Potential Application of Peppermint (Mentha piperita L.), German Chamomile (Matricaria chamomilla L.) and Yarrow (Achillea millefolium L.) as Active Fillers in Natural Rubber Biocomposites

In this study, peppermint (Mentha piperita L.), German chamomile (Matricaria chamomilla L.) and yarrow (Achillea millefolium L.) were applied as natural fibrous fillers to create biocomposites containing substances of plant origin. The purpose of the work was to investigate the activity and effectiveness of selected plants as a material for the modification of natural rubber composites. This research was the first approach to examine the usefulness of peppermint, German chamomile and yarrow in the field of polymer technology. Dried and ground plant particles were subjected to Fourier transmission infrared spectroscopy (FTIR) and UV–Vis spectroscopy, thermogravimetric analysis (TGA), goniometric measurements (contact angle) and scanning electron microscopy (SEM). The characterization of natural rubber composites filled with bio-additives was performed including rheometric measurements, FTIR, TGA, cross-linking density, mechanical properties and colour change after simulated aging processes. Composites filled with natural fillers showed improved barrier properties and mechanical strength. Moreover, an increase in the cross-linking density of the materials before and after the simulated aging processes, compared to the reference sample, was observed.     

Environmentally Friendly Polymer Compositions with Natural Amber Acid

Few scientific reports have suggested the possibility of using natural phenolic acids as functional substances, such as stabilizers for polymeric materials. The replacement of commercial stabilizers in the polymer industry can be beneficial to human health and the environment. The aim of this study was to obtain biodegradable composition of polylactide (PLA) and polyhydroxyalkanoate (PHA) with natural amber (succinic) acid. The materials were subjected to controlled thermooxidation and solar aging. The research methodology included thermal analysis, examination of surface energy, mechanical properties and spectrophotometric analysis of the color change after aging. The samples of aliphatic polyesters containing from 1 to 2 parts by weight of succinic acid were characterized by increased resistance to oxidation (DSC analysis). Natural acid, preferably at a concentration of 1–1.5 parts by weight, acted as a stabilizer in the polymer compositions. On the other hand, materials that had amber acid above 2 parts by weight added were more susceptible to oxidation (DSC). They also showed the lowest aging coefficients (K). The addition of acid at 2.5–4 parts by weight caused a pro-oxidative effect and accelerated aging. By adding amber acid to PLA and PHA, it is possible to design their time in service and their overall lifetime.     

Thermal properties and aging characteristics of chemically modified oil palm ash-filled natural rubber composites

The chemically modified oil palm ash (OPA) with the cetyltrimethylammonium bromide (CTAB) solution was prepared prior to compounding with the natural rubber and other curing ingredients. The aging resistance and thermal stability of CTAB-modified OPA-filled natural rubber composites were evaluated in the same manner as non-modified OPA samples. The retention tensile properties after thermal aging was measured and based on the result shown, the CTAB-modified OPA-filled natural rubber composites imparted insignificant effect to aging resistance as compared to the non-modified OPA-filled natural rubber composites at very low OPA loading; however, the effect became apparent beyond 3 phr OPA loading where the CTAB-modified OPA-filled natural rubber composites provided better aging resistance than the corresponding non-modified OPA-filled natural rubber composites. The thermogravimetric analysis indicated that the CTAB-modified OPA-filled natural rubber composites exhibited lower thermal stability which showed lower temperature at their respective weight loss and lesser char residue than that of non-modified OPA-filled natural rubber composites. This was attributed to the CTAB which started to decompose at the temperature of 210 °C. However, for the range from ambient temperature to 210 °C, the CTAB-modified OPA-filled natural rubber composites produce better thermal stability than those of non-modified OPA-filled natural rubber composites.     

