CN100551818C - The method of preparing hydrogen by decomposing hydrogen sulfide - Google Patents

The method of preparing hydrogen by decomposing hydrogen sulfide Download PDF

Info

Publication number
CN100551818C
CN100551818C CNB2005101060299A CN200510106029A CN100551818C CN 100551818 C CN100551818 C CN 100551818C CN B2005101060299 A CNB2005101060299 A CN B2005101060299A CN 200510106029 A CN200510106029 A CN 200510106029A CN 100551818 C CN100551818 C CN 100551818C
Authority
CN
China
Prior art keywords
hydrogen
sulfide
hydrogen sulfide
sulphur
rosin
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.)
Expired - Fee Related
Application number
CNB2005101060299A
Other languages
Chinese (zh)
Other versions
CN1955107A (en
Inventor
陆海深
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to CNB2005101060299A priority Critical patent/CN100551818C/en
Publication of CN1955107A publication Critical patent/CN1955107A/en
Application granted granted Critical
Publication of CN100551818C publication Critical patent/CN100551818C/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30Hydrogen technology
    • Y02E60/36Hydrogen production from non-carbon containing sources, e.g. by water electrolysis

Landscapes

  • Catalysts (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)

Abstract

The invention discloses a kind of method of using the hydrogen sulfide preparing hydrogen by decomposing.This method comprises multinomial invention, as: the production of invention A. hydrogen sulfide; Invention B preparing hydrogen by decomposing hydrogen sulfide; The desulfurization of invention C cuprous sulfide.The method that invention A hydrogen sulfide is produced, this method comprise uses sulphur and rosin mixture to react under 350-400 ℃ temperature.The method of invention B preparing hydrogen by decomposing hydrogen sulfide, this method comprise under the temperature of using thin copper wire and hydrogen sulfide 400-480 ℃ reacts.The method of invention C cuprous sulfide desulfurization.This method is included under the temperature that heats 500-600 ℃ in the air reacts.

