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Turner, D.B., "Workbook of Atmospheric Dispersion Estimates: An Introduction to Dispersion Modeling," 2nd ed., Lewis Publishing/CRC Press, Florida, 1994.
STANDARD DEVIATION, METERS
Turner, D.B., Workbook of Atmospheric Dispersion Estimates, U.S. Department of Health, Education, and Welfare, Washington, DC, 1970.
( )
Cu
Q
max, m2
( )
Cu
Q
max = e
[a + b lnH + c (lnH) 2 + d(lnH) 3]
Values of Curve-Fit Constants for Estimating (Cu/Q) max from H as a Function of Atmospheric Stability
Constants
Stability a b c d
A 1.0563 2.7153 0.1261 0
B 1.8060 2.1912 0.0389 0
C 1.9748 1.9980 0 0
D 2.5302 1.5610 0.0934 0
E 1.4496 2.5910 0.2181 0.0343
F 1.0488 3.2252 0.4977 0.0765
Adapted from Ranchoux, R.J.P., 1976.
Turner, D.B., "Workbook of Atmospheric Dispersion Estimates: An Introduction to Dispersion Modeling," 2nd ed., Lewis Publishing/CRC Press, Florida, 1994.
dp
Particle Size Ratio
d pc
Ne = 1 = Lb + c G, where
L
H 2
Ne = number of effective turns gas makes in cyclone,
H = inlet height of cyclone (m),
Lb = length of body cyclone (m), and
Lc = length of cone of cyclone (m).
where
D = dissolved oxygen deficit (mg/L) m
DO = dissolved oxygen concentration (mg/L) 2
Si
where ni = for i = 1 to n
Ksi + Si
1 + ktCo 1 + kCo
(4kCo + 1) 2 1
2k
a
Co = initial concentration or influent concentration; Ct = final condition or effluent concentration.
b
Time conditions are for ideal batch reactor only.
Davis, M.L. and S.J. Masten, Principles of Environmental Engineering and Science, McGraw-Hill, New York, 2004.
p
SWp = SWi + Point Source Attenuation
a + bp
SPL (dB) = 10 log10 (r1/r2)2
where
SWp = specific weight of the waste material at pressure Line Source Attenuation
p (lb/yd3) (typical 1,750 to 2,150) SPL (dB) = 10 log10 (r1/r2)
SWi = initial compacted specific weight of waste
(lb/yd3) (typical 1,000) where
SPL (dB) = sound pressure level, measured in decibels
p = overburden pressure (lb/in2)
P = sound pressure (Pa)
a = empirical constant (yd3/in2)
P0 = reference sound pressure (2 105 Pa)
b = empirical constant (yd3/lb)
SPLtotal = sum of multiple sources
Gas Flux SPL (dB) = change in sound pressure level with distance,
Dh 4 3 aCAatm - CA fill k measured in decibels
NA = r1 = distance from source to receptor at point 1
L
r2 = distance from source to receptor at point 2
where
NA = gas flux of compound A, [g/(cm2 s)][lb mol/(ft2 d)] POPULATION MODELING
CAatm = concentration of compound A at the surface of the Population Projection Equations
landfill cover, g/cm3 (lb mol/ft3) Linear Projection = Algebraic Projection
CAfill = concentration of compound A at the bottom of the Pt = P0 + kt
landfill cover, g/cm3 (lb mol/ft3)
L = depth of the landfill cover, cm (ft) where
Pt = population at time t
Typical values for the coefficient of diffusion for methane P0 = population at time zero
and carbon dioxide are 0.20 cm2/s (18.6 ft2/d) and 0.13 cm2/s k = growth rate
(12.1 ft2/d), respectively.
t = elapsed time in years relative to time zero
D = diffusion coefficient, cm2/s (ft2/d)
gas = gas-filled porosity, cm3/cm3 (ft3/ft3) Log Growth = Exponential Growth = Geometric Growth
= porosity, cm3/cm3 (ft3/ft3) Pt = P0ekt
ln Pt = ln P0 + kt
where
Pt = population at time t
P0 = population at time zero
k = growth rate
t = elapsed time in years relative to time zero
= half-life
where I1, 2 = Radiation intensity at locations l and 2
Flux at distance 2 = (Flux at distance 1) (r1/r2)2
R1, 2 = Distance from the source at locations l and 2
The half-life of a biologically degraded contaminant assuming
a first-order rate constant is given by:
t1 2 = 0.693
k
k = rate constant (time1)
t1/2 = half-life (time)
EPA Document "EPA/600/889/046" Soil Sampling Quality Assurance User's Guide, Chapter 7.
