Report No, 78-CUS-7
                 ASARCO COPPER  SMELTER

                    EL  PASO, TEXAS
   ENVIRONMENTAL  PROTECTION AGENCY
  ce of Air and Waste Management
flf Air Quality Planning and Standards
 Emission Measurement Branch
,ircii Triangle Park. North Carolina

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EMISSION TESTING OF ASAflCO COPPER  SMELTER

             EL PASO, TEXAS
                   TO
     ENVIRONMENTAL PROTECTION ASENCY

          Contract #68-02-2812
           Work Assignment 17

             April 25, 1978
                 TRW
       ENVIRONMENTAL ENGINEERING DIVISION

 One Space Park, Redondo Beach,  Ca.  90278

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                          TABLE OF CONTENTS
                                                             PAGE
INTRODUCTION	     1
SUMMARY AND DISCUSSION OF RESULTS  	     2
PROCESS DESCRIPTION (EPA)	,	
LOCATION OF SAMPLING POINTS  	    20
SAMPLING AND ANALYTICAL PROCEDURES (ARSENIC, PARTICULATES,
      S02,PARTICLE SIZING	    28
APPENDICES
      A)  FIELD AND LABORATORY DATA	    36
      B)  SAMPLE CALCULATIONS  	   147
      C)  DAILY ACTIVITY LOG	148

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                           LIST OF FIGURES


FIGURE                                                         PAGE

  1       INLET TO CONVERTER FUGITIVE EMISSIONS BAGHOUSE ...   22

  2       OUTLET FROM CONVERTER BUILDING FUGITIVE EMISSION
          BAGHOUSE	23

  3       ROASTER CALCINING FUGITIVE EMISSIONS DUCT  	   24

  4       OUTLET FROM THE ROASTER/REVERBERATORY FURNACE ESP  ,   25

  5       OUTLET FROM ROASTER/REVERB SPRAY CHAMBER &
          ELECTROSTATIC PRECIPITATOR 	   26

  6       MATTE TAPPING REVERBERATORY FURNACE OUTLET 	   27

  7       METHOD 5 SAMPLING TRAIN SCHEMATIC  	   29

  8       BRINKS IMPACTOR SAMPLING SYSTEM SCHEMATIC  	   35
                           LIST OF TABLES

TABLES
  1       BAGHOUSE INLET P ARTICULATE/SO,, RESULTS 	  .    4
                       •                ^
  2       BAGHOUSE OUTLET PARTICULATE/S02 RESULTS	    5

  3       CALCINE FUGITIVE PARTICULATE/S02 RESULTS 	    6

  4       BAGHOUSE INLET ARSENIC RESULTS 	    7

  5       BAGHOUSE OUTLET ARSENIC RESULTS  	    8

  6       CALCINE FUGITIVE ARSENIC RESULTS	    J.

  7       MATTE TAPPING PARTICULATE/S02 RESULTS	10

  8       MATTE TAPPING ARSENIC RESULTS  	   11

  9       PARTICLE SIZING RESULTS  	   32

 10       ROASTER/REVERB ELECTROSTATIC PRECIPITATOR OUTLET
          PARTICULATE RESULTS  	 	   13

 11       ROASTER/REVERB ELECTROSTATIC PRECIPITATOR OUTLET
          S02 RESULTS	14

 12       PROCESS SAMPLE RESULTS .	15

 13       MASS SPECTROMETRY ANALYSIS RESULTS 	   16-19

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                                INTRODUCTION

     Fugitive dust emissions from copper smelting operations  are a  significant
source of airborne particulates.   These particulates  also contain varying
concentrations of arsenic which may pose a public health hazard. The fugitive
emissions of dust from operating equipment are controlled by  placing hoods
over the equipment and ducting the emissions to a control device.  From
January 17 to 27, 1978 TRW personnel  tested fugitive  emissions from several
copper smelting processes at the Asarco copper smelter in El  Paso,  Texas.   These
tests were performed to provide data to the EPA for the establishment of
fugitive emissions standards for copper smelting.
     The testing consisted of isokinetic sampling of  emissions from the converter
building, matte tapping, and calcining processes to determine particulate,
arsenic, and sulfur dioxide emissions.  The testing of converter building
fugitive emissions was done simultaneously at the inlet and outlet  of a baghouse
in order to determine the efficiency of this device.   Two particulate samples
and an SOp sample were taken at the outlet from a spray chamber and electrostatic
precipitator to determine the amount of uncontrolled  emissions from this process.
TRW personnel also performed particle sizing tests with a Brinks impactor  at the
inlet and outlet from the converter building fugitive emissions baghouse and on the
fugitive emissions from the calcining process.
     This report presents the results of the testing  program.  The  following sec-
tions of the report contain a summary of the results, descriptions  of the  sampling
points, a description of the processes, delineation of sampling and analytical
procedures, and appendices containing field and laboratory data and calculations.
                                        -1-

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                       SUMMARY & DISCUSSION OF RESULTS

     The results of the emission testing at the five test locations  are
summarized in this section of the report.   Three sets of tests were  performed
at the inlet and outlet of the converter building fugitive emissions baghouse
and calcining fugitive emissions duct.   These tests  included three tests  each
for particulate/S02 (Tables 1,2, and 3), three tests each for arsenic/trace
elements (Tables 4, 5 and 6), and several  tests each for particle sizing
(Table 9).  Testing at the matte tapping fugitive emissions duct included
particulate/S02 (Table 7), arsenic/trace elements (Table 8).  Testing at  the
outlet from the roaster/reverb spray chamber and electrostatic precipitator
included particulates (Table 10) and SO,, (Table 11).  In addition, analyses
were performed on composited process samples taken by plant personnel on  the
days that the fugitive emission testing was being performed.  This data  is
summarized in Table 12 & 13.
     The particulate sampling of the converter building fugitive emissions
baghouse showed efficiency for the equipment of up to 99%.  The  average  ef-
ficiency for the three tests was 88%, based on the grain loading of  collected
particulates in and out of the unit.  The efficiency of the unit for arsenic
removal based on arsenic analysis of-collected particulates averaged 96%  for
the three tests.  Particle sizing tests showed an approximately  equal proportion
of particles in the 1-5 micron range on the inlet and outlet, but the outlet
had less particles in the greater than 5 micron range,  and a higher  percentage
of particles in the less than one micron range.
     Sulfur dioxide tests on the converter building fugitive emissions show an
average concentration of 64 parts per million.  Sulfur dioxide emissions  are
quite variable on this source with maximum emissions occurring when  the  con-
verters are being charged.  Since the inlet and outlet tests were not exactly
simultaneous, they reflect this fluctuation in sulfur dioxide concentration.
     Particulate tests on the calcine fugitive duct showed an average concentra-
tion of .218 grains per standard cubic foot.  The great majority of  these were  in-
organic condensables (0.187 grains per standard cubic feet).  Particle sizing
tests showed that the particles were primarily greater than 5 microns (85%).

-------
Sulfur dioxide emissions were highly variable, averaging 67 parts per million.
The arsenic concentration averaged 2.5 parts per million.
     Particulate testing at the matte tapping fugitive emissions duct showed
generally lower particulate concentrations than at the two other locations.
The average particulate concentration was 0.097 grains per standard cubic foot.
The sulfur dioxide concentration averaged 110 parts per million.  The arsenic
concentration averaged 1.7 parts per million.
     Particulate testing of the balloon flue showed an average particulate con-
centration of 0.091 grains per standard cubic foot.  The sulfur dioxide of the
gas stream was 5098 parts per million.
                                     -3-

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TABLE 1.  BAGHOUSE INLET PARTICULATE/SC^ RESULTS

RUN NUMBER


1 DATE
II STACK PARAMETERS
PST - STATIC PRESSURE, "He (wHc)
Ps - STACK GAS PRESSURE, 'He ABSOLUTE (HMHG)
X C02 - VOLUME X DKY
I 02 - VOLUME I DRY
I CO - VOLUME I DRY
I »2 - VOLUME I DRY
Ts - AVERAGE STACK TEMPERATURE °F (°C>
X HoO - X MOISTURE IN STACK GAS, BY VOLUME
As - STACK AREA, FT2 (M2)
Ho - MOLECULAR WEIGHT OF STACK GAS, DRY BASIS
Ms - MOLECULAR WEIGHT OF STACK GAS, WET BASIS
Vs - STACK GAS VELOCITY, FT/SEC, (N/SEC)
OA - STACK GAS VOLUMETRIC FLOW AT STACK CONDITIONS, ACFM (NM /MIN)
Os - STACK GAS VOLUMETRIC FLOW AT STANDARD CONDITIONS, DSCFM (NM /MIN)
X EA - PERCENT EXCESS AIR
III TEST CONDITIONS
PB - BAROMETRIC PRESSURE, "HG CMMHG)
DN - SAMPLING NOZZLE DIAMETER, IN. (MM)
T - SAMPLING TIME, MIN
VM - SAMPLE VOLUME, ACF 
GRS/SSCF, (MG/M3)
*/HR, (KG/HR)
E) TOTAL SO-t (MG)
PPM
(BG/M5)
ff/HR, (KG/HR)
1

ENGLISH
UNITS
1/17/78 .

-.18
25.87
0.0
20.5
0.0
79.5
115.1
1.2
125.36
28.82
28.69
73.H
591,386.1
135,126.8
1.76

26.05
.185
IDS
84.9
20
.m
61.0
2.18
1.35

.89
75.61
1.2
28.69
73.11
109.7

_

_
_

.026
98.25

.
.002
7.15

.253
90.11
.
.255
350.26

.281
1,08.51
-
172.23
-
717.97
METRIC
UNITS
1/17/78

1,57
657.10
0.0
20.5
0.0
'79.5
16.1
1.2
11.311
28.82
28.69
22.38
15,721.9
12,335.0
1.76

E61.E7
1.70
103
2.1
20
.81
16.1
55.37
19.0
311.29

.03
2.1
1.2
28.69
22.38
109.7

31.0
-
98.1
129.1

60.33
W.66

9.1
. 11.39
' 3.25
L239.20
579.13
£8,69
UOB.6
•583.52
43L*
1,577.7
SB.85
1176.60
982.8
172.23
159.30
339.99
2

ENGLISH
UNITS
1/18/78

-.18
25.32
0.0
20.5
0.0
79.5
113.0
1.1
125.95
28.82
28.67
86.15
653,302.6
511,278.7
1.76

26.10
.185
100
83.8
20
.81
72.0
2.21
1.88

l.W
73.26
1.1
28.67
86.15
91.5

-
-
-
-

.003
101.86

t
.000
.18

.215
1,078,90
.
.215
1,079.08
_
.253
1,180.91
-
11.80
.
61.12
METRIC
UNITS
1/18/78

-1.5
658.37
. 0.0
20.5
0.0
79.5
'6.0
l.'l
11.31
28.82
28.67
26.37
18,5rt7.2
11,568.8
'1.76

662.91
1.70
100
2.1
20
.81
22.2
56.9
22.0
17.75

.03
2.1
1.1
28.67
26.37
91.5

38.8
-
71.0
109.8

52.96
16,30

.2
.10
.08
L163.0
560.95
190.13
UE3.2
551.05
«o.a
L273.0
611.01
536.81
66.2
11,80
31.93
27.92
3

ENGLISH
UNITS
1/21/78

-.18
26.02
0.0
20.5
0.0
79.5
115.0
1.1
125.96
28.82
28.67
85.75
618,n]2.7
510,318.2
'1.76

26.20
.12
100
82.6
20
.81
6C.O
2.29
1.85

1.01
71.10
1.1
28.67
85.75
96.3

-
-
'(_-
-

.031
131.52

-
-
-
_ •
-

-
-
-
-
.031
131.52
-
7.60

39.23
METRIC
UNITS
1/21/78

-1.57
660.91
0.0
20.5
0.0
79.5
16.1
1.1
11.31
28.82
28.67
26.11
18,357.3
1",156.6
1.76

