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1.0
INTRODUCTION
As early as the 1970’s, the
United States Department of the Interior, Bureau of Mines, became interested
in the possibility of using glass as a flux for brick clays. The Bureau of Mines’ studies concluded that
“Substitution of glass for one-half of the clay in a red [brick clay] body
reduced the firing temperature 500°F [from 2120°F to 1650°F], which made possible a 30
percent increase in production.”
[1]
These studies took place following the first energy crisis in the
United States, when the Department of the Interior was interested in reducing
energy use by targeted industries.
Since the 1970’s, additional
unpublished proprietary data has been collected by several sources, and it
is possible that a significant amount of glass is being used today as a clay
body flux in proprietary processes. The
CWC became interested in the potential of clay bodies as an alternative use
for finely graded glass.
The
action of vitrified material in a body has been described as follows:
As the temperature of firing increases beyond
red heat, other changes occur in the clay called vitrification. Vitrification is the hardening, tightening,
and finally the partial glassification of clay. Vitrification gives to fired clay its characteristic hard, durable,
dense, and rocklike properties. . . . Vitrification proceeds gradually, at
first causing the clay to be rather loosely compacted and then, with the advance
of temperature, causing it to become increasingly hard, up to the point of
melting and deformation. The same
clay can be either very soft or very dense, hard, and impervious, depending
upon the temperature at which it is fired.
[2]
The function of a body flux
has been described as “The fluxes control the fusion or hardening point of
the clay and make it fire to a satisfactory degree of density at whatever
temperature is used.”
[3]
In January, 1998, Seattle Pottery
Supply won a Technology Validation grant, funded by the United States National
Institute for Standards and Technology (NIST), managed by the CWC. The purpose of the project was to develop some
public information on the function of recycled glass as a body flux in clay
bodies.
1.1 Soda-lime Glass
More than 95% of all manufactured glass is made from
sodium oxide, calcium oxide, and silicon dioxide, commonly referred to as
a soda-lime-silica composition. A
typical average chemical content of the oxides in container and window glass
is given by the following:
OXIDE PERCENTAGE BY WEIGHT
Na2O
13.7
CaO
8.8
Al2O3 .1
Fe2O3 .12
K2O
.04
SO3
.26
The facts that soda
lime glass is already a vitreous silicate, that vitreous silicates are generated
during the maturation of clay bodies, and that vitreous silicates act as fluxes,
reducing clay body maturation temperatures, were strong evidence that
the addition of soda lime glass to clay body raw materials could increase
the efficiency of clay body firing and therefore be a value-added application
for recycled glass fines.
Glass for this project was furnished by TriVitro Corporation
of Kent, Washington. TriVitro manufactures
a variety of crushed glass products from post-consumer and post-industrial
glass. Included in TriVitro’s product
line are abrasives (Vitro-GritÔ), fusable glass (Vitro-HueÔ) and filtration media (Vitro-CleanÔ). TriVitro
furnished two grades of fine glass for this project, their grades 140F and
325F. Gradation analyses are shown
in Figure 1. Except where noted, the
best batches in this project were made using the 325F grade TriVitro glass.

