SFti Emission Reduction
Partnership for the Magnesium Industry
Characterization of Cover Gas and
Byproduct Emissions from
Secondary Magnesium
Ingot Casting at Advanced
Magnesium Alloys Corporation
(AMACOR)
Office of Air and Radiation
Office of Atmospheric Programs, Climate Change Division
-------
Characterization of Cover Gas and Byproduct Emissions from
Secondary Magnesium Ingot Casting at Advanced Magnesium Alloy
Corporation (AMACOR)
Prepared By:
ICF International
1725 Eye St., NW, Suite 1000
Washington, DC 20006
Industrial Monitoring and Control Corporation
800 Paloma Dr., Suite 100
Round Rock, TX 78665
Prepared For:
Kirsten Cappel
U.S. Environmental Protection Agency
Climate Change Division
1200 Pennsylvania Avenue, NW
Washington, DC 20460
June 2009
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Table of Contents
Page
Acknowledgement vi
Executive Summary ES-1
1.0 Introduction 1-1
2.0 Methodology 2-1
2.1 Principles of FTIR Monitoring 2-1
2.2 Principles of RGA Monitoring 2-6
2.3 Ambient Air Dilution Considerations 2-8
3.0 Monitoring Results 3-1
3.1 Casting Hood Monitoring 3-1
3.2 Worker Exposure Monitoring 3-5
4.0 Cover Gas Destruction 4-1
4.1 Determining Dilution 4-1
4.2 Determining Cover Gas Destruction 4-3
5.0 Discussion 5-1
5.1 Cover Gas Test Observations 5-1
5.2 Climate Change Potential Discussion 5-3
5.3 Uncertainty Discussion 5-4
Appendix A. Calibration and Diagnostic Checks A-l
Appendix B. Measurement Study Protocol B-l
in
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List of Tables
Page
ES-1 Cover Gas Average Concentrations and Observed Destruction ES-2
ES-2 Global Warming Potential of Alternative Cover Gas Mixtures ES-3
1-1 Test Schedule and Process Conditions 1-2
1-2 Magnesium Ingot Casting Machine Parameters 1-2
2-1 FTIR Analysis Method Parameters and Minimum Detection Limits 2-3
2-2 Extractive FTIR Configurations and Operating Parameters 2-4
2-3 Relative Isotopic Abundance for Argon and Neon 2-7
3-1 Data Summary for SF6 Cover Gas Mixture 3-2
3-2 Data Summary for MTG-Shield™ using Novec™ 612 3-3
3-3 Data Summary for S02 Cover Gas Mixture 3-4
3-4 Worker Exposure Monitoring 3-5
4-1 Average Concentrations of Neon and CO2 for Determining Dilution 4-2
4-2 Dilution Percentages (DP) Calculated by Ne Tracer and CO2 Measurement 4-3
4-3 Percent Destruction for Cover Gas Testing: Dilution Percent 4-4
5-1 Comparison of 100-year GWP Estimates from the Intergovernmental Panel on
Climate Change (IPCC) Second (1996) Assessment Report 5-3
5-2 Normalized GWP Comparison of Measured Emissions from Inside the Casting
Hood 5-6
5-3 GWP (Weighted by Flow Rate) Comparison of Measured Emissions from Inside the
Casting Hood 5-7
iv
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List of Figures
Page
2-1 Casting Hood and Sampling System Schematic 2-5
2-2 RGA Component Block Diagram 2-6
4-1 RGA Dilution Measurements, 18 December 2008 4-2
v
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Acknowledgements
The analytical measurements, data interpretation, and report preparations were funded by
the U.S. Environmental Protection Agency under contract EP-W-07-068 to ICF International.
The authors wish to express their appreciation and thanks to Advanced Magnesium Alloys
Corporation (AMACOR) and staff, especially Judge Morton, for contributing not only their
facilities but also their valuable assistance and advice to this measurement study. The support of
Polycontrols Inc. and 3M™ for providing the cover gases, their expertise, and trial staff for this
study is also gratefully acknowledged.
vi
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Executive Summary
To protect molten magnesium from oxidation, the cover gas sulfur hexafluoride (SF6) is
widely used throughout magnesium production and processing industry. The U.S. Environmental
Protection Agency (EPA) has set a goal of eliminating the use of SF6 for this application by
2010; and in order to support the achievement of this goal EPA has been evaluating the use of
alternative gases to serve the same function as SF6. The purpose of this study is to continue the
evaluation of greenhouse gas (GHG) emissions and occupational exposure associated with the
SF6 and alternative cover gas technologies. In this study cover gas emissions are continuously
monitored through multiple sample points, and cover gas mixtures are tested in an ingot casting
hood environment. An ingot casting machine located at the Advanced Magnesium Alloys
Corporation (AMACOR) facility in Anderson, Indiana was used to examine the use of SF6,
pentafluoroethylhepafluoro-isopropylketone (Novec™ 612), and sulfur dioxide (SO2).1 For each
cover gas regime tested, process and operating parameters were maintained at similar levels
through the evaluation process. Sampling locations were spaced throughout the hot and cold
zones of the ingot casting hood; which upon injection of each cover gas mixture, allows for the
characterization of the hood environment as the cover gases are interacting with the magnesium
melt surface and undergoing thermo-degradation. Results are presented for three sample points
in the casting hood: one in the cold zone and two in the hot zone. Details and results from
sampling in the casting hood are summarized in Table ES-1; the cover gas destruction rates have
been corrected for dilution effects.2
Observed Percent Destruction for Cover Gases
Destruction estimates calculated in this study were corrected for dilution effects (i.e., the
effects of air ingression into the ingot casting hood). For every cover gas that was tested, a
destruction estimate was determined by the percent difference between the expected dilution
corrected delivery concentration and the measured concentration in the casting area. These
corrected destruction estimates are shown in Table ES-1. Average destruction estimates for
Novec™ 612 and SF6 were on the order of 3.7 percent and 1.5 percent, respectively. Destruction
estimates for S02 were on the order of 5.9 percent for this study. It should be noted that high
levels of dilution found in this study and associated measurement uncertainty resulted in
calculated destruction rates for some tests being unreasonable (i.e., negative) and these values
were treated as zero destruction results.
1 Testing for dilute S02 was inhibited by technical difficulties with the gas mixing system in the very low
temperatures of the facility; this cover gas was only monitored for very brief periods of time.
2 The term destruction is utilized throughout the remainder of this report to represent the thermo-degradation and
disassociation of the cover gas agent resulting in byproduct formation and melt protection.
ES-1
-------
The destruction rates estimated for SF6 in this study were significantly lower than what
was estimated during previous research evaluating die casting holding furnaces (on the order of
20 to 30 percent). This is likely due to the much higher levels of dilution and reduced thermo-
chemical intensity of the casting hood environment. This result is consistent with the prior ingot
casting study that also found very low destruction rates for SF6.
Table ES-1. Cover Gas Average Concentrations and Observed Destruction
Test
Number
and
Location
Cover Gas
Mixture
Components
Flow3
(1pm)
Direct Cover
Gas Delivery
Conc.b
(ppmv)
Cover Gas
Measured
Cone, (ppmv)
Dilution
Percentage
(percent)
Estimated Cover
Gas Destruction
Factor0 (percent)
1CZ
sf6/cda
68
4241
723.9
83.7
4.4
1HZA
sf6/cda
132
4241
386.3
94.9
~0
1HZB
sf6/cda
132
4241
1022.7
85.2
~0
2CZ
Novec™
6I2/CDA/CO2
68
2172
376.6
83.7
2.9
2HZA
Novec™
6I2/CDA/CO2
132
2172
107.3
94.9
8.1
2HZB
Novec™
6I2/CDA/CO2
132
2172
429.4
85.2
~0
3CZ
so2/cda
68
20,000
2935.7
83.7
17.8
3HZA
so2/cda
132
20,000
1351.1
94.9
~0
3HZB
so2/cda
132
20,000
3177.1
85.2
~0
a Approximate, estimated by reading flow rates on gas delivery manifold rotameters (uncalibrated). It was assumed that 17% of
the total flow went to the cold zone, 33% went to hot zone A, 33% went to hot zone B, and the remaining 17%) went to a third hot
zone, which was not sampled in this experiment. The total flow to the casting hood was approximately 400 1pm.
b Measured directly at manifold; only for primary gases of concern (SF6, Novec™ 612, and S02) for the three cover gas systems.
c High levels of dilution resulted in the negative calculated destruction rates. These values were treated as zero destruction results.
