Absorbance Detection Research Articles

Superconducting quasiparticle-amplifying transmon: A qubit-based sensor for meV-scale phonons and single terahertz photons

With great interest from the quantum computing community, an immense amount of R&D effort has been invested into improving superconducting qubits. The technologies developed for the design and fabrication of these qubits can be directly applied to applications for ultralow-threshold particle detectors, e.g., low-mass dark matter and far-infrared photon sensing. We propose a novel energy-resolving sensor based on the transmon qubit architecture combined with a signal-enhancing superconducting quasiparticle amplification stage. We refer to these sensors as SQUATs: superconducting quasiparticle-amplifying transmons. We detail the operating principle and design of this new sensor and predict that, with minimal R&D effort, solid-state-based detectors patterned with these sensors can achieve sensitivity to single terahertz photons, and sensitivity to 1meV phonons in the detector absorber substrate on the microsecond timescale. Published by the American Physical Society 2024

Light-emitting diode-based absorbance detectors for flow-through analysis in analytical chemistry: A tutorial

The development of light-emitting diodes (LEDs) has played a significant role supporting many recent advances made in chemical analysis. Their small size, low power consumption, and semi-monochromaticity make them ideal light sources for portable photometric devices used in field and on-site analysis, environmental monitoring, and industrial applications, such as process analytical technology (PAT) and continuous real-time analysis. This tutorial provides an overview and critical comparison of the key components in LED-based absorbance detectors, including light sources, optical fibres, flow cells, and photodetectors. Fundamental aspects of LEDs relating to their use in such simple detectors are discussed in detail, along with the development of multi-wavelength detectors that incorporate multiple LEDs. The tutorial also details the different methodologies for assessing and characterising the LED-based absorbance detectors. Finally, this tutorial presents some selected applications of LED based photometric detectors in gas sensing, flow injection analysis (FIA), and coupled with separation techniques such as ion chromatography, liquid chromatography, and capillary zone electrophoresis (CZE).

A RAPIDLY COLORIMETRIC DETECTION OF ARSENIC AND MERCURY IONS BASED ON SURFACE PLASMON RESONANCE ABSORBANCES OF FUNCTIONALIZED AuNPs IN COSMETICS

In this study, a novel colorimetric method is developed for the detection of arsenic and mercury ions, utilizing the surface plasmon resonance (SPR) properties of AuNPs ([Formula: see text] nanoparticles) functionalized with APT ([Formula: see text]-(3-aminophenyl) tetrazole). Theoretical calculations confirm the findings from UV–Visible spectroscopy and transmission electron microscopy analyses, indicating that APT is electrostatically bound to the surfaces of the AuNPs. The introduction of [Formula: see text] and [Formula: see text] ions triggers a coordination reaction with APT, resulting in a reduced interparticle distance among the AuNPs. This change leads to a visible color shift of the solution from wine red to bluish-gray. The detection limits for [Formula: see text] and [Formula: see text] are determined to be 0.6 and 0.24 [Formula: see text] g⋅[Formula: see text], respectively, distinguishable to the naked eye. A robust linear correlation is observed between the absorbance ratios and the ion concentrations, with correlation coefficients ([Formula: see text]) of 0.990 for [Formula: see text] and 0.998 for [Formula: see text]. These findings demonstrate that AuNPs functionalized with APT are effective for the quantitative analysis of arsenic and mercury ions. The sensor exhibits high selectivity and excellent resistance to interference, indicating its potential applicability for monitoring [Formula: see text] and [Formula: see text] in tap water and cosmetic products.