Six standard clay mixes sold by Seattle Pottery Supply
were chosen for experimentation. The
clay recipes were for multi-purpose clay bodies. They were chosen to represent a variety of
firing temperatures and uses.
The mixes were designated:
§
D06 Red
§
D06 White
§
D6 Red
§
D6 White
§
D06 Casting Slip
The symbol “D06” represents “pyrometric cone 06,” or just Cone 06. The cone rating designates the firing temperature expected for the clay mixture to reach maturity during firing. The following temperatures correspond to the end points of the cones used in this project, when heated at 36°F per hour: [4]
§
D06 = 1841 °F
§
D04 = 1922 °F
§
D1 = 2057 °F
§
D6 = 2174 °F
The constituents of the standard mixes were as follows:
Weight Weight
percent Ingredient
Recipe Name: D06 Red
7.5 gm 55.0 Red Art Fireclay
3.75 gm 27.5 Old Mine 4 Ball Clay (OM-4)
.06 gm .4 Barium Carbonate
.13 gm 1.0 Bentonite Clay
.31 gm 2.2 Clay Grade Iron
1.88 gm 13.8 Talc
Material substituted for: Talc
Recipe Name: D06 White
7.5 gm 46.0 Old Mine 4 Ball Clay (OM-4)
2.5 gm 15.3 Plastic Vitrox (PV) Ball Clay
.07 gm .4 Bentonite Clay
6.25 gm 38.3 Talc
Material substituted for: Talc
Recipe Name: D6 Red
6.25 gm 41.7 Lincoln Fireclay
5 gm 33.3 Newman Fireclay
1.25 gm 8.3 Old Mine 4 Ball Clay (OM-4)
.31 gm 2.1 Bentonite Clay
.31 gm 2.1 Clay Grade Iron
1.25 gm 8.3 Nepheline Syenite (Neph Sy)
.625 gm 4.2 Talc
Material substituted for: Talc and neph sy
Recipe Name: D6 White
7.5 gm 52.1 Lincoln Fireclay
1.25 gm 8.7 Old Mine 4 Ball Clay (OM-4)
1.88 gm 13.1 EPK Kaolin
1.88 gm 13.1 30 mesh Sand
.44 gm 3.1 Ione 412 Porcelain Grog
.19 gm 1.3 Bentonite Clay
1.25 gm 8.7 Talc
Material substituted for: Talc
Recipe Name: D06 Casting Slip
3783 gm 33 Old Mine 4 Ball Clay (OM-4)
3783 gm 33 SGP Ball Clay
3783 gm 33 Plastic Vitrox (PV) Ball
Clay
.117 gm ND Barium Carbonate
.235 gm ND Soda Ash
1.6 oz.
Sodium Silicate
Material substituted for: see Casting Slip section below
Each of the clay bodies was mixed in a 35lb. capacity
clay mixer for approximately 40 minutes. All of the ingredients were first mixed dry until uniform, then
a measured amount of water was added. After
the clay was thoroughly mixed, it was wedged, or de-aired.
Samples were made by rolling the clay into a flat slab
1cm. thick. Test samples were cut
from this slab to 5cm wide by 30 cm long.
On each piece a carefully measured 20cm mark was scribed and each one
was marked for identification.
After drying, all samples were fired to the desired
temperature (or cone) using a programmable kiln controller. After firing, shrinkage and absorption tests
were performed.
·
Shrinkage -
after firing, the scribed 20cm mark was re-measured.
The difference in length was calculated as the percent of shrinkage.
·
Absorption -- after
firing, each piece was weighed. After
weighing, the pieces were soaked in water for 24 hours. When taken out they were patted down with a
dry rag and weighed again. The difference
in weight was calculated as the percentage of absorption.
Graphical results and percentage substitutions are
shown in Figures 2 through 7. Care
must be taken in making assumptions or attempting to reproduce these results. Conducting these tests in potters’ kilns is
not an exact science. Mixing and firing
properties of clays vary depending on many factors.
Figure 2 CONE 06 RED


Figure 3 CONE 06 WHITE

Figure 4 CONE 6 RED TALC SUBSTITUTION


Figure 5
CONE 6 RED NEPH SY SUBSTITUTION

Figure 6 CONE 6 WHITE (GLASS)

