Solid-state dye laser with modified poly(methyl methacrylate)-doped active elements

Laser generation with modified poly(methyl methacrylate) (MPMMA)-doped matrices with several different types of Rhodamine-based dyes was obtained. Pumping with a frequency-doubled Q-switched Nd:YAG laser was used. During the experiments, high conversion efficiency was achieved. The strong nonlinear dependence of the operating lifetime and the conversion efficiency of material tested on the pump-pulse-repetition rate was observed. Possible mechanisms responsible for the conversionefficiency drop and the useful lifetime of the material are discussed.     

Hot-press molded poly(methyl methacrylate) matrix for solid-state dye lasers

A hot-press molding method was used to fabricate dye-doped poly(methyl methacrylate) (PMMA) slabs. Three rhodamine dyes, Rh640 (ClO(4)), Rh6G(ClO(4)), and Rh6G (Cl), were impregnated into the PMMA matrix first by dissolving the dye and granular PMMA in a solvent mixture of chloroform and methanol and then heating the mixture in vacuo at 175 degrees C to obtain a spongy preform. The powdered preform was molded into slabs at 175 degrees C and at <1 mbar, to eliminate the formation of bubbles in the slabs. We annealed the slabs for several hours to improve its optical homogeneity and hence its lasing efficiency. When pumped by a 1.5-mJ nitrogen laser, we obtained peak lasing efficiencies of 8% and 7.8%, respectively, for Rh6G (ClO(4)) and Rh640 (ClO(4)) in PMMA matrices. The lasing efficiency of Rh6G (ClO(4))-doped PMMA suffered a reduction rate of 0.012%/shot compared with 0.15%/shot for Rh640 (ClO(4))-doped PMMA. In contrast, Rh6G (Cl) in a hot-press molded PMMA slab suffered thermal bleaching that resulted in a low lasing efficiency of <1%; this can be explained by its absorption and fluorescence characteristics.     

Comparison between poly(methyl methacrylate)-carbon black and polyaniline conductive coatings

This work aims to develop and compare two types of conductive, polymer-based coatings via a dip coating process. The first type of coatings was made by dispersing and incorporating carbon black (CB) nanoparticles in a poly(methyl methacrylate) (PMMA) solution followed by dip coating. The CB content and dipping parameters were varied to explore their effects on the particle dispersion, coating thickness, and conductivity of the coatings. The dispersion of the CB particles in the polymer matrix was examined by scanning electron microscopy (SEM), while the coating thickness and conductivity were measured with a surface profilometer and a four-point probe electrometer, respectively. The good dispersion of carbon nanoparticles in the PMMA matrix was observed in the coatings. The conductivity of the PMMA-CB composite coatings was found to be mainly affected by CB content, particle dispersion as well as coating thickness. On the other hand, polyaniline (PANI) was used to make conductive coatings by dip coating and doping, and the advantages and limitations of the PANI coatings were compared with the PMMA-CB coatings.     

Environmentally-affected indentation fracture in poly(ethersulphone) and poly(methyl methacrylate)

The effect of plasticization on the ductile-to-brittle fracture transitions (DBFT) in the ball indentation of poly (ethersulphone) (PES) and poly(methyl methacrylate) (PMMA) has been studied. The DBFT in various organic liquids are governed by a size effect related to the indenter radius, in accordance with the Puttick theory of fracture transitions. In addition, abrasive wear rates of the polymers in these liquids are shown to correlate with the critical indenter radius needed to produce a fracture transition, owing to the connection with fracture toughness.     

Preparation of hydroxyapatite/poly(methyl methacrylate) and calcium silicate/poly(methyl methacrylate) interpenetrating hybrid composites

