CN105727892A - Compound type water purifying material and preparation method thereof - Google Patents

Compound type water purifying material and preparation method thereof Download PDF

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Publication number
CN105727892A
CN105727892A CN201610269390.1A CN201610269390A CN105727892A CN 105727892 A CN105727892 A CN 105727892A CN 201610269390 A CN201610269390 A CN 201610269390A CN 105727892 A CN105727892 A CN 105727892A
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China
Prior art keywords
parts
attapulgite
scavenging material
composite water
water scavenging
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CN201610269390.1A
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Chinese (zh)
Inventor
费金华
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Suzhou Shengpula New Material Technology Co Ltd
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Suzhou Shengpula New Material Technology Co Ltd
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Priority to CN201610269390.1A priority Critical patent/CN105727892A/en
Publication of CN105727892A publication Critical patent/CN105727892A/en
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/22Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising organic material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/02Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
    • B01J20/04Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising compounds of alkali metals, alkaline earth metals or magnesium
    • B01J20/043Carbonates or bicarbonates, e.g. limestone, dolomite, aragonite
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/02Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
    • B01J20/04Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising compounds of alkali metals, alkaline earth metals or magnesium
    • B01J20/046Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising compounds of alkali metals, alkaline earth metals or magnesium containing halogens, e.g. halides
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/02Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
    • B01J20/06Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising oxides or hydroxides of metals not provided for in group B01J20/04
    • B01J20/08Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising oxides or hydroxides of metals not provided for in group B01J20/04 comprising aluminium oxide or hydroxide; comprising bauxite
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/02Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
    • B01J20/10Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising silica or silicate
    • B01J20/12Naturally occurring clays or bleaching earth
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/02Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
    • B01J20/20Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising free carbon; comprising carbon obtained by carbonising processes
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/28Treatment of water, waste water, or sewage by sorption
    • C02F1/288Treatment of water, waste water, or sewage by sorption using composite sorbents, e.g. coated, impregnated, multi-layered
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2220/00Aspects relating to sorbent materials
    • B01J2220/40Aspects relating to the composition of sorbent or filter aid materials
    • B01J2220/46Materials comprising a mixture of inorganic and organic materials
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2101/00Nature of the contaminant
    • C02F2101/10Inorganic compounds
    • C02F2101/20Heavy metals or heavy metal compounds
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2303/00Specific treatment goals
    • C02F2303/16Regeneration of sorbents, filters

Abstract

The invention discloses a compound type water purifying material.The compound type water purifying material is prepared from, by weight, 30-50 parts of attapulgite, 10-20 parts of aluminum oxide, 15-25 parts of 1-nitryl-2-propyl alcohol, 20-30 parts of activated carbon, 8-12 parts of p-toluenesulfonic acid, 3-9 parts of potassium fluozirconate, 10-18 parts of isonicotinic acid, 2-6 parts of magnesium carbonate, 12-20 parts of butanediol salicylate and 20-30 parts of triethylene glycol monomethyl ether.By adopting the compound type water purifying material, the purpose of efficiently purifying sewage can be achieved with few materials, and the material can be recycled after being easily processed.

