Effects of zinc oxide Nanospheres on the Separation performance of Hollow fiber poly(piperazine-amide) composite nanofiltration membranes

The inner-skinned hollow fiber composite (HFC) nanofiltration (NF) membranes were modified through the incorporation of zinc oxide nanospheres in the poly(piperazine amide) layer during the interfacial polymerization (IP) process. The active layer was coated on the inner surface of polysulfone (PSF) support membrane via Two-way coating technique. The chemical composition and morphology of HFC membrane surface were evaluated through the Attenuated Total Reflectance Fourier Transform Infrared spectroscopy (ATR-FTIR) and Scanning Electronic Microscopy (SEM). The effects of zinc oxide (ZnO) nanospheres on membrane performance including the hydrophilicity, separation performance and chlorine resistance were investigated. The results showed that the modified HFC membranes with low concentration ZnO nanospheres (1.5 wt%) had an improved flux (33.8 L·m^-2·h^-1) meanwhile the salt rejection of MgSO₄ was well maintained (92.2 %) at 0.7 MPa. The introduction of ZnO also dramatically enhanced the chloride resistance of composite NF membranes in comparison with the control membranes prepared without ZnO. Therefore, nano metallic oxide like ZnO could be considered as a potential modifier to improve the performance of HFC nanofiltration membranes.     

Effect of organic,inorganic and slow-release urea fertilisers on CH<Subscript>4</Subscript> and N<Subscript>2</Subscript>O emissions from rice paddy fields

Vietnam is one of the world’s top two rice exporting countries. However, rice cultivation is the primary source of agriculture’s greenhouse gas (GHG) emissions in Vietnam. In particular, strategies are required to reduce GHG emissions associated with the application of organic and inorganic fertilisers. The objective of this study was to assess the effects of various combinations of biochar (BIOC), compost (COMP) and slow-release urea (SRU) on methane (CH₄) and nitrous oxide (N₂O) emissions. In total, 1170 gas samples were collected from closed gas chambers in rice paddies at Thinh Long commune and Rang Dong farm in northern Vietnam between June and October 2014. The gas samples were analysed for CH₄-C and N₂O-N fluxes using gas chromatography. The application of BIOC alone resulted in the lowest CH₄ emissions (4.8–59 mg C m^?2 h^?1) and lowest N₂O emissions (0.15–0.26 µg N m^?2 h^?1). The combined application of nitrogen–phosphorus–potassium (NPK) + COMP emitted the highest CH₄ (14–72 mg C m^?2 h^?1), while ½NPK + BIOC emitted the highest N₂O (1.03 µg N m^?2 h^?1 in the TL commune), but it was the second lowest (0.495 µg N m^?2 h^?1) in the RD farm. Green urea and orange urea reduced N₂O emissions significantly (p < 0.05) compared to white urea, but no significant differences were observed with respect to CH₄ emissions. SRU fertilisers and BIOC alone measured the lowest greenhouse gas intensity, i.e. <2.5 and 3 kg CO₂ eq. kg^?1 rice grain, respectively. Based on these results, application of fertilisers in the form of BIOC and/or orange or green urea could be a viable option to reduce both CH₄ and N₂O emissions from rice paddy soils.     

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.     

Macropores regulate CO<Subscript>2</Subscript> behavior in an andisol soil

Macropores resulting from soil pedogenesis, biological activity, and agricultural practices play important roles in soil water, chemical and gas transport; however, seldom studies focus on the effect of soil macropores on CO₂ behavior. In this study, a 150-day soil column incubation experiment was conducted to investigate the CO₂ behavior in a homogeneous soil column and a soil column with an artificial macropore, which have the same total porosity. The results showed that the cumulative CO₂ fluxes observed in the soil with a macropore (57.2 g m^?2) were higher than those in the homogeneous soil (52.7 g m^?2). The soil cumulative CO₂ fluxes measured using column incubation can fit the kinetic model, and a higher carbon mineralization rate in the soil with the macropore was found. The results of the incubation experiment also suggest that macropore increased the gas diffusivities, and thus decreased the CO₂ concentrations in the soil profile. This study proposed a simulation experiment and quantified the effect of macropore on soil CO₂ behavior, which could help to understand the mechanism of CO₂ emission from soil with macropores especially caused by agricultural practices.     

