Oil Filter Final RPT
Oil Filter Final RPT
Suite 1300
Washington, DC 20036-4700
www.steel.org
January 2002
By
Metserv
Ralph M. Smailer, Principal Investigator
Gregory L. Dressel, Investigator
Jennifer Hsu Hill, Investigator
Metserv
9800 A McKnight Road
Suite 310
Pittsburgh, PA 15237-6006
Tel: (412) 348-0015
Fax: (412) 348-0017
E-mail: [email protected]
AISI Contract TRP-9
Project No. 0041
A Feasibility Study for Recycling Used Automotive Oil Filters in a Blast Furnace
Table of Contents
A Feasibility Study for Recycling Used Automotive Oil Filters in a Blast Furnace
This feasibility study has indicated that of the approximately 120,000 tons of low
residual steel available to be recycled from used oil filters (UOF’s), a maximum blast
furnace charge of 2% (40 lb/NTHM) of the burden may be anticipated for short term use
of a few months due to limited availability of the UOF’s. The oil contained in the most
readily processed UOF’s being properly hot drained and crushed is approximately 12%
to 14% by weight. This oil (and filter media) charged (about 10 lb/NTHM) will be
pyrolized into lighter hydrocarbons of 98% of the oil and media charge weight, resulting
in additional fuel gas of 68% (7 lb/NTHM) and a condensable hydrocarbon fraction of
30% (7 lb/NTHM), with the remaining 2% (1 lb/NTHM) resulting as carbon being added
into the burden.
Based upon the writer’s collected information and assessment of the calculations on
the pyrolysis of the motor oil, there does not appear to be any operational problems
relating to the recycling of UOF’s to the blast furnace. Any free draining of oil in the
transportation, handling, and storage of UOF’s prior to their charging must be contained.
Although, the EPA does not consider UOF’s hazardous, five states have enacted
legislation banning the placement of UOF’s into state landfills.
Upon reviewing the preliminary study work with steel plant personnel, it was learned
that one USA blast furnace operator has been routinely charging UOF’s at about 100
tons to 200 tons per month for many years. The current cost of these UOF’s is about
$30 per gross ton delivered to the company’s plant. Discussions with the company’s
operating and scrap purchasing personnel have indicated no adverse effect to their blast
furnace operation or in the handling and storage of the UOF’s with their specification of
“no free flowing oil”. The remaining oil content in these UOF’s is not presently known.
The following sections will provide detailed information regarding the generation rate
of used oil filters, their geographical disposition, and their potential quantities available
for recycling. Although the contained oil quantities are a relatively small percentage of
the blast furnace burden, extensive analysis and calculations have been done to indicate
the most probable result of the pyrolysis of the oil within the blast furnace. There does
not appear to be any toxic consideration as a result of this pyrolysis within the blast
furnace. However, a hydrocarbon condensate in the “gasoline” fraction will condense in
the blast furnace scrubber water and may require additional processing in the water
treatment system to remove the light oils from the condensate.
Used oil filters represent an additional source of high quality iron units that may be
effectively added to the charge of a blast furnace for beneficial value to the operator and
to the removal of this resource from landfills.
2.0 Introduction
This study is the result of a solicitation by the American Iron & Steel Institute for
“A Feasibility Study for Recycling Used Automotive Oil Filters in a Blast Furnace” as
dispatched by e-mail 11 May 2001. In the AISI, “Steel Technology Road Map”, March,
1998, section 3.2.3 AUTOMOTIVE, there is a commentary on recycling of automotive
scrap. Oil filters represented the greatest potential source of currently un-recycled
automotive steel scrap. The Steel Technology Roadmap indicated potential iron units of
65,000 tons from oil filters to be available. This is contrasted with more than 12,000,000
tons of shredded steel scrap from automobiles in 1994.1
There has been considerable work done over the past ten years concerning the
potential for recycling of used automotive oil filters. Professor K. D. Peaslee of the
University of Missouri-Rolla, Department of Metallurgical Engineering, has done a
significant amount work over many years regarding the potential for recycling of used
automotive oil filters. Much of this work is summarized in a current technical bulletin. 2
This AISI feasibility study has relied mainly on published work and information
gathering via the Internet to obtain the background information regarding the generation
rate and location of used oil filters (UOF’s) in the United States. This information is
presented in detail in the following sections of the study. A 100% recycling rate of
current UOF’s has the potential for 120,000 tons of steel to be available for recycling.
This is to be placed in perspective to the approximately 50,000,000 tons/year of blast
furnace iron production in the United States. Therefore, in the writer’s opinion, the most
likely maximum charging rate of UOF’s to the blast furnace would be less than 2% of the
burden.
Section 3.3 Composition, then focuses on the oil content of the UOF’s along with
any potential metals contamination. The results show the metal to be a high quality, low
residual source of iron units. Particular emphasis is placed on the pyrolysis of oil as the
UOF’s enter the blast furnace and become heated within the burden. This study will
show that 98% of the oil entering the blast furnace in the UOF will leave with the top gas
as both fuel gas and a condensable hydrocarbon fraction.
1
AISI, “Steel Technology Roadmap”, March 1998, section 2.2.3 A UTOMOTIVE, pg 77.
2
Technical Bulletin, “The Future of Used Oil Filter Recycling in Missouri: An Evaluation of Potential
Processes, Product Quality, Recycling Locations, and Economics”, February 15, 1997, K.D. Peaslee and
D.E. Roberts, II, University of Missouri-Rolla, Department of Metallurgical Engineering.
3
“Report of the Findings on the Waste Classification of Used Automotive Oil Filters”, The Convenient
Automotive Services Institute, April 1991.
discussions with the US Steel operators identified that they have been charging UOF’s
at the Gary Works for many years as indicated in section 8.0.
As an aid to assist persons who may not be familiar with the iron blast furnace, a
pictorial representation of the blast furnace process has been downloaded from the AISI
web site4 as shown below in Figure 1.
4
“The Process,” From “An Introduction to Blast Furnace Technology”, ATSI Engineering Services,
http://www.steel.org/learning/howmade/blast_furnace.htm, 12/17/2001.
Used oil filters are generated from a number of sources. Light duty pickup
trucks, derivatives thereof and automobiles generate the most oil filters. Other
applications producing used oil filters would be medium and heavy duty trucks,
stationary internal combustion engines, off road vehicles, motorcycles, construction
machinery, hydraulic power generation units, railroad locomotives, aircraft and auxiliary
power units.
A used oil filter is produced every time an oil filter in use is replaced with a new
filter. Very few oil lubrication filters are cleaned and reused. The current state of the art
filters are designed to trap particles as small as 8 to 10 microns in a fibrous media that
precludes flushing and regeneration. 5
Certain cars today have oil change indicators lights built into the instrument
cluster. An algorithm based on the number of engine starts, total engine revolutions,
miles driven, and etc., since the last oil change flashes a signal when an oil change is
needed. However, in order to keep the warranty in force, a driver needs to follow the
written recommendations included with the owner’s manual.
Lubricant analysis for predictive analysis of oil changes and engine conditions
has become a useful tool for railroads, automotive and trucks fleets and aircraft
businesses. On a regular basis, a sample of oil is taken from an internal combustion
engine and checked for viscosity, physical appearance, metal content, water, and
coolant contamination. 6 A major consumer of lubricating oil may set up a complete
laboratory while private analysis service for individual automobile owners are available
through the oil companies.7 While widespread adoption of this method would lead to
better prediction of a used oil filter generation rate, however cost and inconvenience
would preclude the normal owner of a motor vehicle from this service.
5
“AC Delco – Parts Information-Oil Filters-Ultraguard Gold,”
http://www.acdelco.com/pi_filt_oil_gold_feature.htm, 9/24/01
6
F.E. Lockwood and R. Dailey, “Lubricant Analysis,” Friction, Lubrication and Wear Analysis, 1992,
ASM Handbook, Vol. 18, pp. 299-312
7
“Online Sample Report, Oil Sampling Guidelines, ” http://www.thetakgroup.com/pennzoil-
quakerstate/pqs/login.asp, 10/25/01
On the one hand, the commercial oil change facilities are advocating more
frequent oil changes while on the other hand, there will be a large percentage of drivers
who greatly extend the mileage or time between oil filter changes.
In the USA and Puerto Rico in 1999 there were 222,564,582 registered motor
vehicles.8 This total includes all automobiles, trucks and motorcycles in private and
public service. The Oil Filter Recycling Council estimates that approximately
440,000,000 used oil filters will be generated in the USA in year 2001 while historical
trends indicate about a 1% increase per year; 9 this is roughly two oil filter changes for
every registered motor vehicle in the USA. The generation of 440,000,000 oil filters per
year seems reasonable given the number of registered motor vehicles and the fact that it
is impossible for one person to operate more than one vehicle at a time.
From 1998 to 1999 the oil filter-recycling rate increased from 33 to 50% as
indicated in a survey of filter recyclers.10 For year 2001 the Oil Filter Recycling Council
estimated a recycling rate of between 40 to 50%. 11 The recycling rate is dependent on
state laws and growth of oil change facilities sending filters to recyclers. The recycling
rate is expected to exhibit continued growth.
To predict the number of used oil filters generated for recycling in a blast furnace
up to the year 2005, one needs the total annual oil filter units of production and the
increase in recycling rates. A production rate increase of 1% per year is known. For
the purposes of this study, a 5% per year increase in recycling is assumed.
Year Total New Oil Filter Oil Filter Recycling Oil Filter Units
Units Rate Available for
Recycling
2001 440,000,000 50 % 220,000,000
2002 444,400,000 55 % 244,400,000
2003 448,800,000 60 % 269,300,000
2004 453,300,000 65 % 294,700,000
2005 457,900,000 70 % 320,500,000
In all 50 states and Puerto Rico disposal of motor oil on or in the ground is illegal.
Used oil filters are classified by the EPA as a non-hazardous material if they are not
terne plate (coated with a mixture of tin and lead). As a result all commercially available
8
“State Motor Vehicle Registration 1999 Table MV-1, ”
http://wwwcf.fhwa.dot.gov/ohim/hs99/tables/mv1.pdf, 10/25/2001
9
Brent Hazelett, ”Private Communications,” Oil Filter Manufacturers Council, September 25, 2001.
10
“Recycle Rate for Used Oil Filters.” http://www.filtercouncil.org/news/May2000.html, (Filter
Manufacturers Council, FMC PR 01-00, May 4, 2000).
