The effect of the glazed layer and firing conditions (temperature and duration) on the thermal shocks behavior of tableware porcelains has been studied. Two types of glazed layers and three firing conditions, used industrially in the commercial porcelains manufacture, are used in this investigation. Repeated thermal shock tests showed that the glazed layer with higher alumina/silica ratio is more resistant to thermal shocks and that the slow firing cycle, even at a relatively low temperature, is very beneficial for the thermal shock resistance of the porcelain matrix. Three-point bending tests showed that the crazing phenomenon, which affects the glazed layers as well as the porcelain matrix, does not affect significantly the mechanical resistance of these materials.
1. Introduction
The fine and translucent porcelains are used generally to produce tableware, household kitchen utensils, sanitary ware, laboratory materials, electric insulators, sparkplugs for combustion engines, and biomedical organs (such as teeth, disc, or body). Tableware porcelains are often coated with a silica-glazed layer to increase their water resistance, whitening, smoothing, and shining properties. However, repeated thermal shocks lead to the formation of randomly distributed surface cracks and crazes which are attributed principally to the relaxation of compressive stresses and to the difference between the thermal expansion coefficients of the glazed layer and the porcelain matrix [1–3]. The nucleation and the evolution of these cracks depend also on the chemical composition of the glazed layer and the firing process [1, 4–16].
During the last few decades, many works have been devoted to the study of thermal shock resistance of metallic-coated or -glazed porcelains used in dental biomaterials. In particular, the phenomenon of crazing has been extensively investigated due to its detrimental consequences when these crazes become a nesting site for bacteria [17, 18]. However, studies devoted to the tableware porcelains are very limited and do not reflect the commercial importance and the general use of these materials in our daily life. The few performed studies are aimed at determining the effect of parameters such as microstructure, firing conditions, and quartz content on the mechanical and physical properties of porcelains. These results which are sometimes contradictory have been based on three main hypotheses such as the presence of fine mullite needles [5, 6, 8], the dispersion strengthening of the vitreous porcelain structure [9], and the reinforcement of the matrix by the development of compressive residual stresses [1, 7, 10, 11].
The thermal shock resistance of porcelain, as one of a ceramic family, is usually evaluated by the water-quenching method in which specimens are heated to a particular temperature and then quenched in water bath. This test method for the determination of thermal shock resistance by water quenching is commonly used and has been standardized in the ASTM C1525. Thermal shock resistance is graded by the critical temperature difference (ΔTMax) which describes the maximum change in instantaneous temperature that can occur without the initiation of cracks.
The main objective of this work is to present a comparative study in order to determine the effects of glazed layers and firing conditions on the thermal shock resistance of an industrial tableware porcelain. Repeated thermal shock tests are performed on six porcelain grades to reproduce the thermal crazing similar to the one that appeared in service on the same materials. The crack nucleation and propagation have been studied in terms of number and length. The results are analyzed as a function of the number of thermal shocks applied to the material. The evolution of the mechanical properties of the studied materials as a function of the number of thermal shock cycles has been studied using three-point bending tests.
2. Experimental Procedure2.1. Materials and Sample Preparation
The samples used in this investigation, provided by the Tunisia porcelain company, are prepared from porcelain of 50% kaolin, 25% quartz, and 25% feldspar. The samples are classified in two glazed layer families: 230 and 302. The chemical compositions of the two glazed layers are indicated in Table 1. Three grades (1, 2, and 3) have been prepared from each family using different firing conditions (temperatures and duration) as follows:
(1) firing at 1340°C during 25 hours using a tunnel furnace;
(2) firing at 1360°C during 7.5 hours using a fast-firing furnace (length 36 m);
(3) firing at 1370°C during 7.5 hours using a fast-firing furnace (length 60 m).
Chemical composition (wt.%) of the glazed layers.
Family
SiO2
Al2O3
TiO2
Fe2O3
MgO
CaO
Na2O
K2O
230
72,29
12,48
0,90
0,54
2,51
6,45
0,56
4,27
302
66,90
17,20
0,90
0,54
2,22
7,70
0,45
4,09
For example, grade 230-2 designates the porcelain sample from the family 230 subjected to firing at 1360°C during 7.5 hours using a fast-firing furnace (length 36 m).
Test samples (Figure 1) of prismatic shape (87×34×5.5) are obtained with the same manufacturing processes. These samples present a glazed face and a normal face that represent the original structure of the porcelain material. Designations which are glazed face and normal face will be preserved carefully in this study in order to determine their thermal shock behavior.
Sample geometry.
Sample geometry (size in mm)
Sample photography
2.2. Bending Tests
The mechanical properties of the six porcelain grades used in this investigation have been determined using a 3-point bending tests with a span (l) of 50 mm and a crosshead speed of 1 mm/min on a MTS system. Young’s modulus and the maximum stress have been determined by expressions (1) and (2), respectively:
(1)E=Cl348IGz,(2)σmax=32FMaxlbh².
