CN1164503C - Multi-kernel high-molecular inorganic flocculant - Google Patents

Multi-kernel high-molecular inorganic flocculant Download PDF

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CN1164503C
CN1164503C CNB011317752A CN01131775A CN1164503C CN 1164503 C CN1164503 C CN 1164503C CN B011317752 A CNB011317752 A CN B011317752A CN 01131775 A CN01131775 A CN 01131775A CN 1164503 C CN1164503 C CN 1164503C
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component
acid soln
present
water
hydrochloric acid
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CN1343632A (en
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聪 王
王聪
郭秋宝
郑远洋
牛莉芹
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Tiancheng Environment Protection Science And Technology Development Co Ltd Xian
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Tiancheng Environment Protection Science And Technology Development Co Ltd Xian
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Abstract

The present invention relates to a multi-core inorganic macromolecular flocculant which is composed of 20% to 70% of A component, 10% to 60% of B component and 20% and 60% of C component, wherein the A component is a 10% to 30% hydrochloric acid solution composition of magnesium hydrochloride, ferrum hydrochloride and aluminium polyhydrochloride, or a 10% to 30% sulfuric acid solution composition of magnesium sulfate, ferrum sulfate and aluminium polymeric sulfate, the B component is aluminium polymeric hydrochloride or aluminium polymeric sulfate, and the C component is a 10% to 30% acidic solution of soluble silicate. The preparation method comprises: the A component is filled in a reaction kettle, the C component is filled in the reaction kettle to be heated at the temperature of 30 DEG C to 110 DEG C, the B component is filled in the reaction kettle, and the components are cooled into a paste form.

Description

Inorganic polymer flocculant
Technical field
The invention belongs to water, waste water, technical field of sewage, be specifically related to the flocculation or the precipitation of suspended impurity.
Background technology
Used flocculation agent mainly contains five big classes in the processing of trade effluent at present, comprises low-molecular inorganic flocculation agent, inorganic polymer flocculant, natural organic high-molecular flocculant, synthetic organic polymer flocculation agent, microbial flocculant.The low-molecular inorganic flocculation agent mainly contains ferrous sulfate, iron protochloride, Tai-Ace S 150, aluminium chlorohydroxide etc., inorganic polymer flocculant mainly contains polymerize aluminum chloride, bodied ferric sulfate, because the inorganic flocculating agent raw material sources are abundant, cost is low, easy to use, effect is obvious, occupy an leading position in flocculant product always.
However, still there are shortcomings such as consumption is big, flocculation rate is slow, performance is single, PH subject range is narrow, the low temperature result of use is bad in inorganic flocculating agent, very inapplicable as the sewage big to sewage quantity, that flow velocity is fast, very not obvious etc. to the tap water that contains heavy metal ion and wastewater treatment efficiency.
On the other hand, many flocculation agents are liquid, store in the tank filling usually and transportation, are not easy to transportation, and have intensive corrodibility to be easy to etching apparatus.For industrial sewage, oilfield sewage, contain heavy metal ion sewage processing very inapplicable.
Summary of the invention
One object of the present invention is to overcome the shortcoming of above-mentioned flocculation agent, provides that a kind of flocculation rate is fast, flco is closely knit, precipitate and separate efficient height, inorganic polymer flocculant that use range is wide.
Another object of the present invention is to provide the inorganic polymer flocculant that a kind of dissolution rate is fast, be convenient to storage and transport.
Further purpose of the present invention is to provide a kind of preparation method of inorganic polymer flocculant.
For achieving the above object, it is to be that raw material is made by following component and weight proportion for the solution that the present invention adopts:
The A component is the hydrochloride of Mg, the hydrochloride of Fe, 10~30% hydrochloric acid soln compositions of the polysalt hydrochlorate of Al, in its proportioning, the polysalt hydrochlorate of the hydrochloride of the hydrochloride of Mg: Fe: Al: the weight ratio of 10~30% hydrochloric acid solns is 1: 1~3: 1~3: 7~15, or the A component is the vitriol of Mg, the vitriol of Fe, 10~30% sulphuric acid soln compositions of the polymerised sulphur hydrochlorate of Al, in its proportioning, the polymerised sulphur hydrochlorate of the vitriol of the vitriol of Mg: Fe: Al: the weight ratio of 10~30% sulphuric acid solns is 1: 1~3: 1~3: 7~15, and the A components contents is 20~70%.
