Abstract: In a method for preparing a blood sample for subsequent processing in a mass spectrometry laboratory, substances of interest are extracted from whole blood, blood plasma or blood serum immediately after the blood sample has been taken from a subject. The extraction is carried out by means of reversible immobilization on a surface, for example, the surface of a blood extraction vessel. Only the extracted substances of interest are sent in the immobilized state to the mass spectrometry laboratory.

Abstract: The invention relates to the detection of the binding of analyte molecules, for example biopolymer molecules, to immobilized capture substance molecules. The invention consists in using semiconductor wafers (chips) with electrical circuits in spatial proximity to a surface area coated with capture substance molecules and loading the binding of the analyte molecules to the capture substance molecules with co-bound electrically conductive nanoparticles so that the nanoparticles can act upon the electrical circuits either through changes in the electrical stray capacitance or by generating electric currents, thus making the binding of the analyte molecules electronically detectable.

Abstract: A transport system for spinning bobbins and bobbin tubes comprises a transport path with two essentially vertical sections and an essentially horizontal section connected therebetween. The spinning bobbins and bobbin tubes are transported on pallets whose foot portion comprises an element consisting of magnetizable material. A conveyor belt runs along the transport path at the back side of which belt stationarily arranged permanent magnets are arranged to exert magnetic forces to hold the pallets on the conveyor belt.

Abstract: A device for centering tubes during their processing, for example in a tube cleaning station of a textile machine. In a textile machine provided with several batches of tubes of differing length, diameter and/or material, which cannot be processed together in known cleaning devices, the present device has a rotatably seated holder with at least two differing centering devices adapted for different tubes for selective positionability relative to the tubes to be centered according to sensor devices which detect the differing physical characteristics of the tubes.

Abstract: The device for storing money in a cab is distinguished by the fact that it exhibits, in a lockable housing, one or more openings for the introduction of notes and/or coins, mechanisms for dispensing notes and/or coins, mechanisms for determining the amount to be dispensed and mechanisms for invalidating at least the notes in the event of forcible tampering.

Abstract: The invention concerns the novel compound, 4-methyl-3-pentyl-2 (5H)-furanone, I, a process for the manufacture of I and fragrance and flavor compositions containing I.

Abstract: A process for the manufacture of 3-hydroxy-2-alkyl-4-pyrones of formula I is provided. ##STR1## The process comprises cyclizing a compound of formula II, ##STR2## an acidic medium and hydrolyzing the ester formed thereby to produce compound I. R.sup.1 represents methyl or ethyl; R.sup.2 represents lower alkanoyl or optionally substituted benzoyl; R.sup.3 represents --OH or --NR.sup.4 R.sup.5 ; and, R.sup.4 and R.sup.5 may be alike or different and represent lower alkyl. The pyrones of formula I wherein R.sup.1 represents methyl or ethyl are known flavorants and odorants.

Abstract: A process for the manufacture of 3-hydroxy-2-alkyl-4-pyrones of formula I is provided. ##STR1## The process comprises cyclizing a compound of formula II, ##STR2## in acidic medium and hydrolyzing the ester formed thereby to produce compound I. R.sup.1 represents methyl or ethyl; R.sup.2 represents lower alkanoyl or optionally substituted benzoyl; R.sup.3 represents --OH or --NR.sup.4 R.sup.5 ; and, R.sup.4 and R.sup.5 may be alike or different and represent lower alkyl. The pyrones of formula I wherein R.sup.1 represents methyl or ethyl are known flavorants and odorants.

Abstract: A sampling device for inspection vehicles equipped with an environmental inspection system, the system comprising an analyzer having a receiving head (21), to which the substances to be examined are supplied by means of a movable collecting body (4) having a ground-engageable contact surface. The collecting body is formed by a rope-like material (4) which is wound up on a supply drum (2) and passed between two rollers (10, 11) arranged at a certain distance therefrom. By displacing the material (4) in its longitudinal direction, the material can be moved into a first position in which an end section (41) of the material hangs down and contacts the ground (42), and a second position in which the end section (41), which had been in contact with the ground (42), is positioned opposite the receiving head (21). Consumed end portions (41) can be cut off by means of a separating device.

