STUDY THE EFFECT OF SILICA NANOPARTICLE ON RHEOLOGY IN OIL BASED MUD

Limitations of conventional drilling fluid with macro and micro size are not suitable for extreme environment in drilling or completion operation. Macro and micro type fluid additive is impossible to fulfil challenging drilling and production operation requirement due to their inadequate physical, mechanical, chemical, thermal and environment characteristic. Introduction of nanotechnology in oil and gas industry produce a promising nanoparticle which are able to satisfy the requirements; physically small, chemically and thermally stable to design a smart fluid. This project will determine the effect of silica nanoparticle on rheology in oil based to analysis the changes the rheology properties of drilling fluid with and without silica nanoparticle after and before aging process. The ability of silica nanoparticle as an additive in drilling fluid will be evaluate through a few experiments; rheology and high pressure high temperature (HPHT) fluid loss test. Analysis of experiments results will determine the suitability of silica nanoparticle to be used in oil based mud. As a final result, combination of silica nanoparticle in oil based mud enhances the rheology of oil based mud compare to the oil based mud without silica nanoparticle

Readout fidelity of coaxial holographic digital data page recording in nanoparticle–(thiol–ene) polymer composites

We report on an experimental investigation of nanoparticle-concentration and thiol-to-ene stoichiometric ratio dependences of symbol error rates (SERs) and signal-to-noise ratios (SNRs) of digital data pages recorded at a wavelength of 532 nm in thiol–ene based nanoparticle–polymer composite (NPC) films by using a coaxial holographic digital data storage method. We show that SERs and SNRs at the optimized material condition can be lower than 1 × 10−4 and higher than 10, respectively, without error correction coding. These results show the usefulness of thiol–ene based NPCs as coaxial holographic data storage media

Electrostatically gated membrane permeability in inorganic protocells

Although several strategies are now available to produce functional microcompartments analogous to primitive cell-like structures, little progress has been made in generating protocell constructs with self-controlled membrane permeability. Here we describe the preparation of water-dispersible colloidosomes based on silica nanoparticles and delineated by a continuous semipermeable inorganic membrane capable of self-activated, electrostatically gated permeability. We use crosslinking and covalent grafting of a pH-responsive copolymer to generate an ultrathin elastic membrane that exhibits selective release and uptake of small molecules. This behaviour, which depends on the charge of the copolymer coronal layer, serves to trigger enzymatic dephosphorylation reactions specifically within the protocell aqueous interior. This system represents a step towards the design and construction of alternative types of artificial chemical cells and protocell models based on spontaneous processes of inorganic self-organization

Cellular membrane trafficking of mesoporous silica nanoparticles

This dissertation mainly focuses on the investigation of the cellular membrane trafficking of mesoporous silica nanoparticles. We are interested in the study of endocytosis and exocytosis behaviors of mesoporous silica nanoparticles with desired surface functionality. The relationship between mesoporous silica nanoparticles and membrane trafficking of cells, either cancerous cells or normal cells was examined. Since mesoporous silica nanoparticles were applied in many drug delivery cases, the endocytotic efficiency of mesoporous silica nanoparticles needs to be investigated in more details in order to design the cellular drug delivery system in the controlled way. It is well known that cells can engulf some molecules outside of the cells through a receptor-ligand associated endocytosis. We are interested to determine if those biomolecules binding to cell surface receptors can be utilized on mesoporous silica nanoparticle materials to improve the uptake efficiency or govern the mechanism of endocytosis of mesoporous silica nanoparticles. Arginine-glycine-aspartate (RGD) is a small peptide recognized by cell integrin receptors and it was reported that avidin internalization was highly promoted by tumor lectin. Both RGD and avidin were linked to the surface of mesoporous silica nanoparticle materials to investigate the effect of receptor-associated biomolecule on cellular endocytosis efficiency. The effect of ligand types, ligand conformation and ligand density were discussed in Chapter 2 and 3. Furthermore, the exocytosis of mesoporous silica nanoparticles is very attractive for biological applications. The cellular protein sequestration study of mesoporous silica nanoparticles was examined for further information of the intracellular pathway of endocytosed mesoporous silica nanoparticle materials. The surface functionality of mesoporous silica nanoparticle materials demonstrated selectivity among the materials and cancer and normal cell lines. We aimed to determine the specific organelle that mesoporous silica nanoparticles could approach via the identification of harvested proteins from exocytosis process. Based on the study of endo- and exocytosis behavior of mesoporous silica nanoparticle materials, we can design smarter drug delivery vehicles for cancer therapy that can be effectively controlled. The destination, uptake efficiency and the cellular distribution of mesoporous silica nanoparticle materials can be programmable. As a result, release mechanism and release rate of drug delivery systems can be a well-controlled process. The deep investigation of an endo- and exocytosis study of mesoporous silica nanoparticle materials promotes the development of drug delivery applications

