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Design of a secondary ionization target for direct production of a C− beam from CO2 pulses for online AMS

机译:用于直接生产C-光束的二级电离靶标的CO2脉冲在线AMS

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摘要

We designed and optimized a novel device “target” that directs a CO2 gas pulse onto a Ti surface where a Cs+ beam generates C from the CO2. This secondary ionization target enables an accelerator mass spectrometer to ionize pulses of CO2 in the negative mode to measure 14C/12C isotopic ratios in real time. The design of the targets were based on computational flow dynamics, ionization mechanism and empirical optimization. As part of the ionization mechanism, the adsorption of CO2 on the Ti surface was fitted with the Jovanovic–Freundlich isotherm model using empirical and simulation data. The inferred adsorption constants were in good agreement with other works. The empirical optimization showed that amount of injected carbon and the flow speed of the helium carrier gas improve the ionization efficiency and the amount of 12C produced until reaching a saturation point. Linear dynamic range between 150 and 1000 ng of C and optimum carrier gas flow speed of around 0.1 mL/min were shown. It was also shown that the ionization depends on the area of the Ti surface and Cs+ beam cross-section. A range of ionization efficiency of 1–2.5% was obtained by optimizing the described parameters.
机译:我们设计并优化了一种新型设备“目标”,该设备将CO2气体脉冲引导到Ti表面上,在该表面上Cs + 束从CO2生成C -。该次级电离目标使加速器质谱仪能够以负模式电离CO2脉冲,从而实时测量 14 C / 12 C同位素比。目标的设计基于计算动力学,电离机理和经验优化。作为电离机理的一部分,使用经验数据和模拟数据将Jovanovic–Freundlich等温线模型拟合到Ti表面上CO2的吸附。推断的吸附常数与其他工作吻合良好。实验优化表明,注入的碳量和氦载气的流速提高了电离效率,产生的 12 C -量达到饱和点。显示了150到1000 ng C之间的线性动态范围,最佳载气流速约为0.1 mL / min。还表明,电离取决于Ti表面的面积和Cs + 束的横截面。通过优化所描述的参数可获得1-2.5%的电离效率范围。

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