Depolymerization of Turkish lignites. I. Effect of substituted phenols

A lignite (C, 67.4 wt%) was depolymerized with phenol, p-nitrophenol and o-chlorophenol using sulphuric acid as catalyst. The solubility of the lignite was enhanced by these treatments, with phenol being the most reactive reagent whereas p-nitrophenol was the least reactive. The distribution of nitro- and chloro-groups in the solubilized products was investigated by infrared spectrometry and it was found that these groups were redistributed among the pyridine- and methanol-soluble materials. It is suggested that benzene-soluble material is produced by self-depolymerization of coal or by degradation of pyridine- and methanol-soluble material.     

Catalytic oxidation of hydrogen sulphide on activated carbons

Activated carbon is a suitable adsorbent for removal of hydrogen sulphide from natural, synthesis or other product gases. The process depends predominantly on physical adsorption, though catalytic oxidation is also involved. During catalytic oxidation the H₂S is converted in the presence of oxygen to elemental sulphur, which is adsorbed onto the internal surface of the activated carbon, thus leading to a sulphur load of up to 120% by weight. The oxidation rate depends on the partial pressure of both reactants, H₂S and O₂ and is largely controlled by the characteristics of the activated carbon. The activity of the catalyst can be improved by impregnating the activated carbon with promoters such as iron and iodine. The regeneration of spent carbon is currently carried out using hot gas desorption methods at temperatures around 450 °C.     

Combined hydration of tricalcium silicate and β-dicalcium silicate

The mutual interaction of tricalcium silicate (C₃S) and β-dicalcium silicate (β-C₂S) in their combined hydration was studied. The rate of β-C₂S hydration was accelerated significantly in the presence of C₃S. The rate of C₃S hydration was retarded, but only in the presence of large amounts of β-C₂S. The stoichiometric composition and the pore structure of the hydrates formed was altered only unsignificantly when both compound hydrated simultaneously.     

Bücherschau

Ohne Zusammenfassung VDI     

Micro molding for double-sided micro structuring of SU-8 resist

Advances in micro and nano fabrication technologies for MEMS require high-level measurement techniques with regard to sampling and sensitivity. For this purpose at the Institute of Microtechnology (IMT) highly sensitive piezoresistive 3D force sensors based on SU-8 polymer have been developed. In this paper we present an improved micro fabrication process for a double-sided micro structured design. The sensors are produced by multilayer processing techniques such as UV lithography and coating methods. The double-sided micro structured design demands a photoresist application method which simultaneously features a top side structuring and a casting from a mold. We use a new micro molding process to meet the demands. The micro fabrication technology is described, focusing on the development of the molding structure for shaping of the bottom side and a capable release process for the detachment of the molded structures. The fabrication process of the SU-8 mold layer is optimized to fabricate molding structures with heights from a few μm up to 350 μm. Therefore different SU-8 formulations, namely with classification numbers 5, 25, 50, and 100, have been used. The fundamental limitations for the mold design result from the lithography process, which defines the smallest lateral resolution, and from the characteristics of a molding process, e.g. the impossibility to realize an undercut. To allow for reliable release, the molding structures have to be coated with a sacrificial layer. Silicon nitride is deposited onto the substrate with accompanying monitoring of the deposition temperature during the PECVD process.     

An Asymptotic Preserving Method for Linear Systems of Balance Laws Based on Galerkin’s Method

We apply the concept of asymptotic preserving schemes (SIAM J Sci Comput 21:441–454, 1999) to the linearized \(p\) -system and discretize the resulting elliptic equation using standard continuous Finite Elements instead of Finite Differences. The fully discrete method is analyzed with respect to consistency, and we compare it numerically with more traditional methods such as Implicit Euler’s method.     

Underpotential alloy formation in the system Ag(hkl)/Cd2+

The underpotential deposition (UPD) of Cd on “real” and “quasi-ideal” silver single crystal surfaces of (111) and (100) crystallographic orientation as well as on polycrystalline silver substrate has been investigated in 0.5 M Na₂SO₄ supporting electrolyte solutions. At high underpotentials 100 < ΔE < 350 mV, the UPD is characterized by a quasi-reversible adsorption/desorption of Cd whereas at low underpotentials. ΔE < 50 mV, an increase of the anodic stripping charge with the polarization time is found due to the formation of an AgCd alloy at the substrate surface. The time dependence of this process can be described by a parabolic rate law, the rate constant of which is a function of ΔE and temperature T. Relatively low activation energies of about 70 kJmol^?1 were determined from measurements at 293 ? T ? 338 K. The results are discussed in terms of a semi-infinite-linear diffusion model. The alloy formation process is assumed to be initiated by a place exchange between Ag substrate atoms and vacancy sites within a mobile Cd adsorbate layer thus forming the initial stage of a highly distorted AgCd alloy. The further growth will take place by the movement of Ag atoms through the vacancy-rich surface alloy and the simultaneous deposition of Cd at the interface AgCd/Cd²⁺.     

Study of the Catalytic Ozonation of Humic Substances in Water and Their Ozonation Byproducts

It is shown that using transition metals, especially Mn(II) and Ag(I), during ozonation of humic substances in water allows important reductions in the content of organic matter. Characterization of the organic compounds resulting from ozonation was made by concentrating the sample through liquid-liquid extraction or derivation with PFBOA.HCl, along with the GC/MS and GC/ECD techniques. In total, 110 different organic compounds were identified using GC/MS; mainly carboxylic acids, aromatics, hydrocarbons, aldehydes, ketones, and furan-carboxylic acids. The percentages of elimination or formation levels reached during ozonation are discussed.     

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.