Experimental Heat Release Analysis and Emissions of A HSDI Diesel Engine Fueled With Ethanol-Diesel Fuel Blends
Experimental Heat Release Analysis and Emissions of A HSDI Diesel Engine Fueled With Ethanol-Diesel Fuel Blends
Abstract
An experimental study is conducted to evaluate the effects of using blends of ethanol with conventional diesel fuel, with 5%, 10% and
15% (by vol.) ethanol, on the combustion and emissions of a standard, fully instrumented, four-stroke, high-speed, direct injection
(HSDI), ‘Hydra’ diesel engine located at the authors’ laboratory. The tests are conducted using each of the above fuel blends or neat
diesel fuel, with the engine working at a speed of 2000 rpm and at four different loads. In each test, combustion chamber and fuel
injection pressure diagrams are obtained using a specially developed, high-speed, data acquisition and processing system. A heat release
analysis of the experimentally obtained cylinder pressure diagrams is developed and used, with the pertinent application of the energy
and state equations. From the analysis results, plots of the history in the combustion chamber of the gross heat release rate and other
related parameters reveal some very interesting features, which shed light on the combustion mechanism when using these blends.
Moreover, for each test, volumetric fuel consumption, exhaust smokiness and exhaust regulated gas emissions are measured. The
differences in the performance and exhaust emission parameters from the baseline operation of the diesel engine, i.e., when working with
neat diesel fuel, are determined and compared. The heat release analysis results for the relevant combustion mechanism, combined with
the widely differing physical and chemical properties of the ethanol against those for the diesel fuel, are used to aid the correct
interpretation of the observed engine behavior.
r 2007 Elsevier Ltd. All rights reserved.
Keywords: Diesel engine; Ethanol–diesel blends; Heat release analysis; Combustion; Emissions
0360-5442/$ - see front matter r 2007 Elsevier Ltd. All rights reserved.
doi:10.1016/j.energy.2007.03.005
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1792 C.D. Rakopoulos et al. / Energy 32 (2007) 1791–1808
the added advantage of being renewable fuels that can be by this research group [11], which evaluates and compares
replenished through the growth of plants or production of the performance and environmental behavior of a multi-
livestock, showing an ad hoc advantage in reducing the tude of vegetable oils and their bio-diesels, in blend ratios
emitted carbon dioxide [10,11]. There is a commitment by with diesel fuel of up to 20
80.
the USA government to increase bio-energy three-fold in Because of its high octane number, ethanol is a good
10 years, which has added impetus to the search for viable spark-ignition engine fuel, while vegetable oils and bio-
bio-fuels [12]. diesels are good diesel engine fuels owing to their reason-
Concerning the environmental aspect, rational and ably high cetane number. It is true that alcohols, mainly
efficient end-use technologies are identified as key options ethanol and to a much lesser extent methanol, have been
for the achievement of the Kyoto targets of greenhouse gas considered as alternative fuels for diesel engines too
emissions reduction. For the transport sector of European [12,20,21]. Methanol can be produced from coal or petrol
Union (EU), energy savings of 5–10% in the medium term based fuels with low cost production, but it has a restrictive
and an aggregated of 25% in the long term (2020) are solubility in the diesel fuel. On the other hand, ethanol is a
aimed at, with an expected cut of carbon dioxide (CO2) biomass based renewable fuel, which can be produced by
emissions by 8% by the year 2010. The EU has issued a alcoholic fermentation of sugar from vegetable materials,
directive on the use of bio-fuels accounting to at least 2% such as corn, sugar cane, sugar beets, barley, sweet
of the market for gasoline and diesel fuel sold as transport sorghum, cassava, molasses and the like, and agricultural
fuels by the end of 2005, increasing in stages to a minimum residues, such as straw, feedstock and waste woods by
of 5.75% by the end of 2010 [11,13]. using already improved and demonstrated technologies
Bio-fuels made from agricultural products (oxygenated [19]. Therefore, it has the advantage over methanol of
by nature), may not only offer benefits in terms of exhaust higher miscibility with the diesel fuel and of being of
emissions, but also reduce the world’s dependence on oil renewable nature (bio-ethanol).
imports. Moreover, local agricultural industries can be
supported and farming incomes enhanced, besides provid- 2. Use of ethanol in diesel engines: short literature review
ing a better energy security for many developing countries.
Among these, bio-alcohols and vegetable oils or their The initial investigations into the use of ethanol in diesel
derived bio-diesels (methyl or ethyl esters) are considered engines were carried out in South Africa in the 1970s and
as very promising fuels [14–19]. A work has been presented continued in Germany and the USA during the 1980s.
