|
Code:
TP13
|
Time Slot/Poster Number:
090
|
Session:
Raman Instrumentation
|
Development of Highly Sensitive Compact Raman Scanner for Mass Screening of Chemical Dyes
|
| Dinish U. S; Chit Yaw Fu; Malini Olivo
|
Singapore Bioimaging Consortium, 11 Biopolis Way, Singapore
|
|
| View Abstract PDF |
| Summary |
In the Raman analysis of various chemicals, it is often required to do mass screening of dyes and their derivatives. In most cases, it is impractical to screen each dye one by one on a commercial Raman system, which is catered to screen one analyte at a time. In this context, we proposed the design of simple, cost effective and compact ‘Raman Scanner’ developed using commercial laser, detector and optical components. The high throughput screening capability of the system is demonstrated by acquiring the SERS spectra of various molecules adsorbed on to gold colloid in a 96 well plate.
|
|
Code:
TP13
|
Time Slot/Poster Number:
091
|
Session:
Raman Instrumentation
|
In-Situ Raman monitoring of UO2/H2O interfaces under He2+ irradiation
|
| Aurélien Canizares1; Guillaume Guimbretiere1; Yeny Alexandra Tobon-Correa1; Nicole Raimboux1; Michel Perdicakis2; Benoist Muzeau3; Mohammad S. Alam3; Marie-France Barthe1; Catherine Corbel1, 3; Patrick Simon1
|
1CNRS UPR 3079 CEMHTI, Orleans , France; 2CNRS-Nancy Université LCPME, Nancy, France; 3CNRS-CEA-Ecole Polytechnique LSI, Palaiseau, France
|
|
| View Abstract PDF |
| Summary |
An in-situ Raman device is developed to monitor the behavior of UO2/H2O solid/liquid interfaces, during irradiation by a He2+ beam supplied by a cyclotron. This allows access to the alteration mechanisms of the solid, through decomposition of water under alpha-radioactivity and the appearance of stable and transient reactive radiolytic species. The progressive appearance of oxidized U(VI) alteration phases phases is evidenced. These experiments intend to give a better knowledge of nuclear spent fuel behavior in case of contact with water in underground storage. Besides, this in-situ Raman device can be applied to any other material under irradiation.
|
|
Code:
TP13
|
Time Slot/Poster Number:
092
|
Session:
Raman Instrumentation
|
Quantitative Stand-off Raman Scattering
|
| Bernhard Zachhuber1; Maria C. Alcudia-Leon1, 2; Bernhard Lendl1
|
1Vienna University of Technologie, Vienna, Austria; 2University of Cordoba, Cordoba, Spain
|
|
| View Abstract PDF |
| Summary |
Here we present a multivariate analysis of stand-off Raman spectra of xylene isomer mixtures as an example of how techniques, more commonly applied to conventional Raman spectroscopy, can also be applied to stand-off detection.
A multivariate calibration has shown that quantitative analysis of stand-off Raman spectra from liquid, multicomponent mixtures is achievable. The validation of this method indicates that for m- and p-xylene prediction of concentration is accurate to ±0.5%, and ±1.5% for o-xylene.
As stand-off Raman spectroscopy improves and finds its way into more routine analyses there will be increasing requirements for quantification of the signals obtained.
|
|
Code:
TP13
|
Time Slot/Poster Number:
096
|
Session:
Raman Instrumentation
|
Construction of Multichannel Low-Frequency Raman Microspectrometer of Spectral Coverage to 20 cm-1 with Gratings Formed in Glass Plates
|
| Atsuko Tsurumi; Yasuaki Naito; Koichi Iwata
|
Department of Chemistry, Gakushuin University, Tokyo, Japan
|
|
| View Abstract PDF |
| Summary |
We have constructed a multichannel Raman microspectrometer with new Notch filters and examined its performance. A grating is formed inside the glass plate of each Notch filter. We measured the Raman spectrum of L-cyctine that has a number of Raman bands in the low frequency region with our Raman microspectrometer. It is possible to record the low frequency region down to 20 cm-1 with this multichannel Raman microspectrometer.
