Thermal degradation of corn starch based biodegradable plastic plates and determination of kinetic parameters by isoconversional methods using thermogravimetric analyzer

Oil shortage and awareness of environment pollution leads to the extensive use of biodegradable starch-based materials against synthetic plastics. The accumulated wastes of these plastics takes more time for natural recycling and the process is complex. Therefore the best option of recycling would be to convert these polymers into a source of energy by pyrolysis. So to understand the pyrolytic behaviour, kinetics of such waste plastics is studied by using thermogravimetric analysis at different heating rates of 10 °C, 20 °C, 40 °C, 60 °C, 80 °C and 100 °C in nitrogen atmosphere followed by characterization of the pyrolysis products. The kinetic parameters are obtained for two major stages of decomposition in two different temperature ranges 250–620 °C and 620–855 °C by iso-conversional methods such as Friedman, Coats-Redfern, FWO and Kissinger methods. The regression coefficient data (>0.9) of kinetic plots obtained for different methods best fits to the kinetic equation. Empirical formula of the compound is determined by ultimate analysis is CH_2.214S_0.0018O_0.6910. Proximate analysis gives the idea of volatile component which is74.33%. The range of average value of activation energy is 120.7013 kJ/mol to 140.7707 kJ/mol for the biodegradable plastic plate with different conversion (0.1–0.6) and (0.1–0.3) respectively at two different temperatures. The pyrolysis products obtained using a semi-batch reactor are characterized to know their composition and other properties.     

绿色包装材料——生物降解塑料

对绿色包装材料-生物降解塑料的降解机理、特点，国内外研究现状和进展及存在的问题和发展前景进行了介绍。     

The mechanical property and phase structures of wheat proteins/polyvinyl alcohol blends studied by high-resolution solid-state NMR

The phase structures of thermally processed wheat proteins (WP) and polyvinyl alcohol (PVOH) blends were studied by solid-state high-resolution NMR spectroscopy. The intermolecular interactions among the multi-component systems and the behavior of each component in the blends on scales of nanometers were examined. The mechanical properties of the blends were also measured and related to the phase structure studies. The results indicated that the polymer chains of WP could be homogeneously mobilized when thermally processed with glycerol and water as plasticisers, but the glycerol predominately associated with WP rather than PVOH in the blends. The intermolecular hydrogen bonding interactions between WP and PVOH caused some extent of miscibility in the system on scales of nanometers especially when the PVOH content was low. The tensile strength and modulus of the blends were improved as compared to WP. However, the intermolecular interactions were relatively weak and could not be further enhanced by increasing PVOH component in the blends. The particle miscible WP/PVOH blends contained plasticised WP and PVOH phases in conjunction with the miscible WP/PVOH phase. Increasing the PVOH content in the blends did not result in an increase of the percentage of the miscible phase and the blends tented to be immiscible while the elongation of the blends was reduced when increasing the PVOH content in the blends.     

Synthesis of biodegradable poly(trans-4-hydroxy-N-benzyloxycarbonyl-l-proline)-block-poly(ε-caprolactone) copolymers and micellar characterizations

A series of novel types of diblock poly(trans-4-hydroxy-N-benzyloxycarbonyl-l-proline)-block-poly(ε-caprolactone) (PHpr10-b-PCL) copolymers were synthesized by ring-opening polymerization from macroinitiator poly(trans-4-hydroxy-N-benzyloxycarbonyl-l-proline) (PHpr10) and ε-caprolactone (ε-CL) in the presence of organocatalyst dl-lactic acid (dl-LA). The M_n of the copolymers increased from 3370 to 19,040 g mol⁻¹ with the molar ratio (10-100) of ε-CL to PHpr10. These products were characterized by differential scanning calorimetry (DSC), ¹H NMR, and gel permeation chromatography. According to DSC, the glass-transition temperature (T_g) of the diblock copolymers depend on the molar ratio of monomer/initiator that were added. The hydrolytic degradation behavior of PHpr-b-PCLs was evaluated from weight-loss measurements and the change of M_n and M_w/M_n. With higher PCL contents resulted in a slower weight loss, while having a higher molecular weight loss percentage. Their micellar characteristics in an aqueous phase were investigated by fluorescence spectroscopy, transmission electron microscopy (TEM), and dynamic light scattering (DLS). The block copolymers formed micelles in the aqueous phase with critical micelle concentrations (CMCs) in the range of 1.33-4.22 mg L⁻¹. The micelles exhibited a spindly shape and showed a narrow monodisperse size distribution. The obtained micelles have a relatively high drug-loading of about 26% when the feed weight ratio of amitriptyline hydrochloride (AM) to polymer was 1/1. An increase of molecular weight and hydrophobic components in copolymers produced a higher CMC value and greater loading efficiencies were observed.     

