CN1580196A - Dearsenicating agent for removing high boiling point arsonium compound in liquid-state petroleum hydrocarbon at low temperature and normal temperature - Google Patents
Dearsenicating agent for removing high boiling point arsonium compound in liquid-state petroleum hydrocarbon at low temperature and normal temperature Download PDFInfo
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- CN1580196A CN1580196A CN 03142116 CN03142116A CN1580196A CN 1580196 A CN1580196 A CN 1580196A CN 03142116 CN03142116 CN 03142116 CN 03142116 A CN03142116 A CN 03142116A CN 1580196 A CN1580196 A CN 1580196A
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Abstract
The invention is a kind of agent which is used to deprive the arsenide of high boiling point in petroleum hydrocarbon at low or normal temperature. The agent contains a type of carrying agent, which loads helpactive component of one or two kinds of rare earth metal or noble metal or their oxide. The agent can deprive the arsenide of high boiling point in petroleum hydrocarbon at low or normal temperature. The preparation method is easy and safe, besides, the invention will not produce devil liquor containing arsenic and pollute environment. Invention name
Description
Technical field
The present invention relates to a kind of low temperature or normal temperature and remove the dearsenic agent of high boiling point arsenide in the liquid condition petroleum hydrocarbon.
Background technology
Arsenide extensively is present in the petroleum hydrocarbon, and they have nonvolatil toxication to the many catalyzer in the petroleum hydrocarbon processing, have a strong impact on activity of such catalysts and work-ing life, and therefore the arsenide that removes in the petroleum hydrocarbon has crucial meaning.
Arsenide in the petroleum hydrocarbon is mainly the organic arsine title complex of trivalent, and the organic arsine title complex with different boiling is with in the middle of the various fractions that enter into respectively after the crude oil fractionation.Liquid condition petroleum hydrocarbon is except containing a certain amount of lower boiling arsenide such as AsH
3And CH
3AsH
2Deng outside, also contain the high boiling point arsenide such as the As (CH of a great deal of
3)
3, As (C
2H
5)
3Deng.The arsenide boiling point is high more or the alkyl chain length is long more, and it is not easy to be removed more, requires also high more to dearsenic agent.
Removing arsentic from liquid hydrocarbon method commonly used at present has:
1, oxidation dearsenification
With potassium permanganate and hydrogen phosphide cumene (CHP) etc. is the oxidizer treatment petroleum hydrocarbon, removes inorganic arsenide through water elution again, and this method wastewater treatment capacity is big, and environmental pollution is serious.
2, shortening dearsenification
This method needs to move under High Temperature High Pressure, complicated operating process, and the running cost height, easily coking causes life cycle short.
3, absorption dearsenification
The sial bead of this method employing sial bead and load copper sulfate removes the trace arsenide in the liquid condition petroleum hydrocarbon, and for most of application scenarios, the technology of absorption dearsenification is simple, but difficulty removes high boiling point arsenide, the dearsenification degree of depth is not high, and the loading capacity of arsenic is little, and work-ing life is short.
U.S. Pat 5064626, US 5085844, US 5096681, US 5096682 have related to removing of trialkyl arsine (trimethylammonium arsine) and relevant dearsenic agent, but above-mentioned patent documentation does not relate to the liquid condition petroleum hydrocarbon system.
Chinese patent CN 1030440A relates to the process of removing phosphorus and arsenide from the hydrocarbon polymer that is generally liquid state, under the condition of heating, liquid hydrocarbon contacts with a kind of catalyzer that contains 50% metal state nickel at least, and this process can be applicable to the purification of gasoline and petroleum naphtha.Simultaneously, Chinese patent CN 1136070A relates to a kind of preparation method that fraction oil of petroleum contains the Ni-based dearsenic catalyst of arsenic liquid hydrocarbon that is used for.In addition, Chinese patent CN 1113261A discloses a kind of Ni-based dearsenic catalyst, and this catalyzer can effectively be removed arsenic and/or phosphorus from liquid condition petroleum hydrocarbon.U.S. Pat 2003/0111391A1 has also announced a kind of dearsenic catalyst that contains group vib such as Mo and VIII family such as Ni, is used for the dearsenification of liquid condition petroleum hydrocarbon.Those of ordinary skill in the art as can be known, said process and/or dearsenic agent only are adapted to the removing arsentic from liquid hydrocarbon under high temperature, the hydro condition.