Occupational Exposure Monitoring
Workers near the casting hood may be exposed to harmful emissions as a result of using
each cover gas; in particular the dilute SO2 or the possibility of the production of the byproduct
HF. Due to the stringent occupational exposure limits of these compounds, a sampling point was
situated near the hood viewing window in addition to inside the casting hood. This sampling,
which was preformed using a separate FTIR, continuously, monitored the ambient air near a
worker station for observing newly cast ingots in the hood. The results for the occupational
exposure monitoring undertaken during this study can be referenced in Table 3-4. SF6 was
detected during all cover gas runs, albeit in very small harmless concentrations (max = 1.034
ppmv). Novec™ 612, which has an Occupational Safety and Health Administration (OSHA)
Permissible Exposure Limit (PEL) of 150ppmv, was detected during the Novec™ 612 cover gas
runs at small, harmless concentrations (max = 2.761 ppmv). HF was detected only during the
Novec™ 612 runs at very small concentrations (max = 0.138 ppmv), well below the OSHA PEL
of 3.0 ppmv. SO2 was detected during the SO2 cover gas runs at 1.4 and 2.7 ppmv; SO2 was not
ES-2
-------
detected when SF6 or Novec™ 612 was the cover gas in use. The detection of SO2 above the
OSHA PEL of 2 ppmv highlights the safety concerns associated with usage of this cover gas.
Potential Climate Impact
The motivation behind this study is to determine viable alternative cover gases to SF6,
which has one of the highest composite global warming potentials (GWPs) known. Global
warming potentials are based on the heat-absorbing capability and atmospheric lifetime of each
gas relative to that of carbon dioxide. Since all GWPs are expressed in terms of carbon dioxide
equivalents, a basis for comparison of effects of various gases is created. An aggregate global
warming impact was determined for every cover gas and its associated destruction byproducts
through the utilization of the GWP values from the Intergovernmental Panel on Climate Change
(IPCC) Second Assessment Report (SAR).3 Using each cover gas regime's measured average
concentrations of each individual gas, their molecular weights, and the delivery cover gas flow
rate, the over total GWP-weighted gas emissions rate was determined. These total GWP-
weighted emissions rate, expressed in amount of CO2 equivalents, were then compared to the
amount of CO2 equivalent emissions of the current cover gas regime of SF6/CDA.
Based on this approach, results indicate that both the Novec™ 612 cover gas mixture and
the S02 cover gas mixture have a GHG emission impact - weighted by cover gas flow - that is at
least 99 percent lower than SF6. Results for the analysis of the GWPs of the two alternative
cover gas regimes, Novec™ 612 / CDA / C02 and S02 / CD A, are presented in Table ES-2.
Table ES-2. Global Warming Potential of Alternative Cover Gas Mixtures
Cover Gas Mixture
GHG Emissions Relative to
Existing SF6 system
(percent reduction)
Novec™ 612/CDA/C02
>99
S02 / CDA
100
3 IPCC, Climate Change 1996: The Scientific Basis. Intergovernmental Panel on Climate Change, 1996, Cambridge
University Press. Cambridge, U.K.
ES-3
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1. Introduction
The intent of this report is to summarize and interpret the results of an emissions
measurement study of air-entrained cover gas blends in a magnesium ingot casting hood. The
measurements were performed by Industrial Monitoring and Control Corporation (IMACC) on a
single magnesium alloy ingot casting machine at the Advanced Magnesium Alloys Corporation
(AMACOR) facility in Anderson, Indiana. The study was conducted over the course of the week
of 14 December 2008. Through the use of Fourier Transform Infrared (FTIR) Spectroscopy and
Quadrupole Mass Spectrometry (QMS), cover gas in the casting hood and ambient air were
monitored and analyzed in near-real time. Employing these measurement technologies allowed
for the simultaneous quantification of multiple concentrations in the cover gas environments at
ppmv-level sensitivities.
Cover gases are used in magnesium production to protect molten magnesium against
potential surface ignition or burning. This study analyzed three cover gas regimes, whose base
gases were sulfur hexafluoride (SF6), pentafluoroethylhepafluoroisopropylketone (known by
trade name Novec™ 612), and sulfur dioxide (S02). The primary objectives of this study are the
following.
• Characterize the cover gas destruction at this particular ingot casting tool. Destruction
rates of cover gases have an impact on the overall greenhouse gas (GHG) emissions from
magnesium casting. Destruction, which is the percentage of base cover gas consumed by
the process, may occur by breakdown to a magnesium fluoride (MgF2) film and
subsequent chemical byproducts, or by direct conversion to byproducts from the thermal
conditions and chemistries residing in the casting space environment.
• Characterize the ambient air dilution into the ingot casting and cooling environments.
The casting hood in both the hot zone and cold zone sections is not completely sealed, so
a considerable amount of air intrusion was expected to occur. To correctly report
destruction rate, which must be separated from overall concentration reductions, the
ambient air dilution must be factored into the cover gas consumption considerations.
• Characterize the chemical byproducts created for each cover gas mixture during ingot
casting. The base cover gas and the concentrations at which it is used can have a greatly
varied effect on the types and relative amounts of byproducts generated from casting.
Some byproducts may contribute to the overall global warming potential of the cover gas
mixtures.
• Identify and detect low concentration occupational exposure emissions for each cover gas
mixture. Using the most sensitive FTIR system available, monitor the casting hood
operator area for base cover gas and byproduct emissions.
1-1
-------
The measurement schedule and test conditions are summarized in Table 1-1. Rather than
being fixed, these conditions were what was encountered during facility operations at the time of
testing and resulted in a variety of cover gas mixture compositions over different alloy castings.
The ingot casting machine parameters are summarized in Table 1-2.
Table 1-1. Test Schedule and Process Conditions
Date
(mm/dd/yy)
Approx.
Casting Time
(Local Time)
Cover Gas Mixture
Components3
Approximate
Cover Gas
Mixture Flowsb
(1pm)
Base Cover
Gas Delivery
Conc.e
(ppmv)
Alloy Type
12/15/08
01:00-06:00
sf6/cda
400
4241
AM 60
12/15/08-12/16/08
23:15-03:15;
03:45-05:15
sf6/cda
400
4241
AM60
12/15/08
Noncasting run
sf6/cda
400
4241
AM 60
12/18/08-12/19/08
Dilution run
sf6/cda
400
4241
AZ 91
12/17/08
00:30-04:30
Novec-612/ CDA /C02
400
3300-1500
AM 60
12/17/08
Noncasting run
Novec-612/ CDA /C02
400
1650
AM 60
12/17/08-12/18/08
23:25-02:00
Novec-612/CDA/C02
400
1650
AM 60
12/15/08
23:45-00:00
S02 / CDA
400
20,000
AM 60
12/16/08
03:00-03:45
S02 / CDA
400
20,000
AM 60
a CDA = compressed dry air
b Approximate, estimated by reading flow rates on gas delivery manifold rotameters (uncalibrated)
c Either measured directly at cover gas mix (SF6), or calculated from flow settings (S02, Novec-612)
Table 1-2. Magnesium Ingot Casting Machine Parameters
Parameter
Machine Specification11
Facility
AMACOR: Anderson, IN
Ingot Casting Machine Type
Belt Caster
Ingot Weight (lbs)
25
Holding Furnace Capacity (lbs)
Continuous Flow
Alloy Type
All
Ingot Casting Rate (seconds/ingot)
10
Mg Pump Type
Centrifugal
Metal Throughput (lbs/hr)
8,000
Heat Casting Duration (hours)
6 (variable)
Ingot Mold Temperature (°F)
=120
Ingot Residence Time - Hot Zone (min)
~2
Ingot Residence Time - Cold Zone (min)
~2
Ingot Pour Control
Automatic
aAs provided by AMACOR
1-2
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2. Methodology
All gas samples from the casting hood environments and worker exposure area were
extracted continuously from single points in space. There were three sampling points inside the
casting hood, two in the hot zone and one in the cold zone. The hot zone was, in effect, divided
into two zones, one where the molten magnesium was poured into rotating casting molds and one
where the filled molds were conveyored through a partially enclosed hood with an observation
window before reaching the cold zone. A more detailed description of the sampling system may
be found in Section 2.1.2; the sampling schematic is presented as Figure 2-1.
In the following section of the report the method used to determine ambient air dilution
and the field analytical methods used to survey gas samples are presented. The two analytical
approaches used, FTIR and QMS, are explained in Sections 2.1 and 2.2 respectively.
2.1. Principles of FTIR Monitoring
FTIR monitoring is based on the principal that almost every chemical compound known
absorbs some amount of infrared (IR) light in a particular region of the mid-IR spectrum. A
compound's absorption properties can be used to classify and quantify a specific chemical in a
complex mixture of gases. Through Beer's Law an empirical relationship is developed between
the magnitude of the IR absorbance by a compound, and the optical depth of the compound.
