Absorption cross-sections IR 2015

The GEISA-2015 sub-database on
infrared absorption coss-sections

General content

Description of columns :
Column 1 : molecular species common or chemical names
Column 2 : spectral coverage (cm-1)
Column 3 : overall temperature range (K)
Column 4 : total pressure range (Pa)
Column 5 : number of associated temperature-pressure sets
Column 6 : related reference
Column 7 : reference number

In green: updated molecular species, already implemented in GEISA-11
In blue: newly implemented molecular species in GEISA-2015
Molecule Spectral coverage (cm-1) Temperature range (K) Pressure range (Pa) Number of associated Temperature/Pressure (T/P) sets References Ref No
CFC-11 210 – 2000 296 93325 1 Christidis (1997)
Hurley (2003)		 3
7
500 – 1600 297 0 1 Heathfield (1998)
MSF/RAL
Smith (2003)		 5
9
15
810 – 1120 190 – 296 1000 – 101325 55 Li & Varanasi (1994)
Varanasi (2000)		 8
19
CFC-12 850 – 1190 253 – 287 0 3 Clerbaux (1993) 2
210 – 2000 296 93325 1 Hurley(2003) 7
800 – 1200 190 – 296 1000 – 101392 57 Varanasi & Nemtchinov (1994)
Varanasi (2000)		 18
19
800-1300 101325.72 1 Myhre et al. (2006) 59
Pure 1
CFC-13 765 – 1235 203 – 293 0 6 GEISA (1997) 24
CFC-14 220 – 2000 296 93325 1 Hurley (2003) 7
1250 – 1290 180 – 296 1005 – 101458 55 Nemtchinov & Varanasi (2003a) 19
CFC-113 780 – 1232 203 -293 0 6 GEISA (1997) 24
CFC-114 815 – 1285 203 -293 0 6 GEISA (1997) 24
CFC-115 955 – 1260 203 -293 0 6 GEISA (1997) 24
HFC-32 204 – 2000 296 93325 1 Pinnock et al. (1995)
Hurley (2003)		 14
7
995 – 1475 203 – 297 0 – 100000 17 MSF/ RAL
Smith (2003)		 9
15
HFC-125 700 – 1465 287 0 1 Clerbaux (1993) 2
495 – 1504 203 -293 0 – 80000 16 Di Lonardo (2000) 4
208 – 2000 296 93325 1 Pinnock et al. (1995)
Hurley (2003)		 14
7
HFC-134 210 – 2000 296 93325 1 Christidis et al. (1997)
Hurley (2003)		 3
7
600 – 1700 203 – 297 0 – 100000 9 MSF/ RAL
Smith (2003)		 9
15
HFC-134a 815 – 1485 253 – 287 0 3 Clerbaux (1993) 2
203 – 2000 296 93325 1 Pinnock (1995)
Hurley (2003)		 14
7
600 – 1600 203 – 296 0 – 100000 15 MSF/ RAL
Smith (2003)		 9
15
1035 – 1340 190 – 296 2666 – 101376 33 Nemtchinov & Varanasi (2004) 13
HFC-143 204 – 2000 296 93,325 1 Pinnock et al. (1995)
Hurley (2003)		 14
7
HFC-143a 694 – 1504 203 – 293 0 – 80000 19 Di Lonardo (2000) 4
200 – 2000 296 93325 1 Pinnock (1995) et al.
Hurley (2003)		 14
7
580 – 1500 203 – 297 0 – 100000 9 MSF/ RAL
Smith (2003)		 9
15
HFC-152a 700 – 1600 203 – 293 0 – 80000 16 Vander Auwera (2000) 16
840 – 1490 253 – 287 0 3 Clerbaux (1993) 2
200 – 2000 296 93325 1 Pinnock et al. (1995)
Hurley (2003)		 14
7
HCFC-21 785 – 840 296 133 1 Massie et al. (1985) 10
HCFC-22 700 – 1500 203 – 293 0 – 80000 8 Vander Auwera (2003); Ballard et al. 17
765 – 1380 253 – 287 0 3 Clerbaux (1993) 2
208 – 2000 296 93325 1 Pinnock et al. (1995)
Hurley (2003)		 14
7
760 – 1195 181 – 297 2666 – 101936 51 Varanasi et al. (2001, 1992, 1994) 20,21
HCFC-123 740 – 1450 253 – 287 0 3 Clerbaux (1993) 2
204 – 2000 296 93325 1 Pinnock et al. (1995)
Hurley (2003)		 14
7
HCFC-124 675 – 1425 287 0 1 Clerbaux (1993) 2
208 – 2000 296 93325 1 Pinnock et al. (1995)
Hurley (2003)		 14
7
HCFC-141b 209 – 2000 296 93325 1 Pinnock et al. (1995)
Hurley (2003)		 14
7
710 – 1470 253 – 287 0 3 Clerbaux (1993) 2
HCFC-142b 650 – 1475 253-287 0 3 Clerbaux (1993) 2
200 – 2000 296 93325 1 Pinnock et al. (1995)
Hurley (2003)		 14
7
HCFC-225ca 695 – 1420 253 – 287 0 3 Clerbaux (1993) 2
600 – 2000 296 93325 1 Pinnock et al. (1995)
Hurley (2003)		 14
7
HCFC-225cb 715 – 1375 253 – 287 0 3 Clerbaux (1993) 2
600 – 2000 296 93325 1 Pinnock et al. (1995)
Hurley (2003)		 14
7
N2O5 540 – 1380 205 – 293 0 5 Wagner & Birk (2003) 22
SF6 650 – 2000 296 93325 1 Hurley (2003) 7
925 – 955 180 – 295 2693 – 101350 29 Varanasi (2001) 20
ClONO2 500 – 1330 190 – 297 0 – 15580 25 Wagner & Birk (2003) 22
1265 – 1325 201 – 222 0 3
GEISA (1997)
 24
CCl4 750 – 812 208 – 297 1070 – 101272 32 Nemtchinov & Varanasi (2003b) 12
C2F6 1061 – 1285 180 – 296 3320 – 101363 43 Zou & al. (2004) 6
210 – 2000 296 93325 1 Highwood et al. (1999)
Hurley (2003)		 6
7
600 – 2750 203 – 293 0 – 80000 15 MSF/ RAL
Smith (2003)		 9
15
C2H2 450 – 2000 296 93325 1 Highwood et al. (1999)
Hurley (2003)		 6
7
C2H4 220 – 2000 296 93325 1 Highwood et al. (1999)
Hurley (2003)		 6
7
C2H6 220 – 2000 296 93325 1 Highwood et al. (1999)
Hurley (2003)		 6
7
2545 – 3315 194 – 297 6591 – 101789 14 Harrison et al. (2010) 72
C3H8