The B component is the polysalt hydrochlorate of Al or the polymerised sulphur hydrochlorate of Al, and its content is 10~60%.
The C component is 10~30% acidic solutions of soluble silicate, and its content is 20~60%.
The preferred weight proportioning of each raw material of the present invention is:
A component 20~50%
B component 20~60%
C component 20~30%
The optimum weight proportioning of each raw material of the present invention is:
A component 50%
B component 20%
C component 30%
C component soluble silicate of the present invention is water glass or potassium silicate, and the acidic solution of C component soluble silicate is hydrochloric acid soln or sulphuric acid soln.
In proportioning of the present invention, its main ingredient is that the content of the hydrochloride of the polysalt hydrochlorate of Al or polymerised sulphur hydrochlorate and iron or vitriol is higher, accelerated to be suspended in the flocculation rate of dirt in the sewage, increased the alumen ustum settling velocity, reduced sludge volume, and the flco after flocculation is closely knit, has added soluble silicate in proportioning of the present invention, improved the stability and the flocculating effect of product, be applicable to that low temperature uses.
Another solution that the present invention adopts is: this flocculation agent be shaped as ointment shape.
Its preparation method of solution that also has that the present invention adopts is: the A component of liquid state is joined in the reactor, add the C component with heater heats to 30 ℃~110 ℃, being stirred to agitator becomes homogeneous solution, add the B component then, stir with agitator again, make its uniform mixing, stop to stir cooling gradually and become the ointment shape, after quality control standards (QCS) check of the present invention, packing gets product of the present invention.
To join the preferred Heating temperature scope after the A component be 40 ℃~100 ℃ to the C component among the preparation method of the present invention.
To join the optimum heating temperature after the A component be 70 ℃ to the C component among the preparation method of the present invention.
Adopt the ointment shape flocculation agent of the present invention consignment test unit of preparation method of the present invention preparation to carry out simultaneous test, test-results shows: it is fast that flocculation agent of the present invention has flocculation rate.Flco is closely knit.Precipitate and separate efficient height.Advantages such as use range is wide can be used for the processing of oilfield sewage.The processing of trade effluent, and the removal of arsenic and fluorine is handled in the tap water.
Embodiment
The present invention is described in more detail below in conjunction with embodiment, but the invention is not restricted to these embodiment.
Embodiment 1
With production product 100kg of the present invention is that used raw material of example and proportioning thereof are:
The A component is the composition of magnesium chloride, iron(ic) chloride, polymerize aluminum chloride, 20% hydrochloric acid soln, magnesium chloride: iron(ic) chloride: polymerize aluminum chloride: 20% hydrochloric acid soln=1: 2: 2: 11 weight proportions are made hydrochloric acid soln 50kg, the B component is polymerize aluminum chloride 20kg, and the C component is water glass 20% hydrochloric acid soln 30kg.
Its preparation method is: the A component is joined in the reactor, add the C component, with heater heats to 70 ℃, being stirred to stirrer becomes homogeneous solution, add the B component then, restir makes its thorough mixing, places to be cooled to the ointment shape, after quality test, packing promptly gets product.
Embodiment 2
With production product 100kg of the present invention is that used raw material of example and proportioning thereof are:
The A component is the composition of magnesium chloride, iron(ic) chloride, polymerize aluminum chloride, 10% hydrochloric acid soln, magnesium chloride: iron(ic) chloride: polymerize aluminum chloride: 10% hydrochloric acid soln=1: 1: 1: 7 weight proportions are made hydrochloric acid soln 20kg, the B component is polymerize aluminum chloride 60kg, and the C component is water glass 20% hydrochloric acid soln 20kg.
Its preparation method is: the C component joins in the A component with heater heats to 30 ℃, and other technological process is identical with embodiment 1.
