Thermal modeling of high-current solid targets

Production demands at TRIUMF have pushed present target designs to the limit of their beam current capacity. A thermal analysis of the present high-current solid production targets has been carried out in order to increase radioisotope production rates through maximizing current handling capability. This paper describes the optimization of a 5° incident angle solid target for radioisotope production in service on the TRIUMF TR-30 cyclotron. Target materials compared include silver and Glidcop^®,¹ a dispersion-strengthened copper composite. A summary of comparative results is presented.     

Constitutive modeling and computational implementation for finite strain plasticity

This paper describes a simple alternate approach to the difficult problem of modeling material behavior. Starting from a general representation for a rate-type constitutive equation, it is shown by example how sets of test data may be used to derive restrictions on the scalar functions appearing in the representation. It is not possible to determine these functions from experimental data, but the aforementioned restrictions serve as a guide in their eventual definition. The implications are examined for hypo-elastic, isotropically hardening plastic, and kinematically hardening plastic materials. A simple model for the evolution of the “back-stress,” in a kinematic-hardening plasticity theory, that is entirely analogous to a hypoelastic stress-strain relation is postulated and examined in detail in modeling a finitely plastic tension-torsion test. The implementation of rate-type material models in finite element algorithms is also discussed.     

Development of a new frame finite element for crash analysis, using a mixed variational principle and rotations as independent variables

This paper deals with the development and application of a new space curved frame finite element to be used for crash analysis (non-linear). The frame finite element has been developed using a mixed variational principle (complementary form) and using rotations as independent variables. The formulation has been validated for problems of large deflection and rotation, and for problems involving initially curved members. Based on the validation performed, it is expected that crash problems may be modelled using a single element per member thus retaining computational efficiency while performing an accurate analysis. An illustrative example (modelling of an S-leg seat) is presented here to illustrate the benefits of the proposed approach to a designer.     

Determination of vapor pressures using gas chromatography

The determination of vapor pressures, p0, of compounds with low vapor pressures (10(-8) Pa < p0 < 10(3) Pa) is becoming increasingly important as a result of the need to measure p0 for environmentally sensitive compounds such as organophosphorus pesticides, biphenyls, dioxins and alkylbenzenes. Under strict conditions, the components of gas-liquid chromatography (GLC) (a volatile solute, an involatile solvent and a mobile carrier gas) are in equilibrium and as a result it is possible to use the technique to measure equilibrium properties such as vapor pressure. The technique is rapid, reliable and reproducible. These advantages have tempted many workers to measure physiochemical properties, including vapor pressures, under conditions for which the basic theories do not hold. In this review, the GLC techniques used to measure vapor pressures from GLC data together with the basic theory, limitations of the techniques and some recent measurements are discussed.     

Development of a new assay for the screening of hypochlorous acid scavengers based on reversed-phase high-performance liquid chromatography

A new assay for the screening of hypochlorite/hypochlorous acid (XOCl) scavengers, based on the reversed-phase high performance liquid chromatographic analysis of human serum albumin (HSA, 0.2% in 100 mM sodium phosphate, pH 7), before and after oxidation by XOCl (1.6 mM), was developed. XOCl induced a significant decrease of the area under the chromatographic peak of HSA at 280 nm due to the oxidation of the aromatic amino acids tryptophan and tyrosine, as suggested by the literature and by the chromatographic analyses and the electrochemical study performed here. The assay was validated by testing known XOCl scavengers such as ascorbic acid, cysteine, glutathione, S-methylglutathione and alpha-lipoic acid and other antioxidants such as carnosine and chlorogenic acid, which inhibited the oxidation of HSA. Quantitative activities were calculated using an original formula based on the changes of the area of the albumin peak. Electrochemical data collected here in a homogeneous medium showed that the anodic potentials of the antioxidants tested are less positive (ascorbic acid, chlorogenic acid and cysteine) or similar (alpha-lipoic acid) compared with those of the aromatic residues (tryptophan and tyrosine) of HSA oxidized by XOCl. However, as expected, carnosine, glutathione and S-methylglutathione were inactive at a glassy-carbon, gold or platinum electrode.     

Spin state variation in nickel(II) complexes of a redox-active Schiff base

Summary Nickel(II) complexes of a redox-active tetradentate Schiff base ligand with ethylene/propylene linkages have been prepared and characterized by spectroscopic and magnetic studies. The complexes are diamagnetic in the solid state and exhibit paramagnetic behaviour in solution. Reflectance spectra of the samples indicate a shift of the main d-d band envelope to lower energies as the bridge is changed from ethylene to propylene.Author to whom all correspondence should be directed.     