The effect of floating vegetation on CH<Subscript>4</Subscript> and N<Subscript>2</Subscript>O emissions from subtropical paddy fields in China

Duckweed (Lemna minor), a floating macrophyte belonging to the Lemnaceae family, is commonly found in subtropical paddy fields. This plant rapidly takes up nutrients from water and forms dense floating mats over the water surface that may impact the biogeochemical processes and greenhouse gas production in paddy fields. In this study, we measured CH₄ and N₂O emissions from duckweed and non-duckweed plots in a subtropical paddy field in China during the period of rice growth using static chamber and gas chromatography methods. Our results showed that CH₄ emission rate ranged from 0.19 to 26.50 mg m^?2 h^?1 in the duckweed plots, and from 1.02 to 28.02 mg m^?2 h^?1 in the non-duckweed plots. The CH₄ emission peak occurred about 1 week earlier in the duckweed plots compared to the non-duckweed counterparts. The mean CH₄ emission rate in the duckweed plots (9.28 mg m^?2 h^?1) was significantly lower than that in non-duckweed plots (11.66 mg m^?2 h^?1) (p < 0.05), which might be attributed to the higher water and soil Eh in the former. N₂O emission rates varied between ?50.11 and 201.82 µg m^?2 h^?1, and between ?28.93 and 54.42 µg m^?2 h^?1 in the duckweed and non-duckweed plots, respectively. The average N₂O emission rate was significantly higher in the duckweed plots than in the non-duckweed plots (40.29 vs. 11.93 µg m^?2 h^?1) (p < 0.05). Our results suggest that the presence of duckweed will reduce CH₄ emission, but increase N₂O flux simultaneously. Taking into account the combined global warming potentials of CH₄ and N₂O, we found that growing duckweed could reduce the overall greenhouse effect of subtropical paddy fields by about 17 %.     

Carbon dioxide and methane gas permeations in thermally annealed and chemically cross-linked commercial polyimide hollow fiber membrane

Two types of modifications were performed on a commercial polyimide (PI) hollow fiber membrane for carbon dioxide (CO₂) and methane (CH₄) gas permeations. Thermal annealing was conducted between 50- and 200 °C while chemical cross-linking was performed using 0.1- to 1.0 wt% of N, (1-Naphthyl) ethylene-diamine dihydrochloride (NED). Membrane characterization revealed densification of the thermally annealed PIs. But formation of macrovoids was observed in PIs annealed near its glass transition temperature (207 °C). Fourier transform infrared spectroscopy confirmed the successful cross-linking of NED with PI. Highest CO₂ permeance was obtained from pristine PI (P/L=225 GPU) but it also had the lowest selectivity (α=72). The performances of thermally annealed (P/L=160–219 GPU, α=76–106), NED crosslinked (P/L=68–139 GPU, α=65–95) and thermally induced NED cross-linked (P/L=51-91 GPU, α=98–138) PIs varied according to modification conditions. Among the modified membranes, highest CO₂ permeance was obtained from thermally annealed PI at 100 °C (P/L=211GPU, α=106) while thermally induced NED cross-linked PI (100 °C, 0.5 wt% NED) exhibited the highest selectivity (P/L=91, α=138). Both modified membranes are the best candidates for CO₂/CH₄ separation.     

