CN108970350A - A kind of flue gas low-temperature denitration method - Google Patents

A kind of flue gas low-temperature denitration method Download PDF

Info

Publication number
CN108970350A
CN108970350A CN201810627857.4A CN201810627857A CN108970350A CN 108970350 A CN108970350 A CN 108970350A CN 201810627857 A CN201810627857 A CN 201810627857A CN 108970350 A CN108970350 A CN 108970350A
Authority
CN
China
Prior art keywords
flue gas
nitre
absorbing liquid
cooling
temperature
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
CN201810627857.4A
Other languages
Chinese (zh)
Inventor
刘明
刘森
张菡英
赵莉
钤小平
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.)
Shandong Normal University
Original Assignee
Shandong Normal University
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 Shandong Normal University filed Critical Shandong Normal University
Priority to CN201810627857.4A priority Critical patent/CN108970350A/en
Publication of CN108970350A publication Critical patent/CN108970350A/en
Pending legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D46/00Filters or filtering processes specially modified for separating dispersed particles from gases or vapours
    • B01D46/02Particle separators, e.g. dust precipitators, having hollow filters made of flexible material
    • 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
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/46Removing components of defined structure
    • B01D53/48Sulfur compounds
    • B01D53/50Sulfur oxides
    • B01D53/501Sulfur oxides by treating the gases with a solution or a suspension of an alkali or earth-alkali or ammonium compound
    • 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
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/46Removing components of defined structure
    • B01D53/54Nitrogen compounds
    • B01D53/56Nitrogen oxides
    • 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
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/74General processes for purification of waste gases; Apparatus or devices specially adapted therefor
    • B01D53/76Gas phase processes, e.g. by using aerosols
    • 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
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/74General processes for purification of waste gases; Apparatus or devices specially adapted therefor
    • B01D53/77Liquid phase processes
    • B01D53/78Liquid phase processes with gas-liquid contact
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2251/00Reactants
    • B01D2251/10Oxidants
    • B01D2251/102Oxygen
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2251/00Reactants
    • B01D2251/20Reductants
    • B01D2251/206Ammonium compounds
    • B01D2251/2062Ammonia
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2251/00Reactants
    • B01D2251/30Alkali metal compounds
    • B01D2251/304Alkali metal compounds of sodium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2251/00Reactants
    • B01D2251/30Alkali metal compounds
    • B01D2251/306Alkali metal compounds of potassium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2251/00Reactants
    • B01D2251/40Alkaline earth metal or magnesium compounds
    • B01D2251/402Alkaline earth metal or magnesium compounds of magnesium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2251/00Reactants
    • B01D2251/40Alkaline earth metal or magnesium compounds
    • B01D2251/404Alkaline earth metal or magnesium compounds of calcium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2251/00Reactants
    • B01D2251/60Inorganic bases or salts
    • B01D2251/604Hydroxides
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2258/00Sources of waste gases
    • B01D2258/02Other waste gases
    • B01D2258/0283Flue gases

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Environmental & Geological Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Biomedical Technology (AREA)
  • Analytical Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Dispersion Chemistry (AREA)
  • Treating Waste Gases (AREA)

Abstract

The present invention relates to flue gas processing technology field, in particular to a kind of flue gas low-temperature denitration method.The following steps are included: (1) cooling flue gas in flue is to 40 DEG C or less;(2) prepare nitre absorbing liquid, and be introduced into absorption tower;(3) flue gas is passed through absorption tower, flue gas is in contact with nitre absorbing liquid, and absorbing liquid absorbs the nitre in flue gas;(4) flue gas after denitration is emptied.Present invention process is simple and easy, and use cost is low, can carry out denitration using both having ready conditions using power plant, steel mill.The present invention will generate huge environmental benefit, more preferably generate good economic effect, have very big social and economic effect.

