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  • 1.
    Ali pour, Nazanin
    et al.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Enebro, J.
    Strömberg, Emma
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Qualitative characterization of nanoclay particle emissions from PP nanocomposites after thermal degradation2015Inngår i: ICCM International Conferences on Composite Materials, International Committee on Composite Materials , 2015Konferansepaper (Fagfellevurdert)
    Abstract [en]

    The use of nanomaterials in polymeric materials is a rapidly expanding field, and the polymer nanocomposites are being introduced into various markets. But there is still little known about the fate of nanocomposites and nanoparticles during service life and end-of-life of the materials. To avoid possible environmental, health and safety problems, simulating different scenarios for nanoparticles release from the polymer matrix plays a key role in commercialization of these advanced materials. The polymer/nanoclay nanocomposites show superior material properties in comparison with the pure polymers, such as improved mechanical properties, heat resistance, flame retardancy and decreased gas permeability. Polypropylene (PP) nanocomposites have attracted a considerable interest due to the material's low cost, low density and extensive production volumes. In this study, in order to obtain reliable results regarding the release of nanoclays from PP nanocomposites, homogenous composite with predetermined content of nanoclay was produced and characterized to obtain information regarding content, dispersion and size of the nanoclays in the matrix. The PP nanocomposite was degraded under controlled conditions and the surface morphology as well as oxidation of the material was characterized with scanning electron microscopy (SEM) and infrared spectroscopy during degradation. A prototype environmental chamber was designed in order to collect nano-sized particles in a controlled manner and subsequent characterization of the released or formed particles was performed with transmission electron microscopy (TEM) and the exposed nanocomposite was analysed with thermogravimetric analysis (TGA). 

  • 2.
    Alipour, Nazanin
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknik, Polymera material.
    Structure and Mechanical/Transport properties of Single and Multilayer Polyethylene-based Materials2014Licentiatavhandling, med artikler (Annet vitenskapelig)
    Abstract [en]

    The current study discusses the structure, mechanical and transport properties of polyethylene-based materials into two parts. The first part deals with the migration and chemical depletion of active substance such as insecticides from moulded polyethylene sheets. Deltamethrin (DM) and synergist piperonyl butoxide (PBO) are often used for insect control purpose. It was found that DM as a powder was incapable of recrystallization and remained in liquid state after cooling to room temperature, and that the evaporation of a DM/PBO solution was greater than that predicted from the evaporation rates of pristine separate material components. Infrared spectroscopy and liquid chromatography showed that the loss of DM and PBO through polyethylene sheets was negligible over 30 days, when aged in air at 80 °C (60 and 80 %RH). However, significant migration of the active species was observed in aged polyethylene sheets which were exposed in liquid water (at 80 and 95 °C). In the second part, the structure and properties of multi–layered polymer films were studied in terms of crystallization kinetics, mechanical and transport properties. Previously, it has been shown that when the layer thickness decreases from micrometre-scale to nanometre-scale, leading to improvement of the film performance such as crack propagation and oxygen barrier properties. In this work, two multi-layered systems were considered based on compatible (i) or incompatible layers (ii). In the first case (i), metallocene polyethylene (mPE) and low-density polyethylene (LDPE) where investigated as 2, 24, and 288 adjacent layers. In the second case (ii) poly(ethylene-co-vinyl alcohol) (EVOH) and polyethylene adhesive was evaluated as 5 and 19 layers. The crystallization kinetic studies showed that the crystallization rate was retarded as the layers became thinner with increasing number of layers in the multi-layered films as compared to the reference films (2 and 5 layers). The observation was suggested to stem from greater association between layers (inter layer mixing) in the case of mPE/LDPE films with 2 layers. Furthermore, the crack growth resistance increased with increasing number of layers. The x-ray scattering and tensile testing showed that the films were orientated more in extrusion direction than in the transverse direction, besides the EVOH films (the incompatible system) showed higher orientation in the extrusion direction than mPE/LDPE films. The uptake of n-hexane was reduced significantly in multi-layered EVOH films due to the effective protective role of EVOH. Furthermore, it was revealed that non-homogenous swelling causing a folding/curling of bilayer films when exposed to the vapour of the solvent.

