Nazia Rahman

Preparation and Characterization of the Mechanical Properties of the Photocured Chitosan/Starch Blend Film

The chitosan/starch blend films of 2:1 ratio were prepared by solution casting. Tensile strength (TS) and elongation at break (%Eb) of chitosan/starch blend film were found to be 9.33 MPa and 3.6%, respectively. The blend films (2% Chitosan) were soaked in six different formulations of methylmethacrylate (MMA) monomer and aliphatic urethane diacrylate oligomer (M-1200) at different time intervals (1–5 min) and irradiated under UV radiation at different intensities (5–35 pass). Formulations containing 43% MMA and 15% oligomer in methanol solution showed 209% increase in TS at 25th UV pass for 4 min soaking time. SEM and FTIR were used to investigate the molecular interaction and morphology of the blend film, respectively.

Selective Hg(II) adsorption from aqueous solutions of Hg(II) and Pb(II) by hydrolyzed acrylamide-grafted PET films.

Selective Hg(II) adsorption from aqueous solutions of Hg(II) and Pb(II) using hydrolyzed acrylamide (AAm)-grafted polyethylene terephthalate (PET) films was examined to explore the potential reuse of waste PET materials. Selective recovery of Hg(II) from a mixture of soft acids with similar structure, such as Hg(II) and Pb(II), is important to allow the reuse of recovered Hg(II). An adsorbent for selective Hg(II) adsorption was prepared by γ-ray-induced grafting of AAm onto PET films followed by partial hydrolysis through KOH treatment. The adsorption capacity of the AAm-grafted PET films for Hg(II) ions increased from 15 to 70 mg/g after partial hydrolysis because of the reduction of hydrogen bonding between –CONH2 groups and the corresponding improved access of metal ions to the amide groups. The prepared adsorbent was characterized by Fourier transform infrared spectroscopy and scanning electron microscopy. The absorbent film showed high selectivity for the adsorption of Hg(II) over Pb(II) throughout the entire initial metal concentration range (100–500 mg/L) and pH range (2.2–5.6) studied. The high selectivity is attributed to the ability of Hg(II) ions to form covalent bonds with the amide groups. The calculated selectivity coefficient for the adsorbent binding Hg(II) over Pb(II) was 19.2 at pH 4.5 with an initial metal concentration of 100 mg/L. Selective Hg(II) adsorption equilibrium data followed the Langmuir model and kinetic data were well fitted by a pseudo-second-order equation. The adsorbed Hg(II) and Pb(II) ions were effectively desorbed from the adsorbent film by acid treatment, and the regenerated film showed no marked loss of adsorption capacity upon reuse for selective Hg(II) adsorption.

Modification of Gelatin Films Using Trimethylolpropane Trimethacrylate (TMPTMA) by Photo-Curing

Thin gelatin films were prepared via casting at 70°C. Tensile strength (TS) and elongation at break (Eb%) of the gelatin films were found to be 20 MPa and 8.7% respectively. To improve the mechanical and thermal properties, gelatin films were cured with trimethylolpropane trimethacrylate (TMPTMA) using UV radiation. Monomer concentration, soaking time of gelatin films in the monomer solution and UV radiation intensity were optimized on the basis of mechanical properties of the cured films. The highest TS was found to be 28.8 MPa for 3% monomer solution at 10th pass of UV for 5 min soaking time. Thermal properties, water uptake and water aging properties of the gelatin films were also studied.

Synthesis of Potato Starch-Acrylic-Acid Hydrogels by Gamma Radiation and Their Application in Dye Adsorption

Several kinds of acrylic-acid-grafted-starch (starch/AAc) hydrogels were prepared at room temperature (27°C) by applying 5, 10, 15, 20, and 25 kGy of gamma radiation to 15% AAc aqueous solutions containing 5, 7.5, and 15% of starch. With increment of the radiation dose, gel fraction became higher and attained the maximum (96.5%) at 15 kGy, above which the fraction got lowered. On the other hand, the gel fraction monotonically increased with the starch content. Swelling ratios were lower for the starch/AAc hydrogels prepared with higher gamma-ray doses and so with larger starch contents. Significant promotions of the swelling ratios were demonstrated by hydrolysis with NaOH: for 15 kGy radiation-dosed [5% starch/15% AAc] hydrogel, while the maximum swelling ratio was ~200% for those without the treatment. The authors further investigated the availability of the starch/AAc hydrogel as an adsorbent recovering dye waste from the industrial effluents by adopting methylene blue as a model material; the hydrogels showed high dye-capturing coefficients which increase with the starch ratio. The optimum dye adsorption was found to be 576 mg per g of the hydrogel having 7.5 starch and 15% AAc composition. Two kinetic models, (i) pseudo-first-order and (ii) pseudo-second-order kinetic models, were applied to test the experimental data. The latter provided the best correlation of the experimental data compared to the pseudo-first-order model.

Selective Cu(II) Adsorption from Aqueous Solutions Including Cu(II), Co(II), and Ni(II) by Modified Acrylic Acid Grafted PET Film

Acrylic acid (AAc) grafted polyethylene terephthalate (PET) films were prepared by γ irradiation. The graft films showed little metal ion adsorption due to compact structure of the graft chains as shown by the scanning electron microscopy (SEM) images which restricted the access of metal ions to the functional groups. Therefore, the graft films were modified with KOH treatment for expansion of the graft chains to facilitate the access of metal ions to the functional groups. The modified films were used to study the selective Cu2

Study on the Water-Aging Properties of Gelatin-Glucose and Gelatin-Urea Films: The Effect of Gamma Radiation

Thin gelatin films (about 0.25 mm thickness) were prepared from granular gelatin via casting. The mechanical properties of gelatin films such as tensile strength (TS), elongation at break (Eb%), water uptake and water aging properties were investigated. To improve the water aging properties of gelatin films, gelatin-glucose and gelatin–urea films were prepared. Effect of gamma radiation on the tensile properties, water uptake and water aging properties of gelatin-glucose and gelatin-urea films were also studied. The results of the investigation show that both glucose and urea can improve the water stability of the gelatin films.

