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To avoid a catastrophic failure of insulation in high-voltage (HV) applications, a monitoring of partial discharges (PD) is necessary. Fluorescently labelled polymer optical fibres (F-POF) offer an electrically passive method for PD detection in HV facilities. F-POF could be embedded into HV cable insulation material, which are usually made of silicone rubber. Due to the difficult accessibility of HV cable accessories, a self-healing silicone rubber, based on incorporated capsules, with prolonged service life after PD detection represents an attractive material design for HV electrical insulation.
The aims of the Research Unit „Acting Principles of Nano-Scaled Matrix Additives for Composite Structures“ (DFG FOR 2021) are based on different synergetic pathways. Challenges are to achieve an improved damage tolerance combined with unchanged processability and a proof of the nano-based effect from molecular scale up to structural level. First of all, a comprehensive understanding of the acting mechanisms of nano-scaled ceramic additives onto polymer matrices of continuous fibre reinforced polymer composites with respect to improved matrix dominated properties is in focus. To proof of the nanoscopic and microscopic effects up to structural level; experimental investigations start on the functional correlation between the particle properties and the resulting properties of the epoxy as suspension and in the solid state. This includes tests for the resulting composite structures as well. Along the entire process chain different multi-scale simulations are performed from molecular modelling up to the macroscopic, structural level. The combination of experimental investigations and simulation methods enables a holistic understanding of the acting principles and basic mechanisms.
Specialized techniques based on Scanning Force Microscopy are the basis of our analysis of physicochemical properties of the boehmite nanoparticles and their polymer environment. A surface map of mechanical properties as an input for simulations facilitate a deeper understanding of such composites across all scales. This enables us to understand the macroscopic structure-property relationship and to predict failure mechanisms as well as routes for optimization.
The demand for high-performance materials has strongly increased over the last decade. One way to improve their performance is to introduce material gradients as found in Nature (for example squid beaks, spider fangs, mussel byssal threads).
One path towards the achievement of such material gradients is the synthesis of hybrid (gradient) copolymers, for instance based on silane and organic monomers. Since not all gradient copolymers can be synthesized by utilising the reactivity ratios of the monomers, forced gradients have to be used. However, in order to obtain gradient copolymers at high conversions, living or pseudo-living copolymerizations have to be performed and so far only few hybrid (organic / inorganic) gradient copolymers have been reported. In this contribution we will present the synthesis of a novel organic / inorganic hybrid copolymer via controlled radical polymerization.
Unilamellar vesicles self-assembled in water from natural and synthetic phospholipids (liposomes), amphiphilic block copolymers (polymersomes), and more recently amphiphilic Janus dendrimers (dendrimersomes) as hollow soft structures in the nano size regime have attracted increasing interest as they can mimic primitive and contemporary biological membranes, and can be configured into biomimetic nanocapsules with application in nanomedicine such as gene, proteins and drug carriers or theranostics. Compared to other amphiphilic structures, the molecular structure of Janus dendrimers can be precisely controlled: by using the vast range of tools from organic chemistry their size, architecture, density, generation as well as the number of endgroups of the individual dendrons can be modified as desired. Unfortunately, the controlled production of the supramolecular aggregates made thereof is still a challenging task. Conventional batch-based techniques such as the solvent injection method or the film hydration method typically go along with a lack of control over mixing and thus over size, morphology and size distribution. The micromixer technology is a promising method for the controlled preparation of supramolecular assemblies as it allows control of mixing at microscale level. In addition, such microfluidic systems benefit from a high mixing efficiency, a low mixing time as well as from a reproducible and continuous synthesis.
Herein, we report on the microfluidic-controlled self-assembly of Janus dendrimers as dendrimersomes and the impact of the mixing parameters on the self-assembly process.
UCST-type thermoresponsive polymers that phase separate from solution upon cooling present a tremendous potential not only in aqueous media where they can be used in drug delivery, diagnostic and microfluidic applications, but also in water/alcohol mixtures, where they can be used for instance in sensing systems for alcohol-soluble drugs. However, only a few thermoresponsive polymers have been reported that present an UCST in a relevant temperature range and “green” solvents such as water or ethanol. In this context, acrylamide-based monomers can be very useful building blocks for designing novel UCST-type polymers because of their hydrophilic nature (with the right side chain) and propensity to form hydrogen bonds.
We want to present our latest results on the copolymer poly(acrylamide-co-acrylonitrile) (P(AAm-co-AN)) that present a UCST in water as well as on two homopolymers based on an acrylamide derivative of 2,6-diaminopyridine, namely poly(N-(6-aminopyridin-2-yl)acrylamide) (PNAPAAm) and poly(N-(6-acetamidopyridin-2-yl)acrylamide) (PNAcAPAAm) that show UCST-type thermoresponsiveness in water/alcohol mixtures.
