CN106492620A - A kind of deoxidation type drier - Google Patents

A kind of deoxidation type drier Download PDF

Info

Publication number
CN106492620A
CN106492620A CN201610915480.3A CN201610915480A CN106492620A CN 106492620 A CN106492620 A CN 106492620A CN 201610915480 A CN201610915480 A CN 201610915480A CN 106492620 A CN106492620 A CN 106492620A
Authority
CN
China
Prior art keywords
magnesia
deoxidation
magnesium chloride
type drier
drier
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
CN201610915480.3A
Other languages
Chinese (zh)
Inventor
覃宝
刘照龙
苏卓欣
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.)
SUPER DRY DESICCANT (SHENZHEN) CO Ltd
Original Assignee
SUPER DRY DESICCANT (SHENZHEN) CO Ltd
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 SUPER DRY DESICCANT (SHENZHEN) CO Ltd filed Critical SUPER DRY DESICCANT (SHENZHEN) CO Ltd
Priority to CN201610915480.3A priority Critical patent/CN106492620A/en
Publication of CN106492620A publication Critical patent/CN106492620A/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
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/74General processes for purification of waste gases; Apparatus or devices specially adapted therefor
    • B01D53/81Solid phase processes
    • 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
    • B01D53/26Drying gases or vapours
    • B01D53/28Selection of materials for use as drying agents
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/02Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
    • B01J20/0203Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising compounds of metals not provided for in B01J20/04
    • B01J20/0225Compounds of Fe, Ru, Os, Co, Rh, Ir, Ni, Pd, Pt
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/02Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
    • B01J20/04Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising compounds of alkali metals, alkaline earth metals or magnesium
    • B01J20/041Oxides or hydroxides
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/02Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
    • B01J20/04Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising compounds of alkali metals, alkaline earth metals or magnesium
    • B01J20/046Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising compounds of alkali metals, alkaline earth metals or magnesium containing halogens, e.g. halides
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/02Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
    • B01J20/10Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising silica or silicate
    • B01J20/14Diatomaceous earth
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/02Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
    • B01J20/20Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising free carbon; comprising carbon obtained by carbonising processes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2257/00Components to be removed
    • B01D2257/10Single element gases other than halogens
    • B01D2257/104Oxygen
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2257/00Components to be removed
    • B01D2257/80Water
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2220/00Aspects relating to sorbent materials
    • B01J2220/40Aspects relating to the composition of sorbent or filter aid materials
    • B01J2220/42Materials comprising a mixture of inorganic materials

Landscapes

  • Chemical & Material Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • General Chemical & Material Sciences (AREA)
  • Environmental & Geological Engineering (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Biomedical Technology (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)
  • Drying Of Gases (AREA)

Abstract

The invention provides a kind of deoxidation type drier, including the component of following mass ratio:15~45% magnesia;30~45% magnesium chloride;9~24% diatomite;9~30% iron powder;0.1~10% carbon dust.Its advantage is:There is very strong deoxidation amount and wettability power, maximal oxygen uptake can reach 100ml, under conditions of 25 DEG C, humidity are 90%, hydroscopicity can reach more than the 200% of own wt, and there are no at present hydroscopicity under similarity condition state reach own wt more than 200% drier while having deoxidation effect.

