共查询到20条相似文献,搜索用时 93 毫秒
1.
2.
3.
Ti/Sb2O5-SnO2/PbO2电极电催化氧化对氨基苯酚 总被引:2,自引:0,他引:2
以电沉积法制备的Ti/Sb2O5-SnO2/PbO2电极作阳极,恒电流电解水溶液中的对氨基苯酚(PAP),利用紫外光谱探讨了对氨基苯酚电催化氧化的反应历程,系统地考察了电解时间、反应温度,pH值、电流密度以及对氨基苯酚初始浓度对COD去除率的影响,提出了电催化氧化对氨基苯酚的最佳条件.结果表明,对氨基苯酚电催化反应为逐级氧化历程,主要中间产物为苯醌、丁烯二酸和草酸,最终产物为CO2和水.20℃,对初始浓度10mg/L的对氨基苯酚水溶液(pH=6),恒定电流密度100mA/cm^2,电解1h,COD去除率可达98.5%.该方法作为废水中对氨基苯酚的最小化处理.具有良好的应用前景. 相似文献
4.
电解还原法生产的对氨基苯酚纯度及杂质的高效液相色谱分析 总被引:3,自引:0,他引:3
研究了用高效液相色谱法对电化学生产的对氨基苯酚及杂质4,4'-二氨基二苯醚和联苯胺含量的测定。方法简单、重现性好,适合工业生产中的快速控制分析,对氨基苯酚产品的相对标准偏差小于1.5%,4,4'-二氨基二苯醚和联苯胺的相对标准偏差分别小于2.5%和3.0%。 相似文献
5.
6.
以对氨基苯酚和正丁酸为原料,合成了4-丁酰氨基乙酰氧基苯,讨论了反应的影响因素。本方法收率高,易于纯化。 相似文献
7.
利用二氧化硫脲制备对氨基苯酚 总被引:3,自引:0,他引:3
利用二氧化硫脲制备对氨基苯酚顾尚香姚卡玲(兰州大学化学系甘肃730000)对氨基苯酚的制备方法之一是用铁粉在盐酸存在下生成的新生态氢将对硝基苯酚中的硝基还原为氨基,产率约80%左右,但铁泥的处理非常麻烦;另一方法是用苯酚为原料先制备出对亚硝基苯酚,然... 相似文献
8.
9.
对氨基苯酚是一种重要的化工原料及医药中间体。 由硝基苯合成对氨基苯酚具有明显的原料优势,并且具有流程短、能耗低等优点;但该方法通常以传统液体强酸为催化剂,存在设备腐蚀、需要用碱中和反应后的残余酸,产生大量盐固体废弃物等问题。 因此,开发硝基苯加氢合成对氨基苯酚的绿色工艺具有重要的意义,也是近年研究的热点。 现阶段的研究主要集中在开发可替代传统液体酸的催化剂,如固体酸、酸性离子液体、路易斯酸、二氧化碳-水以及固体酸负载金属纳米粒子双效催化剂等,并取得了较大的进展。 本文主要综述和评价如上绿色酸催化体系中硝基苯加氢合成对氨基苯酚的最新进展并对其未来发展进行了展望。 相似文献
10.
对氨基苯酚在L-半胱氨酸修饰金电极上的电化学行为及其在分析中的应用 总被引:2,自引:0,他引:2
宋远志 《理化检验(化学分册)》2008,44(10):986-988,993
在金电极上组装了L-半胱氨酸,采用循环伏安法研究了对氨基苯酚在L-半胱氨酸修饰金电极上的电化学行为.结果表明:在pH 6.54的磷酸盐缓冲介质中,扫描速率为100 mV·s-1时,L-半胱氨酸修饰金电极上对对氨基苯酚具有良好的电催化活性,并显示对氨基苯酚在此修饰电极上的反应过程与裸金电极相比有良好的可逆性.将此优化的反应条件,应用于测定饮用水中对氨基苯酚的含量.对电催化机理也作了简要探讨. 相似文献
11.
Long-term afterglow emission (AG) of poly(arylene phthalide) films (PAP) irradiated with visible light has been discovered.
Recombination nature of the AG was experimentally proven as in the case of UV irradiation. Features of the observed AG spectra
were analyzed in comparison with the photo-, electro-, and thermoluminescence spectra of the PAP films in relation to the
commonness of the AG generation mechanism, which is associated with the involvement of the two-photon reactions and triplet
states in the photoprocesses in PAP. 相似文献
12.
A reliable and simple electrochemical method has been proposed for the simultaneous determination of paracetamol (PAR) and p‐aminophenol (PAP) in pharmaceutical formulations. The oxidation and reduction peak potentials in cyclic voltammetry (CV) for PAR on carbon ionic liquid electrode (CILE) were occurred at 370 and 225 mV vs. Ag/AgCl, respectively at pH 7.0, while those for PAP on CILE appeared at 128 mV and 68 mV, respectively at the scan rate of 0.05 V s?1. In comparison to the conventional carbon paste electrode, the apparent reversibility and kinetics of the electrochemical reactions of PAR and PAP were significantly improved on CILE. In differential pulse voltammetric technique, the peak potentials for PAR and PAP appeared at 345 and 130 mV, respectively, with the peak separation of 215 mV, sufficient for their simultaneous determination in samples containing these two species. The proposed method was used for simultaneous determination of PAR and PAP in tablets. PAR and PAP can be determined in the ranges of 2.0×10?6–2.2×10?3 M and 3.0×10?7–1.0×10?3 M, with the detection limits of 5.0×10?7 and 1.0×10?7 M (calculated by 3σ), respectively. The relative standard deviations for the determination of PAR and PAP were less than 2%. 相似文献
13.
