{"id":448,"date":"2026-04-11T04:48:30","date_gmt":"2026-04-10T21:48:30","guid":{"rendered":"http:\/\/www.tneutron.net\/pangan\/?p=448"},"modified":"2026-04-10T10:17:18","modified_gmt":"2026-04-10T03:17:18","slug":"chemical-parameters-quality-tapioca","status":"publish","type":"post","link":"https:\/\/www.tneutron.net\/pangan\/chemical-parameters-quality-tapioca\/","title":{"rendered":"Chemical Parameters Quality Tapioca"},"content":{"rendered":"<p><span class=\"notranslate\"><strong>h) The degree of white<\/strong><\/span> <strong><br \/>\n<\/strong> <span class=\"notranslate\"> <strong>Principle:<\/strong><\/span> <strong><br \/>\n<\/strong> <span class=\"notranslate\"> Beam reflection measurement standard sample with MgO.<\/span><br \/>\n<span class=\"notranslate\"> Equipment: Photometer.<\/span><br \/>\n<span class=\"notranslate\"> Reagent: Standard MgO 99% pa<\/span><br \/>\n<span class=\"notranslate\"> Ways of working:<\/span><br \/>\n<span class=\"notranslate\"> (1) Insert the sample into the sample container similar to that used for container MgO;<\/span><br \/>\n<span class=\"notranslate\"> (2) Measure the reflection index of the sample (A) and the reflection index of MgO (B);<\/span><br \/>\n<span class=\"notranslate\"> (3) Each completed measurement 10 times the sample, the photometer must be calibrated with MgO to get a smaller deviation.<\/span><\/p>\n<p><span class=\"notranslate\"> <strong>i) The degree of acid<\/strong><\/span> <strong><br \/>\n<\/strong> <span class=\"notranslate\"> <strong>Principle:<\/strong><\/span><br \/>\n<span class=\"notranslate\"> Dissolution of organic acids in a sample by using certain organic solvents (alcohol 95%) followed by penitaran with alkali (NaOH).<\/span><\/p>\n<p><span class=\"notranslate\"> Equipment:<\/span><br \/>\n<span class=\"notranslate\"> a) Balance analytical accuracy of 0.1 mg calibrated;<\/span><br \/>\n<span class=\"notranslate\"> b) 250-ml Erlenmeyer;<\/span> <span class=\"notranslate\"> and<\/span><br \/>\n<span class=\"notranslate\"> c) Buret 25 mL.<\/span><br \/>\n<span class=\"notranslate\"> Reagent:<\/span><br \/>\n<span class=\"notranslate\"> (1) Ethanol, C2H5OH 95% neutral;<\/span><br \/>\n<span class=\"notranslate\"> (2) A solution of sodium hydroxide, NaOH, 0.05 M;<\/span><br \/>\n<span class=\"notranslate\"> (3) phenolphthalein indicator, PP 1% in 60% alcohol.<\/span><br \/>\n<span class=\"notranslate\"> Ways of working:<\/span><br \/>\n<span class=\"notranslate\"> (1) Weigh carefully the 10 g sample (a), then insert it into the 250-ml Erlenmeyer;<\/span><br \/>\n<span class=\"notranslate\"> (2) Add 100 mL ethanol 95% neutral and allow 24 hours while occasionally shaken then strained;<\/span> <span class=\"notranslate\"> and<\/span><br \/>\n<span class=\"notranslate\"> (3) Titration of the filter with 50 mL of 0.05 M NaOH (c) in ethanol using PP indicator (b).<\/span><\/p>\n<p><span class=\"notranslate\"> <strong>j) metal contaminants: Cadmium (Cd) and lead (Pb)<\/strong><\/span> <strong><br \/>\n<\/strong> <span class=\"notranslate\"> <strong>Principle:<\/strong><\/span><br \/>\n<span class=\"notranslate\"> Destruction example by dry ashing at a temperature of 450 \u00b0 C followed by dissolution in acid solution.<\/span> <span class=\"notranslate\"> Dissolved metal calculated using the tool Atomic Absorption Spectrophotometer (AAS) with a maximum wavelength of 228.8 nm to 283.3 nm for Cd and Pb.