Description

A kind of composite water scavenging material and preparation method thereof
Technical field
The invention belongs to technical field of water treatment, be specifically related to a kind of composite water scavenging material and preparation method thereof.
Background technology
Along with the quickening of China's ur-banization speed, various places industrial sector scale is constantly expanded, and city size constantly expands, raw The demand applying flexibly water and water for industrial use is the most in short supply.In order to alleviate the predicament of water resources shortage, using water wisely, repeat profit again The focus of research is become with water source.The most common method for treating water mainly has bioanalysis, chemical precipitation, absorption method etc.;Chemistry Heavy metal ions in sewage is mainly formed precipitation by addition chemical substance in sewage by the sedimentation method, goes scrubbing after filtering Heavy metal ion in water;The amount that this method needs is relatively big, and likely brings secondary pollution;Though in existing adsorption method So purification sewage there is is certain effect, but it is non-renewable to still suffer from adsorbent, the deficiencies such as reusing is poor.
Summary of the invention
For above technical problem present in prior art, the present invention provides a kind of composite water scavenging material and system thereof Preparation Method, by using this composite water scavenging material can be realized the purpose of high-efficient purification sewage by less material, This material is through simple post processing i.e. reproducible utilization simultaneously.
Technical scheme: a kind of composite water scavenging material, including the composition of following parts by weight: attapulgite 30-50 part, Aluminium sesquioxide 10-20 part, 1-nitro-2 propanol 15-25 part, activated carbon 20-30 part, p-methyl benzenesulfonic acid 8-12 part, potassium fluorozirconate 3-9 part .gamma.-pyridinecarboxylic acid 10-18 part, magnesium carbonate 2-6 part, butanediol salicylate 12-20 part, triethylene glycol methyl ether 20-30 part.
Further, described attapulgite 35-40 part, aluminium sesquioxide 15-18 part, 1-nitro-2 propanol 18-22 part, work Property charcoal 25-28 part, p-methyl benzenesulfonic acid 9-11 part, potassium fluorozirconate 4-7 part .gamma.-pyridinecarboxylic acid 12-16 part, magnesium carbonate 3-5 part, butanediol water Poplar acid esters 14-18 part, triethylene glycol methyl ether 23-27 part.
Further, described attapulgite 37 parts, aluminium sesquioxide 16 parts, 1-nitro-2 propanol 20 parts, activated carbon 26 parts, P-methyl benzenesulfonic acid 10 parts, potassium fluorozirconate 6 parts, 14 parts .gamma.-pyridinecarboxylic acid, magnesium carbonate 4 parts, butanediol salicylate 17 parts, triethylene glycol first 25 parts of ether.
The preparation method of a kind of composite water scavenging material, comprises the steps:
S1: attapulgite 30-50 part, aluminium sesquioxide 10-20 part and triethylene glycol methyl ether 20-30 part are added reactor In, at temperature 120-140 DEG C, stirring reaction 2-4h, obtains the attapulgite of modification after filtration drying;
S2: by 1-nitro-2 propanol 15-25 part, activated carbon 20-30 part, p-methyl benzenesulfonic acid 8-12 part and butanediol salicylic acid Ester 12-20 part mixes, stirring reaction 1-3h at temperature 100-120 DEG C;
S3: with adding potassium fluorozirconate 3-9 part and magnesium carbonate 2-6 part in backward step S2, stir 20-30min;Add step Attapulgite modified described in S1, adds .gamma.-pyridinecarboxylic acid 10-18 part, impregnation 2-4h;Reactant liquor through filter, washing, It is dried, obtains described composite water scavenging material after roasting.
Further, temperature described in step S1 is 125 DEG C, stirring reaction 3.5h.
Further, temperature described in step S2 is 115 DEG C, stirring reaction 2h.
Further, in step S3, the time of stirring is 25min, impregnation 2.5h.
Further, the temperature of roasting described in step S3 is 550-600 DEG C, roasting time 15-20min.
Beneficial effect: the preparation method of a kind of composite water scavenging material of the present invention, by with attapulgite and work Property charcoal be main carriers, simultaneously in addition modified by other chemical substances, prepare the compound of activated carbon parcel attapulgite Type water purification material;Dirty impurities in water can substantially be removed by this scavenging material, and after simple process, i.e. reproducible utilization and warp should After scavenging material processes, sewage color and luster is greatly improved.
Detailed description of the invention
Embodiment 1
S1: attapulgite 30 parts, aluminium sesquioxide 10 parts and triethylene glycol methyl ether 20 parts are added in reactor, in temperature At 120 DEG C, stirring reaction 2h, obtains the attapulgite of modification after filtration drying;
S2: 1-nitro-2 propanol 15 parts, activated carbon 20 parts, p-methyl benzenesulfonic acid 8 parts and butanediol salicylate 12 parts is mixed Close, stirring reaction 1h at temperature 100 DEG C;