ARTICLE IN PRESS
C.D. Rakopoulos et al. / Energy 32 (2007) 1791–1808 1793
Most of these works related to the use in farm equipment proof or lower), which is more economical to produce and
(tractors and combines) or to the reduction in smoke and find, or owing to water absorption by its hygroscopic
particulate emissions [22–26]. nature, an emulsifying agent is required to form the opaque
Nonetheless, there are several critical issues to consider macro-emulsion; this, however, could be separated into the
with the use of ethanol in the diesel fuel. While anhydrous two phases if allowed to stagnate over a long period [22].
ethanol is soluble in gasoline, additives must be used in Blends with up to 15% (by volume) ethanol in diesel fuel
order to ensure solubility of anhydrous ethanol (that is can be considered relatively safe from the engine durability
highly hygroscopic and thus practically impossible to stay viewpoint.
as such) in the diesel fuel under a wide range of conditions. Most of the reported researches with ethanol–diesel fuel
Especially at lower temperatures, the miscibility is limited; refer to higher capacity diesel engines (usually turbo-
it was determined that the aromatic content (having a charged) or smaller stationary ones. The present work
co-solvent action), intermediate distillate temperatures and deals with a standard experimental, Ricardo/Cussons
wax content of diesel fuel had a significant impact on the ‘Hydra’, high-speed, direct injection (DI), naturally aspi-
miscibility limits. Furthermore, adding ethanol to diesel rated engine of the automotive type, which possesses a high
fuel can reduce lubricity and create potential wear versatility and control over the variation of its operating
problems in sensitive fuel pump designs. Ethanol possesses parameters. The experiments were conducted without any
also lower viscosity and lower calorific value, with the modification on the engine. An emulsifying agent by ‘Betz
latter imposing minor changes on the fuel delivery system GE’ was used to satisfy ethanol–diesel fuel mixture
to establish the maximum power delivered by the use of the homogeneity and prevent phase separation, while no
neat diesel fuel [12,27,28]. ignition-improving additives were used.
By all estimates, ethanol has a very low cetane number The work evaluates the effects of using various blends of
that reduces the cetane level of the diesel-ethanol blend, ethanol with normal diesel fuel, with 5%, 10% and 15%
requiring normally the use of cetane enhancing additives, (by volume) ethanol, on the performance and exhaust
which improve ignition delay and mitigate cyclic irregu- emissions at various loads. The differences in the perfor-
larity [26,29–31]. Ethanol has much lower flash point than mance and exhaust emission parameters, from the baseline
the diesel fuel and higher vapor formation potential in operation of the diesel engine (working with diesel fuel),
confined spaces, thus requiring extra precautions to ensure are determined and compared. In a recently appeared
safe handling and use of these blends [12]. publication [42], consideration of theoretical aspects of
Therefore, various techniques involving ethanol–diesel diesel engine combustion and of the widely differing
dual fuel operation have been developed, to make diesel physical and chemical properties of the ethanol against
engine technology compatible with the properties of those for the diesel fuel were used to aid, in a rather
ethanol-based fuels. Broadly speaking, they can be divided qualitative way, the interpretation of the observed engine
into the following three categories: behavior with these blends.
At this point it is stated that there seems to be an obvious
(i) Ethanol fumigation to the intake air charge, by using scarcity of theoretical models scrutinizing the formation
carburetion or manifold injection. There seems to be mechanisms of combustion-generated emissions when
limits to the amount of ethanol that can be used in this using liquid bio-fuels, unlike the advanced models existing
manner, due to incipience of engine knock at high for the study of diesel engines when using conventional
loads, and prevention of flame quenching and misfire diesel fuel [43–47]. Recently, a detailed multi-zone combus-
at low loads [22,32–34]. tion modeling with these ethanol–diesel blends has been
(ii) Dual injection system that is not considered very submitted [48], along the lines of a recent paper by the first
practical, as requiring an extra high-pressure injection three authors [49] applied for the engine in hand when
system for the ethanol and, thus, a related major using vegetable oils or their derived bio-diesels, which has
design change of the cylinder head [22]. in turn expanded on a similar multi-zone one that has dealt
(iii) Blends (emulsions) of ethanol and diesel fuel by using only with the related physical processes [17].
