Enhanced physico-mechanical properties of polyester resin film using CaCO<Subscript>3</Subscript> filler

Bio-based CaCO₃ powder was synthesized via size reduction method from waste eggshells. The XRD analysis revealed that eggshell powder consists of CaCO₃ in calcite form. The inclusion level of CaCO₃ contents were varied of 5, 10, 15, 20 and 25 wt.% of prepared CaCO₃-polyester film. Effects of different proportions of prepared chicken eggshell and commercial CaCO₃ filler on the polyester resin composites films were compared by means of mechanical and physical test. It was found that the addition of CaCO₃ filler to the polyester films leads to improve the mechanical properties. The findings revealed that the best and optimum CaCO₃ filler content was 10 wt.% and among the prepared polyester films, eggshell CaCO₃-polyester films showed the best performance. The mechanical properties of CaCO₃-polyester films were measured in terms of tensile strength, elongation-at-break, tensile modulus, flexural strength and impact strength. For eggshell CaCO₃- polyester films, the maximum values of the aforementioned mechanical properties were 52.70 MPa, 4.63 %, 1868.70 MPa, 101.20 MPa and 8.40 kJ/m², respectively, whereas for commercial CaCO₃-polyester films those values were 48.12 MPa, 4.50 %, 1790.30 MPa, 97.50 MPa and 8.21 kJ/m², respectively. Further, water absorption of the composite films as a function of time had also been investigated at 10 wt.% filler content.     

Thermal and mechanical properties of modified CaCO3 filled poly (ethylene terephthalate) nanocomposites

Poly(ethylene terephthalate) (PET)/CaCO₃ and PET/modified-CaCO₃ (m-CaCO₃) nanocomposites were prepared by melt blending. The morphology indicated that m-CaCO₃ produced by reacting sodium oxalate and calcium chloride, was well dispersed in PET matrix and showed good interfacial interaction with PET compared to CaCO₃. No significant differences in the thermal properties such as, glass transition, melting and degradation temperatures, of the nanocomposites were observed. The thermal shrinkage of PET at 120 °C was 10.8 %, while those of PET/CaCO₃ and PET/m-CaCO₃ nanocomposites were 2.9–5.2 % and 1.2–2.8 %, respectively depending on filler content. The tensile strength of PET/CaCO₃ nanocomposite decreased with CaCO₃ loading, whereas that of PET/m-CaCO₃ nanocomposites at 0.5 wt% loading showed a 17 % improvement as compared to neat PET. The storage modulus at 120 °C increased from 1660 MPa for PET to 2350 MPa for PET/CaCO₃ nanocomposite at 3 wt% loading, and 3230 MPa for PET/m-CaCO₃ nanocomposite at 1 wt% loading.     

Effect of CaCO3 contents on the properties of polyethylene nanocomposites sheets

Nanocomposites of high-density polyethylene/linear low-density polyethylene (HDPE/LLDPE) filled with untreated and surface treated nano-calcium carbonate (nCC) were prepared. The influence of isopropyl tri-(dioctylpyrophosphato) titanate (JN114) treatment of nCC on the morphology, mechanical, crystallization and flow properties of the nanocomposites were studied. The results of scanning electron microscopy (SEM) showed that JN114 treated nCC was better dispersion in the matrix than the untreated one. A fine dispersion of the treated nanoparticles in the nanocomposites was observed by transmission electron microscopy (TEM). The FTIR spectrum analysis revealed that the JN114 could change the surface properties of nCC, resulting in greater hydrophobicity of the surface and enhanced compatibility with nonpolar matrices. The tensile elastic modulus (E _c ) and Izod impact strength (SIC) of nanocomposites increased with the increasing of nCC content while tensile fracture strength (σ _b ) decreased. The JN114 treated nanocomposites had superior mechanical properties to those of the untreated ones. The compatibility of these nanocomposites was examined by DSC to estimate melting point (T _m ) and crystallization temperature (T _c ). Furthermore, the melt flow index (MFI) of the nanocomposite materials were measured. It was found that the MFI decreased with the addition of weight fraction of the nCC particles.     

