CN109374618A - 一种亚硝酸根的检测方法 - Google Patents
一种亚硝酸根的检测方法 Download PDFInfo
- Publication number
- CN109374618A CN109374618A CN201811638472.4A CN201811638472A CN109374618A CN 109374618 A CN109374618 A CN 109374618A CN 201811638472 A CN201811638472 A CN 201811638472A CN 109374618 A CN109374618 A CN 109374618A
- Authority
- CN
- China
- Prior art keywords
- ruthenium
- nitrite anions
- binuclear ruthenium
- binuclear
- detection method
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- -1 nitrite anions Chemical class 0.000 title claims abstract description 51
- 238000001514 detection method Methods 0.000 title claims abstract description 37
- 229910052707 ruthenium Inorganic materials 0.000 claims abstract description 47
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims abstract description 44
- 150000001768 cations Chemical class 0.000 claims abstract description 6
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 16
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 claims description 14
- 238000002835 absorbance Methods 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 11
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims description 11
- 150000001450 anions Chemical class 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 8
- 229910019142 PO4 Inorganic materials 0.000 claims description 7
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 claims description 7
- 239000010452 phosphate Substances 0.000 claims description 7
- 238000010992 reflux Methods 0.000 claims description 7
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical class OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 claims description 6
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 6
- 239000012327 Ruthenium complex Substances 0.000 claims description 6
- 229940006460 bromide ion Drugs 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 6
- 238000009938 salting Methods 0.000 claims description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 5
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 claims description 5
- 238000002360 preparation method Methods 0.000 claims description 5
- GWOGSJALVLHACY-UHFFFAOYSA-N 2-pyridin-2-ylpyridine;ruthenium Chemical compound [Ru].N1=CC=CC=C1C1=CC=CC=N1 GWOGSJALVLHACY-UHFFFAOYSA-N 0.000 claims description 4
- IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical group ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 4
- 229910001961 silver nitrate Inorganic materials 0.000 claims description 4
- 238000011088 calibration curve Methods 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 3
- 238000002798 spectrophotometry method Methods 0.000 claims description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
- NPYPAHLBTDXSSS-UHFFFAOYSA-N Potassium ion Chemical compound [K+] NPYPAHLBTDXSSS-UHFFFAOYSA-N 0.000 claims description 2
- FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 claims description 2
- 238000002425 crystallisation Methods 0.000 claims description 2
- 230000008025 crystallization Effects 0.000 claims description 2
- IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 claims description 2
- 229910001414 potassium ion Inorganic materials 0.000 claims description 2
- 229910001415 sodium ion Inorganic materials 0.000 claims description 2
- 238000005259 measurement Methods 0.000 claims 1
- 230000035945 sensitivity Effects 0.000 abstract description 5
- 230000036039 immunity Effects 0.000 abstract description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical group CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 25
- 239000000243 solution Substances 0.000 description 17
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 16
- 235000019441 ethanol Nutrition 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 235000010288 sodium nitrite Nutrition 0.000 description 8
- 229960004756 ethanol Drugs 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 6
- 150000002500 ions Chemical class 0.000 description 6
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 4
- 229960000935 dehydrated alcohol Drugs 0.000 description 4
- 125000003963 dichloro group Chemical group Cl* 0.000 description 4
- JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- 229910021607 Silver chloride Inorganic materials 0.000 description 3
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000004587 chromatography analysis Methods 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 235000013305 food Nutrition 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 230000001376 precipitating effect Effects 0.000 description 3
- 238000002390 rotary evaporation Methods 0.000 description 3
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000001632 sodium acetate Substances 0.000 description 3
- 235000017281 sodium acetate Nutrition 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- CYDQOEWLBCCFJZ-UHFFFAOYSA-N 4-(4-fluorophenyl)oxane-4-carboxylic acid Chemical compound C=1C=C(F)C=CC=1C1(C(=O)O)CCOCC1 CYDQOEWLBCCFJZ-UHFFFAOYSA-N 0.000 description 2
- DDFHBQSCUXNBSA-UHFFFAOYSA-N 5-(5-carboxythiophen-2-yl)thiophene-2-carboxylic acid Chemical compound S1C(C(=O)O)=CC=C1C1=CC=C(C(O)=O)S1 DDFHBQSCUXNBSA-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 235000019270 ammonium chloride Nutrition 0.000 description 2
- 239000008280 blood Substances 0.000 description 2
- 210000004369 blood Anatomy 0.000 description 2
- 238000005251 capillar electrophoresis Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003446 ligand Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000012544 monitoring process Methods 0.000 description 2
- 238000003969 polarography Methods 0.000 description 2
