Meter-scale conditioned hydrodynamic optical-field-ionized plasma channels.

We demonstrate through experiments and numerical simulations that low-density, low-loss, meter-scale plasma channels can be generated by employing a conditioning laser pulse to ionize the neutral gas collar surrounding a hydrodynamic optical-field-ionized (HOFI) plasma channel. We use particle-in-cell simulations to show that the leading edge of the conditioning pulse ionizes the neutral gas collar to generate a deep, low-loss plasma channel which guides the bulk of the conditioning pulse itself as well as any subsequently injected pulses. In proof-of-principle experiments, we generate conditioned HOFI (CHOFI) waveguides with axial electron densities of n_{e0}≈1×10^{17}cm^{-3} and a matched spot size of 26µm. The power attenuation length of these CHOFI channels was calculated to be L_{att}=(21±3)m, more than two orders of magnitude longer than achieved by HOFI channels. Hydrodynamic and particle-in-cell simulations demonstrate that meter-scale CHOFI waveguides with attenuation lengths exceeding 1 m could be generated with a total laser pulse energy of only 1.2 J per meter of channel. The properties of CHOFI channels are ideally suited to many applications in high-intensity light-matter interactions, including multi-GeV plasma accelerator stages operating at high pulse repetition rates.

Brilliant X-rays using a Two-Stage Plasma Insertion Device.

Particle accelerators have made an enormous impact in all fields of natural sciences, from elementary particle physics, to the imaging of proteins and the development of new pharmaceuticals. Modern light sources have advanced many fields by providing extraordinarily bright, short X-ray pulses. Here we present a novel numerical study, demonstrating that existing third generation light sources can significantly enhance the brightness and photon energy of their X-ray pulses by undulating their beams within plasma wakefields. This study shows that a three order of magnitude increase in X-ray brightness and over an order of magnitude increase in X-ray photon energy is achieved by passing a 3 GeV electron beam through a two-stage plasma insertion device. The production mechanism micro-bunches the electron beam and ensures the pulses are radially polarised on creation. We also demonstrate that the micro-bunched electron beam is itself an effective wakefield driver that can potentially accelerate a witness electron beam up to 6 GeV.

Effect of crystallization heat treatment on the microstructure of niobium-doped fluorapatite glass-ceramics.

Our goal was to study the effect of heat treatment temperature and heating rate on the microstructure and crystalline phases and assess the domain of existence of submicrometer fluorapatite crystals in niobium-doped fluorapatite glass-ceramics for biomedical applications. Glass-ceramic specimens were prepared by casting and heat treatment between 700 and 1200°C using a fast or a slow heating rate. The microstructure was characterized by atomic force microscopy and scanning electron microscopy. Crystalline phases were analyzed by x-ray diffraction. AFM of the as-cast glass revealed that amorphous phase separation occurred in this system. XRD confirmed the presence of fluorapatite in all specimens, together with forsterite and enstatite at higher temperatures. Both heating rate and heat treatment temperature strongly influenced microstructure and crystallinity. A dual microstructure with submicrometer fluorapatite crystals and polygonal forsterite crystals was obtained when slow heating rates and crystallization temperatures between 950 and 1100°C were used. Needle-shaped fluorapatite crystals appeared after heat treatment above 1100°C. Fast heating rates led to an increase in crystal size. Heat treatment temperatures should remain below 1100°C, together with slow heating rates, to prevent crystal dissolution, and preserve a dual microstructure of finely dispersed submicrometer crystals without growth of needle-shaped crystals.

Effect of heat treatment after accelerated aging on phase transformation in 3Y-TZP.

Our purpose was to investigate the effect of heat treatment on the reversibility of the tetragonal to monoclinic transformation in 3Y-TZP, and associated surface roughness. The goals were to determine the onset temperature of the reverse transformation, and characterize surface roughness after accelerated aging, and after aging followed by heat treatment. 3Y-TZP disc-shaped specimens were sintered at temperatures from 1300 to 1550 degrees C. The reversibility of the transformation was investigated by X-ray diffraction (XRD) after accelerated aging, followed by heat treatment at temperatures from 350 degrees C up to 850 degrees C. The surface roughness (R(rms)) was measured by atomic force microscopy after polishing, after accelerated aging for 1 or 10 h, and after aging followed by heat treatment. XRD showed that the fraction of m-phase increased linearly with grain size after aging for 10 h (1.0-29.8%). The transformation was reversed for all groups after heat treatment at 850 degrees C/min., with only trace amounts of m-phase remaining for the group sintered at 1550 degrees C. A significant increase in mean surface roughness was observed after accelerated aging (1.59-7.45 nm), compared to polished groups (0.83-1.0 nm). However, the mean surface roughness after accelerated aging for either 1 or 10 h, followed by heat treatment at 850 degrees C/min. (1.18-2.1 nm), was not significantly different from that of the polished groups. This was attributed to the reverse transformation. XRD revealed that the monoclinic to tetragonal transformation, was complete after heat treatment at 500 degrees C for 1 min, for specimens sintered at 1550 degrees C and aged 10 h.

