118 resultados para Smoke detectors


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气体探测器是历史最悠久的核探测器之一气体探测器具有成本低廉、制备简单、性能可靠和使用方便等特点。而且气体探测器的形状和尺寸可任意设计,厚度可随气体气压的变化而改变,适合做大面积位置灵敏、大立本角探测和有较宽的动态测量范围。所以气体探测器在各自的应用范围内发挥着巨大的作用。在兰州放射性束流线(RIBLL)上开展次级束实验的过程中,束流的定位和发散度测定都是非常重要的。我们研制了两种高性能的双维位置灵勘平行板雪崩计数器(PPAC),一种为传统的三个极板结构,另外一种为五个极板的多极结构,分别适用于较重粒子和轻粒子的位置测量。对于五个极板的多极结构的探测器,灵敏面积为100mm×100mm,采用电荷分除法读出位置,我们用3组分α源测试,工作气体选用异丁烷。测试在6.5mb气压下,位置分辨为0.55mm(FWHM),探测效率大于99.2%,位置离散小于士0.2mm。一系列的性能指标都达到了同类探测器的最好水平。该探测器和以前研制的三极板PPAC的性能均已满足RIBLL的要求,将会用作RIBLL重要的束诊元件和位置探测器。同时改进后还能在即将建成的兰州重离子加速器冷却存储环(HIRFL-CSR)上的束流诊断过程中发挥重要的作用。同时,为在RIBLL上开展超重元素和超重核素的合成实验研制了一种多阳极横向场气体电离室(MAIC)。在100mbP10气体下,对应第四块大灵敏区域,5.806MeV~(244)Cm的α粒子的能量损失为1.30MeV,得出该探测器的能量分辨为41.1keV(FwHM),相对分辨为3.16%。该探测器适合于较重粒子的鉴别,性能指标已经满足RIBLL鉴glI灼子的要求。

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In the experiment of nuclear reaction, it is important to measure the mass, charge, energy and emitted direction of particles. For multiparameter measurement, we must use a detector or a group of detectors which can give the time, energy, and position information. The Large Area position sensitive Ionization Chamber(LAIC) is one of the eight experiment terminals of HIRFL. It is built for researching nuclear reactions from low energy to intermediate energy. It is an excellent equipment for energy measurements and atomic number identification of emitted fragments in this energy region. It is also designed to give the time and position information of the emitted fragments by itself. Obviously, an IC can not supply a good timing signal. Moreover, the mechanical installation is different from the original design by some other reasons. In this case, it is not enough to obtain the correct direction information of the emitted fragments. To obtain good timing signals and the correct direction information, some modifications must be made. It is well known that a PPAC can give us excellent timing signals. It also can be easily built as a position sensitive detector. For this reason, a specially designed PPAC is installed in the entrance of the LAIC. For the different purposes, two types of PPACs were designed and tested. Both are OCTPSACs (OCTunit one dimension Position Sensitive Avalanche Counter). In this paper, both OCTPSACs will be introduced. Based on the requirements of the LAIC, the OCTPSACs consist of eight position sensitive PPACs. Each PPAC has an anode and a cathode. In both cases, the sizes are same. But different type of cathodes are used. In one type of OCTPSAC, its cathode is made of wire plane. It consists of gold-plated tungsten wires with the diameter of 20μm, spaced 0.5 mm apart from each other. The anode is a mylar foil which was evaporated by gold layer with the thickness of 50μg/cm~2 mounted on a printed plate in the shape of rectangle. the thickness of mylar foil is 1.5μm. The gap between anode and cathode is 3mm. The performance of the OCTPSAC has been tested by using a ~(252)Cf source in flowing isobutylene gas at the pressure of 3.4mb. The intrinsic time resolution of 289ps and position resolution of 2 mm have been obtained. In another type of OCTPSAC, the cathode is made of mylar foil, which is composed of gold strip by vacuume evaporation method with a special mask on the mylar foil. The thickness and the width of the gold strip is 50μg/cm~2 and 1.7mm. The strips are spaced 0.3 mm apart from each other. The anode is the same as the former type. We have obtained the time resolution of 296ps and position resolution of 2mm by using ~(241)Am-a source when the gas pressure is 6 mb and high voltage is 600V. The working gas is heptane

