Biodegradability of conventional and bio-based plastics and natural fiber composites during composting,anaerobic digestion and long-term soil incubation

Plastics are a major constituent of municipal solid waste that pose a growing disposal and environmental pollution problem due to their recalcitrant nature. To reduce their environmental impacts and allow them to be transformed during organic waste recycling processes, various materials have recently been introduced to improve the biodegradability of plastics. These include conventional plastics amended with additives that are meant to enhance their biodegradability, bio-based plastics and natural fiber composites. In this study, the rate and extent of mineralization of a wide range of commercially available plastic alternative materials were determined during composting, anaerobic digestion and soil incubation. The biodegradability was assessed by measuring the amount of carbon mineralized from these materials during incubation under conditions that simulate these three environments and by examination of the materials by scanning electron micrography (SEM). The results showed that during a 660 day soil incubation, substantial mineralization was observed for polyhydroxyalkanoate plastics, starch-based plastics and for materials made from compost. However, only a polyhydroxyalkanoate-based plastic biodegraded at a rate similar to the positive control (cellulose). No significant degradation was observed for polyethylene or polypropylene plastics or the same plastics amended with commercial additives meant to confer biodegradability. During anaerobic digestion for 50 days, 20–25% of the bio-based materials but less than 2% of the additive containing plastics were converted to biogas (CH₄ + CO₂). After 115 days of composting, 0.6% of an additive amended polypropylene, 50% of a plastarch material and 12% of a soy wax permeated paper pulp was converted to carbon dioxide. SEM analysis showed substantial disintegration of polyhydroxyalkanoate-based plastic, some surface changes for other bio-based plastics and coconut coir materials but no evidence of degradation of polypropylene or polypropylene containing additives. Although certain bio-based plastics and natural fibers biodegraded to an appreciable extent in the three environments, only a polyhydroxyalkanoate-based resin biodegraded to significant extents during the time scale of composting and anaerobic digestion processes used for solid waste management.     

A clever strategy for permeability studies of methyl bromide and some organic compounds through high-barrier plastic films

An analytical strategy has been proposed and optimized to study the permeability of several flexible plastic materials, some of them with high-barrier properties, versus naphthalene, methyl bromide, toluene, ethylbenzene, and ortho- and para-xylenes. The strategy involves using a system of concentric plastic bags made from the materials to be tested polyethylene (PE) and used as permeable plastics to facilitate the homogeneous distribution of a solid compound, such as naphthalene, in vapour phase. After the permeation test, the vapour phase containing the pollutants that cross the plastic barrier is trapped in a 12% ethanol–water solution and further analysed by SPME in headspace mode. Several experimental conditions as well as different samples were tested. The results obtained are shown and discussed.     

Multielemental evaluation of garbage bags by EDXRF

Garbage bags have been broadly used for collecting household waste in Brazil and worldwide. Many of these bags are made from recycled polymers, and the presence of harmful elements is a matter of concern. In this study, an energy dispersive X-ray fluorescence (EDXRF) approach for direct analysis of garbage bags is proposed. The concentrations of K, Ca, Ti, Cr, Mn, Fe, Ni, Cu, Zn, Br, Rb, Sr and Pb were determined in 14 garbage bags of different brands purchased from local markets in Piracicaba, São Paulo State, Brazil. The EDXRF technique proved to be an effective technique for multielemental, environmentally friendly and direct garbage bag monitoring. For most samples, Ca and Ti presented at minor concentration ranges and K, Cr, Mn, Fe, Ni, Cu, Zn and Pb at minor and trace levels. The EDXRF limits of quantification were K: 220; Ca: 112; Ti: 42; Cr: 19; Mn: 13; Fe: 9.2; Ni: 5.7; Cu: 5.3; Zn: 5.2; Br: 12; Rb: 20; Sr: 28 and Pb:17 μg g^–1. The samples had variable thicknesses, with a superficial density variation of 1.5 to 23% among the triplicates. The trueness of the method was checked by analysing the National Institute of Standards and Technology standard reference material SRM2783.     

Separation of phthalates by cyclodextrin modified micellar electrokinetic chromatography: Quantitation in perfumes

A new CE method has been developed for the simultaneous separation of a group of parent phthalates. Due to the neutral character of these compounds, the addition of several bile salts as surfactants (sodium cholate (SC), sodium deoxycholate (SDC), sodium taurodeoxycholate (STDC), sodium taurocholate (STC)) to the separation buffer was explored showing the high potential of SDC as pseudostationary phase. However, the resolution of all the phthalates was not achieved when employing only this bile salt as additive, being necessary the addition of neutral cyclodextrins (CD) and organic modifiers to the separation media. The optimized cyclodextrin modified micellar electrokinetic chromatography (CD-MEKC) method consisted of the employ of a background electrolyte (BGE) containing 25 mM β-CD-100 mM SDC in a 100 mM borate buffer (pH 8.5) with a 10% (v/v) of acetonitrile, employing a voltage of 30 kV and a temperature of 25 °C. This separation medium enabled the total resolution of eight compounds and the partial resolution of two of the analytes, di-n-octyl phthalate (DNOP) and diethyl hexyl phthalate (DEHP) (Rs ~ 0.8), in only 12 min. The analytical characteristics of the developed method were studied showing their suitability for the determination of these compounds in commercial perfumes. In all the analyzed perfumes the most common phthalate was diethyl phthalate (DEP) that appeared in ten of the fifteen analyzed products. Also dimethyl phthalate (DMP), diallyl phthalate (DAP), dicyclohexyl phthalate (DCP), and di-n-pentyl phthalate (DNPP) were found in some of the analyzed samples.     