11
Brent Hazelett, ”Private Communications,” Oil Filter Manufacturers Council, September 25, 2001.
oil filters are now provided with a galvanized or tinplate coating. Depending on state
laws, a “do it yourselfer” or oil change facility can dispose of properly drained used oil
filters in a landfill. Future improvements in oil filter recycling rates may be dependent on
eliminating landfills as a place of oil filter disposal and economic incentives for recycling
oil filters.
Wherever there are internal combustion engines, there are used oil filters. The
U.S. Department of Transportation compiles statistics on motor vehicle registrations by
state including Puerto Rico. By using the assumption of two oil filter changes per year
as was previously discussed and a 50 % recycling rate, one can estimate the number of
recyclable oil filters generated yearly in each state as shown in Appendix 1.
New oil filter weights vary considerably depending on the size of the filter. Listed
below are some designations and gross weights for oil filters, Table 2. The gross weight
includes all components including steel, filter media material and rubber.
Since there are over 100 different types of commercially available oil filters, a
weighted average weight would involve determining both the amount sold in each
category and individual weights. For purposes of this feasibility study a simple average
12
Brent Hazelett, ”Private Communications,” Oil Filter Manufacturers Council, September 25, 2001.
13
Nishaj Attassery, “Private Communications,” 16 Oct 2001, Email Letter, ArvinMeritor
14
Ibid
15
Mike Whitman, “Private Communications,” 12 Oct 2001, Fax Memo, Delphi Corporation
16
Ibid
of the above gross weights will be used as the basis for calculation. The gross average
weight includes all oil filter components for new filters.
Coated steels are used in oil filters. Tin plate or galvanized steels are used for
the can, top and bottom plates and center tube.17 18Wix, Delphi, Fram and ArvinMeritor
reported using tin plate and uncoated steels in their filters.19 20 21 22A coating of 0.25 lb.
tin per base box is usually specified for oil filter applications. 23 A base box is 31360
square inches. The tin coating is always applied to both sides of a sheet for an oil filter
application. This would mean that approximately 0.125 lb tin is present every 31360
square inches of surface area. This works out to a 15 micro inch thick tin coating on
each side.
If galvanized steel is specified for an oil filter the coating weight is usually 0.10 oz
per square foot of surface area for one side. 24 This means the zinc coating thickness is
275 micro inches per side. Zinc is electrolytically applied to both sides for oil filter
applications.
The cans for oil filters are made using a drawn and iron process. Steel thickness
will be reduced around 20% during the drawing operation. Likewise the coating
thickness is reduced 20 % at the same time. The amount of thickness reduction and
associated steel elongation is highly dependent on the design of the irons and dies used
in the process. Stamped parts such as the top and bottom plates will not experience
thickness reduction.
If an oil filter manufacturer uses galvanized steel for the can it is possible to
roughly estimate the weight of the zinc coating. Based on known zinc coating weights
per square foot, the weight of zinc may be determined, as shown in Appendix 4. The
information used to estimate the surface area of the can was obtained from a study of oil
filter construction and quality. 27 The estimate is based on the calculated surface area for
17
“Tin Plate,” http://www.weirton.com/products/tin/tinplate.html , 24 Sep 2001
18
“Weirzin,” http://www.weirton.com/products/galv/weirzin.html, 24 Sep 2001
19
Brent Hazellet, “Private Communications,” Oil Filter Manufacturers Council, 18 Oct 2001
20
Mike Whitman, “Private Communications,” 13 Oct 2001, Phone Message, Delphi Corporation
21
Scott Jacobs, “Private Communications,” 24 Oct 2001, Email Letter, Fram Brand, Honeywell Corp.
22
Nishaj Attassery, “Private Communications,” 16 Oct 2001, Email Letter, ArvinMeritor
23
Edward Adamczyk, “Private Communications,” Weirton Steel, Phone Message, 11 Oct 2001.
24
Ibid
25
Kent D. Peaslee, “Recycling Used Automotive Filters,” Journal of Metals, February, 1994, pg. 46
26
Harold E. McGannon, ed., The Making Shaping and Treating of Steel, (Pittsburgh: United States Steel,
1971), pg. 456
27
“Engine Oil Filter Study,” http://www.scuderiaciriani.com/rx7/oil_filter_study/, 11 Oct 2001.
both the inside and outside of the can, and the thickness reduction due to drawing and
original zinc coating weight.
Data was given for the cartridge cylinder dimensions in the study. The cartridge
is the filtration media element inside the can. Surrounding the filter media cartridge is
the can. By increasing the filter cartridge diameter and height by 10 and 20 %
respectively, the surface area of the can cylinder can be readily calculated.
Based on this calculation, an average filter using a zinc coating on the can will
contain 0.00369 lbs Zn (0.059 oz, 1.67 g). This would result in a minimum zinc content
of 0.54% in the average filter.
3.3.3 Fuels
When a filter is removed from an engine it contains oil. While there are various
methods for draining the filter prior to and after removal, some residual oil will always
remain as shown in Table 3. As measured by ArvinMeritor and Delphi, oil filters can hold
anywhere from 8 oz. (227 ml) to 22 oz (624 ml).28 29An average oil filter will contain
around 16 oz (liquid) of oil. 30 Just after removal, an improperly drained filter will contain
70 % of its original oil volume. Even after properly hot-draining a filter, studies have
shown that approximately 40% of the weight of a used filter remains due to used oil (6 to
8 ounces).31 Proper draining and crushing of used oil filters will remove up to 88 % of
the oil in a used filter. 32
The main parts of a disposable spin-on oil filter are the can, base plate, center
tube, top and bottom plates, springs, filter media cartridge and rubber gasket. In some
filters a dusting of Teflon is blown onto the rubber gasket. Corrosion proof TiO 2 based
paint is used to coat the outside of the filter for protection from the elements and brand
identification.
28
Nishaj Attassery, “Private Communications,” 16 Oct 2001, Email Letter, ArvinMeritor
29
Mike Whitman, “Private Communications,” 17 Oct 2001, Phone Message, Delphi Corporation
30
Brent Hazelett, ”Private Communications,” Oil Filter Manufacturers Council, September 25, 2001.
31
Ibid.
32
Kent D. Peaslee, “Recycling Used Automotive Filters,” Journal of Metals, February 1994, pg. 44.
33
Note: Lubricating Oil Specific Gravity can vary from 0.856 to 0.913. For purposes of this study a value
of 0.88 will be used. “Material Data Safety Sheet,” Havoline Motor Oil,
http://www.equivatexacomsds.com/rd/getsinglemsds.asp?ID=191113, 18 Sep 2001.
(1) The Filter Body or Can is a container for filter parts, which is made of steel
specifically designed to withstand the normal automotive operating environment
as well as start-up pressure surges. Weirton Steel lists the use of tinplate and
galvanized sheet steel for this application. 34
(2) The Base Plate is a thick metal plate which supports the filter and provides
secure engine mounting for easy spin on installation. This is normally made from
an uncoated hot or cold rolled low carbon steel.
(3) The Center Tube provides support to the filtering media. The center tube is
usually made out of tin plate or galvanized steel and perforated with holes to
allow the passage of oil.
(4) The Top and Bottom Plates are a metal disks positioned on the top and bottom of
the filter media. The plates are used to slightly compress and keep the filtration
media in proper position. They are usually made from tin plate or galvanized
steel.
(5) Springs are used in the anti backflow valve. The combination valve assembly
includes a pressure relief (bypass) valve to assure oil flow to the engine if the
filter should plug from extended use beyond the recommended service life or
when the weather is cold and the oil is thick and flows slowly. They are normally
made from plain carbon steel.
(6) The Filter Media Cartridge is the component of the system, in which the oil is
actually filtered to remove the particulate contamination. Almost all filter media is
made out of paper with a very small percentage made from synthetic fibers.
(7) The Gasket is the resilient rubber material (nitrile rubber) that provides a positive
seal between the filter and engine mount.
34
Weirton Steel Internet Site
35
Kent D. Peaslee and Darrell E. Roberts, “Characterization of used automotive oil filters for recycling,”
Resources, Conservation and Recycling 19 (1997), pg 86.
By adding up the weights for the steel components one finds that the weight of
steel in an average oil filter is 8.81 oz (249.8 g).
An energy value used by a major electrical provider is 133,000 Btu per gallon
for used motor oil.36 At a specific gravity of 0.88 this is approximately 18,000 Btu/lb of
used motor oil. Energy values for dry paper (filter media) typically average around
10,000 Btu/lb.37 Due to the small weights involved, energy values for the paint on the oil
filter and nitrile rubber gasket are minimal and will not be considered in this study.
Used oil filters obtained by recyclers are generally crushed into pucks, shredded,
or made into scrap bales. In many scrap-processing operations, a shredder, which
includes a hammermill, both shreds and pounds the pieces into mill nuggets.38 Oil flows
out of the shredder into a collector box. A magnetic drum is used to separate the ferro-
magnetic metallic parts from the paper element and rubber gasket. The metal parts can
then be screened into 1 in, 2 in, 3 in, 4 in or larger fragments. 39 40The paper is then sold
36
Santee Cooper Electric Utility, “GOFER, Give Oil For Energy Recovery,”
http://www.scgofer.org/about.html, November 12, 2001
37
Wisconsin Energy Bureau. “Paper Pellets for Industrial Fuel,” www.wifocusonenergy.com, November
11,2001.
38
Bill Vajdek, “Private Communications,” American Resource Recovery, Ltd., Maywood, IL, November
15, 2001
39
Tammi Jones, “Private Communications,” Commercial Filter Recycling, Los Angeles, California,
October 27, 2001.
40
Gregory C. Potter, “Private Communications,” Oil Filter Recyclers, Inc. Easton, IL, November 13, 2001.
to a waste heat generator. Apparent metallic bulk density after shredding is reported to
be about 37 lb/ ft 3.
Scrap baling is another method of processing used oil filters. Several scrap
processors use this method to supply used oil filter metallics to EAF shops. Apparent
bulk density for scrap bales was reported around 60 to 80 lb/ ft 3. Scrap bundles may be
as small as 1ft³ up to 2 ft³. This material would be too large for charging to a blast
furnace.
Another method is crushing the filters in a hydraulic press to form a “puck”. One
operator then “cooks” the pucks to drive off the remaining oil. 41 All dimensions of a filter
are reduced by about 50 % so the maximum dimension may range from 2 in up to 8 in.
