大型强子对撞机上的CMS探测器

CMS探测器是大型强子对撞机（LHC）上的4个实验之一,它的设计思想是在质心能量为14TeV及积分亮度为1034 cm-2s-1的条件下对质子-质子对撞进行研究.它的特点是非常紧凑,其μ子室几乎覆盖了4π立体角.另外,CMS探测器还有可提供超强磁场的超导磁铁和由超导磁铁环绕的径迹室以及电磁量能器和强子量能器.CMS探测器对于末态为电子、光子、特别是μ子的物理过程有很好的测量精度.     

判别分析法用于ALEPH实验的π-μ鉴别

利用多元统计的判别分析方法,对ALEPH实验的强子量能器模型以及实际探测器的强子量能器和μ子探测器进行了π-μ粒子鉴别的研究.     

在大型强子对撞机上的CMS实验

LHC(large hadron collider)是目前世界上能量最高的强子对撞机.CMS(compact muon solenoid,中文译名是紧凑型缪子螺线管探测器)是LHC上的主要实验计划之一,其目标就是要寻找Higgs粒子或者超出标准模型的其他新粒子,探清自然界的电弱破缺机制,以及寻找暗物质.CMS实验位于高能量和高亮度的最前沿,是21世纪初人类认识微观世界最重要的物理实验之一.中国参加了这项国际合作,制作了部分μ子探测器、磁铁支架、电子学和地板等,目前转入物理研究工作,争取在物理研究中作出有显示度的贡献.文章简要介绍了CMS探测器以及CMS实验的目标和意义.     

在大型强子对撞机上的CMS实验

LHC（large hadron collider）是目前世界上能量最高的强子对撞机.CMS(compact muon solenoid,中文译名是紧凑型缪子螺线管探测器)是LHC上的主要实验计划之一,其目标就是要寻找Higgs粒子或者超出标准模型的其他新粒子,探清自然界的电弱破缺机制,以及寻找暗物质.CMS实验位于高能量和高亮度的最前沿,是21世纪初人类认识微观世界最重要的物理实验之一.中国参加了这项国际合作,制作了部分μ子探测器、磁铁支架、电子学和地板等,目前转入物理研究工作,争取在物理研究中作出有显示度的贡献.文章简要介绍了CMS探测器以及CMS实验的目标和意义.     

符合计数法测量宇生μ子的通量

搭建了宇生 μ子探测器,采用符合计数法测量了宇生μ子通量和空间分布.探讨了甄别器阈值标定、宇生μ子计数率与工作电压的关系、塑料闪烁体板间间距对计数率的影响.通过改进测量装置的几何结构,研究了宇生μ子空间角的分布情况,验证了宇生μ子计数率与探测器摆放天顶角呈co s2θ关系.     

BES实验数据离线刻度

概述了北京谱仪(BES)各子探测器的实验离线数据刻度,包括主漂移室、飞行时间计数器、簇射计数器和μ子鉴别器.给出了BES1994年D_s运行期间的探测器运行性能,以及数据质量情况.     

二维多丝室探测器读出方法的优化

中国散裂中子源将建设一台基于~3He气体的二维多丝室,作为多功能反射谱仪束线的中子探测器.基于已有的研究,为优化选择二维多丝室探测器的丝结构,本文研究了三种不同的丝结构,并采用重心读出方法和数字读出方法进行了探测器的性能测量,得到了满足多功能反射谱仪探测器需求的读出方法.实验结果表明:对同种丝结构的二维多丝室探测器,重心读出方法的位置分辨和成像性能都好于数字读出方法;基于重心法读出的多丝室探测器位置分辨率可以达到约160μm,基于数字读出方法的多丝室探测器位置分辨率可以达到约400μm.优化设计的丝结构为:基于重心读出法的阳极丝间距1.5 mm、读出通道间距4 mm,基于数字读出法的阳极丝间距1.5 mm、读出通道间距2 mm.优化设计的丝结构均能满足谱仪的位置分辨要求.     

北京谱仪BESⅢ

北京谱仪是北京正负电子对撞机上的大型通用磁谱仪。对撞机中的正负电子束团在谱仪中心对撞,产生的末态带电粒子和中性粒子的空间位置、动量、能量等特性由谱仪记录,经过数据处理后进行粲-τ能区的物理研究。在BEPC上先后安装了北京谱仪BESⅠ和BESⅡ。在BEPCⅡ上安装的是新研制的北京谱仪BESⅢ包括主漂移室、电磁量能器、飞行时间计数器、μ子探测器和超导磁体,具有     