Mononuclear and binuclear manganese(II) complexes with tridentate bis-benzimidazolyl ligands

Summary Manganese(II) complexes of bis(2-benzimidazolylmethyl) ether (DGB), bis(2-benzimidazolylmethyl) sulphide (TGB) and the n-butyl derivative of DGB (BDGB) were prepared and characterised. The solution e.p.r. spectrum of [Mn(TGB)Cl₂] in DMF at 143 K is commensurate with an axially distorted monomeric manganese(II) complex, room temperature magnetic moment (6.04 B.M.) per manganese(II) atom being in the range found for other d⁵ monomeric manganese(II) complexes. The solution e.p.r. spectrum of [Mn(BDGB)Cl₂]-2H₂O in DMF at 143 K indicates the presence of two equivalent manganese(II) ions coupled by an exchange interaction, fostered by bridging chlorides. Evidence for this is provided by a nearly isotropic 11 line hyperfine structure of ⁵⁵Mn, with a coupling constant 45 ± 5G. Contact-shifted ¹H n.m.r. data also supports an exchange coupled dimeric manganese complex. The room temperature magnetic moment, 5.64 B.M., per manganese(II) indicates quenching of the magnetic moment below that of monomeric manganese(II) ion. The [Mn(DGB)Cl₂]·H₂O complex exhibits a magnetic moment of 6.02 B.M. per manganese, indicating a monomeric manganese complex. E.p.r. data of the complex diluted in an analogous Zn-DGB complex (1∶20) correlates well for D = 0.22cm⁻¹ and λ ∼- 0.267. The [Mn(DGB)-(C1O₄)₂] and [Mn(BDGB)(ClO₄)₂] complexes, diluted in analogous Zn-DGB and Zn-BDGB complexes (1∶20), show a strong single e.p.r. line at g _eff ∼- 2. The complexes have low magnetic moments; 4.44 B.M./Mn and 4.39 B.M./Mn, at room temperature.     

Hybrid aniline/silica xerogel cation adsorption and thermodynamics of interaction

Aniline groups chemically immobilized on silica through the sol-gel process were employed to extract divalent nickel and manganese from aqueous solutions at room temperature. The maximum adsorption capacity of the xerogel was studied from adsorption isotherms using a batch technique. The isotherms obtained were adjusted following the Langmuir equation. The xerogel adsorbent appears to have better affinity for nickel than manganese. From calorimetric titration, thermodynamic data on cation/nitrogen basic atom interaction in the solid/liquid interface were determined. The enthalpic values, -0.46 +/- 0.02 and -.029 +/- 0.02 kJ mol(-1) for nickel and manganese, respectively, are in agreement with the low availability of the basic nitrogen atom on the aniline group and also the possible steric hindrance of the phenyl group bonded to nitrogen. However, thermodynamics indicated the existence of favorable conditions for such cation-nitrogen interactions.     

Reference values of urinary 3,5,6-trichloro-2-pyridinol in the Italian population--validation of analytical method and preliminary results (multicentric study)

The interlaboratory validation of analytical procedures for the assay of urinary 3,5,6-trichloro-2-pyridinol (TCP) in the general Italian population is reported. The determinations were performed by high-resolution gas chromatography (HRGS) with electron capture detection and HRGS with mass spectrometry (MS) in 2 laboratories. The urine samples were from 42 participants from 3 regions of Italy. The results were evaluated by interlaboratory quality control. Urinary TCP concentrations were above the detection limit (1.2 micrograms/L) in 88% of the population, with a mean detectable concentration [GM (GSD)] of 2.8 (1.9) micrograms/g creatinine (creat). (GM, geometric mean; GSD, geometric standard deviation.) The Mann-Whitney U test showed that wine consumption was a statistically significant variable (p < 0.05) for urinary concentrations of TCP. Analysis of variance of the logarithm of urinary TCP versus wine consumption and diet showed a statistically significant fit. The model used explained 30% of the total variance: wine consumption and diet accounted for 37 and 17% respectively of the explained variance.     

Molecularly Defined Nanostructures Based on a Novel AAA–DDD Triple Hydrogen‐Bonding Motif

A facile and flexible method for the synthesis of a new AAA–DDD triple hydrogen‐bonding motif is described. Polytopic supramolecular building blocks with precisely oriented AAA and DDD groups are thus accessible in few steps. These building blocks were used for the assembly of large macrocycles featuring four AAA–DDD interactions and a macrobicyclic complex with a total of six AAA–DDD interactions.