CN109019654A - A kind of preparation method and device of pencil carbonic acid strontium crystal - Google Patents
A kind of preparation method and device of pencil carbonic acid strontium crystal Download PDFInfo
- Publication number
- CN109019654A CN109019654A CN201811226211.1A CN201811226211A CN109019654A CN 109019654 A CN109019654 A CN 109019654A CN 201811226211 A CN201811226211 A CN 201811226211A CN 109019654 A CN109019654 A CN 109019654A
- Authority
- CN
- China
- Prior art keywords
- partitions
- precipitation tank
- crystal
- material trough
- added
- 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.)
- Granted
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
- C01F11/00—Compounds of calcium, strontium, or barium
- C01F11/18—Carbonates
- C01F11/186—Strontium or barium carbonate
- C01F11/187—Strontium carbonate
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2002/00—Crystal-structural characteristics
- C01P2002/70—Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data
- C01P2002/72—Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data by d-values or two theta-values, e.g. as X-ray diagram
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/01—Particle morphology depicted by an image
- C01P2004/03—Particle morphology depicted by an image obtained by SEM
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/60—Particles characterised by their size
- C01P2004/64—Nanometer sized, i.e. from 1-100 nanometer
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/80—Compositional purity
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Nanotechnology (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- General Physics & Mathematics (AREA)
- Physics & Mathematics (AREA)
- Crystallography & Structural Chemistry (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- Life Sciences & Earth Sciences (AREA)
- Geology (AREA)
- Inorganic Chemistry (AREA)
- Composite Materials (AREA)
- Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
Abstract
The present invention a kind of preparation method and device of pencil carbonic acid strontium crystal, in reaction unit, using six water strontium chlorides and ammonium hydrogen carbonate as reactant, gelatin is bionical inducer, prepares pencil carbonic acid strontium crystal.After completion of the reaction, through being filtered, washed, and in 105 DEG C of dry 1 h, the pencil carbonic acid strontium crystal being made of crystal bar is obtained.The reaction unit is made of No.1 material trough, precipitation tank and No. two material troughs.The diameter of crystal bar is the nm of 30 nm~50 in pencil strontium carbonate, and length is the nm of 200 nm~700;Product purity >=99%, yield are 96%~98%.Product of the present invention has purity is high, and yield is high, and diameter is small, and crystal draw ratio is big, and low in raw material price, method is simple, low energy consumption, the features such as being convenient for industrialized production.
Description
Technical field
The present invention a kind of preparation method and device of pencil carbonic acid strontium crystal, more particularly to one kind with six water strontium chlorides and
Ammonium hydrogen carbonate is reactant, with gelatin for bionical inducer, the method for preparation pencil carbonic acid strontium crystal.Particular technique neck of the present invention
Domain is the preparation of pencil carbonic acid strontium crystal.
Background technique
Strontium carbonate is important one of inorganic basic chemical raw materials, it is the important additives of electronic component, extensive
Applied to manufacture optical glass, high dielectric material, chemical sensor catalyst etc., purposes is throughout light industry, electronic information, chemical industry etc.
More than ten of industry and field, tool have been widely used.The application of strontium carbonate product is related with the size of its particle and pattern, so
Synthesis form, size and structure are an important research direction of modern material science by the inorganic material of artificial adjustment.
In past decades, people have attempted many methods to synthesize the carbonic acid strontium crystal of different-shape, main method
For liquid phase reactor method, including hypergravity reaction precipitation, microwave reaction method, biomineralization method etc., hypergravity reaction is benefit
With Elevated Gravity is provided under conditions of high speed rotation, the specific surface area synthetic crystal nano particle of filler is improved, but this side
Method must react inside high gravity rotating packed bed, the high requirements on the equipment, so at high cost;Microwave reaction method utilizes non-thermal
The heating method of delivery type, heats reaction, but provides thermal energy to reaction and then need to consume other more energies, does not meet
The characteristics of low power consuming in present Green Chemistry;Biomineralization method is that the biological enzyme generated using the metabolism of microorganism is passed through
The CO that enzymeization effect generates3 2-With Sr2+Reaction generates carbonic acid strontium crystal, but what the method used is microorganism living, so
Poor controllability.Not only there is disadvantage mentioned above in existing method, but also general cost of material is relatively expensive, the condition of control is more,
Trivial operations, the pencil crystal being generally made of crystal bar are required to complete under heating conditions, consume other energy.
