CL Emission Research Articles

Enhanced chemiluminescence with sub-1 nanometer CuO-PMA nanosheets for the sensitive detection of quercetin

BackgroundChemiluminescence (CL) analysis, characterized by its simple instrumentation, high signal-to-noise ratio, wide linear range, and minimal background interference, has garnered increasing attention from researchers. Nanomaterials (NMs) have been explored to enhance CL intensity. Notably, sub-1 nanometer scale NMs are considered to hold significant untapped potential due to their size effects. The application of these sub-1 nanometer NMs in enhancing CL is anticipated to yield favorable results. Additionally, the low water solubility and bioavailability of quercetin glycosides lead to their presence in bodily fluids at only trace levels, highlighting the urgent need for efficient and rapid detection methods. ResultsIn this work, phosphomolybdic acid (PMA) was incorporated into CuO to synthesize sub-1 nanometer CuO-PMA nanosheets (SNSs) using a cluster-core co-assembly strategy. Conformational and structural characterization confirmed the successful synthesis of these nanosheets. The CuO-PMA SNSs were employed to enhance the CL emission of the luminol-H2O2 system, resulting in an increase of over 1000 times. The catalytic properties of CuO-PMA SNSs significantly facilitated the decomposition of H2O2, leading to an enhanced production of reactive oxygen species, which in turn induced the CL enhancement. Given that the antioxidant effect of quercetin would consume the reactive oxygen species generated during the catalysis, a decrease in CL intensity was anticipated. A CL sensor for quercetin detection was developed based on the CuO-PMA SNSs-luminol-H2O2 system, demonstrating a strong linear relationship (R2 = 0.9969) and a low detection limit of 0.31 nM. SignificanceThis research provides a strategy to enhance the CL intensity of the luminol-H2O2 system by using CuO-PMA SNSs, offering a highly sensitive assay for detecting quercetin concentrations. The method is characterized as a simple and cost-effective analytical strategy making CL analysis very attractive for chemical analysts.

Cathodoluminescent and Characteristic X-Ray-Emissive Rare-Earth-Doped Core/Shell Protein Labels for Spectromicroscopic Analysis of Cell Surface Receptors.

Understanding the localization and the interactions of biomolecules at the nanoscale and in the cellular context remains challenging. Electron microscopy (EM), unlike light-based microscopy, gives access to the cellular ultrastructure yet results in grey-scale images and averts unambiguous (co-)localization of biomolecules. Multimodal nanoparticle-based protein labels for correlative cathodoluminescence electron microscopy (CCLEM) and energy-dispersive X-ray spectromicroscopy (EDX-SM) are presented. The single-particle STEM-cathodoluminescence (CL) and characteristic X-ray emissivity of sub-20 nm lanthanide-doped nanoparticles are exploited as unique spectral fingerprints for precise label localization and identification. To maximize the nanoparticle brightness, lanthanides are incorporated in a low-phonon host lattice and separated from the environment using a passivating shell. The core/shell nanoparticles are then functionalized with either folic (terbium-doped) or caffeic acid (europium-doped). Their potential for (protein-)labeling is successfully demonstrated using HeLa cells expressing different surface receptors that bind to folic or caffeic acid, respectively. Both particle populations show single-particle CL emission along with a distinctive energy-dispersive X-ray signal, with the latter enabling color-based localization of receptors within swift imaging times well below 2 min per 2 while offering high resolution with a pixel size of 2.78 nm. Taken together, these results open a route to multi-color labeling based on electronspectromicroscopy.

Glow-type luminol chemiluminescence based on a supramolecular enhancer of cyclodextrin

