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1.
Detection of trace-level hydrogen sulfide(H2 S) gas is of great importance whether in industrial production or disease diagnosis.This research presents a novel H2 S gas sensor based on integrated resonant dual-microcantilevers which can identify and detect trace-level H2 S in real-time.The sensor consists of two integrated resonant microcantilever sensors with different functions.One cantilever sensor can identify H2 S by outputting positive frequency ...  相似文献   

2.
A method for the determination of ammonia and hydrogen sulfide in aqueous solution is presented. This method involves the use of a gas-permeable membrane which isolates the piezoelectric crystal device from the solution yet allows the desired gases to pass. Concentrations up to 0.45 M for NH3, and 9 · 10-4 M for H2S give linear calibration curves of concentration vs. frequency change.  相似文献   

3.
A method for the selective detection and determination of hydrogen sulfide in the atmosphere is presented. This method utilizes the reversible adsorption of H2S on a piezoelectric quartz crystal coated with an acetone extract of soots resulting from the burning of organochlorine compounds. The extract of a soot prepared from chlorobenzoic acid provided the best substrate. The method is useful in the concentration range 1–60 ppm.  相似文献   

4.
Herein we report the fabrication of an advanced sensor for the detection of hydrogen sulfide (H2S) at room temperature, using thin films of rare‐earth metal (RE)‐based metal–organic framework (MOF) with underlying fcu topology. This unique MOF‐based sensor is made via the in situ growth of fumarate‐based fcu ‐MOF (fum‐ fcu ‐MOF) thin film on a capacitive interdigitated electrode. The sensor showed a remarkable detection sensitivity for H2S at concentrations down to 100 ppb, with the lower detection limit around 5 ppb. The fum‐ fcu ‐MOF sensor exhibits a highly desirable detection selectivity towards H2S vs. CH4, NO2, H2, and C7H8 as well as an outstanding H2S sensing stability as compared to other reported MOFs.  相似文献   

5.
Hydrogen sulfide (H2S) as small molecular signal messenger plays key functions in numerous biological processes. The imaging detection of intracellular hydrogen sulfide is of great significance. In this work, a ratiometric fluorescent probe BH based on an asymmetric BODIPY dye for detection of H2S was designed and synthesized. After the interaction with hydrogen sulfide, probe display colorimetric and ratiometric fluorescence response, with its maximum emission fluorescence wavelength red-shifted from 542 nm to 594 nm, which is attributed to the sequential nucleophilic reaction of H2S leading to enhanced molecular conjugation after ring formation of the BODIPY skeleton. A special response mechanism has been fully investigated by NMR titration and MS, so that the probe has excellent detection selectivity. Furthermore, probe BH has low cytotoxicity and fluorescence imaging experiments indicate that it can be used to monitor hydrogen sulfide in living cells.  相似文献   

6.
采用旋转甩涂法将硫堇掺杂的聚乙烯醇薄膜固定在K+交换玻璃光波导表面,研制出一种高灵敏硫化氢气体传感器。 传感膜与硫化氢(H2S)气体作用时,薄膜颜色从紫色变为无色,从而降低薄膜对倏逝波的吸收,使传感器的输出光强度(信号)增强。 采用流动注射法对H2S气体进行检测。 实验结果表明,H2S传感器对浓度在0.14~56 mg/m3范围的H2S气体具有良好的线性响应(r=0.99667),检出限为0.11 mg/m3(S/N=3),相对标准偏差为4.0%,响应时间(t90)<2 s。 该传感器具有灵敏度高、响应快、可逆性和重复性好等特点。  相似文献   

7.
8.
There is a great demand for high-performance hydrogen sulfide(H2S) sensors with low operating temperatures. Ag/In2O3 hexagonal tubes with different proportions were prepared by the calcination of Ag+-impregnated indium-organic frameworks(CPP-3(In)), and the developed sensors exhibit enhanced gassensing performance toward H2S. Gas sensing measurements indicate that the response of Ag/In2O3(2.5 wt%) sensor to 5 ppm H2S ha...  相似文献   

