The ν4 and ν2 + ν5 high resolution infrared bands of FClO3 and FClO3

The high resolution infrared spectra of monoisotopic F³⁵Cl¹⁸O₃ and F³⁷Cl¹⁸O₃ have been studied in the region of the ν₄ fundamentals, centered at 1278.3 and 1263.3 cm⁻¹, respectively. Large perturbations are observed in both bands due to a Fermi type anharmonic resonance with the ν₂ + ν₅ combination bands, centered at 1270.7 cm⁻¹ in F³⁵Cl¹⁸O₃ and 1257.3 cm⁻¹ in F³⁷Cl¹⁸O₃. In particular, they affect the kl > 0 levels of the v₄ = 1 and v₂ = v₅ = 1 states which cross at kl ? 18 in F³⁵Cl¹⁸O₃ and kl ? 3 in F³⁷Cl¹⁸O₃, due to the opposite values of and . The Δl = Δk = ±2 and Δl = 0, Δk = ±3 essential resonances are also effective in the excited states of the dyad in F³⁵Cl¹⁸O₃, while in F³⁷Cl¹⁸O₃ only the Δl = Δk = ±2 one is active. In the spectrum of F³⁵Cl¹⁸O₃ 3423 transitions have been assigned, 10% of them belonging to ν₂ + ν₅. The rovibrational parameters and the interaction constants between the v₄ = 1 and v₂ = v₅ = 1 levels have been obtained. The depertubed band origins of ν₄ and ν₂ + ν₅ are 1277.310567(165) and 1271.753733(195) cm⁻¹, respectively, and the anharmonic resonance constant is 2.804416(153) cm⁻¹. For F³⁷Cl¹⁸O₃, 3022 transitions have been assigned, 38% belonging to the ν₂ + ν₅ combination band. The depertubed band origins are 1260.856338(123) and 1259.872338(134) cm⁻¹, for ν₄and ν₂ + ν₅ and the constant is 2.9350669(405) cm⁻¹. The equilibrium geometry of perchloryl fluoride, r_e (ClO) = 139.7(3) pm, r_e (ClF) = 161.0(5) pm, and α_e (OClO) = 115.7(4) degree, has been determined using the A_e and B_e equilibrium constants of the four symmetric isotopologues of perchloryl fluoride, F^35/37Cl¹⁶O₃ and F^35/37Cl¹⁸O₃.     

Comparative study between dispersive and non-dispersive dielectric permittivity in spectral remittances of chiral sculptured zirconia thin films

The transmission and reflection spectra from a right-handed chiral sculptured zirconia thin film are calculated using the piecewise homogeneity approximation method and the Bruggeman homogenization formalism using both dispersive and non-dispersive functions for axial and non-axial states. The comparison of spectral results shows that the dispersion of the dielectric function has a considerable effect on the results. In axial excitation of cross-polarized reflectances and co-polarized transmittances the dispersion effect becomes more pronounced at wavelengths further away from the homogenization wavelength. This is also true in the case of non-axial excitation of circular transmittances, while there are considerable differences for cross-polarized reflectances where (wavelength) the first Bragg peak occurs. At wavelengths in the vicinity of the homogenization wavelength the dispersion effect of the dielectric function in R_RR becomes more significant.     

From kaonic atoms to kaonic nuclei: A search for antikaon-mediated bound nuclear systems

Strong interaction processes were intensively studied at low energy with exotic atoms, touching one of the fundamental problems in hadron physic today — the still unsolved question of how hadron masses are generated. The question of the origin of the large hadron masses made up of light quarks, the current mass of the up (u) and down (d) quarks (m_u,d≈5 MeV) is two orders of magnitude smaller than a typical hadron mass of about 1 GeV, will be discussed in the context with the experimental work done in the field of exotic atoms expanded to exotic nuclei.An overview of the properties of exotic hydrogen atoms made of pions and kaons are presented, using high precision experiments unrevealing the nature of strong interaction physics at low energy. A new field which contributes to the understanding of the origin of the large hadron mass is the study of the mass modification in a nuclear medium. Antikaon mediated bound nuclear systems would be an ideal tool, if they exist, to look for chiral restoration at high density and zero temperature or even more exotic to look for phase transitions.     