A sensitive and selective method was developed for the determination of N-acetyl-p-aminophenol (APAP) and p-aminophenol (PAP) using poly(3,4-ethylenedioxythiophene) (PEDOT)-modified glassy carbon electrode (GCE). Cyclic voltammetry and differential pulse voltammetry were used to investigate the electrochemical reaction of APAP and PAP at the modified electrode. Both APAP and PAP showed quasireversible redox reactions with formal potentials of 367 mV and 101 mV (vs. Ag/AgCl), respectively, in phosphate buffer solution of pH 7.0. The significant peak potential difference (266 mV) between APAP and PAP enabled the simultaneous determination both species based on differential pulse voltammetry. The voltammetric responses gave linear ranges of 1.0 × 10−6-1.0 × 10−4 mol L−1 and 4.0 × 10−6-3.2 × 10−4 mol L−1, with detection limits of 4.0 × 10−7 mol L−1 and 1.2 × 10−6 mol L−1 for APAP and PAP, respectively. The method was successfully applied for the determination of APAP and PAP in pharmaceutical formulations and biological samples. 相似文献
14.
Determination of albumin in biological fluids by flow injection analysis using the peroxyoxalate chemiluminescent system in micellar medium 总被引:2,自引:0,他引:2
A novel chemiluminescence (CL) method for the determination of papaverine (PAP) has been developed by combining the flow injection technique and its sensitizing effect on the weak CL reaction between sulfite and acidic permanganate. A mechanism for the CL reaction has been proposed on the basis of fluorescent and chemiluminescence spectra. The CL response is proportional to the concentration of PAP over the range 0.2-10 micro mol L(-1). The detection limit of PAP is 0.10 micro mol L(-1) (3 s) with a relative standard deviation (RSD) of 2.0% for 10 repetitive determinations of 1.0 micro mol L(-1) PAP. Interferences from other alkaloids in the opium, such as morphine and codeine, are negligible except that of narcotine. The method has been satisfactorily used for the determination of PAP in injections and compound liquorice tablets. 相似文献
15.
以苯胺五聚体(AP)与聚乳酸(PLA)的三嵌段共聚物(PAP)与表面接枝低聚乳酸的纳米羟基磷灰石(op-HA)和聚丙交酯-乙交酯(PLGA)的复合物共混,制备了电活性可降解纳米复合材料PAP/op-HA/PLGA,采用紫外-可见光谱、循环伏安扫描和标准四探针法分析其电化学特性及电导率.采用ESEM观察其膜表面形貌,用接... 相似文献
16.
In this study, Ti-Si-Sn-Sb/GAC particle electrodes were prepared by sol–gel method. The particle electrodes were characterized by SEM, XRD, EDX, and BET then used to carry out three-dimensional (3D) electrocatalytic oxidation degradation on simulated refractory p-aminophenol (PAP) wastewater. The effects of initial pH, cell voltage, aeration flow rate and initial PAP concentration on degradation experiments were investigated. Under the optimal conditions, the PAP and COD removal rates were 89.45% and 75.17% respectively. In addition, the possible degradation mechanism of PAP was further investigated by UV–Vis and HPLC. Finally, it was found that the Ti-Si-Sn-Sb/GAC particle electrodes with high catalytic activity and excellent stability could significantly improve the PAP wastewater removal efficiency. 相似文献
17.
18.
Martínez-Cabot A Varela B Lloveras M Campos R Marco MP Messeguer A 《Analytical and bioanalytical chemistry》2008,391(2):617-624
The fatty acid esters of 3-(N-phenylamino)propane-1,2-diol (PAP) are biomarkers of toxic oil batches that caused toxic oil syndrome (TOS), an intoxication
that caused over 400 deaths and affected 20,000 people in Spain in 1981. PAP esters are converted into PAP by human pancreatic
lipase. The in vivo biotransformation of PAP in two mouse strains generated potentially toxic metabolites. Here we report
an enzyme-linked immunosorbent assay (ELISA) for PAP detection incorporating antibodies generated using PAP-hapten derivatives
1 and 2. The immunizing haptens were designed to recognize the phenylamino and hydroxymethylene moieties of the PAP structure. The
antisera raised against 1-HCH showed greater affinity for free PAP, as demonstrated in competitive experiments using either 1-BSA or 2-BSA as coating antigens. The developed ELISA detects PAP at a threshold of 130 μg L−1 and can be used over a wide range of pH and ionic strength values. The assay can be applied to human urine samples, after
a simple treatment method, with good recovery according to the correlation obtained when analyzing blind spiked urine samples.
Figure Development of an ELISA for PAP in human urine 相似文献
19.
An efficient magnetic nanoparticle‐supported palladium (Fe3O4/SiO2‐PAP‐Pd) catalyst is reported for the Suzuki cross‐coupling and Stille reactions. This method provides a novel and much improved modification of the Suzuki and Stille coupling reactions in terms of phosphine‐free catalyst, short reaction time, clean reaction and small quantity of catalyst. Another important feature of this method is that the catalyst can be easily recovered from the reaction mixture and reused with no loss of its catalytic activity. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
20.
HUANG Wei-Ping ZHANG Xin-Jie WU Shi-HuaMA Shu-Yin ZHANG Shu-Ji ZHAO Wei-Jun 《天然气化学杂志》1997,6(3):252-257
IntroductionIn1962,N.V.Kutepow'SgroupfirstusedcomplexesofFe,CoandNiascatalyststocatalyzecarboXylationofethanoltopreparepropanoicacidanditsderivants.Thereactionpressurewashighandtheyieldwaslow.LateronPaulalsandhiscolleagueusedabC13andiodineascatalyst,which… 相似文献