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Wan Mohd Arif W Ibrahim
Preferred name
Wan Mohd Arif W Ibrahim
Official Name
Wan Mohd Arif, W Ibrahim
Alternative Name
Arif, W. M.
Arif, W. I.Wan Mohd
Ibrahim, Wan Mohd Arif Wan
Main Affiliation
Scopus Author ID
55543554600
Researcher ID
CDS-3018-2022
Now showing
1 - 5 of 5
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PublicationPhase transformation of Kaolin-Ground Granulated Blast Furnace Slag from geopolymerization to sintering process( 2021)
;Mohamad Hasmaliza ;Ikmal Hakem A. Aziz ;Bartłomiej JeżMarcin NabiałekThe main objective of this research was to investigate the influence of curing temperature on the phase transformation, mechanical properties, and microstructure of the as-cured and sintered kaolin-ground granulated blast furnace slag (GGBS) geopolymer. The curing temperature was varied, giving four different conditions; namely: Room temperature, 40, 60, and 80 °C. The kaolin-GGBS geopolymer was prepared, with a mixture of NaOH (8 M) and sodium silicate. The samples were cured for 14 days and sintered afterwards using the same sintering profile for all of the samples. The sintered kaolin-GGBS geopolymer that underwent the curing process at the temperature of 60 °C featured the highest strength value: 8.90 MPa, and a densified microstructure, compared with the other samples. The contribution of the Na2O in the geopolymerization process was as a self-fluxing agent for the production of the geopolymer ceramic at low temperatures.12 1 -
PublicationInfluences of SiO2, Al2O3, CaO and MgO in phase transformation of sintered kaolin-ground granulated blast furnace slag geopolymer( 2020)
;Hasmaliza Mohamad ;Jitrin Chaiprapa11 9 -
PublicationPhase transformation of Kaolin-ground granulated blast furnace slag from geopolymerization to sintering process( 2021-03-01)
;Hasmaliza M. ;Aziz I.H.A. ;Jeż B.Nabiałek M.The main objective of this research was to investigate the influence of curing temperature on the phase transformation, mechanical properties, and microstructure of the as-cured and sintered kaolin-ground granulated blast furnace slag (GGBS) geopolymer. The curing temperature was varied, giving four different conditions; namely: Room temperature, 40, 60, and 80◦ C. The kaolin-GGBS geopolymer was prepared, with a mixture of NaOH (8 M) and sodium silicate. The samples were cured for 14 days and sintered afterwards using the same sintering profile for all of the samples. The sintered kaolin-GGBS geopolymer that underwent the curing process at the temperature of 60◦ C featured the highest strength value: 8.90 MPa, and a densified microstructure, compared with the other samples. The contribution of the Na2 O in the geopolymerization process was as a self-fluxing agent for the production of the geopolymer ceramic at low temperatures.2 -
PublicationSelf-Fluxing mechanism in geopolymerization for Low-Sintering temperature of ceramic( 2021)
;Hasmaliza Mohamad ;Penphitcha Amonpattaratkit ;Joanna Gondro ;Wojciech SochackiNorfadhilah IbrahimKaolin, theoretically known as having low reactivity during geopolymerization, was used as a source of aluminosilicate materials in this study. Due to this concern, it is challenging to directly produce kaolin geopolymers without pre-treatment. The addition of ground granulated blast furnace slag (GGBS) accelerated the geopolymerization process. Kaolin–GGBS geopolymer ceramic was prepared at a low sintering temperature due to the reaction of the chemical composition during the initial stage of geopolymerization. The objective of this work was to study the influence of the chemical composition towards sintering temperature of sintered kaolin–GGBS geopolymer. Kaolin–GGBS geopolymer was prepared with a ratio of solid to liquid 2:1 and cured at 60 °C for 14 days. The cured geopolymer was sintered at different temperatures: 800, 900, 1000, and 1100 °C. Sintering at 900 °C resulted in the highest compressive strength due to the formation of densified microstructure, while higher sintering temperature led to the formation of interconnected pores. The difference in the X-ray absorption near edge structure (XANES) spectra was related to the phases obtained from the X-ray diffraction analysis, such as akermanite and anothite. Thermal analysis indicated the stability of sintered kaolin–GGBS geopolymer when exposed to 1100 °C, proving that kaolin can be directly used without heat treatment in geopolymers. The geopolymerization process facilitates the stability of cured samples when directly sintered, as well as plays a significant role as a self-fluxing agent to reduce the sintering temperature when producing sintered kaolin–GGBS geopolymers.2 11 -
PublicationAlkaline-Activation technique to produce low-temperature sintering activated-HAp ceramic( 2023)
;Hasmaliza Mohamad ;Andrei Victor Sandu ;Petrica Vizureanu ;Madalina Simona BaltatuPatimapon SukmakThe fabrication of hydroxyapatite (HAp) ceramics prepared by existing conventional sintering requires high-temperature sintering of 1250 °C to 1300 °C. In this paper, the activated metakaolin (MK)/HAp specimens were prepared from varied mix design inputs, which were varied solid mixtures (different amounts of MK loading in HAp) and liquid-to-solid (L/S) ratios, before being pressed and sintered at 900 °C. Phase analysis, thermal analysis, surface morphology, and tensile strength of the specimens were investigated to study the influences of the Al, Si, Fe, Na, and K composition on the formation of the hydroxyapatite phase and its tensile strength. XRD analysis results show the formation of different phases was obtained from the different mix design inputs HAp (hexagonal and monoclinic), calcium phosphate, sodium calcium phosphate silicate and calcium hydrogen phosphate hydrate. Interestingly, the specimen with the addition of 30 g MK prepared at a 1.25 L/S ratio showed the formation of a monoclinic hydroxyapatite phase, resulting in the highest diametrical tensile strength of 12.52 MPa. Moreover, the increment in the MK amount in the specimens promotes better densification when sintered at 900 °C, which was highlighted in the microstructure study. This may be attributed to the Fe2O3, Na2O, and K2O contents in the MK and alkaline activator, which acted as a self-fluxing agent and contributed to the lower sintering temperature. Therefore, the research revealed that the addition of MK in the activated-HAp system could achieve a stable hydroxyapatite phase and better tensile strength at a low sintering temperature.3 10