t,' ij HAK r.jiilik QD478.N82015 desdestabilizing agent for solid state hydrogen storage / Nurul Shafikah Mohd Mustafa.

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AN KA TA US RP PE AH AN LT SU R NU H RA HI ZA

I ---- -.. tesis QD478.N82015 1100093779 Modification of magnesium hydride properties by catalysts and desdestabilizing agent for solid state hydrogen storage / Nurul Shafikah Mohd Mustafa. PUSAT PEMBELAJARAN DIGITAL SULTANAH NUR ZAHIRAH UNIVERSITI MALAYSIA TERENGGANU (UMT) Zl030 KUALA TERENGGANU 11 0 0 0 9 3 t,' ij, Lihat Sebelah HAK r.jiilik PUSAT PfMeEUjA?J!t D :!TAI. SUlTANAH NUR lahirah

MODIFICATION OF MAGNESIUM HYDRIDE PROPERTIES BY CATALYSTS AND DESTABILIZING AGENT FOR SOLID STATE HYDROGEN STORAGE Thesis Submitted in Fulfillment of the Requirement for the Degree of Master of Science in the School of Ocean Engineering Universiti Malaysia Terengganu January 2015 II

ABSTRACT Abstract of thesis presented to the Senate ofuniversiti Malaysia Terengganu in fulfillment of the requirement for the degree of Master of Science MODIFICATION OF MAGNESIUM HYDRIDE PROPERTIES BY CATALYSTS AND DESTABILIZING AGENT FOR SOLID STATE HYDROGEN STORAGE NURUL SHAFIKAH BINTI MOHD MUSTAFA January 2015 Main Supervisor Dr. Mohammad bin Ismail School School of Ocean Engineering Solid state hydrogen storage has been an attractive option due to the high gravimetric hydrogen capacity and favourable safety considerations compared with compressed and liquid hydrogen storage. Among the solid state materials, magnesium hydride is one of the potential candidates for hydrogen storage material. The major drawbacks of magnesium hydride are the slow absorption and desorption kinetic and high temperature required for efficient hydride decomposition. The purpose of this study is to improve the hydrogen sorption properties of magnesium hydride by modifying with catalysts and destabilized with other hydrides. All the samples studied were prepared by ball milling for 1 h and the hydrogen sorption properties, structural characterization, thermal properties and surface morphology were investigated. The effect of addition the K2TiF6 additive doped with MgH2 indicated that the onset desorption temperature has been reduced and the dehydrogenation and rehydrogenation kinetics ofthe doped MgH2 were III

also significantly improved compared to the undoped MgH2 due to the formation of active species of KH, TiH2, MgF2 and Ti that believed to work as a real catalyst for improving the hydrogen storage properties of MgH2. Apart from introducing a catalyst, the destabilization concept has also been used to improve the hydrogen storage properties of MgH2. The complex hydride with a high gravimetric density, LiAIH4 has been used as agent to destabilize MgH2. It was found that the formation of intermediate phase of Lio.92Mg4.o8 and Al12Mg17 during the dehydrogenation process resulted from the destabilization of MgH2 by the LiAIH4 may plays a critical role in the enhancement of the hydrogen sorption properties of the MgH2+LiAIH4 destabilized system. It was shown that the optimize MgH2+LiAIH4 destabilized system in this study was the composite of molar ratio 4: 1. In order to improve the hydrogen storage properties of the MgH2+LiAIH4 destabilized system two types of catalyst which is Fe203 and K2TiF6 has been added on this system. The effect of 5 wt.% of Fe203 on the 4MgH2+LiAIH4 composite demonstrated that the formation of ternary Li-Fe oxide species help to enhance the thermodynamic properties of the system and reduce the activation energy. It was believed that the formation of Ti-containing and AI-containing species together with a small amount of Li-containing species during the ball milling or the dehydrogenation process might be actually responsible for the catalytic effects, which strengthens the interaction between MgH2 and LiAIH4 and thus, further improved the dehydrogenation of the K2TiF6- added 4MgH2-LiAIH4 composite system. IV