|
|
Code:
TP13
|
Time Slot/Poster Number:
097
|
Session:
Raman Instrumentation
|
Towards Stand-Off Resonance Raman Spectroscopy
|
| Alison Hobro; Bernhard Zachhuber; Bernhard Lendl
|
Vienna University of Technology, Vienna, Austria
|
|
| View Abstract PDF |
| Summary |
Stand-off Raman is advantageous where samples are dangerous, fragile or difficult to access. Exploiting resonance Raman through careful laser excitation choice, increases the sensitivity of Raman spectroscopy and also means that the spectra obtained are selective for the part of the analyte associated with the chromophore. Therefore, combining these spectroscopies is likely to yield an analysis technique that can be used to probe a sample for specific molecules from a distance. Here we present our work towards stand-off resonance Raman with examples including the detection of carotinoids in leaves.
|
|
Code:
TP13
|
Time Slot/Poster Number:
098
|
Session:
Raman Instrumentation
|
Vibrational Spectroscopic Studies and DFT calculations of 2,6 Diphenyl 4 Piperidone
|
| Sridevi C1; G Velraj2; R Palanivel3
|
1Sona college of Technology, Salem, India; 2Department of Physics, Periyar University, Salem-636011, Tamilnadu, India; 3Department of Physics, Annamalai University, Annamalainagar-608002,Tamilnadu, India
|
|
| View Abstract PDF |
| Summary |
In the present investigation, Vibrational spectroscopic studies and DFT calculation have been performed on 2,6 Diphenyl 4 Piperidone. Laser Raman and FTIR spectra were recorded and their tentative vibrational assignments are discussed clearly. The theoretical results obtained from the studies shows good agreement with experimental values. Comparision of the observed fundamental frequencies of 2,6 Diphenyl 4 Piperidone and the results calculated by HF and DFT methods indicate that B3LYP is superior to scaled HF approach for vibrational problems.
|
|
Code:
TP13
|
Time Slot/Poster Number:
099
|
Session:
Raman Instrumentation
|
FT-IR and Laser Raman Spectroscopic Analysis
of 4-Amino-3-Bromopyridine
|
| Velraj G1; R Sudha1; N Senguttuvan2
|
1Periyar University, Salem, India; 2Department of Physics,Kandaswami Kandar’s College, Paramathi Velur, Tamilnadu, India
|
|
| View Abstract PDF |
| Summary |
Pyridine derivatives are one of the most used frame works for medicines, food flavorings, dyes, agrochemicals, rubber chemicals, and adhesives in drug discovery. In the present investigation, an attempt have been made to record the FTIR and Laser Raman spectra for 4–amino –3–bromo pyridine and their tentative vibrational assignments are discussed clearly.
|
|
Code:
TP13
|
Time Slot/Poster Number:
100
|
Session:
Raman Instrumentation
|
Brillouin Scattering in Ethanol-Water Mixtures
|
| Augustinus Asenbaum1; Bernarda Kezic2; Christian Pruner1; Franjo Sokolic2; Emmerich Wilhelm1
|
1Experimental Physics, University of Salzburg, Salzburg, AUSTRIA; 2Department of Physics, University of Split, Split, CROATIA
|
|
| View Abstract PDF |
| Summary |
We present Brillouin scattering measurements on ethanol-water mixtures at 293.15 K. The spectrometer was a 6-pass tandem Fabry-Perot interferometer with a finesse of about 80, FSR = 15.00 GHz. The scattering angle was 90°. Ultrasonic speed measurements at 3 MHz and index of refraction data at 514.5 nm are also reported. Of particular note is the sound dispersion between 0.1 and 0.6 mole fraction ethanol. The structural relaxation times derived from the experimental Brillouin spectra in the region around 0.2 mole fraction are in rough agreement with dielectric relaxation times.
|
|
Code:
TP13
|
Time Slot/Poster Number:
101
|
Session:
Raman Instrumentation
|
Microfluidic Raman Spectroscopy for Bio-analyte Detection
|
| Praveen Ashok; Gajendra Singh; Khay Tan; Kishan Dholakia
|
University of St. Andrews, St. Andrews, United Kingdom
|
|
| View Abstract PDF |
| Summary |
We report a novel fiber probe based Raman detection system on a microfluidic platform where a split Raman probe is directly embedded into a Polydimethylsiloxane (PDMS) chip. The sensitivity of the system is evaluated by quantitative estimation of urea and the system could detect human physiological level of urea. The prospect of a Raman detection system built on PDMS based microfluidic platform makes this technology inexpensive and biocompatible. Unlike conventional bulk optics based Raman detection schemes in microfluidics, our approach will help to develop point of care, environmental microfluidic monitoring, biotechnological and forensic portable detection devices utilizing Raman spectroscopy.