Chinese patent CN 1197052A discloses a kind of method of removing arsenic from liquid hydrocarbons feedstocks, and the dearsenic agent that this method is used is to be deposited on the oxide compound of the copper on the carrier or the sulfide of copper, and this method is moved under the low temperature that does not have hydrogen to exist, low pressure condition.This patent proposes the dearsenic agent of protection, and its preparation relates to complicated sulfidation, so dearsenification active constituent to the sulfide of small part with copper exists.Analyzing from the technical data that patent documentation provides, is that active constituent is unsatisfactory to the removal effect of high boiling point arsenide with simple copper compound, the arsenic off-capacity 0.1% of dearsenic agent.
Summary of the invention
The purpose of this invention is to provide a kind of dearsenic agent that high boiling point arsenide in the petroleum hydrocarbon is had good removal performance, can more successfully remove the arsenide in the petroleum hydrocarbon under normal temperature or low temperature (＜100 ℃) condition.
The dearsenic agent that low temperature of the present invention or normal temperature remove high boiling point arsenide in the liquid condition petroleum hydrocarbon contains carrier, on the carrier load a kind of main active constituent to three kinds of transition metal or its oxide compound, and load simultaneously a kind of active constituent that helps to two kinds of rare earth metals and/or precious metal or their oxide compound.
The weight percentage that the main active constituent transition metal of load or its oxide compound account for the dearsenic agent total amount on the described carrier is 0.5～50%, preferred 2～20%.
The weight percentage that helps active constituent rare earth metal and/or precious metal or their oxide compound to account for the dearsenic agent total amount of load is 0.0005～10% on the described carrier, preferred 0.005～5%.
In the present invention, the transition metal as main active constituent is the period 4 transition metal.Be selected from a kind of in lanthanum, cerium, the samarium as the rare earth metal that helps active constituent, precious metal is selected from one or both in gold and silver, rhodium, the palladium.
The mean pore size of described carrier is 1～100nm, preferred 3～20nm; Pore volume is 0.1～1.5mL/g, preferred 0.3～1.0mL/g.
Described carrier is preferably from ZSM-5 molecular sieve, mesoporous molecular sieve, USY molecular sieve, gac, aluminum oxide (Al
2O
3), silicon-dioxide (SiO
2), zinc oxide (ZnO), cupric oxide (CuO), chromic oxide (Cr
2O
3), titanium dioxide (TiO
2), sieve and silica-sesquioxide (Al
2O
3-SiO
2) in one or both mixture.
The active constituent of dearsenic agent of the present invention is sulfur compound not, but the dearsenification performance is not influenced by the sulfide in the liquid condition petroleum hydrocarbon.
Dearsenic agent of the present invention is applicable under low temperature (＜100 ℃) or normal temperature and pressure, removes liquid condition petroleum hydrocarbon such as liquid alkane, alkene, alkynes, aromatic hydrocarbons or contains arsenide in the liquid organic mixture of arbitrary proportion above-claimed cpd.Liquid condition petroleum hydrocarbon is except that containing under the normal temperature and pressure for the liquid or solid-state high boiling point arsenide, and also may contain normal temperature and pressure under is gasiform lower boiling organic or inorganic arsenide.
The arsenic capacity of dearsenic agent of the present invention reaches more than 1.0%, and under certain process conditions, raw material arsenic content can be from reducing to below the 10ppb up to 500ppb.
