CN106563334A - Method for trapping nitric oxide by utilizing phenol anion functionalized ionic liquid - Google Patents

Method for trapping nitric oxide by utilizing phenol anion functionalized ionic liquid Download PDF

Info

Publication number
CN106563334A
CN106563334A CN201611031893.1A CN201611031893A CN106563334A CN 106563334 A CN106563334 A CN 106563334A CN 201611031893 A CN201611031893 A CN 201611031893A CN 106563334 A CN106563334 A CN 106563334A
Authority
CN
China
Prior art keywords
nitric oxide
phenol
phosphorus
ion liquid
high power
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201611031893.1A
Other languages
Chinese (zh)
Inventor
王从敏
施桂玲
陈凯宏
李浩然
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Zhejiang University ZJU
Original Assignee
Zhejiang University ZJU
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Zhejiang University ZJU filed Critical Zhejiang University ZJU
Priority to CN201611031893.1A priority Critical patent/CN106563334A/en
Publication of CN106563334A publication Critical patent/CN106563334A/en
Pending legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/14Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by absorption
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/14Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by absorption
    • B01D53/1418Recovery of products
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/14Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by absorption
    • B01D53/1425Regeneration of liquid absorbents
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/14Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by absorption
    • B01D53/1493Selection of liquid materials for use as absorbents
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2252/00Absorbents, i.e. solvents and liquid materials for gas absorption
    • B01D2252/30Ionic liquids and zwitter-ions
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2257/00Components to be removed
    • B01D2257/40Nitrogen compounds
    • B01D2257/404Nitrogen oxides other than dinitrogen oxide

Abstract

The invention discloses a method for trapping nitric oxide by utilizing phenol anion functionalized ionic liquid. Ionic liquid with a phenol anion is used as an absorbent, so as to absorb a nitric oxide gas; the absorption pressure is 0.0001MPa to 0.2MPa; the absorption temperature is 20 to 100 DEG C; the absorption time is 1 to 16 hours; the absorbed nitric oxide is desorbed more easily; the desorption temperature is 60 to 120 DEG C; the desorption time is 0.1 to 3 hours; in comparison with a conventional method for trapping the nitric oxide, the ionic liquid functionalized by the phenol anion is utilized for method for trapping the nitric oxide by utilizing the phenol anion functionalized ionic liquid to react with the nitric oxide to generate NONOates; thus, the absorption efficiency of the nitric oxide is greatly improved; and 4.10 moles of the nitric oxide can be trapped at most by every mole of the ionic liquid.

