ABSTRACT:In an attempt to provide polyolefins such as low-and high-density polyethylene and polypropylene with autohesive properties, hydrophilic monomers such as methacrylic acid (MAA), acrylic acid (AA), and 2-(dimethylamino)ethyl methacrylate (DMAEMA) were photografted onto their surfaces. The wettabilities of the grafted plates stayed constant above full coverage of the substrate surfaces with grafted polymer chains, except for the AA-grafted plates. The amount of absorbed water for the grafted layers formed increased with an increase in the number of grafted polymer chains. The autohesive strength increased with an increase in the wettability and water absorptivity of the grafted plates as well as the temperature and load on heat pressing. For all grafted plates substrate breaking at autohesive strength measurements was observed for grafted amounts 2-3 times as much as those at adhesive strength measurements. The substrate breakings for the HDPE and PP plates photografted with AA and DMAEMA at adhesive strength measurements were observed at lower grafted amounts compared with those photografted with MAA. This study has made it clear that the photografting of hydrophilic monomers onto polyolefin materials can markedly enhance autohesivity without any adhesives as well as the adhesivity for high grafted amounts. Therefore, polyolefin materials with improved autohesivity and adhesivity can be widely applied in adhesive fields, including for novel uses.
A new olivine reference material – MongOL Sh11‐2 – for in situ analysis has been prepared from the central portion of a large (20 × 20 × 10 cm) mantle peridotite xenolith from a ~ 0.5 My old basaltic breccia at Shavaryn‐Tsaram, Tariat region, central Mongolia. The xenolith is a fertile mantle lherzolite with minimal signs of alteration. Approximately 10 g of 0.5–2 mm gem quality olivine fragments were separated under binocular microscope and analysed by EPMA, LA‐ICP‐MS, SIMS and bulk analytical methods (ID‐ICP‐MS for Mg and Fe, XRF, ICP‐MS) for major, minor and trace elements at six institutions world‐wide. The results show that the olivine fragments are sufficiently homogeneous with respect to major (Mg, Fe, Si), minor and trace elements. Significant inhomogeneity was revealed only for phosphorus (homogeneity index of 12.4), whereas Li, Na, Al, Sc, Ti and Cr show minor inhomogeneity (homogeneity index of 1–2). The presence of some mineral and fluid‐melt micro‐inclusions may be responsible for the inconsistency in mass fractions obtained by in situ and bulk analytical methods for Al, Cu, Sr, Zr, Ga, Dy and Ho. Here we report reference and information values for twenty‐seven major, minor and trace elements.
The deep-sea clay that covers wide areas of the pelagic ocean bottom provides key information about open-ocean environments but lacks age-diagnostic calcareous or siliceous microfossils. The marine osmium isotope record has varied in response to environmental changes and can therefore be a useful stratigraphic marker. In this study, we used osmium isotope ratios to determine the depositional ages of pelagic clays extraordinarily rich in fish debris. Much fish debris was deposited in the western North and central South Pacific sites roughly 34.4 million years ago, concurrent with a late Eocene event, a temporal expansion of Antarctic ice preceding the Eocene–Oligocene climate transition. The enhanced northward flow of bottom water formed around Antarctica probably caused upwelling of deep-ocean nutrients at topographic highs and stimulated biological productivity that resulted in the proliferation of fish in pelagic realms. The abundant fish debris is now a highly concentrated source of industrially critical rare-earth elements.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.