The present invention is at high cost in existing method, the problems such as poor controllability, trivial operations, greenization is poor, proposes one kind
High-purity, high yield, diameter is small, and crystal draw ratio is big, low in raw material price, and technology stability is high, easy to operate, and method is easy
It is easy, low energy consumption, the preparation method for the pencil carbonic acid strontium crystal being convenient for industrialized production.
Summary of the invention
The purpose of the present invention is at high cost in existing method, the problems such as poor controllability, trivial operations, greenization is poor, mentions
A kind of high-purity out, high yield, diameter is small, and crystal draw ratio is big, low in raw material price, and technology stability is high, easy to operate, side
Method is simple and easy to do, low energy consumption, the preparation method for the pencil carbonic acid strontium crystal being convenient for industrialized production.
The present invention a kind of preparation method and device of pencil carbonic acid strontium crystal are reaction with six water strontium chlorides and ammonium hydrogen carbonate
Raw material, gelatin are bionical inducer, prepare pencil carbonic acid strontium crystal.
The preparation method specifically: the No.1 valve (4) being first turned in reaction unit and No. two valves (6) are pressed
It is six water strontium chlorides: ammonium hydrogen carbonate=1 according to mass ratio: 1.0~1.1, divide 3 batches and be added in reaction unit, 3 batches of reactants are each
From quality remain unchanged.First six water strontium chloride is added to No.1 material trough (10) by No.1 feed inlet (1), leads to simultaneously
It crosses No. two feed inlets (9) and first ammonium hydrogen carbonate is added to No. two material troughs (12), mass fraction is added in precipitation tank (11)
For 0.020% gelatin solution to assigned scale;Under room temperature, 24 h of reaction are stood;It is six water strontium chlorides according to mass ratio:
Ammonium hydrogen carbonate=1: 1.0~1.1, six water strontium chloride of second batch is added to No.1 material trough (10) by No.1 feed inlet (1), is led to
It crosses No. two feed inlets (9) and second batch ammonium hydrogen carbonate is added to No. two material troughs (12);Under room temperature, 24 h of reaction are stood;It presses
It is six water strontium chlorides: ammonium hydrogen carbonate=1 according to mass ratio: 1.0~1.1, six water chlorinations of third batch are added by No.1 feed inlet (1)
Third batch ammonium hydrogen carbonate is added to No. two material troughs (12) to No.1 material trough (10), by No. two feed inlets (9) in strontium, stands anti-
After answering 48 h, No.1 valve (4) and No. two valves (6) are closed, the product in precipitation tank (11) is filtered, are distilled water washing 3 times,
In 105 DEG C of dry 1 h, the pencil carbonic acid strontium crystal being made of crystal bar is obtained;The diameter of crystal bar is the nm of 30 nm~50, and length is
The nm of 200 nm~700, product purity >=99%, yield are 96%~98%;
The reaction unit are as follows: reaction unit is made of No.1 material trough (10), precipitation tank (11) and No. two material troughs (12);
No.1 material trough (10), precipitation tank (11) and the length and width of No. two material troughs (12) and height are 100 cm, 30 cm, 50 cm, body
Product is 150 L;No.1 material trough (10) is provided with No.1 feed inlet (1), No.1 partition (2) and No. two partitions (3);No.1 into
Material mouth (1) and the interface height of No.1 material trough (10) are 10 cm;A length of 35 cm of No.1 partition (2), width are 30 cm;Two