Description

One kind traps nitric oxide production method using phenol anion functionalized ion liquid
Technical field
The invention mainly relates to a kind of trap nitric oxide production method, it is that one kind utilizes phenol anion work(specifically Ionic liquid can be changed and trap nitric oxide production method.
Background technology
Nitrogen oxides (NOx) are the main components of atmospheric pollution, and NOx is also to form haze, acid rain and destruction lake, forest Deng the arch-criminal of ecosystem.The main selective catalytic reduction method (SCR) of traditional NOx trap method and selective non-catalytic are also Former method (SNCR).But these methods have certain limitation, such as, for SCR, its is relatively costly, and the sulfur in flue gas Compound easily causes catalyst inactivation;And for SNCR, its NOx trap is less efficient, and have waste gas generation.Therefore, design Synthesis application is significant in the new material of efficient NOx trap.
Ionic liquid as a kind of new green solvent, with low-steam pressure, wide liquid journey, high stability, designability The advantages of, the sour gas trapping technique for Development of Novel provides chance.How to be set by the structure of functionalized ion liquid Meter, is the crucial and heat of current Ionic Liquids Acidity gas trapping research while realizing NO gas high power capacity, the trapping of low energy consumption Point problem.
On the other hand, NO is a kind of biological messenger molecule, and it has in cardiovascular system, immune system, nervous system etc. Critically important effect, and star molecule is elected as by Science in 1992.American scientist Luo Baifoqi is Gothic (Robert F.Furchgott), Louis Lu Yigenaluo (LouisJ.Ignarro) and take and auspicious admire rad (Ferid Murad) Nobel's life of 1998 is obtained because of " nitric oxide plays signaling molecule effect in cardiovascular system " is found Of science or Medicine.The trapping of NO also has far-reaching significance to studying applications of the NO in organism.
The content of the invention
It is an object of the invention to provide a kind of utilization phenol anion functionalized ion liquid carries out nitric oxide trapping Method, the mainly ionic liquid of the different phenol anion functionalization of design synthesis, in being applied to nitric oxide production trapping, utilize Phenol anion with alkalescence generates NONOates with nitric oxide reaction, so as to realize the nitric oxide production one kind of efficient absorption New method.
The present invention is achieved through the following technical solutions:
The present invention is a kind of method using nitric oxide trapping is carried out using phenol anion functionalized ion liquid, is made Nitric oxide gas are absorbed with the ionic liquid with phenol anion as absorbent, absorption pressure is 0.0001~ 0.2MPa, it is 20 DEG C~100 DEG C to absorb temperature, and soak time is 1~16 hour, and the nitric oxide of absorption is to be easier to desorption , at 60~120 DEG C, desorption time was at 0.1~3 hour for desorption temperature.
Used as further improving, energy of the present invention traps nitric oxide production alkali anion functionalized ion liquid and is The hexyl phosphorus phenol of myristyl three, the hexyl phosphorus p bromophenol of myristyl three, the hexyl phosphorus paranitrophenol of myristyl three, 14 The hexyl phosphorus p-trifluoromethyl-phenol of alkyl three, the hexyl phosphorus p-methyl phenol of myristyl three, ethyl tributyl phosphorus phenol, ethyl three Butyl phosphorus p bromophenol, ethyl tributyl phosphorus paranitrophenol, ethyl tributyl phosphorus p-trifluoromethyl-phenol, ethyl tributyl phosphorus P-methyl phenol, ethylmethylimidazolium phenol, ethylmethylimidazolium p bromophenol, ethylmethylimidazolium paranitrophenol, ethyl Methylimidazole. p-trifluoromethyl-phenol, ethylmethylimidazolium p-methyl phenol, butyl methyl imidazoles phenol, butyl methyl imidazoles pair Bromophenol, butyl methyl imidazoles paranitrophenol, butyl methyl imidazoles p-trifluoromethyl-phenol, butyl methyl imidazoles are to methylbenzene Any one in phenol.
Used as further improving, alkali anion functionalized ion liquid of the present invention is the hexyl of myristyl three Phosphorus paranitrophenol.
As further improving, nitric oxide absorption pressure of the present invention 0.01 to 0.1MPa atmospheric pressure it Between.
Used as further improving, nitric oxide of the present invention absorbs temperature between 30 DEG C~90 DEG C.
Used as further improving, desorption temperature of the present invention is at 70~90 DEG C.
Used as further improving, desorption time of the present invention was at 1~3 hour.
The invention discloses a kind of phenol anion functionalized ion liquid is energy-efficient to trap nitric oxide production method, lead to Cross phenol anion to generate NONOates to absorb with realizing nitric oxide production high-efficient high-capacity three amount with nitric oxide reaction, be one The industry trapping of nitrogen oxide provides a kind of potential method.Compared with the nitric oxide production method of tradition trapping, the present invention is utilized The ionic liquid of phenol anion functionalization generates NONOates with nitric oxide reaction, so as to drastically increase nitric oxide Absorption efficiency, reach as high as every mole of ionic liquid and trap 4.10 moles of nitric oxide.
Specific embodiment
Technical scheme is described further below by way of specific embodiment.
Embodiment 1
In an internal diameter is for the 5ml glass containers of 1cm, ionic liquid ethylmethylimidazolium paranitrophenol 0.80g is added (0.001mol) in, being subsequently placed in the hermetically sealed can of nitric oxide pressure 0.1MPa, it is 30 DEG C to control to absorb temperature, during absorption equilibrium Between be 9 hours, weigh and show in the ionic liquid that nitric oxide production absorptive capacity is 3.39 moles/mole ionic liquids.
Embodiment 2-4
Similar to embodiment 1, nitric oxide gas pressure is controlled for 0.1MPa, 30 DEG C of temperature of absorption, change ionic liquid Species, nitric oxide absorb result such as following table (table 1):
The impact that the different anions of table 1 are trapped to nitric oxide
Embodiment 5-12
Similar to embodiment 1, the hexyl phosphorus paranitrophenol of myristyl three is adopted for absorbent, absorb nitric oxide gas Body, changes and absorbs temperature, and the condition such as nitric oxide pressure and soak time absorbs result such as following table (table 2):
The impact that the different acceptance conditions of table 2 absorb to nitric oxide
Embodiment 13
An internal diameter for 1cm 5ml glass containers in, addition absorbed nitric oxide production ionic liquid myristyl three oneself Base phosphorus paranitrophenol 0.80g (0.001mol), is subsequently placed in the vacuum drying oven of pressure 0.005MPa, controls desorption temperature For 80 DEG C, desorption time is controlled for 1 hour, the nitric oxide amount for showing to be remained in the ionic liquid of weighing is 2.10mol/mol IL。
Impact of the different condition of table 3 to nitric oxide desorption
Listed above is only some embodiments of the present invention, it is clear that the invention is not restricted to above example, may be used also To have many deformations, all changes that one of ordinary skill in the art can directly derive from present disclosure or associate Shape, is considered as protection scope of the present invention.

