共查询到20条相似文献,搜索用时 15 毫秒
1.
Christian Cruzat Contreras Octavio Peña Manuel F. Meléndrez Judith Díaz-Visurraga Galo Cárdenas 《Colloid and polymer science》2011,289(1):21-31
This work proposes the synthesis, characterization and investigation of the stabilization capabilities of chitosan doped with
magnetic nanoparticles. Nanoparticles of Fe, Co, Co(II,III) oxide, Ni and Ni/Ag mixture in 2-propanol were synthesized by
chemical liquid deposition and the incorporation on the polymeric matrix was performed by solvated metal atom dispersion.
Colloids and nanoparticles supported on chitosan were characterized by ultraviolet, Fourier-transform infrared, thermogravimetric
analysis, electron diffraction X-ray and magnetic behaviour; transmission and field electronic scanning electron microscopy.
The particle size distribution of colloids ranges from 6 to 50 nm with low particle stability due to flocculation after 120 days.
The nanoparticles supported on chitosan had a particle size distribution of approximately between 10 and 80 nm, with low particle
distribution; however, these particles do not flocculate because the matrix increases the stabilization of nanoparticles.
All compounds present superparamagnetic behaviour at low temperature. 相似文献
2.
3.
《Analytical letters》2012,45(6):982-998
Molecular surface-imprinted polymers nanoparticles encapsulating magnetite modified with oleic acid, for recognition of salicylic acid was prepared by three-step miniemulsion polymerization. The important factors including polymerization process, solvents, miniemulsifying approaches, and co-stabilizer have been investigated to obtain magnetic molecular imprinting polymers (MMIPs) nanoparticles (NPs) with high saturation magnetization (Ms), regular morphology, and good monodispersion. The results showed that the amount of magnetite encapsulated in MMIPs NPs was 43.4 wt% and Ms was 33.584 emu/g. Thus, MMIPs NPs could be separated easily within 2 minutes by an external magnetic field. The transmission electron microscope (TEM) showed MMIPs NPs were of regular sphere with core-shell structure, where magnetite NPs were uniformly encapsulated in homogeneous polymer shells. The average diameter of MMIPs NPs was 98 nm with RSD of 6.6%. Good recognition and high loading of target molecule were achieved by MMIPs NPs in batch rebinding tests. 相似文献
4.
Friedemann K Turshatov A Landfester K Crespy D 《Langmuir : the ACS journal of surfaces and colloids》2011,27(11):7132-7139
A model system for multicompartment nanofibers was fabricated by colloid electrospinning. The obtained nanostructured material consisted of fluorescent polymer nanoparticles that were synthesized in a miniemulsion and then embedded in fluorescently labeled polymer nanofibers. Because of the absence of contrast between both polymers, the immobilized nanoparticles cannot be reliably identified in the nanofibers via electron microscopy or other techniques. Here, we describe investigations on the hybrid material with two-color STED microscopy to localize the nanoparticles and to quantify their distribution along nanofibers with particle and fiber radii down to 50 nm. 相似文献
5.
Abraham Chemtob Benjamin Kunstler Céline Croutxé-Barghorn Samuel Fouchard 《Colloid and polymer science》2010,288(5):579-587
This study describes the radical photopolymerization of acrylate monomers in miniemulsion. Starting from nanosized acrylate
droplets (<100 nm) which encapsulate a type I radical photoinitiator (BAPO), UV irradiation led after a few minutes to the
formation of polymer nanoparticles of similar size. The present study deals with the kinetics aspects of this reaction and
the colloidal properties of the resulting polymer dispersions. Real-time Fourier transform near-infrared spectroscopy in transmission
was implemented to follow continuously the fast photopolymerization process. In addition, the spatial resolution of the photoinduced
process allowed the online monitoring of the evolution of the miniemulsion size during the UV irradiation through dynamic
light scattering. 相似文献
6.
Anke Ziegler Katharina Landfester Anna Musyanovych 《Colloid and polymer science》2009,287(11):1261-1271
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. 相似文献
7.
Wang Y Xu H Ma Y Guo F Wang F Shi D 《Langmuir : the ACS journal of surfaces and colloids》2011,27(11):7207-7212
A one-pot colloidal reaction strategy was developed to synthesize asymmetric magnetic composite particles (AMCPs) with high anisotropy and magnetic content. The asymmetricity was established by having two portions of the particle composed of both polystyrene and silica, among which the latter was conjugated with magnetite nanoparticles. Phase separation was found to be critical in developing the asymmetric structure between the inorganic and polymer components during miniemulsion polymerization and the sol-gel reaction. Morphological control of the magnetic composite particles was achieved in a straightforward fashion by adjusting the processing parameters. These asymmetric nanomaterials with superparamagnetic and amphiphilic properties will have significant potential in biomedical applications. 相似文献
8.
