Siriphannon, Punnama
Loading...
Preferred name
Siriphannon, Punnama
Alternative Name
Siriphannon, P.
Main Affiliation
Email
punnama.si@kmitl.ac.th
17 results
Now showing 1 - 10 of 17
- Some of the metrics are blocked by yourconsent settings
Item type:Publication, Hydrothermal growth of ZnO nanostructures from nano-ZnO seeded in P(MMA-co-BA) matrix(2011-11-01); ; Nookaew, JitiNano-ZnO synthesized by hydrothermal reaction were embedded in poly(methyl methacrylate-co-butyl acrylate) matrix (P(MMA-co-BA)) to produce the nano-ZnO/P(MMA-co-BA) nanocomposites via in-situ polymerization at 85 °C. The nano-ZnO/P(MMA-co-BA) nanocomposites were hydrothermal treated in the mixture solution of Zn(NO <inf>3</inf>) <inf>2</inf>•6H <inf>2</inf>O and NH <inf>4</inf>OH at 90 °C under various pH (i.e.7, 8, 9 and 10) and treatment time (i.e. 4, 6, 8, 10, 12 and 24 hrs). The nano-ZnO could act as seeding particles for hydrothermal growth of ZnO nanostructures on the surfaces of nanocomposites. The higher pH of basic solutions used in the hydrothermal treatment, the higher amount of Zn(OH) <inf>4</inf> <sup>2-</sup> nuclei would be created, leading to a modification of the ZnO morphology from nano-nuclei to nanorods, nanorods bushes (flower-like nanostructure) and nanofibers with nanospine. The increase of hydrothermal treatment time resulted in the increases of amount and length of multidirectional grown ZnO nanorods. Data of the contact angle measurement exhibited the increase of hydrophobicity of the nano-ZnO/P(MMA-co-BA) nanocomposites after hydrothermal growth of ZnO nanostructures. The nanocomposites treated at pH∈=∈10 for 24 hrs shows the highest hydrophobicity with the contact angle of 121. In addition, the thermal stability of the nano-ZnO/P(MMA-co-BA) could be improved by the formation of hydrothermal grown ZnO nanostructure on the nanocomposite surface. © 2011 Springer Science+Business Media B.V. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Nanoencapsulation of n-octadecane phase change material in self-assembled polyelectrolyte by soft solution technique(2014-01-01) - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Mechanical properties and bioactivity of calcium silicate/poly(ethylene terephthalateco-caprolactone) composites(2013-12-01); Calcium silicate/poly(ethylene terephthalate-co-caprolactone) (CS/PET-co-PCL) composites were prepared via ring opening polymerisation (ROP) technique. The CS/PET-co-PCL composites were prepared by mixing 60 wt-% of CS, 40 wt-% of cyclics and dibutyl tinoxide catalyst (3 mol.-% with respect to cyclics). The cyclics consisted of the mixture of cyclic oligo(ethylene terephthalate) (COET) and e-caprolactone (CPL) with varying molar ratio of C-OET/CPL, i.e. 7 : 3, 8 : 2 and 9 : 1. The precomposites were then ring opening polymerised at 200°C for 24 h. The ROP-PET-co-PCL in the composites was present as a continuous phase impregnated with the CS particles. The 1HNMR spectra of ROP-PET-co-PCL extracted from the CS/PET-co-PCL composites showed heterolinkage signals between PET and PCL at d 4·4 and d 4·6 ppm, indicating successful copolymerisation. When the PCL content increased, the ROP-PET-co-PCL changed in the copolymer structure from block to random structure. The presence of CS powders in the CS/PETco- PCL composites resulted in high stiffness of the composites and inhibited heat dissipation during the dynamic mechanical analysis performed between 250 and 200°C. The compressive strengths of all the composites were in the range of 16-21 MPa. The higher the PET content, the stronger the CS/PET-co-PCL composites obtained. Composites containing 9 : 1 of C-OET/CPL polymerised at 200°C possessed the highest compressive strengths of 21·3 MPa, falling in the range of cartilage bone, i.e. 14-59 MPa. Bioactivities of the CS/PET-co-PCL composites were studied by soaking in simulated body fluid for 7 days. All CS/PET-co-PCL composites could induce the formation of hydroxyapatite nanocrystals on the composite surfaces, indicating the bioactivity of the CS/PET-co-PCL composites. © W. S. Maney & Son Ltd. 2013. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, In situ ring-opening polymerization of hydroxyapatite/poly(ethylene adipate)-co-(ethylene terephthalate) biomimetic composites(2013-02-01); Hydroxyapatite/poly(ethylene adipate)-co-poly(ethylene terephthalate) biomaterials (HAp/PEA-co-PET) have been prepared by ring opening polymerization (ROP) of cyclic oligo(ethylene adipate)-co-oligo(ethylene terephthalate) (C-OEA-co-C-OET) in the porous hydroxyapatite (HAp) scaffolds at 250 °C for 24 h under vacuum. The content of ROP-PEA-co-PET in the HAp/PEA-co-PET composite was about 20 wt% with the values of number average molecular weight (Mn) and weight average molecular weight (MW) of 3380 and 7160 g/mol, respectively. Compressive strength and modulus of the HAp/PEA-co-PET composites were about 29 and 246 MPa, respectively. These mechanical properties were higher than those of the porous HAp templates and natural cancellous bone. In vitro bioactivity of the HAp/PEA-co-PET composites was studied by soaking in simulated body fluid (SBF) under the flowing system at the rate of 130 mL/day for 7, 14, 21 and 28 days. The formation of hydroxyapatite nanocrystals was observed on the composite surfaces through the consumption of calcium and phosphorus from the SBF solution, indicating the bioactivity of these HAp/PEA-co-PET composites. These results indicated the competency of HAp/PEA-co-PET composites for biomedical applications. © Indian Academy of Sciences. