<4D6963726F736F667420576F7264202D20DFC7D9E320E6D1C7C8CDC920E6E3CDE3CF> Al-Khwarizmi Engineering Journal Al-Khwarizmi Engineering Journal,Vol. 13, No. 3, P.P. 131- 141 (2017) Recovery of Platinum and Palladium from Scrap Automotive Catalytic Converters Mohammed Qasim Hammadi* Rabiha Saleh Yassen** Kadhim Noori Abid*** *,**Department of Production and Metallurgy Engineering/ University of Technology ***General Directorate for Vocational Education/Ministry of Education mohamedqassim94@yahoo.com * Email: doc_nori@yahoo.comEmail: ** rabihazw@yahoo.comEmail: *** (Received 15 January 2017; accepted 3 April 2017) https://doi.org/10.22153/kej.2017.04.002 Abstract The hydrometallurgical method was used to platinum and palladium leaching with aqua regia solution (3HCl: HNO3). The leaching experiments were designed to obtain the optimum conditions by using Taguchi method with 16 experiments at three different factors (time, temperature and solid to liquid ratio), and each factor has four different levels. In this study, leaching the powder sample of catalytic converter that contains platinum and palladium was conducted on the basis of the formation of chloro complexes platinum and palladium (PtCl6 2-, PdCl4 2-) with different concentrations in the acidic solution. The optimum conditions for leaching process are (time = 120 minutes, temperature = 100°C, and solid to liquid ratio = 1/20).The best efficiency for platinum and palladium leaching at these conditions were 97.58%, 93.23%, respectively. After leaching process at optimum conditions, platinum was firstly precipitated in the form of (NH4)2PtCl6 (ammonium chloroplatinate) by adding (5ml/l) of ammonium chloride (NH4Cl) as a precipitant agent .Then, palladium was precipitated in the form of (NH4)2PdClO3 (palladium ammonium chlorate) by adding (5g/l) of sodium chlorate (NaClO3) as a precipitant agent to the remaining solution after the removal of platinum. The best efficiency for platinum and palladium recovery at optimum leaching conditions were 91.94%, and 98.82%, respectively. .33HCl:HNO converter,Platinum, Palladium, recovery, catalytic PGMs, catalytic converter, Aqua regia, :wordsKey 1. Introduction Commitment to the European standards to keep pollution-free environment, all cars manufactured after 1993 should be equipped with catalytic converter. Catalytic converters Contain precious metals like Pt, Pd and Rh, which work on the oxidation (CO), and (HC), and the reduction of (NOx) to lower the required levels of emissions [1].The formation of catalytic converter carrier vary depending upon engine capacity and kind of used fuels [2].Recovery of platinum group metals from secondary sources was an important mean of making materials economically in addition to environmental considerations. Recycling of automobiles catalysts to recover platinum, palladium, and rhodium had received a lot of attention in last few years; there are many works provision for the extraction of precious metals by using different ways. platinum group metals are extracted from scrap by melting them with collector metal like copper, or leaching in strong acidic solutions .The extraction methods can be classified as hydrometallurgical, and pyrometallurgical [3,4,and 5]. About 125,000 kg of platinum, palladium, and rhodium was recovered around the world from new and old scrap in 2015; 55,000 kg was recovered from spent catalytic converters in the United States. 25% of Palladium replaced platinum because it is less expensive in most gasoline engines catalytic converters, the proportion can be as much as 50% in some applications [6].The carrier is made up of a ceramic or metallic substances as shown in Mohammed Qasim Hammadi Al-Khwarizmi Engineering Journal, Vol. 13, No. 3, P.P. 131- 141 (2017) 132 Fig.