Shock Tube/Laser Diagnostics for Fuel and Surrogate ... · temperatures (

35
Shock Tube/Laser Diagnostics for Fuel and Surrogate Kinetics Fuel and Surrogate Kinetics R. K. Hanson, D. F. Davidson D Haylett A Farooq S Vasu S Ranganath D. Haylett, A. Farooq, S. Vasu, S. Ranganath Mechanical Engineering, Stanford University NIST Fuel Summit: Sept 7 10 2008 NIST Fuel Summit: Sept 7-10, 2008 Advances in Experimental Techniques Kinetic Results for Alkanes New Directions: Shock Tube Research 1 Sponsor: AFOSR/USC

Transcript of Shock Tube/Laser Diagnostics for Fuel and Surrogate ... · temperatures (

Page 1: Shock Tube/Laser Diagnostics for Fuel and Surrogate ... · temperatures (

Shock Tube/Laser Diagnostics for Fuel and Surrogate KineticsFuel and Surrogate Kinetics

R. K. Hanson, D. F. DavidsonD Haylett A Farooq S Vasu S RanganathD. Haylett, A. Farooq, S. Vasu, S. Ranganath

Mechanical Engineering, Stanford University

NIST Fuel Summit: Sept 7 10 2008NIST Fuel Summit: Sept 7-10, 2008

Advances in Experimental Techniquesd a p a qu

Kinetic Results for Alkanes

New Directions: Shock Tube Research

1Sponsor: AFOSR/USC

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Long-Term Program Objectives

Build an accurate, multi-target, multi-species experimental database for hydrocarbon combustion – practical fuels and surrogates - utilizing modern shock tube and laser diagnostic techniques

Collaboratively develop, evaluate and refine detailed kinetic mechanismsf i l t f l ltifor single-component fuels, multi-component surrogate blends, and practical fuels to establish predictive capabilities for the kinetics of current pand future fuels

2

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Advances in Experimental Techniques

Virtues of Shock Tubes and Lasers for Combustion Kinetics: Accurately known reaction mixtures and initial conditions accessibility to wide Accurately known reaction mixtures and initial conditions, accessibility to wide

range of conditions (P, T), wide range of time scales (s to ms), negligible influence of transport phenomena, ready access for LOS optical diagnostics

Sensitive, species-specific time-histories via LOS laser absorption diagnostics, p p p g

Advances in Experimental Techniques:

1. Extension of shock tube test time to access low temperature ignition regime

2. Shock tube geometry modification to maintain constant reaction conditions

3. Development of aerosol shock tube to handle low-vapor-pressure fuels

4. Extension of species detection capabilities to provide time-histories of fuel, intermediate and product species – the holy grail

5. Development of shock tube reactive gasdynamics codes to improve kinetic

3

5. Development of shock tube reactive gasdynamics codes to improve kinetic modeling and extend to post-ignition regime

Work sponsored by ARO and AFOSR

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Overview of Stanford Shock Tube Facilities

Transmitted Beam Detector

PressureGas

Chromatograph

D2Lamp

DriverSection

Shock TubeDriven Section

essu ePZTPMT

Excimer photolysis

Shock Tubes (4 + 1 under construction) Low-Pressure Tubes (15 cm and 14 cm) High-Pressure Tube (5 cm) heatable to 150C

UV/Vis/IREmissionDetectors

sideKinetic

Spectrograph ARASMRAS

g ( ) Aerosol Shock Tube (11 cm) Imaging Shock Tube (10 cm sq. under construction)

Optical Diagnostics Absorption (VUV, UV, Vis, Near-IR, Mid-IR)

Ring Dye Laser(UV & Vis) Absorption (VUV, UV, Vis, Near IR, Mid IR)

Kinetic Spectrograph (200-300nm) Emission (UV, Vis, IR) ARAS: H, O, C, N atom detection

Supporting Equipment

( )

Diode Laser(Near IR & IR)