Number a length of 45 cm of partition (3), width are 30 cm;The distance between No.1 partition (2) and No.1 feed inlet (1) side panel are 40
Cm is 30 cm between No.1 partition (2) and No. two partitions (3), edge and edge on No.1 material trough (10) on No.1 partition (2)
The distance between be 15 cm, the lower edge of No. two partitions (3) with No.1 material trough (10) bottom at a distance from be 5 cm;Precipitation tank
(11) No. three partitions (5), a length of 45 cm of No. three partitions (5) are provided with, width is 30 cm;No. three partitions (5) are away from precipitation tank
(11) 50 cm of two sides, the lower edge of No. three partitions (5) are 5 cm at a distance from precipitation tank (11) bottom;No. two material troughs (12) set
It is equipped with No. two feed inlets (9), No. four partitions (7) and No. five partitions (8);No. two feed inlets (9) connect with No. two material trough (12)
Open height is 10 cm;A length of 45 cm of No. four partitions (7), width are 30 cm;The length of No. five partitions (8) is 35 cm, wide
For 30 cm;The distance between No. five partitions (8) and No. two feed inlet (9) side panels are 40 cm, No. four partitions (7) with No. five every
Be 30 cm between plate (8), on No. five partitions (8) along on No. two material troughs (12) along the distance between be 15 cm, No. four
The lower edge of partition (7) is 5 cm at a distance from No. two material trough (12) bottoms;No.1 material trough (10) and precipitation tank (11) it
Between detachable connecting pipe is installed, No.1 valve (4) are provided on pipeline;Precipitation tank (11) and No. two material troughs (12) with
Between detachable connecting pipe is installed, No. two valves (6) are provided on pipeline.
Beneficial effects of the present invention: 1) with high purity.The pencil carbonic acid strontium crystal being made of prepared by the present invention crystal bar
Purity >=99%.2) yield is high.Yield is 96%~98%.3) diameter is small, and crystal draw ratio is big.The diameter of crystal bar is 30 nm~50
Nm, length are the nm of 200 nm~700, and draw ratio range is 4~25.3) production cost is low.Low in raw material price, it is used
Raw material is six water strontium chlorides, ammonium hydrogen carbonate and gelatin, and three kinds of raw materials are cheap and easy to get.4) technology stability is high.Response parameter
Easy to control, extraneous factor is very small to the interference of reaction;Only need control reaction in bionical inducer concentrations and plus raw material when
Between, the complete pencil carbonic acid strontium crystal of growth and development can be obtained.5) low energy consumption, method is simple.Raw material, room need to only be added
Reaction, filtering are stood under the conditions of temperature, drying can be obtained the pencil carbonic acid strontium crystal being made of crystal bar, be convenient for industrialized production.
Detailed description of the invention
Fig. 1 is the SEM figure of pencil carbonic acid strontium crystal prepared by the present invention;
Fig. 2 is the XRD diagram of pencil carbonic acid strontium crystal prepared by the present invention;
Fig. 3 is the reaction unit schematic diagram of pencil carbonic acid strontium crystal prepared by the present invention;
Wherein, 1, No.1 feed inlet;2, No.1 partition;3, No. two partitions;4, No.1 valve;5, No. three partitions;6, No. two valves
Door;7, No. four partitions;8, No. five partitions;9, No. two feed inlets;10, No.1 material trough;11, precipitation tank;12, No. two material troughs.
Specific embodiment
Combined with specific embodiments below to a kind of preparation method and device work of pencil carbonic acid strontium crystal of the present invention
It further describes.