(Propane)

 220 – 2000 296 93325 1 Highwood et al. (1999)
Hurley (2003)		 6
7
2540 – 3300 195 – 296 5346 – 101681 12 Harrison (2010) 73
C4F8 500 – 1600 203 – 297 0 – 65000 19 MSF/ RAL (2003) 9
HNO4 770 – 830 268 93 1 Massie et al. (1985) 10
SF5CF3 600 – 2000 296 93325 1 Hurley (2003) 7
600 – 2500 213-323 101325 5 Rinsland et al (2003) 25
HCH-365mfc 665 – 1480 287 0 1 Clerbaux (1993) 2
(CH3)2CO
(Acetone)		 600-1800 214-297 0-93326 21 Waterfall (2003) 26
830-1950 194-298 6686-93326 19 Harrison (2011a) 74
2615-3300 195-296 6509-101198 12 Harrison (2011b) 75

C2H3NO5
(PAN)
 560-2000 250-297 100 3 Allen et al (2005) 30,31
C6H6
(Ethane)		 600-6500 223-298 101325 3 Rinsland et al (2008) 27
CH3CN
(Acetonitrile)		 624-4574 276-324 101325 3 Kleinböhl et al (2005)
Rinsland et al (2008)		 28
29
880-1700 203-297 6642-101298 12 Harrison & Bernath (2012) 76
2550-3300 208-296 6666-101365 11 Allen et al. (2011) 77
6814-7067 293 500 1 O’Leary et al. (2012) 81
CF2=CF2 100-2600 293 Pure 1 Acerboni et al. (2001) 60
CF3CF=CF2 100-2600 293 Pure 1 Acerboni et al. (2001) 60
CF2=CFCF=CF2 100-2600 293 Pure 1 Acerboni et al. (2001) 60