4

Supporting Equipment Gas Chromatography Excimer Photolysis Mid-IR Lasers

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Overview of Laser Absorption Diagnostics for Species Time-History Measurements

Using Ring Dye/Ar+ LasersCH 431 nmNCO 440 nm

Recent AdditionsBenzyl 266 nmToluene 266 nmNCO 440 nm

NO2 472 nm

With Frequency DoublingCH3 216 nm

Toluene 266 nmPropargyl 335 nmNCN 329 nmCO2 244/266 nmCO 2 3 mNO 225 nm

OH 306 nmNH 336 nmCN 388 nm

CO 2.3 mCO2, H2O, T 2.7 m Tunable DFB lasersHC Fuels 3.3-3.55 m Tunable DFG lasersC2H4 10.5 m CO2 laser

With Frequency ModulationNH2 597 nm HCO 614 nm

Using Diode/HeNe LasersH2O 1.4 mFuel 3.4 mCO 4.6 m

5

NO 5.2 m

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Advances in Experimental Techniques:1) Extended Test Time in Shock Tubes

Challenge: Longer shock tube test times (> 2 ms) needed for studies at lower(> 2 ms) needed for studies at lower temperatures (<900 K) to study NTC regime

Our Approach: Significant improvements in pp g pshock tube test time are possible with:

Step 1: Driver gas tailoring(N2/He driver mix for NTC region) Reflected Shock Temperature [K](N2/He driver mix for NTC region)

~ 10 ms test time Step 2: Driver length change

(2x driver length) 30

40

[ms]

652 820 1015 1550 2175

Ideal Test TimeArgon Driven Gas8.5 m Driven SectionTailored Driver Gas

~ 40 ms test time

10

20

(L = 6 m)2x Driver

Idea

l Tes

t Tim

e

61.0 1.5 2.0 2.5 3.00

10

(L = 3 m)

Incident Mach Number

Existing Driver

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Application: Extended Shock Tube Test Times Provide Access to Low Temperature n-Heptane Ignitionp p g

New driver length and tailored 100

1000K1110K 833K

714K

ggas mixtures provide access to long ignition time region Strong pressure dependence

2

25 ms

9 atmms]

35 ms1 atm

in NTC region: t ign ~ P-2

Current models capture trend but not accurate values

10

gniti

on T

ime

[m

n-Heptane/21% O2/Ar = 0.5

1

2 ms

I

Chalmers University Heptane Model

New shock tube data provides targets for model refinement in NTC region

0.8 0.9 1.0 1.1 1.2 1.3 1.4 1.5

1000/T [1/K]

77

New shock tube data provides targets for model refinement in NTC region At long test times must monitor and minimize non-ideal flow variations

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Advances in Experimental Techniques:2) Shock Tube Geometry Modification (Driver Inserts) Alleviate

Facility-Related Pressure VariationsFacility Related Pressure Variations

5

4

m] Ideal Pressure

Non‐Reactive CaseTailored Driver gas mixture:

50% N2, 50% He;

2

3

Pre

ssur

e [a

tm

Ideal Pressure Driven gas: Ar Reflected shock conditions:

900 K, 4 atm

1

P

T5 = 912 K, 1-L driver without insert T5 = 897 K, 1-L driver with insert

dP/dt (without insert): 1.7%/ms dP/dt (with insert): 0%/ms

8

0 5 10 150

Time [ms]

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Application: Resolve ignition time discrepancy in H2/O2 mixtures at low temperatures2/ 2 p

Significant difference seen between conventional shock tubebetween conventional shock tube experiments and constant volume models of low-temperature H2/O2ignition

Facility effects (dP/dt) at long test times in low-temperature shock tube measurements influence ignition times g

99

Strong sensitivity of H2/O2 ignition delay time to pressure and temperature requires improved gasdynamic model for accurate comparison: CHEMSHOCK

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Advances in Experimental Techniques:3) Aerosol Shock Tube

Experimental challenge:Many practical fuels and propellants have low vapor pressures, requiring heated research facilities to fully vaporize the fuel with the possibility of pre-test fuel decomposition/oxidation

