nice almost 11 gram silver from that cool ;) ill gona have alot of them later black and yellow ;) i have alot of silver oskylaters as well ;) great video
I have worked in industry, I am a metallurgical technician also in large-scale and small-scale industrial recycling plants for precious metals. By the chemical law in October I graduated higher in I+D Chairs of the research and development institute. And since I no longer work for someone else, I am a Goldsmith and your recovery of metals is bad, very inefficient and your workplace is not adequate 👎 This is not my language Si Google no tradujo el chat de manera inexacta no es mi culpa y tampoco me importa eso solo le interesa al gobierno castellano e inglés porque solo ocurre estos errores entre estos idiomas recovery is again inefficient. Industrial acetone / 3, nitric acid volume 65 / 1 Mix 10 ml Erlenmeyer glass at 1 minute drip and refrigeration base. 500ml of solution is capable of destroying 100kg of this element. 3lt glass pilex magnetic stirring pill add the diluent and the components until covered. Scrap may still contain silver but is processed by electroplating 1.A 6.9V For each equitable solution to 100ml we add 10ml muriatic acid when we process the total acid we proceed to heat with the magnetic stirrer. Remember the pill only supports 50°C if it is marnerica if it is a magnetic vase and magnetable pill it will be necessary to remove it and the temperature should not reach boiling 80 to 90°C This is only to speed up the evaporation of acetone and muriatic acid will disintegrate metals that nitric acid itself could not. At room temperature without drastically cooling the solution, we will pass to an Elermeyer beaker type that removes jumps. Strainer glass, flat laboratory funnel or common funnel, add its respective perforated stopper or vacuum gasket. Transfer the solution to a straight glass and add another highly saturated solution 500ml distilled water 400g sodium chloride. This solution will be added gradually without stirring the precipitate. Alert, you have not obtained metallic silver, it is silver nitrate, the direct function causes losses of 68% of expected metal. Elermeyer beaker 50% from the bottom with sulfuric acid and vacuum stopper to which we added a drip funnel. Distilled water 1ltx10g iron nitrate will be added to the drip. This is the reagent not that you put 10 liters on the Elermeyer. This exercise involves 2 elermeyer jumper cups and bubble pipe added to the vacuum plug and metrapropylene hoses on the jumper tubes. 🥛Sulfuric acid and iron nitrate dripping 🥤 50% Distilled water and the silver nitrate pipe is placed submerged to catalyze the sulfuric acid gas and in turn mentalize the silver which turns from nitrate to chloride. This will be noticeable when it turns from metallic white to gray but still not ready for every 100g 1mg of ammonia is added. Silver chloride will transform into metallic silver oxide. The fusion 1x1 silver oxide borax dip the total in alcohol to burn and drain and caking 🔥 You will create an amalgam for the crucible that prevents the borax from spitting metal out of the crucible. In my case it doesn't matter to me I use induction cupela. Sufion and relative times affect ambient temperatures. Butane or propane oxynene torch 30 minutes ~ 1 hour 👎 30m ~ 40m Mini Oxidoacetylene Torch Gas torch and compressed air bellows 20m ~ 30m Preheated Coal Furnace Crucible with Lid 10m ~ 15m Bitrofusion furnace requires this element plus microwave oven energy efficiency 0 ambient temperature does not affect it but it can put the metal at evolution temperature or worse 10m ~ 15m Tesla induction furnace mine includes simple casting or lost wax casting ingot melting time 1 ~ 5m investment casting cup 5m efficiency 100% since the ingots present 0 direct Regular or low-end Tesla induction furnace does not cost more than €300 but we ensure the total octection of precious metal and allow alloys for jewelry
Hello, can you tell me how to recover silver from silver plated iron as i tried dissolving the iron in nitric acid and then when i added hydrochloric acid it got something cloudy white but it didn't convert to silver when i added aluminum.
What about the tantalum ?
Was there more silver in the beakers?
yes broo 👍👍👍
دستت درد نکنه ارزو دارم همیشه موفق باشی
saret salamat agha mehdiye gol
nice almost 11 gram silver from that cool ;)
ill gona have alot of them later black and yellow ;)
i have alot of silver oskylaters as well ;)
great video
its very good bro thanks for watching my videos 🌹🌹🌹🌹👍
@@ImanGoldRecovery ;)
@@JohnnySwedishScrapper 🌹
Follow 😊✊
@@Goldhayday thanks for watching
is there any silver in the remaining water
yes a small amount that settles over time
Видео наглядно показывает как обесценить вещи))) эти детальки то стоят дороже если их продать так...
thanks for watching sir
Será una moda? el de que los afinadores usen sandalias para trabajar!
hahahah thanks for watching brooo👍🌹🌹
Love from india sir ❤️
thanls for watching brooo 👍👍🌹🌹🌹
hello colleague, I also processed such capacitors, the output is normal from them. come visit.
thanks for watching
Active hno3 in the salutation make problems
yes broo 👍🌹🌹🌹
👍👍❤️
thanks for watchn
Сжег тантала на 1200р получив 600р серебром Гений
Причемвидео хатянуто типа калифорний извлекал
Вообще,я тоже окуел....можно было и то и то достать...
