scholarly journals New Polymers and Polymer Materials based on Plant Oils

Author(s):  
Andriy Voronov
Keyword(s):  
2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Guoqiang Zhu ◽  
Chengguo Liu ◽  
Chaoqun Zhang

Abstract Polymer materials derived from natural resources have gained increasing attention in recent years because of the uncertainties concerning petroleum supply and prices in the future as well as their environmental pollution problems. As one of the most abundant renewable resources, plant oils are suitable starting materials for polymers because of their low cost, the rich chemistry that their triglyceride structure provides, and their potential biodegradability. This chapter covers the structure, modification of triglycerides and their derivatives as well as synthesis of polymers therefrom. The remarkable advances during the last two decades in organic synthesis using plant oils and the basic oleochemicals derived from them are selectively reported and updated. Various methods, such as condensation, radical/cationic polymerization, metathesis procedure, and living polymerization, have also been applied in constructing oil-based polymers. Based on the advance of these changes, traditional polymers such as polyamides, polyesters, and epoxy resins have been renewed. Partial oil-based polymers have already been applied in some industrial areas and recent developments in this field offer promising new opportunities.


Vestnik MGSU ◽  
2018 ◽  
pp. 1491-1498 ◽  
Author(s):  
Еlena M Gotlib ◽  
Anh Nguyen ◽  
Аlla G. Sokolova

Introduction. Application of renewable raw materials for manufacturing non-toxic components of polymer materials is of great practical interest. Cyclic carbonates on the base of epoxidated rubber tree oil could be seen as a promising alternative of fossil fuels. The ability of compounds containing cyclic carbonates to interact with primary amines and to form urethane and hydroxyl groups makes them rather efficient modifiers of amine-toughened epoxy compounds on the base of low-molecular diane oligomers. Introduction of cyclic carbonates enhances impact behavior of epoxy materials as well as their adhesion and strength properties. Materials and methods. Epoxy resin ED-20 was used for the research, as a cross-linking agent for cold toughening aminealkylphenol AF-2 was used; cyclic carbonates of epoxidated soy oils and rubber tree oil were applied as modifiers. Adhesional strength of bond joints has been determined in compliance with the GOST 28840-90, abrasive hardness of epoxy compound samples has been tested by the vertical optical caliper IZV-1. Results. When applying two-stage technology for obtaining epoxy cyclic carbonate compounds, there has been appeared a significant increase of adhesion to aluminum. This effect could be even more noticeable with increasing temperature during the stage of mixture of the amine toughener with the cyclic carbonate modifier. High viscosity of cyclic carbonate modifiers complicates the process of mixing components of the epoxy compound and correspondingly its application as a backing of glues and linings. The authors researched cyclic carbonates of epoxidated soy oil with various averaged functionality as modifiers. Application of epoxy materials CESO-75 as a modifier has proven to be more forward-thinking for the reasons of cost-efficiency and for operating and technological properties. CESO lowers the coefficient of static friction for epoxy materials together with enhancing their abrasion hardness. Conclusions. Cyclic carbonates of epoxidated plant oils (soy oil and rubber tree oil) as rather efficient non-toxic modifiers of epoxy polymers are of practical interest. They are produced on the base of annually renewable plant raw materials. Their application enables to enhance abrasion hardness and adhesion properties of epoxy compounds and also improve their antifriction properties.


Author(s):  
D.T. Grubb

Diffraction studies in polymeric and other beam sensitive materials may bring to mind the many experiments where diffracted intensity has been used as a measure of the electron dose required to destroy fine structure in the TEM. But this paper is concerned with a range of cases where the diffraction pattern itself contains the important information.In the first case, electron diffraction from paraffins, degraded polyethylene and polyethylene single crystals, all the samples are highly ordered, and their crystallographic structure is well known. The diffraction patterns fade on irradiation and may also change considerably in a-spacing, increasing the unit cell volume on irradiation. The effect is large and continuous far C94H190 paraffin and for PE, while for shorter chains to C 28H58 the change is less, levelling off at high dose, Fig.l. It is also found that the change in a-spacing increases at higher dose rates and at higher irradiation temperatures.


Author(s):  
J. Petermann ◽  
G. Broza ◽  
U. Rieck ◽  
A. Jaballah ◽  
A. Kawaguchi

Oriented overgrowth of polymer materials onto ionic crystals is well known and recently it was demonstrated that this epitaxial crystallisation can also occur in polymer/polymer systems, under certain conditions. The morphologies and the resulting physical properties of such systems will be presented, especially the influence of epitaxial interfaces on the adhesion of polymer laminates and the mechanical properties of epitaxially crystallized sandwiched layers.Materials used were polyethylene, PE, Lupolen 6021 DX (HDPE) and 1810 D (LDPE) from BASF AG; polypropylene, PP, (PPN) provided by Höchst AG and polybutene-1, PB-1, Vestolen BT from Chemische Werke Hüls. Thin oriented films were prepared according to the method of Petermann and Gohil, by winding up two different polymer films from two separately heated glass-plates simultaneously with the help of a motor driven cylinder. One double layer was used for TEM investigations, while about 1000 sandwiched layers were taken for mechanical tests.


Author(s):  
H.-J. Cantow ◽  
M. Kunz ◽  
M. Möller

In transmission electron microscopy the natural contrast of polymers is very low. Thus the contrast has to be enhanced by staining with heavy metals. The resolution is limited by the size of the staining particles and by the fact that electrons with different energy are focused in different image planes due to the chromatic aberration of the magnetic lenses. The integration of an electron energy loss spectrometer into the optical coloumn of a transmission electron microscope offers the possibility to use monoenergetic electrons and to select electrons with a certain energy for imaging. Thus contrast and resolution are enhanced. By imaging only electrons with an element specific energy loss the element distribution in the sample can be obtained. In addition, elastic bright field images and diffraction patterns yield excellent resolution. Some applications of the method on multicomponent polymer materials are discussed.Bulk polymer samples were prepared by ultramicrotoming at room temperature or well below the glass transition temperature. Very thin films for the direct observation of the structure in semicrystalline polymers were obtained by melt-spinning. Specimens were examined with a ZEISS CEM 902 operated at 80 kV.


Author(s):  
Patricia M. Wilson ◽  
David C. Martin

Efforts in our laboratory and elsewhere have established the utility of low dose high resolution electron microscopy (HREM) for imaging the microstructure of crystalline and liquid crystalline polymers. In a number of polymer systems, direct imaging of the lattice spacings by HREM has provided information about the size, shape, and relative orientation of ordered domains in these materials. However, because of the extent of disorder typical in many polymer microstructures, and because of the sensitivity of most polymer materials to electron beam damage, there have been few studies where the contrast observed in HREM images has been analyzed in a quantitative fashion.Here, we discuss two instances where quantitative information about HREM images has been used to provide new insight about the organization of crystalline polymers in the solid-state. In the first, we study the distortion of the polymer lattice planes near the core of an edge dislocation and compare these results to theories of dislocations in anisotropic and liquid crystalline solids. In the second, we investigate the variations in HREM contrast near the edge of wedge-shaped samples. The polymer used in this study was the diacetylene DCHD, which is stable to electron beam damage (Jc = 20 C/cm2) and highly crystalline. The instrument used in this work was a JEOL 4000 EX HRTEM with a beam blanidng device. More recently, the 4000 EX has been installed with instrumentation for dynamically recording scattered electron beam currents.


2018 ◽  
Vol 4 (2) ◽  
pp. 85-90
Author(s):  
Y. M. Dovydenko ◽  
N. A. Ivanova ◽  
S. A. Chizhik ◽  
V. E. Agabekov

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