BackgroundChemiluminescence (CL) bioassay is one of the most advanced and used detection method in clinical diagnosis and biomedical research because of the advantages of low background, easy operation, and wide-field imaging without a light source or microscope. The luminol/hydrogen peroxide/horseradish peroxidase (luminol/H2O2/HRP) system is the most popular CL system, but its application in high-throughput imaging detection is challenged due to its low luminescence efficiency and flash-type emission which is difficult in ensuring the reproducibility and consistency of detection results. ResultsWe reported a glow-type CL system of luminol@CD/H2O2/HRP by using a supramolecular enhancer of cyclodextrin (CD). This luminol@CD/H2O2/HRP system exhibited a luminescence lifetime of 41 min for sensitive and accurate imaging analysis. The long-lasting CL emission was attributed to the formation of a 1:1 host–guest complex between luminol and CD, which could stabilize the emitter and effectively reduce nonradiative relaxation. The formation of luminol@CD complex was determined through NMR experiments and theoretical analysis. Under optimum conditions, the luminol@CD/H2O2/HRP system showed higher sensitivity and much better precision than classical luminol/H2O2/HRP system for imaging detection of HRP. Especially, this glow-type luminol@CD/H2O2/HRP system realized CL imaging of microwell arrays on microfluidic chips. In addition, the luminol@CD/H2O2/HRP system was successfully applied for point-of-care detection of 17β-estradiol based on a competitive mechanism of host–guest recognition. SignificanceAn efficient CL system is crucial for obtaining reproducible and consistent results for accurate detection. Our luminol@CD/H2O2/HRP system emitted strong and persistent luminescence, resulting in reliability and efficiency at both CL macroscopic and microscopic imaging detection. We expected the luminol@CD/H2O2/HRP CL system to be applied in various detection fields.

Cobalt-Modified Black Phosphorus Nanosheets-Enabled Ferrate (VI) Activation for Efficient Chemiluminescence Detection of Thiabendazole.

The development of chemiluminescence-based innovation sensing systems and the construction of a sensing mechanism to improve the analytical performance of compounds remain a great challenge. Herein, we fabricated an advanced oxidation processes pretreated chemiluminescence (AOP-CL) sensing system via the introduction of cobalt-modified black phosphorus nanosheets (Co@BPNs) to achieve higher efficient thiabendazole (TBZ) detection. Co@BPNs, enriched with lattice oxygen, exhibited a superior catalytic performance for accelerating the decomposition of ferrate (VI). This Co@BPNs-based ferrate (VI) AOP system demonstrated a unique ability to selectively decompose TBZ, resulting in a strong CL emission. On this basis, a highly selective and sensitive CL sensing platform for TBZ was established, which exhibited strong resistance to common ions and pesticides interference. This was successfully applied to detecting TBZ in environmental samples such as tea and kiwi fruits. Besides, the TBZ detection mechanism was explored, Co@BPNs-based ferrate (VI) AOP system produced a high yield of ROS (mainly 1O2), which oxidized the thiazole-based structure of TBZ, generating chemical energy that was transferred to Co@BPNs via a chemical electron exchange luminescence (CIEEL) mechanism, leading to intense CL emission. Notably, this study not only proposed an innovative approach to enhance the chemical activity and CL properties of nanomaterials but also offered a new pathway for designing efficient CL probes for pollutant monitoring in complex samples.

Bifunctional MOF-Encapsulated Cobalt-Doped Carbon Dots Nanozyme-Powered Chemiluminescence/Fluorescence Dual-Mode Detection of Aflatoxin B1.

A novel bifunctional MOF-encapsulated cobalt-doped carbon dots nanozyme (Co-CD/PMOF) with excellent peroxidase-mimic catalytic activity and fluorescence property was synthesized and employed to fabricate a chemiluminescence/fluorescence (CL/FL) dual-mode immunosensor for AFB1 detection. Co-CD/PMOF could catalyze the luminol/H2O2 system to generate robust and long-lasting CL signals due to the slow diffusion effect and continuous generation of •OH, O2•-, and 1O2 species. Differing from traditional flash-type CL emissions, this glow-type CL emission is helpful to fabricate a sensitive and accurate CL sensing platform. Then the CL/FL dual-mode detection of AFB1 was developed using antibody-functionalized Co-CD/PMOF as the signal-amplifying nanoprobe. The CL mode assay based on indirect competitive immune principle was carried out on a chemiluminescence optical fiber platform, where the AFB1-OVA-functionalized optical fiber probe was employed for biorecognition, separation, and signal conducting. The AFB1 detection range and LOD were 0.63-69.36 ng/mL and 0.217 ng/mL, respectively. Using AFB1 antibody-functionalized immunomagnetic beads for capturing and separation, the FL mode detection of AFB1 was established based on the sandwich immune principle. A linear range of 0.54-51.91 ng/mL and a LOD of 0.027 ng/mL were obtained. This work designed a sensitive, rapid, and reliable nanozyme-powered dual-mode assay strategy and provided technical support in the field of environmental monitoring and food safety.

