Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Synthesis of phosphonate-functionalized polystyrene and poly(methyl methacrylate) particles and their kinetic behavior in miniemulsion polymerization.

ABSTRACT: Phosphonate-functionalized polymer nanoparticles were synthesized by free-radical copolymerization of vinylphosphonic acid (VPA) with styrene or methyl methacrylate (MMA) using the miniemulsion technique. The influence of different parameters such as monomer and surfactant type, amount of vinylphosphonic acid on the average particle size, and size distribution was studied using dynamic light scattering and transmission electron microscopy. Depending on the amount and type of the surfactant used (ionic or non-ionic), phosphonate-functionalized particles in a size range from 102 to 312 nm can be obtained. The density of the phosphonate groups on the particle surface was higher in the case of using MMA as a basis monomer than polystyrene. The kinetic behavior of VPA copolymerization with styrene or MMA using a hydrophobic initiator was investigated by reaction calorimetry. Different kinetic curves were observed for miniemulsion (co)polymerization of styrene- and MMA-based nanoparticles indicating different nucleation mechanisms.

SUBMITTER: Ziegler A

PROVIDER: S-EPMC2763176 | biostudies-other | 2009 Nov

REPOSITORIES: biostudies-other

ACCESS DATA

Json Xml

Similar Datasets

Effect of Molecular Weight on Phase Equilibrium in the Polystyrene-Poly(methyl methacrylate) System.

Project description:Data on the solubility of oligomer polystyrene (PS) and poly(methyl methacrylate) (PMMA) of various molecular weights have been obtained. The binodal and spinodal curves of the phase state diagram with the upper critical solution temperature (UCST) are constructed through simulation within the framework of the Flory-Huggins theory. The influence of the molecular weight of polymers on the contribution to their mixing has been compared, and correlation curves have been plotted. The interaction parameters were calculated and the mixing thermodynamics of the components was evaluated. The largest contribution was made by the entropy component. Also, it has been shown using IR spectroscopy that there is no interaction between the functional groups of polystyrene and poly(methyl methacrylate) in a homogeneous mixture.

| S-EPMC10343856 | biostudies-literature

Luminescent Properties of Surface Functionalized BaTiO₃ Embedded in Poly(methyl methacrylate).

Project description:As-received BaTiO₃ nanopowders of average grain sizes 50 nm and 100 nm were functionalized by (3-aminopropyl)triethoxysilane (APTES) and mixed with poly(methyl methacrylate)/toluene solution. The nanocomposite solution was spin coated on Si substrates to form thin films. The photoluminescence spectrum of the pure powder was composed of a bandgap emission at 3.0 eV and multiple bands centered about 2.5 eV. Surface functionalization of the BaTiO₃ powder via APTES increases overall luminescence at room temperature while only enhancing bandgap emission at low-temperature. Polymer coating of the functionalized nanoparticles significantly enhances bandgap emissions while decreasing emissions associated with near-surface lattice distortions at 2.5 eV.

| S-EPMC5453151 | biostudies-other

Stress Relaxation Behavior of Poly(Methyl Methacrylate)/Graphene Composites: Ultraviolet Irradiation.

Project description:The graphene/poly (methyl methacrylate) (PMMA) composites are a promising candidate for electronic, optoelectrical, and environmental applications. Understanding the mechanical degradation of PMMA-based materials is of practical importance in improving the reliability and lifespan of the associated structures and systems. In this study, we investigate the effects of functionalized graphene (FG) and UV irradiation on the stress-relaxation of PMMA. Uniaxial tensile and stress -relaxation tests are performed to evaluate the mechanical properties of the composites. The mechanical strength and elongation at the break increase with the graphene concentration but decrease with the increase of the irradiation dose. Raman spectroscopy and intrinsic viscosity measurement are applied to examine the root cause of the degradation in the composites. UV irradiation leads to polymer chain scission and loss of molecular weight. The Kelvin representation of the standard linear solid model (SLSM) is used to describe the stress-relaxation curves of the composites. The value of the elastic modulus in the Kelvin element decreases with the increase in temperature. The viscosity follows the Arrhenius equation. The activation energy of viscosity increases with the increasing FGs concentration because the FGs hinder the chain motion of PMMA. However, UV irradiation makes chain scission of PMMA/FGs composite so that the polymer chain moves more easily and the activation energy of stress relaxation lowers. The steady-state stress follows the van 't Hoff equation that stress relaxation is an exothermal deformation process. Although Maxwell's representation of SLSM is mathematically identical to the Kelvin representation of SLSM, the former cannot interpret the stress-relaxation behavior of PMMA/FGs composite, which is against the concept of Young's modulus as a decreasing temperature function.

| S-EPMC9573155 | biostudies-literature

Block Copolymer Membranes from Polystyrene-b-poly(solketal methacrylate) (PS-b-PSMA) and Amphiphilic Polystyrene-b-poly(glyceryl methacrylate) (PS-b-PGMA).