9.
It is known that the localized surface plasmon resonance (LSPR) wavelength of plasmonics is highly dependent on compositions and geometry of plasmonics as well as the surrounding environments. Here, monodispersed Au@Ag core-shell nanoparticles (Au@Ag NPs) were prepared by carefully optimizing the shell thickness of Au@Ag NPs, and the presence of hydrogen sulfide (H2S) would significantly alter the LSPR wavelength. On the basis of this, a photothermal paper sensor for on-site recognition of H2S was constructed with a visual detection limit of 12.8 ng/L.  相似文献   

10.
《中国化学快报》2021,32(10):3155-3158
Accurate detection of hydrogen sulfide (H2S) is of great significance for environmental monitoring and protection. We propose a colorimetric method for the detection of H2S by the use of mixed-node Cu-Fe metal organic frameworks (Cu-Fe MOFs) as highly efficient mimic enzymes for target-induced deactivation. The Cu-Fe MOFs were synthesized by a simple solvothermal method and could catalyze the H2O2 mediated oxidation of 3,3′,5,5′-tetramethylbenzidine (TMB) to oxTMB with a blue color. The presence of dissolved H2S would deactivate the mimic enzymes, and then the blue color disappeared. The mechanism of the sensor was discussed by steady-state kinetic analysis. The designed assay was highly sensitive for H2S detection with a linear range of 0−80 μmol/L and a detection limit of 1.6 μmol/L. Moreover, some potential substances in the water samples had no interference. This method with the advantages of low cost, high sensitivity, selectivity, and visual readout with the naked eye was successfully applied to the determination of H2S in industrial wastewater samples.  相似文献   

11.
A promising hydrogen sulfide (H2S) sensor was prepared by electrodeposition of Au nanoclusters on glassy carbon electrode (GCE) and the surface structure was characterized by SEM and EDAX. These flower-like form Au nanoclusters, which were made up of highly dense clustering Au nanorods with an average diameter of 20 nm and length up to 80 nm, had an average size about 600 nm and uniformly distributed on the GCE surface. The electrocatalytic oxidation of H2S in gasoline was performed on this modified electrode, which had a satisfactory liner response to H2S in the range of 1–80 ppm and a detection limit of 0.45 ppm (s/n = 3). This sensor was sensitive, selective and stable.  相似文献   

12.
Various reusable and sensitive piezoelectric (PZ) quartz crystal membrane sensors with home‐made computer interfaces for signal acquisition and data processing were developed to detect organic/inorganic vapors and organic/inorganic/biologic species in solutions, respectively. Fullerene(C60), fullerene derivatives and artificial macrocyclic polyethers, e.g., crown ethers and cryptands, were synthesized and applied as coating materials on quartz crystals of the PZ crystal sensors. The oscillating frequency of the quartz crystal decreased due to the adsorption of organic or inorganic species onto coating material molecules on the crystal surface. The crown ether‐coated PZ crystal gas detector exhibited high sensitivity with a frequency shift range of 10–340 Hz/(mg/L) for polar organic gases, a short response time (< 2.0 min.), good selectivity, and good reproducibility. The Ag(I)/crptand22 and Ru(III) / crptand22 coated PZ gas detectors were also prepared for nonpolar organic vapors, e.g., alkynes and alkenes. The frequency shifts of the nonpolar PZ sensors were in the order: alkynes > alkenes > alkanes. A Ti(IV)/Cryptand22‐coated PZ crystal sensor was also developed to detect the inorganic air pollutants, e.g., CO and NO2. A piezoelectric gas sensor for both polar/nonpolar organic vapors based on C60‐cryptand22 was also prepared. The cryptand22‐coated PZ gas sensor was also employed as a GC detector for organic molecules. The cryptand22‐coated piezoelectric GC detectors compared well with the commercial thermal conductivity detector (TCD). The interaction between fullerene C60 and organic molecules was studied with a fullerene coated PZ gas detector. A multi‐channel PZ organic gas detector with PCA(Principal Component Analysis) and BPN (Back Propagation Neural) analysis methods was developed. Various liquid piezoelectric crystal sensors based on long‐chain macrocyclic polyethers, e.g., C10H21‐dibenzo‐16‐crown‐5, C18H37‐benzo‐15‐crown‐5, (C17CO)2‐cyptand22 and fullerene derivatives, e.g., C60‐NH‐cryptand22 and dibenzo‐16‐crown‐5‐C60, were also developed as HPLC detectors for metal ions, anions, and various organic compounds in solutions. The sensitive and highly selective PZ bio‐sensors based on enzymes, polyvinylaldehyde, polycinnaldehyde‐C60 and C60‐cryptand22 were developed to detect various biologic species, e.g., proteins, glucose, and urea. A quite sensitive EQCM (Electrochemical Quartz Crystal Micro‐balance) detection system was also developed for detection of trace heavy metal ions.  相似文献   

