WO2022110089A1 - Waste water treatment composition for printing and dyeing wastewater, and preparation method therefor - Google Patents
Waste water treatment composition for printing and dyeing wastewater, and preparation method therefor Download PDFInfo
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- WO2022110089A1 WO2022110089A1 PCT/CN2020/132548 CN2020132548W WO2022110089A1 WO 2022110089 A1 WO2022110089 A1 WO 2022110089A1 CN 2020132548 W CN2020132548 W CN 2020132548W WO 2022110089 A1 WO2022110089 A1 WO 2022110089A1
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- WIPO (PCT)
- Prior art keywords
- printing
- treatment composition
- sewage treatment
- dyeing wastewater
- preparation
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 46
- 238000004043 dyeing Methods 0.000 title claims abstract description 34
- 239000002351 wastewater Substances 0.000 title claims abstract description 32
- 238000002360 preparation method Methods 0.000 title claims description 16
- 238000004065 wastewater treatment Methods 0.000 title abstract description 10
- 229920002472 Starch Polymers 0.000 claims abstract description 36
- 239000008107 starch Substances 0.000 claims abstract description 36
- 239000003463 adsorbent Substances 0.000 claims abstract description 27
- 239000003109 Disodium ethylene diamine tetraacetate Substances 0.000 claims abstract description 17
- ZGTMUACCHSMWAC-UHFFFAOYSA-L EDTA disodium salt (anhydrous) Chemical compound [Na+].[Na+].OC(=O)CN(CC([O-])=O)CCN(CC(O)=O)CC([O-])=O ZGTMUACCHSMWAC-UHFFFAOYSA-L 0.000 claims abstract description 17
- 239000000440 bentonite Substances 0.000 claims abstract description 17
- 229910000278 bentonite Inorganic materials 0.000 claims abstract description 17
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 claims abstract description 17
- 235000019301 disodium ethylene diamine tetraacetate Nutrition 0.000 claims abstract description 17
- 239000000701 coagulant Substances 0.000 claims abstract description 10
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 36
- 239000010865 sewage Substances 0.000 claims description 36
- 239000000243 solution Substances 0.000 claims description 36
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 35
- 239000011259 mixed solution Substances 0.000 claims description 30
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims description 24
- 238000003756 stirring Methods 0.000 claims description 23
- 238000006243 chemical reaction Methods 0.000 claims description 14
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 12
- 235000019270 ammonium chloride Nutrition 0.000 claims description 12
- 229910000402 monopotassium phosphate Inorganic materials 0.000 claims description 12
- 235000019796 monopotassium phosphate Nutrition 0.000 claims description 12
- PJNZPQUBCPKICU-UHFFFAOYSA-N phosphoric acid;potassium Chemical compound [K].OP(O)(O)=O PJNZPQUBCPKICU-UHFFFAOYSA-N 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 8
- 239000002245 particle Substances 0.000 claims description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 5
- 229920002401 polyacrylamide Polymers 0.000 claims description 5
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 4
- 239000008187 granular material Substances 0.000 claims description 4
- OYYAGAJDVFTKCK-UHFFFAOYSA-K sulfuric acid trichloroalumane Chemical compound Cl[Al](Cl)Cl.OS(O)(=O)=O OYYAGAJDVFTKCK-UHFFFAOYSA-K 0.000 claims description 4
- 229910052684 Cerium Inorganic materials 0.000 claims description 2
- 229910052691 Erbium Inorganic materials 0.000 claims description 2
- 229910052693 Europium Inorganic materials 0.000 claims description 2