Description

A kind of deoxidation type drier
Technical field
The present invention relates to a kind of while deoxidation drying agent with high hydroscopicity, high deoxidation amount function, especially a kind of ore deposit The deoxidation drying agent composition of species.
Background technology
Drier is the most frequently used material of industrial and civilian damp-prrof packing, and deoxidier is then that industrial and civilian antirust is anti-mildew The most frequently used material, and moistureproof and mildewproof is become rustization function set deoxidation drying agent together and is not found in industry.
Typically existing drier commodity have physics moisture absorption type:Silica-gel desiccant, mineral agent, activated carbon drier, Montmorillonite drier, fiber desiccant etc., its hydroscopicity typically up to can only achieve 30% or so, also chemical hygroscopic type:Chlorine Change calcium drier, magnesium chloride drier etc. moisture-proof role is provided by the hygroscopy of salt, a gang of hydroscopicity of the drier of this type More than 150% can be reached, with high hygroscopic property.But as the deliquescence of salt is so as to change the state of drier itself, from powder Or lenticular changes into liquid or gelinite, the safety issue that reveals on shipping storage is caused.Wherein magnesium chloride drier is inhaled Wet condition is more slightly higher than the security of general chemical hygroscopic drying agent, the magnesite material formed by magnesium chloride, magnesia etc., is inhaling Solid state can be transitioned into from powder or crystal state directly in wet process, so as to avoid the product of the safety issues such as leakage Raw.
In prior art, such as Chinese invention patent ZL 200710068572.3 discloses a kind of drier of high hydroscopicity And its formula is selected, with magnesium chloride, magnesia and silica as raw material, its optimum proportioning is 30: 68 :2, obtain Drier hydroscopicity up to more than 200%, into loose bulk after moisture absorption, with preferable security performance.
What existing deoxidier application was wider has iron series deoxidizers and enzyme system deoxidier.Enzyme system deoxidier is to pH, Aw, salt The change of content, temperature and other factors is all very sensitive, also needs the participation of water in reaction, therefore, in the food of low moisture content In product, application effect is bad.Due to its low cost, raw material are easy to get becomes most widely used in the market to iron series deoxidizers Deoxidier.And temperature, humidity, the ratio of each composition of deoxidier, the size of iron particles, deoxidier and antioxidant or other are anti- Answer mechanism deoxidier whether compound all be affect iron series deoxidizers deoxy performance key factor.Therefore with regard to food deoxidant root According to different food products pack environment requirement made by formula just have many kinds.Main formula material is main with reduced iron powder Raw material, auxiliary material then, based on the materials such as activated carbon, mineral, diatomite, salt, can provide corresponding moisture, reaction temperature for iron powder The required environment of the reduction reactions such as degree.
But now widely used drier and deoxidier are functionally all relatively simple, it is impossible to protect one more comprehensively Low humidity is required, is easily aoxidized, rustization, the product of qualitative change.
Content of the invention
For this purpose, the present invention is solution above-mentioned technical problem, there is provided a kind of deoxidation type drier.
The present invention realizes that the technical scheme that goal of the invention is adopted is:The present invention provides a kind of hydroscopicity height, and deoxidation amount is high, plus Work, deoxidation type drier easy to use, including the component of following mass ratio:15~45% magnesia;30~45% chlorination Magnesium;9~24% diatomite;9~30% iron powder;0.1~10% carbon dust.
Preferably, the deoxidation type drier also NaOH containing 0.1~10%.
Preferably, the deoxidation type drier is grouped into by the group of following mass ratio, 15~20% magnesia;30~40% Magnesium chloride;0.1~1% carbon dust;19~24% diatomite;20~30% iron powder.
Preferably, the deoxidation type drier is grouped into by the group of following mass ratio, 15~20% magnesia;30~40% Magnesium chloride;0.1~1% carbon dust;19~24% diatomite;20~30% iron powder;0.1~10% NaOH.
Preferably, the magnesium chloride is anhydrous magnesium chloride.
Preferably, the iron powder is also secondary originality iron powder.
Preferably, the magnesia is mixing for light calcined magnesia, activated magnesia or light calcined magnesia and activated magnesia Compound.Described magnesia preferably uses the mixture of light calcined magnesia and activated magnesia, wherein light calcined magnesia and activity The mass ratio of magnesia is 3:1-3, light calcined magnesia are preferably 3 with the mass ratio of activated magnesia:1.5 ~ 2.5, most Preferred mass ratio is 3: 2.
The moisture absorption deoxidation principle of deoxidation drying agent of the present invention is that magnesia is anti-with anhydrous magnesium chloride and water effect generation aquation Should, the compound that formula is aMgO bMgCl cH2O is formed, in addition MgO can also generate magnesium hydroxide, nothing with water independent role Aqueous magnesium chloride can also generate the magnesium chloride for carrying the crystallization water with water independent role, and diatomite and activated carbon have certain moisture absorption And adsorption capacity, diatomite and activated carbon are act as by magnesia and anhydrous magnesium chloride and water and provides changing for salt and water Environment, promote iron powder occur with air in sample occur redox reaction, its react skeleton symbol be 4Fe+6O2+6H2O → 4Fe (OH) 3, and appropriate NaOH is to adjust the alkaline environment regulation deoxidation amount that deoxidation is dried according to oxygen demand demand.
