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A novel analysis technique of elements at ambient conditions has been developed. The technique is based on microwave-assisted laser-induced breakdown spectroscopy (MW-LIBS) applied to acoustically levitated samples. The technique has been demonstrated using three solid samples with different properties and compositions. These are ore containing multiple elements (OREAS 520), aluminium oxide (Al3O2) and gypsum (CaSO4·2H2O). The mass of samples was 21 mg, 23 mg, and 55 mg for gypsum, mineral ore, and Al3O2, respectively. Significant signal enhancements were recorded for a variety of elements, using microwave-assisted laser-induced breakdown spectroscopy and levitation (MW-LIBS-Levitation). The signal enhancement for Mn I (403.07 nm), Al I (396.13 nm) and Ca II (393.85 nm) was determined as 123, 46, and 63 times, respectively. Moreover, it was found that MW-LIBS-Levitation minimises the self-absorption of the Ca I (422.67 nm) and Na I (588.99 nm and 589.59 nm) spectral lines. In addition to the signal enhancements, the levitation process produces a spinning motion in the solids with an angular frequency of 7 Hz. This feature benefits laser-based analysis as a fresh sample is introduced at each laser pulse, eliminating the need for the usual mechanical devices. Based on the single-shot analysis, it was found that ∼80% of the laser pulses produced successful MW-LIBS-Levitation detection, confirming an impressive repeatability of the process. This contactless analytical technique can be applied in ambient pressure and temperature conditions with high sensitivity, which can benefit disciplines such as forensics science, isotope analysis, and medical analysis, where the sample availability is often diminutive.

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Dendrimers─nanosized macromolecules that can function as hosts for encapsulation of guest molecules─provide new avenues to engineer gain media for lasing systems. In this context, this study investigates the interplay between the geometric features of a model porous scattering medium, nanoporous anodic alumina (NAA), and the chemical features of a model fluorophore-dendrimer encapsulation system to maximize random lasing. The inner surface of the NAA platforms is functionalized with fluorophore molecules encapsulated within dendrimers via an electrostatic interaction. The resulting solid-state composite structures emit well-resolved, intense random lasing when subjected to optical pumping. By engineering fluorophore-dendrimer and geometric features of scattering medium, we can precisely tune the characteristics of random lasing emissions. It is found that lasing structures with low porosity and thickness functionalized with fluorophore molecules encapsulated in second-generation dendrimers provide the best platforms for lasing generation, resulting in a strongly polarized laser at ∼594 nm that has a high quality-gain product of ∼1588 au, a polarization quality of ∼0.86, and a lasing threshold of ∼0.05 mJ pulse-1. Comparative analysis indicates that dendrimers achieve 2.5 times better random lasing than conventional surfactants due to improved encapsulation and minimization of photobleaching. Our results reveal the importance of the fluorophore encapsulation method and design of scattering media in the engineering of random lasing platforms for applications in optical and optoelectrical systems.

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Suspension microsphere immunoassays are rapidly gaining attention in multiplex bioassays. Accurate detection of multiple analytes from a single measurement is critical in modern bioanalysis, which always requires complex encoding systems. In this study, a novel bioassay with Raman-coded antibody supports (polymer microbeads with different Raman signatures) and surface-enhanced Raman scattering (SERS)-coded nanotags (organic thiols on a gold nanoparticle surface with different SERS signatures) was developed as a model fluorescent, label-free, bead-based multiplex immunoassay system. The developed homogeneous immunoassays included two surface-functionalized monodisperse Raman-coded microbeads of polystyrene and poly(4-tert-butylstyrene) as the immune solid supports, and two epitope modified nanotags (self-assembled 4-mercaptobenzoic acid or 3-mercaptopropionic acid on gold nanoparticles) as the SERS-coded reporters. Such multiplex Raman/SERS-based microsphere immunoassays could selectively identify specific paratope-epitope interactions from one mixture sample solution under a single laser illumination, and thus hold great promise in future suspension multiplex analysis for diverse biomedical applications.