- 229910052688 Gadolinium Inorganic materials 0.000 claims description 2
- 229910052765 Lutetium Inorganic materials 0.000 claims description 2
- 229910052779 Neodymium Inorganic materials 0.000 claims description 2
- 229910052777 Praseodymium Inorganic materials 0.000 claims description 2
- 229910052775 Thulium Inorganic materials 0.000 claims description 2
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 claims description 2
- UYAHIZSMUZPPFV-UHFFFAOYSA-N erbium Chemical compound [Er] UYAHIZSMUZPPFV-UHFFFAOYSA-N 0.000 claims description 2
- OGPBJKLSAFTDLK-UHFFFAOYSA-N europium atom Chemical compound [Eu] OGPBJKLSAFTDLK-UHFFFAOYSA-N 0.000 claims description 2
- UIWYJDYFSGRHKR-UHFFFAOYSA-N gadolinium atom Chemical compound [Gd] UIWYJDYFSGRHKR-UHFFFAOYSA-N 0.000 claims description 2
- 229910052746 lanthanum Inorganic materials 0.000 claims description 2
- FZLIPJUXYLNCLC-UHFFFAOYSA-N lanthanum atom Chemical compound [La] FZLIPJUXYLNCLC-UHFFFAOYSA-N 0.000 claims description 2
- OHSVLFRHMCKCQY-UHFFFAOYSA-N lutetium atom Chemical compound [Lu] OHSVLFRHMCKCQY-UHFFFAOYSA-N 0.000 claims description 2
- QEFYFXOXNSNQGX-UHFFFAOYSA-N neodymium atom Chemical compound [Nd] QEFYFXOXNSNQGX-UHFFFAOYSA-N 0.000 claims description 2
- PUDIUYLPXJFUGB-UHFFFAOYSA-N praseodymium atom Chemical compound [Pr] PUDIUYLPXJFUGB-UHFFFAOYSA-N 0.000 claims description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims 2
- NGDQQLAVJWUYSF-UHFFFAOYSA-N 4-methyl-2-phenyl-1,3-thiazole-5-sulfonyl chloride Chemical compound S1C(S(Cl)(=O)=O)=C(C)N=C1C1=CC=CC=C1 NGDQQLAVJWUYSF-UHFFFAOYSA-N 0.000 claims 1
- MOVRNJGDXREIBM-UHFFFAOYSA-N aid-1 Chemical compound O=C1NC(=O)C(C)=CN1C1OC(COP(O)(=O)OC2C(OC(C2)N2C3=C(C(NC(N)=N3)=O)N=C2)COP(O)(=O)OC2C(OC(C2)N2C3=C(C(NC(N)=N3)=O)N=C2)COP(O)(=O)OC2C(OC(C2)N2C3=C(C(NC(N)=N3)=O)N=C2)COP(O)(=O)OC2C(OC(C2)N2C(NC(=O)C(C)=C2)=O)COP(O)(=O)OC2C(OC(C2)N2C3=C(C(NC(N)=N3)=O)N=C2)COP(O)(=O)OC2C(OC(C2)N2C3=C(C(NC(N)=N3)=O)N=C2)COP(O)(=O)OC2C(OC(C2)N2C3=C(C(NC(N)=N3)=O)N=C2)COP(O)(=O)OC2C(OC(C2)N2C(NC(=O)C(C)=C2)=O)COP(O)(=O)OC2C(OC(C2)N2C3=C(C(NC(N)=N3)=O)N=C2)COP(O)(=O)OC2C(OC(C2)N2C3=C(C(NC(N)=N3)=O)N=C2)COP(O)(=O)OC2C(OC(C2)N2C3=C(C(NC(N)=N3)=O)N=C2)COP(O)(=O)OC2C(OC(C2)N2C(NC(=O)C(C)=C2)=O)COP(O)(=O)OC2C(OC(C2)N2C3=C(C(NC(N)=N3)=O)N=C2)COP(O)(=O)OC2C(OC(C2)N2C3=C(C(NC(N)=N3)=O)N=C2)COP(O)(=O)OC2C(OC(C2)N2C3=C(C(NC(N)=N3)=O)N=C2)CO)C(O)C1 MOVRNJGDXREIBM-UHFFFAOYSA-N 0.000 claims 1
- 230000015271 coagulation Effects 0.000 claims 1
- 238000005345 coagulation Methods 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 230000000694 effects Effects 0.000 abstract description 10
- 238000004042 decolorization Methods 0.000 abstract description 7
- 239000003795 chemical substances by application Substances 0.000 description 8
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 238000004090 dissolution Methods 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 238000000967 suction filtration Methods 0.000 description 6
- 238000005406 washing Methods 0.000 description 6
- 230000008901 benefit Effects 0.000 description 4
- 229920001661 Chitosan Polymers 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 239000004753 textile Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- HSJPMRKMPBAUAU-UHFFFAOYSA-N cerium(3+);trinitrate Chemical compound [Ce+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O HSJPMRKMPBAUAU-UHFFFAOYSA-N 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 239000010881 fly ash Substances 0.000 description 2
- RUTXIHLAWFEWGM-UHFFFAOYSA-H iron(3+) sulfate Chemical compound [Fe+3].[Fe+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O RUTXIHLAWFEWGM-UHFFFAOYSA-H 0.000 description 2
