Evaluation of PET Degradation Using Artificial Microbial Consortia

Polyethylene terephthalate (PET) biodegradation is regarded as an environmentally friendly degradation method. In this study, an artificial microbial consortium composed of Rhodococcus jostii, Pseudomonas putida and two metabolically engineered Bacillus subtilis was constructed to degrade PET. First, a two-species microbial consortium was constructed with two engineered B. subtilis that could secrete PET hydrolase (PETase) and monohydroxyethyl terephthalate hydrolase (MHETase), respectively; it could degrade 13.6% (weight loss) of the PET film within 7 days. A three-species microbial consortium was further obtained by adding R. jostii to reduce the inhibition caused by terephthalic acid (TPA), a breakdown product of PET. The weight of PET film was reduced by 31.2% within 3 days, achieving about 17.6% improvement compared with the two-species microbial consortium. Finally, P. putida was introduced to reduce the inhibition caused by ethylene glycol (EG), another breakdown product of PET, obtaining a four-species microbial consortium. With the four-species consortium, the weight loss of PET film reached 23.2% under ambient temperature. This study constructed and evaluated the artificial microbial consortia in PET degradation, which demonstrated the great potential of artificial microbial consortia in the utilization of complex substrates, providing new insights for biodegradation of complex polymers.

Polyacrylate Decorating Poly(ethylene terephthalate) (PET) Film Surface for Boosting Oxygen Barrier Property

Polymeric barrier materials are critical in contemporary industries for food, medicine, and chemical packaging. However, these materials, such as PET films, are impeded by the optimization of barrier properties by virtue of molecular design. Herein, a new methyl methacrylate-methyl acrylate-diallyl maleate-maleic acid (MMA-MAc-DAM-MA) was synthesized to tailor the surface properties of PET films for maximizing oxygen barrier properties. During the MMA-MAc-DAM-MA coating and curing process, the chemical structure evolutions of MMA-MAc-DAM-MA coatings were characterized, indicating that the cross-linking conversion and proportion of –COOH groups are critical for the oxygen barrier properties of coatings. The inherent –COOH groups are transformed into designed structures, including intramolecular anhydride, inter-chain anhydride and retained carboxylic acid. Therein, the inter-chain anhydride restraining the activity of coated polymer chain mainly contributes to enhanced barrier properties. The thermal properties of novel coatings were analyzed, revealing that the curing behavior is strongly dependent on the curing temperatures. The impacts of viscosity of the coating solution, coating velocity, and coating thickness on the oxygen permeability (Po2) of the coatings were investigated using a gas permeability tester to explore the optimum operating parameters during practical applications, which can reduce the Po2 of PET film by 47.8%. This work provides new insights on advanced coating materials for excellent barrier performance.

A Study on Fabrication Process of Gold Microdisk Arrays by the Direct Imprinting Method Using a PET Film Mold

In this study, an efficient nanofabrication process of metal microdisk arrays using direct imprinting was developed. This process was comprised of three steps; sputter etching on the quartz glass substrate, gold thin film deposition on an etched surface of a substrate, and transfer imprinting using a polyethylene terephthalate (PET) film mold on the Au thin film. A new idea to utilize a PET film mold for disk patterning by the nano transfer imprinting was examined. The PET film mold was prepared by thermally embossing the pillar pattern of a master mold on the PET film. The master mold was prepared from a silicon wafer. The PET film mold was used for transfer imprinting on a metal film deposited on a quartz substrate. The experimental results revealed that the PET film mold can effectively form gold micro-disk arrays on the Au film despite the PET film mold being softer than the Au film. This method can control the distribution and orientation of the nano-arrays on the disk. The plasmonic properties of the gold micro-disk arrays are studied and the absorbance spectrum exhibit depends on the distribution and orientation of gold micro-disk patterns. The nano-transfer imprinting technique is useful for fabricating metallic microdisk arrays on substrate as a plasmonic device.