Anderson N. Mendes Isabela Hubber Mônica Siqueira Gleyce Moreno Barbosa Davyson de Lima Moreira Carla Holandino José Carlos Pinto Marcio Nele 《Macromolecular Symposia》2012,319(1):34-40
Summary: This work aimed to produce poly(methyl methacrylate) nanoparticles for use in drug encapsulation. The polymer nanoparticles were produced using miniemulsion polymerization technique. Monomer miniemulsion showed moderate stability and polymer average particle size was about 90 nm. PMMA nanoparticles were tested for toxicity in human leukemic cell strain K562 and they did not show any adverse effect on cell viability. Therefore, poly(methyl methacrylate) nanoparticles are suitable to encapsulate antitumor agents. 相似文献
9.
Styrene polymer/ZnO nanocomposite latex was fabricated using miniemulsion polymerization in the presence of coupling agent
3-aminopropyltriethoxysilane (APTES) and hexadecane as hydrophobe. The size distribution and morphology of the composite latex
particles were characterized by dynamic light scattering and transmission electron micrograph. X-ray photoelectron spectroscopy
and Fourier transform infrared spectrophotometer results demonstrate that ZnO nanoparticles were encapsulated into polymer
phases. The coupling treatment of ZnO with APTES can improve the dynamic contact angles of ZnO nanoparticle with water to
enhance its hydrophobicity. When 0.6% APTES to ZnO (wt/wt) is used to modify ZnO, the encapsulation efficiency of ZnO reaches
to 95%. It shows that the high encapsulation efficiency improves dispersion of ZnO nanoparticles in polymer film by scanning
electron microscope. The stable structural hybrid latex can adequately exert unique function of nanoparticles in coatings.
It indicates that the coatings added the composite latex exhibits perfect antibacterial activity, which has a tremendous potentiality
in the field of coating materials. 相似文献
10.
Kim Y. van Berkel Craig J. Hawker 《Journal of polymer science. Part A, Polymer chemistry》2010,48(7):1594-1606
A simple and modular synthetic approach, based on miniemulsion polymerization, has been developed for the fabrication of composite polymer–metal nanoparticle materials. The procedure produces well‐defined composite structures consisting of gold, silver, or MnFe2O4 nanoparticles (~10 nm in diameter) encapsulated within larger spherical nanoparticles of poly(divinylbenzene) (~100 nm in diameter). This methodology readily permits the incorporation of multiple metal domains into a single polymeric particle, while still preserving the useful optical and magnetic properties of the metal nanoparticles. The morphology of the composite particles is retained upon increasing the inorganic content and also upon redispersion in organic solvents. Finally, the ability to tailor the surface chemistry of the composite nanoparticles and incorporate steric stabilizing groups using simple thiol‐ene chemistry is demonstrated. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 1594–1606, 2010 相似文献
11.
We aimed at preparing magnetic iron oxide particles by the oxidation-precipitation method in order to encapsulate these particles in polymer matrices composed of poly(acrylamide-styrene sulfonic acid sodium salt). Nanocomposites were synthesized by the incorporation of surface treated magnetic nanoparticles in the synthesized polymers via in situ inverse mini-emulsion polymerization process. The study parameter was the ionic monomer content in the synthesized polymers. The structure and the morphology of the magnetic nanogels were characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), dynamic light scattering (DLS), thermal gravimetric analysis (TGA) and scanning electron microscopy (SEM). FTIR and XRD showed that pure magnetite was formed and successfully encapsulated in the composite nanoparticles. The polymer encapsulation could reduce the susceptibility to leaching and could protect the magnetite particle surfaces from oxidation. The ionic monomer content had a great effect on the magnetization behavior. Magnetite prepared by the oxidation precipitation method, of 50 nm mean particle size, was embedded successfully into the polymer nanogels with a reasonable magnetic response, as proved by vibrating sample magnetometer measurement. Magnetic nanocomposites were proven to be super-ferromagnetic materials. 相似文献
12.