Stanford approach:- Generate liquid aerosols in shock tube and vaporize behind incident shock

P id l t d id i f f l t h ith t- Provides complete and rapid conversion of fuel to vapor phase without pre-test fuel decomposition/oxidation- Enables fundamental shock tube studies of practical fuels

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Work on Aerosol Shock Tube (AST) supported by ARO

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Aerosol Shock Tube: 1st Generation

Two Color DFG Laser

UV LaserMIR Lasers

Near-IR Laser

Differential extinction yields vapor concentration

or vapor and temperature

NIR extinction yields droplet loading as f(t)

UV radical speciesMIR product species

Fill shock tube with fuel aerosol/oxidizer mixture (3 m diam. droplets) Fully evaporate aerosol behind incident shock wave

Confirm evaporation with non-resonant NIR laser extinction D t i f l l di ( d t t ) ith 2 l DFG l

11

Determine fuel loading (and temperature) with 2 color DFG laser Measure HC time-histories behind reflected shock waves with DFG laser,

radicals with UV laser, products with NIR and MIR TDLs

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Aerosol Shock Tube: Complete Conversion to Vapor Behind Shock Waves: n-Dodecane

1. Incident shock arrives T2=446 K, P2=0.78 atm

2. Droplets accelerate and are compressed

3. Droplets evaporate

2

13 4

6Droplet/Vapor Signal

sorp

tion D

roplet

4. Point of complete conversion to vapor

5. Uniform gas phase formed by diffusion

3.39m

1

54 ’s

DropletSignalVa

por

Abs t Extinctio

formed by diffusion6. Reflected shock arrives

T5=618 K, P5=2.4 atm

Signal n

Multi-wavelength diode laser extinction enables determination of droplet size distribution and loading, and confirms complete evaporation 3.39 m laser absorption data enables determination of fuel mole fraction before arrival

4

12

pof reflected shock wave at Next step: study thermal decomposition and oxidation behind reflected shocks in

5

6

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Aerosol Shock Tube Provides Access to Diesel DF-2 Ignition TimesDF 2 Ignition Times

1197 K, 7.2 atm, =0.5, 21%O2

Aerosol shock tube provides first high-concentration ignition time data for diesel (DF-2) with no fuel cracking by mixture heating

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Aerosol Shock Tube : 2nd Generation

Motivation: reduce volume of tube filled with aerosol increase controlfilled with aerosol, increase control of fuel loading, improve uniformity

Use of holding tank for fuel/oxidizer

SlurryValve

GateValve

Use of holding tank for fuel/oxidizer mixture higher fuel loadings possible, smaller droplets

Reduced aerosol filling volume in Control

Shock Tube

shock tube reduced contamination of shock tube

Improved aerosol spatial uniformity by experiment

ControlValve

by experiment

Status: prototype valves and mixture tank are being tested Mixertank are being tested Array of Nebulizers

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Advances in Experimental Techniques:4) Extend Species Detection Capability

Challenge: Species time-histories for fuel, intermediate species, and products needed to aid

mechanism development and validationStanford approach:

N li id h l b i id i i i i i i Narrow-linewidth laser absorption provides sensitive, quantitative, in situdetection of critical combustion species – previously we used this primarily for radicals (OH, benzyl, CH, NCN, CH3 …)

New tunable two-color mid-IR detection provides speciation for HC fuels New tunable two-color mid-IR detection provides speciation for HC fuels, intermediates and products: n-heptane, n-dodecane, ethylene, propene, methane, propane, CH2O …

New tunable mid-IR laser at 2.7 m provides access to product species CO2, H2O, p p p 2, 2 ,and T

New tunable CO2 laser at 10.5 m for C2H4 (applicable to C3H6)

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Research on diode laser diagnostics and supporting spectroscopy sponsored by AFOSR

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Stanford’s Novel 2-Color Mid-IR Laser System