Project description:In this paper; we compare double hydrophobic polystyrene-b-poly(solketal methacrylate) (PS-b-PSMA) and amphiphilic polystyrene-b-poly(glyceryl methacrylate) (PS-b-PGMA) diblock copolymer membranes which are prepared by combining the block copolymer self-assembly in solution with a non-solvent induced phase separation (SNIPS). Diblock copolymers (i.e., PS-b-PSMA) were synthesized by sequential living anionic polymerization, whereas polystyrene-b-poly(glyceryl methacrylate) (PS-b-PGMA) were obtained by acid hydrolysis of the acetonide groups of the polysolketal methacrylate (PSMA) blocks into dihydroxyl groups (PGMA). Membrane structures and bulk morphologies were characterized by scanning electron microscopy (SEM) and transmission electron microscopy (TEM); respectively. The resulting PS-b-PGMA diblock copolymers produce an ordered hexagonal cylindrical pore structure during the SNIPS process, while membranes fabricated from the double hydrophobic (PS-b-PSMA) do not under similar experimental conditions. Membrane performance was evaluated by water flux and contact angle measurements.

| S-EPMC6432498 | biostudies-literature

Polystyrene-Poly(methyl methacrylate) Silver Nanocomposites: Significant Modification of the Thermal and Electrical Properties by Microwave Irradiation.

Project description:This work compares the preparation of nanocomposites of polystyrene (PS), poly(methyl methacrylate) (PMMA), and PSMMA co-polymer containing silver nanoparticles (AgNPs) using in situ bulk polymerization with and without microwave irradiation (MWI). The AgNPs prepared were embedded within the polymer matrix. A modification in the thermal stability of the PS/Ag, PMMA/Ag, and PSMMA/Ag nanocomposites using MWI and in situ was observed compared with that of neat PSMMA, PS, and PMMA. In particular, PS/Ag, and PSMMA/Ag nanocomposites used in situ showed better thermal stability than MWI, while PMMA/Ag nanocomposites showed improved thermal stability. The electrical conductivity of the PS/Ag, PMMA/Ag, and PSMMA/Ag composites prepared by MWI revealed a percolation behavior when 20% AgNPs were used as a filler, and the conductivity of the nanocomposites increased to 103 S/cm, 33 S/cm, and 40 mS/cm, respectively. This enhancement might be due to the good dispersion of the AgNPs within the polymer matrix, which increased the interfacial interaction between the polymer and AgNPs. The polymer/Ag nanocomposites developed with tunable thermal and electrical properties could be used as conductive materials for electronic device applications.

| S-EPMC5456822 | biostudies-literature

Adsorption Kinetics of Polystyrene and Poly(9-anthracenyl methyl methacrylate) onto SiO2 Surface Measured by Chip Nano-Calorimetry.

Project description:The alternating current (AC) chip nano-calorimetry is a powerful tool to investigate the physical properties of polymer thin films. In this paper, we report on the adsorption kinetics of polymers in which an AC chip nano-calorimetry was used for the first time. This technique allows for the real-time measurement of the adsorption kinetics of polymer chains onto the SiO2 surface. We used polystyrene (PS) and poly(9-anthracenyl methyl methacrylate) (PAMMA), which have different chemical natures and side group sizes. It was confirmed that the observed adsorption kinetics for PS were consistent with previously reported results obtained by dielectric spectroscopy. For PAMMA, we found characteristic adsorption kinetics, which shows a clear kink at the crossover between the early and later stages, while PS exhibits a lesser tendency of showing the kink as demonstrated by previously reported results.

| S-EPMC8839510 | biostudies-literature

Inorganically modified particles FeAl-LDH@SiO<sub>2</sub> as reinforcement in poly (methyl) methacrylate matrix composite.

Project description:Silica particles were obtained from rice husk to which layered double hydroxide particles were deposited (weight ratio 1 : 1). Fe2+-Al3+ layered double hydroxides (FeAl-LDH) were synthesized by co-precipitation with ratios Fe : Al of 3 : 1 in the presence of SiO2 particles from the rice husk. Characterization of the synthesized FeAl-LDH@SiO2 particles was performed by X-ray diffraction, Fourier transforms infrared spectroscopy (FTIR) and scanning electron microscopy with EDS. Prepared FeAl-LDH@SiO2 particles were used as reinforcing agents in 1, 3 and 5 wt% quantity in poly (methyl) methacrylate matrix. The aim of this study was to examine whether FeAl-LDH@SiO2 particles affect the mechanical properties of polymer composite materials. The morphology of the composites was examined using a field emission scanning electron microscope. Microindentation, tensile and impact testing determined the mechanical properties of the obtained composites.

| S-EPMC8479365 | biostudies-literature

Nile Red-Poly(Methyl Methacrylate)/Silica Nanocomposite Particles Increase the Sensitivity of Cervical Cancer Cells to Tamoxifen.