Abstract: Wholly aromatic thermotropic polyesters are based on(A) 30 to 60 mol % of 4-hydroxybenzoic acid,(B) 20 to 35 mol % of terephthalic acid and(C) 20 to 35 mol % of a mixture of(C.sub.1) trimethylhydroquinone and(C.sub.2) resorcinolthe molar ratio of C.sub.1 :C.sub.2 being within the range from 0.4:1 to 0.7:1 and the molar ratio of B:C within the range from 0.9:1 to 1.1:1.

Abstract: Wholly aromatic liquid-crystalline condensates which form a liquid-crystalline fiber-forming melt below 320.degree. C. and are diphase within the range from the glass transition temperature Tg to the melting point and are composed of(a) not less than 10 mol % of repeat units of the formula I ##STR1## (b) from 5 to 30 mol % of repeat units of the formula II ##STR2## (c) from 0 to 20 mol % of one or more of the repeat units of the formulae III, IV or V ##STR3## (d) from 0 to 20 mol % of one or more of the repeat units of the formulae VI, VII, VIII or IX ##STR4## (e) a molar amount corresponding to the total amount of components (b), (c) and (d) of repeat units of the formula X ##STR5## the mole percentage of components (a), (b), (c), (d) and (e) adding up to 100 mol % in each case, the preparation thereof and filaments, fibers, films, moldings and surface coating prepared therefrom.

Abstract: Wholly aromatic mesomorphic polyester amides which form a liquid-crystalline fiber-forming melt below 320.degree. C., composed of(a) from 3 to 30 mol % of repeat units of the formula I ##STR1## (b) from 3 to 30 mol % of repeat units of the formula II and/or III ##STR2## (c) from 2 to 25 mol % of one or more of the repeat units of the formula IV, V or VI, ##STR3## (d) a molar amount corresponding to the total amount of components (a), (b) and (c) excluding the repeat unit of the formula III, of the repeat units of the formula VII ##STR4## which, if desired, can in part be replaced by repeat units of the formula VIII ##STR5## (e) if desired from 5 to 25 mol % of repeat units of the formula IX ##STR6## (f) repeat units of the formula X ##STR7## the molar proportions of components (a), (b), (c), (d), (e) and (f) in each case adding up to 100 mol %, and preparation thereof.

Abstract: Nonionic substances which form disk-shaped micelles in aqueous solution and are of the formula ##STR1## where R is H or ##STR2## R.sup.1 is C.sub.1 -C.sub.4 alkyl, R.sup.2 is H or CH.sub.3, x is from 3 to 12 and y is from 3 to 15, and polymers of compounds of the formula I where R is ##STR3## processes for the preparation of the compounds of the formula I and of the polymers, and the use of the compounds described as additives to detergents and cleaning agents, for other surfactant applications and as liquid crystals for optical, electronic and optoelectronic applications.

Abstract: Fully aromatic thermotropic polyesters based on(A) from 30 to 60 mol % of 4-hydroxybenzoic acid,(B) from 20 to 35 mol % of a mixture of(B.sub.1) terephthalic acid,(B.sub.2) isophthalic acid and(B.sub.3) from 0.5 to 5 mol % of a dicarboxylic acid of the general formula I ##STR1## where X is --O--, --S--, --SO.sub.2 --, --CO--, --CH.sub.2 -- or --C(CH.sub.3).sub.2 --, n is 0 or 1 and the two imide nitrogen atoms are meta or para to X, or their C.sub.1 -C.sub.8 -alkyl, C.sub.1 -C.sub.8 -alkoxy, aryl, chlorine or bromine derivatives which are substituted in the nucleus,the molar ratio of B.sub.1 to B.sub.2 being from 1.04:1 to 19:1, and(C) from 20 to 35 mol % of a mixture of(C.sub.1) hydroquinone and(C.sub.2) 4,4'-dihydroxydiphenyl,the molar ratio of C.sub.1 to C.sub.2 being from 0.1:1 to 2.67:1 and the molar ratio of B to C being from 0.9:1 to 1.1:1.

Abstract: Liquid-crystalline carbamyl-containing polycondensates composed of(a) aromatic hydroxycarboxylic and/or aminocarboxylic acids in which the hydroxyl and amino groups are not vicinal to the carboxyl group,(b) from 0.1 to 20 mol % of urea,(c) aromatic dihydroxy, diamino and/or hydroxy-amino compounds in which the hydroxyl and amino groups are not vicinal,(d) a molar amount equivalent to the total amount of components b and c of an aromatic dicarboxylic acid in which the carboxyl groups are not vicinal,the preparation thereof and fibers, films and moldings prepared therefrom.