(1).The used type of catalytic converters for the cars are honeycomb cordierite skeleton type (2MgO-2Al2O3-5SiO2),which is coated with( platinum, palladium, and rhodium) with a density of 60–120 cells/cm2 and the thickness of the walls between the cells is about 150 µ m . The internal surface of the cell is coarse and it is covered with high porosity wash coat about 50-200 µ m that made up of about 90% γ-Al2O3 and a mixture of basic added minerals are oxides of Cerium, Zirconium, Lanthanum, Nickel, Iron and alkaline earths that helps improving the stability of catalytic converter [7]. Fig. 1. Carrier auto catalytic converter with the honeycomb structure [8]. The amount of PGMs in catalytic converter is 2 to 6 gram per car and from 6 to 30 gram per sports cars where the exhaust gases are in large quantity. The proportion of platinum to palladium depends on the level of emission control, metals prices, and the type of car. Platinum is used in catalytic converters for diesel engines, while platinum and palladium are used in vehicles powered by gasoline [9]. The total content of platinum group metals in secondary sources is many times higher than in the ore and the benefit from these sources is very attractive .Concentrations of PGMs are to be different in catalysts depending on the manufacturer, the age and the ability of the catalyst .The concentration of PGMs in the Earth crust are measure by micro grams per kilogram. Concentration of PGMs in ores are (Ruthenium = 0.1 µ g/kg); (Rhodium = 0.06µ g/kg) ;(Palladium= 0.4µ g/kg) ;(Osmium and Iridium = 0.05µ g/kg); and (Platinum=0.4µ g/kg).While, the concentration of Platinum in a new automotive catalytic converter is about 0.3 to 1.0μg/kg, Palladium from 0.2 to 0.8μg/kg and Rhodium from 0.05 to0.1μg/kg [5, and 10]. Auto catalysts recycling, platinum, palladium, and rhodium recovered were about 1.16(Moz), 3.15(Moz), and 3.4(Moz) respectively in 2015. Fig. (2) shows the recovery of Pt , Pd ,and Rh during the years from (2010 to 2015) [11]. Fig. 2. Recovery of Pt, Pd, and Rh from auto catalysts during years from2010 to 2015 [11]. When PGMs dissolved by aqua regia, forming Cl2 and NOCl, which has a high oxidation energy and high concentration of chloride ions act as complex agent. Based on the reactions described in (1), and (2) [12]. HNO� � 3HCl .⇔ NOCl � Cl� � 2H�O ... (1) NOCl � H�O .⇔ HNO� � HCl … (2) PGMs are very resistant to acid dissolving .Chloro complexes (PtCl6 2-, PdCl4 2-, RhCl6 3-)were formed when Pt,Pd, and Rh leach in acidic chloride solutions, which required to oxidizing agent with a reduction potential >0.74 V. Thus, better oxidizers can be used as oxidizing agents are HNO3 and H2O2[2]: NO�� � 4H� � 3e� .⇔ NO � 2H�O �E˚ � 0.96V� … (3) H�O� � 2H � �2e� .⇔ 2H�O �E˚ � 1.77V� … (4) Mohammed Qasim Hammadi Al-Khwarizmi Engineering Journal, Vol. 13, No. 3, P.P. 131- 141 (2017) 133 Electrode potentials for the half reactions of chloro complexes are [13]: PtCl��� � 4e� .⇔ Pt � 6Cl� �E˚ � 0.74V� …(5) PdCl!�� � 2e� .⇔ Pd � 4Cl� �E˚ � 0.62V� … (6) RhCl��� � 3e� .⇔ Rh � 6Cl� �E˚ � 0.44V� … (7) Leaching of platinum and palladium by aqua regia solution is a redox reaction according to reactions (8), and(9)[14,and 15]. 3Pt(%) � 18HCl(()) � 4HNO�(()).⇔ 3�PtCl����(()) � 6H�(()) � 4NO(*) � 8H�O …(8) 3Pd(%) � 12HCl(()) � 2HNO�(()).⇔ 3�PdCl!���(()) � 6H�(()) � 2NO(*) � 4H�O … (9) There are two stages to precipitate platinum and palladium [16]:- 1- Leaching platinum by aqua regia was represented by the following reaction: Pt � 4HNO� � 6HCl .⇒ H�(PtCl�) � 4NO� � 4H�O … (10) Platinum is precipitated as ammonium hexachloroplatinate (NH4)2(PtCl6) by adding ammonium chloride to the platinum chloride solution according to the following reaction: H�(PtCl�) � 2NH!Cl .⇒ (NH!)�(PtCl�) � 2HCl … (11) Ignition of ammonium hexachloroplatinate (NH4)2(PtCl6) is carried out by placing it into a glazed refractory evaporating dish and heat strongly to obtain metal called platinum sponge as represented by the following reaction: (NH!)�(PtCl�) .⇒ Pt � 2NH� � 2HCl � 2Cl� … (12) 2-Finally, palladium is precipitated as diamine palladium (II) chloride by addition ammonia to the palladium chloride solution. Then HCl is added to be precipitated to a yellow salt as shown in the reactions below. A sponge of palladium metal is obtained by ignition of the palladium compound. PdCl!