Claims (7)

1. it is a kind of to trap nitric oxide production method using phenol anion functionalized ion liquid high power capacity, it is characterised in that profit With with phenol anion and Effect of Nitric Oxide, carrying out efficient absorption nitric oxide gas, absorption pressure is 0.0001~ 0.2MPa, it is 20 DEG C~100 DEG C to absorb temperature, and soak time is 1~16 hour, and the nitric oxide of absorption is to be easier to desorption , at 60~120 DEG C, desorption time was at 0.1~3 hour for desorption temperature.
2. utilization basic functionalized ionic liquid high power capacity according to claim 1 traps nitric oxide production method, and it is special Levy and be, it is described can the nitric oxide production alkali anion functionalized ion liquid of trapping be the hexyl phosphorus phenol of myristyl three, ten The hexyl phosphorus p bromophenol of tetraalkyl three, the hexyl phosphorus paranitrophenol of myristyl three, the hexyl phosphorus of myristyl three are to trifluoromethyl Phenol, the hexyl phosphorus p-methyl phenol of myristyl three, ethyl tributyl phosphorus phenol, ethyl tributyl phosphorus p bromophenol, ethyl three Butyl phosphorus paranitrophenol, ethyl tributyl phosphorus p-trifluoromethyl-phenol, ethyl tributyl phosphorus p-methyl phenol, ethyl-methyl miaow Azoles phenol, ethylmethylimidazolium p bromophenol, ethylmethylimidazolium paranitrophenol, ethylmethylimidazolium are to trifluoromethylbenzene Phenol, ethylmethylimidazolium p-methyl phenol, butyl methyl imidazoles phenol, butyl methyl imidazoles p bromophenol, butyl methyl imidazoles Any one in paranitrophenol, butyl methyl imidazoles p-trifluoromethyl-phenol, butyl methyl imidazoles p-methyl phenol.
3. utilization phenol anion functionalized ion liquid high power capacity according to claim 2 traps nitric oxide production side Method, it is characterised in that described to trap nitric oxide production alkali anion functionalized ion liquid for the hexyl phosphorus of myristyl three Paranitrophenol.
4. the utilization phenol anion functionalized ion liquid high power capacity according to claim 1 or 2 or 3 traps nitric oxide Method, it is characterised in that described nitric oxide absorption pressure is 0.01 between 0.1MPa atmospheric pressure.
5. utilization phenol anion functionalized ion liquid high power capacity according to claim 4 traps nitric oxide production side Method, it is characterised in that described nitric oxide absorbs temperature between 30 DEG C~90 DEG C.
6. the utilization phenol anion functionalized ion liquid high power capacity according to claim 1 or 2 or 3 or 5 traps an oxygen The method for changing nitrogen, it is characterised in that described desorption temperature is at 70~90 DEG C.
7. utilization phenol anion functionalized ion liquid high power capacity according to claim 6 traps nitric oxide production side Method, it is characterised in that described desorption time was at 1~3 hour.
CN201611031893.1A 2016-11-22 2016-11-22 Method for trapping nitric oxide by utilizing phenol anion functionalized ionic liquid Pending CN106563334A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201611031893.1A CN106563334A (en) 2016-11-22 2016-11-22 Method for trapping nitric oxide by utilizing phenol anion functionalized ionic liquid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201611031893.1A CN106563334A (en) 2016-11-22 2016-11-22 Method for trapping nitric oxide by utilizing phenol anion functionalized ionic liquid

Publications (1)

Publication Number Publication Date
CN106563334A true CN106563334A (en) 2017-04-19

Family

ID=58542902

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201611031893.1A Pending CN106563334A (en) 2016-11-22 2016-11-22 Method for trapping nitric oxide by utilizing phenol anion functionalized ionic liquid