Bulk density is around 40 to 45 lb/ ft 3 for this material. Another scrap dealer compresses
the filters into 45 lb, 10 in diameter cylinders with hemispherical tops.42
As an estimate, uncrushed filters may have an average cylinder size height of 4.5
in and a diameter of 3.5 inches at a weight of 10.89 oz. This gives a specific density for
an average filter of 27.2 lb/ft3. If the dry filters are put into steel barrel with an assumed
40 % void space, the apparent bulk density would be 16.3 lb/ ft3.
For charging to a blast furnace, used oil filters would need to be screened to
accommodate operators, unless size control is a part of the process. The scrap yard
processors indicated that it would be possible to give blast furnace operators a specified
size range of oil filters.
An oil filter is considered recycled when the metal portion of the filter is melted by
a steel producer or iron foundry and reused for new products. 43 The US Army has done
research into the disposal of used oil filters and the Steel Recycling Institute provided the
following list, to the US Army, of primary steel or foundry companies as possible sources
for melting used oil filters:44
41
Jim Nickerson, “Private Communications,” Nickro Recycling Inc., Pittsburg, TX, November 13, 2001.
42
Terry Jones, “Private Communications,” Bernell Recycling, Ranch Cucamonga, CA, November 14,
2001.
43
Brent Hazelett, “Private Communications,” Oil Filter Manufacturers Council November 9, 2001.
44
“Disposal of Terne-Plated and Non Terne-Plated Oil Filters,” http://chppm-
www.apgea.army.mil/hwmp/Factsheets/OilFilters.html, January, 2001.
The 2001 recycling rate at 220,000,000 UOF’s, or 50% is in the range of 87,000
tons to 115,000 tons depending on the residual oil content of Hot Drained and Crushed
UOF’s and Hot Drained UOF’s only. These recycled UOF’s are melted in iron foundry
cupolas and electric arc furnace steelmaking plants, with a small amount, at about 2,000
tons melted in the blast furnace (see section 8.1).
A summary of the relevant rules encompassing used oil filter disposal by state is
given in Appendix 4.
45
“Used Filter Management Regulations,” Oil Filter Manufacturers Council, http://filtercouncil.org/regs/
As of October 21, 2001 there are 19 separate steel plants with at least one
operating blast furnace as detailed in Table 5.
Most of the listed steel plants have multiple blast furnaces. Due to economic
surges and declines the steel plants will “light up” or “bank” blast furnaces as needed.
For calculations purposes in this study one blast furnace is always assumed to be able
to accept used oil filters at the various steel plants.
In North American blast furnace practice, the coke and iron ore represent about
85% of the operating costs of a net ton of hot metal (NTHM). The availability of
significant quantities of relatively low priced, imported coke results in an approximate
46
“Blast Furnace Roundup,” Iron and Steelmaker, Vol. 28, No. 8, August 2001, pp. 75-77.
equal cost sharing between the iron ore and the balance of imported coke and domestic
coke for the operating costs of the blast furnace.
4.2.1 Fuel
The dominant fuel to the blast furnace is coke. Other fuels are also utilized to
both enhance productivity and also to reduce fuel cost. These include injection of
pulverized coal or granulated coal, and the routine practice of heavy oil or tar injection
into the hot blast at the tuyers of the blast furnace. The air blast is preheated in the blast
furnace stoves to approximately 2,000°F, to create the combustion reaction within the
raceway of the blast furnace producing heat and releasing CO and H into the burden for
chemical reduction.
The coke is added with the burden charging equipment to the top of the furnace
and performs a vital role in maintaining a good permeability of the burden to facilitate a
high volume and uniformly distributed flow of gases through the burden with a minimal
pressure drop.
Besides the fuel value in the coke, the coke also provides many necessary
mechanical and physical characteristics to facilitate the free flow of gases through the
burden and to physically support the weight of the charge.
Iron oxide pellets provide the dominant source of iron units into the blast furnace.
Fluxed sinter, which may provide a means of recycling steel plant iron bearing wastes,
as well as steel making slag, both contribute additional iron units to the burden.
The most likely operating candidate for consideration of used oil filters into the
blast furnace would be an operation that currently has stockhouse bins allocated to the
charging of metallic materials.
4.2.3 Metallics
The majority of the metallic output from an iron blast furnace is derived from the
charging of iron ore in both lump and pellet form. Fine iron ores, and other plant waste
iron oxides may be agglomerated in a sintering process. In making the ingredients for
the sinter plant, additional fluxing agents may be deliberately added so as to incorporate
the flux materials within the sintered iron oxide charge.
Basic oxygen steel making slag contains a sufficient quantity of metallic steel
droplets contained within the slag to make recovery worthwhile. The recovery of this
metal from steel making slag is often referred to as “B scrap”. Depending upon
free flowing characteristics for the furnace charge. The addition of metallic materials into
the blast furnace usually represents a minor portion of the charge, commonly less than
20% to 2%.
4.2.4 Fluxes
Limestone has been the traditional fluxing agent to the blast furnaces along with
gravel containing silica. In some operations, the limestone and silica are substituted by
fluxed sinter, fluxed pellets, or a portion of steel making slag components recycled to the
blast furnace.
The charging of UOF’s to the blast furnace does not appear to indicate any
change to current flux practices. This is because the UOF’s do not contain any
appreciable quantities of either acidic or basic oxides that would offset the chemical
balance of the blast furnace slag.
4.2.5 Production
The average production rate of USA blast furnaces is about 1.5 million tons per
year each. At 90% of calendar days available for production, this would average 4,570
tons per day for a typical blast furnace.
The above-mentioned “B” scrap (metallic droplets recovered from steel making
slag) is commonly utilized in a range of 40-80 lb/NTHM, or about 2% to 4% of the
metallic output. The study assumes a reasonable upper limit for the charging of UOF’s
to the blast furnace of 2%, or 40 lb/NTHM.
The average blast furnace would produce slag at the rate of about 4,570
NTHM/d. A typical hot metal chemistry is shown in Table 6.47
C 4.50%
Fe 94.29%
Si 0.60%
P 0.049%
Mn 0.51%
S 0.052%
47
D. Wakelin, “The Making, Shaping, and Treating of Steel “, 11th Edition, Ironmaking Volume, p751,
AISE Steel Foundation, 1999.
The average blast furnace can be expected to produce about 1,020 t/day. Slag
would have the approximate chemistry as shown in Table 7.48
SiO 2 37.73%
Al2 O3 8.99%
CaO 39.73%
MgO 10.45%
MnO 0.97%
S 1.45%
The blast furnace top gas leaves the furnace at a temperature of approximately
300°F to 400°F. The gas is directed into a dust collector where in the lager particles of
dust are trapped before the gas is further directed into a high intensity wet scrubber for
removing the bulk of the particulate.
The major use of contact process water is in the scrubber system of the venturi
scrubber. Approximately 3,200 gal/NTHM of water is re-circulated in the process. This
water is directed first to a thickener, with 96% of water re-circulated back to the process
after passing through a cooling tower or heat exchanger. Effluent water from the
process of about 70 gal/NTHM goes to a wastewater treatment plant for processing to
meet environmental criteria for discharge.
At a 100 % recycling rate, 122,500 tons of steel from used oil filters are available
for recycling and if 19 blast furnaces are available, this would mean that each steel plant
would melt 6447 tons of oil filters per year. The average annual production rate of 36
listed blast furnaces is 1.49 million tons. This average includes currently banked blast
furnaces. On this basis, an average blast furnace could expect used oil filters to
constitute less than 0.43 % of the total hot metal output depending on yield. Based on
the current 50% recycle rate, steel from used oil filters would constitute less than 0.22 %
of the annual hot metal output.
furnaces operating west of the Mississippi River. Geneva Steel located in Vineyard,
Utah has three blast furnaces but only No. 2 with an annual production rate of 1.3 million
tons is listed as currently operating as of October 21, 2001. Oil filters from Hawaii,
Alaska, Washington, Oregon, California (California has 12 % of the total registered
motor vehicles in the USA), Idaho, Nevada, Arizona, Montana, Wyoming, Colorado and
New Mexico could be shipped to Geneva Steel. This would be a total of 86,739,696
units or 19.5 % of the total used filters generated in the USA each year at a 100 %
recycling rate. The gross weight of the filters would be 27,106 tons while the steel
content would be 23,881 tons. The steel charge weight of used oil filters would
constitute less than 1.84 % of the annual hot metal output. At a recycling rate of 50 %
the steel content of used oil filters would make up less than 0.92 % of the annual hot
metal output.
In Table 8, the charging weights and percentages of the itemized oil filter
components are calculated for an even distribution to 19 blast furnaces. A skewed
distribution-charging pattern of oil filters obtained from the Western States to only one
blast furnace is used as a worst-case scenario. Table 8 is based on a 50 % recycling
rate using current rates of oil filter generation.
Table 8: Charging Weights and Percentages of Used Average Oil Filter Components at a 50 %
Recycling Rate Based on Current Oil Filter Generation Data
48
Assumed 0.030 % Sn in melted steel components, which exhibited a 76 % metallic yield.
The writers recognize that it is not cost effective to consider shipping oil filters
from remote distances to a blast furnace, unless economic incentives are provided to
facilitate overcoming the transportation cost disadvantage. The major advantage for
blast furnace operators using UOF’s would be the low cost of quality iron units.
49
Assumed 0.030 % Sn in melted steel components, which exhibited a 76 % metallic yield.
The typical blast furnace requires approximately 2 tons of solid charged materials
for each net ton of hot metal (NTHM) produced. A nominal blast furnace operation will
handle 9,000 t/day of bulk materials.
The blast furnace raw materials are normally delivered to the site in railroad cars
which are then unloaded either directly into material bins by bottom discharge, or
through a series of conveyor belt transfer into the blast furnace stockhouse bins.
The potential recycling of used automotive filters into the blast furnace will
require that the UOF’s be compatible with the overall bulk material handling system.
This includes factors such as free flowing through gates and bins, sizing compatible with
bin flow and gate control devices, screens, and sufficient density to avoid being removed
from the top of the furnace by the velocity of the top gases.
A major consideration is the degree to which oil may be discharged from used oil
filters while being stored in bins prior to entering the furnace. Any oil that may leak from
the filters into the bin poses a potential problem of dripping from the bottom of the bins
(which are only designed to contain solids, not liquids) and may find its way into the
drainage system beneath the stockhouse. This would create additional problems of
wastewater treatment to remove any contained used motor oil from the drainage
collection system.
UOF’s, which have been properly drained, still contain about 40% by weight
motor oil. Additionally the low bulk density at about 16.3 lb/ft3 would occupy excessive
volume in the skip-charging car to the furnace. Excess oil leaking from the filters would
cause significant oil contamination problems in the material handling system.