Embodiment 3
With production product 100kg of the present invention is that used raw material of example and proportioning thereof are:
The A component is the composition of magnesium chloride, iron(ic) chloride, polymerize aluminum chloride, 30% hydrochloric acid soln, magnesium chloride: iron(ic) chloride: polymerize aluminum chloride: 30% hydrochloric acid soln=1: 3: 3: 15 weight proportions are made hydrochloric acid soln 70kg, the B component is polymerize aluminum chloride 10kg, and the C component is water glass 30% hydrochloric acid soln 20kg.
Its preparation method is: the A component is joined in the reactor, add the C component, with heater heats to 110 ℃, other technological process is identical with embodiment 1.
Embodiment 4
With production product 100kg of the present invention is that used raw material of example and proportioning thereof are:
The A component is the composition of magnesium chloride, iron(ic) chloride, polymerize aluminum chloride, 10% hydrochloric acid soln, magnesium chloride: iron(ic) chloride: polymerize aluminum chloride: 10% hydrochloric acid soln=1: 3: 1: 11 weight proportions are made hydrochloric acid soln 30kg, the B component is polymerize aluminum chloride 10kg, and the C component is water glass 10% hydrochloric acid soln 60kg.
Its preparation method is identical with embodiment 1.
Embodiment 5
With production product 100kg of the present invention is that used raw material of example and proportioning thereof are:
The A component is the composition of magnesium chloride, iron(ic) chloride, polymerize aluminum chloride, 30% hydrochloric acid soln, magnesium chloride: iron(ic) chloride: polymerize aluminum chloride: 10% hydrochloric acid soln=1: 1: 3: 11 weight proportions are made hydrochloric acid soln 70kg, the B component is polymerize aluminum chloride 10kg, and the C component is water glass 10% hydrochloric acid soln 20kg.
Its preparation method is identical with embodiment 1.
Embodiment 6
With production product 100kg of the present invention is that used raw material of example and proportioning thereof are:
The A component is the composition of magnesium chloride, iron(ic) chloride, polymerize aluminum chloride, 10% hydrochloric acid soln, magnesium chloride: iron(ic) chloride: polymerize aluminum chloride: 10% hydrochloric acid soln=1: 1: 1: 7 weight proportions are made hydrochloric acid soln 20kg, the B component is polymerize aluminum chloride 60kg, and the C component is water glass 20% hydrochloric acid soln 20kg.
Its preparation method is identical with embodiment 1.
Embodiment 7
With production product 100kg of the present invention is that used raw material of example and proportioning thereof are:
The A component is the composition of magnesium chloride, iron(ic) chloride, polymerize aluminum chloride, 30% hydrochloric acid soln, magnesium chloride: iron(ic) chloride: polymerize aluminum chloride: 10% hydrochloric acid soln=1: 3: 3: 15 weight proportions are made hydrochloric acid soln 30kg, the B component is polymerize aluminum chloride 10kg, and the C component is water glass 10% hydrochloric acid soln 60kg.
Its preparation method is identical with embodiment 1.
Embodiment 8
With production product 100kg of the present invention is that used raw material of example and proportioning thereof are:
The A component is the composition of magnesium chloride, iron(ic) chloride, polymerize aluminum chloride, 30% hydrochloric acid soln, magnesium chloride: iron(ic) chloride: polymerize aluminum chloride: 10% hydrochloric acid soln=1: 3: 1: 11 weight proportions are made hydrochloric acid soln 70kg, the B component is polymerize aluminum chloride 10kg, and the C component is water glass 30% hydrochloric acid soln 20kg.
Its preparation method is identical with embodiment 2.
Embodiment 9
With production product 100kg of the present invention is that used raw material of example and proportioning thereof are:
The A component is the composition of magnesium chloride, iron(ic) chloride, polymerize aluminum chloride, 10% hydrochloric acid soln, magnesium chloride: iron(ic) chloride: polymerize aluminum chloride: 10% hydrochloric acid soln=1: 1: 3: 11 weight proportions are made hydrochloric acid soln 20kg, the B component is polymerize aluminum chloride 60kg, and the C component is water glass 10% hydrochloric acid soln 20kg.
