CN110227395A - The preparation method of air-flow nanometer - Google Patents

The preparation method of air-flow nanometer Download PDF

Info

Publication number
CN110227395A
CN110227395A CN201910618487.2A CN201910618487A CN110227395A CN 110227395 A CN110227395 A CN 110227395A CN 201910618487 A CN201910618487 A CN 201910618487A CN 110227395 A CN110227395 A CN 110227395A
Authority
CN
China
Prior art keywords
temperature
air
micro
dry
fluidized bed
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.)
Withdrawn
Application number
CN201910618487.2A
Other languages
Chinese (zh)
Inventor
李功伟
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.)
Guangdong Benyuan Science And Technology Development Co Ltd
Original Assignee
Guangdong Benyuan Science And Technology Development 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 Guangdong Benyuan Science And Technology Development Co Ltd filed Critical Guangdong Benyuan Science And Technology Development Co Ltd
Priority to CN201910618487.2A priority Critical patent/CN110227395A/en
Publication of CN110227395A publication Critical patent/CN110227395A/en
Withdrawn legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D50/00Combinations of methods or devices for separating particles from gases or vapours
    • B01D50/20Combinations of devices covered by groups B01D45/00 and B01D46/00
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J13/00Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
    • B01J13/02Making microcapsules or microballoons
    • B01J13/04Making microcapsules or microballoons by physical processes, e.g. drying, spraying
    • B01J13/043Drying and spraying
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2/00Processes or devices for granulating materials, e.g. fertilisers in general; Rendering particulate materials free flowing in general, e.g. making them hydrophobic

Abstract

Disclosed by the invention is a kind of preparation method of air-flow nanometer, it is combined using stirring and emulsifying, shearing homogeneous and biofilm filtration and obtains nanoscale emulsifying materials system, spray drying granulation is carried out using the mixed airflow of upper air inlet, upper air draft, the dry, granulation with the novel all-in-one integrated fluidized bed of three points of warm areas again, it improves drying efficiency, reduce particle diameter, there is energy conservation and environmental protection, flexibility height, prepare the technical characterstics such as simple, at low cost, green non-pollution.