<\/span><br \/>\n<span class=\"notranslate\"> <strong>Equipment:<\/strong><\/span><br \/>\n<span class=\"notranslate\"> (1) Atomic Absorption Spectrophotometer (AAS) along with the accessories (cathode lamps Cd and Pb) calibrated (preferably using graphite furnace AAS);<\/span><br \/>\n<span class=\"notranslate\"> (2) The furnace is calibrated with a precision of 1 \u00b0 C;<\/span><br \/>\n<span class=\"notranslate\"> (3) Balance analytical calibrated to the nearest 0.1 mg;<\/span><br \/>\n<span class=\"notranslate\"> (4) electric heater;<\/span><br \/>\n<span class=\"notranslate\"> (5) water bath;<\/span><br \/>\n<span class=\"notranslate\"> (6) Pipette 0.05 mL measuring scale or micro burette calibrated;<\/span><br \/>\n<span class=\"notranslate\"> (7) flask 1000 mL, 100 mL, and 50 mL, calibrated;<\/span><br \/>\n<span class=\"notranslate\"> (8) Measuring cup capacity of 10 ml;<\/span><br \/>\n<span class=\"notranslate\"> (9) The glass cup 250 mL;<\/span><br \/>\n<span class=\"notranslate\"> (10) Bottle polypropylene;<\/span><br \/>\n<span class=\"notranslate\"> (11) porcelain cup \/ platinum \/ quartz 50 mL to 100 mL;<\/span> <span class=\"notranslate\"> and<\/span><br \/>\n<span class=\"notranslate\"> (12) Filter paper with specifications not berabu liquid particle retention of 20 to 25 lm.<\/span><br \/>\n<span class=\"notranslate\"> Reagent:<\/span><br \/>\n<span class=\"notranslate\"> (1) Nitric acid, HNO3;<\/span><br \/>\n<span class=\"notranslate\"> (2) Hydrochloric acid, concentrated HCl;<\/span><br \/>\n<span class=\"notranslate\"> (3) The solution of nitric acid, HNO3 0.1 N;<\/span> <span class=\"notranslate\"> 7 mL dilute HNO3 with distilled water in a 1000 mL volumetric flask and dilute to mark the line.<\/span><br \/>\n<span class=\"notranslate\"> (4) A solution of hydrochloric acid, HCl 6 N;<\/span> <span class=\"notranslate\"> 500 mL of concentrated HCl diluted with distilled water in a 1000 mL volumetric flask and dilute to mark the line.<\/span><br \/>\n<span class=\"notranslate\"> (5) standard solution 1000 mg \/ mL Cd;<\/span> <span class=\"notranslate\"> dissolve 1.000 g Cd with 7 ml of HNO3 in a 250-ml beaker and insert it into the measuring flask 1000 mL then dilute with distilled water to mark the line.<\/span> <span class=\"notranslate\"> Alternatively, it could be used Cd standard solution 1000 mg \/ mL ready to use.<\/span><br \/>\n<span class=\"notranslate\"> (6) standard solution 200 mg \/ mL Cd;<\/span> <span class=\"notranslate\"> pipette 10 ml of standard solution of 1000 mg \/ mL Cd into 50 mL volumetric flask and then diluted with distilled water up to mark the line then shaken.<\/span> <span class=\"notranslate\"> The second standard solution has a concentration of 200 ug \/ mL Cd.<\/span><\/p>\n<p><span class=\"notranslate\"> (7) the raw solution 20 mg \/ mL Cd;<\/span> <span class=\"notranslate\"> pipette 10 ml of standard solution of 200 ug \/ mL cadmium into 100 mL volumetric flask and then diluted with distilled water up to mark the line then shaken.<\/span> <span class=\"notranslate\"> The third standard solution has a concentration of 20 ug \/ mL Cd.<\/span><br \/>\n<span class=\"notranslate\"> (8) working standard solution of Cd;<\/span> <span class=\"notranslate\"> pipette into a 100 mL volumetric flask respectively of 0 mL, 0.5 mL, 1 mL;<\/span> <span class=\"notranslate\"> 2 mL;<\/span> <span class=\"notranslate\"> 4 mL;<\/span> <span class=\"notranslate\"> 7 mL and 9 ml standard solution 20 mg \/ mL and then add 5 mL of HNO3 1 N or 6 N HCl, and dilute with distilled water to mark the line and shake.