Effect of coloring with various metal oxides on the microstructure, color, and flexural strength of 3Y-TZP.

The purpose of this study was to investigate the effect of cerium and bismuth coloring salts solutions on the microstructure, color, flexural strength, and aging resistance of tetragonal zirconia for dental applications (3Y-TZP). Cylindrical blanks were sectioned into disks (2-mm thick, 25-mm in diameter) and colored by immersion in cerium acetate (CA), cerium chloride (CC), or bismuth chloride (BC) solutions at 1, 5, or 10 wt %. The density, elastic constants, and biaxial flexural strength were determined after sintering at 1350 degrees C. The crystalline phases were analyzed by X-ray diffraction before and after aging in autoclave for 10 h. The results showed that the mean density of the colored groups was comparable with that of the control group (6.072 +/- 0.008 g/cm(3)). XRD confirmed the presence of tetragonal zirconia with a slight increase in lattice parameters for the colored groups. A perceptible color difference was obtained for all groups (DeltaE* = 2.57 +/- 0.48 to 14.22 +/- 0.98), compared with the control. The mean grain size increased significantly for the groups colored with CC or CA at 10 wt %, compared with the control group (0.318 +/- 0.029 mm). The mean biaxial strength of CA1%, CA5%, and BC1% groups was not significantly different from that of the control group (1087.5 +/- 173.3 MPa). The flexural strength of all other groups decreased linearly with increasing concentration for both cerium salts (860.7 +/- 172 to 274.4 +/- 67.3 MPa). The resistance to low temperature degradation was not affected by the coloring process. Coloring with cerium or bismuth salts produced perceptible color differences even at the lowest concentrations. A decrease in flexural strength at the higher concentrations was attributed to an increase in open porosity.

Effect of crystallization heat treatment on the microstructure and biaxial strength of fluorrichterite glass-ceramics.

The purpose of this study was to evaluate the effect of crystallization heat treatment on the flexural strength of potassium fluorrichterite glass-ceramics for biomedical applications. After melting and casting, discs were sectioned from the glass ingots, randomly divided into 10 groups, and heat treated at various temperatures ranging between 890 degrees C and 925 degrees C for various durations. One group was air-abraded after heat treatment. XRD revealed the presence of fluorrichterite and fluormica for all heat-treated groups. SEM confirmed the presence of both fluorrichterite and fluormica crystals. Crystal size increased with temperature and duration of the heat treatment. The mean flexural strength after air abrasion was not significantly different than that of the other groups except the group heat treated at 925 degrees C. The mean flexural strength was maximum after heat treatment at 900 degrees C for 1 h (497.6 +/- 25.5 MPa) and decreased linearly with the longer durations of heat treatment at 900 degrees C.

Microstructural and crystallographic surface changes after grinding zirconia-based dental ceramics.

The purpose of this study was to evaluate microstructural and crystallographic phase changes after grinding 3Y-TZP dental ceramics. Ceramic blanks were sintered according to manufacturer's recommendations and divided into four groups: (A) as-sintered control, (B) diamond-ground manually under water, (C) ground and polished, and (D) ground and annealed at 1000 degrees C for 1 h. Bulk specimens were analyzed by X-ray diffraction to characterize the crystalline phases. The microstructure was investigated by SEM. XRD analyses showed that the control group and the group that was ground and annealed contained only tetragonal zirconia. However, after grinding or after grinding followed by polishing, rhombohedral zirconia and strained tetragonal zirconia were present, without any detectable amount of monoclinic zirconia. Annealing led to the disappearance of both residual lattice strain and the rhombohedral phase. The microstructure of the ground and polished specimens was characterized by significant residual surface damage associated with grain pullout to a depth of about 20 microm. This type of damage could have an impact on the long-term fatigue behavior of 3Y-TZP.

