Concentration Detection Limit Research Articles

Metal-organic framework derived cobalt and iron oxide nanosheets for ppb-concentration and highly selective hydrogen sulfide sensing

Hydrogen sulfide (H2S) sensing with ppb concentration detection limit and high selectivity is highly desired in future exhaled diagnoses of halitosis, asthma and down syndrome, however, needs further developing. Here, a ppb-concentration and highly selective H2S sensing has been developed with the two-dimensional cobalt and iron oxide nanosheets (CoFexOy NSTs), which is transformed from leaf-shaped zeolitic imidazolate frameworks {ZIF-L(Co)} by combined Fe2+ ion-etching and annealing. Typically, as-prepared CoFexOy NSTs are of ∼ 10 nm thick with rough surface. Beneficially, the CoFexOy NSTs present outstanding selectivity to H2S against other interfering gases and exhibit a detection limit as low as 50 ppb. Remarkably, the sensor prototypes exhibit high response to 10 ppm H2S (Ra/Rg = 23.8) and fast response speed (∼13 s to 10 ppm H2S). Theoretically, such excellent H2S sensing might be attributed to the high surface ratio of CoFexOy NSTs providing enriched adsorption sites for H2S molecules. Practically, a H2S sensing device built with the CoFexOy NSTs sensor prototype is simulated for detecting H2S with reliable response, which is potential in future intelligent healthcare.

Enhanced luminol chemiluminescence with oxidase-like properties of prussian blue/MXene nanocomposite without H2O2 for the sensitive detection of uric acid

Novel two-dimensional MXene materials as low-cost carriers have received increasing attention in the development of nanozymes with peroxidase or oxidase-like activities. In this study, the novel materials combining Prussian blue and MXene (referred to as PB/MXene) were proposed by a facile method. In this case, MXene acted as reducing agent and nanocarrier. Compared with the single component, the obtained nanocomposites had excellent oxidase activity without foreign oxidant intervention such as hydrogen peroxide (H2O2). Furthermore, the addition of uric acid (UA) solution was able to directly burst the chemiluminescence (CL) intensity of the constructed PB/MXene-luminol platform. Based on the above process, we developed PB/MXene nanocomposites with oxidase activity as the CL biosensors for detecting UA, displaying good linearity with UA concentration (0.2–30 μM) and low detection limit (0.19 μM). This work not only provided novel biosensors for the detection of UA but also significantly expanded the potential applications of MXene-based functional materials in the fields of biological monitoring and clinical diagnosis.

In Situ growth of high-crystallinity MOF@CTF core-shell hybrid heterostructures and their application in photoelectrochemical sensing of vancomycin

Vancomycin is a first-line drug for the treatment of methicillin-resistant Staphylococcus aureus (MRSA) and multidrug-resistant bacterial infections. It is of great significance to develop rapid detection methods for vancomycin in different matrices. In this work, a novel method for the in-situ preparation of MOF@CTF core-shell hybrid heterogeneous structures was proposed and applied to the photoelectrochemical detection of vancomycin. The insolubility of the imine precursor structure in homogeneous solvents and the Lewis acidic centers in the MOF structure induced the initial arrangement of CTF on the surface of PCN-224. By encapsulating a layer of highly crystalline CTF structure onto the initial morphology of PCN-224, a MOF@CTF heterogeneous structure was formed. Importantly, the introduction of anthracene-based electron-donating groups into the CTF structure and the formation of a donor-acceptor system with triazine rings enhanced the photoconversion efficiency of the heterogeneous structure by establishing a continuous separated built-in electric field within the core-shell structure. The successful in-situ synthesis of the core-shell hybrid heterogeneous structure was confirmed through microscopic morphology, PXRD, XPS, and FT-IR. Furthermore, investigations into the semiconductor properties of the heterogeneous structure, including semiconductor type, bandgap, and photo-voltage, were conducted. Results showed that the heterogeneous structure exhibited a doubled photocurrent density compared to the original PCN-224. Additionally, a molecularly imprinted photoelectrochemical sensor (MIPECS) for vancomycin was constructed. Under optimized conditions, the sensor demonstrated a superior concentration response range (0.1 nM - 1 μM) and detection limit (0.031 nM, 3σ/S, n = 11). Simultaneously, the potential applicability of the sensor in animal-derived foods, serum, and environmental water samples was evaluated, yielding satisfactory results.