Due to the existing interest in new hybrid particles in the colloidal range based on both magnetic and polymeric materials for applications in biotechnological fields, this work is focused on the preparation of magnetic polymer nanoparticles (MPNPs) by a single-step miniemulsion process developed to achieve better control of the morphology of the magnetic nanocomposite particles. MPNPs are prepared by surfactant-free miniemulsion polymerization using styrene (St) as a monomer, hexadecane (HD) as a hydrophobe, and potassium persulfate (KPS) as an initiator in the presence of oleic acid (OA)-modified magnetite nanoparticles. The effect of the type of cross-linker used [divinylbenzene (DVB) and bis[2-(methacryloyloxy)ethyl] phosphate (BMEP)] together with the effect of the amount of an aid stabilizer (dextran) on size, particle size distribution (PSD), and morphology of the hybrid nanoparticles synthesized is analyzed in detail. The mixture of different surface modifiers produces hybrid nanocolloids with various morphologies: from a typical core-shell composed by a magnetite core surrounded by a polymer shell to a homogeneously distributed morphology where the magnetite is uniformly distributed throughout the entire nanocomposite. 相似文献
13.
Stable dispersions of polyacrylonitrile (PAN) nanoparticles in the size range between 100 nm < d < 180 nm were made by polymerization in miniemulsion and characterized by dynamic light scattering, transmission electron microscopy (TEM), and wide angle X‐ray scattering (WAXS). Due to the insolubility of the polymer in its monomer, such particles are not accessible by classical emulsion polymerization. The pure PAN particles are composed of ca. 10 nm large polymer nanocrystals, i. e., the formed polymer precipitates and crystallizes direct after formation. As a consequence, the final latexes do not adopt spherical shape, but show a well defined, narrowly distributed boulder‐like phenotype which is called “crumpled latexes”. Copolymerization with styrene results in a continuous transition between the crumpled and a smooth spherical morphology, which is again related to a decreased degree of crystallinity. 相似文献
14.
Surface modification and characterization of magnetic polymer nanospheres prepared by miniemulsion polymerization 总被引:10,自引:0,他引:10
Liu X Guan Y Ma Z Liu H 《Langmuir : the ACS journal of surfaces and colloids》2004,20(23):10278-10282
A novel and effective protocol for the surface modification and quantitative characterization of magnetic polymeric nanospheres prepared by miniemulsion polymerization is reported. Composite nanospheres consisting of polymer-coated iron oxide nanoparticles were prepared by the miniemulsion polymerization of methyl methacrylate and divinylbenzene in the presence of magnetic fluid. Surface modification reaction of the magnetic polymer with poly(ethylene glycol) (PEG) was employed to obtain a hydrophilic hydroxyl-group-functionalized magnetic nanospheres. An affinity dye, Cibacron blue F3G-A (CB), was then coupled covalently to prepare a magnetic nonporous affinity adsorbent. The morphology and magnetic property of the polymer nanospheres obtained were examined by transmission electron microscopy and a vibrating sample magnetometer. The contents of surface groups modified were quantitatively measured by using diffusive reflectance Fourier transform infrared spectroscopy on the basis of a linear relationship between the intensity ratio of IC-O-C/IC=O and the content of PEG. X-ray photoelectron spectroscopy (XPS) was used to examine the surface of magnetic nanospheres. It was confirmed by the comparison of XPS spectra of both dye-coated and uncoated magnetic nanospheres to which the CB ligand was coupled, and the surface of the PEG-modified nanospheres had an exact 3:7 atomic ratio of sulfur to nitrogen. 相似文献
15.
Well-defined nanoparticles composed of a tetraphenylmethane-based microporous polymer network with an average particle diameter of 30-60 nm were fabricated by a miniemulsion polymerization technique. Strong green emission was observed and efficient excitation energy transfer from nanoparticles to surface-bound dye molecules was explored. 相似文献
16.
I. Csetneki M. Kabai Faix A. Szilgyi A. L. Kovcs Z. Nmeth M. Zrinyi 《Journal of polymer science. Part A, Polymer chemistry》2004,42(19):4802-4808
Magnetic iron oxide (magnetite, Fe3O4) nanoparticles were encapsulated with polystyrene to give a stable water‐based magnetic polymer latex, using the miniemulsion polymerization technique. The resulting magnetic latexes were characterized with transmission electron microscopy (TEM), dynamic light scattering (DLS), vibrating sample magnetometer measurements (VSM), and 57Fe Mössbauer spectroscopy measurements. TEM revealed that all magnetite nanoparticles were embedded in the polymer spheres, leaving no empty polystyrene particles. The distribution of magnetite particles within the polystyrene spheres was inhomogeneous, showing an uneven polar appearance. The DLS measurements indicated a bimodal size distribution for the particles in the latexes. According to our magnetometry and Mössbauer spectroscopy data, the encapsulated magnetite particles conserve their superparamagnetic feature when they are separated in the polymer matrix. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 4802–4808, 2004 相似文献
17.