Effect of niobium content on the microstructure and thermal properties of fluorapatite glass-ceramics.

Niobium oxide has been shown to improve biocompatibility and promote bioactivity. The purpose of this study was to evaluate the effect of niobium oxide additions on the microstructure and thermal properties of fluorapatite glass-ceramics for biomedical applications. Four glass-ceramic compositions with increasing amounts of niobium oxide from 0 to 5 wt % were prepared. The glass compositions were melted at 1,525 degrees C for 3 h, quenched, ground, melted again at 1,525 degrees C for 3 h and furnace cooled. The coefficient of thermal expansion was measured by dilatometry. The crystallization behavior was evaluated by differential thermal analysis. The nature of the crystalline phases was investigated by X-ray diffraction. The microstructure was studied by SEM. In addition, the cytotoxicity of the ceramics was evaluated according to the ASTM standard F895--84. The results from X-ray diffraction analyses showed that fluorapatite was the major crystalline phase in all glass-ceramics. Differential thermal analyses revealed that fluorapatite crystallization occurred between 800 and 934 degrees C depending on the composition. The coefficient of thermal expansion varied from 7.6 to 9.4 x 10(-6)/ degrees C. The microstructure after heat treatment at 975 degrees C for 30 min consisted of submicroscopic fluorapatite crystals (200--300 nm) for all niobium-containing glass-ceramics, whereas the niobium-free glass-ceramic contained needle-shaped fluorapatite crystals, 2 microm in length. None of the glass-ceramics tested exhibited any cytotoxic activity as tested by ASTM standard F895--84.

Effect of heat pressing on the mechanical properties of a mica-based glass-ceramic.

Previous work has shown that heat pressing of mica-based glass-ceramics can lead to crystal alignment along the direction of pressing. The purpose of this study was to evaluate the effect of heat pressing on the fracture toughness of mica-based glass-ceramics. Glass rods (12 x 60 mm) were prepared by melting the glass composition at 1400 degrees C for 2 h. Ingots (12 x 12 mm; n = 5) and discs (12 x 1.5 mm; n = 10) were cut from the rods. The discs were heat treated to simulate heat pressing and served as controls. A machinable mica-based glass- ceramic (Dicor MGC) also served as control. Bar-shaped wax patterns (2 x 4 x 22 mm) were invested and heat pressed at 875 degrees C. The elastic constants were determined with the use of the pulsed ultrasonic velocity method. The fracture toughness was measured by the indentation strength technique. The degree of texture was assessed qualitatively by X-ray diffraction and quantitatively on digital SEM micrographs. The results showed that the mean fracture toughness of the heat-pressed specimens (1.96 +/- 0.19 MPa. m(0.5)) was significantly higher than that of the heat-treated controls (1.51 +/- 0.21 MPa. m(0.5)) or the proprietary mica glass-ceramic (Dicor MGC; 1.66 +/- 0.04 MPa. m(0.5)) (p <.001). It was concluded that heat pressing led to a significant increase in fracture toughness in mica glass-ceramics because of crystal alignment along the direction of pressing.

Elastic constants, Vickers hardness, and fracture toughness of fluorrichterite-based glass-ceramics.

OBJECTIVES: To determine the elastic constants, Vickers hardness, and indentation fracture toughness of fluorrichterite glass-ceramics in the system SiO2-MgO-CaO-Na2O-K2O-F. METHODS: Five glass compositions were prepared with increasing sodium content. The compositions were melted at 1400 degrees C for 2 h and cast into 60 x 12 mm rods. Discs (1.5 x 12 mm) were cut from the glass rods, nucleated in the temperature range 600-650 degrees C for 1 h and crystallized at 900 degrees C for 0.5 h. The density of the glass-ceramics was measured by Archimedes' method. The elastic constants were determined by standard ultrasonic velocity technique. The fracture toughness was evaluated by the indentation technique. The indentation crack patterns and microstructure were investigated by scanning electron microscopy. The crystalline phases were identified by X-ray diffraction. A commercially available lithium disilicate glass-ceramic served as control. RESULTS: The fluorrichterite glass-ceramics containing 3.8 and 5.6 wt% sodium had the lowest mean fracture toughness. The glass ceramic containing 1.9 wt% sodium and the control material had the highest mean fracture toughness. The values obtained for these two materials (2.26 +/- 0.15 MPa m0.5 and 2.29 +/- 0.31 MPa m0.5, respectively), were not significantly different (p = 0.997). There was no linear relationship between the amount of sodium present in the glass-ceramic composition and the mean fracture toughness. The fluorrichterite glass ceramics exhibited a dual microstructure consisting of both fluorrichterite and mica crystals. SIGNIFICANCE: Higher fracture toughness appeared to be associated with a higher density of fluorrichterite crystals.

