CN1127304A - Palladium recovering method from waste palladium carbon catalyst - Google Patents
Palladium recovering method from waste palladium carbon catalyst Download PDFInfo
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- CN1127304A CN1127304A CN 95104435 CN95104435A CN1127304A CN 1127304 A CN1127304 A CN 1127304A CN 95104435 CN95104435 CN 95104435 CN 95104435 A CN95104435 A CN 95104435A CN 1127304 A CN1127304 A CN 1127304A
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Abstract
The method for recovering palladium from waste palladium-carbon catalyst includes such steps of roasting, acid-boiling, chlorination, ion exchange, ammonia complexation and reduction. Said invented method is simple in technological process, its production cost is low, palladium recovery is greater than 99% and palladium purity is up to 99.95%.
Description
The present invention relates to the solid waste regenerative use technology, particularly a kind of method that from waste palladium carbon catalyst, reclaims palladium.
Palladium-carbon catalyst is used for the refining PTA hydrogenation reaction of petrochemical industry, and this support of the catalyst intensity is little, rapid wear is broken, and work-ing life, short (about half a year) scrapped about more than 100 tons of this catalyzer domestic present every year, recyclable more than 300 kilograms of palladiums.To the technical study that this spent catalyst reclaims palladium, domesticly do not appear in the newspapers as yet.Because the palladium that this catalyzer uses costs an arm and a leg, resource shortage is so it is imperative to reclaim palladium from this spent catalyst.
Abroad developed to handle and given up the technology of C catalyst, for example the technical process of U.S. Ying Gehade company as shown in Figure 1.
This technical process is long, operation is many, and the rate of recovery of palladium is not high.
The purpose of this invention is to provide the method that from waste palladium carbon catalyst, reclaims palladium that a kind of technology is simple, the rate of recovery is high, cost is low.
Method of the present invention is: waste palladium carbon catalyst is put into stoving oven oxidizing roasting, furnace temperature can be 500~700 ℃, the roasting ash boils removal of impurities with sulphuric acid soln acid, ash after the removal of impurities leaches palladium with chlorination process, leach liquor exchanges further removal of impurities through Zeo-karb, the exchange liquid close purification through ammino, reduce palladium sponge.
To be described chlorination process put into the solution that contains hydrochloric acid, sodium chlorate, sodium-chlor for the ash that acid is boiled after the removal of impurities to a kind of preferred scheme of the inventive method, weight proportion is: bake around ash: hydrogenchloride: sodium chlorate: sodium-chlor: water=1: (1~3): (0.1~0.3): (0.1~0.3): (4~6), temperature is 70~90 ℃, and the time is 3~5 hours during immersion.Describedly boil with sulphuric acid soln acid that used sulfuric acid concentration expressed in percentage by weight is 10~30% in the step, sulphuric acid soln is 1: 5~8 with the weight proportion of ash, temperature is 90~120 ℃, the acid time of boiling is 2~4 hours, for preventing a small amount of palladium solution loss, also can add a small amount of formic acid, the formic acid add-on is every kilogram of ash 250~400ml.
Described sun from exchange power fat be preferably 720 type cationic exchange power fat especially.
Can filter after described ammino closes, use hcl acidifying, after the sedimentation and filtration washing, get palladium sponge, get palladium metal through hydrogen reduction again with hydrazine hydrate reduction.
Method technology of the present invention is simple, and production cost is low, rate of recovery height (palladium recovery rate 〉=99%), and palladium purity can reach 99.85%.
Establish acid in the method for the present invention and boil and cationic exchange two steps, make and separate the greatly simplification of purifying, improved the rate of recovery of palladium again.
In acid is boiled, add inhibitor formic acid especially, prevented the solution loss of palladium when removal of impurities.The purpose of carrying out cationic exchange is that a small amount of impurities further purifies again, only need just close through an ammino can reach>99.95% palladium purity requirement.If handle without above-mentioned two steps, then impurity is many, just needs that the repeated multiple times ammino closes, acidifying, and complexing slag, acidifying tail washings amount are just many like this, can cause the loss of palladium.