In the present invention, magnesia and magnesium chloride belong to the composition of drier as a kind of salt, because generally deoxidier also can Add trace salt, thus magnesia and magnesium chloride simultaneously can also as the auxiliary element of deoxidier, in the present invention magnesia and Magnesium chloride is substantial amounts of as the content of salt, while acting on drier forms synergy with deoxidant ingredient, this Plant synergy to cause in the case of phase homogenous quantities, drying effect and deoxidation effect can be more preferably.
Drier of the present invention has the advantage that:
There is very strong wettability power and deoxidation amount, under conditions of 25 DEG C, humidity are 90%, hydroscopicity can reach itself More than the 200% of weight, at 30 DEG C, under conditions of humidity is 80%, maximal oxygen uptake can reach 100ml, and there are no at present Under similarity condition state, hydroscopicity reaches the drier of more than the 200% of own wt while having deoxidation effect.
There is the good feature of environmental protection, the material environment friendly of selection is nontoxic, the product after moisture absorption is easy to decompose in nature.
There is very high cost performance, the raw material magnesia for using, anhydrous magnesium chloride, diatomite, iron powder, activated carbon are valency The abundant raw material of the cheap resources of production of lattice, wettability power are 2 ~ 6 times of general physical dryness agent, and the proterties after moisture absorption is loose Scatter mass structure, its security performance are better than general chemical drier, while there is deoxidation effect again, which is of many uses, are suitable for various The use of occasion.
Specific embodiment
Below, describe the present invention in conjunction with specific embodiments.
Embodiment 1
Following components is uniformly mixed, as required with moisture permeable material quantitative package.The mass percent composition of raw material For:
Magnesia 20%
Magnesium chloride 30%
Carbon dust 1%
Diatomite 24%
Iron powder 25%.
Embodiment 2
Following components is uniformly mixed, as required with moisture permeable material quantitative package.The mass percent composition of raw material For:
Magnesia 20%
Magnesium chloride 35%
Carbon dust 1%
Diatomite 21%
Iron powder 23%.
Embodiment 3
Following components is uniformly mixed, as required with moisture permeable material quantitative package.The mass percent composition of raw material For:
Magnesia 20%
Magnesium chloride 40%
Carbon dust 1%
Diatomite 19%
Iron powder 20%.
Embodiment 4
Following components is uniformly mixed, as required with moisture permeable material quantitative package.The mass percent composition of raw material For:
Magnesia 15%
Magnesium chloride 35%
Carbon dust 1%
Diatomite 19%
Iron powder 30%.
Embodiment 5
Following components is uniformly mixed, as required with moisture permeable material quantitative package.The mass percent composition of raw material For:
Magnesia 20%
Magnesium chloride 30%
Carbon dust 1%
Diatomite 19%
Iron powder 30%.
Embodiment 6
Following components is uniformly mixed, as required with moisture permeable material quantitative package.The mass percent composition of raw material For:
Magnesia 20%
Magnesium chloride 30%
Carbon dust 1%
Diatomite 20%
Iron powder 22%
NaOH 7%.
Embodiment 7
Following components is uniformly mixed, as required with moisture permeable material quantitative package.The mass percent composition of raw material For:
Magnesia 40%
Magnesium chloride 40%
Carbon dust 1%
Diatomite 9%
Iron powder 10%.
In above example, magnesia is from light calcined magnesia and the mixture of activated magnesia, light calcined magnesia particle diameter Generally less than 8mm is a kind of by magnisite stone, shepardite and by the magnesium hydroxide Mg (OH) extracted in seawater or bittern2, Through the light calcined magnesia obtained by 700 ~ 1000 DEG C of temperature lower calcinations.The light calcined magnesia particle diameter distribution adopted in above example Between 0 ~ 8mm, existing little particle has thinner powder again.Commercially available light calcined magnesia can be used, manufacturer such as Dandong Yongxing mining industry Co., Ltd, the grand magnesite product Manufacturing Co., Ltd of Haicheng City etc..
The activated magnesia particle diameter of above example preferably uses 40 ~ 80 mesh typically in 40 ~ 350 mesh, Particle pollution, The large percentage of surface atom and body phase atomicity and there is high chemism and physical absorption ability, due to exhibiting high surface Atom and the presence of surface defect, the diffusion velocity of surface atom are very high, and therefore there is good sintering character.Commercially available activity Magnesia can be used, manufacturer such as Dandong Yongxing mining industry Co., Ltd, the grand magnesite product Manufacturing Co., Ltd of Haicheng City Etc..
The present invention is as used merely activated magnesia, although can meet use on moisture sorption effect, but dry after moisture absorption Agent is in sticky pulpous state, easily reveals, and appropriate interpolation light calcined magnesia can still keep comparing after drier moisture absorption Loose state.If merely using light calcined magnesia, although in good condition after drier moisture absorption, but wettability power can under Drop, and it is harder to lump after moisture absorption, and the interpolation of activated magnesia can improve drier activity, drier and water after moisture absorption Carry out can accelerate and carry out more thorough.
