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Aromatic polyester, PEN-2,6, is improved through cross-linking effected by radiation. Polymer retains properties of high tensile strength and toughness and stability at high temperatures.
Fatigue life tests of polyester film tape recorder belts
Linear aliphatic polyesters preparation by acid chloride synthesis, acid exchange and ester exchange, stressing products purification
Gel permeation chromatography of nominally linear aliphatic polyesters, using tetrahydrofuran solvent at 37 degrees C
Linear aliphatic polyesters unit cell dimensions and crystalline densities
Linear aliphatic polyesters, calculating conformational contribution to heats and entropies of fusion
Linear aliphatic polyesters melting point, fusion heat and entropy correlations to molecular parameters
Polyester formation by Escherichia coli ribosome catalyzed alpha-hydroxy acid incorporation into polymer chain
The relative toxicity in rats resulting from a 30 minute exposure to the combustion products of two materials, Tedlar and fluorenone-polyester film was assessed. The combustion products were generated into a static exposure system using a laboratory-scale furnace. The toxicity was assessed using the primary measurements employed in a more detailed overall toxicity evaluation. The toxicological events observed during the 30 minute exposure are reported.
An unsaturated polyester, such as propylene glycolmaleic acid phthalic acid prepolymer dissolved in styrene is interpolymerized with an ultraviolet absorber and/or an antioxidant. The unsaturated chain may be filled with H or lower alkyl such as methyl and tertiary alkyl such as tertiary butyl. A polymer stable to exposure to the outdoors without degradation by ultraviolet radiation, thermal and/or photooxidation is formed.
A tapered tubular polyester sleeve is described to serve as the flexible foundation for a spacesuit limb covering. The tube has a large end and a small end with a length to be determined. The ratio of taper is also determined by scale factors. All the warp yarns extend to the large end. A requisite number of warp yarns extend the full length of the sleeve. Other warp yarns extend from the large end but are terminated along the length of the sleeve. It is then woven with a filling yarn which extends in a full circle along the full length of the sleeve to thereby define the tapered sleeve. The sleeve after fabrication is then placed on a mandrel, heated in an oven, and then attached to the arm or other limb of the spacesuit.
A useful method for kinetic study of the hydrolysis of polyester elastomer is established which uses the number-average molecular weight. The reasonableness of this method is confirmed and the effect of magnetic particles on hydrolysis is considered.
A tapered tubular polyester sleeve as set forth. It has a large end 12 and a small end 14 with a length to be determined. The ratio of taper is also determined by scale factors. All the warp yarns extend to the large end 12. A requisite number of warp yarns 16 extend the full length of the sleeve. Other warp yarns exemplified at 18, 22, 26, 28, 30 and 32 extend from the large end but are terminated along the length of the sleeve. It is then woven with a filling yarn 40 which extends in a full circle along the full length of the sleeve to thereby define the tapered sleeve. The sleeve after fabrication is then placed on a mandrel 42, heated in an oven 44 and is thereafter placed on the arm or other limb of a space suit exemplified at 50.
Chemically recyclable, circular polymers continue to attract increasing attention, but rendering both catalysts for depolymerization and high-performance polymers recyclable is a more sustainable yet challenging goal. Here we introduce a dual catalyst/polymer recycling system in that recyclable inorganic phosphomolybdic acid catalyzes selective depolymerization of high-ceiling-temperature biodegradable poly(δ-valerolactone) in bulk phase, which, upon reaching suitable molecular weight, exhibits outstanding mechanical performance with a high tensile strength of ≈66.6 MPa, fracture strain of ≈904 %, and toughness of ≈308 MJ m –3 , and thus markedly outperforms commodity polyolefins, recovering its monomer in pure state and quantitative yield at only 100 °C. In sharp contrast, the uncatalyzed depolymerization not only requires a high temperature of >310 °C but is also low yielding and non-selective. Importantly, the recovered monomer can be repolymerized as is to reproduce the same polymer, thereby closing the circular loop, and the recycled catalyst can be reused repeatedly for depolymerization runs without loss of its catalytic activity and efficiency.
A polyurethane (PU)-degrading fungus designated as strain S45 was isolated from a solid waste-dumping site in Islamabad, Pakistan. Strain S45 was identified as Aspergillus sp. through microscopic, morphologic as well as 18S rRNA sequencing (99% similarity with Aspergillus fumigatus). The degradation ability of strain S45, was analyzed through measurement of weight loss and evolution of CO{sub 2} as a result of breakdown of PU film. The degradation was confirmed through scanning electron microscopy, fourier transform infrared (FTIR) spectroscopy and differential scanning calorimetry (DSC). Surface changes like pits, cracks and holes were observed in scanning electron micrographs upon degradation of PU film by strain S45. FTIR spectra were carefully examined, changes were observed in various peaks at different wavelength ranges that also correspond to degradation of PU film. Differential scanning calorimetric technique was used to measure the melting temperature of PU film pieces before and after incubation with strain S45. DSC curve indicated an increase in melting temperature of PU from 191 to 196 °C that might be due to increase in crystallinity of the exposed PU after degradation of amorphous soft segment. A gradual increase in specific activity of esterase was observed up to the maximum of 15th day of incubation with PU film in mineral salt medium. Enzyme activity was further confirmed by tween 20 agar plates, demonstrated by formation of calcium complex. It is concluded from the results that Aspergillus sp. strain S45 might be applied for the treatment of plastics-contaminated environments.
The original version of this article unfortunately contained mistakes in the placement of Figs. 5, 7–10 and their captions.
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Future advances and usage of all-organic polymeric materials with permanent void spaces and high surface areas, in applications such as separations or as supports, depends heavily on the development of processing techniques to produce complex geometry objects. Here, the high free volume glassy microporous polymer PIM-1 was fabricated, as a major component in a polymer blend, into complex and customizable 3D objects by fused filament fabrication (FFF). PIM-1 was found to be compatible with polycaprolactone (PCL) and polylactic acid (PLA) and thus could be processed by extrusion into filaments with high loadings of PIM-1 (50% by mass). Ternary PCL/PLA/PIM-1 composite filaments provided an optimal balance of durability and melt flow characteristics for consistent FFF 3D printing of intricate structures. As printed, the micropores of PIM-1 were blocked and inaccessible to N2 during sorption experiments; however, the ternary composite structures displayed significant meso- and macroporosity and nanostructured phase separation. Postprinting immersion in 3-chloro-1-propanol was identified to selectively remove PCL within the composites, re-expose the characteristic micropores of PIM-1, and retain the macrostructure of the printed object. After postprinting treatments, specific surface areas by the Brunauer–Emmett–Teller method (as high as 460 m2 g–1) were found to directly correlate with the PCL content originally present. In conclusion, the extrusion-based processing methodology provides a new approach for production of intrinsically porous polymer objects in custom and complex shapes by reinforcement with thermoplastics (PCL and PLA).