ABSTRAK Abstrak tesis yang dikemukakan kapada Senat Universiti Malaysia Terengganu sebagai memenuhi keperluan untuk ijazah Master Sains. PENGUBAHSUAIAN SIFAT-SIFAT MAGNESIUN HIDRIDA DENGAN KATALIS DAN AGEN PENYAHSTABILAN UNTUK PENYIMPANAN HIDROGEN DALAM BENTUK PEPEJAL NURUL SHAFIKAH BINTI MOHD MUSTAFA January 2015 Penyelia Utama : Dr. Mohammad bin Ismail Pusat Pengajian : Pusat Pengajian Kejuruteraan Kelautan Penyimpanan hydrogen dalam bentuk pepejal menjadi satu pilihan yang menarik berikutan kapasiti gravimetrik hidrogen yang tinggi dan lebih selamat berbanding penyimpanan dalam bentuk mampatan gas dan cecair. Antara bahan-bahan keadaan pepejal, magnesium hidrida adalah satu calon yang berpotensi untuk bahan penyimpanan hidrogen. Keburukan utama magnesium hidrida adalah kinetik penyerapan dan perlepasan hidrogen yang perlahan dan suhu yang tinggi untuk penguraian hidrida yang cekap. Tujuan kajian ini adalah untuk meningkatkan sifat penyerapan hidrogen dalam magnesium hidrida dengan pengubahsuaian menggunakan pemangkin dan menambah jenis hidrida lain. Semua sampel yang dikaji telah dikisar selama 1 jam dan sifat penyerapan hydrogen, pencirian struktur, sifat termal dan permukaan morfologi telah disiasat. Pengaruh penambahan pemangkin K2TiF6 yang ditambah dengan magnesium hidrida menggunakan kisaran bola menunjukkan suhu awal pelepasan v

hidrogen telah berkurang dan peningkatan dalam penyerapan dan pelepasan kinetik disebabkan oleh pembentukan spesies aktif KH, TiH2, MgF2 dan Ti yang dipercayai bertindak sebagai pemangkin sebenar untuk sifat penyerapan hydrogen dalam magnesium hidrida. Selain dari menambah pemangkin, konsep ketidakstabilan juga telah digunakan untuk memperbaiki sifat-sifat penyimpanan hidrogen magnesium hidrida. Kompleks hidrida dengan kepadatan gravimetrik yang tinggi, LiAIH4 telah digunakan sebagai agen untuk menjejaskan kestabilan magnesium hidrida. Didapati pembentukan fasa pertengahan Li., 92Mg4.08 dan Al12Mg17 semasa proses dehidrogenasi akibat daripada ketidakstabilan MgH2 oleh LiAIH4 boleh memainkan peranan penting dalam sifat penyerapan hydrogen dalam sistem MgH2+LiAIH4. Keputusan menunjukkan gabungan dari nisbah molar 4: 1 adalah yang paling optimum untuk sistem ini. Untuk meningkatkan lagi sifat penyimpanan hydrogen dalam sistem MgH2+LiAIH4 dua jenis pemangkin iaitu Fe203 dan K2TiF 6 telah ditambah ke dalam sistem. Kesan 5 wt.% of Fe203 ke atas komposit MgH2+LiAIH4 menunjukkan pembentukan spesies oksida Li- Fe membantu untuk meningkatkan sifat termodinamik sistem dan mengurangkan tenaga pengaktifan. Manakala, pernbentukan spesies Ti dan Al bersama dengan jumlah kecil spesis Li semasa proses kisaran bola atau dehidrogenasi dipercayai bertanggungjawab dalam kesan pemangkinan, yang memperkuat interaksi antara MgH2 dan LiAIH4 dan seterusnya meningkatkan dehidrogenasi sistem MgH2+LiAIH4 yang ditambah dengan K2TiF6. VI