Our focus for P(AAm-co-AN)) is its aggregation behaviour above and below its phase transition temperature as the size of thermoresponsive polymeric systems is of prime importance for biomedical applications (as size dependent processes take place in the body) and is linked to the optical properties of a material that matter in materials science.
In the case of PNAPAAm and PNAcAPAAm, we focused on the co-solvency/co-non solvency effect on the phase transition temperature in water/alcohol mixture. Indeed, polymers with UCST behavior below 60°C in water/alcohol mixtures are extremely promising for the preparation of “smart” materials for sensing.
Im Arbeitskreis von Herrn Prof. Dr. Menzel (TU Braunschweig) wurde in Sievershausen ein Vortrag zum Thema „Self-healing and mechanically reinforced silicone rubber by the use of multifuctional capsules“ gehalten. Der Vortrag beginnt mit einer kurzen Motivation und einem Überblick über selbstheilende Materialien. Daraufhin werden die Ergebnisse zur Entwicklung eines selbstheilenden Silikonelastomers auf Basis von Kapseln, bestehend aus einem PDMS Kern und einer POS Hülle, dargestellt. Es folgt die Analytik, die auf DLS, TGA, UV/Vis und Fluoreszenzspektroskopie sowie SEM beruht. Der Vortrag endet mit einem Ausblick über zukünftige Arbeiten auf dem Gebiet.
UCST-type thermoresponsive polymers (i.e. that phase separate from solution upon cooling) present a tremendous potential not only in aqueous media where they can be used in drug delivery, diagnostic and microfluidic applications but also in water/alcohol mixtures, where they can be used for instance in sensing systems for alcohol-soluble drugs. However, only a few thermoresponsive polymers have been reported that present an UCST in a relevant temperature range and “green” solvents such as water or ethanol.
In this context, acrylamide-based monomers can be very useful building blocks for designing novel non-ionic UCST-type polymers because of their hydrophilic nature (with the right side chain) and propensity to form hydrogen bonds. We will present our latest results on the UCST-type thermoresponsive behaviour of acrylamide- and 2,6-diaminopyridine-based homopolymers and copolymers in water or water/alcohol mixtures, and give some insights about the rational design of UCST polymers relying on H-bonding.
To avoid a catastrophic failure of insulation in high-voltage (HV) applications, a monitoring of partial discharges (PDs) is necessary. Fluorescently labelled polymer optical fibers (F-POF) offer an electrically passive method for PD detection in HV facilities. F-POFs could be embedded in HV cable accessories, which are usually made of silicone rubber. Herein they detect the light emitted by the PD and convert it into an electrical signal that can be monitored. Due to the difficult accessibility of HV cable accessories, a self-healing silicone rubber with prolonged service life after PD detection represents an attractive material design for HV accessories. With this contribution, we would like to present and discuss the possibilities of combining self-healing materials with POF-based sensors for PD detection in HV applications.
Vesicles self-assembled in water from natural and synthetic phospholipids (liposomes), amphiphilic block copolymers (polymersomes), and more recently amphiphilic Janus dendrimers (dendrimersomes) as hollow soft structures in the nano size regime have attracted increasing interest as they can mimic primitive and contemporary biological membranes, and can be configured into biomimetic nanocapsules with application in nanomedicine such as gene, proteins and drug carriers or theranostics.
Compared to other amphiphilic structures, the molecular structure of Janus dendrimers can be precisely controlled: by using the vast range of tools from organic chemistry their size, architecture, density, generation as well as the number of end groups of the individual dendrons can be modified as desired.
Unfortunately, the controlled production of the supramolecular aggregates made thereof is still a challenging task. Conventional batch-based techniques such as the solvent injection method or the film hydration method typically go along with a lack of control over mixing and thus over size, morphology and size distribution. The micromixer technology is a promising method for the controlled preparation of supramolecular assemblies as it allows control of mixing at microscale level. In addition, such microfluidic systems benefit from a high mixing efficiency, a low mixing time as well as from a reproducible and continuous synthesis.
Herein, we report on the microfluidic-controlled self-assembly of Janus dendrimers as dendrimersomes and the impact of the mixing parameters on the self-assembly process.