Compared with prior art, the present invention has the following advantages:
One, dearsenic agent of the present invention to high boiling point arsenide, as triphenylarsine, triethyl arsine, has better removal performance under normal temperature or cold condition, can remove the arsenide in the petroleum hydrocarbon more up hill and dale.
Two, dearsenic agent of the present invention uses under the conditions of non-hydrogen of low temperature or normal temperature, operate easier, condition is more preferential, security is better.
Three, dearsenic agent of the present invention in use can not produce and contain arsenic waste solution and contaminate environment.
Embodiment
Further specify the present invention with embodiment below, but the present invention is in no way limited to these embodiment.
Embodiment 1
Be averaged aperture 10～12nm, the silicon-dioxide (SiO of pore volume 0.8mL/g
2) carrier 200 grams, be impregnated into 300 milliliters of finite concentration Fe (NO
3)
3And Pd (NO
3)
2Mixing solutions in, after dipping spends the night, on electric furnace, use little fire drying, further 120 ℃ down dry, calcination made respectively and is numbered 1 to 11 dearsenic agent (seeing Table 1) after 12 hours in 400 ℃ High Temperature Furnaces Heating Apparatus then, and is standby with the vacuum drier preservation.
Get respectively and be numbered 1 to 11 dearsenic agent 50 grams, load in the middle of internal diameter is the fixed-bed reactor of 33mm, activation was cooled to below 50 ℃ after 2 hours in 150～300 ℃ nitrogen atmosphere, squeezed into volume pump then and was furnished with 500ppb arsenic (with AsPh
3The form existence) petroleum naphtha (sulfur-bearing 300ppm) keeps the liquid air speed at 2.5h
-1, handle 200 hours continuously after, detect the outlet arsenic concentration, test-results sees Table 1.
Table 1
| Numbering | ???Fe 2O 3(％) | ????Pd(％) | Concentration (ppb) before the dearsenification | Concentration after the dearsenification (ppb) |
| ????1 | ???0.5 | ????0.05 | ?500 | ?＜20 |
| ????2 | ???2.0 | ????0.05 | ?500 | ?＜10 |
| ????3 | ???10.0 | ????0.05 | ?500 | ?＜5 |
| ????4 | ???20.0 | ????0.05 | ?500 | ?＜5 |
| ????5 | ???30.0 | ????0.05 | ?500 | ?＜10 |
| ????6 | ???50.0 | ????0.05 | ?500 | ?＜20 |
| ????7 | ???10.0 | ????0.0005 | ?500 | ?＜20 |
| ????8 | ???10.0 | ????0.005 | ?500 | ?＜10 |
| ????9 | ???10.0 | ????0.5 | ?500 | ?＜5 |
| ????10 | ???10.0 | ????5.0 | ?500 | ?＜5 |
| ????11 | ???10.0 | ????10.0 | ?500 | ?＜5 |
Embodiment 2
In reactor, add aluminum nitrate (Al (NO
3)
39H
2O) 187.6 gram (0.5mol) and zinc nitrate (Zn (NO
3)
26H
2O) 59.5 grams (0.2mol), cupric nitrate (Cu (NO
3)
23H
2O) 40.6 gram and Silver Nitrate (AgNO
3) 2.06 grams, add deionized water 100mL then, abundant stirring and dissolving, 50～55 ℃ of constant temperature drip 40wt%Na
2CO
3Solution is between the pH value of solution value 7.5～9, and the centrifugal solid materials that gets after 0.5 hour wears out.Solid materials is washed and starched with deionized water again and is washed with abundant removal soluble inorganic salt, and dry under 120 ℃ after the moulding, calcination was preserved standby with vacuum drier after 12 hours in 400 ℃ High Temperature Furnaces Heating Apparatus then.
Get gained dearsenic agent 50 grams, press the filling of embodiment 1 method, pre-treatment dearsenic agent, squeeze into volume pump then and be furnished with 500ppb arsenic (with AsPh
3The form existence) petroleum naphtha keeps the liquid air speed at 2.5h
-1, handle 200 hours continuously after, the outlet arsenic concentration less than 5.0ppb.