Its preparation method is identical with embodiment 1.
Embodiment 10
With production product 100kg of the present invention is that used raw material of example and proportioning thereof are:
The A component is the composition of sal epsom, ferric sulfate, polyaluminium sulfate, 20% sulphuric acid soln, sal epsom: ferric sulfate: polyaluminium sulfate: 20% sulphuric acid soln=1: 2: 2: 11 weight proportions are made sulphuric acid soln 50kg, the B component is polyaluminium sulfate 20kg, and the C component is water glass 20% sulphuric acid soln 30kg.
Its preparation method is identical with embodiment 1.
Embodiment 11
With production product 100kg of the present invention is that used raw material of example and proportioning thereof are:
The A component is the composition of sal epsom, ferric sulfate, polyaluminium sulfate, 10% sulphuric acid soln, sal epsom: ferric sulfate: polyaluminium sulfate: 10% sulphuric acid soln=1: 1: 1: 7 weight proportions are made sulphuric acid soln 20kg, the B component is polyaluminium sulfate 60kg, and the C component is water glass 20% sulphuric acid soln 20kg.
Its preparation method is identical with embodiment 2.
Embodiment 12
With production product 100kg of the present invention is that used raw material of example and proportioning thereof are:
The A component is the composition of sal epsom, ferric sulfate, polyaluminium sulfate, 30% sulphuric acid soln, sal epsom: ferric sulfate: polyaluminium sulfate: 30% sulphuric acid soln=1: 3: 3: 15 weight proportions are made sulphuric acid soln 70kg, the B component is polyaluminium sulfate 10kg, and the C component is water glass 20% sulphuric acid soln 20kg.
Its preparation method is identical with embodiment 3.
Embodiment 13
The A component is the composition of sal epsom, ferric sulfate, polyaluminium sulfate, 10% sulphuric acid soln, sal epsom: ferric sulfate: polyaluminium sulfate: 10% sulphuric acid soln=1: 3: 1: 11 weight proportions are made sulphuric acid soln 30kg, the B component is polyaluminium sulfate 10kg, and the C component is water glass 10% sulphuric acid soln 60kg.
Its preparation method is identical with embodiment 1.
Embodiment 14
With production product 100kg of the present invention is that used raw material of example and proportioning thereof are:
The A component is the composition of sal epsom, ferric sulfate, polyaluminium sulfate, 30% sulphuric acid soln, sal epsom: ferric sulfate: polyaluminium sulfate: 10% sulphuric acid soln=1: 1: 3: 11 weight proportions are made sulphuric acid soln 70kg, the B component is polyaluminium sulfate 10kg, and the C component is water glass 10% solution 20kg.
Its preparation method is identical with embodiment 1.
Embodiment 15
With production product 100kg of the present invention is that used raw material of example and proportioning thereof are:
The A component is the composition of sal epsom, ferric sulfate, polyaluminium sulfate, 10% sulphuric acid soln, sal epsom: ferric sulfate: polyaluminium sulfate: 10% sulphuric acid soln=1: 1: 1: 7 weight proportions are made sulphuric acid soln 70kg, the B component is polyaluminium sulfate 10kg, and the C component is water glass 20% sulphuric acid soln 20kg.
Its preparation method is identical with embodiment 1.
Embodiment 16
With production product 100kg of the present invention is that used raw material of example and proportioning thereof are:
The A component is the composition of sal epsom, ferric sulfate, polyaluminium sulfate, 30% sulphuric acid soln, sal epsom: ferric sulfate: polyaluminium sulfate: 10% sulphuric acid soln=1: 3: 3: 15 weight proportions are made sulphuric acid soln 30kg, the B component is polyaluminium sulfate 10kg, and the C component is water glass 10% sulphuric acid soln 60kg.
Its preparation method is identical with embodiment 1.