Description

The preparation method of air-flow nanometer
Technical field
The invention belongs to air-flow nano particle preparation technical field more particularly to a kind of preparation methods of air-flow nanometer.
Background technique
Spray drying granulation technology is widely used in the fields such as food, medicine, chemical industry.Currently, spray drying granulation method Traditional Single-stage spray drying granulating system and more complicated multi-stage spray drying-granulating system, traditional single-stage can be divided into Spray drying granulation system uses the airflow design of air draft under upper air inlet, and there are drying effects to be difficult to control, product grain diameter It is unevenly distributed, embedding effect is unstable, the problems such as dust pollution is difficult to control, and more complicated multi-stage spray drying-granulating System preferable can must control particle diameter and drying although solving the problems, such as that some Single-stage spray drying granulating systems exist Stability, still, its own is there is also bulky, and structure is complicated, and energy consumption is high, and material passes through multiple drying equipment mutabilities The defects of.
Currently, using the spray drying granulation method used in production, either traditional single stage drying-granulating system, still Multi-stage spray drying system cannot produce the nanoscale microcapsule granule that particle diameter is less than 50um, with food, health care product, Medical and health, the continuous development of manufacturing field, to the smallest particles diameter of micro- granulation, more stringent requirements are proposed, the micro- glue of nanoscale Capsule particle has dimensionally stable, and anti-extrusion easily absorbs, and is easy to be mixed into the features such as going further processing with unclassified stores, With extensive demand and application prospect
Summary of the invention
The present invention is directed to above-mentioned problem, provides a kind of preparation method of air-flow nanometer.
In order to achieve the above object, the technical solution adopted by the present invention is,
A kind of preparation method of air-flow nanometer, the preparation method include the following steps:
Step 1): material is added in emulsion chamber with the speed of 1-500km/h, with the stirring of 30-2000rpm revolving speed, cream Change 15-50min, then be placed under the pressure conditions of 1-20Mpa, shear homogeneous 15-60min, obtains emulsifying materials liquid;
Step 2): the biofilm filtration that the emulsifying materials liquid that step 1) is obtained is 1-500um through pore size filter obtains micro- Nanoscale emulsion;If 3) emulsifying materials liquid enters step by biofilm filtration aperture, otherwise, flows back into 1- through pipeline Continue to shear homogeneous under the pressure conditions of 20Mpa, the biofilm filtration for being 1-500um using filter opening diameter obtains micro/nano level Emulsion;
Step 3): the micro/nano level emulsion that step 2) obtains is added to multi-stage spray with the speed of 1-500km/h and is done In dry tower, it is passed through dry hot-air from multi-stage spray drying tower upper end, is spray-dried, agglomeration is granulated, the first drying of acquisition Micro/nano level microcapsule granule, and dry hot-air is discharged from multi-stage spray drying tower upper end;
Step 4): the micro/nano level microcapsule granule dry for the first time that step 3) is obtained is added to integrated built in multi-temperature zone In fluidized bed, dry hot-air is passed through into fluidized bed integrated built in multi-temperature zone, dry, cooling, agglomeration is granulated, and obtains finished product Micro/nano level microcapsule granule, dry hot-air is arranged from multi-stage spray drying tower upper end in integrated fluidized bed built in the multi-temperature zone Out;
Step 5): the dry air being discharged in step 3), step 4) is passed through in cyclone separator, in cyclone separator Cyclonic separation dedusting is carried out, obtains the lesser material fine powder of particle, and tail gas is discharged into bag filter and is dusted processing, The material fine powder in tail gas is collected, then by the purified air filtration of bag filter, discharge;
Step 6): the material fine powder collected in step 5) is done by pipeline into multi-stage spray drying tower by spraying Dry, agglomeration is granulated, and obtains micro/nano level microcapsule granule dry for the first time, and micro/nano level microcapsule granule dry for the first time is added to Dry in integrated fluidized bed built in multi-temperature zone, cooling, agglomeration is granulated, and obtains finished product micro/nano level microcapsule granule, or directly will The material fine powder collected in step 5) is transported to dry in integrated fluidized bed, cooling, agglomeration built in multi-temperature zone and is granulated, obtain at Product micro/nano level microcapsule granule.