Electrospun in-situ hybrid polyurethane/nano-TiO<Subscript>2</Subscript> as wound dressings

By combining the organic-inorganic hybridization, wet phase inversion, and electrospinning, novel electrospun polyurethane (PU) membranes with in-situ generated nano-TiO₂ were prepared, which satisfied the requirements of an ideal wound dressing. The morphology of the PU-TiO₂ mats and the cross sectional morphologies of the membranes were characterized by a scanning electron microscopy (SEM). The average diameter of the individual fibers obtained from the solutions was 341±12 nm. SEM micrographs with higher magnification further showed that the in-situ generated TiO₂ particles were well-separated and dispersed homogeneously in the membranes. The average sizes of TiO₂ particles were increased from 31 to 57 nm, with the increase of nano-TiO₂ concentration. The water vapor transmission rates (WVTRs) of the membranes were in the range of 373.55–3121.86 g/m²·d and decreased gradually with the increase of nano-TiO₂ concentration. The water absorption of various PU membranes was in the range of 210.90–397.98 % which was enough to prevent wound beds from exudate accumulation. Shake flask testing indicated that the PU membrane exhibited antibacterial efficiency against Pseudomonas aeruginosa (Ps. aeruginosa) and Staphylococcus aureus (S. aureus) due to in-situ generated of nano-TiO₂. These electrospun nanofibrous membranes also had no toxic effect and showed good and immediate adherence to L929 cells.     

Preparation and characterization of a novel nanofiltration membrane

In this study, poly[2-(N, N-dimethyl amino)ethyl methacrylate] (PDMAEMA) was prepared by bulk polymerization using AIBN as an initiator. Aqueous PDMAEMA solution was then purified by hollow fiber ultrafiltration membrane technology to remove oligomers. PDMAEMA/polysulfone (PSF) positively charged nanofiltration (NF) membrane was developed by interfacial polymerization by using PSF ultrafiltration membrane as the substrate, PDMAEMA aqueous solution as the coating solution and p-xylylene dichloride dissolved in n-heptane as the organic crosslinker. Effects of substrate material, concentration of monomer, pH value of PDMAEMA, coating time and crosslinking time were then carefully examined on the separation properties of the prepared NF membrane. Data suggested that the rejection rate of the composite NF membrane to 1 g/l of MgSO₄ was around 86.7 %, and the water flux was about 18.4 L·m⁻²·h⁻¹. Therefore, the developed NF membrane is suitable for rejection and desalination of alkaline dyes.     

One-step fabrication of high selective hollow fiber nanofiltration membrane module

A novel hollow fiber composite Nanofiltration (NF) membrane was fabricated by an improved preparation procedure. Using hollow fiber ultrafiltration (UF) membrane modules as the supporting modules, hollow fiber composite NF modules were fabricated by the one-step interfacial polymerization method. The effects of preparation conditions (such as concentration of the monomers, reaction time of monomers and ambient relative humidity, etc.) on the performance of the hollow fiber composite membranes were studied. When tested at 0.6 MPa, room temperature, the hollow fiber composite membrane had a rejection sequence of MgSO₄>Na₂SO₄>MgCl₂>NaCl and a permeate flux sequence of NaCl>Na₂SO₄> MgSO₄>MgCl₂. The nagative charge character of the membrane surface was examined by streaming potential methods. The effect of the surface electrolyte properties on the membrane separation performance was investigated. The morphologies of the hollow fiber composite Nanofiltration membranes were studied by scanning electron microscopy (SEM) and atomic force microscopy (AFM).     

Multifunctional modification of wool fabric using graphene/TiO<Subscript>2</Subscript> nanocomposite

