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A long-term sustainable tungsten cathode-solution anode glow discharge (SAGD) source for atomic emission spectrometry was developed for the determination of heavy metal elements. The tungsten cathode of this source was cooled by a compact refrigeration semiconductor, which is simple in design and able to operate at atmospheric pressure for long periods. When the equipment operates at its optimal conditions (75 mA discharge current, 2.0 mm discharge gap, 3.8 mL min−1 flow rate, and solution pH value of 2.0), the detection limits of Ag (338.24 nm), Cd (228.80 nm), Hg (253.66 nm), Pb (368.28 nm), Tl (337.52 nm), and Zn (213.79 nm) were explored, and the values were 0.030, 1.7, 7.2, 17, 0.24, and 25 μg L−1, respectively. The interference of coexisting ions in water, such as K+, Ca2+, Na+, Mg2+, and Li+, on the analytical performance of the solution anode glow discharge-atomic emission spectrometry (SAGD-AES) for Cd, Hg, Pb, and Zn were investigated. The results showed that coexisting metal ions' interferences are insignificant. The SAGD-AES system was successfully applied for analyzing water samples from the Yangtze River and Baixi River, and its accuracy and practicality were verified by comparison with inductively coupled plasma-optical emission spectrometry (ICP-OES) results. [ABSTRACT FROM AUTHOR]

In order to determine metal ions in aqueous solution, a millisecond pulsed solution cathode glow discharge (SCGD) source coupled with a portable spectrometer was developed for atomic emission spectrometry (AES). The millisecond pulsed SCGD source was operated with two high-voltage DC power supplies and a high-voltage pulse switch, specifically boosting the analyte excitation and sustain the glow discharge. The method to excite the plasma discharge contrasts with traditional approaches that employ a single power source. The influence of operating parameters, including pulsed voltage, pulsed frequency, duty ratio, and sample flow rate, were optimized to construct a system having good stability and improved excitation of metal ions. The optimum detection limits for Na, K, Li, Mg, Ag, Cs, Rb, and Sr were 0.17, 0.32, 0.38, 0.50, 2.65, 1.30, 0.22, and 74.02 µg·L−1, respectively. Furthermore, mountain spring, Yangtze River, and reservoir water were spiked with Ag, Rb, and Cs; the recoveries ranged from 105% to 106%, 106% to 107%, and 107% to 108% indicating that the developed system has favorable analytical performance. [ABSTRACT FROM AUTHOR]

This study reports a syringe injection pump for sample introduction for solution cathode glow discharge (SCGD) atomic emission spectroscopy (AES). The experimental conditions are optimized at 60 mA discharge current, 2.5 mm gap spacing, 2.0 mm distance from the glass capillary to cathode, 1.60 mL/min flow rate, and pH 1.0 based on the detection limits (DLs) obtained for Li, Cd, Cu, Ag, Mn, Pb, Cr, and Zn. The detection limits for Li, Cd, Cu, Ag, Mn, Pb, Cr, and Zn were 0.24, 12.26, 12.08, 1.09, 46.42, 25.81, 183.05, and 29.01 µg/L, respectively, significantly lower than using the traditional peristaltic pump. The detection limits decreased by 1.4, 1.8, 2.2, 5.0, 1.4, 1.4, 1.4, 1.6, and 2.2-fold for these elements. The flow rate and the solution consumed per unit time were significantly reduced using this design. The spectral detection revealed stable and practical operation of the system with relative standard deviations <0.85%. Water samples from Yangtze River, Baixi River, and Baiyun Reservoir are analyzed using the modified SCGD system and its evaluation is based upon comparison to inductively coupled plasma—optical emission spectroscopy (ICP-OES). The modified device operates at atmospheric pressure without inert gas and integrates a syringe injection pump and a compact spectrometer to optimize solution utility, analytical performance, and operation size for industrial and environmental monitoring applications. [ABSTRACT FROM AUTHOR]

In order to investigate the influence of laser wavelength on the detection of the metals in Artemisia annua, pulsed lasers operating at wavelengths of 1064 nm and 532 nm for laser induced breakdown spectroscopy (LIBS) have been employed to generate the plasma. The spectral lines of Mg (II) at 279.54 nm, CN at 388.29 nm, Ca (II) at 393.37 nm and Fe (II) at 404.27 nm were used to evaluate the optical emission at various delay times for the 532 nm and the 1064 nm laser. The effects of the data acquisition delay time on the line intensity, signal-to-background ratio and the characteristic parameters of laser plasma have been investigated as well. The results show that the 1064 nm beam induced plasmas with higher signal-to-background ratios and temperatures than the 532 nm beam. However, the 532 nm laser beam produced plasma with higher electron densities than the 1064 nm laser beam. In addition, a significant influence has been found: the spectral intensities of the ions were stronger than the spectral intensities of the atoms independent of whether the laser was operated at 532 nm or 1064 nm. [ABSTRACT FROM AUTHOR]

A hollow anode-solution cathode glow discharge (HA-SCGD) was designed as a plasma excitation source for optical emission spectrometry. The operation parameters such as the discharge current, argon flow rate and solution flow rate were investigated. The spatial distribution profiles of normalized results of spectral bands and spectral lines were investigated and analyzed. The detection limits of Na, Li, K, Ca, Mg, Pb, Sr, Mn, Rb, Cs and Zn were 0.22, 0.69, 1.33, 240.37, 21.55, 529, 619.43, 209.51, 2.94, 7.13 and 206.95 µg L−1, respectively. The repeatability, expressed as the relative standard deviation for these elements, was determined to be within the range from 0.53 to 2.70%. The Ca, Fe, K, Mg and Na concentrations in a certified reference material were quantitatively analyzed, and the results obtained by the HA-SCGD system agreed well with the reference values. The results show that the HA-SCGD system accurately and stably determined metals in aqueous solution. [ABSTRACT FROM AUTHOR]

