广西师范大学学报(自然科学版)
廣西師範大學學報(自然科學版)
엄서사범대학학보(자연과학판)
JOURNAL OF GUANGXI NORMAL UNIVERSITY(NATURAL SCIENCE EDITION)
2006年
1期
68-71
,共4页
蒋治良%邹明静%梁爱惠%尹传磊
蔣治良%鄒明靜%樑愛惠%尹傳磊
장치량%추명정%량애혜%윤전뢰
碘酸根%吖啶红%缔合微粒%共振散射
碘痠根%吖啶紅%締閤微粒%共振散射
전산근%아정홍%체합미립%공진산사
IO3-%acridine red%association particle%resonance scattering
在过量的I-存在的稀盐酸介质中,当有IO3-存在时,IO3-与过量的I反应生成I3-,I3-与吖啶红、吖啶橙染料均可形成离子缔合微粒.吖啶红、吖啶橙分别在540、480 nm有较强吸收峰,在550、520 nm有较强荧光峰,吖啶红体系在605 nm处产生1个较强的共振散射(RS)峰,IO3-浓度在1.0×10-7~4.0×10-6 mol/L与605 nm波长处的共振散射光强度成线性关系.吖啶橙体系在560 nm处产生1个较强的共振散射(RS)峰,碘酸根浓度在2.0×10-7~1.2×10-5mol/L与560 nm波长处的共振散射光强度成线性关系.据此建立测定食盐中碘酸根的一种共振散射光谱法.采用此体系测定食盐中碘酸根,结果满意.
在過量的I-存在的稀鹽痠介質中,噹有IO3-存在時,IO3-與過量的I反應生成I3-,I3-與吖啶紅、吖啶橙染料均可形成離子締閤微粒.吖啶紅、吖啶橙分彆在540、480 nm有較彊吸收峰,在550、520 nm有較彊熒光峰,吖啶紅體繫在605 nm處產生1箇較彊的共振散射(RS)峰,IO3-濃度在1.0×10-7~4.0×10-6 mol/L與605 nm波長處的共振散射光彊度成線性關繫.吖啶橙體繫在560 nm處產生1箇較彊的共振散射(RS)峰,碘痠根濃度在2.0×10-7~1.2×10-5mol/L與560 nm波長處的共振散射光彊度成線性關繫.據此建立測定食鹽中碘痠根的一種共振散射光譜法.採用此體繫測定食鹽中碘痠根,結果滿意.
재과량적I-존재적희염산개질중,당유IO3-존재시,IO3-여과량적I반응생성I3-,I3-여아정홍、아정등염료균가형성리자체합미립.아정홍、아정등분별재540、480 nm유교강흡수봉,재550、520 nm유교강형광봉,아정홍체계재605 nm처산생1개교강적공진산사(RS)봉,IO3-농도재1.0×10-7~4.0×10-6 mol/L여605 nm파장처적공진산사광강도성선성관계.아정등체계재560 nm처산생1개교강적공진산사(RS)봉,전산근농도재2.0×10-7~1.2×10-5mol/L여560 nm파장처적공진산사광강도성선성관계.거차건립측정식염중전산근적일충공진산사광보법.채용차체계측정식염중전산근,결과만의.
Under the conditions of HCl-KI,acridine red (AR) has a max absorption peak at 540 nm,the max absorption peak of acridine orange (AO) at 480 nm. There is a fluorescence peak at 550 nm for AR and at 520nm for AO. When there is IO3-,it reacts with excessive I- to form I3-. The two dyes and I3- all combine to form an association particle, respectively. To the systems of AR,it exhibits a strong resonance scattering (RS) peak at 605 nm. IO3- concentration in 1. 0× 10-7~4. 0× 10-6 mol/L is proportional to the resonance scattering peak at 605 nm. There is hypochromic effect at absorption wavelength of 540 nm,and fluorescence quenching at 550 nm. To the systems of AO,the RS peak at 560 nm is most sensitive with IO3- concentration in 2. 0× 10-7~1.2× 10-5 mol/L. The system of AR is applied to the determination of IO3- in table salt.