A thick semi-monolithic scintillator detector for clinical PET scanners.

Both monolithic and semi-monolithic scintillator positron emission tomography (PET) detectors can measure the depth of interaction with single-ended readout. Usually scintillators with a thickness of 10 mm or less are used since the position resolutions of the detectors degrade as the scintillator thickness increases. In this work, the performance of a 20 mm thick long rectangular semi-monolithic scintillator PET detector was measured by using both single-ended and dual-ended readouts with silicon photomultiplier (SiPM) arrays to provide a high detection efficiency. The semi-monolithic scintillator detector consists of nine lutetium-yttrium oxyorthosilicate slices measuring 1.37 × 51.2 × 20 mm3 with erythrocyte sedimentation rate foils of 0.065 mm thickness in between the slices. The SiPM array at each end of the scintillator detector consists of 16 × 4 SiPMs with a pixel size of 3.0 × 3.0 mm2 and a pitch of 3.2 mm. The 64 signals of each SiPM array are processed by using the TOFPET2 application-specific integrated circuit individually. All but the edge slices can be clearly resolved for the detectors with both single-ended and dual-ended readouts. The single-ended readout detector provides an average full width at half maximum (FWHM) Y (continuous direction) position resolution of 2.43 mm, Z (depth direction) position resolution of 4.77 mm, energy resolution of 25.7% and timing resolution of 779 ps. The dual-ended readout detector significantly improves the Y and Z position resolutions, slightly improves the energy and timing resolution at the cost of two photodetectors required for one detector module and provides an average FWHM Y position resolution of 1.97 mm, Z position resolution of 2.60 mm, energy resolution of 21.7% and timing resolution of 718 ps. The energy and timing resolution of the semi-monolithic scintillator detector in this work are worse than those of the segmented scintillator array detector and need to be further improved. The semi-monolithic scintillator detector described in this work reduces costs as compared to the traditional segmented scintillator array detector and reduces the edge effect as compared to the monolithic scintillator detector.

Unusual dielectric strength of Debye relaxation in monohydroxy alcohols upon mixing.

The dielectric strength of the Debye relaxation in the binary mixtures of two isomeric monohydroxy alcohols, 2-ethyl-1-butanol (2E1B) and 4-methyl-2-pentanol (4M2P), is studied at low temperature near glass transition. Enhanced dielectric strength is exhibited in the mixtures, remarkably different from the mixing behaviors of the structural (α-) relaxation of generic liquids. A similar result is observed when analyzing the dielectric data of the binary mixtures of 2-ethyl-1-hexanol and 2-methyl-1-butanol reported in an early study. The unusual behavior of the dielectric strength in the mixtures reveals a new feature of the Debye relaxation in monohydroxy alcohols. Yet, the calorimetric measurements of the glass transition temperature in 2E1B-4M2P mixtures show a distinct negative deviation from the ideal mixing law. The explanation of the Debye relaxation is discussed with the results.

Kinetic fragility of binary and ternary glass forming liquid mixtures.

The experimental studies of liquid fragility in miscible binary and ternary glass forming mixtures reveal a general observation of the negative deviation in fragility upon mixing from the linear average of those of the components. Further analyses from ideal, near ideal to non-ideal mixing modes show that the deviation magnitude does not increase monotonically with mixing enthalpy, and a moderate intermolecular interaction would generate a largest reduction in fragility. Four eutectic systems, methyl-o-toluate-methyl-p-toluate, ZnCl(2)-AlCl(3), glycerol-water, and fructose-water, are studied to locate the composition where the largest fragility deviation occurs in phase diagrams. It is found that the compositions with the fragility minima do not coincide with the eutectic points. The results partly explain the experimental observation that the best glass forming region is not located at the eutectic composition.

Component dynamics in miscible mixtures of water and methanol.

In binary mixtures with hydrophilic substances, water is usually the more mobile component and its relaxation time is shorter than those of the other components. An exception is the case of the mixture of 1-propanol with 45 mol % water, where the α-relaxation of water is slower than the α-relaxation of 1-propanol and even slower than the local relaxation of water confined in various spaces of nanometer size. This unusual result, so far obtained in a mixture of 1-propanol with water at a single composition, deserves confirmation by experiments in another mixture at more than one composition. Toward this goal, we have chosen mixtures of methanol with water at concentrations of water ranging from 10 to 40 mol % and investigated the dynamics of the slower water and the faster methanol components by broad-band dielectric relaxation measurements. The α-relaxation time of the water component becomes shorter with increasing content of the faster methanol component in the mixture as expected and is much shorter than in the mixture of 1-propanol with 45 mol % water. In mixtures with lower water contents of 10-20 mol %, the α-relaxation of the methanol component has a narrow frequency dispersion and no resolved Johari-Goldstein ß-relaxation, indicating a low degree of intermolecular coupling or cooperativity of methanol. An increase of the content of the slower water component effectively enhances intermolecular coupling of the methanol component. Consequently, the α-relaxation of the methanol component becomes more cooperative, as evidenced by broadening of its frequency dispersion and the appearance of a resolved Johari-Goldstein ß-relaxation of methanol when the water concentration is higher than 30 mol %. The observations are rationalized by application of the coupling model.

 Dielectric relaxation dynamics in glass-forming mixtures of propanediol isomers.

The relaxation dynamics of 1,2-propanediol-1,3-propanediol mixtures is studied in supercooled liquid regions across a wide composition range. The composition dependences of liquid fragility and nonexponential parameter ß(KWW) are presented in the hydrogen-bonded mixtures with ideal mixing. The fragility index and glass transition temperature are shown to develop inversely with ß(KWW), in analogy to the dynamic behaviors in mixtures of van der Waals liquids. Negative mixing effects on liquid fragility and ß(KWW) are observed, and the strongest dependence of ß(KWW on relaxation dynamics is revealed at the equimolar concentration. The glass formation in isomeric liquids is also addressed.