Further specify the present invention below by embodiment.
Embodiment
Get 25 kilograms of waste palladium carbon catalysts (doing), wherein contain palladium 77500mg, put into stoving oven and carry out oxidizing roasting, temperature is about 600 ℃, the roasting ash adds 20% aqueous sulfuric acid, and solid-to-liquid ratio is 1: 6, and the amount with every kilogram of grey 350ml adds formic acid again, be heated to and boiled about 100 ℃ 3 hours, after the filtration, acid is boiled in the liquid and discharging, and lime-ash adds and contains hydrochloric acid, sodium chlorate, in the aqueous solution of sodium-chlor the palladium chlorination is leached, wherein grey: hydrogenchloride: sodium chlorate: sodium-chlor: water is 1: 2: 0.2: 0.2: 3, about 80 ℃ of temperature, leaching time 4 hours is after the filtration, slag returns roasting, filtrate exchanges further removal of impurities with 732 type Zeo-karbs, and exchange liquid closes through ammino, filters, the complexing slag reclaims, complexing Huaihe River hcl acidifying, the acidifying tail washings reclaims, after the sedimentation and filtration washing, obtain palladium sponge with hydrazine hydrate reduction, get palladium metal through hydrogen reduction again.
Handled two batches of waste palladium carbon catalysts with aforesaid method, its test-results is as follows:
Experiment lot number project | ????I | ????II | ||
Contain pd (mg) | ?% | Contain pd (mg) | ?% | |
25 kilograms of waste palladium carbon catalysts (doing) | 77500 | ?100 | ?77500 | ?100 |
Liquid is boiled in acid | 3.1 | ?0.004 | ?3.1 | ?0.004 |
Close palladium in the slag | 47.5 | ?0.061 | ?42.5 | ?0.055 |
Residual palladium in the filter paper | 170.5 | ?0.22 | ?192.1 | ?0.248 |
Palladium sponge | 77278.9 | ?99.715 | ?77262 | ?99.693 |
Add up to | 77500 | ?100 | ?77500 | ?100 |
During the test-results table, the rate of recovery of palladium 〉=99%, the purity of palladium is 99.95%.
Claims (9)
1, a kind of method that from waste palladium carbon catalyst, reclaims palladium, it is characterized in that waste palladium carbon catalyst is put into stoving oven oxidizing roasting, the roasting ash boils removal of impurities with sulphuric acid soln acid, ash after the removal of impurities leaches palladium with chlorination process, leach liquor exchanges further removal of impurities through Zeo-karb, the exchange liquid close purification through ammino, reduce palladium sponge.
2, method as claimed in claim 1 is characterized in that described maturing temperature is 500~700 ℃.
3, method as claimed in claim 1, it is characterized in that described step puts into the solution that contains hydrochloric acid, sodium chlorate, sodium-chlor for the ash that acid is boiled after the removal of impurities, weight proportion is an ash: hydrogenchloride: sodium chlorate: sodium-chlor: water=1: (1~3): (0.1~0.3): (0.1~0.3): (4~6), temperature is 70~90 ℃, and soak time is 3~5 hours.
4, method as claimed in claim 1 is characterized in that it is that the roasting ash is added in the sulphuric acid soln of 10~30% (weights) that step is boiled in described acid, and solid-to-liquid ratio is 1: 5~8, and temperature is 90~120 ℃, and the acid time of boiling is 2~4 hours.
5,, it is characterized in that described acid boils in the step every kilogram of ash and add 250~400ml formic acid as the method for claim 1 or 4.
6, method as claimed in claim 1 is characterized in that described chloridizing leach solution exchanges further removal of impurities through 732 type Zeo-karbs.
7, method as claimed in claim 1 is characterized in that described exchange liquid closes after-filtration through ammino, the complex liquid hcl acidifying.
8,, it is characterized in that described reduction step is for to obtain palladium sponge with hydrazine hydrate reduction as the method for claim 1 or 7.
9, method as claimed in claim 1 is characterized in that described palladium sponge gets palladium metal through hydrogen reduction.