In order to reach good wettability power, the magnesium chloride used by above example is anhydrous magnesium chloride(Do not tie Brilliant water), although with the crystallization water(Such as with the crystallizations water such as 2,4,6)Magnesium chloride can also use but the crystallization water is more few more sharp In the wettability power for improving drier.The purity of anhydrous magnesium chloride is more high also beneficial to the wettability power for improving drier, preferably pure Spend for more than 97%.Anhydrous magnesium chloride has very strong moisture absorption, forms the compound of many water crystallizations at different temperatures with water, with The particle diameter of the anhydrous magnesium chloride that upper embodiment is selected is generally less than 8mm, is distributed between 0 ~ 8mm, and existing little particle has thinner again Powder.General commercial anhydrous magnesium chloride can be used, manufacturer such as Qinghai source of iron Mei Ye Co., Ltd, Shouguang Ding Hao Trade Co., Ltd.s etc..
In order to reach higher oxygen absorbed, reduced iron of the oxygen consumption Duration Ratio of secondary reduction iron powder in reduced iron powder The time of powder will be grown, and the iron powder that therefore above example is used is preferably secondary reduction iron powder.Secondary reduction iron powder is using once Reduced iron powder is formed through melting deep processing, and iron-holder reaches more than 99%, and particle diameter is generally 40 mesh ~ 100 mesh, above example It is preferred that 80 ~ 100 mesh are used.Typically commercially available secondary reduction iron powder can be used, manufacturer's such as prosperous powder of Gongyi City's bridge ditch gold Metallurgical Factory, the thunderous mineral products processing tea in Lingshou County etc..
, by adding appropriate diatomite, after can making drier moisture absorption, product quality is slightly loose, otherwise high for above example Harder bulk can be formed after circumstances moisture absorption, the further dilution inside lump can be like this hindered, reduce overall suction Wet ability.Simultaneously because the loose porous of its quality, can store moisture and there is good permeability, secondary going back may be preferably inspired Former iron powder reaction, improves deoxidation duration and the deoxidation amount of deoxidation drying agent.Diatomaceous particle diameter typically in 1 ~ 4mm, with Upper embodiment preferably 2 ~ 3mm, if particle diameter is carefully easy to very much produce airborne dust, is unfavorable for processing and uses, and particle diameter slightly affects very much to make Use effect.Typically commercially available diatomite can be used, manufacturer's such as fine products factory of Shengzhou East Zhejiang province diatomite etc..
By adding appropriate carbon dust, the initiator as deoxidation drying agent deoxidation is added above example.Typically can be with From commercially available activated carbon, wood chip activated carbon, mao bamboon activated carbon and cocoanut active charcoal is included.As mao bamboon activated carbon is compared with wood chip Activated carbon, the reference area with 3 times of wood chip activated carbons, with higher adsorption capacity, therefore above example is preferably active Bamboo charcoal.Although cocoanut active charcoal with high mechanical properties, pore structure is flourishing, and specific surface area is big, and adsorption rate is fast, and absorption is held Amount is high, it is easy to regenerate, and the features such as durable in use, but to obtain scope less so that relatively costly, inventive formulation due to raw material Product can be used according to the economic worth of corresponding use product.150 mesh ~ 300 mesh are generally from activated carbon particle size, preferably 300 mesh, such as Dongguan City station wood Feng Lin filtering materials business department etc. of manufacturer.
The NaOH of embodiment 7 can adjust deoxidation drying agent according to the oxygen demand using product using directly interpolation Oxygen absorbed, typically commercially available NaOH can be used.
Wettability power and deoxidizing capacity contrast experiment
Deoxidation drying agent prepared by embodiment 1~7 and 3 kinds of commercially available drier and deoxidier carry out moisture absorption respectively and deoxidation is surveyed Try, test condition is:1. deoxidation test(Ambient temperature and moisture)2. moisture absorption test(25 DEG C of temperature, humidity 90%)
Test result is as follows:
Drier is originated Hydroscopicity after 7 days Deoxidation amount after 7 days State after 7 days
Embodiment 1 150.8% 100ml Dry tack free, blocking loosening
Embodiment 2 166.3% 77ml Dry tack free, lumps slightly loose
Embodiment 3 174.4% 74ml Dry tack free, lumps slightly loose
Embodiment 4 155.6% 94ml Dry tack free, blocking loosening
Embodiment 5 146.0% 86.5ml Dry tack free, blocking loosening
Embodiment 6 126.0% 80ml Dry tack free, lumps slightly loose
Embodiment 7 220% 8ml Surface moisture, lumps harder
Deoxidier 0.0% 167ml Dry tack free, does not loosely lump
Commercial silica gel drier 34.8% 0ml/g iron powders Without significant change
Commercially available ore deposit drier living 30.8% 0ml/g iron powders Surface wettability, blocking loosening
Commercially available fiber desiccant 98.3% 0ml/g iron powders Surface is in shape is soaked, thick
From test result it can be seen that the deoxidation drying agent of the present invention has very strong wettability power, wettability power is existing all kinds of 2~6 times of drier;There is very strong deoxidizing capacity also simultaneously, deoxidizing capacity is the 60% of existing pure deoxidier.
Presently preferred embodiments of the present invention is the foregoing is only, not in order to limit the present invention, all in essence of the invention Within god and principle, any modification, equivalent substitution and improvements that is made etc. should be included within the scope of the present invention.

