Research on a deconvolution algorithm for laser-induced fluorescence diagnosis based on the maximum entropy principle

Laser-induced fluorescence(LIF)spectroscopy is employed for plasma diagnosis,necessitating the utilization of deconvolution algorithms to isolate the Doppler effect from the raw spectral signal.However,direct deconvolution becomes invalid in the presence of noise as it leads to infinite amplification of high-frequency noise components.To address this issue,we propose a deconvolution algorithm based on the maximum entropy principle.We validate the effectiveness of the proposed algorithm by utilizing simulated LIF spectra at various noise levels(signal-to-noise ratio,SNR=20–80 d B)and measured LIF spectra with Xe as the working fluid.In the typical measured spectrum(SNR=26.23 d B)experiment,compared with the Gaussian filter and the Richardson–Lucy(R-L)algorithm,the proposed algorithm demonstrates an increase in SNR of 1.39 d B and 4.66 d B,respectively,along with a reduction in the root-meansquare error(RMSE)of 35%and 64%,respectively.Additionally,there is a decrease in the spectral angle(SA)of 0.05 and 0.11,respectively.In the high-quality spectrum(SNR=43.96 d B)experiment,the results show that the running time of the proposed algorithm is reduced by about98%compared with the R-L iterative algorithm.Moreover,the maximum entropy algorithm avoids parameter optimization settings and is more suitable for automatic implementation.In conclusion,the proposed algorithm can accurately resolve Doppler spectrum details while effectively suppressing noise,thus highlighting its advantage in LIF spectral deconvolution applications.

FLUORESCENCE SPECTRUM ANALYSIS OF ETHER-WATER SOLUTION BASED ON GAUSSIAN DECOMPOSITION METHOD

The fluorescence spectrum of the ether-water solution excited by the ultraviolet light with the wavelength of 245 nm is experimentally detected. Based on the second derivative analysis, the fluorescence spectrum of the ether-water solution is used as Gaussian decomposition and seven Gaussian spectral lines are obtained. The center wavelength, the peak intensity and the half peak bandwidth of each Gaussian spectral line are measured, and the multi-peak fitting is made by using Gaussian primitive parameters. The highest and the lowest oscillation energy level differences in the ground state of each Gaussian spectrum are calculated. It is found that there are seven types of luminescent association molecules formed by ether and water molecules in different configurations existed in the solution. The location of each optimum absorption wavelength and the half peak bandwidth of the Gaussian spectral line is different. The energy level difference with the central wavelength of 304 nm attains the maximum value The result can contribute to the study of the molecular association in ether-water solution.

Detecting H2S Gas Concentration by 1,8-Naphthalimides Fluorescent Probe

针对传统硫化氢检测方法灵敏度低的问题,以1,8-萘酰亚胺为荧光基团,基于H_2S的还原性,通过在荧光分子结构上引入具有氧化性的硝基,合成一种可与硫化氢气体发生氧化还原反应生成有荧光响应的小分子荧光探针。该探针本身荧光十分微弱,且荧光峰值在λ=467nm和λ=522nm处。与H_2S反应之后,522nm处的荧光效应消失,467nm处的荧光效应显著增强。测定小分子荧光探针在通入H_2S气体前后的荧光光谱,分析467nm处的荧光强度与气体浓度关系。结果表明:荧光光谱法检测出的H_2S气体浓度与荧光强度之间存在很强的线性关系,相关系数为0.979 3,最低可检测极限可达0.88×10^(-6 )mol·L^(-1)量级。表明基于1,8-萘酰亚胺衍生物的荧光光谱检测法可为油气田H_2S气体浓度的的快速测定提供参考。

Spectrum Correction in Study of Solvation Dynamics by Fluorescence Non-collinear Optical Parametric Amplification Spectroscopy

Femtosecond time-resolved fluorescence non-collinear optical parametric amplification spec- troscopy can extract the curve of spectral gain from its parametric superfluorescence. This unique spectrum correction method enables fluorescence non-collinear optical parametric amplification spectroscopy acquiring the genuine transient fluorescence spectrum of the studied system. In this work we employ fluorescence non-collinear optical parametric amplification spectroscopy technique to study the solvation dynamics of DCM dye in ethanol solution, and confirm that genuine solvation correlation function and shift of peak frequency can be derived from transient fluorescence spectra after the spectral gain correction. It demonstrates that fluorescence non-collinear optical parametric amplification spectroscopy can benefit the research fields, which focuses on both fluorescence intensity dynamics and fluorescence spectral shape evolution.