Temperature Field-Assisted Ultraviolet Nanosecond Pulse Laser Processing of Polyethylene Terephthalate (PET) Film

Understanding the mechanism of and how to improve the laser processing of polymer films have been important issues since the advent of the procedure. Due to the important role of a photothermal mechanism in the laser ablation of polymer films, especially in transparent polymer films, it is both important and effective to adjust the evolution of heat and temperature in time and space during laser processing by simply adjusting the ambient environment so as to improve and understand the mechanism of this procedure. In this work, studies on the pyrolysis of PET film and on temperature field-assisted ultraviolet nanosecond (UV-ns) pulse laser processing of polyethylene terephthalate (PET) film were performed to investigate the photothermal ablation mechanism and the effects of temperature on laser processing. The results showed that the UV-ns laser processing of PET film was dominated by the photothermal process, in which PET polymer chains decomposed, melted, recomposed and reacted with the ambient gases. The ambient temperature changed the heat transfer and temperature distribution in the laser processing. Low ambient temperature reduced the thermal effect and an increase in ambient temperature improved its efficiency (kerf width: 39.63 μm at −25 °C; 48.30 μm at 0 °C; 45.81 μm at 25 °C; 100.70 μm at 100 °C) but exacerbated the thermal effect.

Cost-Normalized Circular Economy Indicator and Its Application to Post-Consumer Plastic Packaging Waste

This work presents an adaptation of the material circularity indicator (MCI) that incorporates economic consideration. The Ellen MacArthur Foundation (EMF) has developed the MCI to characterize the sustainability, viz., the “circularity”, of a product by utilizing life cycle assessment data of a product range rather than a single product unit. Our new “circo-economic” indicator (MCIE), combines product MCI in relation to total product mass, with a cost-normalization against estimated plastic recycling costs, for both separately collected and municipal solid waste. This is applied to assess Dutch post-consumer plastic packaging waste comprising polyethylene (PE), polypropylene (PP), polyethylene terephthalate (PET), film, and mixed plastic products. Results show that MCIE of separate plastic collection (0.81) exceeds municipal solid waste (0.73) for most plastics, thus suggesting that under cost normalization, there is greater conformity of separately collected washed and milled goods to the circular economy. Cost sensitivity analyses show that improvements in plastic sorting technology and policy incentives that enable the production of MSW washed and milled goods at levels comparable to their separately collected counterparts may significantly improve their MCI. We highlight data policy changes and industry collaboration as key to enhanced circularity—emphasized by the restrictive nature of current Dutch policy regarding the release of plastic production, recycling, and costing data, with a general industry reluctance against market integration of weight-benchmarked recycled plastics.

Waste size and lay up sequence strategy for reusing/recycling carbon fiber fabric in laminate composite: Mechanical property analysis

Carbon fiber fabrics have been largely used in composite structures as they provide high mechanical strength and potential weigh reduction, allowing more efficiency in product design. However, the production of the parts generates scraps that is discarded as a waste, becoming a challenge to recycle the carbon fiber with predictable mechanical strength. Within this context, this research analyzed strategies of laying up carbon woven fabrics based scraps, in order to reach a desirable mechanical properties in bending loading. Three types of laminates were manufactured using varied fabric size and number of discontinuities in the layup combined with polyethylene terephthalate (PET) film as a matrix. The obtained composites were tested under four-point-bending test and an energy-strength based analysis was conducted. This analysis explained a strategic position of fabric scrap to maximize the bending strength: providing a value of 106.33 MPa for a composite with high number of discontinuities against 83.11 MPa for another with less discontinuity.

