Presence Of Polyamide Research Articles

Microplastics provide new hotspots for frequent transmission of antibiotic resistance genes during anaerobic digestion of sludge containing antibiotics

Antibiotics and microplastics are emerging contaminants of widespread concern. Individual exposure to either antibiotics or microplastics may facilitate the dissemination of antibiotic resistance genes (ARGs). However, little is known about how the co-exposure of antibiotics and microplastics drives the dissemination of ARGs during sludge anaerobic digestion. This study established a series of long-term operational anaerobic digesters and found that 20 mg/L ofloxacin facilitated the dissemination of ARGs, whereas 200 mg/L ofloxacin led to a decrease in the absolute abundance of ARGs. However, the coexistence of polyamide and ofloxacin further increased the abundance of five ARGs by 4.4–359.1 % compare to singular ofloxacin exposure. The presence of polyamide not only complicated the microbial community structure but also increased the abundance of ARGs hosts by 12.2–108.7 %. Metagenome-assembled genomes indicated that 42 out of 53 ARGs hosts were functional microorganisms, and their enrichment under polyamide exposure facilitated the conversion of substrates into methane. Further mechanism exploration found that ofloxacin and polyamide promoted the formation of biofilm and enhanced the adhesion and communication among microorganisms. The upregulation of functional genes related to antioxidant, DNA repair, and type IV secretion systems provided evidence for the stimulated horizontal transfer of ARGs under the co-exposure of ofloxacin and polyamide. Partial least squares path modeling analysis identified that mobile genetic elements predominantly determined the variation of ARGs in this study. These findings emphasized that the coexistence of microplastics and antibiotics in sludge may further exacerbate the risk of antibiotic resistance transmission.

Microplastic-Assisted Removal of Phosphorus and Ammonium Using Date Palm Waste Derived Biochar.

Microplastics (MPs) are emerging environmental pollutants worldwide, posing potential health risks. Moreover, MPs may act as vectors for other contaminants and affect their fate, transport, and deposition in the environment. Therefore, efficient and economical techniques are needed for the removal of contemporary MPs and contaminants from the environment. The present research study investigated the sorption of phosphorus (P) and ammonium (NH4+) onto date palm waste-derived biochar (BC) from an aqueous solution in the presence of polyamide (PA) and polyethylene (PE) MPs. The BC was prepared at 600 °C, characterized for physio-chemical properties, and applied for P and NH4+ removal via isotherm and kinetic sorption trials. The results of the sorption trials demonstrated the highest removal of NH4+ and P was obtained at neutral pH 7. The highest P sorption (93.23 mg g-1) by BC was recorded in the presence of PA, while the highest NH4+ sorption (103.76 mg g-1) was found with co-occurring PE in an aqueous solution. Sorption isotherm and kinetics models revealed that P and NH4+ removal by MP-amended BC followed chemisorption, electrostatic interaction, precipitation, diffusion, and ion exchange mechanisms. Overall, co-existing PA enhanced the removal of P and NH4+ by 66% and 7.7%, respectively, while co-existing PE increased the removal of P and NH4+ by 55% and 30%, respectively, through the tested BC. Our findings suggested that converting date palm waste into BC could be used as a competent and economical approach to removing P and NH4+ from contaminated water. Furthermore, microplastics such as PE and PA could assist in the removal of P and NH4+ from contaminated water using BC.

Carbon fibre waste recycling into hybrid nonwovens for electromagnetic interference shielding and sound absorption

The increasing global use of carbon fibre (CF) in different industries has resulted in production of significant amounts of waste in the forms of CF-reinforced composites and dry CF scrap. The latter group which is mainly in the form of short fibres is generated during manufacturing of CF-reinforced composites and comprises a significant portion of total CF waste. However, little attention has been paid to recycling these waste fibres. This research provides a comprehensive understanding on the processability of CF waste into nonwovens using conventional textile machineries of carding and needle-punching, for applications in areas of electromagnetic interference (EMI) shielding and sound absorption. The carding of CF was carried out in the presence of polyamide 6 (PA6) fibres to minimise damages to CF during the recycling process. Hybrid CF/PA6 nonwovens were produced and the effects of operating parameters such as the number of carding passages, the ratio of CF/PA6 fibres (20/80, 50/50, and 80/20), and the number of cross-lapped web layers during the needle-punching process on the obtained features were explored. The results demonstrated that excellent EMI shielding effectiveness was achieved with the highest performance being 85 dB from the CF/PA6 80/20 samples. Increasing the content of CF, the number of carding passages and the thickness of nonwovens all positively contributed to enhancing the EMI shielding performance. The sound absorption performance of nonwovens was found to depend on the CF/PA6 ratio and the thickness of the tested samples. However, the second carding process negatively impacted on the sound absorption performance by reducing the fibres mass in final products. In addition, the relations between the composition of samples and employed methodologies with production yield, areal density, electrical conductivity and actual CF content of the developed nonwovens were all discussed.