Hydrothermal Synthesis,Crystal Structure and Fluorescence Spectrum Studies of a Supramolecular Compound {[2-(2-Pyridyl)benzimidazoleH_2]^(2+)·[SbCl_5]^(2-)}_2

A new supramolecular compound, { [2-（2-pyridyl）benzimidazoleH2]2＋.[SBC15]2-}2, was synthesized by the hydrothermal reaction of o-diaminobenzene, 2-pyridinecarboxylie acid and SbCl3 in 1：1 HC1 solution, and characterized by chemical analysis, elemental analysis, IR spectra, thermogravimetfic analysis and fluorescence spectra. The crystal structure was deter- mined by X-ray single-crystal diffraction. The crystal belongs to the monoclinic system, space group P211c, with a = 16.0397（13）, b = 14.3189（12）, c = 15.6370（13） A, β = 105.8980（10）°, V = 3454.0（5） A3, Z = 4, C24H22Cl10N6Sb2, Mr = 992.48, Dc = 1.909 g/cm3,/z = 2.366 mm-1, S = 1.010, F（000） = 1920, R = 0.0254 and wR = 0.0555. The coordination anion, [SbCl5]2- which is a distorted tetragonal pyramid, is composed by coordinating action with Sb3＋ ion and five adjacent chloride ions. Every four coordination anions of [SbCl5]2- form a biquaternion ring structure through the secondary bonding of Sb...Cl. Moreover, the compound adopts a three-dimensional network supramolecular structure because of the hydrogen bonds and π-π stacking between the rings and the 2-（2-pyridyl）benzimidazole divalent cations. The title compound also shows good fluorescent behaviors.

Chemical Modification and Fluorescence Spectrum of Tryptophan Residues in Pullulanase

Tryptophan（Trp） residues in a pullulanase were modified by N-bromosuccinimide（NBS）. The results of the Spande method indicate that there are 18 Trp residues in the pullulanase and nine of them are located on the surface af the enzyme. Three of these Trp residues are nonessential residues which show the fastest reaction rate according to the Zou＇s plot. Two of the seven relative faster reacting residues are essential for the activity of the enzyme. The other eight are the slowest in the reaction rate or non-reactive residues for the reaction. The fluorescence and circular dichroism（CD） spectra of the pullulanase have been changed after the reaction with NBS. Potassium iodide（KI） and acrylamide also have remarkable influences on the fluorescence spectra of the pullulanase.

Synthesis and Characteristic Study on Complexes of Europium(Ⅲ) and Maleic Acid Doped with Non-Fluorescent Ions

Complex of europium （Ⅲ） with maleic acid, and binuclear complexes of europium（Ⅲ）with maleic acid doped with non-fluorescent ions gadolinium, lanthanum and yttrium, were synthesized. The compositions and structures of complexes were characterized with elemental analysis, single crystal X-ray diffraction, IR and DSC-TG. Fluorescent properties were studied with fluorescence spectrum. The results indicated that the strongest fluorescent complexes were obtained when the ratio of europium and non-fluorescent ion was 8：2. The order of Eu^3＋ fluorescence strengthened by three doped rare earths was Gd^3＋ 〉La^3＋ 〉Y^3＋

Fluorescence spectrum characteristic of ethanol-water excimer and mechanism of resonance energy transfer

The steady-state fluorescence spectrum characteristic of ethanol-water excimer has been studied in this paper. By analysing the features of the sharp emission spectrum with fine structures in a shortwave band and the characteristics of the broad and featureless fluorescence peaks in the longwave band, one can conclude that the excimers are formed between the new ethanol-water cluster molecules in the excited state and the ground state through the interaction among different chromophores. The excitation spectra in the two fluorescence bands have been studied, and their emission mechanisms have been ascertained based on the energy transfer theory. Furthermore, the critical distance of the resonance energy transfer has been calculated.