Claims (8)

1. a kind of deoxidation type drier, including the component of following mass ratio:15~45% magnesia;30~45% magnesium chloride; 9~24% diatomite;9~30% iron powder;0.1~10% carbon dust.
2. deoxidation type drier according to claim 1, it is characterised in that:The deoxidation type drier also containing 0.1~ 10% NaOH.
3. deoxidation type drier according to claim 1, it is characterised in that:The deoxidation type drier is by following quality The group of ratio is grouped into, 15~20% magnesia;30~40% magnesium chloride;0.1~1% carbon dust;19~24% diatomite; 20~30% iron powder.
4. deoxidation type drier according to claim 2, it is characterised in that:The deoxidation type drier is by following quality The group of ratio is grouped into, 15~20% magnesia;30~40% magnesium chloride;0.1~1% carbon dust;19~24% diatomite; 20~30% iron powder;0.1~10% NaOH.
5. the deoxidation type drier according to any one of claim 1-4, it is characterised in that:The magnesium chloride is anhydrous chlorine Change magnesium.
6. deoxidation type drier according to claim 5, it is characterised in that:The iron powder is secondary reduction iron powder.
7. deoxidation type drier according to claim 5, it is characterised in that:The magnesia is light calcined magnesia, activity Magnesia or the mixture of light calcined magnesia and activated magnesia.
8. deoxidation type drier according to claim 7, it is characterised in that:The magnesia is light calcined magnesia and work Property magnesia mixture, the mass ratio of light calcined magnesia and activated magnesia is 3: 1-3.
CN201610915480.3A 2016-10-20 2016-10-20 A kind of deoxidation type drier Pending CN106492620A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610915480.3A CN106492620A (en) 2016-10-20 2016-10-20 A kind of deoxidation type drier

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610915480.3A CN106492620A (en) 2016-10-20 2016-10-20 A kind of deoxidation type drier

Publications (1)

Publication Number Publication Date
CN106492620A true CN106492620A (en) 2017-03-15

Family

ID=58318090

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610915480.3A Pending CN106492620A (en) 2016-10-20 2016-10-20 A kind of deoxidation type drier

Country Status (1)