<\/span> <span class=\"notranslate\"> The working standard solution has a concentration of 0 mg \/ mL;<\/span> <span class=\"notranslate\"> 0.1 mg \/ mL;<\/span> <span class=\"notranslate\"> 0.2 mg \/ mL;<\/span> <span class=\"notranslate\"> 0.4 mg \/ mL;<\/span> <span class=\"notranslate\"> 0.8 mg \/ mL;<\/span> <span class=\"notranslate\"> 1.4 mg \/ mL and 1.8 mg \/ mL Cd.<\/span><br \/>\n<span class=\"notranslate\"> (9) standard solution 1000 mg \/ mL Pb;<\/span> <span class=\"notranslate\"> dissolve 1,000 g Pb with 7 ml of HNO3 in a 250-ml beaker and insert it into the measuring flask 1000 mL then dilute with distilled water to mark the line.<\/span> <span class=\"notranslate\"> Alternatively, it could be used Pb standard solution of 1.000 mg \/ mL ready to use.<\/span><br \/>\n<span class=\"notranslate\"> (10) the raw solution 50 mg \/ mL Pb;<\/span> <span class=\"notranslate\"> and pipette 5.0 ml of standard solution of 1.000 mg \/ mL Pb into a 100 mL volumetric flask and dilute with distilled water to mark the line and shake.<\/span> <span class=\"notranslate\"> The second standard solution has a Pb concentration of 50 ug \/ mL.<\/span><br \/>\n<span class=\"notranslate\"> (11) working standard solution of Pb.<\/span> <span class=\"notranslate\"> pipette into a 100 mL volumetric flask respectively of 0 mL, 0.2 mL;<\/span> <span class=\"notranslate\"> 0.5 mL;<\/span> <span class=\"notranslate\"> 1 mL;<\/span> <span class=\"notranslate\"> 2 mL;<\/span> <span class=\"notranslate\"> 3 mL and 4 mL standard solution 50 mg \/ mL and then add 5 mL of HNO3 1 N or 6 N HCl, and dilute with distilled water to mark the line and shake.<\/span> <span class=\"notranslate\"> The working standard solution has a concentration of 0 mg \/ mL;<\/span> <span class=\"notranslate\"> 0.1 mg \/ mL;<\/span> <span class=\"notranslate\"> 0.25 mg \/ mL;<\/span> <span class=\"notranslate\"> 0.5 mg \/ mL;<\/span> <span class=\"notranslate\"> 1.0 mg \/ mL;<\/span> <span class=\"notranslate\"> 1.5 mg \/ mL and 2.0 mg \/ mL Pb.<\/span><br \/>\n<span class=\"notranslate\"> Ways of working:<\/span><br \/>\n<span class=\"notranslate\"> (1) Weigh 10 g to 20 g of sample accurately in a porcelain cup \/ platinum \/ quartz (m);<\/span><br \/>\n<span class=\"notranslate\"> (2) Place the dish containing the test sample on top of electric heating and heat gradually until the test sample does not smoke anymore;<\/span><br \/>\n<span class=\"notranslate\"> (3) Continue incineration in a furnace at a temperature of (450 \u00b1 5) \u00b0 C until the ash is white, free from carbon;<\/span><br \/>\n<span class=\"notranslate\"> (4) If the ashes are not free from carbon which is characterized by a grayish color, lightly mist with a few drops of water and add dropwise HNO3 Approximately 0.5 mL to 3 mL;<\/span><br \/>\n<span class=\"notranslate\"> (5) Dry the cup above the electric heater and reinsert it into the furnace at a temperature of (450 \u00b1 5) \u00b0 C and continue heating until white ash.<\/span> <span class=\"notranslate\"> Addition of HNO3 may be repeated if the ash is grayish;<\/span><br \/>\n<span class=\"notranslate\"> (6) Dissolve white ash in 5 mL of 6 N HCl, while heated over an electric heater or a water bath until dry, then dilute with 0.1 N HNO3 and enter into a 50 mL measuring flask and then align to mark the lines with distilled water (V), if necessary, filter the solution using a filter paper into a polypropylene bottle;<\/span><br \/>\n<span class=\"notranslate\"> (7) Prepare a blank solution by the addition of reagents and the same treatment as an example;<\/span><br \/>\n<span class=\"notranslate\"> (8) Read the absorbance of the working standard solution and the sample solution against the blank using AAS at a wavelength maximum of about 228.8 nm to 283.3 nm for Cd and Pb;<\/span><br \/>\n<span class=\"notranslate\"> (9) Create a calibration curve between metal concentrations (mg \/ mL) as the X-axis and absorbance as the Y axis;<\/span><br \/>\n<span class=\"notranslate\"> (10) Plot the readings solution is an example of the calibration curve (C);<\/span> <span class=\"notranslate\"> and<\/span><br \/>\n<span class=\"notranslate\"> (11) Calculate the metal content in the sample.