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Immobilization of zinc oxide nanoparticles on cotton fabrics using poly 4-styrenesulfonic acid polyelectrolyte(2012-05-31) - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Facile synthesis of chitosan/CuO nanocomposites for potential use as biocontrol agents(2018-06-01); Iamphaojeen, Y.Chitosan/CuO nanocomposites (Chi/CuO) were prepared by facile and eco-friendly technique. The 2%w/v chitosan solution was mixed with 0.5 %w/w sodium tripolyphosphate (STPP), resulting in the formation of ionically crosslinked chitosan. The crosslinked chitosan was soaked in an aqueous solution containing 0.001, 0.01 or 0.1 mol/L CuSO<inf>4</inf>•5H<inf>2</inf>O for 24 hrs, in which the Cu<sup>2+</sup> ions were absorbed into the chitosan network, forming as the chitosan/Cu<sup>2+</sup> precursors. The chitosan/Cu<sup>2+</sup> precursors were hydrothermally reacted in two different basic media, i.e. NaOH and NH<inf>4</inf>OH, at 100°C for 24 hrs, resulting in the nano-sized CuO crystals hydrothermally grew and embedded in the crosslinked chitosan matrix. The CuO grown in the NaOH possessed larger crystallite size and higher crystallinity than that in the NH<inf>4</inf>OH. In addition, the CuO crystallite size in the nanocomposites increased with the increase of initial concentration of Cu<sup>2+</sup> starting agent due to the increase of Cu<sup>2+</sup> quantity in the chitosan/Cu<sup>2+</sup> precursors. The chitosan/CuO nanocomposites prepared by using 0.01 and 0.1 mol/L Cu<sup>2+</sup> could exhibit the antibacterial activities after intimate contact with Staphylococcus aureus and Escherichia coli under JIS L 1902:1998 (Qualitative) test method, indicating their potential use as biocontrol agents. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Poly(methyl methacrylate-co-butyl acrylate)/organophosphate-modified montmorillonite composites(2011-11-03); ; Poly(methyl methacrylate-co-butyl acrylate)/tetrabutylphosphonium modified montmorillonite (P(MMA-co-BA)/P-MMT) composite films were prepared by simple solution casting technique. P(MMA-co-BA) was synthesized through solution polymerization in the presence of benzoyl peroxide (BPO) as an initiator. After modification via cation exchange reaction by tetrabutylphosphonium bromide, the organoclay was dispersed in toluene and added into P(MMA-co-BA) solution. The well-dispersed mixture was cast by doctor blade technique to obtain the composite films. The P-MMT content in the composites was varied (i.e., 1, 2, 3 and 6 wt%) in order to study its effects on thermal stability, mechanical properties and UV shielding ability. The structure of P-MMT in the composites was investigated by XRD technique. The composites containing 1 and 2 wt% of P-MMT showed the d<inf>001</inf> peak slightly shifted to lower 2θ, indicating mainly intercalated structure occurred with some agglomerations of particles. The intercalated structure of P(MMA-co-BA)/P-MMT 2% composites was observed by TEM technique. The TGA results showed that degradation of the composites occurred at higher temperatures compared to that of their virgin polymer and the degradation point increased with P-MMT content. Tensile strength and Young's modulus of composites were higher than those of their original copolymer. By addition of 1-3 wt% of P-MMT, it could be seen that the higher the P-MMT loading, the higher would be the tensile strength and Young's modulus. The P(MMA-co-BA)/P-MMT composite films showed their screening ability in UV region, especially in the UV-B range, which is rather higher than that in the visible region. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Polyelectrolyte-Assisted Immobilization of Oil-Based Nanocapsules on Cotton Fabric(2016-01-01) - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Facile Refluxing Synthesis of Hydroxyapatite Nanoparticles(2015-01-01) - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Water-soluble chitosan intercalated montmorillonite nanocomposites for removal of basic blue 66 and basic yellow 1 from aqueous solution(2013-04-05); ; Water-soluble chitosan intercalated montmorillonite (wCTS/MMT) nanocomposites were modified and characterized by using Fourier transform infrared, thermogravimetric analysis, and X-ray diffractometer techniques. Two types of wCTS, namely, low molecular-weight chitosan (L-wCTS) and hydroxyethylacryl chitosan (H-wCTS) were synthesized and applied. The batch adsorption experiments on these nanocomposites were conducted by using basic dyes, that is, Basic Blue 66 and Basic Yellow 1 (BY1). The adsorption capacities of sodium montmorillonite (Na-MMT), chitosan, L-wCTS/MMT, and H-wCTS/MMT were measured and compared. The results showed that the adsorption capacities of wCTS/MMT nanocomposites were higher than those values of Na-MMT and chitosan. The adsorption kinetics of wCTS/MMT nanocomposites for BY1 were studied. It was described that the adsorption processes were better fitted by pseudo-second-order equation. The Langmuir and the Freundlich models were used to fit the adsorption isotherm. It was indicated that the adsorption isotherms followed the Langmuir model. The values of the maximum adsorption capacity of L-wCTS/MMT and H-wCTS/MMT adsorbents were at 188.7 and 294.1 mg/g, respectively. © 2012 Wiley Periodicals, Inc.