Nano-SiO2 filled rice husk/polypropylene composites: Physico-mechanical properties

In this research, reinforcing effect of hybrid filler including rice husk (RH), beech bark (BB) and nano-SiO₂, in polypropylene has been investigated. In the sample preparation, four levels of filler loading were used for waste lignocellulosic materials (55-58 wt.%) and nano-SiO₂ (0-4 wt.%). In order to increase the interphase adhesion, polypropylene grafted with maleic anhydride was added as a coupling agent to all the composites studied. The physical properties, viz. the thickness swelling and water absorption, and mechanical properties, namely, the tensile, flexural and notched Izod impact strengths, of the composites were determined. Generally, high amount of filler content in composites can lead to the reduction of interfacial adhesion between matrix polymer and filler, and it limits their applications. The results showed that while flexural properties and elongation at break were moderately improved by the increase in the amount of filler in the matrix, tensile and Izod impact strengths decreased dramatically. However, the composites had acceptable mechanical strength levels. The mechanical properties of composites filled with RH are generally greater than BB composites. The thickness swelling and water absorption of the composites increased with the increase in the filler loading, but to a negligible extent as compared with the wood-based composites and the solid woods. Nano-SiO₂ addition showed little positive effect on the mechanical properties. It can be concluded from this study that the used waste lignocellulosic materials are attractive reinforcements from the standpoint of their physico-mechanical properties.     

Preparation of collagen fiber/CaCO3 hybrid materials and their applications in synthetic paper

The collagen fiber/CaCO₃ hybrid materials were successfully prepared via in situ organic-inorganic hybrid technique. The surface morphology, hybrid mechanism, thermal and hydrothermal stability of these materials were investigated, respectively. Scanning electron microscopy (SEM) analysis showed that the size scale and distribution of CaCO₃ particles in collagen fiber relied on the concentration of CaCl₂. When the CaCl₂ was at low concentration, for example 6 wt%, the in-situ produced CaCO₃ particles were distributed evenly around the collagen fiber, the particle size could be controlled in the range of 2–4 µm and no apparent coagulation of CaCO₃ particles was found. Fourier transform infrared spectroscopy (FTIR) study revealed the interactions between the collagen fiber and CaCO₃ particles. The water solubility test and TGA analysis indicated that the solubility of collagen fiber in hot water decreased significantly after hybridization with CaCO₃ particles, whereas, the decomposition temperature was improved with increasing of the production of CaCO₃ particles. Moreover, the hybrid materials were used in conjunction with polyurethane and CaCO₃ powder to fabricate a novel synthetic paper. The result showed that the synthetic paper had good writing and printing.     

Influence of synergism caused by organic montmorillonite and nanometer calcium carbonate on mechanical properties and crystallization of polyamide 1010-based composites

This account showed that nanometer-active calcium carbonate (CaCO₃) improved polyamide 1010/organic montmorillonite (OMMT) composites and OMMT boosted polyamide 1010/CaCO₃. The mechanical performance suggested the composites to be reinforced through adsorption forces present between the nanofillers and the matrix. The synergistic effect of CaCO₃ and OMMT increased the yields and shrunk cavities when observed by scanning electron microscopy. The obvious resulting synergism was verified by X-ray scattering techniques after the addition of OMMT. The concentration of CaCO₃ did not change lamellar-size or influence the crystal growth. The effect of CaCO₃ on melting behavior was found less significant than that exert on crystallization behavior.     