Optical depth is the product of the sample cell optical path length and the concentration of that
specific compound in the gaseous mixture. With the use of extractive FTIR instrumentation
levels in the ppb are measurable. Detection of levels on this scale are achievable due to the
utilization of a series of mirrors in the measurement cell, which magnify the optical path length
by reflecting the IR beam within the cell numerous times before the detector is reached. Using
the series of mirrors, the optical path length in the FTIR measurement cell can be fixed to
provide a length that is optimal for the mixture of gases being tested. However, in the interest of
obtaining for each cover gas the most accurate quantifications over a linear dynamic
measurement range, the strongest fundamental absorption bands with the largest integrated areas
were chosen for analysis. Under the ppm to percentage level concentrations that the cover gases
existed within the casting hood environments very short path lengths were required to prevent IR
absorption saturation. Single pass sample cells without mirrors were used. As a result, optical
path lengths of 8 m (for worker exposure monitoring), 0.1m (for hot zone casting head space
monitoring), and 0.15 m (for cold zone casting head space monitoring) were utilized for this
study.
2-1
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2.1.1. The FTIR Spectrum Analysis Method
Analytical FTIR spectrum analysis utilizes an identification method that involves
matching the features of an observed spectrum to spectra of references gases whose
concentration path length products are known. In the case that multiple features are found within
one region, the compounds are quantified by using a linear combination of these references.
Standards of gases of known concentrations are scaled in accordance with the observed band
intensities in the sample, which is an action that helps to match the unknown concentrations. It
takes approximately one second to collect and analyze a sample. However, spectra are typically
averaged over longer integration periods of one to five minutes. This time enhanced averaging
allows for production of adequate signal to noise limits and sub-ppm detection levels.
The absorption spectra of scaled references are combined by matrix addition which, in
effect, produces a composite spectrum that best characterizes the sample. To match this reference
absorption profile to the observed spectrum of the sample in a specified region of spectral
analysis, a classic least squares mathematical fitting procedure is used. Within any analysis
region the compounds that are expected to cause spectral interference in addition to the target
compounds in question are included.
The spectrum analysis methods used for this study were developed by selecting the
spectral regions that were least affected by primary IR absorbers (in this case, H20 and CO2)
while also producing the best detection limits, accuracies, and linearities possible for cover gas
compounds and potential byproducts. Target compounds were determined prior to sampling
based on previous tests of similar cover gas compositions. The analysis methods were iteratively
refined by analyzing representative sets of IR spectra while varying quantitative analysis
parameters until optimum methods were established. Methods were optimum when the 95
percent confidence levels (the errors indicating goodness-of-fit) and the absolute bias of all
analytes were minimized. Table 2-1 lists the signal-to-noise limited detection limits, as they
pertain to their respective cover gas mixture for all the compounds considered in the AMACOR
casting hoods. Each analysis method has its respective compounds categorized according to
their primary spectral analysis regions. This represents a comprehensive list of potential and
existing contaminants, as well as potential process constituents (such as CH4, CO, C2H2 and
C2H4). The worker exposure monitoring system, which possessed a sample cell path length
almost two orders of magnitude longer than the casting hood sample cells, maintained detection
limits on the order of 100 times lower than those indicated in Table 2-1.
2-2
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Table 2-1. FTIR Analysis Method Parameters and Minimum Detection Limits, in ppmv,
within the Casting Hoods*
SFr/CDA Analysis Method
Spectral Analysis
Region
(wavenumbers)
sf6 mdl
HF MDL
ch4mdl
CO MDL
C2H2 MDL
c2h,mdl
840-1000
0.4
8.2
3990-4150
4.0
2073-2114
15.4
2876-3180
10
706-786
1.2
S02/CDA Analysis Method
Spectral Analysis
Region
(wavenumbers)
S02 MDL
h2so4
MDL
ch4mdl
CO MDL
C2H2 MDL
c2h,mdl
h2s
MDL
1091-1403
10.0
200
800-1000
100
8.2
2073-2114
15.4
2876-3180
10.0
706-786
1.2
Novec-612/CDA/CO;
Analysis Method
Spectral Analysis
Region
(wavenumbers)
Novec612
MDL
cof2
MDL
cf4
MDL
C2F6
MDL
HF
MDL
CO
MDL
co2
MDL
c2h2
MDL
c2h,
MDL
ch4
MDL
900-1020
41.7
8.2
1090-1400
2.3
0.2
4.5
3990-4150
4.0
706-786
1.2
2228-2282
167
2876-3180
10.0
2073-2114
15.4
*Atmospheric constituents (H20, C02 and N20) were subtracted out before SF6 or S02 analysis, to minimize spectral
interferences. C02 is a major component of the Novec-612 mix, so it is included in the quantitative analysis method.
2.1.2. The Extractive FTIR Systems
Three extractive FTIR systems were used in this study. A single FTIR spectrometer
provided modulated infrared (IR) radiation to two sample cells for simultaneous hot zone(s) and
worker exposure analysis. An IR beam splitter and appropriate focusing optics allowed optimal
signal-to-noise through-put from a cell designed for the relatively high concentrations (hundreds
of ppmv) at the hot zone casting hood environments, as well as from a cell designed for the
relatively low concentrations (sub-ppmv) outside the hoods. The simultaneous detection scheme
required special electronic triggering and signal processing incorporated in a software
application. A second FTIR spectrometer provided modulated IR radiation to another high
concentration sample cell for cold zone analysis. The FTIR/sample cell configurations and
spectrometer operating parameters are listed in Table 2-2 below:
2-3
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Table 2-2. Extractive FTIR Configurations and Operating Parameters
Hot Zones
Cold Zone
Worker Exposure
Cell Windows
ZnSe
ZnSe
ZnSe
Cell Material
Ni-Coated A1
Ni-Coated A1
Ni-Coated A1
Cell Volume
100 ml
150 ml
5 L
Pathlength
0.10m
0.15 m
7.2 m
Typical Cell Sampling Pressure
0.90 atm
0.90 atm
0.90 atm
Cell Temperature
35° C
35° C
35° C
IR Detector
HgCaTe (MCT)
MCT
MCT
Spectral Resolution
0.5 cm"1
0.5 cm"1
0.5 cm"1
Spectral Bandwidth
600 - 4500 cm"1
600-4500 cm"1
600 - 4500 cm"1
Sample Interval
120 sec
120 sec
120 sec
Number of scans per sample interval
64
64
64
Each FTIR sample cell had its own dedicated Fox model number 611210-030 mini-
eductor (venturi pump) that continuously pulled gas samples through it. Stainless steel sample
probes (3/8-inch outside diameter (OD)) were used to extract gas samples from the three casting
hood environments (hot zone at metal pour, hot zone at hood adjacent to metal pour, and cold
zone at hood adjacent to hot zone hood) to perfluoroalkoxy (PFA) Teflon lines (1/4-inch OD). A
single PFA line (H-inch OD) attached to the 8 meter sample cell system acted as the sample
probe at the worker exposure location. Flows on the order of 3 1pm were maintained through
each extraction system. Sample cell temperatures were maintained at 35°C. The switching of
sample streams from the hot zone at metal pour (hot zone "A") to the hot zone adjacent to metal
pour (hot zone "B") and vice versa was performed manually by turning a three-way valve for
periods of continuous sampling at each location. The sampling probe extended approximately 6-
12 inches into each casting hood, but it was elevated about a foot above the metal surfaces for
logistical reasons; the cover gas manifolds had prevented access close to the ingot molds.
Approximate dimensions and configurations are indicated in the sampling schematic (Figure 2-
1).
2-4
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Figure 2-1. Casting Hood and Sampling System Schematic
Slipstream Atmospheric
f j —— Sampling
RGA
FTlR
0.1 mcell
FTIR
0.15 fin cell
Casting Hood
Observation
Window
Conveyor Direction
HZA
CZ
HZB
FTIR
S m cell
Sampling Lines
¦ Cover Gas Nozzles
NOT TO SCALE
2-5
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2.2. Principles of RGA Monitoring
A mass spectrum is obtained by converting components of a sample into rapidly moving
gaseous ions and resolving them on the basis of their mass-to-charge ratios. The principles of
mass spectrometry are straightforward; a block diagram showing the major components of the
QMS based Residual Gas Analyzer (RGA) is displayed in Figure 2-2.
Figure 2-2. RGA Component Block Diagram
Sample
1Z
Chamber
Aperture
Inlet System
Ion Source
+
Mass Analyzer
+
Detector
Signal Processor
Vacuum
System
Vacuum
System
Data Archival and
Control
Descriptions of these components are included in Section 2.2.2. As molecules from the
sample are ionized in the analyzer chamber, the detector registers a response for a given mass-to-
charge (m/e) ratio at an intensity proportional to the absolute molecule count. The following
section reports the desired m/e ratios for argon and neon, which were monitored during dilution
measurements.
2.2.1. The RGA Spectrum Analysis Method
The RGA quadrupole mass analyzer breaks down molecules (or, in this case, the natural
atomic species argon or neon) into fragments of varying m/e ratios. Therefore the specific m/e
2-6
-------
for each compound of interest that leads to the greatest response at the detector was targeted.