Highly sensitive detection of Rydberg atoms with fluorescence loss spectrum in cold atoms

Fluorescence loss spectrum for detecting cold Rydberg atoms with high sensitivity has been obtained based on lock-in detection of fluorescence of 6 P3/2 state when cooling lasers of the magneto-optical trap are modulated.The experiment results show that the signal to noise ratio has been improved by 32.64 dB when the modulation depth(converted to laser frequency)and frequency are optimized to 4 MHz and 6 kHz,respectively.This technique enables us to perform a highly sensitive non-destructive detection of Rydberg atoms.

Preliminary investigations on Arctic microalgae by jointapplication of fluorescent instruments

In vivo fluorescence has a wide application in analyzing microalgae, including assessing phytoplankton biomass, rates of primary production and physiological status. This study describes a preliminary investigation on the joint application of the three kinds of fluorescence analysis in the physiological study of microalgae. Flow cytometry and fluorescence spectrometry were used to obtain the in vivo static fluorescence information of pigments, and a Pulsed-Amplitude-Modulation chlorophyll fluorometer was used to detect the dynamic fluorescence of chlorophyll. The validity of the joint application was proved by analyzing two labora- tory cultured Arctic microalgae, Pseudo-nitzschia delicatissima （Bacillariophyceae） and Thalassiosira sp. The higher value of minimum fluorescence yield in dark-adapted state （Fo）, actual photochemical efficiency of PSll （ФPSII）, and electron transport rate （ETR） exhibited positive results in a higher cell abundance and chlorophyll a content of P. delicatissima; whereas higher fl-carotene content of Thalassiosira sp. played an important role in the protection of photosynthesis.

Quantitative energy-dispersive X-ray fluorescence analysis for unknown samples using full-spectrum least-squares regression

The full-spectrum least-squares(FSLS) method is introduced to perform quantitative energy-dispersive X-ray fluorescence analysis for unknown solid samples.Based on the conventional least-squares principle, this spectrum evaluation method is able to obtain the background-corrected and interference-free net peaks, which is significant for quantization analyses. A variety of analytical parameters and functions to describe the features of the fluorescence spectra of pure elements are used and established, such as the mass absorption coefficient, the Gi factor, and fundamental fluorescence formulas. The FSLS iterative program was compiled in the C language. The content of each component should reach the convergence criterion at the end of the calculations. After a basic theory analysis and experimental preparation, 13 national standard soil samples were detected using a spectrometer to test the feasibility of using the algorithm. The results show that the calculated contents of Ti, Fe, Ni, Cu, and Zn have the same changing tendency as the corresponding standard content in the 13 reference samples. Accuracies of 0.35% and 14.03% are obtained, respectively, for Fe and Ti, whose standard concentrations are 8.82% and 0.578%, respectively. However, the calculated results of trace elements (only tens of lg/g) deviate from the standard values. This may be because of measurement accuracy and mutual effects between the elements.

Chemical Modification of Tryptophan Residues in Superoxide Dismutase from Camellia Pollen and Its Fluorescence Spectrum

The amino acid composition of the superoxide dismutase（SOD） from camellia pollen was measured and the tryptophan（Trp） residues were modified by using N-bromosuccinimide（NBS）. The results show that there are 21 Trp residues in an SOD molecule and seven of which are located on the surface of the enzyme. By researching the fluorescence spectra of the native SOD and the modified SOD, we have found that the emission wavelength of Trp is at 335 nm and the fluorescence intensity will decrease when the enzyme is modified. The results also show that potassium iodide（KI） can significantly quench the fluorescence of the native SOD, but it has a less pronounced effect on the modified enzyme. Glycerin as a surface activation reagent can stabilize the fluorescence of the modified enzyme.

Tryptophan Modification and Fluorescence Spectrum of Hyaluronidase

Tryptophan residues in hyaluronidase （HAase） were modified by N-bromosuccinimide （NBS）, the results indicated that there were eleven tryptophan residues in HAase, one of which was exposed and essential for the activity of the enzyme. The study on fluorescence quenching showed that KI could not quench all of the fluorescence from Trp residues in HAase, while acrylamide （Acr） could quench almost all of the fluorescence from Trp residues in HAase. The collisional quenching constants （KD） of HAase at different concentrations of Acr were calculated in terms of Stern-Volmer equation. The results implied that some of the Trp residues were buried in the interior of HAase and the Trp residue on the surface of HAase was not located in the hydrophobic pocket.