Fusariotoxins Concentration in Common Wheat Grain Depending on the Farming System (Organic vs. Integrated vs. Conventional) and Changes During Grain Processing

Currently, the EU is focusing on less intensive agrotechnology and sustainable development. It is important to minimize the occurrence of mycotoxins (including Fusariotixins) in food, and to monitor mycotoxin concentration in the food chain. Therefore, this study evaluated Fusarium mycotoxin contamination, specifically type A and B trichothecenes and ergosterol concentration, in wheat grain from a three-year field experiment (2019–2021) conducted at IUNG-PIB in Osiny (Poland), along with its byproducts (bran, flour, bread). Four wheat cultivars were grown under different farming systems: organic (ORG), integrated (INT), and conventional (CONV). Ergosterol was analyzed using HPLC with an absorbance detector while Type A and B trichothecenes were analyzed using gas chromatography and mass spectrometry. Results showed that the farming system significantly influenced type B trichothecenes concentration in grain, with the highest concentration established in ORG-grown wheat. However, the grain concentration from the INT farming system was comparable to that from CONV. Type A trichothecenes concentrations were low and not significantly affected by the farming system. Bran exhibited the highest ergosterol and mycotoxin concentration, while flour and bread exhibited the lowest.

Coupling solid phase microextraction to integrated optical sensors with microfluidic open interface

Increasing number of regulations today is very demanding, so many fields need to rely to screening techniques to separate samples whose content need to be confirmed with that field's gold standard approach. Therefore, the development of simple and fast approaches is very much needed. This manuscript presents the development of a microfluidic open interface integrated with ultraviolet-visible (UV–Vis) absorption detection for rapid screening applications. The system was designed as a rapid sensor readout for compounds enriched by solid-phase microextraction devices. Two azo dyes from a liquid water enhancer solution served as model analytes. These two dyes were extracted with the solid phase microextraction fiber and introduced to the system for analysis. Experimental results demonstrated that the system could effectively detect dyes with absorbance at 403 nm, indicating its potential for quantitating analytes with UV–Vis chromophores. Although this sensing method exhibits limited selectivity, it offers a cost-effective, straightforward approach to rapid screening that can be conveniently miniaturized for on-site applications. Further advances could focus on integrating low-cost sensors with specific responses in place of the UV–Vis unit, as well as simplification and miniaturization of the system to improve on-site analysis. Additionally, incorporating autosampler systems could enable high-throughput determinations, broadening the method's applicability. The developed solid phase microextraction method reliably samples and enriches small molecules from complex systems, delivering clean extracts to the selective sensor for readout without interference from the investigated sample matrix.

Overcoming the Strong Sample Solvent Effect for Sustainability Measurement Challenges in Liquid Chromatography. Example for Bisphenol-A.

This paper describes an approach to achieve low parts per billion (ppb) concentration level detection using a reversed-phase ultrahigh-performance liquid chromatographic ultraviolet absorbance detection method with large-volume feed injection (FI) for analytes in dichloromethane (DCM). FI is a novel technology that allows sample injection at a defined speed into the LC mobile phase. We demonstrate this approach for a mixture of bisphenol A and its diglycidyl ether derivatives in DCM. DCM is a very strong injection solvent at reversed-phase LC conditions and is typically immiscible with a starting reversed-phase gradient mobile phase containing a high percentage of water. As a result, reduced separation performance and even peak splitting are seen with classic flow-through injection. The method setup comprised an octyl-bonded core-shell stationary phase (150 × 4.6 mm i.d., 2.7 μm particle size) with a water/acetonitrile mobile phase gradient and an exceptionally high injection volume of 45 μL of DCM solution using FI. Optimization of feed speed (1%) and isocratic hold duration (4 min) was crucial for final separation conditions. FI delivered more than a 20-fold improvement in the limit of detection (LOD) compared to standard flow-through injection while maintaining peak resolution. The LOD of the final method ranged between 1 and 10 ppb in the polymer resin. This methodology has high potential for trace analysis in a large variety of applications that suffer from the "strong solvent effect".

