5 research outputs found

    Durable 3D Porous Superhydrophobic Composites for Versatile Emulsion Separation in Multiple Environments

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    Polydopamine as a multifunctional biomimetic polymer with nonselective strong adhesion properties has become a hot research topic in recent years. However, there are a few reports on the durable and effective emulsion separation of polydopamine composites from other materials. Therefore, it is necessary to construct durable polydopamine composites to achieve selective adsorption of materials. In this work, polypyrrole (PPy)-PDA was obtained on sponges by an in situ polymerization reaction, followed by the attachment of SiO2 nanoparticles to the surface by polydimethylsiloxane to achieve superhydrophobicity. As a result, previously unreported selective superhydrophobic adsorbents for PPy-PDA coatings were obtained. The prepared sponges have an excellent adsorption capacity for oils and organic solvents. Not only can the sponges absorb 19–39 g of organic solvents per gram but they can also absorb oil from oil-in-water emulsions. The chemical oxygen demand value of the emulsion can be reduced to 219 mg/L after separation. More importantly, the performance remains good in the cycle test, and due to the construction of a durable superhydrophobic sponge, it can still maintain its relatively good performance in artificial seawater, acid–base environments, and can achieve relatively stable emulsion separation. At the same time, the potential of the polymer material composited with PDA in lasting and stable emulsion separation was also verified

    PCR products of DSPP alleles in splicing vector pLRT transfected into 293T and COS-1 cells.

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    <p>From left to right: D2000 marker, 293T cell control, naïve pLRT, mutant DSPP allele and wild type DSPP allele in 293T cells, D2000 marker, COS-1 cell control, naïve pLRT, mutant DSPP allele and wild type DSPP allele in COS-1 cells.</p

    Sequencing raw data of subjects V<sub>6</sub> (an unaffected member) and V<sub>8</sub> (an affected member).

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    <p>The data are from the reverse complementary sequencing with the primer DSPP_New3R. The arrows show the complementary nucleotide of g.8662 site. V<sub>6</sub> has homozygous A while V<sub>8</sub> has heterozygous A/G.</p
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