Graded‐index plastic optical fiber with high mechanical properties enabling easy network installations. I

A doped poly(methyl methacrylate) (PMMA)–based graded‐index plastic optical fiber (GI POF) with high mechanical strength is reported for the first time. Although the POF is generally believed to have a good mechanical flexibility even if it has a large‐core diameter, such a high mechanical strength has been provided by making the polymer chains in the POF highly oriented in its axial direction. If such an orientation of polymer chains is eliminated, the POF becomes brittle, which is similar to silica‐based fibers. On the other hand, too high an orientation of the polymer chains induces fiber deformation in a high‐temperature atmosphere resulting from orientation relaxation. This study reports how high mechanical strengths such as the tensile strength and the large elongation are provided to the GI POF. By selecting the optimum heat‐drawing conditions, the GI POF has a mechanical strength comparable to that of the commercially available step index (SI) POF. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 404–409, 2004     

Thermal and optical properties of PMMA–titania hybrid materials prepared by sol‐gel approach with HEMA as coupling agent

A series of sol‐gel derived organic–inorganic hybrid materials consisting of organic poly(methyl methacrylate) (PMMA) and inorganic titania (TiO₂) were successfully synthesized by using 2‐hydroxyethyl methacrylate (HEMA) as coupling agent. In this work, HEMA is first copolymerized with methyl methacrylate monomer at specific feeding ratios by using benzoyl peroxide (BPO) as initiator. Subsequently, the as‐prepared copolymer (i.e., sol‐gel precursor) is then cohydrolyzed with various contents of titanium butoxide to afford chemical bondings to the forming titania networks to give a series of hybrid materials. Transparent organic–inorganic hybrid materials with different contents of titania are always achieved. Effects of the material composition on the thermal stability, optical properties, and morphology of neat copolymer and a series of hybrid materials, in the form of both coating and free‐standing film, are also studied by differential scanning calorimetry, thermogravimetric analysis, UV–Vis transmission spectra, refractometer, and atomic force microscopy, respectively. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 400–405, 2004     

The synthesis of poly(3‐hydroxybutyrate)‐g‐poly(methylmethacrylate) brush type graft copolymers by atom transfer radical polymerization method

Brush type of poly (3‐hydroxy butyrate), PHB, copolymer synthesis has been reported. Natural PHB was chlorinated by passing chlorine gas through PHB solution in CHCl₃/CCl₄ mixture (75/25 v/v) to prepare chlorinated PHB, PHB‐Cl, with the chlorine contents varying between 2.18 and 39.8 wt %. Toluene solution of PHB‐Cl was used in the atom transfer radical polymerization (ATRP) of methyl methacrylate, MMA, in the presence of cuprous bromide (CuBr)/2,2′‐bipyridine complex as catalyst, at 90°C. This “grafting from” technique led to obtain poly (3‐hydroxybutyrate)‐g‐poly(methylmethacrylate) (PHB‐g‐PMMA) brush type graft copolymers (cylindrical brush). The polymer brushes were fractionated by fractional precipitation methods and the γ values calculated from the ratio of the volume of nonsolvent to volume of solvent of brushes were ranged between 2.8 and 9.5 depending on the molecular weight, grafting density, and side chain length of the brushes, while the γ values of PHB, PHB‐Cl, and homo‐PMMA were 2.7–3.8, 0.3–2.4, and 3.0–3.9, respectively. The fractionated brushes were characterized by gel permeation chromatography, ¹H‐NMR spectrometry, thermogravimetric analysis (TGA), and differential scanning calorimetry techniques. PHB‐g‐PMMA brush type graft copolymers showed narrower molecular weight distribution (mostly in range between 1.3 and 2.2) than the PHB‐Cl macroinitiator (1.6–3.5). PHB contents in the brushes were calculated from their TGA thermograms and found to be in range between 22 and 42 mol %. The morphologies of PHB‐g‐PMMA brushes were also studied by scanning electron microscopy. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Effect of ultrasonic oscillations on weld line strength of PS,PMMA, and their blends

The effect of ultrasonic oscillations on the weld line strength of amorphous polystyrene (PS), polymethyl methacrylate (PMMA), and PS/PMMA (20/80, 50/50, 80/20) blends at various temperatures was investigated. By facilitating the molecular diffusion across the weld line, the introduction of ultrasonic oscillations could evidently improve the weld line strength of PS, PMMA, and their blends. The different effects on the weld line strength of PS/PMMA (20/80, 50/50, 80/20) blends were investigated. The ultrasonic oscillations could greatly increase the weld line strength of PS/PMMA (80/20) by ～ 70%, but was less efficient to PS/PMMA (50/50, 20/80) blends, due to the great difference of weld line morphologies of these blends. The dispersed phase of PS/PMMA (80/20) in the weld line was spherical while two different morphologies in the weld line of PS/PMMA (50/50) were observed. And the stripe‐like morphology of PS perpendicular to the flow direction in the weld line of PS/PMMA (20/80) is responsible for the little effect of ultrasonic oscillations. The fractured surfaces of PS, PMMA, and PS/PMMA (80/20) with weld line became much rougher due to the introduction of ultrasonic oscillations. The morphology study of PS/PMMA (80/20) showed that the spherical dispersed phase of PS/PMMA at the skin turned smaller under ultrasonic oscillations. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 2990–2997, 2006     

