Organic fertilizer from recycled biowaste was identified as a vehicle for entry of microplastic particles into the environment.

Simple salts are known to influence the cloud point temperature of the aqueous solution of thermoresponsive compounds, such as poly-(N-isopropylacrylamide), PNIPAM. The effect of one series of anions (six potassium salts) and two series of cations (five alkali-metal hydroxides and chlorides, respectively) on the cloud point temperature of PNIPAM oligomers is investigated. All salts with the exception of low (<0.5 M) concentrations of KI are found to lower the cloud point temperature; the relationship between the temperature and the concentration of the added salt tends to be linear. The intensity of the effect of a given salt corresponds to its position in the Hoffmeister series. However, while the anions differ significantly in force, the cations-with the exception of Li + -show little difference in this regard. The observed effects are interpreted based on the structure making/structure breaking potential of the involved ions as evidenced by their viscosity B coefficients. While a relationship could be established for the anions this is less obvious for the cations. Moreover, while the structure breaking ability of the I --anion to some extent explains its salting in ability at low concentrations, it does not account for the linear salting out effect observed at higher concentrations. The second attempt to interpret the results is based on the solvophobic theory, i.e., takes the contribution of both electrostatic and hydrophobic interactions into account. Thermodynamic data on the phase separation obtained through differential scanning calorimetry are used to calculate the unitary free Gibbs energy as a function of the molal salt concentration.

Nonviral gene delivery with the help of polycations has raised considerable interest in the scientific community over the past decades. Herein, we present a systematic study on the influence of the molecular weight and architecture of poly(2-(dimethylamino)ethyl methacrylate) (PDMAEMA) on the transfection efficiency and the cytotoxicity in CHO-K1 cells. A library of well-defined homopolymers with a linear and star-shaped topology (3- and 5-arm stars) was synthesized via atom transfer radical polymerization (ATRP). The molecular weights of the polycations ranged from 16 to 158 kDa. We found that the cytotoxicity at a given molecular weight decreased with increasing number of arms. For a successful transfection a minimum molecular weight was necessary, since the polymers with a number-average molecular weight, M(n), below 20 kDa showed negligible transfection efficiency at any of the tested polyelectrolyte complex compositions. From the combined analysis of cytotoxicity and transfection data, we propose that polymers with a branched architecture and an intermediate molecular weight are the most promising candidates for efficient gene delivery, since they combine low cytotoxicity with acceptable transfection results.

2850 wileyonlinelibrary.com large amounts of liquids and are excellent fi lters. Sponges with a volume of 1000 cm 3 can process up to 3000 L water h −1 . Furthermore, they can conduct light as discovered recently by Brümmer et al. [ 2 ] In addition, Natalio et al. reported on the formation of sponge skeletons shown to feature great bending strength and on the role of silicatein-α in the biomineralization of silicates in sponges, which accounts for the high reversible compressibility of sponges in spite of low densities. [ 3 ] Aizenberg et al. pointed out on the example of the so-called glass sponges ( Euplectella ) the important role of the hierarchical design from the nanometer to macroscopic length scale for structural materials. [ 4 ] The structural base of sponges are multiarmed spicules of silicate or calcium carbonate, which form highly porous structures of several hierarchical layers as shown in Figure 1 A,B. This leads to highly porous ultralight 3D materials (ultralight is defi ned when the density of material is <10 mg cm −3 ).[ 5 ] In recent literature, a variety of highly porous ultralight 3D materials were reported based on carbon, ceramics, and cellulose, which were characterized by porosities >99% and relatively high compressive strength. [6][7][8][9][10] Carbon and cellulose based sponges show ultralow densities and excellent mechanical properties but soft sponges with similar mechanical integrity are missing.Since spicules of natural sponges conspicuously resemble polymer fi bers, formation of such fi brous structures by electrospinning [ 11 ] could be a promising concept for the preparation of polymer-based biomimetic analogous of natural sponges and would open the huge potential of electrospun materials for 3D sponge-type structures. Indeed, 3D porous structures were prepared by electrospinning which was nicely summarized in comprehensive review in recent literature. [ 7 ] However, previous efforts of making 3D highly porous electrospun materials, for example, via ultrasonic treatment, resulted in higher densities and correspondingly lower porosities of <99%, [ 12 ] as well as relatively poor mechanical performance. Remarkably, Eichhorn et al. claimed that theoretically ultrahigh porosities of electrospun nonwovens >99% could not be achieved. [ 13 ] In contrast to these reports, we present here the formation of ultralight weight highly porous 3D electrospun polymer fi ber-based spongy structures with densities as low as 2.7 mg cm −3 corresponding to a porosity of 99.6%. They were prepared by electrospinning of a photo cross-linkable polymer followed by UV cross-linking, mechanical cutting, suspending cut fi bers in liquid dispersion, and freezedrying. These polymer sponges showed in analogy to natural Ultralight, Soft Polymer Sponges by Self-Assembly of Short Electrospun Fibers in Colloidal DispersionsGaigai Duan , Shaohua Jiang , Valérie Jérôme , Joachim H. Wendorff , Amir Fathi , Jaqueline Uhm , Volker Altstädt , Markus Herling , Josef Breu , Ruth Freitag , Seema Agarwal , and Andreas Gre...

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