Influence of laser surface remelting on microstructure and degradation mechanism in simulated body fluid of Zn-0.5Zr alloy

In this study, the Zn-0.5 wt%Zr (Zn-Zr) alloy was treated by laser surface remelting (LSR), and then the microstructure and degradation mechanism of the remelting layer were investigated and compared with the original as-cast alloy. The results reveal that after LSR, the bulky Zn₂₂Zr phase in the original Zn-Zr alloy is dissolved and the coarse equiaxed grains transform into fine dendrites with a secondary dendrite arm space of about 100 nm. During the degradation process in simulated body fluid (SBF), the corrosion products usually concentrate at some certain areas in the original alloy, while the corrosion products distribute uniformly and loosely in the LSR-treated surface. After removing the corrosion products, it was found that the former suffers obvious pitting corrosion and then localized corrosion. The proposed mechanism is that corrosion initiates at grain boundaries and develops into the depth at some locations, and then leads to localized corrosion. For the LSR-treated sample, corrosion initiates at some active sites and propagates in all directions, corrosion takes place in the whole surface with distinctly uniform thickness reduction, while the localized corrosion and peeling of bulky Zn₂₂Zr particles were eliminated. The electrochemical results also suggest the uniform corrosion of LSR-treated sample and localized corrosion of original sample. Based on the results, a new approach to regulate the corrosion mode of the biodegradable Zn alloy is proposed.     

淀粉基生物降解塑料的研究现状

简述了淀粉的加工特性,挤出流变行为,简要介绍了国内外淀粉基生物降解塑料的研究现状及展望。     

淀粉基生物降解塑料

简述了淀粉的基本性持和淀粉塑料分类,分析了各类淀粉塑料的优缺点,介绍了目前的研究动态,指出了淀粉塑料目前存在的问题以及发展方向     

Surface modification of biodegradable plastics by ion beams

Biodegradable plastics can be used as conventional plastics, while on disposal they decompose to water and carbon dioxide by microorganisms existing in natural environment. Products using biodegradable plastics have recently been developed in many companies pursuing ecology. In this study, surface modification of biodegradable plastics was carried out by inert ion beams for improvement of photo deterioration under an ultraviolet ray. The hardness of biodegradable plastics tended generally to decrease with irradiation of an ultraviolet ray. In this method, the hardness of ion-bombarded biodegradable plastics was kept at an initial value under an ultraviolet ray, because the modified layer by ion bombardment intercepted an ultraviolet ray. The hardness of He⁺ ion-bombarded biodegradable plastics showed larger value than that of Ar⁺ ion bombardment. He⁺ ion bombardment at ion energy of 10 keV produced the suitable property with both of high transmittance of a visible ray and high interception of an ultraviolet ray in a surface layer of biodegradable plastics.     

A comparison of the tribological behaviour of steel/steel, steel/DLC and DLC/DLC contacts when lubricated with mineral and biodegradable oils

Diamond-like carbon (DLC) coatings, which can nowadays be applied to many highly loaded mechanical components, sometimes need to operate under lubricated conditions. It is reasonable to expect that in steel/DLC contacts, at least the steel counter body will behave according to conventional lubrication mechanisms and will interact with lubricants and additives in the contact. However, in DLC/DLC contacts, such mechanisms are still unclear. For example, the “inertness” of DLC coatings raises several questions about whether they are able to provide real boundary “lubrication” or whether they are just a “passive” member in these contacts. On the other hand, biodegradable oils, in particular vegetable base oils, possess a good lubricating ability, often much better than mineral or conventional synthetic oils as a result of the large amount of un-saturated and polar components that can promote the lubricity of DLC coatings. Accordingly, in this study, we present the results of experiments under severe boundary-lubrication conditions during reciprocating sliding. We look at the effect of the type of mating surfaces - steel/DLC, DLC/DLC and steel/steel - and the type of oil on the tribological performance of DLC coatings. We compare the wear and friction behaviours of two types of DLC coatings, i.e., a “pure” non-doped a-C:H DLC coating (denoted as a-DLC) and a WC-containing multilayer coating (denoted as W-DLC) tested with a mineral oil and a biodegradable vegetable oil. These oils, which have very different chemical compositions, were used as base oils and also with mild AW and strong EP additives. Among other things, the results confirm the following: (1) coating/coating lubricated contacts can resemble metal-lubrication mechanisms; (2) additives reduce wear in coating/coating contacts by up to 80%; (3) better wear and friction performance are obtained with oils that contain large amounts of polar and un-saturated molecules; (4) a coating/coating combination generally results in less wear than a steel/coating combination.     

Toughening of Polylactic Acid: An Overview of Research Progress

To overcome the limitations of polylactic acid, alterations are needed to enhance its toughness, to improve handling and for various applications. Extensive studies were reported, mainly in the area of blends with renewable resource polymer blends. Better phase dispersion between the blend materials is achieved either by reactive mixing of the two components or by incorporation of a block copolymer compatibilizer, finally showing highly enhanced property. In this article, the recent research progress of different toughening processes of PLA via blending is reviewed and a detailed understanding about toughening of PLA using biodegradable or renewable polymers has been established.