Characterization of Oleogels Based on Waxes and Their Hydrolyzates

In this paper, the structuring of liquid oils, also known as oleogelation, is systematically investigated for the first time using a quasi-quaternary mixing system approach. Native waxes with different quantities of wax esters (WE), n-alkanes (hydrocarbons (HC)), fatty acids (FA), and fatty alcohols (FaOH) are applied in mixtures with hydrolyzed waxes to systematically change the composition. Hydrolyzed waxes contain high levels of FA and FaOH. The model systems are investigated on microscopic level (brightfield light microscopy (BFM), cryogenic scanning electron microscopy (cryo-SEM)) as well as on their macroscopic properties (rheology, gel hardness) and calorimetric behavior (differential scanning calorimetry (DSC)). It is found that sunflower wax (SFW)-based gels (12% structurant) become less hard on any admixture. Beeswax (BW)-based gels show significant increases in hardness when 25% and 50% (w/w) hydrolyzate are admixed. This could be related to stepwise crystallization. Further analysis reveals that the dissolution/melting behavior of the wax ester mixtures can be surprisingly well described as ideal solubility of a single pseudocomponent. The approach to unravel the individual contributions of the different species present in waxes is successful and marks a first step to better understand the systematic of wax functionality as oleogelators. Practical Application: The substitution of hardstock fats in structured oil phases is of interest for two reasons. The improved nutritional profile oleogels offer are beneficial for public health while the elimination of palm oil based ingredients appears to be a general public desire. Among the technical solutions for non-TAG oil structuring waxes are very promising. This is primarily due to their availability, prior consumption, potentially low cost for functionality. Currently waxes are technically and scientifically wrongly treated as single components. In order to better utilize the potential of waxes and design future sourcing strategies it is necessary to understand the wax functionality at a compositional/molecular level. This contribution marks the first step into this direction by considering classes of molecules with respect to their contribution to functionality. This understanding is considered as a key for future compositional design.     

Binary phase behavior of 1,3-distearoyl-2-oleoyl-sn-glycerol (SOS) and 1,3-distearoyl-2-linoleoyl-sn-glycerol (SLS)

The binary phase behavior of SOS (1,3-distearoyl-2-oleoyl-sn-glycerol) and SLS (1,3-distearoyl-2-linoleoyl-sn-glycerol) was examined by using DSC and conventional and synchrotron radiation X-ray diffraction. The solid-solution phases were observed in the metastable α and γ forms in all concentration ranges. Results indicated that the miscible γ form did not transform to the β′ form when the mixtures were subjected to simple cooling from a high-temperature liquid to a low-temperature solid phase. However, and α-melt-mediated transformation into β′ and β₂ resulted in the formation of immiscible phases in concentration ranges of SLS below 30%. By contrast, at SLS concentration ranges above 30%, the α-melt-mediated transformation caused crystallization of only the γ form, and β′ and β₂ crystals did not appear. These results show that the specific interactions between SOS and SLS are operative in the phase behavior of the mixture states of SOS and SLS.     

13C- and 23Na-NMR investigations on alkali cellulose

Summary Solid state ²³Na- and ¹³C-NMR spectra of alkali cellulose are presented as a function of NaOH-concentration of the steeping lye, steeping temperature and amount of adhering lye (press factor). Results are discussed with regard to chemical binding of NaOH to the cellulose chain in the system cellulose/ NaOH/H₂O.Presented at the 22nd Microsymposium, Characterization of Structure and Dynamics of Macromolecular Systems by NMR Methods, Prague, CSSR, July 20–23,1981     

