Basf Aktiengesellschaft

Basf Aktiengsellschaft

Juergen Koch

Gerhard Heinz

Peter Ittemann

Hartmut Zeiner

Hermann Buchert

Wolfgang Eberle

Jochem Henkelmann

Manfred Eggersdorfer

Michael Kopietz

Peter Wolf

Robert R Lieder

Helmut Reichelt

Alexander Aumueller

Helmut Muenstedt

Georg N Simon

Bernd Hupfeld

Karin Elbl-Weiser

Wolfgang Stegmaier

Christiane Husemann

Polyimides can be obtained by reacting a dianhydride component comprising 3,4,3',4'-bisphenyltetracarboxylic dianhydride, oxydiphthalic dianhydride and in addition further aromatic dianhydrides, and a diamine component comprising diamines of the formula ##STR1## and in addition further aromatic diamines.

Recrystallizable polyimides

Stabilized polyaryl ether ketone molding compositions containing as essential components

Stabilized polyaryl ether ketone molding compositions

A process for preparing polyaryl ethers of the formula I or Ia ##STR1## by condensation of at least one appropriate bisphenol with at least one appropriate aromatic dichloride in the presence of an alkali metal carbonate in a dipolar aprotic solvent, is carried out in the presence of a catalyst selected from the alkali metal nitrites and the group of compounds of the formula II ##STR2## where r.sup.1 and r.sup.3 are each hydrogen, C.sub.7 -C.sub.16 -phenylalkyl, C.sub.1 -C.sub.12 -alkoxy, fluorine, chlorine, bromine, iodine or nitro, and R.sup.2 is nitro or nitroso, or ##STR3## where R.sup.4 is hydrogen, C.sub.1 -C.sub.4 alkyl, fluorine, chlorine, bromine or iodine.

Preparation of polyaryl ethers with nitrogen compound catalysts

An N-substituted polyamideimide essentially composed of identical or different repeating units of the formula I ##STR1## where R.sup.1 is one of the following tetravalent aromatic radicals ##STR2## and X is a bond or one of the following linkers ##STR3## where R.sup.2 and R.sup.4 are each, independently of one another, one of the following divalent aromatic radicals ##STR4## and where X has the abovementioned meanings and where R.sup.3 is hydrogen or a monovalent radical such as C.sub.1 -C.sub.6 -alkyl or phenyl, and the C.sub.1 -C.sub.6 -alkyl-, C.sub.1 -C.sub.6 -alkoxy-, aryl- or halogen-substituted derivatives thereof, and precursors (monomers) therefor, are described.

N-substituted polyamide-imides

An N-substituted polyamide-imide essentially composed of identical or different repeating units of the formula I ##STR1## where R.sup.1 is one of the following tetravalent aromatic radicals ##STR2## and X is a bond or one of the following linkers ##STR3## where R.sup.2 and R.sup.4 are each, independently of one another, one of the following divalent aromatic radicals ##STR4## and where X has the abovementioned meanings and where R.sup.3 is hydrogen or a monovalent radical such as C.sub.1 -C.sub.6 -alkyl or phenyl, and the C.sub.1 -C.sub.6 -alkyl-, C.sub.1 -C.sub.6 -alkoxy-, aryl- or halogen-substituted derivatives thereof, and precursors (monomers) therefor, are described.

N-substituted polyamide-imide

Polyaryl ether ketones which contain units of the formula ##STR1## are prepared by electrophilic polycondensation in an inert solvent in the presence of a Lewis acid and in the presence or absence of a Lewis base using a carbonyl halide as monomer component, said carbonyl halide being an oxalyl dihalide or a mixture thereof with another carbonyl halide.

Preparation of polyaryl ether ketones by electrophilic polycondensation

Thermoplastic molding compositions suitable for producing interior components for vehicles for the conveyance of passengers, in particular aircraft, which show a low smoke gas density and low heat release characteristics in the event of a fire, are based on a heat-resistant plastic which contains as a filler from 0.5 to 50 % by weight of an oxide of an element of main group III, IV or V, of a salt of an oxygen acid of an element of main group III, IV or V or of a compound which on heating forms such an oxide or salt.

Heat-resistant thermoplastic molding compositions

The addition of compounds which convert carboxylic acids into their halides in the course of electrophilic polycondensation for preparing polyaryl ether ketones improves the controllability and reproducibility of the process and the properties of the products.

Polyaryleneetherketones are prepared by a quasicontinuous process, by Friedel-Crafts polycondensation of a reaction mixture containing

Preparation of polyaryleneetherketones

Thermoplastic molding compositions suitable for producing interior components for vehicles for the conveyance of passengers, in particular aircraft, which show a low smoke gas density and low heat release characteristics in the event of a fire, are based on a heat-resistant plastic which contains as a filler from 0.5 to 50% by weight of an oxide of an element of main group III, IV or V, of a salt of an oxygen acid of an element of main group III, IV or V or of a compound which on heating forms such an oxide or salt.

Polyaryl ethers which are stable at high temperatures essentially consist of

Polyaryl ethers which are stable at high temperatures and have improved

Polyaryl ether ketones essentially consist of

Polyaryl ether ketones having improved processibility

Highly heat-resistant polyaryl ether ketones are composed of

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Neuhofen, Germany

Juergen Koch