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    <subfield code="a">Synthesis and characterization of cationic-diutan gum to enhance  thermal stability for oil &amp; gas application /</subfield>
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    <subfield code="a">Water-based fluids have been used for centuries in oil and gas applications.  Technological advancements, particularly the addition of clay, polymer material, and  many other substances into the water-based fluids, were made to create a robust fluid  system to suit the demands of various reservoir conditions and to enhance oil and gas  production. The fluids can be tailored for water-soluble polymers with viscosifying or  gelling properties. As the oil and gas in the shallow wells become depleted, the oil and  gas exploration has moved into deeper and more extreme reservoir conditions, which  limited the performance of the currently available gelling fluids. At high temperatures,  the gelling fluids will experience degradation and lose their viscosity. To preserve environmental safety, it is more favorable to improve 'green' gelling fluid produced from biopolymer material instead of changing focus towards synthetic polymers with only slightly better thermal stability. Amongst the biopolymers, diutan gum (DG) was  chosen due to its high molecular weight and double helical structure. The application of  DG can still be considered new in the oil and gas industry; therefore, many of its  potentials need to be explored. The cationization of DG was conducted in this research  to further enhance the properties of DG. Cationic diutan gum (CDG) biopolymer was  developed to improve the thermal and rheological properties of water-based gelling  systems for upstream petroleum applications. The modification process involved  incorporating a quaternary amine group onto the diutan gum (DG) structure by mixing  DG with varying concentrations of N-(3-chloro-2-hydroxypropyl) trimethyl ammonium  chloride (CHPTAC) in the presence of sodium hydroxide as a catalyst. The  cationization resulted in a decrease in %H from 5.54% to 3.81% and an increase in %N  from 0.72 to 0.83, indicating the successful formation and grafting of CHPTAC onto  the polysaccharide structure. Fourier transform infrared spectroscopy (FTIR) confirmed  the incorporation of cationic moieties into the CDG chains, observed through an  increase in the intensity of the C&#x2013;N stretching vibration peak at 1411 cm-1 . Field  emission scanning electron microscopy (FESEM) revealed that the smooth surface of  DG transformed into a connective spherical reticular structure upon CHPTAC  modification. The viscosity of the CDG gelling fluid increased due to electrostatic chain  interaction, except for CDG with higher CHPTAC concentrations, which exhibited  decreased viscosity. Additionally, the viscoelasticity properties displayed a plateau-like  region, indicating a stable gel response towards frequency and excellent suspension  capability of CDG. Thermogravimetric analysis (TGA) and differential scanning  calorimetry (DSC) demonstrated a slight improvement in thermal characteristics for  CDG compared to DG. Furthermore, the thermal stability analysis using a static thermal  aging test confirmed that CDG remained stable up to 170 &#xB0;C, highlighting its potential  to meet the high-temperature requirements of the upstream petroleum industry. In  conclusion, the development of cationic diutan gum (CDG) presents a promising  approach for enhancing the thermal and rheological properties of water-based gelling  systems, making it a potential candidate for various challenging oil and gas reservoir  conditions</subfield>
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