Small-angle neutron scattering from branched epoxide resins

Small-angle neutron scattering experiments in the range of q² from 0.01 to 25 nm⁻² have been carried out on branched epoxide resins based on bisphenol-A at the Institute Laue—Langevin (I.L.L) in Grenoble (q=(4π/λ) sin(θ/2)). Measurements were made with six samples in the range of M_W from 1500 to 19 000 and four concentrations between 1.3 and 10% (w/w) in deuterated diglyme. The results are as follows: (i) The mean square radius of gyration follows a relationship S²_z=4.69×10⁻⁴M^1.20_W (nm²). (ii) In all cases fairly large second virial coefficients A₂ are obtained which, however, decrease strongly with molecular weight. Above M_W=2500, the virial coefficient follows the relationship A₂=1.6M^−0.85_W (mol cm³g⁻²). (ii) The reciprocal particle scattering factor as a function of q² exhibits only a slight upturn and otherwise shows the behaviour of a randomly branched polycondensate. The slight upturn is discussed as being caused by the finite volume of the monomeric unit. Possible reasons for the high exponent in the S²_z versus M_W dependence are briefly discussed.     

Application of K2CO3 catalysts in the coal gasification process using nuclear heat

Conventional gasification processes use coal not only as feedstock to be gasified but also for supply of energy for reaction heat, steam production, and other purposes. With a nuclear high temperature reactor (HTR) as a source for process heat, it is possible to transform the whole of the coal feed into gas. This concept offers advantages over existing gasification processes: saving of coal, as more gas can be produced from coal; less emission of pollutants, as the HTR is used for the production of steam and electricity instead of a coal-fired boiler; and a lower production cost for the gas. However, the process has the disadvantage that the temperature is limited to the outlet temperature (950 °C max) of the helium cooling gas of the HTR. Therefore the possibility of catalytic steam gasification was examined. Model calculations based on experimental results show that use of 3–4 wt% relative to coal of K²CO³ catalyst increases the throughput of a large scale nuclear gasification plant by ≈65%, while gas production costs decrease by ≈15%. Corrosion by catalysts is not significant at low concentration (< 5 wt%) and low temperature (< 900 °C).     

Estimation of impact forces during multi-point collisions involving small deformations

Multibody System Dynamics - Collision between hard objects causes abrupt changes in the velocities of the system, which are characterized by very large contact forces over very small time...     

Realization strategies of dedicated path protection: A bandwidth cost perspective

Communication networks have to provide a high level of availability and instantaneous recovery after failures in order to ensure sufficient survivability for mission-critical services. Currently, dedicated path protection (or 1 + 1) is implemented in backbone networks to provide the necessary resilience and instantaneous recovery against single link failures with remarkable simplicity. However, in order to satisfy strict availability requirements, connections also have to be resilient against Shared Risk Link Group (SRLG) failures. In addition, switching matrix reconfigurations have to be avoided after a failure in order to guarantee instantaneous recovery. For this purpose, there are several possible realization strategies improving the characteristics of traditional 1 + 1 path protection by lowering reserved bandwidth while conserving all its favorable properties. These methods either utilize diversity coding, network coding, or generalize the disjoint-path constraint of 1 + 1.In this paper, we consider the cost aspect of the traditional and the alternative 1 + 1 realization strategies. We evaluate the bandwidth cost of different schemes both analytically and empirically in realistic network topologies. As the more complex realizations lead to NP-complete problems even in the single link failure case, we propose both Integer Linear Programming (ILP) based optimal methods, as well as heuristic and meta-heuristic approaches to solve them. Our findings provide a tool and guidelines for service providers for selecting the path protection method with the lowest bandwidth cost for their network corresponding to a given level of reliability.     

A 3D face matching framework for facial curves

Among the many 3D face matching techniques that have been developed, are variants of 3D facial curve matching, which reduce the amount of face data to one or a few 3D curves. The face’s central profile, for instance, proved to work well. However, the selection of the optimal set of 3D curves and the best way to match them has not been researched systematically. We propose a 3D face matching framework that allows profile and contour based face matching. Using this framework we evaluate profile and contour types including those described in the literature, and select subsets of facial curves for effective and efficient face matching. With a set of eight geodesic contours we achieve a mean average precision (MAP) of 0.70 and 92.5% recognition rate (RR) on the 3D face retrieval track of the Shape Retrieval Contest (SHREC’08), and a MAP of 0.96 and 97.6% RR on the University of Notre Dame (UND) test set. Face matching with these curves is time-efficient and performs better than other sets of facial curves and depth map comparison.