CuO-ZIF-8 modified electrode surface as a new electrochemical sensing platform for detection of free chlorine in aqueous solution

This work has applied metal–organic frameworks (MOFs) with high adsorbability and catalytic activity to develop electrochemical sensors to determine free chlorine (free-Cl) concentrations in aqueous media. A zeolitic imidazolate frameworks, Zn(Hmim)2 (ZIF-8) has been synthesized and incorporated with CuO nanosheets to decorate a glassy carbon electrode (GCE) and provide a new sensor for free-Cl determination. The as-prepared ZIF-8 and CuO-ZIF-8 composites have been characterized by FESEM, EDX, XRD, and FT-IR analyses. Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) utilized to characterize the CuO-ZIF-8/GC modified electrode electrochemically, demonstrated the ability of the sensor to measure free-Cl concentration. Using differential pulse voltammetry (DPV) and under the optimal conditions, the prepared CuO-ZIF-8/GC modified electrode showed a linear response in the 0.25–60 ppm range with a 12 ppb detection limit (LOD) for free-Cl concentration. Finally, the fabricated sensor was applied to analyze free-Cl from actual swimming pool water samples with promising 97.5 to 103.0% recoveries.

Hierarchically In2S3@In2O3 nanorods heterojunctions for enhanced NO2 sensing at lower operating temperature

Hierarchically structured In2S3@In2O3 nanorods were synthesized via a two-step hydrothermal method. Compared to single-component In2O3 based sensors, the as-developed In2S3@In2O3 nanorods based chemiresistive-type sensor exhibited significantly enhanced response and reduced operating temperature. The sensor displayed a response of approximately 51.2 to 3 ppm NO2 at 120℃, with a response time and recovery time of 76 and 48 seconds, respectively, and a detection limit of NO2 concentration to 0.014 ppm. By constructing In2S3@In2O3 heterojunctions, the optimal operating temperature has been effectively lowered from 160℃ to 120℃. The improved sensing performance is attributable to the nano-heterojunctions formed between In2S3 and In2O3, which increase the specific surface area to provide additional active adsorption sites, and as well, prevent the shielding effect of surface-adsorbed oxygen on NO2. Density functional theory (DFT) calculations demonstrated that the introduction of heterojunctions of In2S3@In2O3 enhances the adsorption energy and charge transfer between NO2 and the sensing material.

Crafting Ultra–Sensitive and selective fluorescent probes for CH3Hg+ detection in groundwater: A 3–in–1 strategy

Development of ultra–sensitive and selective fluorescent probes exclusively targeting CH3Hg+, especially against Hg2+, in real ecosystems like groundwater remains a critical yet formidable challenge. In this contribution, we present a series of fluorescent carbazole boronic acids (probes 1–4) designed for the highly sensitive and selective detection of Hg2+ and CH3Hg+ using an innovative 3–in–1 strategy. Notably, probe 4 exhibited exceptional performance in mercury detection in real groundwater, achieving a limit of detection concentration as low as 1.0 ppb for both Hg2+ and CH3Hg+, even in the presence of elevated levels of interfering cations or anions. Subsequently, a new fluorescent probe system was established by embedding probe 4 into cationic micelles, employing a microphase separation protocol. This resulted in exclusive selectivity towards CH3Hg+ over Hg2+ and other interfering ions with sensitivity as low as 10.0 ppb. This advancement not only addresses a critical gap in environmental monitoring but also demonstrates the potential for broader applications of these probes in sensitive detection methodologies.

Proposed Detection Limits for Radioactivity Concentrations in Water in the Decommissioning and Dismantling of Nuclear Facilities

The Dismantling and Decommissioning (D&D) of nuclear facilities poses several challenges for radioactivity measurement laboratories involved in environmental radiation monitoring plans. One of them is the definition of the detection limits to be achieved for the radionuclides analysis in different samples. The detection limits should be set in such a way that the obtained concentration values for each radionuclide are easily discriminated from certain maximum activity concentration levels. These maximum activity concentration levels are usually set in view of the respective dose contributions from each radionuclide. There are some national legislations that settle detection limits for drinking water. However, there is no regulation containing detection limits for groundwater or surface water. In this way, different institutions or companies require very different detection limits for radioactivity concentration assessment in those types of water associated with D&D activities. In this work, we focus on the detection limits required for the D&D activities in rainwater, surface water and groundwater. We propose detection limits obtained by applying the WHO methodology for maximum activity concentration levels and compare with those requested by radioactive waste management agencies and regulatory bodies. Some real cases where our proposal allows identification of events are analysed and conclusions are extracted.