Preparation and Characterization of an Alginate/Clay Nanocomposite for Optoelectronic Application

Sodium Alginate/bentonite clay composites of different compositions were prepared by solution casting method. The electrical properties (Conductivity, Dielectric constant) of the composites were investigated by standard methods with Impedance Analyzer. The electrical properties were found to improve with the incorporation of bentonite clay. The thermal, physical and mechanical properties of sodium alginate/bentonite clay composite were investigated by Thermo-Mechanical Analyzer (TMA), X-ray Deffraction (XRD), and Universal Testing Machine respectively. . Tensile Strength (TS) and Elongation at break (Eb) of 2% clay containing composite film were found to be 7.6 MPa and 55% respectively. The XRD demonstrates the enhancing crystallinity of sodium alginate/bentonite clay composite with the increasing clay content. TMA results showed a higher thermal stability in the composite. Water absorption properties of the sodium alginate/clay composite were studied and found to decrease with the increase of clay content. . The inter action between sodium alginate and bentonite clay were studied by Fourier transform infrared spectroscopy (FT-IR). All of the results indicate that the developed composite is promising for use in a wide variety of optoelectronic applications.

Preparation and Characterization of Iminodiacetate Group Containing Nonwoven Polyethylene Fabrics and Its Application in Chromium Adsorption

An iminodiacetate (IDA) group containing nonwoven polyethylene (PE) film was prepared by radiation induced graft polymerization of an epoxy group containing monomer, glycidyl methacrylate (GMA) onto nonwoven PE fabric and subsequent chemical modification to IDA group. The effect of solvents (water, methanol, ethanol, isopropyl alcohol and dimethyl sulfoxide) on modification of epoxy group of GMA grafted PE (GMA-g-PE) fabric to IDA group was investigated. Ethanol provided a higher density of IDA group on GMA-g-PE fabric. Fourier transform infrared spectroscopy, scanning electron microscopy, thermogravimetric analysis and dynamic mechanical analysis of IDA-GMA-PE adsorbent, GMA-g-PE fabric and pure PE fabric were studied. The ability of resultant IDA adsorbent to absorb chromium from aqueous medium was evaluated by batch method. The parameters such as feeding chromium concentration, pH of chromium solution and adsorption time of IDA adsorbent were discussed. The obtained results illustrate that the IDA adsorbent could be fruitful to absorb chromium from water. The equilibrium experimental data for the adsorption of chromium on IDA adsorbent fitted Langmuir isotherm model.

Preparation of gelatin/poly(vinyl alcohol) film modified by methyl methacrylate and gamma irradiation

ABSTRACT The properties of gelatin–polyvinyl alcohol (G–PVA) blend films were improved by methyl methacrylate (MMA) and γ irradiation for a practical viewpoint. The films were prepared by the casting method, modified by glycerol and MMA monomer, and their mechanical properties were also studied. The gelatin-based films were successfully prepared using γ irradiation (3.1 kGy) and gelatin: PVA = 97:3 (w/w) as optimized. Tensile properties of the films were studied and thermal properties of the films were characterized by thermogravimetric analysis and dynamic mechanical analysis pointed out that MMA treated both gelatin films, and G–PVA blend films showed less thermal degradation than untreated films. In addition, structural and morphological features of the gelatin-based films were examined by Fourier transform infrared and scanning electron microscopy, respectively. The ultimate results of the present study showed remarkable enhancement in tensile properties (> 40%) and a reduction in elongation at break of the films, thanks to the MMA addition and γ irradiation.

UV RADIATION INDUCED GRAFT COPOLYMERIZATION OF ALLYL ACETATE ONTO POLY(ETHYLENE TEREPHTHALATE) (PET) FILMS FOR FUEL CELL MEMBRANES

Ultraviolet (UV)-induced graft copolymerization of allyl acetate (AA) monomer onto poly(ethylene terephthalate) (PET) films and the subsequent sulfonation on the monomer units in the grafting chain using chlorosulfonic acid (ClSO3H) were carried out to prepare proton exchange membranes (PEMs) for fuel cells. A maximum grafting value of 12.8% was found for 35 vol% allyl acetate after 3 h radiation time. Optimum concentration of ClSO3H was selected for the sulfonation reaction to be 0.05 mol/L based on the degree of sulfonation and the tensile strength studies of the membrane. The degree of sulfonation increased as the sulfonation reaction temperature and sulfonation time were increasing. The radiation grafting and the sulfonation have been confirmed by titrimetric and gravimetric analyses as well as FTIR spectroscopy. The maximum ion exchange capacity (IEC) of 0.04125 mmol g−1 was found at 12.1% degree of sulfonation and the maximum proton conductivity was found to be 0.035 S cm−1 at 30°C and a relative humidity of 60%. The various physical and chemical properties of the PEMs such as water uptake, mechanical strength, thermal durability and oxidative stability were also studied. To investigate the suitability of the prepared membrane for fuel cell applications, its properties were compared with those of Nafion 117.