Embodiment 1
0.60 kg is added by No.1 feed inlet (1) in the No.1 valve (4) being first turned in reaction unit and No. two valves (6)
0.66 kg ammonium hydrogen carbonate is added to No. two material troughs to No.1 material trough (10), by No. two feed inlets (9) in six water strontium chlorides
(12), mass fraction is added in precipitation tank as 0.020% gelatin solution to assigned scale;Under room temperature, reaction 24 is stood
h;0.60 kg, six water strontium chloride is added to No.1 material trough (10) by No.1 feed inlet (1), is added by No. two feed inlets (9)
Enter 0.66 kg ammonium hydrogen carbonate to No. two material troughs (12);Under room temperature, 24 h of reaction are stood, are added by No.1 feed inlet (1)
Enter 0.60 kg, six water strontium chloride to No.1 material trough (10), 0.66 kg ammonium hydrogen carbonate is added to two by No. two feed inlets (9)
Number material trough (12) stands 48 h of reaction under room temperature;No.1 valve (4) and No. two valves (6) are closed, it will be in precipitation tank
Product filtering, distill water washing 3 times, in 105 DEG C of dry 1 h, pencil carbonic acid strontium crystal that acquisition is made of crystal bar.Crystal bar
Diameter is the nm of 30 nm~50, and length is the nm of 200 nm~700, product purity >=99%, yield 97%.
The reaction unit are as follows: reaction unit is made of No.1 material trough (10), precipitation tank and No. two material troughs (12).
No.1 material trough (10), precipitation tank and the length and width of No. two material troughs (12) and height are 100 cm, 30 cm, 50 cm, and volume is equal
For 150 L.No.1 material trough (10) is provided with No.1 feed inlet (1), No.1 partition (2) and No. two partitions (3);No.1 feed inlet
It (1) is 10 cm with the interface height of No.1 material trough (10);A length of 35 cm of No.1 partition (2), width are 30 cm;No. two every
A length of 45 cm of plate (3), width are 30 cm;Between No.1 partition (2) and No.1 feed inlet (1) side panel of No.1 material trough (10)
Distance be 40 cm, be 30 cm between No.1 partition (2) and No. two partitions (3), edge and No.1 material on No.1 partition (2)
The distance between edge is 15 cm on slot (10), and the lower edge of No. two partitions (3) is 5 at a distance from No.1 material trough (10) bottom
cm.Precipitation tank is provided with No. three partitions (5), a length of 45 cm of No. three partitions (5), and width is 30 cm;No. three partitions (5) are away from precipitating
50 cm of slot two sides, the lower edge of No. three partitions (5) are 5 cm at a distance from precipitating trench bottom.No. two material troughs (12) are provided with two
Number feed inlet (9), No. four partitions (7) and No. five partitions (8);The interface height of No. two feed inlets (9) and No. two material troughs (12)
For 10 cm;A length of 45 cm of No. four partitions (7), width are 30 cm;The length of No. five partitions (8) is 35 cm, and wide is 30
cm;The distance between No. two feed inlet (9) side panels of No. five partitions (8) and No. two material troughs (12) are 40 cm, No. four partitions
It (7) is 30 cm between No. five partitions (8), edge is on No. five partitions (8) with the distance between edge on No. two material troughs (12)
15 cm, the lower edge of No. four partitions (7) are 5 cm at a distance from No. two material trough (12) bottoms.No.1 material trough (10) and heavy
Detachable connecting pipe is installed between the slot of shallow lake, No.1 valve (4) are provided on pipeline;In precipitation tank and No. two material troughs (12)
Detachable connecting pipe is installed between, No. two valves (6) are provided on pipeline.
Embodiment 2
0.60 kg is added by No.1 feed inlet (1) in the No.1 valve (4) being first turned in reaction unit and No. two valves (6)
0.64 kg ammonium hydrogen carbonate is added to No. two material troughs to No.1 material trough (10), by No. two feed inlets (9) in six water strontium chlorides
(12), mass fraction is added in precipitation tank as 0.020% gelatin solution to assigned scale;Under room temperature, reaction 24 is stood
h;0.60 kg, six water strontium chloride is added to No.1 material trough (10) by No.1 feed inlet (1), is added by No. two feed inlets (9)
Enter 0.64 kg ammonium hydrogen carbonate to No. two material troughs (12);Under room temperature, 24 h of reaction are stood, are added by No.1 feed inlet (1)
Enter 0.60 kg, six water strontium chloride to No.1 material trough (10), 0.64 kg ammonium hydrogen carbonate is added to two by No. two feed inlets (9)
Number material trough (12) stands 48 h of reaction under room temperature;No.1 valve (4) and No. two valves (6) are closed, it will be in precipitation tank
Product filtering, distill water washing 3 times, in 105 DEG C of dry 1 h, pencil carbonic acid strontium crystal that acquisition is made of crystal bar.Crystal bar
Diameter is the nm of 30 nm~50, and length is the nm of 200 nm~700, product purity >=99%, yield 96%.