Local H i absorption towards the magellanic cloud foreground using ASKAP

ABSTRACT We present the largest Galactic neutral hydrogen H i absorption survey to date, utilizing the Australian SKA Pathfinder Telescope at an unprecedented spatial resolution of 30 arcsec. This survey, GASKAP-H i, unbiasedly targets 2714 continuum background sources over 250 square degrees in the direction of the Magellanic Clouds, a significant increase compared to a total of 373 sources observed by previous Galactic absorption surveys across the entire Milky Way. We aim to investigate the physical properties of cold (CNM) and warm (WNM) neutral atomic gas in the Milky Way foreground, characterized by two prominent filaments at high Galactic latitudes (between $-45^{\circ }$ and $-25^{\circ }$). We detected strong H i absorption along 462 lines of sight above the 3$\sigma$ threshold, achieving an absorption detection rate of 17 per cent. GASKAP-H i’s unprecedented angular resolution allows for simultaneous absorption and emission measurements to sample almost the same gas clouds along a line of sight. A joint Gaussian decomposition is then applied to absorption-emission spectra to provide direct estimates of H i optical depths, temperatures, and column densities for the CNM and WNM components. The thermal properties of CNM components are consistent with those previously observed along a wide range of Solar neighbourhood environments, indicating that cold H i properties are widely prevalent throughout the local interstellar medium. Across our region of interest, CNM accounts for $\sim$30 per cent of the total H i gas, with the CNM fraction increasing with column density towards the two filaments. Our analysis reveals an anticorrelation between CNM temperature and its optical depth, which implies that CNM with lower optical depth leads to a higher temperature.

Line-shape parameters of the oxygen first rotational triplet

A lines shape of the first triplet of rotational band of oxygen molecule was studied beyond the Voigt profile in the framework of the quadratic approximation of speed dependence of collision relaxation rate. Recordings of the lines broadened by O2 and N2 were obtained at room temperature using two fundamentally different spectrometers, in particular, a video spectrometer and a spectrometer with radio-acoustic detection of absorption. A set of line-shape parameters was determined based on the line recording analysis. Data accuracy and reliability was evaluated from a comparative analysis of the parameters obtained from different techniques and with previous data.

Enhanced osseointegration and antimicrobial properties of 3D-Printed porous titanium alloys with copper-strontium doped calcium silicate coatings.

The 3D printing of porous titanium scaffolds reduces the elastic modulus of titanium alloys and promotes osteogenic integration. However, due to the biological inertness of titanium alloy materials, the implant-bone tissue interface is weakly bonded. A calcium silicate (CS) coating doped with polymetallic ions can impart various biological properties to titanium alloy materials. In this study, CuO and SrO binary-doped CS coatings were prepared on the surface of 3D-printed porous titanium alloy scaffolds using atmospheric plasma spraying and characterized by SEM, EDS, and XRD. Both CuO and SrO were successfully incorporated into the CS coating. The in vivo osseointegration evaluation of the composite coating-modified 3D-printed porous titanium alloy scaffolds was conducted using a rabbit bone defect model, showing that the in vivo osseointegration of 2% CuO-10% SrO-CS-modified 3D-printed porous titanium alloy was improved. The in vitro antimicrobial properties of the 2% CuO-10% SrO-CS-modified 3D-printed porous titanium alloy were evaluated through bacterial platform coating, co-culture liquid absorbance detection, and crystal violet staining experiments, demonstrating that the composite coating exhibited good antimicrobial properties. In conclusion, the composite scaffold possesses both osteointegration-promoting and antimicrobial properties, indicating a broad potential for clinical applications.

Quartz Clouds in the Dayside Atmosphere of the Quintessential Hot Jupiter HD 189733 b

Recent mid-infrared observations with JWST's Mid-Infrared Instrument Low Resolution Spectrometer (MIRI LRS) have resulted in the first direct detections of absorption features from silicate clouds in the transmission spectra of two transiting exoplanets, WASP-17 b and WASP-107 b. In this Letter, we measure the mid-infrared (5–12 μm) dayside emission spectrum of the benchmark hot Jupiter HD 189733 b with MIRI LRS by combining data from two secondary-eclipse observations. We confirm the previous detection of H2O absorption at 6.5 μm from Spitzer's Infrared Spectrograph (IRS) and additionally detect H2S as well as an absorption feature at 8.7 μm in both secondary-eclipse observations. The excess absorption at 8.7 μm can be explained by the presence of small (∼0.01 μm) grains of SiO2[s] in the uppermost layers of HD 189733 b’s dayside atmosphere. This is the first direct detection of silicate clouds in HD 189733 b’s atmosphere, and the first detection of a distinct absorption feature from silicate clouds on the dayside of any hot Jupiter. We find that models including SiO2[s] are preferred by 6–7σ over clear models and those with other potential cloud species. The high-altitude location of these silicate particles is best explained by formation in the hottest regions of HD 189733 b’s dayside atmosphere near the substellar point. We additionally find that HD 189733 b’s emission spectrum longward of 9 μm displays residual features not well captured by our current atmospheric models. When combined with other JWST observations of HD 189733 b’s transmission and emission spectra at shorter wavelengths, these observations will provide us with the most detailed picture to date of the atmospheric composition and cloud properties of this benchmark hot Jupiter.