Abstract: Wholly aromatic polyesters which form a liquid-crystalline fiber-forming melt below 300.degree. C. and composed of(a) from 5 to 35 mol % of repeat units of the formula I ##STR1## (b) from 3 to 15 mol % of repeat units of the formula II ##STR2## (c) a molar amount corresponding to the total amount of (a) and (b) of repeat units of the formula III ##STR3## and (d) not less than 10 mol % of repeat units of the formula IV ##STR4## the molar proportions of components a, b, c and d adding up to 100 mol % in each case, the preparation thereof and fibers, films, moldings and surface coating materials prepared therefrom.

Abstract: Wholly aromatic thermotropic polyesters are based on(A) from 25 to 60 mol % of a mixture of(A.sub.1) 4-hydroxybenzoic acid and(A.sub.2) 3-hydroxybenzoic acid, 4-aminobenzoic acid and/or 3-aminobenzoic acid or their chlorine, bromine, C.sub.1 -C.sub.8 -alkyl or C.sub.1 -C.sub.8 -alkoxy derivatives substituted in the nucleus,the molar ratio of A.sub.1 to A.sub.2 being from 5:1 to 41:1,(B) from 20 to 37.5 mol % of a mixture of(B.sub.1) terephthalic acid and(B.sub.2) isophthalic acid,the molar ratio of B.sub.1 to B.sub.2 being from 1.04:1 to 19:1, and(C) from 20 to 37.5 mol % of a mixture of(C.sub.1) hydroquinone and(C.sub.2) 4,4'-dihydroxydiphenyl,the molar ratio of C.sub.1 to C.sub.2 being from 0.1:1 to 2.67:1 and the molar ratio of B to C being from 0.9:1 to 1.1:1.

Abstract: Wholly aromatic polyester carbamides which form a liquid-crystalline fiber-forming melt below 300.degree. C. and are composed of(a) not less than 20 mol % of repeat units of the formula I ##STR1## (b) from 5 to 15 mol % of repeat units of the formula II ##STR2## (c) from 5 to 15 mol % of repeat units of the formula III ##STR3## (d) from 1 to 10 mol % of units of the formula IV ##STR4## (e) a molar amount corresponding to the total amount of components (b), (c) and (d) of repeat units of the formula V ##STR5## the molar proportions of components (a), (b), (c), (d) and (e) adding up to 100 mol % in each case, the preparation thereof and fibers, films moldings and coatings prepared therefrom.

Abstract: Fully aromatic themotropic polyesters are based on(A) from 30 to 60 mol % of 4-hydroxybenzoic acid,(B) from 20 to 35 mol % of a mixture of(B.sub.1) terephthalic acid and(B.sub.2) isophthalic acid,the molar ratio of B.sub.1 to B.sub.2 being from 1.04:1 to 19:1, and(C) from 20 to 35 mol % of a mixture of(C.sub.1) hydroquinone,(C.sub.2) 4,4'-dihydroxydiphenyl and(C.sub.3) from 0 to 5 mol % of a dihydroxy compound of the general formula I ##STR1## where R and R' are each C.sub.1 -C.sub.4 -alkyl, halogen or aryl, n is 1, 2 or 3 and m is 0 or 1,the molar ratio of C.sub.1 to C.sub.2 being from 0.1:1 to 2.67:1 and the molar ratio of B to C being from 0.9:1 to 1.1:1.

Abstract: Wholly aromatic, mesomorphic polyesters which give a homogeneous liquid crystalline melt at below 320.degree. C. consist of(a) not less than 10 mol % of repeating units of the formula I ##STR1## (b) from 1 to 25 mol % of repeating units of the formula II ##STR2## (c) from 5 to 20 mol % of one or more of the repeating units of the formulae III to VII ##STR3## (d) from 5 to 15 mol % of repeating units of the formula VIII ##STR4## and (e) from 10 to 60 mol % of repeating units of the formula IX ##STR5## the sum of the molar amounts of (a), (b), (c), (d) and (e) being 100 mol % in each case and the molar ratio of the components (b)+(c)+(d) to component (e) being from 0.9:1 to 1.1:1.