Fabrication and characterization of nano Al<Subscript>2</Subscript>O<Subscript>3</Subscript> filled PVA:NH<Subscript>4</Subscript>SCN electrolyte nanofibers by electrospinning

Present paper reports a method of preparing polymer composite electrolyte nanofiber mat using polyvinyl alcohol (PVA), ammonium thiocynate (NH₄SCN) salt, and aluminium oxide (Al₂O₃) nano particles based on electrospinning technique. Two-stage process of preparation of nanofibers, namely, preparation of nano particles filled PVA electrolyte gel solution followed by its electrospinning has been used. The so obtained nanofibers have been characterized by XRD, DSC, SEM, and Conductivity measurements. XRD patterns affirm the formation of nanocomposite while SEM pictures reveal formation of fibers on a nano scale format (300–800 nm). Fibers of the electrolytes are seen to be thermally stable. Ionic conductivity of electrolyte fiber is seen to improve in the presence of nano filler at room temperature with a maximum at 5.31×10⁻³ Scm⁻¹ for 4 wt% filler concentration, which is comparable to that for corresponding dried gel electrolyte films.     

Mechanical and rheological properties of calcium carbonate-filled ethylene propylene diene elastomer reinforced by metallic acrylate salt

High performance ethylene propylene diene methylene elastomer (EPDM)/calcium carbonate (CaCO₃)/aluminum triacrylate (ALTA) hybrids have been prepared by a melt compounding process. The mechanical properties of the peroxide cured EPDM/CaCO₃/ALTA vulcanizates were investigated by tensile, hardness, resilience, abrasion and fatigue life tests. The results showed that the ALTA can greatly improve the modulus at 100 %, tensile strength, abrasion resistance and fatigue life of the EPDM/CaCO₃/ALTA vulcanizates, while retaining their high elongation at break. ALTA as a reactive filler had accelerating effect on the vulcanization reaction of and increased the crosslink density of the EPDM/CaCO₃ composites. This phenomenon is due to increasing the ionic bonds arise from both homo-polymerization of ALTA and graft co-polymerization of it onto the EPDM. Scanning electron microscopy (SEM) revealed the presence of ALTA causes to the roughness of the fracture surface of CaCO₃-filled EPDM compounds demonstrating high interaction between the fillers and EPDM improved by introduction of ALTA. Dynamic mechanical analysis revealed that the glass transition temperature (T _g ) and dissipation peak (tan δ) of EPDM composites decreases with increasing ALTA content. Decrease in tan δ value and inward shifting of T _g were related to improved interaction of filler and EPDM.     

Controlling the Properties of OPEFB/PLA Polymer Composite by Using Fe<Subscript>2</Subscript>O<Subscript>3</Subscript> for Microwave Applications

Microwave-absorptive polymer composite materials provide protection against interference to communication systems caused by microwave-inducing devices. Microwave-absorptive polymer composites were prepared from polylactic acid (PLA) biocomposite blended with oil palm empty fruit bunch (OPEFB) fiber and commercial Iron oxide (Fe₂O₃) as filler using the melt-blending method. The composites characterization was carried out using the scanning electron microscopy (SEM) and X-ray diffraction (XRD) analyses. The coefficient of reflection S₁₁ and coefficient of transmission S₂₁ of the composites for various Fe₂O₃ filler percentages were determined using a rectangular waveguide in connection with microwave vector network analyser (HP/Agilent model PNA N5227). These coefficients were then used to calculate microwave-absorption properties (in decibels). XRD analysis showed that increasing amounts of reinforced material (Fe₂O₃) reduces the crystallinity of the composites. SEM data indicated that Fe₂O₃ filler ratio increased in the composites, and adhesion to the cellulose fiber grew gradually until the highest percentage of filler was added. The complex relative permittivity and relative permeability were obtained within the broad frequency range of 8–12 GHz at room temperature for various percentages of filler and were measured by the transmission/reflection method using a vector network analyser. Fe₂O₃ embedment in OPEFB/PLA was observed to have resulted in enhancing the dielectric and magnetic properties. The values of permittivity and permeability increased with increasing Fe₂O₃ filler content. Theoretical simulation studied the relation between ε′ and ε″ of the relative complex permittivity in terms of Cole-Cole dispersion law. The result indicated that the processes of Debye relaxation in Fe₂O₃/OPEFB/PLA, the unique dielectric characteristics of Fe₂O₃ cannot be accounted for by both the Debye dipolar relaxation and natural resonance. Results further showed that the material transmission, reflection, and absorption properties could be controlled by changing the percentage of Fe₂O₃ filler in the composites.     