裂变室探测器组合研制

裂变室探测器己广泛应用于中子的辐射强度、中子产额以及剂量测量，是一种气体计数器，内有裂变材料，在热核聚变研究中，需研制两种裂变室探测器组合，即微裂变室探测器组合和通用型多裂变室探测器组合。微裂变室探测器是铅笔大小的气体计数器，它作为裂变堆的堆芯监察器而被研制。     

塑料闪烁体探测器测量宇宙射线μ子寿命实验

本文设计了基于快时间响应的塑料闪烁体和光电倍增管组成的宇宙射线μ子探测器.带电粒子在探测器中产生的电脉冲信号波形由数字化仪读出并记录在计算机.通过离线数据分析完成μ子衰变事例选择、脉冲信号定时和寿命拟合等步骤.实验中脉冲信号上升时间小于20 ns,噪声小于3 mV,经估算使用前沿定时方法得到的探测器时间分辨率可达到纳秒量级.μ子平均寿命测量值为2.188±0.045μs,与粒子数据表(PDG)给出的μ子寿命测量值在误差范围内是符合的.     

Theoretical Study of the Collision-Induced Double Transition CO(2) (nu(3) = 1) + N(2) (nu(1) = 1) <-- CO(2) (nu(3) = 0) + N(2) (nu(1) = 0) at 296 K

A procedure is presented for the calculation of the double vibrational collision-induced absorption CO(2) (nu(3) = 1) + N(2) (nu(1) = 1) <-- CO(2) (nu(3) = 0) + N(2) (nu(1) = 0) on the basis of quantum lineshapes computed using an isotropic potential and dipole-induced dipole functions. The linestrengths and energies of the vibration-rotation transitions are treated explicitly for N(2), utilizing the HITRAN database for CO(2). The theoretical absorption profile is compared to recent experimental results. By narrowing the width of the individual lines contributing to the overall absorption profile relative to their values determined for N(2)-N(2) collision-induced absorption, excellent agreement between theory and experiment is obtained. Copyright 2000 Academic Press.     

First Observation of the nu(17)-nu(4) Difference Bands of Diborane (10)B(2)H(6) and (11)B(2)H(6)

An analysis of the nu(17)-nu(4) difference bands near 800 cm(-1) of two isotopic species, (10)B(2)H(6) and (11)B(2)H(6), of diborane has been carried out using infrared spectra recorded with a resolution of ca. 0.003 cm(-1). In addition, the nu(17) band of (10)B(2)H(6) has been recorded and assigned. Since this band in (11)B(2)H(6) had already been studied (R. L. Sams, T. A. Blake, S. W. Sharpe, J.-M. Flaud, and W. J. Lafferty, J. Mol. Spectrosc. 191, 331-342 (1998)), it was possible to derive precise energy levels and Hamiltonian constants for the 4(1) vibrational states of both isotopic species. Copyright 2000 Academic Press.     

The 2(3)Delta(g) State of (7)Li(2)

Using pulsed perturbation-facilitated optical-optical double resonance (PFOODR) spectroscopy, the 2(3)Delta(g) state of (7)Li(2) (electronic configuration (varsigma(g)2s) (4ddelta(g)), effective principal quantum number n* = 4.101) has been observed and assigned. Molecular constants and a RKR potential energy curve were obtained. The major molecular constants are Copyright 2000 Academic Press.     

The Perturbation between the G(1)Pi(g) and 2(1)Delta(g) States of (7)Li(2)

We have observed the rotational levels in the v = 2, 3, 5, 6, 7, and 8 vibrational manifolds of the 2(1)Delta(g) state of (7)Li(2) via the A(1)Sigma(+)(u) intermediate levels by DeltaLambda = 2 transitions. This violation of the DeltaLambda = 0, +/-1 selection rule is due to the interaction with the G(1)Pi(g) state. Band-by-band deperturbations of the G(1)Pi(g) approximately 2(1)Delta(g) (v(Pi), v(Delta)) = (11, 2), (12, 3), (15, 5), (16, 6), (18, 7), and (19, 8) bands have been performed. Deperturbed molecular constants and rotational-electronic interaction parameters are reported here. Copyright 2000 Academic Press.     

Rovibrational Intensities of the (00(0)3) <-- (10(0)0) Dyad Absorption Bands of (12)C(16)O(2)

Absolute line intensities of (12)C(16)O(2) are experimentally measured for the first time for the (00(0)3)(I) <-- (10(0)0)(II) band at 5687.17 cm(-1) and the (00(0)3)(I) <-- (10(0)0)(I) band at 5584.39 cm(-1). The spectra were obtained using a Bomem DA8 Fourier transform spectrometer and a 25-m base-path White cell at NASA-Ames Research Center. The rotationless bandstrengths at a temperature of 296 K and the Herman-Wallis parameters are S(0)(vib) = 6.68(30) x 10(-25) cm(-1)/(molecule/cm(2)); A(1) = 1.4(9) x 10(-4), and A(2) = -1.1(5) x 10(-5) for the (00(0)3)(I) <-- (10(0)0)(II) band and S(0)(vib) = 6.07(22) x 10(-25) cm(-1)/(molecule/cm(2)); A(1) = 5.2(1.5) x 10(-4) and A(2) = -4.0(7) x 10(-5) for the (00(0)3)(I) <-- (10(0)0)(I) band.     

