Design and study of a high-current 5-cell superconducting rf cavity

The Advanced Photon Source （APS） at Argonne National Laboratory is considering the development of a superconducting linac-based fourth-generation hard X-ray source to meet future scientific needs of the hard X-ray user community. This work specifically focuses on the design of an optimized 5-cell superconducting radio-frequency structure well suited for a high-energy, high-beam-current energy recovery linac. The cavity design parameters are based on the APS storage ring nominal 7 GeV and 100 mA beam operation. A high-current 5-cell cw superconducting cavity operating at 1.4 GHz has been designed. In order to achieve a high current, the accelerating cavity shape has been optimized and large end-cell beam pipes have been adopted. The beam break-up threshold of the cavity has been estimated using the code TDBBU, which predicts a high threshold beam current for a 7 GeV energy recovery linac model. A copper prototype cavity has been fabricated that uses half-cell modules, initially assembled by clamping the cells together.     

DFT study on a fullerene doped with Si and N

DFT calculations are applied for some stable C₆₀, C₅₉Si, and C₅₉N hetero fullerenes. Sn and Ge atoms are doped at the same position of C₆₀. Computations are carried out at the B3LYP/cc pVDZ levels. In this work the effects of the heteroatoms, Si and N, on the structural properties of the fullerene have been studied. The structure, energetic and relative stabilities of the compounds were compared and analyzed with each other. In addition, vibrations spectra of proposed stable neutral species, as well as the infrared intensities are calculated. From the data obtained from calculation, we found that there is strong correlation between the stability of pure C₆₀ fullerene molecule and the numbers of different C-C bonds.     

Tetrathiaoxa Macrocycles with Dibenzo-subunits: A Search for New Tl(I)- and Ag(I)-Selective Ionophores

Novel S⁴O ⁿ mixed donor macrocycles (1, n=1; 2, n=2) were synthesized by the coupling reactions of corresponding dichlorides with dithiols under high dilution conditions. Synthesis and crystal structures of Tl⁺ and Ag⁺ complexes, [Tl(2)⁺ and Ag(2)⁺], with macrocycle 2 are described. The electrode based on macrocycle 2 showed excellent potentiometric sensing ability for Tl⁺ and Ag⁺ ions. This remarkable sensing of the proposed electrode can be understood in terms of the synergy effect of a soft–soft acid–base interaction and π-coordination, especially for the Tl⁺ ion, which was observed from the crystal structure of the corresponding complex.     

EFFECT OF COMPOSITION AND PROCESSING CONDITION ON MICROSTRUCTURAL PROPERTIES AND DURABILITY OF FLUOROPOLYMER/ACRYLIC BLENDS

Fluoropolymer blends have been widely used as binders for exterior coatings because of their excellent resistance to ultra-violet (UV) radiation as well as to many corrosive chemical agents.It is known that the fluorinated component usually has a lower glass transition temperature and easily crystallizes in the final structure depending upon the blend composition and sample annealing condition.We investigated the effect of blend composition and annealing process (slow and fast cooling) on the surface mor...     

SELF-SIMILAR CRACK EXPANSION METHOD FOR THE STRESS INTENSITY FACTOR ANALYSIS

The Self-Similar Crack Expansion (SSCE) method is proposed to evaluate stress intensi-ty factors at crack tips, whereby stress intensity factors of a crack can be determined by the crackopening displacement over the crack, not just by the local displacement around the crack tip. The crackexpansion rate is estimated by taking advantage of the crack self-similarity. Therefore, the accuracy ofthe calculation is improved. The singular integrals on crack tip elements are also analyzed and are pre-cisely evaluated in terms of a special integral analysis. Combination of these two techniques greatly in-creases the accuracy in estimating the stress distribution around the crack tip. A variety of two-dimen-sional cracks, such as subsurface cracks, edge cracks, and their interactions are calculated in terms ofthe self-similar expansion rate. Solutions are satisfied with errors less than 0.5% as compared with theanalytical solutions. Based on the calculations of the crack interactions, a theory for crack interactionsis proposed such that for a group of aligned cracks the summation of the square of SIFs at the right tipsof cracks is always equal to that at the left tips of cracks. This theory was proved by the mehtod ofSelf-Similar Crack Expansion in this paper.     

