Kristalline und flüssigkristalline copolyester substituierter und unsubstituierter 4-hydroxybenzoesären

Three synthetic strategies were explored to lower the melting point of poly(4-hydroxybenzoate) below 400°C. Binary copolyesters of 4-hydroxybenzoic acid and 3-substituted 4-hydroxybenzoic acid were highly crystalline, regardless of composition, and did not melt below 400°C. In contrast ternary and quartenary copolyesters containing 3-bromo-4-hydroxybenzoic acid may possess melting points below 360°C. Binary copolyesters of 4-mercaptobenzoic acid and 3-substituted 4-hydroxybenzoic acids melt in the range of 360–400°C. Random copolyesters of 3-(4-hydrophenyl) propionic acid and 4-hydroxybenzoic acid are mainly amorphous with glass-transition temperatures between 50 and 15°C. They contain liquid-crystalline domains, which in the case of the 1:1 copolyester are stable over a range of ca. 400°C. The heat-distortion temperatures are low (60–80°C) due to the predominant influence of the amorphous matrix.     

Aus Sand erbaut – Saugspannungen infolge Teil sättigung ermöglichen scheinbar Unmögliches

Built of sand – tension from unsaturation enable unimaginable sculptures. Partly saturated sand enables to form astonishing figures and sculptures of sand. Curvers are forming sculptures, which are presented in open air exhibitions. It can be shown, that suction caused by waterfilms in the pores of the soil is the physical reason for the tension stress of unsaturated soils.     

COMPLEX FORMATION AND LIQUID-LIQUID EXTRACTION OF SILVER WITH CYCLIC AND OPEN-CHAIN OXATHIA ALKANES

The complex forming and extraction properties of various open-chain and two cyclic oxathia alkanes towards silver have been studied. The investigations confirm the direct proportionality between extraction constants and related complex stability constants.The extraction of silver by open-chain oxethie alkenee is greeter than by structurally analogoue thicacrown compounds. This fact and the determined stability constants show an absence of a macrocyclic effect during complex formation. The differences of extraction power between the various open-chain compounds can be interpreted on the basic o f the coordinative saturation and stereochemiatry of the silver ion, on the size o f the poesible chelate rings, and on the complexing capability o f the ether oxygen atoms.     

LIQUID-LIQUID EXTRACTION STUDIES OF METAL IONS WITH DIAZACROWN AND STRUCTURE ANALOGOUS OPEN-CHAIN COMPOUNOS

1,10-diaze [8]crown-6, their N,N'-dibutyl- and dioctyl-substituted derivatives and the structure analogous open-chein tetreoxedieza slkanee have been synthesized in order to examine the extraction properties for Na⁺, K⁺, Sr²⁺ and Hg²⁺. It wes found, that the extraction of strontium, potassium and sodium picratee with azacrown compounds ie much higher than that with open-chein oxaaze alkanes. 1,10-diaze [18] erown-6 has a good selectivity for the extraction of Sr²⁺ over K⁺ and Na in alkaline solution. In the case of Sr²⁺ the diffarencea between tha various azacrown compounds are email, whereea in the caee of K⁺ and Na the substituted derivativee are better extractante. Theserssulte correspond qualitativsly with tha order of stebility conetantB in protic solvsnts. The extrectebility of N,N'-dioctyl-l, 10-dieze[18]crown-6 for HgCl₂ is very high. Contrerv to the order of stability conetants the uneubetituted conpound do not extract mercury under the choeen experimental condition*. The extraction power of open-chain conpounde ie aleo high and strong Influenced by the alkyl eubatltuente at the nitrogen donor stons,     

Photo‐induced Charge Transfer and Relaxation of Persistent Charge Carriers in Polymer/Nanocrystal Composites for Applications in Hybrid Solar Cells

The photo‐induced charge transfer and the dynamics of persistent charge carriers in blends of semiconducting polymers and nanocrystals are investigated. Regioregular poly(3‐hexylthiophene) (P3HT) is used as the electron donor material, while the acceptor moiety is established by CdSe nanocrystals (nc‐CdSe) prepared via colloidal synthesis. As a reference system, organic blends of P3HT and [6,6]‐phenyl C₆₁‐butyric acid methyl ester (PCBM) are studied as well. The light‐induced charge transfer between P3HT and the acceptor materials is studied by photoluminescence (PL), photo‐induced absorption (PIA) and light‐induced electron spin resonance spectroscopy (LESR). Compared to neat P3HT samples, both systems show an intensified formation of polarons in the polymer upon photo‐excitation, pointing out successful separation of photogenerated charge carriers. Additionally, relaxation of the persistent charge carriers is investigated, and significant differences are found between the hybrid composite and the purely organic system. While relaxation, reflected in the transient signal decay of the polaron signal, is fast in the organic system, the hybrid blends exhibit long‐term persistence. The appearance of a second, slow recombination channel indicates the existence of deep trap states in the hybrid system, which leads to the capture of a large fraction of charge carriers. A change of polymer conformation due to the presence of nc‐CdSe is revealed by low temperature LESR measurements and microwave saturation techniques. The impact of the different recombination behavior on the photovoltaic efficiency of both systems is discussed.     

Einlaufverhalten nasslaufender Lamellenkupplungen im Schlupfbetrieb

Forschung im Ingenieurwesen - Nasslaufende Lamellenkupplungen weisen zu Betriebsbeginn eine Phase des Einlaufens auf, in der sich das Reibungsverhalten durch Anpassung der Reibflächen...