Evaluating the Mechanical Behavior of Basalt Fibers/Epoxy Composites Containing Surface-modified CaCO<Subscript>3</Subscript> Nanoparticles

Polymer matrix composites (PMCs) owing to their outstanding properties such as high strength, low weight, high thermal stability and chemical resistance are broadly utilized in various industries. In the present work, the influence of silanized CaCO₃ (S-CaCO₃) with 3-aminopropyltrimethoxysilane (3-APTMS) coupling agent at different values (0, 1, 3 and 5 wt.% with respect to the matrix) on the mechanical behavior of basalt fibers (BF)/epoxy composites was examined. BF-reinforced composites were fabricated via hand lay-up technique. Experimental results from three-point bending and tensile tests showed that with the dispersion of 3 wt.% S-CaCO₃, flexural strength, flexural modulus, tensile strength and tensile modulus enhanced by 28 %, 35 %, 20 % and 30 %, respectively. Microscopic examinations revealed that the development of the mechanical properties of fibrous composites with the incorporation of modified CaCO₃ was related to enhancement in the load transfer between the nanocomposite matrix and BF as well as enhanced mechanical properties of the matrix part.     

Sound absorption properties of spiral vane electrospun PVA/nano particle nanofiber membrane and non-woven composite material

In this research, we fabricated a series of PVA membranes loaded with 0 wt.%, 1 wt.%, 3 wt.%, 5 wt.% ZrC and 0 wt.%, 1 wt.%, 3 wt.%, 5 wt.% TiO₂ using a spiral vane electrospun machine respectively. There were 2 sizes of TiO₂ nano particles: 10 nm and 200 nm. We tested sound absorption properties of needle-punched nonwovens as well as the composite of nano membranes and needle-punched nonwovens by an impedance tube at the frequency range from 500 Hz to 6500 Hz. Besides, we tested morphological characterization of nano membranes by scanning electron microscope (SEM) and crystalline properties by X-ray diffraction (XRD). We investigated the sound absorption properties of composites as well as the effect of ZrC, TiO₂, nano particle sizes and cavity depth on sound absorption properties. Results showed that sound absorption properties of composites increased at the whole range of frequency compared to those of needle-punched nonwovens. When loaded with ZrC nano particles, sound absorption properties of composite shifted to a higher frequency region, and with increasing content of ZrC, sound absorption properties were better above 2500 Hz. However, when loaded with TiO₂, sound absorption properties were better at lower frequency. With 3 wt.% TiO₂, sound absorption coefficient reached the best at the frequency range from 500 Hz to 1500 Hz. Besides, 200 nm TiO₂ was more conductive to the increase of sound absorption properties at lower frequency region compared to 10 nm TiO₂. Sound absorption properties of composites with air back cavity shifted to a lower frequency region, too. SEM showed that there was nano particle aggregation when loaded TiO₂ nano particles. XRD showed that ZrC nano particles loaded in PVA nano fiber retained their crystalline structure while TiO₂ didn’t. It appeared from the results that nano particles had an effect on sound absorption materials, with different kinds and different sizes, sound absorption properties will improve in different ranges of frequency     

Effect of calcium carbonate nanoparticles on barrier properties and biodegradability of polylactic acid

