Mxene Quantum Dot Nanosurface Molecularly Imprinted Polymer Resonance Rayleigh Scattering Probe for Highly Sensitive and Selective Determination of Thiocyanate.

In this article, a nanosurface molecularly imprinted polymer (MQD@MIP) resonance Rayleigh scattering (RRS) spectral probe for SCN- was prepared by sol-gel method, using Mxene quantum dot as a matrix, thiocyanate (SCN-) as a template ion, (3-aminopropyl) triethoxysilane (APTES) as a functional monomer, tetraethoxysilane (TEOS) as the cross-linker, and ammonia as the initiator. The probe produced an RRS peak at 370 nm and exhibits a strong RRS energy transfer (RRS-ET) effect when the MQD@MIP probe identifies SCN-. As the concentration of SCN- increased, the RRS-ET was enhanced, and the signal value of the system decreased linearly at 370 nm, with a determination range of 0.87-5.22 µg/L, and a detection limit of 0.37 µg/L SCN-. This detection method has the characteristics of simplicity, sensitivity, and specific recognition. The RRS method was used to determine SCN- in the sample, with relative standard deviation of 1.95-10.98% and recovery of 89.0-102.8%.

A Dimode Scattering Method for Ultratrace Dinitrofuran Detection with Nanopalladium Molecularly Imprinted Polymer Nanocatalytic Probe.

With four nanoparticles as the nanomatrix, dinotefuran (DNF) as the template molecule, N-isopropylacrylamide as the functional monomer, trimethylolpropane and trimethacrylate as the cross-linker, four nanosurface molecularly imprinted polymer (MIP) bifunctional probes were prepared by microwave synthesis. It was found that palladium nanosurface MIP (Pd@MIP) not only recognized DNF but also had the strongest catalytic effect on the new nanogold indicator reaction of acrylic acid-HAuCl4, which was evaluated quickly with the slope procedure developed by us. The generated gold nanoparticles (AuNPs) not only possessed the resonance Rayleigh scattering (RRS) effect but also strong surface-enhanced Raman scattering (SERS) activity. The combination of Pd@MIP with DNF enhanced the catalytic effect by coupling the nanosurface electrons with π-electrons, thus enhancing both scattering signals. A new Pd@MIP nanoprobe catalytic-SERS/RRS dual-mode analytical platform was developed for the specific and sensitive detection of DNF. The linear ranges of the SERS and RRS methods were 0.075-0.75 and 0.1-0.75 nmol/L, and the limits of detection were 0.03 and 0.06 nmol/L, respectively. The standard deviations were 0.54-2.39%, and the recoveries were 93-105%.

A new copper nanocluster surface molecular imprinted polymethacrylic acid probe for ultratrace trichlorophenol based on in situ-generated nanogold SPR effects.

A new coinage metal nanocluster surface molecularly imprinted polymethacrylic acid nanoprobe (NC@MIP) for the selective determination of 2,4,6-trichlorophenol (TCP) was prepared via microwave synthesis using 2,4,6-trichlorophenol as a template molecule, copper nanoclusters (CuNC) as a nanosubstrate, and methacrylic acid as a polymer monomer. It was found that the copper nanocluster MIP (CuNC@MIP) shows the strongest catalytic performance for the reduction of HAuCl4 by hydrazine hydrate for the on-site generation of gold nanoparticles (AuNPs) with the surface plasmon resonance (SPR) effects of resonance surface-enhanced Raman scattering (SERS) and resonance Rayleigh scattering (RRS) as well as absorption (Abs). When TCP was added, the CuNC@MIP nanoprobe and TCP-formed CuNC@MIP-TCP nanoenzyme with stronger catalytic activity generated more AuNPs, and the trimodal analytical signal was enhanced linearly. Therefore, a new SERS/RRS/Abs trimodal sensing platform for TCP was constructed, which was simple, rapid, sensitive, and selective. For each mode, the linear ranges were 0.0075-0.075, 0.010-0.10, and 0.010-0.10 nmol L-1, and the detection limits were 0.0010, 0.021, and 0.043 nmol L-1, respectively. The relative deviation of TCP in different water quality was 0.47%-2.5% and the recovery rate was 94.6%-108.6%.

A new and highly efficient CuMOF-based nanoenzyme and its application to the aptamer SERS/FL/RRS/Abs quadruple-mode analysis of ultratrace malachite green.

