Departamento de QuÄ±Â´mica, Universidade Federal do MaranhaËo, Brazil Centro de Energia Nuclear na Agricultura, Universidade de SaËo Paulo, Av. CentenaÂ´rio, 303, Box 96, 13400-970, Piracicaba, SP, Brazil A multicommutated ï¬ow system for simultaneous determination of iron and chromium in steel alloys by photometry is described. The ï¬ow network consisted of an automatic injector and four solenoid valves assembled to form two independent analytical pathways, each one comprising reaction coils and a ï¬ow cell. The light source (LED) and detector (photodiode) were attached to the ï¬ow cells to form a compact unit. The ï¬ow system was microcomputer controlled by Quick BASIC 4.5 software, which carried out all steps of the analytical procedure. The feasibility of the system was proved by the determination of iron and chromium in steel alloys and its accuracy was accessed by comparing results with those obtained by plasma atomic emission spectrometry (ICP-AES). No signiï¬cant diï¬erence at the 95% conï¬dence level was observed. Other proï¬table features such as low reagent consumption (0.33 mg 1,10-phenantroline and 0.03 mg 1,5-diphenylcarbazide per determination); relative standard deviations (n Â¼ 5) of 0.4% for iron and 1.2% for chromium; and an analytical throughput of 160 determinations per h were also achieved. A light-emitting diode (LED) has been employed as a radiation source in some photometric procedures, its advantages being robustness and low current consumption [8, 9]. Nevertheless, depending on the LED type, the width of the emission band can range from 30 to 100 nm [10â13]. However, by carefully selecting the methods, LEDs can became a good option as a radiation source in ï¬ow system when multidetermination is performed with photometric detection employing non-expensive instrumentation [14â17]. The ï¬ow network for multicomponent determination can became complex, mainly when the selected spectrophotometric methods required two reagent solutions per analyte [3, 18]. This diï¬culty can be minimized by employing the multicommutation approach that allowed facilities to handle several reagent solutions using a single pumping channel [19, 20]. In the present work, the intention is to develop a photometric ï¬ow set-up for the determination of two analytes at the same time using LEDs as the radiation source and a photodiode as the detector. The ï¬ow network was designed based on the multicommutation approach [21, 22], which aimed to implement a compact and inexpensive ï¬ow system for simultaneous determination of iron and chromium in steel alloys, also presenting a low reagent consumption, which is an inherent feature of the multicommutated ï¬ow system [22, 23]. As chromogenic reagents, 1,10-phenantroline and 1,5-diphenylcarbazide were selected for iron and chromium, respectively. Introduction The simultaneous determination of two or more analytes at a time by ï¬ow-injection analysis became very attractive after the work proposed by Stewart and Ruzicka (1976) . Afterwards, a large number of ï¬ow procedures for multiparameter determination per sample using diï¬erent detection techniques have been described [2â6]. When a multidetermination ï¬ow system is implemented using UV-Vis spectrophotometry as the detection technique, the reagentsâ incompatibility is one diï¬culty that may appear. This drawback has been surmounted by designing ï¬ow systems based on merging zones [2, 3] or on sandwich-technique approaches . When analytes compound absorb radiation at the same wavelengths, the ï¬ow networks have been designed to determine each analyte at a diï¬erent time . On the other hand, if chemical species absorb at a diï¬erent wavelength, simultaneous determination had been carried out, nevertheless equipment with the ability to sweep automatically the wavelengths have been employed [6, 7]. * To whom correspondence should be addressed. e-mail: email@example.com Experimental Reagents, standards and samples All solutions were prepared with analytical-grade reagents, and freshly distilled and deionized water was used throughout. A 0.06% (w/v) 1,5-diphenylcarbazide solution was prepared by dissolving 0.06 g in 2 ml 96% (v/v) ethanol and making the volume up to 100 ml with water. This solution, which was stored in refrigerator, could be use for at least 1 week. Before use, a 20-ml aliquot was equilibrated to laboratory temperature. A 0.25% (w/v) 1,10-phenantroline solution was prepared by dissolving 0.5 g in 100 ml of hot water (ï¬708C). After cooling to room temperature, the volume was made up to 200 ml with water. This solution was stable by 1 week. Journal of Automated Methods & Management in Chemistry