Hydroxyapatite/poly(methyl methacrylate) (HAp/PMMA) and calcium silicate/poly(methyl methacrylate) (CS/PMMA) composites were prepared by interpenetrating bulk polymerization of methyl methacrylate (MMA) monomer in porous structures of HAp and CS. The porous HAp and CS templates were prepared by mixing their calcined powders with poly(vinyl alcohol) (PVA) solution, shaping by uniaxial pressing and then firing at 1,100 °C for HAp and 900 °C for CS. The templates were soaked in the solution mixture of MMA monomer and 0.1 mol% of benzoyl peroxide (BPO) for 24 h. The pre-composites were then bulk polymerized at 85 °C for 24 h under nitrogen atmosphere. The microstructures of the composites showed the interpenetrating of PMMA into the porous HAp and CS structures. Thermogravimetric analysis indicated that the PMMA content in the HAp/PMMA and CS/PMMA composites were 13 and 26 wt%, respectively. Weight average molecular weights ( ) of PMMA were about 491,000 for HAp/PMMA composites and about 348,000 for CS/PMMA composites. Compressive strengths of these composites were about 90–131 MPa in which they were significantly higher than their starting porous templates.     

Blends of poly(methyl methacrylate) and polyamides

The morphology of PMMA blends with different polyamides (PA-6, 6/9 and 12) was investigated by transmission electron microscopy, recognizing PA-6/PMMA as the most miscible pair. Blends of these polymers were prepared from solutions in m-cresol and formic acid and the morphology was highly dependent on the solvent. The morphology and the segregation degree of extruded PA-6/PMMA blends was investigated by scanning electron microscopy and dynamic-mechanical analysis. The compatibilization succeeded by the introduction of a block copolymer of polyamide and poly(ethylene oxide).     

Mechanical behaviour of poly(methyl methacrylate)

A series of tensile and three-point bending studies was conducted at various temperatures and loading rates using a commercial poly(methyl methacrylate) (PMMA). Tensile properties and fracture toughness data were obtained for the various conditions. In general, both tensile strength and fracture toughness increase with increasing loading rate and decreasing temperatur E. However, when the temperature reaches the glass transition region, the relationships between fracture toughness, loading rate, and temperature become very complex. This behaviour is due to the simultaneous interaction of viscoelasticity and localized plastic deformation. In the glass transition region, the fracture mechanism changes from a brittle to a ductile mode of failure. A failure envelope constructed from tensile tests suggests that the maximum elongation that the glassy PMMA can withstand without failure is about 130%. The calculated apparent activation energies suggest that the failure process of thermoplastic polymers (at least PMMA) follows a viscoelastic process, either glass or transition. The former is the case if crack initiation is required.Deceased.     

In-situ synthesis and performance of titanium oxide/poly(methyl methacrylate) nanocomposites

Polymer nanocomposites have elicited extensive research efforts due to their potential to exhibit spectacular properties. They have immense potential and are befitting materials to serve as an ideal and futuristic alternative for varied applications. Poly(methyl methacrylate) (PMMA) and titanium oxide (TiO2) nanocomposites used in this study were fabricated by an in-situ free radical polymerization process. Three point bend tests were conducted with a modified universal microtribometer to evaluate fracture toughness. The results indicated that the stress intensity values increase as the concentration of titanium oxide increases up to 1 vol% and subsequently decrease at higher concentrations. Scanning electron microscopy (SEM) images of fracture surfaces afforded clues as to the possible deformation mechanism. Ultraviolet-visible spectroscopy (UV-vis) evaluated the degree of transparency of the nanocomposites. It was observed that samples became opaque as the concentration was increased beyond 0.01% volume fraction. X-ray diffraction characterized the TiO2 crystalline phase and Scherrer's equation was used to calculate the crystallite size. Among the concentrations considered the 3% volume fraction sample had the largest crystallite size. Finally, microhardness measurements further characterized the mechanical properties of the composites.     

Electrospun poly(methyl methacrylate) nanofibers and microparticles

Electrospinning at relatively low polymer concentrations results in particles rather than fibers. This particle-formation process can be termed as electrospray. So electrospinning/electrospray is a highly versatile method to process fibers and particles with different morphologies. In this work, poly(methyl methacrylate) (PMMA) micro- and nanostructures with different morphologies (fibers, spheres, cup-like, and ring-like) have been produced by a facile electrospinning/electrospray method. PMMA was electrospun into various morphologies from only DMF without any other solvents. Field emission scanning electron microscope (FESEM) images demonstrate the different morphologies and prove this technique to be an effective method for obtaining morphology-controllable polymer materials by changing the processing parameters. These micro- and nanostructured polymer materials may find applications in drug delivery and filtration media.     