Table 2-3 lists the relative isotopic abundances in nature for argon and neon.
Table 2-3. Relative Isotopic Abundances for Argon and Neon
Isotope
Accurate Mass
(amu)
Abundance
(percent)
36-Ar
35.967546
0.34
38-Ar
37.962732
0.063
40-Ar
39.962383
99.60
20-Ne
19.992439
90.60
21-Ne
20.993845
0.26
22-Ne
21.991384
9.20
According to the information in Table 2-2, the derived m/e value for the "parent" argon
ion is 40 and for neon is 20. As a result, rather than scanning across each m/e channel within its
measurement range of 2 to 100 amu, the analyzer was focused directly to either m/e = 40 or m/e
= 20. A few other m/e values were scanned during monitoring periods for diagnostic purposes,
including parent ions for nitrogen and oxygen. In order to enable measurements of dilution
percentage, the RGA detector response at a given m/e value (representative of the partial
pressure of a species) was ratioed against the total RGA chamber pressure at the same time, then
compared to the partial/total pressure at the same m/e when measuring the cover gas mixture
directly sans dilution. Dilution determinations are reported in Section 4.
2.2.2. The Extractive RGA System
Traditionally, mass spectrometers are used in a vacuum. Coupled with the development
of atmospheric samplers and closed ion sources, recent advancements of this technology have
enabled atmospheric sampling. The "high pressure" RGA used in this study is smaller, more
robust, and much more portable than its laboratory predecessors. Gas samples were brought to
the mass analyzer vacuum chamber as slip-streams from the FTIR sample inlets via a venturi
pump. The pump provided the sample matrix at less-than-atmospheric (-500 torr) pressures and
with small residence times within the sample line tubing. The venturi pump extraction region,
which is basically the inlet of the pump, was interfaced to the RGA sample chamber with a small
orifice valve that was manually tuned to maintain a reasonable leak rate into the sample chamber.
This orifice valve was separated from the mass analyzer chamber by a small diameter (< 100
|j,m) aperture. The inlet system was set to maintain a sample pressure of ~5 x 10"5 torr, which
was an increase of 2-3 orders of magnitude over the mass analyzer chamber background pressure
and which was maintained by turbomolecular pump. Detection sensitivities for argon and neon
of approximately 100 ppmv was achieved.
2-7
-------
The RGA detection system housed in the main (mass analyzer) chamber was a
Micropole™ mass analyzer manufactured by Horiba. It consisted of an integrated package that
operated a tungsten filament (the ionizer) coupled to a series of focusing lenses and a miniature
array of quadrupoles (the mass analyzer) that allowed the ions to strike a Faraday Cup (the
detector). The mass range for this analyzer was 2 to 100 amu with a resolution of 1 amu. A
RS232 digital interface to a laptop and appropriate software allowed continuous operation and
data archival.
2.3. Ambient Air Dilution Considerations
Though the ingot casting machine hot and cold zones were somewhat contained in a
hooded enclosure, they were not completely sealed. A significant amount of ambient air dilution
was anticipated and must be considered when computing destruction rates based on
concentration measurements. As a result, the ambient air dilution within the casting hood was
experimentally considered using three distinct approaches.
1) Neon tracer: A benefit of this was that neon background concentrations and cover
gas mixture contributions were negligible, thus minimizing dilution rate bias. A
challenge presented on-site involved providing adequate neon spiking flow rates
and RGA measurement sensitivity, since the overall cover gas flow rates into the
casting hoods were excessive.
2) Cover gas measurements during non-casting periods: Because casting operations at
AMACOR were constant while the cover gas was being applied, measurements
taken from the casting hood during normal testing conditions (a moving ingot mold
conveyer belt with metal present) could be compared to a situation with a moving
belt but no metal present. Since no magnesium was present in the casting hood
zones to react with or degrade the cover gas, any reduction in the concentration of
the cover gas constituents would be solely attributable to ambient air dilution. This
test was run once for the SF6 and Novec-612 cover gases (not the SO2). A potential
anticipated drawback to this procedure was that the ambient air/cover gas dilution
dynamics may be different in a casting hood without molten magnesium and its
resulting convective effects, though ingot molds are pre-heated. The dilution
estimates determined through this approach were then used to determine cover gas
destruction.
3) FTIR measurement of CO2 during Novec-612 casting runs: Given that the Novec-
612 cover gas mixture consisted of Novec-612 mixed with mostly CO2 (on the
order of 70 percent), and ambient air contains a negligible amount (several hundred
ppm) in comparison, a straight ratio of CO2 concentrations measured in the casting
hoods to CO2 concentrations measured directly from the cover gas mixing manifold
2-8
-------
was considered the most accurate approach to determining process dilution. The
potential impact of CO2 interaction with molten magnesium was considered not to
be a significant factor since the low surface areas and temperatures of the melt
surfaces should have a minimal effect on such a large concentration of gas. As a
result, continuous monitoring of CO2 within the casting hoods during ingot casting
runs provided direct and nonintrusive measurements of dilution under process
conditions.
2-9
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3. Monitoring Results
3.1. Casting Hood Monitoring
Each cover gas mixture has the potential to generate a variety of chemical byproducts that
are due to local thermal plasma effects near the ingot melt surfaces. The amount of air dilution
was expected to impact the type and relative amounts of these byproducts, but the extent of this
impact is not completely understood. For example, air dilution provides a source of hydrogen as
a chemical pathway so that fluorinated cover gas mixtures (SF6 and Novec™ 612) were expected
to produce a hydrogen fluoride (HF) byproduct. Also, the thermal plasmas within the local
volumes around each ingot mold were expected to break down the base cover gas mixture
components into reactive atomic and free radical species. These species would then recombine
into other byproducts that were mostly fluorinated. This would be especially true for Novec™
612 mixtures, as perfluorocarbons (PFCs) have previously been observed during tests conducted
on magnesium die casting holding furnaces.4
However, for this measurement study, the expected byproducts normally produced at
ppmv levels in holding furnaces were not analytically detected because of the small surface areas
of the magnesium melts and the high degree of dilution in the ingot casting hood. This result is
consistent with the findings from the previous measurement study on an ingot casting machine.
Table 3-1 summarizes the cover gas, ambient air, and combustion-type compounds and the
expected destruction byproducts for the SF6 cover gas runs. Unobserved compounds/byproducts
are reported as unknown values less than their FTIR Minimum Detection Limits (MDLs) listed
in Table 2-1. Table 3-2 summarizes the compounds for the Novec™ 612 cover gas runs and
Table 3-3 summarizes those for the SO2 cover gas mixture.
The monitoring results in the three tables provide a direct measurement of the cover gas
concentration being fed into the casting hood along with the minimum, average, and maximum
values recorded for the sample points inside the casting hood itself. The monitoring results for
inside the casting hood are grouped by test period.
It should be noted that the mixer used to deliver the dilute SO2 cover gas experienced
operational difficulties and measurements were only feasible for very brief periods of time. The
complications were believed to be due in part to the very low temperatures in the facility and
condensation of the gaseous SO2 in the mixer. The portable gas delivery systems used in these
trials are not as robust as what would be installed on a permanent basis for melt protection.
4 US EPA. Characterization of Emissions and Occupational Exposure Associated with Five Cover Gas
Technologies for Magnesium Die Casting, 2007
3-1
-------
Table 3-1. Data Summary for SF6 Cover Gas Mixture
Test Number
and Location
SFs(ppmv)
CO (ppmv)
CH4 (ppmv)
HF (ppmv)
c2H2
(ppmv)
C2H4
(ppmv)
Direct
4241
1HZA
Mill
273.2
Max
469.7
Avg
386.3
MDL
15.4
10.0
4.0
1.2
8.2
1HZB
Mill
895.5
Max
1120.2
Avg
1022.7
MDL
15.4
10.0
4.0
1.2
8.2
1CZ
Mill
657.3
Max
817.9
Avg
723.9
MDL
15.4
10.0
4.0
1.2
8.2
1HZA
noncast
Mill
161.6
Max
183.4
Avg
172.3
MDL
15.4
10.0
4.0
1.2
8.2
1HZB
noncast
Mill
810.0
Max
930.5
Avg
860.9
MDL
15.4
10.0
4.0
1.2
8.2
1CZ
noncast
Mill
819.4
Max
985.1
Avg
912.8
MDL
15.4
10.0
4.0
1.2
8.2
MDL is reported if the compound was not detected; all the byproducts listed met this criteria.