- 229910000360 iron(III) sulfate Inorganic materials 0.000 description 2
- FYDKNKUEBJQCCN-UHFFFAOYSA-N lanthanum(3+);trinitrate Chemical compound [La+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O FYDKNKUEBJQCCN-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 239000004964 aerogel Substances 0.000 description 1
- 230000003064 anti-oxidating effect Effects 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000006065 biodegradation reaction Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000005189 flocculation Methods 0.000 description 1
- VQEHIYWBGOJJDM-UHFFFAOYSA-H lanthanum(3+);trisulfate Chemical compound [La+3].[La+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O VQEHIYWBGOJJDM-UHFFFAOYSA-H 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- GJENVQFRSQOLAE-UHFFFAOYSA-H lutetium(3+);trisulfate Chemical compound [Lu+3].[Lu+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O GJENVQFRSQOLAE-UHFFFAOYSA-H 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- CFYGEIAZMVFFDE-UHFFFAOYSA-N neodymium(3+);trinitrate Chemical compound [Nd+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O CFYGEIAZMVFFDE-UHFFFAOYSA-N 0.000 description 1
- RHVPCSSKNPYQDU-UHFFFAOYSA-H neodymium(3+);trisulfate;hydrate Chemical compound O.[Nd+3].[Nd+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O RHVPCSSKNPYQDU-UHFFFAOYSA-H 0.000 description 1
- KBJMLQFLOWQJNF-UHFFFAOYSA-N nickel(ii) nitrate Chemical compound [Ni+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O KBJMLQFLOWQJNF-UHFFFAOYSA-N 0.000 description 1
- 230000001546 nitrifying effect Effects 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- YWECOPREQNXXBZ-UHFFFAOYSA-N praseodymium(3+);trinitrate Chemical compound [Pr+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O YWECOPREQNXXBZ-UHFFFAOYSA-N 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/28—Treatment of water, waste water, or sewage by sorption
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/52—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities
Definitions
- the invention belongs to the field of sewage treatment, and in particular relates to a sewage treatment composition for printing and dyeing wastewater and a preparation method thereof.
- the wastewater discharged from printing and dyeing, textile, dye and papermaking industries has the characteristics of large water volume, complex composition, high pollutant concentration, deep chromaticity, etc., and has certain anti-oxidation and anti-biodegradation properties. important source of pollution.
- the decolorization treatment of such high-concentration and high-chroma wastewater has always been one of the difficult problems of various discharge enterprises, and it must be effectively treated to reduce the pollution and harm to the environment.
- the Chinese invention patent with the application number CN202010259781.1 discloses a sewage treatment agent for printing and dyeing textile industry and a preparation method thereof.
- the sewage treatment agent is prepared from the following raw materials in parts by weight: coconut shell activated carbon/chitosan composite 30-40 parts, 5-10 parts of polyaluminum chloride, 1-5 parts of nickel nitrate, 5-10 parts of aerogel silica gel, 3-5 parts of polyferric sulfate, 5-8 parts of polyacrylamide, 5-10 parts of nitrifying bacteria
- the sewage treatment agent has a good effect on the treatment of printing and dyeing textile sewage, and the treated sewage meets the national discharge standard, can be recycled, and saves water resources. It is an efficient sewage treatment agent.