Preferably, integrated fluidized bed built in the multi-temperature zone includes high-temperature region, middle warm area, low-temperature space, it is described first Dry micro/nano level microcapsule granule is added sequentially to integrated fluidized bed high temperature area, middle warm area, low-temperature space built in multi-temperature zone, It is set the product exit collection in low-temperature space, obtains finished product micro/nano level microcapsule granule.
Preferably, the high-temperature region temperature is 300-380 DEG C, the middle warm area temperature is 200-260 DEG C, the low temperature Area's temperature is 80-100 DEG C.
Preferably, it is 150-200 DEG C that multi-stage spray drying tower upper end, which is passed through dry hot air temperature, the multistage It is 60-100 DEG C that dry hot air temperature, which is discharged, in spray drying tower upper end.
Preferably, when the material fine powder collected in step 5) being directly transported to integrated fluidized bed built in multi-temperature zone, The material fine powder of collection is transported to the high-temperature region built in multi-temperature zone in integrated fluidized bed, or the material fine powder of collection is conveyed To the low-temperature space built in multi-temperature zone in integrated fluidized bed.
Preferably, the finished product micro/nano level microcapsule granule diameter obtained in step 4) or step 6) is 100nm-20um.
Compared with prior art, the advantages and positive effects of the present invention are,
1, nanoscale is obtained using the novel emulsion system that stirring and emulsifying, high shear homogeneous and biofilm filtration combine Emulsifying materials system;The airflow design for changing air draft under conventionally spray-dried Granulation Equipments upper air inlet, using upper air inlet, upper air draft Mixed airflow, improve drying efficiency;It is dry with the novel all-in-one integrated fluidized bed of three points of warm areas, one is carried out to material The drying cooling and agglomeration of step formula are granulated, compared with the existing technology in fluidized bed, can be more energy-saving and environmentally friendly, efficient stable;It can Secondary agglomeration granulation is carried out so that non-compliant fine powder is returned to hothouse, ensure that the stability of granulation;Back-mounted rotary The fine powder of wind separator collection can according to the production requirement of variable grain diameter, by pipeline return to hothouse re-start it is attached It is poly- to be granulated, it also can transport integrated fluidized bed high-temperature region or low-temperature space, flexibility is high;Preparation process is simple, at low cost, green It is pollution-free;High-temperature region temperature is 300-380 DEG C, and middle warm area temperature is 200-260 DEG C, and low-temperature space temperature is 80-100 DEG C and sets It sets, so that efficient stable obtains finished product micro/nano level microcapsule granule, if deviateing temperature setting, particle diameter cannot be produced and be less than The nanoscale microcapsule granule of 50um;Being passed through dry hot air temperature is 150-200 DEG C, and it is 60-100 that dry hot air temperature, which is discharged, DEG C, drying efficiency is improved, while being conducive to an efficient step and completing the preparation of finished product micro/nano level microcapsule granule, reduces step 5), step Rapid operation 6);The covering of the finished product micro/nano level microcapsule granule of acquisition is hard, and solid, content is more stable.
Detailed description of the invention
In order to illustrate the technical solution of the embodiments of the present invention more clearly, required use in being described below to embodiment Attached drawing be briefly described, it should be apparent that, drawings in the following description are some embodiments of the invention, for ability For the those of ordinary skill of domain, without any creative labor, it can also be obtained according to these attached drawings others Attached drawing.
Fig. 1 is structural schematic diagram of the invention;
Fig. 2 is preparation flow figure of the invention.
Specific embodiment
To better understand the objects, features and advantages of the present invention, with reference to the accompanying drawings and examples The present invention will be further described.It should be noted that in the absence of conflict, in embodiments herein and embodiment Feature can be combined with each other.