Demonstration of record sensitivity for water vapor detection by means of comb-locked cavity ring-down spectroscopy

We report on the development, characterization, and test of a comb-locked cavity ring-down spectrometer (CL-CRDS) operating in the spectral region around 1.39 µm. The system is based on the use of a hemispherical optical resonator with a finesse as high as ∼507000, which gives an empty-cavity ring-down time of about 285 µs. An Allan-Werle analysis on repeated acquisitions of the ring-down time at a fixed laser frequency suggests a minimum detectable absorption coefficient of 2×10−12cm−1 for the optimum integration time of 45 s. This limit can be exceeded by adopting the strategy of long-term spectral averaging. Taking advantage of the frequency stability guaranteed by the optical frequency comb, the CL-CRDS spectra were averaged over more than two days, thus removing efficiently the effect of mechanical, acoustic, and thermal noises. As a result, we could achieve a minimum detectable absorption coefficient as low as 3.7×10−13cm−1, which corresponds to a limit of detection for H2O in N2 of nine parts per trillion and a H2O partial pressure of 2×10−8 Pa (or 2×10−10 mbar). The potentialities of our approach are demonstrated by recording the absorption features of HD16O and HD18O in flows of ultra-high-purity N2 and ambient air, respectively.

Highly sensitive assaying study based on three-dimensional graphene/cerium oxide nanoparticle nanozyme for the detecting of organophosphate pesticides in vegetable

As an important chemical pollutant affecting the safety of agricultural products, the on-site and efficient detection of pesticide residues has become a global trend and hotspot in research. Herein, this work present a highly sensitive assaying study based on three-dimensional graphene/cerium oxide nanoparticle nanozyme for the detection of organophosphate pesticides (OPs) in vegetable. The detection mechanism is because OPs can inhibit the activity of alkaline phosphatase (ALP). Cerium oxide nanoparticles exhibited intrinsic biomimetic oxidase activity and catalyzed the oxidation of the colorless 3,3′,5,5′-tetramethylbenzidine (TMB) into blue oxidized oxTMB. Upon the introduction of ALP, L-ascorbic acid-2-phosphate can be dephosphorylated to ascorbic acid, which aroused the disintegration of cerium oxide nanoparticles into Ce3+ ions. This disintegration weakened the enzyme-mimicking activity, thus impeding the oxidation of TMB. The absorbance at 652 nm exhibited a linear relationship with the concentration of phorate in the range of 0.15–50 μg/mL, generating a limit of detection of 0.13 μg/mL, Phorate recovery in the spiked samples for the absorption detection mode was 81.0 %–96.7 %. The relative standard deviations (RSD) of the absorption were in the range of 2.18 %–4.12 %. The results in terms of detecting pesticide residues collected from food samples via this method satisfactorily agree with those obtained via gas chromatography–mass spectrometry. This simple assay is therefore suitable for sensing pesticides in complex samples, especially in combination with other portable platforms.

A tutorial on optical photothermal infrared (O-PTIR) microscopy.

