Academic literature on the topic 'Electrosteric stabilization'

In a circular economy approach, paint waste is recycled and reformulated to be transformed into new paints. In this regard, the lifespan of recycled paints must be properly assessed and extended beyond their preliminary specifications. This study aimed to improve the stability of waterborne acrylic paints by adding dispersing agents. Seventeen dispersing agents were added to two formulations of recycled paints: one stable, and one showing signs of instability. Their stability was characterized by analytical centrifugation and quantification of the supernatant. Among the tested dispersing agents, four showed a significant improvement in stability in both tests. These dispersants belong to the four possible categories of stabilization mechanisms: electrostatic, steric, electrosteric, and controlled stabilization. Electrosteric dispersing agents are especially effective in both paints. The combination of two dispersants does not have a synergistic effect.

Nanocrystal suspensions proved to be a potent enabling principle for biopharmaceutics classification system class II drugs with dissolution limited bioavailability. In the example of itraconazole (ITZ) as a model drug combined with electrosteric stabilization using hydroxypropyl cellulose (HPC-SL), sodium dodecyl sulfate (SDS) and polysorbate 80 (PS80), the impacts of formulation and process parameters of a dual centrifugal mill on material attributes such as particle size, zeta potential, particle morphology, storage stability and especially solid-state characteristics were evaluated. A minimal concentration of 0.9% (w/w) HPC-SL, 0.14% (w/w) SDS and 0.07% (w/w) PS80 was necessary for sufficient nanoparticle stabilization. Despite the minor effect of PS80, its presence was beneficial for electrosteric stabilization. Choosing lower stabilizer concentrations resulted in a pronounced increase in particle size due to agglomeration, which was confirmed by SEM imaging and a decrease in zeta potential in combination with an amorphization of the particles. Milling temperature had no significant impact on the particle size, whereas milling speed and the size of the milling beads used were found to have a strong impact on the critical material attributes such as particle size and polydispersity index. The smallest particle sizes could be obtained by using the smallest milling bead size. However, the smallest obtainable particle size could only be achieved by using two-fold stabilizer concentrations, as smaller particles exhibit a larger specific surface area.

The kinetics of electrosterically stabilized emulsion systems was studied. The aim of this was to understand the impact that steric and electrosteric stabilizers have on the kinetics of particle growth and particle formation in the area of emulsion polymerization. The well-established mechanisms that govern these processes for emulsions stabilized by conventional low molecular weight surfactants were used as a reference point for comparative purposes. Model latexes were synthesized that comprised of a poly(styrene) core stabilized by a corona of poly(acrylic acid). The advent of successful controlled radical polymerization techniques in heterogeneous media (via RAFT polymerization) allowed for latexes to be synthesized under molecular weight control. For the first time, the degree of polymerization of the stabilizing block on the particle surface was able to be controlled and verified experimentally using mass spectrometry techniques. Three latexes were made with different average degrees of polymerization of the stabilizing block; five, ten and twenty monomer units respectively. A methodology was developed to remove the RAFT functionality from the polymer chains present in the emulsion while retaining the desired particle morphology. Oxidation with tertbutylhydroperoxide (TBHP) was proven to be successful at eliminating the living character provided by the thiocarbonyl end-group. Extensive dialysis and cleaning of the latex was performed to ensure no residual TBHP or reaction by-products remained. Latexes with poly(styrene) cores were chosen for this work as poly(n-butyl acrylate) latexes were shown to be influenced by chain transfer to polymer, providing an additional kinetic complication. The three electrosterically stabilized emulsions were used as seed latexes in carefully designed kinetic experiments to measure the rate of polymerization as a function of time. Two independent techniques (chemically initiated dilatometry and γ-relaxation dilatometry) were used to measure the rate coefficients of radical entry (ρ) and exit (k) in these systems – the two parameters that essentially govern the rate of particle growth. The latexes were chosen such that they satisfied ‘zero-one’ conditions (i.e. that any given latex particle contains at most one growing radical at any given time) in order to simplify data analysis. Three different chemical initiators were used, each yielding a radical with a different electric charge. Results from γ-relaxation experiments demonstrated that the three electrosterically stabilized latexes gave very long relaxation times when removed from the radiation source, ultimately yielding very small k values. These values were up to a factor of 10 smaller than that predicted by the ‘transfer-diffusion’ model for exit for particles of that size. This reduction was attributed to a ‘restricted diffusion’ effect, where the exiting monomeric radical has to diffuse through a dense layer of polymer on the particle surface, where its mobility will be restricted. Modification of the Smoluchowski equation for diffusion-controlled adsorption/desorption to account for this postulate led to the development of a model that gave excellent semi-quantitative agreement with experiment. Chemically