In the following description, numerous specific details are set forth in order to facilitate a full understanding of the present invention, still, the present invention may be used also To be implemented using other modes described herein are different from, therefore, the present invention is not limited to the specific of specification is described below The limitation of embodiment.
Embodiment 1
It is as shown in Figs. 1-2 a kind of specific embodiment of the preparation method of air-flow nanometer, which includes following step It is rapid:
Step 1): material is added in emulsion chamber with the speed of 1km/h, with the stirring of 30rpm revolving speed, emulsification 20min, then It is placed under the pressure conditions of 1Mpa, shears homogeneous 30min, obtain emulsifying materials liquid;
Step 2): the biofilm filtration that the emulsifying materials liquid that step 1) is obtained is 1um through pore size filter obtains micro-nano Otherwise grade emulsion, does not pass through biological membrane aperture if 3) emulsifying materials liquid is entered step by biofilm filtration aperture Drop, which is flowed back into through pipeline under the pressure conditions of 1Mpa, to be continued to shear homogeneous, and the biofilm filtration for being 1um using filter opening diameter obtains Obtain micro/nano level emulsion;
Step 3): the micro/nano level emulsion that step 2) obtains is added to multi-stage spray drying tower with the speed of 1km/h In, it is passed through dry hot-air from multi-stage spray drying tower upper end, is spray-dried, agglomeration granulation, obtains the micro- of drying for the first time Nanoscale microcapsule granule, and from the dry hot-air of multi-stage spray drying tower upper end discharge, spray-drying process, from multi-stage spray It is 150 DEG C that drying tower upper end, which is passed through dry hot air temperature, and it is 60 that dry hot air temperature, which is discharged, in multi-stage spray drying tower upper end ℃;
Step 4): integrated fluidized bed built in multi-temperature zone includes 300 DEG C of high-temperature region, 200 DEG C of middle warm area, 80 DEG C low Warm area is passed through dry hot-air into fluidized bed integrated built in multi-temperature zone, by the micro-nano of the drying for the first time of step 3) acquisition Grade microcapsule granule is added sequentially to integrated fluidized bed high temperature area, middle warm area, low-temperature space built in multi-temperature zone, dry, cooling, attached It is poly- to be granulated, it is set the product exit collection in low-temperature space, obtains the finished product micro/nano level microcapsule granule that particle diameter is 80nm, Hot-air dry in fluidized bed integrated built in multi-temperature zone is discharged from multi-stage spray drying tower upper end;
Step 5): the dry air being discharged in step 3), step 4) is passed through in cyclone separator, in cyclone separator Cyclonic separation dedusting is carried out, obtains the lesser material fine powder of particle, and tail gas is discharged into bag filter and is dusted processing, Collect tail gas in material fine powder, then by the purified air filtration of bag filter, be discharged in atmosphere;
Step 6): the material fine powder collected in step 5) is done by pipeline into multi-stage spray drying tower by spraying Dry, agglomeration is granulated, and obtains micro/nano level microcapsule granule dry for the first time, and micro/nano level microcapsule granule dry for the first time is successively added Enter to fluidized bed high temperature area integrated built in multi-temperature zone, middle warm area, low-temperature space, dry, cooling, agglomeration is granulated, and obtains particle Diameter is the finished product micro/nano level microcapsule granule of 80nm;Or directly the material fine powder collected in step 5) is fed sequentially into mostly warm Integrated fluidized bed high temperature area, middle warm area, low-temperature space built in area, dry, cooling, agglomeration are granulated, and are obtained particle diameter and are The material fine powder collected in step 5) is directly transported to built in multi-temperature zone by the finished product micro/nano level microcapsule granule of 80nm taking When dry in integrated fluidized bed, cooling, agglomeration is granulated, two ways can be divided into: one, the material that will be collected in step 5) Fine powder is transported to the high-temperature region built in multi-temperature zone in integrated fluidized bed, then by middle warm area, low-temperature space processing, obtains particle Diameter is the finished product micro/nano level microcapsule granule of 80nm;Two, the material fine powder collected in step 5) is transported to built in multi-temperature zone Low-temperature space processing in integrated fluidized bed, obtains the finished product micro/nano level microcapsule granule that particle diameter is 80nm, a variety of processing Step, flexibility are high.