665.18
1.70
100
2.1
20
.«
15.6
58.17
22.0
16.99

.03
2.1
1.1
28.67
26.11
96.3

H.I
.
95.7
117.8

70.18
Q.15

II.D.
-
-
N.D.
-
-
n.n.
-
-
117.8
70.13
61,15
13.1
7.60
20.55
17.83
AVERAGE

ENGLISH
UNITS


-.18
25.93
0.0
20.5
0.0
79.5
111.3
1.3
125.95
28.82
28.67
81.88
618,767.1
186,671.6
1.76

26.11
.185
102
83.8
20
.81
61.3
2.21
1.69

.99
71.32
1.3
28.67
81.88
100.2

-
-
-
-

,021
111,51

-
.001
3.66
.
.219
1011.00
-
0.169
L011.67
-
.m
787.99
-
63.87
-
282.87
METRIC
UNITS


-1.57
658.79
0.0
20.5
0.0
79.5
15.7
1.3
11.31
28.82
28.67
21.9f
17,528.8
13,786.8
1.76

663.36
1.70
102
2.1
20
,81
18.0
56.81
21.0
13.01

.03
2.10
1.3
28.67
21.96
100.2

W.3
-
88.6
128.9

61.26
50.70

3.2
2.21
1.66
L201.0
STO.fft
159.56
1,205.9
572.29
161.22
932.83
W2.78
358.187
361.0
63.37
170.59
128.58
                     -4-

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TABLE 2.
BAGHOUSE OUTLET PARTICULATE/S02 RESULTS

RON NUMBER


1 DATE
II STACK PARAfOERS
PST - STATIC PRESSURE, "Ho (MnHc)
Ps - STACK GAS PRESSURE, "He ABSOLUTE (NMHG)
t CO? - VOLUME I DRV
X 0, - VOLUME X DRV
I CO - VOLUME I DRV
I N2 - VOLUME X DRV
Ts - AVERAGE STACK TEMPERATURE °F (°C>
X H20 - X MOISTURE IN STACK GAS, Bv VOLUME
As - STACK AREA, FT2 (M2)
Hn - COLECULAR WEIGHT OF STACK GAS, DRV BASIS
Us - MOLECULAR HEIGHT F STACK GAS, WET BASIS
Vs - STACK GAS VELOCIT , FT/SEC, (M/SEC)
OA - STACK GAS VOLUMET ic FLOW AT STACK CONDITIONS, ACFr1 (NMVMIH)
Os - STACK GAS VOLUMET ic FLOW AT STANDARD CONDITIONS, DSCFM (NM /MIH)
X EA - PERCENT EXCESS IR
III TEST CONDITIONS
PB - BAROMETRIC PRESSURE, "He (NMHG)
DN - SAMPLING NOZZLE DIAMETER, IN. (MM)
T - SAMPLING TIME, MIN
VM - SAMPLE VOLUME, ACF 
Np - NET SAMPLING POINTS
Cp - PITOT TUBE COEFFICIENT
TM - AVERAGE METCR TEMPERATURE °F (°O
PM - AVERAGE ORIFICE PRESSURE DROP, "H20 (mH^O)
VLC - C.ONDENSATE COLLECTED (IMPINGERS AND GEL), MLS
6P - STACK VELOCITY HEAD "H20 (MnH20)
IV TEST CALCULATIONS
VH - CONDENSED WATER VAPOR, SDCF (Nn3)
VM - VOLUME OF GAS SAMPLED AT STANDARD CONDITIONS, DSCF (Hn5)
X H20 - PERCENT MOISTURE, Bv VOLUME
Ms - MOLECULAR WEIGHT OF STACK GAS, WET BASIS
Vs - STACK VELOCITY, FT/SEC (M/SEC)
X I - PERCENT ISOKINETIC
V ANALYTICAL DATA
A) PARTICULATES FRONT HALF
PROBE (MG)
CYCLONE (MG)
FILTER (MG)
PARTICULATES FRONT HALF TOTAL (MG)
GRS/SDCF, (MG/M3)
0/HH, KG/HR)
B) PARTICULATES - CONDENSABLES
ORGANIC (MG)
GRS/SDCF, (MG/M3)
tlm, (KG/MB)
INORGANIC (HG)
GRS/SDCF, (MO/M3)
U/HR, (KG/HR)
n p^pTTfin »TF« - TOTAL C(INTIFNSARLES (MG)
GRS/SDCF, (MG/M3)
0/HR, (KG/HR)
D) TOTAL PARTICULATES (MG)
GRS/SDCF, (MG/M3)
Urn. (KG/HR)
E) IflliL-SOj (MG)
PPM
(MG/M3)
»/HR, (KG/HR)
1

ENGLISH
UNITS
1/17/78

-.17
25.83
0.0
20.5
0.0
79.5
114.0
1.0
180.60
23.82
2B.71
61.84
657,872
526,039.2
4,76

26.05
.185
]20
74.5
W
.04
61.5
1.07
.96

.66
55.28
•1.0
28.71
61.84
98.0



.
_
_
.00501
22.87

-
.Q3Q7
3.19
.
.1060
177.78

.1067
180.97
.
,1U£
503.3H
-
'129.64
METRIC
UNITS
1/17/78

-1.32
657.35
0.0
20.5
0.0
79.5
15.6
1.0
16.20
28.82
28.71
18.85
18,919.9
11,899.2
1.76

661.67
1.70
120
1.8
10
.84
20.0
27.B
14.0
21.38

.02
1.8
1.0
28.71
18.85
33.0


21.5
-
0.0
21.5
11.607
10.37

. 3.0
1.62
1.15
448.6
212.82
217.17
451.6
244.14
218.62
173.1
256.05
228.99
iffl.il
81.E8
213.36
195.29
2

ENGLISH
UNITS
1/18/78

-.07
26.03
0.0
20,5
0.0
79.5
118.0
.9
180
28.82
23.72
55.11
593,428.0
47U90.8
4.76

26.10
.185
160
90.5
40
.34
71,8
.88
.77

.75
81.04
.9
23.82
28.72
97.7


-
-
-
-
.001]
1.45

-
.001
6.30
.
.1337
556.63
.
.1391
562.33
.
.140!
567.38
-
153.57
METRIC
UNITS
MS/78

-1.78
661.15
0.0
20.5
0.0
79.5
17.8
.9
16.20
23.82
28.72
16.39
16.952.6
13,341.4
4.76

KZ.9U
1.70
160
2.3
10
.54
13.9
22.35
16.0
19.56

.02
2.3
.9
28.82
28.72
37,7


5.C
_
0.0
5.8
2.522
2.02

8.2
3.53
2.86
721.10
315,86
253.01
732.6
319.11
255.87
738.4
321.03
257.C9
HB.3
93.61
263.05
210.71
3

ENGLISH
UNITS
1/21/78

. -.07
26.13
0.0
20.5
0.0
79.5
114.0
1.1
ISO
28.82
28.70
57.92
625,536.0
49E,907.0
4.76

26.20
.ITS
160
37.4
10
.81
61.0
.91
.85

.99
86.93
.9
28.70
57.9!
103.7


-


.
.0001
1.95

-
.0033
1.360
-
.01
30.97
_
.0073
32.33
_
,KW
3i;.29
_
22.66
"ETRIC
UNITS
1/21/78

-1.78
663.70
0.0
20.5
0.0
79.5
15.6
• 1.1
15.20
28.82
28.70
17.05
17.720.6
14,072.7
4.76

665.18
1.70
160
2.5
40
.84
16.1
23.88
21.0
21.59

.03
2.5
1.1
28.70
17.66
103.7


2.6
.
0.0
2.6
1.05
.89

. 1.80
.73
.62
11.0
16.67
11.07
42.9
17.44
14.73
15.4
18.50
15.62
30.0
1.57
12.19
10.30
AVERAGE

ENGLISH
UNITS


-.02
26.01
0.0
20.5
0.0
79.5
115
1.0
180
28.82
23.71
58.33
629,964.0
498,032.3
4.76

26.12
.125
116
87.17
10
.84
G5.7
.96
.86

.80
77.75
1.0
28.74
58.33
101.2


-
-
_
_
,03219
9.76

-
.00033
3.62
_
.083
33.12
_
.0345
358.71
_
.0367
368.50
_
305.29
METRIC
UNITS


-2.63
660.71
0.0
20.5
0.0
79.5
46.3
1.0
16.20
28.82
23.74
17.80
17,846.0
14,105.4
4.76

663.36
4.70
146
2.2
10
.81
16.7
24.17
17.0
21.81

.02
2.2
1.0
28.74
17.80
M.2


9.97
-
0.0
9.97
5.03
4.13

1.3
1.977
1.64
TO. 60
191.78
161.11
409.0
193.76
1E3.0S
418.0)
133.83
167.50
345.6
61.69
161.53
138.76
                      -5-

-------
TABLE 3.
CALCINE FUGITIVE PARTICULATE/S02 RESULTS

RUN NUMBER


1 MTE 1978
II STACK PARAMETERS
PST - STATIC PRESSURE, "Ho (wife)
Ps - STACK CAS PRESSURE, "Ho ABSOLUTE 
I COj - VOLUMI 1 DRV
X On • VOLUME I DRV
X CO - VOLUME I DRV
I N2 - VOLUME I DRV
Ts - AVERAGE STACK TEMPERATURE °F (°C)
I H20 - I NOISTURE IN STACK GAS, Bv VOLUME
As - STACK AREA, FT* (M2)
No - MOLECULAR HEIGHT OF STACK GAS, DRV BASIS
Us - MOLECULAR HEIGHT OF STACK GAS, NET BASIS
Vs - STACK GAS VELOCITY, FT/SEC, (H/SEC)
QA - STACK GAS VOLUMETRIC FLOW AT STACK CONDITIONS, ACFM (NH'/MIN)
Qs - STACK GAS VOLUMETRIC FLOW AT STANDARD CONDITIONS, DSCFM (NNVMIN)
I EA - PERCENT EXCESS AIR
III TEST CONDITIONS
PB - BAROMETRIC PRESSURE, 'He (MMHG)
DN - SAMPLING NOZZLE DIAMETER, IN. (MM)
T - SAMPLING TIME, NIN
VH - SAMPLE VOLUME, ACF («')
NP - NET SAMPLING POINTS
CP - PITOT TUBE COEFFICIENT
TM - AVERAGE METER TEMPERATURE °F (°C)
PN - AVERAGE ORIFICE PRESSURE DROP, "t^O (M«H20>
VLC - CONOENSATE COLLECTED (IMPINGERS AND GEL), MLS
fcp - STACK VELOCITY. HEAD "H20 (wH20)
IV TEST CALCULATIONS
VH - CONDENSED MATER VAPOR, SDCF (KM3)
VH - VOLUME OF GAS SAMPLED AT STANDARD CONDITIONS, DSCF (Nx3)
I H20 - PERCENT MOISTURE, Bv VOLUME
Ms - MOLECULAR HEIGHT OF STACK GAS, HET BASIS
Vs - STACK VELOCITY, FT/SEC (M/SEC)
t 1 - PERCENT ISOKINETIC
V ANALYTICAL DATA
A) PARTICULATES FRONT HALF
PROBE (NG)
CYCLONE (MG)
FILTER 
-------
TABLE 4.  BAGHOUSE INLET ARSENIC RESULTS
RW NUMBER



