HIRFL-CSR注入引出KICKER磁铁

以难度最大的快引出 KICKER磁铁为例 ,介绍了兰州重离子加速器冷却储存环注入引出 KICKER磁铁和电源设计的基本概念和所达到的指标

The influence of fractionation on cell survival and premature differentiation after carbon ion irradiation

Carbon ion radiotherapy/Fractionated irradiation/R-BE/Premature terminal differentiation. To investigate the influence of fractionation on cell survival and radiation induced premature differentiation as markers for early and late effects after X-rays and carbon irradiation. Normal human fibroblasts NHDF, AG1522B and WI-38 were irradiated With 250 kV X-rays, or 266 MeV/u, 195 MeV/u and I I MeV/u carbon ions. Cytotoxicity was measured by a clonogenic survival assay or by determination of the differentiation pattern. Experiments with high-energy carbon ions show that fractionation induced repair effects are similar to photon irradiation. The RBE10 values for clonogenic survival are 1.3 and 1.6 for irradiation in one or two fractions for NHDF cells and around 1.2 for AG1522B cells regardless of the fractionation scheme. The RBE for a doubling of post mitotic fibroblasts (PMF) in the population is I for both single and two fractionated irradiation of NHDF cells. Using I I MeV/u carbon ions, no repair effect can be seen in WI-38 cells. The RBE10 for clonogenic survival is 3.2 for single irradiation and 4.9 for two fractionated irradiations. The RBE for a doubling of PMF is 3.1 and 5.0 for single and two fractionated irradiations, respectively. For both cell lines the effects of high-energy carbon ions representing the irradiation of the skin and the normal tissue in the entrance channel are similar to the effects of X-rays. The fractionation effects are maintained. For the lower energy, which is representative for the irradiation of the tumor region. RBE is enhanced for clonogenic survival as well as for premature terminal differentiation. Fractionation effects are not detectable. Consequently, the therapeutic ratio is significantly enhanced by fractionated irradiation with carbon ions.

Study on shunt impedance and voltage distribution of 4-rod RFQ cavity

A high current RFQ (radio frequency quadrupole) is being studied at the Institute of Modern Physics, CAS for the direct plasma injection scheme. Shunt impedance is air important parameter when designing a 4-rod RFQ cavity, it reflects the RF efficiency of the cavity, and has a direct influence on the cost of the structure. Voltage distribution of a RFQ cavity has an effect on beam transmission, and particles would be lost if the actual voltage distribution is not as what, it should be. The influence of cell length, stern thickness and height on Shunt impedance and voltage distribution have been studied, in particular the effect of projecting electrodes has been investigated in detail.

保护性耕作对土壤线虫c-p类群及功能团的影响

以辽宁彰武县保护性耕作示范推广基地土壤为研究对象,通过实地调查和取样分析,对比研究了传统犁耕和6a保护性耕作(免耕秸秆覆盖)条件下的土壤线虫c-p(colonizer-persister)类群及功能团,为评价保护性耕作的土壤生态效应提供理论依据。研究发现,与犁耕相比,保护性耕作显著增加了土壤线虫各c-p类群及绝大多数功能团的多度,但显著减少了Ba4和Om5功能团多度。此外,保护性耕作还改变了土壤线虫生活史和功能团的结构特征:在大部分研究土层,c-p1和c-p2线虫的相对多度显著提高,而c-p3、c-p4以及c-p3-5类群显著降低;Ba1、Ba2、Ba3、Fu4和H5功能团的相对多度显著提高,而Ba4、H3和Om5的相对多度显著降低,Fu2、H2和Om4相对多度的变化较复杂,在表土层表现为显著抑制,在15~30cm土层则为促进作用。土壤线虫c-p类群和功能团的多度及结构特征可能适合作为评价保护性耕作对土壤质量影响的生物学指标。

Femtosecond pump-probe mass spectra on the dissociative photoionization of CF3I

The multi-photon dissociative photoionization dynamics of CF3I has been studied with femtosecond two-color pump-probe time-of-flight mass spectra at a pump pulse of 265 nm and a probe pulse of 398 nn. This enables the A band and 5ppi(3)7ssigma((2)Pi(1/2)) Rydberg state to be accessed with the pump beam. The observed fast and slow decay components of CF3+ and I+ reflect the fast repulsive A band and some higher lying ion-pair states may be responsible for the decay of the 5ppi(3)7ssigma((2)Pi(1/2)) Rydberg state. The results provide information on the different multi-photon pathways producing these ions and the de-excitation mechanism of the 5ppi(3)7ssigma((2)Pi(1/2)) Rydberg state. (C) 2003 Elsevier Science B.V. All rights reserved.

耕地土壤交换性钙镁比值的研究

对沈阳市郊区1994个耕地表土(0～20cm)样点和4个典型剖面中交换性Ca/Mg的比值进行了对比研究。结果表明:不同土属耕层土壤中Ca、Mg交换量有较大差别,交换性Ca/Mg的比值主要受母质等成土因素的影响;棕壤的各个土属的Ca/Mg在4左右,石灰性草甸土和草甸沼泽土的Ca/Mg则在8以上。棕壤和草甸土典型剖面不同层次中的Ca/Mg比值有着随深度加深而降低的趋势;由于Ca的植物返还率较Mg高,同一土壤类型中Ca/Mg比值的最大值出现在表土层,母质层中的Ca/Mg则相对稳定。对土壤Ca/Mg进行研究可以丰富土壤离子交换性能研究和土壤发生学特性研究的内容。

有机质、CaCl_2和MgCl_2对细颗粒泥沙絮凝沉降的影响

在CaCl2和MgCl2浓度为0~1.0mmol/L,泥沙浓度为10g/L时,用吸管法研究了有机质、CaCl2和MgCl2对细颗粒泥沙静水絮凝沉降的影响,结果表明,去除有机质后,细颗粒泥沙絮凝沉降加快,其絮凝所需的最佳电解质浓度降低;CaCl2和MgCl2的絮凝能力无明显差异,有机质含量对其几乎没有影响;在相同盐度下,细颗粒泥沙的絮凝沉降速度随电解质摩尔浓度的增大而增大.