Embodiment 2
It is as shown in Figs. 1-2 a kind of specific embodiment of the preparation method of air-flow nanometer, which includes following step It is rapid:
Step 1): material is added in emulsion chamber with the speed of 250km/h, with the stirring of 1015rpm revolving speed, emulsification 40min, then be placed under the pressure conditions of 10.5Mpa, homogeneous 60min is sheared, emulsifying materials liquid is obtained;
Step 2): the biofilm filtration that the emulsifying materials liquid that step 1) is obtained is 250um through pore size filter obtains micro-nano Otherwise meter level emulsion, does not pass through biological membrane aperture if 3) emulsifying materials liquid is entered step by biofilm filtration aperture Drop flowed back into through pipeline under the pressure conditions of 10.5Mpa and continue to shear homogeneous, the biomembrane for being 250um using filter opening diameter Filtering obtains micro/nano level emulsion;
Step 3): the micro/nano level emulsion that step 2) obtains is added to multi-stage spray drying with the speed of 250km/h In tower, it is passed through dry hot-air from multi-stage spray drying tower upper end, is spray-dried, agglomeration granulation, obtains drying for the first time Micro/nano level microcapsule granule, and from the dry hot-air of multi-stage spray drying tower upper end discharge, spray-drying process, it is sprayed from multistage It is 175 DEG C that mist drying tower upper end, which is passed through dry hot air temperature, and multi-stage spray drying tower upper end is discharged dry hot air temperature and is 80℃;
Step 4): integrated fluidized bed built in multi-temperature zone includes 325 DEG C of high-temperature region, 220 DEG C of middle warm area, 90 DEG C low Warm area is passed through dry hot-air into fluidized bed integrated built in multi-temperature zone, by the micro-nano of the drying for the first time of step 3) acquisition Grade microcapsule granule is added sequentially to integrated fluidized bed high temperature area, middle warm area, low-temperature space built in multi-temperature zone, dry, cooling, attached It is poly- to be granulated, it is set the product exit collection in low-temperature space, obtains the finished product micro/nano level microcapsule granule that particle diameter is 70nm, Hot-air dry in fluidized bed integrated built in multi-temperature zone is discharged from multi-stage spray drying tower upper end;
Step 5): the dry air being discharged in step 3), step 4) is passed through in cyclone separator, in cyclone separator Cyclonic separation dedusting is carried out, obtains the lesser material fine powder of particle, and tail gas is discharged into bag filter and is dusted processing, The material fine powder in tail gas is collected, then by the purified air filtration of bag filter, discharge;
Step 6): the material fine powder collected in step 5) is done by pipeline into multi-stage spray drying tower by spraying Dry, agglomeration is granulated, and obtains micro/nano level microcapsule granule dry for the first time, and micro/nano level microcapsule granule dry for the first time is added to Dry in integrated fluidized bed built in multi-temperature zone, cooling, agglomeration is granulated, and it is micro- to obtain the finished product micro/nano level that particle diameter is 70nm Capsule particle;Or directly the material fine powder collected in step 5) is transported to built in multi-temperature zone and is dried in integrated fluidized bed, is cooling, Agglomeration is granulated, and obtains finished product micro/nano level microcapsule granule, take directly the material fine powder collected in step 5) is transported to it is more When dry in integrated fluidized bed built in warm area, cooling, agglomeration is granulated, two ways can be divided into: one, will be received in step 5) The material fine powder of collection is transported to the high-temperature region built in multi-temperature zone in integrated fluidized bed, then handles by middle warm area, low-temperature space, Obtain the finished product micro/nano level microcapsule granule that particle diameter is 70nm;Two, the material fine powder collected in step 5) is transported to more Low-temperature space processing built in warm area in integrated fluidized bed, obtains the finished product micro/nano level microcapsule granule that particle diameter is 70nm, A variety of processing steps, flexibility are high.
Embodiment 3
It is as shown in Figs. 1-2 a kind of specific embodiment of the preparation method of air-flow nanometer, which includes following step It is rapid:
Step 1): material is added in emulsion chamber with the speed of 500km/h, with the stirring of 2000rpm revolving speed, emulsification 35min, then be placed under the pressure conditions of 20Mpa, homogeneous 30min is sheared, emulsifying materials liquid is obtained;
Step 2): the biofilm filtration that the emulsifying materials liquid that step 1) is obtained is 500um through pore size filter obtains micro-nano Otherwise meter level emulsion, does not pass through biological membrane aperture if 3) emulsifying materials liquid is entered step by biofilm filtration aperture Drop flowed back into through pipeline under the pressure conditions of 20Mpa and continue to shear homogeneous, the biomembrane mistake for being 500um using filter opening diameter Filter obtains micro/nano level emulsion;
Step 3): the micro/nano level emulsion that step 2) obtains is added to multi-stage spray drying with the speed of 500km/h In tower, it is passed through dry hot-air from multi-stage spray drying tower upper end, is spray-dried, agglomeration granulation, obtains drying for the first time Micro/nano level microcapsule granule, and from the dry hot-air of multi-stage spray drying tower upper end discharge, spray-drying process, it is sprayed from multistage It is 200 DEG C that mist drying tower upper end, which is passed through dry hot air temperature, and multi-stage spray drying tower upper end is discharged dry hot air temperature and is 100℃;
Step 4): integrated fluidized bed built in multi-temperature zone includes 350 DEG C of high-temperature region, 230 DEG C of middle warm area, 100 DEG C Low-temperature space is passed through dry hot-air into fluidized bed integrated built in multi-temperature zone, the micro-nano dry for the first time that step 3) is obtained Meter level microcapsule granule is added sequentially to integrated fluidized bed high temperature area, middle warm area, low-temperature space built in multi-temperature zone, dry, is cooling, Agglomeration is granulated, and is set the product exit collection in low-temperature space, is obtained the finished product micro/nano level micro-capsule that particle diameter is 20um Hot-air dry in fluidized bed integrated built in multi-temperature zone is discharged grain from multi-stage spray drying tower upper end;
Step 5): the dry air being discharged in step 3), step 4) is passed through in cyclone separator, in cyclone separator Cyclonic separation dedusting is carried out, obtains the lesser material fine powder of particle, and tail gas is discharged into bag filter and is dusted processing, The material fine powder in tail gas is collected, then by the purified air filtration of bag filter, discharge;
Step 6): the material fine powder collected in step 5) is done by pipeline into multi-stage spray drying tower by spraying Dry, agglomeration is granulated, and obtains micro/nano level microcapsule granule dry for the first time, and micro/nano level microcapsule granule dry for the first time is added to Dry in integrated fluidized bed built in multi-temperature zone, cooling, agglomeration is granulated, and it is micro- to obtain the finished product micro/nano level that particle diameter is 20um Capsule particle;Or directly the material fine powder collected in step 5) is transported to built in multi-temperature zone and is dried in integrated fluidized bed, is cooling, Agglomeration is granulated, and obtains finished product micro/nano level microcapsule granule, take directly the material fine powder collected in step 5) is transported to it is more When dry in integrated fluidized bed built in warm area, cooling, agglomeration is granulated, two ways can be divided into: one, will be received in step 5) The material fine powder of collection is transported to the high-temperature region built in multi-temperature zone in integrated fluidized bed, then handles by middle warm area, low-temperature space, Obtain the finished product micro/nano level microcapsule granule that particle diameter is 20um;Two, the material fine powder collected in step 5) is transported to more Low-temperature space processing built in warm area in integrated fluidized bed, obtains the finished product micro/nano level microcapsule granule that particle diameter is 20um, A variety of processing steps, flexibility are high.
The above described is only a preferred embodiment of the present invention, being not that the invention has other forms of limitations, appoint What those skilled in the art changed or be modified as possibly also with the technology contents of the disclosure above equivalent variations etc. It imitates embodiment and is applied to other fields, but without departing from the technical solutions of the present invention, according to the technical essence of the invention Any simple modification, equivalent variations and remodeling to the above embodiments, still fall within the protection scope of technical solution of the present invention.