Paper-based radial chromatographic assay for rapid in situ measurement of gelatinized starch concentration

Starch gelatinization is pivotal in food processing, impacting viscosity, texture, and functionality. However, current methods for determining concentration and viscosity of gelatinized starch (GS), such as falling ball and rotational viscometers, are impractical for in situ measurements due to bulky equipment. Here, we introduce a paper-based radial chromatographic assay (PRCA) method for rapidly measuring the concentration of gelatinized starch (GS). We utilized Evans Blue (EB) as a chromatic agent to label GS and generate color-ring patterns on a nitrocellulose membrane based on the “Coffee-ring” effect. The resulting PRCA patterns varied depending on the GS concentrations, yielding a good linear correlation (R2 > 0.967) between grayscale value and viscosity. This method enables rapid measurement of GS concentration within 10 s, even with varying ratios of amylose to amylopectin. PRCA demonstrates a detection limit for GS concentration between 0.027% and 0.051%, which is 10-20 fold lower than that of traditional rotational-viscometer. The intensity of PRCA patterns at pH 3 (45.8) was significantly lower than those at higher pH levels (5 to 9), consistent with the decreased viscosity measured by the viscosimeter. The intensity of PRCA patterns did not change with increasing temperature from 25°C to 90°C, despite the significant decrease in viscosity from 345 mPa•s to 195 mPa•s. Additionally, PRCA can monitor changes in starch viscosity during the hydrolysis process, which decreases from 744 mPa•s to 6 mPa•s. This capability provides an efficient means of measuring the concentration and viscosity of GS during food processing.

Fluorescence Sensing of Eclampsia Biomarkers via the Immunosorbent Atom Transfer Radical Polymerization Assay.

Accurate and quantitative detection of pre-eclampsia markers is crucial in reducing pregnancy mortality rates. This study introduces a novel approach utilizing a fluorescent biosensor by the immunosorbent atom transfer radical polymerization (immuno-ATRP) assay to detect the pre-eclampsia protein marker CD81. The critical step used in this sensor is the novel signal amplification strategy of fluorescein polymerization mediated by ferritin-enhanced controlled radical polymerization, which combines with a traditional enzyme-linked immunosorbent assay (ELISA) to further reduce the detection limit of the CD81 protein concentration. The fluorescence intensity was linear versus logarithmic CD81 protein concentration from 0.1 to 10,000 pg mL-1, and the detection limit was 0.067 pg mL-1. Surprisingly, in 30% normal human serum (NHS), the sensor can also detect target protein over 0.1-10,000 pg mL-1, with 0.083 pg mL-1 for the detection limit. Moreover, the proposed biosensor is designed to be cost-effective, making it accessible, particularly in resource-limited settings where expensive detection techniques may not be available. The affordability of this method enables widespread screening and monitoring of preeclampsia, ultimately benefiting many pregnant women by improving their healthcare outcomes. In short, developing of a low-cost and susceptible direct detection method for preeclampsia protein markers, such as CD81, through the use of the immuno-ATRP assay, has significant implications for reducing pregnancy mortality. This method holds promise for early detection, precise treatment, and improved management of preeclampsia, thereby contributing to better maternal and fetal health.

Advancing Simultaneous Extraction and Sequential Single-Particle ICP-MS Analysis for Metallic Nanoparticle Mixtures in Plant Tissues.

Engineered nanoparticles (ENPs) have been increasingly used in agricultural operations, leading to an urgent need for robust methods to analyze co-occurring ENPs in plant tissues. In response, this study advanced the simultaneous extraction of coexisting silver, cerium oxide, and copper oxide ENPs in lettuce shoots and roots using macerozyme R-10 and analyzed them by single-particle inductively coupled plasma-mass spectrometry (ICP-MS). Additionally, the standard stock suspensions of the ENPs were stabilized with citrate, and the long-term stability (up to 5 months) was examined for the first time. The method performance results displayed satisfactory accuracies and precisions and achieved low particle concentration and particle size detection limits. Significantly, the oven drying process was proved not to impact the properties of the ENPs; therefore, oven-dried lettuce tissues were used in this study, which markedly expanded the applicability of this method. This robust methodology provides a timely approach to characterize and quantify multiple coexisting ENPs in plants.

Development and application of a TaqMan-probe-based multiplex real-time PCR assay for simultaneous detection of porcine circovirus 2, 3, and 4 in Guangdong province of China.

