Made available in DSpace on 2014-12-17T14:07:18Z (GMT). No. of bitstreams: 1 LaureniceMP_DISSERT.pdf: 7523564 bytes, checksum: 3bb1b06da6a21522b0974a84935760a3 (MD5) Previous issue date: 2014-12-28 / Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior / The development of new materials to fill the demand of technological advances is a challenge for many researchers around the world. Strategies such as making blends and composites are promising alternatives to produce materials with different properties from those found in conventional polymers. The objective of this study is to evaluate the effect of adding the copolymer poly(ethylene methyl acrylate) (EMA) and cotton linter fibers (LB) on the properties of recycled poly(ethylene terephthalate) (PETrec) by the development of PETrec/EMA blend and PETrec/EMA/LB blend composite. In order to improve the properties of these materials were added as compatibilizers: Ethylene - methyl acrylate - glycidyl methacrylate terpolymer (EMA-GMA) and maleic anhydride grafted polyethylene (PE-g-MA). The samples were produced using a single screw extruder and then injection molded. The obtained materials were characterized by thermogravimetry (TG), melt flow index (MFI) mensurements, torque rheometry, pycnometry to determinate the density, tensile testing and scanning electron microscopy (SEM). The rheological results showed that the addition of the EMA copolymer increased the viscosity of the blend and LB reduces the viscosity of the blend composite. SEM analysis of the binary blend showed poor interfacial adhesion between the PETrec matrix and the EMA dispersed phase, as well as the blend composite of PETrec/EMA/LB also observed low adhesion with the LB fiber. The tensile tests showed that the increase of EMA percentage decreased the tensile strength and the Young s modulus, also lower EMA percentage samples had increased the elongation at break. The blend composite showed an increase in the tensile strength and in the Young`s modulus, and a decrease in the elongation at break. The blend formulations with lower EMA percentages showed better mechanical properties that agree with the particle size analysis which showed that these formulations presented a smaller diameter of the dispersed phase. The blend composite mechanical tests showed that this material is stronger and stiffer than the blend PETrec/EMA, whose properties have been reduced due to the presence of EMA rubbery phase. The use of EMA-GMA was effective in reducing the particle size of the EMA dispersed phase in the PETrec/EMA blend and PE-g-MA showed evidences of reaction with LB and physical mixture with the EMA / O desenvolvimento de novos materiais para atender as necessidades dos avan?os tecnol?gicos ? um desafio enfrentado por pesquisadores de todo o mundo. No que diz respeito aos materiais polim?ricos, estrat?gias como a confec??o de blendas e comp?sitos s?o alternativas promissoras para atender a demanda por materiais com propriedades diferentes das encontradas nos pol?meros convencionais. O objetivo deste trabalho ? avaliar o efeito da adi??o do copol?mero poli(etileno-acrilato de metila) (EMA) e da fibra de linter de algod?o (LB) nas propriedades do poli(tereftalato de etileno) reciclado (PETrec). Para isto, foram desenvolvidos a blenda PETrec/EMA e o comp?sito da blenda PETrec/EMA/LB. Com o intuito de melhorar as propriedades destes materiais foram adicionados agentes compatibilizantes: terpol?mero etileno-acrilato de metila-metacrilato de glicidila (EMA-GMA) e o polietileno enxertado com anidrido mal?ico (PE-g-MA). As misturas foram produzidas por meio de uma extrusora monorosca e, em seguida, moldados por inje??o. As caracteriza??es realizadas foram termogravimetria (TG), medida de ?ndice de fluidez (MFI), reometria de torque, determina??o da densidade por picnometria, ensaio de tra??o uniaxial e microscopia eletr?nica de varredura (MEV). Os resultados reol?gicos mostraram que a adi??o do copol?mero EMA aumentou a viscosidade da mistura e o LB reduziu a viscosidade da blenda PETrec/EMA. A an?lise por MEV da blenda bin?ria mostrou baixa ades?o interfacial entre a matriz de PETrec e a fase dispersa de EMA, assim como no comp?sito da blenda PETrec/EMA/LB, tamb?m observou-se uma baixa ades?o com a fibra de LB. Os ensaios de tra??o mostraram que o aumento da porcentagem de EMA diminuiu a resist?ncia m?xima e o m?dulo de elasticidade, e, para as formula??es com menor porcentagem de EMA verificou-se um aumento do alongamento na ruptura. O comp?sito da blenda apresentou um aumento na resist?ncia m?xima e no m?dulo de elasticidade, e uma redu??o no alongamento de ruptura. As formula??es da blenda com menores porcentagens de EMA apresentaram propriedades mec?nicas melhores, que corrobora com as an?lises de tamanho de part?cula que mostraram que estas formula??es apresentaram menor di?metro m?dio de fase dispersa. Os resultados de ensaios mec?nicos do comp?sito da blenda mostraram que essa mistura resultou em um material com maior resist?ncia mec?nica e rigidez do que a blenda PETrec/EMA, cujas propriedades foram reduzidas em fun??o da fase borrachosa EMA. O uso do EMA-GMA foi eficiente na redu??o do tamanho de part?culas da fase dispersa do EMA na blenda PETrec/EMA e o PE-g-MA apresentou ind?cio de rea??o com o LB e mistura f?sica com o EMA

