CN106669639A - Preparation method of chemical drying agent - Google Patents
Preparation method of chemical drying agent Download PDFInfo
- Publication number
- CN106669639A CN106669639A CN201510744753.8A CN201510744753A CN106669639A CN 106669639 A CN106669639 A CN 106669639A CN 201510744753 A CN201510744753 A CN 201510744753A CN 106669639 A CN106669639 A CN 106669639A
- Authority
- CN
- China
- Prior art keywords
- percent
- preparation
- calcium chloride
- pigment
- citric acid
- 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
Links
- 239000000126 substance Substances 0.000 title claims abstract description 14
- 238000002360 preparation method Methods 0.000 title claims abstract description 12
- 239000002274 desiccant Substances 0.000 title abstract 4
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims abstract description 36
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 claims abstract description 15
- 239000001110 calcium chloride Substances 0.000 claims abstract description 14
- 229910001628 calcium chloride Inorganic materials 0.000 claims abstract description 14
- 229910021536 Zeolite Inorganic materials 0.000 claims abstract description 12
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 claims abstract description 12
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 claims abstract description 12
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 claims abstract description 12
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000000049 pigment Substances 0.000 claims abstract description 12
- 239000000843 powder Substances 0.000 claims abstract description 12
- 239000010457 zeolite Substances 0.000 claims abstract description 12
- 229920001661 Chitosan Polymers 0.000 claims abstract description 7
- 238000001816 cooling Methods 0.000 claims abstract description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 7
- 238000001035 drying Methods 0.000 claims abstract description 6
- 238000001914 filtration Methods 0.000 claims abstract description 6
- 239000002994 raw material Substances 0.000 claims abstract description 6
- 239000007787 solid Substances 0.000 claims abstract description 6
- 238000003756 stirring Methods 0.000 claims abstract description 6
- 239000000243 solution Substances 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 abstract description 13
- 238000010438 heat treatment Methods 0.000 abstract 1
- 238000002156 mixing Methods 0.000 abstract 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- 229910021529 ammonia Inorganic materials 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation 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
- B01D53/26—Drying gases or vapours
- B01D53/28—Selection of materials for use as drying agents
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
- B01J20/04—Solid 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
- B01J20/046—Solid 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
- B01J20/10—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising silica or silicate
- B01J20/16—Alumino-silicates
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/22—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising organic material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/22—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising organic material
- B01J20/24—Naturally occurring macromolecular compounds, e.g. humic acids or their derivatives
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/22—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising organic material
- B01J20/26—Synthetic macromolecular compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2253/00—Adsorbents used in seperation treatment of gases and vapours
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2220/00—Aspects relating to sorbent materials
- B01J2220/40—Aspects relating to the composition of sorbent or filter aid materials
- B01J2220/44—Materials comprising a mixture of organic materials
- B01J2220/445—Materials comprising a mixture of organic materials comprising a mixture of polymers
Landscapes
- Chemical & Material Sciences (AREA)
- Analytical Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Abstract
The invention discloses a preparation method of a chemical drying agent. The preparation method of the chemical drying agent comprises the following steps: (1) selecting raw materials comprising 60 to 70 percent of calcium chloride, 10 to 15 percent of zeolite powder, 2 to 6 percent of chitosan, 1.5 to 3.5 percent of hydroxypropyl methyl cellulose, 2 to 4 percent of citric acid, 0.5 to 2 percent of pigment and the balance of water; (2) mixing the zeolite powder and the hydroxypropyl methyl cellulose uniformly, heating at the temperature of 220 to 240 DEG C for 40 to 70 minutes, and naturally cooling to room temperature to be viscous; (3) putting the prepared viscous product into a chitosan solution, stirring uniformly, adding the calcium chloride, the citric acid and the pigment, and filtering; (4) baking, drying and cooling the filtered solid to obtain the drying agent. The preparation method has the advantages that the production process is adjusted reasonably, so that the production process is simple and the production cost is greatly reduced.
Description
Technical field
The invention belongs to chemicals field, and in particular to a kind of preparation method of chemical drier.