Description

A kind of flue gas low-temperature denitration method
(1) technical field
The present invention relates to flue gas processing technology field, in particular to a kind of flue gas low-temperature denitration method.
(2) background technique
Gas denitrifying technology can be divided into dry and wet two major classes at present, wherein the selective catalytic reduction in Dry denitration (SCR) and selective non-catalytic reduction (SNCR) technology be market most widely used (accounting for about 80% denitrating flue gas market), technology most Mature denitration technology, principle are the spray reducing agents such as ammonium hydroxide or urea into flue gas, direct at high temperature (or the association of catalyst With under) with flue gas in NOx occur redox reaction, NOx is reduced into nitrogen and water.But the office that the technology also has it very big Sex-limited, since chemical reaction needs to carry out at high temperature, and for medium small boiler and Industrial Boiler, exhaust gas temperature is remote High temperature required for chemical reaction cannot be reached, so, denitration effect is bad when low temperature.In addition, even if high-temperature boiler denitration is imitated When fruit is good, the reducing agents such as a large amount of ammonia or urea are also consumed, and some new pollutions can be generated simultaneously again.
For this problem, existing relevant unit releases the relevant technologies at present, but mainly based on low-temperature SCR, therefore each list Position puts into a large amount of financial resources and energy, carries out the research and development of low temperature catalyst.Nevertheless, the use of catalyst to be related to it is high at The problem of this and hardly possible operate.Also there is technology to abandon the use of catalyst, use oxidizing process instead to absorb the NO in flue gas.It considers Cost and denitration effect, the oxidant used in oxidizing process at present are mainly ozone and hydrogen peroxide.But the system of ozone and hydrogen peroxide It is standby to consume a large amount of energy again, economically, it is difficult to be subject to promotion and implementation.
In view of the above technical problems, the present invention provides a kind of oxidizing process flue tail gas method of denitration of brand new ideas, the party Method had both been not necessarily to denitration at high temperature, without catalyst is used, did not also need the oxidation of the highly energy-consumings such as similar ozone and hydrogen peroxide Agent, but only original exhaust emissions technique is transformed, that is, it can reach good denitration effect.
The present invention has abandoned traditional denitration idea and method completely, will not only generate huge ring
Benefit is protected, good economic effect is more preferably generated, there is very big social and economic effect.
(3) summary of the invention
In order to compensate for the shortcomings of the prior art, the present invention provides a kind of flue gas low-temperature denitration methods.
The present invention is achieved through the following technical solutions:
A kind of flue gas low-temperature denitration method, it is characterised in that:
The following steps are included:
(1) flue gas in flue is cooled down to 40 DEG C or less;
(2) prepare nitre absorbing liquid, and be introduced into absorption tower;
(3) flue gas is passed through absorption tower, flue gas is in contact with nitre absorbing liquid, and absorbing liquid absorbs in flue gas Nitre;
(4) flue gas after denitration is emptied.
Further, the type of cooling of the flue gas in step (1) is that heat exchanger is cooling, water-washing method is cooling, air-cooled side One of formula cooling or its combination.
Further, the temperature of flue gas is not higher than 30 DEG C in step (1).
Further, the temperature of flue gas is not higher than 20 DEG C in step (1).
Further, purified treatment first is carried out to flue gas before step (1), purified treatment includes desulfurization and dust removal process.
Further, in step (2) nitre absorbing liquid be potassium hydroxide, sodium hydroxide, calcium hydroxide, magnesium hydroxide aqueous solution And one of ammonium hydroxide or several combinations.