This tutorial reviews the rapidly growing field of optical photothermal infrared (O-PTIR) spectroscopy and chemical imaging. O-PTIR is an infrared super-resolution measurement technique where a shorter wavelength visible probe is used to measure and map infrared (IR) absorption with spatial resolution up to 30× better than conventional techniques such as Fourier transform infrared and direct IR laser imaging systems. This article reviews key limitations of conventional IR instruments, the O-PTIR technology breakthroughs, and their origins that have overcome the prior limitations. This article also discusses recent developments in expanding multi-modal O-PTIR approaches that enable complementary Raman spectroscopy and fluorescence microscopy imaging, including wide-field O-PTIR imaging with fluorescence-based detection of IR absorption. Various practical subjects are covered, including sample preparation techniques, optimal measurement configurations, use of IR tags/labels and techniques for data analysis, and visualization. Key O-PTIR applications are reviewed in many areas, including biological and biomedical sciences, environmental and microplastics research, (bio)pharmaceuticals, materials science, cultural heritage, forensics, photonics, and failure analysis.

Unveiling the self-healing behavior of marine exposed concrete: Nondestructive ultrasonic detection and Vickers hardness characterization

Cracking is a widespread phenomenon throughout the service of concrete structures for marine and offshore engineering. In this paper, the effect of sulfate ions and related cations on the crack closure behavior of cracked mortar in chloride-containing environments was studied. To this end, the mortars are cracked before transferring to the pure chloride solution as well as composite chloride and sulfate solutions (CNS and CMS series). The self-healing behavior is assessed by the evolution of crack width, water absorption, and nondestructive ultrasonic detection. The Vickers hardness test is applied to evaluate the micro-hardness of self-healing products generated in the crack gaps. Thermodynamic modeling of the phase volume expansion from the mortar matrix to the crack surface is conducted using Gibb’s free energy theory to explore the self-healing mechanisms. Experiment results suggest that the existence of sulfate ions in chloride-containing solutions is beneficial for crack closure, and self-healing could be more obvious if the cations that bind to sulfate are magnesium ions. The distributions of Vickers hardness on the mortar surface across the crack reveal that the brucite layer diminishes the overall Vickers hardness of the mortar matrix, whereas it is favorable for the micro-hardness enhancement of self-healing products in the CMS series. Thermodynamic modeling interprets the expansion rates relative to the original unhydrated cement under the action of different soaking solutions.

Open-Source Absorbance Detector with Multiple Deep UV-LEDs for On-Capillary Multiwavelength Detection at a Single Point.

On-capillary ultraviolet photometric detection (UV-PD) in a multiwavelength mode provides comprehensive analytical information. However, achieving single-point multiwavelength UV-PD for capillary-scale instruments typically requires high-cost and complex devices. This study presents the development of a cost-effective, open-source absorbance detector for on-capillary multiwavelength detection. The detector employs three deep UV light-emitting diodes emitting at 235, 255, and 278 nm as light sources, each coupled with its own photodetector for independent detection channels. The components are housed using 3D-printed parts, with an Arduino board used for data acquisition. Three individual optical paths, formed by three slits (60 μm width ×1 mm length), surround the measured capillary and converge at the same detection point. The detector demonstrates simultaneous multiwavelength detection of medicines for both HPLC and CE. This development represents an advancement in portable, low-cost analytical instrumentation, with broad implications for various fields of application.

A nitrogen-specific detector for high performance liquid chromatography

We describe a nitrogen-specific detector (NSD) for aqueous mobile phase-based high performance liquid chromatography (HPLC). It is based by means of total hydrophilic organic nitrogen detection. Separated analytes are photooxidized online and converted to nitrate, followed by an ultravilet absorbance detector. It features response dependant on the product of nitrogen number in the molecule and its molar concentration, no matter what is ultravilet-absorbing or not. The HPLC equipped with NSD can quantify nitrogen-containing analytes via a sole standard of potassium nitrate for calibration. This results in identical calibration curve for all nitrogen-containing analytes, obviating individual calibration. The limit of detection of NSD is 4.3 μM N/L, and its linear range is up to 4 mM N/L.