Priority Applications (1)
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CN95104435A CN1040665C (en) | 1995-05-29 | 1995-05-29 | Palladium recovering method from waste palladium carbon catalyst |
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CN95104435A CN1040665C (en) | 1995-05-29 | 1995-05-29 | Palladium recovering method from waste palladium carbon catalyst |
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CN1127304A true CN1127304A (en) | 1996-07-24 |
CN1040665C CN1040665C (en) | 1998-11-11 |
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Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1062492C (en) * | 1996-12-30 | 2001-02-28 | 韦士平 | Process for reclaiming waste catalyst with low palladium content |
CN100537800C (en) * | 2007-06-22 | 2009-09-09 | 厦门金达威维生素股份有限公司 | From the waste loading palladium hydrogenation catalyst, reclaim the method for palladium metal and Palladous chloride |
CN102978409A (en) * | 2012-12-26 | 2013-03-20 | 安徽工业大学 | Method for recovering heavy metal palladium from waste carbon-based catalytic agent |
CN103451431A (en) * | 2013-08-27 | 2013-12-18 | 罗治 | Method for extracting arsenic and precious metals from dead catalysts containing precious metals |
CN103555957A (en) * | 2013-11-20 | 2014-02-05 | 浙江省冶金研究院有限公司 | Method for recovering high-purity metal palladium from organic waste palladium contained catalyst |
CN104032143A (en) * | 2014-05-15 | 2014-09-10 | 浙江省冶金研究院有限公司 | Recycling and purifying method of waste palladium-carbon catalyst |
CN104060095A (en) * | 2014-06-17 | 2014-09-24 | 励福实业(江门)贵金属有限公司 | Method of recovering palladium from palladium-loading aluminum oxide waste catalyst |
CN108285978A (en) * | 2018-03-06 | 2018-07-17 | 北京科技大学 | A kind of recovery method of the palladium from palladium-containing catalyst |
CN111203425A (en) * | 2020-01-10 | 2020-05-29 | 泉州丰鹏环保科技有限公司 | Process and device for crushing and recovering alumina framework of waste FCC catalyst |
-
1995
- 1995-05-29 CN CN95104435A patent/CN1040665C/en not_active Expired - Fee Related
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1062492C (en) * | 1996-12-30 | 2001-02-28 | 韦士平 | Process for reclaiming waste catalyst with low palladium content |
CN100537800C (en) * | 2007-06-22 | 2009-09-09 | 厦门金达威维生素股份有限公司 | From the waste loading palladium hydrogenation catalyst, reclaim the method for palladium metal and Palladous chloride |
CN102978409A (en) * | 2012-12-26 | 2013-03-20 | 安徽工业大学 | Method for recovering heavy metal palladium from waste carbon-based catalytic agent |
CN103451431A (en) * | 2013-08-27 | 2013-12-18 | 罗治 | Method for extracting arsenic and precious metals from dead catalysts containing precious metals |
CN103451431B (en) * | 2013-08-27 | 2015-08-12 | 江西南城鑫业环保处置有限公司 | A kind of method extracting arsenic and precious metal from spent noble metals bearing catalysts |
CN103555957A (en) * | 2013-11-20 | 2014-02-05 | 浙江省冶金研究院有限公司 | Method for recovering high-purity metal palladium from organic waste palladium contained catalyst |
CN104032143A (en) * | 2014-05-15 | 2014-09-10 | 浙江省冶金研究院有限公司 | Recycling and purifying method of waste palladium-carbon catalyst |
CN104060095A (en) * | 2014-06-17 | 2014-09-24 | 励福实业(江门)贵金属有限公司 | Method of recovering palladium from palladium-loading aluminum oxide waste catalyst |
CN108285978A (en) * | 2018-03-06 | 2018-07-17 | 北京科技大学 | A kind of recovery method of the palladium from palladium-containing catalyst |
CN111203425A (en) * | 2020-01-10 | 2020-05-29 | 泉州丰鹏环保科技有限公司 | Process and device for crushing and recovering alumina framework of waste FCC catalyst |
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CN1040665C (en) | 1998-11-11 |
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