Embodiment 3
Get dearsenic agent 50 grams by the preparation of embodiment 2 methods, load in the middle of internal diameter is the fixed-bed reactor of 33mm, 300～350 ℃ down with hydrogen nitrogen mixed gas (H
2/ N
2(v/v)=1: 1) reduce after 4 hours, be cooled to below 50 ℃.Squeeze into volume pump then and be furnished with 500ppb arsenic (with AsPh
3The form existence) petroleum naphtha keeps the liquid air speed at 2.5h
-1, handle 200 hours continuously after, after testing, the outlet arsenic concentration less than 5.0ppb.
Embodiment 4
Take by weighing 3.51 gram cerous nitrates and 110 grams, 50% manganese nitrate solution, be dissolved in the 100mL deionized water, add sieve and silica-sesquioxide (Al
2O
3-SiO
2) carrier 97 grams, flooded 12 hours, little fire drying on electric furnace, calcination gets dearsenic agent in 500 ℃ High Temperature Furnaces Heating Apparatus then.Get this dearsenic agent 50 grams and estimate the dearsenification activity by embodiment 1 method, handle 200 hours continuously after, the outlet arsenic concentration is reduced to below the 10.0ppb.
Embodiment 5
Take by weighing 6.72 gram Silver Nitrate (AgNO
3) and 36.75 gram copper sulfate, be dissolved in the 100mL deionized water, add aluminum oxide (Al
2O
3) carrier 97 gram dipping 12 hours, little fire drying on electric furnace, calcination is decomposed Silver Nitrate and is got dearsenic agent in 500 ℃ High Temperature Furnaces Heating Apparatus then.
Get gained dearsenic agent 50 grams, press embodiment 1 and load, handle dearsenic agent, squeeze into volume pump then and be furnished with 500ppb arsenic (with AsPh
3The form existence) petroleum naphtha keeps the liquid air speed at 2.0h
-1, handle 500 hours continuously after, the outlet arsenic concentration less than 5.0ppb.
Embodiment 6
Take by weighing 47.2 gram nitrate trihydrate copper and 0.25 gram lanthanum nitrate is dissolved in the 100mL deionized water, add silicon-dioxide (SiO
2) carrier 97 gram dipping 12 hours, little fire drying on electric furnace is impregnated into 100mL concentration then and is in 20% the iron nitrate solution, after the little fire drying in 500 ℃ High Temperature Furnaces Heating Apparatus calcination get dearsenic agent.Get this dearsenic agent 50 grams and estimate the dearsenification activity by embodiment 1 method, handle 200 hours continuously after, the solution arsenic concentration is reduced to less than 10.0ppb by 500ppb.
Embodiment 7
Get embodiment 6 gained dearsenic agents 50 grams, method filling, pre-treatment and the evaluation dearsenification activity of pressing embodiment 2 are at liquid air speed 3.0h
-1Condition under handle after 250 hours continuously, the solution arsenic concentration is reduced to less than 5.0ppb by 500ppb.
Embodiment 8
Take by weighing 39.72 gram neutralized verdigris (Cu (OOCCH
3)
2H
2O) and 0.012 the gram RhCl
3Be dissolved in the 100mL deionized water, add silicon-dioxide (SiO
2) carrier 97 gram dipping 12 hours, little fire drying on electric furnace, calcination is decomposed manganese acetate and is got dearsenic agent in 300 ℃ High Temperature Furnaces Heating Apparatus then.Get this dearsenic agent 50 grams and estimate the dearsenification activity by embodiment 1 method, handle 200 hours continuously after, arsenic concentration is reduced to less than 3.0ppb by 500ppb.
Claims (10)
1, a kind of low temperature or normal temperature remove the dearsenic agent of high boiling point arsenide in the liquid condition petroleum hydrocarbon, comprise carrier, it is characterized in that: on the described carrier load a kind of to three kinds of transition metal or its oxide compound, and load simultaneously a kind of to two kinds of rare earth metals and/or precious metal or their oxide compound.