The properly drained and crushed UOF’s would represent the least cost
processing for recycling to the blast furnace, although it still contains approximately 13%
oil in the filter media. Further observation will be required to see whether or not such
crushed and drained UOF’s would continue to leak amounts of oil that would considered
excessive by the blast furnace operator.
UOF’s, which have been shredded and the non-metallic materials removed,
would have oil content of less than 2% (mainly surface adhering oil) but would be too low
in density to remain within the furnace due to the high top gas velocity. Additional
compressing of shredded oil filter metallics would be required to achieve the density
necessary for blast furnace operations, although this entails additional processing costs.
This feasibility study for recycling used oil filters in the iron blast furnace was
based upon two main factors: the recovery of iron units from the steel container, and the
potential recovery of energy from the contained motor oil. The only fuel routinely added
to the top of a blast furnace is coke. Coke, as a result of the pyrolysis of coal in coke
oven plants, does not have any appreciable remaining volatility. Other fuels used in the
blast furnace include tar, fuel oil, granulated and pulverized coal, and natural gas: all of
which are injected along with the hot blast through the tuyeres.
Also shown in Figure 2, the box shape, which represents a UOF, entering the top
of the furnace, undergoing pyrolysis, and ultimately melting into the liquid iron bath at
around 7 hours schematically represents the position of used oil filters in the blast
furnace as a function of time.
50
R. Jeschar, A Theoretical Model Coupling Kinetics of Ore Reduction and Coke Gasification in Cocurrent
and Countercurrent Reactors, Fifth International Iron and Steel Congress, Washington, April 6-9, p 992,
Iron & Steel Society, 1986.
51
A. Poos, and N. Pongjis, 1994 Turkdogan Symposium Proceedings, Application of Process Models for
the design of an Optimized Blast Furnace Process, p 45, Iron & Steel Society, 1994.
400°F (200°C)
0 Hours
750°F (400°C)
1 Hours
1110°F (600°C)
2 Hours
1470°F (800°C)
70 ft 3 Hours
1560°F (850°C)
4 Hours
1650°F (900°C)
5 Hours
1830°F (1000°C)
6 Hours
2190°F (1200°C)
7 Hours
30 ft
2820°F
Tuyere (1550°C)
8 Hours
Tap Hole
Item 0 Hr 1 Hr 2 Hr 3 Hr 4 Hr 5 Hr 6 Hr 7 Hr 8 Hr
Temp°F 400 750 1110 1470 1560 1650 1830 2190 2820
CO % 24 24 30 32.2 34 41.2 43.6 39.6 40
CO2% 21 21 15 12.9 11.2 4.1 1.8 .4 0
H2% 2.5 2.5 2.5 2.4 2.3 2.2 2.1 2 2
N2% 52.5 52.5 52.5 52.5 52.5 52.5 52.5 58 58
Total 100 100 100 100 100 100 100 100 100
Fresh Motor Oils typically contain C18 to C32 paraffinic, napthenic and aromatic
hydrocarbons with boiling points starting around 620 °F. 52 The ingredients of three
different brands of motor oil are given in Table 10.
53
Table 10: Ingredients of Fresh Motor Oil
Table 10 shows that fresh motor oil consists of primarily paraffins, which are non-
cyclic, saturated hydrocarbons. The effects of additives were not considered in this
study since they make up a small percentage of the oil.
An analysis of the composition of used motor oil is shown in Table 11. Used Motor Oils
contain heavy polycyclic aromatic hydrocarbons (PAHs), which are aromatics with two or
more rings. The structure of some of the PAHs is shown in Appendix 7.
Some PAHs are known carcinogens although for many others the effects are not
determined. Shown in Table 12, is the concentration of various PAHs found in a sample
of motor oil. The total PAH concentration in this sample is low, 0.17%, and most of the
PAHs have high boiling points, and so will remain in the furnace until they have broken
down. Table 13 shows the metal content of used oil, and Table 14 shows the nitrogen
and sulfur content.
The chemistry of used motor oil is highly variable. To assist the reader in this
regard, Table 15: Compositions of Used Oil and Other Fuels, has been partially
reproduced to illustrate a sampling of Virgin Lube, Used Gasoline Engine Oil, and Used
Diesel Engine Oil.
52
Robert A. Meyers. Environmental Analysis and Remediation, v. 6. John Wiley & Sons, New York,
1998. p. 3669
53
Internet
The time of acquisition of used motor oil samples for chemical analysis that is
referenced in a later section is not known. Although the early references to toxicology of
used motor oil make an inferred relationship to studies involving fresh water trout
species and PAH’s compounds (polycyclic aromatic hydrocarbons), the very high lead
content may also be a toxicity factor. This is discussed in section 4.3.3.1.1, composition
of properties in motor oil.
The lead content shown in Table 15 at 47.2 ppm to 57 ppm is markedly lower
than that shown in
54
Table 11: Hydrocarbon Group Analysis of used motor oil .
Hydrocarbon Group Weight %
Saturates 76.6-86.3
Aromatics 4.1-12.9
Polars 0.8-3.8
Asphaltenes 0
Volatiles 3.2
55
Irwin, Roy J. et al. Environmental Contaminants Encyclopedia, Used Motor Oil Entry. National Park
Service, 1997. http://nature.nps.gov/toxic/oilused.pdf.
54
Table 12: Concentrations of PAHs found in one sample of motor oil
54
Table 13: Metal Content of Used Oil
54
Table 14: Non-Metal Inorganic Content of Used Oil
55
D.J. Graziano and E.J. Daniels, Assessment of Opportunities to Increase the Recovery and Recycling
Rates of Waste Oils. Energy Systems Division Argonne National Laboratory, Contract W-31-109-Eng-38,
for the United States Department of Energy, pg 54, August 1995.
With the use of the thermal profile and the pressure profile given in Figure 2,
flash calculations for the distillation of the oil, as in Appendix 4, were performed to
calculate the vapor-liquid equilibrium properties of the oil in each temperature section.
The NIST Chemistry Web Book 56 provided Antoine Equation 57 parameters for
calculating saturated pressure. Table 16 lists the Antoine equation parameters available
for various paraffins and pyrene. Since Antoine parameters were only available for the
paraffins listed, the flash calculations were done using only these components plus
pyrene since it is a PAH that is reported to have a higher concentration. The calculation
using only these components should give an adequate understanding since the boiling
points should be similar.
Species A B C
C18 H38 4.332 2068.96 -111.927
C21 H44 5.92073 3571.218 -19.953
C23 H48 6.557 4200.069 1.864
C26 H54 6.5763 4224.36 -30.387
C27 H56 6.256 3654.27 -86.045
Pyrene 2.68713 1086.824 -262.849
Flash Calculations show that at 0 hours and 400°F, all of the oil will be in liquid
form, at 1 hour and 750°F, 99.8% of the oil will be vaporized and 0.2% of the oil will be in
liquid form and go down to the next stage during hour 2. At that point the remaining oil
will then be vaporized. Therefore the oil will remain in the 1-hour stage until it has
decomposed into products with boiling points below 400°F, which would include
hydrocarbons with 11 or less Carbons, or it will react to form products that act as
petroleum coke. The products of these reactions will be discussed further in the next
section.
56
“NIST Chemistry Web Book”,
“http://WebBook.nist.gov/cgi/cbook.cgi?ID=C593453&Units=SI&Mask=4.”.
57
J.M. Smith and H.C. Van Ness. “Introduction to Chemical Engineering Thermodynamics”. McGraw-
Hill, Inc. New York, 1987.
58
James Speight. The Chemistry and Technology of Petroleum 3 rd ed. Marcel Dekker, Inc., New York,
1999.
into the system which typically involves the cleavage of a C-C bond in heavy paraffins.
(2)Propagation – a series of reactions that converts reactants to products while leaving
the radical concentrations unchanged. (3) Termination – the combination of radicals to
give stable products.59
The primary reactions that occur during free radical reactions of hydrocarbons
are decomposition reactions such as: 58
CH 3 − CH 2 − CH 2 − CH 3
→ CH 3 − CH = CH 2 + CH4 .
The secondary reactions are those where the primary product form higher
molecular weight products, i.e.:58
CH 2 = CH 2 + CH2 = CH 2
→ CH 3 CH 2 CH = CH 2 ,
or
R - CH = CH 2 + R ′ − CH = CH 2
→ Cracked Residuum + coke + other products .
Table 17: Results of the pyrolysis of partially hydrogenated gas oil with a temperature profile
60
between 1292-1526°F
Figure 3 outlines the results given in Table 17, and shows the final destination of
the products. About 90% of the products would have boiling points below 400°F and
would therefore leave the top of the furnace. Of this, about 28 wt % of the feed (gasoline
fraction) will condense in the scrubber at 80°F and 62 % (Gas fraction) is not
condensable at that temperature and will be used as fuel gas. The gasoline fraction
contains 9 wt % (of the feed) oil as benzene and toluene. Benzene is considered toxic in
exposure levels above 25 ppm for an 8 hour shift, and toluene above 300 ppm.
Benzene has been identified as a carcinogen. The remaining products consist of 9 wt %
(of the feed) of fuel oil with tboil> 392°F and 0.9 wt% of coke. The fuel oil should undergo
59
Lyle F. Albright, et al. Pyrolysis: Theory and Industrial Practice. Academic Press, New York, 1983.
Iron can act as a catalyst to produce surface carbon.6
60
Nowak et al. Chem Tech. v. 31 p. 496-500, 1979.
further cracking to form more volatile products and coke. The deposit of coke may
contain high boiling point PAHs in the form of tars, and ordered or disordered carbon,
formed in the gas phase or on a surface. Any such PAH in the coke will be destroyed in
the high temperature zones of the process. Iron can act as a catalyst to produce surface
carbon.
Cracked gas ≤ C4
(62.1 %)
+ Gasoline
Gasoline (C 5 to Tboil < 392 °F) Fuel Gas == 30.3%
67.9%
Condensed in scrubber
(27.7% )
(80 °F)
Oil
charged
into BF Pyrolysis
at top
100%
Fuel Gas Gasoline
5.8% 2.6%
Coke
+ Coke 1.8%
(0.9%)
0.9% Coke
Figure 3: Flow diagram outlining the pyrolysis of Gas Oil shown in Table 15
During the pyrolysis reactions, the 9.3% of pyrolyized fuel oil in the burden at 1 hour
will undergo further pyrolysis into lighter hydrocarbons and coke, approximating a
distribution of 5.8% as fuel gas, 2.6% as gasoline, and 0.9% as additional coke.