In current enterprises, simulations are being utilized to lessen the cost of product advancement.  Along this line, there is an awesome enthusiasm for enhancing precision and accuracy of simulations. For an accurate and reliable simulation, it is essential to use an accurate material model and provide it with accurate material information. In exhibit industries, orthotropic materials are being simulated utilizing isotropic material model, as orthotropic material model requires more material data which is not promptly accessible. This proposal intends to test and identify orthotropic materials and simulate them using orthotropic material model in ABAQUS. Materials utilized as a part of this proposal are Aluminium, LDPE, PET. Required material data was gotten by performing Uni-directional tensile tests, DIC, and an algorithm we developed in light of Inverses method. To get highly accurate material data from DIC, a few kinds of patterns were examined, and a superior pattern was resolved for camera configuration being utilized.

The course of polymer film functioning has been a crucial concern in the advent of packaging technology. The thesis project aims towards obtaining an understanding of mechanical properties for a class of these materials, namely LDPE and PET. A constitutive understanding of this behavior in the case of LDPE is acquired through incorporating a plastic stress strain relationship in an iterative approach with focus put on the sensitivity of a few parameters by following a simple linear curve-fit technique in a way that the global as well as the local response are predictable. FE-models also developed in this way are validated with experimental data. An inverse analysis testing validity or usefulness of DIC technique in identifying a material model is done and some discussions are drawn towards this area. A relative numerical study with respect to experimentally obtained global response for tearing of these polymers is done through use of a similar material model developed from tensile tests and the challenges faced in this area have been addressed.

D. Tech. (Department of Mechanical Engineering, Faculty of Engineering and Technology), Vaal University of Technology. / Cracked concrete slabs are a problem due to several factors such as poor maintenance, insufficient reinforcement or steel corrosion leading to crack propagation. There is a need to increase the load-bearing capacity of concrete slabs and increase their life span. The use of waste Polyethylene Terephthalate (PET) fibres and fly ash in a hybrid composite slab dramatically alleviates the problem of crack propagation and failure sustainably. This study aimed to optimize a waste PET fibre/fly ash hybrid cement composite for use in slabs. This study characterized the raw materials used, including fly ash and aggregates. After that, concrete test specimens were fabricated using the PET fibres and fly ash following the full factorial experimental design. The developed specimens were then tested to ascertain their material strength properties. Model development was carried out using Minitab Software Version 14, and subsequent experimental validation was carried out. After that, the PET and fly ash optimisation for maximum favourable response outcome was carried out. The fly ash was found to belong to the Class F category with particle size ranging from 0.31 μm to 800 μm. The fly ash was mainly spherical and consisted of Ca, Al, P, Si, and trace amounts of Ti and Mg. The spherical shape of the fly ash helped improve the concrete's workability. The river sand had a fineness modulus of 3.69, considered coarse sand. The fine aggregate showed uniform particle size distribution with a uniformity coefficient of 4.007. The coarse aggregate characterisation was carried out and revealed that the aggregate particle size was 13 mm in size. The coarse aggregate had a uniformity coefficient of 4.007, which implied the aggregate was well graded. The coarse aggregate had a high flakiness index of 74.82 % and an acceptable elongation index of 46.72 %. Full factorial methodology experimental design was employed to fabricate the test specimens by simultaneously varying the independent factors to develop a model for overall response variation. The slump value was observed to increase with the addition of fly ash. However, the addition of PET fibre decreased the slump value with incremental amounts of fibre. The combined effect of fibre addition and fly ash showed a general decreasing slump value for all quantities of fly ash content. The compressive strength of PET fibre only composite had maximum strength at 0.5% fibre addition, and the composite with fly ash alone had the maximum compressive strength at 15%. The combined optimum compressive strength for fibre and fly ash was at 0.5 % and 15 %, respectively, with a 15.54 N/mm2. The split tensile strength decreased with an increase in fibre content. However, the fibre provided crack retardation. Fly ash increased the split tensile strength significantly to a peak of 2.35 N/mm2 for 20 % fly ash addition. The combined addition of fibre and fly ash had an optimum split tensile strength of 2.79 N/mm2 at 0.5 % fibre and 20 % fly ash. The addition of fibre had an optimum split