Embodiment 17
With production product 100kg of the present invention is that used raw material of example and proportioning thereof are:
The A component is the composition of sal epsom, ferric sulfate, polyaluminium sulfate, 30% sulphuric acid soln, sal epsom: ferric sulfate: polyaluminium sulfate: 10% sulphuric acid soln=1: 3: 1: 11 weight proportions are made sulphuric acid soln 70kg, the B component is polyaluminium sulfate 10kg, and the C component is water glass 30% sulphuric acid soln 20kg.
Its preparation method is identical with embodiment 1.
Embodiment 18
With production product 100kg of the present invention is that used raw material of example and proportioning thereof are:
The A component is the composition of sal epsom, ferric sulfate, polyaluminium sulfate, 10% sulphuric acid soln, sal epsom: ferric sulfate: polyaluminium sulfate: 10% sulphuric acid soln=1: 1: 3: 11 weight proportions are made sulphuric acid soln 20kg, the B component is polyaluminium sulfate 60kg, and the C component is water glass 10% sulphuric acid soln 20kg.
Its preparation method is identical with embodiment 1.
Embodiment 19
C component water glass also can adopt potassium silicate in above embodiment 1~18, and its weight is identical with water glass among the corresponding embodiment, and the preparation method is identical with the preparation method of corresponding embodiment.
In order to verify the beneficial effect of flocculation agent of the present invention, the applicant adopts flocculation agent of the present invention (name is called the XN21-DW multi-kernel high-molecular inorganic flocculant during test) the consignment test unit of the embodiment of the invention 1 preparation to carry out simultaneous test, and test situation is as follows:
One, flocculation agent of the present invention (name is called the XN21-DW multi-kernel high-molecular inorganic flocculant during test) is tested different water body flocculating effects
1, test sample
Test sample: flocculation agent of the present invention
Simultaneous test sample: polymerize aluminum chloride, bodied ferric sulfate
2, test water sample
Tap water pipe network end, High-Tech Development Zone, 1# Xi'an is water slightly
Shenmu County, 2# Shaanxi red alkali mire lake water
Yantai, 3# Shandong seawater
3, test apparatus
50ml volumetric flask, stopwatch.
4, test method: get the 50ml water sample and move in the volumetric flask, add 1ml flocculation agent of the present invention, clock to the alumen ustum generation time.
5, test-results
Test-results sees Table 1.
Table 1 flocculation agent of the present invention and polymerize aluminum chloride and bodied ferric sulfate treating water be table as a result
Water sample Flocculant concentration Polymerize aluminum chloride Bodied ferric sulfate Flocculation agent of the present invention
Tap water 10% 20 seconds Do not react in 60 seconds 15 seconds
Lake water 10% Went up lower leaf in 15 seconds 16 seconds not stratified 8 seconds lower floors
Lake water 1% 30 seconds upper stratas Went up lower leaf in 22 seconds 6 seconds lower floors
Seawater 1% 26 seconds 60 seconds not stratified 16 seconds
6, conclusion (of pressure testing):
Flocculation agent of the present invention and polymerize aluminum chloride have throwing out to tap water, lake water, seawater, and bodied ferric sulfate does not have throwing out to tap water, seawater.Flocculation scope: flocculation agent>polymerize aluminum chloride of the present invention>bodied ferric sulfate.Flocculation agent of the present invention has the flocculating effect of various water bodies, multiple water quality.
Two, flocculation agent of the present invention (name is called the XN21-DW multi-kernel high-molecular inorganic flocculant during test) was tested the alumen ustum rise time
Test objective: more various flocculation agent alumen ustum formation speeds.
Use instrument and test method: same.Test-results: test-results sees Table 2, table 3.
The different water sample alumen ustum rise time tables of table 2
Flocculation agent The alumen ustum rise time Mean time
Polymerize aluminum chloride 15-30 second 25 seconds
Bodied ferric sulfate 16-60 second 39 seconds
Flocculation agent of the present invention 6-16 second 11 seconds
The same water sample different concns alumen ustum rise time table of table 3
Water sample Flocculant concentration Polymerize aluminum chloride Bodied ferric sulfate Flocculation agent of the present invention
Lake water 10% 15 seconds 16 seconds 8 seconds
Lake water 1% 30 seconds 22 seconds 6 seconds
Mean value 22 seconds 19 seconds 7 seconds
Conclusion (of pressure testing)
1, the different water sample alumen ustum rise times: flocculation agent<polymerize aluminum chloride of the present invention<bodied ferric sulfate;
2, the same water sample different concns flocculation agent alumen ustum rise time: flocculation agent<polymerize aluminum chloride of the present invention<bodied ferric sulfate;
3, different water sample alumen ustum rise time flocculation agents of the present invention are 0.55 times of polymerize aluminum chloride, and same water sample alumen ustum rise time flocculation agent of the present invention is 0.32 times of polymerize aluminum chloride.