|
|
Code:
TP13
|
Time Slot/Poster Number:
102
|
Session:
Raman Instrumentation
|
On axis Resonance Raman microspectroscopy
combined with macromolecular crystallography
at the Swiss Light Source
|
| Martin R. Fuchs1; Guillaume Pompidor1; Vincent Thominet1; Robin L. Owen2; Arwen Pearson3; Clemens Schulze-Briese1
|
1Swiss Light Source, Paul Scherrer Institute, Villigen, Switzerland; 2Diamond Light Source, Didcot, United Kingdom; 3University of Leeds, Leeds, United Kingdom
|
|
| View Abstract PDF |
| Summary |
Macromolecular crystallography is a powerful method to obtain structural information of biomolecules and molecular assemblies down to atomic resolution.
Optical spectroscopic techniques such as UV/Vis absorption, fluorescence and (resonance) Raman spectroscopy can provide valuable complementary information that can not be inferred from the crystal structure alone.
A multimode microspectrophotometer for in-crystallo optical spectroscopy has been developed at beamline X10SA of the Swiss Light Source. It can be configured for UV/Vis, fluorescence and Raman spectroscopy.
We present selected results obtained with the Raman configuration of the spectrometer and discuss the current instrument design as well as upgrades currently being implemented.
|
|
Code:
TP13
|
Time Slot/Poster Number:
104
|
Session:
Raman Instrumentation
|
Molecular and vibrational structure of 3-amino-2-bromo pyridine: FT-IR, FT-Raman and Quantum chemical calculations
|
| Velraj G1; Kandasamy M2
|
1Periyar University, Salem, India; 2Arignar Anna Government Art College, Namakkal-636 001,Tamilnadu, India
|
|
| View Abstract PDF |
| Summary |
One of the most successful selective scaling schemes, developed with deep understanding of the nature of molecular vibrations, is the so-called Scaled Quantum Mechani¬cal (SQM) force field method. Based on the SQM force field obtained by DFT calculations at B3LYP/6-311+G** levels, complete vibrational properties of ABP32 have been investigated by FT-IR and FT-Raman spectroscopic techniques. The roles of amino and bromine groups in the vibrational frequencies of the title compounds are discussed and their tentative vibrational assignments are explained in detailed.
|
|
Code:
TP13
|
Time Slot/Poster Number:
105
|
Session:
Raman Instrumentation
|
Near-Infrared Raman Spectroscopy Using Hollow-Core Photonic Bandgap Fibers
|
| K. M. Eddie Tan; Gajendra P. Singh; C. S. Herrington; C. T. A. Brown
|
University of St. Andrews, St. Andrews, United Kingdom
|
|
| View Abstract PDF |
| Summary |
We report a NIR Raman spectroscopy system incorporating hollow-core photonic bandgap fibers (HC-PBFs) in both the excitation and collection paths. Raman excitation was achieved at NIR laser wavelength of 785 nm. We demonstrate that using HC-PBFs, Raman spectroscopy can be performed without the use of an additional longpass filter on the collection side. A narrow bandpass filter on the excitation side is also not required. These results provide a framework where HC-PBF based Raman probes can be developed and used in space restricted biomedical and sensing applications.
|
|
Code:
TP13
|
Time Slot/Poster Number:
106
|
Session:
Raman Instrumentation
|
Raman microscopy imaging: improving detection through nonlinear optical interaction
|
| Vladislav Yakovlev
|
University of Wisconsin - Milwaukee, Milwaukee, WI
|
|
| View Abstract PDF |
| Summary |
Raman spectroscopy based on spontaneous scattering cannot compete with nonlinear Raman spectroscopy, when the sample volume is large enough to take advantage of the coherent nature of nonlinear optical interactions. However, when the interaction volume is small, the number of optical photons generated through spontaneous Raman scattering can be larger than the number of photons generated by coherent Raman process. In this work, the signal-to-noise ratio for Raman spectroscopy is carefully evaluated, and, by optically amplifying the weak Raman signal, Raman spectra, free of background noise are achieved.
