Er3+Incorporated Transparent Ternary Nanocomposite as Active Core Material in Polymer Optical Preform with Improved Photo-emission Performance

2021 ◽  
Vol 04 ◽  
Author(s):  
Ipsita Chinya ◽  
Ranjan Sen ◽  
Anirban Dhar

Background: A polymer as a host in the optical waveguide has many advantages and, when doped with rare-earth (RE) elements, offers an efficient connection, compared to its glass-based counterparts as an amplifier. However, a polymer matrix causes the concentration quenching effect of REs in the polymer matrix, making the fabrication of RE-doped polymer waveguides more complicated as compared to the fabrication of glass-based complements. Moreover, controlling scattering loss at the particle-polymer interface for maintaining the optical clarity of the composite is also a great challenge. Objective: The main aim of the present study was to optimize the synthesis of Er2O3grafted Polymethylmethacrylate (PMMA)-Polystyrene (PS) composite based transparent ternary nanocomposite and its characterization to implement them as a potential material for active core in Polymer Optical Preform (POP). Methods: Nano Erbium Oxide (Er2O3) was successfully synthesized by the wet-chemical method and encapsulated by a polymerizable surfactant, i.e., 3-Methacyloxypropyltrimethoxy silane (MPS). The encapsulated nanoparticles were further subjected to grafting with PMMA using in-situ polymerization of methyl methacrylate (MMA) followed by blending with PS via solvent mixing technique. Results: The optical transparency of the ternary composite was achieved by fine-tuning the diameter (15-20 nm) of the PMMA coated Er2O3. The crystallinity present in Er2O3 was significantly reduced after PMMA coating. The comparatively higher refractive index obtained at 589 nm wavelength for the synthesized material indicated its usability as active core material in the presence of a commercial acrylate cladding tube. A photoluminescence (Pl) study indicated that the technique might be used for a higher level of Er3+doping in polymer matrix without sacrificing its transparency. Conclusion: The obtained results indicated that the sample synthesized with the adopted technique gives better Pl intensity compared to the other methods of Er3+ incorporation in polymer optical preform (POP).

2014 ◽  
Vol 1015 ◽  
pp. 381-384
Author(s):  
Li Liu ◽  
Li Hai Cai ◽  
Dan Liu ◽  
Jun Xu ◽  
Bao Hua Guo

The poly (butylene succinate) (PBS) and 3 wt% attapulgite (ATP) reinforced PBS/ATP nanocomposites with 1,6-hexanediol were fabricated using an in situ polymerization method. The crystallization behaviors indicated that ATP had effectively acted as nucleating agent, resulting in the enhancement on the crystallization temperature. The SEM results showed a superior interfacial linkage between ATP and PBS. Also, ATP could disperse as a single fiber and embed in the polymer matrix, which resulted in the improved mechanical properties.


Polymers ◽  
2020 ◽  
Vol 12 (1) ◽  
pp. 211 ◽  
Author(s):  
Valentina Sabatini ◽  
Tommaso Taroni ◽  
Riccardo Rampazzo ◽  
Marco Bompieri ◽  
Daniela Maggioni ◽  
...  

Polyamide 6 (PA6) suffers from fast degradation in humid conditions due to hydrolysis of amide bonds, which limits its durability. The addition of nanotubular fillers represents a viable strategy for overcoming this issue, although the additive/polymer interface at high filler content can become privileged site for moisture accumulation. As a cost-effective and versatile material, halloysite nanotubes (HNT) were investigated to prepare PA6 nanocomposites with very low loadings (1–45% w/w). The roles of the physicochemical properties of two differently sourced HNT, of filler functionalization with (3-aminopropyl)triethoxysilane and of dispersion techniques (in situ polymerization vs. melt blending) were investigated. The aspect ratio (5 vs. 15) and surface charge (−31 vs. −59 mV) of the two HNT proved crucial in determining their distribution within the polymer matrix. In situ polymerization of functionalized HNT leads to enclosed and well-penetrated filler within the polymer matrix. PA6 nanocomposites crystal growth and nucleation type were studied according to Avrami theory, as well as the formation of different crystalline structures (α and γ forms). After 1680 h of ageing, functionalized HNT reduced the diffusion of water into polymer, lowering water uptake after 600 h up to 90%, increasing the materials durability also regarding molecular weights and rheological behavior.