Porcine circoviruses disease (PCVD), caused by porcine circovirus (PCVs), is an important swine disease characterized by porcine dermatitis, nephrotic syndrome and reproductive disorders in sows. However, diseases caused by PCV2, PCV3, or PCV4 are difficult to distinguish, so a simple, rapid, accurate and high-throughput diagnostic and identification method is urgently needed to differentiate these three types. In this study, specific primers and probes were designed based on the conserved region sequences of the Rep gene of PCV2, and the Cap gene of PCV3 and PCV4. A multiplex qPCR assay was developed and optimized that the limit of detection concentration could reach as low as 3.8 copies/μL, with all correlation coefficients (R2) exceeding 0.999. Furthermore, the method showed no cross-reaction with other crucial porcine viral pathogens, and both intra-repeatability and inter-reproducibility coefficients of variation were below 2%. The assay was applied to the detection of 738 pig samples collected from 2020 to 2021 in Guangdong Province, China. This revealed positive infection rates of 65.18% for PCV2, 29.27% for PCV3, and 0% for PCV4, with a PCV2/PCV3 co-infection rate of 23.17%. Subsequently, complete genome sequences of 17 PCV2 and 4 PCV3 strains were obtained from the above positive samples and pre-preserved positive circovirus samples. Nucleotide sequence analysis revealed that the 17 PCV2 strains shared 96.7-100% complete nucleotide identity, with 6 strains being PCV2b and 11 strains being PCV2d; the 4 PCV3 strains shared 98.9-99.4% complete nucleotide identity, with 2 strains being PCV3a-1 and 2 strains being PCV3b. This research provides a reliable tool for rapid PCVs identification and detection. Molecular epidemiological investigation of PCVs in pigs in Guangdong Province will help us to understand PCV2 and PCV3 epidemiological characteristics and evolutionary trends.

Nitroxyl donating and visualization with a coumarin-based fluorescence probe

Nitroxyl (HNO), the single-electron reduction product of nitric oxide (NO), has attracted great interest in the treatment of congestive heart failure in clinical trials. In this paper, we describe the first coumarin-based compound N-hydroxy-2-oxo-2H-chromene-6-sulfonamide (CD1) as a dualfunctional HNO donor, which can release both an HNO signaling molecule and a fluorescent reporter. Under physiological conditions (pH 7.4 and 37 °C), the CD1 HNO donor can readily decompose with a half-life of ∼90 min. The corresponding stoichiometry HNO from the CD1 donor was confirmed using both Vitamin B12 and phosphine compound traps. In addition to HNO releasing, specifically, the degradation product 2-oxo-2H-chromene-6-sulfinate (CS1) was generated as a fluorescent marker during the decomposition. Therefore, the HNO amount released in situ can be accurately monitored through fluorescence generation. As compared to the CD1 donor, the fluorescence intensity increased by about 4.9-fold. The concentration limit of detection of HNO releasing was determined to be ∼0.13 μM according to the fluorescence generation of CS1 at physiological conditions. Moreover, the bioimaging of the CD1 donor was demonstrated in the cell culture of HeLa cells, where the intracellular fluorescence signals were observed, inferring the site of HNO release. Finally, we anticipate that this novel coumarin-based CD1 donor opens a new platform for exploring the biology of HNO.

NiS-modified zeolite imidazolic acid frame-67 as a bi-functional catalyst: A non-enzymatic lactic acid sensor and supercapacitor

The ZIF-67/NiS composite electrode was prepared on nickel foam (NF) matrix by hydrothermal method. NiS has been widely studied in sensors and supercapacitors due to its good electron transfer ability and good pseudocapacitor performance. Therefore, we prepared ZIF-67/NiS composite electrode. The synthesised ZIF-67/NiS composite electrode not only has certain electrochemical performance of battery type electrode, but also is sensitive to lactic acid (LA), and can be used as a non-enzymatic LA sensor and a dual-function material for supercapacitors. The detection limit of LA concentration in alkaline solution is 0.8 μM, and the sensitivity is 1.34 μA μM−1 cm−2. Indicating that the electrode has good electrochemical sensing performance. The GCD test results show that the charging capacity of the ZIF-67/NiS is 2.5 times that of the ZIF-67. The ZIF-67/NiS composite has good cyclic performance, and the capacitance retention rate of the ZIF-67/NiS composite is 87% at 10 A/g current density.