Three, flocculation agent of the present invention (name is called the XN21-DW multi-kernel high-molecular inorganic flocculant during test) is to the test of different quality water sample flocculation removal effect
1, tap water arsenic, fluorine are removed test
Water sample: Xi'an army provides the water in the well for oneself, and the content of arsenic, fluorine surpasses national standard 0.5-1.7 doubly in the water.
Test method: get the 500ml processed water respectively, add the 50mg flocculation agent, observe alumen ustum rise time and flocculation rate, get supernatant liquor quantitative analysis removal effect.Analytical effect sees Table 4.
Analytical procedure and use instrument: undertaken by three editions regulations of State Bureau of Environmental Protection " water and tailing water analysis method ".
Table 4 analytical results table
Polymerize aluminum chloride Poly-propionic acid amide Flocculation agent of the present invention
The arsenic clearance 87% 80% 92.3%
The fluorine clearance 70% 69% 70%
Conclusion (of pressure testing):
1) flocculation agent of the present invention can be used in the tap water arsenic-containing water matter and handles, and is respond well, remedied the technological deficiency that the chlorion of polymerize aluminum chloride increases; 2) the flocculation agent consumption is when 100mg/l reduces to 50mg/l and 25mg/l, and polymerize aluminum chloride, poly-propionic acid amide do not have flocculating effect, and flocculation agent of the present invention still has alumen ustum to produce.
2, the red alkali mire in Shenmu County fishery water flocculation test
Water sample: the water of fish farm, hair Wu Su desert, Shenmu County, Shaanxi Province, the basicity of water is higher, the water body muddiness.
Use instrument and test method: undertaken by three editions regulations of State Bureau of Environmental Protection " water and tailing water analysis method ".
Test-results: test-results sees Table 5, table 6.
Table 5 flocculating effect information slip
Flocculating effect (10%) Flocculating effect (1%)
Polymerize aluminum chloride Alumen ustum is two-layer up and down Alumen ustum is on the upper strata
Bodied ferric sulfate Muddy not stratified Alumen ustum is two-layer up and down
Flocculation agent of the present invention The alumen ustum lower sediment The alumen ustum lower sediment
Change of water quality table before and after table 6 flocculation
PH value before handling Handle the back pH value
Polymerize aluminum chloride >9 7
Bodied ferric sulfate >9 8-9
Flocculation agent of the present invention >9 7
Conclusion (of pressure testing):
1) flocculation agent of the present invention was handled the alumen ustum lower sediment that water produces, and helped separating;
2) flocculation agent of the present invention can reduce the content of impurity in the fishery cultivating water, is convenient to impurity is separated.
Four, flocculation agent of the present invention (name is called the XN21-DW multi-kernel high-molecular inorganic flocculant during test) is handled the chemical flocculation of dyeing and printing sewage
Test sample: flocculation agent of the present invention
Simultaneous test sample: PAC (alkali formula aluminium), PFS (bodied ferric sulfate), Tai-Ace S 150 [Al 2(SO 4) 3]
Simultaneous test index: COD Cr, colourity, SS, PH
The test water sample: Shaanxi Hua Chang dyeing clothing limited liability company Sewage Plant equalizing tank outlet sewage, its major ingredient is PAV, auxiliary agent, dyestuff (azoic dyestuff, substantive dyestuff, reactive dyestuffs, matching stain, cationic red etc.).
Test apparatus: DBJ-621 type six stirrers, PHs-3C type, CS101-AB type electric drying oven with forced convection, TG328B type electroanalysis balance.