an emulsifier to mix the two fuels in order to prevent As a ‘bridging’ agent for correctly interpreting the
separation; these require no technical modifications on present ethanol–diesel blends results and with a view to
the engine side [22,35–41]. assist the related multi-zone combustion modeling, a heat
release analysis for the relevant combustion mechanism,
It is reminded that stable emulsions usually refer to both combined with the widely differing physical and chemical
solutions of anhydrous ethanol in diesel fuel (transparent) properties of the ethanol against those for the diesel fuel,
and micro-emulsions of ethanol in diesel fuel (translucent). are used in the present study. As known, concerning the
Anhydrous ethanol (200 proof) does not require an study of the combustion process in diesel engines, either of
emulsifying agent or so-called ‘surfactant’ (from, surface the DI or the IDI (indirect injection) type, a very important
active agent) to form a transparent solution in diesel fuel, means to analyze combustion characteristics is the calcula-
but these solutions can tolerate only 0.5% water. Then, in tion and analysis of heat release rates according to actual
the practical cases of using lower proof ethanol (say 190 measurements of pressures in the (main) chamber (and the
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1794 C.D. Rakopoulos et al. / Energy 32 (2007) 1791–1808
The engine is mounted on a fully automated test bed and 3.3. Exhaust gas analyzers system
coupled to a ‘‘McClure’’ DC motoring dynamometer,
having load absorbing and motoring capabilities, which is The exhaust gas analysis system consists of a group of
equipped with a load cell for the engine torque measure- analyzers for measuring soot (smoke), nitrogen oxides
ments. There is one electric sensor for speed and one for (NOx), carbon monoxide and total unburned hydrocar-
load (torque), with these signals fed to indicators on the bons (HC). The smoke level in the exhaust gas was
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C.D. Rakopoulos et al. / Energy 32 (2007) 1791–1808 1795
Fig. 1. Schematic arrangement of the engine test bed, instrumentation and data logging system.
measured with a ‘Bosch’ RTT-100 opacimeter, the readings signal. The signal from a ‘‘Tektronix’’ TDC magnetic pick-
of which are directly provided as Hartridge units (% up marker is used for time reference.
opacity) or equivalent smoke (soot) density (milligrams of The output signals from the magnetic pick-up and the
soot per cubic meter of exhaust gases). two piezoelectric transducers signals, while they were
The carbon monoxide concentration in ppm (parts per continuously monitored on a dual beam ‘‘Tektronix’’
million, by volume) in the exhaust was measured with a storage oscilloscope, are connected to the input of a
‘Signal’ Series-7200 non-dispersive infrared analyzer ‘‘Keithley’’ DAS-1801ST A/D board installed on an IBM
(NDIR). The nitrogen oxides concentration in ppm in the compatible Pentium III PC. This board can acquire input
exhaust was measured with a ‘Signal’ Series-4000 chemi- data at a total throughput rate of 312.5 ksamples/s from up
luminescent analyzer (CLA). The total unburned hydro- to eight differential analogue inputs, utilizing also dual-
carbons concentration (in ppm) in the exhaust was channel direct memory access (DMA) operation. It is then
measured with a ‘Ratfisch-Instruments’ flame-ionization appropriate for the recording of high frequency engine
detector (FID). The last two analyzers were fitted with signals, with the added advantage of high signal resolution
thermostatically controlled heated lines. (much less than 1 1CA, depending also on the number of
simultaneous recorded signals). This high acquisition rate
capability secures the nearly simultaneous sampling of all
3.4. Transducers measuring set-up and data acquisition input signals too.
system Control of this high-speed data acquisition system is
achieved by developing a computer code based on the
For measuring the pressure in the cylinder, a ‘‘Kistler’’ ‘‘TestPoint’’ control software. The resultant program,
miniature piezoelectric transducer is used, flush mounted to specially designed for steady or transient internal combus-
the cylinder head and connected to a ‘‘Kistler’’ charge tion engine applications, is an object-oriented functional
amplifier. Also, a ‘‘Kistler’’ piezoelectric transducer is code. It allows the direct on-screen selection of the desired
connected on the injector side of the pipe linking the values of all acquisition parameters, namely: engine type
injection pump and injector to provide the fuel pressure (two- or four-stroke); engine speed (in rpm); desired
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1796 C.D. Rakopoulos et al. / Energy 32 (2007) 1791–1808
number of recorded cycles; selection of the acquired of 29 1CA before TDC, and four loads corresponding to
channels; and sampling interval (in degrees CA). brake mean effective pressures of 0.00 (no-load), 1.40, 2.57
After the selection of the above values, the resulting and 5.37 bar, respectively. Owing to the differences among
sampling rate per channel is displayed on screen. When the lower calorific values ‘Y’ and oxygen contents of the
acquisition starts, data are initially stored in the computer’s fuels tested, the comparison must be effected at the same
memory. This secures the continuous gap-free acquisition engine brake mean effective pressure, i.e., load, and not at
for the large amount of multi-channel input data. When the the same injected fuel mass or air–fuel ratio. For the no-
desired amount of engine cycles is recorded, the data are load conditions, only pressure measurements were taken.
transferred from the memory to a corresponding file in the In each test, volumetric fuel consumption rate Vfc (in m3/s),
hard disk and directly displayed on-screen (as X–Y graphs). exhaust gas temperature, exhaust smokiness and exhaust
Special warning signs and other secondary options are also regulated gas emissions such as nitrogen oxides, carbon
available. monoxide and total unburned hydrocarbons are measured.
