, erroneous decisions can lead to error accumulation in ethanol estimation and in MAF sensor correction. In this paper, we present a cylinder air flow estimation scheme that accounts for MAF sensor drift or bias using an intake manifold absolute pressure (MAP) sensor. The proposed fusion of the MAF, MAP and λ sensor measurements prevents severe mis-estimation of ethanol content in flex fuel vehicles.


2016 ◽  
Author(s):  
Hilkka Timonen ◽  
Panu Karjalainen ◽  
Erkka Saukko ◽  
Sanna Saarikoski ◽  
Päivi Aakko-Saksa ◽  
...  

Abstract. The effect of fuel ethanol content (10 %, 85 %, 100 %) on primary emissions and on subsequent secondary aerosol formation was investigated for a EURO5 flex-fuel gasoline vehicle. Emissions were characterized during the New European Driving Cycle (NEDC) using a comprehensive setup of high time resolution instruments. Detailed chemical composition of exhaust particulate matter (PM) was studied using a soot particle aerosol mass spectrometer (SP-AMS) and secondary aerosol formation using a potential aerosol mass (PAM) chamber. For the primary gaseous compounds, an increase in total hydrocarbon emissions and a decrease of aromatic BTEX (benzene, toluene, ethylbenzene and xylenes) compounds was observed when the amount of ethanol in fuel increased. In regard to particles, largest primary particulate matter concentrations and potential to form secondary particles were measured for the E10 fuel (10 % ethanol). As the ethanol content of the fuel increased, a significant decrease in average primary particulate matter concentrations over the NEDC cycle was found, PM emissions being 0.45, 0.25 and 0.15 mg m−3 for E10, E85 and E100, respectively. Similarly, a clear decrease in secondary aerosol formation potential was observed with larger contribution of ethanol in fuel. Secondary to primary PM ratios were 13.4, and 1.5 for E10 and E85, respectively. For E100 a slight decrease in PM mass was observed after the PAM chamber, indicating that the PM produced by secondary aerosol formation was less than the PM lost via e.g. wall losses or degradation of POA in the chamber. For all fuel blends, the formed secondary aerosol consisted mostly of organic compounds. For E10 the contribution of organic compounds containing oxygen increased from 35 %, measured for primary organics, to 62 % after the PAM chamber. For E85 the contribution of organic compounds containing oxygen increased from 42 % (primary) to 57 % (after the PAM chamber), whereas for E100 the amount of oxidized organics remained the same (approximately 62 %) with the PAM chamber when compared to the primary emissions.


Wear ◽  
2018 ◽  
Vol 406-407 ◽  
pp. 105-117 ◽  
Author(s):  
Dinecio dos Santos Filho ◽  
André Paulo Tschiptschin ◽  
Hélio Goldenstein

2017 ◽  
Author(s):  
Renato Souza ◽  
Carlos Carvalho ◽  
Rosalvo Bertolucci

2017 ◽  
Vol 17 (8) ◽  
pp. 5311-5329 ◽  
Author(s):  
Hilkka Timonen ◽  
Panu Karjalainen ◽  
Erkka Saukko ◽  
Sanna Saarikoski ◽  
Päivi Aakko-Saksa ◽  
...  

Abstract. The effect of fuel ethanol content (10, 85 and 100 %) on primary emissions and on subsequent secondary aerosol formation was investigated for a Euro 5 flex-fuel gasoline vehicle. Emissions were characterized during a New European Driving Cycle (NEDC) using a comprehensive set-up of high time-resolution instruments. A detailed chemical composition of the exhaust particulate matter (PM) was studied using a soot particle aerosol mass spectrometer (SP-AMS), and secondary aerosol formation was studied using a potential aerosol mass (PAM) chamber. For the primary gaseous compounds, an increase in total hydrocarbon emissions and a decrease in aromatic BTEX (benzene, toluene, ethylbenzene and xylenes) compounds was observed when the amount of ethanol in the fuel increased. In regard to particles, the largest primary particulate matter concentrations and potential for secondary particle formation was measured for the E10 fuel (10 % ethanol). As the ethanol content of the fuel increased, a significant decrease in the average primary particulate matter concentrations over the NEDC was found. The PM emissions were 0.45, 0.25 and 0.15 mg m−3 for E10, E85 and E100, respectively. Similarly, a clear decrease in secondary aerosol formation potential was observed with a larger contribution of ethanol in the fuel. The secondary-to-primary PM ratios were 13.4 and 1.5 for E10 and E85, respectively. For E100, a slight decrease in PM mass was observed after the PAM chamber, indicating that the PM produced by secondary aerosol formation was less than the PM lost through wall losses or the degradation of the primary organic aerosol (POA) in the chamber. For all fuel blends, the formed secondary aerosol consisted mostly of organic compounds. For E10, the contribution of organic compounds containing oxygen increased from 35 %, measured for primary organics, to 62 % after the PAM chamber. For E85, the contribution of organic compounds containing oxygen increased from 42 % (primary) to 57 % (after the PAM chamber), whereas for E100 the amount of oxidized organics remained the same (approximately 62 %) with the PAM chamber when compared to the primary emissions.


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