Poly(Lactic Acid) Filled with Cassava Starch-g-Soybean Oil Maleate

Poly(lactic acid), PLA, is a biodegradable polymer, but its applications are limited by its high cost and relatively poorer properties when compared to petroleum-based plastics. The addition of starch powder into PLA is one of the most promising efforts because starch is an abundant and cheap biopolymer. However, the challenge is the major problem associated with poor interfacial adhesion between the hydrophilic starch granules and the hydrophobic PLA, leading to poorer mechanical properties. In this paper, soybean oil maleate (SOMA) was synthesized by grafting soybean oil with various weight percents of maleic anhydride (MA) using dicumyl peroxide (DCP) as an initiator. Then, SOMA was employed for the surface modifying of cassava starch powder, resulting in SOMA-g-STARCH. The obtained SOMA-g-STARCH was mixed with PLA in various weight ratios using twin-screw extruder, resulting in PLA/SOMA-g-STARCH. Finally, the obtained PLA/SOMA-g-STARCH composites were prepared by a compression molding machines. The compatibility, thermal properties, morphology properties, and mechanical properties were characterized and evaluated. The results showed that the compatibility, surface appearance, and mechanical properties at 90 : 10 and 80 : 20 ratios of PLA/SOMA-g-STARCH were the best

Phosphonic Acid Functionalization of Hyperbranched Polyamidoamine Grafted Ultrafine Silica to Prepare the Flame Retardant for Cotton Fabric

Polyamidoamine (PAMAM) dendrimers, the starburst polymers with a plurality of terminal functional groups have attracted considerable interest due to their novel functionalities such as nanoscopic containers, delivery devices, ultrafine colloid stabilizers and nanocomposite materials [1-8]. Surface modifications of terminal groups with different functionalities such as acetamide, hydroxyl, carboxyl or quaternized PAMAM dendrimers further increase the versatile applicability of these materials[9-13]. Focused on nanoparticle fillers such as carbon black and silica, these materials are widely used for rubber and plastics. A good uniform dispersion of extremely fine particle size for most of their applications is important.Grafting of hyperbranched polyamidoamine (PAMAM) dendrimer onto ultrafine silica followed by the introduction of phosphonic acid groups onto branch ends was carried out. First, an initiating site was incorporated into silica surface by reacting the silica silanol group with 3-aminopropyltriethoxysilane, producing amino-functionalized silica. The free amine group content was controlled by varying ratios of methanol to water in the hydrolysis step of sol-gel reaction. Then grafting of PAMAM was performed by repetitive reactions between Michael addition of silica amino groups to methyl acrylate and amidation of the resulting terminal methyl ester groups with ethylenediamine. Amino group content in each generation was determined. This was found to be significantly lower than theoretical value due to unavoidable side reactions. After the G3.0 hyperbranched PAMAM grafted onto silica was synthesized, phosphonic acids functionalization of the terminal amino groups by the Mannich type reaction was carried out. The phosphorylated hyperbranched PAMAM grafted silica was achieved and its application on cotton fabric to produce phosphonated cellulose was studied

Morphology and crystallization of polypropylene/microfibrillated cellulose composites

Microfibrillated cellulose (MFC) was prepared by controlling the re-precipitation of cellulose prepared in the mixture form of NaOH/Urea solubilized microcrystalline cellulose (MCC) and starch. The cellulose re-precipitation was carried-out in an HCl bath, resulting in a MFC form having relatively lower crystallinity than MCC. The XRD pattern of MFC indicated the partially crystalline structure arising from the imperfect orientation of a cellulose chain obstructed by a starch molecule in the precipitation step. Interestingly, the MFC morphology exhibited a web-like structure with a diameter in the range of 10-20 nm. The water retention value of MFC was extraordinarily high due to its extremely small diameter having high surface area. Further, surface silanization of MFC with organosilane was carried out. Then, the modified MFC was melt-mixed with polypropylene (PP) matrix via a simple melt mixing technique. The morphology and crystallization of the PP/MFC composites were measured. The morphology of organosilane treated MFC exhibited agglomeration of 10 microns in diameter with layered structures arising from the packing of microfibrils. The FTIR spectra showed hydrophobic characteristics of treated MFC observed by the disappearance of original cellulose hydroxyl group and bound water. The crystallinity of treated MFC increased when compared to the untreated MFC, indicating that cellulose chains of unmodified MFC underwent re-orientation occurring in the modification step due to its high crystallinity characteristic. For the PP/MFC-composite containing MFC loading, faster crystallization and higher spherulite growth rate, in case of higher MFC loading, were observed. In addition, the spherulite size decreased with an increase in the crystallization temperature. However, the degree of crystallinity was fairly independent on the MFC-loading. Therefore it can be concluded that the addition of MFC might enable shorter cycle times, resulting in cheaper processing cost in a view point of polymer processing

Effects of Soybean Oil Modified Cellulose Fibril and Organosilane Modified Cellulose Fibril on Crystallization of Polypropylene