Description

The method of preparing hydrogen by decomposing hydrogen sulfide
Technical field
The present invention relates to a kind of method of hydrogen, the present invention especially relates to a kind of method with preparing hydrogen by decomposing hydrogen sulfide.
Background technology
Shortage of energy sources has retrained expanding economy.Hydrogen is a kind of pollution-free combustible gas, and it is having a wide range of applications aspect industry, the Aeronautics and Astronautics etc.Up to the present, hydrogen mainly is to produce hydrogen as raw material, its complex process, inefficient shortcoming with fossil oils such as coal, oil, Sweet natural gases.
Summary of the invention
The method that the purpose of this invention is to provide a kind of hydrogen, this method comprises multinomial invention, overcome the problems referred to above of ordinary method, application present method scale operation at short notice goes out to have highly purified hydrogen, and cuprous sulfide is reusable after treatment (for example: copper).
In achieving the above object, comprise multinomial invention according to this method of the method that the invention provides a kind of hydrogen, as: the production of A. hydrogen sulfide, the decomposition of B. hydrogen sulfide, the desulfurization of C. cuprous sulfide.
The method that invention A hydrogen sulfide is produced, this method comprises uses raw material rosin, sulphur and catalyzer potassium permanganate, and rosin is exactly the resin of pine tree, its structural formula:
Figure C20051010602900041
Its molecular formula C 19H 29COOH, it is just can directly be used by rosin removal impurity and moisture content, and sulphur can use the industrial sulphur powder, has the catalyzer potassium permanganate that accounts for rosin 2%-10% to exist down, rosin and sulphur mixture react the system hydrogen sulfide under 350-400 ℃ temperature, its chemical equation:
Figure C20051010602900042
Since rosin, the physical properties difference of sulphur, and rosiny density is at 0.9-0.95g/cm 3Between, boiling point is about 360 ℃, and the density of sulphur is 2g/cm 3, boiling point is 444 ℃.Because rosiny density, boiling point are all little than sulphur, thus public fragrant heat respectively with sulphur after, again because of sulphur will on the temperature more than 360 ℃ could with the rosin rapid reaction. react in the rosin in that sulphur is from top to bottom dripped into.The quality of rosin, sulphur is calculated by following formula and is carried out adapted.
The method of invention B preparing hydrogen by decomposing hydrogen sulfide, this method comprise uses thin copper wire and hydrogen sulfide.Thin copper wire preferably uses diameter 0.1-0.15mm's.Hydrogen sulfide is removed sulphur steam through purifying, rosin steam and water vapor etc., 400---its chemical equation of reaction under 480 ℃ the temperature:
Figure C20051010602900051
Wherein, the quality of copper use what calculate by chemical equation and carry out adapted.
The method of invention C cuprous sulfide desulfurization: this method comprises the use powdered rice hulls, the cuprous sulfide monolithic porous.
According to the method for this invention, at first on monolithic porous, keep flat the powdered rice hulls about one deck 0.5cm, cuprous sulfide is not directly contacted with high temperature heater (HTH).Below monolithic porous, heat then in that cuprous sulfide is placed on above the powdered rice hulls, when powdered rice hulls burns, make cuprous sulfide reach 500-600 ℃ of desulfurization and generate sulfurous gas and copper with airborne oxygen reaction.After the reaction beginning, the heat energy of emitting is proceeded till naturally cooling reaction.Make cuprous sulfide fully and burning rapidly, cuprous sulfide pulverized, in the cuprous sulfide powder, add some combustible fuel again, play its reactive chemistry equation of effect that ignites and be incubated as powdered rice hulls hybrid reaction powdered rice hulls and be:
Figure C20051010602900052
If use high light, as tungsten lamp pipe reacting by heating, though very fast of reaction, cuprous sulfide that can only desulfurization 0.1-0.5cm, its reaction equation is:
The cuprous sulfide desulphurization reaction can not react in pure oxygen.
The industrialization desulfurization can be reelected a little and can use with the fluidizing furnace in the gas washing in SA production equipment.
Description of drawings
Accompanying drawing is the synoptic diagram according to preparing hydrogen by decomposing hydrogen sulfide Special Equipment of the present invention.
Embodiment
Sulphur is added sealing the molten sulphur device 2 from advancing sulphur mouth 3, again rosin 4 is added in the reactor 5, then molten sulphur device 2 is connected and seals with reactor 5.Again thin copper wire is put into sealing in the reactor 7, then reactor 5 and reactor 7 usefulness airways are coupled together and seal.Then all well heaters 8 are connect electrically heated.The sulphur of the heat fused hydrogen sulfide that reaction generates from the rosin 4 of porous plate 9 drippage heat fused is from pneumatic outlet 10 guiding cleaners 11, again by in the cleaner 11 directed response devices 7, in reactor 7, generate hydrogen with the thin copper wire reaction, derive hydrogen from pneumatic outlet 14, after water-cooled, can directly utilize.After reacting completely, again SO 215 feed the residual hydrogen sulfide of removal in the reactor 5 from the gas inlet.Then the resultant carbon in the reactor 5 is taken out.Again the cuprous sulfide of reactor 7 is taken out.Repeat to continue hydrogen according to above-mentioned method.
Embodiment
The production implementation method of invention A hydrogen sulfide according to the data proportioning that chemical equation calculates, is used rosin 250g to raw material sulphur, rosin, and sulphur 344.4g makes 530g hydrogen sulfide chemical equation:
Figure C20051010602900061
The method of invention B hydrogen sulfide and copper reaction hydrogen is thin copper wire and invent the stink damp precursor reactant that A makes.Calculate with copper 1317.6g and hydrogen sulfide 350g reaction its chemical equation according to chemical equation:
Make 20gH 2
The data that the gas that makes according to the present invention and chemical equation calculate are variant, this be because of
Cause for incomplete reaction.
Description of reference numerals:
1. sulphur 14. gas vents
2. molten sulphur device 15. gas inletes
3. advance the sulphur mouth
4. rosin
5. reactor
6. thin copper wire
7. reactor
8. well heater
9. porous plate
10. pneumatic outlet
11. cleaner
12. gas inlet
13. porous plate