tensile strength at 0.5% of 1.82 N/mm2. The fly ash increased the flexural strength, with optimum strength at 15 %. The combined addition of fibre and fly ash created optimum flexural strength at 0.5% and 30 %, respectively. The trend observed by the rebound number followed that of the compressive strength. However, the non-destructive rebound hammer method gave significantly lower strength values than the destructive test method. The addition of fly ash had the effect of lowering the cost of producing the slab. However, the addition of fibres marginally increased the cost. The combined effect of fibre and fly ash resulted in a significant cost saving. Numerical optimisation was carried out concerning the fibre reinforced concrete's fresh and hardened mechanical properties. Predictive modified quadratic equations were developed for slump value, compressive, flexural, split tensile strength and total cost. Analysis of variance test carried out for all the responses indicated that the model could predict the slump value and mechanical properties of the fibre reinforced concrete correctly and effectively with a coefficient of determination in the range of 0.4151 to 0.9467. The developed model can predict the required fibre reinforced fresh and hardened properties in order to assist in decision making in construction in slabs. The optimum constituent combination for maximum mechanical strength at the lowest possible cost was found to be 15.7576 % Fly ash and 0.3232 % PET fibre with optimum responses as shown in Table 4-26. These predictions were validated experimentally, and a good correlation was observed between the actual and predicted values based on the observed standard deviations of 0.1335, 0.031, 0.005, 0.676, 0.02 for compressive strength, flexural strength, tensile strength, slump value and cost, respectively. Concrete slabs were optimised for various possible end uses, and the optimum PET fibre % and fly ash % were ascertained as shown in Table 4-27.

The crystallization and melting behaviors of an ethylene/1-hexene copolymer and series of narrow molecular weight linear polyethylene and poly(ethylene oxide) fractions were studied using a combination of ultra-fast and conventional differential scanning calorimetry, optical microscopy, small angle X-ray scattering, and wide angle X-ray diffraction. In the case of linear polyethylene and poly(ethylene oxide), the zero-entropy production melting temperatures of initial lamellae of isothermally crystallized fractions were analyzed in the context of the non-linear Hoffman-Weeks method. Using the Huggins equation, limiting equilibrium melting temperatures of 141.4 ± 0.8oC and 81.4 ± 1.0oC were estimated for linear polyethylene and poly(ethylene oxide), respectively. The former and the latter are about 4oC lower and 12.5oC higher than these predicted by Flory/Vrij and Buckley/Kovacs, respectively. Accuracy of the non-linear Hoffman-Weeks method was also examined using initial lamellar thickness literature data for a linear polyethylene fraction at different crystallization temperatures. The equilibrium melting temperature obtained by the Gibbs-Thomson approach and the C2 value extracted from the initial lamellar thickness vs. reciprocal of undercooling plot were similar within the limits of experimental error to those obtained here through the non-linear Hoffman-Weeks method. In the next step, the Lauritzen-Hoffman (LH) secondary nucleation theory was modified to account for the effect of stem length fluctuations, tilt angle of the crystallized stems, and temperature dependence of the lateral surface free energy. Analysis of spherulite growth rate and wide angle X-ray diffraction data for 26 linear polyethylene and 5 poly(ethylene oxide) fractions revealed that the undercooling at the regime I/II transition, the equilibrium fold surface free energy, the strength of the stem length fluctuations and the substrate length at the regime I/II transition are independent of chain length. The value of the equilibrium fold surface free energy derived from crystal growth rate data using the modified Lauritzen-Hoffman theory matches that calculated from lamellar thickness and melting data through the Gibbs-Thomson equation for both linear polyethylene and poly(ethylene oxide). Larger spherulitic growth rates for linear polyethylene than for poly(ethylene oxide) at low undercooling is explained by the higher secondary nucleation constant of poly(ethylene oxide). While the apparent friction coefficient of a crystallizing linear polyethylene chain is 2 to 8 times higher than that of a chain undergoing reptation in the melt state, the apparent friction coefficient of a crystallizing poly(ethylene oxide) chain is about two orders of magnitude lower. This observation suggests that segmental mobility on the crystal phase plays a significant role in the crystal growth process. In case of the statistical ethylene/1-hexene copolymer, the fold surface free energies of the copolymer lamellae at the time of crystallization and melting increase with increasing undercooling, approaching the same magnitude at high undercooling. As a result of this temperature dependence, the experimental melting vs. crystallization temperature plot is parallel to the Tm = Tc line and the corresponding