In these equations, C=FMax/yMax is the slope of the force-deflection curve, IGz=bh3/12 is the quadratic moment, FMax and yMax are force and deflection at fracture, respectively, l is the span, and b and h are the width and the thickness of the sample, respectively.
2.3. Thermal Shock Tests
To reduce the error margin, thermal shock tests have been applied simultaneously to sets of three different samples. The thermal cycle applied to each set is illustrated in Figure 2. It consists of a heating phase to T for 20 minutes followed by water quenching to ambient temperature T0=20±2C°. The intermediate transfer phase of the samples between the furnace and the water bath has been neglected since it is done very quickly (few seconds). The thermal shock resistance (ΔTmax) is estimated [19] using the following relationship:
(3)ΔTmax=(1-ν)σmaxEα,
where σmax is the maximum fracture stress, E is Young’s modulus, ν is Poisson’s ratio, and α is the thermal expansion coefficient of glazed layers.
Thermal shock cycle applied to samples.
2.4. Cracks Characterization
The samples used in the thermal shock tests have been initially examined by macrographic observations in order to verify the absence of surface defects (scratches, scraping, bubbles, etc.). After every thermal shock cycle, both glazed face and normal face of the sample are macrographically examined, and the generated cracks due to the thermal shocks are scanned for qualitative and quantitative analyses.
3. Results3.1. Mechanical Resistance of the Initial State Material
Three-point bending test results obtained on the studied material in the initial state for different grades are summarized in Table 2. The evaluated properties are the mechanical stress, Young’s modulus, and the thermal shock resistance. All these properties are determined using (1), (2), and (3), respectively, with a Poisson’s ratio v=0,25, thermal expansion coefficient α=44×10-7(C°)-1 for 230 family, and α=43×10-7(C°)-1 for 302 family. The results are shown in Table 3.
Maximum force and deflection for the studied porcelain grades.
Grade
230-1
230-2
230-3
302-1
302-2
302-3
Average maximum force FMax(N)
750
1025
700
850
950
800
Average maximum deflection yMax (mm)
0.11
0.12
0.11
0.12
0.13
0.11
Estimated mechanical and thermal properties of the studied porcelain grades.
Grade
230-1
230-2
230-3
302-1
302-2
302-3
Mechanical stress σmax (MPa)
55
75
51
62
69
58
Young’s modulus E (GPa)
38
47
35
39
40
40
Thermal shock resistance ΔTMax (°C)
236
258
236
258
279
236
3.2. Thermal Shock Resistance
We assume that the nucleation stage is achieved, after a number of thermal shock cycles, when the surface of the sample presents one or several detectable cracks that could be observed by macrographic examination [2]. For example, Figure 3 shows the cracks’ cartography of the glazed face and normal face of the grade 302-3 produced by cyclic thermal shocks at ΔT=230°C.
Surface cracks evolution by thermal shocks of the grade 302-3 at ΔT=230C°.
3.2.1. Number of Cracks
The number of cracks is defined by the number of all observed cracks, by macrographic examination, on the sample surface. For example, Figure 4 illustrates the number of cracks as a function of thermal shock cycles at ΔT=230°C for the studied grades.
Number of cracks as a function of the number of thermal shock cycles at ΔT=230°C.
Glazed face
Normal face
3.2.2. Length of Cracks
The total length of cracks is defined as the sum of lengths of all existing cracks. Figure 5 illustrates the evolution of the crack length as a function of the number of thermal shock cycles generated at ΔT=230°C for the studied grades.
Total length (mm) of cracks as a function of the number of thermal cycles ΔT=230°C.
Glazed face
Normal face
Results of thermal shock tests showed that the number and the total length of the formed cracks stabilize in both faces at a maximum of 20 cycles for ΔT=230°C and after the first 2 cycles for ΔT=280°C. For ΔT=180°C, no cracks have been detected after 30 thermal shock cycles.
For ΔT=230C°(T=250C°) the following can be shown.
The number of cracks on the normal face for grades 2 and 3 is higher than that on the glazed face, whereas it is comparable on both faces for grade 1. This number decreases in some cases where certain cracks undergo junction by coalescence that often occurs by the creation of triple points or by the interconnection of two cracks.
No new cracks appeared after the first five cycles on both faces for all the studied grades.
The total length of cracks is higher on the normal faces than on the glazed faces for all the grades.
For the porcelain matrix, the slow-firing process applied to grade 1, although is performed at a relatively low temperature, seems to have a beneficial influence on the thermal shock resistance (Figure 6);
The crack propagation is very brutal on the normal face, whereas these cracks grow much slower and often stopped on the glazed face (Figure 3).
Cracks cartography on the normal face of grades 230-1 and 230-2 after cyclic thermal shocks at ΔT=230°C.