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论文的结构分为空间望远镜系统的设计和硅(锂)探测器研制两个部分。第一部分主要介绍了空间望远镜系统的设计,该空间望远镜系统能鉴别Z≤26、M≤56范围内的空间带电粒子,该系统的设计在国内是首例,它将使我国空间高能带电粒子的鉴别和测量上一个新的台阶;第二个部分主要介绍适合于探测空间粒子的硅(锂)探测器的研制及其性能的测试过程。该探测器的研制成功为空间高能带电粒子的探测提供了必要的准备。 我们已经提供给空间科学与应用研究中心二十多块硅(锂)探测器。我们用ThC'-C源和137Cs源对硅(锂)探测器进行了测试,我们在120V时便可得到137Cs电子谱;我们在250V常温常压得到α粒子谱,其能量分辨可好于37Kev,长期加压测试时硅(锂)探测器的反向电流变化稳定,在持续20天加压250V时,其中直径为12mm的硅(锂)探测器的电流变化可达1.10±0.50微安,信噪比可达420倍。

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LiCaBO3 was synthesized by high-temperature solid-state reaction. The influence of different rare earth dopants, i.e. Dy3+, Tb3+. TM3+ and Ce3+, on thermoluminescence (TL) of LiCaBO3 phosphor was discussed. We studied the TL properties and some dosimetric characteristics of Ce3+-activated LiCaBO3 phosphor in detail. The effect of the concentration of Ce3+ on TL was investigated, the result of which showed that the optimum Ce3+ concentration was 1 mol%. The TL kinetic parameters of LiCaBO3:0.01 Ce3+ were studied by computer glow curve deconvolution (CGCD) method.

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Amphiphilic biodegradable star-shaped polymer was conveniently prepared by the Sn(Oct)(2)-catalyzed ring opening polymerization of c-caprolactone (CL) with hyperbranched poly(ester amide) (PEA) as a macroinitiator. Various monomer/initiator ratios were employed to vary the length of the PCL arms. H-1 NMR and FTIR characterizations showed the successful synthesis of star polymer with high initiation efficiency. SEC analysis using triple detectors, RI, light scattering, and viscosity confirmed the controlled manner of polymerization and the star architecture.

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The thermoluminescence (TL) properties of Ce3+ doped NaSr4(BO3)(3) phosphor under the beta-ray irradiation were reported. The polycrystalline sample was synthesized by high temperature solid-state reaction. The TL glow curve of NaSr4(BO3)(3):Ce3+ phosphor was composed of only one peak. TL kinetic parameters of NaSr4(BO3)(3):Ce3+ were deduced by the peak shape method, the activation energy (E) was 0.590 eV and the frequency factor was 1.008x10(6) s(-1). TL dose response was linear in the range of measurement. The 3-dimensional (3D) TL emission spectrum was also recorded, the emission spectrum consisted of two bands located at 441 and 479 nm respectively, corresponding to the characteristic 4f(0)5d(1)-> F-2((5/2,7/2)) transitions of the Ce3+ ion. The fading behavior of the NaSr4(BO3)(3):Ce3+ phosphor over a period of 15 d was also studied.

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A new straightforward strategy for synthesis of novel hyperbranched poly (ether amide)s from readily available monomers has been developed. By optimizing the reaction conditions, the AB(2)-type monomers were formed dominantly during the initial reaction stage. Without any purification, the AB(2) intermediate was subjected to further polymerization in the presence (or absence) of an initiator, to prepare the hyperbranched polymer-bearing multihydroxyl end-groups. The influence of monomer, initiator, and solvent on polymerization and the molecular weight (MW) of the resultant polymers was studied thoroughly. The MALDI-TOF MS of the polymers indicated that the polymerization proceeded in the proposed way. Analyses of H-1 NMR and C-13 NMR spectra revealed the branched structures of the polymers obtained. These polymers exhibit high-moderate MWs and broad MW distributions determined by gel permeation chromatography (GPC) in combination with triple detectors, including refractive index, light scattering, and viscosity detectors. In addition, the examination of the solution behavior of these polymers showed that the values of intrinsic viscosity [eta] and the Mark-Houwink exponent a were remarkably lower compared with their linear analogs, because of their branched nature.