Background technology
Drier is a kind of extremely strong adsorbent of adsorption capacity.The material of moisture in moist material is removed using drier.At present, conventional drier is divided into physical dryness agent and chemical drier due to the difference of application category.Chemical drier is dried by being combined generation hydrate with water, such as calcium sulfate, calcium chloride, and calcium chloride therein can not absorb ammonia, it is typically at ambient temperature mixed gas to be passed through into anhydrous calcium chloride when dry ammonia, at this moment this complex compound is not easily decomposed once generating.
Existing technical scheme complex manufacturing, production cost is high and absorption efficiency is low.
The content of the invention
Present invention aims to the deficiencies in the prior art, now provide a kind of simple production process, the preparation method of the chemical drier of low production cost.
For achieving the above object, the technical scheme is that:A kind of preparation method of chemical drier, its innovative point is:Comprise the steps:
(1)The selection of raw material:Calcium chloride 60-70%, zeolite powder 10-15%, shitosan 2-6%, hydroxypropyl methyl cellulose 1.5-3.5%, citric acid 2-4%, pigment 0.5-2%, balance of water;
(2)Heated after zeolite powder is well mixed with hydroxypropyl methyl cellulose, the temperature is 220-240 DEG C, the heat time is 40-70 minutes, is then naturally cooled to after room temperature into thick;
(3)Obtained thick product is put into chitosan solution, calcium chloride, citric acid and pigment is stirring evenly and then adding into, is then filtered;
(4)By the solid after filtration carry out roasting, drying, cooling drier is obtained.
Beneficial effects of the present invention are as follows:The present invention passes through Reasonable adjustment production technology so that simple production process, production cost is greatly reduced.
Specific embodiment
Hereinafter embodiments of the present invention are illustrated by particular specific embodiment, the content that those skilled in the art can be by disclosed by this specification understands easily other advantages and effect of the present invention.
Embodiment 1
A kind of preparation method of chemical drier, comprises the steps:
(1)The selection of raw material:Calcium chloride 60%, zeolite powder 10%, shitosan 2%, hydroxypropyl methyl cellulose 1.5%, citric acid 2%, pigment 0.5%, balance of water;
(2)Heated after zeolite powder is well mixed with hydroxypropyl methyl cellulose, temperature is 220 DEG C, the heat time is 40 minutes, is then naturally cooled to after room temperature into thick;
(3)Obtained thick product is put into chitosan solution, calcium chloride, citric acid and pigment is stirring evenly and then adding into, is then filtered;
(4)By the solid after filtration carry out roasting, drying, cooling drier is obtained.
Embodiment 2
A kind of preparation method of chemical drier, comprises the steps:
(1)The selection of raw material:Calcium chloride 70%, zeolite powder 15%, shitosan 6%, hydroxypropyl methyl cellulose 3.5%, citric acid 4%, pigment 2%, balance of water;
(2)Heated after zeolite powder is well mixed with hydroxypropyl methyl cellulose, temperature is 240 DEG C, the heat time is 70 minutes, is then naturally cooled to after room temperature into thick;
(3)Obtained thick product is put into chitosan solution, calcium chloride, citric acid and pigment is stirring evenly and then adding into, is then filtered;
(4)By the solid after filtration carry out roasting, drying, cooling drier is obtained.
Embodiment 3
A kind of preparation method of chemical drier, comprises the steps:
(1)The selection of raw material:Calcium chloride 65%, zeolite powder 13%, shitosan 4%, hydroxypropyl methyl cellulose 2.5%, citric acid 3%, pigment 1.3%, balance of water;
(2)Heated after zeolite powder is well mixed with hydroxypropyl methyl cellulose, temperature is 230 DEG C, the heat time is 55 minutes, is then naturally cooled to after room temperature into thick;
(3)Obtained thick product is put into chitosan solution, calcium chloride, citric acid and pigment is stirring evenly and then adding into, is then filtered;
(4)By the solid after filtration carry out roasting, drying, cooling drier is obtained.
The present invention passes through Reasonable adjustment production technology so that simple production process, production cost is greatly reduced.
Above-described embodiment is presently preferred embodiments of the present invention; it is not the restriction to technical solution of the present invention; as long as without the technical scheme that creative work can be realized on the basis of above-described embodiment, in the rights protection scope for being regarded as falling into patent of the present invention.