Figure 7
CONE 6 WHITE (140 GLASS)
Two trends can be discerned from Figures 2 through
7. First, the line for shrinkage vs.
percent substitution of glass is fairly flat.
This means that the amount of shrinkage of the clay body was relatively
unaffected by the glass substitution. In
contrast, the line for absorption drops significantly with increasing percentages
of glass. Lower absorption correlates
to both increased strength and improved resistance to freeze/thaw cycles.
Lower absorption is also indicative of lower temperature clay body
maturation during firing.
In general, these results support the work of the Bureau
of Mines cited above, to the effect that using glass as a clay body flux lowers
the maturation temperatures of clay bodies.
Appendix A contains the raw data from the tests.
3.1 Problems with Clays
The major problem of all these clay bodies to a varying
degree was solidification. After a
very short time, a clay that was soft and malleable when mixed would stiffen
to the point where it was unusable. This was particularly evident in clays with more than 20% glass
substitution. Clays with high glass
substitutions of 50% or more were very "short" or non-plastic. This made them unusable for most practical
applications.
Probably the best application for any of these clay
bodies would be press molding, which does not require a highly plastic clay
body.
3.2 Slip Casting
Casting slips are clay mixtures made to be formed in
plaster molds. Casting slips became
one of the most interesting results of these tests. The high glass content slips were extremely vitrified at low temperatures.
The surface of the castings were self-glazed, or took on a glass-like
quality.
To keep the high amount of glass suspended, extra suspending
agents (dispersants) were added. While
the first casting was often successful, it would appear to leave scumming
(most likely ball clay) on the surface of the mold. This would leave the mold unusable for subsequent
castings.
The other problem with these slips was settling.
Even with extra suspension agents, after a day or so, the glass would
settle to the bottom of the mixture and solidify, making it practically impossible
to remix even with a power mixer.
To experiment with casting slips, a basic ball clay
mix was made of:
§
1 part OM-4 Ball
Clay
§
1 part SGP Ball Clay
§
1 part Plastic Vitrox
(PV) Ball Clay
Using this ball clay mix, the following experiments
were performed. All tests were fired
to Cone 06:
1)
12.5 lb. BALL CLAY
MIX
12.5 lb. 325 GLASS
.117 gm Barium Carbonate
.235 gm Soda Ash
1.6 oz. Sodium Silicate
Results: Fast Setting; high vitrification;
self glazing. Clogs mold after multiple
castings. Very fragile green ware
2)
5 lb. Ball Clay Mix
10 lb. 140 Glass
10 lb. 325 Glass
.117 gm Barium Carb
.235 gm Soda Ash
.3 oz. Dispersant (Darvan)
2 1/8 Gal. H20
Results: Uncastable cracks in mold
3)
8.75 lb. Ball Clay
Mix
8.13 lb. 140 Glass
8.13 lb. 325 Glass
.117 gm Barium Carb
.235 gm Soda Ash
2 gal. H20
Results: Good consistency but cracks
in mold
4)
12.5 lb. Ball Clay
Mix
6.25 lb. 325 Glass
6.25 lb. 140 Glass
.117 gm Barium Carb
.235 gm Soda Ash
2 oz. Dispersant (Darvan)
4 oz. VEE Gum
2 gal. H20
Results: Good consistency but cracks
in mold. Sticks to mold. Self-glazing.
5)
12.5 lb. Ball Clay
Mix
12.5 lb. 325 Glass
.118 gm Barium Carbonate
.235 gm Soda Ash
2 oz. Dispersant
4 oz. VEE Gum
1 lb. Dry Celulose Fiber
2 gal. H20
Results: Good casting. Strong Green Strength. Sticks to mold after multiple castings. Self glazing.
All slips are highly vitrified. It appears that Ball Clay leaches to the surface
of the casting. This causes problems
with sticking.
4.0 CONCLUSION
This project confirms that finely graded glass is an
effective body flux when substituted for other fluxing materials in clay mixes.
Glass body flux lowers clay maturation temperatures and has the potential
to improve the efficiency of clay production facilities.
Additional work is needed to confirm specific clay body applications
which will benefit most from the addition of glass.
The workability of mixtures containing glass is different
from standard mixtures. More research
in this area could be focused on finding additives (dispersants, plasticizers,
etc.) that will improve the functionality of glass as a clay body flux.
APPENDIX A
RAW DATA FROM TESTS
DATA POINTS FOR CONE 06 RED

DATA POINTS FOR CONE 06 WHITE

DATA POINTS FOR CONE 6 RED TALC SUBSTITUTION

DATA POINTS FOR CONE 6 RED NEPH SY SUBSTITUTION

DATA POINTS FOR CONE 6 WHITE (GLASS)

DATA POINTS FOR CONE 6 WHITE (140 GLASS)