Cathodoluminescence differentiates sedimentary organic matter types

High-resolution scanning electron microscopy (SEM) visualization of sedimentary organic matter is widely utilized in the geosciences for evaluating microscale rock properties relevant to depositional environment, diagenesis, and the processes of fluid generation, transport, and storage. However, despite thousands of studies which have incorporated SEM methods, the inability of SEM to differentiate sedimentary organic matter types has hampered the pace of scientific advancement. In this study, we show that SEM-cathodoluminescence (CL) properties can be used to identify and characterize sedimentary organic matter at low thermal maturity conditions. Eleven varied mudstone samples with a broad array of sedimentary organic matter types, ranging from the Paleoproterozoic to Eocene in age, were investigated. Sedimentary organic matter fluorescence intensity and CL intensity showed an almost one-to-one correspondence, with certain exceptions in three samples potentially related to radiolytic alteration. Therefore, because CL emission can be used as a proxy for fluorescence emission from sedimentary organic matter, CL emission during SEM visualization can be used to differentiate fluorescent from non-fluorescent sedimentary organic matter. This result will allow CL to be used as a visual means to quickly differentiate sedimentary organic matter types without employing correlative optical microscopy and could be widely and rapidly adapted for SEM-based studies in the geosciences.

Structural, morphological and luminescence properties of hafnia nanoparticles obtained by hydrothermal synthesis

Hafnia is a novel material for optoelectronic applications, fabrication methods are focused to obtain hafnium oxide nanomaterials included thin films and nanoparticles. HfO2 nanoparticles synthesized and studied in this work are crystalline without subsequent heat treatment and were processed by hydrothermal method at 200 °C during 1.3, 2 and 4 h. SEM and TEM analysis revealed the presence of spherical and oval nanoparticles, with range size from 60 to 70 nm and 90–110 nm for spherical and oval nanoparticles, respectively. Raman spectroscopy and X-ray diffraction confirmed that nanoparticles exhibit a stable monoclinic phase. Crystal growth is typical with the presence of the characteristic monoclinic plane (1‾11) but for reaction times of 2 and 4 h and pH over 12 it turns in the plane (220) which is perpendicular to typical growth. Cathodoluminescence measurements revealed strong blue emission intensity showing a broadband in all visible range and a maximum peak at 460 nm. The presences of VO3 and VO4 in HfO2 crystalline structure are responsible for this inherent CL emission corroborated by photoluminescence studies.

Interpretation of the effects of anthropogenic chlorine on nitrate formation over northeast Asia during KORUS-AQ 2016

The Weather Research and Forecasting–Community Multiscale Air Quality (WRF-CMAQ) model, implemented with anthropogenic chlorine (Cl) emissions, was evaluated against ground and NASA DC-8 aircraft measurements during the Korea-United States Air Quality (KORUS-AQ) 2016 campaign. The latest anthropogenic Cl emissions, including gaseous HCl and particulate chloride (pCl−) emissions from the Anthropogenic Chlorine Emissions Inventory of China (ACEIC-2014) (over China) and a global emissions inventory (Zhang et al., 2022) (over outer China), were used to examine the impacts of Cl emissions and the role of nitryl chloride (ClNO2) chemistry in N2O5 heterogeneous reactions on secondary nitrate (NO3−) formation across the Korean Peninsula. The model results against aircraft measurements clearly showed significant Cl- underestimations due mainly to the high gas-particle (G/P) partitioning ratios at aircraft measurement altitudes such as 700–850 hPa, but the ClNO2 simulations were reasonable. Several simulations of CMAQ-based sensitivity experiments against ground measurements indicated that although addition of Cl emission did not significantly alter NO3− formation, the activated ClNO2 chemistry with Cl emissions showed the best model performance with the reduced normalized mean bias (NMB) of 18.7 % compared to a value of 21.1 % for the Cl emissions-free case. In our model evaluation, ClNO2 accumulated during the night but quickly produced Cl radical due to ClNO2 photolysis at sunrise, which modulated other oxidation radicals (e.g., ozone [O3] and hydrogen oxide radicals [HOx]) in the early morning. In the morning hours (0800–1000 LST), the HOx were the dominant oxidants, contributing 86.6 % of the total oxidation capacity (sum of major oxidants such as O3 and HOx species), while oxidability was enhanced by up to ∼6.4 % (increase in 1 h HOx average of 2.89 × 106 molecules·cm−3) in the early morning mainly due to the changes in OH (+7.2 %), hydroperoxyl radical (HO2)(+10.0 %), and O3 (+4.2 %) over the Seoul Metropolitan Area, during the KORUS-AQ campaign. Our results improve understanding of the atmospheric changes in the PM2.5 formation pathway caused by ClNO2 chemistry and Cl emissions over northeast Asia.