Systematic Review: Efektivitas Ideonella sakaiensis dan Chlamydomonas reinhardtii sebagai Agen Biodegradasi Plastik Berbahan Dasar PET

<p>Bakteri <em>Ideonella sakaiensis</em> dan microalga<em> Chlamydomonas reinhardtii</em> dapat mendegradasi plastik PET (Poly-ethylene terephthalate) dengan mensintesiskan enzim PETase. Tujuan penelitian ini adalah untuk mengetahui efektivitas dari bakteri<em> Ideonella sakaiensis</em> dan <em>Chlamydomonas reinhardtii</em> sebagai agen biodegradasi plastik berbahan dasar PET. Penelitian ini merupakan <em>systematic review</em>, yang dilakukan dengan membandingkan dan menganalisis artikel-artikel yang diambil dari database digital seperti Springer Link dan Semanthic Schoolar. Artikel–artikel yang telah dicari dengan keyword yang telah ditentukan, kemudian dieksklusi sesuai dengan parameter yang ditetapkan, sehingga didapat 2 artikel rujukan. Hasil review menunjukkan bakteri <em>I. sakaiensis</em> mampu mendegradasi PET menjadi MHET (Monoterephtalic Hydroxyethyl Terephtalate) yang lebih dominan dibanding BHET (Bis-hydroxyethyl Terephtalate) &amp; TPA (Terephthalate Acid), sedangkan <em>C. reinhardtii</em> mendegradasikan PET menjadi TPA. Bakteri <em>I. sakaiensis</em> memerlukan waktu 18 jam untuk dapat mendegradasi 30 % dari PET film sedangkan <em>C.reinhardtii</em> memerlukan waktu 4 minggu untuk dapat mendegradasi 35,17% dari PET powder. Kedua mikroorganisme tersebut memiliki keefektifan yang berbeda dalam setiap parameter, yaitu hasil degradasi dan lama waktu pendegradasian.</p>

Fabrication of Flexible Electrode with Sub-Tenth Micron Thickness Using Heat-Induced Peelable Pressure-Sensitive Adhesive Containing Amide Groups

In response to the increasing demand for flexible devices, there is increasing effort to manufacture flexible electrodes. However, the difficulty of handling a thin film is an obstacle to the production of flexible electrodes. In this study, a heat-induced peelable pressure-sensitive adhesive (h-PSA) was fabricated and used to manufacture a flexible electrode with sub-tenth micron thickness. Unlike the control PSA, the incorporation of amide groups made the h-PSA fail through adhesive failure at temperatures ranging from 20 to 80 °C. Compared to the peeling adhesion (1719 gf/in) of h-PSA measured at 20 °C, the value (171 gf/in) measured at 80 °C was decreased by one order of magnitude. Next, the 8 μm thick polyethylene terephthalate (PET) film was attached on a thick substrate (50 μm) via h-PSA, and Mo/Al/Mol patterns were fabricated on the PET film through sputtering, photolithography, and wet-etching processes. The thick substrate alleviated the difficulty of handling the thin PET film during the electrode fabrication process. Thanks to the low peel force and clean separation of the h-PSA at 80 °C, the flexible electrode of metal patterns on the PET (8 μm) film was isolated from the substrate with little change (<1%) in electrical conductivity. Finally, the mechanical durability of the flexible electrode was evaluated by a U-shape folding test, and no cracking or delamination was observed after 10,000 test cycles.

Diamine vapor treatment of viscoelastic graphene oxide liquid crystal for gas barrier coating

A layered graphene oxide/ethylenediamine (GO/EDA) composite film was developed by exposing aqueous GO liquid crystal (GOLC) coating to EDA vapor and its effects on the gas barrier performance of GO film were systematically investigated. When a GO/EDA coating with a thickness of approximately 1 μm was applied to a neat polyethylene terephthalate (PET) film, the resultant film was highly impermeable to gas molecules, particularly reducing the gas permeance up to 99.6% for He and 98.5% for H2 in comparison to the neat PET film. The gas barrier properties can be attributed to the long diffusion length through stacked GO nanosheets. The EDA can crosslink oxygen-containing groups of GO, enhancing the mechanical properties of the GO/EDA coating with hardness and elastic modulus values up to 1.14 and 28.7 GPa, respectively. By the synergistic effect of the viscoelastic properties of GOLC and the volatility of EDA, this coating method can be applied to complex geometries and EDA intercalation can be spontaneously achieved through the scaffold of the GOLC.