In this study, the effect of calcium carbonate (CaCO₃) nanoparticles on the barrier properties and biodegradability of polylactic acid (PLA) was investigated. For this purpose, nanocomposite films with various CaCO₃ nanoparticle contents (0, 3, 5, 10, and 15 wt%) were prepared by solution casting method. The gas permeability of nitrogen (N₂), oxygen (O₂), and carbon dioxide (CO₂) was evaluated through a constant volume and variable pressure apparatus at different pressures and temperatures. According to results, barrier properties were improved by loading CaCO₃ nanoparticles up to 5 wt%, and the gas permeability of CO₂, O₂, and N₂ was decreased from 1.4, 0.31, and 0.07 Barrer to 0.48, 0.095, and 0.019 Barrer, respectively. In addition, it was also observed that the gas permeability of samples was decreased by increasing feeding pressure and increased by enhancing temperature. Furthermore, morphological results confirmed the formation of agglomerations and large clusters over 5 wt% CaCO₃ nanoparticles. Finally, the thermal properties and biodegradability of PLA were increased by employing CaCO₃ nanoparticles. These results suggested PLA nanocomposites as favorable candidates for food packaging applications.     

Mechanical and Dynamic Mechanical Studies on Epoxy-Cobaltous Sulfate Polymer Hybrids

Cobaltous sulfate heptahydrate (CoSO₄·7H₂O) was incorporated as filler into diglycidyl ether of bisphenol A (DGEBA) based epoxy resin system, to prepare organic-inorganic polymer hybrid materials. Mechanical tensile studies and dynamic mechanical analysis (DMA) were carried out in order to study the static and dynamic mechanical properties of the prepared hybrid films. Mechanical tensile studies were carried out at room temperature, at a test speed of 30 mm/min. Highest tensile strength of 24.74±2.42 MPa was achieved for 4.44 wt% filler level (FL), along with an increase in the value of Young’s modulus. Storage modulus (E′), loss modulus (E″), damping factor (tan δ) were obtained by DMA studies. Glass transition temperature (T_g) was obtained for pure epoxy and filled epoxy, for various FLs varying from 0.28 wt% to 5.00 wt%. Pure epoxy showed highest T_g value compared to filled epoxy hybrids. Highest storage modulus of 9.5 GPa was obtained for 2.22 wt% FL, which also showed highest loss modulus peak. Parameters like effectiveness coefficient (C) and crosslink density were calculated from the storage modulus data. Loss modulus and tan δ curves were analyzed to study the energy dissipation properties of prepared hybrid films. Activation energy (E_a) value for glass transition was obtained from damping factor (tan δ), which showed highest E_a value of 630.5 kJmol^-1, for 4.44 wt% FL. DMA studies for various FLs were carried out at different test frequencies in order to study the changes in dynamic mechanical properties of the prepared hybrid materials with respect to frequency     

Nanocellulose reinforced PVA composite films: Effects of acid treatment and filler loading

Nanocellulose was prepared by acid hydrolysis of microcrystalline cellulose (MCC) at different hydrobromic acid (HBr) concentrations. Polyvinyl alcohol (PVA) composite films were prepared by the reinforcement of nanocellulose into a PVA matrix at different filler loading levels and subsequent film casting. Chemical characterization of nanocelluloses was performed for the analysis of crystallinity (X_c), degree of polymerization (DP), and molecular weight (M_w). The mechanical and thermal properties of the nanocellulose reinforced PVA films were also measured for tensile strength and thermogravimetric analysis (TGA). The acid hydrolysis decreased steadily the DP and M_w of MCC. The crystallinity of MCC with 1.5 M and 2.5 M HBr showed a significant increase due to the degradation of amorphous domains in cellulose. Higher crystalline cellulose showed the higher thermal stability than MCC. From X-ray diffraction (XRD) analysis, nanocellulose samples showed the higher peak intensity than MCC cases. Reduction of MCC particle by acid hydrolysis was clearly observed from scanning electron microscope (SEM) images. The tensile and thermal properties of PVA composite films were significantly improved with the increase of the nanocellulose loading.     