Malachite green (MG) is highly toxic, persistent, and carcinogenic, and its widespread use is a danger to the ecosystem and a threat to public health and food safety, making it necessary to develop new sensitive multimode molecular spectroscopy methods. In this work, a new copper-based nanomaterial (CuNM) was prepared by a high-temperature roasting using a copper metal-organic framework (CuMOF) as precursor. The as-prepared CuNM was characterized using X-ray diffraction (XRD), X-ray photoelectron spectroscopy, transmission electron microscopy (TEM), and BET surface area analysis. CuNM was found to catalyze the oxidation of 3,3',5,5'-tetramethylbenzidine (TMB) by H2O2 to produce the oxidation product TMBOX; however, subsequently, the MG aptamer (Apt) could be adsorbed on the CuNM surface by intermolecular interaction, which would inhibit the catalytic performance. After the addition of MG to be tested, the CuNM previously adsorbed by the Apt was transformed into its free state, thus restoring its catalytic activity. This new nanocatalytic indicator reaction could be monitored by surface-enhanced Raman scattering (SERS)/resonance Rayleigh scattering (RRS)/fluorescence (FL)/absorption (Abs) quadruple-mode methods. The SERS determination range was 0.004-0.4 nmol L-1 MG, with a limit of detection of 0.0032 nM. In this way, a rapid, stable, and sensitive method for the determination of MG residues in the environment was established.

Single-atom Fe catalytic amplification-gold nanosol SERS/RRS aptamer as platform for the quantification of trace pollutants.

Bisphenol A (BPA), as a typical endocrine disruptor, poses a serious threat to human health. Therefore, it is urgent to establish a rapid, sensitive, and simple method for the determination of BPA. In this paper, based on the aptamer-mediated single-atom Fe carbon dot catalyst (SAFe) catalyzing the HAuCl4-ethylene glycol (EG) nanoreaction, a new SERS/RRS di-mode detection method for BPA was established. The results show that SAFe exhibits a strong catalytic effect on the HAuCl4-EG nanoreaction, which could generate purple gold nanoparticles (AuNPs) with resonance Rayleigh scattering (RRS) signals and surface-enhanced Raman scattering (SERS) effects. After the addition of BPA aptamer (Apt), it could encapsulate SAFe through intermolecular interaction, thus inhibiting its catalytic action, resulting in the reduction of AuNPs generated and the decrease of RRS and SERS signals of the system. With the addition of BPA, Apt was specifically combined with BPA, and SAFe was re-released to restore the catalytic ability; the generated AuNPs increased. As a result of this RRS and SERS signals of the system recovered, and their increment was linear with the concentration of BPA. Thus, the quantification of 0.1-4.0 nM (RRS) and 0.1-12.0 nM (SERS) BPA was realized, and the detection limits were 0.08 nM and 0.03 nM, respectively. At the same time, we used molecular spectroscopy and electron microscopy to study the SAFe-HAuCl4-ethylene glycol indicator reaction, and proposed a reasonable SAFe catalytic reaction mechanism. Based on Apt-mediated SAFe catalysis gold nanoreaction amplification, a SERS/RRS di-mode analytical platform was established for targets such as BPA.

A novel N/Au co-doped carbon dot probe for continuous detection of silicate and phosphate by resonance Rayleigh scattering.

Co-doped carbon dots are new multifunctional carbon nanomaterials. Their fast preparation and new analytical applications such as in continuous detection and resonance Rayleigh scattering (RRS) probes are of interest to people. Herein, the N/Au co-doped carbon dots (CDN/Au) were prepared quickly by a microwave synthesis method using fructose as the carbon source and urea and HAuCl4 as dopants, and it exhibited an excellent RRS effect at 555 nm. Based on both silicate (SiO32-) and phosphate (PO43-) reacting with ammonium molybdate to form silicomolybdate heteropoly acid (SiMo) and phosphomolybdate heteropoly acid (PMo), PMo decomposed by the addition of citric acid, and SiMo/PMo combined with CDN/Au to show good RRS analytical properties, and a new strategy was developed to detect SiO32- and PO43- by the CDN/Au probes continuously. With the increase of SiO32- (PO43-), SiMo (PMo) reacted with CDN/Au probes to form more big particles which resulted in the RRS intensity enhancement at 555 nm, and had a good linear relationship with the SiO32- (PO43-) concentration in the range of 1.11 µg L-1-19.98 µg L-1, with detection limits of 0.3 µg L-1 SiO32- and 0.3 µg L-1 PO43-. Accordingly, a new RRS method was established for continuous detection of SiO32- and PO43- using CDN/Au as the probe.