Chemiluminescence sensor array for oxidase discrimination based on ternary transition metal sulfide

Simultaneous discrimination of multiple enzymes in clinical diagnosis is significance and remains a great challenge. Herein, we reported a facile synthesis of three ternary transition metal sulfide (TTMS) nanoparticles, i.e. FeCo2S4, CuCo2S4 and FeCu2S4, by using L-cysteine as sulphur source for oxidase discrimination. The CL emission from luminol oxidation by hydrogen peroxide (H2O2) was greatly enhanced by TTMS, with the maximal three orders of magnitude CL signal amplification for FeCo2S4. Hence, an ultra-sensitive CL assay was developed for H2O2 detection down to 0.5 pM. Because H2O2 is generated via biocatalytic reaction between substrate and corresponding oxidase, thus, CL sensor arrays can be developed to discriminate different oxidases. The sensing principle is based on the fact that different substrates/oxidases produced different amounts of H2O2. For each substrate/oxidase couple, the sensor array produces a peculiar CL intensity pattern able to be distinguished via linear discriminant analysis. As a proof-of-concept study, four oxidases, i.e. glucose-, sarcosine-, choline- and cholesterol-oxidase, were selected to demonstrate the array’s discrimination performance and were identified successfully with an accuracy of 100%, and achieved the accurate discrimination of oxidases in serum samples. This work demonstrated the potential of the TTMS-based CL sensor array to discriminate multiple oxidases.

High-Contrast Visualization Chemiluminescence Based on AIE-Active and Base-Sensitive Emitters.

Peroxyoxalate chemiluminescence (PO-CL) is one of the most popular cold light sources, yet the drawback of aggregation-caused quenching limits their use. Here, we report a new kind of efficient bifunctional emitter derived from salicylic acid, which not only exhibits typical aggregation-induced emission (AIE) character but also has the ability to catalyze the CL process under basic conditions based on base sensitivity. By taking advantage of these unique features, we successfully confine the CL process on the surface of solid bases and provide a high-contrast visualization of CL emission. This method allows most of the common basic salts like sodium carbonate to be invisible encryption information ink and PO-CL solution to be a decryption tool to visualize the hidden information. The current study opens up an appealing way for the development of multifunction CL emitters for information encryption and decryption applications.

Comparing the effect of electron beam, beta and ultraviolet C exposure on the luminescence emission of commercial dosimeters

This paper reports on the luminescence characterization of TLD-100 (LiF: Ti, Mg), TLD-200 (CaF2: Dy), TLD-400 (CaF2: Mn) and GR-200 (LiF: Mg, Cu, P) dosimeters exposed to electro beam, beta and ultraviolet C radiation -UVC-. All of them show high sensitivity to radiation regardless of whether it is ionizing or partially ionizing radiation based on their luminescence properties (cathodoluminescence -CL- or thermoluminescence -TL-). CL emission differs significantly among them in shape and intensity due to their chemical compositions. LiF samples display three maxima at: (i) 300–450 nm linked to intrinsic and structural defects, (ii) a green waveband probably due to F3+ centres or the presence of hydroxyl groups and (iii) the red-infrared emission band associated with F2 centres. However, CL spectra from the CaF2 dosimeters display meaningful differences due to the dopant. TLD-200 is characterized by an emission with four sharp individual peaks in the green-IR spectral region (due to the Dy3+), whilst TLD-400 exhibits a broad maximum peaked at ̴500 nm (linked to the Mn2+). On the other hand, the variation in the TL glow curves allows to discriminate the TLDs exposed to beta and UVC radiation since they give rise to different chemical-physical processes and that have been studied from the estimation of the kinetic parameters by means of the Computerised Glow Curve Deconvolution (CGCD) method.