非导电型各向同性手性介质中非线性旋光的宏观理论

采用经典电磁场理论描述非导电型各向同性手性介质,研究了圆偏振抽运光作用下线偏振信号光的非线性旋光现象．给出了非线性旋光角的解析表达式．用该公式计算的结果与实验结果一致. 关键词：     

Thermal radical initiator derivatives based on O‐imino‐isourea: Synthesis,polymerization, and characterization

The new thermal radical initiators (TRIs) with linear and cyclic type groups based on derivatives of O‐imino‐isourea have been designed and synthesized. The radical polymerization property of the synthesized TRI derivatives as a radical initiator in n‐butyl acrylate was monitored by differential scanning calorimetry analysis. TRI derivatives with linear type groups, such as 3‐PenDCC, 3‐HexDCC, and 4‐HepDCC, showed peak temperatures (T_peak) of 80–84 °C, whereas those with cyclic type groups, such as C‐PenDCC, C‐HexDCC, and C‐HepDCC, exhibited a wide T_peak distribution in the 74–87 °C range. The polymerization efficiency using new TRIs in n‐butyl acrylate was elaborately identified from the molecular weights and conversion obtained using gel permeation chromatography analysis and NMR spectroscopy. To consider their possible application to automotive clearcoats, the real‐time evolution of the rheological properties of clearcoat resins during the crosslinking process with newly synthesized TRI derivatives was measured, confirming the different crosslinking kinetics of TRI derivatives in real thermal curing process. The results were found to be well correlated with data from the radical polymerization experiments of TRIs. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 3593–3600.     

Film characteristics of anodic oxidized AZ91D magnesium alloy by applied power

This study examined the film characteristics of an anodized AZ91D magnesium alloy by varying the direct current and pulse frequency conditions. In order to evaluate the effect of the pulse frequency on film formation, anodic oxidation was carried out by applying direct current and pulse current at a current density of 300 mA/cm². Compared with the sample groups treated with the direct current, a large number of small arcs were generated continuously on the film treated with the pulse current and the film formation rate was found to increase. Homogeneous and compact pores were formed with increasing frequency, and the rate of formation was increased rapidly to the arrival voltage. The film thickness increased and the surface roughness decreased with increasing anodic oxidation time at a fixed frequency of 125 Hz. However, treatment for more than 3 min led to decomposition of the oxidized film onto the previously formed film, which caused an increase in the number of cracks and pores within the film. The most uniform and smallest pores were acquired when the surface was anodized for 3 min at a current density and frequency of 300 mA/cm² and 125 Hz, respectively. X‐ray diffraction revealed the formation of MgO and Mg₂SiO₄ peaks, with a relative decrease in peak intensity for the MgO and Mg substrate. The Vickers hardness value was higher on the treated groups than on the untreated group, and the potentiodynamic polarization test revealed satisfactory corrosion resistance through a decrease in corrosion density and a large improvement in the corrosion potential. Copyright © 2009 John Wiley & Sons, Ltd.     

C 1s -->pi* excitation in variable size benzene clusters

The C 1s -->pi* transition in molecular benzene and benzene clusters is investigated by photoion yields at high energy resolution. The vibrationally resolved band shows the same shape in clusters as in the bare molecule, but it is redshifted by 50 meV in small clusters, i.e. near the threshold of cluster formation. This redshift increases to 70 meV with increasing cluster size. The results are assigned in comparison with ab initio calculations on model structures of dimers, trimers, and tetramers. These indicate that different carbon sites in the molecular moieties give rise to distinct spectral shifts, where carbon sites that are pointing to the pi-system of another molecule show a larger redshift than the other ones. Such structural properties are found in solid benzene, so that the gas-to-solid shift of C 1s -->pi* excited benzene is derived to be a redshift which is of the order of 100-180 meV.