A review on flammability of epoxy polymer,cellulosic and non‐cellulosic fiber reinforced epoxy composites

Natural fiber is well‐known reinforcement filler in polymer‐matrix composites. Composite components like organic polymers and natural fibers are natural fire conductors as the natural fiber consists of cellulose, hemicellulose, and lignin, and hence are as highly flammable as wood. Natural fiber reinforced composite materials are progressively being used in a variety of applications where their fire response is a hazardous consideration, for example, in the automotive (transportation) and building‐construction industries. As a result, an awareness of their performance or response during a fire and the use of conventional fire retardants are of great importance, as they are subject to thermal decomposition when exposed to intensive high heat or fire sources. In this review paper, fire flammability is the main concern for cellulosic and non‐cellulosic fiber‐reinforced polymer composites, especially epoxy composites. This paper reviews the literature on the recent developments in flammability studies concerning polymers, epoxy polymers, cellulosic‐fibers, and non‐cellulosic fiber‐reinforced epoxy bio‐composites. The prime objective of this review is to expand the reach of “fire retardants for polymer materials and composites” to the science community, including physicists, chemists, and engineers in order to broaden the range of their applications. Copyright © 2015 John Wiley & Sons, Ltd.     

Cellulose--model films and the fundamental approach

This critical review describes the recent arrival of ultrathin films of cellulose. The methodology of preparation as well as the applications of the films for fundamental research is fully covered. The review places cellulose in a wider scientific context where cellulose research is no longer a field of interest for specialised scientists only. Cellulose and cellulosic materials should interest communities such as biochemists, physical chemists, surface chemists, organic chemists, polymer chemists and also physicists working close the disciplines mentioned. (149 references.).     

Investigating the mechanical performance deterioration of Mediterranean cellulosic cypress and pine/polyethylene composites

The synergy of the materials physical characteristics, performance and recyclability become vital for industrial sustainability. However, finding a suitable cellulosic fiber type to form potential cellulosic-based composite and investigating performance deteriorations are of paramount importance to expand sustainable design possibilities for various applications. In this work investigations of the mechanical performance deterioration of both Mediterranean cellulosic pine and cypress fibers are experimentally investigated. This was achieved by utilizing the fibers with polyethylene matrix to reveal their potential capabilities for industrial applications. Numerous composites with various parameters like fiber types, fiber loading, fiber size, and reinforcement conditions were designed to study several characteristics of the cellulosic composites, their mechanical performance deteriorations, as well as determining the optimal fiber loading condition for each particular studied mechanical property of the composites. Results demonstrate that mechanical properties are significantly changed with fiber loading. In addition, the failure mode in the high fiber loading composites is an obvious indication of the improper or ineffective load transfer between the matrix and the cellulosic fiber. Moreover, it is revealed here that the performance of cypress fibers with polyethylene matrix is much better than that of pine for the considered properties with reference to the neat polyethylene matrix. The overall performance of both types of fibers with polyethylene clearly demonstrates that the performance of cypress fibers is much better than that of pine for all considered properties.     

Ecofriendly Biocomposites from Natural fibers: Mechanical and Weathering study

Increasing environmental concerns and depletion of petroleum resources has forced researchers around the globe to find new green materials. In the present research work, a particular interest was focused on the effective use of lignocellulosic natural fibers as reinforcement using polymer resin as a novel matrix. Green composites were prepared using the compression molding technique with different fiber contents. The physicomechanical and thermal characteristics of the different composite samples were investigated as a function of fiber contents. The results obtained suggest that the properties of the polymer matrix are positively affected by the incorporation of natural cellulosic fibers.     

Mechanically-induced dimensional extensibility of fibers towards tough fiber networks

The beneficial effect of materials with high aspect ratio as composite reinforcement has prompted continuous interest towards cellulosic fibers. Besides providing stiffness, fibers can potentially contribute to composite extensibility. While mechanical treatments are typically used to adjust the physical and surface properties of fibers, less is known about ensuing effects on their extensibility and that of associated networks. Fiber network dimensional extensibility of 16% was achieved by processing the precursor aqueous fiber dispersions following a simple mechanical treatment with a judicious combination of low (PFI refining) and high concentrations and temperatures (Wing defibrator). Consequently, deformation of fibers and increased inter-fiber bonding resulted in a three-fold increase in strength to rupture of the fiber network leading to the structures with unprecedented toughness.     