Further, nitre absorbing liquid is water in step (2).
Further, step (2) absorption tower is any one of spray column, plate column or packed tower.
Way of thinking of theories of the invention is that for overwhelming majority chemical reaction, temperature is increased, and reaction rate increases, still 2NO+O2=2NO2 reaction is the decline with temperature and speed is accelerated, though the mechanism of the theory is proved already, extremely The present there is no no technical solution that technology field is applied to carry out oxidation and denitration to NO.
For existing wet desulphurization denitrating technique, either spray process, tower tray method gas immersion method, although can It is enough that flue gas is cooled down, but general cooling temperature is not less than 50 DEG C, if further cooled down, need to consume multipotency Amount, and be no advantage to technique.
Therefore in the prior art, be not directed to the big novelty of of the invention one, i.e., for flue gas itself,
If being cooled to certain temperature, the NO in flue gas can quickly react with O2, and temperature is lower, and reaction speed is got over Fastly, react more abundant.
Flue gas is tested:
The Gas Parameters of certain boiler are as follows: exhaust gas volumn 200000m2/h(operating condition), SO2 concentration 5700mg/m3, dust concentration 1850mg/m3, nitrous oxides concentration 640mg/m3,135 DEG C of flue-gas temperature.
Flue gas treating process are as follows: the flue gas from boiler carries out desulfurization, desulfurization subsequently into desulfurizing tower first through bag-type dust Mode is wet desulphurization, and desulfurizing agent is calcium hydroxide, and desulfurizing tower is spray column.Desulfurizing tower connect chimney, flue gas after desulfurization from Chimney discharge.
In the smoke outlet data measured of desulfurizing tower are as follows: SO2 concentration 87mg/m3, dust concentration 78mg/m3, nitrogen oxidation Object concentration 580mg/m3,62 DEG C of flue-gas temperature, flue gas flow rate 4.2m/s.
Experimentation are as follows:
Partial fume is shunted from desulfurizing tower exit and is exported, into a heat exchanger, the hot journey of heat exchanger is flue gas, and cold journey is cold But medium.The temperature of cooling medium is adjusted, flue gas temperature at heat exchanger exit is adjusted.Flue gas enters after coming out from heat exchanger One absorption tower sets spray thrower in absorption tower, and absorbing liquid is the NaOH solution of 0.1M, keeps the temperature and heat exchanger flue gas of absorbing liquid The temperature in exit is consistent.Thermometer is installed in flue gas heat-exchange unit exit and absorption tower;It is set in adsorption tower smoke exit Nitric oxide detector is set, to measure experimental data.
When flue-gas temperature is 62 DEG C, NO concentration is 601.48ppm after absorption.
When flue-gas temperature is 50 DEG C, NO concentration is 578.16ppm after absorption.
When flue-gas temperature is 40 DEG C, NO concentration is 420.10ppm after absorption.
When flue-gas temperature is 30 DEG C, NO concentration is 194.96ppm after absorption.
When flue-gas temperature is 20 DEG C, NO concentration is 105.60ppm after absorption.
When flue-gas temperature is 18 DEG C, NO concentration is 92.78ppm after absorption.
The beneficial effects of the present invention are:
1, present invention process is simple and easy, and use cost is low, can both be had ready conditions using power plant, steel mill and carry out denitration.
2, present invention process is novel, is not necessarily to denitration at high temperature, without using catalyst,
Also the oxidant for not needing the highly energy-consumings such as similar ozone and hydrogen peroxide, saves cost;
3, the present invention will generate huge environmental benefit, more preferably generate good economic effect, have greatly society and economic shadow It rings.
(4) specific embodiment
Embodiment 1:
The following steps are included:
(1) purified treatment first is carried out to flue gas, purified treatment includes desulfurization and dust removal process;The cooling cigarette in flue Road tail gas is to 50 DEG C;The type of cooling of flue gas is one of cooling heat exchanger, water-washing method cooling, air cooling way cooling Or its combination.