In this study, a new finishing technique is introduced through treatment of wool fabric with graphene/TiO₂ nanocomposite. Graphene oxide/titanium dioxide nanocomposite first applied on the wool fabric by hydrolysis of titanium isopropoxide in graphene oxide suspension and then this coating chemically converted by sodium hydrosulfite to graphene/TiO₂ nanocomposite. The homogenous distribution of the graphene/TiO₂ nanocomposite on the fiber surface was confirmed by field emission scanning electron microscopy (FE-SEM), Energy-dispersive X-ray spectroscopy (EDS) and X-ray mapping. X-ray diffraction patterns proved the presence of titanium dioxide nanoparticles with a crystal size of 127 Å on the treated wool fabric. Also, the defect analysis based on X-ray photoelectron spectroscopy (XPS) established the composition of the nanocomposite. Other characteristics of treated fabrics such as antibacterial activity, photo-catalytic self-cleaning, electrical resistivity, ultraviolet (UV) blocking activity and cytotoxicity were also assessed. The treated wool fabrics possess significant antibacterial activity and photo-catalytic self-cleaning property by degradation of methylene blue under sunlight irradiation. Moreover, this process has no negative effect on cytotoxicity of the treated fabric even reduces electrical resistivity and improves UV blocking activity.     

Ladder-Structured Polysilsesquioxane/Al<Subscript>2</Subscript>O<Subscript>3</Subscript> Nanocomposites for Transparent Wear-Resistant Windows

As a protective layer for deformable displays, we synthesized ladder-type polysilsesquioxanes (LPSQs) containing cyclic epoxy as a curable unit. The mechanical properties after photo- and thermal-curing of LPSQs with a small amount of added Al₂O₃ nanoparticles were compared with those of the pure LPSQs. The prepared LPSQ-Al₂O₃ nanocomposites and the pure LPSQs exhibited comparable optical transparencies and thermal stabilities. In addition, the degree of conversion of the applied epoxy units in LPSQs and the resulting mechanical properties, as monitored by Fourier transform infrared spectroscopy and nanoindentation tests, indicated that the addition of nanoparticles to LPSQs moderately enhanced the epoxy conversion rate and remarkably improved the wear resistance, including hardness, after photo-/thermal-curing processes. The LPSQ-Al₂O₃ nanocomposites achieved higher wear resistance than epoxy-silica nanocomposites containing similar curable functional groups and reinforcing fillers (silica). The excellent mechanical properties of the LPSQ-Al₂O₃ nanocomposites could be attributed to three-dimensionally interconnected networks of organic-inorganic hybrid-type chemical structures in the LPSQ as well as additional reinforcement from amine-functionalized Al₂O₃ nanoparticles covalently interconnected with the LPSQ. We believe that the devised LPSQ-Al₂O₃ nanocomposites could serve effectively as a wear-resistant platform for deformable display windows.     

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.     

Self-cleaning Properties of Nylon 6 Fabrics Treated with Corona and TiO<Subscript>2</Subscript> Nanoparticles under Both Ultraviolet and Daylight Irradiations

Nylon 6 fabric with self-cleaning properties was prepared by corona discharge pre-treatment and coating with TiO₂ nanoparticles (NPs) using pad-dry-cure technique. The self-cleaning property was studied by discoloration of methylene blue (MB), ketchup, tea and coffee stains from the corona+TiO₂ treated nylon-6 fabric. Color difference (ΔΕ*), reflectance (R) and K/S of MB stain were investigated by diffuse reflectance spectrophotometry. The MB stain was almost completely removed from the corona+TiO₂ treated nylon surface after 24 h under UV light/daylight irradiation. Both of these phenomena (corona and TiO₂) led to an increase in the discoloration of stains under UV and daylight irradiations. The EDS analysis showed an increase in the concentration of deposited TiO₂ NPs coating after corona treatment. The FE-SEM images revealed that the surface of nylon 6 was coarser after the corona treatment. Also, the FE-SEM micrographs exhibited that a uniform layer of TiO₂ NPs was formed on the corona treated nylon fabric. The corona+TiO₂ treated nylon illustrated antibacterial activity against E. coli and B. subtillis microorganisms. The EDS and FE-SEM analysis confirmed that after 5 washing cycles, the amount of TiO₂ NPs was higher on the surface of corona+TiO₂ treated nylon than that of the fabric only treated with TiO₂ without corona pretreatment. This result justifies that the corona+TiO₂ treated nylon fabric with appropriate self-cleaning property can be applied cost-effectively in the textile industry.     