initiated dilatometric experiments (using three different types of initiator) gave the unusual result of very low reaction rates and low steady-state values of 'nbar', the average number of radicals per particle. Using the standard kinetic equations for styrene-based systems (where it is assumed that an exited monomeric radical undergoes re-entry), this led to the calculation of impossibly small values of the entry rate coefficient ρ (far below any background or ‘thermal’polymerization rate). However upon removing the assumption of re-entry and assuming that exited radicals undergo termination, the obtained values of ρ were in almost perfect agreement with the values predicted from the ‘control by aqueous phase growth’ entry mechanism. This unexpected result was attributed to chemical reaction with the poly(acrylic acid) stabilizers through chain transfer to polymer (via hydrogen-atom abstraction). This postulate was verified by separate experiments that demonstrated that poly(acrylic acid) could act as a reasonably efficient chain transfer agent for styrene polymerization. The addition of poly(acrylic acid) to the aqueous phase of a conventionally stabilized emulsion also led to the rate reduction seen previously. NMR experiments demonstrated the existence of poly(acrylic acid-graft-styrene), which could only be formed through termination of a poly(styrene) chain with a poly(acrylic acid) chain bearing a mid-chain radical (as the product of a chain transfer reaction). These additional terms of transfer and termination were included in the governing kinetic equations of emulsion systems (the Smith-Ewart equations) to develop a model to account for the behaviour of electrosterically stabilized latexes. The ultimate fate of an exiting radical was now shown to be a competition between fates; successful desorption into the aqueous phase, or chemical reaction (through transfer or termination) within the hairy layer. These additional terms were shown to significantly reduce the theoretical value of nbar, and were in excellent agreement with experiment. For small electrosterically stabilized particles with a densely packed ‘hairy layer,’ it was seen that transfer/termination is the dominant loss mechanism as opposed to desorption. The developed model showed that as the particle size was increased, the dominant loss mechanism once again became successful desorption into the aqueous phase. The model was shown to give excellent agreement with experimental data from ‘uncontrolled’ emulsion systems. To explain the highly unusual secondary nucleation behaviour seen in systems such as these, it was postulated that beta-scission of a poly(acrylic acid) chain bearing a mid-chain radical is an important mechanistic step in the nucleation mechanisms of these systems. Modelling (both steady-state and time-dependent) gave good agreement with experiment with a minimal number of adjustable parameters. Theory (and supporting experimental evidence) demonstrated that this nucleation mechanism is only significant at high particle numbers; under other conditions the well-known ‘homogeneous nucleation’ mechanism is once again dominant.

O presente projeto de trabalho buscou avaliar e estabelecer relações de causa e efeito que justificassem a ocorrência de singularidades no comportamento reológico de formulações complexas contendo elevada carga de sólidos em suspensão incorporada. O mecanismo de estabilização coloidal empregado para preparação das formulações e posterior análise foi o mecanismo de estabilização eletroestérico. O caso particular estudado correspondeu à dispersão de cargas inorgânicas (óxido de alumínio) em meio aquoso auxiliada pela incorporação de conteúdo orgânico com ação dispersante (poliacrilato de amônio) e ligante (emulsão acrílica) respectivamente. A implementação de técnicas analíticas complementares permitiu o estudo detalhado de uma singularidade associada ao comportamento reológico do sistema, exclusivamente evidenciada em função da elevada carga de sólidos, oferecendo, portanto, subsídios para elaboração de um modelo supramolecular fundamentado em possíveis alterações de configuração das cadeias poliméricas para justificativa do fenômeno. A contribuição referente ao pleno entendimento do fenômeno, considerando-se suas causas e efeitos, reside na possibilidade de se estabelecer diretrizes de formulação que propiciem a otimização das quantidades de aditivos incorporados e o respectivo controle do estado de dispersão e estabilidade do sistema. Considerou-se, para efeitos práticos de engenharia de formulação, que o mínimo secundário de viscosidade corresponda ao ponto ótimo de estabilidade do sistema mesmo que a condição de máxima dispersão já tenha sido alcançada para uma concentração de dispersante equivalente ao mínimo primário de viscosidade. A contribuição do efeito estérico associada à reduzida distância de separação entre as partículas (IPS) mostrou-se de vital importância para assegurar a viabilidade de uma dada formulação. A proposta aqui apresentada fundamentou-se no mecanismo de depleção como principal força motriz para desencadear possíveis mudanças de conformação espacial das cadeias poliméricas implicando, portanto, em alterações do raio hidrodinâmico, da fração volumétrica efetiva ocupada e da intensidade de interação (repulsão) entre as partículas. O efeito da dinâmica configuracional sofrida pelo sistema refletiu-se diretamente no comportamento reológico do mesmo. O caráter de inovação do presente trabalho reside na utilização não convencional da técnica de espectroscopia eletroacústica, empregada para avaliação de mudanças do raio hidrodinâmico de partículas em suspensão (sistemas concentrados), integrada com a técnica de turbidimetria dinâmica de varredura para avaliação de desempenho (cinética de sedimentação) de formulações complexas (suspensões).