II STACK PARAMETERS
PST - STATIC PRESSURE, "Ho (MMHG)
Ps - STACK GAS PRESSURE, 'He ABSOLUTE (NNHG)
1 CO? - VOLUME I DRY
I 0, - VOLUME I DRV
I CO ' VOLUME I DRV
X N2 - VOLUKE t DRV
Ts - AVERAGE STACK TEMPERATURE °F t°C)
Z H^O - X HOISTURE IN STACK GAS, Bv VOLUME
As - STACK AREA, FT2 (M2)
(to - MOLECULAR WEIGHT OF STACK GAS, DRY BASIS
Is - MOLECULAR WEIGHT OF STACK GAS, WET BASIS
Vs - STACK GAS VELOCITY, FT/SEC, (H/SEC)
OA - STACK GAS VOLUMETRIC FLOW AT STACK CONDITIONS, ACFM (NM'/MIN)
Qs - STACK GAS VOLUMETRIC FLOW AT STANDARD CONDITIONS, HSCFM (NN'/MIN)
Z EA> - PERCENT EXCESS AIR
III TEST CONDITIONS
Pa - BAROMETRIC PRESSURE, "He (MMHG)
DN - SAMPLING NOZZLE DIAMETER, IN. (MM)
T - SAMPLING llMt, MIN
VM - SAMPLE VOLUME, ACF (M3)
Np - NET SAMPLING POINTS
Cp - PITOT TUBE COEFFICIENT
TM - AVERAGE METER TEMPERATURE °F (°C)
PM - AVERAGE ORIFICE PRESSURE DROP, 'H20 (mHoO)
VLC - CONDENSATE COLLECTED (1MPINGERS AND GEL), MLS
GP - STACK VELOCITY HEAD 't^O (Mri^O)
IV TEST CALCULATIONS
Vw - CONDENSED WATER VAPOR, SDCF (HM3)
VM - VOLUME OF GAS SAMPLED «T STANDARD CONDITIONS, DSCF (NM )
Z H20 - PERCENT MOISTURE, Bv VOLUME
Us - MOLECULAR WEIGHT OF STACK GAS, WET BASIS
Vs - STACK VELOCITY, FT/SEC (M/SEC)
X I - PERCENT ISOKINETIC
V ANALYTICAL DATA
A) ARSENIC'FRONT HALF
PROBE (MG)
CYCLONE (MG)
FILTER (MG)
ARSENIC FRONT HALF TOTAL (MG)
PPM, (MG/M )
rnR, (KG/HR)
B) ARSENIC - IMPINGER COLLECTION
IMPINCER 11. 2 (MO)
PPM, (MG/M3>
J/HR, (KG/KB)
lMpmeER-g3.4.5 (MG)
PPM, (MG/M*)
*/HR, (KG/HR)
D ARSFNIC - [NPINGFR TOTAL (MB)
PPM, (MG/M3)
I/HR, (KG/HR)

D) TOTAL AHSFNIC (MG)
PPM, (MG/M3)

-------
TABLE 5.  BAGHOUSE OUTLET ARSENIC RESULTS
RUN NUMBER



11 STACK PARAMETERS
PST - STATIC PRESSURE, 'Ho (HNHG)
Ps - STACK GAS PRESSURE, 'He ABSOLUTE (MMHG)
t CO; - VOLUME X DRY
X 0, - VOLUME t DRY
X CO < VOLUME X DRV
X N2 - VOLUME X DRV
Ts - AVERAGE STACK TEMPERATURE °F (°C>
X H20 - X MOISTURE IN STACK GAS, Bv VOLUME
As - STACK AREA, FT2 In2)
MD - MOLECULAR WEIGHT OF STACK GAS, DRY BASIS
Ms - MOLECULAR WEIGHT OF STACK GAS, WET BASIS
Vs - STACK GAS VELOCITY, FT/SEC, (M/SEC)
OA - STACK GAS VOLUMETRIC FLOW AT STACK CONDITIONS, ACFM (NM /MIN)
Os - STACK GAS VOLUMETRIC FLOW AT STANDARD CONDITIONS, DSCFM (NM*/MIN)
X EA> - PERCENT EXCESS AIR
III TEST CONDITIONS
PB - BAROMETRIC PRESSURE, "He (MMHG)
DN - SAMPLING NOZZLE DIAMETER, IN. (MM)
T - SAMPLING IIHE, MIN
VM - SAMPLE VOLUME, ACF (M3)
HP - NET SAMPLING POINTS
Cp - PITOT TUBE COEFFICIENT
TM - AVERAGE METER TEMPERATURE °F (°C)
PM - AVERAGE ORIFICE PRESSURE DROP, 'H20 (MnH20)
VLC - CONDENSATE COLLECTED (IMPINGEHS AND GEL), MLS
CP - STACK VELOCITY HEAD "H20 (K«rl20)
IV TEST CALCULATIONS
VK - CONDENSED WATER VAPOR, SDCF (NM3)
VM - VOLUME OF GAS SAMPLED »T STANDARD CONDITIONS, DSCF (NM3)
X K20 - PERCENT MOISTURE, BY VOLUME
Ms - MOLECULAR WEIGHT OF STACK GAS, WET BASIS
Vs - STACK VELOCITY, FT/SEC (M/SEC)
X I - PERCENT ISOKINETIC
V ANALYTICAL DATA
A) ARSENIC' FRONT HALF
PROBE (MG)
CYCLONE (MG)
FILTER (MG)
ARSENIC FRONT HALF TOTAL (MG)
PPM, 'MG/M3)
CHR, (KG/HR)
B) ARSENIC - IMPINGER COLLECTION
IMPIHEFR fll. 2 (NG)
PPM, (MG/M3)
0/HR, (KG/HR)
IMPIHI-.FR -/H.!!.1; (MG)
PPM, (MG/M3)
f/HR, (KG/HR)
O ARSFNIC - IMPINGFR TOTAL (MO)
PPM, (MG/M5)
»/HR, (KG/HR)
D) TOTAI ARSFNIC (ME)
PPM, (MG/M3)
#/HR, (KG/HR)
1
ENGLISH
UNITS
1/18/78

-.07
26.03
0.0
20.5
0.0
79.5
101.0
0.0
180.0
28.82
28.82
49.49
534,492
437,609
1.76

26.10
.185
160
88.4
40
.84
61.0
.80
0.635

0.0
78.10
0.0
28.82
19.49
105.7


_
_

_
.130
.672

0.00
0.00

0.00
0.00
.
0.00
0.00
.130
.672

METRIC
UNITS
1/18/78

-1.78
661.16
0.0
20.5
0.0
79.5
38.3
0.0
16.56
28.82
28.82
15.08
15,137-
12,393
4.76

662.94
4.70
Ifl)
2.5
10
.84
17.8
20.32
0.0
16.129

0.0
2.2
0.0
28.82
15.08
105.7


.040

.830
.87
.390
.305

0.0
0.00
0.00
0.0
0.00
0.00
0.00
O.CO
0.00
.87
.390
.305

2
ENGLISH
WITS
1/19/78

-.07
26.23
0.0
20.5
0.0
79.5
99.0
.7
180.0
28.82
28.74
59.31
W,548.0
526,564.8
4.76

26.30
.185
160
im.o
40
.81
65.0
LIB
.92

.66
89.86
,7
28.74
59.31
101.1


.
_
_
_
.001
.025

.ra
.mi
-
0.00
.om

.002
.015
.006
.010

METRIC
UNITS
1/19/78

-1.78
Gffi.24
0.0
20.5
0.0
79.5
37.0
.7
16.56
28.82
28.71
lli.OB
18.145.8
14,916.8
4.76

668.02
4.70
IS)
2.9
40
.04
1SJ
2f.(7
14.0
23.36

.02
2.5
.7
28.74
18.03
101.1


.005

.027
.032
.01
.011

.ma
inoE
.007
0.00
.000
.025
.007
.ore
.057
.007
.017

3
ENGLISH
UNITS
1/23/78

-.07
25.93
0.0
20.5
0.0
79.5
121.0
1.3
180.0
28.82
28.68
58,62
633,09F,0
'190,154.9
4.76

26.05
.185
200
123.5
10
.84
78.0
.96
.C5

1.11
106.13
1.3
28.68
53.62
102.6


_
_

_
.CO)
.026

0.00
0.00
.
0.00
0.00

0.00
0.00
.001
.027

METRIC
UNITS
1/23/78

-1.78
659.89
0.0
20.5
0.0
79.5
51.1
1.3
16.56
28.82
28.68
17.87
17.W.7
RS53.5
'1.76

661.67
1.70
200
3.5
40
.8"
25.6
24.38
30
21.59

.01
3.ffl
1.3
28.68
17.87
102.6


.019

.024
.013
.005
.012

O.CO
0.00
0.00
.om
O.CO
0.00
.om
0.00
0.00
.015
.012

AVERAGE
ENGLISH
UNITS


-.07
26.08
0.0
20.5
0.0
79.5
108.0
.7
180.0
28.82
28.75
55.50
QO.236.0
'91,062.2
4.76

26.15
.185
173
101.3
10
.81
69
.94
.82

.69
91.36
.7
28.75
56.50
103.14


_



.016
.211

O.CO
.005
-
O.CO
0.00

0.00
.005
.046
.216

METRIC
UNITS


-1.78
662.43
0.0
20.5
0.0
79.5
42.13
.7
16,56
28.82
28.75
17.22
17,287.1
13,911.1
4.76

664.21
4.70
173
2.9
40
.84
20.6
23.79
14.7
20.83

.02
2.6
,7
28.75
17.22
103.14


.021

.2gd
.315
.135
.119

.006
.002
.002
.0006
0.00
0.00
.0066
.002
.002
.3216
.1370
.1190

                   -8-

-------
TABLE 6.  CALCINE FUGITIVE ARSENIC RESULTS
RUN NUMBER



II STACK PARAMETERS
PST - STATIC PRESSURE, 'Ha (HMHo)
Ps - STACK GAS PRESSURE, *Ho ABSOLUTE (Mrflc)
I CO, - VOLUME I DRV
I 02 - VOLUME J DRY
I CO ' VOLUME I DRY
I N2 - VOLUME I DRV
Ts - AVERAGE STACK TEMPERATURE °F (°C)
I H^ - I MOISTURE IN STACK GAS, By VOLUME
As - STACK AREA, FT2 (M2)
MD - MOLECULAR HEIGHT OF STACK GAS, DRV BASIS
Ms - MOLECULAR HEIGHT OF STACK GAS, MET BASIS
Vs - STACK GAS VELOCITY, FT/SEC, (M/SEC)
QA - STACK GAS VOLUMETRIC FLOW AT STACK CONDITIONS, ACFH (NM'/HIN)
Os - STACK GAS VOLUMETRIC FLOW AT STANDARD CONDITIONS, DSCFM (NMVMIN)
t EA> - PERCENT EXCESS AIR
I'll TEST CONDITIONS
PB - BAROMETRIC PRESSURE, "Ho (NMHG)
DN - SAMPLING NOZZLE DIAMETER, IN. (KM)
T - SAMPLING 1mb, MIN
VN - SAMPLE VOLUME, ACF (M3)
NP - NET SAMPLING POINTS
CP - PITOT TUBE COEFFICIENT
TN - AVERAGE METER TEMPERATURE °F (°C)
PM - AVERAGE ORIFICE PRESSURE DROP, "H20 (nMHoO)
VLC - CONOENSATE COLLECTED (INPINGEDS AND GEL), MLS
Cf - STACK VELOCITY HEAD 'H20 (M«H20>
IV tEST CALCULATIONS
VH - CONDENSED HATER VAPOR, SDCF (NM3)
VM - VOLUME OF GAS SAMPLED «T STANDARD CONDITIONS, DSCF (NM5)
I H20 - PERCENT MOISTURE, BY VOLUME
Ms - MOLECULAR HEIGHT OF STACK GAS, MET BASIS
Vs - STACK VELOCITY, FT/SEC (M/SEC)
I 1 - PERCENT ISOKINETIC
V ANALYTICAL DATA
A) ARSENIC' FRONT HALF
PROBE (MO)
CYCLONE (MG)
FILTER (MG)
ARSENIC FRONT HALF TOTAL (MG)
PPM, (MG/M3)
tm, (KG/HR)
B) ARSENIC - IMPINGED COLLECTION
INPINGER #1. 2 (MG)
PPM, (MG/M3)
K/HR, (KG/HR)
lMpnir,FB-«.l|.5 (MB)
PPM, (MG/M3)
»/HR, (KG/HR)
C) ARSENIC - IMPINGER TOTAL (MG)
PPM, (MG/M3)
f/MR, (KG/HR)
D) TOTAL ARSENIC (MG)
PPM, (MG/M3)
»/HR, (KG/HR)
1
ENGLISH
UNITS
1/24/78

-.05
26.00
0,0
20.5
0.0
79.5
56.0
.1
4.43
28.82
28.30
32.65
8,678.1
7,706.2
4.76

26.05
.245
60
35.7
20
.84
54.0
1.26
.30

.05
32.15
.1
28,80
32.65
93.4


.