3-2
-------
Table 3-2. Data Summary for MTG-Shield™ using Novec™ 612
Test
Number
and
Location
Novec™
612
(ppmv)
co2
(%)
CO
(ppmv)
ch4
(ppmv)
HF
(ppmv)
cf4
(ppmv)
c2f6
(ppmv)
c2h2
(ppmv)
c2h4
(ppmv)
cof2
(ppmv)
Direct
2172.1
66.3
2HZA
Min
29.0
1.9
Max
173.8
5.0
Avg
107.3
3.6
MDL
15.4
10.0
4.0
0.2
4.5
1.2
8.2
41.7
2HZB
Mill
358.1
9.0
Max
452.9
10.4
Avg
429.4
9.9
MDL
15.4
10.0
4.0
0.2
4.5
1.2
8.2
41.7
2CZ
Mill
346.7
9.3
Max
398.4
10.4
Avg
376.6
9.7
MDL
15.4
10.0
4.0
0.2
4.5
1.2
8.2
41.7
2HZA
noncast
Mill
66.4
3.0
Max
77.2
3.4
Avg
72.8
3.2
MDL
15.4
10.0
4.0
0.2
4.5
1.2
8.2
41.7
2HZB
noncast
Mill
355.0
8.7
Max
412.2
10.0
Avg
392.5
9.6
MDL
15.4
10.0
4.0
0.2
4.5
1.2
8.2
41.7
2CZ
noncast
Mill
472.0
11.0
Max
526.0
12.3
Avg
500.3
11.8
MDL
15.4
10.0
4.0
0.2
4.5
1.2
8.2
41.7
MDL is reported if the compound was not detected; all the byproducts listed met this criteria.
3-3
-------
Table 3-3. Data Summary for S02 Cover Gas Mixture
Test Number
S02 (ppmv)
h2so4
ch4
CO
c2h2
C2H4
H2S
and Location
(ppmv)
(ppmv)
(ppmv)
(ppmv)
(ppmv)
(ppmv)
Direct
20,000
Mill
918.4
3HZA
Max
1603.3
Avg
1351.1
MDL
100
10.0
15.4
1.2
8.2
200
Mill
2794.8
3HZB
Max
3740.4
Avg
3177.1
MDL
100
10.0
15.4
1.2
8.2
200
Mill
2356.2
3CZ
Max
3249.4
Avg
2935.7
MDL
100
10.0
15.4
1.2
8.2
200
MDL is reported if the compound was not detected; all the byproducts listed met this criteria.
3-4
-------
3.2. Worker Exposure Monitoring
The cover gases evaluated in this study can produce byproducts that may be of concern
from an occupational exposure standpoint. Therefore, a long path (8 m) extractive FTIR system
was used to monitor the ambient air near the casting machine operator station (see Figure 2-1)
for any potential occupational exposure hazards associated with the usage of each cover gas. For
example, SO2 and HF have very low eight-hour time-weighted average exposure limits of 2 and
3 ppmv, respectively.5 The area above the observation window in the hot zone casting hood was
continuously monitored during the testing. Table 3-4 summarizes the concentrations observed,
as well as the pertinent MDLs for the compounds not detected, for those species present in the
casting hood at the highest concentrations - namely the primary cover gas compounds and the
most significant byproduct (HF). The spectra were surveyed for the appearance of features
attributable to compounds outside of those listed in Table 3-4 but none were observed besides
expected ambient air constituents.
Average ambient concentrations of SO2 directly above the viewing window of the casting
hood during two tests did indicate an occupational exposure concern as they were near or above
the permissible exposure limit (PEL) of 2 ppm.6 This is to be expected considering that
convection currents of cover gas escaping from the casting hood would be above the hood itself.
Similar to workers standing above a holding furnace using dilute SO2, special precautions would
need to be taken to ensure safety if a worker was in a position above the casting hood for a
prolonged period of time.
Table 3-4. Worker Exposure Monitoring
Date
(m/dd/yy)
Approx.
Casting Time
(Local Time)
Cover Gas Mixture
Components
Average SF6
(ppmv)
Average S02
(ppmv)
Average
Novec™ 612
(ppmv)
Average
HF
(ppmv)
12/15/08
01:00-06:00
sf6/cda
0.637
<0.1
<0.05
<0.05
12/16/08
00:00-03:00;
03:45-05:15
sf6/cda
1.034
<0.1
<0.05
<0.05
12/15/08
23:45-00:00
so2/cda
0.503
1.448
<0.05
<0.05
12/16/08
03:00-03:45
so2/cda
0.442
2.751
<0.05
<0.05
12/17/08
00:30-04:30
Novec™ 6I2/CDA/CO2
0.128
<0.1
0.282
0.138
12/17/08-
12/18/08
23:25-02:00
Novec™ 6I2/CDA/CO2
0.136
<0.1
2.761
0.091
Compounds listed with values as < X were not observed; their detection limits are reported as the value X.
n/a - not applicable
5 OSHA Permissible Exposure Limit (PELs), http://www.osha.gov
6 It should be noted that elevated levels of S02 cover gas (2 percent) were being used during these brief testing
periods due to complications with the mass flow controllers in the gas mixer. It is likely that a lower optimized
delivery concentration would reduce ambient concentrations found above the casting hood.
3-5
-------
4. Cover Gas Destruction
Throughout each casting run listed in Table 1-1, the primary cover gas components and
byproducts were quantified simultaneously at the casting hood hot zones and the cold zone (see
Figure 2-1). As the cold zone was continuously monitored throughout, roughly half of each
monitoring period was spent sampling the hot zone "A" port (metal pour); the other half was
spent at the hot zone "B" (hot casting hood) port. On some occasions, it was possible to monitor
at these sampling ports while the ingot casting conveyor was moving and still heated but with no
magnesium being poured: this was known as a "noncasting condition". In addition, on some
occasions it was possible to sample the cover gas composition at the outlet of the gas blending
manifold before injection into the casting hood. This was known as a "direct" cover gas mixture
measurement. Average concentrations over the sampling periods were then used to calculate
cover gas destruction percentages via the following approach:
Consider the injection cover gas concentration (after factoring in ambient air dilution)
versus the cover gas concentrations at the sampled locations. Calculate the destruction
factor (DF) as a percentage using
where DP is the dilution percentage, which was determined experimentally by CO2
measurements during Novec™ 612 runs or neon tracer testing, as reported in Section 4.1.
The concentration and DF results for each cover gas mixture are reported in section 4.2.
4.1. Determining Dilution
Figure 4-1 shows a plot of the RGA-measured concentrations, expressed as partial pressure
at m/e = 20 divided by total chamber pressure, for neon. This corresponded to a period of time
when a neon tracer was injected into the cover gas blending manifold with a flow producing
concentrations on the order of 2.5 percent. Notated on the graph is when the monitoring
occurred at a specific sampling location (cold zone, hot zone "A" at metal pour, hot zone "B"
within its hood and cover gas direct). Table 4-1 summarizes the average neon concentrations
and the average CO2 concentration results measured by FTIR during Novec™ 612 casting (an
excerpt of the data from Table 3-2).
DF = 100 x 1
sample cover gas conc. (ppm) 1
x
direct cover gas conc. (ppm)
4-1
-------
RGA Dilution Determination: Ne Tracer (m/e = 20 response at sample zones vs. direct cover gas mix)
0.040-,
Direct Cover Gas Mix Period
0.035-
0.030-
Hot Zone B Period
0.025-
O
0.020-
0.015-
Hot Zone A Period
0.010-
Cold Zone Period
0.005-
^-V^V/pvJ
6700
6800
0.000
6600
6900
7000
7100
Time (seconds from start)
Figure 4-1. RGA Dilution Measurements, 18 December 2008
Table 4-1. Average Concentrations of Neon and C02 for Determining Dilution
Sample Location
Average Neon (%)
Average C02 (%)
Direct
2.681
66.3
Cold Zone
0.168
9.7
Hot Zone "A"
0.028
3.6
Hot Zone "B"
0.524
9.9
4-2
-------
DP calculations were carried out accordingly:
DP = 100 x [1 - sample CCVneon (%) ^ direct CCVneon in cover gas mixture (%)]
The DP values at each location are reported in Table 4-2. Besides experimental
measurement uncertainties, more significant for the RGA (~±20 percent) than FTIR (~±10
percent), there may be inherent sampling variability due to ingot mold movement through the
casting hood and interactions with flows from cover gas nozzles. Still, reasonable agreement did
exist between the two measurement approaches, as indicated in Table 4-2. Dilution was
estimated to be significant, on the order of 80 percent to 98 percent depending on the zone and
calculation method used. Due to the significant variability found in the Ne tracer DP
calculations, the average of the lower of the CO2 measurement DP values was used to estimate
destruction.
Table 4-2. Dilution Percentages (DP) Calculated by Ne Tracer and C02 Measurement
Calculation Method
Cold Zone
(percent)
Hot Zone A
(percent)
Hot Zone B
(percent)
Ne Tracer
93.7(2.8)
98.9(1.1)
80.5(19.9)
C02 Measurement Noncast
82.2(1)
95.2(1)
85.5(1)
C02 Measurement Cast
85.3(1)
94.6(1)
85.0(1)
C02 Measurement Ave.