Compatibility in biobased poly(L‐lactide)/polyamide binary blends: From melt‐state interfacial tensions to (thermo)mechanical properties

ABSTRACTThe melt compatibility between poly(L‐lactide) (PLA) and polyamides (PAs) with related thermomechanical properties is addressed. A particular attention is paid to four commercial PAs with extrusion processing temperatures close to PLA (PA10‐10 to PA12). PLA/PA blend morphologies without a compatibilizer are first revealed by scanning electron microscopy. PA12 displays the best droplet dispersion into PLA (Dn 700 nm), whereas a poor interfacial adhesion is attested for PLA/PA10‐10 blends. Interfacial tensions corroborate the PLA/PA10‐10 incompatibility (γ12 9 mN/m, 240 °C) with decreasing γ12 in the order PLA/PA10‐10 > PLA/PA11 > PLA/PA12 (γ12 2 mN/m). Surface tensions confirm the highest compatibility between PLA and PA12. Ductilities, toughnesses, and thermal resistances of PLA/PA blends are evaluated up to 40‐wt % PA. Brittle‐to‐ductile transitions are observed for PA content higher than 30‐wt % with the highest ductility for PLA/PA12, in accordance with their enhanced compatibility. Impact strengths display similar trends with a twofold increase for PLA/PA12. An outstanding synergy between PLA and PA is highlighted by dynamic mechanical analyses with heat deflection up to 130 °C for PLA/PA blends. The synergy arises from a peculiar crystallization of PLA in the presence of PA. PLA/PA morphologies/interfaces can be consequently tuned by an appropriate PA choice with interesting improvements of thermomechanical properties for high‐performance/durable applications. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020, 137, 48440.

Effect of Polyamide 66 on the Mechanical and Thermal Properties of Post-Industrial Waste Polyamide 6

Post-industrial waste (PIW) polyamide 6 is successfully used in lieu of commercial virgin polyamide 6, in several automotive applications. The presence of polyamide 66 in the final formulation may affect the mechanical and thermal properties of the PIW polyamide 6 materials. Using unreinforced polyamide 6 from PIW and commercial sources, it was found that the addition of polyamide 66 (below 10 wt.%) lowered the crystallization rate and crystallinity level of all polyamide 6 materials. The thermal and mechanical properties of glass fiber (GF) reinforced PIW polyamide 6 compounds with and without polyamide 66 were also studied. Differential scanning calorimetry (DSC) showed that reinforced materials without polyamide 66 had a higher level of crystallinity. Furthermore, dynamic mechanical analysis (DMA) showed that reinforced compounds without polyamide 66 also had a faster storage modulus buildup immediately after injection molding. Reinforced PIW polyamide 6 compounds without polyamide 66 also exhibited higher tensile and higher vibration weld strengths as well as a thicker heat affected zone (HAZ) than those with polyamide 66, leading to the conclusion that polyamide 66 had a detrimental effect on crystallinity level and consequently on the mechanical properties of GF-reinforced PIW polyamide 6 materials.