13.
AuNPs monolayer doping Poly(3,4-ethylenedioxythiophene):polystyrenesulfonate (PEDOT : PSS) film on interdigitated electrode had been fabricated into AuNPs/PEDOT : PSS Janus film sensor to detect hydrogen sulfide (H2S). The results show that the Janus film sensors have a wide measurement range of H2S concentration. The sensitivity of PEDOT : PSS/AuNPs sensor grows up with the thickness of Janus film increases. The resistance response of AuNPs Janus film was affected little by the rough surface states of PEDOT : PSS film. In addition, the PEDOT : PSS/AuNPs film sensor had been used again to detect H2S. This work presents a platform to inspire a novel high sensitive chemiresistive sensor via nanoparticles monolayer.  相似文献   

14.
The emergence of hydrogen sulfide (H2S) as an important signalling molecule in redox biology with therapeutic potential has triggered interest in generating this molecule within cells. One strategy that has been proposed is to use carbonyl sulfide (COS) as a surrogate for hydrogen sulfide. Small molecules that generate COS have been shown to produce hydrogen sulfide in the presence of carbonic anhydrase, a widely prevalent enzyme. However, other studies have indicated that COS may have biological effects which are distinct from H2S. Thus, it would be useful to develop tools to compare (and contrast) effects of COS and H2S. Here we report enzyme‐activated COS donors that are capable of inducing protein persulfidation, which is symptomatic of generation of hydrogen sulfide. The COS donors are also capable of mitigating stress induced by elevated reactive oxygen species. Together, our data suggests that the effects of COS parallel that of hydrogen sulfide, laying the foundation for further development of these donors as possible therapeutic agents.  相似文献   

15.
Shen D  Kang Q  Li X  Cai H  Wang Y 《Analytica chimica acta》2007,593(2):188-195
This paper presents different experimental results of the influence of an immersion angle (θ, the angle between the surface of a quartz crystal resonator and the horizon) on the resonant frequency of a quartz crystal microbalance (QCM) sensor exposed one side of its sensing surfaces to liquid. The experimental results show that the immersion angle is an added factor that may influence the frequency of the QCM sensor. This type of influence is caused by variation of the reflection conditions of the longitudinal wave between the QCM sensor and the walls of the detection cell. The frequency shifts, measured by varying θ, are related to the QCM sensor used. When a QCM sensor with a weak longitudinal wave is used, its resonant frequency is nearly independent of θ. But, if a QCM sensor with a strong longitudinal wave is employed, the immersion angle is a potential error source for the measurements performed on the QCM sensor. When the reflection conditions of the longitudinal wave are reduced, the influence of θ on the resonant frequency of the QCM sensor is negligible. The slope of the plot of frequency shifts (ΔF) versus (ρη)1/2, the square root of the product of solution density (ρ) and viscosity (η), may be influenced by θ in a single experiment for the QCM sensor with a strong longitudinal wave in low viscous liquids, which can however, be effectively weakened by using the averaged values of reduplicated experiments. In solutions with a large (ρη)1/2 region (0-55 wt% sucrose solution as an example, with ρ value from 1.00 to 1.26 g cm−3 and η value from 0.01 to 0.22 g cm−1 s−1, respectively), the slope of the plot of ΔF versus (ρη)1/2 is independent of θ even for the QCM sensor with a strong longitudinal wave in a single experiment. The influence of θ on the resonant frequency of the QCM sensor should be taken into consideration in its applications in liquid phase.  相似文献   