�� � 4NH� .⇒ Pd(NH�)!�� � 4Cl� … (13) Pd(NH�)!�� � 2HCl .⇒ Pd(NH�)� Cl � � 4NH!� … (14) The aim of this study is to develop a hydrometallurgical process to leach honeycomb substrate of spent catalytic converters with aqua regia which is composed of (3HCl:1 HNO3) followed by precipitation process for recovery of platinum and palladium. The optimum conditions for maximum leaching of platinum and palladium is investigate by using Taguchi Design. The various experiments are design by computer simulating software (Minitab) with leaching parameters, such as time, temperature, and S/L ratio. The effect of time, temperature, and S/L ratio on leaching platinum and palladium have been investigated. The possibility of recovery of platinum and palladium from leaching solution is investigate by the chemical precipitation using ammonium chloride (NH4Cl) and sodium chlorate (NaClO3) as precipitant agents for recovery of platinum and palladium, respectively. 2. Experimental Work In this study, spent catalytic converters of BMW car were used for platinum and palladium recovery because the BMW car manufacturing company has a high quality and mandatory agreements in the use of PGM metals as a catalyst .Catalytic converter scrap was assembled from maintenance shops of catalytic converters. Opening way of the catalyst converter is carried out by flame cutting (torch), taking into consideration the clean cut so as not to monolith damage. After taking out monolith structure from the body, then cleaning was done by blowing air to get rid of dust and the remains of the combustion products .Fig.(3) represents flow chart for recovery of Pt, Pd from spent catalytic converter. Comminution is to be a two-stages, crushing, and grinding to get to the required particle size .The first stage was crushing by using cast iron mortar and pestle which it is similar to coffee grinder to reduce the honeycomb structure to a suitable size .The second stage was grinded by using a ball mill machine (Retsch). A ball mill is a fairly simple machinery consisting of a drum inside it three steel balls which rotates horizontally. (1250) grams of the sample powder was fed into the drum, the charge was divided into seven small weights, each run took up 10 minutes, magnet is used to get rid of ferrous contamination. The grinded powder was reduced in size to less than +250 µ m at end of the operation.. Catalyst powder is washed several times with distilled water to get rid of dust and other pollutants. Then, the powder was placed in refractory dish for adding in an electric oven at 100˚C for one hour to remove moisture, and also combustion products, coal, and gas. The powder sample was then sieved to (-250)µ m,(+60 mesh) using mechanical auto sieve shaker (AD60-01) according to ASTM standard sieves . The laboratory technique used Mohammed Qasim Hammadi Al-Khwarizmi Engineering Journal, Vol. 13, No. 3, P.P. 131- 141 (2017) 134 dependent for sampling was by using the Chute Riffler. The chemical analyses of the catalytic powder is carried out by flame atomic absorption spectrometry (NOVAA-350).The analysis results are shown in table (1)as weight percentage. Table 1, Chemical composition of the catalytic powder as determined by the flame atomic absorption spectrometry. Ni Ag Zn Pt Pd 3O2Fe CaO 2SiO 3O2Al Components 0.0106 0.0007 0.046 0.075 0.370 0.054 0.0316 10.502 43.608 Wt.% Fig. 3. Flow chart for recovery of Pt, Pd from spent catalytic converter. The catalytic converter powder was dissolved in strong acidic solutions. Aqua regia solution (3HCl:1HNO3) consisting of high purity hydrochloric acid (37%) and concentrated nitric acid (65%) were employed in all dissolution experiments. 