Maillard reactions of dextrins and starch

When dextrins or starch are heated with propyl-amine in neutral aqueous solution at 100–130° C a brown colouration is observed. From the reaction mixture 3-hydroxy-2-methyl-1-propyl-4(1H)-pyridone11, 1,4-dihy-dro-2-methyl-1-propyl-4-propylimino-3-pyridinol12 and 5-hydroxymethyl-1-propyl-pyrrol-2-aldehyde13 can be extracted with organic solvents and separated by HPLC. Enzymatic hydrolysis effects the release of 1(3-hydroxy-1-propyl-2-pyrrolyl)-1-ethanone10 from a glycosidically bound precursor.

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Maillard Reaktionen von Dextrinen und Stärke

Zusammenfassung Erhitzt man Dextrine oder Stärke mit Propylamin in neutraler wäßriger Lösung auf 100–130 °C, so beobachtet man eine braune Färbung. Aus der Reaktionsmischung lassen sich 3-Hydroxy-2-methyl-1-propyl-4(1H)-pyridon11, 1,4-Dihydro-2-methyl-1-pro-pyl-4-propylimino-3-pyridinol12 und 5-Hydroxymethyl-1-propyl-pyrrol-2-aldehyd13 mit organischen Lösungsmitteln extrahieren und durch HPLC trennen. Nach enzymatischer Hydrolyse der wasserlöslichen Fraktion ist 1(3-Hydroxy-1-propyl-2-pyrrolyl)-1-ethanon10 isolierbar.

     

Modeling of program, erase and retention characteristics of charge-trap gate all around memories

This paper describes the effect of geometry in charge-trap (CT) memory devices. We first theoretically analyze the impact of the curvature radius on the behavior of the gate current in Gate-All-Around devices, and then describe the change to make to planar model in order to fit the cylindrical devices characteristics. This model is used to simulate Nanocrystal and SONOS program, erase and retention behaviors. The dynamics enhancement during program/erase due to the bending of the active region in such cylindrical devices is explained. The scaling perspectives conclude this paper.     

Long time reliability study of soldered flip chips on flexible substrates

Due to the requirements of new light, mobile, small and multifunctional electronic products the density of electronic packages continues to increase. Especially in medical electronics like pace makers the minimisation of the whole product size is an important factor. So flip chip technology becomes more and more attractive to reduce the height of an electronic package. At the same time the use of flexible and foldable substrates offers the possibility to create complex electronic devices with a very high density. In terms of human health the reliability of electronic products in medical applications has top priority.In this work flip chip interconnections to a flexible substrate are studied with regard to long time reliability. Test chips and substrates have been designed to give the possibility for electrical measurements. Solder was applied using conventional stencil printing method. The flip chip contacts on flexible substrates were created in a reflow process and underfilled subsequently.The assemblies have been tested according to JEDEC level 3. The focus in this paper is the long time reliability up to 10,000 h in thermal ageing at 125 °C and temperature/humidity testing at 85 °C/85% relative humidity as well as thermal cycling (0 °C/+100 °C) up to 5000 cycles. Daisy chain and four point Kelvin resistances have been measured to characterise the interconnections and monitor degradation effects.The failures have been analysed in terms of metallurgical investigations of formation and growing of intermetallic phases between underbump metallisation, solder bumps and conductor lines. CSAM was used to detect delaminations at the interfaces underfiller/chip and underfiller/substrate respectively.     

Provably-Secure Time-Bound Hierarchical Key Assignment Schemes

A time-bound hierarchical key assignment scheme is a method to assign time-dependent encryption keys to a set of classes in a partially ordered hierarchy, in such a way that each class can compute the keys of all classes lower down in the hierarchy, according to temporal constraints.     

Selective Functionalization of Microstructured Surfaces by Laser‐Assisted Particle Transfer

Microcavity arrays represent millions of different reaction compartments to screen, for example, molecular interactions, exogenous factors for cells or enzymatic activity. A novel method is presented to selectively synthesize different compounds in arrays of microcavities with up to 1 000 000 cavities per cm². In this approach, polymer microparticles with embedded pre‐activated monomers are selectively transferred into microcavities with laser radiation. After particle patterning, heating of the particle matrix simultaneously leads to diffusion and coupling of the monomers inside each microcavity separately. This method exhibits flexibility, not only in the choice of compounds, but also in the choice of particle matrix material, which determines the chemical reaction environment. The laser‐assisted selective functionalization of microcavities can be easily combined with the intensively growing number of laser applications for patterning of molecules and cells, which is useful for the development of novel biological assays.     