From the first measurement, specific fuel consumption and
4. Properties of fuels thermal efficiency are computed using the fuel sample density
and lower calorific value.
The conventional diesel fuel was supplied by the By knowing the engine brake torque Mt (in N m), i.e.,
Aspropyrgos Refineries of the ‘Hellenic Petroleum SA’ the load, which is set for each experiment and kept
and represents the typical, Greek automotive, low sulphur constant by the engine controllers, the following engine
(0.035%) diesel fuel (gas oil); it forms the baseline fuel of performance quantities were computed, with N the
the present study. The properties of the diesel fuel and the (constant) engine speed (in rpm):
ethanol are summarized in Table 2.
The ethanol (CH3CH2OH) is blended with the normal
5 10
diesel fuel at blend ratios of 95 , 90 and 15
The brake mean effective pressure, b.m.e.p. (in bar)
85 (by volume). For
the present experiments, no cetane improving additives b:m:e:p: ¼ ð4pM t =V h Þ 105 (1a)
(ignition improvers) were used. An emulsifying agent by 2
with Vh ¼ (p/4)D s the (single-cylinder) engine displace-
‘Betz GE’, a division of General Electric, Inc., was used in
ment volume.
proportions of 1.5% by volume, to satisfy mixture
The brake power, P (in W)
homogeneity and prevent phase separation.
The emulsifier replaced a corresponding part of the P ¼ M t ð2pN=60Þ. (1b)
diesel fuel. Thus, the 15
85 blend ratio corresponds to 83.5%
diesel fuel, 1.5% emulsifier and 15% ethanol (by volume), The brake specific fuel consumption, b.s.f.c. (in g/kW h)
and similarly for the other two blends. The mixing protocol
consisted of first blending the emulsifier into the ethanol b:s:f :c ¼ ðV fc rf =PÞ3:6 109 . (1c)
and then blending this mixture into the diesel fuel.
The brake thermal efficiency, b.t.e.
5. Parameters tested and experimental procedure b:t:e: ¼ P=ðV fc rf YÞ. (1d)
6.2. Preliminary treatment of the experimental pressure 0 500 1000 1500 2000 2500
diagrams and determination of various timings Sampling point number
for the first derivative of pressure with respect to crank The difference between the dynamic injection timing and
angle. The sudden changes of the latter one, for the the pump spill timing forms the injection delay.
indicator diagram, would grossly be transferred to the By processing the cylinder pressure diagram, as shown
‘sensitive’ heat release rate diagram (cf. Eq. (6)). for example in Fig. 3b, the ignition timing was located at
By processing the fuel pressure diagram, as shown for the crank angle where the first derivative of this pressure
example in Fig. 3a, the static injection timing (at the with respect to crank angle suddenly changes slope,
injector) was determined at the crank angle where this immediately following the event of the dynamic injection
pressure rises suddenly above the residual (in the connect- timing, going from a negative to a positive value and so
ing pipe) pressure value (point ‘S.inj.’). As no apparatus for presenting a local minimum. The ignition timing was then
measuring the injector needle lift was available, the determined either by using this condition, or by locating
dynamic injection timing was assumed to coincide with the corresponding ‘zeroing’ crank angle of the second
the crank angle where the fuel pressure reaches the value of derivative of pressure with respect to crank angle, assuming
the injector nozzle opening pressure, immediately following that this signal is ‘smooth’ enough; this is shown in Fig. 3b
the event of the static injection timing (point ‘D.inj.’). as point ‘S’. Note that with every differentiation of the
original pressure signal the noise-to-signal ratio increases,
while if over-smoothing is applied this ‘zero’ point might
disappear as being ‘ill conditioned’. The difference between
600 Injection pressure (bar) 100 the ignition timing and the dynamic injection timing forms
Cylinder pressure (bar) the ignition delay.
From the first and second derivatives of the cylinder
80 pressure diagram with respect to crank angle, which are
found numerically, the crank angles of the maximum
400 values of the first derivative of pressure and of the pressure
60 itself can be determined, bearing also in mind that they
immediately follow the ignition timing and in that order.
Injector nozzle
opening pressure 40 6.3. Energy conservation and state equations
200
The heat release rate determination procedure is based
20 on the processing of the cylinder pressure (indicator)
diagram. The properties of the gas content are considered
constant inside each time step, with their values calculated
0 S.inj. D.inj.
0 as described in Section 6.4.
