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The raw material of polylactide (PLA) is lactic acid obtained by biological fermentation. PLA is the most promising degradable polymer to replace traditional plastics to address the pollution problems caused by their non-degradability. However, the application of PLA is hindered by its low softening temperature, easy hydrolysis, and poor toughness. Herein, the ternary composites with PLLA, PDLA and Poly (butylene adipate- co -terephthalate) (PBAT) were prepared by melt blending to balance its thermal stability, hydrolysis, and toughness. The effects of PBAT content (3 %, 6 %, 9 % and 12 %) and isothermal crystallization temperature on composite properties were fully investigated. The results show that the composite of stereo-complexed PLA (sc-PLA) with 6 % PBAT crystallized at 110 °C exhibits good comprehensive properties. Its vicat softening temperature (VST), mass loss rate under alkaline (pH = 12) and breaking elongation are 166 °C, 21.6 % and 4.40 %, respectively. Compared with the pure PLLA sample crystallized at same condition, the VST, mass loss rate and breaking elongation are 159 °C, 24.7 % and 3.76 % respectively, which increased by nearly 5 %, 13 % and 20 %. This indicates that this strategy is feasible to balance the heat resistance, hydrolysis resistance and toughness of PLA, while it sacrifices the tensile strength a little. This work provides a new way to modify and improve the PLA properties. Nonetheless, it is also necessary to coordinate the compatibility of PLA and PBAT. [ABSTRACT FROM AUTHOR]

ABSTRACT Keratin particles with microscale are prepared by ball mill and its influences on the chitosan membrane is evaluated. Composite membranes with various content of keratin are fabricated, and their physical and chemical properties such as morphology, wettability, crystallization, thermal stability, tensile strength, and break elongation are investigated. Optical microscope and situ topographic scan mode of nano-test system are used to examine the dispersion and aggregation of keratin on the surface of chitosan membrane. The result of contact angle (CA) and mechanical testing show that the incorporation of keratin particles decrease the CA from 98.1° to 58.2°. Tensile strength and break elongation of the composite membrane reaches a maximum of 65 ± 8 MPa and 15% when the keratin content is 6%, an increase of 80% and 88% compared with the pristine chitosan membrane. Both the increase in tensile strength and break elongation is result of the incorporation of keratin particles known for their excellent compatibility between keratin and chitosan matrix. These kind of composite material combines the antibacterial properties of chitosan with cell culture preference of keratin which may have potential biomedical application. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017, 134, 44667. [ABSTRACT FROM AUTHOR]

Abstract: Chitosan membrane possesses huge potential application in many fields, such as biomedicine, wastewater purification and environmental protection, however, the poor mechanical property restricts its further development. In this study, chitin whisker was prepared by hydrolysis method, and was firstly used as an interlayer to fabricate the multilayered chitosan membrane through layer-by-layer method, which is inspired by the natural materials' hierarchical structure. From the results of mechanical testing, it is shown that tensile strength of the multilayered chitosan membranes reaches up to 122.8MPa, which is about 2.5 times than that of neat chitosan membrane (i.e. 49.5MPa), and the elongation at break is sharply increased as well. [Copyright &y& Elsevier]

Abstract: In this paper, rod-like chitin whisker was used as a filler to reinforce the chitosan membrane, and a series of composite membranes were prepared by casting–evaporation method. Mechanical testing shows that tensile strength of the resulting composite membrane with 3wt% chitin whisker content reaches up to 110.3MPa, which is about 2.8times than that of neat chitosan membrane (38.5MPa), and moisture regain of all composite membranes presents a decreasing tendency with increasing content of chitin whisker. Furthermore, SEM was used to investigate the morphology difference between neat chitosan membrane and composite membranes, to understand the reinforce mechanism of chitin whisker. Wide angle x-ray diffraction and Fourier transform infrared spectroscopy were used to visualize the structure change before and after the compositing processes. Besides, the bacterostatic test shows that this composite membrane presents effective inhibitory effect on Staphylococcus aureus, Escherchia coli and Corinebaterium michiganence respectively, which indicates it a promising material for packaging and wound dressing. [Copyright &y& Elsevier]