The reaction unit are as follows: reaction unit is made of No.1 material trough (10), precipitation tank and No. two material troughs (12).
No.1 material trough (10), precipitation tank and the length and width of No. two material troughs (12) and height are 100 cm, 30 cm, 50 cm, and volume is equal
For 150 L.No.1 material trough (10) is provided with No.1 feed inlet (1), No.1 partition (2) and No. two partitions (3);No.1 feed inlet
It (1) is 10 cm with the interface height of No.1 material trough (10);A length of 35 cm of No.1 partition (2), width are 30 cm;No. two every
A length of 45 cm of plate (3), width are 30 cm;Between No.1 partition (2) and No.1 feed inlet (1) side panel of No.1 material trough (10)
Distance be 40 cm, be 30 cm between No.1 partition (2) and No. two partitions (3), edge and No.1 material on No.1 partition (2)
The distance between edge is 15 cm on slot (10), and the lower edge of No. two partitions (3) is 5 at a distance from No.1 material trough (10) bottom
cm.Precipitation tank is provided with No. three partitions (5), a length of 45 cm of No. three partitions (5), and width is 30 cm;No. three partitions (5) are away from precipitating
50 cm of slot two sides, the lower edge of No. three partitions (5) are 5 cm at a distance from precipitating trench bottom.No. two material troughs (12) are provided with two
Number feed inlet (9), No. four partitions (7) and No. five partitions (8);The interface height of No. two feed inlets (9) and No. two material troughs (12)
For 10 cm;A length of 45 cm of No. four partitions (7), width are 30 cm;The length of No. five partitions (8) is 35 cm, and wide is 30
cm;The distance between No. two feed inlet (9) side panels of No. five partitions (8) and No. two material troughs (12) are 40 cm, No. four partitions
It (7) is 30 cm between No. five partitions (8), edge is on No. five partitions (8) with the distance between edge on No. two material troughs (12)
15 cm, the lower edge of No. four partitions (7) are 5 cm at a distance from No. two material trough (12) bottoms.No.1 material trough (10) and heavy
Detachable connecting pipe is installed between the slot of shallow lake, No.1 valve (4) are provided on pipeline;In precipitation tank and No. two material troughs (12)
Detachable connecting pipe is installed between, No. two valves (6) are provided on pipeline.
Embodiment 3
0.60 kg is added by No.1 feed inlet (1) in the No.1 valve (4) being first turned in reaction unit and No. two valves (6)
0.68 kg ammonium hydrogen carbonate is added to No. two material troughs to No.1 material trough (10), by No. two feed inlets (9) in six water strontium chlorides
(12), mass fraction is added in precipitation tank as 0.020% gelatin solution to assigned scale;Under room temperature, reaction 24 is stood
h;0.60 kg, six water strontium chloride is added to No.1 material trough (10) by No.1 feed inlet (1), is added by No. two feed inlets (9)
Enter 0.68 kg ammonium hydrogen carbonate to No. two material troughs (12);Under room temperature, 24 h of reaction are stood;Added by No.1 feed inlet (1)
Enter 0.60 kg, six water strontium chloride to No.1 material trough (10), 0.68 kg ammonium hydrogen carbonate is added to two by No. two feed inlets (9)
Number material trough (12) stands 48 h of reaction under room temperature;No.1 valve (4) and No. two valves (6) are closed, it will be in precipitation tank
Product filtering, distill water washing 3 times, in 105 DEG C of dry 1 h, pencil carbonic acid strontium crystal that acquisition is made of crystal bar.Crystal bar
Diameter is the nm of 30 nm~50, and length is the nm of 200 nm~700, product purity >=99%, yield 98%.