Effect of post-processing heat treatment on the fracture strength of a heat-pressed dental ceramic.

The purpose of this study was to evaluate the effect of post-processing heat treatment on the fracture strength of a heat-pressed lithium disilicate dental ceramic (OPC 3G). Bar-shaped wax patterns (2 x 4 x 22 mm; n = 60) were invested and heat pressed in an automated pressing machine according to manufacturer's recommendations. The bars were polished to 1200 grit and annealed at 600 degrees C for 1 h. Two groups were left untreated as controls, one of which was Vickers indented in oil prior to testing in three-point bending. Two groups were indented and then heat treated at either 800 or 825 degrees C for 30 min. The corresponding control groups were heat treated, then indented prior to testing. Optical micrographs of the indentations were taken before and after heat treatment under differential interference contrast. The fracture toughness and/or fracture strength of the specimens was determined by the indentation-strength technique in three-point bending. Indentation-generated cracks were not discernible by optical microscopy after heat treatment at either 800 or 825 degrees C for 30 min, even under 1000 x magnification. ANOVA and Tukey's test showed that heat treatment in air at 825 degrees C for 30 min significantly increased the fracture strength of a heat-pressable lithium disilicate ceramic. This result was attributed to healing of the flaws present in the material.

Fetal exposure to intact immunoglobulin E occurs via the gastrointestinal tract.

BACKGROUND: Consideration of the evolutionary significance of IgE might provide insight into the immunological interactions occurring in utero and during early post-natal life that regulate later atopic disease. OBJECTIVE: We postulated that the fetal gut is exposed to intact amniotic fluid IgE that might interact with local IgE receptors. METHODS: IgE levels in matched maternal blood and amniotic fluid (n = 47) or breast milk (n = 15) collected from pregnant women in the UK (Southampton) and Brazil (Sao Paulo) were studied. Expression of IgE receptors, Fc epsilon RI and Fc epsilon RII (CD23), in fetal gastrointestinal tract (n = 19) and skin (n = 11) was examined immunohistochemically. RESULTS: Human amniotic fluid at 16-18 weeks' gestation contained intact IgE at levels that increased as maternal circulating levels increased (Spearman's rho = 0.897; P < 0.001). Circulating IgE levels from women in Sao Paulo, Brazil, associated positively not only with term (> 37 weeks' gestation) amniotic fluid (rho = 0.993; P < 0.001) but also breast milk IgE levels (rho = 0.785; P = 0.001). Maternal levels of IgE did not change significantly over pregnancy and fetal circulating levels of IgE were very low (< 0.6 IU/mL). Low-affinity IgE receptors (CD23) were expressed in lymphoid follicles of the fetal gut from 16 weeks of gestation (6/8), but not from 11 to 16 weeks (0/11) or in the skin. CONCLUSION: Amniotic fluid contains intact IgE that might bind to CD23+ cells within the lymphoid follicles of the fetal gastrointestinal tract. The evolutionary significance of these interactions might be to prepare the immune system for helminthic parasite exposure at birth via IgE-mediated antigen focusing, or "education" of the developing immune system about the prevailing extrauterine environment. However, at present in societies where helminthosis is not a significant health issue, this pathway may still be operational and associated with the development of atopic disease.

Effect of processing variables on texture development in a mica-based glass-ceramic.

The purpose of this study was primarily to determine the feasibility of heat-pressing a mica-based glass-ceramic with the use of commercially available dental equipment, and secondly to evaluate the effect of various processing variables on the degree of crystal alignment in the pressed glass-ceramic. The hypotheses were that the mica-based glass-ceramic could be successfully heat-pressed and that some degree of crystal orientation would be obtained, depending on the processing variables. The glass composition was melted at 1400 degrees C for 2 h and cast into 12 x 60-mm rods. Ingots (10 x 12 mm) were cut from the glass rods, heat treated, and heat-pressed under various conditions. The microstructure of the pressed specimens was investigated by SEM and compared to that of heat-treated controls. The length of Vickers-induced cracks was measured on heat-pressed specimens and heat-treated controls. The results showed that mica-based glass-ceramics could be successfully pressed with the use of commercially available dental equipment. The resulting degree of crystal alignment (texture) along the direction of pressing varied between 35 +/- 6 and 79 +/- 6. There was a linear relationship between the degree of texture and the apparent aspect ratio of the mica platelets. A significant decrease in the length of the Vickers-induced cracks in the direction perpendicular to pressing was observed, associated with an increase in length in the direction of pressing.