Claims (1)
1. a kind of preparation method of chemical drier, it is characterised in that:Comprise the steps:
(1)The selection of raw material:Calcium chloride 60-70%, zeolite powder 10-15%, shitosan 2-6%, hydroxypropyl methyl cellulose 1.5-3.5%, citric acid 2-4%, pigment 0.5-2%, balance of water;
(2)Heated after zeolite powder is well mixed with hydroxypropyl methyl cellulose, the temperature is 220-240 DEG C, the heat time is 40-70 minutes, is then naturally cooled to after room temperature into thick;
(3)Obtained thick product is put into chitosan solution, calcium chloride, citric acid and pigment is stirring evenly and then adding into, is then filtered;
(4)By the solid after filtration carry out roasting, drying, cooling drier is obtained.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201510744753.8A CN106669639A (en) | 2015-11-06 | 2015-11-06 | Preparation method of chemical drying agent |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201510744753.8A CN106669639A (en) | 2015-11-06 | 2015-11-06 | Preparation method of chemical drying agent |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN106669639A true CN106669639A (en) | 2017-05-17 |
Family
ID=58858798
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201510744753.8A Pending CN106669639A (en) | 2015-11-06 | 2015-11-06 | Preparation method of chemical drying agent |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN106669639A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN107486168A (en) * | 2017-09-09 | 2017-12-19 | 南通意特化工有限公司 | A kind of preparation method of chemical drier |
| CN108889095A (en) * | 2018-06-29 | 2018-11-27 | 杭州维万日用品有限公司 | A kind of dehumidizer and preparation method thereof |
-
2015
- 2015-11-06 CN CN201510744753.8A patent/CN106669639A/en active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN107486168A (en) * | 2017-09-09 | 2017-12-19 | 南通意特化工有限公司 | A kind of preparation method of chemical drier |
| CN108889095A (en) * | 2018-06-29 | 2018-11-27 | 杭州维万日用品有限公司 | A kind of dehumidizer and preparation method thereof |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5771274B2 (en) | Multi-aperture carbon particle air purifier and method for producing the same | |
| CN103657589A (en) | Drying agent with high moisture absorption rate | |
| CN102674346A (en) | Process for preparing high-specific surface area composite pore structure coal-based activated carbon by using low dosage of KOH | |
| CN103964432A (en) | Method for preparing granular activated carbon from lignin | |
| CN105386338A (en) | Preparation method of instant sodium alginate printing gum | |
| CN105056889A (en) | Preparation method for bentonite drying agent | |
| CN105984888A (en) | Process for preparing hydrogen cyanamide by utilizing urea | |
| CN106669639A (en) | Preparation method of chemical drying agent | |
| CN105107344B (en) | A kind of deoxidation drying agent and preparation method thereof | |
| CN103638789A (en) | Production process of chemical drying agent | |
| CN105148859B (en) | A kind of bentonite drier and its preparation technology | |
| CN105251454B (en) | A kind of efficient Spent Radioactive water process adsorbent of modified zeolite with spatial multi network architecture and preparation method | |
| CN102757048A (en) | Method for preparing activated carbon from peonies | |
| CN105017812A (en) | Composite titanium dioxide | |
| CN104117327B (en) | A kind of low temperature method of granulating of powder lactic acid | |
| CN105001679A (en) | Composite titanium dioxide | |
| CN106107054A (en) | The silica-type choline chloride powder of a kind of high effective content and production method thereof | |
| CN104959121A (en) | Chemical desiccant and preparation method thereof | |
| CN106861379A (en) | A kind of drier and preparation method thereof | |
| CN104368311B (en) | A kind of renewable anti-haze mask adsorbent and preparation method thereof | |
| CN103539116A (en) | Process for producing activated carbon by means of phosphoric acid method | |
| CN104016709A (en) | Preparation method of porous sodium-based bentonite particles | |
| CN106040166B (en) | The preparation method of the space division molecular sieve of efficient De contamination | |
| CN107486168A (en) | A kind of preparation method of chemical drier | |
| CN105419391A (en) | Method for preparing ammonium polyphosphate micro-capsules coated by melamine cyanurate |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| WD01 | Invention patent application deemed withdrawn after publication | ||
| WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20170517 |