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 2
- 229910052939 potassium sulfate Inorganic materials 0.000 description 2
- 235000011151 potassium sulphates Nutrition 0.000 description 2
- 239000001509 sodium citrate Substances 0.000 description 2
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 2
- 235000011083 sodium citrates Nutrition 0.000 description 2
- 239000001540 sodium lactate Substances 0.000 description 2
- 229940005581 sodium lactate Drugs 0.000 description 2
- 235000011088 sodium lactate Nutrition 0.000 description 2
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 2
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 2
- 238000001291 vacuum drying Methods 0.000 description 2
- GPRYKVSEZCQIHD-UHFFFAOYSA-N 1-(4-aminophenyl)ethanone Chemical compound CC(=O)C1=CC=C(N)C=C1 GPRYKVSEZCQIHD-UHFFFAOYSA-N 0.000 description 1
- HVBSAKJJOYLTQU-UHFFFAOYSA-N 4-aminobenzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C=C1 HVBSAKJJOYLTQU-UHFFFAOYSA-N 0.000 description 1
- 208000004998 Abdominal Pain Diseases 0.000 description 1
- ROFVEXUMMXZLPA-UHFFFAOYSA-N Bipyridyl Chemical group N1=CC=CC=C1C1=CC=CC=N1 ROFVEXUMMXZLPA-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 description 1
- 206010012735 Diarrhoea Diseases 0.000 description 1
- 208000000059 Dyspnea Diseases 0.000 description 1
- 206010013975 Dyspnoeas Diseases 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 206010016952 Food poisoning Diseases 0.000 description 1
- 208000019331 Foodborne disease Diseases 0.000 description 1
- 206010019233 Headaches Diseases 0.000 description 1
- 206010021143 Hypoxia Diseases 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 206010041349 Somnolence Diseases 0.000 description 1
- 241001122767 Theaceae Species 0.000 description 1
- 229930003268 Vitamin C Natural products 0.000 description 1
- 206010047700 Vomiting Diseases 0.000 description 1
- 238000011481 absorbance measurement Methods 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 229960001413 acetanilide Drugs 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical class N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- ZVSKZLHKADLHSD-UHFFFAOYSA-N benzanilide Chemical compound C=1C=CC=CC=1C(=O)NC1=CC=CC=C1 ZVSKZLHKADLHSD-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- UHYPYGJEEGLRJD-UHFFFAOYSA-N cadmium(2+);selenium(2-) Chemical compound [Se-2].[Cd+2] UHYPYGJEEGLRJD-UHFFFAOYSA-N 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 208000002173 dizziness Diseases 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000000119 electrospray ionisation mass spectrum Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 231100000869 headache Toxicity 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 229940071870 hydroiodic acid Drugs 0.000 description 1