The calculations indicate that for 100% of the weight of used oil charged into the top
of the blast furnace into the burden, all of the oil will remain as a liquid until reaching the
1-hour zone of about 750°F. Within the burden at this temperature zone, about 90% of
the charged oil will vaporize, undergo pyrolysis and exit the blast furnace with the top
61
G.F. Froment, Coke formation in the thermal cracking of hydrocarbons. Reviews in Chemical
Engineering. V. 6, n4, p293-328, 1990.
gas. The overall result of charging oil into the top of the blast furnace is decomposed as
follows:
Oil Input =100.0%
Fuel Gas = 67.9%
Condensate (Gasoline) = 30.3%
Coke = 1.8%
The heavier hydrocarbons oils with 12 or more carbons, about 10%, will undergo
progressive pyrolysis in the lower and higher temperature zones of the burden until
lighter hydrocarbons leave the top of the burden and the heavier hydrocarbons are
converted to coke, at about 2% of the oil charge weight.
f.r.r. f.r.r.
Initial hydrocarbon lighter hydrocarbons products (gases)
+
heavier hydrocarbons
cyclized intermediates
f.r.r. polymerization
Figure 4: Flow Diagram for the production of coke. Any hydrocarbon can yield catalytic carbon in
59
the presence of some materials. (f.r.r. = Free-radical reactions)
The calculations in Table 18 were utilized to obtain an average molecular weight for
fuel gas and the “gasoline” fraction. For the case illustrated at a 2% charge of UOF’s to
the burden, the fuel gas weighing 7 lb would occupy 71 scf at a molecular weight of 35.7
lb. In a similar calculation, the gasoline fraction that will condense at a weight of 3 lb
would occupy a volume of 10.5 scf in the gas phase at a molecular weight of 102.8 lb.
These values are shown in the material balance of Figure 6.
Table 18: Calculated results of the composition of the products of pyrolysis of used motor oil to
obtain average molecular weights
Coke
Carbon 1.8 12 1.00 12
Input Motor Oil 100.0
Because of the very small contribution to the total gas volume made by the fuel
gas, which is equivalent to 1.2 weight% of the total top gas volume, it is not felt to be
practical to develop a detailed chemistry for the overall top gas.
Metallics (Fe) will be recovered at a rate of nearly 100% of the Fe in the charged
materials. Therefore the metallics recovered from UOF’s would be equal to the weight
fraction of Fe in the weight of the UOF. For the drained and crushed UOF in the
illustrated case, a value of 76% of the weight of the UOF is indicated.1
As mention in section 3.3.2 Steel Coatings, coated steels are used in oil filters.
Steel provided to the manufacturer of oil filters is approximated by 50% uncoated, 25%
galvanized (zinc coated) and 25% tin plate. An earlier study referenced in this same
section showed an analysis on melting a charge of 100% UOF’s resulting in a residual
tin level from 0.026 to 0.035 weight%. However, it is not presently known if this
represents a mixture of both coated and uncoated filters.
The crushed and drained oil filter appears to have dimensions approximating 3 in
to 4 in diameter by about 1 in high as observed in Peaslee.1 An observation of Figure 3
in the previously referenced work would indicate that a crushed and drained filter should
be reasonably free flowing in bulk, and of a large enough particle size so as not to
provide restrictions to gas flow in the burden or subsequent decrease in burden
permeability. This comment is the opinion of the authors and will need verification by
blast furnace operators and/or trials.
In order to help clarify and identify to the reader the overall effect of the charging
of UOF’s to the iron blast furnace, two process flow diagrams have been constructed.
The first, Figure 5 shows the blast furnace material balance for a conventional practice.
SLAG
D
BLAST
B
E
HOT METAL
A lb C scf lb
Iron bearing burden Dry top gas 53,718 4376
Pellets 65% Fe 1828 (23.4% CO, 21.2% CO2, 2.5% H2, bal.N2)
Fluxed sinter 51% Fe 1368
Steelmaking slag 28% Fe 52 Moisture 3521 168
62
From: D. H. Wakelin, Blast Furnace Material and Energy Balance. The Making, Shaping and Treating of
Steel, 11th Edition, Ironmaking Volume, p734, sec 10.3.5, 1999.
SLAG
D
BLAST
B
E
HOT METAL
A lb C scf lb
Iron bearing burden Dry top gas 53,546 4362
Pellets 65% Fe 1782 (23.4% CO, 21.2% CO2, 2.5% H2, bal.N2)
Fluxed sinter 51% Fe 1368 Fuel Gas 71 7
Steelmaking slag 28% Fe 52 Moisture 3521 168
Used Oil Filters* 76% Fe 40 Gasoline Fraction 10.5 3
Fuel Coke 919 Flue dust and sludge 87
*UOF (Oil, paper) 24% D lb
Moisture Moisture 132 Slag 543
B scf lb (38% SiO2, 9% Al2O3, 42% CaO, 10% MgO)
Blast Dry air 34,584 2655 (1.3% S)
Enriching oxygen 1227 104 E lb
Moisture 1028 49 Hot metal 2000
(4.5% C, 0.48% Si, 0.59% Mn, 0.029% S)
Fuel Tar 6.6 gal 69 (0.060% P)
Figure 6: Blast furnace material balance for a 2% recycle rate of used oil filters in the burden63
63
As calculated by the writer.
filtered media contained within an oil filter could be an off gas problem if the filter were
not compacted within the steel container.
Any filter material entering the burden within the UOF, would be trapped until
much deeper into the burden where the temperatures would be sufficient for full
pyrolysis of the cellulose material of the filter. Both the pyrolysis of motor oil and of the
filter media would occur simultaneously. Therefore, additional particulate contamination
of the top gas stream does not appear to be a problem.
As pointed out in section 4.3.3.1, The chemistry of Motor Oil in the Blast Furnace,
98.2% of the amount of oil charged into the furnace with the UOF will leave in the top
gas in the vapor phase. The lighter hydrocarbons will remain as fuel gas equal to about
67.9% of the original charged oil weight. The other 30.3% of the somewhat higher
hydrocarbon fraction, referred to as “gasoline”, will condense in the water scrubbing
system.
Once the gasoline fraction is condensed, 14% of this fraction will be benzene and
14% toluene with the balance in the C5 to C10 range. Detailed examination of the water
treatment plant will be required to determine if additional actions need to be taken to
remove these constituents prior to discharge.
About 67.9 % of the oil entering the top of the furnace will undergo pyrolysis and
be converted into lighter hydrocarbons, approximating an average heating value of
methane, CH4. As such, this fuel gas would have a heating value of approximately
1,000 Btu/ft3.
The capital cost associated with charging UOF’s into the blast furnace cannot be
quantitatively expressed until a determination is made as to the weight fraction of burden
that UOF’s will occupy. As previously mentioned, the authors of this study have
subjectively indicated an approximate 2% of the burden as being a potential target figure
for charging UOF’s into the blast furnace. The following capital cost considerations will
be based upon this approximation, but once more definitive charging percentages can
be determined, more accurate cost effects could be developed.
5.1 Storage
The majority of blast furnace burden materials are delivered to the stockhouse by
railroad. These materials are delivered in iron ore cars where by they may be emptied
by means of a rotary car dumper, or in bottom dump hopper cars for discharging directly
into receiving bins. Transfer cars are used to deliver additional materials to the
stockhouse.
The receipt of UOF’s into a storage location will need to accommodate some
amount of oil leakage from the material. Considerations for protected storage to avoid
contamination with rainwater by the used motor oil may be appropriate. The potential
amount of oil that may drain from previously drained and crushed UOF’s is not presently
known and will need to be evaluated to determine the criteria for an engineering solution
for the storage requirements.
The most important criteria in this regard is to keep any free draining oil from
entering sumps and drains associated with the storage facility. Communication and
cooperation between the suppliers and the buyers can be a major factor to reduce
and/or control any free draining oil.
As long as the overall size of UOF’s are below 6 in x 6 in and preferably less than
below 4 in x 6 in, and preferably in the range of 3 in x 4 in, the normal bulk material
handling system should be relatively unaffected. UOF’s in the drained and crushed form
would be reasonably free flowing in normal blast furnace materials handling systems.
One case study for an originator of UOF’s is the New York City Department of
Sanitation Bureau of Motor Equipment. 64 On an annual basis the New York Department
of Sanitation diverted 50 tons of filters from disposal to recycling. The overall cost per
ton of export (UOF’s) was $100/ton. The recycling program avoided a solid disposal
cost of approximately $5,000.00, but the recycling company charged $48,024.00 for a
net program increase of $43,024.00. However it is stated that there is a reduced cost
and liability associated with hazardous waste disposal and minimizing the volume of
waste disposed.
64
Recycling Oil and Fuel Filters, www.nycwasteless.com/citysense/initiaves/dosfilters.htm, 2000.
The above example shows that the immediate cost of recycling oil filters is
significantly higher than landfill. Due to environmental considerations, landfill of UOF’s
may not be feasible in the future.
Charging of UOF’s would not result in any capital costs associated with the dry
particulate cleaning of the top gas.
This study has indicated that approximately 30% of the residual oil contained in the
UOF’s will be pyrolyized into a condensate that would be condensed by the scrubber
wash water at an operating temperature of 80°F. An analysis of this aspect was not
included in the scope of work for this study and may be developed in a later study, if
deemed appropriate.
Because UOF’s are not a regular part of the blast furnace burden, there is no
published market price for this material. US Steel has indicated that UOF’s are currently
delivered FOB their Gary Works at $30 per gross ton. A metallic yield of 80% would
result in low residual iron units at about $35.60 per net ton Fe. The following cost
considerations will be of a qualitative approach to indicate where additional costs and/or
benefits may be obtained and or examined in more detail in the future.
From the above relationship, we may assume that an increase in blast furnace
productivity may be approximated by utilization of the metallic Fe content of the charged
material on the same basis as AK’s experience with the HBI. The use of this relationship
in a calculation for crushed and drained UOF’s having a demonstrated yield of 76%
would result in a production increase for an average blast furnace producing 4,920
NTHM/day of approximately 1.4% with a charging rate of UOF’s of 2% of the burden. 66
65
D.A. Kercsmar, et al., Sustained Production in Excess of 9 Tons Per Day/100 ft 3 WV at Middletown’s No.
