Methodology to resolve the transport equation with the discrete ordinates code TORT into the IPEN/MB-01 reactor

Resolution of the steady-state Neutron Transport Equation in a nuclear pool reactor is usually achieved by means of two different numerical methods: Monte Carlo (stochastic) and Discrete Ordinates (deterministic). The Discrete Ordinates method solves the Neutron Transport Equation for a set of selected directions, obtaining a set of directional equations and solutions for each equation which are the angular flux. In order to deal with the energy dependence, an energy multi-group approximation is commonly performed, obtaining a set of equations depending on the number of energy groups. In addition, spatial discretization is also required and the problem is solved by sweeping the geometry mesh. However, special cross-sections are required due to the energy and directional discretization, thus a methodology based on NJOY99 code capabilities has been used. Finally, in order to demonstrate the capability of this method, the 3D discrete ordinates code TORT has been applied to resolve the IPEN/MB-01 reactor.     

A New Indole Synthesis Promoted by Metal Triflates

A new synthesis of 4- and 7-carbon-substituted indoles is described. The overall sequence involves the addition of a nitrile oxide to 1 carboethoxy-2-(or 3-) allylpyrrole, hydrogenation of the intermediate isoxazoline to β-hydroxy ketone and cyclization of the ketol using magnesium or zinc triflate to the substituted indole. This new indole-forming strategy can also accommodate the introduction of oxygen functionality into the indole 6-position. Possible mechanistic aspects of the reaction are detailed.     

Relative reduction rates of fatty acid isomers by hydrazine

Mixtures of fatty acids and of hydrocarbons have been reduced by hydrazine in ethyl alcohol solution at 50 C. Samples were removed during reduction for analysis and the relative reduction rates calculated by digital computer.cis-15-Octadecenoic acid is reduced 1.3 times as fast as itscis-9-isomer. No differences were found amongcis-6,9- and -12-octadecenoic acids.cis-3-Octadecene was also reduced 1.3 times as fast as thecis-9-isomer andcis-1-octadecene 8.6 times as fast. Elaidic acid was reduced 1.27 times as fast as oleic. Presented at the AOCS Meeting, Chicago, October 1967. No. Utiliz. Res. Dev. Div., ARS, USDA.     

Extraction of lipids from cottonseed tissue: VI. Ultrastructural morphology of isolated pigment glands

Cottonseed pigment glands, isolated from the underflow fraction of the liquid cyclone process, were examined with an electron microscope. The glands were circumscribed by a layer of tangentially flattened cells. Subjacent to the flattened cells were partially lysed cells containing recognizable remnants of cell walls. Within the lumens or matrices of the glands were myriads of pigment spherules measuring 0.1–1.5 µ in diameter. These spherules remained within the glands, even though gland walls were ruptured mechanically. Since aggregates of pigment spherules devoid of gland walls were observed in the gland-rich fraction, it was concluded that maintenance of intact pigment glands was not a requisite for successful separation of gossypol from other cottonseed components with the liquid cyclone process. Avoiding dispersion of aggregated spherules from the glandular matrix was probably just as important as maintaining intact gland walls during mechanical separation of gossypol from other cottonseed components.     

Polymer-Analog Transformations of Polycaproamide—Polyglycidyl Dimethacrylate Graft Copolymers under the Effect of Aromatic Diamine

The kinetic and thermodynamic parameters of amination of PCA—PGMA graft copolymer with p-phenylenediamine (initial reaction rate, reaction order in chemically active groups, and effective activation energy were determined. The high efficacy of p-phenylenediamine in splitting of PGMA -oxide groups, almost at the level of diamines of aliphatic structure, was demonstrated.     

Crack-wake shielding and small-scale crack-tip yielding as potential mechanisms for improving the delayed-failure resistance of silicon nitride at elevated temperatures

Requirements and microstructural design criteria for employing silicon nitride in long-term structural applications at elevated temperatures are discussed according to fracture mechanics concepts. Three least engineering parameters are considered: lifetime, flaw-tolerance and deformation under stress. “Ductile” materials are found by exploitation of small-scale crack-tip yielding which arises from the softening of their grain-boundary phase. These materials, however, are likely to exhibit poor deformation resistance. Materials with a “strong” grain boundary generally show a superior deformation behaviour but are liable to brittle fracture and static-fatigue strength degradation unless shielding mechanisms in the crack-wake be operative. The present analysis evaluates and compares these two classes of materials and the respective approaches commonly followed for their densification.     

Towards a continuous process in heterogeneous coordinated anionic ring opening polymerization

Summary The current article deals with the initial developments of the use of a continuous plug flow reactor using an original heterogeneous catalyst system for the living coordinated anionic polymerization of certain oxygenated rings. This reactor is designed in order to maintain the essential characteristics of the original batch system. One of the pertinent parameters considered here is the residence time of the reactants inside the reactor. The column has been used to investigate ethylene oxide and -caprolactone oligomerization. Initial experiments have pointed out how the molecular weights can depend on the flow rate for a fixed bed length. Some theoretical problems relative to the reactive column are discussed in order to investigate more in depth the properties of this original continuous process and to model it to find the optimal working conditions.     

Viscosity and Thermal Expansion of Mixed-Alkali Borate Glasses

Transformation-range viscosity and thermal expansion measurements were made for five series (Li-Na, Li-K, Li-Cs, Na-Cs, and K-Rb) of mixed-alkali borate glasses containing 30 mol% total alkali oxide. In each case, negative deviations from additivity were observed in the isokom and glass transformation temperatures. Positive deviations from additivity were observed in the thermal expansion coefficients for the Li-Na, Li-K, and K-Rb glasses, while the Li-Cs and Na-Cs glasses exhibited negative deviations. Maximization of the deviation from additivity in the viscosity and glass transformation temperatures occurred when the radius ratio of the two alkali ions was approximately 1.7 to 1.8. Combination of the results of this study with those of earlier studies indicates that the deviations from additivity observed for these properties are independent of the identity of the glass former.