Polyethylene/Ethylene Vinyl Acetate and Ethylene Octene Copolymer/Clay Nanocomposite Films: Different Processing Conditions and Their Effect on Properties

Polymer nanocomposites based on a layered clay used as nanofiller and copolymers ethylene and vinyl acetate matrix (EVA, the content of vinyl acetate (VA) component 19 wt% and 5 wt%) and ethylene octene copolymer (EOC, 17% and 45% of octene) were prepared. KO Buss kneader and double screw extruder were used. The MMT Na+ and four types of commercial products such as Nanofil N5 and N3000, Cloisite 93A and 30B were used as nanofillers—5 wt% in relation to the content of montmorillonite. The aim was to evaluate the influence of copolymer composition and processing on prepared nanocomposite properties. The morphology of samples was examined by means of X‐ray diffraction (XRD) and transmission electronic microscopy TEM. Furthermore, mechanical and especially barrier properties were observed. Despite the fact that the XRD and microscopy results have revealed that complete exfoliation did not take place in any case, mechanical properties as well as the permeability showed that used 5 wt% of clay was enough to achieve the improvement of properties. Cloisite 30B might be the most suitable for the polyethylene/EVA matrix. In case of EOC copolymer the nanofiller Nanofil N3000 and mainly Cloisite 93A seems to be more suitable. The better properties were achieved for the version of EVA with lower VA content and also for EOC 17, but not for each evaluated property. POLYM. ENG. SCI., 59:2514–2521, 2019. © 2019 Society of Plastics Engineers     

Intrathalline Metabolite Profiles in the Lichen <Emphasis Type="Italic">Argopsis friesiana</Emphasis> Shape Gastropod Grazing Patterns

Lichen-gastropod interactions generally focus on the potential deterrent or toxic role of secondary metabolites. To better understand lichen-gastropod interactions, a controlled feeding experiment was designed to identify the parts of the lichen Argopsis friesiana consumed by the Subantarctic land snail Notodiscus hookeri. Besides profiling secondary metabolites in various lichen parts (apothecia, cephalodia, phyllocladia and fungal axis of the pseudopodetium), we investigated potentially beneficial resources that snails can utilize from the lichen (carbohydrates, amino acids, fatty acids, polysaccharides and total nitrogen). Notodiscus hookeri preferred cephalodia and algal layers, which had high contents of carbohydrates, nitrogen, or both. Apothecia were avoided, perhaps due to their low contents of sugars and polyols. Although pseudopodetia were characterized by high content of arabitol, they were also rich in medullary secondary compounds, which may explain why they were not consumed. Thus, the balance between nutrients (particularly nitrogen and polyols) and secondary metabolites appears to play a key role in the feeding preferences of this snail.     

Rational Design and Synthesis of Selective PRMT4 Inhibitors: A New Chemotype for Development of Cancer Therapeutics**

Protein arginine N-methyl transferase 4 (PRMT4) asymmetrically dimethylates the arginine residues of histone H3 and nonhistone proteins. The overexpression of PRMT4 in several cancers has stimulated interest in the discovery of inhibitors as biological tools and, potentially, therapeutics. Although several PRMT4 inhibitors have been reported, most display poor selectivity against other members of the PRMT family of methyl transferases. Herein, we report the structure-based design of a new class of alanine-containing 3-arylindoles as potent and selective PRMT4 inhibitors, and describe key structure–activity relationships for this class of compounds.     

Al2O3·2SiO2 powders synthesized via sol–gel as pure raw material in geopolymer preparation

Geopolymers are inorganic aluminosilicates mainly proposed as environmentally friendly building materials, which are obtained by alkali activation of natural minerals, calcined clay (e.g., metakaolin) and other aluminosilicate sources. The wide range of chemical and mineralogical compositions of these raw materials influences several properties of the obtained geopolymers. In the present work, pure Al₂O₃·2SiO₂ powders were synthesized via the sol–gel technique and proposed as pure aluminosilicate sources to prepare alkali activated geopolymers. Samples differing in the ratio between the SiO₂ precursor and the H₂O used in the sol–gel process were prepared, in order to study the effect of water content on the material structure and reactivity. The chemical structure of all the obtained Al₂O₃·2SiO₂ powders were characterized by Fourier transform infrared (FT‐IR) and solid‐state nuclear magnetic resonance (²⁷Al and ²⁹Si MAS NMR) spectroscopies and compared to that of a reference metakaolin. Moreover, material reactivity was evaluated by alkali activation of the samples. After 28 days of ageing, ²⁷Al and ²⁹Si MAS NMR and FT‐IR spectra ascertained the formation of a geopolymeric network in the activated samples. The results showed that lower water content allows obtaining a homogeneous Al‐rich geopolymer similar to that obtained, using metakaolin as raw material.     