ISSN 1463â9246 print/ISSN 1464â5068 online # 2003 Taylor & Francis Ltd http://www.tandf.co.uk/journals A 0.5 mol lâ1 hexamine buï¬er solution, pH 4.9, was prepared by adjusting the pH with HCl. A 1.0% (w/v) ascorbic acid solution was prepared by dissolving 0.5 g in 50 ml on the examine buï¬er solution. This solution was prepared every day. A 1000 mg lâ1 iron(III) stock solution was prepared by dissolving 1.0 g metallic iron in 10 ml concentrated HCl plus 10 ml HNO3 concentrated. After dissolution, the volume was made up to 1000 ml with water. Working standard solutions 0, 5, 15, 30, 60, 90 and 120 mg lâ1 Fe3+ in 0.5 mol lâ1 HCl medium were prepared by appropriated dilution from the stock solution. A 1000 mg lâ1 chromium(VI) stock solution was prepared by dissolving 3.7535 g potassium dichromate in 1000 ml water. Working standard solutions 0, 5, 15, 30, 45, 60 and 75 mg lâ1 Cr6+ in 0.5 mol lâ1 HCl medium were prepared by appropriated dilution from the stock solution. Sample solutions for iron and chromium determination were prepared as described by elsewhere . Apparatus The equipment set-up consisted of two LEDs-based photometers constructed to implement the work; an IPC8 Ismatec peristaltic pump furnished with Tygon tubes; a home-made automatic commutator injector with two commutation sections, which was controlled by means of two solenoids attached to its sliding bar ; four 161T031 three-way solenoid valves (NResearch, Stow, MA, USA); a 486 microcomputer equipped with a PCL711S interface card (American Advantech, San Jose, CA, USA); and a home-made electronic interface to match voltage and current intensities required to switch on the commutator injector and solenoid valves . Reaction coils and ï¬ow lines were of polyethylene tubing (i.d. Â¼ 0.8 mm). The ï¬ow system was controlled by the microcomputer running a software written in QuickBasic 4.5, which was designed to carry out all steps involved in the proposed analytical procedures comprising solutions handling and data acquisition. Detection system A block diagram of the LEDs-based detectors is shown in ï¬gure 1. The two LEDs (L1, L2) employed as the radiation source presented a maximum wavelength at 560 nm (half wide %50 nm). The maximum absorption of the compounds of iron and chromium occurred at 520 and 536 nm, respectively, thus presenting a good overlap with the emitted radiation band. The photodetectors (Det1, Det2) were based on the photodiode supplied by RS Data Library (Catalogue No. RS 308-067). Each detection set-up had an LED, ï¬ow cells (F1, F2) with 10 mm optical length and 100 ml inner volume, and a photodiode. These devices were assembled in a black acrylic block forming compact units. Both photometers presented similar physical structures and the electronic diagram is shown in ï¬gure 2. The operational ampliï¬er (741) was assembled to work with unitary gain in order to provide the impedance marriage Figure 1. Bloc diagram of the photometers. L1, L2, light-emitting diode (LED), Â¼ 560 nm; F1, F2, ï¬ow cell, 10 mm path length, 100 l inner volume; Det1, Det2, phototransistor; AD0, AD1, input of the analogue/digital interface card; Ii, Io, radiation intensity. Figure 2. Electronic diagram of the photometer. Ft, photodetector; Catalogue No. RS 308-067. and to allow the baseline adjusting. The analytical signal was the potential diï¬erence between pin 2 and the 8.2 V set to pin 1 as reference, which was supplied by the Zener diode in series with the 3.3 k resistor. The reference potential (8.2 V) was also used by means of the variable resistor (R) to adjust the value of the baseline measurement. The LED emission intensity was adjusted by controlling the current intensity applied to the base of the transistor (BC547). High radiation intensity can saturate the detector, thus causing a hindering of its response, by other hand, an excessive reduction of the radiation intensity decreased its linear response range. The signals generated by the photometers were read by the microcomputer through the analogue input of the PCL711S interface card. This task was done by coupling the output of the operational ampliï¬er (741) of the photometers (F1, F2) to the A0 and A1 analogue inputs of the interface card, which were selected by software using the interface analogue multiplex. The control software was developed to carry out the handling of the sample and reagents solutions and to perform data acquisition as indicated on its ï¬ow chart shown in ï¬gure 3. Flow diagram and experimental variables The ï¬ow network was designed to implement the multicommutation and binary sampling approaches and the ï¬ow diagram is shown in ï¬gure 4. When the