Antioxidantien und Stabilisatoren XXVIII. Gelchromatographie nichtflüchtiger phenolischer antioxidantien zur stabilisierung von polymeren

High resolution gel chromatography was applied to the analysis of phenolic antioxidants mixtures formed by an alkylation of 4,4'-isopropylidenebisphenol and used for the stabilisation of polyolefins and rubbers. The calibration by pure model substances provided values of relative zone rates on S-GEL-832 for a series of tert-butyl and tert-octyl derivatives of phenol and 4,4'-isopropylidenebisphenol. The chromatograms show in some cases a separation of isomers differing in size of their molecules in solution.     

The impact of natural and artificial weathering on the visual,colour and structural changes of seven tropical woods

This study investigates the effects of wood weathering on changes in its macroscopic and colour characteristics in connection with changes in its molecular and anatomical structure. Seven hardwoods suitable for outdoor architecture—bangkirai, cumaru, cumaru rosa, ipé, jatobá, kusia, and massaranduba—were exposed to the exterior out of ground contact for 1–36 months according to EN 927-3, and for 1–12 weeks in Xenotest with water spraying according to partly modified EN 927-6. With prolonged weathering, the following changes occurred in the top surfaces of all tropical woods: (1) visual—creation of longitudinal macro-cracks, (2) spectrophotometry and CIE-L ^? a ^? b ^? —darkening in exterior exposure mainly due to pollutants, except for ipé, and vice versa lightening in Xenotest, as well as greening and blueing in both modes of exposure, (3) FTIR—faster decrease of guaiacyl than syringyl lignin, absolute decrease of conjugated and unconjugated carbonyl groups in the newly formed lignin-polysaccharide-extractive substrate in the photo-oxidized and washed-out cell walls, and decrease of cellulose crystallinity, (4) SEM—damaging of cell-walls by micro-cracks, and their degradation by thinning. Connections between changes of the individual characteristics of weathered woods, for example, between the colour (ΔE*, etc.) and the molecular structure (carbonyls, etc.), were also determined.     

Post-translational fate of CAN1 permease of Saccharomyces cerevisiae

To study the post-translational fate of arginine permease (Can1p), the gene coding for this transport protein was placed behind a constitutive promoter of plasma membrane ATPase (PMA1) and furnished with a Myc tag. In exponential-phase cells the amount of Can1p is constant, although turnover can be demonstrated. A rapid decrease in transport activity during the early stationary phase is paralleled by a corresponding net degradation of the protein. The amount of Can1p present in exponential cells grown on various nitrogen sources is the same, except in arginine-grown cells, in which the amount of the protein is markedly lower. This occurs solely when arginine serves as nitrogen source but not as an immediate consequence of, for example, arginine addition to cells growing on other nitrogen sources. It was demonstrated that Can1p is phosphorylated. Since Can1p expression under the PMA1 promoter is glucose-dependent, the amount of the permease expressed in high-glucose-grown cells is higher than in low-glucose-grown ones. Only a part of the Can1p overexpressed in high-glucose-grown cells is phosphorylated, while in low-glucose-grown cells the phosphorylated form probably represents the majority of Can1p. The permease phosphorylation or dephosphorylation is not related to transinhibition. © 1998 John Wiley & Sons, Ltd.     

Polypyrrole and polyaniline prepared with cerium(IV) sulfate oxidant

The conducting polymers, polypyrrole and polyaniline, were synthesized by chemical oxidative polymerization of the corresponding monomers in 0.1 M sulfuric acid using cerium(IV) sulfate as the oxidant at mole ratios of oxidant-to-monomer ranging from 0.5 to 3. The yields of the oxidation products were determined, and the samples were characterized with respect to their elemental composition, molecular structure, and morphology. The conductivity of polypyrrole prepared in 0.1 M sulfuric acid, 10^?1 to 10⁰ S cm^?1, was higher compared with the conductivity of polyaniline prepared under the same conditions, 10^?3 to 10^?1 S cm^?1. The loss of mass after deprotonation with ammonium hydroxide is reported, and discussed in terms of the type of protonation as also reflected by FTIR spectroscopy. The conductivity of polypyrrole bases remained at relatively high level, 10^?5 to 10^?3 S cm^?1, while PANI bases became non-conducting, 10^?12 to 10^?10 S cm^?1. The polymers had a granular morphology in all cases.     

Long-term studies (1871-2000) on acidification and recovery of lakes in the Bohemian Forest (central Europe)

This paper evaluates long-term changes in the atmospheric depositions of S and N compounds, lake water quality, and biodiversity at eight glacial lakes in the Bohemian Forest over the past 130 years. This time interval covers (i) the 'background' pre-acidification status of the lakes, (ii) a period of changes in the communities that can be partly explained by introduction of fish, (iii) a period of strong lake acidification with its adverse impacts on the communities, (iv) the lake reversal from acidity, which includes the recent status of the lakes. The lake water chemistry has followed-with a characteristic hysteresis-both the sharp increase and decline in the deposition trends of strong anions. Remarkable changes in biota have mirrored the changing water quality. Fish became extinct and most species of zooplankton (Crustacea) and benthos (Ephemeroptera and Plecoptera) retreated due to the lake water acidification. Independent of ongoing chemical reversal, microorganisms remain dominant in the recent plankton biomass as well as in controlling the pelagic food webs. The first signs of the forthcoming biological recovery have already been evidenced in some lakes, such as the population of Ceriodaphnia quadrangula (Cladocera) returning into the pelagial of one lake or the increase in both phytoplankton biomass and rotifer numbers in another lake.     

The influence of blast-furnace slag hydration products on microcracking of concrete

New hydration products of ground granulated blast-furnace slag are formed during the hydration process of Portland slag cement concrete. Spatial distribution of microcracks in concrete is related also to newly formed slag hydrates. The chemical composition of hydration products is variable and unstable. The Si/Ca ratios rise in hydration products near the unhydrated slag core significantly. There is also a certain increase of Mg and Al content in the central parts of hydration rims. The scope of the paper is to find a relation between slag hydration products and the process of microcracking. The amount of microcracks was reduced in concretes with a lower content of vitreous fraction where the slag basicity was high. Neoformation of hydration products is accompanied by volume changes, which can lead to concrete microcracking.