In Situ Incorporation of Pores and Nanoparticles into Polymer Surfaces Using Melt Crystallization

2019 ◽  
pp. 1900131 ◽  
Author(s):  
Sangwon Chi ◽  
Jonghwi Lee
1993 ◽  
Vol 304 ◽  
Author(s):  
R. L. Opila ◽  
K. Konstadinidis ◽  
A. O. Ibidunni ◽  
A. J. Davenport ◽  
H. S. Isaacs

AbstractThe interface formed between metals, Ti and Cr, and polymers, epoxy and triazine, have been studied, nondestructively, using x-ray absorption spectroscopy. The metals were sputtered onto the polymer surfaces. Titanium reacts extensively, up to Ti thicknesses of 100 Å while Cr remains primarily metallic. In situ heating at 200°C increases the extent of reaction for both metals. Heating has a greater effect on metal/epoxy interfaces than metal/triazine. Titanium and Cr were ion implanted into the polymer in order to determine the interactions of isolated metal atoms with the polymer. Titanium and Cr appear to form oxides as the final reaction product, and the Ti is tetrahedrally coordinated.


Minerals ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 829
Author(s):  
Jingyao Xu ◽  
Joan Melgarejo ◽  
Qiuli Li ◽  
Lisard Abat ◽  
Montgarri Castillo-Oliver

We present the results of a detailed petrographic study of fresh coherent samples of the Menominee kimberlite sampled at site 73, located in Menominee County, MI, USA. Our objective is to account for its unusual and complex paragenetic sequence. Several generations of olivine, ilmenite, and spinel-group minerals are described. Early olivine and ilmenite are xenocrystic and were replaced or overgrown by primary minerals. Zoned microcrysts of olivine have a xenocrystic core mantled by a first rim in which rutile, geikielite, and spinel s.s. (spinel sensu stricto) cocrystallized. The in situ U–Pb dating of a microcryst of primary rutile yielded 168.9 ± 4.4 Ma, which was interpreted as the age of emplacement. The groundmass consists of olivine, spinel s.s., a magnesian ulvöspinel–ulvöspinel–magnetite (MUM) spinel, calcite, and dolomite. An extremely low activity of Si is suggested by the crystallization of spinel s.s. instead of phlogopite in the groundmass. The presence of djerfisherite microcrysts indicates high activities of Cl and S during the late stages of melt crystallization. The occurrence of two distinct spinel-group minerals (spinel s.s. and qandilite-rich MUM) in the groundmass is interpreted as clear evidence of the mingling of a magnesiocarbonatitic melt with a dominant kimberlitic melt.


2018 ◽  
Vol 6 (15) ◽  
pp. 2240-2249 ◽  
Author(s):  
A. Buslovich ◽  
B. Horev ◽  
Y. Shebis ◽  
V. Rodov ◽  
A. Gedanken ◽  
...  

In the current work, stable nanoparticles (NPs) of vanillin are formed in situ from an aqueous/ethanol solution and deposited on the surface of chitosan, a natural polymer, using a high-intensity ultrasonic method.


2021 ◽  
Vol 12 ◽  
Author(s):  
Annika Vaksmaa ◽  
Katrin Knittel ◽  
Alejandro Abdala Asbun ◽  
Maaike Goudriaan ◽  
Andreas Ellrott ◽  
...  

Plastic particles in the ocean are typically covered with microbial biofilms, but it remains unclear whether distinct microbial communities colonize different polymer types. In this study, we analyzed microbial communities forming biofilms on floating microplastics in a bay of the island of Elba in the Mediterranean Sea. Raman spectroscopy revealed that the plastic particles mainly comprised polyethylene (PE), polypropylene (PP), and polystyrene (PS) of which polyethylene and polypropylene particles were typically brittle and featured cracks. Fluorescence in situ hybridization and imaging by high-resolution microscopy revealed dense microbial biofilms on the polymer surfaces. Amplicon sequencing of the 16S rRNA gene showed that the bacterial communities on all plastic types consisted mainly of the orders Flavobacteriales, Rhodobacterales, Cytophagales, Rickettsiales, Alteromonadales, Chitinophagales, and Oceanospirillales. We found significant differences in the biofilm community composition on PE compared with PP and PS (on OTU and order level), which shows that different microbial communities colonize specific polymer types. Furthermore, the sequencing data also revealed a higher relative abundance of archaeal sequences on PS in comparison with PE or PP. We furthermore found a high occurrence, up to 17% of all sequences, of different hydrocarbon-degrading bacteria on all investigated plastic types. However, their functioning in the plastic-associated biofilm and potential role in plastic degradation needs further assessment.


2015 ◽  
Vol 2015 ◽  
pp. 1-16 ◽  
Author(s):  
Valentina Sabatini ◽  
Hermes Farina ◽  
Luca Basilissi ◽  
Giuseppe Di Silvestro ◽  
Marco A. Ortenzi

Polylactic acid (PLA) nanocomposites were prepared via “in situ” ring opening polymerization (ROP) of lactide using a montmorillonite, Cloisite 15A, employed after surface treatment with 3-Glycidoxypropyltrimethoxysilane. The dispersion of the nanoparticles was checked using Wide Angle X-Ray Scattering (WAXS) and Transmission Electron Microscopy (TEM); both the effects of different amounts of montmorillonite and silane were measured on molecular weights and on thermal and rheological properties, using Size Exclusion Chromatography (SEC), Differential Scanning Calorimetry (DSC), thermogravimetric analyses (TGA), and rheological analyses. It was found that even very low amounts (0.1% w/w) of nanoparticles greatly affect nanocomposites properties. Unmodified montmorillonite tends to decrease molecular weights, deactivating the catalytic system used for ROP of lactide, but when epoxy silane is present molecular weights increase. Melt crystallization temperatures increase with modified nanoparticles, which enhance crystallization process. TGA analyses show that when pure montmorillonite is present, nanocomposites have lower thermal stability with respect to standard PLA; when silane is used thermal stability can get much higher than standard PLA as silane content increases. The rheological behaviour of nanocomposites shows that melt viscosity is far higher than that of standard PLA at low shear rates and also a marked shear thinning behaviour can be achieved.


2013 ◽  
Vol 10 (83) ◽  
pp. 20130171 ◽  
Author(s):  
Dadhichi Paretkar ◽  
Marleen Kamperman ◽  
David Martina ◽  
Jiahua Zhao ◽  
Costantino Creton ◽  
...  

We tested the adhesive response of polymer surfaces structured with arrays of cylindrical fibrils having diameters of 10–20 µm and aspect ratios 1–2.4. Fibrils had two different tip shapes of end-flaps and round edges. A preload-induced mechanical buckling instability of the fibrils was used to switch between the states of adhesion and non-adhesion. Non-adhesion in fibrils with round edges was reached at preloads that caused fibril buckling, whereas fibrils with end-flaps showed adhesion loss only at very high preloads. The round edge acted as a circumferential flaw prohibiting smooth tip contact recovery leading to an adhesion loss. In situ observations showed that, after reversal of buckling, the end-flaps unfold and re-form contact under prevailing compressive stress, retaining adhesion in spite of buckling. At very high preloads, however, end-flaps are unable to re-form contact resulting in adhesion loss. Additionally, the end-flaps showed varying contact adaptability as a function of the fibril–probe alignment, which further affects the preload for adhesion loss. The combined influence of preload, tip shape and alignment on adhesion can be used to switch adhesion in bioinspired fibrillar arrays.


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