Time-intensity transformation and internal stress in UV-curable hyperbranched acrylates

The photocuring of three different highly functional acrylates—Di-pentaerythritol penta/hexaacrylate (DPHA) and two hyperbranched molecules (HBP), one with a stiff polyester and one with a more flexible polyether structure—was investigated by means of photorheology, photo differential scanning calorimetry, and beam bending. Special attention was paid to the influence of the composition of DPHA/HBP reactive blends and UV intensity on gelation and vitrification and the resulting dynamics of the internal stress. It was found that adding HBPs to DPHA did not influence gelation significantly, but shifted the onset of vitrification to higher conversions and thus caused lower internal stresses in the material. Increasing UV intensity increased both the conversion at vitrification, thus retarding the build-up of internal stresses, and the ultimate conversion, thus increasing the final stress level. The obtained conversion, gelation, and vitrification data were assembled into time-intensity transformation diagrams, thus providing a useful tool for optimizing photocuring

MATE, a single front-end ASIC for silicon strip, Si(Li) and CsI detectors

MATE (Must ASIC for Time and Energy) will process signals delivered from the hodoscope MUST2. The hodoscope consists of six large area telescopes (100 cm²), each made up of a double sided Si strip detector followed by a Si(Li) and Csi crystal. MATE has sixteen channels and can deliver three types of analogue information per channel; time of flight and energy loss of the detected particle; value of leakage DC current per channel. MATE also gives a trigger logical signal corresponding to the cross over of an adjustable threshold value. The analogue information is transmitted as differential current through twisted pair to the acquisition system based on VXI-C. The slow control is assured via the I2C industrial protocol. The first version of MATE for Si(strip) is available. An update of MATE will allow it to be used for the Si(Li) and Csi detectors. MATE is a novel R&D project for nuclear physics which includes both energy and time measurements with good resolution and high energy dynamic range

Valorization of byproducts of hemp multipurpose crop: Short non-aligned bast fibers as a source of nanocellulose

Nanocellulose was extracted from short bast fibers, from hemp (Cannabis sativa L.) plants harvested at seed maturity, non-retted, and mechanically decorticated in a defibering apparatus, giving non-aligned fibers. A chemical pretreatment with NaOH and HCl allowed the removal of most of the non-cellulosic components of the fibers. No bleaching was performed. The chemically pretreated fibers were then refined in a beater and treated with a cellulase enzyme, followed by mechanical defibrillation in an ultrafine friction grinder. The fibers were characterized by microscopy, infrared spectroscopy, thermogravimetric analysis and X-ray diffraction after each step of the process to understand the evolution of their morphology and composition. The obtained nanocellulose suspension was composed of short nanofibrils with widths of 5–12 nm, stacks of nanofibrils with widths of 20–200 nm, and some larger fibers. The crystallinity index was found to increase from 74% for the raw fibers to 80% for the nanocellulose. The nanocellulose retained a yellowish color, indicating the presence of some residual lignin. The properties of the nanopaper prepared with the hemp nanocellulose were similar to those of nanopapers prepared with wood pulp-derived rod-like nanofibrils

Elongation and fluctuations of semi-flexible polymers in a nematic solvent

We directly visualize single polymers with persistence lengths ranging from $\ell_p=0.05$ to 16 $\mu$m, dissolved in the nematic phase of rod-like {\it fd} virus. Polymers with sufficiently large persistence length undergo a coil-rod transition at the isotropic-nematic transition of the background solvent. We quantitatively analyze the transverse fluctuations of semi-flexible polymers and show that at long wavelengths they are driven by the fluctuating nematic background. We extract both the Odijk deflection length and the elastic constant of the background nematic phase from the data.Comment: 4 pages, 4 figures, submitted to PR

Nonlinear Elasticity in Biological Gels

Unlike most synthetic materials, biological materials often stiffen as they are deformed. This nonlinear elastic response, critical for the physiological function of some tissues, has been documented since at least the 19th century, but the molecular structure and the design principles responsible for it are unknown. Current models for this response require geometrically complex ordered structures unique to each material. In this Article we show that a much simpler molecular theory accounts for strain stiffening in a wide range of molecularly distinct biopolymer gels formed from purified cytoskeletal and extracellular proteins. This theory shows that systems of semi-flexible chains such as filamentous proteins arranged in an open crosslinked meshwork invariably stiffen at low strains without the need for a specific architecture or multiple elements with different intrinsic stiffnesses.Comment: 23 pages, 5 figures, submitted to Natur

Oxygen permeation, mechanical and structural properties of multilayer diffusion barrier coatings on polypropylene

To improve temperature durability for autoclaving of SiOx diffusion barrier coatings on polypropylene, plasma polymerized hexamethyldisiloxane (pp-HMDSO) is applied by plasma enhanced chemical vapour deposition as interlayer material and compared with results obtained with amorphous hydrogenated carbon-nitrogen (a-C : N : H) and a-Si : C : O : N : H interlayers. The influence of the O2/HMDSO ratio on the chemical structure and related mechanical and oxygen barrier properties is investigated by fragmentation tests, dilatometry, oxygen transmission rate, internal stress and mass density measurements as well as Fourier transform infrared and x-ray photoelectron spectroscopy. Carbon-rich, polymer-like coatings with low density, low internal stress and excellent adhesive and cohesive properties are found for pp-HMDSO at the expense of barrier performance. In the SiO x/pp-HMDSO coating a broad transition in chemical composition was observed, explaining improved mechanical properties responsible for good barrier performance after thermal cycling or autoclaving

Acrylated Hyperbranched Polymer Photoresist for Ultra-Thick and Low-Stress High Aspect Ratio Micropatterns

Different photocurable acrylates, including two hyperbranched monomers, are compared with an epoxy negative-tone photoresist (SU-8) with respect to their suitability for the fabrication of ultra-thick polymer microstructures in a photolithographic process. To this end, a resolution pattern was used and key parameters, such as the maximum attainable thickness and aspect ratio, the minimum resolution and the processing time were determined. Compared to SU-8, all acrylate materials allowed the fabrication of thicker layers with a fast single layer fabrication procedure. Microstructures with thicknesses of up to 850 μm, an aspect ratio of up to 7.7, a 5.5-fold reduction in internal stress and a 6-fold reduction in processing time compared to SU-8 were demonstrated using an acrylated hyperbranched polyether. The specific development process of the hyperbranched polymer combined with channel design moreover enabled us to produce a high-performance valve for micro-battery devices