@@sity1977 Этот парень только серик походу и золото знает Мож какой начинающий))
@@ИванИванов-ш2т9р *Раскусывать каждый конденсатор не захотел, а видео снял для контента! Тантал жалко это факт, Варвар- радиолюбители слёзы льют!* !
@@Gold_Plus Ну мы то профи - вандалы )) Мы и видео снимаем и правельно делаем))
you give a safety warning?! try actual rubber gloves not cloth backed, and get some closed toecap shoes FFS
thanks for watching and help brooo 👍🌹🌹🌹
Lol 😂
Gas propano/ butano.
thanks for wawtching and comment sir
А я их в срезку кидаю))
thanks for watching broooo 🌹🌹🌹👍
Ok
thanks for watching and comment sir
I have worked in industry, I am a metallurgical technician also in large-scale and small-scale industrial recycling plants for precious metals. By the chemical law in October I graduated higher in I+D Chairs of the research and development institute. And since I no longer work for someone else, I am a Goldsmith and your recovery of metals is bad, very inefficient and your workplace is not adequate 👎
This is not my language
Si Google no tradujo el chat de manera inexacta no es mi culpa y tampoco me importa eso solo le interesa al gobierno castellano e inglés porque solo ocurre estos errores entre estos idiomas
recovery is again inefficient.
Industrial acetone / 3, nitric acid volume 65 / 1
Mix 10 ml Erlenmeyer glass at 1 minute drip and refrigeration base.
500ml of solution is capable of destroying 100kg of this element.
3lt glass pilex magnetic stirring pill add the diluent and the components until covered.
Scrap may still contain silver but is processed by electroplating 1.A 6.9V
For each equitable solution to 100ml we add 10ml muriatic acid when we process the total acid we proceed to heat with the magnetic stirrer. Remember the pill only supports 50°C if it is marnerica if it is a magnetic vase and magnetable pill it will be necessary to remove it and the temperature should not reach boiling 80 to 90°C
This is only to speed up the evaporation of acetone and muriatic acid will disintegrate metals that nitric acid itself could not.
At room temperature without drastically cooling the solution, we will pass to an Elermeyer beaker type that removes jumps.
Strainer glass, flat laboratory funnel or common funnel, add its respective perforated stopper or vacuum gasket.
Transfer the solution to a straight glass and add another highly saturated solution 500ml distilled water 400g sodium chloride.
This solution will be added gradually without stirring the precipitate.
Alert, you have not obtained metallic silver, it is silver nitrate, the direct function causes losses of 68% of expected metal.
Elermeyer beaker 50% from the bottom with sulfuric acid and vacuum stopper to which we added a drip funnel.
Distilled water 1ltx10g iron nitrate will be added to the drip. This is the reagent not that you put 10 liters on the Elermeyer.
This exercise involves 2 elermeyer jumper cups and bubble pipe added to the vacuum plug and metrapropylene hoses on the jumper tubes.
🥛Sulfuric acid and iron nitrate dripping 🥤 50% Distilled water and the silver nitrate pipe is placed submerged to catalyze the sulfuric acid gas and in turn mentalize the silver which turns from nitrate to chloride.
This will be noticeable when it turns from metallic white to gray but still not ready for every 100g 1mg of ammonia is added. Silver chloride will transform into metallic silver oxide.
The fusion 1x1 silver oxide borax dip the total in alcohol to burn and drain and caking 🔥 You will create an amalgam for the crucible that prevents the borax from spitting metal out of the crucible. In my case it doesn't matter to me I use induction cupela.
Sufion and relative times affect ambient temperatures.
Butane or propane oxynene torch 30 minutes ~ 1 hour 👎
30m ~ 40m Mini Oxidoacetylene Torch
Gas torch and compressed air bellows 20m ~ 30m
Preheated Coal Furnace Crucible with Lid 10m ~ 15m
Bitrofusion furnace requires this element plus microwave oven energy efficiency 0 ambient temperature does not affect it but it can put the metal at evolution temperature or worse 10m ~ 15m
Tesla induction furnace mine includes simple casting or lost wax casting ingot melting time 1 ~ 5m investment casting cup 5m efficiency 100% since the ingots present 0 direct
Regular or low-end Tesla induction furnace does not cost more than €300 but we ensure the total octection of precious metal and allow alloys for jewelry
Hello,
can you tell me how to recover silver from silver plated iron as i tried dissolving the iron in nitric acid and then when i added hydrochloric acid it got something cloudy white but it didn't convert to silver when i added aluminum.
thansk for watching an info