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Effect of Materials

Design on Properties of
Porcelain Insulators
Substitution of alumina for silica
improved the mechanical properties
of high-voltage porcelain insulators
but did not have a significant effect on
their electrical properties.

Fig. 1 Examples of insulators.

N. Riahi Noori, R. Sarraf Mamoory and S. Mehraeen

High-strength electrical porcelain is needed by the power industry. This need is met by a specific composition of raw materials, which consists of clays and feldspars. These two raw materials, depending on geological and geophysical characteristics, have various compositions and specifications. Three main constituents of
electrical porcelain bodies (Fig. 1) are clays (as plastic materials), fillers (such as silica and alumina) and
refractories (such as feldspars and talc).1
When an electrical porcelain body that contains silica is fired at high temperatures, the corners of the
quartz particles are dissolved into a feldspar-containing corrosive liquid. In the critical case, these particles are
completely dissolved in the liquid phase. The decrease of solid quartz content in the system leads to remarkable decrease in the mechanical strength of the body.
Thus, firing time and temperature of bodies that contain quartz must be controlled carefully. To achieve
the highest strength, quartz particles must be fine, and the bodies must be fired carefully. Long periods of firing, higher firing temperatures and annealing processes completely vitrify the body. This leads to decreases in
strength.2,3
Another imperfection in the electrical properties of porcelain bodies that contain quartz results from the
difference between thermal expansion coefficients of the quartz grains and the body matrix around them. This
difference results in tensile stress in the quartz grains and compressive stress in the surrounding matrix. When
the temperature changes, these stresses intensify. This leads to development of microcracks that are created
in the grinding step of quartz grains and in the - to -phase transformation of the quartz.
These microcracks act as stress localization centers. Therefore, stress near the cracks is remarkably greater
than the applied stress.4 Decrease of strength under load (when the insulator is suspended) usually results in
abrupt fracture of the insulator because of the growth of these microcracks. This problem can be solved by
decreasing the size or content of quartz grains in the body matrix or by substituting a portion of the quartz
with other refractory materials.4
Decrease in silica grain size leads to higher strength, lower workability and higher firing to drying shrinkage. On the other hand, when the content of fine grains increases, fracture toughness decreases. The only
proper substitution for quartz in industrial production of porcelain insulators is alumina, which can replace a
large portion or total content of quartz.46

American Ceramic Society Bulletin, Vol. 86, No. 3

9201

Porcelain Insulators

Bending strength (MPa)

The Experiment

Alumina content (%)

To study the effect of alumina on the


mechanical and electrical properties of electrical porcelain bodies, six body groups were
selected (Table 1). Group 1 had the common
composition of electrical insulator bodies. In
groups 26, silica content decreased gradually and alumina content increased gradually.
In group 6, silica was totally replaced by alumina. The wet method was used for porcelain body preparation. Kaolin, ball clay,
feldspar and silica were used as raw materials.
All of the groups had the same amount of
kaolin, ball clay, and feldspar.

Alumina and silica were smaller in size


Fig. 2 Effect of silica replacement with alumina on bending strength of
than 120 m. The materials were wet milled
porcelain insulators () 1250, (I) 1300 and () 1350C).

Density (g/cm3)

with 80100 wt% water and then cast into


plaster molds to be formed. The samples were
dried at room temperature for 48 h and kept
at 110C for 5 h. The temperature then was
increased to maximum in 4 h. The samples
were fired at this temperature for 2 h and
cooled inside the furnace at its natural rate.

The maximum firing temperatures selected in this study were 1250, 1300, and
1350C. Bending strength (Table 2), thermal shock resistance, density (Table 2) and
porosity were determined in accordance with
ASTM standards. In each case, several samples were tested. Relative permeability factor
Alumina content (%)
(r) and dielectric loss tangent (tan ) at 60
Hz and 1 MHz were measured. The measureFig. 3 Effect of silica replacement with alumina on density of porcelain ment accuracy for was 0.5% and for tan
r
insulators () 1250, (I) 1300 and () 1350C).
was 3%.

Strength
The effect of silica replacement by alumina on bending strength of electrical porcelain bodies was determined (Fig. 2). In the main composition, the body that contained 25% silica without alumina had the lowest strength. When the alumina content was increased and the silica content decreased, the strength of the
samples increased.
On the other hand, as temperature increased, strength increased because dissolution of quartz (silica) in
system increased. Moreover, when firing temperature increased, alumina was partially dissolved into system,
but the rate of dissolution was much less than that of quartz. When the alumina content in the body and
the firing temperature increased, mullite content (Al2O32SiO2) increased, which acted as an agent for
strength increase. Although alumina content in the body was <8%, the formation of mullite phase was possible at temperature as high as 1340C.

