Three-dimensional voltammetry: Use of chronoamperometric E-t-i data to achieve second-order advantage.

This work studied the use of three-dimensional voltammetry, particularly potential-time-current (E-t-i) data, on the development of electroanalytical methods. E-t-i data was obtained by taking chronoamperograms at potentials applied as pulses on a staircase waveform. By using this three-way kind of data and appropriate calibration algorithms, the possibility of achieving the second-order advantage was evaluated in the determination of ferrocyanide in the presence of the uncalibrated interference hydroquinone as a model system. The determination of acetaminophen in urine samples, where ascorbic acid and uric acid play the major roles as interferents was also studied. Parallel factor analysis (PARAFAC) and multivariate curve resolution alternating least-squares (MCR-ALS) were the algorithms employed in this work. Both algorithms successfully achieved the second-order advantage by correctly predicting the concentrations of the validation synthetic samples. Excellent predictions were obtained in the direct analysis of acetaminophen-spiked urine samples by E-t-i data and MCR-ALS.

Complex numbers-partial least-squares applied to the treatment of electrochemical impedance spectroscopy data.

This work investigated the application of partial least-squares regression of complex numbers on multivariate data obtained by electrochemical impedance spectroscopy (EIS). The use of complex numbers-PLS was evaluated in the individual determination of two well-known redox probes: ferrocyanide and hydroquinone. The predictive ability of complex numbers-PLS was evaluated for EIS spectra obtained at different applied potentials and perturbation amplitudes, and was also compared to that obtained with PLS applied to EIS data presented as real numbers - only the real or imaginary part of the complex impedance, or the absolute impedance or the phase angle. It is shown that complex numbers-PLS is more efficient (better prediction models) when more complex electrochemical systems (hydroquinone) are probed. Excellent predictions were obtained for the determination of hydroquinone and catechol in the direct analysis of spiked tap water samples with EIS and complex numbers-PLS.

Biosorption of 17α-ethinylestradiol by yeast biomass from ethanol industry in the presence of estrone.

Yeast biomass from ethanol industry (YB) was evaluated as a biosorbent to 17α-ethinylestradiol (EE) alone and along with estrone (EST). This material is rich in sorption sites and has a good cost-benefit ratio, since it is an industrial residue largely produced (around 30 g for each liter of ethanol). A 2k-factorial design was carried out to evaluate the sorption capacity of YB for EE considering the variables pH, biosorbent dose (BD), and ionic strength (IS), at two hormone concentration (HC) levels. The best conditions assessed for individual EE adsorption (pH = 10, IS = 0.1 mol/L, and BD = 0.5 mg/L) were also established for adsorption carried out in the presence of EST. Individuals EE and EST experimental sorption capacities (SCexp) were, respectively, 24.50 ± 0.07 and 0.80 ± 0.07 mg/g, fairly similar to Qmax (EE, 21.41 ± 1.27 mg/g; EST, 0.93 ± 0.075 mg/g) from Langmuir model. The Freundlich model best fitted the experimental data for EE adsorption (r2 = 0.9925; χ2 = 0.5575). The study carried out in the presence of EST showed an associative/competitive sorption process between EE and EST, which may be explained by their similar chemical structures and organic carbon-water partition coefficients Koc.

Influence of chlorhexidine and zinc oxide in calcium hydroxide pastes on pH changes in external root surface.

The objective of this study was to assess the influence of chlorhexidine (liquid and gel) and zinc oxide in calcium hydroxide (CH) pastes on root pH in simulated external resorption. One hundred human anterior teeth with a single root canal were selected. After decoronation and root canal instrumentation, the specimens were divided into 4 experimental groups and 1 control group (without intracanal paste): CH + saline (CH+S), CH + 2% chlorhexidine liquid (CH+ CHX), CH + 2% chlorhexidine gel (CH+ CHXg), and CH + 2% chlorhexidine gel + zinc oxide (CH+ CHXg+ZnO). pH was measured using a microelectrode at 3 and 24 h, and 1, 2, 3, and 4 weeks after inserting intracanal pastes. Data were analyzed statistically using an ANOVA and Tukey's test (p < 0.05). The CH+CHXg+ZnO group had the highest pH values throughout (p<0.05). The CH+S and CH+ CHX groups had the highest pH values after 1 week and the CH+ CHXg group after 2 weeks. CH+ CHXg maintained the highest pH until the fourth week compared with CH+ CHX (p < 0.05). The control group remained at a neutral pH at all evaluated times. It can be concluded that chlorhexidine solution or gel maintained the alkaline pH of CH, and chlorhexidine gel allowed a slower decrease in pH over time. CH+ CHXg+ZnO showed the highest pH values and was an effective intracanal medication for maintaining alkaline root pH in the area of resorption.

Influence of chlorhexidine and zinc oxide in calcium hydroxide pastes on pH changes in external root surface

Abstract The objective of this study was to assess the influence of chlorhexidine (liquid and gel) and zinc oxide in calcium hydroxide (CH) pastes on root pH in simulated external resorption. One hundred human anterior teeth with a single root canal were selected. After decoronation and root canal instrumentation, the specimens were divided into 4 experimental groups and 1 control group (without intracanal paste): CH + saline (CH+S), CH + 2% chlorhexidine liquid (CH+ CHX), CH + 2% chlorhexidine gel (CH+ CHXg), and CH + 2% chlorhexidine gel + zinc oxide (CH+ CHXg+ZnO). pH was measured using a microelectrode at 3 and 24 h, and 1, 2, 3, and 4 weeks after inserting intracanal pastes. Data were analyzed statistically using an ANOVA and Tukey's test (p < 0.05). The CH+CHXg+ZnO group had the highest pH values throughout (p<0.05). The CH+S and CH+ CHX groups had the highest pH values after 1 week and the CH+ CHXg group after 2 weeks. CH+ CHXg maintained the highest pH until the fourth week compared with CH+ CHX (p < 0.05). The control group remained at a neutral pH at all evaluated times. It can be concluded that chlorhexidine solution or gel maintained the alkaline pH of CH, and chlorhexidine gel allowed a slower decrease in pH over time. CH+ CHXg+ZnO showed the highest pH values and was an effective intracanal medication for maintaining alkaline root pH in the area of resorption.