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Author: Simon, Frank × Start date: 1990 × Has files: Yes × WGL Institute: IPF ×

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Now showing 1 - 10 of 17
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    Bioinspired Polydopamine Coating as an Adhesion Enhancer Between Paraffin Microcapsules and an Epoxy Matrix
    (Washington, DC : ACS Publications, 2020) Fredi, Giulia; Simon, Frank; Sychev, Dmitrii; Melnyk, Inga; Janke, Andreas; Scheffler, Christina; Zimmerer, Cordelia
    Microencapsulated phase change materials (PCMs) are attracting increasing attention as functional fillers in polymer matrices, to produce smart thermoregulating composites for applications in thermal energy storage (TES) and thermal management. In a polymer composite, the filler–matrix interfacial adhesion plays a fundamental role in the thermomechanical properties. Hence, this work aims to modify the surface of commercial PCM microcapsules through the formation of a layer of polydopamine (PDA), a bioinspired polymer that is emerging as a powerful tool to functionalize chemically inert surfaces due to its versatility and great adhesive potential in many different materials. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) evidenced that after PDA coating, the surface roughness increased from 9 to 86 nm, which is beneficial, as it allows a further increase in the interfacial interaction by mechanical interlocking. Spectroscopic techniques allowed investigating the surface chemistry and identifying reactive functional groups of the PDA layer and highlighted that, unlike the uncoated microcapsules, the PDA layer is able to react with oxirane groups, thereby forming a covalent bond with the epoxy matrix. Hot-stage optical microscopy and differential scanning calorimetry (DSC) highlighted that the PDA modification does not hinder the melting/crystallization process of the paraffinic core. Finally, SEM micrographs of the cryofracture surface of epoxy composites containing neat or PDA-modified microcapsules clearly evidenced improved adhesion between the capsule shell and the epoxy matrix. These results showed that PDA is a suitable coating material with considerable potential for increasing the interfacial adhesion between an epoxy matrix and polymer microcapsules with low surface reactivity. This is remarkably important not only for this specific application but also for other classes of composite materials. Future studies will investigate how the deposition parameters affect the morphology, roughness, and thickness of the PDA layer and how the layer properties influence the capsule–matrix adhesion.
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    Sand/Polyethyleneimine Composites with Enhanced Sorption/Desorption Properties toward Pollutants
    (Basel : MDPI, 2022) Bucatariu, Florin; Petrila, Larisa-Maria; Zaharia, Marius-Mihai; Simon, Frank; Mihai, Marcela
    The direct deposition of polyethyleneimine (PEI), a weak polycation with a large content of amino groups, onto sand fractions with different sizes (F70, F100, F200, and F355), resulted in versatile core-shell sorbents for water cleaning. Herein, PEI and the weak polyanion poly(acrylic acid) (PAA) were directly precipitated as an nonstoichiometric polyelectrolyte complex ([PEI]:[PAA] = 2:1) onto a sand surface followed by cross-linking with glutaraldehyde (GA) at three molar ratios ([CHO]:[amine] = 1:10; 1:5; 1:1 = r). Non-crosslinked polyelectrolyte chains were washed out in strongly basic (pH 14) and acidic (pH 0) media. The sand/PEI-GA composites were evaluated to determine the organic shell stability using swelling experiments and X-ray photoelectron spectroscopy. The sorbed/desorbed amount of two model pollutants (copper ions and bromocresol green) in column experiments depended on the sand fraction size and cross-linking degree of the PEI shell. The maximum recorded values, after five loading/release cycles of pollutant species onto F70/PEI-GAr, F100/PEI-GAr, F200/PEI-GAr, and F355/PEI-GAr, were situated between the 0.7–5.5 mg Cu2+/mL column and 3.7–15 mg BCG/mL column. Sand/PEI-GAr composites could act as promising sorbents, low-cost and eco-friendly, which could be applied for water purification procedures.
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    Gold Aerogels: Three-Dimensional Assembly of Nanoparticles and Their Use as Electrocatalytic Interfaces
    (Washington, DC : Soc., 2016) Wen, Dan; Liu, Wei; Haubold, Danny; Zhu, Chengzhou; Oschatz, Martin; Holzschuh, Matthias; Wolf, André; Simon, Frank; Kaskel, Stefan; Eychmüller, Alexander
    Three-dimensional (3D) porous metal nanostructures have been a long sought-after class of materials due to their collective properties and widespread applications. In this study, we report on a facile and versatile strategy for the formation of Au hydrogel networks involving the dopamine-induced 3D assembly of Au nanoparticles. Following supercritical drying, the resulting Au aerogels exhibit high surface areas and porosity. They are all composed of porous nanowire networks reflecting in their diameters those of the original particles (5–6 nm) via electron microscopy. Furthermore, electrocatalytic tests were carried out in the oxidation of some small molecules with Au aerogels tailored by different functional groups. The beta-cyclodextrin-modified Au aerogel, with a host–guest effect, represents a unique class of porous metal materials of considerable interest and promising applications for electrocatalysis.
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    Nickel cobalt oxide hollow nanosponges as advanced electrocatalysts for the oxygen evolution reaction
    (Cambridge : Soc., 2015) Zhu, Chengzhou; Wen, Dan; Leubner, Susanne; Oschatz, Martin; Liu, Wei; Holzschuh, Matthias; Simon, Frank; Kaskel, Stefan; Eychmüller, Alexander
    A class of novel nickel cobalt oxide hollow nanosponges were synthesized through a sodium borohydride reduction strategy. Due to their porous and hollow nanostructures, and synergetic effects between their components, the optimized nickel cobalt oxide nanosponges exhibited excellent catalytic activity towards oxygen evolution reaction.