A comparison of spatial discretization schemes for differential solution methods of the radiative transfer equation

A comparison of discretization schemes required to evaluate the radiation intensity at the cell faces of a control volume in differential solution methods of the radiative transfer equation is presented. Several schemes developed using the normalized variable diagram and the total variation diminishing formalisms are compared along with essentially non-oscillatory schemes and genuinely multidimensional schemes. The calculations were carried out using the discrete ordinates method, but the analysis is equally valid for the finite-volume method. It is shown that the S schemes of the genuinely multidimensional family perform quite well, particularly in problems with discontinuous radiation intensity fields. However, they are time consuming, and so they do not always become more attractive regarding the trade-off between accuracy and computational requirements, in comparison with other high-order schemes that, although being less accurate, are also more economical.     

提高布里渊光时域反射应变仪测量空间分辨力的等效脉冲光拟合法

由于探测光脉冲宽度受到限制,布里渊光时域反射仪(BOTDR)在对光纤上的应变进行分布式测量时,空间分辨力只能达到1 m。针对布里渊光时域反射仪单次采样接收背向布里渊散射信号(BBS)需要一定的时间,提出了基于等效脉冲光的多洛仑兹拟合法以提高其应变测量的空间分辨力。该方法将探测光脉冲在布里渊光时域反射仪完成单次采样所需的时间上进行积分,将积分函数作为等效脉冲光的表达式,再根据等效脉冲光的形状将布里渊光时域反射仪接收到的背向布里渊散射谱(BBS)细分,并对它进行多洛仑兹迭代拟合,准确求得每个细分布里渊散射谱的中心频率,进而利用光纤中布里渊频移与应变的对应关系,得到光纤中与细分布里渊散射谱对应的细分光纤单元上的应变情况。实验结果表明,利用这种方法,可使布里渊光时域反射仪应变测量的空间分辨力提高至0.05 m。     

分辨率对大气中痕量污染气体的DOAS测量性能影响研究

在差分吸收光谱(DOAS)测量过程中,光谱分辨率的选择直接决定了污染气体浓度的测量准确度.主要研究了光谱分辨率对污染气体被榆测到的特征吸收结构形状的影响,以及差分吸收截面随分辨率的变化趋势,从而确定了光谱分辨率对污染气体最低可检测浓度的影响,通过研究分辨率与光强的关系,确定了分辨率与信噪比(S/N)的函数关系式,得出了DOAS测量NO2,O3,和SO2的最佳信噪比范围,对多种污染物标准气体进行了同时监测,计算出标准气体在不同光谱分辨率下的测量误差,确定了对NO2,O3和SO2监测的最适用的分辨率范围.在此分辨率范围既能够实现对痕量气体的准确定性定量测量,又能达到测量所需要的高灵敏度,强选择性和适用的时间分辨率.通过在北京丰台区的实际监测得到了与点式仪器测量结果很好的一致性.     

尺度缩小合成孔径激光成像雷达的孔径合成实验

设计了一种尺度缩小的合成孔径激光成像雷达(SAIL),在实验室平台上模拟实施远场传输条件,相应地解决了波前测量和外差质量监视技术,实现了一个目标点的方位向孔径合成实验,实验结果与理论预测相近.     

基于菲涅耳透镜阵列的红外气体传感器

菲涅耳透镜同时具有分光与会聚特性, 且体积小、重量轻和易复制, 使其在光谱检测中得到逐步应用, 但典型光谱成像仪采用菲涅耳透镜沿光轴扫描的方法来获得连续谱线, 不利于光谱仪的稳定性。考虑到气体探测需求, 选用多通道方式来获得多光谱, 提出了一种基于菲涅耳透镜阵列的新型红外气体传感器, 可实现吸收波长在3～5 μm的CO2,CO,CH4,SO2气体的实时检测。利用球面波的传输理论和瑞利判据, 推导了菲涅耳透镜光谱分辨率与透镜结构参数之间的函数关系, 并以光谱分辨率小于50nm为性能指标, 对1μm工艺的8台阶菲涅耳透镜阵列的结构参数进行了计算和误差分析。结果表明, 透镜阵列所需焦距为47.84 mm, 平均数值孔径大于0.4。     

On the nature of the and from their behavior in chiral dynamics

We study the behavior with the number of colors (N_c) of the Λ(1405) and Λ(1670) resonances obtained dynamically within the chiral unitary approach. The leading order meson–baryon interaction, used as the kernel of the unitarization procedure, manifests a nontrivial N_c dependence of the flavor SU(3) representation for baryons. As a consequence, the SU(3) singlet (or ) component of the Λ(1405) states remains bound in the large N_c limit, while the other components dissolve into the continuum. Introducing explicit SU(3) breaking, we obtain the N_c dependence of the excitation energy, masses and widths of the physical Λ(1405) and Λ(1670) resonances. The N_c behavior of the decay widths is found to be different from the general counting rule for a qqq state, indicating the dynamical origin of these resonances.