2014
DOI: 10.1016/j.powtec.2014.05.047
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Kinetics and mechanism of three stages of thermal transformation of kaolinite to metakaolinite

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Cited by 99 publications
(41 citation statements)
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“…7. The DSC curves exhibited four main regions: i) region 1 (T<200 °C): all samples showed an endothermic peak attributed to elimination of adsorbed and absorbed water [34]; the peak position and intensity increased with increasing additive concentration; this may be due to the presence of high percentage of absorbed water in additives and/or the high pH values (8-9) of additives which improved the kaolin dehydration; ii) region 2 (T=200-820 °C): an endothermic peak centered at 558 °C was assigned to dehydroxylation process of kaolin leading to the transformation of kaolinite to metakaolinite (Al 2 O 3 .2SiO 2 ) and the loss of structural hydroxyl groups; the proposed dehydroxylation mechanism consists of the division of hydroxyl groups into H + and O 2-ions; the H + ions form water molecules with OH -groups while the O 2-ions are bonded to the newly created metakaolinite lattice [35]; it was noticed that the peak position and intensity decreased with the increase of additive concentration; this can be explained by the decrease of kaolin amount in the samples; a new endothermic peak was detected around 780 °C in S30, S50 and S70 samples which may be assigned to the decomposition reactions of carbonate (Eqs. C and E) [14]; iii) region 3 (T=820-1100 °C): the exothermic peak at about 995 °C with a formation enthalpy, ΔH, of -64.24 J/g observed for S0 was related to the transformation of metakaolinite to mullite phase [36]; with the increase of additive concentration, both the peak position and intensity decreased progressively indicating that the mineral formation proportion decreased in all samples; iv) region 4 (T=1100-1500 °C): for the sample S0, an exothermic peak was observed at 1295 °C with a stored enthalpy of about ΔH= -21.30 J/g; this may be due to the crystallization of cristobalite [37]; S10 exhibited two exothermic peaks, the first at 1136 °C corresponding to the formation of albite phase (ΔH= -7.29 J/g) and the second at 1325 °C corresponding to anorthite phase formation (ΔH= -19.24 J/g); sample S30 exhibited two small exothermic peaks at 1194 °C attributed to the albite crystal formation (ΔH= -4.14 J/g) and at 1376 °C (ΔH= -2.81 J/g) corresponding to the anorthite formation; for the sample S50, a small exothermic peak was observed at around 1218 °C which was due to the formation of albite Bulk density (g/cm 3 ) [38]; the same phenomena were observed for the sample S70; the first exothermic peak at 1113 °C corresponded to the formation of albite (ΔH= -4.4 J/g); the endothermic peaks showed the melt points of eutectic 2CaO.SiO 2 -5CaO.…”
Section: [Figura 4: Difratogramas De Raios X Das Cerâmicas Preparadasmentioning
confidence: 99%
“…7. The DSC curves exhibited four main regions: i) region 1 (T<200 °C): all samples showed an endothermic peak attributed to elimination of adsorbed and absorbed water [34]; the peak position and intensity increased with increasing additive concentration; this may be due to the presence of high percentage of absorbed water in additives and/or the high pH values (8-9) of additives which improved the kaolin dehydration; ii) region 2 (T=200-820 °C): an endothermic peak centered at 558 °C was assigned to dehydroxylation process of kaolin leading to the transformation of kaolinite to metakaolinite (Al 2 O 3 .2SiO 2 ) and the loss of structural hydroxyl groups; the proposed dehydroxylation mechanism consists of the division of hydroxyl groups into H + and O 2-ions; the H + ions form water molecules with OH -groups while the O 2-ions are bonded to the newly created metakaolinite lattice [35]; it was noticed that the peak position and intensity decreased with the increase of additive concentration; this can be explained by the decrease of kaolin amount in the samples; a new endothermic peak was detected around 780 °C in S30, S50 and S70 samples which may be assigned to the decomposition reactions of carbonate (Eqs. C and E) [14]; iii) region 3 (T=820-1100 °C): the exothermic peak at about 995 °C with a formation enthalpy, ΔH, of -64.24 J/g observed for S0 was related to the transformation of metakaolinite to mullite phase [36]; with the increase of additive concentration, both the peak position and intensity decreased progressively indicating that the mineral formation proportion decreased in all samples; iv) region 4 (T=1100-1500 °C): for the sample S0, an exothermic peak was observed at 1295 °C with a stored enthalpy of about ΔH= -21.30 J/g; this may be due to the crystallization of cristobalite [37]; S10 exhibited two exothermic peaks, the first at 1136 °C corresponding to the formation of albite phase (ΔH= -7.29 J/g) and the second at 1325 °C corresponding to anorthite phase formation (ΔH= -19.24 J/g); sample S30 exhibited two small exothermic peaks at 1194 °C attributed to the albite crystal formation (ΔH= -4.14 J/g) and at 1376 °C (ΔH= -2.81 J/g) corresponding to the anorthite formation; for the sample S50, a small exothermic peak was observed at around 1218 °C which was due to the formation of albite Bulk density (g/cm 3 ) [38]; the same phenomena were observed for the sample S70; the first exothermic peak at 1113 °C corresponded to the formation of albite (ΔH= -4.4 J/g); the endothermic peaks showed the melt points of eutectic 2CaO.SiO 2 -5CaO.…”
Section: [Figura 4: Difratogramas De Raios X Das Cerâmicas Preparadasmentioning
confidence: 99%
“…8, 12, 14 and 17 then provide the set of important parameters, which can have interesting utilization in many branches of heterogeneous kinetics. For example, it enables to eliminate the constant term from Kissinger Equation [14,15]:…”
Section: J•k à1mentioning
confidence: 99%
“…It was also recognized that the value of B(x) is not affected by the size of crystallites in the sample. Another example could be the dehydroxylation step during the process of thermal decomposition (400-700 C) of kaolinite [15]:…”
Section: J•k à1mentioning
confidence: 99%
“…Kaolinite is the main structure of kaolin mineral. Kaolinite consist of aluminosilicate hidrate compound Al 2 Si 2 O 5 (OH) 4 which consist of Si-O crystal tetrahedral layer (SiO 4 ) connected with alumina crystal octahedral layer (Al (O, OH)6) [1] . During calcination, the main reaction which occured is the breaking off the kaolinite structure.…”
Section: Introductionmentioning
confidence: 99%
“…The heating reaction breaks off -OH chain from the mineral, and collapsing the kaolinite structure, resulting in an amorphous aluminosilicate structure (Al 2 O 3 .2SiO 2 ) known as metakaolinite. Theoritically, there are three stages of thermal transformation of kaolinite to metakaolinite [2][3][4][5]:  When the heating process begin, kaolinite structure will break down and separate the alumina layer and silicate layer and break down the long order structure. This process occured until the heating temperature reach 400 o C, caused by the dehydroxilation of hydroxil structure in the layer which cause the water crystal to evaporate and leave the main structure.…”
Section: Introductionmentioning
confidence: 99%