.
3~62
.326

-
.04
.003
_
.03
.003

.07
.006
3.690
.332
METRIC
UNITS
1/24/78

-1.27
660.40
0.0
20.5
0.0
79.5
13.3
.1
.412
28.82
28.80
9.95
245.8
218.2
4.76

661.67
6.22
60
1.01
20
.84
12.2
32.00
1.0
7.62

0.00
.9
.1
28.80
9.S6
93.4


.60
.
9.70
10.30
11.52
.148

.100
.11
.001
.087
.10
.001
.187
.21
.002
10.49
11.53
.150
2
ENGLISH
UNITS
1/24/78

-.05
26.00
0.0
20.5'
0.0
79.5
57.0
.4
'4.43
28.82
28.78
33.24
8,835,2
7,803.8
4,76

2P.C6
.245
60
39.2
20
.84
56.0
1.46
.31

.14
35.14
.4
28.78
33.24
103.7


.
_
.
.
1.00
.092

-
.01
.001

.020
.on

.030
.002
1.030
.084
METRIC
UNITS
1/24/78

-1.27
6H1.40
0.0
20.5
0.0
70.5
33.9
.4
.412
28.82
28.78
in.B
250.3
221,1
4.76

661.67
C.22
60
1.11
20
.811
133
37.08
3.0
7.87 '

0.00
1.0
.4
28,78
10.B
100.7


J2
_
3.00
3J2
3J.4
.042

.035
'.at
.ora
.0607
.05
.0005
.0857
.090
.001
3.206
3.23
.043

ENGLISH
UNITS
1/24/78

-.06
26.00
0.0
20.5
n.'o
79.5
61.0
.3
4.43
28.82
28.79
32.82
8,723.6
7,659.0
4.76

26.03
.245
60
36.1 .
20
.84
59.0
1.34 '
.30

.09
32.17 .
.3
28.79
32.82
»'.'o •


;
~
-
-
2.49
.223

-
.010
.cm
_
0.00
0.00

,010
.cm
2.500
.224

METRIC
UNITS
1/24/78

-1.27
6G0.40
0.0
20.5
0.0
79.5
16.1
.3
.412
28.82
28.79
10.00
247J
216.9
4.76

661.67
6.22
60
1.02
20
.84
15.0
34.04
2.0
7.62

0.00
.9
.3
28.79
10.00
94.0


1.JB9
_
5.200
7.09
7.79
jm

.018
.02
.0002
0.00
0.00
0.00
.018
.02
.002
7.108
7.810
.103
AVERAGE
ENGLISH
UNITS


-.05
26,00
0,0
20,5
0.0
79.5
58.0
.3
4.43
28.82
28.79
32.90
8,745.7
7,724.3
4.76

26.G5
.245
60
37.0
20
.84
56.3
1.35
.30

.09
33.15
.3
28.79
32.90
96.0


.

m
.
2.37
.2137

-
.020
.0017
_
.017
.0013

.037
.003
2.4067
.2167
METRIC
UNITS


-1.27
660.40
0.0
20.5
0.0
79.5
14.4
.3
,412
28.82
28.79
10.03
247.75
218.82
4.76

661.67
6.22
60
1.06
20
.84
13.5
34.37
2.0
7.70

0.00
.9
.3
28.79
10.03
96.0


.87
_
5.97
6.84
7.42
.0970

,.051D
.057
.0336
.0459
.060
.0X6
.0969
.1067
.0017
6.934
7.523
.M9B7
                   -9-

-------
TABLE 7.
MATTE TAPPING PARTICULATE/SO? RESULTS

RUN NlieER


1 DATE
II STACK PARAMETERS
PST - STATIC PRESSURE, "He (mHo)
Ps - STACK GAS PRESSURE, "He ABSOLUTE (twlta)
I C02 - VOLUME I DRV
I Oo - VOLUME I DRV
I CO - VOLUME X DRV
t N2 - VOLUME X DRV
Ts - AVERAGE STACK TEMPERATURE °F (°C)
I 820 - X MOISTURE IN STACK GAS, Bv VOLUME
As - STACK AREA, FT* (M*)
Ho - MOLECULAR HEIGHT OF STACK GAS, DRV BASIS
Ms - MOLECULAR HEIGHT OF STACK GAS, MET BASIS
Vs - STACK GAS VELOCITV, FT/SEC, (M/SEC)
QA - STACK GAS VOLUMETRIC FLOH AT STACK CONDITIONS, ACFI* (NM'/MIH)
Qs - STACK GAS VOLUMETRIC FLOH AT STANDARD CONDITIONS, DSCFM (NM'/HIN)
X EA - PERCENT EXCESS AIR

III TEST CONDITIONS
PB - BAROMETRIC PRESSURE, "Ho (HMHG)
D» - SAMPLING NOZZLE DIAMETER, IN. (MM)
T - SAMPLING TIME, MIN
VM - SAMPLE VOLUME, ACF («3>
NP - NET SAMPLING POINTS
CP - PITOT TUBE COEFFICIENT
TM - AVERAGE METER TEMPERATURE °F (°C)
PH - AVERAGE ORIFICE PRESSURE DROP, "H20 (MxH-jO)
VLC - CONDEHSATE COLLECTED (IMPINGERS AND GEL), MLS
£P - STACK VELOCITY HEAD "H20 (wH20)
IV TEST CALCUUTIONS
VH - CONDENSED HATER VAPOR, SDCF (HM3>
VH - VOLUME OF GAS SAMPLED AT STANDARD CONDITIONS, DSCF (NM3)
X H20 - PERCENT MOISTURE, Bv VOLUME
Ms - MOLECULAR HEIGHT OF STACK GAS, MET BASIS
Vs - STACK VELOCITV, FT/SEC (M/SEC)
X 1 - PERCENT ISOKIKETIC
V ANALYTICAL DATA
A) PARTICIPATES FRONT HALF
PROBE (BO)
CYCLONE (MG)
FILTER (MG)
PARTICIPATES FRONT HALF TOTAL (MG)
GRS/SnCF, (MG/M3)
#/HR, KG/HK)
B) PARTICULATES - CONDENSABLES
PHGAHIC (MG)
GRS/SDCF, (MG/M3)
. C/HR, (KG/HR)
INORGANIC (MG)
GRS/SDCF, (MG/M3)
fl/HR, (KG/HR)
C) PARTICIII ATES - TQTAJ CDKOFMSABLES (MG)
GRS/SDCF, (MG/M3)
»/HR, (KG/HR)
D) TOTAL PARTICULARS (MG)
ORS/SDCF, (MO/M3)
*/HR, (KG/MR)
E) TOTAL SO; (MG)
PPM
(MG/M )
0/HR, (KG/HR)
1

ENGLISH
UNITS
1/25/78

+.44
26.65
0.0
20.5
0.0
79.5
73.0
.8
5.85
28.82
28.74
87.13
30,687.9
26,871.G
1.76

26,21
.185
389
372.1
24
.80
87
2.52

2.13

2.45
317.8
.8
28.71
87.13
93.7

.
_
.
-
.003
1.07

.
.004
.100
.
.078
18.05
.
,081
18,15

.036
19,12
-
61.55
1C.49
METRIC
UNITS
1/25/78

11.18
676,91
0.0
20.5
0.0
79,5
22,8
.8
,513
28.82
28.71
26.65
£69.'!
760.9
4.76

665,73
1.70
389
9.0
21
.84
30.6
64,01
52
54,10

.07
9.0
.8
28.71
26.65
93.7

12.8

100.2
113.0
10.73
.49

10.3
.98
.045
1,891,6
179,63
8.20
L901.9
180.fl
8.25
2,014.9
191.31
8,74
1,728.4
61.55
164.13
7.50
2

ENGLISH
UNITS
1/26/78

+.44
26.64
0.0
20.5
0.0
79.5
82.0
0.0
5.B5
28.82
28.82
89.90
3L554.9
27,369.8
4,76

26,20
.185
360
3E8.0
24
.84
100.0
2.76

2.22

0.0
307.1
0.0
28.82
84.90
9C.O

.
_
.
-
.016
3,77

.
.001
.199
-
.120
28.17
.
.121
28.37
.
,137
52.14
-
90.04
24.58
METRIC
UNITS
1/26/78

11.1E
676.66
0.0
20,5
0,0
79.5
22.8
0.0
.543
28.82
28.82
27.40
893.9
775,0
'1,76

665.48
4.70
3CO
8.7
24
.84
37.8
70.10
0
5E.39

0.0
8.7
0.0
28,82
27.40
96.0

48.4
_
335.9
384.3
36.90
171

20.2
1.911
.09
2,805.7
275.17
12.80
2,885.9
277.09
12.89
3,270.2
313.99
14.CO
2,500.8
93.04
2)0.13
11.17
!

ENGLISH
UNITS
1/26/78

+.44
26.64
0.0
20.5
0.0
79.5
82.0
0.0
5.85
28.82 .
28.82
88.06
50,903.0
26,802.1
4.76

26,20
.185
360
350.6
24
.84
110.0
3.28

2.33

.08 '
287.9 •
0.0 .
28.82
88.03 ;
91.9

i
_
.
-
.013
3.08

.
.on
.197
-
.126
28,96
.
.127
29.18
_
.140
32.27
.
201.47
53.86
METRIC
UNITS
1/26/78

11.18
276.91
0.0
20.5
0.0
79.5
22.8
0,0
,543
28,22
28.82
26.84
875.6
759.1
11.76

665.48
4.70
360
8.2
24
.84
43.3
83.31
2.0
54.10

Oil
8.2
0.0
28.82
26.84
91.9

32.2
_
273.9
303.9
30.83
1.41

19.5
1.97
.09
2,868,6
289,12
13.17
2,888.1
291.09
13.26
3,194.0
321,92
14.07
5,331.0
201.47
537.29
24.48
AVERAGE

FJtGLlSH
UNITS


+ .44
26.64
0.0
20.5
0.0
79.5
79.0
.3
5.85
28.82
28.79
88.46
31.050.6
27,014.5
4.76

26,20
.185
369
363.6
24
.84
99.0
2.8S

2.16

.84
304.3
.3
28.79
88.46
93.9

_
_
m
-
.011
2.64

.
.002
.165

.108
25.07
_
.085
25.23
_
,087
27.811
.
117.69
31.64
METRIC
UNITS


11.18
676.74
0.0
20.5
0.0
79.5
22.8
.3
.543
28.82
28.79
26.96
879.62
765.3
4.7B

665.56
4.70
360
8.6
24
.84
37.2
72.5
27,0
54.86

.02
8.6
.3
28.79
26.96
93.9

31.13

236.67
267.73
26.15
1.20

16.67
1.63
.075
2,541.97
247.97
11,39
2,558.6
249.60
11.47
2,826,3
275.75
12.07
3,186.7
117.69
313,85 .
14,33
                     -10-