Country Link
CN (1) CN106492620A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107159357A (en) * 2017-06-08 2017-09-15 全椒县崇明米业有限公司 It is a kind of to reduce the big rice processing method of broken rice rate
CN112121606A (en) * 2020-10-10 2020-12-25 杭州家爽包装材料有限公司 Drying agent and preparation method thereof
CN112871130A (en) * 2021-01-15 2021-06-01 杭州干将实业有限公司 Preparation method and preparation device of deoxidizer for medicine
CN115303644A (en) * 2022-09-01 2022-11-08 湖南九典制药股份有限公司 Method for reducing impurity growth rate of levocetirizine capsule
EP4173691A4 (en) * 2020-06-30 2024-01-31 Mitsubishi Gas Chemical Co Oxygen scavenger composition and method for producing same

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101249418A (en) * 2007-05-17 2008-08-27 张红军 High hydroscopicity drier
CN104107678A (en) * 2014-07-18 2014-10-22 杭州干将实业有限公司 Adsorbent with deoxygenation and humidity control functions and preparation method thereof
CN104258696A (en) * 2014-09-04 2015-01-07 青岛市高科专利技术转移平台有限公司 Novel deoxygenation drying agent

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101249418A (en) * 2007-05-17 2008-08-27 张红军 High hydroscopicity drier
CN104107678A (en) * 2014-07-18 2014-10-22 杭州干将实业有限公司 Adsorbent with deoxygenation and humidity control functions and preparation method thereof
CN104258696A (en) * 2014-09-04 2015-01-07 青岛市高科专利技术转移平台有限公司 Novel deoxygenation drying agent

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107159357A (en) * 2017-06-08 2017-09-15 全椒县崇明米业有限公司 It is a kind of to reduce the big rice processing method of broken rice rate
EP4173691A4 (en) * 2020-06-30 2024-01-31 Mitsubishi Gas Chemical Co Oxygen scavenger composition and method for producing same
CN112121606A (en) * 2020-10-10 2020-12-25 杭州家爽包装材料有限公司 Drying agent and preparation method thereof
CN112871130A (en) * 2021-01-15 2021-06-01 杭州干将实业有限公司 Preparation method and preparation device of deoxidizer for medicine
CN115303644A (en) * 2022-09-01 2022-11-08 湖南九典制药股份有限公司 Method for reducing impurity growth rate of levocetirizine capsule

Similar Documents

Publication Publication Date Title
CN106492620A (en) A kind of deoxidation type drier
CN100525898C (en) High hydroscopicity drier
CN107282003A (en) A kind of preparation method of the efficient modified activated carbon for removing formaldehyde in air
CN102847181B (en) Product capable of delaying generation and releasing of chlorine dioxide and preparation method thereof
CN103721533A (en) Deoxidizing and drying agent and preparation method thereof
CN102835421A (en) Stable product containing chlorine dioxide and preparation method of stable product
CN101565338B (en) Method for preparing fertilizer adsorbing volatilizing nitrogen
CN103657589A (en) Drying agent with high moisture absorption rate
CN104107678B (en) Adsorbent with deoxygenation and humidity control functions and preparation method thereof
JPWO2018135612A1 (en) Granular fertilizer containing glutathione
CN108477207A (en) A kind of slow-release chlorine dioxide of solid carrier particle and preparation method thereof
CN102198401A (en) Cobalt molybdenum CO sulfur-tolerant shift catalyst by using attapulgite clay as carrier and its preparation method
CN104548889A (en) Preparation method of bentonite drying agent
TW201524752A (en) Fruit and vegetable fresh packing material and producing method thereof
WO2011158675A1 (en) Composite magnesium hydroxide, method for producing same, and adsorbent
CN1096883C (en) Preservative
CN101948097B (en) Method for preparing stable solid chlorine dioxide
CN108067186A (en) A kind of acticarbon and its preparation process for loading phosphoric acid
CN104768901A (en) Method for limiting the use of an ammonium nitrate fertilizer as a precursor for an explosive and composition therefor
JPH0446615B2 (en)
CN101961593A (en) Dissolved type gas drying material and preparation method thereof
CN102115352A (en) Ammonium nitrate modifier
KR102027778B1 (en) Granular desiccant, a method for producing the same, and a method for recycling the same
CN101433361A (en) Vermiculite double-suction agent/oxygen absorbent
CN103721534A (en) Deoxidizing and drying agent for instruments and meters and preparation method thereof

Legal Events

Date Code Title Description
C06 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: 20170315