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We report a relatively simple configuration of laser-induced breakdown spectroscopy (LIBS) that is suitable for gas flow diagnostics with increased spatial resolution, signal intensity, and stability. In this optical configuration, two laser beams are generated by splitting a single laser beam, and then they are focused and crossed orthogonally at the detection volume from two different optical paths. Different from dual-pulse LIBS, this LIBS configuration uses only one laser source, and thus is of relatively low cost. Several advantages were found for this simple beam-crossing LIBS when it was demonstrated in air in the present work, particularly on signal enhancement and stabilization, confining plasma volume, and controlling plasma position. Both of the latter two advantages are relevant to spatial resolution improvement of LIBS in gases, which has rarely been discussed in previous reports. An enhancement factor of 2 was found for atomic hydrogen, nitrogen, and oxygen emissions with respect to conventional LIBS. Another advantage is that the position of breakdown can be precisely controlled through adjustment of the propagation of the two beams, also resulting in smaller plasma volume and stable emission intensity. Furthermore, the technique is moderately tolerant to dust particles neutrally present in the environment, avoiding the spark occurring at a position out of the detection volume. Beyond LIBS, the new configuration has other potential applications, e.g., laser-induced ignition, which is also briefly discussed.

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In this Letter, we present a particle image/tracking velocimetry (PIV/PTV) technique for simultaneous velocity measurement of both fluid and particle phases, adopting newly developed optical phase discrimination methods and novel optical particles. Spherical acrylic (PMMA) particles of diameter ∼O(100µm) were used as the particle phase, while fine BAM:Eu2+ phosphors of diameter ∼O(1µm) were used as the fluid tracer. Under Nd:YAG 355 nm laser excitation, both the laser-induced fluorescence (LIF) from PMMA and laser-induced phosphorescence (LIP) from BAM:Eu2+ provided sufficiently strong signals for PIV imaging with two non-intensified cameras and were clearly separable for phase discrimination using spectral filters and temporal profiles. The advantages of the PIV/PTV method include the relatively low cost of BAM:Eu2+ phosphors, high sphericity and narrow size distribution of PMMA particles with LIF emission, and direct optical discrimination eliminating artifacts, while requiring much less computational capacity for PIV/PTV processing of complex particle-laden flows.

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An efficient 3.168 kW solid-state solar thermal simulator (SSSTS), capable of supplying ~30,000 suns at a focal plane via a fibre optical delivery, has been developed. The source consists of 41 diode lasers, each operated at a wavelength and power of ~915 nm and ~80 watt, respectively. The SSSTS provides a semi-top hat radiation profile and can be focused to a diameter of ~10.5 mm. The electro-optical power efficiency of the SSSTS was evaluated to be 55%, where the maximum value of the uniform radiation flux exceeds 36.6MW/m2. As such, the present technology is relevant to solar thermal applications that are not wavelength-sensitive or where narrow line-width is desirable. Additionally, the fibre optical delivery feature enables ease of direction onto a suitable target, without the need of large ellipsoidal reflectors usually employed for the conventional arc solar simulators. To demonstrate the new SSSTS, ZnO:Zn particles were introduced into the path of the radiation to investigate the change in their own temperature by using the laser induced phosphorescence technique (LIP). The temperature of the averaged particles was measured at a different radiation flux over a ~87 mm2 cross sectional area. A change in the average particle temperature of up to 225°C was detected within the measurement volume when the SSSTS was operated at a flux of ~30,000 suns. The unique characteristics of the SSSTS, namely, the uniformity, high power flux, efficiency, ease of delivery, and precise control of the radiation flux responds to the current demands of solar thermal research.

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The enhancement of laser-induced breakdown spectroscopy (LIBS) assisted with microwave radiation is demonstrated for an aqueous solution of indium using the 451.13 nm emission line. Microwave power was delivered via a near-field applicator to the LIBS measurement volume where the indium aqueous solution was presented as a liquid jet. The microwave enhancement effect was observed to decrease with increasing laser pulse fluence at 532 nm resulting in a maximum emission intensity occurring at a laser pulse fluence of 85.2 J∙cm(-2), independent of the microwave power used. The detection limits of indium in an aqueous solution were determined to be 10.8 ± 0.7 and 124 ± 5 ppm for the cases of microwave enhanced and standard LIBS, respectively. The 11.5-fold detection limit enhancement obtained in the liquid phase is of the same order of magnitude as that reported for other elements in solid samples, but lower than that obtained in solid phase utilizing a similar experimental setup. This establishes microwave enhancement as an effective technique for the detection of metals in aqueous solutions. In addition, the temporal evolution of plasma emission intensity was investigated and was found to be qualitatively similar to that of plasma produced from solid phase samples, which reveals the same coupling mechanism between laser generated plasma and microwave radiation.