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    Poly(3-hexylthiophene)s Functionalized with N-Heterocyclic Carbenes as Robust and Conductive Ligands for the Stabilization of Gold Nanoparticles
    (Weinheim : Wiley-VCH, 2020) Sun, Ningwei; Zhang, Shi-Tong; Simon, Frank; Steiner, Anja Maria; Schubert, Jonas; Du, Yixuan; Qiao, Zhi; Fery, Andreas; Lissel, Franziska
    Recently, N-heterocyclic carbenes (NHCs) are explored as anchor groups to bind organic ligands to colloidal gold (i.e. gold nanoparticles, Au NPs), yet these efforts are confined to non-conjugated ligands so far—that is, focused solely on exploiting the stability aspect. Using NHCs to link Au NPs and electronically active organic components, for example, conjugated polymers (CPs), will allow capitalizing on both the stability as well as the inherent conductivity of the NHC anchors. Here, we report three types of Br-NHC-Au-X (X=Cl, Br) complexes, which, when used as starting points for Kumada polymerizations, yield regioregular poly(3-hexylthiophenes)-NHC-Au (P3HTs-NHC-Au) with narrow molecular weight distributions. The corresponding NPs are obtained via direct reduction and show excellent thermal as well as redox stability. The NHC anchors enable electron delocalization over the gold/CP interface, resulting in an improved electrochromic response behavior in comparison with P3HT-NHC-Au. © 2020 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH
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    CVD-Grown CNTs on Basalt Fiber Surfaces for Multifunctional Composite Interphases
    (Basel : MDPI, 2016) Förster, Theresa; Hao, Bin; Mäder, Edith; Simon, Frank; Wölfel, Enrico; Ma, Peng-Cheng
    Chemical vapor deposition (CVD) is used as a method for the synthesis of carbon nanotubes (CNT) on substrates, most commonly pre-treated by a metal-catalyst. In this work, the capability of basalt fiber surfaces was investigated in order to stimulate catalyst-free growth of carbon nanotubes. We have carried out CVD experiments on unsized, sized, and NaOH-treated basalt fibers modified by growth temperature and a process gas mixture. Subsequently, we investigated the fiber surfaces by SEM, AFM, XPS and carried out single fiber tensile tests. Growth temperatures of 700 °C as well as 800 °C may induce CNT growth, but depending on the basalt fiber surface, the growth process was differently affected. The XPS results suggest surficial iron is not crucial for the CNT growth. We demonstrate that the formation of a corrosion shell is able to support CNT networks. However, our investigations do not expose distinctively the mechanisms by which unsized basalt fibers sometimes induce vertically aligned CNT carpets, isotropically arranged CNTs or no CNT growth. Considering data from the literature and our AFM results, it is assumed that the nano-roughness of surfaces could be a critical parameter for CNT growth. These findings will motivate the design of future experiments to discover the role of surface roughness as well as surface defects on the formation of hierarchical interphases.
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    The Localization Behavior of Different CNTs in PC/SAN Blends Containing a Reactive Component
    (Basel : MDPI, 2021-3-1) Gültner, Marén; Boldt, Regine; Formanek, Petr; Fischer, Dieter; Simon, Frank; Pötschke, Petra
    Co-continuous blend systems of polycarbonate (PC), poly(styrene-co-acrylonitrile) (SAN), commercial non-functionalized multi-walled carbon nanotubes (MWCNTs) or various types of commercial and laboratory functionalized single-walled carbon nanotubes (SWCNTs), and a reactive component (RC, N-phenylmaleimide styrene maleic anhydride copolymer) were melt compounded in one step in a microcompounder. The blend system is immiscible, while the RC is miscible with SAN and contains maleic anhydride groups that have the potential to reactively couple with functional groups on the surface of the nanotubes. The influence of the RC on the localization of MWCNTs and SWCNTs (0.5 wt.%) was investigated by transmission electron microscopy (TEM) and energy-filtered TEM. In PC/SAN blends without RC, MWCNTs are localized in the PC component. In contrast, in PC/SAN-RC, the MWCNTs localize in the SAN-RC component, depending on the RC concentration. By adjusting the MWCNT/RC ratio, the localization of the MWCNTs can be tuned. The SWCNTs behave differently compared to the MWCNTs in PC/SAN-RC blends and their localization occurs either only in the PC or in both blend components, depending on the type of the SWCNTs. CNT defect concentration and surface functionalities seem to be responsible for the localization differences.
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    Bio-inspired deposition of electrochemically exfoliated graphene layers for electrical resistance heating applications
    (Bristol : IOP Publishing, 2020-12-4) Utech, Toni; Pötschke, Petra; Simon, Frank; Janke, Andreas; Kettner, Hannes; Paiva, Maria; Zimmerer, Cordelia
    Electrochemically exfoliated graphene (eeG) layers possess a variety of potential applications, e.g. as susceptor material for contactless induction heating in dynamic electro-magnetic fields, and as flexible and transparent electrode or resistivity heating elements. Spray coating of eeG dispersions was investigated in detail as a simple and fast method to deposit both, thin conducting layers and ring structures on polycarbonate substrates. The spray coating process was examined by systematic variation of dispersion concentration and volume applied to heated substrates. Properties of the obtained layers were characterized by UV-VIS spectroscopy, SEM and Confocal Scanning Microscopy. Electrical conductivity of eeG ring structures was measured using micro-four-point measurements. Modification of eeG with poly(dopamine) and post-thermal treatment yields in the reduction of the oxidized graphene proportion, an increase in electrical conductivity, and mechanical stabilization of the deposited thin layers. The chemical composition of modified eeG layer was analyzed via x-ray photoelectron spectroscopy pointing to the reductive behavior of poly(dopamine). Application oriented experiments demonstrate the direct electric current heating (Joule-Heating) effect of spray-coated eeG layers.