The combination of crystallization, transparency, and strength is still a challenge for broadening the application of polylactic acid (PLA) films, while it is also difficult to balance. In this work, the long aliphatic chains of octadecylamine (ODA) were grafted onto the surface of cellulose nanocrystal (CNC) by tannic acid oxidation self-polymerization and Michael addition/Schiff base reaction between polytannic acid and ODA. Furthermore, the ODA grafted CNC (g-CNC) was used as green reinforcement for the PLA matrix and a series of PLA/g-CNC nanocomposite films were prepared by the casting method. The DSC, WAXD, POM, UV–vis and stretching test were employed to examine the effect of g-CNC on the properties of the as-prepared PLA/g-CNC nanocomposite films. It shows that the g-CNC is effective to improve the melt crystallization rate of PLA from 11 min to 7.3 min. Most importantly, the crystal size of the PLA spherulites was significantly reduced due to the well dispersion in the amorphous PLA matrix, which would effectively improve the transmittance of the PLA films and synchronously realize the combination of crystallization (62 %) and transparency (80.6 %). Moreover, the improved crystallization could also enhance the heat deformation performance of the PLA films since the heat resistance is closely associated with the crystallinity. Besides, the grafted ODA long chains improve the compatibility between CNC and PLA, leading to the reinforcement of PLA matrix, where the tensile strength reaches 65.05 MPa from 44.31 MPa. Compared with the pristine CNC, the addition of g-CNC makes more comprehensive improvement in the properties of the PLA films. [ABSTRACT FROM AUTHOR]

In this research, nanocellulose crystal (NCC) grafted with lactic acid (LA) oligomer was synthesized by one-pot method and used to reinforce the poly(l -lactic acid) (PLLA) matrix. FT-IR, XRD, and 13C NMR were used to analyze the structure of modified nanocellulose crystal (g-NCC). The results of GPC suggested that the degree of polymerization of the grafted segments was 23, and the degree of hydroxyl substitution of g-NCC was 2.4%. For the g-NCC/PLLA composite, its crystallization rate increases significantly compared with pure PLLA, indicating that g-NCC acted as a nucleating agent to promote the crystallization. Moreover, tensile strength of the composite materials was significantly improved from 41.9 MPa to 53.9 MPa due to the enhanced compatibility. This study provides a fast and effective modification method for g-NCC/PLLA biodegradable composites. According to the above-mentioned experimental results, the g-NCC/PLLA composites can be considered as a potential material in the packaging field, mainly due to its proper biological and physicochemical properties. • Nanocellulose crystal was modified with lactic acid by one-pot method. • The degree of polymerization of the grafted segments is 23, and the degree of hydroxyl substitution of g-NCC is 2.4%. • Tensile strength of G-NCC/PLLA has been improved from 41.9 MPa to 53.9 MPa. [ABSTRACT FROM AUTHOR]

In this research, solutions of styrene-butadiene-styrene block copolymer (SBS) in 2-ethoxyethyl methacrylate (EOEMA) were used to prepare strippable films via rapid visible-light curing, where the mixture of camphorquinone (CQ), diphenylsilane (DPS) and diphenyliodonium hexafluorophosphate (Iod) was employed as the photoinitiating system, LED@405 nm, sunlight or household LED panel light as the light source and no any solvent was involved. The double bond conversion for pure EOEMA under LED@405 nm was firstly monitored by real-time FTIR and it reached 72% within 300 s. The rapid-curing of SBS/EOEMA solutions were systematically investigated and it was found that the solution with 16 wt% SBS became completely dried at the presence of 2.16 mol% crosslinker and 3.6 wt% photoinitiating system after 240 s irradiation under LED@405 nm. The tensile strength, elongation at break and glass transition temperature of the resultant strippable film were determined to be about 4.4 ± 0.5 MPa, 130 ± 11.2% and 6.9 °C, respectively, by mechanical properties testing and DSC measurements. Also, the decontamination efficiencies (DE) of household LED panel light/sunlight cured-strippable film for uranium nitrate on stainless steel, glass, and ceramic surface were evaluated to be higher than 90%. These results indicate that this rapid-curing strippable films would be a good candidate material for large-scale radioactive decontamination. [ABSTRACT FROM AUTHOR]