Water soluble acrylamide polymers, 2. Aging and viscous flow of aqueous solutions of polyacrylamide and hydrolyzed polyacrylamide

The aging of aqueous solutions of polyacrylamide which appears experimentally as a decrease of solution viscosity and which is probably caused by microorganisms may be prevented by the addition of a small amount (0.02 wt.-%) of an antimicrobial agent such as sodium azide. Aluminium chloride causes a very strong decrease of the viscosity during a prolongated storing time. The addition of aluminium ions to the polymer solution leads to a complexing of amidic groups with aluminium cations and probably also to decrease of the dimensions of individual polymer coils. The viscous flow of aqueous solutions of polyacrylamide and hydrolyzed polyacrylamides was studied as a dependence of the shear gradient D on the shear stress τ and was described by the relation D = k · τⁿ, where k and n denote constants. Both constants depend on the polymer concentration, the degree of polymerization and the content of carboxylic groups in the polymer. The greatest deviations from the Newtonian behaviour were found in the range of molecular weights over 2 · 10⁶ g/mol and practically no deviations were observed for polyacrylamide with molecular weights below 1 · 10⁶ g/mol. The dependence of the viscosity on the shearing time at different shear rates (300, 600 and 1200 s^?1) which was observed in solutions of polyacrylamide, hydrolyzed polyacrylamide and poly-(N,N-dimethyl)-acrylamide was explained by an entanglement model.     

Tailoring of Surfaces with Ultrathin Layers for Controlled Binding of Biopolymers and Adhesion and Guidance of Cells

Various strategies are described for the bio-functionalization of solid substrates by design of interfacial architectures. The first approach is based on the self-assembly process of long-chain thiol molecules from solution to a (noble) metal surface. If some of these building blocks carry a binding site (ligand) for proteins (receptors, antibodies, etc.) the metal surface can be tailored for maximum specific binding while simultaneously minimizing nonspecific adsorption. The second concept is based on polymers that are covalently attached to (oxide) surfaces. The preparation of these (end-) grafted functional polymers involves either the binding of preformed macromolecules to corresponding sites at the surface of the support or the recently introduced “grafting-from” method, by which an initiator molecule is first covalently bound to the surface and then activated — either by heat or light — in the presence of suitable monomer units such that a polymer chain grows from the solid/solution interface. Finally, the functionalization of patterned surfaces by peptide chains that mimic the binding domains of cell adhesion proteins is summarized. It is demonstrated that not only the selective adhesion of neuronal cells can then be controlled, but also their development with the outgrowth of dendrites and axons.     

Comparison of Formulae for the Determination of Fluorescent and Non–fluorescent Whiteness

The prediction capabilities of simple whiteness formulae based on photometer reflectance readings (A, G, B) as compared to linear formulae with adjustable parameters based on chromaticity values (x, y, Y) have been investigated. For each formula, the instrumentally determined whiteness was compared with visually estimated whiteness using the plates of the Ciba–Geigy Plastic White (CGPW) Scale as a standard. This was carried out for a set of 48 fluorescent cotton cloth samples previously studied, as well as for a new set of 86 non–fluorescent cotton cloth samples. As expected, the AGB formulae were inferior to those based on chromaticity values; however, the Taube formula performed quite well for fluorescent samples. On the set of non–fluorescent samples, a formula having green hue preference was required; the Berger formula was found to be the most successful among the simple AGB formulae.     

The carbon-isotopic composition of Proterozoic carbonates: Riphean successions from northwestern Siberia (Anabar Massif, Turukhansk Uplift)

Thick carbonate-dominated successions in northwestern Siberia document secular variations in the C-isotopic composition of seawater through Mesoproterozoic and early Neoproterozoic (Early to early Late Riphean) time. Mesoproterozoic dolomites of the Billyakh Group, Anabar Massif, have delta 13C values that fall between 0 and -1.9 permil versus PDB, with values in the upper part of the succession (Yusmastakh Formation) consistently higher than those of the lower (Ust'-Il'ya and Kotuikan formations). Consistent with available biostratigraphic and radiometric data, delta 13C values for Billyakh carbonates compare closely with those characterizing early Mesoproterozoic carbonates (about 1600-1200 Ma) worldwide. In contrast, late Mesoproterozoic to early Neoproterozoic limestones and dolomites in the Turukhansk Uplift exhibit moderate levels of secular variation. Only the lowermost carbonates in the Turukhansk succession (Linok Formation) have delta 13C values that approximate Billyakh values. Higher in the Turukhansk succession, delta 13C values vary from -2.7 to +4.6 permil (with outliers as low as -5.0 permil interpreted as diagentically altered). Again, consistent with paleontological and radiometric data, these values compare well with isotopic values from 1200 to 850 Ma successions elsewhere. Five sections measured in different parts of the Turukhansk basin show nearly identical patterns of variation, confirming that carbonate delta 13C correlates primarily with time and not facies. The Siberian sections illustrate the potential of integrated biostratigraphic and chemostratigraphic data in the intra- and interbasinal correlation of Mesoproterozoic and early Neoproterozoic rocks.     