Density and Porosity


Body composition was important to final density (Fig. 3). When silica was replaced with alumina in the
main composition of the body, the density of the fired bodies increased. In other words, as the silica content of the body decreased, the density of the bodies increased because of decreased porosity induced from
microcracks around silica grains.
Open porosity content (available pores in bodies) versus increased alumina content in the system was
determined (Fig. 4).

9202

American Ceramic Society Bulletin, Vol. 86, No. 3

Porcelain Insulators
The microstructures of two samples, one
with 30% alumina and another with 30%
silica, were observed using SEM. The porosity in the silica bodies was studied in particular (Fig. 5).

Water Absorption

Table 1 Composition of Prepared Bodies


Group

Feldspar

Kaolin

Ball clay

Alumina

Silica

number

(wt%)

(wt%)

(wt%)

(wt%)

(wt%)

15

35

25

25

15

35

25

20

15

35

25

10

15

25

15

10

25

20

25

25

The water absorption of bodies decreased


4
15
35
with increased firing temperature because
5
15
35
pores and open porosities of the bodies
6
15
35
decreased and there was increased glassy
phase content in the body. In addition, as
the silica content in the body decreased
(and alumina increased), water absorption of the bodies decreased because of
decreased microcracks and pores. Water absorption of high-voltage insulators
must be zero.7

Thermal Shock
Thermal shock resistance was determined by heating samples to 100C for 1
h and then immersing them in 0C ice water to be cooled completely. This cycle
was repeated n times.
The number of cycles before crack creation is the criteria for thermal shock
resistance. For samples prepared in this study, n = 30. The literature requires n
20 for electrical ceramics in a similar condition.

Table 3 Loss Tangent


Group
No.

Dielectric loss
tangent (103)

24.5

24.7

24.8

25

25.1

25

Dielectric Properties
Dielectric loss tangent was measured at 60 Hz and 20C (Table 3). The dielectric loss tangent was similar for the various bodies (~25 103). The dielectric loss tangent of bodies at 1 MHz decreased to 12 103
that again was similar for all bodies.
The relative permeability factor for all bodies at 60 Hz was 67.

About the Authors


N. Riahi Noori is a Researcher at the Niroo Research Institute, Tehran, Iran, and is a Ph.D. student at
Tarbiar Modares University, Tehran. R. Sarraf Mamoory is Associate Professor, Tarbiat Modares University.
S. Mehraeen is a Researcher in the Ceramic and Polymer Group, Niroo Research Institute.

References
1S.I.

Warshaw and R. Seider, Comparison of Strength of Triaxial Porcelains Containing Alumina and Silica, J. Am.
Ceram. Soc., 50, 337 (1967).

2R.S.
3J.E.

Gorour, et al., Outdoor Insulators, Ravi S. Gorur Inc., Ariz., 1999; pp. 215.

Schroeder, Inexpensive High-Strength Electrical Porcelain, Am. Ceram. Soc. Bull., 57, 526 (1978).

4P.

Johnson and W.G. Robinson, Development of Pottery BodiesElectrical Porcelain; presented at the 22nd
Meeting of the Pottery Section (Trentham Gardens, Stoke-on-Trent, U.K., 1947), pp. 23.

5A.M. Bisha, B.H F. Al-Khayat and F.A. Awni, Dielectric and Physicomechanical Properties of Electrical Porcelain
Bodies, Am. Ceram. Soc. Bull., 64, 598 (1985).
6J.

Liebermann, Reliability of Materials for High-Voltage Insulators, Am. Ceram. Soc. Bull., 42 [5] 670 (2000).

7M.

Nemamcha, S. Rouaiguia, A. Belbah and B. Belfarhi, Dielectric Properties of Alumino-Silicate Ceramic


Materials, IEEE, 22, 413 (1995).

American Ceramic Society Bulletin, Vol. 86, No. 3

9203

Table 2 Properties of Bodies


Group

Sintering

Bending

No.

temperature (C)

1250

2.37

1300

2.41

50

1350

2.43

45

strength (MPa)
39

1250

2.43

53

1300

2.46

60

1350

2.48

59

1250

2.48

62

1300

2.51

75

1350

2.55

83

1250

2.53

70

1300

2.58

83

1350

2.61

98

1250

2.59

75

1300

2.66

88

1350

2.70

105

1250

2.65

80

1300

2.70

92

1350

2.74

110

Porosity (%)

Density

(g/cm3)

Alumina content (%)


Fig. 4 Effect of silica replacement with alumina on water absorption of
porcelain insulator () 1250, (I) 1300 and () 1350C).

(a)

(b)

Fig. 5 SEM photographs of body with (a) 30% silica and


(b) 30% alumina.

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