-40 -20 0 20 40 It is understood that all the differentiations to follow
CRANK ANGLE (deg.) with respect to time ‘t’ can be converted to differentiations
Pressure (bar) with respect to degrees crank angle ‘j’, by multiplying by
1st Press. Deriv. (bar/deg) the factor (where the engine speed ‘N’ is expressed in rpm)
100 2nd Press. Deriv. (bar/deg**2) 2 6
dt 1
¼ . (2)
dj 6N
80 4
By applying the first law of thermodynamics in
differential form, for an open system, the net heat release
1
rate is determined as [1,2,58]:
60 2
dQn dme dU dV
he ¼ þp , (3a)
dt dt dt dt
40 0 where the dme/dt ¼ (dme/dj)6N term stands for the (out-
S
0 flowing) blowby rate, calculated in Section 6.6, having the
specific enthalpy he of the cylinder contents. The terms
20 -2
U and he are defined as the gas sensible internal energy and
sensible specific enthalpy, respectively. The corresponding
sensible term for the fuel, hf (dmf/dt), has been omitted
0 -1 -4
from the above equations as being very small.
-40 -20 0 20 40
Thus, the net heat release rate, so computed, represents
CRANK ANGLE (deg.)
the difference between the combustion energy-release rate
Fig. 3. Determination of static (point ‘S.inj.’) and dynamic (point ‘D.inj.’) (gross) and the rate of heat transferred (loss) to the
injection timings in (a), and of ignition timing (point ‘S’) in (b). chamber walls.
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C.D. Rakopoulos et al. / Energy 32 (2007) 1791–1808 1799
Considering the working medium as a perfect gas, with 6.4. Combustion reaction and working medium properties
m the instantaneous cylinder mass, Eq. (3a) results in
In this subsection only the combustion phase is
dT dQn pdV dme addressed, since the compression and expansion phases
mcv ¼ he . (3b)
dt dt dt dt can be considered as simple sub-cases (absence of chemical
The perfect gas state equation for the cylinder gas reaction and constant composition in time for compres-
content reads sion). Although dissociation could be included
[43,44,58,59], it was opted to neglect it for keeping the
pV ¼ mRT ! T ¼ pV =mR (4a) analysis simple. Moreover, in the light of the inherent
uncertainties involved in experimental heat release analysis
or in differential form as calculations, it was felt that its inclusion would not
dV dp dT dm add much.
p þV ¼ mR þ RT . (4b) The basic stoichiometric chemical equation for the fuel
dt dt dt dt
(with chemical formula CnHmOr)—oxygen reaction is
Combining Eqs. (3b) and (4b), we get the following [2,60],
expression for the first law equation:
Cn Hm Or þ ½n þ ðm=4Þ ðr=2ÞO2 ! nCO2 þ ðm=2ÞH2 O:
pðdV =dtÞ þ V ðdp=dtÞ RTðdm=dtÞ
cv (10)
R
dQn dV dme The number of kmoles bi of the constituents (i ¼ 1,2,3,4
¼ p he . ð5Þ
dt dt dt and 5 for CO2, H2O, O2, N2 and CnHmOr, respectively) at
any time t (or corresponding crank angle j), for complete
Substituting the value of T from Eq. (4a) into Eq. (5), we
combustion in air, are calculated from the following
can calculate the net heat release rate from
expressions:
dQn cv dV dp pV dm dV dme
¼ p þV þp þ he . (6) b1 ¼ nwf ; b2 ¼ ðm=2Þwf ; b3 ¼ b1 b2 =2 þ wf G=F,
dt R dt dt m dt dt dt
b4 ¼ 3:76wf G=F; b5 ¼ w0f wf , ð11aÞ
The instantaneous mass m in the cylinder, needed in
Eqs. (4a) and (6), at any crank angle j (corresponding ‘t’) where G ¼ n+(m/4)(r/2), and wf ¼ mfb/Mf is the number
is calculated from of kmoles of fuel burned up to that time out of a total of
Z j w0f, with b5 ¼ 0 when Fp1.
dme 1 The fuel–air equivalence ratio F, i.e., the actual fuel–air
mðjÞ ¼ mðjivc Þ dj, (7)
jivc dt 6N ratio (by mass) divided by its stoichiometric value, is
computed with the cumulative values (up to the crank
where a computation of mass (air and possibly residual angle in question) of the air and fuel burned (calculated in
gases) is accomplished at the point of IVC (inlet valve the previous subsection), as follows:
closure), with known pressure and temperature there for
the engine in hand. F ¼ ½mfb =ðm mfb Þ=FAst (11b)
Therefore, the corresponding gross heat release rate,
which is the energy released from the combustion of fuel, is with
given by
FAst ¼ ð12n þ m þ 16rÞ=½4:76ðn þ m=4 r=2Þ28:96.