Influence of a Natural Plant Antioxidant on the Ageing Process of Ethylene-norbornene Copolymer (Topas)

In the field of polymer technology, a variety of mainly synthetic additives are used to stabilize the materials during processing. However, natural compounds of plant origin can be a green alternative to chemicals such as synthetic polyphenols. An analysis of the effect of hesperidin on the aging behavior of ethylene-norbornene copolymer was performed. The evaluation of changes in the tested samples was possible by applying the following tests: determination of the surface energy and OIT values, mechanical properties analysis, colour change measurements, FT-IR and TGA analyses. The obtained results proved that hesperidin can be effectively used as natural stabilizer for polymers. Furthermore, as a result of this compound addition to Topas-silica composites, their surface and physico-mechanical properties have been improved and the resistance to aging significantly increased. Additionally, hesperidin can act as a dye or colour indicator and only few scientific reports describe a possibility of using flavonoids to detect changes in products during their service life, e.g., in food packaging. In the available literature, there is no information about the potential use of hesperidin as a stabilizer for cycloolefin copolymers. Therefore, this approach may contribute not only to the current state of knowledge, but also presents an eco-friendly solution that can be a good alternative to synthetic stabilizers.     

Direct Observation of Triplet Reactions of Anthraquinone Vat Dyes Using Nanosecond Laser Photolysis

The triplet-triplet spectra of three commercial anthraquinone vat dyes (C.I. 67300, C.I. 59100 and C.I. 60515) were studied in solution at room temperature using laser photolysis. The triplet states of these dyes react with oxygen, and the rate constants for the quenching process were measured, together with the rates of energy transfer from the triplet state to anthracene. These observations are considered in relation to the photoreactivity of these dyes.     

A comparison between the static and fatigue properties of glass‐fiber and carbon‐fiber reinforced polyetherimide composites after prolonged aging

The static and fatigue behavior of two fiber‐reinforced composites was characterized after samples were subjected to both natural and accelerated aging. The composites consisted of a thermoplastic matrix (PEI: polyetherimide) reinforced with glass or carbon fabric. Natural aging involved exposing samples to the elements over a period of two years, while accelerated aging was conducted in a saline solution during 200 days. Subsequently, static (tensile and interlaminar shear) and fatigue tests were carried out with the aim of determining the mechanical properties of the materials after exposure. A negligible decrease in the value of these properties was observed, while different behavior was detected depending on the type of aging of the material.     

In situ generation of sulfur using silica as a carrier in the wet mixing of natural rubber latex

Using sodium thiosulfate and hydrochloric acid as the raw materials and a silica aqueous dispersion as the carrier, sulfur is generated in situ by a chemical precipitation method, and an in situ sulfur-silica/natural rubber (in situ S-Silica/NR) composite is prepared. The in situ sulfur is characterized, and its effects on the natural rubber composites' cross-linking density, vulcanization characteristics, mechanical properties, aging properties, dynamic mechanical properties, and Payne effect are studied. The experimental results show that the particle size of in situ sulfur is small, with a maximum of 5 μm, and the cross-linking ability is stronger than commercial sulfur. Due to the strong surface adsorption force of silica, the interfacial bonding strength is enhanced, and the dispersion of the two components in the rubber matrix is improved. Compared with commercial sulfur-silica/natural rubber (S-Silica/NR) composites, the tensile strength is 20.3% higher, the elongation at break is 28.5% higher, and it better retains its aging properties and has a lower rolling resistance. This study provides a theoretical basis for the development of functional rubber vulcanizing agents and the preparation of high-performance rubber composites.     

A review on the processing–morphology–property relationship in biodegradable polymer composites containing carbon nanotubes and nanofibers

Carbon nanofillers containing biodegradable polymer composites have become an emerging frontier in materials science and engineering because of their potential as environmentally friendly materials in multiple applications, from load-bearing to advanced packaging to biomedical applications. Herein, we present the effect of processing parameters on the final morphology and the resulting properties of the biodegradable polymer composites containing carbon nanotubes (CNTs) or carbon nanofibers (CNFs). Various strategies can be employed to develop such composites; however, the type of morphology, which results during processing, significantly affects the final properties of the obtained composites. Therefore, various processing strategies such as melt-blending, additive manufacturing, and electrospinning are critically reviewed, together with the potential applications in load-bearing, tissue engineering, electromagnetic shielding, gas sensing, and packaging. Finally, we discuss the existing challenges and future directions in designing CNTs/CNFs containing biodegradable polymer composites with desired properties.     