  • 3.
    Alipour, Nazanin
    et al.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi.
    Andersson, Richard L.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi.
    Olsson, Richard T.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi.
    Gedde, Ulf W.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi.
    Hedenqvist, Mikael S.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi.
    VOC-Induced Flexing of Single and Multilayer Polyethylene Films As Gas Sensors2016Inngår i: ACS Applied Materials and Interfaces, ISSN 1944-8244, E-ISSN 1944-8252, Vol. 8, nr 15, s. 9946-9953Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The differential swelling and bending of multilayer polymeric films due to the dissimilar uptake of volatile organic compounds (VOCs; n-hexane, limonene) in the different layers was studied. Motions of thin polyethylene films triggered by the penetrant were investigated to learn more about how their deformation is related to VOC absorption. Single layers of metallocene or low-density polyethylene, and multilayers (2-288-layers) of these in alternating positions were considered. Single-, 24-, and 288 layer films displayed no motion when uniformly subjected to VOCs, but they could display simple curving modes when only one side of the film was wetted with a liquid VOC. Two-layer films displayed simple bending when uniformly subjected to VOCs due to the different swelling in the two layers, but when the VOC was applied to only one side of the film, more complex modes of motion as well as dynamic oscillations were observed (e.g., constant amplitude wagging at 2 Hz for ca. 50 s until all the VOC had evaporated). Diffusion modeling was used to study the transport behavior of VOCs inside the films and the different bending modes. Finally a prototype VOC sensor was developed, where the reproducible curving of the two-layer film was calibrated with n-hexane. The sensor is simple, cost-efficient, and nondestructive and requires no electricity.

  • 4.
    Alipour, Nazanin
    et al.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Polymera material.
    Gedde, Ulf W.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Polymera material.
    Hedenqvist, Mikael S.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknologi, Polymera material.
    Yu, Shun
    Roth, Stephan
    Brüning, Karsten
    Vieyres, Arnaud
    Schneider, Konrad
    Structure and properties of polyethylene-based and EVOH-based multilayered films with layer thicknesses of 150 nm and greater2015Inngår i: European Polymer Journal, ISSN 0014-3057, E-ISSN 1873-1945, Vol. 64, s. 36-51Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    This paper presents the structure and properties of two multilayered systems where polymers in adjacent layers were either miscible or immiscible. The miscible system consisted of 2, 17, 18, 24 and nominally 288 layers of alternating low-density (LDPE) and low-density/linear-low density (mPE) polyethylene layers with observed thicknesses ranging from 150 nm to 20 urn. The immiscible system consisted of 5 and 19 layer films with a combination of poly(ethylene-co-vinyl alcohol) (EVOH) (thickness: 9 and 1 gm, respectively), LDPE (17 and 7 gm) and a polyethylene adhesive (3 and 1 gm). The purpose of the multi-layering was to increase the crack growth resistance and, in the EVOH-based system, to decrease the oxygen transmission rate. Indeed, the crack growth resistance, as measured on tensile-tested notched films, increased with increasing number of layers. The thinnest polyethylene and polyethylene adhesive layers showed a clear ductile failure when fractured even in liquid nitrogen. Simultaneous synchrotron wide-angle/small-angle X-ray scattering and tensile testing indicated no new deformation features with changes in the layer thickness. The oxygen permeability was the same in the 5- and 19-layer EVOH-based films, but the uptake of n-hexane was strongly reduced in the 19-layer films, demonstrating the effective protective role of the EVOH layers. The n-hexane desorption data of the 2-layer LDPE/mPE film was successfully modeled using the diffusivities and solubilities of the single layers. Crystallization was slower and more confined in the films with thinner layers. The interlayer mixing in the melt (measured by isothermal crystallization from melts of initially layered polyethylene-based systems) was, as expected, significantly faster in the 24- and 288-multilayer films than in the 2-layer film.