A sensitive SERS quantitative analysis method for Ni2+ by the dimethylglyoxime reaction regulating a graphene oxide nanoribbon catalytic gold nanoreaction.

The nanogold reaction between HAuCl4 and trisodium citrate (TCA) proceeded very slowly at 60°C in a water bath. The as-prepared graphene oxide nanoribbons (GONRs) exhibited strong catalysis during the reaction to form gold nanoparticles (Au NPs) and appeared as a strong surface-enhanced Raman scattering (SERS) peak at 1616 cm-1 in the presence of the molecular probe Victoria blue 4R (VB4r). With increase in GONR concentration, the SERS peak increased due to increased formation of Au NPs. Upon addition of dimethylglyoxime (DMG) ligand, which was adsorbed onto the GONR surface to inhibit GONR catalysis, the SERS peak decreased. When Ni2+ was added, a coordination reaction between DMG and Ni2+ took place to form stable complexes of [Ni (DMG)2 ]2+ and the release of free GONR catalyst that resulted in the SERS peak increasing linearly. A SERS quantitative analysis method for Ni2+ was therefore established, with a linear range of 0.07-2.8 µM, and a detection limit of 0.036 µM Ni2+ .

A simple gold nanoplasmonic SERS method for trace Hg2+ based on aptamer-regulating graphene oxide catalysis.

The as-prepared graphene oxide (GO) exhibited a strong catalytic effect on reduction of HAuCl4 by trisodium citrate to form gold nanoplasmons (AuNPs) with a strong surface-enhanced Raman scattering (SERS) effect at 1615 cm-1 in the presence of molecular probe Victoria blue 4R (VB4r). SERS intensity increased with nanocatalyst GO concentration due to the formation of more AuNP substrates. The aptamer (Apt) of Hg2+ can bind to GO to form Apt-GO complexes, which can strongly inhibit nanocatalysis. When target Hg2+ is present, the formed stable Hg2+ -Apt complexes are separated from the GO surface, which leads to GO catalysis recovery. The enhanced SERS signal was linear to Hg2+ concentration in the range 0.25-10 nmol/L, with a detection limit of 0.08 nmol/L Hg2+ . Thus, a new gold nanoplasmon molecular spectral analysis platform was established for detecting Hg2+ , based on Apt regulation of GO nanocatalysis.

A new silver nanochain SERS analytical platform to detect trace hexametaphosphate with a rhodamine S molecular probe.

Using AgNO3 as the precursor, stable silver nanochain (AgNC) sols, orange-red in color, were prepared using hydrazine hydrate. A strong surface plasmon resonance Rayleigh scattering (RRS) peak occurred at 420 nm plus two surface plasmon resonance (SPR) absorption peaks at 410 nm and 510 nm. Rhodamine S (RhS) cationic dye was absorbed on the as-prepared AgNC substrate to obtain a RhS-AgNC surface-enhanced Raman scattering (SERS) nanoprobe that exhibited a strong SERS peak at 1506 cm(-1) and a strong RRS peak at 375 nm. Upon addition of the analyte sodium hexametaphosphate (HP), it reacted with RhS, which resulted in a decrease in the SERS and RRS peaks that was studied in detail. The decreased SERS and RRS intensities correlated linearly with HP concentration in the range of 0.0125-0.3 µmol/L and 0.05-1.0 µmol/L, with a detection limit of 6 nmol/L and 20 nmol/L HP respectively. Due to advantages of high sensitivity, good selectivity and simple operation, the RhS molecular probes were used to determine HP concentration in real samples.

A sensitive fluorescence method for detection of E. Coli using rhodamine 6G dyeing.