Confidence level: 1 (Probability of a Type I error) = 1 = size probability of not making a Type I error.
Power = 1 (Probability of a Type II error) = 1 = probability of not making a Type II error.
CV = (100 * s)/ x
CV = coefficient of variation
s = standard deviation of sample
x = sample average
Minimum Detectable Relative Difference = Relative increase over background [100 (s B)/B] to be detectable with a
probability (1 )
50
10
Comparative Acutely Lethal Doses
Actual
Ranking LD 50 (mg/kg) Toxic Chemical
No.
1 15,000 PCBs
2 10,000 Alcohol (ethanol)
3 4,000 Table saltsodium chloride
Ferrous sulfatean iron
4 1,500
supplement
5 1,375 Malathionpesticide
6 900 Morphine
7 150 Phenobarbitala sedative
8 142 Tylenol (acetaminophen)
9 2 Strychninea rat poison
10 1 Nicotine
11 0.5 Curarean arrow poison
Williams, P.L., R.C. James, and S.M. Roberts, Principles of Toxicology: Environmental and Industrial
12 0.001 2,3,7,8-TCDD (dioxin) Applications, 2nd ed., Wiley, New Jersey, 2000.
Flammable
Describes any solid, liquid, vapor, or gas that will ignite easily
and burn rapidly. A flammable liquid is defined by NFPA and
DOT as a liquid with a flash point below 100F (38C).
182
Reactivity Group
No. Name
Acid, Minerals, 1
1 Non-Oxidizing
Acids, Minerals, 2
2 Oxidizing KEY
G 3
3 Acids, Organic H REACTIVITY
H H CODE CONSEQUENCES
4 Alcohols & Glycols H 4
F P
H HEAT GENERATION
H H H
ENVIRONMENTAL ENGINEERING
5 Aldehydes P F P
5 F FIRE
H G INNOCUOUS & NON-FLAMMABLE GAS
6 Amides H 6
GT GT TOXIC GAS GENERATION
Amines, Aliphatic & H GF FLAMMABLE GAS GENERATION
7 H H H 7
Aromatic GT
E EXPLOSION
Azo Compounds, H H H H
8 H 8 P POLYMERIZATION
Diazo Comp, Hydrazines G GT G G
S SOLUBILIZATION OF TOXIC MATERIAL
H H H
9 Carbamates G G
9 U MAY BE HAZARDOUS BUT UNKNOWN
GT
H H H H H 10
10 Caustics G
GT GT GT EXAMPLE:
11 Cyanides GF GF GF G 11
H H H GF H
12 Dithiocarbamates GF GF GF GT U G 12 H HEAT GENERATION,
F F GT
F FIRE, AND TOXIC GAS
H H 13
13 Esters H F G H GT GENERATION
H
14 Ethers H F 14
15 Fluorides, Inorganic GT GT GT 15
16 Hydrocarbons, Aromatic H 16
F
H H H
H F H H 17
17 Halogenated Organics GT GT G GF
GT
H H
H F H H H H P H U
18 Isocyanates G G P P G G 18
GT G
19 Ketones H H H H H 19
F G
Mercaptans & Other H H
20 GT F H H H 20
Organic Sulfides GF G
GT
Metal, Alkali & Alkaline GF GF GF GF GF GF GF GF GF GF GF GF GF
21 H H H H H GT H GF GF GF 21
Earth, Elemental H H H H H H H E H H H
F F F F F H
Oxidizing Agents, H F H H H H H H
104 H H H H F GT H F E F H H H H F H F F
GT GT F F E F F F GT F 104
Strong GT H GT GT GT GT GT GE
H H GF H GF GF GF H
105 Reducing Agents, H H H GF H H H H
GF F GF GF H GF G F T H H H F 105
Strong GT F F GT E
106 Water & Mixtures H H G H GF GF
Containing Water G H GT 106
107 Water Reactive EXTREMELY REACTIVE! Do Not Mix With Any Chemical or Waste Material 107
Substances
NO THRESHOLD LINEAR
AT LOW DOSE
CARCINOGENIC DOSE
RESPONSE CURVE
Noncarcinogens
NONCARCINOGENIC DOSE
RESPONSE CURVE
Dose is expressed
d n
mass of chemical
body weight : exposure time
Risk Assessment Guidance for Superfund. Volume 1, Human Health Evaluation Manual (part A). U.S. Environmental Protection Agency, EPA/540/1-89/002, 1989.