2006 ◽  
Vol 15 (5) ◽  
pp. 096369350601500 ◽  
Author(s):  
Jingyu Wang ◽  
Guoping Chen ◽  
Quan Zhou

A method to synthesize completely delaminated polymer/lamellar aluminophosphate (Mu-4) nanocomposites has been successfully developed, wherein organo-modification of Mu-4 followed by in situ polymerization was applied. It can be found that the long chain n-dodecylamine molecules can favor the intercalation of Mu-4 and thus readily make the Mu-4 layers delaminated in the polymer matrix compared with the short chain N,N-dimethylpropane-1,3-diamine.


Polymers ◽  
2020 ◽  
Vol 12 (10) ◽  
pp. 2366 ◽  
Author(s):  
Xiaoxing Yan ◽  
Yu Tao ◽  
Xingyu Qian

Microcapsules were prepared by in situ polymerization with urea formaldehyde resin as the wall material and Dulux waterborne acrylic acid as the core material. The effects of the core–wall ratio, water bath temperature and depositing time on the morphology, particle size, yield and encapsulation ratio of microcapsules were investigated by orthogonal experiment of three factors and two levels. The results showed that the core–wall ratio had the greatest influence on the performance of microcapsules. When the core–wall ratio was 0.58:1, the water bath temperature was 70 °C, and the depositing time was 5 d, the microcapsule performance was the best. With the increase in depositing time, the yield of microcapsule particles increased gradually, and the microcapsules appeared to show an adhesive phenomenon. However, the long-term depositing time did not lead to complete deposition and agglomeration of microcapsules. When 10.0% concentration of the waterborne acrylic microcapsules with 0.58:1 of core–wall ratio was added to the coatings, the mechanical and optical properties of the coatings did not decrease significantly, but the elongation at break increased significantly. Therefore, this study offers a new prospect for using waterborne acrylic microcapsules to improve the toughness of waterborne paint film which can be cured at room temperature on a wood surface.


2012 ◽  
Vol 583 ◽  
pp. 236-239
Author(s):  
Xiao Min Fang ◽  
Yuan Qing Xu ◽  
Tao Ding

In order to develop efficient “three in one” intumesent flame retardants, a novel caged bicyclic phosphate, tris(1-oxo-2,6,7-trioxa-1-phosphorbicyclo[2.2.2]octane methylene-4)phosphate (trimer) as the core material was encapsulated by melamine resin and etherified melamine resin as nitrogen resource respectively via in situ polymerization. The two microencapsulations were characterized by SEM, XPS and thermal gravimetric analysis. When they were used as intumesent flame retardant in epoxy they all exhibit good properties. With 20wt% loading amount the flame-retarded epoxy all can pass UL94 V-0 rating.


2010 ◽  
Vol 148-149 ◽  
pp. 1031-1035
Author(s):  
Yang Zhao ◽  
Wei Zhang ◽  
Le Ping Liao ◽  
Wu Jun Li ◽  
Yi Xin

With the development of the embedded microcapsule concept for self-healing material, the preparation of microcapsule has been paid more attentions. A new series of microcapsules were prepared by in situ polymerization technology in an oil-in-water emulsion with polyoxymethylene urea (PMU) as shell material and a mixture of epoxy resins as core material. The PMU microcapsules were characterized by Fourier transform infrared spectroscopy (FTIR), scanning electronic microscopy (SEM), particle size analyzer and thermo gravimetric analyzer (TGA) to investigate their chemical structure, surface morphology, size distribution and thermal stability, respectively. The results indicate that PMU microcapsules containing epoxy resins can be synthesized successfully. The optimized reaction parameters were obtained as follow: agitation rate 600 rpm, 60°C water bath, pH=3.5, core material 20ml and hot water dilution by in-situ polymerization. The size is around 116 μm. The rough outer surface of microcapsule is composed of agglomerated PMU nanoparticles. The microcapsules basically exhibit good storage stability at room temperature, and they are chemically stable before the heating temperature is up to approximately 200°C.