83.7
94.9
85.2
Parenthetical values represent (±) one absolute standard deviation.
4.2. Determining Cover Gas Destruction
Table 4-3 presents the cover gas flow rate, delivery concentration; FTIR measured
concentration, dilution percentage, and calculated DF value for each available sampling site for
each cover gas test. An average of the CO2 measurement dilution percentage values is presented
and used for estimating destruction. For SO2, a noncasting run was not conducted because of
logistical reasons. A direct sample of the SO2 cover gas composition was also not possible from
the temporary setup used during processing, so the direct SO2 concentrations were estimated by
calculation from the mass flow controller settings on the gas mixing system. DF values could be
determined somewhat reliably at the cold zone, and were 4.4 percent, 2.9 percent and 17.8
percent for SF6, Novec-612 and SO2, respectively, when calculated by CCVbased dilution
percentages.
Determining DF values involved several experimental measurements to derive
concentrations and DP values. As will be discussed in Section 5, the DF values determined by
dilution considerations carry significant uncertainties because the DP values are rather large and
contain significant variance. The DP values determined by CO2 measurements, possessing lower
4-3
-------
uncertainties than those determined by RGA, were utilized in the DF calculations. Also for this
particular study, the DF values determined by casting/noncasting considerations carry significant
variance because of sample port limitations from processing logistics (discussed in Section 5).
These variances resulted in the generation of negative destruction values in some cases because
the destruction is very low and near zero.
Table 4-3. Percent Destruction for Cover Gas Testing
Test
Number
and
Location
Cover Gas
Mixture
Components
Flow3
(1pm)
Direct Cover
Gas Delivery
Conc.b (ppmv)
Cover Gas
Measured
Cone,
(ppmv)
Dilution
Percentage
(percent)
Estimated Cover
Gas Destruction
Factor0
(percent)
1CZ
SFg/CDA
68
4240.9
723.9
83.7
4.4
1HZA
SFs/CDA
132
4240.9
386.3
94.9
~0
1HZB
SFs/CDA
132
4240.9
1022.7
85.2
~0
2CZ
Novec™
612/CDA/C02
68
2172.1
376.6
83.7
2.9
2HZA
Novec™
612/CDA/C02
132
2172.1
107.3
94.9
8.1
2HZB
Novec™
612/CDA/C02
132
2172.1
429.4
85.2
~0
3CZ
so2/cda
68
20,000
2935.7
83.7
17.8
3HZA
so2/cda
132
20,000
1351.1
94.9
~0
3HZB
so2/cda
132
20,000
3177.1
85.2
~0
a Approximate, estimated by reading flow rates on gas delivery manifold rotameters (uncalibrated). It was assumed that 17% of
the total flow went to the cold zone, 33% went to hot zone A, 33% went to hot zone B, and the remaining 17% went to a third hot
zone, which was not sampled in this experiment. The total flow to the casting hood was approximately 400 1pm.
b Measured directly at manifold; only for primary gases of concern (SF6, Novec™ 612, and S02) for the three cover gas systems.
c High levels of dilution resulted in the negative calculated destruction rates. These values were treated as zero
destruction results.
4-4
-------
5. Discussion
5.1. Cover Gas Test Observations
Compared to the die casting crucibles previously studied, the design of typical
magnesium ingot casting hoods suggested that the cover gas destruction would be low and
difficult to estimate due to increased ambient air dilution and variability. This assumption was
made due to the five factors listed below.
1. The overall surface area of molten magnesium to be covered in an ingot caster is
smaller than typical die casting crucibles. Assuming that about six ingot molds
containing molten metal are within the hot zone at the same time, and given that each
mold has a surface area of about 800 cm2, the total surface area of the covered molds
is about 4,800 cm2. A 1.2 meter diameter die casting crucible has a surface area of
about 12,000 cm2. A smaller covered surface area means that less of the cover gas is
coming into direct continuous contact than with a larger covered holding furnace.
2. The freshly poured ingots within the hot zone begin cooling immediately after
injection of molten magnesium. Alloying crucibles and holding furnaces must keep
the metal in a liquid state throughout processing. This implies that less cover gas will
interact and break down at the ingot surface as it cools, leading to lower destruction
rates.
3. The casting hood volumes are greatly affected by ambient air dilution. Excessive
dilution makes differential measurements difficult to carry out because the amount of
dilution must be precisely and consistently characterized.
4. The casting hood volumes are quite large and the ingot protection atmosphere is very
turbulent due to high cover gas flow rates and movement of the ingot molds. These
characteristics create difficulties for continuous real-time extraction of representative
gas samples, which makes analytical measurement precision challenging and greatly
influences destruction calculations.
5. The dilution dynamics with the casting hood are presumably different during ingot
casting, when molten metal is present, than during noncasting. Convection currents
due to heat emanating from the ingot surfaces could lead to stratification of cover gas
concentrations within the hood, making placement of the gas extraction probe
critically important (if not impossible) for representative sampling.
These factors were born-out in the actual measurement results. Several reasonable
estimations and observable trends can be gleaned from the results reported in Section 4. These
observations would include the following:
• Destruction was generally low under all cases, with the exception of SO2, which
exhibited the highest destruction percentages (17.8 percent at the cold zone).
5-1
-------
• Unrealistic, negative DF values were prevalent whether determined by dilution
percentages or casting versus noncasting. This is a product of very low or near zero
destruction and measurement uncertainty.
• Surprisingly, the most consistently reliable destruction percentages for both measurement
methods were calculated at the cold zone sampling location, where DF values should be
at their lowest.
For measurements during ingot casting, this study yields the following primary
recommendations for future research: (1) maximize the representativeness of concentration
analysis by setting up as many sampling points as possible for simultaneous gas extraction from
the casting hood, and then (2) characterize ambient air dilution effects by basing the destruction
calculations upon casting-versus-noncasting conditions. Instead of employing single point
extraction probes, an area monitoring scheme, such as open-path FTIR, could possibly be better
suited to averaging out stratification effects and dilution variability because the extent to which
(1) can be applied is highly dependent upon logistical and process concerns. For this study it
was not feasible to set up more than a single sampling port on the conveyor belt per casting hood
zone, and rather removed from the ingot surfaces, without interfering with process activities such
as metal pouring, cover gas manifold, and conveyor belt operation. An additional
recommendation is to account for air turbulence effects during monitoring periods. For example,
extend casting and noncasting events over longer continuous blocks of time to help smooth out
the averaging and subsequent comparison of concentrations during the casting-versus-noncasting
conditions. These analytic methodology improvements continue to be elusive given the
constraints of an operating foundry with limited resources and stringent production requirements.
One benefit of the low destruction values and profuse air dilution is that the
concentrations of cover gas byproducts were negligible within the casting hood and, by
extension, also within the operator (ambient) environment. The tables in Section 3 indicate that
the only measurable byproduct was HF and its average concentrations were well under 1 ppmv.
Sulfur dioxide was detected at concentrations of 2 ppm directly above the casting hood near the
ingot viewing window which indicates that occupational exposure concerns would need to be
addressed with operational procedures for staff.
This study also indicates that there is significant uncertainty regarding the exact mixture
of cover gas being applied using the current rotameter-based control system. Monitoring of the
cover gas system currently utilized at the facility indicates that there may be significant over-
protection occurring and that optimization to minimize cover gas usage would be achievable if
the current rotameter-based controls were replaced or upgraded to a more accurate and consistent
delivery control method.
5-2
-------
5.2. Climate Change Potential Discussion
One of the benefits of using Novec™ 612 or SO2 as cover gases for magnesium melt
protection is their contribution to global climate change is significantly lower when compared to
SF6. This is evident when comparing their estimated global warming potentials (GWPs). Table
5-1 presents the GWPs of the cover gases used in this study.
Table 5-1. Comparison of 100-Year GWP Estimates for
Cover Gases Tested during this Study
Gas
IPCC GWP
so2
0
Novec™ 612a
1
Sulfur Hexafluoride (SF6)b
23,900
a D'Anna B, Sellevag S.R., Wirtz K., and Nielsen C.J. Photolysis Study of
Perfluoro-2-methyl-3-pentanone Under Natural Sunlight Conditions
Environ Sci and Tech 2005 39(22) 8708-8711
b IPCC (1996), Climate Change 1996: The Scientific of Climate Change.
Intergovernmental Panel on Climate Change, Cambridge University Press.
Cambridge, U.K.
To compare the climate change potential of the alternative cover gases, the average
concentrations (parts per million by volume) for each of the component cover gases was
multiplied by their respective GWP factors (obtained from the Second Assessment Report of the
Intergovernmental Panel on Climate Change) to obtain a GWP-weighted value. The average of
the GWP-weighted values (or the "CO2 equivalent values") for each cover gas were then
compared to the average CO2 equivalent values corresponding to SF6.