Modification of NovaWave Laser

High-Power Single TDL

Polarization Control

PPLNDFG

Fiber Combiner

Tunable Telecom DFB #1

I TunableMid-IR

Yb/Er Fiber Amplifier

Polarization Control

Alternate current to two DFB lasers to

DFB #1

Tunable Telecom

I

Light at 1 & 2

Mid-IR generation usies robust NIR componentsT l NIR l t id IR l th 100 1

rapidly switch between colorsDFB #2Time

Telecom NIR lasers can tune mid-IR wavelengths ~ 100 cm-1

Stanford modification provides two alternating output wavelengths Wavelength tunability enables optimization for specific application/species

C b d f i ti f bt ti f d l t/ ti l t ti ti

16

Can be used for speciation, for subtraction of droplet/particulate extinction, or for simultaneous species and temperature

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Polyatomic Hydrocarbon Fuels Have Strong Mid-IR Absorption, with Some Differences

8x105

T = 673 K8x105

41 433 T = 673 K

N-HeptaneIso-Octane

1

6

4

on [c

m2 /m

ole]

6

4

on [c

m2 /m

ole] 3.

4

3.4

2

2

0

Cro

ss S

ectio

Tuning Range of DFG Lasers

2

0

Cro

ss S

ectio

Tuning Range of DFG Lasers

Hydrocarbon Fuels:

0

3.603.553.503.453.403.353.30Wavelength [m]

0

3.603.553.503.453.403.353.30Wavelength [m]

C-H stretch vibrations have strong absorption strength near 3000 cm-1 (3.3 m) Rotational structure blended into broad features for pure polyatomic hydrocarbon

compounds and fuel blends – but each fuel has different spectrum C l it T d d f ti t i lt l f l d T

17

Can exploit T-dependence of cross-sections to simultaneously measure fuel and T

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Fuel Measurements in Heptane Decomposition:Measurement Using Mid-IR Laser Absorption

Mid-IR laser absorption provides reactant (and product) measurement capability Measurements complement direct rate determination using CH3 laser absorption First direct measurements of n heptane decomposition rate near 1000 K

18

First direct measurements of n-heptane decomposition rate near 1000 K

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Advances in Shock Tube Modeling:5) New Kinetic Code: CHEMSHOCK)

The capability to measure product species (CO2 and H2O) and temperature p y p p ( 2 2 ) pnow enables study of post-ignition phenomena in reflected shock studies

But current constant volume modeling constraint fails with large energy But, current constant-volume modeling constraint fails with large energy release after ignition, prohibiting use of species time-histories after ignition, and fails to account for non-ideal facility effects

The solution: Development of a new Chemkin-based code CHEMSHOCK enables modeling of 1-D behavior, e.g. due to non-ideal facility effects and energy release from initial decomposition through ignition to finalenergy release, from initial decomposition through ignition to final combustion products

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Use of a New Reflected Shock Code CHEMSHOCKfor Reactive Systems with Energy Release

2000 2.5

N-Heptane Oxidation1 5

1600 2.0

Constant V model

CHEMSHOCK tm]

re [

K] Constant V model

TDL Data

1.0

1.5

atio

n [%

]

CHEMSHOCK

TDL Data

1200 1.5

Pre

ssur

e [a

t

Tem

pera

tu

CHEMSHOCK input

Initial Conditions:0.2% Heptane/O2/Ar1385 K 1 4 atm =1 2

0.5

H2O

Con

cent

ra

0 1 2 3 4 5

800 1.0

Time [ms]

CHEMSHOCK inputpressure data and fit

1385 K, 1.4 atm, =1.2

0 1 2 3 4 50.0

Time [ms]

Pressure, temperature and concentration well modeled using isentropic compression/expansion model for shock tube ignition with energy release

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Allows modeling of 1-D behavior (non-ideal facility effects and energy release)

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Kinetics Results for Alkanes

Review of previous high-pressure jet fuel/surrogate ignition time data Review of previous high pressure jet fuel/surrogate ignition time data