The size and polydispersity of silica nanoparticles under simulated hot spring conditions

The nucleation and growth of silica nanoparticles in supersaturated geothermal waters was simulated using a flow-through geothermal simulator system. The effect of silica concentration ([SiO2]), ionic strength (IS), temperature (T) and organic additives on the size and polydispersity of the forming silica nanoparticles was quantified. A decrease in temperature (58 to 33°C) and the addition of glucose restricted particle growth to sizes <20 nm, while varying [SiO2] or ISdid not affect the size (30-35 nm) and polydispersity (±9 nm) observed at 58°C. Conversely, the addition of xanthan gum induced the development of thin films that enhanced silica aggregation

Self-Assembly of Silica Nanoparticles on Glass Surface

In this work, silica nanoparticles were synthesised using Stöber Method. Compared to other synthesis techniques like, Stöber Method is regarded as one of the simplest and most effective route for silica nanoparticle synthesis. Low temperature stabilises the nanosilica suspension, and low ratio of NH3/TEOS avoids coagulation of particles. These nanoparticles (average size less than 1 ?m) were self-assembled on a glass surface using sodium carboxymethyl cellulose (CMCNa) and oxalic acid template. The silica nanoparticle self-assembly was validated by the observed fractal-pattern in a sessile drop. For preparing superhydrophilic film, sequential adsorption (layer-by-layer coating) of a polyelectrolyte and silica nanoparticle suspension on the surface was done for appropriate number of cycles. Layer-by-Layer assembly is an economical, easy and a fast technique for coating of substrates with alternate layers. It is known that superhydrophilicity (and superhydrophobicity) increases with increase in surface roughness. By this technique, two different coatings with equal number of depositions were created – one consisting of polyelectrolyte and silica nanoparticles and other consisting of polyelectrolyte and silica nanoparticle with sodium carboxymethyl cellulose and oxalic acid. Contact angle measurement done on these two coating validated the superhydrophilic property of the films. The second-type coating had a lower contact angle (less than 10°) while the first-type coating had a contact angle slightly greater than 10°

Effect of crosslinker length on the elastic and compression modulus of poly(acrylamide) nanocomposite hydrogels

Polymer hydrogelshave shown to exhibit improved properties upon the addition of nanoparticles; however, the mechanical underpinnings behind these enhancements have not been fully elucidated. Moreover, fewer studies have focused on developing an understanding of how polymer parameters affect the nanoparticle-mediated enhancements. In this study, we investigated the elastic properties of silica nanoparticle-reinforced poly(acrylamide) hydrogels synthesized using crosslinkers of various lengths. Crosslinker length positively affected the mechanical properties of hydrogels that were synthesized with or without nanoparticles. However the degree of nanoparticle enhancement was negatively correlated to crosslinker length. Our findings enable the understanding of the respective roles of nanoparticle and polymer properties on nanoparticle-mediated enhancement of hydrogels and thereby the development of next-generation nanocomposite materials

Polymeric Nanocapsule from Silica Nanoparticle@Cross-linked Polymer Nanoparticles via One-Pot Approach

A facile strategy was developed here to prepare cross-linked polymeric nanocapsules (CP nanocapsules) with silica nanoparticles as templates. The silica nanoparticle@cross-linked polymer nanoparticles were prepared by the encapsulation of the silica nanoparticles by the one-pot approach via surface-initiated atom transfer radical polymerization of hydroxyethyl acrylate in the presence ofN,N′-methylenebisacrylamide as a cross-linker from the initiator-modified silica nanoparticles. After the silica nanoparticle templates were etched with hydrofluoric acid, the CP nanocapsules with particle size of about 100 nm were obtained. The strategy developed was confirmed with Fourier transform infrared, thermogravimetric analysis and transmission electron microscopy