software was run, it request the actual values of the system control variables summarized in table 1. Afterwards, all the steps in the analytical process were carried out without any operator assistance. Table 1. System control variables. Valve Time duration (s) 0.2 0.2 0.2 0.2 0.2 0.2 0.2 0.2 25 Step Sampling/Cr Sampling/Fe Insertion/Cr Insertion/Fe Data acquisition V1 0 0 I 0 0 0 0 0 0 V2 I 0 0 0 0 0 0 0 0 V3 0 0 0 0 I 0 0 0 0 V4 0 0 0 0 0 0 I 0 0 Cycle 4 10 10* 20* Symbols I and 0 indicate valves switched on and oï¬, respectively. * Number of reagentsâ slugs inserted in the sample zones. Figure 3. Flow chart of the software. Initially, all solenoid valves were switched oï¬ (ï¬gure 4) and the carrier solutions (C1, C2) were ï¬owing by aspiration through the valves (V3, V4) and reaction coils (B2, B3) towards the detectors (Det1, Det2). The software was designed to work following the sequence depicted in the valves timing course of ï¬gure 1, i.e. the basic strategy of the binary sampling concept [19â23]. To begin the analytical process, the microcomputer sent through the PCL711 interface card a control signal to displace the injector-sliding bar to the sampling position (ï¬gure 4). This was done by switch on during a time interval (di Â¼ 1 s) one of the solenoids attached to the injector sliding bar . Afterwards, valves V1 and V2 were switched on/oï¬ several times as indicated in the valvesâ timing course. This was done to maintain the time intervals as deï¬ned in table 1. When valve V2 was switched on, the carrier solution stream (C2) was halted and the sample solution (S) ï¬owed through this valve and coil B1 towards the sampling loop L2. When valve V1 was switched on, the stream of solution sample (S) was halted and the reagent solution (R1) ï¬owed through this valve towards the sampling loop L1. When valves V1 and V2 were switched oï¬, the initial solutions ï¬owed again. Henceforth, an on/oï¬ valve switching will be referred as a sampling cycle. A sampling cycle was repeated several times to ï¬ll the sampling loops. Under this condition, sampling loops L1 and L2 were loaded with strings comprising sample slugs in tandem with slugs of reagent solution R1 and carrier solution C2, respectively. After the sampling step had been completed, the injector sliding bar was displaced to the injection position (hatched surface) by powering the other solenoid attached to injector sliding bar . Afterwards, the solenoid valves V3 and V4 were switched on/oï¬ several times (table 1) to insert into the reaction coils B2 and B3 a sequence of sample slugs in tandem with slugs of the reagent solutions R2 and R3. Mixing of the solutions occurred while the sample zones Figure 4. Flow diagram of the system. The three-rectangular surface is an overview of the injector. The hatched area is the alternative position of the sliding bar (central part) and the dashed lines are inner holes; V1, V2, V3, V4, three-way solenoid valves, solid lines into the valves symbols were the ï¬uid pathway, while valves were oï¬ and dashed lines were the alternative pathway when valves were switched on; L1, L2, sampling loops, 25 and 8 cm long, respectively; B1, dilution coil, 25 cm long; B2, B3, reaction coils, 100 cm long; Det1, Det2, photometers; Bp, peristaltic pump; C1, carrier solution for iron determination, 0.5 mol l â1 hexamine buï¬er solution at pH 4.9; C2, carrier solution for chromium determination, 0.5 mol l â1 HCl; W, waste; R1, 1.0% ascorbic acid solution; R2, 0.06% (w/v) 1,5-diphenylcarbazide solution; R3, 0.25% (w/v) 1,10-phenantroline solution. T1, T2, T3, T4 Â¼ valves V1, V2, V3, V4 timing course; d, injector displacement; SL , sample loading step; Rl, reagentsâ loading step; SR, signal reading step. Sampling loops, coils and ï¬ow lines were of polyethylene tubing, 0.8 mm i.d. The high level of the timing course line indicates that the related valve was switched on. were displaced by the carrier solutions towards the detectors Det1 and Det2. The signals related to chromium and iron concentrations were read by a mean of the PEL711s interface card coupled to the detector outputs as a time function and stored for further treatment to determine the concentration of the analytes. While this task was in progress, the data were also displayed on the microcomputer screen while the analytical process was run. The data acquisitions were carried out by sharing the analogue/digital converter of the PCL711 interface card, which aï¬ord facilities to read up to eight analogue signals sequentially. Afterwards, the sliding bar of the injector was displaced to the initial position to begin the next analytical run. The experimental