dQg dQn dQw (11c)
¼ þ , (8)
dt dt dt
The specific internal energies (considering only their
where the ‘dQw/dt’ term stands for the rate of heat sensible part) of the components are given as 4th order
transferred to the walls of the combustion chamber, which polynomial expressions of the absolute temperature [60].
is calculated as described in Section 6.5. Similar expressions are then derived for the specific
Obviously, by knowing the fuel lower calorific value Y, enthalpies, specific heat capacities and specific heat
the fuel burned mass rate in the chamber is computed from capacities ratio, by applying the simple thermodynamic
dmfb 1 dQg relations connecting these quantities for a perfect gas
¼ . (9) [1,58]. The mixture properties in the chamber are then
dt Y dt
computed by knowing the prevailing gas composition
If now we integrate Eqs. (8) and (9), from the point of as calculated from Eqs. (11a)–(11c) and the gas tempera-
IVC event up to any crank angle ‘j’ (corresponding ‘t’) of ture T calculated from Eq. (4a). Owing to the small
the closed part of the cycle (along the lines of Eq. (7)), we variation of the mixture molecular weight ‘M’ with
can obtain the respective cumulative values in the chamber composition, the mixture specific constant R ¼ Rmol/M
of the heat released by the fuel Qg and the fuel burned mfb. was considered as constant.
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1800 C.D. Rakopoulos et al. / Energy 32 (2007) 1791–1808
6.5. Gas heat transfer sub-model where atmospheric pressure is assumed to exist. The value
of the discharge coefficient cd is chosen in a way to match
The heat transfer between the chamber trapped mass and the measured blowby rate from the engine. The analysis is
surrounding walls is calculated by using the formula of taken to include also the effect of the mass flow rate
Annand [61], with the heat flux given by leakage through the engine valves (a relatively very
small amount), without making its distinction from the
dQw =dt kgas
¼a ðReÞb ðT T w Þ þ c ðT 4 T 4w Þ, (12) blowby one.
A D
where A is the heat transfer surface area of the combustion
6.7. Cylinder volume and its rate of change against crank
chamber walls, Re ¼ rgasDup/vgas is the Reynolds number,
angle
up ¼ 2Ns/60 is the mean piston speed, and kgas, vgas are the
gas thermal conductivity and dynamic viscosity, respec-
The instantaneous volume in the cylinder is given by
tively, which are available as polynomial expressions of the
[1,2,59,63]
gas temperature T. qffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffi
In the above equation, exponent b ¼ 0.75 and constant
V ¼ V c þ Apc r½ð1 cos fÞ þ l l2 sin2 j, (14a)
1
c¼0 for the compression period, otherwise
c ¼ 3.3 108 W/m2 K4, which are their most usual values where Vc is the cylinder clearance volume, r ( ¼ s/2) the
[44,60]. Finally, constant ‘a’ is evaluated by iteration, in a crank radius, Apc the piston cross section area, and l the
way that the total fuel burned in the chamber, mfbtot, found ratio of crank radius to piston rod length.
by integration, from the IVC event to the EVO event of the Its rate of change against crank angle is,
closed part of the cycle, of Eq. (9) coincides with its qffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffi
corresponding experimental value mfc/(N/120), where mfc is dV =df ¼ Apc r½sin jð1 þ l cos j= 1 l2 sin2 jÞ. (14b)
the measured fuel consumption rate.
Although it is expected that the value of the ‘c’
(radiation) constant is lower for the cases of ethanol
blends due to their lower flame luminosity, it is kept the 6.8. Numerical solution procedure and computer program
same with any differences incorporated in the value of the
‘a’ constant. The equations of the thermodynamic model, presented in
the previous subsections, are solved numerically step-by-
step using a simple time marching technique, with a time
6.6. Blowby rate sub-model
step size corresponding to 0.51CA. The differential
equations are converted to algebraic ones using a simple
For the evaluation of the mass blowby rate (of total
Euler scheme [64].
amount of 1% of the cylinder full charge) a simple model is
Before the start of calculations, the design characteristics
adopted, by assuming an equivalent blowby area the
of the engine are inputted into the program. The
greatest part of which is the piston ring gap. It was felt that
computations start at IVC event and end at EVO event.
the use of more elaborate models, such as for example the
At the IVC event, reasonable estimates must be made for
ones developed by the present research group taking into
the prevailing pressure and temperature in the cylinder.
account the piston rings motion [62], would not add much
The pressure is taken equal to the atmospheric one [2,65].
to this analysis.