A Catalog of 71 Coronal Line Galaxies in MaNGA: [Ne v] Is an Effective AGN Tracer

Despite the importance of active galactic nuclei (AGNs) in galaxy evolution, accurate AGN identification is often challenging, as common AGN diagnostics can be confused by contributions from star formation and other effects (e.g., Baldwin–Phillips–Terlevich diagrams). However, one promising avenue for identifying AGNs is “coronal emission lines” (“CLs”), which are highly ionized species of gas with ionization potentials ≥100 eV. These CLs may serve as excellent signatures for the strong ionizing continuum of AGNs. To determine if CLs are in fact strong AGN tracers, we assemble and analyze the largest catalog of optical CL galaxies using the Sloan Digital Sky Survey's Mapping Nearby Galaxies at Apache Point Observatory (MaNGA) catalog. We detect CL emission in 71 MaNGA galaxies, out of the 10,010 unique galaxies from the final MaNGA catalog, with ≥5σ confidence. In our sample, we measure [Ne v]λ3347, λ3427, [Fe vii]λ3586, λ3760, λ6086, and [Fe x]λ6374 emission and crossmatch the CL galaxies with a catalog of AGNs that were confirmed with broad-line, X-ray, IR, and radio observations. We find that [Ne v] emission, compared to [Fe vii] and [Fe x] emission, is best at identifying high-luminosity AGNs. Moreover, we find that the CL galaxies with the least dust extinction yield the most iron CL detections. We posit that the bulk of the iron CLs are destroyed by dust grains in the galaxies with the highest [O iii] luminosities in our sample, and that AGNs in the galaxies with low [O iii] luminosities are possibly too weak to be detected using traditional techniques.

Effect of Nd3+ Doping on Structural, Near-Infrared, and Cathodoluminescent Properties for Cadmium Tantalate Phosphors

Cd1-xTa2O6:xNd3+ (x=0.5, 1.5, 3, 5, 7, and 10 mol%) phosphor series were fabricated by conventional solid state method at 1100 °C for 17 hours. The samples of cadmium tantalate were investigated by structural (XRD, SEM) and spectroscopic (CL, PL) analyses. In XRD results, the symmetry of CdTa2O6 phase with orthorhombic columbite structure was confirmed between 0.5 and 10 mol% Nd3+ doping concentrations. SEM analysis of the grains revealed round and shapeless morphology while grain sizes ranged from submicron to several microns. The emission spectra of Cd1-xTa2O6:xNd3+ (x=0.5, 1.5, 3, 5, 7 and 10 mol%) phosphor series recorded with the transitions of 4F3/2→4I9/2 and 4F3/2→4I11/2. Among these transitions, the transition 4F3/2→4I9/2 (at 889 nm) has a high near-infrared emission intensity, which can be attributed to the laser potential of the phosphor. The NIR emission of the phosphor increased with increasing concentration of Nd3+ up to 5 mol% and then declined because of concentration quenching phenomenon. The CL emission peak at about 450 nm found in all samples is related to the intrinsic emission of the cadmium tantalate host. In addition, Nd3+ doped phosphors exhibited the 4F3/2→4I9/2 transition of Nd3+ and defect-related CL emissions at 670 nm. Decreasing crystallinity with increasing Nd3+ concentration caused a decrease in host emission intensity at 450 nm.

High resolution imaging of ultrafine bubbles in water by Atmospheric SEM-CL

Various analytical methods such as high-resolution observation of ultrafine bubbles in water are required to clarify the mechanisms and interrelationships of various effects brought about by ultrafine bubbles. In this study, we used atmospheric scanning electron microscopy-cathodoluminescence (ASEM-CL) method for observing ultrafine bubbles in water. ASEM can observe samples in water, and the fine electron beam provides high spatial resolution. Furthermore, the gas in the bubble can be estimated from the CL emission spectrum. We have measured characteristics such as bubble size and particle number density. Also, the CL spectra has shown that the ultrafine bubbles contained nitrogen.

