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11• Moir <br /> � � � I• li♦ I1i• � I11• 1111• I� si• � �� �� � <br /> Henry's Law Constant Solubility In Water Adsorption Coefficient Blodegredatlon Half-life (Hours) <br /> ComtMele atm m3hnol mg/1 at 20 deg C Koc 5oll Air 5urface Water Groundwater <br /> Benzene 5 38E-03 1780 70 120-384 501-501 120-384 240-17280 <br /> rtoluene 6 70E 03 515 132 96-528 10-104 96-528 168-672 <br /> Ethyloenzene 6 60E-03 152 4 72-240 8 56-85 6 72-240 144-5472 <br /> o-Xylene 5 27E-03 152 129 168-672 4444 168-672 336-8640 <br /> m-Xylene 7 OOE-03 158 1585 168-672 26-26 168-672 336-8640 <br /> xylene 710E-03 200' 204 165-672 42-42 168-672 336-8640 <br /> Acenaphthene 0000195, 3 93' 18 299-24-48 0879-579 30300 590-4896 <br /> Acenaphthylene 2150E 04 3 93' 4786 1020-1440 0191-127 1020-1440 2040-2880 <br /> Anthracene 140E-03 0041 20,300 1200-11040 058-17 058-i7 2400-22080 <br /> Dernzo(a)anthraGene 6 60E-07 0 011 1380384 2448-16320 10-30 10-30 4896-32640 <br /> Bcnzo(a) rene 240E-06 0 003 882267 1368-12720 037-11 0 37 11 2736-25440 <br /> Dvizo(b)fluoranthcnc 120E-05 0 014 645654 8640-14640 143-143 87-720 17280-29280 <br /> Senzo(g,h,1) eryfene 140E-07 0 00026' 7762471 14160-15600 0 321-3 21 14160-15600 28320-31200 <br /> 13cnzo(k)fluoranthene 104E-03 000055' 4365158 21840-51360 110-110 38-499 42680-102720 <br /> Chrysene 7 26E-20 00018, 245471 8904-24000 0 802-8 02 44-13 17808-48000 <br /> Dbenzo(a,h)w0racene 7 33E-09 0 005 1659587 8664-22060 0 428-4 28 6-782 17328-45120 <br /> Fluoranthene 0016' 0166 41687 3360-10560 202-202 21-63 6720-21120 <br /> Fluorene 210E 04 08 5012 768-1440 6 81-681 768-1440 1536-2880 <br /> 1ndeno(1,2,3-CD) rene 2 96E-20' 0 062 3090295 14400-17520 0 629-6 29 3000-6000 28800-35040 <br /> Naphthalene 4 60E-04 377 1819701 398-1152 2 96-29 6 12-480 1 24-6192 <br /> rhenanthrene 130E-03 118, 14289 384-4600 1 201-201 30-25 768-9600 <br /> i yrene 109E-05 0165 78524 5040-45600 10668-204 0 68-2 04 10080-91200 <br /> 'Valuer,measured at 25 degrees Celsius <br /> Table 4-1 Summary of physical and chemical characteristics of BTEX and PAII compounds Sources <br /> Montgomery and Welko t1, 1990, ChemBank, 1992 <br /> au�nr ntiti xs <br />