Negatively charged bacteria combined with positively charged alkaline dye rhodamine 6G (Rh6G) in NaH2 PO4 -Na2 HPO4 buffer solution pH 7.4, by electrostatic interaction. The dyed bacteria exhibited a strong fluorescence peak at 552 nm and fluorescence intensity was directly linear to Escherichia coli (E. coli), Bacillus subtilis (B. subtilis) and Staphylococcus aureus (S. aureus) concentrations in the range of 7.06 × 10(4) to 3.53 × 10(7) , 4.95 × 10(5) to 2.475 × 10(8) and 32.5 to 16250 colony forming unit/mL (cfu/mL) respectively, with detection limits of 3.2 × 10(4) cfu/mL E. coli, 2.3 × 10(5) cfu/mL B. subtilis and 16 cfu/mL S. aureus, respectively. Samples were cultured for 12 h, after which the linear detection range for E. coli was 2 to 88 cfu/mL. This simple, rapid and sensitive method was used for the analysis of water and drinking samples. Copyright © 2015 John Wiley & Sons, Ltd.

[A Facile Nanogold Surface Plasmon Resonance Absorption Method for CO Tracing].

The detection of gas pollutants in atmosphere and indoor air is very important to human health and safety. Monoxide carbon (CO) is a common gas pollutant with high toxicity that mainly comes from the inadequacy oxidization of carbon such as oil, coal and petrol inadequacy combustion, auto-gas and some natural disasters whose limit value in air is lower than 6.0 mg·m-3 in the national standard. Due to its toxicity and uneasy detection, it is one of very dangerous component in the silent killer. Recently, several methods, including infra-red absorption, gas chromatography, potentiometry, Hg replacement, spectrophotometry, I2O5 and PdCl2 nake-eye, semiconductor sensor have been reportedly used for the detection of CO. To our best knowledge, there are no SPR absorption methods for CO, based on the NG SPR absorption. In this paper, the reaction between CO and HAuCl4 was studied with absorption spectrophotometry and transmission electron microscopy (TEM)while a simple and rapid SPR absorption method was developed for the determination of trace CO. In pH 7.2 phosphate buffer solutions, monoxide carbon reduced HAuCl4 to form nanogold (NG) particles with the size of about 45 nm that exhibited surface plasmon resonance (SPR) absorption peak at 540 nm and three energy spectral peaks at 1.70 keV, 2.20 and 9.70 keV for gold element. The analytical conditions were examined, and a pH 7.2 phosphate buffer solution with a concentration of 40 mmoL·L-1 PO3-4, a concentration of 40.0 µg· mL-1 HAuCl4 and a reaction time of 5 min was selected for use. Under the selected conditions, the SPR absorption peak value was linear to CO concentration in the range of 0.2～8.75 µg· mL-1, with a detection limit of 0.1 µg· mL-1 CO. According to the procedure, the influence of coexistent substances on the determination of 1.0 mg·L-1 CO was tested, with a relative error of ±5%. Results indicated that 200 times SO2-3, PO3-4, SO2-4, CO2-3 and NO-3, 100 times Zn2+, K+, BrO-3, Na2S, ethanol, methanol, 80 times Ni2+, Cr3+, Co2+, Ca2+, Mg2+, Fe3+, glucose, Pb2+, Al3+, SeO2-3, Na2S2O3, formaldehyde, 50 times Mn2+ do not interfere with the determination. It showed that this SPR method had good selectivity. The CO content in air samples was determined with the SPR method, with a relative standard deviation (RSD) of 1.8%～4.2%, the SPR method results were agreement with that of the gas chromatography (GC).

[A Hydride Generation-Catalytic Resonance Rayleigh Scattering Method for Detection of Trace Arsenic].

Arsenic is a toxic metal element and the establishment of a highly sensitive and selective method for As has great significance to human health and environment protection. In sulfuric acid medium, As(Ⅲ) was reduced by NaBH4 to form AsH3 gas that was trapped by the Ce(Ⅳ)-I- catalytic absorption solution to cause Ce(Ⅳ) concentration decreased and As particle increased, which resulted in the resonance Rayleigh scattering (RRS) and fluorescence increased at 370 and 351 nm respectively. The increased RRS and fluorescence intensities were linear to As(Ⅲ) concentration in the range of 0.006~0.76 and 0.006~0.28 mg·L(-1) respectively, with a detection of As of 3.0 µg·L(-1). The new hydride generation-catalytic RRS method was applied for detection of trace As(Ⅲ) in milk samples, and the results were in agreement with that of hydride generation-atomic absorption spectrometry.

A label-free DNAzyme-cleaving fluorescence method for the determination of trace Pb(2+) based on catalysis of AuPd nanoalloy on the reduction of rhodamine 6G.