3 Blast Furnace, Iron & Steelmaker, p 33, July 1994.
66
K.D. Peaslee & D.E. Roberts, II, “ The Future of Used Oil Filter Recycling in Missouri: An Evaluation
of Potential Processes, Product, Quality, Recycling Locations, & Economics”, Missouri Department of
Natural Resources, p 19, February 15, 1997.
The used motor oil contained in the UOF’s will undergo a distillation such that for
each 100% of oil entering the furnace, 67.9% would exit the top gas as fuel gas and
30.3% would exit as a gasoline fraction in the vapor phase. In the demonstration case of
a 2% UOF charge to the burden, or 40 lb UOF’s/NTHM, for the case of drained and
crushed filters this would represent a 13% weight of oil or 5.2 lb/ton of motor oil that
would be released into the top gas as 3.5 lb/ton fuel gas and 1.6 lb of gasoline in the
vapor phase. The 3.5 lb/NTHM of CH4 would be equivalent to approximately 378 scf. At
a natural gas energy value of $2.50/1,000 scf, this would represent a value increase in
the fuel gas of $0.94/NTHM credit.
The C5 and higher hydrocarbons in the gasoline fraction will be condensed in the
scrubber.
There is no change to operating costs for the dry portion of the top gas cleaning
operation.
Some additional process water/waste water treatment costs will increase due to
the vapor fraction in the hydrocarbon range referred to as “gasoline”, C5 to C10 will
condense in the gas cleaning system within the scrubber. This will result in
hydrocarbons within the gasoline fraction to be removed from the process water and the
wastewater stream for prior to discharge.
The cost of wastewater treatment has not been included within the scope of work for
this study. Therefore, it is not known at this time whether or not the condensate would
be removed within the normal process water/wastewater treatment plant for a modern
blast furnace, or not.
7.0 Analysis
In section 4.3 Recycling of Used Oil Filters to the Blast Furnace, calculations were
made to show the recycling capability of 19 blast furnaces in the U.S. consuming all
available filters as well as one western blast furnace consuming all filters west of the
Mississippi as an extreme hypothetical case. Under conditions that assume a future
growth of oil filter recycling and increased production of oil filters, and a 70% recycling
rate in the year 2005 results in an average charge of only 0.3% of steel components
from the UOF’s recycled to the average blast furnace. This would obviously be too small
an amount for an operator to deal with, and so the calculations showed an increase
concentration going to one furnace as an example at a steel-charging rate of 1.3% to the
burden.
Another way to look at the potential for balancing UOF generation rate against BF
capacity on a regional basis may be demonstrated by the following example. In this
case, two regional markets Chicago and Pittsburgh have been selected.
In the case of the Chicago market, and assuming 100% UOF recycling from the
adjoining states of Iowa, Illinois, Indiana, Michigan, and Wisconsin, a total of 31.2 million
UOF’s at an average weight of 0.79 lb would result in 12,300 tons of UOF’s (including
the oil) for recycle to one Chicago blast furnace. This would be an equivalent charging
rate of 0.82% UOF’s to one blast furnace at a rate of 1.5 Mtpy.
The overall usage rate within this study encompassed an average of 2% crushed
and drained UOF’s, per NT HM. The writer’s opinion is that this may represent a
reasonable average charging rate upon which to base the calculations for this study.
Actual operations may significantly change this average charging rate to a smaller
fraction or a much greater fraction depending upon the operating philosophy. However,
operating at a rate greater than 2% UOF’s/NTHM would necessarily mean an
intermittent operation as the availability of UOF’s would be limited.
The writers have assumed that the used oil filters, having been first properly hot
drained and then subsequently crushed, would represent a reasonable, least cost supply
of UOF’s to the blast furnace. Any filter media remains within the crushed and drained
UOF, will act as a sponge to inhibit further draining of oil. Additional examination of
crushed and drained UOF’s in bulk will be required to evaluate whether or not such UOF
processing will relieve the problems of oil contamination from material handling and
storage considerations at the blast furnace storage and stockhouse.
Charging of crushed and drained UOF’s to the blast furnace at a bulk density of
50 lb/ft3 is a metallic charging practice that may be similar to other scrap charges used in
the blast furnace. In section 4.3.3.1 The Chemistry of Motor Oil in the Blast Furnace, a
detailed approach to the behavior of motor oil in entering the upper zone of the blast
furnace with the charged materials has been shown. Motor oil has a high boiling point,
such that it would remain liquid at 400°F, thereby entering the burden within the drained
and crushed UOF. During the next one to two hours as temperatures increase from
750°F to 1100°F, the motor oil would pyrolyize into lighter hydrocarbons which would
leave the burden with the top gas and heavier hydrocarbons which would undergo
further pyrolysis until becoming coke. The resulting coke from the pyrolysis of the motor
oil would represent about 2% of the weight of motor charged into the furnace. Although
some concerns have been expressed about the possibility of polycyclic aromatic
hydrocarbons (PAH’s) because of the possibility of connection to known carcinogens,
this risk appears to be exceedingly small as these heavier PAH’s would be pyrolyized in
the higher temperature zones of the furnace.
The lighter weight fractions of the motor oil input to the furnace would be
discharged from the blast furnace as fuel gas, 67.9% of the weight of motor oil charged,
and a “gasoline” fraction representing 30.3% of the weight of motor oil charged which
would condense in the wet scrubber of the off gas system. The absolute quantities of
“gasoline” condensate at a charging rate of 2% UOF’s/NTHM would be1.6 lb/NTHM.
The effect of this 1.6 lb “gasoline” fraction lb/NTHM may have on the process
water and wastewater treatment is outside of the scope of this study. If subsequent
study of this water treatment issue would indicate it to represent a significant cost item,
then the processing of UOF’s to the blast furnace would require shredding of the filters
by the processor and briquetting of the shredded material into “bricks” or “pucks”. There
are some UOF processors within the United States that do shredding of the UOF’s. This
has been commented in section 3.5 Processing.
In the event that a UOF shredding operation would be required, the resulting
metallic units recovered form this process would have no adverse affect on blast furnace
operations and, could be handled as any other metallic charged to the blast furnace.
At this stage of the feasibility study, it is not possible to accurately quantify additional
costs and/or benefits to derived in a $/NTHM of hot metal produced. The best approach
at this stage is to identify, in a qualitative manner, the areas that will be expected to see
either an increase cost or a benefit to be derived from the charging of UOF’s to the blast
furnace.
Table 19, Relative Cost vs. Benefit of Charging Used Oil Filters to the Blast Furnace,
has been constructed to show these relationships, in the writer’s opinion, which may
result from the charging of UOF’s to the blast furnace.
Table 19: Relative Cost vs. Benefit of Charging Used Oil Filters to the Blast Furnace
Item Higher Cost Benefit
Storage +
Iron Ore +
Metallics +
Fluxes 0 0
Coke +
Production +
Hot Metal Analysis 0 0
Slag Production 0 0
Slag Analysis 0 0
Gas Cleaning 0 0
Water Treatment +
Fuel Value +
Maintenance ? ?
With the present knowledge base, it may be expected that additional cost may be
incurred relative to UOF storage and in water treatment resulting from the condensation
of “gasoline fraction” hydrocarbon phases in the gas cleaning scrubber water for
treatment. An unknown factor is whether or not the additional hydrocarbon vapors may
result in additional maintenance problems, and/or possible oil leakage from the UOF’s
that may require additional maintenance considerations.
On the benefit side, there exists a reduction in iron ore pellet requirements, the
potential for reduced metallics costs, an increase in the production rate and less coke
due to charging metallics, a higher fuel value in the blast furnace top gas, and an
unknown cost/benefit relationship relative to maintenance.
At this stage of the feasibility study, it appears that there is potential incentive to
determine what is required to conduct additional industrial trials for the recycling of
UOF’s to the blast furnace. To assist in this aspect, the section 8.0 Review with Blast
Furnace Operators, which follows, will serve to highlight the past experiences that have
been brought to the attention of this feasibility study by operators solicited by AISI and
the writer.
William Obenchain of the AISI provided the writer with blast furnace operator
contacts at Bethlehem Steel, Dofasco, Ispat Inland, USS and WCI Steel.
During the review of this feasibility study with blast furnace personnel at US
Steel, it was learned that USS reported continuing experience in charging UOF’s into
their iron blast furnace at the Gary Works. This work has been underway for at least five
or six years. The current cost of the UOF’s is about $30 per gross ton delivered to the
Gary Works.
USS has been receiving approximately 100 tons to 200 tons of UOF’s per month.
These are delivered by dump truck at about 20 tons per load. The UOF’s are dumped
onto the scrap blending concrete pad. A front-end loader is used to distribute the UOF’s
throughout the scrap (B scrap, and other steel plant metallics) for blending.
The blended metallic charges are then loaded by front-end loader into a transfer
car to be discharged into the metallic/scrap bin at the stock house. The skip car is
loaded by a material gathering conveyor, which receives all burden materials from the
stockhouse for delivery into the skip car.
The UOF’s are blended with scrap at a rate of 100 tons to 200 tons UOF’s per
30,000 tons to 40,000 tons of scrap per month or about 0.3% to 0.5% UOF in the scrap
blend. At a concentration of 0.5% UOF in the scrap blend, and assuming a 400 lb scrap
per NTHM charging rate, this would represent a UOF charging rate of 0.1% in the overall
burden.
The discussion USS personnel indicated that no problems had been experienced
with respect to oil draining from the UOF’s and that because the scrap is blended on a
concrete pad, any potential drainage would be contained. Additionally, there were no
known operational problems with respect to the blast furnace operations or its top gas
treatment and water treatment. The charging rate at 0.1% in the overall burden is a very
small amount and may be insufficient to disclose potential problems if larger amounts
may be charged.
The other blast furnace operators representing Bethlehem Steel, Dofasco, Ispat
Inland and WCI Steel all expressed concerns relating to the contained oil. The initial
concerns are that any free flowing oil from the filters may be a material storage and
handling problem resulting in contamination of the ground and/or ground water.
Communications between buyers and suppliers of UOF’s in the supply chain should
be able to properly address any concerns over freely draining oil.
The next major concern expressed by all of these operators was the extent to which
oil would vaporize in the top of the furnace. The concern is that the vaporized oil would
condense and contaminate the scrubber wash water system.
Other concerns expressed were the potential difficulties based on the final size of the
oil filter in charging with a Paul Worth top and also with potential problems in conveyor
charging systems due to concerns on poor material flowability.