Soybean oil modified cellulose fibril (Oil-g-CF) and organosilane modified cellulose fibril (Silane-g-CF) were prepared using maleinized soybean oil and hexadecyltrimethoxysilane, respectively. Thus obtained modified cellulose fibril was added to polypropylene by a simple melt mixing on a hotplate. PP/modified CF composites with 4.0 wt% filler content were prepared. The composites were subject to a polarized optical microscope to investigate particle dispersion, supramolecular morphology, and crystallization behavior. It was found that Silane-g-CF exhibited smaller particle sizes with better particle distribution when compared to Oil-g-CF. In addition, the etched composite samples unveiled an increase in a number of spherulite crystals as well as a decrease in the spherulite size. The nonisothermal crystallization study of composites revealed that both Oil-g-CF and Silane-g-CF were capable of nucleating PP by facilitating faster crystallization process and raising the number of spherulites. The DSC results indicated that Silane-g-CF was able to perform a more effective nucleation than Oil-g-CF, judged by a higher crystallization temperature. Moreover, PP composites containing Oil-g-CF and Silane-g-CF had higher crystallinity by 7% and 10%, for the first and the latter, respectively, when compared to neat PP

Preparation and Characterizations of PSS/PDADMAC Polyelectrolyte Complex Hydrogel

Polyelectrolyte complex (PEC) hydrogel, formed via physically electrostatic crosslinks between polyanion and polycation, is an interesting hydrogel in terms of its nontoxicity and solvent-free technique. In this work, poly (sodium 4-styrenesulfonate) (PSS)/poly (diallyl dimethyl ammonium chloride) (PDADMAC) complex hydrogels were prepared. Firstly, the PSS/PDADMAC complex aggregates using various PSS/PDADMAC mole fractions that were prepared in the presence of NaCl solution. Then, the aggregates were resolubilized under stirring at 70 °C for 2 h to obtain a homogeneous PEC solution. Finally, the PEC solution was dialyzed using a dialysis membrane with 3500 molecular cut-off for 1 day. The dialysis bath was changed every interval period of 2 h to control the rate of reversible electrostatic interaction, resulting in the homogenous PEC hydrogel with porous morphology as revealed by SEM and BET investigations. The dimensional stability and viscoelasticity of the PEC hydrogel was studied by DMA experiment, which showed the viscoelastic behavior at a compressive force ranging from 0 to 0.1 N. Finally, PSS/PDADMAC hydrogels showed a high water absorbency property and excellent affinity to textile anionic dyes

Effects of the Amount and Type of Diol Ring Openers on the Properties of Oligolactide Acrylates for UV-Curable Printing Inks

This study aimed to synthesize low viscosity oligolactide acrylates for UV-curable inks from oligolactide diols. Firstly, low molecular weight oligolactide diols were prepared by ring opening reaction of L-lactide with diols. Oligolactide acrylates were then synthesized by functionalizing the oligolactide diols with acrylic acid. In this study, three diol ring openers having short and long alkyl chain length were used to investigate the effects of the amount and type of diols on the properties of the oligolactide acrylates. The obtained oligomers were characterized, and the viscosities of oligolactide acrylates were measured. Results showed that oligolactide acrylates were successfully synthesized in all cases of ring openers, as confirmed by 1H-NMR (proton nuclear magnetic resonance spectroscopy) and FTIR (Fourier transform infrared spectroscopy). An increase in the alkyl chain length of the ring openers resulted in oligomers with lower viscosity and a decrease in Tg. Following that, the obtained oligolactide acrylates were employed for the formulation of UV-curable screen printing inks and their properties were investigated. Results showed that the inks formulated from oligomers with lower molecular weight exhibited better ink flow. Additionally, all ink films cured by UV radiation were very flexible with excellent adhesion, high impact resistance, and excellent water resistance

Chitosan-Coated Bacterial Cellulose (BC)/Hydrolyzed Collagen Films and Their Ascorbic Acid Loading/Releasing Performance: A Utilization of BC Waste from Kombucha Tea Fermentation

SCOBY bacterial cellulose (BC) is a biological macromolecule (considered as a by-product) that grows at the liquid–air interface during kombucha tea fermentation. In this study, BC:HC (hydrolyzed collagen) blend films coated with 1 wt% chitosan (CS) were loaded with ascorbic acid to study loading/releasing performance. At first, the mechanical properties of the blend films were found to be dependent on HC ratio. After chitosan coating, the coated films were stronger due to intermolecular hydrogen bonding interaction and the miscibility of two matrixes at the interface. The antibacterial activity test according to the AATCC Test Method revealed that chitosan-coated BC/HC films exhibited excellent antimicrobial activity against S.aureus growth from the underneath and the above film when compared to BC and BC:HC films. Moreover, chitosan was attractive to ascorbic acid during drug loading. Consequently, its releasing performance was very poor. For BC:HC blend films, ascorbic acid loading/releasing performance was balanced by water swellability, which was controlled using blending formulation and coating. Another advantage of BC films and BC:HC blend films was that they were able to maintain active ascorbic acid for a long period of time, probably due to the presence of plenty of BC hemiacetal reducing ends (protective group)