CHF2OCF2OCHF2
 25-3250 298 Pure 1 Myhre et al. (1999) 61

CHF2OCF2CF2OCHF2
 25-3250 298 Pure 1 Myhre et al. (1999) 61
(CF3)2CHOCH2F

(Sevoflurane)

 400-4000 298 Pure 1 Ryan et al. (2010) 62
CHF2OCHClCF3

(Isoflurane)

 400-4000 298 Pure 1 Ryan et al. (2010) 62

(CF3)2CFC(O)CF2CF3
 450-2000 298 Pure 1 D’Anna et al. (2005) 63

CHF2CF2CH2OCH3
 450-3200 298 Pure 1 Oyaro et al. (2004) 64

CF3CF2CH2OCH3
 450-3200 298 Pure 1 Oyaro et al. (2004) 64

CF3CH2OCH2CF3
 450-3200 298 Pure 1 Oyaro et al. (2004) 64
(CF3)2CHOCH3 450-3200 298 Pure 1 Oyaro et al. (2004) 64
CHF2CHFOCF3 440-3200 298 Pure 1 Oyaro et al. (2005) 65
CF3CHFOCF3 440-3200 298 Pure 1 Oyaro et al. (2005) 65
CHF2OCHFCF3 440-3200 298 Pure 1 Oyaro et al. (2005) 65

CF3CHFCF2OCH2CH3
 440-3200 298 Pure 1 Oyaro et al. (2005) 65

CF3CF2CF2OCHFCF3
 440-3200 298 Pure 1 Oyaro et al. (2005) 65

CHF2OCH2CF3
 440-3200 298 Pure 1 Oyaro et al. (2005) 65
CF3CH2OCH3 440-3200 298 Pure 1 Oyaro et al. (2005) 65
CH2FCH2OH 80-4800 293 Pure 1 Sellevag et al. (2004) 66
CHF2CH2OH 70-4800 293 Pure 1 Sellevag et al. (2004) 66
CF3CH2OH 70-4800 293 Pure 1 Sellevag et al. (2004) 66
CF3CF2CH2OH 400-4000 298 Pure 1 Sellevag et al. (2007) 67
500-4000 298 773.3-13065.6 1 Antinolo et al. (2012) 69
Pure (129.3-533.3) 1 Antinolo et al. (2012) 69
CHF2CF2CH2OH 400-4000 298 Pure 1 Sellevag et al. (2007) 67
500-4000 298 746.6-12798.9 1 Antinolo et al. (2012) 69
Pure (41.3-200.0) 1 Antinolo et al. (2012) 69
CF3CF2CF2CH2OH 400-4000 298 Pure 1 Sellevag et al. (2007) 67
CF3CH2CH2OH 400-4000 298 Pure 1 Sellevag et al. (2007) 67
500-4000 298 666.6-20797.9 1 Jimenez et al. (2010) 68
CF3(CH2)2CH2OH 500-4000 298 666.6-21864.5 1 Jimenez et al. (2010) 68
CF3CHO 400-2500 298 Pure 1 Jimenez et al. (2010) 68
CF3CH2CHO 400-3500 298 Pure 1 Sellevag et al. (2004) 70
500-4000 298 626.6-7999.2 1 Antinolo et al. (2011) 71
CF3(CH2)2CHO 500-4000 298 493.3-9065.7 1 Antinolo et al. (2011) 71
CH3OH
(Methanol)		 877-1167 204-295 6689-101498 12 Harrison et al. (2012) 78
2600-3250 204-296 6789-101432 12 Harrison et al. (2012) 78]
CHF3
(HFC-23)		 950-1500 188-294 3066-101645 27 Harrison (2013) 79
CH3CHO
(Acetaldehyde)		 2400-3400 200-298 6694-101623 16 Tereszchuk et al. (2011) 80
CH3I
(Methyl iodide)		 7473-7497 295 6500 1 Farago et al. (2013) 82
CH3O2
(Methyldioxidany)		 7474-7497 295 6500 1 Farago et al. (2013) 82
H2CO
(Formaldehyde)		 6547-7051 291 200 1 Ruth et al. (2015) 83
HO2
(Hydroperoxy radical)		 6604-6696 295 6650 1 Thiebaud et al. (2007)
Ibrahim et al. (2007)		 84
85
HONO
(Nitrous acid)		 6624-6645 295 5332 1 Jain et al. (2011) 86
NH3
(Ammonia)		 6850-6997 293 1150 1 O’Larry et al. (2008) 87

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