Comparison of the Characteristics of Recycled Carbon Fibers/Polymer Composites by Different Recycling Techniques

In this study, three recycling methods, namely, mechanical grinding, steam pyrolysis, and the supercritical solvent process, which are used to acquire recycled carbon fibers (RCFs), were compared for their application in synthesizing polymer-matrix composites. RCF-reinforced polyethylene (PE) composites were prepared to compare the mechanical properties of the composites generated using the three recycling methods. The PE/RCF composites exhibited 1.5 times higher mechanical strength than the RCF-reinforced PE composites, probably because of the surface oxidation effects during the recycling processes that consequently enhanced interfacial forces between the RCF and the matrix. Further, the steam pyrolysis process showed the highest energy efficiency and can thus be applied on a large production scale in domestic recycled CF markets.     

Post-Consumer Poly(ethylene terephthalate) (PET) Depolymerization by Yarrowia lipolytica: A Comparison between Hydrolysis Using Cell-Free Enzymatic Extracts and Microbial Submerged Cultivation

Several microorganisms have been reported as capable of acting on poly(ethylene terephthalate) (PET) to some extent, such as Yarrowia lipolytica, which is a yeast known to produce various hydrolases of industrial interest. The present work aims to evaluate PET depolymerization by Y. lipolytica using two different strategies. In the first one, biocatalysts were produced during solid-state fermentation (SSF-YL), extracted and subsequently used for the hydrolysis of PET and bis(2-hydroxyethyl terephthalate) (BHET), a key intermediate in PET hydrolysis. Biocatalysts were able to act on BHET, yielding terephthalic acid (TPA) (131.31 µmol L⁻¹), and on PET, leading to a TPA concentration of 42.80 µmol L⁻¹ after 168 h. In the second strategy, PET depolymerization was evaluated during submerged cultivations of Y. lipolytica using four different culture media, and the use of YT medium ((w/v) yeast extract 1%, tryptone 2%) yielded the highest TPA concentration after 96 h (65.40 µmol L⁻¹). A final TPA concentration of 94.3 µmol L⁻¹ was obtained on a scale-up in benchtop bioreactors using YT medium. The conversion obtained in bioreactors was 121% higher than in systems with SSF-YL. The results of the present work suggest a relevant role of Y. lipolytica cells in the depolymerization process.     

紫外激光标记空气开关的工艺研究

激光器的打标速度、频率、填充间隔、电流、离焦量等工艺参数直接影响空气开关的打标效果。实验根据5因素4水平正交表L16(45)改变激光工艺参数,利用分光测色计和二维码扫描器对激光标记分别进行色差和读码率的测量,通过正交分析法和极差法研究激光工艺参数对打标效果的影响。研究表明：色差与读码率的数据趋于正比关系,并且存在一个阈值色差;当激光参数的速度为1 000 mm/s、频率为20~30 kHz、填充间隔为0.04 mm、电流为28 A、离焦量为-1 mm时,在空气开关上打标出点密度合适、色差对比度高、易于读取的二维码。     

Cutting of aramide fiber-reinforced plastics by Co2 laser

Comparative characteristics of aramide fiber reinforced plastics (AFRP) made by laser cutting or machining are presented. It is found that the strength of the specimens cut out by laser is 4–25% higher, while the moisture absorption is at least 2 times lower as compared to those cut out by machining. The deviation of the cutting edge size for AFRP 2 mm thick does not exceed 0.4 mm. Calculated and experimental data are given. The possibilities and conditions of cutting the AFRP up to 6 mm thick are determined.Translated from Mekhanika Kompozitnykh Materialov, Vol. 35, No. 3, pp. 375–384, May–June, 1999.     

Influence of technological processing parameters on the properties of carbon filled thermoplastics

The effect of processing parameters of injection molding on the mechanical and tribotechnical properties of carbon plastics based on polyacetals is investigated. The copolymer of 1,3,5-trioxane with 1,3-dioxolane is used as the polymer matrix. Hydrated cellulose Ural LO-24 carbon fibers are used as the reinforcing filler. The effect of molding temperature, pressing time, and temperature of the casting mould on the properties of carbon plastics is investigated. It has been found that for improving the mechanical properties of carbon plastics it is necessary to raise the molding temperature up to 200–210°C. Prolongation of the technological cycle leads to thermal degradation of the polymer in the cylinder of a casting machine. The mould temperature only slightly affects the composite strength properties, but lower temperatures create better conditions for polymer crystallization. As a result of our investigations, the optimal processing parameters of the above carbon plastics are determined.Ukrainian State University of Chemical Technology, Dnepropetrovsk, Ukraine. Translated from Mekhanika Kompozitnykh Materialov, Vol. 35, No. 3, pp. 385–392, 1999.     

新型光学塑料——EA光学塑料

新型光学塑料—EA光学塑料系采用合成双酚A环氧丙烯酸双酯,再与苯乙烯共聚固化成型制成的一种光学塑料材料。它的光学性能优越R_D=1.5836,v=32,内应力是现有塑料中最小的,成像分辨率是现有光学塑料中最好的,可以做成像透镜材料。该项成果为光学塑料增添了一个新品种。