摘要
在醋酸/醋酸钠缓冲溶液(pH=4.5)中,亚锡离子对层状二硫化钼(MoS_2)纳米片催化过氧化氢(H_2O_2)氧化邻苯二胺(OPD)的显色反应有很强的抑制作用,据此构建了一种检测亚锡离子的比色传感器.实验结果表明,与不加Mo S2纳米片的OPD/H_2O_2比色传感体系相比,MoS_2/OPD/H_2O_2体系检测亚锡离子的灵敏度显著提高,线性范围变宽.在优化的条件下,MoS_2/OPD/H_2O_2传感体系检测亚锡离子的线性范围为0.02~3.0μmol/L,检出限为8 nmol/L(S/N=3).该传感体系对检测亚锡离子具有高的选择性,可用于湖水中亚锡离子的检测.
In acetate / sodium acetate buffer( pH = 4. 5),tin( Ⅱ) ion displayed strong inhibitory effect on the color reaction of o-phenylendiamine( OPD) oxidized by hydrogen peroxide( H_2O_2) in the presence of layered molybdenum disulfide( MoS_2) nanosheets-based catalysts. This phenomenon was exploited to develop a colorimetric sensor for detection of tin( Ⅱ) ions. The experimental results showed that compared with the OPD /H_2O_2 colorimetric sensory system without Mo S2 nanosheets,MoS_2/ OPD / H_2O_2 colorimetric sensory system exhibited increased sensitivity,low detection limit,and wide linear range toward tin( Ⅱ) ions. Under the optimum experimental conditions,the tin( Ⅱ) sensor based on MoS_2/ OPD / H_2O_2 system provided a linear range of 0. 02—3. 0 μmol / L with a low detection limit of 8 nmol / L( S / N = 3). Moreover,the MoS_2/ OPD /H_2O_2 system displayed a high selectivity for tin( Ⅱ) detection,and can be used for the detection of tin( Ⅱ)ions in lake water samples.
引文
[1]Malla M.E.,Alvarez M.B.,Batistoni D.A.,Talanta,2002,57(2),277—278
[2]Mino Y.,J.Health Sci.,2006,52(1),67—72
[3]Skowronska B.P.,Kaczorowska P.,Skowronski T.,Environ.Pollut.,1997,97(1/2),65—69
[4]Gholivand M.B.,Babakhanian A.,Rafiee E.,Talanta,2008,76(3),503—508
[5]Amjadi M.,Manzoori J.L.,Hamedpour V.,Food Anal.Methods,2013,6(6),1657—1664
[6]Lan H.C.,Wen Y.,Shi Y.M.,Liu K.Y.,Mao Y.Y.,Yi T.,Analyst,2014,139(20),5223—5229
[7]Wang J.Q.,Lv M.Y.,Wang Z.W.,Zhou M.,Gu C.Q.,Guo C.,J.Photochem.Photobiol.A,2015,309,37—45
[8]Adhikari S.,Mandal S.,Ghosh A.,Guria S.,Das D.,Dalton Trans.,2015,44(32),14388—14393
[9]Guan X.Y.,Huang M.Z.,Wang Y.,Chen C.,Cao Z.Q.,Chem.J.Chinese Universities,2013,34(4),841—845(管相宇,黄梅珍,汪洋,陈超,曹庄琪.高等学校化学学报,2013,34(4),841—845)
[10]Feng J.J.,Zhao Y.M.,Wang H.Y.,Chem.J.Chinese Universities,2015,36(7),1269—1274(冯娟娟,赵祎曼,王海燕.高等学校化学学报,2015,36(7),1269—1274)
[11]Ganatra R.,Zhang Q.,ACS Nano,2014,8(5),4074—4099
[12]Joswig J.O.,Lorenz T.,Wendumu T.B.,Gemming S.,Seifert G.,Acc.Chem.Res.,2015,48(1),48—55
[13]Zhu C.B.,Mu X.K.,Aken P.A.V.,Yu Y.,Maier J.,Angew.Chem.Int.Ed.,2014,53(8),2152—2156
[14]Tang H.J.,Wang J.Y.,Yin H.J.,Zhao H.J.,Wang D.,Tang Z.Y.,Adv.Mater.,2015,27(6),1117—1123
[15]Liang Y.L.,Yoo H.D.,Li Y.F.,Shuai J.,Calderon H.A.,Hernandez F.C.R.,Grabow L.C.,Yao Y.,Nano Lett.,2015,15(3),2194—2202
[16]Lukowski M.A.,Daniel A.S.,Meng F.,Forticaux A.,Li L.,Jin S.,J.Am.Chem.Soc.,2013,135(28),10274—10277
[17]Splendiani A.,Sun L.,Zhang Y.B.,Li T.S.,Kim J.,Chim C.Y.,Galli G.,Wang F.,Nano Lett.,2010,10(4),1271—1275
[18]Voiry D.,Salehi M.,Silva R.,Fujita T.,Chen M.W.,Asefa T.,Shenoy V.B.,Eda G.,Chhowalla M.,Nano Lett.,2013,13(12),6222—6227
[19]Quinn M.D.J.,Ho N.H.,Notley S.M.,ACS Appl.Mater.Interfaces,2015,5(23),12751—12756
[20]Pumera M.,Loo A.H.,Trends Anal.Chem.,2014,61,49—53
[21]Guo X.R.,Wang Y.,Wu F.Y.,Ni Y.N.,Kokot S.,Analyst,2015,140(4),1119—1126
[22]Zhang K.,Mao L.Y.,Cai R.X.,Talanta,2000,51(1),179—186
[23]Huang K.J.,Wang L.,Liu Y.J.,Liu Y.M.,Wang H.B.,Gan T.,Wang L.L.,Int.J.Hydrogen Energy,2013,38(32),14027—14034
[24]Lin T.R.,Zhong L.S.,Guo L.Q.,Fu F.F.,Chen G.N.,Nanoscale,2014,6(20),11856—11862
[25]Tarcha P.J.,Chu V.P.,Whittern D.,Anal.Biochem.,1987,165(1),230—233
[26]Igov R.P.,Mitic V.D.,Pecev T.G.,Stankov V.P.,J.Serb.Chem.Soc.,2001,66(9),631—636
[27]Rancic S.M.,Nikolic S.D.,Bojic A.L.,Hem.Ind.,2013,67(6),989—997
[28]Capitán-Vallvey L.F.,Valencia M.C.,Mirón G.,Anal.Chim.Acta,1994,289(3),365—370
[29]Omar M.,Bowen H.J.M.,Analyst,1982,107(1275),654—658