Enhanced Foam Stability Using Nanoparticle in High Salinity High Temperature Condition for Eor Application

The capability of commercial nanoparticles to perform as foam stabilizer were investigated at reservoir temperature of 96°C. Al2O3, Fe3O4, Co3O4, CuO, MgO, NiO, ZrO2, ZnO and SiO2 nanoparticles that were characterized using XRD, FTIR, FESEM-EDX, TEM and PSA, were blended in the in-house formulated surfactant named IVF respectively at a particular ratio. The test was performed with and without the presence of reservoir crude oil. Results showed that formulation with nanoparticles enhanced foam stability by having longer foam half-life than the IVF surfactant alone, especially in the absence of oil. Only SiO2 nanoparticles were observed to have improved the foam stability in both test conditions. The unique properties of SiO2 as a semi-metal oxide material may have contributed to the insensitivity of SiO2 nanoparticle towards crude oil which is known as a foam destabilizer. The physical barrier that was formed by SiO2 nanoparticles at the foam lamella were probably unaffected by the presence of crude oil, thus allowing the foams to maintain its stability. In thermal stability tests, we observed the instability of all nanoparticles in the IVF formulation at 96°C. Nanoparticles were observed to have separated and settled within 24 hours. Therefore, surface modification of nanoparticle was done to establish steric stabilization by grafting macro-molecule of polymer onto the surface of SiO2. This in-house developed polymer grafted silica nanoparticles are named ZPG nanoparticles. The ZPG nanoparticles passed the thermal stability test at 96°C for a duration of 3 months. In the foam wetness analysis, ZPG nanoparticles were observed to have produced more wet foams than IVF formulation alone, indicating that ZPG is suitable to be used as foam stabilizer for EOR process as it showed catalytic behaviour and thermally well-stable at reservoir temperature.

Methanol to Formaldehyde: An Overview of Surface Studies and Performance of an Iron Molybdate Catalyst

Formaldehyde is a primary chemical in the manufacturing of various consumer products. It is synthesized via partial oxidation of methanol using a mixed oxide iron molybdate catalyst (Fe2(MoO4)3–MoO3). This is one of the standard energy-efficient processes. The mixed oxide iron molybdate catalyst is an attractive commercial catalyst for converting methanol to formaldehyde. However, a detailed phase analysis of each oxide phase and a complete understanding of the catalyst formulation and deactivation studies is required. It is crucial to correctly formulate each oxide phase and influence the synthesis methods precisely. A better tradeoff between support and catalyst and oxygen revival on the catalyst surface is vital to enhance the catalyst’s selectivity, stability, and lifetime. This review presents recent advances on iron molybdate’s catalytic behaviour for formaldehyde production—a deep recognition of the catalyst and its critical role in the processes are highlighted. Finally, the conclusion and prospects are presented at the end.

Nickel Phosphide Catalysts as Efficient Systems for CO2 Upgrading via Dry Reforming of Methane

This work establishes the primordial role played by the support’s nature when aimed at the constitution of Ni2P active phases for supported catalysts. Thus, carbon dioxide reforming of methane was studied over three novel Ni2P catalysts supported on Al2O3, CeO2 and SiO2-Al2O3 oxides. The catalytic performance, shown by the catalysts’ series, decreased according to the sequence: Ni2P/Al2O3 > Ni2P/CeO2 > Ni2P/SiO2-Al2O3. The depleted CO2 conversion rates discerned for the Ni2P/SiO2-Al2O3 sample were associated to the high sintering rates, large amounts of coke deposits and lower fractions of Ni2P constituted in the catalyst surface. The strong deactivation issues found for the Ni2P/CeO2 catalyst, which also exhibited small amounts of Ni2P species, were majorly associated to Ni oxidation issues. Along with lower surface areas, oxidation reactions might also affect the catalytic behaviour exhibited by the Ni2P/CeO2 sample. With the highest conversion rate and optimal stabilities, the excellent performance depicted by the Ni2P/Al2O3 catalyst was mostly related to the noticeable larger fractions of Ni2P species established.

Solvothermal Synthesis of Bi2s3 Nanoparticles for Active Photocatalytic and Energy Storage Device Applications

High edge energy storage with large life-span stable materials have become the most significant and major requirement in near future. Bismuth sulfide (Bi2S3) Nanoparticles (NPs) was effectively synthesized by utilizing Bismuth diethyldithiocarbamate (Bi[DTC]) complex as single-source antecedent. The synthesized Bi2S3 NPs were affirmed by structural, morphological and thermal analysis with various analytical studies. The electrochemical performance of Bi2S3 NPs reveals that, exhibit redox behavior from cyclic voltammetry analysis, the charge-discharge analysis was examined by the galvanostatic chronopotentiometry. Bi2S3 NPs exhibit excellent supercapacitor behavior with value of the specific capacitance 470 Fg-1 at current density 0.5 Ag-1 and the retentivity of 79 % after 1000 cycles. The Bi2S3 NPs were further utilized as photocatalytic discoloration of Congo Red (CR) dye in aqueous medium under UV-light irradiation. Which shows, excellent catalytic behaviour, up to 98% of CR dye degrade within 150 min. and it is exhibit good catalytic stability and reusability.

Alkaline modified A-site deficient perovskite catalyst surface with exsolved nanoparticles and functionality in biomass valorisation

Environmental problems associated with the use of fossil fuels and increase in energy demands due to rise in population and rapid industrialisation, are the driving forces for energy. Catalytic conversion of biomass to renewable energies is among the promising approaches to materialize the above. This requires development of robust catalysts to suppress deactivation due to carbon deposition and agglomeration. In this work, surface properties and chemistry such as exsolution of B-site metal catalyst nanoparticles, particle size and distribution, as well as catalyst-support interactions were tailored through the use of alkaline dopants to enhance catalytic behaviour in valorisation of glycerol. The incorporation of alkaline metals into the lattice of an A-site deficient perovskite modified the surface basic properties and morphology with a consequent robust catalyst-support interaction. This resulted in promising catalytic behaviour of the materials where hydrogen selectivity of over 30% and CO selectivity of over 60% were observed. The catalyst ability to reduce fouling of the catalyst surface as a result of carbon deposition during operation was also profound due to the robust catalyst-support interaction occurring at the exsolved nanoparticles due to their socketing and the synergy between the dopant metals in the alloy in perovskite catalyst systems. In particular, one of the designed systems, La0.4Sr0.2Ca0.3Ni0.1Ti0.9O3±δ, displayed almost 100% resistance to carbon deposition. Therefore, lattice rearrangement using exsolution and choice of suitable dopant could be tailored to improve catalytic performance.