-------
TABLE 8.  MATTE TAPPING ARSENIC RESULTS
RUN NUMBER



II STACK PARAMETERS
PST - STATIC PRESSURE. "He (mHc)
Ps - STACK GAS PRESSURE, "He ABSOLUTE (MHNG)
I CO? • VOLUM X DRY
t 0, - VOLIWE I DRY
I CO ' VOLUME I DRV
I N2 - VOLUME X DRV
Ts - AVERAGE STACK TEMPERATURE °F <°C>
X H20 - X MOISTURE IN STACK GAS, BY VOLUME
As - STACK AREA, fr Or)
It - MOLECULAR HEIGHT OF STACK GAS, DRV BASIS
Ms - MOLECULAR HEIGHT OF STACK GAS, NET BASIS
Vs - STACK GAS VELOCITY, FT/SEC, (H/SEC)
DA - STACK GAS VOLUMETRIC FLO* AT STACK CONDITIONS, ACFM (NMVMIH)
us - STACK GAS VOLUMETRIC FLO* AT STANDARD CONDITIONS, DSCFH (Hx'/Min)
I EA> - PERCENT EXCESS AIR
III TEST CONDITIONS
PB - BAROMETRIC PRESSURE, 'Ho MG)
DN - SAMPLING NOZZLE DIAMETER, IN. (MM)
T - SAMPLING TIMI, MIN
VM - SAMPLE VOLUME, ACF (N3>
NP - NET SAMPLING POINTS
CP - PITOT TUBE COEFFICIENT
TM - AVERAGE METER TEMPERATURE °F (°C)
PN - AVERAGE ORIFICE PRESSURE DROP, 'H20 (MMHiO)
VLC - CONDENSATE COLLECTED (IHPINGERS AND GEL), MLS
Cf - STACK VELOCITY HEAD "H20 (MMH20)
IV TEST CALCULATIONS
VM - CONDENSED WATER VAPOR, SDCF (NH3)
VH - VOLUME OF GAS SAMPLED «T STANDARD CONDITIONS, DSCF (KM3)
X l<20 - PERCENT MOISTURE, BY VOLUME
Ms - MOLECULAR HEIGHT OF STACK GAS, HET BASIS
Vs - STACK VELOCITY, FT/SEC (M/SEC)
X 1 - PERCENT ISOPUNETIC
V ANALYTICAL DATA
A) ARSENIC' FRONT HALF
PROBE (MG)
CYCLONE (HG)
FILTER (MG)
ARSENIC FRONT HALF TOTAL (MG)
PPM, (MG/M3)
AIR, (KG/MR)
B) ARSENIC - 1 WINGER COLLECTION
IMPINGED 41. 2 (MG)
PPM, (MG/M')
Htm, (KG/HR)
IMPINGED •«}. 4. 5 (MG)
PPM, (MG/M3)
0/HR, (KG/HR)
O ARSENIC - IMPINGER TOTAL (MG)
PPM, (nc/N3)
0/HR, (KG/HR)
D) TOTAL APSFNIC (HG>
PPM, (MG/M3)
»/HR, (KG/HR)
1
ENGLISH
UNITS
1/20/78

+.44
26.54
0.0
20.5
0.0
79.5
1D5.0
,3
5.85
28.82
28.79
80.27
28,174,8
23,295,8
4.76

26.10
.185
240
205.2
24
,84
93,0
2,04
1.69

,45
171,48
.3
28.79
80.27
94.5

..
. ^
.
-
2.12
.578

-
00,2
.001
_
.0036
,001

.0056
.002

2.126
.50)
METRIC
UNITS
1/20(98

11.18
674.12
0.0
20.5
.0.0
79.5
40,6 '
.3
.543
28.82
28.79
24.17
733.2
659.7
4.76

662.94
4.70
240
5.81
24
.84
35.6
51.82
9.5
42.93

.m
4,9
.3
28.79
24.47
94.5

1.18

31.00
32.18
6,63
,263

,045
.as
.0003
.065
.011
.com
.1003
.020
.0007
32.28
6.65
.264
2
ENGLISH
UNITS
1/20/78

+.44
26.54
0.0
20.5
0.0
79.5
98.0
0.0
5.85
28.82
28,82
89.52
3L421.5
26,367.0
4.76

26.10
.125
240
222.3
24
.84
98,0
2.50
2.13

.05
185.30
0.0
28.82
89.52
90.2

_
_
_
-
1.94
.598

.
00.23
.001
_
.0027
.001

.0(5
.002

1.945
.600
METRIC
UNITS
1/20/78

11.18
674.12
0.0
20.5
0.0
79.5
3R.7
0,0
.543
28.82
28,82
27.29
890.1
74C.6
4.76

662.94
4.70
240
5.2
24
,84
36.7
63.50
1.0
54.10

0.0
5.2
0.0
28.82
27.29
90.2

.19

51.00
31.79
6.06
.272

.035
.007
.0005
.045
.009
,0003
.03
.016
.0006
31.87
6.076
.273
3
ENaiSH
UNITS
1/25/78

+.44
26.65
0.0
20.5
P.O
79.5
73.0
0.0
5.85
28.82
28.82
o5,!3
3X074.0
27,417.9
4.76

26.21
.185
396
361.2
24
.84
91.0
2.50
2.19

0.0
306.23
0,0
28.82
88.53
86.9

_
_
.
-
.90
.288

_
.0007
.0002
_
.0002
.0001

.0009
.0003

.9009
.2883
METRIC
UNITS
0/25/78

11.18
676.91
0.0
20.5
0.0
79.5
22,8
0.0
.543
28.82
28.82
26.93
880.3
776.71
4.76

665.73
4.70
396
10.23
24
.84
32.8
63.50
0.0
55.63

0.0
8.7
0,0
28.82
26.93
86.9

.87

23.5
24 J7
2.81
.151

.020
.002
.on
.007
.0008
.0000
.027
.0028
.001
34.397
2.813
.132
AVERAGE
ENGLISH
UNITS


+.44
26.58
0.0
20.5
0.0
79.5
92.0
.1
5.85
28.G2
28.81
86.11
30.223.4
25,693.6
4.76

26.14
.185
292
262.9
24
,84
95.0
2.34
2.00

,17
221.00
.1
28.81
86.11
90.5

_
_
_
-
1.B
.488

_
.0017
.0007
_
,0022
,0007

.0039
.0014

1.654
.489
METRIC
WITS


11.18
675.05
0.0
20.5
0.0
79.5
33.37
.1
.543
28.82
28.81
26.25
856.2
727.9
4.76

663.9
4.70
292
7.45
24
.84
35.0
59.60
3.5
50.88

0.00
6,26
,1
28.81 .
26.25
90.5

.95

28.5
29.45
5.17
.222

.033
.006
,0005
.036
,0069
.0002
.069
.0129
.0007
29.519
5.1829
.2227
                   -11-

-------
                         TABLE  9   PARTICLE  SIZING  SUMMARY (LOCATION-ASARCO PLANT, EL PASO, TEXAS)
ro
i

LOCATION
Baghouse Inlet
Baghouse Inlet
Baghouse Inlet
Baghouse Inlet
Baghouse Inlet
Baghouse Outlet
Baghouse Outlet
Calcining Duct
Calcining Duct
Calcining Duct
Calcining Duct
TEST
303-ABI-la
303-ABI-lb
303-ABI-lc
303-ABI-ld
303-ABI-le
302-ABE-la
302-ABE-lb
334-DBE-l
335-DBE-2
336-DBE-3
337-DBE-4
PARTICLE SIZE DISTRIBUTION %
>5*
7.0
52.0
49.0
8.0
42.0
16.0
23.0
89.0
81.0
91.0
79.0
3-5 M
10.0
8.0
9.0
9.0
10.0
11.0
9.0
3.0
6.0
2.5
6.0
1-3 M
39.0
15.0
18.0
30.0
20.0
27.0
23.0
3.5
8
3.5
9.5
lM
44.0
25.0
24.0
53.0
28.0
46.0
45.0
4.5
5.0
3.0
5.5

-------
TABLE 10.  ROASTER/REVERB ELECTROSTATIC PRECIPITATOR
           OUTLET PARTICULATE RESULTS

RUN NIHER
iV

1 DATE
II STACK PARAMETERS
PST - STATIC PRESSURE, 'He (MMHO)
Ps - STACK GAS PRESSURE, "Ho ABSOLUTE dwHc)
I C02 - VOLUME Z DRV
I Oo - VOLUME I DRY
I CO - VOLUME I Our
I N2 - VOLUME I Dfiy
Ts - AVERAGE STACK TEMPERATURE °F (°C)
t H20 - I MOISTURE in STACK GAS, By VOLUME
As - STACK AREA, rr (ir)
No - MOLECULAR HEIGHT OF STACK GAS, DRY BASIS
Ms - MOLECULAR WEIGHT OF STACK GAS, NET BASIS
Vs - STACK GAS VELOCITY, FT/SEC, (M/SEC)
QA - STACK GAS VOLUMETRIC FLOH AT STACK CONDITIONS, ACFM (NMVMIH)
Os - STACK GAS VOLUMETRIC FLOM AT STANDARD CONDITIONS, DSCFM (NMVHIN)
X EA - PERCENT EXCESS AIR
III TEST CONDITIONS
PB - BAROMETRIC PRESSURE, "Ho (MMHe)
DN - SAMPLING NOZZLE DIAMETER, IN. (MM)
T - SAMPLING TIME, MIN
VM - SAMPLE VOLUME, ACF 
NP - NET SAMPLING POINTS
CP - PITOT TUBE COEFFICIENT
TM - AVERAGE METER TEMPERATURE °F (°C)
PH - AVERAGE ORIFICE PRESSURE DROP, "^0 (nnHoO)
VLC - CONDENSATE COLLECTED (InPINGERS AND GEL), MLS
6P - STACK VELOCITY HEAD "H20 
-------
TABLE 11.  ROASTER/REVERB ELECTROSTATIC PRECIPITATOR
           OUTLET S00 RESULTS

RUN NUKED


1 DATE
II STACK PARAMETERS
PIT - STATIC PRESSURE, 'Ho (mHo)
Pt - STACK GAS PRESSURE, "Ho ABSOLUTE (wHo)
I CO, - VOLUME I DRY
I 02 - VOLUME I DRY
I CO - VOLUME I DRV
I N2 - VOLUME I DRY
Ts - AVERAGE STACK TEMPERATURE °F (°C)
I H20 - X MOISTURE IN STACK GAS, Br VOLUME
As - STACK AREA, rr (M2)
MD - MOLECULAR HEIGHT OF STACK GAS, DRV BASH
Ms - MOLECULAR HEIGHT OP STACK GAS, MET BASIS
Vs - STACK GAS VELOCITY, FT/SEC, (M/SCC)
QA - STACK GAS VOLUMETRIC FLOH AT STACK CONDITIONS, ACFH (Ntr/MIN)
09 - STACK GAS VOLUMETRIC FLOH AT STANDARD CONDITIONS, DSCFM (NM'/MIN)
I EA - PERCENT EXCESS AIR
III TEST CONDITIONS
PB - BAROMETRIC PRESSURE, 'Ho (HMHo)
ON - SAMPLING NOZZLE DIAMETER, IN, (MM)
T • SAMPLING TIME, MIN
VM - SAMPLE VOLUME, ACF (M3)
NP - NET SAMPLING POINTS
CP - PITOT TUBE COEFFICIENT
TM - AVERAGE METER TEMPERATURE °F (°C>
PM - AVERAGE ORIFICE PRESSURE DROP, '(^O (wtHoCO
VLC - CONDENSATE COLLECTED (IMPINGERS AND GEL), MLS
OP • STACK VELOCITY HEAD 'H20 (MMH20)
IV TEST CALCULATIONS
V* - CONDENSED CATER VAPOR, SDCF 
VM - VOLUME OF GAS SAMPLED AT STANDARD CONDITIONS, DSCF (NH})
t HjO - PERCENT MOISTURE, Bv VOLUME
Ms - MOLECULAR HEIGHT OF STACK GAS, MET BASIS
Vs - STACK VELOCITY, FT/SEC (M/SEC)
t 1 - PERCENT ISOKINETIC
V ANALYTICAL DATA
A) PARTICULATES FRONT HALF
PROBE (MO)
CYCLONE (MG)
FILTER (MG)
PARTICULATES FRONT HALF TOTAL (MO)
ORS/SDCF, (MO/M3)
I/MI, KG/HR)
B) PARTICULATES - COXDENSABLES
QRBAHIC (MG)
GRS/SIKF, (MO/M3)
I/H», (KG/HR)
INORCAIIIC (MG)
GRS/SDCF, (MO/M3)
ff/MR, (KG/HR)
C.) pAimcijQATFt • TOTAI, CnNDFNXAfu ra (MO)
CRS/SDCF, (MO/M3)
I/MR, (KG/HR)
D) TOTAL PARTICULARS (MG)
GRS/SDCF, (MO/M3)
I/KR, (KO/HR)
E) TOTAL SO; (HO)
PPM
(MO/M3)
I/HR, (KG/HR)
1