This fact was used to ‘reference’ the pressure transducers,
The well-known relation for gas mass flow through a
taking as the value of point at IVC event the average of 5
restriction is used, accounting for one-dimensional, quasi-
points before and 5 after its position, in order to minimize
steady, compressible flow [1,63], as follows:
vffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffiffi
ffi the potential error of relying on only one measured point
u " ðgþ1Þ=g # [51,55]. The corresponding temperature was selected 30 K
dme pu u t 2gR u T u p d
2=g
p
¼ cd F d higher than the atmospheric one [65]. The associated
dt Ru T u g1 pu pu computer program was written in Fortran V language and
(13a) executed on a Pentium-IV Personal Computer.
diagrams (of neat diesel fuel against the E15-D blend) that 100
are relatively well discernible in this case.
The results of this section refer to all four loads
considered, corresponding to brake mean effective pres-
80
sures of 0.00 (no-load), 1.40, 2.57 and 5.37 bar, respec-
400 decreases with engine load for both fuels, while the heat
release rate values become higher. For the higher loads,
both parts of combustion, i.e., the premixed combustion
(the part under the first ‘abrupt peak’) and the diffusion
combustion (the last part under the second ‘rounded
peak’), are apparent, with the diffusion combustion
200 diminishing with load decrease.
One can again observe, from this figure, that for each
load considered, the ignition delay for the E15-D blend is
higher than the corresponding one for the neat diesel fuel
case, while its premixed combustion peak is much higher
and sharper. It is the lower cetane number of ethanol
0
(cf. values in Table 2) that causes the increase of ignition
-40 -20 0 20
delay and so the increased amount of ‘prepared’ fuel (to
CRANK ANGLE (deg.)
this end may also assist the easier evaporation of ethanol)
Fig. 4. Fuel (injection) pressure against crank angle diagrams, at the four for combustion after the start of ignition. However, as
loads, for the neat diesel fuel and the 15% ethanol blend. noticed in Fig. 5, this is not translated into higher pressures,
ARTICLE IN PRESS
1802 C.D. Rakopoulos et al. / Energy 32 (2007) 1791–1808
50 2000
GROSS HEAT RELEASE RATE (J/deg.)
40
1600
TEMPERATURE (K)
30
1200
20
800
10
400
0
0
-10
-20 0 20 40
-20 0 20 40 60 80
CRANK ANGLE (deg.)
CRANK ANGLE (deg.)
50 Fig. 7. Cylinder temperature against crank angle diagrams, at the four
loads, for the neat diesel fuel and the 15% ethanol blend.
GROSS HEAT RELEASE RATE (J/deg.)
40
800 0.6
CUMULATIVE GROSS HEAT RELEASE (J)
600
EQUIVALENCE RATIO
0.4
400
200
0.2
-200
0
-20 0 20 40 60 80
-40 -20 0 20 40 60
CRANK ANGLE (deg.)
CRANK ANGLE (deg.)
Fig. 8. Cumulative gross heat release against crank angle diagrams, at the
four loads, for the neat diesel fuel and the 15% ethanol blend. Fig. 10. Fuel–air equivalence ratio against crank angle diagrams, at the
four loads, for the neat diesel fuel and the 15% ethanol blend.
300 proves that the engine runs overall a little ‘leaner’ with the
E15-D blend, for the same engine load and speed
conditions. It is stated that the calculation of F was based
on Eqs. (11b) and (11c) by considering all the fuel-bound
oxygen, hoping this is released in crucial local ‘rich’ areas
CUMULATIVE HEAT LOSS (J)
200
(zones).
160 ethanol in its blends with diesel fuel. One can observe that
Diesel
the NOx emitted by the ethanol blends are slightly lower
than those for the corresponding neat diesel fuel case, with
5% Ethanol the reduction being higher the higher the percentage of
10% Ethanol ethanol in the blend. This may be attributed to the engine
120 running overall ‘leaner’ and the temperature lowering effect
15% Ethanol of the ethanol having the dominating influence (cf. Figs. 7
and 10), against the opposing effect of the lower cetane
Soot Density (mg/m3)
320
800
NOX (ppm)
600
240
CO (ppm)
400
160
200
0 80
b.m.e.p. : 1.40 bar 2.57 bar 5.37 bar
Fig. 12. Bar chart diagram of the emitted nitrogen oxides (NOx), at the
three loads, for the neat diesel fuel and the 5%, 10% and 15% ethanol
blends.