Test method: COD adopts potassium dichromate process, SS to adopt gravimetry, colourity to adopt extension rate method, PH to adopt instrumental method.
Test-results: test-results sees Table 7, table 8.
Table 7 flocculation agent of the present invention and simultaneous test sample preparation dyeing and printing sewage be table as a result
COD Cr(mg/L) colourity (doubly) SS (mg/L) PH
The former water water outlet of former water water outlet η (%) former water water outlet η (%) former water water outlet η (%)
Flocculation agent 1129.80 830.40 26.50 400 76 81 378.79 9.00 97.62 11 5.8 of the present invention
PAC 1129.80 929.04 17.78 400 130 68 378.79 57,00 84.95 11 6.9
PFS 1129.80 822.36 27.21 400 125 69 378.79 287.50 24.10 11 5.6
Al 2(SO i) 31129.80 855.12 24.31 400 75 81 378.79 17.00 95.51 11 6.5
Table 8 flocculation agent of the present invention and simultaneous test sample preparation dyeing and printing sewage flocculating effect table
Title flocculation agent PAC of the present invention PFS Al 2(SO 4) 3
Optimal coagulant dose (mg/L) 414 571 923 857
The flco size is maximum large, medium and small
Settling property has the rising phenomenon good job well
Flco time of occurrence (s) 15 12 15 30
Conclusion (of pressure testing): for being up to 97.62%, optimal coagulant dose is low, settling property good, the flco time period occurs to the clearance of SS for flocculation agent of the present invention.Clearance and PFS to COD quite are best.Chroma removal rate and AI 2(SO 4) 3Quite be best.
Five, flocculation agent of the present invention (name is called the FA-M flocculation agent during test) is handled viscous crude production waste indoor comparative test with polymerize aluminum chloride
1. test sample
1# simultaneous test polymerize aluminum chloride is produced by the tenth chemical plant, Yingyang City.
2# flocculation agent of the present invention is provided by the consignor.
2. the fresh sewage in the viscous crude production that provides by one section of Test Production Co., Henan Petroleum Survey Bureau's viscous crude joint station with sewage of test.
3. test method
Two kinds of flocculation agents are mixed with 10% the aqueous solution, are added to according to a certain percentage in the quantitative sewage sample, stir 20 times, standing sedimentation is observed its flocculation rate.The size of alumen ustum and degree of compactness, and the sewage of getting after the processing does reference with clear water, surveys its absorbancy.
4. test-results: test-results sees Table 9.
Table 9 flocculation agent of the present invention and polymerize aluminum chloride are handled viscous crude production waste table as a result
Sample number Consumption Flocculation rate The alumen ustum size. degree of compactness Absorbancy
1 # 100ppm+5ppm Slowly Alumen ustum is big. and loose 0.223
2 # 100ppm+5ppm Hurry up Alumen ustum is little. and closely knit 0.053
Remarks: 1. sewage is the sewage that is produced in the viscous crude production; 2. the sewage after handling does not carry out oily water separation, just its absorbancy of integration test.
Six, flocculation agent of the present invention (name is called the FA-M flocculation agent during test) is to the comparison test of sewage from oil refinery handling property
1, test sample
1 #: Al 2(SO 4) 318H 2O is the simultaneous test flocculation agent;
2 #: ZB4109 (A, B) is the simultaneous test flocculation agent.
3 #: flocculation agent of the present invention is provided by the consignor.
2, test sewage
The refinery oily(waste)water.
3, test apparatus
SC series six experiment stirrers, four in 1000ml beaker.
4, test method
Three kinds of flocculation agents are mixed with 1% use solution, in four beakers, respectively add 1000ml oily(waste)water (one of them compare observe with) and place six online on, stir with balancing speed, requirement according to dosage adds an amount of flocculation agent use solution in sewage, on six experiment stirrers, stirred 2 minutes, left standstill 20 minutes, apparent proterties behind the observation sewage flocculation is got supernatant liquor and is measured COD.
5, test-results
The apparent proterties of raw waste water: the original water gauge face has one deck pool flower, muddiness, and blackout, COD is 661mg/l.
