Renewable resources are used increasingly in the production of polymers. In particular, monomers such as carbon dioxide, terpenes, vegetable oils and carbohydrates can be used as feedstocks for the manufacture of a variety of sustainable materials and products, including elastomers, plastics, hydrogels, flexible electronics, resins, engineering polymers and composites. Efficient catalysis is required to produce monomers, to facilitate selective polymerizations and to enable recycling or upcycling of waste materials. There are opportunities to use such sustainable polymers in both high-value areas and in basic applications such as packaging. Life-cycle assessment can be used to quantify the environmental benefits of sustainable polymers.

/pdf/sustainable-polymers-from-renewable-resources-3zc6tmi7nv.pdf

Sustainable polymers from renewable resources

Each year vast amounts of plastic are produced worldwide. When released to the environment, plastics accumulate, and plastic debris in the world's oceans is of particular environmental concern. More than 60% of all floating debris in the oceans is plastic and amounts are increasing each year. Plastic polymers in the marine environment are exposed to sunlight, oxidants and physical stress, and over time they weather and degrade. The degradation processes and products must be understood to detect and evaluate potential environmental hazards. Some attention has been drawn to additives and persistent organic pollutants that sorb to the plastic surface, but so far the chemicals generated by degradation of the plastic polymers themselves have not been well studied from an environmental perspective. In this paper we review available information about the degradation pathways and chemicals that are formed by degradation of the six plastic types that are most widely used in Europe. We extrapolate that information to likely pathways and possible degradation products under environmental conditions found on the oceans' surface. The potential degradation pathways and products depend on the polymer type. UV-radiation and oxygen are the most important factors that initiate degradation of polymers with a carbon-carbon backbone, leading to chain scission. Smaller polymer fragments formed by chain scission are more susceptible to biodegradation and therefore abiotic degradation is expected to precede biodegradation. When heteroatoms are present in the main chain of a polymer, degradation proceeds by photo-oxidation, hydrolysis, and biodegradation. Degradation of plastic polymers can lead to low molecular weight polymer fragments, like monomers and oligomers, and formation of new end groups, especially carboxylic acids.

/pdf/pathways-for-degradation-of-plastic-polymers-floating-in-the-110uao8lbz.pdf

Pathways for degradation of plastic polymers floating in the marine environment

The majority of commodity plastics and materials are derived from petroleum-based chemicals, illustrating the strong dependence on products derived from non-renewable energy sources. As the most accessible, renewable form of carbon (in comparison to CO2), lignocellulosic biomass (defined as organic matter available on a renewable basis) has been acknowledged as the most logical carbon-based feedstock for a variety of materials such as biofuels and chemicals. This Review focuses on methods developed to synthesize polymers derived from lignin, monolignols, and lignin-derived chemicals. Major topics include the structure and processing of lignocellulosic biomass to lignin, polymers utilizing lignin as a macromonomer, synthesis of monomers and polymers from monolignols, and polymers from lignin-derived chemicals, such as vanillin.

Strategies for the Conversion of Lignin to High-Value Polymeric Materials: Review and Perspective

http://www.if.ufrrj.br/biolig/art_citados/Physico-chemical%20characterization%20of%20lignins%20from%20different%20sources%20for%20use%20in%20phenol-formaldeyde%20resin%20synthesis.pdf

Physico-chemical characterization of lignins from different sources for use in phenol–formaldehyde resin synthesis

Towards lignin-based functional materials in a sustainable world

New cellulose–lignin hydrogels and their application in controlled release of polyphenols

Lignin role in a complex polyolefin blend

Unbleached and bleached Kraft cellulose pulp fibers modified with a long chain carboxylic acid, i.e. oleic acid in cold plasma conditions have been used as reinforcements in low density polyethylene (LDPE). The purpose of the modification is to enhance the interfacial adhesion between cellulose and matrix and to increase the dispersability. Composites containing up to 10 wt.% of untreated and modified cellulose pulp fibers with LDPE were prepared by melt mixing. The samples were characterized by processing behavior, mechanical and rheological properties, SEM, contact angle measurements, TGA and DSC. It was found that when the modified pulp fibers were incorporated into composites matrix, most of the properties have been improved.

Low density polyethylene composites containing cellulose pulp fibers

The polysaccharides are important materials in food, pharmaceutical, cosmetic and related biomedical applications. Xanthan gum is a microbial polysaccharide of great commercial significance. It is well known as one of the best thickening polymers due to its high intrinsic stiffness related to the helical conformation stabilized in the presence of excess salt. It is used in a wide variety of foods for a number of important reasons, including emulsion stabilization, temperature stability, compatibility with food ingredients, and its pseudoplastic rheological properties. Due to its properties in thickening aqueous solutions, as a dispersing agent, and stabilizer of emulsions and suspensions, xanthan gum is used in pharmaceutical formulations, cosmetics, and agricultural products, as well as in textile printing pastes, ceramic glazes, slurry explosive formulations, and rust removers. In this work the crosslinking of a mixture of xanthan and lignins in the presence of the epichlorohydrin, leading to superabsor...

Semi-interpenetrating Polymer Networks Containing Polysaccharides. I Xanthan/Lignin Networks

In the present study, the compatibility, properties and degradability of polyolefin/lignin blends have been studied. Blends of three maleic anhydride grafted copolymers of ethylene-propylene rubbers containing various content of functional groups with epoxy-modified lignosulfonate have been investigated by microscopy, X-ray diffraction, surface and mechanical indices determination, electron spin resonance, IR spectroscopy, differential scanning calorimetry and thermogravimetry. To assess the environmental degradation characteristics, the behavior of the blends during soil burial test has been investigated. The influence of the buried polymer blends on the physiological vegetative processes of the Vicia X hybrida hort plant has been monitored.

Polyolefin/Lignosulfonate Blends, 9

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