Singlet oxygen and dye-triplet-state quenching in solid-state dye lasers consisting of pyrromethene 567-doped poly(methyl methacrylate)

Solid-state dye lasers based on poly(methyl methacrylate) (PMMA) doped with Pyrromethene 567 dye (P567) have been investigated. The preparation techniques employed provided high photostability and laser damage threshold for P567 in pure PMMA with 270,000 pulses emitted before the conversion efficiency fell to half its initial value for a pump fluence of 0.16 J cm(-2). When PMMA was modified with 1, 4-diazobicyclo [2, 2, 2] octane singlet oxygen quencher, the longevity increased to 550,000 pulses, corresponding to a normalized photostability of 270 GJ mol(-1). Modification of PMMA with a triplet quencher (perylene) yielded no improvement, but in ethanol solutions both additives enhanced photostability. It is possible that in PMMA, stabilization by means of triplet quenching that depends on dye diffusion is prevented but that stabilization by means of singlet oxygen quenching that depends on the faster oxygen diffusion rate will succeed.     

Mechanical properties of blends of poly(methyl methacrylate) and poly(vinylidene fluoride)

The mechanical properties of blends of the crystallizable polymer poly(vinylidene fluoride) and the amorphous material poly(methyl methacrylate) have been investigated as a function of composition both for glassy amorphous materials and for partially crystalline materials. The data obtained were interpreted in terms of the molecular and super-molecular structure of the blends and in terms of their dynamic properties.The main conclusions were that the mechanical properties are not strongly dependent on details of the distribution of the two components in the material nor on the crystal modifications present. The mechanical properties were found to depend primarily on the location of the glass transition temperature relative to the elongation temperature and on the presence or absence of crystalline regions. The degree of crystallinity was found to play an important role in determining the properties only at lower values of this quantity. The advantage of these blends is that the important parameters, namely, the degree of crystallinity and the location of the glass transition temperature, can be adjusted at will by varying the composition appropriately. This allows well-defined variations of the mechanical properties to be achieved.     

Feasibility study of friction spot welding of dissimilar single-lap joint between poly(methyl methacrylate) and poly(methyl methacrylate)-SiO2 nanocomposite

In this work, the feasibility of friction spot welding (FSpW) of a commercial poly(methyl methacrylate) (PMMA) GS grade and a PMMA 6 N/2 wt% silica (SiO₂) nanocomposite was investigated. Single-lap joints welded at rotational speeds of 1000, 2000 and 3000 rpm were produced. The analysis of the joint microstructure and material flow pattern indicated that joints could be produced using all of the tested welding conditions. However, the joint produced at 1000 rpm displayed sharp weld lines (weak links), indicating insufficient heat input, while the welds produced at 3000 rpm displayed excessive plastic deformation (bulging of the bottom plate), volumetric defects and a lack of material mixing in the welded area, associated with higher heat input. The weld produced at a rotational speed of 2000 rpm resulted in improved material mixing, which was indicated by the absence of weld lines and volumetric defects due to the more correct heat input. This welding condition was selected for further mechanical testing. Lap shear testing of PMMA GS/PMMA 6 N/2 wt% SiO₂ nanocomposite single lap joints welded at 2000 rpm resulted in an average ultimate lap shear strength of 3.9 ± 0.05 MPa. These weld strength values are equal to or better than those obtained using state-of-the-art welding techniques for PMMA materials, thereby demonstrating the potential of friction spot welding for thermoplastic nanocomposites.     

Wettability of poly(methyl methacrylate) surfaces in dental use

Poly(methyl methacrylate) is widely used in dentistry. In contact with water, there is an increase in the polar surface free energy from 9.5 to 21 mJ m^–2. Various other surface modification treatments have been examined (chemical treatment, gold deposition and flaming), which also bring about a surface polar component increase and thus produce a better wettability in contact with water or saliva. The water modification seems to be the best treatment.     