<\/span><\/p>\n<p><span class=\"notranslate\"> <strong>k) Metal Contamination: Tin (Sn)<\/strong><\/span> <strong><br \/>\n<\/strong> <span class=\"notranslate\"> <strong>Principle:<\/strong><\/span><br \/>\n<span class=\"notranslate\"> Examples didekstruksi with HNO3 and HCl then add KCl to reduce interference.<\/span> <span class=\"notranslate\"> Sn read using Atomic Absorption Spectrophotometer (AAS) at a wavelength of 235.5 nm with a maximum of N2O-C2H2 flame oxidation.<\/span><br \/>\n<span class=\"notranslate\"> Equipment:<\/span><br \/>\n<span class=\"notranslate\"> (1) Atomic Absorption Spectrophotometer (AAS) along with the accessories (cathode lamps Sn) calibrated;<\/span><br \/>\n<span class=\"notranslate\"> (2) The furnace is calibrated with precision 1oC;<\/span><br \/>\n<span class=\"notranslate\"> (3) Balance analytical calibrated to the nearest 0.1 mg;<\/span><br \/>\n<span class=\"notranslate\"> (4) electric heater;<\/span><br \/>\n<span class=\"notranslate\"> (5) water bath;<\/span><br \/>\n<span class=\"notranslate\"> (6) flask 1000 ml, 100 ml and 50 ml, calibrated;<\/span><br \/>\n<span class=\"notranslate\"> (7) Pipette 0.1 mL calibrated measuring scale;<\/span><br \/>\n<span class=\"notranslate\"> (8) 250 ml Erlenmeyer flask;<\/span><br \/>\n<span class=\"notranslate\"> (9) glass measuring 50 mL;<\/span> <span class=\"notranslate\"> and<\/span><br \/>\n<span class=\"notranslate\"> (10) Glass cup of 250 mL.<\/span><br \/>\n<span class=\"notranslate\"> Reagent:<\/span><br \/>\n<span class=\"notranslate\"> (1) A solution of potassium chloride, 10 mg \/ mL K;<\/span> <span class=\"notranslate\"> dissolve 1.91 g of KCl with water to 100 mL.<\/span><br \/>\n<span class=\"notranslate\"> (2) Nitric acid, HNO3;<\/span><br \/>\n<span class=\"notranslate\"> (3) Hydrochloric acid, concentrated HCl;<\/span><br \/>\n<span class=\"notranslate\"> (4) standard solution 1000 mg \/ mL Sn;<\/span> <span class=\"notranslate\"> and dissolve 1.000 g Sn with 200 mL of concentrated HCl in 1000 mL volumetric flask, add 200 ml of distilled water, cooled to room temperature and dilute with distilled water to mark the line.<\/span><\/p>\n<p><span class=\"notranslate\"> (5) working standard solution of Sn.<\/span><br \/>\n<span class=\"notranslate\"> Pipette 10 mL of concentrated HCl and 1.0 mL of KCl into each 100 mL volumetric flask.<\/span> <span class=\"notranslate\"> Add each 0 mL;<\/span> <span class=\"notranslate\"> 0.5 mL;<\/span> <span class=\"notranslate\"> 1.0 mL;<\/span> <span class=\"notranslate\"> 1.5 mL;<\/span> <span class=\"notranslate\"> 2.0 mL and 2.5 mL of standard solution of 1000 mg \/ mL Sn and dilute with distilled water to mark the line.<\/span> <span class=\"notranslate\"> The working standard solution has a concentration of 0 mg \/ mL;<\/span> <span class=\"notranslate\"> 5 mg \/ mL;<\/span> <span class=\"notranslate\"> 10 mg \/ mL;<\/span> <span class=\"notranslate\"> 15 mg \/ mL;<\/span> <span class=\"notranslate\"> 20 mg \/ mL and 25 mg \/ mL Sn.