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Planar infrared visualization of species in flames is challenging due to the severe thermal radiation background and relatively weak fluorescence quantum yields from ro-vibration transitions. In this express, we report imaging of molecular species in a flame via an absorption-based coherent optical method, namely infrared polarization spectroscopy (IRPS). Single-shot, planar imaging of hydrogen fluoride (HF) has been achieved in a premixed CH(4)/O(2) Bunsen flame, being seeded with a small amount of SF(6). The HF molecule was excited through a rovibrational transition at around 2.5 µm, which belongs to the fundamental vibration band. High spatial resolution was guaranteed using an orthorgonal pump-probe geometry, and an effective suppression of thermal background emission was achieved owing to the coherent nature of the demonstrated two-dimensional IRPS. Other advantages, e.g. high temporal resolution and species-specificity, are also features of this laser-based technique, which make it suitable for imaging of non-fluorescent but infrared active gaseous molecules in harsh environments.

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During the combustion of coal or biomass, the inherent alkali metals in the fuel will be released to the gas phase. The released alkali species condensed during the cooling of the flue gas, which may subsequently cause problems with ash deposition and corrosion in thermal fuel conversion systems. Laser Induced Breakdown Spectroscopy (LIBS) is an effective technique to measure the alkali species in the plume of burning coal or biomass. In this study, an LIBS experimental system with a flat flame burner was set up, and the Flame Emission Spectroscopy (FES) and LIBS of K in the flat flame environment were measured using different ICCD gate-width times. The experimental results revealed that with the same ICCD gate-width time, the LIBS intensity of K was higher than the FES intensity of K in the flat flame. With the increase of the ICCD gate-width time, both intensities increased, but their increase rates were different: the increase rate of the LIBS intensity of K was firstly fast then became slow, but the increase rate of the FES intensity of K was constant. Furthermore, the intensity ratio of LIBS to FES of K increased monotonically with the ICCD gate-width time in the range of 0-8 µs, until reaching approximately 4. Then, further increasing the ICCD gate-width time, such ratio decreased slowly with an asymptote value of 1. After analyzing the influences of the FES on the LIBS measurement of K in a flame condition, it is proposed that to minimize such influence, the optimization of the ICCD gate-width time was necessary, which maximized the intensity ratio of LIBS to FES-of K and facilitated the measurement accuracy of K in the flame environment using LIBS.

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This paper presents the first demonstration of the pulsed laser ablation technique to seed a laminar non-reacting gaseous jet at atmospheric pressure. The focused, second harmonic from a pulsed Nd : YAG laser is used to ablate a neutral indium rod at atmospheric pressure and temperature. The ablation products generated with the new seeding method are used to seed the jet, as a marker of the scalar field. The neutral indium atoms so generated are found to be stable and survive a convection time of the order of tens of seconds before entering the interrogation region. The measurements of planar laser-induced fluorescence (PLIF) with indium and laser nephelometry measurements with the ablation products are both reported. The resulting average and root mean square (RMS) of the measurements are found to agree reasonably well although some differences are found. The results show that the pulsed laser ablation method has potential to provide scalar measurement for mixing studies.

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Narrow laser beams directed from aircraft may at times pass through the exhaust plume of the engines and potentially degrade some of the laser beam characteristics. This paper reports on controlled studies of laser beam deviation arising from propagation through turbulent hot gases, in a well-characterized laboratory burner, with conditions of relevance to aircraft engine exhaust plumes. The impact of the temperature, laser wavelength, and turbulence length scale on the beam deviation has been investigated. It was found that the laser beam displacement increases with the turbulent integral length scale. The effect of temperature on the laser beam angular deviation, σ, using two different laser wavelengths, namely 4.67 µm and 632.8 nm, was recorded. It was found that the beam deviation for both wavelengths may be semiempirically modeled using a single function of the form, σ=a(b+(1/T)(2))(-1), with two parameters only, a and b, where σ is in microradians and T is the temperature in °C.