Thermal properties of poly(ethylene terephthalate) recovered from municipal solid waste by steam autoclaving

The steam autoclaving of municipal solid waste followed by size separation was shown to be a way to recover virtually 100% of recyclable poly(ethylene terephthalate) (PET); this is a yield not attainable by a typical material recovery facility. The polymer properties of the recovered PET, which had undergone various degrees of thermal processing, were evaluated by thermogravimetric analysis, differential scanning calorimetry, gel permeation chromatography, viscometry, and solid‐state NMR to assess the commercial viability of polymer reuse. The weight‐average molecular weight (M_w) decreased as a result of autoclaving from 61,700 g/mol for postconsumer poly(ethylene terephthalate) (pcPET) to 59,700 g/mol for autoclaved postconsumer poly(ethylene terephthalate) [(apcPET)]. M_w for the reclaimed poly(ethylene terephthalate) (rPET) was slightly lower, at 57,400 g/mol. The melting temperature increased with two heat cycles from 236°C for the heat‐crystallized virgin poly(ethylene terephthalate) (vPET) pellets to 248°C for apcPET and up to 253°C for rPET. Correspondingly, the cold crystallization temperature decreased with increased processing from 134°C for vPET to 120°C for apcPET. The intrinsic viscosity varied from 0.773 dL/g for the vPET to 0.709 dL/g for rPET. Extruded samples were created to assess the potential commercial applications of the recovered rPET samples. The M_w values of the extruded apcPET and rPET samples dropped to 37,000 and 34,000 g/mol, respectively, after extrusion (three heat cycles); this indicated that exposure to heat dictated that these materials would be better suited for downcycled products, such as fibers and injected‐molded products. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2012     

Neuroprotective Effects of Erucin against 6-Hydroxydopamine-Induced Oxidative Damage in a Dopaminergic-like Neuroblastoma Cell Line

Oxidative stress (OS) contributes to the cascade leading to the dysfunction or death of dopaminergic neurons during Parkinson’s disease (PD). A strategy to prevent the OS of dopaminergic neurons may be the use of phytochemicals as inducers of endogenous antioxidants and phase 2 enzymes. In this study, we demonstrated that treatment of the dopaminergic-like neuroblastoma SH-SY5Y cell line with isothiocyanate erucin (ER), a compound of cruciferous vegetables, resulted in significant increases of both total glutathione (GSH) levels and total antioxidant capacity at the cytosolic level. The increase of GSH levels was associated with an increase in the resistance of SH-SY5Y cells to neuronal death, in terms of apoptosis, induced by 6-hydroxydopamine (6-OHDA). The pretreatment of SH-SY5Y cells with ER was also shown to prevent the redox status impairment, in terms of intracellular ROS and O₂^•− formation, and loss of mitochondrial membrane potential, early events that are initiators of the apoptotic process, induced by 6-OHDA. Last, the antiapoptotic and antioxidant effects of ER were abolished by buthionine sulfoximine, supporting the main role of GSH in the neuroprotective effects recorded by ER. These results suggest that ER may prevent the oxidative damage induced by 6-OHDA.     

Scanning electron microscopy study of raw and chemically modified sisal fibers

Mercerization and acetylation treatments were applied to sisal fibers to enhance adhesion with polymer matrices in composites. The structures of the untreated and treated fibers were assessed with scanning electron microscopy. The waste from sisal‐fiber decortication consisted of mechanical, ribbon, and xylem fibers, and their ultimate cells varied considerably in size and shape. After mercerization and acetylation, the fibers and conductive‐vessel surfaces were successfully changed. The parenchyma cells were partially removed, and the fibrils started to split, because of the alkali action. This increased the effective surface area available for contact with the matrix. The mercerized and acetylated fibers were coated with cellulose acetate by the grafting of the acetyl group in the fibrils. The treatment used to remove lignin and hemicellulose caused changes in the fiber surface but did not damage the fiber structure because the fibrils remained joined in a bundle. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 2333–2340, 2004     

Prevention of Swelling Phenomenon of Alginate Beads To Improve the Stability and Recyclability of Encapsulated Horse Liver Alcohol Dehydrogenase

Horse Liver Alcohol Dehydrogenase (HLADH) has been immobilized on calcium-alginate beads and used for both oxidation and reduction reactions. To avoid swelling of the beads and their subsequent breakage, calcium ions were added to both reaction and storage solutions, allowing the beads to maintain the initial structural features. The techniques used for this purpose revealed that 2 mM Ca²⁺ is the optimal concentration, which does not significantly change the weight of the beads, the amount of water in them, and their external and internal structure. The optimized experimental procedure has been used to verify the properties of the enzyme in terms of reusability, storage, and thermal stability. The addition of calcium ions allows the enzyme to retain more than 80 % of its initial activity for fourteen cycles and approximately 50 % at the twentieth cycle. Moreover, when the biocatalyst has been stored in a buffer solution containing 2 mM Ca²⁺, the retention of enzyme activity after 30 days was 100 %, compared to that measured before incubation. The encapsulated enzyme exhibits greater thermal stability than free HLADH up to at least 60 °C, preventing dimer dissociation into the two subunits.