Some morphological aspects of PVC processing

The efficiency of unplasticised polyvinylchloride (UPVC) extrusion from dry blends of high-attrition mixers largely depends on powder characteristics of the dry blends. Better understanding of the morphological features of the powder blend and its processed form would therefore underlie the optimisation of the efficiency of the overall process. This is the theme, and therefore the raison d'être, for the present study. [Continues.

Effect of equilibrium contact angle on water equilibrium film thickness for the carbon dioxide–brine–mineral system based on surface force theory

Abstract The thickness of the thin wetting film depends on disjoining pressure forces, and it evolves with pH evolution due to brine acidification at the physical and chemical conditions of geological carbon dioxide storage becoming thinner in response to dewetting. In the literature, molecular dynamic simulation (MDS) studies have been employed to understand the effect of pressure/capillary pressure on the thin wetting film evolution. In this paper, a theoretical approach based on the Frumkin–Derjaguin Equation (FDE), models of electric double layer repulsion, and van der Waals forces have been used for the calculation of the wetting film thickness. The approach excluded hydration forces contribution to disjoining pressure forces due partly to its poorly understood nature, and partly to the high salinity conditions encountered in geological carbon storage. Due to its promising global storage capacity compared to other lithologies, the carbon dioxide–brine–silica systems was chosen to simulate sandstone saline aquifers. The validation of the model benefited much from literature resources on data and a universal model of carbon dioxide–brine interfacial tension. Calculated results confirm pH-induced dewetting and they follow trends controlled by pH and pressure as found in the literature. The novelty of the paper can be seen from the fact that it has demonstrated a theoretical supplement to MDS studies in addition to justifying the fundamental utility and versatility of the FDE. Moreover, the paper links for the first time, a transcendental equation to the thin wetting film theory encountered in the carbon dioxide–solid–brine system found in geological carbon storage

Theoretical Interpretation of pH and Salinity Effect on Oil-in-Water Emulsion Stability Based on Interfacial Chemistry and Implications for Produced Water Demulsification

The petroleum industry produces thousands of barrels of oilfield waters from the initial stage driven by primary production mechanisms to the tertiary stage. These produced waters contain measurable amounts of oil-in-water emulsions, the exact amounts being determined by the chemistry of the crude oil. To meet strict environmental regulations governing the disposal of such produced waters, demulsification to regulatory permissible levels is required. Within the electric double layer theory, coupled with the analytical solutions to the Poisson–Boltzmann Equation, continuum electrostatics approaches can be used to describe the stability and electrokinetic properties of emulsions. In the literature, much of the surface charge density and zeta potential relationship to emulsion stability has been confined to systems with less salinity. In this paper, we have exploited the theoretical foundations of the electric double layer theory to carry out theoretical evaluations of emulsion salinity based on zeta potential and surface charge density calculations. Most importantly, our approaches have enabled us to extend such theoretical calculations to systems of the higher salinity characteristic of oil-in-water emulsions found in oilfield-produced waters, based on crude oil samples from the literature with varying surface chemistry. Moreover, based on the definition of acid crude oils, our choice of samples represents two distinct classes of crude oils. This approach enabled us to evaluate the stability of emulsions associated with these produced oilfield waters in addition to predicting the potential of demulsification using demulsifiers. Given that the salinity range of this study is that encountered with the vast majority of produced oilfield waters, the findings from our theoretical predictions are perfect guides as far as emulsion stability is concerned

Interrelationship of Electric Double Layer Theory and Microfluidic Microbial Fuel Cells: A Review of Theoretical Foundations and Implications for Performance

Microbial fuel cells and their related microfluidic systems have emerged as promising greener energy alternatives for the exploitation of avenues related to combined power and wastewater treatment operations. Moreover, the potential for their application in biosensing technology is large. However, while the fundamental principles of science that govern the design and operation of microbial fuel cells (MFCs) and microfluidic microbial fuel cells (MMFCs) are similar to those found in colloid science, the literature shows that current research lacks sufficient reference to the electrostatic and electrokinetic aspects, focusing mostly on aspects related to the architecture, design, anodes, microbial growth and metabolism, and electron transfer mechanisms. In this regard, research is yet to consider MFCs and MMFCs in the context of electrostatic and electrokinetic aspects. In this extensive review, we show, for the first time, the interrelationship of MFCs and MMFCs with electric double layer theory. Consequently, we show how the analytical solution to the mean field Poisson–Boltzmann theory relates to these systems. Moreover, we show the interrelationship between MFC and MMFCs’ performance and the electric double layer and the associated electrostatic and electrokinetic phenomena. This extensive review will likely motivate research in this direction

Spontaneous Imbibition and an Interface-Electrostatics-Based Model of the Transition Zone Thickness of Hydrocarbon Reservoirs and Their Theoretical Interpretations

The transition zone (TZ) of hydrocarbon reservoirs is an integral part of the hydrocarbon pool which contains a substantial fraction of the deposit, particularly in carbonate petroleum systems. Consequently, knowledge of its thickness and petrophysical properties, viz. its pore size distribution and wettability characteristic, is critical to optimizing hydrocarbon production in this zone. Using classical formation evaluation techniques, the thickness of the transition zone has been estimated, using well logging methods including resistivity and Nuclear Magnetic Resonance, among others. While hydrocarbon fluids’ accumulation in petroleum reservoirs occurs due to the migration and displacement of originally water-filled potential structural and stratigraphic traps, the development of their TZ integrates petrophysical processes that combine spontaneous capillary imbibition and wettability phenomena. In the literature, wettability phenomena have been shown to also be governed by electrostatic phenomena. Therefore, given that reservoir rocks are aggregates of minerals with ionizable surface groups that facilitate the development of an electric double layer, a definite theoretical relationship between the TZ and electrostatic theory must be feasible. Accordingly, a theoretical approach to estimating the TZ thickness, using the electrostatic theory and based on the electric double layer theory, is attractive, but this is lacking in the literature. Herein, we fill the knowledge gap by using the interfacial electrostatic theory based on the fundamental tenets of the solution to the Poisson–Boltzmann mean field theory. Accordingly, we have used an existing model of capillary rise based on free energy concepts to derive a capillary rise equation that can be used to theoretically predict observations based on the TZ thickness of different reservoir rocks, using well-established formation evaluation methods. The novelty of our work stems from the ability of the model to theoretically and accurately predict the TZ thickness of the different lithostratigraphic units of hydrocarbon reservoirs, because of the experimental accessibility of its model parameters

Correlation of tangible quality parameters of vegetable-based transformer fluids

Due to the inherent environmental footprint of petroleum derived transformer fluids, the power industry is gradually exploring the potential of vegetable oils as alternatives. The impetus comes mostly from vegetable oils renewability and their inherent biodegradability.However, the major drawback in the use of vegetable oils as dielectric fluids is their lower oxidative stability and higher kinematic viscosity compared to mineral oils. The results obtained clearly demonstrate the correlation between spectroscopic data induction time, kinematic viscosity, acid value, and peroxide value. Quantitatively, the absorption frequencies of functional groups in vegetable oil transformer fluids that can be correlated to the mentioned quality parameters show noticeable changes with aging/oxidative degradation. The study also demonstrates the utility of integrating spectroscopic data to understand trends in induction time and kinematic viscosity of oil samples heated under transformer service conditions