- the Chinese invention patent with the application number CN201410503661.6 discloses a preparation method of a printing and dyeing wastewater treatment agent, comprising the following steps: (1) Weighing 10 parts of fly ash with a 100-mesh sieve, adding a mass concentration of 1.2% 50-150 parts of chitosan-based acetic acid solution of 50-150 parts of chitosan acetic acid solution, stirring rapidly for 0.5h; (2) then stirring at a slow speed, and mixing with 5% sodium hydroxide solution to neutrality while stirring to obtain a paste; (3) mixing the above After the paste is matured, it is filtered with suction, dried at a constant temperature of 110°C, and then passed through an 80-mesh sieve to obtain the desired printing and dyeing wastewater treatment agent.
- the printing and dyeing wastewater treatment agent realizes waste utilization, does not cause pollution to the environment, and fully utilizes the residual value of fly ash; using the printing and dyeing wastewater treatment agent, the decolorization rate of wastewater can reach 98% Above, the COD removal rate can reach more than 95%.
- the inventors actively conduct research and innovation with rich practical experience and professional knowledge engaged in such products for many years, and cooperate with the application of theory, in order to create a sewage treatment composition for printing and dyeing wastewater and its preparation
- the method can effectively remove harmful substances in printing and dyeing wastewater.
- the main purpose of the present invention is to overcome the deficiencies in the prior art, and to provide a sewage treatment composition for printing and dyeing wastewater and a preparation method thereof.
- the composition can effectively remove harmful substances in printing and dyeing wastewater.
- the invention provides a sewage treatment composition for printing and dyeing wastewater.
- the composition includes the following components and the content of each component is: flocculant 40-60%, modified nano-starch adsorbent 30-60% 50%, bentonite 5-10%, coagulant aid 1-5%, disodium EDTA 1-5%.
- the aforementioned sewage treatment composition for printing and dyeing wastewater wherein, in terms of weight percentage, the composition includes the following components and the content of each component is: flocculant 50%, modified nanostarch adsorbent 35%, bentonite 8% , 3% coagulant aid, 4% disodium EDTA.
- the aforementioned sewage treatment composition for printing and dyeing wastewater wherein, in terms of weight percentage, the composition includes the following components and the content of each component is: flocculant 50%, modified nanostarch adsorbent 40%, bentonite 5% , 3% coagulant aid, 2% disodium EDTA.
- the flocculant is selected from any one of polyferric sulfate aluminum chloride, polyferric sulfate, polyacrylamide, and polyaluminum chloride.
- the aforementioned sewage treatment composition for printing and dyeing wastewater wherein the coagulant is selected from the nitrate and sulfate of lanthanum, cerium, praseodymium, neodymium, lutetium, europium, gadolinium, erbium, thulium, yttrium or more.
- the invention provides a preparation method of a sewage treatment composition for printing and dyeing wastewater, which comprises the following steps:
- the mass ratio of the nano-starch particles, citric acid and potassium dihydrogen phosphate in the step (1) is 1:(0.1-0.5):(0.1-0.5).
- the concentration of the ammonium chloride solution in the step (1) is 0.1-0.5 mol/L.
- the concentration of the acrylamide solution in the step (1) is 0.1-0.5 mol/L.
- reaction conditions in the step (2) are: the temperature is 20-40° C., and the time is 1-3 hours.
- the present invention has at least the following advantages: the sewage treatment composition of the present invention has good stability and is suitable for treating printing and dyeing wastewater.
- the sewage treatment composition provided by the invention adopts nano-starch as the base material, and has excellent wastewater treatment effect, no secondary pollution, economical and environmental protection, and abundant and renewable raw materials, and has a huge application prospect.
- the sewage treatment composition of the invention has good treatment effect on waste water, can generate larger flocs during the flocculation process, the decolorization rate reaches over 98.8%, and the COD removal rate reaches over 99.8%.
- the special sewage treatment composition for printing and dyeing wastewater of the present invention has the advantage of good decolorization effect. It has many of the above advantages and practical value, and there is no similar design published or used in similar products and methods, but it is indeed an innovation. It has great improvements in both methods and functions. It has made great progress, and has produced easy-to-use and practical effects. Compared with the existing products, it has improved many functions, so it is more suitable for practical use, and has the value of extensive use in the industry. It is a novel, progressive, and Practical new design.