The preparation of TiO2–nitrogen doped by calcination of TiO2·xH2O under ammonia atmosphere for visible light photocatalysis

The investigation on incorporating nitrogen group into titanium dioxide in order to obtain powdered visible light-active photocatalysts is presented. The industrial hydrated amorphous titanium dioxide (TiO₂·xH₂O) obtained directly from sulphate technology installation was modified by heat treatment at temperatures of 100–800 °C for 4 h in an ammonia atmosphere. The photocatalysts were characterized by UV–VIS–DR and XRD techniques. The UV–VIS–DR spectra of the modified catalysts exhibited an additional maximum in the VIS region (, ) which may be due to the presence of nitrogen in TiO₂ structure. On the basis of XRD analysis it can be supposed that the presence of nitrogen does not have any influence on the transformation temperature of anatase to rutile. The photocatalytic activity of the modified photocatalysts was determined on the basis of decomposition rate of phenol and azo-dye (Reactive Red 198) under visible light irradiation. The highest rate of phenol degradation was obtained for catalysts calcinated at 700 °C (6.55%), and the highest rate of dye decomposition was found for catalysts calcinated at 500 and 600 °C (ca. 40–45%). The nitrogen doping during calcination under ammonia atmosphere is a very promising way of preparation of photocatalysts which could have a practical application in water treatment system under broader solar light spectrum.     

Surface hydrocarbon components of two species ofNasutitermes from Trinidad

Colonies ofNasutitermes costalis (Holmgren) andN. ephratae (Holmgren) were collected from five locations in Trinidad. Cuticular hydrocarbons were characterized by gas chromatography-electron impact mass spectrometry and quantified by capillary gas chromatography. Sixteen major components were identified; all but one component (12, 16-dimethyltriacontane) were common to both species. The methyl-branched hydrocarbons were predominant inN. costalis, while the majority of the hydrocarbon components inN. ephratae weren-alkanes. One hydrocarbon (11,15-dimethylheptacosane) was found in abundance in samples ofN. ephratae from Trinidad but was not previously reported from collections of this species in Panama. In addition to the morphology of the soldiers and alates and the architecture of the arboreal nests,N. costalis andN. ephratae from Trinidad can easily be separated by chromatograms of the hydrocarbons.N. costalis has an enormous 13,17-dimethylhentriacontane peak (mean = 42.4% of total hydrocarbon). InN. ephratae this peak is much smaller and the 12,16-dimethyltriacontane peak is completely missing.N. costalis from Trinidad andN. corniger from Panama appear to have cuticular hydrocarbon profiles that are more similar to one another than are those ofN. ephratae from Trinidad and Panama.Isoptera: Termitidae: Nasutitermitinae.     

The location of inhibitory specificities in human mucus proteinase inhibitor (MPI): separate expression of the COOH-terminal domain yields an active inhibitor of three different proteinases

Human mucus proteinase inhibitor (MPI) consists of 107 aminoacids arranged in two domains showing high homology to eachother. This protein is an inhibitor of different serine proteinasesincluding trypsin, chymotrypsin, leukocyte elastase and cathepsinG. On the basis of sequence comparisons it has been suggestedthat the first domain inhibits trypsin, whereas the second onewas thought to be active against chymotrypsin and elastase.To prove the location of the different inhibitory activitiesgene fragments for both domains have been cloned separatelyand expressed in Escherichia coli. Inhibition assays with theisolated recombinant domains showed that the second domain isactive against chymotrypsin, neutrophil elastase and trypsin,whereas for the first domain only a weak activity against trypsincould be detected. These results suggest that the inhibitoryactivities of the native molecule towards these three proteinasesare all located in the second domain.     

Passivation of pyrite due to surface treatment

Two samples of naturally occurring pyrite were treated with acetyl acetone, silanes, humic acids, lignin-NaOH mixture, and oxalic acid. The corrosion rate of pyrite was observed to decrease significantly due to the surface treatment by the chemicals used in this study. Surface characterization methods indicate that phenyl triacetoxy silane forms a passive coating a few Angstroms thick on the pyrite, thus preventing its dissolution in 1M H₂SO₄.