Table 5-2 shows that when comparing the CO2 equivalent values, the alternate cover
gases have a much lower impact. The source for this reduction is the comparatively high GWP
of SF6 shown in Table 5-1. Novec™ 612's GWP is likely to be extremely low (i.e., Novec™
612 is assumed to have an atmospheric lifetime of approximately 5 days and a GWP of 1), and
the carrier gas CO2 has a GWP value of 1. Sulfur dioxide is not an IR absorber and therefore has
no global warming potential. Compared to using SF6, switching to Novec™ 612 with CO2 as a
carrier gas produces a reduction in overall global warming impact of at least 99.54 percent.7
Changing the cover gas from SF6 to SO2 reduces the global warming impact by 100 percent but
introduces a more complex operational scenario due to toxicity concerns. For reasons described
below this calculation assumed that no cover gas destruction byproducts were formed.
As described in Section 2 above, single-pass FTIR cells were used in the casting hood,
which allowed for accurate measurements down to the 1-10 ppmv level. This allowed for the
most accurate measurement of cover gas concentrations and the best estimate for the cover gas
destruction factors, but did not allow for the measurement of destruction byproducts at the ppb
level. For this reason a "sensitivity analysis" was done assuming that all possible byproducts
were detected at their minimum detection limit (see tables 3-1, 3-2, and 3-3). The sensitivity
7 Please refer to Section 5-3 for a discussion regarding the uncertainty associated with this methodology.
5-3
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analysis confirmed that, even using a liberal estimate of byproduct formation, byproducts have
very little influence on the overall normalized CO2 equivalent values. The Novec™ 612 cover
gas regime exhibited at least a 99.54 percent reduction from SF6, as it did assuming no byproduct
formation.
The above comparison does not include the specific flow rates for each cover gas. In
order to provide a more comprehensive analysis of composite GWP, an additional comparison
was conducted. Using the ideal gas law, the molecular weights of each gas and the delivery flow
rate of the cover gas was used to estimate the composite emission rate in grams per hour (g/hr).
This equation can be described as follows:
Emission Rate \ ^rams j = ppmv x MW x Ipm x ^ mm (3 8.6 liters / mole / 10' )
^ hour J hour
ppm = measured average concentration in parts per million
MW = molecular weight in grams per mole
lpm = gas flow in liters per minute
These values were multiplied by the appropriate GWP to provide the CO2 equivalent
value that was weighted by the cover gas flow rate. The average flow weighted CO2 equivalent
values were then compared against the corresponding values for the SF6/CDA system. Based on
this approach, Novec™ 612 with CO2 as a carrier gas was observed to reduce GHG emissions by
at least 99.87 percent relative to SF6. SO2 was observed to reduce GHG emissions by 100
percent relative to SF6. Details of the flow-weighted GHG emission impacts are presented in
Table 5-3.
A sensitivity analysis was also conducted for the flow rate-weighted CO2 equivalent
values. The normalized CO2 equivalent values, weighted by cover gas flow rate, for the
Novec™ 612 regime exhibited at least a 99.87 percent reduction from SF6, as it did assuming no
byproduct formation.
5.3. Uncertainty Discussion
The results of this measurement study should not be interpreted to represent an absolute
analysis of GHG emissions associated with Novec™ 612, SO2, and SF6 cover gas usage. While
this study does present a relatively accurate measurement analysis and approximate comparison
of GHG emissions, there are several areas of uncertainty inherent with this methodology. These
areas of uncertainty include FTIR and RGA error, error associated with blending gases, dilution
correction, and analytical and operational variation of the ingot casting machine evaluated. The
high levels of dilution - on the order of 90 percent - results in significant uncertainty associated
with destruction estimates.
5-4
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Measurements taken by the FTIR and RGA are subject to variability inherent with highly
complex analytical equipment. While all prudent steps were taken during the measurement study
to minimize this contributor to uncertainty (see Section 2 and Appendix A), a small degree of
error is unavoidable.
5-5
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Table 5-2. Normalized GWP Comparison of Measured Emissions from Inside the Casting Hood
Test Number
and Location
Cover Gas Mixture
Components
Cover Gas
Delivery Cone. a
(ppmv)
Cover Gas
Measured Cone,
(ppmv)
GWP
Weighted
Cover Gas"
GWP
Weighted
co2
Normalized C02
Equivalent
Average by
cover gas
Chg from
SF6(%)
1CZ
sf6/cda
4,241
723.9
17,300,904
0
17,300,904
16,992,448c
1HZA
sf6/cda
4,241
386.3
9,233,008
0
9,233,008
1HZB
sf6/cda
4,241
1,022.7
24,443,433
0
24,443,433
2CZ
Novec™
612/CDA/C02
2,172
376.6
376.6
97,000
97,376.6
77,638
>99%
2HZA
Novec™
6I2/CDA/CO2
2,172
107.3
107.3
36,000
36,107.3
2HZB
Novec™
6I2/CDA/CO2
2,172
429.4
429.4
99,000
99,429.4
3CZ
so2/cda
20,000
2,935.7
0
0
0
0.00
100%
3HZA
so2/cda
20,000
1,351.1
0
0
0
3HZB
so2/cda
20,000
3,177.1
0
0
0
a Measured directly at cover gas manifold
b GWP weighting based on dilution corrected concentration for the primary cover gas constituent (e.g., Novec™ 612, SF6)
c SF6 composite GWP baseline estimate for comparison with other tests.
5-6
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Table 5-3. GWP (Weighted by Cover Gas Flow) Comparison of Measured Emissions from Inside the Casting Hood
Test Number
and Location
Cover Gas Mixture
Components
Cover Gas
Delivery Cone. a
(ppm)
Cover Gas
Measured
Cone,
(ppm)
GWP
Weighted
Cover Gas"
(g/hr)
GWP Weighted
C02 (g/hr)
Normalized C02
GWP Equivalent
(g/hr)
Average by
cover gas
(g/hr)
Chg from
SF6 (%)
1CZ
sf6/cda
4,241
723.9
267,059
0
267,059
425,383c
1HZA
sf6/cda
4,241
386.3
276,660
0
276,660
1HZB
sf6/cda
4,241
1,022.7
732,429
0
732,429
2CZ
Novec™
612/CDA/C02
2,172
376.6
12.6
451.2
463.8
572.6
>99%
2HZA
Novec™
612/CDA/C02
2,172
107.3
7.0
325.1
332.1
2HZB
Novec™
6I2/CDA/CO2
2,172
429.4
27.9
894.0
921.9
3CZ
so2/cda
20,000
2,935.7
0
0
0
0
100%
3HZA
so2/cda
20,000
1,351.1
0
0
0
3HZB
so2/cda
20,000
3,177.1
0
0
0
a Measured directly at cover gas manifold
b GWP weighting based on dilution corrected concentration for the primary cover gas constituent (e.g., Novec™ 612, SF6)
c SF6 composite GWP baseline estimate for comparison with other tests.
5-7
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Appendix A - Calibrations and Diagnostic Checks
This section summarizes the on-site FTIR/RGA calibration and diagnostic procedures
carried out before and during the sampling tests.
A.1. FTIR Calibrations and System Checks
A series of on-site calibration and system checks was performed on each FTIR and
respective sampling system prior to testing to ensure data quality. These checks are described in
the remainder of this Section.
A.1.1. FTIR Sample Cell Integrity Checks
The integrity of each FTIR sample cell was confirmed prior to sampling by (1) drawing a
terminal vacuum of < 200 torr, then (2) sealing off the sample cell while still under vacuum, then
(3) monitoring any pressure rise (i.e., leak rate) within the cell by observing its pressure
transducer reading over a several-minute period. A cell was considered leak-tight when a leak
rate of < 2 torr min"1 was observed. The evacuated pressure on each FTIR sample cell did not
rise above measurable values over a 1-min period.
A.1.2. Infrared Detector Linearity Checks
For best results, the IR detector in each FTIR system must yield a linear response
throughout the measurement absorbance ranges within the measurement frequency range of all
sample spectra. An electronic linearizer circuit was used to continuously adjust the MCT
detector preamp signal to achieve the desired linear response. To optimize the linearizer,
background spectra were acquired with and without a polystyrene film in the IR beam.
Comparison of the strongly absorbing polystyrene bands in the low-, mid-, and high-frequency
regions against a clean background enables the user to appropriately set the linearizer trimpot.
This procedure was run prior to the start of testing for each FTIR detector, and subsequent
spectra were periodically visually checked to confirm that linearity was maintained.