Laser-induced Fluorescence Excitation Spectrum of NiS in 15500-17200 cm^-1

The laser-induced fluorescence excitation spectrum of jet-cooled NiS molecule has been recorded in the energy range of 15500 17200 cm-1. Fifteen bands have been assigned as three transition progressions：[15.65]^3Ⅱ1（v′=0-4）-X^3∑0^-（v″=0）,[15.69]^3∑0^-（v′=0-4）-X^3∑0^-（v″=0）,and [15.81]^3Ⅱ1（v′=0-4）-X^3∑0^-（v″=0）.Spectroscopic constants for the three newly identified electronically excited states have been determined for the first time. In addition,the lifetimes for most observed vibronic bands have also been measured.

3-D Fiber Optic Fluorescent Detection System for Mineral Oilin Water

Parameter quantification principle of three-dimensional(3-D) fluorescent spe ctrum and its realization technique are studied. The portab le fiber-optic fluorescent measurer for mineral oil is given. Thr ee parameters of the exciting light wavelength, the wavelength and the intensity of the fluorescent light excited by the measured oil are expressed with 3-D co ordinates and are processed so as to be sampled again and to be curve fitted.

Study on the Regulation of Diorganogermanium Compounds on the Maillard Reaction of Histidine and Glycine by Fluorescence Spectrum

The suppression of diorganogermanium compounds on the Maillard reaction of histidine(His) and glycine (Gly) with glucose has been determined by fluorescence spectrum underphysiological conditions. The title compounds show inhibition for the fluorescence intensity (FI) ofglycosylated andno acids stronger than Ge-132.

海面乳化溢油水包油乳化液的LIF接收光功率饱和强度分析

海面溢油的水包油乳化液对海洋造成严重的危害,水包油乳化液的识别以及定量分析,对于海洋污染的处理以及海洋环境的恢复具有重要意义。近年来一些研究对较薄的乳化溢油进行了定量分析,然而对于油层较厚的乳化溢油却鲜有深入的研究。激光照射到海面的水包油乳化液产生的荧光,在一定条件下会开始出现饱和而不再变化,针对这一饱和临界点以及相关范围的水包油乳化液的光谱特征进行研究。根据LIF探测系统接收到的光功率与BRRDF数值的关系,使用BRRDF模型对荧光光谱进行仿真。分析的油品使用Romashkino油和Petrobaltic油,分别代表深色不透明的油和明亮透明的油。提出一种针对厚度较大的水包油乳化液的荧光强度计算方法,计算出两种油在不同浓度和乳化时间下的乳化液出现荧光饱和的厚度。对计算结果进行比较可以看出饱和厚度随着浓度的增加而降低,随着乳化时间的增加而降低。分析结果显示,对于海水中的深色不透明的油的水包油乳化液,LIF接收到的荧光强度通常会出现饱和,因此单独使用LIF系统无法判断出超过饱和厚度的乳化液层的厚度。设计了一个4层神经元的神经网络,对饱和临界点附近的荧光光谱对乳化液浓度的识别能力进行验证。验证结果显示,不同浓度的水包油乳化液,只要达到或超过饱和厚度,其荧光光谱就具有较好的鉴别能力,可以用来区分不同浓度的乳化液。对于那些距离饱和厚度比较远的样本,荧光光谱具有分辨乳化液是否达到饱和厚度的能力。这些实验和结论将对较厚的水包油乳化液的识别和定量分析研究提供参考。