The substrate chain of double-stranded DNA (dsDNA) could be specifically cleaved by Pb(2+) to release single-stranded DNA (ssDNA) that adsorbs onto the AuPd nanoalloy (AuPdNP) to form a stable AuPdNP-ssDNA complex, but the dsDNA can not protect AuPdNPs in large AuPdNP aggregates (AuPdNPA) under the action of NaCl. AuPdNP-ssDNA and large AuPdNPA could be separated by centrifugation. On increasing the concentration of Pb(2+) , the amount of released ssDNA increased; AuPdNP-ssDNA increased in the centrifugation solution exhibiting a catalytic effect on the slow reaction of rhodamine 6G (Rh6G) and NaH2 PO2 , which led to fluorescence quenching at 552 nm. The decrease in fluorescence intensity (ΔF) was linear to the concentration of Pb(2+) within the range 0.33-8.00 nmol/L, with a detection limit of 0.21 nmol/L. The proposed method was applied to detect Pb(2+) in water samples, with satisfactory results.

SERS quantitative detection of trace human chorionic gonadotropin using a label-free Victoria blue B as probe in the aggregated immunonanogold sol substrate.

Nanogold particles (NG) were modified by anti-rabbit antibody (RAb) against human chorionic gonadotropin to obtain an immunonanogold probe (ING). In pH 7.0 Na2HPO4-citrate buffer solution containing KCl, ING probes formed large aggregates in which Victoria blue B (VBB) molecules were adsorbed on the surface and which exhibited strong surface-enhanced Raman scattering (SERS) at a peak of 1612 cm(-1). After addition of human chorionic gonadotropin (hCG) an immune reaction with the ING probe occurred to form dispersive ING-hCG complexes with non-SERS activity that led to a decreased SERS peak at 1612 cm(-1). The decreased SERS intensity was linear to the concentration of hCG over 2.4-73.2 ng/mL. The ING reaction was studied in detail by SERS, scanning electron microscope (SEM), resonance Rayleigh scattering (RRS), surface plasmon resonance (SPR) absorption and laser scattering techniques. SERS quenching was observed and discussed.

[Determination of Trace Boron Based on Gold Nanorod Plasmonic Resonance Rayleigh Scattering Energy Transfer to the Coordinate].

B is a necessary trace element for human and animals, but the excess intake of B caused poison. Thus, it is very important to determination of B in foods and water. The target of this study is development of a new, sensitive and selective resonance Rayleigh scattering energy transfer (RRS-ET) for the determination of B. The combination of energy transfer with resonance Rayleigh scattering (RRS) has developed a new technology called RRS-ET, which can realize selective and sensitive detection of boric acid. The gold nanorods in diameter of 12 nm and length of 37 nm were prepared by the seed growth procedure. In pH 5. 6 NH4 Ac-HAc buffer solution and in the presence of azomethine-H (AMH), the gold nanorod particles exhibited a strong resonance Rayleigh scattering (RRS) peak at 404 nm. In the presence of boric acid, it reacts with AMH to form AMH-boric acid (AMH-B) complexes. When the complexe as a receptor close to the gold nanorod as a donor, the resonance Rayleigh scattering energy transfer (RRS-ET) take placed that resulted in the Rayleigh scattering signal quenching. With the increase of the concentration of boric acid, the formed complexes increased, the scattering light energy of gold nanorod transfer to the complexes increased, resulting in the Rayleigh scattering intensity linearly reduced at 404 nrn. The decreased RRS intensity responds linearly to the concentration of boron over 10~750 ng . mL-1 B, with a regress equation of ΔI404 nm =3. 53c+24 and a detection of 5 ng mL-1 B. The influence of coexistence substances on the RRS-ET determination of 2. 3 X 10(-7) mol . L-1 B was considered in details. Results showed that this new RRS-ET method is of high selectivity, that is, 4 X 10(-4) mol . L-1 Mn2+, Cd2+, Zn2+, Bi+, Na+, Al3+, glucose, Hg2+, IO3-, F-, SO(2-)3, SiO3-, NO3-, CIO4-, H2O2, mannitol, glycerol, and ethylene glycol, 4X 10(-5) mol . L-1 L-tyrosine, and 2 X 10(-4) mol . L-1 L-glutamic acid do not interfere with the determination. Based on this, a new sensitive, selective, simple and rapid RRS-ET method has been developed for the determination of trace boron in six mineral water samples that contain 24. 9, 29. 3, 57. 9, 59. 0, 84. 9, and 105. 1 ng . mL-1 B, with relative standard deviation of 1. 6%~ 4. 1% and recovery of 95. 61~9. 6%.