Effect of additives on the microstructure and thermal properties of a mica-based glass-ceramic.

Previous work has shown that lithium mica glass-ceramics were excellent potential candidates as dental ceramics. The purpose of this study was to evaluate the effect of various additives on the microstructure and thermal properties of a mica glass-ceramic in the system Li(2)O-K(2)O-SiO(2)-MgO-F. Five glass compositions were prepared: a base composition and four compositions with various additives. The compositions were melted at 1400 C for 2 h and cast into 50 x 8 mm ingots. Differential thermal analyses were performed on the glasses up to 1400 C. Bars (4 x 8 x 25 mm) were cut from the ingots and heat treated at various temperatures. The crystalline phases were analyzed by x-ray diffraction. The microstructure was investigated by scanning electron microscopy. The percent crystallinity, crystal density, and average particle size were calculated from stereology measurements. X-ray diffraction revealed that the major crystalline phase was taeniolite for all glass-ceramics. Differential thermal analyses showed that the crystallization exotherm occurred in the temperature range 600--700 C. The addition of calcium fluoride was most efficient in promoting the growth of mica crystals. Larger mica plate diameter could be beneficial to the crack-propagation resistance of the glass-ceramic. The addition of aluminum phosphate promoted nucleation rather than crystal growth and led to a significantly lower glass transition temperature and crystallization exotherm temperature.

Effect of sodium content on the crystallization behavior of fluoramphibole glass-ceramics.

The purpose of this study was to evaluate the effect of sodium content on the crystallization behavior of glass-ceramics in the system SiO(2)-MgO-CaO-Na(2)O-K(2)O-F. Five glass compositions were prepared with increasing sodium content. The compositions were melted at 1400 degrees C for 2 h and cast into 60 x 12-mm ingots. Differential thermal analyses were performed on the glasses up to 1400 degrees C. Discs (1.5 x 12 mm) were cut from the ingots, nucleated in the temperature range 600-650 degrees C for 1-2 h, and crystallized in the temperature range 900-1000 degrees C for 0.5-4 h. The crystalline phases were analyzed by x-ray diffraction. The microstructure was investigated by scanning electron microscopy. Differential thermal analyses showed that the crystallization exotherm occurred in the temperature range 600-750 degrees C. There was a linear relationship between the amount of sodium and the transformation temperatures. X-ray diffraction revealed the presence of mica and diopside as major crystalline phases in the sodium-free composition. Mica, diopside, and fluorrichterite were present in all other glass-ceramics. The microstructure of the sodium-free glass-ceramic was characterized by the presence of hexagonal mica crystals and prismatic diopside crystals. All other compositions exhibited needle-shaped fluorrichterite crystals (2-5 microm in length) in addition to mica and diopside crystals.

Expression of the high-affinity IgE receptor on peripheral blood dendritic cells: differential binding of IgE in atopic asthma.

BACKGROUND: Dendritic cells can express the high-affinity IgE receptor (FcepsilonRI), which, in the presence of specific IgE, facilitates the uptake of allergen, leading to increased activation of allergen-specific T cells. FcepsilonRI expression by dendritic cells is higher in the airways of atopic asthmatic subjects than in those of healthy, nonatopic control subjects. OBJECTIVE: The aims of this study were to determine whether a similar difference in FcepsilonRI expression occurs between dendritic cells in the peripheral blood of atopic asthmatic subjects and healthy individuals and also whether an altered ability of FcepsilonRI(+) peripheral blood dendritic cells to bind IgE accompanies the atopic asthmatic state. METHODS: Flow cytometry was used to analyze the surface expression of FcepsilonRI and exogenously bound IgE on dendritic cells identified as lineage negative (CD3, CD14, CD16, CD19, and CD56) and HLA-DR bright. RESULTS: The total expression of FcepsilonRI on the surface of dendritic cells from healthy and asthmatic subjects was not significantly different. However, in vivo, dendritic cells from atopic asthmatic subjects had higher levels of receptor occupancy by IgE and bound exogenous IgE in vitro more efficiently than dendritic cells from healthy subjects. CONCLUSION: The similar levels of expression of FcepsilonRI on peripheral blood dendritic cells from healthy and asthmatic subjects suggest that the local environment in the airway is responsible for the upregulation of surface FcepsilonRI on airway dendritic cells in asthma. The results also suggest that the functional ability of FcepsilonRI to bind IgE is differentially controlled in the atopic state.

