Debye Temperature and Electrical Conduction of Fe2O3-CaO-SiO2 Glasses

The electrical conductivity of iron-containing silica glasses was measured from 80 to 350 K. The conductivity data were analyzed based on the hopping conduction theory. The hopping binding energy (W_p) and disorder energy W_D) were calculated from the activation energy at high and low temperatures. The disorder energy obtained was much lower than reported for FeO-P₂O₅ glasses, but similar to that for vandium-containing glasses.     

Diffusion of cobalt,chromium, and titanium in Ni3Al

Diffusion studies of cobalt, chromium, and titanium in Ni₃Al (γ′) at temperatures between 1298 and 1573 K have been performed using diffusion couples of (Ni-24.2 at. pct Al/Ni-24.4 at. pct Al-2.91 at. pct Co), (Ni-24.2 at. pct Al/Ni-23.1 at. pct Al-2.84 at. pct Cr), and (Ni-24.2 at. pct Al/Ni-20.9 at. pct Al-3.17 at. pct Ti). The diffusion profiles were measured by an electron probe microanalyzer, and the diffusion coefficients of cobalt, chromium, and tita-nium in γ′ containing 24.2 at. pct Al were determined from those diffusion profiles by Hall’s method. The temperature dependencies of their diffusion coefficients (m[su2]/s) are as follows: ~D_(Co) = (4.2 ± 1.2) × 1O^-3exp {-325 ± 4 (kJ/mol)/RT} ~D_(Cr) = (1.1 ± 0.3) × 10^-1 exp {-366 ± 3 (kJ/mol)/RT} and D_(Ti) = (5.6 ± 3.1) × 10¹ exp {-468 ± 6 (kJ/mol)/RT} The values of activation energy increase in this order: cobalt, chromium, and titanium. These activation energies are closely related to the substitution behavior of cobalt, chromium, and titanium atoms in the Ll₂ lattice sites of γ′; the cobalt atoms occupying the face-centered sites in the Ll₂ structure diffuse with the normal activation energy, whereas the titanium atoms oc-cupying the cubic corner sites diffuse with a larger activation energy that includes the energy due to local disordering caused by the atomic jumps. The chromium atoms which can occupy both sites diffuse with an activation energy similar to that of cobalt atoms.     

Repetition bend properties of Cu-Cr and Cu-Cr-Sn alloys

Repetition numbers of bending of Cu-0.81 wt% Cr, Cu-0.81 wt% Cr-0.14 wt% Sn and Cu-0.26 wt% Cr-0.10 wt% Sn alloys were investigated. After solution treatment, the first two types of copper alloys have a primary chromium phase; this is not so in the last alloy. The primary chromium phase does not influence the repetition numbers of bending of cold-rolled specimens; the repetition numbers of bending of specimens aged at 723 K for 1.8 × 10³ sec after cold rolling are higher than those of cold-rolled specimens. The cause of this is considered to be a recovery of work-hardening during ageing.     

A substrain mouse serologically classified in ddN strain and its behavioral characteristics

Since the publication of Masters and Johnson's Human Sexual Inadequacy in 1970, sex therapy has become an established, though controversial, new approach to the treatment of sexual disorders. Masters and Johnson adopted the position that any other form of psychotherapy should be avoided or suspended during the two- or three-week period of sex therapy. Helen Kaplan, in considering sex therapy to be a type of psychotherapy, has stressed that the skillful trained psychotherapist uses his awareness of the psychodynamics and unconscious conflicts of the couple in modifying and tailoring the sex therapy program to their individual needs. In the present study, sex therapy, utilizing a second therapist, was introduced into an ongoing psychoanalytic psychotherapy.     

Decarboxylation of the 6-nitrobenzisoxazole-3-carboxylate anion catalyzed by cross-linked poly(4-vinylpyridinium) salts

Summary Catalysis of cationic polyelectrolytes for the decarboxylation of 6-nitrobenzisoxazole-3-carboxylate anion was studied in a buffer solution (pH=9.0). Cross-linked poly (4-vinylpyridinium) salts prepared from 4-vinylpyridine and , -dibromides were used as cationic catalysts. The cross-linked catalysts were found to accelerate markedly the decarboxylation in comparison with the linear water-soluble analogues. Effect of the polymer structure such as the length of (CH₂)_x linkages between positive charges on the catalytic activity was examined. It was suggested that the acceleration by the cross-linked polymer catalysts would be due to the hydrophobic microenvironment around the catalytic sites.     