塔河油田盐下地区原油地球化学特征及不同期次油气成藏贡献

对于多旋回叠合盆地,油气藏形成的过程往往伴随着多期次的原油充注,但并非每一期原油充注都对现今油藏形成起到关键作用。流体包裹体方法只能对原油充注期次和时间进行限定,而无法确定各期充注原油对油藏的贡献。针对上述问题,以塔河油田盐下地区奥陶系碳酸盐岩油藏为例,采用原油地球化学、流体包裹体法、荧光光谱和单井模拟分析方法,系统揭示了研究区原油的荧光特征、油气成藏期次和成藏时间。原油生物标志化合物参数分析结果表明,其母质相同且沉积于海相弱还原环境,再通过与研究区烃源岩进行油源对比,确定了原油均来自下寒武统玉尔吐斯组烃源岩。原油芳烃中甲基菲指数和二苯并噻吩参数是定量评价原油成熟度的有效指标,计算得到塔河油田盐下地区原油成熟度(R_(o))在0.90%~1.47%之间,可能对应了多期油气充注。此外,在对盐下地区奥陶系储层油包裹体荧光光谱分析、共生盐水包裹体测温和测盐的基础上,结合单井埋藏史和热史模拟,确定盐下地区存在加里东中期(420 Ma)、海西中期(318 Ma)和喜马拉雅晚期(10 Ma)3期原油充注。对比原油和3期油包裹体荧光光谱参数,认为喜马拉雅晚期是盐下地区的主成藏期,为盐下地区的奥陶系油藏贡献了最多的原油。

紫云英长期还田对稻田土壤DOM和Cd形态影响研究

长期种植和翻压紫云英能够显著提高土壤中有机质(SOM)和水溶性有机物(DOM)的含量,影响土壤颗粒对重金属镉(Cd)的吸附行为和Cd在土壤中的形态,了解该条件下Cd在不同土层中的特征对紫云英的进一步推广种植具有重要意义。以余江区(YJ)、南昌县(NC)、丰城市(FC)3地长期种植和翻压紫云英处理(F+M)和化肥处理(F)的定位试验点为研究对象,测试了不同层次土壤中SOM、水溶性有机碳(DOC)含量、Cd总量和形态、DOM三维荧光,以期探明紫云英长期还田模式下不同土层中DOM成分的差异及其对Cd含量和形态影响。结果显示,NC和FC试验点F+M处理耕作层土壤(0-20 cm)中SOM的含量显著高于F处理,分别提高16.8%和10.5%。同一土层中土壤Cd活性呈现F+M处理>F处理的趋势。紫云英DOM主要在耕作层和中层(20-40cm)土壤中迁移,YJ、NC、FC试验点中,F+M处理耕作层土壤中DOC含量比F处理分别提高17.0%、58.1%和33.7%,中层土壤中DOC含量分别提高43.0%、36.7%和11.2%。种植和翻压紫云英降低了DOM中类蛋白质组分的占比,增加了类腐殖质组分的占比,耕作层、中层和深层土壤(40-60 cm)中,3个试验点F处理DOM中类蛋白质的平均占比分别为7.34%、16.7%、23.9%,占比分别是F+M处理的1.26、1.92和1.54倍。类蛋白质组分的深层迁移能力大于类腐殖质组分。逐步回归分析表明,有生物活性的Cd形态占比与土壤SOM、类色氨酸含量存在负相关关系,与类富里酸含量存在正相关关系,其系数分别为-2.170、-0.760和0.239。常年种植和翻压紫云英通过影响土壤SOM总量以及DOM组分对土壤Cd表现出一定的活化潜力。

沥青老化前后宏-微观性能相关性

为探索沥青老化过程中微观结构变化对其宏观力学性能的内在影响机制,结合动态剪切流变仪测定的流变学参数与红外光谱仪及荧光显微镜获取的化学官能团和微观结构数据,揭示了基质沥青与SBS改性沥青在不同老化阶段的宏-微观性能关联。研究发现,SBS改性沥青的微观空间网络结构赋予其卓越的黏弹特性。识别了SBS改性剂特有的红外光谱特征峰,为快速识别和评估SBS改性沥青提供了一种方法。通过灰色关联度分析,发现官能团指数与复数剪切模量的关联度排序为:亚砜基官能团指数>芳香环官能团指数>羰基官能团指数,与沥青表面能的关联度顺序为:芳香环官能团指数>羰基官能团指数>亚砜基官能团指数。研究进一步证实,沥青老化过程中官能团的氧化和微观形貌的重构是影响其复数剪切模量变化的关键因素,为沥青材料的老化行为提供了新的理论解释。