Invention Grant
US08206675B2 Nontoxic polyethoxysiloxane material or the production of biologically resorbable and/or bioactive articles containing polyethoxysiloxane material, the production thereof, and the use thereof 有权
无毒的聚乙氧基硅氧烷材料或生产含有聚乙氧基硅氧烷材料的生物可再吸收和/或生物活性制品,其生产及其用途

  • Patent Title: Nontoxic polyethoxysiloxane material or the production of biologically resorbable and/or bioactive articles containing polyethoxysiloxane material, the production thereof, and the use thereof
  • Patent Title (中): 无毒的聚乙氧基硅氧烷材料或生产含有聚乙氧基硅氧烷材料的生物可再吸收和/或生物活性制品,其生产及其用途
  • Application No.: US12602773
    Application Date: 2008-06-03
  • Publication No.: US08206675B2
    Publication Date: 2012-06-26
  • Inventor: Axel Thierauf
  • Applicant: Axel Thierauf
  • Applicant Address: DE Duesseldorf
  • Assignee: Bayer Innovation GmbH
  • Current Assignee: Bayer Innovation GmbH
  • Current Assignee Address: DE Duesseldorf
  • Agency: Norris McLaughlin & Marcus PA
  • Priority: DE102007026043 20070604
  • International Application: PCT/DE2008/075002 WO 20080603
  • International Announcement: WO2008/148384 WO 20081211
  • Main IPC: C01B15/14
  • IPC: C01B15/14
Nontoxic polyethoxysiloxane material or the production of biologically resorbable and/or bioactive articles containing polyethoxysiloxane material, the production thereof, and the use thereof
Abstract:
The present invention relates to a polyethoxysiloxane (PES) material to be obtained in that (a) a first hydrolysis condensation reaction of a maximum of one group X of one or more different Si compounds of the formula (I) SiX4 (I) in which the groups X are the same or different and represent hydroxy, hydrogen, or ethoxy (EtO), are catalyzed in an acidic fashion at an initial pH value of 0 to ≦7, is conducted in the presence of ethanol (EtOH) or an ethanol-water mixture as a solvent over a time period of 1 to 24 hours at a temperature of 0° C. to 78° C, (b) a second hydrolysis condensation reaction of the material obtained in step (a) is conducted while simultaneously removing the solvent by successive evaporation in a gas diffusion-tight container at a pressure of 100 to 1013 mbar, preferably at a slight negative pressure of 300 mbar to 800 mbar and a temperature of 50-78° C. until a drastic increase in viscosity (at a shear rate of 10 s−1 at 4° C.) to 0.5 to 2 Pa·s until a constant weight is attained and a cyclotetrasiloxane of the general formula ((SiO(OH)0,75(OEt)1,25× 1/64H2O)4 and a molar mass of 4*approx. 114 g=approx. 456 g; (c) said PES material is cooled in a closed container over a time period from a few minutes to a few hours, and (d) the PES material obtained from step (c) is converted into an rPES material by a third hydrolysis condensation reaction.
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