Behavior of coal-chlorine in chemical looping combustion

This work focuses on two aspects: (i) the behavior of coal-derived chlorine in chemical looping combustion (CLC); (ii) the potential adverse impacts of primary gaseous chlorine (i.e., HCl) on Cu-based oxygen carrier (OC). The inactivation mechanism of the sol-gel-derived CuO/Al2O3 OC is investigated. Systematic experiments are conducted in a batch fluidized reactor. First, in CLC of coal, chlorine distribution including HCl, Cl2, Cl adsorbed in the outlet tube and Cl in solid phase is studied under various bed inventories, temperatures and gas atmospheres. The main gaseous Cl from coal is HCl, which shows a high reactivity towards CuO and is partially physically adsorbed by Al2O3. Unconverted HCl is 15.63 ± 0.20%, which could result in corrosion of the CO2 transportation line and compression equipment. What's more, the coal ash exhibits a dechlorination function by forming KCl and CaCl2. The CO2 atmosphere and high temperature in fuel reactor show a promotion on the conversion of coal-Cl to HCl. Then, the corrosion of various OC components is evaluated by a mixture gas with 400 ppm HCl, i.e., Cu-Al (whole OC), CuO (active phase) and Al2O3 (inert support phase). It is found that a part of HCl is converted to Cl2 via the Deacon reaction (4HCl + O2 = 2H2O + 2Cl2) and oxidized by CuO (2CuO + 4HCl = 2CuCl + Cl2 + 2H2O). At the high concentration of HCl (400 ppm) atmosphere, CuO is partially lost from the OC, producing the gaseous copper chlorides, i.e., CuCl and (CuCl)3, which are found to be condensed in the outlet tube. Besides, the solid-phase copper chlorides also degrade the oxygen donation capacity of the OC. Finally, the migration path of coal-chlorine during CLC is summarized. This work will contribute to the development of Cl-resistance OCs and control approaches for Cl emission.

Quantification of dimethoate and chlorpyrifos residues in green leafy vegetables by laser-induced breakdown spectroscopy

The presence of pesticide residues in food represents a significant threat to consumers, mainly due to their toxicity to humans. Evidence has even been found that determines the relationship between many diseases and deaths from ingestion, contact, or mishandling. The need to introduce controls on pesticide residues has become an issue of central concern to society, given the increasing knowledge about the potential dangers associated with the use of pesticides. So the objective of the present study was to evaluate and analyze the feasibility of using the laser-induced breakdown spectroscopy technique as a potential tool for the quantification of dimethoate and chlorpyrifos in green leafy vegetables. For this purpose, reference samples with powdered chard were made using the aforementioned pesticides, with increasing concentrations in a range of 0–80 mg kg−1 and 0–250 mg kg−1, respectively. By applying calibration curves, it was possible to quantify pesticide residues by measuring S (416.26 nm), P (460.21 nm), and Cl (837.59 nm) emission lines, with limits of detection of 1.7 mg kg−1, 0.8 mg kg−1, and 6.9 mg kg−1 respectively. Clear evidence of the applicability of this technique as a potential tool for the study of pesticides in food matrices was established. It was achieved by minimum sample preparation, ensuring a rapid analysis, low application costs, and without toxic waste production. In this way, its use as a preliminary evaluation technique or complementary to the analytical methods traditionally already used is evidenced.

BASS. XXVIII. Near-infrared Data Release 2: High-ionization and Broad Lines in Active Galactic Nuclei* * Based on observations collected under programs 086.B-0135(A), 089.B-0951(A), 090.A-0830(A), 091.B-0900(B), 093.A-0766(A), 098.A-0635(B), 099.A-0403(B), 0101.A-0765(A), and 0102.A-0433(A) with X-shooter at the Very Large Telescope of the Paranal Observatory in Chile, operated by the European Southern Observatory.