Claims (6)

1. a kind of preparation method of air-flow nanometer, which is characterized in that the preparation method includes the following steps:
Step 1): material is added in emulsion chamber with the speed of 1-500km/h, with the stirring of 30-2000rpm revolving speed, emulsification 15- 50min, then be placed under the pressure conditions of 1-20Mpa, homogeneous 15-60min is sheared, emulsifying materials liquid is obtained;
Step 2): the biofilm filtration that the emulsifying materials liquid that step 1) is obtained is 1-500um through pore size filter obtains micro-nano Grade emulsion;If 3) emulsifying materials liquid enters step by biofilm filtration aperture, otherwise, flows back into 1-20Mpa through pipeline Pressure conditions under continue shear homogeneous, using filter opening diameter be 1-500um biofilm filtration, obtain micro/nano level emulsification Liquid;
Step 3): the micro/nano level emulsion that step 2) obtains is added to multi-stage spray drying tower with the speed of 1-500km/h In, it is passed through dry hot-air from multi-stage spray drying tower upper end, is spray-dried, agglomeration granulation, obtains the micro- of drying for the first time Nanoscale microcapsule granule, and dry hot-air is discharged from multi-stage spray drying tower upper end;
Step 4): the micro/nano level microcapsule granule dry for the first time that step 3) is obtained is added to integrated fluidisation built in multi-temperature zone In bed, dry hot-air is passed through into fluidized bed integrated built in multi-temperature zone, dry, cooling, agglomeration is granulated, and obtains finished product micro-nano Meter level microcapsule granule, dry hot-air is discharged from multi-stage spray drying tower upper end in integrated fluidized bed built in the multi-temperature zone;
Step 5): the dry air being discharged in step 3), step 4) is passed through in cyclone separator, is carried out in cyclone separator Cyclonic separation dedusting obtains the lesser material fine powder of particle, and tail gas is discharged into bag filter and is dusted processing, collects Material fine powder in tail gas, then by the purified air filtration of bag filter, discharge;
Step 6): the material fine powder collected in step 5) is spray-dried by pipeline into multi-stage spray drying tower, Agglomeration is granulated, and obtains micro/nano level microcapsule granule dry for the first time, micro/nano level microcapsule granule dry for the first time is added to more Dry in integrated fluidized bed built in warm area, cooling, agglomeration is granulated, and obtains finished product micro/nano level microcapsule granule, or directly will step Rapid 5) the middle material fine powder collected is transported to dry in integrated fluidized bed, cooling, agglomeration built in multi-temperature zone and is granulated, acquisition finished product Micro/nano level microcapsule granule.
2. a kind of preparation method of air-flow nanometer according to claim 1, it is characterised in that: the built-in integration of the multi-temperature zone Formula fluidized bed includes high-temperature region, middle warm area, low-temperature space, and the micro/nano level microcapsule granule dry for the first time is added sequentially to mostly warm Integrated fluidized bed high temperature area, middle warm area, low-temperature space built in area, be set low-temperature space product exit collection, obtain at Product micro/nano level microcapsule granule.
3. a kind of preparation method of air-flow nanometer according to claim 2, it is characterised in that: the high-temperature region temperature is 300-380 DEG C, the middle warm area temperature is 200-260 DEG C, and the low-temperature space temperature is 80-100 DEG C.
4. a kind of preparation method of air-flow nanometer according to claim 1, it is characterised in that: the multi-stage spray drying tower It is 150-200 DEG C that upper end, which is passed through dry hot air temperature, and multi-stage spray drying tower upper end is discharged dry hot air temperature and is 60-100℃。
5. a kind of preparation method of air-flow nanometer according to claim 2, it is characterised in that: will directly be collected in step 5) Material fine powder when being transported to integrated fluidized bed built in multi-temperature zone, the material fine powder of collection is transported to integration built in multi-temperature zone High-temperature region in formula fluidized bed, or the material fine powder of collection is transported to the low-temperature space built in multi-temperature zone in integrated fluidized bed.
6. a kind of preparation method of air-flow nanometer according to claim 1, it is characterised in that: obtained in step 4) or step 6) The finished product micro/nano level microcapsule granule diameter obtained is 100nm-20um.
CN201910618487.2A 2019-07-10 2019-07-10 The preparation method of air-flow nanometer Withdrawn CN110227395A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201910618487.2A CN110227395A (en) 2019-07-10 2019-07-10 The preparation method of air-flow nanometer