2011 ◽  
Vol 391-392 ◽  
pp. 1427-1430
Author(s):  
Guo Lun Zhong ◽  
Ru Yi Bi ◽  
Hong Lei Mao ◽  
Yong Hong Wang ◽  
Jin Bao Xu

A new method for fabrication of core-shell functional polymer coated nanoparticles was proposed in this work. At first the magnetite particles were wrapped with single-layer oleic acid for getting a hydrophobic surface. Then the monomer molecules of 4-vinylbenzoic acid were fabricated onto this layer by self-assembly and finally in-situ polymerization was taken place for obtaining the functional polymer coated nanoparticles with –COOH groups outside. The nanoparticles were characterized by FTIR, TEM, magnetic property, etc. The results showed that the size of the particle was less than 20 nm in diameter and had a very good property of superparamagnetism.


2013 ◽  
Vol 712-715 ◽  
pp. 105-110 ◽  
Author(s):  
Yi Shen Huang ◽  
Ji Ju Guan ◽  
Guo Wei Ma ◽  
Zhong Ya Li ◽  
Xue Feng Xu

With butyl stearate (BS) as the core material and melamine-formaldehyde resin (MF) as the wall material, BS-MF resin microcapsules were synthesized under in situ polymerization method. The microcapsules were characterized using FTIR, SEM and other methods. The four-ball friction method was performed to test the tribological property of the microcapsules when polyethylene glycol was taken as the base fluid. The results showed that base fluid with 3% microcapsules had a friction coefficient as small as 0.053 and the wear scar diameter could be 0.326mm (4%) under 314N. The microcapsules were ruptured under the action of friction and then the reactive group formed physical adsorption film. The physical adsorption film, together with the subsequently formed friction polyester film, presented a synergistic lubricating effect.


2016 ◽  
Vol 1819 ◽  
Author(s):  
Jenaro L. Varela Caselis ◽  
Marco Morales Sánchez ◽  
José A. Galicia Aguilar ◽  
Efraín Rubio Rosas

ABSTRACTPolymer-clay nanocomposites are compounds in which nanoclay particles are distributed in a polymer matrix. Epoxy-clay nanocomposites have become a very interesting topic among researchers in the past two decades because nanoclays have a positive effect on the mechanical, thermal and especially barrier anticorrosive performance of the polymers. In this study, epoxy-montmorillonite organoclay (OMMT) nanocomposite coatings were prepared and deposited on carbon steel substrates. The coatings were prepared through in situ polymerization and by UV-curing technique. The OMMT was added to epoxy resin at loadings between 0 wt.% and 5 wt.%, the particles of OMMT were dispersed using forced agitation-sonication and deposited on carbon steel coupons. The nanocomposite coatings obtained have been characterized by scanning electron microscopy (SEM), spectroscopy Fourier transform infrared (FTIR), X-ray diffraction (XRD), thermogravimetric analysis (TGA), and evaluated their corrosion protection effect on cold rolled carbon steel coupons by performing visual analysis. The X-ray analysis showed that exfoliation occurred for the OMMT in the polymer matrix, the SEM analysis showed that OMMT was homogenous dispersed in the polymer matrix and the coatings were uniform. The FTIR analysis showed the characteristic bands of epoxy resin and OMMT in the composite. The results showed that 1 wt.% OMMT coating exhibit better anticorrosive properties than pure epoxy.


2016 ◽  
Vol 40 (4) ◽  
pp. 3612-3621 ◽  
Author(s):  
Gholamhossein Mohammadnezhad ◽  
Mohammad Dinari ◽  
Roozbeh Soltani

The addition of nanoboehmite as a nanofiller into the polymer matrix led to the improvement of the thermal properties and increased the active sites of nanocomposites for Cu(ii) removal.


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