2018
DOI: 10.1088/1757-899x/440/1/012008
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Synthesis and characterization of hydrophilic polymer nanoparticles using n-isopropylacrylamide (NIPAM) via emulsion polymerization technique

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Cited by 7 publications
(5 citation statements)
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“…Preparation of PNIPAM Particles via Emulsion Polymerization. Emulsion polymerization of NIPAM was performed according to the method that was previously reported by Azmi et al 26 N-Isopropylacrylamide monomer (450 mg), SDS (0.225 mg), and Triton X-100 (1 mg) as surfactants, BIS (0.065 mg) as a cross-linker, and NaHCO 3 (0.02 mg) were dispersed in DI water (50 mL). The prepared solution was transferred into a 250 mL four-neck roundbottom reactor equipped with a magnetic stirrer, a refluxcondenser, argon gas inlet, and thermometer.…”
Section: Methodsmentioning
confidence: 99%
“…Preparation of PNIPAM Particles via Emulsion Polymerization. Emulsion polymerization of NIPAM was performed according to the method that was previously reported by Azmi et al 26 N-Isopropylacrylamide monomer (450 mg), SDS (0.225 mg), and Triton X-100 (1 mg) as surfactants, BIS (0.065 mg) as a cross-linker, and NaHCO 3 (0.02 mg) were dispersed in DI water (50 mL). The prepared solution was transferred into a 250 mL four-neck roundbottom reactor equipped with a magnetic stirrer, a refluxcondenser, argon gas inlet, and thermometer.…”
Section: Methodsmentioning
confidence: 99%
“…CMC is defined as the concentration of surfactant above the micellization becomes thermodynamically favorable and any additional surfactant added to the system forms micelles [72]. From the research, it can be proved that different CMC did affect the emulsion polymerization, in which different morphology detected by the scanning electron microscope (SEM) and different thermal stability was obtained via thermogravimetric analysis (TGA) [23]. Besides, it proves that the equivalent CMC for the surfactant showed more stability in terms of thermal degradation based on the highest onset temperature.…”
Section: Figure 6 Emulsion Polymerization Processmentioning
confidence: 99%
“…When the temperature is below LCST, the hydrophilic amide group dissolved by the water molecules resulting in the PNIPAM soluble in water caused by a highly structured hydration shell made by hydrogen bonding and made it remains in a coil-like conformation. While it will collapse into coil-to-globule when the temperature is elevated because the hydrogen bonding is weakened and following that the interactions among the hydrophobic group become strong and result in the release of water from structure [27,23]. On top of that, it is often misinterpreted that PNIPAM is hydrophobic above LCST, although it contains both hydrophobic and hydrophilic moieties [22].…”
Section: Poly (N-isopropyl Acrylamide) (Pnipam)mentioning
confidence: 99%
“…The composites were washed several times with deionized water show a typical FT-IR spectrum of PNIPAM. The most intense peak at 1677 cm -1 is attributed to C=O and the second most intense peak at 1563 cm -1 is due to amide groups (N-H and C-N); characteristic bimodal peaks of isopropyl groups could be observed at 1390, and 1379 cm -1 ; methylene peaks could be seen at 2987 and 2942 cm -1 (18); the broad peak at 3310 cm -1 is caused by N-H stretching (19). However, the peaks of PNIPAM@60 are much more intensive than those of PNIPAM@20 because heating at higher temperature provides more oxygen-involved radicals to readily crosslink NIPAM.…”
Section: Sponge Fabricationmentioning
confidence: 99%