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201910618487.2A CN110227395A (en) 2019-07-10 2019-07-10 The preparation method of air-flow nanometer

Publications (1)

Publication Number Publication Date
CN110227395A true CN110227395A (en) 2019-09-13

Family

ID=67854936

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201910618487.2A Withdrawn CN110227395A (en) 2019-07-10 2019-07-10 The preparation method of air-flow nanometer

Country Status (1)

Country Link
CN (1) CN110227395A (en)

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040108608A1 (en) * 2002-11-25 2004-06-10 Amorepacific Corporation Method for stabilizing active components using polyol/polymer microcapsule, and cosmetic composition containing the microcapsule
CN1803272A (en) * 2005-12-02 2006-07-19 杨第伦 Air bubble liquid membrane method for producing nanometer granule material
CN102908967A (en) * 2012-11-09 2013-02-06 北京泰克来尔科技有限公司 High-pressure high-shearing crystallization kettle, and application of high-pressure high-shearing crystallization kettle to clean preparation of layered composite metal hydroxide
CN103277985A (en) * 2013-06-04 2013-09-04 无锡市阳光干燥设备厂 Multistage spray and fluidized drying equipment
CN207405148U (en) * 2017-03-24 2018-05-25 清华大学 The preparation system of porous micro- ice cellula adhesiae dimensional culture carrier
CN108160000A (en) * 2017-12-25 2018-06-15 杭州鑫伟低碳技术研发有限公司 A kind of micro/nano level granulation preparation
CN108927080A (en) * 2018-10-11 2018-12-04 本溪恒康制药有限公司 The equipment for preparing lipid microspheres

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040108608A1 (en) * 2002-11-25 2004-06-10 Amorepacific Corporation Method for stabilizing active components using polyol/polymer microcapsule, and cosmetic composition containing the microcapsule
CN1803272A (en) * 2005-12-02 2006-07-19 杨第伦 Air bubble liquid membrane method for producing nanometer granule material
CN102908967A (en) * 2012-11-09 2013-02-06 北京泰克来尔科技有限公司 High-pressure high-shearing crystallization kettle, and application of high-pressure high-shearing crystallization kettle to clean preparation of layered composite metal hydroxide
CN103277985A (en) * 2013-06-04 2013-09-04 无锡市阳光干燥设备厂 Multistage spray and fluidized drying equipment
CN207405148U (en) * 2017-03-24 2018-05-25 清华大学 The preparation system of porous micro- ice cellula adhesiae dimensional culture carrier
CN108160000A (en) * 2017-12-25 2018-06-15 杭州鑫伟低碳技术研发有限公司 A kind of micro/nano level granulation preparation
CN108927080A (en) * 2018-10-11 2018-12-04 本溪恒康制药有限公司 The equipment for preparing lipid microspheres

Similar Documents

Publication Publication Date Title
CN103920299B (en) A kind of spray drying system of easily sticky wall material
CN204193911U (en) A kind of microcapsules spray-drying installation
CN103277985A (en) Multistage spray and fluidized drying equipment
CN111780495B (en) Closed cycle process for continuously producing vitamin D3 microcapsule powder
CN105651031B (en) A kind of rotary flashing drying equipment and rotary flashing drying method
CN100579879C (en) Delivery spray nozzle, polytetrafluoroethylene fine particle processing method and apparatus using the spray nozzle
CN102788488A (en) High-speed centrifugal drying method and drying system for implementing method
CN109734102A (en) The preparation method and its preparation facilities of silica micron ball
CN207913720U (en) A kind of system and device that nanoscale is granulated
CN202315347U (en) Centrifugal spray drying system with deduster
CN103820253B (en) Technique and the device of powdery MES particle is prepared in a kind of serialization
CN110227395A (en) The preparation method of air-flow nanometer
CN108160000B (en) Micro-nano-grade granulation preparation method
CN106390495B (en) A kind of air energy spray drying device
CN209060564U (en) A kind of spray drying production equipment of low-temperature SCR catalyst powder
CN100556545C (en) A kind of is the production method of the catalyst of active component with copper zinc
CN209237365U (en) A kind of Chinese medical spray drying system
CN214701468U (en) Spray drying equipment
CN204447350U (en) Drying spraying automated production equipment under cryogenic conditions
CN206867746U (en) A kind of multistage continuous drier for being used to dry powder body material
CN101059308A (en) Double-cone shape spray-drying tower body
CN104258784B (en) A kind of Swine blood protein separator
CN107101469A (en) A kind of drying system of nano-powder
CN206881162U (en) A kind of feed SDPP spray drying device
CN103127733A (en) Secondary high-efficient drying device for transforming medical liquid to solidified powder

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
WW01 Invention patent application withdrawn after publication

Application publication date: 20190913

WW01 Invention patent application withdrawn after publication