Current program: low-pressure (C5-C9) n-alkane ignition delay time data

Current program: use of intermediate and high pressure C12 ignition data to test JetSurF mechanism

21

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Review of Jet Fuel and Surrogate Database:High-Pressure Ignition Delay Timesg g

Heated high-pressure h k t b id

10000

4Fuel/air, =1.0, 20 atmStanford data 2 shock tube provides access

to smaller alkanes, i.e. <C12 Aerosol shock tube

id t l

5

1

[s]

Stanford data 23

provides access to larger alkanes, i.e >C9

1000

1) Toluene2) Iso-octane

gniti

on D

elay

Evidence of NTC behavior below 1000 K in all alkanes and jet fuel

100

2) Iso octane3) MCH4) Jet-A5) n-Dodecane

Ig

n-Dodecane and MCH (methylcyclohexane) are potential candidates for high

0.7 0.8 0.9 1.0 1.1 1.2 1.3 1.4 1.51000/ T, [1/K]

22

( y y ) p gtemperature jet fuel surrogate; MCH better for lower temperature (at high P)

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Current Program Preliminary Results :Large N-Alkane Low-Pressure Ignition Survey

1 0

n-Nonane/ O2/ Ar

Example n-Nonane Data

Hi h l

0.8

1.0

ut [V

]

2

= 1.0 XO2 = 0.04 T5 = 1367 K P5 = 1.86 atm

High-temperature, low-pressure survey of large n-alkanes to support jet surrogate (dodecane)

0.4

0.6

Ampl

ifier

Out

pu dP5/dt = 4%/ms

Side

surrogate (dodecane) mechanism development

First n-nonane ignition delay

0.0

0.2End

A

Sidewall Pressure Sidewall OH* Endwall OH*

First n nonane ignition delay data: low vapor pressure (~2 torr at 20C) requires heated shock tube (25C)

-200 0 200 400 600 800

Time [s]

( )

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Current Program Preliminary Results :Large N-Alkane Low-Pressure Ignition Survey

High temperature

n-Pentane10000

n-Pentane/ O2/ Ar1 5 atm 4% O = 1 0

10000

n-Hexane/O2/Ar1.5 atm, 4% O, = 1.0

1429K 1333K 1250K

n-Hexane

g psurvey of C5-C9 alkanes shows similar ignition times at 1 5 atm100

1000

C t St d

nitio

n Ti

me

[s]

1.5 atm, 4% O2, = 1.0

100

1000

nitio

n Ti

me

[s]

times at 1.5 atm, =1

Agreement with0.60 0.65 0.70 0.75 0.80 0.85

10

100 Current Study JetSurF (2008) Horning et al. (2002)

Ign

1000/T [1/K]0.65 0.70 0.75 0.80 0.85

10

100

Current Study JetSurF (2008) Horning et al. (2002)

Ign

1000/T [1/K] Agreement with Horning et al. (2002) n-alkane correlation

1000/T5 [1/K] 1000/T5 [1/K]

10000

n-Octane/ O2/ Ar1.5 atm, 4% O2, = 1.0

1429K 1333K 1250K 10000 1250K1333K

n-Nonane/ O2/ Ar1.8 atm, 4% O2, = 1.0

1429K

n-Octane n-Nonane

Next step: expand T, P, and mixture

100

1000

gniti

on T

ime

[s]

100

1000

Igni

tion

Tim

e [

s]

range

240.65 0.70 0.75 0.80 0.8510

Current Study JetSurF (2008) Horning et al. (2002)

Ig

1000/T5 [1/K]

0.65 0.70 0.75 0.80 0.8510

Current Study JetSurF (2008) Horning et al. (2002)

I

1000/T5 [1/K]

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Current Program High-Pressure n-Dodecane Results: Use of HP data to Test JetSurF Mechanism

20 atm n-Dodecane Ignition

H d hi h h k1250 K 1000 K 833 K 714 K

Heated high-pressure shock tube (HHPST) and aerosol shock tube (AST) provides C12 ignition data