Project description:Tamoxifen (TAM) is a hormonal drug and is mainly used as an anti-estrogen in breast cancer patients. TAM binds to estrogen receptors (ERs), resulting in inhibition of estrogen signaling pathways and thus, a downregulation of cell proliferation. Cancer cells with negative or low ER expression will not uptake TAM and will show low response. Poly (methyl methacrylate) (PMMA) nanoparticles were prepared using surfactant-free emulsion polymerization, then were loaded with Nile red (NR), which resulted in PMMA-NR. To enhance TAM delivery to cervical cancer cells (HELA), which is considered ER-negative, we loaded TAM and polymethyl methacrylate nanoparticles-Nile-red into silica (PMMA-NR-Si-TAM). The uptake and intracellular distribution were visualized by confocal laser scanning microscopy, and the in vitro cytotoxic activity was evaluated by MTT (3-(4,5-Dimethylthiazol-2-yl)-2,5-Diphenyltetrazolium Bromide) assay using HELA and non-tumorigenic cell line HFF-1. The sensitivity of HELA (LC50: 207.31 µg/mL) and HFF-1 (LC50: 234.08 µg/mL) to free TAM was very low. However, after the encapsulation of TAM with PMMA-NR, the sensitivity significantly increased HELA (LC50: 71.83 µg/mL) and HFF-1 (LC50: 37.36 µg/mL). This indicates that TAM can be used for the treatment of ER-negative cervical cancer once conjugated to PMMA-NR nanoparticles. In addition, the PMMA-NR formulation appears to be highly suitable for cancer imaging and drug delivery.

| S-EPMC7408027 | biostudies-literature

Transparent Polymer Blends of Poly(methyl methacrylate) and Poly(propylene glycol).

Project description:Polymer blends, obtained by polymerization of methyl methacrylate in the presence of poly(propylene glycol), are investigated. Poly(propylene glycol) acts as a plasticizer, significantly lowering poly(methyl methacrylate)'s glass transition temperature and decreasing its elasticity modulus and yield stress. The mixture of methyl methacrylate with poly(propylene glycol) is more stable than its mixture with currently used poly(ethylene glycol), which leads to more uniform distribution and higher possible content of the plasticizer. Unlike low molecular weight plasticizers, poly(propylene glycol) is less prone to migration and exudation during manufacturing process and in use, and has low toxicity. Dynamic mechanical thermal analysis, compression testing and X-ray diffraction were used to investigate how the properties of the material depend on the content and molecular weight of the poly(propylene glycol) in the polymer blend. It was shown that the dependence of the glass transition temperature of methyl methacrylate polymerized in the presence of poly(propylene glycol) on the molar fraction of propylene glycol units is linear, and poly(propylene glycol) with lower molecular weight affects properties of the material stronger than poly(propylene glycol) with higher molecular weight. Therefore, the addition of poly(propylene glycol) allows to control the properties of poly(methyl methacrylate) easily and within wide range.

| S-EPMC9183039 | biostudies-literature

Copper (0) Mediated Single Electron Transfer-Living Radical Polymerization of Methyl Methacrylate: Functionalized Graphene as a Convenient Tool for Radical Initiator.

Project description:Polymer nanocomposites have been synthesized by the covalent addition of bromide-functionalized graphene (Graphene-Br) through the single electron transfer-living radical polymerization technique (SET-LRP). Graphite functionalized with bromide for the first time via an efficient route using mild reagents has been designed to develop a graphene based radical initiator. The efficiency of sacrificial initiator (ethyl α-bromoisobutyrate) has also been compared with a graphene based initiator towards monitoring their Cu(0) mediated controlled molecular weight and morphological structures through mass spectroscopy (MOLDI-TOF) and field emission scanning electron microscopy (FE-SEM) analysis, respectively. The enhancement in thermal stability is observed for graphene-grafted-poly(methyl methacrylate) (G-g-PMMA) at 392 °C, which may be due to the influence ofthe covalent addition of graphene, whereas the sacrificial initiator used to synthesize G-graft-PMMA (S) has low thermal stability as analyzed by TGA. A significant difference is noticed on their glass transition and melting temperatures by DSC. The controlled formation and structural features of the polymer-functionalized-graphene is characterized by Raman, FT-IR, UV-Vis spectroscopy, NMR, and zeta potential measurements. The wettability measurements of the novel G-graft-PMMA on leather surface were found to be better in hydrophobic nature with a water contact angle of 109 ± 1°.

| S-EPMC7240427 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data