0
b.m.e.p. : 1.40 bar 2.57 bar 5.37 bar
Fig. 12 shows in a bar chart diagram, at the three loads Fig. 13. Bar chart diagram of the emitted carbon monoxide (CO), at the
considered, the nitrogen oxides (NOx) exhaust emissions three loads, for the neat diesel fuel and the 5%, 10% and 15% ethanol
for the neat diesel fuel and the various percentages of the blends.
ARTICLE IN PRESS
C.D. Rakopoulos et al. / Energy 32 (2007) 1791–1808 1805
120 500
Diesel 10% Ethanol
5% Ethanol 15% Ethanol
80 300
HC (ppm)
60 200
40 100
20 0
0 5 10 15
Ethanol in fuel blend (% by vol.)
0 Fig. 15. Brake specific fuel consumption for the neat diesel fuel and the
b.m.e.p. : 1.40 bar 2.57 bar 5.37 bar 5%, 10% and 15% ethanol blends, at the three loads.
Fig. 14. Bar chart diagram of the emitted total unburned hydrocarbons
(HC), at the three loads, for the neat diesel fuel and the 5%, 10% and 15% fuel. The fuel blend mass flow rate is calculated from the
ethanol blends. respective measured volume flow rate value and the blend
density. Since the comparison is made at the same load
percentages of the ethanol in its blends with diesel fuel. One (b.m.e.p.) and speed, which is translated into the same
can observe that the HC emitted by the ethanol–diesel fuel engine power (cf. Eqs. (1a) and (1b)), the brake specific fuel
blends are higher than those for the corresponding neat consumption values are then effectively directly propor-
diesel fuel case, with the increase being higher the higher tional to the fuel mass flow rate (cf. Eq. (1c)). It is observed
the percentage of ethanol in the blend. This is the behavior that for all the ethanol–diesel fuel blends, the specific fuel
reported by almost all investigators on various types of consumption is a little higher than the corresponding diesel
engines and conditions [21]. fuel case, with the increase being higher the higher the
As it is known, the formation of unburned hydrocarbons percentage of ethanol in the blend. This is the expected
originates from various sources in the engine cylinder and behavior due to the lower calorific value of the ethanol
their theoretical study is still at its infancy. It is argued [20] compared to that for the neat diesel fuel, given that the
that, presumably, the increase of HC with the addition of comparison is effected at the same load.
ethanol is due to the higher heat of evaporation of the Fig. 16 shows, at the three loads, the brake thermal
ethanol blends causing slower evaporation and so slower efficiency for the neat diesel fuel and the various
and poorer fuel–air mixing, to the increased spay penetra- percentages of the ethanol in its blends with diesel fuel.
tion causing unwanted fuel impingement on the chamber It is to be noted that the brake thermal efficiency is simply
walls (and so flame quenching) and cushioning in the ring the inverse of the product of the specific fuel consumption
land areas, and to the increase with ethanol of the so-called and the lower calorific value of the fuel (cf. Eqs. (1c)
‘lean outer flame zone’ where flame is unable to exist and (1d)). Given the above-mentioned close interrelation
[1,2,33]. To this end may also contribute the late escape between brake thermal efficiency and specific fuel con-
into the cylinder of the fuel left in the nozzle sac volume, sumption, the results of this figure can be explained. It is
because with the addition of ethanol this is easier observed that for all the ethanol–diesel fuel blends, the
evaporated (as heated) and ‘slipped’ into the cylinder (at brake thermal efficiency is slightly higher than that for the
low velocity, late in the expansion stroke) [1,58]. Further, corresponding neat diesel fuel case, with the increase being
some observed phenomena of cyclic irregularity [30,56,57], higher the higher the percentage of ethanol in the blend.
especially with the higher ethanol content blends (to be This means that the increase of brake specific fuel
reported and analyzed in a following paper), may consumption for the ethanol–diesel blends is lower than
contribute towards this side [1]. the corresponding decrease of the lower calorific value of
Fig. 15 shows, at the three loads considered, the brake the blends. This can be attributed to the higher premixed
specific fuel consumption for the neat diesel fuel and the combustion part possessed by the ethanol blends because
various percentages of the ethanol in its blends with diesel of the lower cetane number of ethanol, leading to higher
ARTICLE IN PRESS
1806 C.D. Rakopoulos et al. / Energy 32 (2007) 1791–1808
0.4 the corresponding neat diesel fuel case (cf. Fig. 7), with this
decrease being higher the higher the percentage of ethanol
in the blend. This is in accordance with the corresponding
trend of slightly higher thermal efficiency, as justified
0.3
above, by denoting a better expansion process; to this side
may also be corroborating the higher latent heat of
Brake thermal efficiency
0.2 9. Conclusions
On the contrary, the unburned hydrocarbons (HC) [14] Graboski MS, McCormick RL. Combustion of fat and vegetable oil
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