Fatigue failure of poly(methyl methacrylate) in alcohol environments

Fatigue tests of poly(methyl methacrylate) were conducted in environments of methanol, 1-butanol, and 1-octanol at room temperature under cyclic tensile loading at 10 Hz. The fatigue lifetime increased as the molar volume of the environmental alcohol increased, and indicated no correlation with the solubility parameter. The scanning electron micrographs of the fracture surfaces reveal that crazes strongly participate in the fatigue fracture, and suggest that a great increase in the fatigue lifetime in methanol brought about by pre-soaking the specimen in methanol for a period below 100 h, which has been previously reported, is caused by the combined effects both of the case II diffusion of methanol producing the softened matter and the internal compressive stress in the swollen surface layer and of a cooperative work of crazing, shear flow and/or shear cracking taking place under cyclic tensile loading.     

Contact conductivity detection in poly(methyl methacrylate)-based microfluidic devices for analysis of mono- and polyanionic molecules

An on-column contact conductivity detector was developed for the analysis of various mono- and polyanionic compounds separated by electrophoresis chips fabricated in poly(methyl methacrylate) (PMMA) using hot embossing techniques from Ni electroforms. The detector consisted of a pair of Pt wires (127 microm diameter) with an end-to-end spacing of approximately 20 microm and situated within the fluidic channel. The waveform applied to the electrode pair was a bipolar pulse with a frequency of 5.0 kHz and was used to reduce the charging current from measurement so that the current recorded at the end of one pulse is more representative of the solution conductivity. Using the detector, separations of amino acids, peptides, proteins, and oligonucleotides were demonstrated. For the amino acids and peptides, free-solution zone electrophoresis was performed. A calibration plot for the amino acid alanine was found to be linear from approximately 10 to 100 nM in a carrier electrolyte consisting of 10 mM triethylamonium acetate. The concentration detection limit was found to be 8.0 nM, with the corresponding mass detection limit equal to 3.4 amol (injection volume = 425 pL). The protein separations with conductivity detection were performed using MEKC, in which the carrier electrolyte contained the anionic surfactant sodium dodecyl sulfate (SDS) above its cmc. Near baseline resolution was achieved in the PMMA microchip for a solution containing 8 different proteins. In the case of the DNA fragments, capillary electrochromatography was used with a C18-modified PMMA chip and a carrier electrolyte containing an ion-pairing agent.     

Strength of poly(methyl methacrylate) with indentation flaws

Controlled flaws were introduced into poly(methyl methacrylate) samples in the presence of liquid acetone using a Vickers indenter over a range of indentation loads from 100 to 1400 N. Due to the large plastic zone underneath the indenter, the radial crack formed by indentation consisted of two halves, known as Palmqvist cracks, instead of a single semicircular crack. The strengths of the samples were measured in air either immediately following indentation or after a stress-relief anneal. The strength of the as-indented samples was about 6% less than that of the annealed samples; however, the dependence of strength on indentation load was similar for both sets of samples. These results were interpreted in terms of an indentation fracture mechanics model. The analysis is consistent with poly(methyl methacrylate) having a rising fracture toughness with increasing crack size.     

聚甲基丙烯酸甲酯包覆十二醇微胶囊的制备及表征

以相变物质正十二醇(DA)为芯材,聚甲基丙烯酸甲酯(PMMA)为壁材,采用悬浮聚合法制备了正十二醇-聚甲基丙烯酸甲酯(DA@PMMA)微胶囊。通过差示扫描量热仪(DSC),扫描电镜(SEM),透射电镜(TEM),傅里叶变换红外光谱仪(FIIR)和热重分析仪(TGA)等仪器对微胶囊进行检测表征。结果表明:当工艺为苯乙烯-马来酸甘钠盐(SMA)加入量占DA质量的7.5%,偶氮二异丁腈(AIBN)加入量占单体甲基丙烯酸甲酯(MMA)质量的7.5%,芯材壁材质量比为2∶1,搅拌速度为1 000r/min时,所制备的微胶囊整体性能最好。DA@PMMA微胶囊为球形,平均粒径26μm,DA@PMMA微胶囊中DA的质量分数为66%。DA@PMMA微胶囊的熔化焓和结晶焓分别是137.6J/g和132.8J/g。TGA和FIIR的分析表明,DA@PMMA微胶囊具有良好的性能。