- 230000007954 hypoxia Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000004020 luminiscence type Methods 0.000 description 1
- 238000001819 mass spectrum Methods 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- WZRRZVUZWWMSKH-UHFFFAOYSA-N n'-naphthalen-1-ylethane-1,2-diamine;hydrochloride Chemical compound Cl.C1=CC=C2C(NCCN)=CC=CC2=C1 WZRRZVUZWWMSKH-UHFFFAOYSA-N 0.000 description 1
- OEZDYMAFWLGKFC-UHFFFAOYSA-N n-(2,5-diethoxyphenyl)benzamide Chemical class CCOC1=CC=C(OCC)C(NC(=O)C=2C=CC=CC=2)=C1 OEZDYMAFWLGKFC-UHFFFAOYSA-N 0.000 description 1
- XTBLDMQMUSHDEN-UHFFFAOYSA-N naphthalene-2,3-diamine Chemical compound C1=CC=C2C=C(N)C(N)=CC2=C1 XTBLDMQMUSHDEN-UHFFFAOYSA-N 0.000 description 1
- GQPLMRYTRLFLPF-UHFFFAOYSA-N nitrous oxide Inorganic materials [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 230000033116 oxidation-reduction process Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 235000014786 phosphorus Nutrition 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 235000007686 potassium Nutrition 0.000 description 1
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 1
- 229910000160 potassium phosphate Inorganic materials 0.000 description 1
- 235000011009 potassium phosphates Nutrition 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000002096 quantum dot Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 229950000244 sulfanilic acid Drugs 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 235000013616 tea Nutrition 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 235000019154 vitamin C Nutrition 0.000 description 1
- 239000011718 vitamin C Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/75—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated
- G01N21/77—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator
- G01N21/78—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator producing a change of colour
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
- C07F15/0046—Ruthenium compounds
- C07F15/0053—Ruthenium compounds without a metal-carbon linkage
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
- G01N21/25—Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
- G01N21/31—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
- G01N21/25—Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
- G01N21/31—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry
- G01N21/35—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using infrared light
- G01N21/359—Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using infrared light using near infrared light
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/75—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated
- G01N21/77—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator
- G01N2021/775—Indicator and selective membrane
Landscapes
- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Spectroscopy & Molecular Physics (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Plasma & Fusion (AREA)
- Investigating Or Analysing Materials By The Use Of Chemical Reactions (AREA)
Abstract
本发明涉及一种亚硝酸根的检测方法，用双核钌配合物作为检测亚硝酸根的可见光或近红外光显色剂，所述双核钌配合物的阳离子具有如式Ⅰ所示的结构。本发明的亚硝酸根的检测方法方便易行，灵敏度高，抗干扰性强，可以快速检测亚硝酸根。
Description
技术领域
本发明涉及一种利用可见光-近红外光显色检测亚硝酸根的方法，属于检测技术领域。
背景技术
亚硝酸盐是一种常用的防腐剂，广泛使用在各种腌制食品中，提升了食品的色泽度和保存时间。水体中的含氮化合物如氨基酸等在细菌作用下也极易产生亚硝酸盐。在污染严重的空气中，也发现了明显的亚硝酸根存在。所以，亚硝酸盐存在于人们生活中的各种环境中。科学家已经发现亚硝酸盐引起食物中毒的几率较高，它能氧化血液中的低铁血红蛋白，导致其失去携氧能力而引起细胞、组织、器官缺氧，引起头晕、头疼、乏力、心跳加速、嗜睡或烦躁、呼吸困难、恶心、呕吐、腹痛、腹泻等症状。因此，科学家极为注重监控环境中的亚硝酸根。
Li先生课题组利用CdSe量子点通过电化学发光法实现了对亚硝酸根的检测(Luminescence ,2013 ,28:551–556)。Andreas Nussler等人采用2，3-二氨基萘与亚硝酸根反应通过荧光变化和增强实现了对亚硝酸根的检测(Nature Protocols ,2006 ,1 ,2223–2226)。而Shin-ichi Wakida则使用毛细管电泳法检测了浓度低至2.6μM的亚硝酸根。(Journal of Chromatography A ,2004 ,1051:185-191)。这些报道，却极少涉及对其他各种共存离子干扰的研究和报道。此外，还有GB5009.33—2016 中使用的离子色谱法等。在这些众多方法中，离子色谱法、毛细管电泳法处理复杂且仪器昂贵，需专业人员操作，不利于监管人员和品控人员现场的大量筛查检测工作。近年来有大量依靠观察颜色变化判读结果的亚硝酸盐快速检测的试剂盒快速检测试纸，依然存在检测试纸灵敏度相对较低，试纸吸附不均匀导致显色不均匀，检测重复性差，不利于结果判读等缺点。因此，发展检测亚硝酸根的方法成为食品安全管理、环境监测、医疗检测中必不可少的手段。
中国专利文献CN108872226A（申请号：201811000105.1）公开了一种利用N-苯甲酰替苯胺、2 ',5 '-二乙氧基苯酰替苯胺、3-氨基-4-甲氧乙氧基乙酰替苯胺、4 ,4 '-二氨基苯酰替苯胺或N-乙酰苯胺和浓的高氯酸、氢碘酸、盐酸或硫酸结合后，检测水中亚硝酸根的方法。中国专利文献CN108303414 A（申请号：201810016076.1）公开了一种通过复配的：氯化钠、对氨基苯磺酸、N-1-萘基乙二胺盐酸盐、苯甲酸钠、维生素C、茶多酚混合体系检测亚硝酸根。但是，上述这些配方体系复杂，要求比例掌控比较精确。许多方法还不能满足对亚硝酸根检测中的灵敏度和快速检测的要求，发展新的亚硝酸根的可见光检测方法还是十分必要的。
发明内容
本发明要解决的技术问题是提供一种方便易行，灵敏度高，抗干扰性强，可以快速检测亚硝酸根的检测方法。
本发明为解决上述技术问题提出的一种技术方案是：一种亚硝酸根的检测方法，用双核钌配合物作为检测亚硝酸根的可见光或近红外光显色剂，所述双核钌配合物的阳离子具有如式Ⅰ所示的结构，
。
上述双核钌配合物的阴离子是高氯酸根、硫酸根、氟离子、溴离子、磷酸根或乙酸根。
上述亚硝酸根的检测方法具体步骤是：将所述双核钌配合物配制成浓度为1×10- 9mol/L～1×10-4mol/L的溶液，将待测物加入双核钌配合物的溶液中，采用分光光度法测定波长为436nm或705nm位置处的吸光度，吸光度与亚硝酸根含量成正比，根据吸光度判断待测物中的亚硝酸根含量。
上述亚硝酸根的检测方法，先用双核钌配合物的溶液检测不同浓度的亚硝酸钠标准品，绘制标准品的含量曲线，再用双核钌配合物的溶液检测待测物，采用标准曲线法计算待测物的亚硝酸根含量。
本发明为解决上述技术问题提出的一种技术方案是：一种双核钌配合物，其阳离子具有如式Ⅰ所示的结构，
。
上述双核钌配合物的阴离子是高氯酸根、硫酸根、氟离子、溴离子、磷酸根或乙酸根。
本发明为解决上述技术问题提出的一种技术方案是：将溶解于有机溶剂中的2，2-联吡啶钌配合物和1，1-双（吡啶-2-甲亚氨基）苯乙醇混合，然后加入硝酸银，加热至回流，然后加入盐溶液，结晶生成双核钌配合物，所述盐溶液的阴离子是高氯酸根、硫酸根、氟离子、溴离子、磷酸根或乙酸根，所述盐溶液的阳离子是钠离子、钾离子或铵离子。本发明采用一锅法生成双核钌配合物。
上述有机溶剂是无水乙醇，所述2，2-联吡啶钌配合物与1，1-双（吡啶-2-甲亚氨基）苯乙醇的摩尔比为1:1至2:1，所述回流反应时间为15分钟～2小时，所述反应温度为78℃（乙醇沸点，加热回流的温度），所述硝酸银的与2，2-联吡啶钌配合物摩尔比为2:1。
本发明具有积极的效果：
（1）本发明的亚硝酸根的检测方法采用具有特殊结构的双核钌配合物作为亚硝酸根的显色剂，与亚硝酸根相互作用时会发生吸光强度变化的显色现象，具体原理是亚硝酸根结合到Ru(II)离子上，引起配合物中金属d轨道到配体以及配体到金属的LMCT电荷转移跃迁吸收带变化。同时，导致双核钌的长程电子作用，形成混合价态[RuII-RuIII]（可以由极谱法图2看到）。混合价态[RuII-RuIII]的形成不能由氯离子、硝酸根、高氯酸根、乙酸根、磷酸根、硫酸根、四苯硼酸根等阴离子引发的。从而达到检测亚硝酸根的目的，并能与其他各种阴离子区别开实现选择性检测。与亚硝酸根形成复合物，检测的吸光度位置是波长为436nm和705nm。该方法方便易行，灵敏度高，抗干扰性强，可以快速检测亚硝酸根，尤其适用于快各种阴离子共存的复杂水体的亚硝酸根含量测定。
（2）本发明的亚硝酸根的检测方法只需要按照一定浓度将双核钌配合物配制成水或醇性溶液，水溶液更加实用且使用方便，浓度优选1×10-7mol/L～1×10-6mol/L，可以采用分光光度法进行吸光度测定，采用标准曲线法用标准品绘制含量，从而进行具体含量的计算。
附图说明
图1为实施例1的双核钌配合物的电喷雾质谱图。
图2为采用实施例1的双核钌配合物作为显色剂检测不同浓度的亚硝酸钠溶液的可见光-近红外光光谱图。
