化学研究与应用
化學研究與應用
화학연구여응용
CHEMICAL RESEARCH AND APPLICATION
2014年
10期
1539-1544
,共6页
贾晶%刘琼燕%李桂芳%何晓英
賈晶%劉瓊燕%李桂芳%何曉英
가정%류경연%리계방%하효영
萘酚异构体%乙炔黑%交流阻抗法%线性扫描伏安法%半微分技术
萘酚異構體%乙炔黑%交流阻抗法%線性掃描伏安法%半微分技術
내분이구체%을결흑%교류조항법%선성소묘복안법%반미분기술
naphthol isomers%acetylene black%EIS%liner sweep voltammetry( LSV)%semi-derivative technique
制备了乙炔黑修饰电极(AB/GCE),运用交流阻抗法研究了电极表面的特性。研究了1-萘酚(α-N)和2-萘酚(β-N)在该修饰电极上的循环伏安行为,探讨了修饰剂用量、底液种类及pH、浓度和扫速对伏安行为的影响。在pH6.0的B-R缓冲液中,α-N和β-N均出现一明显的不可逆氧化峰。在60~240mV·s-1扫速范围内,二者氧化峰电流与扫速均呈线性关系,表明该电极过程是受吸附控制的不可逆过程。计算了电极过程的部分动力学参数。运用线性扫描伏安法结合半微分技术对α-N和β-N进行了同时定量测定,发现α-N和β-N的半微分氧化峰电流值与其浓度在5.00×10-5~6.50×10-4mol·L-1范围内呈良好的线性关系(rα-N=0.996;rβ-N=0.997)。α-N和β-N 的检出限(S/N=3)分别为5.04×10-7mol·L-1,6.69×10-7mol·L-1。加标回收率分别为97.20%~100.20%和95.40%~102.50%。
製備瞭乙炔黑脩飾電極(AB/GCE),運用交流阻抗法研究瞭電極錶麵的特性。研究瞭1-萘酚(α-N)和2-萘酚(β-N)在該脩飾電極上的循環伏安行為,探討瞭脩飾劑用量、底液種類及pH、濃度和掃速對伏安行為的影響。在pH6.0的B-R緩遲液中,α-N和β-N均齣現一明顯的不可逆氧化峰。在60~240mV·s-1掃速範圍內,二者氧化峰電流與掃速均呈線性關繫,錶明該電極過程是受吸附控製的不可逆過程。計算瞭電極過程的部分動力學參數。運用線性掃描伏安法結閤半微分技術對α-N和β-N進行瞭同時定量測定,髮現α-N和β-N的半微分氧化峰電流值與其濃度在5.00×10-5~6.50×10-4mol·L-1範圍內呈良好的線性關繫(rα-N=0.996;rβ-N=0.997)。α-N和β-N 的檢齣限(S/N=3)分彆為5.04×10-7mol·L-1,6.69×10-7mol·L-1。加標迴收率分彆為97.20%~100.20%和95.40%~102.50%。
제비료을결흑수식전겁(AB/GCE),운용교류조항법연구료전겁표면적특성。연구료1-내분(α-N)화2-내분(β-N)재해수식전겁상적순배복안행위,탐토료수식제용량、저액충류급pH、농도화소속대복안행위적영향。재pH6.0적B-R완충액중,α-N화β-N균출현일명현적불가역양화봉。재60~240mV·s-1소속범위내,이자양화봉전류여소속균정선성관계,표명해전겁과정시수흡부공제적불가역과정。계산료전겁과정적부분동역학삼수。운용선성소묘복안법결합반미분기술대α-N화β-N진행료동시정량측정,발현α-N화β-N적반미분양화봉전류치여기농도재5.00×10-5~6.50×10-4mol·L-1범위내정량호적선성관계(rα-N=0.996;rβ-N=0.997)。α-N화β-N 적검출한(S/N=3)분별위5.04×10-7mol·L-1,6.69×10-7mol·L-1。가표회수솔분별위97.20%~100.20%화95.40%~102.50%。
A new modified electrode( AB/GCE) was prepared by acetylene black and was used to determine naphthol isomers. The properties of electrode surface were characterized by Nyquist plots. Cyclic voltammetry was used to study the electrochemical behav-iors of α-N and β-N on AB/GCE. The influences of modifier dosage,type of buffer solution,pH,concentration of naphthol isomers and scan rate were discussed by Cyclic voltammetry(CV). The results indicated that there were two sensitive oxidation peaks re-spectively belong toα-N andβ-N in pH6. 0B-R buffer solution. The oxidation peak currents of bothα-N andβ-N were linearly withυ in the range of 60~240mV·s-1 ,showed that the electrode processes ofα-N andβ-N were controlled by adsorption. Some impor-tant parameters of these electrochemical processes were also determined. The linear sweep voltammetry( LSV) with semi-derviative technique was used to determine naphthol isomers quantitatively. A good linear relationship between the peak currents and concen-trations of α-N andβ-N was observed in the range of 5. 00×10-5 ~6. 50×10-4mol·L-1. The detection limit ofα-N is 5. 04×10-7mol ·L-1 and β-N is 6. 69×10-7mol·L-1(S/N=3). The spiked recoveries of the two samples were 97. 20% ~100. 20%and 95. 40% ~102. 50%,respectively.