S3: with adding potassium fluorozirconate 3 parts and magnesium carbonate 2 parts in backward step S2, stir 20min;Add institute in step S1 State modified attapulgite, add 10 parts .gamma.-pyridinecarboxylic acid, impregnation 2h;Reactant liquor through filtering, washing, vacuum is done at 80 DEG C Described composite water scavenging material is i.e. can get after dry, 550 DEG C of roasting 15min.
Comparative example 1
S1: attapulgite 30 parts, aluminium sesquioxide 10 parts and triethylene glycol methyl ether 20 parts are added in reactor, in temperature At 120 DEG C, stirring reaction 2h, obtains the attapulgite of modification after filtration drying;
S2: with adding magnesium carbonate 2 parts in backward step S1, stir 20min;Add described in step S1 modified concavo-convex Rod soil, impregnation 2h;Reactant liquor through filtering, washing, be vacuum dried at 80 DEG C, i.e. to can get water after 550 DEG C of roasting 15min clean Formed material.
Embodiment 2
S1: attapulgite 50 parts, aluminium sesquioxide 20 parts and triethylene glycol methyl ether 30 parts are added in reactor, in temperature At 140 DEG C, stirring reaction 4h, obtains the attapulgite of modification after filtration drying;
S2: 1-nitro-2 propanol 25 parts, activated carbon 30 parts, p-methyl benzenesulfonic acid 12 parts and butanediol salicylate 20 parts is mixed Close, stirring reaction 3h at temperature 120 DEG C;
S3: with adding potassium fluorozirconate 9 parts and magnesium carbonate 6 parts in backward step S2, stir 30min;Add institute in step S1 State modified attapulgite, add 18 parts .gamma.-pyridinecarboxylic acid, impregnation 4h;Reactant liquor through filtering, washing, vacuum is done at 80 DEG C Described composite water scavenging material is i.e. can get after dry, 600 DEG C of roasting 20min.
Comparative example 2
S1: attapulgite 50 parts, aluminium sesquioxide 20 parts and triethylene glycol methyl ether 30 parts are added in reactor, in temperature At 140 DEG C, stirring reaction 4h, obtains the attapulgite of modification after filtration drying;
S2: with adding magnesium carbonate 6 parts in backward step S1, stir 30min;Add described in step S1 modified concavo-convex Rod soil, impregnation 4h;Reactant liquor through filtering, washing, be vacuum dried at 80 DEG C, i.e. to can get water after 600 DEG C of roasting 20min clean Formed material.
Embodiment 3
S1: attapulgite 35 parts, aluminium sesquioxide 15 parts and triethylene glycol methyl ether 23 parts are added in reactor, in temperature At 120 DEG C, stirring reaction 2h, obtains the attapulgite of modification after filtration drying;
S2: 1-nitro-2 propanol 18 parts, activated carbon 25 parts, p-methyl benzenesulfonic acid 9 parts and butanediol salicylate 14 parts is mixed Close, stirring reaction 2h at temperature 100 DEG C;
S3: with adding potassium fluorozirconate 4 parts and magnesium carbonate 3 parts in backward step S2, stir 20min;Add institute in step S1 State modified attapulgite, add 12 parts .gamma.-pyridinecarboxylic acid, impregnation 2h;Reactant liquor through filtering, washing, vacuum is done at 80 DEG C Described composite water scavenging material is i.e. can get after dry, 600 DEG C of roasting 20min.
Embodiment 4
S1: attapulgite 40 parts, aluminium sesquioxide 18 parts and triethylene glycol methyl ether 27 parts are added in reactor, in temperature At 130 DEG C, stirring reaction 3h, obtains the attapulgite of modification after filtration drying;
S2: 1-nitro-2 propanol 22 parts, activated carbon 28 parts, p-methyl benzenesulfonic acid 11 parts and butanediol salicylate 18 parts is mixed Close, stirring reaction 3h at temperature 120 DEG C;
S3: with adding potassium fluorozirconate 7 parts and magnesium carbonate 5 parts in backward step S2, stir 30min;Add institute in step S1 State modified attapulgite, add 16 parts .gamma.-pyridinecarboxylic acid, impregnation 3h;Reactant liquor through filtering, washing, vacuum is done at 80 DEG C Described composite water scavenging material is i.e. can get after dry, 550 DEG C of roasting 15min.
Embodiment 5
S1: attapulgite 37 parts, aluminium sesquioxide 16 parts and triethylene glycol methyl ether 25 parts are added in reactor, in temperature At 125 DEG C, stirring reaction 3.5h, obtains the attapulgite of modification after filtration drying;
S2: 1-nitro-2 propanol 20 parts, activated carbon 26 parts, p-methyl benzenesulfonic acid 10 parts and butanediol salicylate 17 parts is mixed Close, stirring reaction 2h at temperature 115 DEG C;
S3: with adding potassium fluorozirconate 6 parts and magnesium carbonate 4 parts in backward step S2, stir 25min;Add institute in step S1 State modified attapulgite, add 14 parts .gamma.-pyridinecarboxylic acid, impregnation 2.5h;Reactant liquor through filtering, washing, vacuum at 80 DEG C It is dried, i.e. can get described composite water scavenging material after 600 DEG C of roasting 18min.
The water purification material of each embodiment and comparative example gained is applied in the waste water of metal ion, 20 DEG C of suctions Attached 50h, obtains following result:
Experiment Removal of heavy metal ions rate (%)
Comparative example 1 43
Embodiment 1 96
Comparative example 2 41
Embodiment 2 97
Embodiment 3 98
Embodiment 4 97.5
Embodiment 5 98.5
Select composite water scavenging material described in embodiment 5 to wash through simple alcohols, wash, be dried, after 120 DEG C of low-temperature bakes Being recycled and reused in the waste water of metal ion, demonstrate preferable regenerability, concrete outcome is as follows:

Claims (8)

1. a composite water scavenging material, it is characterised in that include the composition of following parts by weight: attapulgite 30-50 part, Aluminium sesquioxide 10-20 part, 1-nitro-2 propanol 15-25 part, activated carbon 20-30 part, p-methyl benzenesulfonic acid 8-12 part, potassium fluorozirconate 3-9 part .gamma.-pyridinecarboxylic acid 10-18 part, magnesium carbonate 2-6 part, butanediol salicylate 12-20 part, triethylene glycol methyl ether 20-30 part.
A kind of composite water scavenging material the most according to claim 1, it is characterised in that described attapulgite 35-40 part, Aluminium sesquioxide 15-18 part, 1-nitro-2 propanol 18-22 part, activated carbon 25-28 part, p-methyl benzenesulfonic acid 9-11 part, potassium fluorozirconate 4-7 part .gamma.-pyridinecarboxylic acid 12-16 part, magnesium carbonate 3-5 part, butanediol salicylate 14-18 part, triethylene glycol methyl ether 23-27 part.
A kind of composite water scavenging material the most according to claim 2, it is characterised in that described attapulgite 37 parts, three Al 2 O 16 parts, 1-nitro-2 propanol 20 parts, activated carbon 26 parts, p-methyl benzenesulfonic acid 10 parts, potassium fluorozirconate 6 parts .gamma.-pyridinecarboxylic acid 14 Part, magnesium carbonate 4 parts, butanediol salicylate 17 parts, triethylene glycol methyl ether 25 parts.
4. the preparation method of a composite water scavenging material, it is characterised in that comprise the steps:
S1: attapulgite 30-50 part, aluminium sesquioxide 10-20 part and triethylene glycol methyl ether 20-30 part are added in reactor, At temperature 120-140 DEG C, stirring reaction 2-4h, obtains the attapulgite of modification after filtration drying;
S2: by 1-nitro-2 propanol 15-25 part, activated carbon 20-30 part, p-methyl benzenesulfonic acid 8-12 part and butanediol salicylate 12-20 part mixes, stirring reaction 1-3h at temperature 100-120 DEG C;
S3: with adding potassium fluorozirconate 3-9 part and magnesium carbonate 2-6 part in backward step S2, stir 20-30min;Add in step S1 Described modified attapulgite, adds .gamma.-pyridinecarboxylic acid 10-18 part, impregnation 2-4h;Reactant liquor through filtering, wash, being dried, Described composite water scavenging material is obtained after roasting.
The preparation method of a kind of composite water scavenging material the most according to claim 4, it is characterised in that institute in step S1 Stating temperature is 125 DEG C, stirring reaction 3.5h.
The preparation method of a kind of composite water scavenging material the most according to claim 4, it is characterised in that institute in step S2 Stating temperature is 115 DEG C, stirring reaction 2h.
The preparation method of a kind of composite water scavenging material the most according to claim 4, it is characterised in that stir in step S3 The time mixed is 25min, impregnation 2.5h.
The preparation method of a kind of composite water scavenging material the most according to claim 4, it is characterised in that institute in step S3 The temperature stating roasting is 550-600 DEG C, roasting time 15-20min.
CN201610269390.1A 2016-04-27 2016-04-27 Compound type water purifying material and preparation method thereof Pending CN105727892A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111790356A (en) * 2020-06-23 2020-10-20 山东海邦水务科技有限公司 Water treatment material and water purification method thereof

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63287593A (en) * 1987-05-19 1988-11-24 Toray Ind Inc Straw-type water purifier
CN1648064A (en) * 2004-12-25 2005-08-03 李玉堂 Water purifier for removing fluorine and arsenic and preparing method
WO2008129551A1 (en) * 2007-04-18 2008-10-30 H2Q Water Industries Ltd. Filter medium

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63287593A (en) * 1987-05-19 1988-11-24 Toray Ind Inc Straw-type water purifier
CN1648064A (en) * 2004-12-25 2005-08-03 李玉堂 Water purifier for removing fluorine and arsenic and preparing method
WO2008129551A1 (en) * 2007-04-18 2008-10-30 H2Q Water Industries Ltd. Filter medium

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111790356A (en) * 2020-06-23 2020-10-20 山东海邦水务科技有限公司 Water treatment material and water purification method thereof

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