Removal of volatile organic compounds using amphiphilic cyclodextrin-coated polypropylene

• Ludmilla Lumholdt,
• Sophie Fourmentin,
• Thorbjørn T. Nielsen and
• Kim L. Larsen

Beilstein J. Org. Chem. 2014, 10, 2743–2750, doi:10.3762/bjoc.10.290

• production and running costs due to the need of advanced equipment and/or relatively low uptake capacity or low cavity coverage. Choi et al. [20] produced hollow polysulfone fibres containing CDs that were used to remove di-(2-ethylhexyl)phthalate (one of the endocrine disruptors mentioned in the Water

Synthesis and characterization of a novel carboxyl group containing (co)polyimide with sulfur in the polymer backbone

• Miroslav Mrsevic,
• David Düsselberg and
• Claudia Staudt

Beilstein J. Org. Chem. 2012, 8, 776–786, doi:10.3762/bjoc.8.88

• )polyimides show cutoff wavelengths over 400 nm and were yellow in color. Compared to their respective homopolymers 6FDA-3,3′-DDS (84%) and 6FDA-4,4′-SDA (86%) [21] the (co)polyimides exhibited approximately the same transparency and color. In comparison to commercially available polymers such as polysulfone

Functionalized copolyimide membranes for the separation of gaseous and liquid mixtures

• Nadine Schmeling,
• Roman Konietzny,
• Daniel Sieffert,
• Patrick Rölling and
• Claudia Staudt

Beilstein J. Org. Chem. 2010, 6, 789–800, doi:10.3762/bjoc.6.86

• separations are currently not possible because suitable membrane materials are not commercially available. It has been found that polymeric membranes, e.g., silicone rubber, polysulfone, cellulose acetate, PDMS, 1,2-polybutadiene and polyethylene are not suitable for this kind of separation because the

Synthesis, characterization and photoinduced curing of polysulfones with (meth)acrylate functionalities

• Cemil Dizman,
• Sahin Ates,
• Lokman Torun and
• Yusuf Yagci

Beilstein J. Org. Chem. 2010, 6, No. 56, doi:10.3762/bjoc.6.56

• -dimethoxy-2-phenylacetophenone (DMPA) as the photoinitiator undergo rapid polymerization upon irradiation forming insoluble networks. The photo-curing behavior was investigated by photo-DSC and the effects of the molecular weight of the polysulfone precursor and type of functionality on the rate of

• polymerization and conversion were evaluated. Thermal properties of the photochemically cured films were studied by differential scanning calorimeter (DSC) and thermal gravimetric analysis (TGA). Keywords: acrylates; photoinitiated polymerization; polysulfone; UV-curable oligomers; Introduction Polysulfones

• )acrylate telechelics with polysulfone backbones. The curing behavior of these telechelics was studied by photo-DSC with 2,2-dimethoxy-2-phenylacetophenone (DMPA) as the photoinitiator. As shown below, the rigid aromatic polysulfones with different molecular weights were deliberately used so as to