Thermal Aging Properties of Graphite Fiber Reinforced Peek and Graphite Fiber Reinforced Bmi Composites

Graphite fiber reinforced poly(ether ether ketone) (PEEK) and graphite fiber reinforced bismaleimide (BMI) composite materials are two kinds of advanced fiber-reinforced polymer matrix composites with good thermal stability and excellent mechanical properties at high temperature. They are currently receiving considerable attention. the main limitation on their application is the lack of knowledge regarding their behaviors during extended use at high temperature. Thermal aging properties are the main parameters for new polymer matrix composites that will be used in advanced spacecraft structural components. From the results of thermal aging effects on the properties—including interlaminar shear strength, drop-weight impact strength, and impact energy—of graphite/PEEK and graphite/BMI composites, it is found that unidirectional graphite fiber reinforced composites retain higher strength compared to multidirectional, and that multidirectional graphite/PEEK composites keep higher property retentions than multidirectional graphite/BMI composites after thermal aging at 190°C. From scanning electron photomicrographs, it is also found that graphite/PEEK composites have better fiber/resin adhesion, intraply adhesion, and microcrack resistance compared to graphite/BMI composites after thermal aging.     

Plant-Origin Stabilizer as an Alternative of Natural Additive to Polymers Used in Packaging Materials

Over the past 25 years, cannabis plants have gained major popularity in the research community. This study aimed to evaluate the antioxidant capacity and stabilization efficiency of cannabidiol (CBD) extract in two different polymers: polylactide (PLA) and ethylene–norbornene copolymer (Topas) that are used in packaging materials more often. The research technology included weathering in a special chamber, surface free energy and color change measurements, surface morphology and Fourier-transform infrared spectroscopy (FTIR) analysis, thermogravimetry, and determination of the oxidation induction time or temperature (OIT) values, based on which the effectiveness of the cannabidiol extract could be estimated. Obtained results showed that the addition of CBD to polymer mixtures significantly increased their resistance to oxidation, and it can be used as a natural stabilizer for polymeric products. Moreover, samples with cannabidiol changed their coloration as a result of weathering. Therefore, this natural additive can also be considered as a colorimetric indicator of aging that informs about the changes in polymeric materials during their lifetime. On the other hand, surface properties of samples with cannabidiol content did not alter much compared to pure Topas and PLA.     

Sugarcane bagasse ash as a reinforcing filler in thermoplastic elastomers: Structural and mechanical characterizations

The incorporation of residues as reinforcing fillers in polymer composites has emerged as a viable solution, enabling improvements in the mechanical properties of these materials, and has also resulted in a reduction in the cost of the final product. In this work, sugarcane bagasse ash (SBA) was used as a reinforcing filler in comparison with commercial silica (CS) in thermoplastic elastomers prepared from the compatibility of low‐density polyethylene (LDPE) with natural rubber (NR). The composites were obtained by a physical mixture of LDPE and NR with different proportions of CS and SBA using a Haake rotational rheometer. The samples were analyzed by Raman spectroscopy, Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and tensile testing. The results show that SBA has similar properties to CS, thus making its use feasible as a reinforcing filler in thermoplastic elastomers. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41466.     

Photofading of anthraquinone disperse dyes in epoxy resin films: Photoreduction,energy transfer and photostabilisation processes

The photofading of three anthraquinone disperse dyes, 1- and 2-piperidino- and 1-hydroxy-4-(p-toluidino)-anthraquinone has been examined in a number of epoxy resin systems using UV-visible absorption spectroscopy. Compared with a relatively inactive polymer system such as cellulose triacetate the epoxy resins accelerate photofading through a reduction mechanism, which is, in turn, dependent on the structure of the dye and functionality of the hardener. A number of stabiliser systems are examined on the fading rate of one of the dyes and one of them, an N-oxy radical, is highly effective in inhibiting photoreduction. A regenerative mechanism involving the hydroxylamine is discussed. Evidence for a triplet-to-singlet energy transfer process from the polymer to the 2-piperidino derivative is also presented.     