10

1001250 K

n-Dodecane/air20 atm, =1.0

[ms]

ignition data

Current JetSurF mechanism captures trends of high-

1 on

Del

ay T

ime

captures trends of highpressure, low-temperature (NTC) ignition regime for n-dodecane0 01

0.1 Current Study USC/Wang (2008)

Igni

tio

0.8 1.0 1.2 1.40.01

1000/T, [1/K]

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New Directions for Shock Tube Kinetics Research

PLIF imaging in shock tube to characterize flow uniformity/non-uniformity behind reflected shock waves

Accurate temperature measurement using WMSccu ate te pe atu e easu e e t us g S

Mid-IR laser absorption diagnostics for fuels, intermediates, CO2, H2O and Tand T

Apply multi-species diagnostics: capability for simultaneous time-histories of up to 6 species and Thistories of up to 6 species and T

26

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Laser Diagnostics for Shock Tube Kinetics Studies

Issue 1: Variations of temperature (T5) may be present, under some conditions, potentially

BifurcationCurved Shock and

Boundary Layer

Shock Tube Imaging

impacting kinetics due to attenuation, curved shocks, shock bifurcation, weak ignition, …

Diagnostic Solution: High-sensitivity PLIF of T and species in new imaging shock tube Reflected Incident

T5

and species in new imaging shock tube, combined with new non-reactive and reactive gasdynamic models; sensitive detection of T(t) by TDLAS

ReflectedShock Wave

IncidentShock Wave

Species Time-Histories

Issue 2: Ignition delay times alone do not

Products

StableIntermediatesac

tion Fuel

ignition

sufficiently test detailed reaction mechanisms Diagnostic Solution: Multi-species time-histories

of fuel, radicals, intermediates, products and T

SmallRadicals

Intermediates

Mol

e Fr

a

2727

Time

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OH PLIF Imaging in a Shock Tube:Past Work on Strong and Weak Ignition

Strong Ignition Limit Weak Ignition LimitHighly uniform planar wave

observedobserved

Slightly non-uniform OH reaction front

Imaged Area27 x 27 mm

OH ReactionFront

1440 K, 1.9 atm, = 1H2/O2/ 90% Ar

1110 K, 1.3 atm, = 1H2/O2/ 90% ArShock Tube Endwall

ReflectedShock Wave

H2/O2/ 90% Ar H2/O2/ 90% Ar

OH PLIF proven for examining inhomogeneities in H2/O2 ignition (McMillin et al. 1990)

What is needed now: study of non-uniformities in weak ignition limit at longer times

i ti fl t l PLIF f iti i i f T

Shock Tube Endwall

2828

in non-reacting flows use toluene PLIF for sensitive imaging of T

in reacting flows use PLIF of OH & T to image spatial variations in reaction progress

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PLIF Imaging in a Shock Tube: Status Report

Toluene LIF for Sensitive ThermometryICCD camera 1

Toluene in 1 atm N

Mirror

Optical filter

Laser sheet

Data acquisition computer

0.01

0.1

Toluene in 1 atm N2

266 nm Excitation

LIF(

300) 7%

in LIF

Beam dump Sheet 

forming optics

1E-3

0.011% in T

LIF(

T) /

L

New Imaging Shocktube

Excimer  or dye laser

400 600 800 1000 12001E-4

Temperature [K]

New imaging shock tube is under construction Toluene strategy offers prospects for <1% imaging of T! New reactive gasdynamic modeling effort underway

29

Unsteady 1-D & 2-D with kinetics Bifurcation, curved/oscillating shock, corners, walls, weak ignition, etc.