|
|
Code:
TP13
|
Time Slot/Poster Number:
109
|
Session:
Raman Instrumentation
|
High Performance Resonance Raman Spectroscopy Using Volume Bragg Gratings as Tunable Light Filters
|
| Marc Verhaegen1; Matthieu Paillet2; François Meunier3; Sébastien Blais-Ouellette1; Richard Martel2
|
1Photon etc, Montreal, Canada; 2Département de Chimie, Université de Montréal, Montréal, Canada; 3Département de Physique, Université de Montréal, Montréal, Canada
|
|
| View Abstract PDF |
| Summary |
We designed a near infrared tunable resonance Raman spectroscopy system based on a tandem of thick volume Bragg gratings (VBGs). VBGs are here the constituents of two light filtering units: a tunable laser line filter (LLF) and a tunable notch filter (NF). When adapted in a micro-Raman setup with a single stage monochromator, the tandem of LLF and NF allowed measurements of Raman signals down to 20 cm-1. The good performance and fast tunability of the VGB Raman system was demonstrated on a sulfur powder and on a bulk single-walled carbon nanotube sample.
|
|
Code:
TP13
|
Time Slot/Poster Number:
112
|
Session:
Raman Instrumentation
|
New Directions in AFM-Raman BioImaging in Liquids
|
| Aaron Lewis1; Anatoly Komisar2; Rimma Dekhter2; David Lewis2
|
1Hebrew University of Jerusalem, Jerusalem, Israel; 2Nanonics Imaging Ltd., Jerusalem, Israel
|
|
| View Abstract PDF |
| Summary |
A new feedback mechanism for AFM imaging in liquids will be introduced. This new approach is based on tuning fork technology which has been shown to be the most effective method of AFM feedback. Thanks to their high Q factors, tuning forks allow for improving feedback sensitivity and imaging quality. It will be shown how these unique characteristics can now be extended to liquid environments for bioimaging.
|
|
Code:
TP13
|
Time Slot/Poster Number:
113
|
Session:
Raman Instrumentation
|
Very Low Frequency Stokes and Anti-Stokes Raman Spectra Accessible with a Single Multichannel Spectrograph and Volume Bragg Grating Optical Filters
|
| Alexandra Rapaport1, 2; Bernard Roussel1, 2; Hans-Juergen Reich1, 2; Fran Adar1, 2; Alexei Glebov 3; Oleksiy Mokhun3; Vadim Smirnov3; Leonid Glebov3
|
1Horiba Scientific, Edison, ; 2HORIBA Scientific, Villeneuve d'Ascq, France; 3OptiGrate Corp, 3267 Progress Dr.,, Orlando, Florida 32826
|
|
| View Abstract PDF |
| Summary |
Multichannel measurement of Raman bands with frequencies very close to the excitation line has traditionally been possible with the use of triple monochromator systems. These systems are very flexible, but they can be complex to use, large, low in throughput, and expensive. We have recently demonstrated the use of a single monochromator Raman system where the Rayleigh filtering elements are made of Volume Bragg Gratings (VBGs); such a system enabled recording of Stokes and anti-Stokes modes with frequencies less than 10 cm-1.
|
|
Code:
TP13
|
Time Slot/Poster Number:
114
|
Session:
Raman Instrumentation
|
Development of 1064 nm Excited Multichannel Raman Microspectrometer and Its Application to in vivo Measurements of Cyanobacteria
|
| Masahiro Ando1; Miwa Sugiura2; Hidenori Hayashi2; Hiro-o Hamaguchi1, 3
|
1The University of Tokyo, Tokyo, Japan; 2Ehime University, Matsuyama, Japan; 3National Chiao Tung University, Hsinchu, Taiwan
|
|
| View Abstract PDF |
| Summary |
Near-infrared (NIR) excited Raman microspectroscopy is highly useful for in vivo studies of biological samples, which often show strong fluorescence that interfere the Raman measurements. However, some biological samples emit strong fluorescence even with NIR excitation at 800 nm. For the purpose of further overcoming this difficulty, we have developed a 1064 nm deep NIR excited multichannel Raman microspectrometer with the sensitivity high enough for measurements of single living cells. In this presentation, its application to the in vivo Raman measurements of cyanobacteria, which emit strong fluorescence with 800 nm excitation, is also reported.
|