Fast simulation of the forward tracking detector of HPLUS

The necessity of installing a forward tracking detector stack is discussed for the Hadron Physics LanzhoU Spectrometer(HPLUS). A local tracker is developed to solve the multi-track finding problem. The track candidates are searched iteratively via Hough Transform. The fake tracks are removed by a least square fitting process. With this tracker we have studied the feasibility of pp -> pp + phi(-> K+K-), a typical physical channel proposed on HPLUS. The single track momentum resolution due to the uncertainty of the positioning in FTD is 1.3%. The multiple scattering effect contributes about 20% to the momentum resolution in the FTD coverage. The width and the signal-to-background ratio of the reconstructed phi are 1.51 MeV and 4.36, respectively, taking into account the direct Kaon channel pp -> pp + K+K- as background. The geometry coverage of FTD for phi events is about 85.4%. Based on the current fast simulation and estimation, the geometrical configuration of FTD meets the physical requirement of HPLUS under the current luminosity and multiplicity conditions. The tracker is applicable in the full simulation coming next and is extendable to other tracking component of HPLUS.

基于SLEUTH模型的沈阳-抚顺都市区城市规划

利用SLEUTH模型,在3种规划预案下研究沈阳-抚顺都市区城市规划。结果表明,低生态保护的城市增长预案导致了城市快速扩张和农田、林地等其他景观类型面积迅速减少.严格的生态保护规划预案虽然能很好地保持聚集的城市增长格局,减少对其他景观的侵占,但限制了城市增长速度,与区域经济发展现状相矛盾.如果扩散的城市增长格局能得到进一步的控制,适当生态保护的城市增长预案将是沈阳-抚顺都市区未来发展的推荐预案.

推广旱作农业技术是促进西部农业发展的重要环节

依据朱钅容基总理 1 999年 8月 7日讲话精神 ,以及旱作农业的技术体系 ,文章阐述了培肥地力、轮作倒茬、化学技术、选育品种、节水、立体种植、地膜覆盖、水土保持耕作法这八种技术的内涵和特点 ,分析了其充分利用光、热、水、气、土、肥资源而取得的社会效益、经济效益和生态效益 ,着重强调旱作技术在农业持续、稳定、健康发展中的作用和改善农业生态环境的显著地位 ,供同类地区的决策者和研究者借鉴。

黄土高原典型土壤矿物固定态铵变化的南北差异

采集从北向南依次分布的干润砂质新成土(神木)、黄土正常新成土(延安)和土垫旱耕人为土(杨陵)等典型土壤剖面0—200 cm土层土样,通过测定土样全氮和矿物固定态铵,以阐明黄土高原典型区域土壤全氮和矿物固定态铵及二者比率随地理位置和土层的变异规律,为全面了解黄土高原土壤相对稳定氮库累积提供科学数据。结果表明,不同地理位置、不同土层全氮和矿物固定态铵含量存在显著差异。从南到北全氮和矿物固定态铵呈下降趋势,但各土壤全氮和矿物固定态铵的分布显著不同,全氮含量在0—60 cm随土层深度增加下降很明显,60—120 cm有一定下降,120 cm以下低而稳定。矿物固定态铵在全剖面上的分布比较均匀,随土层深度的变化差异不显著,不同土层间的差异基本在误差范围内,土垫旱耕人为土、黄土正常新成土和干润砂质新成土表层(0—10 cm)矿物固定态铵平均含量分别为215.80±7.45、165.80±8.73和146.50±1.83 mg/kg,表层以下(10—200 cm)平均含量分别为193.40±9.67、157.14±5.75和142.02±5.47 mg/kg。从地理位置分析,干润砂质新成土、黄土正常新成土和土垫旱耕人为土表层...

从Σ-协议到公共参考串模型下可否认零知识的高效编译器

给出公共参考串(CRS)模型下可否认零知识的一个正面结果:从Σ-协议到CRS模型下的可否认零知识的高效转化.由Pass在CRYPTO 2003中给出的下界可知,我们的编译器取得了最优的轮效率.此外,转化所增加的通信复杂度较小.