One operator indicated that they have optimized the blast furnace process to a
controlled temperature of the top gas. They did not think it would be worthwhile to re-
optimize furnace practices for a small percentage of a material that could potentially
cause problems.
Most operators felt that the UOF’s would need to be priced at a low level relative to
other metallics, or they would not be interested in interrupting normal material balances
to the process.
The only remaining concern of blast furnace operators not answered in the feasibility
study is with respect to the effect of the vaporized oil components on the operating cost
and capital cost of the top gas cleaning system to comply with all regulations.
At the time this study was authorized, it was not known that US Steel at Gary Works
had a continuing program of charging UOF’s into their blast furnaces.
Due to the fact that US Steel does have operating experience with recycling UOF’s
into the blast furnace, consideration may be given to conducting a study of the
operational results at that blast furnace site. This has the benefit of not incurring any
significant cost to conduct a demonstration for the feasibility of this concept. However, it
must be consistent with US Steel’s policies and procedures regarding any proprietary or
confidential operating practices and procedures.
If an analysis of the USS Gary experience can be shared with other blast furnace
operators, then the potential for significant additional recycling of UOF’s to the blast
furnace may readily occur.
It will be necessary to collect additional information with respect to motor oil that may
drain from crushed and drained UOF’s during transportation and storage prior to
charging into the blast furnace. In the event that free draining of motor oil from the
UOF’s is found to be in excess of steel plant requirements, then consideration needs to
be given toward the shredding and separation of oil and filter media from the steel
components, and the compaction and/or briquetting of the shredded steel components
for blast furnace charging.
10.0 Conclusions
The least cost delivery of UOF’s to the blast furnace would be properly hot draining
followed by crushing of the filter. This is expected to result in approximately 13% oil
remaining in the filter media within the crushed filter. The chemistry of the used oil,
when charged in to the top of the blast furnace, indicates that about 98% of the weight of
this oil would be removed from the furnace in the blast furnace top gas as both fuel gas
and as a condensable “gasoline fraction” that would condense in the scrubber water.
The fuel gas is a positive benefit, but it is not known to what extent the condensable
“gasoline fraction” would represent additional water treatment costs.
In the event that a 13% contained oil in crushed and drained UOF’s is excessive,
then a UOF processing route that encompasses shredding of the filter, separation of
filter media, collection of used motor oil for its recycling, and compaction of the shredded
metal may be required to provide a charge material to the blast furnace. This
subsequently shredded and compacted charged material should, in the writer’s opinion,
have no detrimental effect to the recycling of this material through the blast furnace with
respect to top gas chemistry or any contamination of the hot metal chemistry, but it
would incur additional cost.
The charging of metallic iron units to the top of the blast furnace is a routine practice
in the industry. To be acceptable to the blast furnace operator, recycling of steel from
used oil filters must be conducted in a way that will not cause environmental remediation
costs and/or operational problems, which outweigh the potential cost benefits of
recycling this material.
Due to the fact that used oil filters are presently being recycled in the blast furnaces
at US Steel, Gary Works, a study of this practice would benefit the industry. Such a
study would need to be consistent with the policies and confidentiality requirements of
US Steel. The current cost of the UOF’s is about $30 per gross ton delivered to the
Gary Works.
The analysis conducted in this study has been mainly oriented to the use of a 2%
charge of UOF’s to the blast furnace burden. The US Steel practice at 0.1% UOF’s may
be too low to indicate any potential problems. However, on a geographically distributed
basis, there may not be nearly enough total volume of UOF’s generated to charge more
than about 0.5 weight percent of the burden to a blast furnace. In this case, provided
transportation costs are not excessive, sufficient blast furnace capacity exists to recycle
all UOF’s that may be reasonably delivered to the steel plant.
Currently electric furnace steel plants as well as iron foundries consume significant
amounts of the existing recycled UOF’s.
Future work should be directed to establishing the criteria for processing of UOF’s to
be acceptable to the blast furnace from a size, density and residual oil content basis.
Additionally, a more detailed assessment of wastewater treatment costs may be required
to properly accommodate the condensable fraction of the vaporized oil species.
There is strong indication that additional states may enact legislation banning the
disposal of UOF’s into landfills. This will result in increased cost to the public for
disposal of these necessary maintenance activities on their automobile, unless beneficial
recycling can be organized. Through a combination of developing the requirements of
UOF’s for blast furnace recycling, publicity to the originating sources of UOF’s, and
development of an appropriate and responsible transportation link; the recycling of
UOF’s into the blast furnace may be mutually beneficial to the environment and to the
steel industry.
11.0 Acknowledgements
The writers would like to acknowledge participation and advice from the following
companies and their personnel.
12.0 Appendix
Mississippi 2,348,984 0
67
“State Motor Vehicle Registration 1999 Table M V-1, ”
http://wwwcf.fhwa.dot.gov/ohim/hs99/tables/mv1.pdf, 10/25/2001
Storage Limits:
1. Less than 1 ton – 1 year
2. 1 ton or more-180 days
Let L equal the moles of liquid with mole fractions {x i}, and let V be the moles of vapor
with mole fractions {y i}. The material balance equations are written as
L +V =1
z i = x i L + y iV ( i = 1, 2, K, N )
where {zi} are the overall mole fractions. Eliminating L from the equations, we get
z i = x i (1 − V ) + y i V ( i = 1, 2, K, N ) Eq. 1
Raoult’s law for vapor-liquid equilibrium is given by
yi = K i xi
where Ki is the “K-value” and is given here by
K i = Pi sat / P
Psat is calculated using the Antoine Equation given by
B
log 10 P sat = A − Eq. 2
T +C
Substituting x i=yi/Ki in Eq. 1 and solving for y i gives
zi K i
yi = (i = 1, 2,K , N ) Eq. 3
1 + V ( K i − 1)
zi K i
∑ 1 + V (K
i − 1)
=1 Eq. 4
i
Since T, P, and {zi} are known, the only unknown in Eq. 3 is V. The solution is
obtained iteratively.
1
Pd =
∑ yi / Pi sat
i
with {y i}={zi}.
First using values of zi and Pisat shown below, the Bubble Pressure of the oil at 750 °F is
calculated:
Pb = ∑ z i Pi sat
i
= 0.19 * 4.337 + 0.18 * 2.772 + 0.19 * 2.105 + 0.18 * 0.980 + 0.19 * 1.043 + 0.07 *1.071
= 2.17 bar
The Dew Pressure for the oil is also calculated:
1
Pd =
∑ yi / Pi sat
i
1
=
0.19 / 4.337 + 0.18 / 2.772 + 0.19 / 2.105 + 0.18 / 0.980 + 0.19 / 1.043 + 0.07 / 1.071
= 1.59 bar
Since the pressure, P=1.92 bar, is between the bubble pressure and the dew pressure, the
flash calculation can be performed. If the pressure was greater than the bubble pressure
than the mixture would be all vapor and if the pressure was less than the dew pressure,
the mixture would be all liquid.
i zi Pisat(bar) Ki yi xi
K i = Pi sat / P
Component (overall B (vapor (liquid
A−
composition,
arbitrarily P sat = 10 T +C
composition) composition)
set) (T in Kelvin) zi K i y
yi = xi = i
1 + V ( K i − 1) Ki
C18 H38 0.19 4.337 2.256 0.1902 0.0843
C21 H44 0.18 2.772 1.442 0.1801 0.1249
C23 H48 0.19 2.105 1.095 0.1900 0.1736
C26 H54 0.18 0.980 0.510 0.1797 0.3525
C27 H56 0.19 1.043 0.543 0.1897 0.3496
pyrene 0.07 1.071 0.557 0.0699 0.1254
The value of V, the fraction of the mixture that is vaporized, is obtained iteratively by
using the MS Excel “Goal Seek” function to change V in order to set
∑y i =1
i
“Goal Seek” calculated V to be 0.998 so 99.8% of the oil is vaporized in that section at
750 °F.
Figure 7: Some typical aromatics from hydr ocarbon pyrolysis.57 Molecules with 2 or more rings are
known as polycyclic aromatic hydrocarbons (PAH)
13.0 References
1
AISI, “Steel Technology Roadmap”, March 1998, section 2.2.3 A UTOMOTIVE, pg 77.
2
Technical Bulletin, “The Future of Used Oil Filter Recycling in Missouri: An Evaluation of Potential
Processes, Product Quality, Recycling Locations, and Economics”, February 15, 1997, K.D. Peaslee and
D.E. Roberts, II, University of Missouri-Rolla, Department of Metallurgical Engineering.
3
“Report of the Findings on the Waste Classification of Used Automotive Oil Filters”, The Convenient
Automotive Services Institute, April 1991.
4
“The Process,” From “An Introduction to Blast Furnace Technology”, ATSI Engineering Services,
http://www.steel.org/learning/howmade/blast_furnace.htm, 12/17/2001.
5
“AC Delco – Parts Information-Oil Filters-Ultraguard Gold,”
http://www.acdelco.com/pi_filt_oil_gold_feature.htm, 9/24/01
6
F.E. Lockwood and R. Dailey, “Lubricant Analysis,” Friction, Lubrication and Wear Analysis, 1992,
ASM Handbook, Vol. 18, pp. 299-312
7
“Online Sample Report, Oil Sampling Guidelines, ” http://www.thetakgroup.com/pennzoil-
quakerstate/pqs/login.asp, 10/25/01
8
“State Motor Vehicle Registration 1999 Table MV-1, ”
http://wwwcf.fhwa.dot.gov/ohim/hs99/tables/mv1.pdf, 10/25/2001
9
Brent Hazelett, ”Private Communications,” Oil Filter Manufacturers Council, September 25, 2001.
10
“Recycle Rate for Used Oil Filters.” http://www.filtercouncil.org/news/May2000.html, (Filter
Manufacturers Council, FMC PR 01-00, May 4, 2000).
11
Brent Hazelett, ”Private Communications,” Oil Filter Manufacturers Council, September 25, 2001.
12
“State Motor Vehicle Registration 1999 Table MV-1, ”
http://wwwcf.fhwa.dot.gov/ohim/hs99/tables/mv1.pdf, 10/25/2001
13
Brent Hazelett, ”Private Communications,” Oil Filter Manufacturers Council, September 25, 2001.