[Fluorescence Determination of Trace Se with the Hydride-K13-Rhodamine 6G System].

Se is a necessary trace element for human and animals, but the excess intake of Se caused poison. Thus, it is very important to determination of Se in foods and water. The target of this study is development of a new, sensitive and selective hydride generation-molecular fluorescence method for the determination of Se. In 0. 36 mol . L-1 sulfuric acid, NaBH4 as reducing agent, Se (IV) is reduced to H2 Se. Usin3-g I solution as absorption liquid3, I- is reduced to I- by H2Se. When adding rhodamine 6G, Rhodamine 6G and I3- form association particles, which lead to the fluorescence intensity decreased. When Se(IV) existing, Rhodamine 6G and I3- bind less, And the remaining amount of Rhodamine 6G increase. So the fluorescence intensity is enhanced. The analytical conditions were optimized, a 0. 36 ml . L-1 H2SO4, 21. 6.g . L-1 NaBH4, 23.3 µm . L-1 rhodamine 6G, and 50 µmol . L-1 KI3 were chosen for use. When the excitation wavelength is at 480nm, the Rayleigh scattering peak does not affect the fluorescence recording, and was selected for determination of Se. Under the selected conditions, Se(IV) concentration in the 0. 02~0. 60 µg . mL-1 range and the increase value of the fluorescence intensity (ΔF) at 562 nm linear relationship. The linear regression equation is ΔF562 nm =12. 6c + 20. 9. The detecton limit was 0.01 µ.g . L-1. The influence of coexistence substances on the hydride generatin-molecular fluorescence determination of 5. 07 X10(-6) mol . L-1 Se(IV) was considered in details. Results showed that this new fluorescence method is of high selectivity, that is, 0. 5 mmol. L-1 Ba2+, Ca2+, Zn2+ and Fe3+, 0. 25 mmol . L-1 . Mg2+, 0. 05 mmol . L-1 K+, 0. 2 mmol . L-1 Al3+, 0. 025 mmol . L-1 Te(VI) do not interfere with the determination. The influence of Hg2+, CD2+ and Cu2+ that precipitate with Se(IV), can be eliminated by addition of complex reagent. This hydride generation-molecular fluorescence method has been applied to determination of trace Se in water samples,

A simple and sensitive resonance Rayleigh scattering method for determination of As(III) using aptamer-modified nanogold as a probe.

A simple and selective aptamer (ssDNA)-modified nanogold probe (AussDNA) was prepared for the determination of trace As(III) in HEPES buffer solution (pH 8.2) containing 0.05 mol/L NaCl. The method coupled the aptamer reaction of AussDNA-As(III) and the resonance Rayleigh scattering (RRS) of nanogold aggregations at 278 nm. When the As(III) concentration increased, the RRS intensity at 278 nm increased to form more nanogold aggregation and a stable As(III)-ssDNA complex. Under selected conditions, the increased RRS intensity (ΔI) was linear to the concentration of As(III) in the range 3.8-230.4 ng/mL, with a detection limit of 1.9 ng/mL. This RRS method was applied to detect As(III) in water samples, with simplicity, sensitivity and selectivity.

A simple and sensitive fluorescence method for the determination of trace ozone in air using acridine red as a probe.

The ozone in an air sample was trapped by H3 BO3 -LK solution to produce iodine (I2) that interacted with excess I(-) to form I3(-). In pH 4.0 acetate buffer solutions, the I3(-) reacted with acridine red to form acridine red-I3 ion association particles that resulted in the fluorescence peak decreased at 553 nm. The decreased value ΔF553 nm is linear to the O3 concentration in the range 0.08-53.3 × 10(-6) mol/L, with a detection limit of 4 × 10(-8) mol/L. This fluorescence method was used to determine ozone in air samples, and the results were in agreement with that of indigo carmine spectrophotometry.

[Resonance Rayleigh scattering determination of trace ozone based on the cationic surfactant association particles].