3. Taguchi Method In this study, experiments are designed by using Taguchi method to create three parameters, time, temperature, and solid/liquid ratio for the purpose of determining optimal conditions of leaching processes, unlike previous research that used the old traditional ways (classic ways). Three controlled factors and their levels are designed as given in table (2). Table 2, Three controlled factors and their levels are used in leaching process of the catalytic powder by aqua regia solution 4. Selection of Orthogonal Array Taguchi orthogonal array (OA) designs are usually used in design experiments on many factor levels. These standard arrays give the method to reduces the minimal number of experiments which could give the complete information of all the factors that have effects on the performance parameters .Orthogonal array notation is La(bc) where L represents the orthogonal array notation in the table ,a is mean number of experiments ,b is mean number of levels ,and c is mean number of parameters[18].The design used in the experiments of leaching processes is Taguchi orthogonal arrays. By using the array selector, see table (3) three parameters and four levels were selected the proper array was L16(4 3). Levels Controlled factors L4 L3 L2 L1 120 90 60 30 Time (min) 100 75 50 25 Temp(˚C) 1/20 1/15 1/10 1/5 Solid/Liquid Ratio (wt/wt) Mohammed Qasim Hammadi Al-Khwarizmi Engineering Journal, Vol. 13, No. 3, P.P. 131- 141 (2017) 135 ,3 Table ].71Array selector [ Table 4, Design of experiments used in the leaching process for the catalytic converter. 5. Signal–Noise(S/N) Ratio At parameters design, the factors were divided into two kinds: control factors which can be easily controlled by the experimenters and noise factors which can be difficult or expensive to control during operation. To determine (S/N) ratio, there are three types of formulations as shown in table (5).In this study, the second formula is used which represents the larger signal to noise ratio giving the best leaching efficiency [18]. Table 5, S/N Ratios Formulations [19]. 6. Analysis of Variance (ANOVA) Analysis of variance was used to evaluate the response value in percent (%) for each variable in the orthogonal experiments. In this study, it was used to identify two tries result for three parameters of leaching. The main calculation of ANOVA was that the total sums of the squares are equal to the sum of the SS for all parameters(time ,temperature, and solid/liquid ratio) and error as shown in equation (15) [20]. ,,- � ,,./01 � ,,.102. � ,,3/5 � ,,16676 … (15) ,,- � 8 9/� − ; < = > ? … (16) ,,@ � ∑ BC − ;< = … (17) Where :SST is total sums of squares parameters and error; G is sum of the results data for all the experiments; F is total number for all the experiments; G is level number; C is one of the tested parameters;∑9/ is sum of results for all experiments; i.e, at parameter c, and at level G; H is number of parameters. Degree of freedom was calculated by the following equation: Solid/Liquid Ratio (wt/wt) Temp (˚C) Time (min) Exp. 1/5 25 30 1 1/10 50 30 2 1/15 75 30 3 1/20 100 30 4 1/10 25 60 5 1/5 50 60 6 1/20 75 60 7 1/15 100 60 8 1/15 25 90 9 1/20 50 90 10 1/5 75 90 11 1/10 100 90 12 1/20 25 120 13 1/15 50 120 14 1/10 75 120 15 1/5 100 120 16 I J = -10 log(8 KLM N N LOP ) I J = -10 log(8 P NKLM N LOP ) I J = 10 log(8 KLM IM N LOP ) 1-Lower is the better 2-Higher is the better 3-Nominal is the better Mohammed Qasim Hammadi Al-Khwarizmi Engineering Journal, Vol. 13, No. 3, P.P. 131- 141 (2017) 136 QRST � U − 1 … (18) QRS- � V − 1 … (19) Where; C represents the levels for each parameter (controlled factor),T represents the number of experiments. Also, contribution percentage (ρ%) was calculated for each controlled factor and for the error from the following equation[21]: W% � YYZYY[ … (20) When: ρerror≤ 15%,so the chosen controlled factors are not active. ρerror≥ 50%, so chosen controlled factors are active. Table 6, ANOVA for the Platinum leaching by aqua regia solution for each controlled factor. Table 7, ANOVA for the Palladium leaching by aqua regia solution for each controlled factor. 