Solution cathode glow discharge-atomic emission spectrometry (SCGD-AES) has attracted wide attention globally in recent years. The technology has the advantages of on-line detection of various metal elements, small volume, and convenience. In this work, the original spectrometer based on SCGD-AES technology was replaced by filter-wheel, photomultiplier tube (PMT) and picoammeter, which was named FPP spectral discrimination device. Analytical performance of the device with narrow-band monochromator (0.08 nm) was compared to its performance with wide-bandpass filters (10 nm) with optimized spatial. The relative standard deviation of SCGD-FPP for Na, K, Ca, Li, Sr, Rb, and Cs ranged from 0.2 to 0.8%, comparable to the 0.6 to 1.4% with the monochromator. With optimized spatial resolution, the detection limits ranged from 0.15 to 350 μg/L, and the optimal plasma spectral collected points of Na, K, Ca, Li, Sr, Rb, and Cs at 0.8 mm, 0.8 mm, 0.6 mm, 0.4 mm, 0.2 mm, 0.6 mm, and 0.6 mm, respectively. The deviation analysis of the samples containing Na, K, Ca, and Li were analyzed under optimal conditions. The results show that a SCGD-FPP source with spatial resolution improved the detection performance. [ABSTRACT FROM AUTHOR]

A novel-pulsed electrolyte cathode atmospheric pressure discharge (pulsed-ECAD) plasma source driven by an alternating current (AC) power supply coupled with a high-voltage diode was generated under normal atmospheric pressure between a metal electrode and a small-sized flowing liquid cathode. The spatial distributions of the excitation, vibrational, and rotational plasma temperatures of the pulsed-ECAD were investigated. The electron excitation temperature of H Texc(H), vibrational temperature of N2 Tvib(N2), and rotational temperature of OH Trot(OH) were from 4900 ± 36 to 6800 ± 108 K, from 4600 ± 86 to 5800 ± 100 K, and from 1050 ± 20 to 1140 ± 10 K, respectively. The temperature characteristics of the dc solution cathode glow discharge (dc-SCGD) were also studied for the comparison with the pulsed-ECAD. The effects of operating parameters, including the discharge voltage and discharge frequency, on the plasma temperatures were investigated. The electron number densities determined in the discharge system and dc-SCGD were 3.8-18.9 × 1014 cm-3 and 2.6 × 1014 to 17.2 × 1014 cm-3, respectively. [ABSTRACT FROM AUTHOR]

In sample measurements, matrix effects are unavoidable. The matrix effects are one of the main factors affecting the accuracy of the pulsed electrolyte cathode atmospheric pressure discharge detection system. The stability of sodium, potassium, and magnesium, under optimized parameters is measured; the relative standard deviation of spectral intensity is found to be no more than 2%; and the relative standard deviation of background intensity is less than 2%. The matrix effects on the elements potassium, sodium, and magnesium were studied, and the experiments showed that high concentrations of sodium and potassium interfere with each other. A concentration of 200 mg L−1K+affected the sodium signal with an enhancement of more than 120%; and the K+intensity increased 20% in the presence of a high concentration of 200 mL−1Na+. In high concentrations of sodium or potassium, the elemental signal for magnesium enhancement was approximately 8%. Sodium, potassium, and magnesium were quantitatively determined using a mixed calibration sample. When sodium, potassium, and magnesium are present at low concentrations in solution, there were no obvious matrix effects. The sodium, potassium, and magnesium in the calibration samples are quantitatively determined. The relative error and precision are less than 3%, and the recoveries are less than 105%. The detection limits for sodium, potassium, and magnesium were found to be 2.1, 3.4, and 92.6 µg L−1, respectively. [ABSTRACT FROM AUTHOR]

Chinese herbal medicine has attracted increasing attention because of the unique and significant efficacy in various diseases. In this paper, three types of Chinese herbal medicine, the roots of Angelica pubescens, Codonopsis pilosula, and Ligusticum wallichii with different places of origin or parts, are analyzed and identified using laser-induced breakdown spectroscopy (LIBS) combined with principal component analysis (PCA) and artificial neural network (ANN). The study of the roots of A. pubescens was performed. The score matrix is obtained by principal component analysis, and the backpropagation artificial neural network (BP-ANN) model is established to identify the origin of the medicine based on LIBS spectroscopy of the roots of A. pubescens with three places of origin. The results show that the average classification accuracy is 99.89%, which exhibits better prediction of classification than linear discriminant analysis or support vector machine learning methods. To verify the effectiveness of PCA combined with the BP-ANN model, this method is used to identify the origin of C. pilosula. Meanwhile, the root and stem of L. wallichii are analyzed by the same method to distinguish the medicinal materials accurately. The recognition rate of C. pilosula is 95.83%, and that of L. wallichii is 99.85%. The results present that LIBS combined with PCA and BP-ANN is a useful tool for identification of Chinese herbal medicine and is expected to achieve automatic real-time, fast, and powerful measurements. [ABSTRACT FROM AUTHOR]

A solution-cathode glow discharge was used for atomic emission spectrometry. The acidic reagent, discharge current, and flow rate were optimized. The detection limits for sodium, potassium, calcium, and magnesium were 1.51, 4.13, 131, and 54.9 µg L−1, respectively. The relative standard deviation for five replicates was from 0.52 to 3.00%. Sodium, potassium, calcium, and magnesium were determined in mineral water by solution-cathode glow discharge–atomic emission spectrometry. The results demonstrate that the protocol is suitable for the elemental analysis of mineral water. [ABSTRACT FROM AUTHOR]