ENGLISH
UNITS
1/27/78

0,0
26,20
3.0
20.5
0.0
76.5
219,0'
6.0
180,0
29.30
28,62
28.09
513,002.0
200,352,4
4.93

26,20
.306
15
3.674
1
,84
72.25

_
.183


3.190
_
28.62
28.99

.
'
.
.
—
.
•

.
.
-
-
-
-
-
-
-
.
-
KU54.W
METRIC
UNITS
1/27/78

0.0
665.48
3,0
20.5
0.0
76.5
103.9
6.0
16,2
29,30
28,62
8,8>l
8,8(9.5
5,673.4
4,95

665,48
7.C2
JS
.104
1
.84
22.36
.
.
4.57


.09

28.K
8.84

.
-
.
m
m
.
•

.
.
-
-
•
•
-
-
-
L223.4
5,081.52
13,551.62
4x615.67
2

ENGLISH
UNITS



















































METRIC
UNITS



















































J

ENGLISH
UNITS



















































METRIC
UNITS



















































AVERAGE

ENGLISH
UNITS



















































(ETHIC
UNITS



















































                       -14-

-------
TABLED2.  Process Samples From ASARCO, El Paso
LOCATION

WEDGE
ROASTER
CALCINE





RAM
REVERB
SLAG



H.F.
REVERB
SLAG



DATE SAMPLED % As
1-17-78 0.149
1-18-78 0.131
1-19-78 0.568
1-20-78 0.481
1-21-78 0.050
1-22-78 0.135
1-23-78 0.641
1-24-78 0.197
1-25-78 0.342
1-17-78 0.096
1-18-78 0.088
1-19-78 0.157
1-22-78 0.083
1-23-78 0.086
1-24-78 0.203
1-25-78 0.201
1-17-78 0.074
1-18-78 0.146
1-19-78 0.156
1-20-78 0.108
1-21-78 0.102
1-22-78 0.058
1-23-78 0.058
1-24-78 0.184
1-25-78 0.171
1-28-78 0.075
'
LOCATION

CONVERTER
SLAG





REVERB
MATTE



WEDGE
ROASTER
CONC.
FEED



ROASTER/
REVERB SPRAY
CHAM.
DATE SAMPLED % As
1-17-78 0.044
1-18-78 0.060
1-19-78 0.088
1-20-78 0.044
1-21-78 0.090
1-22-78 0.048
1-23-78 0.046
1-24-78 0.128
1.25-78 0.049
1-17-78 0.059
1-18-78 0.082
1-19-78 0.101
1-20-78 0.083
1-21-78 0.083
1-22-78 0.072
1-23-78 OJ)62
1-24-78 0.119
1-18-78 0.083
1-19-78 0.109
1-20-78 0.090
1-21-78 0.075
1-22-78 0.301
1-23-78 0.125
1-24-78 0.016
1-25-78 0.384
1-26-78 0.430
1-23-78 0.805
                               -15-

-------
               TABLE 13



  MASS SPECTROMETRY ANALYSIS RESULTS








      Prepared by CDM/ACCU LABS



11485 W. 48th Ave./WheatRidge CO. 80033

-------
COM/ACCU-LABS
11485 W. 48th Ave./WheatRidge CO 80033
(303) 423-2766
Baghouse Outlet
 1/17-21/78
TRW DATE: April 28, 1978
onA; * • « T3 i ^ ALRNo: 273-6312-4-1
ss-ssxsr ssLu 9o26e ~frr° NEo«sest #1
-t ILL wllttOC \-rl UGL ii W • .Lj vF^l A ^XvJ Vj*O "'
CONCENTRATION IN ug/ml
Uranium <0. 003
Thorium <0. 002
Bismuth 0. 52
Lead 13
Thallium 0. 036
Mercury NR
Gold
Platinum
Iridium
Osmium
_L . Internal
Rhenium standard
Tungsten <0. 003
Tantalum <0. 002
Hafnium <0. 010
Lutecium
Ytterbium <0. 005
Thullium <0. 002
Erbium <0. 006
rlolmium
Dysprosium
Terbium
Gadolinium <0. 004
Europium <0. 002
Samarium <0. 005
Neodymium <0. 005
Praseodymium 0. 007
Cerium 0. 004
Lanthanum 0. 004
Barium 0. 88
Cesium 0. 008
Iodine 0. 010
Tellurium
Antimony 0. 035
Tin 0. 082
T ,. Internal
Indlum Standard
Cadmium 0. 086
Silver 0. 027
Palladium
Rhodium

Ruthenium
Molybdenum 0.26
Niobium 0. 024
Zirconium 0. 030
Yttrium 0. 002
Strontium 0. 29
Rubidium 0. 18
Bromine 1. 3
Selenium 2. 0
Arsenic 250
Germanium
Gallium 0. 003
Zinc 6. 8
Copper 7. 1
Nickel 0. 025
Cobalt 0. 013
Iron 2. 6
Manganese 0. 063
Chromium 0. 16

Vanadium
Titanium
Scandium
Calcium
Potassium
Chlorine
Sulphur
Phosphorus
Silicon
Aluminum
Magnesium
Sodium
Fluorine
Oxygen
Nitrogen
Carbon
Boron
Beryllium
Lithium

0.005
0.050
<0. 003
26
29
1.1
39
0.14
6.2
9.5
19
760
1.3
NR
NR
NR
NR
<0. 003
0.016

       All elements for which values are not entered <0. 001 jjg/ml.
NOTES:  NR - Not Reported                            „ ..,    .
                                    _16_           ^Jto^JTR
                                                   Supervisor
                                                   Hess Spectrometry

-------
COM/ACCU-LABS
11485 W. 48th Ave./WheatRidge CO 80033
(303) 423-2766
To.     Mr. Dave Ringwald
        TRW
              Matte Tapping
              1/20-25/78
DATE:     April 28, 1978
ALRNo:   273-6312-4-2
Sample Identification No.  CME Composite
Purchase Order No.
CONCENTRATION IN pig/ml
Uranium <0. 003
Thorium -0. 022
Bismuth 70
Lead 150
Thallium 0. 64
Mercury NR
Gold
Platinum
Iridium
Osmium
Rhenium _. , ,
Standard
Tungsten <0. 004
Tantalum <0, 003
Hafnium <0. 013
Lutecium <0. 002
Ytterbium <0, 006
Thullium <0. 003
Erbium <0. 008
Holmium
Dysprosium <0. 002
Terbium
Gadolinium <0. 005
Europium <0. 002
Samarium <0. 007
Neodymium 0. 015
Praseodymium 0. 008
Cerium 0. 010
Lanthanum 0. 006
Barium 0.89
Cesium <0. 020
Iodine 0. 035
Tellurium 0. 42
Antimony 4. 7
Tin 1. 9
T ,. Internal
Indium „, , ,
Standard
Cadmium 11
Silver 0. 036
Palladium
Rhodium

Ruthenium'
Molybdenum 2. 1
Niobium
Zirconium 0. 036
Yttrium 0. 016
Strontium 0. 17
Rubidium 0. 87
Bromine 0. 38
Selenium 2. 6
Arsenic >0. 5%
Germanium 0. 045
Gallium 0. 004
Zinc 490
Copper 72
Nickel 0. 34
Cobalt 0.17
Iron 65
Manganese 0. 59
Chromium 0. 090

Vanadium 0. 21
Titanium 0. 44
Scandium 0. 003
Calcium 44
Potassium 68
Chlorine 0. 43
Sulphur 290
Phosphorus 0. 19
Silicon 470
Aluminum 36
Magnesium 42
Sodium 380
Fluorine 1.8
Oxygen NR
Nitrogen NR
Carbon NR
Boron NR
Beryllium <0. 004
Lithium 0. 052

NOTES-   AU elements for which values are not entered <0. 001 us/ml
        NR - Not Reported                              - --
                                         -17-
                                                       Supervisor           "
                                                       Mass jpeotrometry

-------
COM /ACCU- LABS
11485 W. 48th Ave./WheatRidge CO 80033
(303) 423-2766
To:     Mr. Dave Ringwald
        TRW
               Baghouse  Inlet
               1/18-21/78
DATE:    April 28,  1978
ALRNo:  273-6312-4-4
Sample Identification No. AMI Composite
Purchase Order No.
CONCENTRATION IN  jig/ml
Uranium 0. 004
Thorium <0. 003
Bismuth 20
Lead 370
Thallium 0. 52
Mercury
Gold
Platinum
Iridium
Osmium
Internal
Rhenium Standard
Tungsten <0. 003
Tantalum <0. 003
Hafnium <0. 010
Lutecium
Ytterbium <0. 005
Thullium <0. 002
Erbium <0. 007
ttolmium
Dysprosium
All elements
NOTES: NR - Not Re]
Terbium
Gadolinium <0. 004
Europium <0. 002
Samarium <0. 006
Neodymium 0. Oil
Praseodymium 0. 008
Cerium 0. 012
Lanthanum 0. 012
Barium 4. 8
Cesium 0. 015
Iodine 0. 028
Tellurium 0. 29
Antimony 1. 8
Tin 0. 89
T ,. Internal
Indium _, , ,
Standard
Cadmium 3. 3
Silver 0. 58
Palladium
Rhodium
for which values are nx
ported
«
Ruthenium
MolybdenumS. 9
Niobium
Zirconium 0. 029
Yttrium 0. 013
Strontium 0. 63
Rubidium 0. 40
Bromine 0. 13
Selenium 3. 3
Arsenic 590
Germanium 0. 014
Gallium 0. 003
Zinc 310
Copper 220
Nickel 0. 54
Cobalt 0. 18
Iron 280
Manganese 1. 6
Chromium 0. 51
)t entered <0. 001 pg/
Ct >
\1 A
Vanadium
Titanium
Scandium
Calcium
Potassium
Chlorine
Sulphur
Phosphorus
Silicon
Aluminum
Magnesium
Sodium
Fluorine
Oxygen
Nitrogen
Carbon
Boron
Beryllium
Lithium
'ml.
1 !\& V"^ i^
Supervisor
0. 012
0.74
<0. 003
84
16
0.70
330
1.6
10
35
20
230
0.63
NR
NR
NR
NR
<0. 003
0.018
"iSUAV-A
^/VAlr •» "^

-------
COM/ACCU-LABS
11485 W. 48th Ave./WheatRidge CO 80033
(303) 423-2766
 To:     Mr. Dave Ringwald
        TRW
                                            Calcine Fugitive  Duct
                                                 1/24/78
                                    DATE:     April 28,  1978
                                    ALR No:    273-6312-4-3
                                    Sample Identification No.  DME Composite
                                    Purchase Order No.
                                    CONCENTRATION IN  jig/ml
Uranium 0. 010
Thorium <0. 003
Bismuth 6. 9
Lead 250
Thallium 0. 31
Mercury NR
Gold
Platinum
Iridium
Osmium
Rhenium _. , ,
Standard
Tungsten <0. 004
Tantalum <0. 003
Hafnium <0. 013
Lutecium <0. 002
Ytterbium <0. 006
Thullium <0. 003
Erbium 
-------
                         LOCATION OF SAMPLING POINTS

1)  Inlet to the Converter Building Fugitive Emissions  Baghouse
     Samples from the inlet to the converter building fugitive baghouse  were
     taken from a 152" diameter horizontal  duct which is  50 feet above the
     ground.  Sampling ports on the top and side of the duct allowed  for vertical
     and horizontal traverses of the duct during sampling.   The  nearest  upstream
     flow disturbance was a bend 90 feet (7 diameters)  away from the  sampling
     point.  The nearest downstream disturbance was a bend  100 feet (8 diameters)
     downstream.  Forty traverse points were chosen so that the  sampling period
     would coincide with that at the outlet from the baghouse.  Figure 1  is a
     diagram of the sampling location.