From agricultural cellulosic waste to food delivery packaging: A mini-review

The growing food delivery service market has boosted the consumption of packaging materials, and this trend is projected to continue in the following years. The gap between industrial supply and consumer demand from a sustainable viewpoint leads to a need for agricultural cellulosic waste-based materials that bring the idea of trash-to-treasure to fruition. In this paper, we review up-to-date advancements surrounding the food delivery packaging that are derived from agricultural cellulosic waste. Two scenarios in which agricultural feedstock is used as a host or guest material are summarized, and sketch on the individual processing routine is depicted. We further evaluate how the chemical compositions and processing parameters influence the properties of the final products. Current challenges and gaps in developing sustainable packaging materials are identified, with perspectives on these important issues highlighting the importance of process innovation as well as economic and environmental-impact assessment for agricultural cellulosic waste to food delivery packaging.     

Materials chemistry and the futurist eco-friendly applications of nanocellulose: Status and prospect

Cellulose, a linear biopolymer, is present naturally in all plants. Apart from being the planet’s predominant natural polymer, it also offers a variety of features including excellent biocompatibility, lower density, substantial strength and the most beneficial mechanical characteristics, inexpensive in cost. Applying the mechanical or chemical techniques, cellulosic materials are transformed into cellulose nanofibres (CNFs) and even cellulose nanocrystals (CNCs). These CNFs and CNCs exhibit excellent capabilities in comparison with native cellulose fibre. Nowadays, nanocellulose is being used in a variety of practical applications such as product packaging, papers as well as paperboard, food sector, healthcare, hygiene products, paints, skin care products and sensors. The current review article summarizes the cellulose, processing methods for nanocellulose, techniques used for chemical modification of cellulose surface and consequently its application as reinforcement in polymeric materials. This article also provides a comprehensive discussion of the historical development in the area of nanocellulose.     

Preparation of cellulosic soft and composite materials using ionic liquid media and ion gels

Cellulose - Ionic liquids (ILs) are powerful media for the modification and functionalization of cellulose. This review article discusses the preparation of cellulosic soft and composite materials...     

Electrokinetic Investigations of Oriented Cellulose Polymers

Summary: Electrokinetic investigations of different cellulosic fibres were reviewed with special emphasis on polymer composite materials and textile applications of cellulose fibres. The possibilities in the interpretation of zeta-potential data regarding chemical and physical modification, specific adsorption, swelling and changes in hydrophobicity/hydrophilicity of cellulose polymers are discussed. Using recent data from literature, advantages and limitations of electrokinetic measurements of oriented polymers are described, finding that the zeta-potential is a valuable parameter in polymer surface characterisation.     

Paracrystalline lattice disorder in cellulose. I. Reappraisal of the application of the two-phase hypothesis to the analysis of powder x-ray diffractograms of native and hydrolyzed cellulosic materials

An examination of powder x-ray diffractograms of native and hydrolyzed cellulosic materials obtained from widely different sources revealed the presence of materials having a higher degree of molecular order than ramie hydrolyzate, the conventional crystalline standard for cellulose. With the use of these materials as new crystalline standards, a critical reappraisal has been made of the validity of the application of the two-phase (i.e., fringed-micelle) hypothesis to the fine structure of cotton and related cellulosic materials. It is concluded that the lattice structure of cotton and related celluloses of plant or bacterial origin is liquid-like or paracrystalline.     

Fiber-matrix interactions in cement mortar composites reinforced with cellulosic fibers

With the aim of gaining a better understanding of the phenomena responsible of the loss of durability of cement mortar composites reinforced with vegetable fibers, this paper focuses on the analysis of the fiber-matrix interactions. More specifically we analyze the effects of the vegetable fibers on the cementitious matrix after their mixture for different periods of time and vice versa. Three kinds of cellulosic fibers with differences on its physic-chemical properties were studied: bamboo fibers, kraft pulp and cotton linters. The results show that the cellulosic fibers modify the total amount of heat released during the hydration process in the cement paste, this effect differing depending on the purity of the fibers. The high alkalinity of the cementitious matrix causes the partial dissolution of chemical components of the fibers and a harmful precipitate of the inorganic particles on its surface and/or lumen, damaging the fibers and hence decreasing its reinforcement capacity.     