(2) prepare nitre absorbing liquid, and be introduced into absorption tower;Nitre absorbing liquid is potassium hydroxide, sodium hydroxide, hydroxide One of calcium, the aqueous solution of magnesium hydroxide and ammonium hydroxide or several combinations.Wherein nitre absorbing liquid may be water.It absorbs Tower is any one of spray column, plate column or packed tower.
(3) flue gas is passed through absorption tower, flue gas is in contact with nitre absorbing liquid, and absorbing liquid absorbs in flue gas Nitre;
(4) flue gas after denitration is emptied.
Embodiment 2:
The following steps are included:
(1) purified treatment first is carried out to flue gas, purified treatment includes desulfurization and dust removal process;The cooling cigarette in flue Road tail gas is to 40 DEG C;The type of cooling of flue gas is one of cooling heat exchanger, water-washing method cooling, air cooling way cooling Or its combination.
(2) prepare nitre absorbing liquid, and be introduced into absorption tower;Nitre absorbing liquid is potassium hydroxide, sodium hydroxide, hydroxide One of calcium, the aqueous solution of magnesium hydroxide and ammonium hydroxide or several combinations.Wherein nitre absorbing liquid may be water.It absorbs Tower is any one of spray column, plate column or packed tower.
(3) flue gas is passed through absorption tower, flue gas is in contact with nitre absorbing liquid, and absorbing liquid absorbs in flue gas Nitre;
(4) flue gas after denitration is emptied.
Embodiment 3:
The following steps are included:
(1) purified treatment first is carried out to flue gas, purified treatment includes desulfurization and dust removal process;The cooling cigarette in flue Road tail gas is to 30 DEG C;The type of cooling of flue gas is one of cooling heat exchanger, water-washing method cooling, air cooling way cooling Or its combination.
(2) prepare nitre absorbing liquid, and be introduced into absorption tower;Nitre absorbing liquid is potassium hydroxide, sodium hydroxide, hydroxide One of calcium, the aqueous solution of magnesium hydroxide and ammonium hydroxide or several combinations.Wherein nitre absorbing liquid may be water.It absorbs Tower is any one of spray column, plate column or packed tower.
(3) flue gas is passed through absorption tower, flue gas is in contact with nitre absorbing liquid, and absorbing liquid absorbs in flue gas Nitre;
(4) flue gas after denitration is emptied.
Embodiment 4:
The following steps are included:
(1) purified treatment first is carried out to flue gas, purified treatment includes desulfurization and dust removal process;The cooling cigarette in flue Road tail gas is to 20 DEG C;The type of cooling of flue gas is one of cooling heat exchanger, water-washing method cooling, air cooling way cooling Or its combination.
(2) prepare nitre absorbing liquid, and be introduced into absorption tower;Nitre absorbing liquid is potassium hydroxide, sodium hydroxide, hydroxide One of calcium, the aqueous solution of magnesium hydroxide and ammonium hydroxide or several combinations.Wherein nitre absorbing liquid may be water.It absorbs Tower is any one of spray column, plate column or packed tower.
(3) flue gas is passed through absorption tower, flue gas is in contact with nitre absorbing liquid, and absorbing liquid absorbs in flue gas Nitre;
(4) flue gas after denitration is emptied.
Embodiment 5
The following steps are included:
(1) purified treatment first is carried out to flue gas, purified treatment includes desulfurization and dust removal process;The cooling cigarette in flue Road tail gas is to 18 DEG C;The type of cooling of flue gas is one of cooling heat exchanger, water-washing method cooling, air cooling way cooling Or its combination.
(2) prepare nitre absorbing liquid, and be introduced into absorption tower;Nitre absorbing liquid is potassium hydroxide, sodium hydroxide, hydroxide One of calcium, the aqueous solution of magnesium hydroxide and ammonium hydroxide or several combinations.Wherein nitre absorbing liquid may be water.It absorbs Tower is spray column, plate column or filler
Any one of tower.
(3) flue gas is passed through absorption tower, flue gas is in contact with nitre absorbing liquid, and absorbing liquid absorbs in flue gas Nitre;
(4) flue gas after denitration is emptied.