Dynamic mechanical study of epoxy,epoxy/glass,and glass/epoxy/wood hybrid composites aged in various media

It was proposed and subsequently established that wrapping of red oak wood crossties with epoxy impregnated glass fiber composites will impart longer service life and better stiffness and strength characteristics to these hybrid ties than conventional ones and will help them better withstand environmental extremes. The objective was to understand the degrading effects of aqueous (distilled water), saline (NaCl), acidic (HCl), and alkaline (NaOH) solutions, as well as accelerated aging and freeze/thaw cycling environments on the dynamic and static mechanical properties of these hybrid materials (i.e., wood, wrapped with fiber reinforced resin) and their components. Also micrographs of composite samples, obtained through scanning electron microscopy (SEM), were studied to determine the failure mechanism of composite specimens aged in different environments. Results showed that immersion in aging media lowered the glass transition temperature (T_g) and enhanced apparent phase separation in the samples because of polymer plasticization. In water immersion, the T_g and the stiffness increased with time owing to continued resin curing. At ambient temperature, sustained load had little effect on the mechanical behavior of the aged samples. The extent of degradation was the least for samples aged in salt solution. Soaking in room‐temperature acid solution was most damaging to pure red oak wood samples. Six‐cycle aging did not damage the neat resin or the hybrid samples, whereas it damaged pure wood specimens. Therefore, the composite wrapping around the wood core of the hybrid sample protected it sufficiently, thereby preventing damage to the hybrid specimen during the aging process. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers     

Raw and chemically treated bio-waste filled (Limonia acidissima shell powder) vinyl ester composites: Physical,mechanical, moisture absorption properties,and microstructure analysis

The rapid growth of environmentally sustainable and eco-friendly materials tends to the utilization of biowastes as filler in polymer matrix composites. The particulate composite with improved wettability of fillers and advanced approach can evolve polymer composites that exhibit promising applications in packaging, automobile, marine, construction, and aerospace. In the present work, one of the biowaste fillers were synthesized from Limonia acidissima shells via a top-down approach (pulverizing) and the surfaces were chemically modified using sodium hydroxide (NaOH) before they were used as fillers in vinyl ester polymer composites by different weight percentage (0, 5, 10, 15, and 20 wt%). The prepared particulate composites were characterized by mechanical properties, moisture absorption behavior, and morphology. At different filler loading the tensile strength, tensile modulus, flexural strength, flexural modulus, impact strength, hardness, density, and moisture intake tests were performed. The results reveal that the properties increased for composites filled with alkaline treated fillers for the same filler loading and found to be higher at filler loading of 15 wt%. The morphological analysis confirms the better interfacial bonding between alkali-treated particles and matrix due to the removal of non-cellulose materials from the surface of the particles.     

Recent advances in vegetable oil-based polymers and their composites

The development of viable alternatives to petroleum-based polymeric materials is a compelling contemporary challenge attributable to environmental concerns and the effects of fluctuating oil prices. Triglycerides, the primary components of vegetable oils, are an abundant, renewable, and widely investigated alternative feedstock for polymeric materials. Efforts are made on a global scale to develop innovative technologies to transform these natural resources into novel monomers and polymers. Some of these technologies have already generated competitive industrial products with properties comparable to conventional petrochemical polymers. Fillers and fibers have also been incorporated into these bio-based polymer matrices to improve the physical and thermal-mechanical properties of the resulting composite materials. The development of multifunctional composite materials facilitates the application of these materials in new areas, e.g., sensors, structural parts, medical device, construction units, flame retardant parts. This article reviews recent advances in polymeric materials from vegetable oils in terms of preparation, characterization, and properties. Nano-composites and fiber reinforced composites based on bio-polymers matrices will also be reviewed. This chapter will conclude with an overview of current and potential future applications of these materials in packaging, automotive, construction, electrical, and medical devices.     

Properties and Degradation of Novel Fully Biodegradable PLA/PHB Blends Filled with Keratin

The utilization of keratin waste in new materials formulations can prevent its environmental disposal problem. Here, novel composites based on biodegradable blends consisting of poly(lactic acid) (PLA) and poly(3-hydroxybutyrate) (PHB), and filled with hydrolyzed keratin with loading from 1 to 20 wt % were prepared and their properties were investigated. Mechanical and viscoelastic properties were characterized by tensile test, dynamic mechanical thermal analysis (DMTA) and rheology measurements. The addition of acetyltributyl citrate (ATBC) significantly affected the mechanical properties of the materials. It was found that the filled PLA/PHB/ATBC composite at the highest keratin loading exhibited similar shear moduli compared to the un-plasticized blend as a result of the much stronger interactions between the keratin and polymer matrix compared to composites with lower keratin content. The differences in dynamic moduli for PLA/PHB/ATBC blend filled with keratin depended extensively on the keratin content while loss the factor values progressively decreased with keratin loading. Softening interactions between the keratin and polymer matrix resulted in lower glass transitions temperature and reduced polymer chain mobility. The addition of keratin did not affect the extent of degradation of the PLA/PHB blend during melt blending. Fast hydrolysis at 60 °C was observed for composites with all keratin loadings. The developed keratin-based composites possess properties comparable to commonly used thermoplastics applicable for example as packaging materials.     

