Atomic Force Microscopy and Molecular Dynamic Simulation of Adsorption of Polyacrylamide with Different Chemistries onto Calcium Carbonate.

This study investigates the interaction of polyacrylamide (PAM) of different functional groups (sulfonate vs. carboxylate) and charge density (30% hydrolysed vs. 10% hydrolysed) with calcium carbonate (CaCO) via atomic force microscopy (AFM) and partly via molecular dynamic (MD) simulations.

Atomic Force Microscopy of Hydrolysed Polyacrylamide Adsorption onto Calcium Carbonate.

In this work, the interaction of hydrolysed polyacrylamide (HPAM) of two molecular weights (F3330, 11-13 MDa; F3530, 15-17 MDa) with calcium carbonate (CaCO) was studied via atomic force microscopy (AFM). In the absence of polymers at 1.7 mM and 1 M NaCl, good agreement with DLVO theory was observed.

Molecular Dynamics Simulation of Polyacrylamide Adsorption on Calcite.

In poorly consolidated carbonate rock reservoirs, solids production risk, which can lead to increased environmental waste, can be mitigated by injecting formation-strengthening chemicals. Classical atomistic molecular dynamics (MD) simulation is employed to model the interaction of polyacrylamide-based polymer additives with a calcite structure, which is the main component of carbonate formations. Amongst the possible calcite crystal planes employed as surrogates of reservoir rocks, the (1 0 4) plane is shown to be the most suitable surrogate for assessing the interactions with chemicals due to its stability and more realistic representation of carbonate structure.

Non-linear response of colloid monolayers at high-frequency probed by ultrasound-driven microbubble dynamics.

Hypothesis: High-frequency interfacial rheology of complex interfaces remains challenging yet it is central to the performance of multiphase soft matter products. We propose to use ultrasound-driven bubble dynamics to probe the high-frequency rheology of a colloid monolayer used as model system with controlled interactions and simultaneous monitoring of the microstructure. We hypothesize that by comparing the response of colloid-coated bubbles with that of a bare bubble under identical experimental conditions, it is possible to detect the non-linear response of the monolayer and use it to extract interfacial rheological properties at 10s.

Adsorption of Hydrolysed Polyacrylamide onto Calcium Carbonate.

Carbonate rock strengthening using chemical techniques is a strategy to prevent excessive fines migration during oil and gas production. We provide herein a study of the adsorption of three types of hydrolysed polyacrylamide (HPAM) of different molecular weight (F3330S, 11-13 MDa; F3530 S, 15-17 MDa; F3630S, 18-20 MDa) onto calcium carbonate (CaCO) particles via spectrophotometry using a Shimadzu UV-2600 spectrometer. The results are compared to different adsorption isotherms and kinetic models.

Signature of elastic turbulence of viscoelastic fluid flow in a single pore throat.

When a viscoelastic fluid, such as an aqueous polymer solution, flows through a porous medium, the fluid undergoes a repetitive expansion and contraction as it passes from one pore to the next. Above a critical flow rate, the interaction between the viscoelastic nature of the polymer and the pore configuration results in spatial and temporal flow instabilities reminiscent of turbulentlike behavior, even though the Reynolds number Re≪1. To investigate whether this is caused by many repeated pore body-pore throat sequences, or simply a consequence of the converging (diverging) nature present in a single pore throat, we performed experiments using anionic hydrolyzed polyacrylamide (HPAM) in a microfluidic flow geometry representing a single pore throat.

Layer-by-layer adsorption: Factors affecting the choice of substrates and polymers.

The electrostatic layer-by-layer technique for fabrication of multi-layered structures of various sizes and shapes using flat and colloidal templates coupled with polyelectrolyte layer-forming materials has attracted significant interest among both academic and industrial researchers due to its versatility and relative simplicity of the procedures involved in its execution. Fabrication of the multi-layered structures using the electrostatic layer-by-layer method involves several distinct stages each of which holds great importance when considering the production of a high-quality product. These stages include selection of materials (both template and a pair of construction polyelectrolytes), adsorption of the first polyelectrolyte layer onto the selected templates, formation of the second layer comprised of the oppositely charged polyelectrolyte and guided by the interactions between the two chosen polyelectrolytes, and multi-layering, where a selected number of layers are produced, and which is conditioned by both intrinsic properties of the involved construction materials and external fabrication conditions such as temperature, pH and ionic strength.

Layer-by-layer encapsulated nano-emulsion of ionic liquid loaded with functional material for extraction of Cd ions from aqueous solutions.

Ionic liquids can serve as an environmentally-friendly replacement for solvents in emulsions, therefore they are considered suitable to be used as an emulsified medium for various active materials one of which are extractors of metal ions. Increasing the extraction efficiency is considered to be one of the key objectives when working with such extraction systems. One way to improve the extraction efficiency is to increase the contact area between the extractant and the working ionic solution.

Fabrication of polyelectrolyte multilayered nano-capsules using a continuous layer-by-layer approach.

The layer-by-layer approach is a highly versatile method for the fabrication of multilayered polymeric films and capsules. It has been widely investigated in research for various polyelectrolyte pairs and core template particles. However, the fabrication of nano-sized capsules at the larger scale is difficult and time consuming, due to the necessity of washing and centrifugation steps before the deposition of each polyelectrolyte layer.

Microfluidic processing of concentrated surfactant mixtures: online SAXS, microscopy and rheology.