  • 5.
    Alipour, Nazanin
    et al.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi.
    Vinneras, Bjorn
    SLU Swedish Univ Agr Sci, Dept Energy & Technol, POB 7032, SE-75007 Uppsala, Sweden..
    Gouanve, Fabrice
    Univ Lyon 1, Univ Lyon, Ingn Mat Polymeres, CNRS,UMR 5223, 15 Bd Andre Latarjet, F-69622 Villeurbanne, France..
    Espuche, Eliane
    Univ Lyon 1, Univ Lyon, Ingn Mat Polymeres, CNRS,UMR 5223, 15 Bd Andre Latarjet, F-69622 Villeurbanne, France..
    Hedenqvist, Mikael S.
    KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Polymera material.
    A Protein-Based Material from a New Approach Using Whole Defatted Larvae, and Its Interaction with Moisture2019Inngår i: Polymers, ISSN 2073-4360, E-ISSN 2073-4360, Vol. 11, nr 2, artikkel-id 287Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    A protein-based material created from a new approach using whole defatted larvae of the Black Soldier fly is presented. The larvae turn organic waste into their own biomass with high content of protein and lipids, which can be used as animal feed or for material production. After removing the larva lipid and adding a plasticizer, the ground material was compression molded into plates/films. The lipid, rich in saturated fatty acids, can be used in applications such as lubricants. The amino acids present in the greatest amounts were the essential amino acids aspartic acid/asparagine and glutamic acid/glutamine. Infrared spectroscopy revealed that the protein material had a high amount of strongly hydrogen-bonded beta-sheets, indicative of a highly aggregated protein. To assess the moisture-protein material interactions, the moisture uptake was investigated. The moisture uptake followed a BET type III moisture sorption isotherm, which could be fitted to the Guggenheim, Anderson and de Boer (GAB) equation. GAB, in combination with cluster size analysis, revealed that the water clustered in the material already at a low moisture content and the cluster increased in size with increasing relative humidity. The clustering also led to a peak in moisture diffusivity at an intermediate moisture uptake.

  • 6.
    Nawaz, Sohail
    et al.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknik, Polymera material.
    Ali Pour, Nazanin
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknik, Polymera material.
    Hedenqvist, Mikael S.
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknik, Polymera material.
    Gedde, Ulf
    KTH, Skolan för kemivetenskap (CHE), Fiber- och polymerteknik, Polymera material.
    Migration and chemical consumption of deltamethrin and piperonyl butoxide from polyethylene in aqueous media2013Inngår i: Polymers from Renewable Resources, ISSN 2041-2479, Vol. 4, nr 1, s. 1-18Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Deltamethrin (DM), an important insecticide (synthetic pyrethroid) together with synergist piperonyl butoxide (PBO), is used for food storage and insect control purposes. It is often impregnated in polymers for controlled and effective release of insecticide. The migration and chemical consumption of DM and PBO from moulded polyethylene sheets was studied. The thermal behaviour of pristine DM and the prepared polyethylene compound was studied by differential scanning calorimetry. DM did not crystallize and remained in a liquid state after cooling to room temperature. Evaporation rates and activation energies of evaporation were determined by thermogravimetry for pristine DM, PBO, a solution of DM and PBO and for the PE compound. Evaporation from the DM/PBO solution was greater than that predicted from the evaporation rates of the individual compounds, which suggested that the DM/PBO solution obeyed non-ideal solution properties. The migration of DM and PBO from the polyethylene was studied in liquid water at 80 and 95 °C and in air of different relative humidities (60 and 80%) at 80 °C. Exposure to liquid water caused degradation and hydrolysis of the ester bond in DM, present in the prepared material, and generated species containing hydroxyl groups. Liquid chromatography and infrared spectroscopy showed a significant migration of the active species in liquid water, whereas the loss of DM and PBO in air at 80°C (60 and 80 %RH) was negligible over 30 days.

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