16.
We report a photochemical bismuth vanadate (BiVO4) sensing material, which possesses a large proportion of (110) and (011) facets combined with the additional (111) facets, for the selective detection of ultra-low concentration hydrogen sulfide (H2S) driven by visible light. Specifically, the obtained octadecahedron BiVO4 (Octa-BiVO4) performs a high response value (67) and short response time (47.4 s) to 100 ppm H2S with good stability for nearly 100 days, as well as undisturbedness by moist air. With the combination of experimental and theoretical calculation results, the adsorption and carrier transfer behaviors of H2S molecules on the Octa-BiVO4 crystal surface are investigated. By adjusting the ratio of different crystal facets and controlling the facets with characteristic adsorption, we achieve improved anisotropic photoinduced carrier separation and high selectivity for a specific gas. Furthermore, this facial facet engineering can be extended to the synthesis of other sensing materials, offering huge opportunities for fundamental research and technological applications.  相似文献   

17.
《Analytical letters》2012,45(4):661-676
Abstract

A novel amperometric sensor of hydrogen peroxide was constructed. Hemoglobin (Hb) was successfully immobilized on nanometer‐sized SiO2, which was supported by chitosan. Chitosan was acted as dispersant. The determination of hydrogen peroxide was performed in the presence of an electron mediator hydroquinone. Hb immobilized on the SiO2/chitosan composite film displayed excellent electrocatalytical activity to the reduction of H2O2. The linear range of detection towards H2O2 was from 6.25×10?7 to 1.63×10?4mol/L with a detection limit of 1.8×10?7mol/L (S/N=3). The apparent Michaelis‐Menten constant (K app M) was found to be 0.75mmol/L.  相似文献   

18.
A method is presented for the detection and determination of hydrogen sulfide. It is based on the selective and reversible adsorption of hydrogen sulfide on the surface of a piezoelectric crystal coated with a cadmium iodide/urea/-glycerol solution. The proposed detector has a response time of 30 s with linear response over the concentration range 2–25 μl l?1 (ppm).  相似文献   

19.
A novel strategy to fabricate hydrogen peroxide (H2O2) sensor was developed by electrodepositing palladium? silver nanoparticles (NPs) on a glassy carbon electrode. The morphology of the modified electrode was characterized by Scanning electron microscopy (SEM). The result of electrochemical experiments showed that such constructed sensor had a favorable catalytic ability, high sensitivity, excellent selectivity towards reduction of hydrogen peroxide (H2O2). The response to H2O2 is linear in the range between 0.30 μM to 2.50 mM, and the detection limit is 0.1 μM (at an S/N of 3).  相似文献   

20.
Hydrogen sulfide (H2S) is an important signaling molecule whose up‐ and down‐regulation have specific biological consequences. Although significant advances in H2S up‐regulation, by the development of H2S donors, have been achieved in recent years, precise H2S down‐regulation is still challenging. The lack of potent/specific inhibitors for H2S‐producing enzymes contributes to this problem. We expect the development of H2S scavengers is an alternative approach to address this problem. Since chemical sensors and scavengers of H2S share the same criteria, we constructed a H2S sensor database, which summarizes key parameters of reported sensors. Data‐driven analysis led to the selection of 30 potential compounds. Further evaluation of these compounds identified a group of promising scavengers, based on the sulfonyl azide template. The efficiency of these scavengers in in vitro and in vivo experiments was demonstrated.  相似文献   

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