Preparation of compatible blends of poly(methyl methacrylate) used in dentistry with a reactive terpolymer containing maleic anhydride and their thermomechanical characterization

This study focuses on the preparation of compatible blends with the poly(methyl methacrylate) (PMMA) using a reactive terpolymer maleic anhydride–styrene–vinyl acetate (MA–St–VA). In the first series of experiments, binary blends of the PMMA and the MA–St–VA terpolymer have been prepared in tetrahydrofurane. The PMMA and the MA–St–VA terpolymer formed the compatible blends. The effects on thermomechanical properties of MA–St–VA terpolymer ratio in the blends were studied. The glass transition temperatures (T_g), thermal expansion coefficient (α), and other thermomechanical parameters for the blends have been established by TMA method and the compatibility of two polymers has been evaluated by these TMA parameters. The addition of MA–St–VA terpolymer to PMMA made a plasticizing effect on PMMA. This effect regularly changed with the increasing of the terpolymer in the blends. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 363–367, 2006     

涂布层压法制备抗静电塑料

探索和开发出一种新型制备抗静电塑料方法。在PVC、PMMA或PC基材板(片)上,涂布有一层表面1 .0～1 .5μm厚的导电涂料的离型PET薄膜,叠放时导电涂料层向下与基材板接触,PET膜向外。为了提高导电涂层与基材板间的粘合强度,还可以在两层间加上一层粘合膜。     

热压法快速制作微流控芯片模具

提出了一种微流控芯片模具的快速批量制作方法。应用光刻与湿法腐蚀技术制作玻璃母模,然后采用热压成形技术批量制作聚甲基丙烯酸甲酯(PMMA)阳模,再利用阳模浇模、键合批量制作聚二甲基硅氧烷(PDMS)微流控芯片。结果表明,该法制作的PMMA模具及复制得到的PDMS芯片平整度好、一致性高,其沟道宽度和深度的相对标准偏差分别小于0.5%和1.5%。     

Controlled formation of Ag/poly(methyl-methacrylate) thin films by RAFT technique for optical switcher

The functional group of sulfur was introduced into the PMMA terminus by the reversible addition-fragmentation transfer (RAFT) technique and the PMMA/Ag nanocomposite film was prepared by the in situ synthetic method. The third-order nonlinear optical properties of the material were further investigated by the Z-scan technique. The result shows that the χ⁽³⁾ nonlinearity of the material depend on the doped content of Ag nanoparticles and is obtained to be 6.22 × 10⁻⁹ esu at the content of 2.4 wt%. Furthermore, it is found that the material has the potential application on optical switcher at the content of 0.8 wt%.     

Steady ratcheting strains accumulation in varying temperature fatigue tests of PMMA

The evolutions of ratcheting strains of polymethyl methacrylate (PMMA) at different temperatures and stress levels were experimentally investigated. A steady ratcheting strain growth region with a constant rate was observed in all specimens, which occupied significant part of total fatigue failure life. Experimental results also showed that the steady ratcheting growth rate varied with applied temperatures and loading. In this paper, theory of thermally activated process for glassy polymers was used to describe the plastic deformations during the cycle. Based on the correlations between ratcheting strains per cycle and hysteresis loop energy, a new ratcheting strains accumulative model for polymer materials was developed, which quantificationally elucidated the effects of temperature, loading frequency, mean stress and stress amplitude on the accumulative rate of ratcheting strains. Comparing the predications from the proposed model with experimental ratcheting strain data of PMMA, it was found that the model could describe the steady ratcheting strain accumulative behaviors under arbitrary temperatures and loading conditions exactly.     

Mechanical and three-body abrasive wear behaviour of PMMA/TPU blends

The blends of poly(methyl methacrlate) (PMMA) and thermoplastic polyurethane (TPU) were prepared by a Brabender co-twin screw extruder. The mechanical and three-body abrasive wear behaviour of PMMA/TPU blends has been studied. Three-body abrasive wear tests were conducted using rubber wheel abrasion tester (RWAT) under different abrading distances at 200 rpm and 22 N load. A significant reduction in tensile strength and tensile modulus with an increase in TPU content in the blend formulation was observed. Three-body abrasive wear results indicate that the wear volume increases with increase in abrading distance for all the samples studied. However, neat PMMA showed better wear resistance as compared to PMMA/TPU blends. The worn surface features, as examined through scanning electron microscope (SEM), show matrix cracking and deep furrows in PMMA/TPU blends.