图3为采用实施例1的双核钌配合物作为显色剂检测亚硝酸钠溶液的极谱图。
具体实施方式
实施例1
本实施例的双核钌配合物的制备方法是0.10 g（0.6 mmol）的AgNO3与0.17 g（0.3mmol）的二水二氯2，2-联吡啶钌和0.06 g (0.15 mmol)的1，1-双（吡啶-2-甲亚氨基）苯乙醇在100mL的无水乙醇中混合回流30 分钟后，滤去白色的AgCl沉淀，旋转蒸发出去大部分溶剂后加入饱和NaClO4的100mL的乙醇溶液，自然蒸发得到黄色结晶，用乙醇多次洗涤后，真空干燥，得产物0.19 g，产率76%。
本实施例的双核钌配合物的阳离子具有如式Ⅰ所示的结构，阴离子是高氯酸根。
从图1的质谱图可以发现，m/z为1054.05处为结构[(I)ClO4(OH)2]+形成的分子离子峰，同时在m/z为1107.07处为结构[(I)ClO4(OH)2]+•3H2O的水合离子峰，这两处质谱充分说明了配合物的形成。
二水二氯2，2-联吡啶钌具有如式Ⅱ所示的结构。
1，1-双（吡啶-2-甲亚氨基）苯乙醇具有如式Ⅲ所示的结构。
实施例2
本实施例的双核钌配合物的制备方法是0.20 g（0.12 mmol）的AgNO3与0.35 g（0.6mmol）的二水二氯2，2-联吡啶钌和0.12 g (0.3 mmol)的1，1-双（吡啶-2-甲亚氨基）苯乙醇在100mL的无水乙醇中混合回流30 分钟后，滤去白色的AgCl沉淀，旋转蒸发出去大部分溶剂后加入饱和乙酸钠的100mL的的乙醇水溶液（乙醇含量90%），自然蒸发得到黄色结晶，用乙醇多次洗涤后，真空干燥，得产物0.40 g，产率80%。
实施例3
本实施例的双核钌配合物的制备方法是0.10 g（0.6 mmol）的AgNO3与0.17 g（0.3mmol）的二水二氯2，2-联吡啶钌和0.06 g (0.15 mmol)的1，1-双（吡啶-2-甲亚氨基）苯乙醇在100mL的无水乙醇中混合回流45分钟后，滤去白色的AgCl沉淀，旋转蒸发出去大部分溶剂后加入饱和硫酸铵的100mL的乙醇溶液，自然蒸发得到黄色结晶，用乙醇多次洗涤后，真空干燥，得产物0.15g，产率71%。应用例
本应用例的亚硝酸根的检测方法是，采用实施例1制得的双核钌配合物，配制成水/乙醇（体积比70：30）溶液，溶液中双核钌配合物的浓度为1×10-6mol/L。加入待测物，采用分光光度计测定，获得吸光度为纵坐标的光谱图。
本应用例的亚硝酸根的检测方法对浓度分别为1×10–7mol/L、4×10–7 mol/L、8×10–7mol/L、2×10–6 mol/L的亚硝酸钠溶液进行吸光度检测，亚硝酸钠溶液的，获得的可见光-近红外光光谱图如图1所示。由此可知，波长为436nm和705nm位置处的吸光度均与亚硝酸钠含量呈正比。极谱法显示如图2所示，双核钌配合物的半波电位为0.98 和 1.35 V (vsSCE)，分别归属于RuIIIRuII/RuIIRuII2(5+/4+) 和RuIIIRuIII/RuIIIRuII2(6+/5+)氧化－还原电对，对应的两个峰电位的电势差为 ∆E = 0.37 V，当加入亚硝酸钠后，由于亚硝酸根与钌离子的结合，引起双核金属离子的长程电子的运动，导致双核钌的核间作用加强，∆E 减小至0.34 V。
选择性实验
采用本应用例的亚硝酸根的检测方法对含有亚硝酸钠、乙酸钠、柠檬酸钠、乳酸钠、磷酸钾、高氯酸钾、硫酸钾、硝酸钠、氯化铵、氟化铵和溴化钠的混合溶液在可见光-近红外光光谱区域进行吸光度检测。其中，乙酸钠、柠檬酸钠、乳酸钠、磷酸钾、高氯酸钾、硫酸钾、硝酸钠、氯化铵、氟化铵和溴化钠在溶液中的浓度均是1×10–5mol/L，亚硝酸钠在溶液中的浓度为1×10–6mol/L。实验结果证明，这些共存离子也不干扰对亚硝酸根的吸光度。
本发明中所用试剂如无特殊说明浓度均为化学纯。
显然，上述实施例仅仅是为清楚地说明本发明所作的举例，而并非是对本发明的实施方式的限定。对于所属领域的普通技术人员来说，在上述说明的基础上还可以做出其它不同形式的变化或变动。这里无需也无法对所有的实施方式予以穷举。而这些属于本发明的精神所引伸出的显而易见的变化或变动仍处于本发明的保护范围之中。
Claims (10)
1.一种亚硝酸根的检测方法，其特征在于：用双核钌配合物作为检测亚硝酸根的可见光或近红外光显色剂，所述双核钌配合物的阳离子具有如式Ⅰ所示的结构，
。
2.根据权利要求1所述的一种亚硝酸根的检测方法，其特征在于：所述双核钌配合物的阴离子是高氯酸根、硫酸根、氟离子、溴离子、磷酸根或乙酸根。
3.根据权利要求2所述的一种亚硝酸根的检测方法，其特征在于，具体步骤是：将所述双核钌配合物配制成浓度为1×10-9mol/L～1×10-4mol/L的溶液，将待测物加入双核钌配合物的溶液中，采用分光光度法测定波长为436nm或705nm位置处的吸光度，吸光度与亚硝酸根含量呈正比，根据吸光度判断待测物中的亚硝酸根含量。
4.根据权利要求3所述的一种亚硝酸根的检测方法，其特征在于：先用双核钌配合物的溶液检测不同浓度的亚硝酸根标准品，绘制标准品的含量曲线，再用双核钌配合物的溶液检测待测物，采用标准曲线法计算待测物的亚硝酸根含量。
5.根据权利要求3所述的一种亚硝酸根的检测方法，其特征在于：所述双核钌配合物的溶液中双核钌配合物的浓度为1×10-8mol/L～1×10-6mol/L。
6.根据权利要求5所述的一种亚硝酸根的检测方法，其特征在于：所述双核钌配合物的溶液中双核钌配合物的浓度为1×10-7mol/L～1×10-6mol/L。
7.一种双核钌配合物，其特征在于：其阳离子具有如式Ⅰ所示的结构，
。
8.根据权利要求7所述的双核钌配合物，其特征在于：双核钌配合物的阴离子是高氯酸根、硫酸根、氟离子、溴离子、磷酸根或乙酸根。
9.一种如权利要求7所述的双核钌配合物的制备方法，其特征在于：将溶解于有机溶剂中的2，2-联吡啶钌配合物和1，1-双（吡啶-2-甲亚氨基）苯乙醇混合，然后加入硝酸银，加热至回流，然后加入盐溶液，结晶生成双核钌配合物，所述盐溶液的阴离子是高氯酸根、硫酸根、氟离子、溴离子、磷酸根或乙酸根，所述盐溶液的阳离子是钠离子、钾离子或铵离子。
10.根据权利要求9所述的双核钌配合物的制备方法，其特征在于：所述有机溶剂是无水乙醇，所述2，2-联吡啶钌配合物与1，1-双（吡啶-2-甲亚氨基）苯乙醇的摩尔比为1:1至2:1，所述回流反应时间为15分钟～2小时，所述反应温度为78℃，所述硝酸银的与2，2-联吡啶钌配合物摩尔比为2:1。
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