Phase transformations in a leucite-reinforced pressable dental ceramic.

The objectives of this study were to determine the conditions for the formation of sanidine in a pressable dental ceramic (OPC; Jeneric/Pentron). Ceramic discs (16 mm in diameter, 1.3 mm thick; n = 60) were pressed according to the manufacturer's recommendations. One group was left as pressed as the control; the other groups were further heat-treated at temperatures ranging from 700 degrees C to 1100 degrees C for times ranging from 10 min to 24 h. X-ray diffraction was performed on powdered specimens. The microstructure was investigated by scanning electron microscopy (SEM). X-ray diffraction showed that sanidine was the only crystalline phase present after heat treatment at 900 degrees C for 24 h, whereas a mix of tetragonal leucite and sanidine was found in the specimens heat-treated at 900 degrees C for 12 h and 800 degrees C for 24 h. Tetragonal leucite was the only phase present in the control specimens after heat treatment at 950 degrees C and higher, and in the specimens heat-treated up to 1 h at 850 degrees C or 900 degrees C. Tetragonal and cubic leucite were found in the specimens treated at 750 degrees C or 800 degrees C for 30, 60, and 180 min and 700 degrees C for 24 h. SEM confirmed the presence of sanidine in the specimens heat-treated at 900 degrees C for 24 h. All specimens treated for up to 20 min at temperatures ranging from 700 degrees C to 950 degrees CC contained only tetragonal leucite. The clinical significance of this study is that the formation of sanidine is unlikely to occur at the temperature and time ranges needed for the staining or veneering of this leucite-reinforced pressable dental ceramic.

Detection of house-dust-mite allergen in amniotic fluid and umbilical-cord blood.

Mononuclear cells in umbilical-cord blood display allergen-specific reactivity, but how allergen exposure occurs in utero is unknown. We investigated the presence of a common inhalant allergen (Der p 1), to which mothers are exposed throughout pregnancy, by ELISA in matched maternal blood and amniotic fluid samples at 16-17 weeks of gestation, and in matched maternal and umbilical-cord blood at term (> or =37 weeks of gestation). Der p 1 was detectable in 24 of 43 amniotic fluid samples where it was also present in maternal blood, and in 15 of 24 cord-plasma samples at significantly higher concentrations than in the maternal plasma (p=0.022). The detection of Der p 1 in the amniotic fluid and the fetal circulation provides direct evidence of transamniotic and transplacental allergen exposure.

Effect of magnesium content on the microstructure and crystalline phases of fluoramphibole glass-ceramics.

The purpose of this study was to evaluate the effect of magnesium content on the microstructure and crystalline phases of glass-ceramics in the system SiO(2)-MgO-CaO-Na(2)O-K(2)O-F. Four glass compositions were prepared with magnesium content varying from 12-18 wt%. The compositions were melted at 1400 degrees C for 2 h and cast into 30 x 8 mm ingots. Differential thermal analyses were performed on the powdered glasses at a heating rate of 20 degrees C/minute up to 1400 degrees C. Bars (4 x 8 x 25 mm) were cut from the ingots with a low-speed diamond saw, nucleated in the temperature range 600-650 degrees C for 1-2 h and crystallized in the temperature range 900-1000 degrees C for 4-6 h. The crystalline phases were analyzed by X-ray diffraction. The microstructure was investigated by scanning electron microscopy. The Vickers hardness was determined after indentation under a 9.81 N load. Differential thermal analyses revealed that crystallization occurred in the temperature range 700-800 degrees C. X-ray diffraction showed the presence of fluorrichterite as major crystalline phase regardless of the magnesium content in the parent glass or heat treatment temperature. The microstructure consisted of interlocked acicular crystals (5-10 micrometers). The highest magnesium content led to the coexistence of both a mica phase and fluorrichterite. This microstructure promoted crack deflections and arrest.