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A novel Prussian blue chemically modified electrode (CME) was constructed and characterized for liquid chromatography electrochemical detection (LCEC) of catecholamines. Both anodic and cathodic peaks could be obtained by monitoring at constant applied potential at anodic and slightly cathodic potential ranges (0.3-0.7 and -0.2-0.1 V vs. SCE), respectively. When arranged in a series configuration, using the modified electrodes as generating and collecting detectors, extremely high effective collection efficiencies of 0.91 (for norepinephrine) and 0.58 (for dihydroxyphenylacetic acid) were achieved in dual-electrode LCEC for catecholamines; and a linear response range over 3 orders of magnitude and a detection limit of 10 pg were obtained with a downstream CME as the indicating detector.

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The use of chemically modified electrodes (CMEs) for liquid chromatography and flow-injection analysis is reviewed. Electrochemical detection with CMEs based on electrocatalysis, permselectivity, ion flow in redox films, and ion transfer across the water-solidified nitrobenzene interface is discussed in terms of improving the stability, selectivity, and scope of electrochemical detectors, and the detection of electroinactive substances. More than 90 references are included.

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利用激光诱导击穿光谱定量分析了铝合金中多种元素的成分。采用Nd∶YAG脉冲激光器,在空气环境下烧蚀铝合金固体样品获得等离子体。利用多通道光栅光谱仪和CCD检测器对200~980nm波长范围的光谱进行同时检测。研究了检测时延、激光脉冲能量、元素深度分布对光谱强度的影响,考虑这些因素之后对实验参数进行了优化。在优化的实验参数下对国家标准铝合金样品中的八种元素Si,Fe,Cu,Mn,Mg,Zn,Sn及Ni进行了定标,并利用定标曲线对一种铝合金样品进行了定量分析。实验结果表明,测量结果的相对标准偏差(RSD)最大为5.89%,相对误差在-20.99%~15%范围内,说明对铝合金样品成分进行定量分析,激光诱导击穿光谱是一种有效的光谱分析工具,但是分析结果的准确度仍需要提高。

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角点检测应用十分广泛,是许多计算机视觉任务的基础。本文提出了一种快速、高精度的角点检测算法,算法简单新颖,角点条件和角点响应函数设计独特。和以往不同的是:算法在设计上考虑的是角点的局部几何特征,使得处理的数据量大为减少,同时能够很好地保证检测精度等其他性能指标。通过和广泛使用的SUSAN算法、Harris算法在正确率、漏检、精度、抗噪声、计算复杂度等方面进行综合比较,结果表明该算法无论对人工合成图像还是对自然图像均具有良好的性能。

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传统的火灾检测方法一般采用感烟、感温、感光探测器等进行探测。本文提出了一种嵌入式基于图像视觉特征的火灾检测方法,以TI公司的数字多媒体处理器TMS320DM642为核心,设计实现智能前端火灾探测与自动报警系统。通过DM642对视频图像进行采集并结合相应的智能图像处理与模式识别算法,对森林火险进行实时监控。实验结果表明,该系统比传统系统更进一步减少了误报率且具有响应快、监控范围广等优点。

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After revising Russell Motives for Smoking Questionnaire(RMSQ,1974), 317 smoking students and 270 non-smoking students in Beijing are studied. Factor analysis on RMSQ showed that there are four factors: Indulgent, Stimulant/Sedative, Addictive and Social, which cause students to smoke. All the four motives are positively correlated to Psychoticism, and excluding Stimulant /Sedative, the other motives have a negative correlation with the scores on the EPQ Lie sclae. The revised RMSQ has a high reliability and validity in China.