In situ synthesis of a Cu-BTC metal–organic framework (MOF 199) onto cellulosic fibrous substrates: cotton

A mechanism for chemical attachment and growth of a Cu-BTC Metal–Organic Framework, also known as MOF-199 or HKUST-1, onto cellulosic substrates is reported. Four different experimental procedures were attempted in order to elucidate the role of carboxylate groups on the anionic cellulose’s surface. The order of addition of Cu(OAc)₂—copper acetate, BTH3, 1,3,5-benzenetricarboxylic acid and TEA—Triethylamine was found to be a critical factor for the attachment and growth of the MOF-199 crystals onto anionic cellulose. The presence of MOF-199 crystals was probed using XRD and XPS spectra and a strong chemical interaction to the carboxymethylated cellulose fibers was confirmed by intense and vigorous washing of the specimens with water, DMF and methanol. Based on the recognized ability of MOF-199 to capture gases and toxic chemicals, combined with the availability of cellulose-based fibrous materials, the described procedure provides the basis for future fabrication of functionalized fibers and active filtration media.     

Graft Copolymerization of Acrylonitrile on Bleached Holocellulose

The mechanism by which ceric ions interact with cellulosic materials in the presence of vinyl monomers to initiate graft copolymer formation is generally believed to involve propagation by radicals generated on the cellulosic substrate [1–5]. However, the relatively high levels of homopolymerization and low efficiencies of grafting associated with graft copolymerization suggest that loci of initiation other than radicals formed on the cellulosic materials may be important in graft copolymerization [6].     

Hydrophilic–oleophobic coatings on cellulosic materials by plasma assisted polymerization in liquid phase and fluorosurfactant complexation

Materials with hydrophilic–oleophobic properties are of relevance due to their application to different fields such as self-cleaning coatings, liquid–liquid separation membranes and functional textiles for different technical applications. In this work, hydrophilic–oleophobic coatings have been deposited on cellulosic materials (filter paper and bleached cotton) by means of plasma assisted polymerization of acrylic acid solutions in water followed by cationic fluorosurfactant complexation. Chemical composition of the coatings on cellulosic materials was characterized by means of FTIR–ATR and XPS whereas their morphology was studied by SEM. Hydrophilic–oleophobic behavior was characterized by means of contact angle and wetting time. Additionally wetting properties of cationic, anionic and non-ionic surfactant solutions on the hydrophilic–oleophobic coatings were used to characterize the polyelectrolyte electrostatic forces upon the functionalized layer.     

Biodegradable Multiphase Systems Based on Plasticized Starch: A Review

Abstract

The aim of this review is to show the relationships between the structure, the process, and the properties of biodegradable multiphase systems based on plasticized starch (PLS), the so‐called “thermoplastic starch.” These mutiphase materials are obtained when associating association between plasticized starches and other biodegradable materials, such as biodegradable polyesters [polycaprolactone (PCL), polyhydroxyalkanoates (PHAs), polylactic acid (PLA), polyesteramide (PEA), aliphatic, and aromatic copolyesters], or agro‐materials (ligno‐cellulosic fiber, lignin etc.). Depending on materials (soft, rigid) and the plastic processing system used, various structures (blends, composites, multilayers) can be obtained. The compatibility problematic between these hetero‐materials is analyzed. These starchy products show some interesting properties and have some applications in different fields: packaging, sports, catering, agriculture and gardening, or hygiene.     

RAFT mediated polysaccharide copolymers

Graft copolymers were prepared using the RAFT process via a Z-group approach, where xanthate esters were formed directly on a cellulosic substrate. Grafting of vinyl acetate onto the modified cellulosic materials was then carried out via the reversible addition fragmentation chain transfer (RAFT) process. The xanthate RAFT agents on the backbone of the cellulosic materials were identified by Fourier-transform infrared spectroscopy (FT-IR) and ultraviolet-visible spectroscopy (UV-vis). The number average molar masses of the graft copolymers were determined using size exclusion chromatography (SEC) and further characterization was conducted via liquid adsorption chromatography (LAC). The chromatographic results showed that the modified cellulosic materials were successfully grafted with polyvinyl acetate in a controlled manner. Grafted polyvinyl acetate (on the surface) and nongrafted polyvinyl acetate (in the solution) have almost the same molar mass and polydispersity index.     