2)  Outlet from the Converter Building Fugitive Emissions Baghouse
     Samples from the outlet of the converter building fugitive  baghouse were
     taken from a 20' by 9' rectangular duct.  The duct was horizontal and
     the sampling point was 35 feet above the ground.  The  nearest upstream flow
     disturbance was 45 feet (3.5 equivalent diameters) away. The nearest down-
     stream disturbance was 12.5 feet (1 equivalent duct  diameter) away.  Ten
     traverse points were selected at each of the four sampling  ports.   Figure 2
     is a diagram of this location.

3)  Roaster Calcining Fugitive Emissions Duct
     The roaster calcining fugitive emissions were sampled  from  a 28.5  inch'
     diameter circular duct which was 15 feet above the ground and at a  10 degree
     angle to the horizontal.  The nearest upstream flow  disturbance was 75 feet
     away (32 diameters); the nearest downstream disturbance was 8 feet  away
     (3.5 diameters).  Twenty traverse points were selected for  sampling, ten  on
     each of the two traverses.  Figure  3  is a diagram of  this  sampling location.

4)  Outlet from the Roaster/Reverberatory Furnace Electrostatic  PrecipUator
     The duct exiting the roaster/reverberatory furnace electrostatic precipltator
     is a balloon shaped duct twenty-two feet high and twelve feet wide  at the
                                        -2Q-

-------
     top.   The nearest upstream disturbance was  50 feet (   4 diameters)  away;
     the nearest downstream disturbance was 20 feet (   1.5 diameters)  away.
     Sampling was done at 50 traverse points.   Figure   4  is the  plan view diagram
     of this sampling location.  Figure § illgstrates  the cross-sectioned view.
5)  Matte Tapping Reverbatory Furnace Outlet
     The fugitive emissions from the matte tapping reverbatory furnace were
     sampled from a 32.75" diameter horizontal  round duct.   The nearest upstream
     disturbance was 20 fe"et (6 diameters) away; the nearest downstream
     disturbance was 12 feet (4 diameters) away.  Sampling  was done at 24 traverse
     points on two traverses.  Figure 6  is a diagram of this sampling location.
                                      -21-

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                                              TRAVERSE POINT LOCATIONS
           152"
Tra-
verse
Point
Loca-
tions
1
2
3
4
5
6
7
8
9
10
Fraction of
Stack I.D.
0.026
0.082
0.146
0.226
0.342
0.658
0.774
0.854
0.918
0.974
Distance
From Inside
Wall (in)
4.0
12.5
22.2
34.4
52.0
100.0
117.6
129.8
139.5
148.0
    TO
BAGHOUSI
                              FIGURE  1.
           INLET TO CONVERTER FUGITIVE EMISSIONS BAGHOUSE
                                                              FROM

                                                            CONVERTER
                                 -22-

-------
      CROSS SECTION
                                 DISTANCE OF  SAMPLING POINT

                                         FROM PORT
                                              DISTANCE
                                                FROM
                                     TRAVERSE  INSIDE
                                      POINT   WALL (IN)
                SAMPLING POINT
1
2
3
4
5
6
7
8
9
10
12
36
60
84
108
132
156
180
204
228
                                          FROM BAG HOUSE
                         PLAN VIEW
FIGURE 2.  OUTLET FROM CONVERTER BUILDING FUGITIVE EMISSIONS BAGHOUSE

                              -23-

-------
                                                                    TRAVERSE POINT LOCATION
I
ro
TRAVERSE POINT
NUMBERS
1
2
3
4
5
6
7
8
9
10
FRACTION OF
STACK r.D.
0,026
0,082
0,146
0,226
0,342
0,658
0,774
0,851
0,918
0,974
DISTANCE FROM
INSIDE WALL (IN)
1,0
2,25
4,25
6,5
9,75
18,75
22,0
24,25
26,25
27.75
                                                                           FROM  CALCINING
                                                           SIDE VIEW
                                          TO SPRAY CHAMBER

                                          AND  ELECTROSTATIC  PRECIPITATOR


                              FIGURE  3.  ROASTER CALCINING FUGITIVE  EMISSIONS  DUCT

-------
        TO  MAIN STACK
             t
          o o  o  oo
        ELECTROSTATIC
        PRECIPITATOR
                           SAMPLING
                            'POINT
                          SPRAY
                         CHAMBER
PLAN VIEW

             FROM ROASTER/REVERBERATORY  FURNACE
 FIGURE 4.  OUTLET FROM THE ROASTER/REVERBERATORY  FURNACE ESP

                           -25-

-------
                                   4"  0,D,  PORTS
       CROSS SECTION VIEW
                                             22
OUTLET FROM ROASTER  REVERB SPRAY CHAMBER
   AND ELECTROSTATIC PRECIPITATOR
              -26-

-------
                                                             TRAVERSE POINT LOCATIONS
I
ro
Traverse
Point # .
1
2
3
4
5
6
7
8
9
10
11
12
Fraction of
Duct I.D.
0.021
0.067
0.118
0.177
0.250
0.356
0.644
0.750
0.823
0.882
0..933
0.979
Distance
From
Inside Wall
1.0
1.8
3.1
4.7
6.6
9.4
17.1
19.9
21.8
23.4
24.7
25.5
                                                     PLAN VIEW
                           TO MATTE TAPPING  BAGHOUSE
                              FIGURE 6.  MATTE TAPPING REVERBERATORY FURNACE OUTLET

-------
                     SAMPLING AND ANALYTICAL PROCEDURE

A)  Particulate Sampling
     Particulate sampling was performed according.to EPA Method 5,  as  revised
in the Federal Register, Volume 42, Number 160,  Thursday, August 18,  1977.
Figure  7 is a diagram of the sampling train used for the particulate  tests.
     Before each test a velocity traverse of the stack was done to  determine
the average stack temperature and velocity pressure.  The velocity  traverse
was done according to EPA Methods T and 2.  A grab sample of the stack gas  was
taken and analyzed with a Fryrite apparatus for  COp.  Before the first test at
each location the moisture content of the gas stream was estimated  by  either
condensation in impingers as in EPA Method 4, or by wet and dry bulb  thermometer
if the stack gas temperature was below 120°F.
     The particulate samples were taken at traverse points at the center of equal
areas within the stack.  The number of traverse  points was determined  by the
number of duct diameters upstream and downstream from the nearest flow disturbances.
The sampling rate was adjusted to isokinetic conditions using a nomograph which
had been set based on the preliminary velocity traverse data, and moisture  estimate.
     The sampling time per traverse point varied at different sampling locations
depending upon the particulate concentration in  the gas stream at each location.
The sampling times varied from 3 minutes to 5 minutes per traverse point.
     Leak checks of the sampling train were done at the beginning of each test,
just before the sampling port change, and at the end of the test.  At the end of
each test the sampling train was inspected for cracked or broken glassware,
and to assure that the filter remained intact.
Sample Recovery
     After completing the particulate test the sampling probe was removed from
the sampling train, the nozzle wiped off, and the probe rinsed into a  clean
sample container with acetone, using a nylon brush with a teflon handle to
scrub particulates out of the probe.  The filter holder of the sampling train was
then capped and the filter holder and impingers  were removed to the mobile
laboratory for sample recovery.

                                      -28-

-------
ro
10
                                                                                   12
                                                                                       13
                          FIGURE 7.    EPA  METHOD  5  PARTICULATE  SAMPLING TRAIN

-------
                                  KEY
 1.   Calibrated Nozzle
 2.   Heated Probe
 3.   Reverse Type Pi tot
 4.   Cyclone Assembly
 5.   Filter Holder
 6.   Heated Box
 7.   Ice Bath
 8.   Impinger - (Water)
 9.   Impinger - (Water)
10.   Impinger - (Water)
11.   Impinger - (Silica Gel)
12.   Thermometer
13.   Check Valve
14.   Vacuum Line
15.   Vacuum Gauge
16.   Main Valve
17.   Air Tight Pump
18.   By-Pass Va>ve
19.   Dry Test Meter
20.   Orifice
21.   Pi tot Manometer
                                   -29B-

-------
     The collected particulate sample was recovered and placed  in  four containers.
The participate filter was folded and placed in a polyethylene  jar and the  jar
was labeled and sealed.  The acetone rinse of the nozzle,  probe liner, and  front
half of the filter was placed in a 250ml  glass jar with teflon  lined  lid, labeled
and sealed.  The impinger solutions were measured, and placed in a glass jar
along with a water rinse of the impingers.  The front half of the  filter holder,
first three impingers, and connecting glassware were rinsed with acetone; this
rinse was placed in a glass jar with a teflon lid liner, sealed, and  labeled.
Analysis
     The front half acetone rinse and back half acetone rinse were placed in
tared glass beakers and evaporated.  The impinger solutions and water rinse
was extracted with ether and chloroform, and the fractions placed  in  separate
tared beakers and evaporated.  Aqueous fractions were dried on  a steam bath.  The
filter and tared beakers were then placed in a dessicator until they  reached a
constant weight and weighed to a tenth of a milligram.
B)  Particu1ate/Sulfur Pioxide Sampling
     Most of the particulate tests were done concurrently with sulfur dioxide
sampling.  This was accomplished by setting up the sampling train in the same
configuration as for Method 5 particul ate sampling, but replacing the water in
the first two impingers with 3% hydrogen peroxide.  Sulfur dioxide in the sampled
gas was oxidized to SO-" in these first two impingers.
Analysis
     The samples were analyzed for sulfur dioxide by taking an aliquot of the
hydrogen peroxide impinger solutions and titrating with barium perchlorate
solution and thorin indicator as described in EPA Method 6 (Determination of
Sulfur Dioxide Emissions from Stationary Sources).  The remainder of the impinger
solution was then analyzed for organic and inorganic fractions as described in  the
section on particulate sample analysis (Section A).  An aliquot factor was used
                                     -30-

-------
to account for the aliquot withheld for SCL analysis.   The amount of SC^
determined to be in the sample by Barium-Thorin titration was subtracted
from the amount of inorganic condensables determined gravimetrically.

C)  Arsenic Sampling
     The sampling train used for arsenic collection was an EPA Method 5
sampling train modified by adding three 'additional  impingers in series to the
four used in the Method 5 train.  The first two impingers contained 150 milliliters
of distilled water, the third was empty and the fourth, fifth and sixth
contained 200 milliliters of 10% hydrogen peroxide.  The seventh impinc/IN
•contained 200 grams of silica gel.
    "^
     The sampling procedure was identical with that used in Method 5 particulate
sampling.  The sampling was done isokinetically at the centers of equal areas
within the duct, sampling for the same amount of time at each point.

