Biocomposites reinforced with natural fibers: 2000–2010

Adsorption of methylene blue on low-cost adsorbents: A review

Natural-based plasticizers and biopolymer films: A review

Heavy metal adsorption onto agro-based waste materials: A review

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 effects of coupling agents on the mechanical, morphological, and water sorption properties of luffa fiber (LF)/polypropylene(PP) composites were studied. In order to enhance the interfacial interactions between the PP matrix and the luffa fiber, three different types of coupling agents, (3-aminopropyl)-triethoxysilane (AS), 3-(trimethoxysilyl)-1-propanethiol (MS), and maleic anhydride grafted polypropylene (MAPP) were used. The PP composites containing 2–15 wt% of LF were prepared in a torque rheometer. The tensile properties of the untreated and treated composites were determined as a function of filler loading. Tensile strength and Young's modulus increased with employment of the coupling agents accompanied by a decrease in water absorption with treatment due to the better adhesion between the fiber and the matrix. The maximum improvement in the mechanical properties was obtained for the MS treated LF composites. The interfacial interactions improved the filler compatibility, mechanical properties, and water resistance of composites. The improvement in the interfacial interaction was also confirmed by the Pukanszky model. Good agreement was obtained between experimental data and the model prediction. Morphological studies demonstrated that better adhesion between the fiber and the matrix was achieved especially for the MS and AS treated LF composites. Atomic force microscope (AFM) studies also showed that the surface roughness of LFs decreased with the employment of silane-coupling agents.

/pdf/the-effect-of-fiber-surface-treatments-on-the-tensile-and-3pmnygmwaz.pdf

The effect of fiber surface treatments on the tensile and water sorption properties of polypropylene–luffa fiber composites

Dye adsorption behavior of Luffa cylindrica fibers.

https://gcris.iyte.edu.tr/bitstream/11147/1984/1/1984.pdf

Synergistic effect of natural zeolites on flame retardant additives

The effect of interfacial interactions on the mechanical properties of polypropylene (PP)/natural zeolite composites was investigated under dry and wet conditions. Interfacial interactions were modified to improve filler compatibility and mechanical properties of the composites by surface treatment of natural zeolite with a non-ionic surface modifier; 3 wt% polyethylene glycol (PEG) and three different types of silane coupling agents; 3-aminopropyltriethoxysilane (AMPTES), methyltriethoxysilane (MTES) and 3-mercaptopropyltrimethoxysilane (MPTMS), at four different concentrations (0.5–2 wt%). PP composites containing (2–6 wt%) zeolite were prepared by an extrusion technique. The tensile properties of the composites determined as a function of the filler loading and the concentration of the coupling agents were found to vary with surface treatment of zeolite. Silane treatment indicated significant improvements in the mechanical properties of the composites. According to the dry and wet tensile test results, the maximum improvement in the mechanical properties was obtained for the PP composites containing 1 wt% AMPTES treated zeolite. The improvement in the interfacial interaction was confirmed using a semi-empirical equation developed by Pukanszky. Good agreement was obtained between experimental data and the Pukanszky model prediction. Scanning electron microscopy studies also revealed better dispersion of silane treated filler particles in the PP matrix.

https://openaccess.iyte.edu.tr/bitstream/11147/1889/1/1889.pdf

The effect of interfacial interactions on the mechanical properties of polypropylene/natural zeolite composites

https://openaccess.iyte.edu.tr/bitstream/11147/1968/1/1968.pdf

Devrim Balköse

Papers

The effect of fiber surface treatments on the tensile and water sorption properties of polypropylene–luffa fiber composites

Dye adsorption behavior of Luffa cylindrica fibers.

Synergistic effect of natural zeolites on flame retardant additives

The effect of interfacial interactions on the mechanical properties of polypropylene/natural zeolite composites

Thermal stabilisation of poly(vinyl chloride) by organotin compounds