7. Leaching Process All experiments of leaching processes for catalytic powder containing platinum and palladium in aqua regia shown in the table (4) are subject to three variables (time, temperature, and solid/liquid ratio). The weight of the sample in each experiment was 10 grams with particle size (-250)µ m. The dissolution process involved the following steps: 1-The HCl-HNO3 mixture was prepared in a volume ratio 3HCl:1HNO3 to form an acidic solution called aqua regia of a reddish brown color. . 2-Aqua regia is heated by hot plate magnetic stirrer to the specified point according to each experiment in a glass container containing three vents from up for (condenser ,thermometer, and for adding materials) with (400) rpm agitating for all experiments. . 3-The catalytic converter powder is added to the glass container after heated aqua regia to a specific temperature at a specific time according to each experiment. . 4-At the end of leaching process, filtration step is done using glass funnel and ashless filter paper (Whatman England /Circle=12.5cm) to separate the slurry from the solution. 5-After filtration stage, platinum and palladium concentration in the solution were determined by using atomic absorption spectrometry analysis (NOVAA-350). . 6-In order to obtain accurate leaching rate, sixteen experiments of Taguchi method is performed twicely. 7-The percentage of leaching for each experiment is calculated by the following formula: % \]^_`LNa � b.c d.e Pff Where: U= Concentration platinum or palladium after leaching (g/l); g=Volume of solution after leaching (l); h=Weight of catalytic powder in leaching solution (g); i=Percentage of platinum or palladium in catalytic converter powder (%). 8. Precipitation Process The removal of metals (Pt and Pd) from chloride solutions at optimum condition of leaching using (NH4Cl) and (NaClO3) as the precipitant agents are investigated, unlike previous research that used precipitators Other. The percentage of recovery platinum and palladium are calculated by the following formula:- % j]_kl]mn � bP\P − bM\MbP\P Where: b P= The concentration of element before precipitation (g/l); \P=Volume of solution before precipitation (l); bM=The concentration of element after precipitation (g/l); \M=Volume of solution after precipitation(l).The leaching and precipitation process involved the following steps:- 1-Leaching of (20) grams sample of catalyst powder with particle size (-250)µ m in (320) ml of aqua regia at optimum condition (Time=120 min;Temp=100˚C;S/L=1/20).The concentration of platinum and palladium is determined by atomic absorption spectrometry analysis before ρ% SSc DOFc Factors 3.661 11.638 3 Time (min) 13.299 42.265 3 Temp(˚C) 64.447 204.817 3 Solid/Liquid Ratio(wt/wt) 18.591 59.085 6 Error 100 317.805 15 Total ρ% SSc DOFc Factors 1.538 0.977 3 Time (min) 7.259 4.610 3 Temp(˚C) 70.34 44.67 3 Solid/Liquid Ratio(wt/wt) 20.866 13.25 6 Error 100 63.50 15 Total Mohammed Qasim Hammadi Al-Khwarizmi Engineering Journal, Vol. 13, No. 3, P.P. 131- 141 (2017) 137 precipitation is carried out. 2-The diluted solution was prepared by boiling aqua regia solution to 100˚C, which containing platinum and palladium until the solution was condensed and mixed properly. Then cooled to 50˚C for adding HCl to get rid of the nitroso- compounds in the solution. (5) ml of hydrochloric acid were add to the solution every 10 minutes for ten times This process was conducted in moderate temperatures without allowing the solution to evaporate completely .The hot solution was diluted with four volumes of tap water in a large bowl and then filtered. 3-By dissolving (214) grams of ammonium chloride (NH4Cl) in 1 litter of distilled water .The solution is used to precipitate platinum. 4-The diluted solution which contains platinum and palladium was heated at medium temperature (50˚C). Platinum was firstly precipitated by adding (5ml/l) of ammonium chloride solution, slowly with stirring continuously until the formation of yellowish orange solution ,after 1 hour the solution was filtrated , platinum was precipitated as a bright orange powder which is ammonium chloroplatinate (NH4)2PtCl6 then concentration of platinum in the solution was determined by flame atomic absorption spectrometry analysis. 