The present research project pretended to evaluate and establish cause and effect relationships able to justify the singularities evidenced when exploring the rheological behaviour of complex formulations containing elevated solids loading. The stabilization mechanism used for the preparation of the dispersed systems and subsequent analyses corresponded to the electrosteric mechanism. The particular case studied herein corresponded to the dispersion of inorganic colloidal particles (aluminun oxide) in aqueous media assisted by the incorporation of organic components acting respectively as dispersant (ammonium polyacrylate) and binder agent (acrylic emulsion). The implementation of complementary analytical techniques enabled the detailed study of a singularity related to the rheological behaviour of the system that could only be evidenced for high solids loading condition. The results obtained provided the fundamental concepts necessary to propose a supramolecular model based on possible conformational changes associated with the adsorbed polymeric chains and sufficient to justify the phenomenon. Considering the practical aspects related to formulation engineering, it was determined that the secondary minimum viscosity corresponds to the optimum stablity condition although the maximum dispersion condition was achieved for dispersant concentrations equal to the primary minimum viscosity. The contribution of the steric effect associated with the reduced interparticle separation distance (IPS) showed itself to be of vital importance to ensure the viability of a stable formulation. The proposal here presented suggests that the depletion mechanism corresponds to the major cause that imparts possible configurational changes related to the adsorbed polymer chains. As a result of, significant alterations of the hydrodynamic radius, effective volume fraction occupied by and interaction intensity (repulsion) between the particles are expected. The effect of the configurational dynamics experienced by the system reflected directly on the associated rheological behaviour.The innovation character of the present work relies on the employment of the electrosacoustic spectroscopy technique to evaluate possible changes of the hydrodynamic radius of the suspended particles (concentrated systems) integrated with the dynamic turbidimetry technique to evaluate the performance (sedimentation kinetics) of the complex formulations.

Doctor of Philosophy
The kinetics of electrosterically stabilized emulsion systems was studied. The aim of this was to understand the impact that steric and electrosteric stabilizers have on the kinetics of particle growth and particle formation in the area of emulsion polymerization. The well-established mechanisms that govern these processes for emulsions stabilized by conventional low molecular weight surfactants were used as a reference point for comparative purposes. Model latexes were synthesized that comprised of a poly(styrene) core stabilized by a corona of poly(acrylic acid). The advent of successful controlled radical polymerization techniques in heterogeneous media (via RAFT polymerization) allowed for latexes to be synthesized under molecular weight control. For the first time, the degree of polymerization of the stabilizing block on the particle surface was able to be controlled and verified experimentally using mass spectrometry techniques. Three latexes were made with different average degrees of polymerization of the stabilizing block; five, ten and twenty monomer units respectively. A methodology was developed to remove the RAFT functionality from the polymer chains present in the emulsion while retaining the desired particle morphology. Oxidation with tertbutylhydroperoxide (TBHP) was proven to be successful at eliminating the living character provided by the thiocarbonyl end-group. Extensive dialysis and cleaning of the latex was performed to ensure no residual TBHP or reaction by-products remained. Latexes with poly(styrene) cores were chosen for this work as poly(n-butyl acrylate) latexes were shown to be influenced by chain transfer to polymer, providing an additional kinetic complication. The three electrosterically stabilized emulsions were used as seed latexes in carefully designed kinetic experiments to measure the rate of polymerization as a function of time. Two independent techniques (chemically initiated dilatometry and γ-relaxation dilatometry) were used to measure the rate coefficients of radical entry (ρ) and exit (k) in these systems – the two parameters that essentially govern the rate of particle growth. The latexes were chosen such that they satisfied ‘zero-one’ conditions (i.e. that any given latex particle contains at most one growing radical at any given time) in order to simplify data analysis. Three different chemical initiators were used, each yielding a radical with a different electric charge. Results from γ-relaxation experiments demonstrated that the three electrosterically stabilized latexes gave very long relaxation