陆地生态系统水—碳耦合循环与过程管理研究

陆地生态系统的水循环与碳循环是地球表层系统物质循环与能量交换的核心,也是最基本的耦合的两个生态学过程。区域或全球尺度生态系统的水管理与碳管理是全球变化科学与可持续发展研究的两大主题,是人类维持全球生态系统的物质与能量循环、自然资源循环再生的重要生态学途径。我们在综合评述现代应用生态学研究的发展趋势,陆地生态系统水和碳循环与生态系统管理关系的基础上,提出了陆地生态系统水循环与碳循环过程管理的内容与思路,阐述了生态系统水和碳耦合循环机制与模拟综合研究的新设想。

Micropatterning of metal films coated on polymer surfaces with epoxy mold and its application to organic field effect transistor fabrication

In this letter, a simple and versatile approach to micropatterning a metal film, which is evaporated on a Si substrate coated with polymer, is demonstrated by the use of a prepatterned epoxy mold. The polymer interlayer between the metal and the Si substrate is found important for the high quality pattern. When the metal-polymer-Si sandwich structure is heated with the temperature below T-m but above T-g of the polymer, the plastic deformation of the polymer film occurs under sufficiently high pressure applied. It causes the metal to crack locally or weaken along the pattern edges. Further heating while applying a lower pressure results in the formation of an intimate junction between the epoxy stamp and the metal film. Under these conditions the epoxy cures further, ensuring adhesion between the stamp and the film. The lift-off process works because the adhesion between the epoxy and the metal film is stronger than that between the metal film and the polymer. A polymer field effect transistor is fabricated in order to demonstrate potential applications of this micropatterning approach.

Coordination reactions in the extraction of cerium(IV) and fluorine(I) by DEHEHP from mixed nitric acid and hydrofluoric acid solutions

The coordination reactions during the solvent extraction of cerium(IV) and fluorine(l) from mixed nitric acid and hydrofluoric acid solutions by di-(2-ethylhexyl)-2-ethylhexylphosphonate, L (DEHEHP) in heptane have been investigated. The extraction data have been analyzed by graphical methods taking into account all plausible species extracted into the organic phase. Different variables influencing the extraction of Ce(IV), such as the concentrations of nitrate ions, hydrofluroric acid, nitric acid, and extractant have been studied. The results demonstrate that DEHEHP can extract not only Ce(NO3)(4) as Ce(NO3)4.2L and HF as HF (.) H2O (.) L, but both together as Ce(HF)(NO3)(4) (.) L. The extraction equilibrium equations are determined according to slope analysis and IR spectra. The equilibrium constants of the extracted complexes have been calculated, taking into account complexation between the metal ion and inorganic ligands in the aqueous phase and all plausible complexes extracted into the organic phase. It is also shown that boric acid, which was added into the mixed solutions to complex with F(I) is not extracted by DEHEHP, and neither does it affect the extraction of cerium(IV) and HF, nor change the extraction mechanism.

Synthesis and characterization of tris(cyclopentylcyclopentadienyl)lanthanide complexes (C5H9C5H4)(3)NdBrLi(THF)(3) and (C5H9C5H4)(3)SmTHF

(C5H9C5H4)(3)NdBrLi(THF)(4)(1)(C5H9=cyclopentyl) was obtained from the reaction of NdCl3 with C5H9C5H4Na and LiBr (Nd:Na:Li=1:2:1 molar ratio) in THE X-ray crystallography showed that the ten-coordinated neodymium atom is bonded to three cyclopentylcyclopentadienyl(eta(5)) rings and a single bromine atom bridging a lithium which is bonded to three THF molecules. Complex 1 is triclinic, P1 space group with unit dimensions of a= 12.048(2), b= 13.498(3), c= 13.831(3)Angstrom, a = 104.16(3), beta = 104.07(3), gamma =95.96(3)degrees, V=2083.3(7)Angstrom(3), Z=2, D-c=1.35Mg/m(3) and F(000)=874. (C5H9C5H4)(3)SmTHF (2) was synthesized by reaction of anhydrous SmCl3 with C5H9C5H4Na at a molar ratio of 1:3. The structure was determined by X-ray crystallography. The ten-coordinated samarium atom is bonded to three cycloperrtylcyclopentadienyl rings and one oxygen of THF molecule to form a pseudo-tetrahedron. Complex 2 is orthorhombic, Fdd2 space group with unit cell dimensions of a =28.175(5)Angstrom, b =46.24(2) Angstrom, c =9.167(4) Angstrom(3), V=11943(8)Angstrom(3), Z= 16, D-c = 1.38Mg/m(3) and F(000)=5136.