We present the BAT AGN Spectroscopic Survey (BASS) Near-infrared Data Release 2 (DR2), a study of 168 nearby ( z¯=0.04 , z < 0.6) active galactic nuclei (AGN) from the all-sky Swift Burst Array Telescope X-ray survey observed with the Very Large Telescope (VLT)/X-shooter in the near-infrared (NIR; 0.8–2.4 μm). We find that 49/109 (45%) Seyfert 2 and 35/58 (60%) Seyfert 1 galaxies observed with VLT/X-shooter show at least one NIR high-ionization coronal line (CL; ionization potential χ > 100 eV). Comparing the emission of the [Si vi] λ1.9640 CL with the X-ray emission for the DR2 AGN, we find a significantly tighter correlation, with a lower scatter (0.37 dex) than that for the optical [O iii] λ5007 line (0.71 dex). We do not find any correlation between CL emission and the X-ray photon index Γ. We find a clear trend of line blueshifts with increasing ionization potential in several CLs, such as [Si vi] λ1.9640, [Si x] λ1.4300, [S viii] λ0.9915, and [S ix] λ1.2520, indicating the radial structure of the CL region. Finally, we find a strong underestimation bias in black hole mass measurements of Sy 1.9 using broad Hα due to the presence of significant dust obscuration. In contrast, the broad Paα and Paβ emission lines are in agreement with the M–σ relation. Based on the combined DR1 and DR2 X-shooter sample, the NIR BASS sample now comprises 266 AGN with rest-frame NIR spectroscopic observations, the largest set assembled to date.

Back Cover Image: Volume 3 Issue 2

Back cover image: Highly biocompatible and self-illuminating carbon nanogels (CNGs) with dual ability of ROS imaging and PDT have been designed with self-assembled chemiluminescent carbonized polymer dots (CPDs). Different CPDs have been derived from biomass materials and exhibit polymer-like property, enabling their ability of self-assembling into CNGs through the hydrophilic and hydrophobic interaction. With efficient deep-red/near-infrared (NIR) CL emission and distinctive PDT capacity, H2O2-driven water-soluble chemiluminescent carbon nanogels are further designed by assembling the polymeric conjugate and CL donors. Mechanistically, ROS generated in the inflammatory sites can trigger the chemically initiated electron exchange luminescence between the CPDs and intermediate, enabling in vitro and in vivo CL imaging. Meanwhile, the production of such as 1O2, •OH and •–O2 from the chemiluminescent CNGs under the self-illumination can efficiently induce the apoptosis of tumor cell thus inhibit the tumor growth, resulting in cancer therapy. (DOI: 10.1002/smm2.1099)

Chemiluminescence Studies Using Some Non Steroidal Anti-Inflammatory Drugs with Benzoyl Hydroperoxide

The oxidation of luminol with benzoyl hydroperoxide (BzOOH) in alkaline medium was studied. The reaction occurring between luminol and benzoyl hydroperoxide in alkaline medium leads to the production of nitrogen gas with simultaneous emission of CL. The effect of non-steroidal anti-inflammatory drugs (NSAIDS) like diclofenac sodium, analgin &amp; paracetamol has also been studied. The time dependence of the CL intensity of luminol and benzoyl hydroperoxide at different temperature and the CL emission spectra of the reactions have been recorded for better understanding of the reaction.

Chlorine emission characteristics and control status of coal-fired units

Chlorine is a harmful trace element in coal. During coal combustion, the chlorine undergoes complex changes and transfers to the gas, and forms chlorine-containing substances. This paper summarizes the field test data of chlorine emission from domestic coal-fired units, and analyzes the chlorine emission and control characteristics. The results show that during the combustion process, the chlorine in coal is released into flue gas, mainly HCl, and a small amount of Cl2 and particulate Cl. Conventional pollutant control facilities affect the form and concentration of Cl. The impact of dust removal facilities on Cl is mainly reflected in the coordinated removal of particulate Cl. The impact of wet desulfurization facilities on Cl is mainly reflected in the coordinated removal of HCl. The Cl emission concentration in flue gas of coal-fired units is 0.85 mg/m3, which meets the emission requirements. Chlorine is transferred from coal to fly ash, desulfurization wastewater and desulfurization gypsum, so the secondary pollution of chlorine should be paid much attention. HCl in coal-fired flue gas has an adverse effect on wet desulfurization facilities. Based on the material balance of chloride ions in absorption tower slurry, this paper proposes a technical idea for removing HCl from flue gas with alkaline absorbents.