29

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Use of CO2 laser diagnostic for accurate temperature measurement in shock tubes

Use of wavelength modulation spectroscopy (2f/1f) can provide accurate (+/- 4 K) determination of reflected shock temperature

1200 2.4

20

Combined with extended test time techniques and driver inserts can provide ~ 10 ms of high-uniformity test time with 1-L driver, greater than 20 ms with 2-L driver

900 1.8

atur

e [K

]

10

0

K]

300

600

0 6

1.2

952 K 1 197 atm re [a

tm]Te

mpe

ra

10

05 K

T [K

0 K

0 5 100

300

0.0

0.6952 K, 1.197 atm2% CO2 / Ar1-L Driver with insert: 40% N2 / He

Time [ms]

Pre

ssur

0 5 10-20

-10

Ti [ ]

30

Time [ms] Time [ms]

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Holy Grail of Combustion Kinetics:Complete Picture of Fuel Chemistry through Multi-Species Time-Histories

Fuel & Oxygen(e.g., n-heptane, n-dodecane)

CW laser diagnostics can provide time-histories of many species

Fuel using DFG lasers (3 3-3 5 m)

InitialDecomposition

Products

H-Abstraction& Oxidation

Products

time histories of many species

Fuel using DFG lasers (3.3-3.5 m) Radicals using UV/Vis lasers (216-614 nm) Intermediates using IR strategies (2.3-10.5 m )

P d t d T i DFB l (2 5 2 7 )

Intermediate Products

H, OH, H2, C2H4, C2H2, CO, CH2O Products and T using DFB lasers (2.5-2.7 m)

Ignition

CO CO H O

, , 2, 2 4, 2 2, , 2

CO L

DFG Laser

UV/Vi L

DFB Laser

CO, CO2, H2O

Driver Driven Tube

CO2 LaserUV/Vis Laser

Excimerphotolysis

313131

Kinetics Shock Tubes(Dia. = 5, 14, 15, & 15 cm) Ethylene 10.5 m

Fuel /HCs 3.3/3.5 m

OH 306 nm

CO2 /H2O 2.5/2.7 m

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Two Species Example: Sensitive Detectionof n-Heptane at 3.4 microns and Ethylene at 10.5 microns

Hydrocarbon IR Absorption Spectra

Fortuitous CoincidenceWith CO2 Laser

Strong n-heptane absorption at 3.4 m accessible with tunable DFG laser; utilize multiple wavelengths to eliminate interference absorptions

Strong ethylene absorption at 10 53 m accessible with tunable CO2 laser

32

Strong ethylene absorption at 10.53 m accessible with tunable CO2 laser(P14 line) with no significant interfering species

Directly applicable for measuring alkane pyrolysis and oxidation kinetics

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Two Species Example: n-Heptane Pyrolysis and Oxidation

Heptane Pyrolysis Heptane Oxidation

Absorption measurements of fuel, stable intermediates and products provide critical decomposition and oxidation information for alkanes and fuel surrogates Initial data reveal deficiencies in current detailed mechanisms for heptane

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Current Status of Multi-Species Detection Diagnostics:Capability for Time-Histories of up to 6 species and TCapab ty o e sto es o up to 6 spec es a d

Current Diagnostics

Species Wavelength

C2H4 10.5 m

C H T 3 4C7H16, T 3.4 m

C12H26, T 3.4 m

CO2, T 2.7 m

OH 306 nm

H2O, T 2.5 m

Next Species Targets: Fuels: methylcyclohexane, JP- and RP-fuelsRadical Species: CH C H

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Radical Species: CH3, C3H3Stable Intermediates: Butadiene, propene, CH2OProducts: CO, NO, Soot

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Key Accomplishments and Future Work

Development and application of advanced shock tube/lasers techniques: Extended test time x10 and improved uniformity of reaction conditions Extended test time x10 and improved uniformity of reaction conditions Developed aerosol shock tube for low-vapor-pressure fuel Extended detection capability to hydrocarbons, products and T Developed initial modeling capability for facility effects and energy release

Database Development: Ignition times High-pressure Jet fuel and major surrogate components

L C5 C9 lk d id C12 Low-pressure C5-C9 n-alkanes and mid-pressure C12

Future Work: Extend ignition time data to wider T and P regimes and larger alkanes Accurate T measurement using WMS Multi-species time-histories Interact with model developers to design/execute optimized experiments

Di t l t ti t di

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Direct elementary reaction studies