Study of the release of a microencapsulated acid dye in polyamide dyeing using mixed cationic liposomes

The main objective of this work was to increase the retarding effect of the acid dye Telon® Blue RR (C.I. Acid Blue 62; DyStar, Frankfurt, Germany) release on polyamide fibres dyeing by encapsulation of the dye in liposomes as an alternative to synthetic auxiliaries, in order to reduce effluent pollution. The retarding effect achieved with the use of mixed cationic liposomes of dioctadecyldimethylammonium bromide (DODAB)/soybean lecithin (containing a 10% molar fraction of DODAB) was better in comparison with either pure soybean lecithin liposomes or synthetic auxiliaries. The retarding effect of liposomes on the dye release was analysed through changes in the absorption and fluorescence spectra of the acid dye at different conditions. The effect of temperature (in the range of 25 °C - 70 °C) on the spectroscopic behaviour of the dye in the absence and in presence of polyamide was also studied, in order to simulate the dyeing conditions. Exhaustion curves obtained in dyeing experiments showed that, below 45 °C, the retarding effect of the mixed liposomes (lecithin/DODAB (9:1)) was similar to that of the auxiliaries, but better than the one of pure lecithin liposomes. At higher temperatures (above 45 °C), the system lecithin/DODAB presents a better performance, achieving a higher final exhaustion level when compared with the commercial leveling agent without losing the smoothing effect of lecithin.

Matrix polymerization of aniline in the presence of polyamides containing sulfo acid groups

The matrix synthesis of polyaniline in the presence of water-soluble aromatic polyamides containing sulfo acid groups has been studied. It has been shown that the nature of polyacid and the concentration of reagents affect the shape and dynamics of a change in absorption spectra. The S-shaped profile of kinetic curves for spectra variation and the experiments on the seed polymerization provide evidence for the autocatalytic character of polymerization. It has been concluded that, depending on the nature of polyacid, polymer complexes form in which polyaniline macromolecules are situated along main chains of polyacid macromolecules (the two-stream structure) or appear as side chains of polyacid macromolecules (the comb-shape structure). In the latter case, polyaniline macromolecules serve as ionic bridges crosslinking polyacid macromolecules, as is confirmed by the viscometric study of solutions in the course of polymerization.

Thermal Decomposition of Polymer Mixtures Containing Poly(vinyl chloride)

Thermal decomposition of a series of 1 : 1 mixtures of typical polymer waste materials [polyethylene (PE), poly(propylene) (PP), polystyrene (PS), polyacrylonitrile (PAN), polyisoprene, poly(methyl methacrylate) (PMMA), polyamide-6 (PA-6), polyamide-12 (PA-12), polyamide-6,6 (PA-6,6), and poly(1,4-phenylene terephthalamide) (Kevlar)] with poly(vinyl chloride) (PVC) was examined using thermal analysis and analytical pyrolysis techniques. It was found that the presence of polyamides and PAN promotes the dehydrochlorination of PVC, but PVC has no effect on the main decomposition temperature of polyamides. The hydrogen chloride evolution from PVC is not altered when other vinyl polymers or polyolefins are present. The thermal degradation of PAN is retarded significantly, whereas that of the other vinyl polymers is shifted to a slightly higher temperature in the presence of PVC. Among the pyrolysis products of PAN-PVC mixture methyl chloride was found in comparable amount to the other gaseous products at 500°C pyrolysis temperature.

Minor groove DNA-protein contacts upstream of a tRNA gene detected with a synthetic DNA binding ligand

Transcription factor IIIB (TFIIIB) is composed of the TATA box binding protein (TBP) and class III gene-specific TBP-associated factors (TAFs). TFIIIB is brought to a site centered approximately 35 bp upstream from the transcription start site of tRNA genes via protein-protein interactions with the intragenic promoter-recognition factor TFIIIC. Since TBP interacts with TATA elements through the minor groove of DNA, we asked whether TFIIIB interacts with DNA in the minor groove. Polyamides containing pyrrole (Py) and imidazole (Im) amino acids are synthetic DNA ligands that bind to predetermined sequences in the minor groove of double helical DNA. These small molecules have been shown to interfere with protein-DNA interactions in the minor groove. A series of DNA constructs was generated in which the binding site for a Py-Im polyamide was placed at various distances upstream from a tRNA gene transcription start site. We find that a match polyamide will effectively inhibit tRNA gene transcription when its binding site is located within 33 bp of the transcription start site of the Xenopus TyrD tRNA gene. Moreover, in the presence of polyamide, RNA polymerase III is redirected to a new transcription initiation site located approximately one DNA helical turn downstream from the native start site. Our results suggest that a subunit of TFIIIB, possibly TBP, makes an essential minor groove DNA contact centered approximately 30 bp upstream from the tRNA gene.