The reaction unit are as follows: reaction unit is made of No.1 material trough (10), precipitation tank and No. two material troughs (12).
No.1 material trough (10), precipitation tank and the length and width of No. two material troughs (12) and height are 100 cm, 30 cm, 50 cm, and volume is equal
For 150 L.No.1 material trough (10) is provided with No.1 feed inlet (1), No.1 partition (2) and No. two partitions (3);No.1 feed inlet
It (1) is 10 cm with the interface height of No.1 material trough (10);A length of 35 cm of No.1 partition (2), width are 30 cm;No. two every
A length of 45 cm of plate (3), width are 30 cm;Between No.1 partition (2) and No.1 feed inlet (1) side panel of No.1 material trough (10)
Distance be 40 cm, be 30 cm between No.1 partition (2) and No. two partitions (3), edge and No.1 material on No.1 partition (2)
The distance between edge is 15 cm on slot (10), and the lower edge of No. two partitions (3) is 5 at a distance from No.1 material trough (10) bottom
cm.Precipitation tank is provided with No. three partitions (5), a length of 45 cm of No. three partitions (5), and width is 30 cm;No. three partitions (5) are away from precipitating
50 cm of slot two sides, the lower edge of No. three partitions (5) are 5 cm at a distance from precipitating trench bottom.No. two material troughs (12) are provided with two
Number feed inlet (9), No. four partitions (7) and No. five partitions (8);The interface height of No. two feed inlets (9) and No. two material troughs (12)
For 10 cm;A length of 45 cm of No. four partitions (7), width are 30 cm;The length of No. five partitions (8) is 35 cm, and wide is 30
cm;The distance between No. two feed inlet (9) side panels of No. five partitions (8) and No. two material troughs (12) are 40 cm, No. four partitions
It (7) is 30 cm between No. five partitions (8), edge is on No. five partitions (8) with the distance between edge on No. two material troughs (12)
15 cm, the lower edge of No. four partitions (7) are 5 cm at a distance from No. two material trough (12) bottoms.No.1 material trough (10) and heavy
Detachable connecting pipe is installed between the slot of shallow lake, No.1 valve (4) are provided on pipeline;In precipitation tank and No. two material troughs (12)
Detachable connecting pipe is installed between, No. two valves (6) are provided on pipeline.
Claims (1)
1. a kind of preparation method and device of pencil carbonic acid strontium crystal, it is characterised in that: the preparation method is with six water chlorinations
Strontium and ammonium hydrogen carbonate are reactant, and gelatin is bionical inducer, prepare pencil carbonic acid strontium crystal;
The preparation method specifically: the No.1 valve (4) being first turned in reaction unit and No. two valves (6), according to matter
Amount is than being six water strontium chlorides: ammonium hydrogen carbonate=1: 1.0~1.1, divide 3 batches and be added in reaction unit, 3 batches of reactants are respective
Quality remains unchanged;First six water strontium chloride is added to No.1 material trough (10) by No.1 feed inlet (1), while passing through two
First ammonium hydrogen carbonate is added to No. two material troughs (12) in number feed inlet (9), and mass fraction is added in precipitation tank (11) and is
0.020% gelatin solution is to assigned scale;Under room temperature, 24 h of reaction are stood;It is six water strontium chlorides: carbon according to mass ratio
Sour hydrogen ammonium=1: 1.0~1.1, six water strontium chloride of second batch is added to No.1 material trough (10) by No.1 feed inlet (1), is passed through
Second batch ammonium hydrogen carbonate is added to No. two material troughs (12) in No. two feed inlets (9);Under room temperature, 24 h of reaction are stood;According to
Mass ratio is six water strontium chlorides: ammonium hydrogen carbonate=1: 1.0~1.1, six water strontium chlorides of third batch are added by No.1 feed inlet (1)