Structure and performance of<Emphasis Type="Italic">Bombyx mori</Emphasis> silk modified with nano-TiO<Subscript>2</Subscript> and chitosan

Bombyx mori (B. mori) silk was modified with the nano-TiO₂ and chitosan dispersion system by the crosslinking reactions of citric acid (CA) and maleic anhydride (MA). The average size of the nano-TiO₂ particles in the aqueous dispersion system was 36.7 nm. The scanning electron microscopy (SEM) micrographs showed that the nano-TiO₂ particles were spherical and homogeneously dispersed in the dispersion system, and the surface ofB. mori silk fiber treated with the nano-TiO₂ and chitosan dispersion system was rougher than that of the untreated one. X-ray diffraction (XRD) and Fourier transform infrared (FT-IR) Spectrometry indicated that the crystallinity of theB. mori silk fiber increased after treatment. It was also found that the nano-TiO₂ and chitosan contributed to significantly enhance the mechanical properties including breaking strength, breaking elongation, initial modulus, rupture work, and elastic recovery property of theB. mori silk fiber. The wrinkle-resistant performance of the treatedB. mori silk fabrics was also greatly improved.     

Electrospun SiO<Subscript>2</Subscript>/PMIA nanofiber membranes with higher ionic conductivity for high temperature resistance lithium-ion batteries

The nanofiber membrane prepared by electrospinning has been widely applied in lithium-ion batteries. A powerful strategy for designing, fabricating and evaluating Poly-m-phenylene isophthalamide (PMIA) nanofiber membrane with SiO₂ nanoparticles was developed by electrospinning in this paper. The morphology, crystallinity, thermal shrinkage, porosity and electrolyte uptake, and electrochemical performance of the SiO₂/PMIA nanofiber membranes were investigated. It was demonstrated that the nanofiber membrane with 6 wt% SiO₂ possessed notable properties, such as better thermal stability, higher porosity and electrolyte uptake, resulting in higher ionic conductivity (3.23×10^-3 S·cm^-1) when compared with pure PMIA nanofiber membrane. Significantly, the SiO2/PMIA nanofiber membrane based Li/LiCoO₂ cell exhibited more excellent cycling stability with capacity retention of 95 % after 50 cycles. The results indicated that the SiO₂-doped PMIA nanofiber membranes had a potential application as separator in high temperature resistance lithium-ion batteries.     

Immobilization of Cationic Titanium Dioxide (TiO<Subscript>2</Subscript><Superscript>+</Superscript>) on Electrospun Nanofibrous Mat: Synthesis,Characterization, and Potential Environmental Application

We report a facile approach to fabrication and characterization of cationic titanium dioxide (TiO₂⁺) on poly (vinyl alcohol)/poly (acrylic acid) (PVA/PAA) composite electro-spun nanofibrous mat. The aim of this study is to develop a “functional electrospun nanofibrous mat” as a sustainable approach to superior photocatalytic degradation of organic colorants. For that, the PVA/PAA nanofibrous mat was prepared by electrospinning of PVA and PAA solution according to an aspect ratio of 1:1 and later water stability was induced by the thermal cross linking at an elevated temperature of 145 °C for 30 minute. By means of electrostatic layer-by-layer (LbL) assembly, cationic titanium dioxide (TiO₂⁺, ~19 nm) was immobilized on the surface of the water stable nanofibrous mat. As functionalized composited nanofibrous mat was characterized by using scanning electron microscope (SEM), fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD) analysis and thermogravimetric analysis (TGA). Superior competency of the functionalized nanofibrous mat towards photocatalytic degradation of organic dye (methyl blue) in aqueous solution was observed by using UV-visible spectrophotometer with quantitative measuring method. The result indicates a complete degradation of methyl blue within 40 mins and superior reusability upto 5 cycles application. The study signifies the prospect of using electrospun nanofibers to manipulate the catalytic activity, which could be a foundation for further rational design of various composite nanofibrous materials.     