Inhibitory effects of cold plasma-activated water on the generation of advanced glycation end products and methylimidazoles in cookies and mechanistic evaluation using electron paramagnetic resonance

The inhibitory effects of cold plasma-activated water (PAW) on the formation of AGEs and methylimidazoles in cookies was examined. The results showed that different PAW (parameters: 50 W–50 s, 50 W–100 s, 50 W–150 s, 100 W–50 s, 100 W–100 s, and 100 W–150 s) reduced the contents of AGEs and methylimidazoles, in which the maximum inhibition rates were 47.38% and 40.17% for free and bound AGEs and 44.16% and 40.31% for free and bound methylimidazoles, respectively. Moreover, the mechanisms associated with the elimination of carbonyl intermediates and free radicals was determined by electron paramagnetic resonance (EPR) and high performance liquid chromatography-ultraviolet/visible absorption detector (HPLC-UV/Vis). The results showed the quenching of total free radicals, alkyl free radicals, and HO· by PAW, leading to the suppression of glyoxal and methylglyoxal intermediates. These findings support PAW as a promising agent to enhance the safety of cookies.

Using absorbance detection for hs-SV-AUC characterization of adeno-associated virus

Data are presented demonstrating that absorbance detection can be used during high-speed sedimentation velocity analytical ultracentrifugation (hs-SV-AUC) experiments to characterize the size distribution of adeno-associated virus (AAV) drug products accurately. Advantages and limitations of being able to use this detector in this specific type of SV-AUC experiment are discussed.

MALS discovery of a rare H I 21 cm absorber at z ∼ 1.35: Origin of the absorbing gas in powerful active galactic nuclei

We report a new, rare detection of H I 21 cm absorption associated with a quasar (only six quasars are known at 1 < z < 2) toward J2339−5523 at zem = 1.3531, discovered through the MeerKAT Absorption Line Survey (MALS). The absorption profile is broad (∼400 km s−1 ), and the peak is redshifted by ∼200 km s−1 from zem. Interestingly, optical/far-UV spectra of the quasar from the Magellan-MIKE/HST-COS spectrographs do not show any absorption features associated with the 21 cm absorption, despite the coincident presence of the optical quasar and the radio core inferred from a flat-spectrum component with a flux density of ∼65 mJy at high frequencies (> 5 GHz). The simplest explanation would be that no large H I column (N(H I) > 1017 cm−2) is present toward the radio core and the optical active galactic nucleus. Based on the joint optical and radio analysis of a heterogeneous sample of 16 quasars (zmedian = 0.7) and 19 radio galaxies (zmedian = 0.4) with H I 21 cm absorption detection and matched in 1.4 GHz luminosity (L1.4 GHz), a consistent picture emerges according to which quasars primarily trace the gas in the inner circumnuclear disk and cocoon created by the interaction of the jet with interstellar medium. They (i.e., quasars) exhibit a L1.4 GHz – ΔVnull correlation and a frequent mismatch of the radio and optical spectral lines. The radio galaxies show no such correlation and likely trace the gas from the cocoon and the galaxy-wide interstellar medium outside the photoionization cone. The analysis presented here demonstrates the potential of radio spectroscopic observations to reveal the origin of the absorbing gas associated with active galactic nuclei that may be missed in optical observations.

Analytical Determination of Aflatoxin in Ground Corn Check Samples Completed by Multiple Laboratories over Several Years.

Mycotoxins are toxic molecules produced by multiple fungal species, including Aspergillus and Fusarium. Fungal infection of crops can result in mycotoxins entering the animal and human food supply. Enzyme-linked immunosorbent assays and other immunological assays have been developed to detect mycotoxins in foods. To calibrate the response of those methods, reference materials with known amounts of homogeneously dispersed mycotoxins are often utilized, where the mycotoxin concentrations have been determined using high-performance liquid chromatography coupled with absorbance or fluorescence detection methods, or high-performance liquid chromatography coupled with mass spectrometry detection methods. Therefore, it is important that the analytical methods provide accurate and precise quantitation of mycotoxins. The reference materials must also contain homogeneously dispersed known quantities of mycotoxin. To evaluate the accuracy and precision of mycotoxin reference materials and the analytical methods, quantitative results from multiple laboratories were completed each year for several years on ground corn check samples containing known levels of mycotoxins. Results for the quantitation of aflatoxin-containing corn reference samples are presented in this article.