Linker-Preserved Iron Metal-Organic Framework-Based Lateral Flow Assay for Sensitive Transglutaminase 2 Detection in Urine Through Machine Learning-Assisted Colorimetric Analysis.

A groundbreaking demonstration of the utilization of the metal-organic framework MIL-101(Fe) as an exceptionally perceptive visual label in colorimetric lateral flow assays (LFA) is described. This pioneering approach enables the precise identification of transglutaminase 2 (TGM2), a recognized biomarker for chronic kidney disease (CKD), in urine specimens, which offers a remarkably sensitive naked-eye detection mechanism. The surface of MIL-101(Fe) was modified with oxalyl chloride, adipoyl chloride, and poly(acrylic) acid (PAA); these not only improved the labeling material stability in a complex matrix but also achieved a systematic control in the detection limit of the TGM2 concentration using our LFA platform. The advanced LFA with the MIL-101(Fe)-PAA label can detect TGM2 concentrations down to 0.012, 0.009, and 0.010 nM in Tris-HCl buffer, urine, and desalted urine, respectively, which are approximately 55-fold lower than those for a conventional AuNP-based LFAs. Aside from rapid TGM2 detection (i.e., within 20 min), the performance of the MIL-101(Fe)-PAA-based LFA on reproducibility [coefficients of variation (CV) < 2.9%] and recovery (95.9-103.2%) along with storage stability within 25 days of observation (CV < 6.0%) shows an acceptable parameter range for quantitative analysis. A sophisticated sensing method grounded in machine learning principles was also developed, specifically aimed at precisely deducing the TGM2 concentration by analyzing immunoreaction sites. More importantly, our developed LFA offers potential for clinical measurement of TGM2 concentration in normal human urine and CKD patients' samples.

Silver-palladium bimetallic nanoparticles stabilized by elm pod polysaccharide with peroxidase-like properties for glutathione detection and photothermal anti-tumor ability

Noble metal nanoparticles show good application prospects in biosensors and anti-tumor drug research. Herein, the near-spherical silver‑palladium bimetallic nanoparticles supported by elm pod polysaccharide (EPP-AgPd1.5 NPs) were prepared by using the elm pod polysaccharide (EPP). EPP acts as a stabilizer and reducing agent due to its water solubility and weak reducing ability. The particle size of EPP-AgPd1.5 NPs was 33.6 ± 5.5 nm. In addition, EPP-AgPd1.5 NPs had peroxidase-like activity to catalyze 3,3′,5,5′-tetramethylbenzidine (TMB) to oxidized TMB by catalyzing H2O2 to OH. Based on the peroxidase-like activity of EPP-AgPd1.5 NPs, a method for detecting glutathione was established, and the detection limit and linear range of glutathione concentration were 0.279 μM and 0–400 μM, respectively. More importantly, the photothermal conversion efficiency of EPP-AgPd1.5 NPs reached 39.7 %, and their inhibition rate in HeLa cells reached 69.9 %. Silver‑palladium bimetallic nanoparticles stabilized by EPP had good performance in glutathione detection and anti-tumor drugs.

Selective determination of an ovarian cancer biomarker at low concentrations with surface imprinted nanotube based chemosensor

In this study, an electrochemical chemosensor that utilizes a conductive polymer-based molecularly imprinted polymer (MIP) surface for rapid and reliable determination of CA125 was devised. A novel method has been applied to fabricate CA125 imprinted polypyrrole nanotubes (MI-PPy NT) via vapor deposition polymerization (VDP) as a recognition element for highly selective and sensitive determination of CA125. The chemosensor was prepared by immobilizing MI-PPy NT onto screen-printed gold electrodes (Au-SPE) and the performance of the sensor was evaluated by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) in terms of selectivity, sensitivity, linear dynamic concentration range (LDR) and limit of detection (LOD). The MI-PPy NT@Au-SPE sensor exhibited high sensitivity (68.57 μA per decade) to the CA125 concentration ranging from 0.1 U mL−1 to 100 U mL−1 at an LOD of 0.4 U mL−1 with a correlation coefficient of 0.9922. The developed chemosensors with their novel design combined with a facile fabrication method, prove to be promising as future state-of-the-art biosensors.