<\/span><br \/>\n<span class=\"notranslate\"> Ways of working:<\/span><br \/>\n<span class=\"notranslate\"> (1) Weigh sample of 10 g to 20 g (m) carefully into 250-ml Erlenmeyer flask, add 30 mL HNO3 and allow 15 minutes;<\/span><br \/>\n<span class=\"notranslate\"> (2) Heat gently for 15 minutes in a fume hood, avoid the occurrence of excessive spark;<\/span><br \/>\n<span class=\"notranslate\"> (3) Continue heating so that the remaining volume of 3 mL to 6 mL or until the sample was dry on the bottom, avoiding the formation of charcoal;<\/span><br \/>\n<span class=\"notranslate\"> (4) Remove the Erlenmeyer of electric heating, add 25 ml of concentrated HCl, and heat up for 15 minutes until a burst of steam Cl 2 stops;<\/span><br \/>\n<span class=\"notranslate\"> (5) Increase the heating and bring to a boil so that the residual volume of 10 mL to 15 mL;<\/span><br \/>\n<span class=\"notranslate\"> (6) Add 40 ml of distilled water, stir, and pour into a 100 mL volumetric flask, rinse the Erlenmeyer flask with 10 mL of distilled water (V);<\/span><br \/>\n<span class=\"notranslate\"> (7) Add 1.0 mL KCl, let cool at room temperature, align with distilled water up to mark the line and filter;<\/span><br \/>\n<span class=\"notranslate\"> (8) Prepare the reference solution with the addition of reagents and the same treatment as an example;<\/span><br \/>\n<span class=\"notranslate\"> (9) Read the absorbance of the working standard solution and the sample solution against the blank using AAS at a wavelength of 235.5 nm with a maximum of N2O-C2H2 flame oxidation;<\/span><br \/>\n<span class=\"notranslate\"> (10) Create a calibration curve between metal concentrations (mg \/ mL) as the X-axis and absorbance as the Y axis;<\/span><br \/>\n<span class=\"notranslate\"> (11) Plot the readings solution is an example of the calibration curve (C);<\/span><br \/>\n<span class=\"notranslate\"> (12) Perform Duplo construction;<\/span> <span class=\"notranslate\"> and<\/span><br \/>\n<span class=\"notranslate\"> (13) Calculate the Sn content in the sample.<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>h) The degree of white Principle: Beam reflection measurement standard sample with MgO. Equipment: Photometer. Reagent: Standard MgO 99% pa<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"colormag_page_container_layout":"default_layout","colormag_page_sidebar_layout":"default_layout","footnotes":""},"categories":[1820],"tags":[614,616,615,608,617,612,609,610,613,611],"class_list":["post-448","post","type-post","status-publish","format-standard","hentry","category-english","tag-chemical-composition-of-tapioca-starch","tag-chemical-formula-for-tapioca-dextrin","tag-chemical-name-of-tapioca-starch","tag-chemical-tapioca","tag-physical-properties-of-tapioca-starch","tag-tapioca-chemical","tag-tapioca-chemical-composition","tag-tapioca-chemical-formula","tag-tapioca-chemical-reaction","tag-tapioca-chemical-structure"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.9 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Chemical Parameters Quality Tapioca - TN Pangan<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.tneutron.net\/pangan\/chemical-parameters-quality-tapioca\/\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:title\" content=\"Chemical Parameters Quality Tapioca - TN Pangan\" \/>\n<meta name=\"twitter:description\" content=\"h) The degree of white Principle: Beam reflection measurement standard sample with MgO. Equipment: Photometer. 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Equipment: Photometer. 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