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Due to their extreme high hydrogen contents, high molecular weight (HMW-) and ultra-high molecular weight (UHMW-) polyethylene (PE) are a comprehensible choice as neutron radiation shielding material in casks for storage and transport of radioactive materials. But as a direct consequence of inserting radioactive material in such casks, gamma radiation occurs. Hence, the impact of gamma radiation on the molecular structure of polyethylene has to be taken into consideration. Consequently, PE has to withstand any type of gamma radiation induced degradation affecting safety relevant aspects in order to be applicable for long term neutron radiation shielding purposes during the whole storage period (in Germany, for instance, up to 40 years). The scope of our investigation comprises an estimation of the impact of gamma radiation and temperature on the molecular and supra molecular structure of the two types of PE used as neutron radiation shielding cask components. A further point which is worth exploring is to what extent these changes are detectable by conventional analysis methods. Therefore, thermoanalytical measurements were performed such as differential scanning calorimetry (DSC), thermo mechanical analysis (TMA), dynamic mechanical analysis (DMA), and thermo gravimetric analysis (TGA). Additionally optical and weighing methods were applied. With those methods it is possible to detect structural changes in polyethylene induced by exposure to gamma radiation. The observed amounts of changes of the irradiated material are not safety relevant for the application of polyethylene as neutron radiation shielding material; moreover, some properties actually improve via irradiation.
Nanoparticulate networks as fillers for polymer based nanocomposites offer an optimized, surfactant free distribution of the inorganic component. Additionally, their non-aggregated but interconnected nanoparticulate subunits can lead to new properties owing to special inherent solid state properties and/or spacial restrictions to the polymeric parts. In particular, polymer nanocomposites based on poly(methyl methacrylate) (PMMA) or poly(hydroxyethyl methacrylate) (PHEMA), filled with different nanoparticulate networks of AlOOH were synthesized using two advanced synthesis techniques. An ex situ method, in which a preformed AlOOH-gel was solvent exchanged by methyl methacrylate (MMA) and an in situ method, in which the AlOOH scaffold was prepared within hydroxyethyl methacrylate (HEMA), have been used to produce the materials described here through polymerization. On the MMA based composites the particles were removed by etching, yielding porous polymers. Promising for a broad variety of crystallisable networks within polymers, the phase transition of amorphous AlOOH within PMMA towards crystalline boehmite was performed using a hydrothermal method. The materials were characterized using transmission electron microscopy, X-ray diffraction, gel permeation chromatography, differential scanning calorimetry, IR-spectroscopy, UV/Vis spectroscopy and hardness measurements. Special material properties were investigated using thermogravimetry, thermomechanical analysis and dynamic mechanical analysis. Furthermore, interactions between PMMA segments and the AlOOH network were detailed studied using dielectric spectroscopy.
The special properties of high molecular weight polyethylene (HMW-PE) and ultra high molecular
weight polyethylene (UHMW-PE) result basically from their extreme chain lengths and their high
degree of crystallinity. As high-performance polymers, they are used for a variety of applications.
UHMW-PE in particular is often utilized for endoprothesis (due to its excellent slip and wear
properties) and due to its high hydrogen content as a neutron moderator in casks for storage and
transport of radioactive materials.
To prepare the material for instance for its use as a total joint replacement, it is exposed to radiation
for several reasons, such as sterilization and crosslinking, leading to partial improvement of the
mechanical properties (e.g. fracture toughness, crack propagation resistance, wear resistance) and
better chemical stability.
To be applicable for long term radiation shielding purposes for instance over a period of 40 years,
PE has to withstand any type of degradation affecting safety relevant aspects.
The scope of our investigation comprises an estimation of the radiation impact on the molecular and
supra molecular structure of two types of PE and to what extent these changes are detectable by
thermo-analytical (TA) methods, such as Differential Scanning Calorimetry (DSC), Thermo
Mechanical Analysis (TMA), Dynamic Mechanical Analysis (DMA) and Thermo Gravimetric
Analysis (TGA). Additionally FT-IR spectroscopy as well as density and gas sorption
measurements were carried out.
Due to the poor solubility of HMW-PE and UHMW-PE, some classical analytical techniques are
not applicable. But TA-methods represent a feasible approach to detect structural and
morphological features of these materials as well as changes caused by external influences, such as
thermal treatment and/or irradiation. With the combination of the applied TA-techniques it is
possible to distinguish between crosslinking and degradation.