14
Nishaj Attassery, “Private Communications,” 16 Oct 2001, Email Letter, ArvinMeritor
15
Ibid
16
Mike Whitman, “Private Communications,” 12 Oct 2001, Fax Memo, Delphi Corporation
17
Ibid
18
“Tin Plate,” http://www.weirton.com/products/tin/tinplate.html, 24 Sep 2001
19
“Weirzin,” http://www.weirton.com/products/galv/weirzin.html , 24 Sep 2001
20
Brent Hazellet, “Private Communications,” Oil Filter Manufacturers Council, 18 Oct 2001
21
Mike Whitman, “Private Communications,” 13 Oct 2001, Phone Message, Delphi Corporation
22
Scott Jacobs, “Private Communications,” 24 Oct 2001, Email Letter, Fram Brand, Honeywell Corp.
23
Nishaj Attassery, “Private Communications,” 16 Oct 2001, Email Letter, ArvinMeritor
24
Edward Adamczyk, “Private Communications,” Weirton Steel, Phone Message, 11 Oct 2001.
25
Ibid
26
Kent D. Peaslee, “Recycling Used Automotive Filters,” Journal of Metals, February, 1994, pg. 46
27
Harold E. McGannon, ed., The Making Shaping and Treating of Steel, (Pittsburgh: United States Steel,
1971), pg. 456
28
“Engine Oil Filter Study,” http://www.scuderiaciriani.com/rx7/oil_filter_study/, 11 Oct 2001.
29
Nishaj Attassery, “Private Communications,” 16 Oct 2001, Email Letter, ArvinMeritor
30
Mike Whitman, “Private Communications,” 17 Oct 2001, Phone Message, Delphi Corporation
31
Brent Hazelett, ”Private Communications,” Oil Filter Manufacturers Council, September 25, 2001.
32
Ibid.
33
Kent D. Peaslee, “Recycling Used Automotive Filters,” Journal of Metals, February 1994, pg. 44.
34
Note: Lubricating Oil Specific Gravity can vary from 0.856 to 0.913. For purposes of this study a value
of 0.88 will be used. “Material Data Safety Sheet,” Havoline Motor Oil,
http://www.equivatexacomsds.com/rd/getsinglemsds.asp?ID=191113, 18 Sep 2001.
35
Weirton Steel Internet Site
36
Kent D. Peaslee and Darrell E. Roberts, “Characterization of used automotive oil filters for recycling,”
Resources, Conservation and Recycling 19 (1997), pg 86.
13.0 Resumes
[email protected]
Summary:
Manager and engineer operating a variety of steel melt shops. Well experienced in the management and
startup of melt shops using scrap, hot metal and DRI cast into slabs, thin slabs, billets, blooms and beam
blanks.
1977 B.S. The Pennsylvania State University, University Park, PA, USA. Metallurgical Engineering.
1991 MS The University of Massachusetts, Amherst, MA, USA. Engineering Management
Current Employment:
1997 Concast Standard, Zurich, Daye Steel, Huangshi, China Technical and operational
Switzerland supervision of a DC EAF in startup
phase
1996-1997 Namheng Steel, Lopburi, Thailand Namheng Steel, Lopburi, Thailand Management of a DC EAF, AC LF
and billet melt shop in start up
phase
1996 Gallatin Steel, Ghent, KY USA Gallatin Steel, Ghent, KY USA EAF operational training in shop
using DC EAF and Thin Slab
Caster
1996 Kvaerner Metals, St. Chamond, Essar Steel, Surat, India Performance testing of a DC EAF
France using 80 % HBI as a raw material.
SPC training
1996 Kvaerner Metals, Sheffield, Hadeed, Saudi Arabia Engineering Calculations for DRI
England feed rates and EAF Practices
1996 Dressel Technolo gies, Pawleys AISE Automation Conference, Presentation of a paper on melt
Island, SC, USA Nashville, TN, USA shop simulation
1995-1996 ABB Industrie, AG, Baden, Shanghai No. 3 Steel Works, Technical and operational
Switzerland Shanghai, China supervision of two DC EAF’s in
startup phase
1994-1995 Kvaerner Metals, Pittsburgh, PA, Essar Steel, Surat, India Management of two DC EAF’s
USA and AC Ladle Furnaces in startup
phase using 80% HBI
1994-1995 Caribbean Ispat Limited, Trindad Caribbean Ispat Limited, Trindad Steelmaking and SPC Training and
and Tobago, West Indies and Tobago, West Indies Quality Consulting in EAF shop
using 90 % DRI
1994 Van Deilen Industries, Van Deilen Industries, Conceptual engineering for a micro
Lambertville, MI, USA Lambertville, MI, USA steel plant
1994 Dressel Technologies, Dressel Technologies, Established Dressel Technologies
Pawleys Island, SC, USA Pawleys Island, SC, USA as a metallurgical and steel plant
management consulting firm
Former Employers:
1993 to 1994 Florida Steel, Jacksonville, Fl, USA Melt shop process engineer
1987 to 1993 Georgetown Steel, Georgetown, SC, USA. Management of billet caster process engineering
and quality control in a carbon steel melt shop using 50 % direct reduced iron (DRI). Supervision of
various operational personnel. Shop produced a large quantity of high carbon wire rod products.
1980 to 1987 National Steel Research Center, Weirton, WV, USA. Technical management of a number of
steelmaking and slab continuous casting research projects. Supervision of technical personnel.
1978 to 1980 Weirton Steel, Weirton, WV, USA. Operational management of a vacuum degasser and
continuous slab caster operations. Supervision of operational personnel.
Professional License:
State board certified professional engineer, PA and WV.
JENNIFER H. HILL
[email protected]
Graduate Student
Campus Address:
Carnegie Mellon University
Department of Chemical Engineering
5000 Forbes Avenue
Pittsburgh, PA 15213
(412) 268-3039
Home Address:
105 Heston Drive
Cranberry Township, PA 16066
(724) 772-9018
OBJECTIVE To obtain an industrial position in research and development that uses my engineering
skills and knowledge about advanced process control and modeling.
EXPERIENCE AND
QUALIFICATIONS
RELATED
COURSES Mathematical Techniques in Chemical Engineering Engineering Design
Process Systems Engineering and Optimization Process Control
Computational Methods for Large Scale Processes Reactor Design
Linear Systems and Control Thermodynamics
Fluid Dynamics Kinetics
Chemical Plant Design Polymer Science
COMPUTER SKILLS:
Pro II/Provision, MATLAB, Fortran, C, GAMS, LaTex, Unix, Windows
CONFERENCE PRESENTATIONS:
• Hill, Jennifer and Erik Ydstie. “Robust Adaptive Control: How to Stop the
Estimator to Prevent Bursting”. 2001 AIChE Annual Meeting, Reno, NV,
November 2001.
• Hill, Jennifer and Erik Ydstie. “Parameter Estimation and Robust Adaptive
Control”. 2000 AIChE Annual Meeting, Los Angeles, CA, November 2000.
• Hsu, Jennifer and Erik Ydstie. “Robust Adaptive Control with Unknown
Disturbances”.
1999 AIChE Annual Meeting, Dallas, TX, November 1999.
PUBLICATIONS:
• Hill, Jennifer and Erik Ydsite. “Adaptive Control without Parameter Projection
and Unknown Sign of the High Frequency Gain”. Submitted to International
Journal of Adaptive Control and Signal Processing.
• Hill, Jennifer, Erik Ydstie, and Yu Jiao. “Adaptive Control of an Industrial Float
Glass Process”. Submitted to IFAC World Congress, 2002.
• Hill, Jennifer, Erik Ydstie, and Yu Jiao. “Adaptive Predictive Control of Glass
Temperature”. To be submitted to Automatica.
AWARDS:
• Carnegie Mellon University Graduate Fellowship (1997-2002)
• Penn State Engineering Society Scholarship (1993-1997)
• Penn State Academic Excellence Scholarship (1993-1997)
• Graduated Penn State University with Highest Distinction (1997)
. Metserv
9800 A McKnight Road
Suite 310
Pittsburgh, PA 15237-6006
Tel: (412) 348-0015
Fax: (412) 348-0017
E-mail: [email protected]
PROFESSIONAL EXPERIENCE
Technical Publications
“Modeling for DRI Value in Steelmaking”, Smailer R M, Sheftel VM, Holmes R L; Steel
Times International, September, 1999
“The Use of Natural Gas in the FIOR Process”, Smailer RM, Triplett DW, Gas Research
Conference on “Natural Gas Use in the Production of Virgin Iron Units”, Chicago,
Illinois, April 23, 1987
“FIOR Today - Operations and Products”, Whipp, RH, Smailer RM, Kulberg HA, Arab
Steel 127, p. 44-72, 1985.
“Development of the NK-AP Ladle Refining Process:, Smailer RM, Ikegami Y, Iron and
Steel Engineer, 62 (11), p. 29-33, November 1985
“Phosphorus Control in DRI Steelmaking”, Smailer RM, Electric Furnace ’83, Mexico
City, Mexico, June 12-15, 1983, Instituto Latinoamericano del Fierro y El Acero, 1983
“Hot Briquetting of FIOR Fines”, Smailer RM, Whipp RH, Kuby OA, Malakouti N
SME-AIME Fall Meeting and Exhibit, Society of Mining Engineers of AIME, 1981
“FIOR - 300,000 Tons by Water”, Molina MA, Smailer RM, Direct Reduction ’80
Conference, July 27-30, 1980, Instituto Latinoamericana del Fierro y El Acero, 1980
“Handling Storage, and Shipment of Direct Reduced Iron”, Jensen HB, Smailer RM, 39th
Ironmaking Conference, Iron and Steel Society of AIME, Warrendale, Pennsylvania, p.
430-436, 1980
“Transportation and Storage of Direct Reduced Iron”, Smailer RM, Jensen HB, (Chapter
for AIME book on Direct Reduction of Iron, 1980)
“Utilization of Direct Reduction Iron in Electric Steelmaking”, Smailer RM, Jensen HB,
Scott WW, Jr., Electric Furnace Conference Proceedings, Volume 32, p. 29-36, 1975
“Utilization of Direct Reduction Iron in Electric Steelmaking”, Smailer RM, Jensen HB,
Scott WW, Jr., UNIDO (United Nations Industrial Development Organization) Third
Interregional Symposium Iron Steel Industry, Brazil, October 1973
“Vacuum Degassing of Specialty Plate Steel”, McMichael RC, Smailer RM, Edwards
DY, Blast Furnace Steel Plant, March 1969
Book: Direct Reduced Iron: Technology and Economics of Production and Use,
Stephenson, Robert H; Smailer, Ralph M., Iron and Steel Society AIME, Warrendale,
Pennsylvania, 1980
Patents:
Patent No. 3,809,986, “Combination Iron and Iron Oxide Briquetting for
Steelmaking”