2, dearsenic agent as claimed in claim 1 is characterized in that: to account for the weight percentage of dearsenic agent total amount be 0.5～50% for the transition metal of load or its oxide compound on the described carrier.
3, dearsenic agent as claimed in claim 1 is characterized in that: to account for the weight percentage of dearsenic agent total amount be 2～20% for the transition metal of load or its oxide compound on the described carrier.
4, dearsenic agent as claimed in claim 1 is characterized in that: to account for the weight percentage of dearsenic agent total amount be 0.0005～10% for the rare earth metal of load and/or precious metal or their oxide compound on the described carrier.
5, dearsenic agent as claimed in claim 1 is characterized in that: to account for the weight percentage of dearsenic agent total amount be 0.005～5% for the rare earth metal of load and/or precious metal or their oxide compound on the described carrier.
6, dearsenic agent as claimed in claim 1 is characterized in that: described transition metal is the period 4 transition metal.
7, dearsenic agent as claimed in claim 1 is characterized in that: described rare earth metal is selected from lanthanum, cerium, samarium, and described precious metal is selected from gold and silver, rhodium, palladium.
8, as the described dearsenic agent of claim 1 to 5, it is characterized in that: the mean pore size of described dearsenic agent is 1～100nm, and pore volume is 0.1～1.5mL/g.
9, as the described dearsenic agent of claim 1 to 5, it is characterized in that: the mean pore size of described dearsenic agent is 3～20nm, and pore volume is 0.3～1.0mL/g.
10, as the described dearsenic agent of claim 1 to 5, it is characterized in that: described carrier is selected from ZSM-5 molecular sieve, mesoporous molecular sieve, the mixture of one or both in USY molecular sieve, gac, aluminum oxide, silicon-dioxide, zinc oxide, cupric oxide, chromic oxide, titanium dioxide, the sieve and silica-sesquioxide.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB031421164A CN100392046C (en) | 2003-08-07 | 2003-08-07 | Dearsenicating agent for removing high boiling point arsonium compound in liquid-state petroleum hydrocarbon at low temperature and normal temperature |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB031421164A CN100392046C (en) | 2003-08-07 | 2003-08-07 | Dearsenicating agent for removing high boiling point arsonium compound in liquid-state petroleum hydrocarbon at low temperature and normal temperature |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1580196A true CN1580196A (en) | 2005-02-16 |
| CN100392046C CN100392046C (en) | 2008-06-04 |
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ID=34579377
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|---|---|---|---|
| CNB031421164A Expired - Fee Related CN100392046C (en) | 2003-08-07 | 2003-08-07 | Dearsenicating agent for removing high boiling point arsonium compound in liquid-state petroleum hydrocarbon at low temperature and normal temperature |
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Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101591554A (en) * | 2008-05-30 | 2009-12-02 | 北京三聚环保新材料股份有限公司 | A kind of normal temperature composite desulfurating and dearsenic agent and preparation method thereof |
| CN102302935A (en) * | 2011-05-31 | 2012-01-04 | 武汉科林精细化工有限公司 | Catalyst for oil product hydrodearomatization and preparation method thereof |
| CN103316690A (en) * | 2013-07-04 | 2013-09-25 | 西安元创化工科技股份有限公司 | Liquid hydrocarbon de-arsenic agent and preparation method thereof |