Claims (8)

1. a kind of flue gas low-temperature denitration method, it is characterised in that: the following steps are included: (1) cooling cigarette in flue Road tail gas is to 40 DEG C or less;(2) prepare nitre absorbing liquid, and be introduced into absorption tower;(3) flue gas is passed through absorption tower, cigarette Gas is in contact with nitre absorbing liquid, and absorbing liquid absorbs the nitre in flue gas;(4) flue gas after denitration is emptied.
2. flue gas low-temperature denitration method according to claim 1, it is characterised in that: the flue gas in step (1) The type of cooling be that heat exchanger is cooling, water-washing method is cooling, air cooling way is one of cooling or its combination.
3. flue gas low-temperature denitration method according to claim 1, it is characterised in that: flue gas in step (1) Temperature is not higher than 30 DEG C.
4. flue gas low-temperature denitration method according to claim 1, it is characterised in that: flue gas in step (1) Temperature is not higher than 20 DEG C.
5. flue gas low-temperature denitration method according to claim 1, it is characterised in that: first to flue tail before step (1) Gas carries out purified treatment, and purified treatment includes desulfurization and dust removal process.
6. flue gas low-temperature denitration method according to claim 1, it is characterised in that: nitre absorbing liquid is in step (2) One of potassium hydroxide, sodium hydroxide, calcium hydroxide, the aqueous solution of magnesium hydroxide and ammonium hydroxide or several combinations.
7. flue gas low-temperature denitration method according to claim 1, it is characterised in that: nitre absorbing liquid is in step (2) Water.
8. flue gas low-temperature denitration method according to claim 1, it is characterised in that: step (2) absorption tower is spray Any one of tower, plate column or packed tower.
CN201810627857.4A 2018-06-19 2018-06-19 A kind of flue gas low-temperature denitration method Pending CN108970350A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810627857.4A CN108970350A (en) 2018-06-19 2018-06-19 A kind of flue gas low-temperature denitration method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810627857.4A CN108970350A (en) 2018-06-19 2018-06-19 A kind of flue gas low-temperature denitration method

Publications (1)

Publication Number Publication Date
CN108970350A true CN108970350A (en) 2018-12-11

Family

ID=64540577

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810627857.4A Pending CN108970350A (en) 2018-06-19 2018-06-19 A kind of flue gas low-temperature denitration method

Country Status (1)

Country Link
CN (1) CN108970350A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109647132A (en) * 2018-12-29 2019-04-19 山东师范大学 A kind of rotary active carbon flue gas desulfurizing device
CN110893313A (en) * 2019-07-27 2020-03-20 齐金禄 Method for treating waste gas containing nitrogen oxides

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109647132A (en) * 2018-12-29 2019-04-19 山东师范大学 A kind of rotary active carbon flue gas desulfurizing device
CN110893313A (en) * 2019-07-27 2020-03-20 齐金禄 Method for treating waste gas containing nitrogen oxides

Similar Documents

Publication Publication Date Title
CA2978023C (en) Gas denitration process and apparatus
WO2021082308A1 (en) Flue gas low-temperature adsorption denitration method
CN105251326A (en) Reduction and oxidation combined denitration system and denitration method thereof
CN203355611U (en) Device for removing NOX and dioxins in sintering and pelletizing flue gas through SCR (Selective Catalytic Reduction)
CN210035516U (en) Hazardous waste incineration flue gas treatment device
WO2021088525A1 (en) Flue gas multi-pollutant collaborative purification process method and apparatus
WO2021088526A1 (en) Flue gas multi-pollutant synergistic purification process and apparatus
CN108970352A (en) A kind of flue gas low-temperature denitration method
CN113941238A (en) Integrated control method for low-temperature smoke pollutants
CN103100294A (en) Method for removing oxynitride from flue gas through ozone oxidation method
CN105311947A (en) Boiler fume denitration and desulfuration dedusting device and process
CN108970350A (en) A kind of flue gas low-temperature denitration method
CN210021683U (en) Flue gas treatment device of rotary kiln
CN102371110B (en) Flue gas desulfurization and denitration method
CN205073858U (en) DeNOx systems is united with oxidation to reduction
CN205308112U (en) Ozone and device of air in coordination with nitrogen oxide in oxidation flue gas
CN108970351A (en) A kind of flue gas low-temperature denitration method
CN211753781U (en) Smoke multi-pollutant cooperative purification device
CN112023693B (en) Efficient denitration method for hot blast stove and hot blast stove device
CN111359398B (en) Method for denitration and whitening of flue gas
CN108970356A (en) A method of nitric acid is produced using flue gas
CN112354337A (en) High-efficient SOx/NOx control of low temperature flue gas takes off white integration equipment
CN103341306B (en) A kind of method of poor ammonia SNCR reduction and oxidative absorption combined denitration demercuration
CN113952832A (en) Low-temperature flue gas pollutant synergistic removal method
CN109925859B (en) Device and process for deep oxidation, desulfurization and denitrification of industrial flue gas

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

Application publication date: 20181211

RJ01 Rejection of invention patent application after publication