Radiation induced structural changes of HMW-PE and UHMW-PE as detected by thermo-analytical methods
(2009)
Bei der Abschätzung der Beständigkeit von Kunststoffen gegenüber niedermolekularen Flüssigkeiten ist die Kohäsionsenergiedichte CED ein wichtiger Parameter auf molekularer Ebene. Die Vernetzungsdichte ν eines polymeren Festkörpers bildet hierbei einen bedeutsamen Kennwert, der darüber hinaus neben der Löslichkeit wichtige Eigenschaften wie thermische Stabilität und Steifigkeit des Materials charakterisiert. Für die experimentelle Bestimmung von CED und ν eignet sich die Untersuchung des Quellverhaltens in unterschiedlichen Lösungsmitteln. Es werden zwei Messmethoden miteinander verglichen und die Ergebnisse unter Berücksichtigung des molekularen Aufbaus von Proben aus Polyurethan (PU) und hochmolekularem – (HMWPE) und ultrahochmolekularem Polyethylen (UHMWPE) diskutiert. Zum Verständnis des Quellverhaltens dieser Polymerproben in niedermolekularen Lösungsmitteln werden neben den Messergebnissen Literaturdaten zu Grunde gelegt.
Thermosetting moulding compounds are synthetic materials which can be easily formed in the molten state and achieve high temperature stability due to a cross-linking process which takes place during manufacture. To ensure thermal and mechanical properties, post-curing of moulded phenolic resin components is necessary for high quality applications. In the industrial practice, post-curing time-temperature-programs are heuristically acquired. In this paper, dynamical mechanical thermal analysis is employed to determine optimal post-curing conditions for injection moulded parts from phenolic resin.
Dielectric spectroscopy in combination with temperature modulated differential scanning calorimetry and quasielastic/inelastic neutron scattering are employed to investigate the molecular (glassy) dynamics of poly(dimethyl siloxane) (PDMS) and poly(methyl phenyl siloxane) (PMPS) confined to random nanoporous glasses with nominal pore sizes between 2.5 nm and 20 nm. Inside the pores PDMS and PMPS have faster molecular dynamics than in the bulk state. Down to a pore size of 7.5 nm the temperature dependence of the relaxation times (or rates) obeys the Vogel/Fulcher/Tammann (VFT) equation where the data obtained from dielectric and thermal spectroscopy agree quantitatively. At a pore size of 5 nm this VFT-like temperature dependence changes to an Arrhenius behavior. At the same confining length scale the increment of the specific heat capacity at Tg normalized to the weight of the confined polymer vanishes. The results indicate that a minimal length scale seems to be relevant for glassy dynamics in both polymers although the estimated length scale of about 5 nm seems to a bit too large in comparison to other experimental results and theoretical approaches. Neutron scattering is employed to investigate methyl group reorientation and the fast segmental dynamics of both polymers in confinement. Although the methyl group rotation is a localized process these experiments show that a part of the methyl groups is immobilized by the confinement whereas the effects for PDMS are much more pronounced than for PMPS. With regard to the segmental dynamics, neutron scattering reveals a big difference in the behavior of both polymers. Whereas the data obtained for PMPS are in accord with a boundary layer formed at the surfaces of the nanopores, for PDMS a considerable amount of elastic scattering is observed. To explain this result it is assumed that some structure formation of PDMS takes place in the nanopores, although the thermal data show no crystallization or melting effects.
Dielectric spectroscopy and temperature modulated DSC are employed to study the molecular dynamics of oligomeric poly(propylene glycol) (PPG) melts of different molecular weights confined to nanoporous glasses (pore sizes 2.5, 5.0, 7.5 and 20 nm). Moreover the results obtained for the polymer are compared with the corresponding monomer. For large pore sizes an acceleration of the segmental dynamics compared to the bulk state is observed which is already known for low molecular-weight glass forming liquids. For smaller pore sizes the molecular dynamics is slower than in the bulk. The observed behavior is nearly independent of the molar mass of the polymer and of the treatment of internal glass surfaces. The experimental results are discussed in the frame of an interplay of confinement and adsorption effects. Moreover a length scale of about 1.6 nm is estimated as a minimal length scale for the cooperativity for the glass transition. In addition to the ?-relaxation the whole chain dynamics (normal mode relaxation) can be measured by dielectric spectroscopy because PPG has a dipole component parallel to the chain. For virgin internal surfaces the relaxation rate of the normal mode relaxation is shifted dramatically to lower relaxation rates. That can be explained by adsorption effects. For treated surfaces this effect is strongly reduced and it is concluded that also in this case the chain dynamics are influenced by geometric (confinement) effects.