We investigate the effect of microfluidic flow on the microstructure and dynamics of a model surfactant mixture, combining synchrotron Small Angle X-ray Scattering (SAXS), microscopy and rheology. A system comprising a single-chain cationic surfactant, hexadecyl trimethyl ammonium chloride (C16TAC), a short-chain alcohol (1-pentanol) and water was selected for the study due to its flow responsiveness and industrial relevance. Model flow fields, including sequential contraction-expansion (extensional) and rotational flows, were investigated and the fluid response in terms of the lamellar d-spacing, orientation and birefringence was monitored in situ, as well as the recovery processes after cessation of flow.

Towards an understanding of the release behavior of temperature-sensitive liposomes: a possible explanation of the "pseudoequilibrium" release behavior at the phase transition temperature.

It is generally believed that thermal sensitive liposomes (i.e. vesicles) that contain 1,2-dihexadecanoyl-sn-glycero-3-phosphocholine (DPPC) and 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-[methoxy(polyethyleneglycol)-2000 (DSPE.

Preparation and characterization of microgels sensitive toward copper II ions.

An emulsion polymerization technique has been used to prepare chemically crosslinked microgels in aqueous suspension that are sensitive to the presence of copper ions. Poly(N-isopropylacrylamide) (PNIPAM) was copolymerized with different amounts of 1-vinylimidazole (VI), and the resultant microgels exhibited multi-responsive behavior being sensitive to changes in temperature, pH and to the presence of metal ions, particularly copper. These swelling properties of the microgel particles were characterized using dynamic light scattering (DLS), scanning electron microscopy (SEM), and transmission electron microscopy (TEM).

Surface tension-induced gel fracture. Part 2. Fracture of gelatin gels.

The spreading of surfactants on gel layers has been found to be accompanied by an intriguing instability which involves the formation of crack-like patterns on the surface of the gel. In an attempt to extend the findings on the spreading on agar gels presented in part 1 of this series, this paper examines the case of surfactant spreading on gelatin, which is a characteristic example of a protein-based gel. Aqueous solutions of Silwet L-77 of varying concentrations were spread on thick gelatin layers of varying concentrations.

Surface tension-induced gel fracture. Part 1. Fracture of agar gels.

This work involves an experimental investigation of the spreading of liquids on gel layers in the presence of surfactants. Of primary interest is the instability that accompanies the cracking of gels through the deposition and subsequent spreading of a drop of surfactant solution on their surfaces. This instability manifests itself via the shaping of crack-like spreading "arms", in formations that resemble starbursts.

Development of lysolipid-based thermosensitive liposomes for delivery of high molecular weight proteins.

The purpose of the present investigation was to determine the feasibility of using lysolipid-based thermal sensitive liposomes (145nm) for high molecular weight molecule delivery. Fluorescein isothiocyanate conjugate-albumin was used as a model drug (MW 66kDa). Thermal sensitive liposomes, which encapsulated the protein were prepared using a passive encapsulation methodology involving freeze-thawing cycles followed by extrusion.

Interaction forces between particles stabilized by a hydrophobically modified inulin surfactant.

The adsorption isotherm of a hydrophobically modified inulin (INUTEC SP1) on polystyrene (PS) and poly(methyl methacrylate) (PMMA) particles was determined. The results show a high affinity isotherm for both particles as expected for a polymeric surfactant adsorption. The interactions forces between two layers of the hydrophobically modified inulin surfactant adsorbed onto a glass sphere and plate was determined using a modified atomic force microscope (AFM) apparatus.

Manipulating forces between surfaces: applications in colloid science and biophysics.

It is the forces between the microscopic constituents of materials which to a large extent determine the macroscopic properties. For example, it is the differences in bonding between the carbon atoms which determines the different physical properties of carbon and graphite. The same is true in colloidal systems.

Dewetting behavior of aqueous cationic surfactant solutions on liquid films.

Previous experimental work has shown that the spreading of a drop of aqueous anionic surfactant solution on a liquid film supported by a negatively charged solid substrate may give rise to a fingering instability (Afsar-Siddiqui, A. B.; Luckham P, F.

Interaction forces between polyethylene oxide-polypropylene oxide ABA copolymers adsorbed to hydrophobic surfaces.

Block and graft copolymers are frequently used as stabilizing agents in colloidal dispersions. One common material is the range of polymers known as "Pluronics," which is a BASF trade name for ABA block copolymers composed of a propylene oxide anchoring block (B block) and two ethylene oxide buoy or stabilizing blocks (A block); the equivalent ICI (Uneqima) trade name is Synperonic. In the work presented here the interactions between adsorbed layers of these materials immersed in 10(-2) M sodium sulfate solutions are presented.

Investigation of the molecular interactions in a pMDI formulation by atomic force microscopy.

The forces of interaction between inhalable formoterol fumarate dihydrate particles, and the various components of a pressurised Metered Dose Inhaler (pMDI) (e.g. aluminium container, other drug particles and stabilising excipients) were investigated in isolation and combination in the model propellant 2H, 3H perfluoropentane (HPFP).

The spreading of surfactant solutions on thin liquid films.

The spreading of a surfactant solution on a water film at first glance seems a trivial problem. However, in the last 30 years or so this has been shown to be anything like the case. There have been numerous studies which show that Marongoni driven fingering of the spreading surfactant front exists.