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A quantitative point measurement of total sodium ([Na](total)) and potassium ([K](total)) in the plume of a burning particle of Australian Loy Yang brown coal (23 ± 3 mg) and of pine wood pellets (63 ± 3 mg) was performed using laser-induced breakdown spectroscopy (LIBS) in a laminar premixed methane flame at equivalence ratios ( U ) of 1.149 and 1.336. Calibration was performed using atomic sodium or potassium generated by evaporation of droplets of sodium sulfite (Na(2)SO(3)) or potassium sulfate (K(2)SO(4)) solutions seeded into the flame. The calibration compensated for the absorption by atomic alkalis in the seeded flame, which is significant at high concentrations of solution. This allowed quantitative measurements of sodium (Na) and potassium (K) released into the flame during the three phases of combustion, namely devolatilization, char, and ash cooking. The [Na](total) in the plume released from the combustion of pine wood pellets during the devolatilization was found to reach up to 13 ppm. The maximum concentration of total sodium ([Na](max)M(total)) and potassium ([K](max)(total)) released during the char phase of burning coal particles for φ = 1.149 was found to be 9.27 and 5.90 ppm, respectively. The [Na](max)(total) and [K](max)(total) released during the char phase of burning wood particles for φ = 1.149 was found to be 15.1 and 45.3 ppm, respectively. For the case of φ = 1.336, the [Na](max)(total) and [K](max)(total) were found to be 13.9 and 6.67 ppm during the char phase from burning coal particles, respectively, and 21.1 and 39.7 ppm, respectively, from burning wood particles. The concentration of alkali species was higher during the ash phase. The limit of detection (LOD) of sodium and potassium with LIBS in the present arrangement was estimated to be 29 and 72 ppb, respectively.

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We aim to investigate the potential of four different organic solvents, namely, acetone, ethanol, methanol, and isopropanol, and the organic-solvent-water mixtures as a seeding medium for the two-line atomic fluorescence technique. Water is used as the reference case. Indium, which has been previously shown to have suitable spectroscopic attributes, is chosen as the thermometry species in the present study. Acetone and methanol are shown to enhance the fluorescence signal intensity the most (approximately threefold to fivefold at stoichiometric conditions) when used. Acetone and methanol are shown to improve the fluorescence emission over the entire stoichiometric envelope of flame, most significantly in the rich combustion region, as well as a twofold enhancement in the signal-to-noise ratio.

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This work investigates the first demonstration of nonlinear regime two-line atomic fluorescence (NTLAF) thermometry in laminar non-premixed flames. The results show the expediency of the technique in the study of the reaction zone and reveals interesting findings about the indium atomization process. Indium fluorescence is observed to be strongest at the flame-front, where the temperature exceeds 1000 K. The uncertainty in the deduced temperature measurement is approximately 6%. The temperature profile across the reaction zone shows good agreement with laminar flame calculations. The advantages and inherent limitations of the technique are discussed.

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This work aims to advance understanding of the coupling between temperature and soot. The ability to image temperature using the two-line atomic fluorescence (TLAF) technique is demonstrated. Previous TLAF theory is extended from linear excitation into the nonlinear fluence regime. Nonlinear regime two-line atomic fluorescence (NTLAF) provides superior signal and reduces single-shot uncertainty from 250 K for conventional TLAF down to 100 K. NTLAF is shown to resolve the temperature profile across the stoichiometric envelope for hydrogen, ethylene, and natural gas flames, with deviation from thermocouple measurements not exceeding 100 K, and typically ≲30 K. Measurements in flames containing soot demonstrate good capacity of NTLAF to exclude interferences that hamper most two-dimensional thermometry techniques.

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The application of polarization spectroscopy (PS) to detect atomic species in an atmospheric pressure welding plasma has been demonstrated. PS spectra of Na atoms, seeded in the shielding gas flow of a gas tungsten arc welding (GTAW) plasma, are presented at different pump beam energies. The nature of the PS technique was found to be very efficient in suppressing the high background emission associated with the welding plasma. The PS spectral profiles appear to be Lorentzian and Lorentzian cubed for high and low pump beam energy, respectively. The effect of beam steering, due to the thermal gradient in the interaction plasma zone, was addressed. It was found that there is 2% unavoidable error in the detectable PS signal.

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Planar laser polarization spectroscopy has recently been used to image the hydroxyl radical in combustion for small intersection angles of pump and probe beams. We report an experimental configuration that allows planar laser polarization imaging for perpendicular intersection of pump and probe beams. We demonstrate what to our knowledge is the first planar laser polarization spectroscopy imaging at a 90 degree intersection of pump and probe beams for both linearly and circularly polarized pump beams.