Polypropylene/Cellulosic Fiber Composites Chemical Treatment of the Cellulose Assuming Compatibilization Between the Two Materials

Abstract

The present work deals with the realization of composites with a polypropylene (PP) matrix and cellulosic fibers as reinforcement. In order to achieve a good adhesion with the PP matrix, the modification of different cellulosic fibers has been performed with various chemical functions: carboxylic anhydrides, isocyanates, vinylsulfone, and chlorotriazine systems. All these compatibilizing agents carry an alkyl chain or a PP chain. Grafting is evidenced by infrared and ESCA spectroscopies, and the grafting rates for the different chemicals are determined by microweighing measurements. Modification of the surface characteristics is followed by wettability tests and inverse gas chromatography. Determination of the water sorption isotherm for the treated fibers shows an important decrease in water regain in the case of isocyanate treatments in swelling medium. Enhancement of adhesion between fibers and the matrix is demonstrated by mechanical tests: the interfacial shear stress obtained by the microbond test increases by 70% for cellulosic fibers treated with maleated PP. This may be the result of entanglements between PP chains, but for macrocomposites the effect is much more limited due to the predominance of external factors during development of the composite.     

Free Radical–Induced Graft Copolymerization onto Natural Fibers

Surface modification of a natural cellulosic polymer system is required to improve the physicochemical properties of the fibers to be used as reinforcement for green composite applications. Surface modification through graft copolymerization improves the existing properties of the cellulosic fibers for a number of applications. Therefore, in the present study, an attempt was made to synthesize butyl acrylate (BA)-g-Saccaharum cilliare fibers using a redox initiator. Graft copolymers were characterized through FT-IR/SEM/TGA/DTA/DTG techniques, and the effect of grafting percentage on the water absorption properties of raw as well as grafted fibers was also investigated.     

Improvement of Fibre-Matrix-Adhesion of Natural Fibres by Chemical Treatment

Plastics, also called synthetic polymers, are playing an important role in daily living. To raise more applications it is necessary to modify known polymeric systems to reach improved materials/material systems. A possibility to create new optimised materials out of neat polymers is offered by compounding them with different filling material. Besides chemical modification of polymers, mixing, combining or use of different fillers, one possibility is given by the composite technique, whereas the combination of the polymeric matrix and the embedded reinforcement (e.g. fibre) are yielding in optimised materials adjusted to the required properties. Concerning the polymeric matrix, either thermoplastic or thermoset material can be used. In case of the reinforcement, either synthetic (carbon-, glass- or polymeric fibres) or natural fibres are introduced to composites. To obtain an appropriate adhesion of the matrix to the reinforcement system, synthetic fibres are equipped with an avivage. For natural fibres, there are no such materials available and the hydrophilic property of this system surface prevents an adhesion to hydrophobic polymers, as well as to sizings. In this paper, ways are shown to modify the natural fibres via chemical treatment to yield higher physical properties at better adhesion. Also we will explain activities on the use of natural fibres as reaction systems and processing tools as well as the attempt to isolate the different compounds of the neat fibre via selective work-up.     

Surface composition of alloys

The practical importance of alloy surfaces in catalysis, corrosion andother aspects of materials performance is widely recognized. What is needed now is sufficient knowledge of the relationship between externally controllable factors — alloy composition, temperature, environment — and surface properties — composition, structure, chemical activity — to control materials performance in these applications. Our purpose here is to review progress in determining and predicting the relationship between one surface property, composition, and certain externally controllable variables: overall composition, temperature, environment and physical form.We find that theoretical treatments of metal alloy surface composition now include essentially all significant physical effects and can predict values for most parameters of interest. Though improvements are still possible, the accuracy of predictions is more often limited by uncertainties or absence of the basic data for the calculations (e.g., thermochemical values) than by the models themselves.Alloy surface composition can now be measured well. The first monolayercomposition of large alloy slabs can be determined quantitatively over a wide temperature range in ultra-high vacuum. Difficulties with specimens of practical interest still challenge experimentalists. Among these are supported catalysts, surfaces under chemisorbed layers and composition of layers below the first. Significant progress is being made and we expect the next few years will see success.