Gibbs-Thomson plot is non-linear. This behavior is attributed to the fact that longer ethylene sequences form a chain-folded structure with lower concentration of branch points on the lamellar surface at lower undercooling, while shorter ethylene sequences form lamellar structures at higher undercooling exhibiting a higher concentration of branch points on the lamellar surface. Branch points limit the ability of lamellar structures to relax their kinetic stem-length fluctuations during heating prior to melting. / Ph. D. / Morphology of semi-crystalline polymers is strongly affected by their crystallization conditions. Thermodynamic and kinetic models allow us to understand the crystallization mechanism of a semi-crystalline polymer and relate its crystallization conditions to the final morphology. In this research, we studied the molar mass dependence of the crystallization and melting behaviors of narrow molecular weight distribution linear polyethylene (LPE) and poly(ethylene oxide) (PEO) fractions using a modified Lauritzen-Hoffman (LH) secondary nucleation theory. We have shown that the equilibrium melting temperature of LPE and PEO fractions found from the non-linear Hoffman-Weeks method are within the experimental uncertainty identical with these measured directly for extended chain crystals or derived from a Gibbs-Thomson analysis. The value of the equilibrium fold surface free energy derived from crystal growth rate data using the modified LH theory matches that calculated from lamellar thickness and melting data through the Gibbs-Thomson equation for both LPE and PEO. We reported that the higher segmental mobility of PEO in the crystalline phase leads to significantly lower apparent chain friction coefficients during crystal growth compared to LPE. We also studied the role of short-chain branching in the crystal growth kinetics of ethylene/1-hexene copolymers. We observed that the fold surface free energies during crystallization and during melting are both function of the undercooling while the ratio of the former to the latter decreases with increasing undercooling. We proposed that this behavior may be related to the concentration of short-chain branches at the surface of the lamellae, where higher concentration leads to lower relaxation.

Polyethylene Terephthalate (PET) is one of the most important polymers in use today for packaging due to its outstanding properties. The usage of PET has grown at the highest rate compared with other plastic packaging over the last 20 years, and it is anticipated that the increase in global demand will be around 6% in the 2010 ¿ 2015 period. The rheological behaviour, thermal properties, tensile modulus, permeability properties and degradation phenomena of PET/clay nanocomposites have been investigated in this project. An overall, important finding is that incorporation of nanoclays in PET gives rise to improvements in several key process and product parameters together ¿ processability/ reduced process energy, thermal properties, barrier properties and stiffness. The PET pellets have been compounded with carefully selected nanoclays (Somasif MAE, Somasif MTE and Cloisite 25A) via twin screw extrusion to produce PET/clay nanocomposites at various weight fractions of nanoclay (1, 3, 5, 20 wt.%). The nanoclays vary in the aspect ratio of the platelets, surfactant and/or gallery spacing so different effect are to be expected. The materials were carefully prepared prior to processing in terms of sufficient drying and re-crystallisation of the amorphous pellets as well as the use of dual motor feeders for feeding the materials to the extruder. The rheological properties of PET melts have been found to be enhanced by decreasing the viscosity of the PET i.e. increasing the ¿flowability¿ of the PET melt during the injection or/and extrusion processes. The apparent shear viscosity of PETNCs is show to be significantly lower than un-filled PET at high shear rates. The viscosity exhibits shear thinning behaviour which can be explained by two mechanisms which can occur simultaneously. The first mechanism proposed is that some polymer has entangled and few oriented molecular chain at rest and when applying high shear rates, the level of entanglements is reduced and the molecular chains tend to orient with the flow direction. The other mechanism is that the nanoparticles align with the flow direction at high shear rates. At low shear rate, the magnitudes of the shear viscosity are dependent on the nanoclay concentrations and processing shear rate. Increasing nanoclay concentration leads to increases in shear viscosity. The viscosity was observed to deviate from Newtonian behaviour and exhibited shear thinning at a 3 wt.