In the presence of pH 4.0 HAC-NaAC buffer solution, using H3BO3-KI (BKI) as absorption solution, O3 oxidized KI to produce I2, and it reacted with excess I- to form I3- that combined with the cationic surfactant (CS) such as cetylpyridinium chloride (CPCl), tetradecyl pyridinium bromide (TPB), cetyl trimethyl ammonium bromide (CTMAB), and tetradecyl dimethylbenzyl ammonium chloride (TDMAC) to produce stable (CS-I3)n association particles, which exhibited a strong resonance Rayleigh scattering (RRS) peak at 470 nm. Under the chosen conditions, as the concentration of O3 (C) increased, the concentration of I3- increased, and the RRS intensity at 470 nm (1470 nm) increased due to more association particles forming. The increased RRS intensity I470 nm was linear with O3 concentration. For the four CS systems, the linear range was 15-50, 50-100, 5-25 and 1-50 micromol x L(-1) O3 respectively. The regression equation is delta I = 8.81c-4.01, delta I = 5.44c-3.11, delta I = 15.39c-1.55, and delta I = 16.88c + 0.51. The detection limit is 4.9, 12, 2.85 and 0.56 micromol L(-1) O3 respectively. The influence of some foreign substances was examined on the determination of 2.5 x 10(6) mol x L(-1) O3, within +/- 10% relative error. Results showed that a 4.0 x 10(-5) mol x L(-1) Hg2+, 8.7 X 10(-5) mol x L(-1) Fe3+, 5.0 x 10(-5) mol x L(-1) Ca2+, 2.5 x 10(-5) mol L(-1) Zn2+ and Cu2+, 2.8 x 10(-6) mol x L(-1) Pb2+ and Cr3+, 4.2 x 10(-5) mol x L(-1) Mg2+, Mn2+ and Ba2+ do not interfere with the RRS determination. This showed that this RRS method is of good selectivity. The TDMAC system is most sensitive, and was chosen to detect O3 in air samples. The analytical results were in agreement with that of spectrophotometry results. Further more, laser scattering technique was utilized to examine the particle size distribution of (TDMAC-I3)n system. Results indicated that the particle size located in the range of 190-531 nm, in the absence of O3. Upon addition of O3, the excess KI reacted with O3 to produce I3-, and I3- interacted with the TDMAC to form (TDMAC-I3)n associated particles with a size range of 1,106-3,091 nm. This test identified that there are associated particles in the TDMAC system.

[Resonance Rayleigh scattering determination of trace tobramycin using aptamer-modified nanogold as probe ].

Nanogold (NG) was prepared using NaBH4 reduction of HAuCl4. The NG was modified by the tobramycin-aptamer to obtain a stable Apt-NG probe for tobramycin. The three aptamers containing 15, 21 and 27 bases were examined, and results showed that the aptamer with 21 bases was best and was chosen for use. In pH 6. 8 PBS buffer solution and in the presence of NaCl, the Apt-GN probes were not aggregated. When tobramycin was added, it reacted with the Apt of Apt-NG probe to form a very stable Apt-Tbc complex and released NGs that were aggregated into big particles under the action of NaCl with three resonance Rayleigh scattering peaks at 285, 368 and 525 nm respectively. The resonance Rayleigh scattering peak increased at 368 nm due to the formation of big NG particles from the probe. The effect of pH buffer solution, its volume, and Apt-GN probe concentration on the ΔI value was considered. A 200 µL pH 6. 8 PBS buffer solution and 19. 1 nmol · L(-3) Apt-GN, giving max ΔI value, were chosen for use. Under the chosen conditions, the increased resonance Rayleigh scattering intensity ΔI368 nm was linear with Tbc concentration in the range of 1.9-58.3 ng mL(-3), with a regress equation of ΔI = 35.3c-23 and a detection limit of 0.8 ng · mL(-3) Tbc. A 10.0, 20.0 and 30.0 ng mL-3 Tbc was determined five times respectively, and the relative standard deviations were 6.8%, 5.0% and 4.4%. The influence of some foreign substances was examined on the determination of 38.9 ng · mL(-3) Tbc, within ±10% related error. Results showed that a 80 times of Zn2+, 40 times of L-glutamic acid, Cu2+, Mg2+ and Ca2+, 20 times of glucose and terramycin, 10 times of L-phenylalanine and glycin, 2 times of L-aspartic acid, and 6 times of bovine serum albumin (BSA) and human serum albumin (HSA) do not interfere with the RRS determination of Tbc. The results showed that this aptamer-nanogold RRS method is of good selectivity. Tbc in real sample was analyzed, and the analytical result was in agreement with that of reference results, with a relative standard deviation of 6.5%-7.6% and a recovery of 95.0%-107%.