Country Status (1)

Country Link
CN (1) CN106563334A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115430283A (en) * 2022-09-23 2022-12-06 全椒科利德电子材料有限公司 Method for purifying nitrous oxide

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101037388A (en) * 2007-04-17 2007-09-19 华东师范大学 Multifunctional ion liquid system, preparation and application thereof
CN102126968A (en) * 2011-01-11 2011-07-20 中国科学院过程工程研究所 Alkaline ionic liquid as well as preparation and application thereof
CN102274674A (en) * 2011-06-20 2011-12-14 浙江大学 Method for capturing carbon dioxide (CO2) by high-stability substituted phenol ionic liquid
CN105920992A (en) * 2016-06-21 2016-09-07 浙江大学 Method for capturing nitric oxide by basic functionalized ionic liquid

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101037388A (en) * 2007-04-17 2007-09-19 华东师范大学 Multifunctional ion liquid system, preparation and application thereof
CN102126968A (en) * 2011-01-11 2011-07-20 中国科学院过程工程研究所 Alkaline ionic liquid as well as preparation and application thereof
CN102274674A (en) * 2011-06-20 2011-12-14 浙江大学 Method for capturing carbon dioxide (CO2) by high-stability substituted phenol ionic liquid
CN105920992A (en) * 2016-06-21 2016-09-07 浙江大学 Method for capturing nitric oxide by basic functionalized ionic liquid

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
KAIHONG CHEN ETAL.: "Highly Efficient Nitric Oxide Capture by Azole-Based Ionic Liquids through Multiple-Site Abosorption", 《ANGEW.CHEM.INT.ED》 *
白漫等: "碱性离子液体的研究进展", 《化学工程与装备》 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115430283A (en) * 2022-09-23 2022-12-06 全椒科利德电子材料有限公司 Method for purifying nitrous oxide

Similar Documents

Publication Publication Date Title
CN105920992B (en) It is a kind of to trap nitric oxide production method using basic functionalized ionic liquid
Fan et al. Selective catalytic reduction of NOX with ammonia over Mn–Ce–OX/TiO2-carbon nanotube composites
CN101259368A (en) Method for catalytic oxidation NO with ZSM-5 type molecular sieve as catalyst
CN102580525A (en) Method for using activated carbon load copper oxide composite catalyst to absorb nitrogenous oxide
Fei et al. Confined catalysts application in environmental catalysis: current research progress and future prospects
CN105381801A (en) Catalyst capable of directly catalytically decomposing N2O
CN107715845A (en) A kind of flue gas desulfurization and denitrification adsorbent and its preparation and application
CN101822983B (en) Catalyst for catalyzing and oxidizing oxynitride in flue gas and preparation process thereof
CN106362549B (en) It is a kind of to trap nitric oxide production method using amino acid anionic functional ionic liquid
CN105521781B (en) A kind of preparation method of fume desulfurizing agent
CN103816789A (en) Alkaline denitration absorbent
CN102160963B (en) Method for capturing sulfur dioxide by employing imidazolyl ionic liquid
Herring et al. In situ infrared study of the absorption of nitric oxide by 12-tungstophosphoric acid
CN103894160A (en) Carbon dioxide solid absorbent as well as preparation method thereof
CN105413423A (en) Method for eliminating nitrogen oxide waste gas produced in metronidazole production process
CN103111264B (en) The preparation method of a kind of ionic liquid and the two modification bacterium slag active carbon of metal and application
CN104128188A (en) Denitration catalyst used in waste incineration power plant and preparation method thereof
Changjin et al. Recent progress on elimination of NOx from flue gas via SCR technology under ultra-low temperatures (< 150℃)
CN103506121A (en) Low-temperature denitration catalyst with iron loaded on carbon nanotube and preparation method thereof
CN106731491A (en) One kind traps nitric oxide production method using halide anion functionalized ion liquid
CN106563334A (en) Method for trapping nitric oxide by utilizing phenol anion functionalized ionic liquid
CN104069737A (en) Recycling and purifying method of ammonia-containing industrial waste gas
CN105854541A (en) Method for reducing and removing nitrogen oxide by adsorption-oxidation and liquid phase absorption
CN102284287A (en) Titanium dioxide molecular sieve supported platinum cold catalyst for removing formaldehyde in indoor air
CN203022850U (en) Two-carrier-containing structure of automobile three-way catalyst housing

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20170419