% concentration. It is possible that the formation of aggregates of clay is responsible for an increase in shear viscosity. Reducing the shear viscosity has positive benefits for downstream manufacturers by reducing power consumption. It was observed that all ii three nanoclays used in this project act as nucleation agents for crystallisation by increasing the crystallisation temperature from the melt and decreasing the crystallisation temperature from the solid and increasing the crystallisation rate, while retaining the melt temperature and glass transition temperatures without significant change. This enhancement in the thermal properties leads to a decrease in the required cycle time for manufacturing processes thus potentially reducing operational costs and increasing production output. It was observed that the nanoclay significantly enhanced the barrier properties of the PET film by up to 50% this potentially allows new PET packaging applications for longer shelf lives or high gas pressures. PET final products require high stiffness whether for carbonated soft drinks or rough handling during distribution. The PET/Somasif nanocomposites exhibit an increase in the tensile modulus of PET nanocomposite films by up to 125% which can be attributed to many reasons including the good dispersion of these clays within the PET matrix as shown by TEM images as well as the good compatibility between the PET chains and the Somasif clays. The tensile test results for the PET/clay nanocomposites micro-moulded samples shows that the injection speed is crucial factor affecting the mechanical properties of polymer injection moulded products.

Yes / Understanding the structure-property relationships of drug delivery system (DDS) components is critical for their development and the prediction of bodily performance. This study investigates the effects of introducing polyethylene oxide (PEO) homopolymers, over a wide range of molecular weights, into Pluronic injectable smart hydrogel formulations. These smart DDSs promise to enhance patient compliance, reduce adverse effects and dosing frequency. Pharmaceutically, Pluronic systems are attractive due to their unique sol-gel phase transition in the body, biocompatibility, safety and ease of injectability as solutions before transforming into gel matrices at body temperature. This paper presents a systematic and comprehensive evaluation of gelation and the interplay of microscopic and macroscopic properties under both equilibrium and non-equilibrium conditions in controlled environments, as measured by rheology in conjunction with time-resolved Small Angle Neutron Scattering (SANS). The non-equilibrium conditions investigated in this work offer a better understanding of the two polymeric systems’ complex interactions affecting the matrix thermo-rheological behaviour and structure and therefore the future release of an active pharmaceutical ingredient from the injectable DDS.

Condition monitoring (CM) of electrical equipment is an important field in electrical engineering and a considerable amount of research is dedicated to this field. Power cables are one of the most important parts of any electrical network and the variety of techniques available for CM of electrical cables is therefore no surprise. Electrical cables are exposed to operational and environmental stressors which will cause degradation of the insulation material. The degradation will continue to the point where the cable fails. Blackouts caused by failing cables will have an effect on the safety, efficiency and production of an electrical network. It is therefore important to constantly monitor the condition of electrical cables, in order to prevent the premature failure of cables. The research presented in this dissertation sets out to investigate CM techniques for power cables and to design and implement a basic cable CM technique based on the principles of partial discharge (PD) measurements. A comprehensive literature study introduces the fundamental concepts regarding the CM of power cables. The basic construction of electrical cables, as well as the variety of different types is researched in order to lay a foundation for the research that follow. CM techniques for electrical equipment are investigated, with the emphasis on techniques used on cables. Conducted research led to the decision to focus on CM by means of PD measurements. PD as a phenomenon is investigated to be able to better understand the origins and effects of discharge activity. From there the focus shifts to the available techniques for monitoring the condition of electrical cables by means of PD measurements. The research conducted in the literature study chapter forms the basis from which the rest of the study is conducted. Simulation models were used to study PD characteristics. The models are derived from engineering and mathematical principles and are based on the well-known three-capacitor model of PD. The simulations were performed in order to study the effects of discharge activity. The designed simulation models allows for a variety of PD characteristics to be studied. The simulations were performed in the MATLAB® Simulink® environment. The research conducted in the dissertation was used to design an elementary CM technique which can be used to detect the presence of PD within electrical cables. The designed CM technique was used for the practical measurement of PD data. MATLAB® programs were designed in order to analyse the PD data in both the time- and frequency-domain. The analysis of the measured data revealed PD characteristics of the test specimen used for the measurements. The designed CM is used for the detection of PD activity within electrical cables and in combination with other techniques, may be used for complete CM of electrical cables. The experimental setup which was used to take practical PD measurements adds another dimension to the work presented in this dissertation. / MIng (Electrical and Electronic Engineering), North-West University, Potchefstroom Campus, 2015