Morphology and crack toughness behaviour of nanostructured block copolymer/homopolymer blends

The crack initiation and propagation behaviour of styrene-butadiene (SB) star block copolymer/polystyrene blends (ST3/PS) forming PS-rich and polybutadiene (PB)-rich nanosized domains by self-assembling have been investigated using the essential-work-of-fracture (EWF) approach. Three morphological transitions have been observed, which are crucial to understand the crack toughness behaviour: (i) 0-30 wt.% PS homopolymer: A co-continuous domain structure of PS-rich and PB-rich domains has been observed. For PS homopolymer fraction (?_PS) < 10 wt.% PS homopolymer (i.e. only pure ST3) the rubbery PB-rich phase forms the major phase and for ?_PS > 10 wt.% the glassy PS-rich phase. (ii) At 40-60 wt.% PS homopolymer, a layer-like morphology is formed where the PS-rich layer thickness is ?50 nm, a critical dimension, which is crucial for understanding the ductile-to-semiductile transition. (iii) For 80 wt.% PS homopolymer, PS-rich phase starts to form the matrix combined with a transition from shear stress dominated (shear yielding) to normal stress dominated behaviour (PS-like crazes). The co-continuous morphology at 20 wt.% and 30 wt.% PS is capable of improving toughness of block copolymers, demonstrated by the observed maximum in the non-essential work of fracture and thus explaining a new way of toughening of polymers while retaining high transparency. The correspondence between the ductile-to-semiductile transition and the change in the shape of plastic zone from circular to elliptical as revealed from strain field analysis could be clearly reaffirmed by the observed transition from shear to normal force induced deformation in the fractured surface analysis of these blends. The conceptual correspondence of βw_p and w_e with T_J and δ_0.2 respectively reveal that resistance against crack propagation (βw_p and T_J) is morphology sensitive while the resistance against crack initiation (w_e and δ_0.2) is matrix sensitive.     

Securing Passive Objects in Mobile Ad-Hoc Peer-to-Peer Networks

Security and privacy in mobile ad-hoc peer-to-peer environments are hard to attain, especially when working with passive objects (without own processing power, e.g. RFID tags). This paper introduces a method for integrating such objects into a peer-to-peer environment without infrastructure components while providing a high level of privacy and security for peers interacting with objects. The integration is done by associating public keys to passive objects, which can be used by peers to validate proxies (peers additionally acting on behalf of objects). To overcome the problem of limited storage capacity on small embedded objects, ECC keys are used.     

A new approach for handling and transferring of thin semiconductor materials

 Based on the fracture mechanics analysis of crack propagation, the phenomenon of subcritical crack growth was utilized for a controlled debonding of directly wafer-bonded interfaces. The approach allowed the well-defined separation of bonded wafers although the bond strength was high due to thermal annealing. The achieved splitting velocity depended on the wafer material, the wafer thickness ratio, the bonding process parameters, and the environmental conditions during cleaving. In combination with wafer bonding, the method can be used for a temporary stiffening and handling of thin and brittle wafers during fabrication, even if the wafers are exposed to high process temperatures. The approach can also be applied to fabricate micromechanical systems (MEMS). Received: 12 July 2001/Accepted: 26 February 2002 This paper was presented at the Conference of Micro System Technologies 2001 in March 2001.     

DIC image reconstruction on large cell scans

The width of the emission spectrum of a common fluorophore allows only for a limited number of spectral distinct fluorescent markers in the visible spectrum, which is also the regime where CCD-cameras are used in microscopy. For imaging of cells or tissues, it is required to obtain an image from which the morphology of the whole cell can be extracted. This is usually achieved by differential interference contrast (DIC) microscopy. These images have a pseudo-3D appearance, easily interpreted by the human brain. In the age of high throughput and high content screening, manual image processing is not an option. Conventional algorithms for image processing often use threshold-based criteria to identify objects of interest. These algorithms fail for DIC images as they have a range from dim to bright with an intermediate intensity equal to the background, so as to produce no clear object boundary. In this article we compare different reconstruction methods for up to 100 MB-large DIC images and implement a new iterative reconstruction method based on the Hilbert Transform that enables identification of cell boundaries with standard threshold algorithms.