Chemical surface modification of carbon dots with Germanium: A highly sensitive and selective ratiometric fluorescence probe for Mg2+ detection using DFT and TD-DFT

In this study, we chemically modified carbon dots (Cdots) using germanium, enhancing their sensitivity and selectivity as a ratiometric fluorescence probe for precise detection of Mg2+ ions. Excitation of the modified Cdots resulted in a distinct emission peak at 527 nm, enabling accurate measurement of Mg2+ concentrations across a linear range. The surface modification with germanium led to the creation of novel emitting centers on the Cdots' surface. Theoretical calculations using density functional theory (DFT) revealed the effective suppression of these emitting centers through a photo-induced electron transfer (PET) process, utilizing the nitrogen lone pair electrons on the Cdots' surface. Furthermore, adjacent Cdots' surface pyrazino[2,3-f][1,10]-phenanthroline (PPT) nitrogen atoms formed chemical bonds with Mg2+ ions, resulting in the formation of aggregated Cdots. Consequently, the intricate complexation terminated the PET process, resulting in a novel emission peak at longer wavelengths. This study presents a highly sensitive and selective ratiometric fluorescent detection system with exceptional low concentration detection limit for precise Mg2+ ion detection.

Modified spectrophotometry for micromolar H2O2 determination in iron-containing solutions with leuco crystal violet under both aerobic and anaerobic conditions.

Accurately quantifying hydrogen peroxide (H2O2) is essential for elucidating its role across diverse environments. Spectrophotometry is widely employed in laboratories for this purpose due to its convenience, cost-effectiveness, and low detection limits for micromolar H2O2 concentrations. However, accurate measurement of H2O2 in iron-containing solutions presents challenges due to the interference of iron ions. In this study, we propose a modified spectrophotometric method for H2O2 determination in iron-containing solutions by adding two types of iron ion chelators and selecting leuco crystal violet (LCV) as a chromogenic reagent due to its stability. By sequentially adding 1,10-phenanthroline and EDTA, and using a phosphate buffer at pH 4.2 to provide the optimal chromogenic pH condition, this modified method effectively mitigates the interference of iron ions in the LCV chromogenic reaction. The applicability of this method under aerobic and anaerobic conditions was confirmed by comparing the experimental results with theoretical simulations. Under optimal chromogenic conditions, this method achieves a detection limit of 300 nM. This improved method allows better detection of H2O2 in iron-containing systems and investigation of its significance in various environmental processes.

Review of recent advances and sensing mechanisms in solid-state organic thin-film transistor (OTFT) sensors

Advances in processing of active layers of organic thin-film transistor (OTFT)-based chemical and biological sensors have enabled significant developments in their performance, achieving part-per-billion molar concentration limits of detection.

High-sensitivity detection of low-concentration heavy metal ions in solution by multiple reflection enhanced absorption (MREA) spectroscopy.

Heavy metal ions (Cr6+, Co2+, Ni2+, and Cu2+) in the electroplating and electrolysis industries are significantly related to process parameters and product quality, even at lower concentrations. Absorption spectroscopy is widely used for substance qualitative and quantitative analysis, which is an analytical method with the potential for real-time monitoring of heavy metal ions concentration in industrial processes. In this paper, a low-concentration heavy metal ion analysis method based on multiple reflection enhanced absorption (MREA) is proposed. Compared with traditional absorption, MREA has the advantages of low concentration detection limit and high-sensitivity. First, a reflective film (Al-SiO2) was prepared and a multiple reflection optical structure was designed to realize multiple parallel reflections of light in the solution medium. Then absorption spectra of low-concentration Cr6+, Co2+, Ni2+ and Cu2+ solutions were measured by MREA and traditional absorption methods. Finally, spectral bandwidth and incident light spots were optimized to obtain a superior absorption enhancement effect. The results showed that MREA could effectively increase the substance absorbance compared with traditional absorption. At the same time, with the optimal spectral bandwidth (0.4 nm) and incident light spot (1 mm), the detection limit of Cr6+, Co2+, Ni2+ and Cu2+ was reduced by 81.48%, 82.52%, 80.92% and 82.93%, respectively. The sensitivity was improved by 5-6 times, which was more obvious for low-concentration detection. In addition, the MREA method can achieve ion concentration analysis when Cr6+, Co2+, Ni2+, and Cu2+ coexist, and the linear correlative coefficients of the C-A curves were all greater than 0.999. Moreover, by adjusting reflectivity of the reflective film and the number of reflections in the optical structure, the results of the MREA method can be further optimized for the low-concentration heavy metal ion analysis. The MREA method has the advantages of simplicity, rapidity and versatility, which can provide the technical foundation for real-time monitoring method development of low-concentration heavy metal ions in industrial processes.