3.3. Mechanical Resistance Evolution
The mechanical resistance degradation of the porcelain grades used in this study by thermal shock has been studied in terms of the isotropic damage (D) given by the following expression:
(4)D=|σ-σ0|σ0,
where σ0 and σ are the mechanical resistance of the material in the initial state and after the thermal shocks, respectively.
Table 4 gives the damage by thermal shocks after 30 cycles at ΔT=230°C for the different grades. It is clear that the damage by thermal shocks at ΔT=230°C is lower for grade 1, whereas it is comparable for other grades. This result is in good agreement with the rate of cracking (Figure 4). However, a damage of 2.4% has been produced for grade 1 after 30 thermal shock cycles at ΔT=180°C for which no crack has been macrographically observed. Grades subjected to thermal shocks at ΔT=280°C lost 50% of their mechanical resistance after the first applied cycle.
Damage of the studied grades by thermal shocks at ΔT=230°C.
Grade
230-1
230-2
230-3
302-1
302-2
302-3
Damage D (%)
6
12
11,5
6,5
11
10
4. Discussion
At ΔT=180C°(T=200C°), the studied industrial porcelain grades did show good resistance to the thermal shocks and no cracks have been detected until 30 cycles, whereas, for ΔT=230C°(T=250C°), a network of cracks had been developed on both glazed and normal faces of the six studied grades. These results are in good agreement with the theoretical evaluations of the thermal resistance provided in Table 3.
The phenomenon of crack arrest, which is very remarkable on the glazed face, can be attributed to the presence of precipitates in the glazed layer which serve as obstacles to brutal propagation of these cracks. In particular, it has been confirmed [20–22] that the presence of TiO2 in the chemical composition of a vitreous structure facilitates the nucleation and the growth of these precipitates. Furthermore, this precipitation is strongly favorable by the relatively high firing temperature.
The glazed layer of 302 family showed a more attractive behavior than that of 230 family. This result consolidates the assumption that the high alumina/silica ratio improves the mechanical resistance of the glazed layer.
The brutal propagation of cracks in the normal face, occurred usually by coalescence, is confirmed for this type of materials and reflects the amorphous structure of the porcelain matrix. The slow firing process, although performed at a relatively low temperature (grade 1), is very beneficial for the thermal shock resistance of the porcelain matrix. However, this process did not show a considerable effect on the thermal shock behavior of glazed layers. For identical firing durations (grades 2 and 3), the relatively low difference of the firing temperature did not show a significant effect on thermal shock resistance.
The evolution of developed cracks by thermal shocks at ΔT=230°C stops after the first 20 cycles for the six grades. This result can be attributed, as confirmed in the literature [2, 3, 17, 18], to the relaxation of compressive stresses. These last ones are related to the evolution of the porcelain matrix microstructure during firing process, and they are more important when the firing duration is shorter [7, 9–11]. The few crazes observed on the glazed face can be related to the delamination phenomenon [3, 23] occurred at the glazed layer-porcelain matrix interface due to their different thermal expansion rate.
The damage, after 30 cycles of thermal shock at ΔT=230°C is relatively low (the maximum value is 12%). In addition, a damage of 2.4% after 30 cycles thermal shocks at ΔT=180°C has been obtained even though no cracks have been detected by macrographic observation. This puts in question the method usually used to detect and to follow the evolution of generated thermal shock cracks. In addition, these results led to classify the observed cracks into the crazing phenomenon that consists of the generation of randomly oriented superficial cracks which do not affect considerably the mechanical behavior. However, crazed tableware porcelain should be generally avoided for food contact as the cracks can harbor bacteria.
5. Conclusions
Thermal shock tests have been performed on six grades of an industrial porcelain in order to compare their behavior to thermal shocks. The studied grades differ by the glazed layers 230 and 302 and by the firing conditions (1, 2, or 3). Test samples have glazed and normal faces.
At a difference of temperature of ΔT=180°C, the studied industrial porcelain showed a good resistance to thermal shocks. However, for ΔT=230°C, a network of cracks has been developed on the glazed and the normal faces.
The thermal shock resistance of glazed layer is more important than of porcelain matrix. However, the two glazed layers show a similar behavior to thermal shocks in terms of crack initiation and propagation with a minor advantage for the 302 family.
The slow firing, even performed at relatively low temperature (grade 1), has a very beneficial effect on the thermal shock resistance of the porcelain matrix. For the same firing duration (grades 2 and 3), a small difference in firing temperature does not have a considerable effect on the thermal shock resistance.
The crazing produced by thermal shocks does not have considerable effect on the structural damage that varies between 6 and 12% at ΔT=230°C. This damage is attributed to the compression stress relaxations in the porcelain matrix and to the delamination at the interface between the porcelain matrix and the glazed layer.
Acknowledgment
The authors are grateful to Mr. Tarek Kort, in charge of quality group in the Tunisie Porcelaine Society, for the samples’ preparation and technical assistance.
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