| CN103877931A (en) * | 2012-12-19 | 2014-06-25 | 上海工程技术大学 | Metal compound-type arsenic removal agent, preparation method and application thereof |
| CN105582877A (en) * | 2014-10-24 | 2016-05-18 | 中国石油化工股份有限公司 | Normal-temperature desulfurization dearsenic agent and preparation method thereof |
| CN109251764A (en) * | 2018-09-30 | 2019-01-22 | 昆山市精细化工研究所有限公司 | A kind of Hydrodearsenic Catalyst and its preparation method and application |
| CN110639466A (en) * | 2019-09-30 | 2020-01-03 | 四川润和催化新材料股份有限公司 | Dearsenic adsorbent and preparation method thereof |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2644472B1 (en) * | 1989-03-16 | 1991-06-21 | Inst Francais Du Petrole | PROCESS FOR THE REMOVAL OF MERCURY AND POSSIBLY ARSENIC IN HYDROCARBONS |
| FR2673192B1 (en) * | 1991-02-27 | 1994-07-22 | Inst Francais Du Petrole | PROCESS FOR THE ELIMINATION OF MERCURY AND POSSIBLY ARSENIC IN THE LOADS OF CATALYTIC PROCESSES PRODUCING AROMATICS. . |
| FR2701269B1 (en) * | 1993-02-08 | 1995-04-14 | Inst Francais Du Petrole | Process for the elimination of arsenic in hydrocarbons by passage over a presulfurized capture mass. |
| CN1115382C (en) * | 1998-03-20 | 2003-07-23 | 中国石油化工集团公司 | Dearsenic agent for petroleum hydrocarbon and its prepn. method and application |
-
2003
- 2003-08-07 CN CNB031421164A patent/CN100392046C/en not_active Expired - Fee Related
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|---|---|---|---|---|
| CN101591554A (en) * | 2008-05-30 | 2009-12-02 | 北京三聚环保新材料股份有限公司 | A kind of normal temperature composite desulfurating and dearsenic agent and preparation method thereof |
| CN101591554B (en) * | 2008-05-30 | 2013-05-08 | 北京三聚环保新材料股份有限公司 | Normal temperature compound desulfuration and dearsenization agent and preparation method thereof |
| CN102302935A (en) * | 2011-05-31 | 2012-01-04 | 武汉科林精细化工有限公司 | Catalyst for oil product hydrodearomatization and preparation method thereof |
| CN102302935B (en) * | 2011-05-31 | 2014-05-07 | 武汉科林精细化工有限公司 | Catalyst for oil product hydrodearomatization and preparation method thereof |
| CN103877931A (en) * | 2012-12-19 | 2014-06-25 | 上海工程技术大学 | Metal compound-type arsenic removal agent, preparation method and application thereof |
| CN103316690A (en) * | 2013-07-04 | 2013-09-25 | 西安元创化工科技股份有限公司 | Liquid hydrocarbon de-arsenic agent and preparation method thereof |
| CN105582877A (en) * | 2014-10-24 | 2016-05-18 | 中国石油化工股份有限公司 | Normal-temperature desulfurization dearsenic agent and preparation method thereof |
| CN105582877B (en) * | 2014-10-24 | 2019-01-25 | 中国石油化工股份有限公司 | Room temperature desulfurating and dearsenic agent and preparation method thereof |
| CN109251764A (en) * | 2018-09-30 | 2019-01-22 | 昆山市精细化工研究所有限公司 | A kind of Hydrodearsenic Catalyst and its preparation method and application |
| CN109251764B (en) * | 2018-09-30 | 2023-03-21 | 昆山市精细化工研究所有限公司 | Dearsenic agent and preparation method and application thereof |
| CN110639466A (en) * | 2019-09-30 | 2020-01-03 | 四川润和催化新材料股份有限公司 | Dearsenic adsorbent and preparation method thereof |
| CN110639466B (en) * | 2019-09-30 | 2020-12-01 | 四川润和催化新材料股份有限公司 | Dearsenic adsorbent and preparation method thereof |
| WO2021063345A1 (en) | 2019-09-30 | 2021-04-08 | 四川润和催化新材料股份有限公司 | Dearsenification adsorbent and preparation method therefor |
| EP4023329A4 (en) * | 2019-09-30 | 2022-11-23 | Rezel Catalysts Corporation | Dearsenification adsorbent and preparation method therefor |
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| Publication number | Publication date |
|---|---|
| CN100392046C (en) | 2008-06-04 |
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