(C_5H_9C_5H_4)_3NdBrLi(THF)_3和(C_5H_9C_5H_4)_3SmTHF的合成与结构

无水三氯化钕与环戊烷基环戊二烯钠、溴化锂(1:2:1摩尔比)反应,除去不溶物和溶剂后,产物在己烷/四氢呋喃溶剂中冷冻得到兰紫色晶体(C5H9C5H4)3NdBrLi(THF)3(配合物1)。其中心金属Nd3+的配位数为10,以η5与3个环戊二烯基相连,并通过单溴原子桥连锂原子,形成双核结构。该晶体属三斜晶系,P`1空间群。晶体学参数为a=12.048(2)、b=13.498(3)、c=13.831(3);α=104.16(3)、β=104.07(3)、γ=95.96(3); V=2083.3(7)3、Z=2、Dc=1.35Mg/m3、Mr=847.01gmol-1、F(000)=874。无水三氯化钐与环戊烷基环戊二烯钠(1:3)反应,产物在-30oC下的己烷溶剂中结晶得桔红色晶体(C5H9C5H4)3SmTHF(配合物2)。该晶体属正交晶系,Fdd2空间群。晶胞参数a=28.175(5) 、b=46.24(2)、c=9.167(4);V=11943(8)3、Z=16、Dc=1.38Mg/m3、 Mr=622.11 g·mol-1、F(000)=5136。10配位的金属Sm3+与3个环戊二烯基以η5相连,并结合...

16-and 18-electron Cp*Rh complexes with 1,2-dicarba-closo-dodecabofane(12)-1,2-dichalcogenolato ligands, as studied by multinuclear magnetic resonance

The reaction of [Cp*RhCl2](2) 1 with dilithium 1,2-dicarba-closo-dodecaborane(12)-1,2-dithiolate (a) and -diselenolate (b) afforded the 16-electron rhodium(III) half-sandwich complexes Cp*Rh[E2C2(B10H10)] [E=S (3a), Se (3b)]. The 18-electron trimethylphosphane rhodium(III) half-sandwiches Cp*Rh(PMe3)[E2C2(B10H10)] 4a-c were prepared from the reaction of Cp*RhCl2(PMe3) 2 with the same dichalcogenolates, including the ditelluride (c). The complexes 4a,b could also be obtained from the reaction of 3a,b with trimethylphosphane. The molecular geometry of 4b was determined by X-ray structural analysis. The 16-electron complexes 3 an monomeric in solution as shown by multinuclear magnetic resonance (H-1-, B-11-, C-13-, P-31- Se-77-, Rh-103-, Te-125-NMR). also in comparison with the data for the trimethylphosphane analogues 4a-c and for 6a in which the rhodium bears the eta(5)-1,3-C5H3 Bu-t(2) ligand. The Rh-103 nuclear shielding is reduced by 831 ppm (3a) and 1114 ppm (3b) with respect to the 18-electron complexes 4a,b. Similarly, the Se-77 nuclear shielding in 3b is reduced by 676.4 ppm with respect to that in 4b. (C) 1999 Elsevier Science S.A. All rights reserved.

4,5-二溴苯基荧光酮-钛(Ⅳ)-Tween-80分光光度法测定尿蛋白

本文提出了一个借钛-4,5-二溴苯基荧光酮(DBPF)-Tween-80与蛋白质显色反应光度测定微量尿蛋白的高灵敏方法。在pH2.9,血清蛋白能与Ti-DBPF-Tween-80形成蓝色络合物,最大吸收波长为605nm。加入小量乙醇能提高方法的灵敏度和稳定性,牛血清蛋白含量在0～150μg/25ml范围内服从Beer定律。尿液中其它成分不干扰测定。用拟定的方法测定人尿蛋白,获得满意结果。