5- After platinum removal, palladium was precipitated from remaining filtrated solution by adding sodium chlorate (NaClO3) ,the solution was placed in a beaker and boiled it at 100˚C,then it is cooled to just less boiling and (5g/l) of sodium chlorate crystals was added into beaker with shaking carefully until the formation of bright red solution , after 1 hour the solution was filtrated , palladium was precipitated as a bright red powder which is palladium ammonium chlorate (NH4)2PdClO3 then the concentration of palladium in the solution was determined by flame atomic absorption spectrometry analysis. 9. Results& Discussion 9.1. Effect of Time The time of platinum and palladium leaching process was studied. Two experiments whose durations varied (30, 60, 90, and 120) minutes, were carried out to discover the time advance of leaching in aqua regia solution. Figure (4) show platinum and palladium leaching by aqua regia solution as a function of time, respectively. Leaching efficiency of platinum and palladium started rising gradually at different times .The percentage of leaching of platinum was52.8% at 120 minutes, while the percentage of leaching palladium was 62.8% at 120 minutes. Fig. 4. Efficiency of platinum and palladium leaching by aqua regia solution for each level as a function of time. 9.2. Effect of Temperature Platinum and palladium leaching kinetics is studied at four temperature levels (25, 50, 75, and 100) ˚C. Each leaching experiment was conducted at different times and solid to liquid ratios, but an agitation rate was fixed at (400 rpm).Results data of the two experiments of platinum and palladium leaching efficiency as a temperature function are presented in figure (5).They, indicate that the increase in temperature greatly improves the leaching kinetics of platinum and palladium .This Mohammed Qasim Hammadi Al-Khwarizmi Engineering Journal, Vol. 13, No. 3, P.P. 131- 141 (2017) 138 shows that the activation energy of the leaching reactions increases with increased temperatures. Platinum leaching efficiency was 52.9% achieved at 100˚C, while Palladium leaching efficiency was 67% achieved at 100˚C. Fig. 5. Efficiency of platinum and palladium leaching by aqua regia solution for each level as a function of temperature. 9.3. Effect Solid/Liquid Ratio The weight ratio of solid/liquid (wt/wt) was another investigated variable. Four levels 1/5, 1/10, 1/15, and 1/20 of S/L ratios were tested. Platinum and palladium leaching results for the two experiments are obtained as shown in figure (6) as S/L ratios function. The leaching kinetics in aqua regia solution becomes faster with increased S/L ratio. Platinum and palladium leaching efficiency reached to 62.9%, and 73.8%, respectively at1/20 as solid to liquid ratio. Fig. 6. Efficiency of platinum and palladium leaching by aqua regia solution for each level as a function of solid/liquid ratio. 10. Leaching Platinum and Palladium The sample of catalyst powder was dissolved by using aqua regia solution (3HCl:HNO3).HNO3 was added to increase the oxidation of platinum and palladium during leaching .PtCl6 2- and PdCl4 2- were formed during the leaching process that undergone according to the reactions (8), and (9) .The color of chloro complex Pd is darker than of Pt. Color of filtrated leachate is not to be an indicator of platinum and palladium dissolution efficiency. Platinum and palladium were Mohammed Qasim Hammadi Al-Khwarizmi Engineering Journal, Vol. 13, No. 3, P.P. 131- 141 (2017) 139 completely leaching in aqua regia solution; the separation is more complicated between platinum group metals because they have similar chemical and physical properties. Increasing the concentration of hydrochloric acid as a volume unit with three times of nitric acid led to obtain high leaching of platinum and palladium were (97.58% ,93.23%) respectively. 