A.1.3. Noise Equivalent Absorbance (NEA, or Signal-to-Noise Ratio) Tests
NEA tests provide a measure of system noise - more specifically, the sensitivity of the
instrument at the specified spectral resolution (in this case, 0.5 cm"1) and number of co-added
spectra (in this case, 64, or 2 min of signal averaging). A two-min FTIR spectral background
was recorded while the sample cell was purged with dry nitrogen. A subsequent "sample"
spectrum was recorded while the cell was still under nitrogen purge immediately after the
background recording. The two spectra were ratioed to provide a snapshot of instrumental noise.
The NEAs of all three FTIR systems were well below 0.001 absorbance units across all
measurement frequencies prior to sampling, which enabled instrument-limited quantitative
A-l
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analysis sensitivities in the l-100ppmv range (and a factor of 100 better for the long path FTIR
cell) to be achieved for all compounds of interest.
A.1.4. Path Length
The sample cells utilized for this study were geometrically fixed with an FTIR cold zone
system path length of 0.15 m and a hot zone(s) system path length of 0.1 m. The worker
exposure FTIR system contained an adjustable multi-pass White cell that was aligned, set, and
calibrated at a path length of 8 m.
A.1.5. Spectrometer Frequency and Resolution Checks
A real-time check of frequency position and resolution was performed at each FTIR prior
to and directly following each round of testing. These checks were performed by monitoring a
specific water absorption band present in ambient air. The position of this line must not deviate
more than ± 0.005 cm"1 from the reference value over the course of each test. Likewise, the
linewidth of this band, which is directly related to instrument resolution, must not deviate more
than ± 0.05 cm"1 from the reference value over the course of each test.
A.1.6. Spectral Background
A spectral background is essentially a "blank spectrum" in that it does not contain any of
the target compounds normally present in the sample. It was created by purging each cell with
either ambient air or ultra-high-purity (UHP) nitrogen while recording a spectrum. This
spectrum was then used by the analytical software to ratio against each sample spectrum to
produce an absorbance spectrum for quantitative analysis. A new spectral background was
generated each day prior to testing.
A.2. RGA Calibrations and System Checks
A series of on-site system checks was performed on the RGA and sampling system prior
to and during sampling to ensure high data quality. These checks and calibrations are described
in the remainder of this Section.
A.2.1. Sample Inlet and Mass Analyzer Chamber Pressures
Pressure was continuously monitored in the mtorr range via a thermocouple gauge within
the sample inlet chamber, which is considered to be the high pressure side of the chamber
aperture (see block diagram, Figure 2-2). The sample inlet chamber was directly interfaced to
the venturi pump-driven sample extraction line. The venturi pumping speed and valve orifice
maintained a constant pressure of 5 x 10"3 torr within the sample inlet chamber. Given a fixed
chamber aperture previously installed at URS, the 5 x 10"3 torr constant sample inlet chamber
pressure created a 5 x 10"5 torr total pressure within the mass analyzer chamber. Pressures were
continuously monitored by cold cathode gauge. When isolated from the sample inlet, total
A-2
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background chamber pressures (~5 x 10"8 torr) were 2-3 orders of magnitude less than this mass
analyzer chamber total pressure. These pressures allowed RGA sensitivities for neon of -100
ppmv at m/e = 20, as previously mentioned in Section 2.2.2.
A-3
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Appendix B - Measurement Study Protocol
The analytical measurement and data interpretation approach described herein attempts to
determine, by empirical means, the most conservative cover gas destruction possible for a given
type of magnesium process tool and gas flow ranges used during production. This approach is
based on the experience from the AMACOR study and pertains to only those processes that can
allow typical operation and cover gas flow without molten metal in place, as well as normally
with molten metal. Therefore, ingot casting and chilling machines are prime candidates for this
approach, as opposed to alloying and die casting crucibles which are often kept under constant
high temperatures and filled with metal. The approach encompasses all the measurement
variance brought about by the process gas flows (including turbulence invoked by ambient air
dilution) in conjunction with analytical instrument and sampling variability. The variances
associated with each measurement condition needed in calculating the degradation factor are
then properly propagated through the calculations to the final result. The maximum destruction
factor is thus considered by adding the propagated variance to the final calculation result. If the
process under study is normally run over a range of cover gas concentrations, this measurement
approach is to be conducted at both the lowest concentration and highest concentration of that
range; the reportable maximum destruction factor is then the greater of the two.
The Test Plan outlines how the experimental observables and variances needed to
determine the maximum degradation factors are obtained. The Quantitative Data Analysis
section describes how the measurements are used to estimate destruction factors and how the
variances are propagated. A hypothetical example is provided to help illustrate the measurement
approach.
Test Plan
1. Set up a real-time measurement instrument to continuously extract and analyze a low
volume slipstream of the completely blended cover gas mixture prior to injection into the
melt protection area. The extractive analysis technique should not significantly impact
the overall gas flow within normal process operations, and allow enough consecutively
recorded measurements as to be statistically relevant. For instance, an extractive FTIR
system monitoring SF6 concentrations over one-minute of signal averaging will produce
240 data points within a four-hour continuous sampling period.
B-l
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2. Set up a second real-time measurement instrument to continuously extract and analyze a
low volume stream of cover gas within the process environment (i.e., where molten
magnesium is to be covered during casting or chilling). The extractive analysis technique
at this sample location should not significantly impact the overall gas flow throughout the
process environment, should allow the most representative sampling configuration
possible (for instance, equidistant perforated sample probes that traverse the entire width
of process head space a few centimeters from the molten metal surfaces), and also allow
enough consecutively recorded measurements as to be statistically relevant. This
instrument will be sampling coincidentally with the instrument described in step #1, so
the implementation of two identical analysis techniques (for instance, two extractive
FTIR systems) is ideal.
3. With molten magnesium present during production: Simultaneously monitoring both
sampling locations over a sufficiently long time period will produce a mean concentration
during metal production at the point of cover gas injection, MP1, and a mean
concentration during metal production within the process environment, MPe. Also, the
99 percent confidence level of both means, which when expressing as +/- values about
the means would contain virtually all sources of indeterminate measurement error, can be
estimated as 2.58 times the standard deviations (divided by the square root of the number
of measurements) of their respective data sets. Hence, the experimentally determined
MP1/ MPe would carry associated 0\n>' / 0\n>° as total measurement uncertainties (the
squares of which being measurement variances) to be considered when calculating
degradation percentages.
4. With molten magnesium not present during mock production: Simultaneously monitoring
both sampling locations under the same configurations and over a similar length of time
as conducted in step #3 will produce, under nonmetal process conditions, an
experimentally determined NP7NPe pair and associated aNpV 0\-pe measurement
uncertainties. These are needed to effectively estimate the amount of ambient air dilution
present in an open process.
5. Steps #3 and #4 are to be repeated as necessary over the cover gas concentration ranges
utilized during normal production, presumably since the degradations may be
significantly different depending on mixture ratios. This typically means an experimental
B-2
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pair will be run at the lowest and the highest operating concentration, with the highest
destruction percentage reported to be conservative.
6. Standard analytical measurement protocols, pertaining to the technique of choice, must
be run to characterize instrumental accuracy and reproducibility for each experiment (in
effect, any determinate errors associated with the instruments are quantified). Typically,
this means a pre-test and post-test calibration run for all instruments to ensure accurate
and consistent measurements at both sampling locations for each metal/nonmetal test
condition.
Quantitative Data Analysis
• For the noncasting sampling period, the reduction of injected cover gas concentrations
represents only the ambient air dilution in the system because molten magnesium is not
present to react with the cover gas. Therefore,
NPe
Dilution = 1
NP'
• For the casting or metal present sampling period, the reduction of injected cover gas
concentrations represents the ambient air dilution plus destruction in the system, for
molten magnesium is present. Therefore,
MPe
\Degradation + Dilution] = 1
MP'
• To determine solely the destruction factor, DF:
NPe MPe
DF = [Degradation + Dilution] - Dilution = : (1)
NP1 MP'
• Since the sum of relative variances for each ratio yields the relative variance of the result
for each ratio in (1), and the sum of absolute variances for each term in (1) yields the
absolute variance of the difference of terms8, the variances of equation (1) can be
propagated and simplified to produce the variance associated with the destruction factor:
aDp2 Uj +
2 f AlT>e^ \2 ( A /fUesr
NPe°N,
+
NP'
Hence, the measurement uncertainty for DF is:
MPe°MP'
V MP'2 )
MP'
I MP'
B-3
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Example
The noncasting sampling period produced mean SF6 concentrations of 1000 ppmv and
500 ppmv for the cover gas injection point and process environment, respectively. The 99
percent confidence limit (basically, a multiple of the standard deviation) was 50 ppmv for each.
The subsequent metal sampling period produced mean SF6 concentrations of 1000 ppmv and 400
ppmv for the cover gas injection point and process environment, respectively. The 99 percent
confidence limit was also 50 ppmv for each. To summarize,
NP' = 1000 ppmv;
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