variables such as the pumping ï¬ow rates, the time intervals to switch the solenoid valves on/ oï¬, the sampling cycle number to load the sampling loops, the time interval to read the analytical signals (table 1) were settled before the start of the experiment. After the experimental variables had been established, iron and chromium were simultaneously determined in a set of steel alloy samples. Figure 5. Recorder tracing. The sets (a) and (b) refer to iron (100 mg lâ1) and chromium (100 mg lâ1) determination, respectively. Results and discussion As depicted in the valve timing regime in ï¬gure 4, during the sampling step for chromium determination, the solenoid valve V2 underwent an on/oï¬ switching sequence. As indicated in table 1, these time intervals were both ï¬xed at 0.2 s. The ï¬ow rate was maintained at 33.3 ml sâ1, thus when a sampling cycle was carried out (one on/oï¬ valve switching), a sample slug of 6.6 ml was inserted into the dilution coil B1, and afterwards a carrier solution slug with equal volume was inserted while valve V2 was maintained oï¬. Taking into account the concentration range of chromium, the sampling loop L2 and dilution coil B1 were settled at 8 and 25 cm (40 and 125 ml), respectively. To assure the appropriated dilution, four sampling cycles were carried out. Under this condition, a sample solution underwent a dilution >50%, which was required to match the sample concentration with the linear response range of the photometer. The reagent solution (R2) was added to the sample zone by switching valve V3 on/oï¬ 10 times. As in the sampling step, the time intervals (on/oï¬) were both ï¬xed at 0.2 s, therefore a volume of 66 ml 1,5-diphenylcarbazide was used per determination. For iron determination, the length of sampling loop L1 was ï¬xed at 25 cm (125 ml) and the time interval to switch valve V1 on/oï¬ was settled at 0.2 s. The ï¬ow rate was maintained at 33.3 ml sâ1. Thus, to ï¬ll the sampling loop L1, 10 sampling cycles were carried out. Under this condition, the reaction to reduce Fe3+ ions to Fe2+ occurred during the sampling step. The 1,10phenantroline solution (R3) was added to the sample zone by switching valve V4 (on/oï¬) 20 times, thus inserting a solution volume of 132 m l. As can be seen in the ï¬ow diagrams (ï¬gure 4), the two systems were assembled employing the same injector, nevertheless the ï¬ow pathways were completely independent allowing simultaneous solutions handling for both analytes. The control software was designed to read the signals generated by the photometers Det1 and Det2 sequentially. The analogue-to-digital converter of the PCL771S interface card presented a converting time of 25 ms. Thus, when considering this feature, the software was designed to read each photometer continuously for 200 times. In this sense, each datum stored and displayed on the computer screen (ï¬gure 5) was the average of 200 sequential readings of each photometer. Considering other computer tasks related to data acquisition, such as average calculation and datum save, the time interval spent was <50 ms. In this sense, each peak proï¬le shown in ï¬gure 5 was plotted using at least 200 measurements. Both photometers presented good stability (ï¬gure 5) characterized by relative standard deviations (RSD) of 0.4% for iron and 1.2% for chromium. Apart from these recorders, one can deduce that an analytical throughput of 160 determinations per h was achieved. The feasibility of the system was ascertained by processing a set of steel alloy solutions yielding the results shown in table 2. Accuracy was assessed by comparing the results with those obtained with induced coupled argon plasma atomic emission spectrometry (ICP-AES), and no signiï¬cant diï¬erence at the 95% conï¬dence level was observed. Others proï¬table featuresâsuch as linear response, which ranged from 5.0 to 75.0 mg lâ1 for chromium (R Â¼ 0.997) and from 5.0 to 120.0 mg lâ1 for iron (R Â¼ 0.998); and low reagent consumption, 32 and 330 mg per determination for chromium and for iron, respectivelyâwere also achieved. Table 2. Comparison of results. Iron (%) Chromium (%) Proposed System 32.86 Ã 0.37 57.82 Ã 0.53 61.28 Ã 0.63 46.66 Ã 0.45 14.41 Ã 0.23 ICP-AES 31.90 Ã 0.07 56.70 Ã 0.09 58.01 Ã 0.01 46.40 Ã 0.26 15.90 Ã 0.06 Sample 1 2 3 4 5 Proposed System 28.62 Ã 0.42 16.38 Ã 0.10 29.38 Ã 0.74 36.82 Ã 0.27 63.07 Ã 0.60 ICP-AES 28.70 Ã 0.03 15.90 Ã 0.08 28.90 Ã 0.01 35.90 Ã 0.08 62.00 Ã 0.12 Results are the average of three sequential measurements. 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Journal of Automated Methods and Management in Chemistry – Hindawi Publishing Corporation
Published: Sep 14, 2014