Sample Recovery
     The sampling nozzle and probe liner were rinsed with 0.1N NaOH and
brushed out with a nylon bristle brush with a teflon tubing handle.  The re-
mainder of the sampling train was removed to the mobile laboratory.  The front
half of the filter and connecting glassware were rinsed with 0.1N NaOH and this
rinse was added to the nozzle and probe rinse.  The filter was removed from the
filter holder and placed in a polyethylene container, which was labeled and
sealed.  The first two impinger solutions were measured and placed in a glass
sample container along with a 0.1N NaOH rinse of the impingers.  The contents of
the fourth, fifth and sixth impingers were measured and placed in a separate
glass sample container along with a 0.1N NaOH rinse of the impingers.  The
third impinger was rinsed with 0.1N NaOH and placed in a separate glass sample
container.  The silica gel in the seventh impinger was weighed to the nearest
gram, and regenerated.
                                      -31-

-------
Analysis
      1.   Filter - warm filter and loose participate matter with 50ml 0.1N NaOH
for about 15 minutes.  Add 10ml concentrated HN03 and bring to boil for 15
minutes.   Filter solution through no. 41 Whatman paper and wash with hot water.
.Evaporate filtrate, cool, redissolve in 5ml of 1:1 HNO-, transfer to a 50ml
volumetric flask and dilute.
      2.   Probe wash and  impinger solns.  These should be combined and a 200ml
sample withdrawn.  Add 10ml concentrated HN03 and evaporate to a few milliliters.
Redissolve with 5ml 1:1  HN03 and dilute to 50mls.  A reagent blank should be
carried through the same procedure.  The resulting blank solution should be used
in the dilution of standards to matrix match samples and standards.
      3.   All the samples prepared above should be screened by air/acetylene
flame.  The filter samples may require dilution with 0.8N HN03<  Impinger solu-
tions containing more than 25 mg/1 of arsenic should be diluted since linearity
decreases dramatically above that level.
      Since an entrained  hydrogen flame provides about five times as much sensitivity
as the air/acetylene flame, a matrix check of a sample in a hydrogen flame should
be carried out by the method of standard additions, and compared with a value
obtained  from matrix matched standards in a hydrogen flame.  If values are
comparable (- 5%) the air entrained hydrogen flame may be used.
      Due  to high concentrations of copper on the filter an air/acetylene flame
should always be used to dissociate any AsCu compounds stable in the cooler
hydrogen  flame.
      4.   For samples below the lmg/1 level, hydride generation is necessary.
An appropriate aliquot of digested sample in 0.8N HNO- containing less than
                                                     O
about lOug of arsenic is chosen (some screening may be necessary).  Five mis
of concentrated H2S04 is added to the sample which is then placed on a hot
plate until S03 fumes fill the flask.  A reduction in volume to about 5ml or
less may  be necessary.   This step removes HN03 which causes a violent reac-
tion when the reducing agent is added resulting in poor reproducibility and
lowered sensitivity by producing I2, N02 and possibly other species.
                                     -32-

-------
     One ml of 30% KI and 1ml  of 30% SnCl2 are added to the sample,  the former
to act as a catalyst in hydride formation and the latter to reduce all  the
             +3
arsenic to As  .   The sample is then diluted to about 15ml  and 15ml  of  concen^
trated HC1 is added.  Powdered Zn Cor NaBH^} is then added, the reaction vessel
is immediately closed and the  nitrogen or argon carrier fflow initiated.  A  peak
should be produced within a few seconds.
                                       -33-

-------
Particle Sizing
     The size distribution of the participates  was  estimated  with  a  Brinks  six ,
stage impactor.  Figure 8  is a diagram of the  Brinks impactor sampling system
used.
Sampling Procedure
     The Brinks impactor was introduced into the gas stream through  the sampling
port with the nozzle facing the flow of gas. The sampling pump was  turned  on
and the pressure drop across the impactor adjusted with the bypass valve.   The
pressure drop across the impactor was read from the mercury manometer.   The
pressure drop is proportional to the flowrate through the impactor and  to the
particle .sizing cutoffs of each stage.
     Sampling time at each location varied according to grain loading  in the
particular duct being sampled.  The impactor plates were inspected after each
test and the sampling time altered on the succeeding test to  optimize  the amount
of particulate sampled.  Sampling for too long  results in carryover  from one
stage to the next, while sampling for too short a time can result  in insufficient
particulate on one or more of the stages for accurate analysis.
Analysis
     The impactor plates and filters had been dessicated to a constant weight
before the tests, and tare weights taken.  After the test the same procedure
was used to get the final weights of the impactor plates and  filters.   The  dif-
ference between the tare weight and final weight is the weight of  particulate
collected.                        '              •        ,  : ",
     The cummulative percentage of the total particulate catch which was col-
lected in each  stage was plotted on log normal graph paper against  the size
cutoffs for each stage.  The resulting best fit straight line is the estimated
particle size distribution of the collected particulates.
1.  Brink, J.A. "Cascade Impactor for Adiabatic Measurements," Industrial  and
    Engineering Chemistry, Vol. 5, Mo. 4, April 1958, page 647.
                                    -34-

-------
i
CO
en
                     BRINKS  IMPACTOR
                            47 MM  GLASS FIBER  FILTER


                                     SHUT  OFF       ^-BY PASS VALVE
                                                                      ORIFICE
                               MERCURY

                              MANOMETER
                                              PUMP
DRY GAS

 METER
                                                                       MANOMETER
                        FIGURE 8.  BRINKS IMPACTOR PARTICLE SIZING SYSTEM  SCHEMATIC

-------
                         ERRATA SHEET
                             FOR
Report on Parti oil ate and Arsenic Emission Measurements from
                      a Copper Smelter
                   at the ASARCO Smelter in
                       El Paso, Texas
                   EPA Contract 68-02-2812
                     Work Assignment #7
                          Prepared  by:
               TRW  Energy  Systems Group
               Environmental  Engineering  Division
               One  Space Park
               Redondo Beach, California  90278

-------
     The changes that follow pertain to the tests for particulate performed
                      4  •    •                •               • p
at the Roaster and Reverberatory Dottrel! outlet which is a balloon flue
that joins the main stack at its base.
              •
                                                               2
     The area of the duct was incorrectly calculated at 180:ft,   Original
emission rates for this site in this report are erroneously high.  For
quick reference, the end of this errata sheet contains sampling summary
sheets giving correct emission factor for this site.

-------
                                CHANGES
Page 13. Table 10, Section II


                               2  2
     Change AS - Stack area, Ft (m )



          from 180 ft2 to 151 ft2



          from 16.2m2 to 14.03m2
        •. .  *


     Change:  (English Units).
                                                                            *
            •                                               •                 *

          Qa - Stack Gas Volumetric Flow at Stack Conditions. ACFM from:
           o                                      .                   .


          Run 1



          313092 to 262653



          Run 2



          319032 to 267636



          Run 3



          323892 to 271713



          Average



          318672 to 267334



     Change  (Metric Units)



          Q  - Stack Gas  Volumetric Flow at Stack Conditions  (N 3/min)  from:



          Run  1



          8869.5  to 7441



          Run  2



          9037.7  to 7582



          Run  3



          9175.4  to 7697



        .  Average



          9027.5  to 7573

-------
     Change:   (English  Units)
          Q   -  Stack  Gas  Volumetric  Flow  at  Standard  Conditions.   CDSCFM) from:
          Run 1
          200352.4 to 168076
          Run 2
          207295.2 to 173900
              •
          Run 3*                                                              :
          202650.9 to 170004
          Average
          203432.8 to 170660     '                       .   "
     Change:   (Metric Units)
          QS  -  Stack  Gas  Volumetric  Flow  at  Standard  Conditions  (Nm3/min) from:
          Run 1
          5673.4 to 4759
          Run 2
          5870.0 to 4924
          Run 3
          5738.5 to 4814
          Average
•
          5760.6 to 4833
Page 13, Table 10, Section V,(A) Front Half.
      Change:  (English Units)  #/Hr from:
          Run 1
          104.00 to .57.2
          Run 2
          160.74 to 134.8
          Run 3
          71.10 to 59.6
          Average
          111.95 to 93.9

-------
Section V (A).- Change:  (Metric Units)
     Kg/hr  from:
     Run 1
     47.27 to 39.7 .
        •• •  *
  '.'• Run 2
     73.06 to'61.3
     Run 3
     71.1 to 59.6
     Average                                            •   -
     50.88 to 42.7
Page 13, Table 10, Section V(B), Parttculates-Condensables, Organic
     Change:  (English Units) #/Hr from;
     Run 1
     No Change
     Run 2
     .41 to .34
     Run 3
     No Change
     Average
     .14 to .11
     Change:  (Metric  Units)  Kg/Hr
     Run 1
     No. Change
     Run 2
     .187 to  .157
     Run 3 •
     No Change
     Average
      .06  to  .05

-------
Page 13, Table 10, Section V(B), Particulates-Condensables,  Inorganic
     Change:  (English Units)  #/Hr from:
     Run 1
     76.15 to 63.9
     Run 2
     36.57 to 30.7
     t
     Run 3
     24.62 to 20.7
     Average
     45.78 to 38.4
     Change:  (Metric Units)  Kg/Hr from:
     Run 1
     34.62 to 29.0
     Run 2
     16.62 to 13.9
     Run 3
     11,19  to 9.4
     Average
 •  .       --
 '  .  20.81  to 17.5
 Page 13, Table  10,  Section  V(C),  Particulates-Total Condensables
     Change:   (English  Units)   #/Hr from;
     Run  1
     76.15  to 63.9
     Run 2
     36.98  to  31.0
     Run  3
     24.62  to  20.7
     Average
     45.92  to  38.5

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     Change:   (Metric Units)  Kg/Hr. from:
     Run 1
     34.62  to 29.04
     Run 2
        •. .  4
     T6.81  to 14.1
     Run 3
     11.19  to 9.4
     Average
     20.87  to 17.5
Page 13, Table 10, Section V(C), Total Participates
     Change:   (English Units)  #/Hr from:
     Run 1
     180.15 to 151.1
     Run 2
     197.72 to 165.7
     Run 3
     95.72  to 80.3
     Average
     157.86 to 132.4
     Change:  (Metric Units)  Kg/hr from;
     Run 1
     81.89 to 68.7   -
     Run 2
     89.87 to 75.4
     Run 3
     43.51  :to 36.5
     Average
     71.76 to 60.2

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Page 14, Table II, Section II, Stack Parameters
                                                                        3
     Change:  QA Stack Gas Volumetric Flow at Stack Conditions ACFM/ £Nm /min)
     Run 1 .
  .  . English Units - from 313092.0 to 262653
     Metric Units -  "from 8869.5 to 7441.
               •                                         .......         -  .
     Change:  Qs Stack Gas Volumetric Flow at Standard Conditions DSCFM (N  /min)
     Run 1
     English Units - from 200352,4 to 168076
   •  Metric Units  - from 5673.4 to 4759
Page 14, Table II, Section V(E), Total S02
     Change #/Hr   (Kg/Hr)   .
     English Units -  from 10154.48 to 8519
     Metric Units  -  from 4615.67 to 3872
Page 20, Paragraph 4
     Change dimensions on balloon flue from 22  feet high  to  20.6 feet  high
     and the width from  12 feet wide to  10 feet wide.
Page 26
     Change dimension on drawing from  12 feet to  10 feet  and from 22 feet
     to 20.6 feet.   See  attached drawing for actual dimensions.

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CROSS  SECTION
BALLOON FLUE
R ( K COTTRELL OUTLET
ASARCO SMELTER
   .  9A.50,  TEXAS

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