Influence of Graphite Filler on Physicochemical Characteristics of Polymer/Graphite Composites: A Review

In this article, carbon nanofiller, in particular graphite, has been reviewed for the preparation of polymer-based composites. The dispersion of graphite relies on fabrication methods employed such as solution mixing, melt blending, and in situ polymerization. The consequences of surface modification on thermal, mechanical, and electrical characteristics were explored. Moreover, the properties and parameters involved in feature enhancement of graphite-based materials have been highlighted. Topical development in field of thermal, mechanical, and other physical properties of polymer/graphite composites was investigated. Furthermore, worth of materials regarding electrodes, resistors, dye-sensitized solar cells, electromagnetic interference shielding, packaging, and flame retardant applications has been discussed.     

Preparation of an ecofriendly chitosan–ZnO composite for chromium complex dye adsorption

Three chitosan‐ZnO composites were prepared by the chitin deacetylation process using zinc chloride as source material and sodium hydroxide as precipitant. The physical characteristics of chitosan‐ZnO composites were studied using Fourier Transform infrared spectroscopy and scanning electron microscopy. The adsorption of a chromium complex dye onto commercial chitosan, prepared chitosan and chitosan‐ZnO composites was investigated in aqueous dye solution. Dye calibration was carried out by UV‐vis spectroscopy. The calculated dye adsorption values for commercial chitosan, prepared chitosan, and chitosan‐ZnO composite samples are 0.0086, 0.0137, and 0.0214 mg/g respectively, indicating that the chitosan‐ZnO composites have better dye adsorption capacity than commercial chitosan and prepared chitosan. The experimental isotherm data for the composites fitted the Langmuir isotherm model well. Thus, the chitosan‐ZnO composites can be used as an effective biosorbent for the removal of anionic dyes.     

Effects of benzoyl peroxide on some properties of composites based on hemp and natural rubber

The obtaining and characterization of polymer composites based on natural rubber and hemp, in which the elastomer crosslinking has been achieved with benzoyl peroxide, are presented. The mechanical characteristics, gel fraction, crosslink density, water uptake swelling parameters and FTIR of the composites based on natural rubber and hemp fiber vulcanized by dibenzoyl peroxide have been investigated as a function of the hemp content. The hardness, modulus at 100 % elongation, tearing strength, tensile strength and elongation at break have been improving with the increasing of fiber content in composites materials due to the better interaction of fiber in natural rubber composites. These results indicate that hemp has a reinforcing effect on natural rubber. Gel fraction value is over 95 % for all blends and varies irregularly depending on the amount of hemp in the composites. The crosslinking density (ν) of samples increases as the amount of hemp in blends increases, because hemp act as a filler in natural rubber blends and leads to reinforcement of the blends. The water uptake and swelling parameters also increases with the increasing of the amount of fiber content, because of the hemp hydrophilic characteristics.     

Covalently linked biocompatible graphene/polycaprolactone composites for tissue engineering

Two synthesis routes to graphene/polycaprolactone composites are introduced and the properties of the resulting composites compared. In the first method, mixtures are produced using solution processing of polycaprolactone and well dispersed, chemically reduced graphene oxide and in the second, an esterification reaction covalently links polycaprolactone chains to free carboxyl groups on the graphene sheets. This is achieved through the use of a stable anhydrous dimethylformamide dispersion of graphene that has been highly chemically reduced resulting in mostly peripheral ester linkages. The resulting covalently linked composites exhibit far better homogeneity and as a result, both Young’s modulus and tensile strength more than double and electrical conductivities increase by ≈ 14 orders of magnitude over the pristine polymer at less than 10% graphene content. In vitro cytotoxicity testing of the materials showed good biocompatibility resulting in promising materials for use as conducting substrates for the electrically stimulated growth of cells.