Search For Dynamical Resonance In Chemical Reaction

寻找化学反应中的动态共振

• 批准号: 05453025
• 负责人: SUZUKI Toshinori
• 金额: $ 4.54万
• 依托单位: Okazaki National Research Institutes
• 依托单位国家: 日本
• 项目类别: Grant-in-Aid for General Scientific Research (B)
• 财政年份: 1993
• 资助国家: 日本
• 起止时间: 1993 至 1994
• 项目状态: 已结题
• 来源: https://kaken.nii.ac.jp/en/grant/KAKENHI-PROJECT-05453025/
• 关键词: Photodissociation; Imaging; Reactive Scattering; Laser; Resonance Enhanced Multiphoton Ionization; Dynamical Resonance; Computer Tomography; 化学反応; 共鳴; レーザー分光; 量子力学; 画像観測法; エテレン

Two-dimensional ion imaging apparatus has been newly constructed, and its performance has been examined by photodissociation experiments. The spatial resolution of the apparatus was found to be better than hundreds of microns, which provides us the speed resolution of about 10% and the angular resolution of about 5 degree. Photodissociation dynamics of NO_<2, >, N_<2, >O,OCS,Chlorethylenes, Vinylbromide, and acetylene has been investigated in detail. The experimental and theoretical methods have been further developed to investigate polarization of angular momentum in molecular and atomic products. The method will be eventually used to measure multiply differential cross section in inelastic and reactive scattering. The pulsed hydrogen atomic beam has been generated by the photodissociation of H_2S and HI.The duration of this hydrogen beam has been found to be 35 ns. The hydrogen beam was crossed with target beam of (D_2, Ar etc.), but the observation of scattered hydrogen atoms was interfered by background hydrogen signal coming from residual gas in the chamber. The chamber was baked and also liquid nitrogen trap was added to pump down to 10^<-8> Torr, but higher vacuum seems necessary. The modification of the vacuum system is still in progress. Although the ultimate goal of the research project has not been achieved at this point, the present research has established the new theoretical and experimental method to observe dynamical resonance in chemical reaction.

二维离子成像设备已被新构建，并且通过光解离实验检查了其性能。发现该设备的空间分辨率比数百微米要好，这为我们提供了约10％的速度分辨率，角度分辨率约为5度。已经详细研究了NO_ <2，>，>，N_ <2，> O，OC，氯乙烯，乙烯基溴和乙炔的光解离动力学。实验和理论方法已进一步开发，以研究分子和原子产物中角动量的极化。该方法最终将用于测量非弹性和反应性散射中的多重差分横截面。脉冲氢原子束是通过H_2S和HI的光解离并产生的。该氢束的持续时间已被发现为35 ns。将氢束与靶束（D_2，AR等）交叉，但是散射氢原子的观察受到来自腔室中残留气体的背景氢信号的干扰。腔室也被烘烤，并加入液态氮气陷阱以泵送至10^<-8>托尔，但似乎需要更高的真空。真空系统的修改仍在进行中。尽管目前尚未实现该研究项目的最终目标，但目前的研究已经建立了新的理论和实验方法，以观察化学反应中的动力共振。

项目成果

Toshinori Suzuki, Kenichi Tonokura, Lizla.S.Bontuyan, and N.Hashimoto: "Photodissociation of trans-Dichloreoethylene : State-Resolved Speed and Distributions of Cl Atoms Angular" Phys.Chem.98. 13447-13451 (1994)

Toshinori Suzuki、Kenichi Tonokura、Lizla.S.Bontuyan 和 N.Hashimoto：“反式二氯乙烯的光解离：Cl 原子角度的状态分辨速度和分布”Phys.Chem.98。

Simon North, Trevor J.Sears, Gregory E.Hall, and Toshinori Suzuki: "Comment on "Energy Paritioning in Photodissociation of Methyl, Ethyl, and n-Propyl Iodides at 304 nm"" Chem.Phys.(submitted).

Simon North、Trevor J.Sears、Gregory E.Hall 和 Toshinori Suzuki：“对“甲基、乙基和正丙基碘化物在 304 nm 光解离中的能量分配”的评论”“Chem.Phys.（已提交）。

Nobihisa Hashimoto and Toshinori Suzuki: "Energy and State Dependence in Quenching and Predissociation of C_2H_2" J.Chem.Phys.(submitted).

Nobihisa Hashimoto 和 Toshinori Suzuki：“C_2H_2 淬灭和预解离中的能量和状态依赖性”J.Chem.Phys.（已提交）。

N.Hshimoto and T.Suzuki: "Energy and State Dependence in the Quenching and Predissociarion of C2H2" The Journal of Chemical Physics. (submitted).

N.Hshimoto 和 T.Suzuki：“C2H2 淬灭和预解离中的能量和状态依赖性”化学物理杂志。

Kenichi Tonokura and Toshinori Suzuki: "Slicing Photofragment Spatial Distribution by Laser Sheet Ionization" Chem.Phys.Lett.224. 1-6 (1994)

Kenichi Tonokura 和 Toshinori Suzuki：“通过激光片电离切割照片片段空间分布”Chem.Phys.Lett.224。