Grain growth in microwave sintered Si3N4 ceramics sintered from different starting powders

Silicon nitride ceramics have been produced by microwave sintering at 28 GHz with Y₂O₃, Al₂O₃ and MgO as sintering additives. The effect of initial β content of the Si₃N₄ starting powder on the microstructural development has been assessed by scanning electron microscopy (SEM) and quantitative image analysis. Phase transformation behaviour was assessed by X-ray diffraction. Mechanical properties of the sintered bodies were determined through assessment of hardness and fracture toughness. It was found that the samples sintered from powders with lower initial β content developed larger grains than those from higher β content powders, due to fewer nucleation sites during the →β transformation. However, attempts to develop a more bimodal microstructure by using a mixture of the two grades of powder, in an effort to increase both fracture toughness and fracture strength, were unsuccessful. In this case the microstructure was similar to that developed in the materials produced from higher β content powders. The mechanical properties of the sintered bodies were very similar, despite differences in microstructure. This was attributed to the strong bonding between the grains and grain boundary phase resulting in crack paths in all the materials that were predominantly transgranular, with little debonding or crack deflection. Under these circumstances the effect of larger grains is eliminated.     

Fracture Resistance Behavior of Highly Anisotropic Silicon Nitride

The R -curve behavior was characterized by the Vickers indentation flaw technique, for highly anisotropic silicon nitride, a silicon nitride whose fibrous grains are highly aligned. The measured crack lengths ranged from 30 to 500 μm. The fracture resistance of a conventional self-reinforced silicon nitride was determined for comparison using the same procedures. While in the self-reinforced material several hundred micrometers of crack extension were required to obtain a high fracture toughness, the highly anisotropic material exhibited a high toughness from the beginning of the measured crack length range with little increase in the following range. It is suggested that the toughness of the highly anisotropic material steeply rises in a very short crack extension, which is advantageous in avoiding catastropic fractures.     

Investigation of anti-wear additives for low viscous synthetic esters: Hydroxyalkyl phosphonates

Various synthetic esters are widely applied as lubricating fluid to reduce friction and wear at tribological contact. Among them low viscous synthetic esters are expected to improve fuel efficiency by minimizing the fluid friction. These low viscous esters are composed of short-chain fatty acids. Therefore, low viscous synthetic esters are inherently polar molecules. Since efficiency of anti-wear additives decreases with increase of polarity of the base oil, new additive technology is requested.In this work, hydroxyalkyl phosphates [P(O)(OCHRCH₂OH)₃], and hydroxyalkyl phosphonates [P(OH)_n(OCHRCH₂OH)_3−n, where n=1,2] are proposed as novel anti-wear additives for polar synthetic esters. The anti-wear additives are evaluated under the boundary conditions. The additives prevent wear in polar esters, in which conventional anti-wear additives do not work at all. Interestingly, effects of substituent in additive molecule on anti-wear properties are found. Alkyl and aryl derivatives reduce wear remarkably, whereas allyl derivatives exhibit poor results. It is speculated that the anti-wear inefiiciency of allylic compounds is due to auto-oxidation of the additives.A facile preparative method for hydroxyalkyl derivatives characterizes the present additive system. They are prepared in situ by simply mixing phosphonic acid and substituted epoxides. Flexiblity of lubricant design can be made possible by the present additive system.     

Radical polymerization of (phenylethynyl)styrenes and characterization of poly(phenylethynyl)styrenes as a thermally curable material

Summary The radical polymerizations of 2-, 3-, and 4-(phenylethynyl)styrenes (1a–c) and the copolymerizations of 1a–c (M₁) with styrene (M₂) were carried out using AIBN as the initiator in toluene at 60°C. The number-average molecular weights (M _ns) were extremely low for poly(2-phenylethynylstyrene) (2a) and poly[(phenylethynyl)styrene-co-styrene] (3a), and increased in the order of 2a, 3a << 2b, 3b < 2c, 3c. Monomer reactivity ratios were determined as r ₁= 1.80 and r ₂= 0.51 for 1a, r ₁= 1.72 and r ₂= 0.53 for 1b, and r ₁= 3.17 and r ₂= 0.24 for 1c. Polymers 2a–c and 3a–c underwent an exothermic reaction at elevated temperature to form organic solvent-insoluble polymers. Although the decomposition of 2a was observed from 200°C, 2b and 2c exhibited a high heat-resistance property in both nitrogen and air atmospheres, in particular, 2b showed no significant weight loss below 450°C. Received: 28 January 1998/Accepted: 5 March 1998