Functionalization of lyocell fibers with TiO2, SiO2, and GLYMO

In the research self-cleaning coatings based on photocatalytically active nano titanium dioxide (TiO₂) were prepared. When applied directly to cellulose fiber surfaces, TiO₂ coatings form weak bonds with fibers. Therefore 3-glycidooxypropyl-trimethoxysilane was used as a coupling agent. It had been applied on the surface of cellulose fibers before the TiO₂ coating was performed. In this case, the silane is in the interface region, where it can be most effective as an adhesion promoter. Silane coupling agents have unique chemical and physical properties not only to enhance bond strength, but more importantly to prevent de-bonding at the interface during composite aging and use as well. The coupling agent provides a stable bond between two otherwise poorly bonding surfaces. Surface properties of these coatings have been examined, such as surface morphology and surface microstructure. TiO₂ nanoparticles were irreversibly attached to the surface of monodisperse silica (SiO₂) spheres and to the surface of Lyocell fibers coated with an epoxy-containing silane coupling agent. Analysis using scanning electron microscopy showed uniform distribution of nanoparticles in the resulting coatings. Fourier transform infrared spectroscopy revealed changes in the surface microstructure occurring after different modifications. In addition, the influence of photocatalytic activity on the mechanical properties of Lyocell fibers was determined. In addition to that, the results indicated that SiO₂ and the coupling agent provide a protection against high oxidizing power of TiO₂ under exposure to daylight irradiation.     

Nano-SiO2in-situ hybrid polyurethane leather coating with enhanced breathability

A novel in-situ nano hybrid technique combined with industrialized wet phase inversion coating-forming process was developed for the modification of polyurethane (PU) leather coating with nano-SiO₂. During the wet phase inversion process, nano-SiO₂ particles were in-situ generated synchronously as polyurethane resin coagulated. Scanning electron microscope analysis indicated that when the SiO₂ concentration was limited within 1.5 wt%, the size scale of in-situ generated nano-SiO₂ ranged from 70 to 150 nm, which were well-separated and dispersed uniformly throughout the PU coating. After nano hybridization, extra mesopores were detected in the PU coating by nitrogen adsorption/desorption experiment. These mesopores were correlated with enhanced water vapor and gas (hydrogen, nitrogen, and oxygen) permeability, which could improve the breathability or wear comfort of PU leather. In spite of extra mesopores, the hybrid PU coating maintained comparable hydrostatic pressure to control. Nevertheless, when the SiO₂ concentration was increased up to more than 1.5 wt%, micro-SiO₂ particles and agglomerates dominated throughout the PU coating, which obstructed mass transportation and lowered the breathability of the coating. Without disturbing established wet phase inversion coating-forming process in PU leather industry, the novel in-situ nano hybrid technique developed in this study may be of great potential for producing PU leather with improved breathability on an industrial scale.     

Preparation and characterization of (POSS/TiO2)n multi-coatings based on PBO fiber surface for improvement of UV resistance

The application of poly (p-phenylene-2, 6-benzobisoxazole) (PBO) fiber as reinforcement in composite material was restricted by its photo-degradation, therefore, some measures should be considered to protect PBO fiber against UV aging. In this study, A series of multilayer coating for (POSS/TiO₂)_n was prepared on PBO fiber surface via LbL assembly technique for enhancement of UV resistance. TiO₂ as UV absorbing material was used to relieve UV-degradation of PBO. Surface elemental composition, surface morphology, mechanical and interfacial properties, and UV resistance of uncoated and coated PBO fibers were investigated. These experimental results show multilayer coating of (POSS/TiO₂)_n was uniform deposition on fiber surface after treatment, tensile strength decreased to certain extent, interfacial shear strength increased in a small range and UV resistance is obvious enhanced. After the same accelerated aging time under UV irradiation, the retention of tensile strength and intrinsic viscosity of coated PBO fibers were much better than that of untreated PBO fibers.     