To No.1 material trough (10), third batch ammonium hydrogen carbonate is added to No. two material troughs (12) by No. two feed inlets (9), stands reaction
After 48 h, No.1 valve (4) and No. two valves (6) are closed, the product in precipitation tank (11) is filtered, are distilled water washing 3 times, in
105 DEG C of 1 h of drying obtain the pencil carbonic acid strontium crystal being made of crystal bar;The diameter of crystal bar is the nm of 30 nm~50, and length is
The nm of 200 nm~700, product purity >=99%, yield are 96%~98%;
The reaction unit are as follows: reaction unit is made of No.1 material trough (10), precipitation tank (11) and No. two material troughs (12);
No.1 material trough (10), precipitation tank (11) and the length and width of No. two material troughs (12) and height are 100 cm, 30 cm, 50 cm, body
Product is 150 L;No.1 material trough (10) is provided with No.1 feed inlet (1), No.1 partition (2) and No. two partitions (3);No.1 into
Material mouth (1) and the interface height of No.1 material trough (10) are 10 cm;A length of 35 cm of No.1 partition (2), width are 30 cm;Two
Number a length of 45 cm of partition (3), width are 30 cm;The distance between No.1 partition (2) and No.1 feed inlet (1) side panel are 40
Cm is 30 cm between No.1 partition (2) and No. two partitions (3), edge and edge on No.1 material trough (10) on No.1 partition (2)
The distance between be 15 cm, the lower edge of No. two partitions (3) with No.1 material trough (10) bottom at a distance from be 5 cm;Precipitation tank
(11) No. three partitions (5), a length of 45 cm of No. three partitions (5) are provided with, width is 30 cm;No. three partitions (5) are away from precipitation tank
(11) 50 cm of two sides, the lower edge of No. three partitions (5) are 5 cm at a distance from precipitation tank (11) bottom;No. two material troughs (12) set
It is equipped with No. two feed inlets (9), No. four partitions (7) and No. five partitions (8);No. two feed inlets (9) connect with No. two material trough (12)
Open height is 10 cm;A length of 45 cm of No. four partitions (7), width are 30 cm;The length of No. five partitions (8) is 35 cm, wide
For 30 cm;The distance between No. five partitions (8) and No. two feed inlet (9) side panels are 40 cm, No. four partitions (7) with No. five every
Be 30 cm between plate (8), on No. five partitions (8) along on No. two material troughs (12) along the distance between be 15 cm, No. four
The lower edge of partition (7) is 5 cm at a distance from No. two material trough (12) bottoms;No.1 material trough (10) and precipitation tank (11) it
Between detachable connecting pipe is installed, No.1 valve (4) are provided on pipeline;Precipitation tank (11) and No. two material troughs (12) with
Between detachable connecting pipe is installed, No. two valves (6) are provided on pipeline.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201811226211.1A CN109019654B (en) | 2018-10-22 | 2018-10-22 | Preparation method of beam-shaped strontium carbonate crystal |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201811226211.1A CN109019654B (en) | 2018-10-22 | 2018-10-22 | Preparation method of beam-shaped strontium carbonate crystal |
Publications (2)
Publication Number | Publication Date |
---|---|
CN109019654A true CN109019654A (en) | 2018-12-18 |
CN109019654B CN109019654B (en) | 2020-04-28 |
Family
ID=64613540
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201811226211.1A Expired - Fee Related CN109019654B (en) | 2018-10-22 | 2018-10-22 | Preparation method of beam-shaped strontium carbonate crystal |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN109019654B (en) |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105271322A (en) * | 2015-09-28 | 2016-01-27 | 辽宁工程技术大学 | Preparation method of fascicular magnesium carbonate trihydrate crystals |
CN105836780A (en) * | 2016-03-28 | 2016-08-10 | 余国礼 | Method of converting celestite into strontium carbonate under cavitation effect |
CN106927492A (en) * | 2015-12-30 | 2017-07-07 | 吴礼秀 | A kind of high-purity strontium salt preparation method |