Condition monitoring (CM) of electrical equipment is an important field in electrical engineering and a considerable amount of research is dedicated to this field. Power cables are one of the most important parts of any electrical network and the variety of techniques available for CM of electrical cables is therefore no surprise. Electrical cables are exposed to operational and environmental stressors which will cause degradation of the insulation material. The degradation will continue to the point where the cable fails. Blackouts caused by failing cables will have an effect on the safety, efficiency and production of an electrical network. It is therefore important to constantly monitor the condition of electrical cables, in order to prevent the premature failure of cables. The research presented in this dissertation sets out to investigate CM techniques for power cables and to design and implement a basic cable CM technique based on the principles of partial discharge (PD) measurements. A comprehensive literature study introduces the fundamental concepts regarding the CM of power cables. The basic construction of electrical cables, as well as the variety of different types is researched in order to lay a foundation for the research that follow. CM techniques for electrical equipment are investigated, with the emphasis on techniques used on cables. Conducted research led to the decision to focus on CM by means of PD measurements. PD as a phenomenon is investigated to be able to better understand the origins and effects of discharge activity. From there the focus shifts to the available techniques for monitoring the condition of electrical cables by means of PD measurements. The research conducted in the literature study chapter forms the basis from which the rest of the study is conducted. Simulation models were used to study PD characteristics. The models are derived from engineering and mathematical principles and are based on the well-known three-capacitor model of PD. The simulations were performed in order to study the effects of discharge activity. The designed simulation models allows for a variety of PD characteristics to be studied. The simulations were performed in the MATLAB® Simulink® environment. The research conducted in the dissertation was used to design an elementary CM technique which can be used to detect the presence of PD within electrical cables. The designed CM technique was used for the practical measurement of PD data. MATLAB® programs were designed in order to analyse the PD data in both the time- and frequency-domain. The analysis of the measured data revealed PD characteristics of the test specimen used for the measurements. The designed CM is used for the detection of PD activity within electrical cables and in combination with other techniques, may be used for complete CM of electrical cables. The experimental setup which was used to take practical PD measurements adds another dimension to the work presented in this dissertation. / MIng (Electrical and Electronic Engineering), North-West University, Potchefstroom Campus, 2015

It is commonly known that water plays a crucial role in many natural and industrial processes. One of these processes is the formation of water trees, and the subsequent breakdown of polyethylene used for high voltage cable insulation purposes. It has been shown that the mechanism for water molecules diffusing through amorphous polyethylene includes the formation of small water clusters. Gibbs Ensemble Monte Carlo molecular simulations has been performed to study the clustering of vapour phase water under vapour - liquid equilibrium conditions at temperatures ranging from 300 K to 600 K. The increase in vapour density with increasing temperature leads to a radical increase in the fraction of molecules belonging to clusters with two or more water molecules. It is also seen that the size of the clusters increases with temperature. The topologies of the smaller clusters, up to pentamers, have also been studied. A structural transition is observed from a large percentage with cyclic topology, which is the minimum energy configuration, at lower temperatures to predominantly linear clusters, favoured by entropic effects, at higher temperatures. Similar water properties have been obseved in simulations where the vapour phase has been replaced with a hydrocarbon rich phase ( n-alkanes and polyethylene ). Application of an external electric field to the polymer system reduces the water solubility and affects the water structure. A dramatic increase in water solubility in the hydrocarbon phase is observed when two oppositely charged ions are introduced in the hydrocarbon. The structure of the water have changed from several small clusters to a single large cluster with a rod-like shape. The cluster is extremely stable during the simulation. Application of an external electric field may enhance or reduce the effect of the ions depending on the direction of the field. Based on these observations is an alternative mechanism for water tree propagation proposed.