a
For some workplace applications of inhalation exposure, the form of the equation becomes:
Dosage =
( )( BR)( C )( t )
( BW )
where
Dosage = mg substance per kg body weight
= fraction of chemical absorbed by the lungs (assume 1.0 unless otherwise specified)
BR = breathing rate of the individual (1.47 m3/hr for 2 hr or 0.98 m3/hr for 6 hr; varies some with size of individual)
C = concentration of the substance in the air (mg/m3)
BW = body weight (kg), usually 70 kg for men and 60 kg for women
t = time (usually taken as 8 hr in these calculations)
Based on animal data, one may use the above relations to calculate the safe air concentration if the safe human dose (SHD) is known, using the following
relationship:
SHD
C=
( )( BR)( t )
10 kT = k20(1.035)T20
0
n = coefficient relating to media characteristics; modular
0 200 400 600 800 1000 1200 1400 1600 1800 2000 plastic, n = 0.5
TEMPERATURE C SLUDGE AGE, DAYS Tchobanoglous, G. and Metcalf and Eddy, Wastewater Engineering: Treatment, Disposal, and Reuse,
3rd ed., McGraw-Hill, 1991.
VOLATILE SOLIDS REDUCTION IN AN AEROBIC DIGESTER AS A FUNCTION Peavy, HS, D.R. Rowe and G. Tchobanoglous Environmental Engineering, McGraw-Hill, New York,
1985.
OF DIGESTER LIQUID TEMPERATURE AND DIGESTER SLUDGE AGE
ENVIRONMENTAL ENGINEERING 187
Facultative Pond Depth of Sorption Zone
BOD Loading
Zs = Z = G
VZ
Mass (lb/day) = Flow (MGD) Concentration (mg/L) VT - 0 . 5VZ
8.34(lb/MGal)/(mg/L)
Total System 35 pounds BOD5/acre-day where Q in
VZ = VT VB Co
Minimum = 3 ponds
ZS = depth of sorption zone
Depth = 38 ft
Z = total carbon depth Co
Minimum t = 90120 days
VT = total volume treated at
exhaustion (C = 0.95 C0) Z
WATER TREATMENT TECHNOLOGIES Zs
VB = total volume at breakthrough
Activated Carbon Adsorption (C = C = 0.05 C0)
Freundlich Isotherm C0 = concentration of contaminant
x 1 n in influent
m = X = KCe Q out
where Air Stripping Ce
x = mass of solute adsorbed Pi = HCi
m = mass of adsorbent Pi = partial pressure of component i, atm
X = mass ratio of the solid phasethat is, the mass of H = Henrys Law constant, atm-m3/kmol
adsorbed solute per mass of adsorbent
Ci = concentration of component i in solvent, kmol/m3
Ce = equilibrium concentration of solute, mass/volume
K, n = experimental constants
(Q W , C in ) (Q A , A out )
WATER INLET AIR OUTLETS
Linearized Form
ln mx = l n ln C + l n K
e
Langmuir Isotherm
(Q W , C out )
x aKCe WATER OUTLET AIR INLETS (BLOWER)
m = X = 1 + KCe (Q A , A in )
where
a = mass of adsorbed solute required to saturate completely a Aout = H'Cin
unit mass of adsorbent
QW Cin = QA H'Cin
K = experimental constant
QW = QA H'
Linearized Form H' (QA/ QW) = 1
m= 1+ 1 1
x a aK Ce where
Aout = concentration in the effluent air (kmol/m3)
EXHAUSTION QW = water flow rate (m3/s)
0.95C O
QA = air flow rate (m3/s)
Ain = concentration of contaminant in air (kmol/m3)
C, Cout = concentration of contaminants in effluent water
mg/l (kmol/m3)
C = BREAKTHROUGH Cin = concentration of contaminants in influent water
0.05C O (kmol/m3)
VB VZ Stripper Packing Height = Z
THROUGHPUT VOLUME V VT
Z = HTU NTU
Assuming rapid equilibrium:
_Cin Cout i _ RS - 1i + 1
NTU = d n ln f p
RS
RS - 1 RS
SELECTIVELY
Stokes Law
g `t p - t f j d 2
PERMEABLE
WASTE BRINE
MEMBRANE
Vt =
A CONTINUOUS-FLOW 18n
REVERSE OSMOSIS UNIT
where
Water Flux = membrane porosity
Jw = Wp (P ) r = membrane pore size
where P = net transmembrane pressure
Jw = water flux through the membrane [kmol/(m2 s)]
= viscosity
Wp = coefficient of water permeation, a characteristic of the
particular membrane [kmol/(m2 s Pa)] = membrane thickness
P = pressure differential across membrane = Pin Pout (Pa) Jw = volumetric flux (m/s)
= osmotic pressure differential across membrane
in out (Pa)