CN107601543A (en) * | 2017-10-28 | 2018-01-19 | 李志强 | Strontium carbonate and its production method |
CN108675335A (en) * | 2018-09-03 | 2018-10-19 | 南昌航空大学 | A kind of bionical method for preparing carbonic acid strontium crystal |
-
2018
- 2018-10-22 CN CN201811226211.1A patent/CN109019654B/en not_active Expired - Fee Related
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105271322A (en) * | 2015-09-28 | 2016-01-27 | 辽宁工程技术大学 | Preparation method of fascicular magnesium carbonate trihydrate crystals |
CN106927492A (en) * | 2015-12-30 | 2017-07-07 | 吴礼秀 | A kind of high-purity strontium salt preparation method |
CN105836780A (en) * | 2016-03-28 | 2016-08-10 | 余国礼 | Method of converting celestite into strontium carbonate under cavitation effect |
CN107601543A (en) * | 2017-10-28 | 2018-01-19 | 李志强 | Strontium carbonate and its production method |
CN108675335A (en) * | 2018-09-03 | 2018-10-19 | 南昌航空大学 | A kind of bionical method for preparing carbonic acid strontium crystal |
Also Published As
Publication number | Publication date |
---|---|
CN109019654B (en) | 2020-04-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN103435096B (en) | Method for preparing size controllable nano stannic oxide | |
CN102002751B (en) | Method for directly synthesizing basic magnesium sulfate whiskers by brine | |
CN105836807B (en) | A kind of two-dimensional slice self assembly multilevel hierarchy tungsten oxide and its preparation method and application | |
CN104911688B (en) | The preparation method of anhydrous calcium sulfate whisker | |
CN110343259B (en) | Green fluorescent sandwich type zinc coordination polymer and preparation method and application thereof | |
CN108033475A (en) | A kind of method that micro- reaction prepares nano-calcium carbonate | |
CN103359773A (en) | Preparation method of zinc oxide nanorod | |
CN109731583A (en) | A kind of two-step method preparation Zn0.2Cd0.8The method of S/rGO composite material | |
CN110218333A (en) | A kind of pyridine methylene phosphonic acids nickel coordination polymer and its preparation method and application | |
CN105883910B (en) | A kind of perovskite SrTiO3The preparation method and product of porous nano particle | |
CN102718235A (en) | Method for preparing magnesium carbonate trihydrate crystal whiskers by adopting basic magnesium carbonate tetrahydrate | |
CN102703982A (en) | Method for preparing magnesium carbonate trihydrate crystal whisker by utilizing serpentine | |
CN103833086A (en) | Preparation method of flaky iron trioxide | |
CN101704532A (en) | Preparation method of zinc borate | |
CN102583273A (en) | Method for preparing nano nickel selenide with octahedral structure | |
CN109019654A (en) | A kind of preparation method and device of pencil carbonic acid strontium crystal | |
CN101805017B (en) | Preparation method of rutile type titanium dioxide nano particle | |
CN109133136B (en) | Method for preparing strontium carbonate crystal by room temperature self-diffusion | |
CN210973907U (en) | Micro-reaction device for preparing nano calcium carbonate | |
CN103623800B (en) | A kind of preparation method of titanium dioxide ball and products obtained therefrom | |
CN105197969B (en) | Preparation method of millimeter-grade radial nesquehonite crystal | |
CN102502846B (en) | Manganese molybdate material having micron rod structure assembled by nano sheets | |
CN102807485B (en) | Composite cobalt salt bonding promoter and preparation method thereof | |
CN101549874A (en) | Synthesizing process for improving generation rate of nano Y-shaped molecular sieve | |
CN105836799B (en) | A kind of method of regulation and control bromine oxygen bismuth exposure crystal face |
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 | ||
GR01 | Patent grant | ||
GR01 | Patent grant | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20200428 Termination date: 20201022 |
|
CF01 | Termination of patent right due to non-payment of annual fee |