The v(1)+v(3) Bands of the (16)O(17)O(16)O and (16)O(16)O(17)O Isotopomers of Ozone

Using 0.002 cm(-1) resolution Fourier transform absorption spectra of an (17)O enriched ozone sample, an extensive analysis of the v(1)+v(3) bands of the (16)O(17)O(16)O and (16)O(16)O(17)O isotopomers of ozone has been performed for the first time. The experimental rotational levels of the (101) vibrational states were satisfactorily reproduced using a Hamiltonian matrix that takes into account the observed rovibrational resonances. More precisely, for (16)O(17)O(16)O, as for the other C(2v)-type ozone isotopomers, it was necessary to account for the Coriolis type resonances linking the (101) rotational levels with the levels of the (200) and (002) vibrational states and the Darling-Dennison interaction coupling the levels of (200) with those of (002). For the C(s)-type isotopomer, namely (16)O(16)O(17)O, as for (16)O(16)O(18)O and (16)O(18)O(18)O, it proved necessary to also account for an additional DeltaK(a)&equals+/-2 resonance involving the rotational levels from (101) and (002) (J.-M. Flaud and R. Bacis, Spectrochimica Acta Part A 54, 3-16 (1998)). Using a Hamiltonian matrix which takes these resonances explicitly into account, precise vibrational energies and rotational and coupling constants were deduced, leading to the following band centers: v(0)(v(1)+v(3))=2078.3496 cm(-1) for (16)O(17)O(16)O and v(0)(v(1)+v(3))=2098.8631 cm(-1) for (16)O(16)O(17)O. Copyright 2001 Academic Press.     

Multiple magnetic transitions in single crystals of Ce_(12)Fe_(57.5)As_(41) and La_(12)Fe_(57.5)As_(41)

Measurements of magnetic and transport properties were performed on needle-shaped single crystals of Ce_(12)Fe_(57.5)As_(41)and La_(12)Fe_(57.5)As_(41).The availability of a complete set of data enabled a side-by-side comparison between these two rare earth compounds.Both compounds exhibited multiple magnetic orders within 2-300 K and metamagnetic transitions at various fields.Ferromagnetic transitions with Curie temperatures of 100 and 125 K were found for Ce_(12)Fe_(57.5)As_(41)and La_(12)Fe_(57.5)As_(41),respectively,followed by antiferromagnetic type spin reorientations near Curie temperatures.The magnetic properties underwent complex evolution in the magnetic field for both compounds.An antiferromagnetic phase transition at about 60 K and 0.2 T was observed merely for Ce_(12)Fe_(57.5)As_(41).The field-induced magnetic phase transition occurred from antiferromagnetic to ferromagnetic structure.A strong magnetocrystalline anisotropy was evident from magnetization measurements of Ce_(12)Fe_(57.5)As_(41).A temperature-field phase diagram was present for these two rare earth systems.In addition,a logarithmic temperature dependence of electrical resistivity was observed in the two compounds within a large temperature range of 150-300 K,which is rarely found in 3D-based compounds.It may be related to Kondo scattering described by independent localized Fe 3d moments interacting with conduction electrons.     

The (29)Si T(1) and T(2) NMR relaxation in porous paramagnetic material SiO(2)-MnO-Al(2)O(3)

The (29)Si spin-lattice relaxation in porous silica-based material 1, doped by ions Mn(2+) at a Si/Mn ratio of 3.5, is non-exponential, independent of magic-angle spinning (MAS) rates and governed by direct dipolar coupling between electron and nucleus where an electron relaxation time is estimated to be about 10(-8)s. In the absence of mutual energy-conserving spin flips (spin diffusion) in 1, the (29)Si T(2) time increases linearly with spinning rates. None was observed in diamagnetic porous system 2. The unexpected (29)Si T(2) dependence has been interpreted in terms of the large bulk magnetic susceptibility (BMS) effects. It has been shown that editing the (29)Si Hahn-echo MAS NMR spectra eliminates wide lines, belonging to (29)Si nuclei in the proximity of paramagnetic centers, and reduces the BMS broadenings in sideband patterns for nuclei remote from these centers.