Investigation on the effect of titanium dioxide nano particles on camouflage properties of cotton fabrics

Cotton fabrics were dyed with three commercial vat dyes in order to provide camouflage in Vis-NIR regions and imitate reflectance profile of greenish leaves. To investigate the effect of nano particles on camouflage properties of dyed fabric, nano particles of TiO₂ were applied on dyed fabrics using pad-dry-cure method. The nano TiO₂ padded dyed fabrics were investigated using scanning electron microscopy (SEM). Reflectance curves of coated dyed samples with different concentrations of nano TiO₂ were measured. Results showed that in both of the standard shades, nano TiO₂ increases the reflectance value in NIR region and with increasing the concentration of nano TiO₂, the reflectance curves of samples tend to show the maximum reflection of greenish leaves (deciduous leaves) in NIR region. Chromatic values (CIE1976 L*, a*, and b*) and color difference (according to CIECMC color difference ΔE*cmc (2:1)) of each of the coated samples were measured using the reflection spectrophotometer. By considering the influence of white color of nano TiO₂ on green shade of dyed cotton fabrics and increasing the color difference (between coated samples and the standard shades of the 1948 U.S army pattern) in visible range, optimum concentrations of nano TiO₂ for development of camouflage properties on cotton fabrics in both NIR and visible region were determined. These values for NATO and forest green shades were 0.75 % and 0.5 %, respectively. Fastness results showed that both of the samples have acceptable color fastness. The effect of washing and exposure to light on camouflage properties of coated dyed fabrics in visible (in term of chromatic values) and NIR region (in term of spectral reflectance) was investigated when those were coated in optimum concentrations of nano TiO₂. The results showed that the effect of after treatments (washing and exposure to light) on surface color spectral characteristics and camouflage properties was inconsiderable.     

In situ loading TiO<Subscript>2</Subscript> and its photocatalysis and UV resistance on cotton fabric

Anatase TiO₂ nanoparticles was in-situ formed on the cotton fabric by using tetrabutyl titanate (TBT) as a precursor through the normal pressure hydrothermal method. X-ray diffraction (XRD), Scanning electron microscopy (SEM), UV visible spectra (UV-VIS), ATR-IR were used as the characterization techniques. Photocatalytic performance of TiO₂ on the fabric surface was evaluated by methylene blue (MB), 4 kinds of the common living stains and three dyes under ultraviolet and visible light radiation. XRD analysis found that the TiO₂ loaded on the fabric was mainly anatase crystalline phase with particle size of 6.4 nm. SEM observed that a large number of nano TiO₂ particles are distributed on the fabric surface. UV-VIS test indicated that theTiO₂-coated fabric possessed an obvious absorption for ultraviolet. ATR-IR analysis indicated that the nano-TiO₂ possesses a strong affinity with the hydroxyl group of the cotton fabric, and the soaping tests showed that the TiO₂ was firmly bonded with the fabrics. The treated fabrics have good degradation ability for MB aqueous solution, and could degrade azo, anthraquinone and phthalocyanine dyes. The order of degradation of the common life stains was: pepper oil> tea > coffee > soy sauce.     

Analysis of green hemp fibre reinforced composites using bag retting and white rot fungal treatments

The main objective of this project was to investigate two low cost treatment methods, namely bag retting and treatment with white rot fungi, which could be applied to hemp fibre with low environmental impact to improve its interfacial bonding with polypropylene. Wet chemical analysis, FTIR, scanning electron microscopy (SEM), X-ray diffraction (XRD), zeta potential and single fibre tensile testing were used to characterise the effect of treatment on hemp fibres. It was found that all the treatments increased the tensile strength of composites. White rot fungi Schizophyllum commune (S.com) treated fibre composites had the highest tensile strength of 45 MPa, an increase of 28% compared to composites using untreated fibre.