Claims (1)

1. the method for a production compound hydrogen sulfide, this method comprise uses rosin, sulphur, adds catalyzer potassium permanganate 2%-10% in rosin, and sulphur will disperse to drip in the rosin to react under 350-400 ℃ temperature.
CNB2005101060299A 2005-09-21 2005-09-21 The method of preparing hydrogen by decomposing hydrogen sulfide Expired - Fee Related CN100551818C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB2005101060299A CN100551818C (en) 2005-09-21 2005-09-21 The method of preparing hydrogen by decomposing hydrogen sulfide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB2005101060299A CN100551818C (en) 2005-09-21 2005-09-21 The method of preparing hydrogen by decomposing hydrogen sulfide

Publications (2)

Publication Number Publication Date
CN1955107A CN1955107A (en) 2007-05-02
CN100551818C true CN100551818C (en) 2009-10-21

Family

ID=38062707

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB2005101060299A Expired - Fee Related CN100551818C (en) 2005-09-21 2005-09-21 The method of preparing hydrogen by decomposing hydrogen sulfide

Country Status (1)

Country Link
CN (1) CN100551818C (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101817502B (en) * 2010-04-26 2014-03-19 云南云天化国际化工股份有限公司 Method for preparing hydrogen from hydrothion and industrial tail gas
CN110127602B (en) * 2018-02-09 2020-09-25 中国石油化工股份有限公司 Method for decomposing hydrogen sulfide by using catalyst

Also Published As

Publication number Publication date
CN1955107A (en) 2007-05-02

Similar Documents

Publication Publication Date Title
CN103062910B (en) Method and device for integrating chemical-looping combustion with CO<2> trapping
JP6226423B2 (en) Production of synthesis gas from oxidized biomass by heating with hot gas obtained by oxidation of residual product
BRPI0606737B1 (en) method for reforming steam carbonaceous material
EP2408852A1 (en) Environmentally clean process for utilizing pyrolysis products
ES2190695A1 (en) Process and device for autothermic gasification of solid fuels
CN105889949A (en) Organic wastewater incineration and gasification system and incineration and gasification method
CN112811983A (en) System and method for preparing methanol by using sulfur-containing flue gas of boiler
CN211394370U (en) System for pyrolysis of junked tire of boiler flue gas of thermal power plant
CN107777663A (en) A kind of lighter hydrocarbons hydrogen manufacturing and the coupling process of hydrogen from methyl alcohol
KR20030065483A (en) Conversion of methane and hydrogen sulfide in non-thermal silent and pulsed corona discharge reactors
CN113353920B (en) Continuous preparation device and preparation method of carbon nano tube
CN100551818C (en) The method of preparing hydrogen by decomposing hydrogen sulfide
RU2004101734A (en) MAGNETO-HYDRODYNAMIC METHOD FOR PRODUCING ELECTRIC ENERGY AND SYSTEM FOR ITS IMPLEMENTATION
EP3356031B1 (en) Process for energy recovery in carbon black production
CN104876190A (en) Oxygen-enriched combustion-supporting waste acid cracking process
CN113321182B (en) System and method for producing hydrogen by sludge coupling
CN113060704B (en) Organic solid clean high-efficiency hydrogen production device and method
CA2968494C (en) Energy efficient integrated process for production of metals or alloys
CN215855145U (en) System for boiler contains sulfur flue gas and flying dust comprehensive utilization
US11952277B2 (en) Conversion of solid waste into syngas and hydrogen
CN117545809A (en) Method and apparatus for recovery and reuse of tail gas and flue gas components
JPS6235440B2 (en)
CN105623740A (en) Clean gas preparation method and preparation system
CN205957171U (en) High -efficient gas that mixes gas mixes gas device
CA3224728A1 (en) Method and apparatus for recovery and reuse of tail gas and flue gas components

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20091021

Termination date: 20110921