11. Precipitation of platinum and palladium Precipitation is considered one of the separation methods, precipitation step have a major influence on the recovery of platinum and palladium .Firstly ,through adding ammonium chloride (NH4Cl)to the diluted solution, platinum complex (PtCl6 2-)was precipitated because its less soluble according to precipitation reaction (see equ(11)).While, palladium complex(PdCl4 2-) remained dissolved in the diluted solution. Secondly, palladium complex (PdCl4 2-) was precipitated by adding sodium chlorate (NaClO3) to the diluted solution. Temperatures had a clear effect on the precipitation process, all the platinum group metals complexes are fast influenced to hydrolysis, especially at high temperatures. After completion of the precipitation, the results of the analysis show that the platinum and palladium content could completely precipitate from the catalytic converter, and this has been proved possibility of extracting efficiently. The percentage of efficient recovery of platinum and palladium were (91.94%, and 98.82%) respectively. 12. Conclusion Based on this study of the recovery of platinum and palladium from spent catalytic converter, using aqua regia solution, the following conclusions can be drawn: 1. The percentages of platinum and palladium in the powder sample of spent catalytic converter were 0.075% and 0.37%, respectively based on chemical analysis by flame atomic absorption. 2. Leaching experiments have been done and chosen by Taguchi Design to find optimum conditions to leach platinum and palladium by aqua regia. Effect of time, temperature, and S/L ratio on leaching efficiency are investigated .The relationship was direct between effect of time, temperature, and S/L ratio on leaching efficiency. The increase of the level of each effective tends to increase the leaching efficiency of platinum and palladium. 3. The optimum dissolution of platinum and palladium by aqua regia were (97.58%) ,and (93.23%) ,respectively at a time of 120 minutes, temperature 100°C,and solid/liquid ratio 1/20. . 4. Recovery of platinum and palladium was possible by the precipitation using ammonium chloride (NH4Cl) and sodium chlorate (NaClO3) as precipitation agents at 50°C for 1 hour. Recovery efficiency of platinum was 91.94%, while recovery efficiency of palladium was 98.82%. 13. References [1] D. Jimenez de Aberasturi, R. Pinedo, I. Ruiz de Larramendi, J.I. 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Thesis (2016). )2017( 131-141، صفحة 3د، العد13دجلة الخوارزمي الهندسية المجلم محمد قاسم حمادي 141 في السيارات المحول الحفاز مخلفات استرجاع البالتين والبالديوم من كاظم نوري عبيد*** رابحة صالح ياسين** م حمادي* محمد قاس الجامعة التكنولوجية/قسم هندسة االنتاج والمعادن،*** وزارة التربية/ ***المديرية العامة للتعليم المهني mohamedqassim94@yahoo.comاأللكتروني:البريد * doc_nori@yahoo.comالبريد األلكتروني: ** rabihazw@yahoo.comالبريد األلكتروني:*** الخالصة ) .وكانت صممت تجارب االذابة 33HCl: HNO(عنصري البالتين والبالديوم في محلول الماء الملكي الطريقة المائية كانت قد استخدمت في اذابة ب الى لمعرفة الظروف المثالية لالذابة بواسطة طريقة تاكوشي بواقع ستة عشر تجربه عند ثالث عوامل مؤثرة هي درجة الحرارة والوقت ونسبة الصل يحتوي على البالتين والبالديوم التي كانت قد اجريت على اساس تشكيل مركبات كلوريدية من البالتين والبالديوم السائل.اذابة مسحوق المحول الحفاز الذي )-24, PdCl -2 6(PtCl = درجة الحرارة) 100بتراكيز مختلفة في المحلول الحامضي.الظروف المثالية لعملية االذابة كانت°C, =دقيقة ونسبة ١٢٠والوقت ).بعد عملية االذابة عند الظروف المثالية ٩٣٫٢٣والبالديوم(% ) ٩٧٫٥٨اذابة عند هذه الظروف للبالتين(%كفاءة ),وكانت افضل ١/٢٠الصلب الى السائل= مل لكل لتر) من كلوريد االمونيوم ٥بواسطة اضافة 6PtCl2)4(NH ) (ammonium chloroplatinate),كان قد ترسب البالتين اوال على شكل Cl) 4e (NHammonium chlorid كعامل مرسب,بعد ذلك كان ترسب البالديوم على شكل(palladium ammonium chlorate)3 PdClO2)4(NH كعامل مرسب الى المحلول المتبقي بعد ازالة البالتين.وكانت 3sodium chlorate ( NaClO (غم لكل لتر) من كلورات الصوديوم ٥بواسطة اضافة ( ) . على التوالي %98.82 ) و (%91.94 ف االذابة المثالية للبالتين والبالديوم هي افضل كفاءة استرجاع عند ظرو