Gabriela Diaconu José M. Asua Maria Paulis Jose R. Leiza 《Macromolecular Symposia》2007,259(1):305-317
Summary: Waterborne polymer clay nanocomposites (WPCN) were prepared by emulsion and miniemulsion copolymerization of butyl acrylate and methyl methacrylate with enhanced mechanical, thermal and barrier properties for coating applications. Emulsion polymerization was used to synthesize WPCN using pristine Na-MMT (sodium montmorillonite) and miniemulsion polymerization to prepare the WPCNs when the pristine clay was organically modified and hence its incorporation into the polymerization loci was not guaranteed by the conventional emulsion polymerization technique. Both techniques allowed preparing stable nanocomposite latexes of BA/MMA copolymers with partially exfoliated morphologies as demonstrated by wide X-ray difraction (WAXD) and transmission electron microscope (TEM) measurements. Furthermore, latexes with solids contents up to 45 wt% and manageable viscosities were prepared for the first time using seeded semibatch emulsion polymerization. 相似文献
18.
Marie Tschage Klaus Beckerle Khosrow Rahimi Seungwhan Jung Stefan S.‐H. Chang Jörg Stellbrink Jun Okuda 《Journal of polymer science. Part A, Polymer chemistry》2017,55(1):175-180
Poly(styrene) microgels are known, but the influence of tacticity on particle formation and behavior has not been investigated yet. Isotactic poly(styrene) (iPS) with Mn = 15–120 kg/mol is synthesized by coordinate polymerization and cross‐linked by Friedel–Crafts alkylation in a miniemulsion. Nuclear magnetic resonance (NMR) spectroscopy, light microscopy, cryogenic transmission electron microscopy, and wide‐angle powder diffraction are applied to understand the structure of microgels obtained. Typically, spherical microgels with overall diameter of 40–500 nm are found. Isotacticity of the polymer is retained during microgel formation. Increase of cross‐linker content leads to partial crystallinity inside the microgel. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55, 175–180 相似文献
19.
Maryam Kaabipour Saeid Khodadoust Fatemeh Zeraatpisheh 《Journal of separation science》2020,43(5):912-919
In this work, core/shell magnetic molecularly imprinted polymer nanoparticles were synthesized for extraction and pre‐concentration of valsartan from different samples and then it was measured with high‐performance liquid chromatography. For preparation of molecularly imprinted polymer nanoparticles, Fe3O4 nanoparticles were coated with tetraethyl orthosilicate and then functionalized with 3‐(trimethoxysilyl) propyl methacrylate. In the next step, molecularly imprinted polymer nanoparticles were synthesized under reflux and distillation conditions via polymerization of methacrylic acid, valsartan (as a template), azobisisobutyronitrile and ethylene glycol dimethacrylate as cross linking. The properties of molecularly imprinted polymer nanoparticle were investigated by FTIR spectroscopy, field emission scanning electron microscopy, and X‐ray diffraction. Box‐Behnken design with the aid of desirability function was used for optimizing the effect of variables such as the amounts of molecularly imprinted polymer nanoparticles, time of sonication, pH, and volume of methanol on the extraction percentage of valsartan. According to the obtained results, the affecting variables extraction condition were set as 10 mg of adsorbent, 16 min for sonication, pH = 5.5 and 0.6 mL methanol. The obtained linear response (r2 > 0.995) was in the range of 0.005–10 µg/mL with detection limit 0.0012 µg/mLand extraction recovery was in the range of 92–95% with standard deviation less than 6% (n = 3). 相似文献
20.
《印度化学会志》2022,99(11):100744
ZnO nanoparticles are one of the prominent photocatalysts for environmental applications due to its high redox ability, nontoxic and higher stability. This report explains the synthesis of ZnO nanoparticles by a simple solution combustion method using zinc nitrate hexahydrate as an oxidizing agent and incense stick powder as fuel at 400 °C. Several techniques were adopted for the characterization of the obtained product. X-ray diffraction (XRD) pattern shows that a lower concentration of fuel gives pure ZnO and a higher concentration of fuel results in calcium doped ZnO with a cubic phase having a crystallite size of 32–28 nm. UV–vis spectrum shows that as the fuel concentration increases, band gap decreases and reaches to 3.33 eV for 3 g of fuel. Spongy networks with many pores wereobserved in the scanning electron microscope (SEM) and transmission electron microscope (TEM) images showed the average particle size of Ca doped ZnO NPs is about 20 nm. Pure and Ca doped ZnO nanoparticles were examined for photocatalytic degradation of methylene blue (MB) dye under UV light irradiation. The results prove that Ca doped ZnO nanoparticles show good photocatalytic activity. 相似文献