Comparative test result sees Table 10.
Table 10 the present invention coagulates agent and handles oil refining sewerage comparative test result table
Sample number Dosage Sewage is apparent after the flocculation COD
1 # 40ppm (in Al) Muddiness is creamy white, and flocs unit is little 140mg/l
2 # A:15ppm;B:5ppm Water is clear, and is transparent, and floc particle is big 120mg/l
3 # 80ppm Transparent clear, but flco is more tiny 132mg/l
Conclusion: flocculation agent of the present invention has stronger neutralizing effect to colloidal particle in the dirt, but the volume effect of sweeping is relatively poor, and the treatment effect of oil refining sewerage is better than Al 2(SO 4) 318H 2O, but be worse than ZB4109 (A, B) slightly.

Claims (6)

1, a kind of inorganic polymer flocculant is characterized in that it is to make with following materials of weight proportions:
The A component is the hydrochloride of Mg, the hydrochloride of Fe, 10~30% hydrochloric acid soln compositions of the polysalt hydrochlorate of Al, in its proportioning, the polysalt hydrochlorate of the hydrochloride of the hydrochloride of Mg: Fe: Al: the weight ratio of 10~30% hydrochloric acid solns is 1: 1~3: 1~3: 7~15, or the A component is the vitriol of Mg, the vitriol of Fe, 10~30% sulphuric acid soln compositions of the polymerised sulphur hydrochlorate of Al, in its proportioning, the polymerised sulphur hydrochlorate of the vitriol of the vitriol of Mg: Fe: Al: the weight ratio of 10~30% sulphuric acid solns is 1: 1~3: 1~3: 7~15, and the A components contents is 20~70%;
The B component is the polysalt hydrochlorate of Al or the polymerised sulphur hydrochlorate of Al, and its content is 10~60%;
The C component is 10~30% acidic solutions of soluble silicate, and its content is 20~60%;
The preparation method of above-mentioned inorganic polymer flocculant is: the A component of liquid state is joined in the reactor, add the C component with heater heats to 30 ℃~110 ℃, being stirred to agitator becomes homogeneous solution, add the B component then, stir with agitator again, make its uniform mixing, stop to stir cooling gradually and become the ointment shape, after quality control standards (QCS) check of the present invention, packing gets product of the present invention.
2, according to the described inorganic polymer flocculant of claim 1, wherein the weight proportion of each raw material is:
A component 20~50%
B component 20~60%
C component 20~30%
3, according to the described inorganic polymer flocculant of claim 1, wherein the weight proportion of each raw material is:
A component 50%
B component 20%
C component 30%
4, according to claim 1 or 2 or 3 described inorganic polymer flocculants, it is characterized in that: said C component soluble silicate is water glass or potassium silicate, and the acidic solution of C component soluble silicate is hydrochloric acid soln or sulphuric acid soln.
5, according to the described inorganic polymer flocculant of claim 1, wherein to join the Heating temperature scope after the A component be 40 ℃~100 ℃ to the C component.
6, according to the described inorganic polymer flocculant of claim 1, wherein to join the Heating temperature after the A component be 70 ℃ to the C component.
CNB011317752A 2001-11-06 2001-11-06 Multi-kernel high-molecular inorganic flocculant Expired - Fee Related CN1164503C (en)

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CN102010045B (en) * 2010-11-19 2012-08-08 杭州电子科技大学 Preparation method for polysilicate-metal flocculant containing titanium
CN102259963A (en) * 2011-06-22 2011-11-30 哈尔滨工业大学 Polymeric magnesium silicate-sulfate composite flocculant
CN108217894A (en) * 2017-12-13 2018-06-29 赛恩斯环保股份有限公司 A kind of preparation method and application of efficient defluorinate ferro-aluminum complex reagent
CN108996645A (en) * 2018-09-20 2018-12-14 王晓霞 A kind of wastewater from chemical industry flocculant
CN113072152B (en) * 2021-06-04 2021-09-14 赛恩斯环保股份有限公司 Preparation method and application of defluorination and heavy metal removal polynuclear medicament

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