UCST-type thermoresponsive polymers (i.e. that phase separate from solution upon cooling) present a tremendous potential not only in aqueous media where they can be used in drug delivery, diagnostic and microfluidic applications, but also in water/alcohol mixtures, where they can be used for instance in sensing systems for alcohol-soluble drugs. However, only a few thermoresponsive polymers have been reported that present an UCST in a relevant temperature range and “green” solvents such as water or ethanol.
In this context, acrylamide-based monomers can be very useful building blocks for designing novel non-ionic UCST-type polymers because of their hydrophilic nature (with the appropriate side chain) and propensity to form hydrogen bonds. We will present our latest results on the UCST-type thermoresponsive behaviour of acrylamide- and 2,6-diaminopyridine-based homopolymers and copolymers in water or water/alcohol mixtures, and give some insights about the rational design of UCST polymers relying on H-bonding.
Vesicles self-assembled in water from natural and synthetic phospholipids (liposomes), amphiphilic block copolymers (polymersomes), and more recently amphiphilic Janus dendrimers (dendrimersomes) -5 as hollow soft structures in the nano size regime have attracted increasing interest as they can mimic primitive and contemporary biological membranes, and can be configured into biomimetic nanocapsules with application in nanomedicine such as gene, proteins and drug carriers or theranostics.
Compared to other amphiphilic structures, the molecular structure of Janus dendrimers can be precisely controlled: by using the vast range of tools from organic chemistry their size, architecture, density, generation as well as the number of end groups of the individual dendrons can be modified as desired.
Unfortunately, the controlled production of the supramolecular aggregates made thereof is still a challenging task. Conventional batch-based techniques such as the solvent injection method or the film hydration method typically go along with a lack of control over mixing and thus over size, morphology and size distribution. The micromixer technology is a promising method for the controlled preparation of supramolecular assemblies as it allows control of mixing at microscale level. In addition, such microfluidic systems benefit from a high mixing efficiency, a low mixing time as well as from a reproducible and continuous synthesis.
Herein, we report on the microfluidic-controlled self-assembly of Janus dendrimers as dendrimersomes and the impact of the mixing parameters on the self-assembly process.
UCST-type thermoresponsive polymers (i.e. that phase separate from solution upon cooling) present a tremendous potential not only in aqueous media where they can be used in drug delivery, diagnostic and microfluidic applications, but also in water/alcohol mixtures, where they can be used for instance in sensing systems for alcohol-soluble drugs. However, only a few thermoresponsive polymers have been reported that present an UCST in a relevant temperature range and “green” solvents such as water or ethanol.
In this context, acrylamide-based monomers can be very useful building blocks for designing novel non-ionic UCST-type polymers because of their hydrophilic nature (with the appropriate side chain) and propensity to form hydrogen bonds. We will present our latest results on the UCST-type thermoresponsive behaviour of acrylamide- and 2,6-diaminopyridine-based homopolymers and copolymers in water or water/alcohol mixtures, and give some insights about the rational design of UCST polymers relying on H-bonding.
Charakterisierung von Glas-Polymer Verbundmaterialien fur die Hochdruckspeicherung von Wasserstoff
(2017)
In der vorliegenden Arbeit werden Glaskapillaren und Strukturen aus Borosilikatglas (Simax) f¨ur die Hochdruckspeicherung von Wasserstoff betrachtet. Um die mechanischen Belastungen zu analysieren und anschließend ein optimiertes Speicherdesign abzuleiten, findet die Finite Element Methode (FEM) Einsatz.
Die notwendigen Materialkennwerte werden zuvor experimentell ermittelt. Dazu geh¨oren die Festigkeit, die Schubfestigkeit der Grenzfl¨ache Klebung/Glas, der Wasserstoffpermeationskoeffizient, das Temperatur-Zeit-abh¨angige Verhalten, sowie die obere Temperatureinsatzgrenze.
Die Glasfestigkeit ist stark abh¨angig von der Oberfl¨acheng¨ute. Daher werden in dieser Arbeit Kapillaren selber gezogen und beschichtet. Der Einfluss auf die Festigkeit wird mit Hilfe von Berstversuchen untersucht. Die eingesetzten Polymere werden zus¨atzlich mit dem Push-out Versuch, der dynamisch mechanischen Analyse und der Permeationsmessung charakterisiert.
Dar¨uber hinaus wird aus den DMA Versuchen ein viskoelastisches Materialmodell abgeleitet, womit der Temperatur- und Zeiteinfluss auf die mechanische Belastung simuliert wird.
Unter Beachtung der experimentell gewonnenen Erkenntnisse, sowie der durchgef¨uhrten Simulation ist es m¨oglich, ein optimiertes Speicherdesign zu erstellen und Aussagen ¨uber die Einsatzgrenzen zu treffen.