times when removed from the radiation source, ultimately yielding very small k values. These values were up to a factor of 10 smaller than that predicted by the ‘transfer-diffusion’ model for exit for particles of that size. This reduction was attributed to a ‘restricted diffusion’ effect, where the exiting monomeric radical has to diffuse through a dense layer of polymer on the particle surface, where its mobility will be restricted. Modification of the Smoluchowski equation for diffusion-controlled adsorption/desorption to account for this postulate led to the development of a model that gave excellent semi-quantitative agreement with experiment. Chemically initiated dilatometric experiments (using three different types of initiator) gave the unusual result of very low reaction rates and low steady-state values of 'nbar', the average number of radicals per particle. Using the standard kinetic equations for styrene-based systems (where it is assumed that an exited monomeric radical undergoes re-entry), this led to the calculation of impossibly small values of the entry rate coefficient ρ (far below any background or ‘thermal’polymerization rate). However upon removing the assumption of re-entry and assuming that exited radicals undergo termination, the obtained values of ρ were in almost perfect agreement with the values predicted from the ‘control by aqueous phase growth’ entry mechanism. This unexpected result was attributed to chemical reaction with the poly(acrylic acid) stabilizers through chain transfer to polymer (via hydrogen-atom abstraction). This postulate was verified by separate experiments that demonstrated that poly(acrylic acid) could act as a reasonably efficient chain transfer agent for styrene polymerization. The addition of poly(acrylic acid) to the aqueous phase of a conventionally stabilized emulsion also led to the rate reduction seen previously. NMR experiments demonstrated the existence of poly(acrylic acid-graft-styrene), which could only be formed through termination of a poly(styrene) chain with a poly(acrylic acid) chain bearing a mid-chain radical (as the product of a chain transfer reaction). These additional terms of transfer and termination were included in the governing kinetic equations of emulsion systems (the Smith-Ewart equations) to develop a model to account for the behaviour of electrosterically stabilized latexes. The ultimate fate of an exiting radical was now shown to be a competition between fates; successful desorption into the aqueous phase, or chemical reaction (through transfer or termination) within the hairy layer. These additional terms were shown to significantly reduce the theoretical value of nbar, and were in excellent agreement with experiment. For small electrosterically stabilized particles with a densely packed ‘hairy layer,’ it was seen that transfer/termination is the dominant loss mechanism as opposed to desorption. The developed model showed that as the particle size was increased, the dominant loss mechanism once again became successful desorption into the aqueous phase. The model was shown to give excellent agreement with experimental data from ‘uncontrolled’ emulsion systems. To explain the highly unusual secondary nucleation behaviour seen in systems such as these, it was postulated that beta-scission of a poly(acrylic acid) chain bearing a mid-chain radical is an important mechanistic step in the nucleation mechanisms of these systems. Modelling (both steady-state and time-dependent) gave good agreement with experiment with a minimal number of adjustable parameters. Theory (and supporting experimental evidence) demonstrated that this nucleation mechanism is only significant at high particle numbers; under other conditions the well-known ‘homogeneous nucleation’ mechanism is once again dominant.

Our investigation in this study focuses on the chemical and thermal characteristics of Single Walled Nanotubes (SWNTs) in comparison with Double Walled Nanotubes (DWNTs) for their potential to extend the heat flux in the boiling regime. SWNTs and DWNTs were successfully dispersed in an aqueous medium by reducing the surface tension, i.e. adsorption of anionic surfactant (NaDDBS). Two mechanisms of stabilization have been adopted: electrosteric and steric stabilization, and the suspensions were seen to be stable for longer periods. DWNTs have better heat transfer performance in the pool boiling experiment due to their unique structure. Functionalization and surfactant coating of SWNTs may reduce the heat flow because of modification of the structure. The burnout heat flux of the immersed Nichrome wire in water under pool boiling conditions was increased by up to 170% over that for the pure base liquid for DWNT nanofluid. In contrast, SWNT nanofluid enhanced burnout heat flux by 30%. The nature of the deposition on the heating element affects the surface wetting and therefore the pool boiling curve. DWNT coating on the wire is much thinner than SWNT coating; however, it is more porous and enhances CHF.