Spectroscopic studies on charge transfer from Ce3+, to Yb3+ in KMgF3 : Ce, Yb nanocrystals

Nanocrystals of KMgF3 single-doped and codoped with Ce3+ or/and Yb3+ were synthesized separately by the microemulsion method. The X-ray diffraction(XRD) patterns were indexed to show that the KMgF, crystal system was unchanged. The fluorescent spectra of KMgF3:Ce, Yb polycrystal powders were studied and compared with those of the Ce, Yb doped KMgF3 crystals produced using the high-temperature solid phase method. The diffuse reflection spectra and infrared. emission of KMgF3:Ce, Yb were investigated. From the results, the authors could confirm that there were charge transfer processes from Ce3+ to Yb3+ in both KMgF3: Ce,Yb nanocrystals and polycrystal powders.

Synthesis and properties of polyquinolines and polyanthrazolines containing pyrrole units in the main chain

A series of eight new polyquinolines and polyanthrazolines with pyrrole isomeric units in main chain were synthesized and characterized. The new polymers showed high glass transition temperatures (T-g = 242-339 degreesC) and excellent thermal stability (T-5% = 398-536 degreesC in air, TGA). Compared to the series of polyanthrazolines, the series of polyquinolines exhibited higher thermal stability, better solubility in common organic solvents, and lower maximum absorption wavelengths (lambda(max)(a)). Polyanthrazolines with 2,5-pyrrole linkage showed an unusually high lambda(max)(a) (565 nm) and small band gap (2.02 eV). All polymers in solution had low photoluminescence quantum yields between 10(-2%) and 10(-5%) and excited-state lifetimes of 0.28-1.29 ns. The effects of molecular structure, especially pyrrole linkage structures, on the electronic structure, thermodynamics, and some of the optical properties of the polymers were explored. A model of hydrogen bonds in the main chain of the polymers was suggested to explain the difference in the properties of the isomer polymers. In addition, a polyquinoline (PBM) was chosen to examine the proton conductivity; the result indicated that the PBM/H3PO4 complex exhibited a high conductivity of 1.5 x 10(-3) S cm(-1) at 157 degreesC.

固相反应法制备Pt-Ru/C催化剂对乙醇氧化的电催化活性研究

引言近年来,直接甲醇燃料电池(DMFC)由于其燃料来源丰富、价格低廉、甲醇携带和储存安全方便等独特的优越性而越来越受到重视[1]。但是甲醇具有一定的毒性,因此要想实现DMFC在诸如手机、笔记本电脑以及电动车等可移动电源领域的应用,必须探索新的液体燃料以替代有毒性的甲醇。其中乙醇很易从农作物中大量生产,又无毒,因此很有可能用作替代甲醇的质子交换膜燃料电池燃料。近年来乙醇的电催化氧化已被众多的研究者从电催化和乙醇燃料电池的角度进行了广泛的研究[2,3]。但是乙醇在Pt电极上的氧化易导致强吸附物种CO毒化催化剂,Pt鄄Ru合金是目前强吸附毒化物种CO易氧化为CO2的最有效的电催化剂,因此近年来也有一些关于Pt鄄Ru合金催化剂对乙醇的电化学氧化的研究[4~6]。我们研究组首次用固相反应法制备了Pt/C催化剂,发现所制得的Pt/C催化剂对甲醇[7]和乙醇[8]氧化的电催化性能要比用传统的液相反应法制得的Pt/C催化剂好很多。但Pt/C催化剂对甲醇和乙醇氧化的电催化活性还是较低,因此,本文首次研究了用固相反应法制备Pt鄄Ru/C催化剂及这种催化剂对乙醇氧化的电催化性能,发现用固相反应法制备的Pt鄄Ru/C催化剂对乙醇氧...

Blue light-emitting poly(fluorene-co-benzene) containing an oxadiazole moiety

A new kind of polyfluorene containing oxadiazole as the side chain was synthesized. The introduction of oxadiazole moiety as more bulky group prevents the aggregation and reduces the crystallinity of the polymers. Efficient intramolecular energy transfer from oxadiazole moiety to the conjugated backbone has been realized, leading to 70% improvement of photoluminescence quantum efficiency of the designed polymers. Compared with PAF, the PFOXD exhibits significant improvement in electroluminescence properties, with luminous efficiency of 0.8 cd/A and maximum luminance of 1800 cd/m(2).

The reduction of Eu3+ to Eu2+ in BaMgSiO4 : Eu prepared in air and the luminescence of BaMgSiO4 : Eu2+ phosphor

The reduction of Eu3+ to Eu2+ in air has been observed in a silicate matrix for the first time in BaMgSiO4:Eu prepared by high-temperature solid-state reaction. Emission and excitation spectra were employed to detect the presence of Eu2+ ions in the compound and this reduction was explained by a charge compensation model proposed previously. In BaMgSiO4 : Eu2+, Eu2+ ions occupy three different lattice sites by substitution for Ba2+ ions. Eu2+ ions on Ba(1) and Ba(2) sites gave emissions at about 500 nm while that on Ba(3) site showed an emission band at 398 nm. All the emissions of Eu2+ ions in BaMgSiO4 : Eu2+ were not quenched at room temperature.