Nano-TiO<Subscript>2</Subscript> based multilayer film deposition on cotton fabrics for UV-protection

Nano-TiO₂ based multilayer nanocomposite films were fabricated on cationically modified woven cotton fabrics by layer-by-layer molecular self-assembly technique. Cationization process was used to obtain cationic surface charge on cotton fabrics. Attenuated total reflectance Fourier transform infrared spectroscopy analyses were used to verify the presence of cationic surface charge and multilayer films deposited on the fabrics. Scanning electron microscope micrographs of poly(sodium 4-styrene sulfonate)/TiO₂, nano polyurethane/TiO₂, and TiO₂/poly(diallyldimethylammonium chloride) multilayer films deposited on cotton fabrics were taken. With nano-TiO₂ based multilayer film deposition, the protection of cotton fabrics against UV radiation is enhanced. The UV protection durability of the self-assembled multilayer films deposited on the cotton fabrics was analyzed after 10 and 20 washing cycles at 40 °C for 30 min. Air permeability and whiteness value analysis were performed on the untreated and multilayer film deposited cotton fabrics. The effect of layer-by-layer deposition process on tensile strength properties of the warp and weft yarns was determined.     

Hard Surface-adhesive Properties of TiO<Subscript>2</Subscript> Nanoparticles-encapsulated Microparticles Prepared by Spray Drying and Surface Coating Method

The aim of this study is to compare hard surface-adhesive properties of TiO₂ nanoparticles (TNPs)-encapsulated microparticles prepared by spray drying and surface coating method. Thus, TNPs were encapsulated with chitosan by spray drying and poly(L-lysine) by surface coating method, which were selected as positively charged materials. And then, the TNPs-encapsulated microparticles were investigated by particle surface properties and adhesion properties on hydroxyapatite (HAP) surface as model for hard surface-adhesion. The characteristics of TNPs-encapsulated Chitosan microcapsules (CM) and TiO₂ nanoparticles coated with cationic poly(L-lysine) polymer (TNPs-PLL) were determined with scanning electron microscope (SEM) image and zeta-potentials. The hard surface-adhesive properties on HAP surface were confirmed with SEM and whitening test. The zeta-potentials of TNPs and HAP were negative, -13 mV and -18 mV respectively, while TNPsencapsulated CM, and TNPs-PLL of positively charged polymers were positive, 13 mV and 57 mV respectively. Whitening test was carried out on model surface when shaking the samples. TNPs-PLL were adhered to HAP surface very much more than those of TNPs-encapsulated CM. Also, the change value of whiteness of the HAP surface treated with TNPs-PLL is large evidently, compared with TNPs-encapsulated CM.     

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.     

Pervaporation separation of dimethyl carbonate/methanol binary mixtures with poly(vinyl alcohol)-perfluorslulfonic acid/poly(acrylonitrile) hollow fiber composite membranes

Using poly(vinyl alcohol) (PVA) and perfluorslulfonic acid (PFSA) as coating materials, poly(acrylonitrile) (PAN) hollow fiber ultrafiltration membrane as substrate, PVA-PFSA/PAN composite membranes were fabricated by dip-coating method. The fabricated composite membranes were used to the separation of dimethyl carbonate (DMC)/methanol (MeOH) binary mixtures by pervaporation process. SEM images verify that the coated layer is well combined with substrate and the thickness nearly linearly increases with the coating solution concentration. The separation factor increases but at cost of the decline of permeation flux when the concentration of the coating solution or its PVA mass fraction increase. The permeation flux increases and separation factor slightly increases with the feed temperature increasing at 30–60 °C. The increase of feed MeOH concentration leads to an improvement of permeation flux and a decline of separation factor.