- a 0.3 mol/L ammonium chloride solution was added to the water, heated to 80 °C and stirred for 0.5 h to prepare a mixed solution; then a 0.3 mol/L acrylamide solution was added, stirring continued for 3 h, then washing and suction filtration, and After drying, the modified nano-starch adsorbent is obtained.
- nano-starch particles, citric acid and potassium dihydrogen phosphate into water in a mass ratio of 1:0.1:0.5 to complete dissolution, then heat to 140 °C for reaction for 4 hours; then wash, suction, filter, and dry; A 0.1 mol/L ammonium chloride solution was added to the water, heated to 80 °C and stirred for 0.5 h to prepare a mixed solution; then a 0.5 mol/L acrylamide solution was added, stirring continued for 3 h, then washing and suction filtration, and After drying, the modified nano-starch adsorbent is obtained.
- nano-starch particles, citric acid and potassium dihydrogen phosphate into water in a mass ratio of 1:0.1:0.5 to complete dissolution, then heat to 140 °C for reaction for 4 hours; then wash, suction, filter, and dry; A 0.1 mol/L ammonium chloride solution was added to the water, heated to 80 °C and stirred for 0.5 h to prepare a mixed solution; then a 0.5 mol/L acrylamide solution was added, stirring continued for 3 h, then washing and suction filtration, and After drying, the modified nano-starch adsorbent is obtained.
- a 0.5 mol/L ammonium chloride solution was added to water, heated to 90°C and stirred for 0.1 h to prepare a mixed solution; then a 0.5 mol/L acrylamide solution was added, stirring continued for 3 h, then washing and suction filtration, and After drying, the modified nano-starch adsorbent is obtained.
- nano-starch particles, citric acid and potassium dihydrogen phosphate into water in a mass ratio of 1:0.2:0.3 to complete dissolution, then heat to 150 °C for reaction for 3 hours; then wash, suction, filter, and dry; A 0.1 mol/L ammonium chloride solution was added to water, heated to 70°C and stirred for 1 h to prepare a mixed solution; then a 0.3 mol/L acrylamide solution was added, stirring continued for 3 h, then washed and suction filtered, and dried treatment to obtain a modified nano-starch adsorbent.
- nano-starch particles, citric acid and potassium dihydrogen phosphate into water in a mass ratio of 1:0.2:0.3 to complete dissolution, then heat to 150 °C for reaction for 3 hours; then wash, suction, filter, and dry; A 0.1 mol/L ammonium chloride solution was added to water, heated to 70°C and stirred for 1 h to prepare a mixed solution; then a 0.3 mol/L acrylamide solution was added, stirring continued for 3 h, then washed and suction filtered, and dried treatment to obtain a modified nano-starch adsorbent.
- nano-starch particles, citric acid and potassium dihydrogen phosphate into water in a mass ratio of 1:0.3:0.1 to complete dissolution, then heat to 140 °C for reaction for 3 hours; then wash, suction, filter, and dry; A 0.3mol/L ammonium chloride solution was added to water, heated to 80°C and stirred for 1 h to prepare a mixed solution; then a 0.3mol/L acrylamide solution was added, stirring continued for 3h, then washing, suction filtration, and drying treatment to obtain a modified nano-starch adsorbent.
- nano-starch particles, citric acid and potassium dihydrogen phosphate into water in a mass ratio of 1:0.2:0.3 to complete dissolution, and heat to 140 °C for reaction for 3 hours; then wash, suction, filter, and dry; A 0.3mol/L ammonium chloride solution was added to water, heated to 80°C and stirred for 1 h to prepare a mixed solution; then a 0.3mol/L acrylamide solution was added, stirring continued for 3h, then washing, suction filtration, and drying treatment to obtain a modified nano-starch adsorbent.
- Test method The compositions prepared in Examples 1-8 were applied to the wastewater treatment test of printing and dyeing wastewater.
- the main water quality indicators of the original printing and dyeing wastewater are shown in Table 1.
- the specific method is as follows: in the treatment process, the composition is directly added to the waste water according to the feeding ratio of 20 mL per liter of water, first stirred at a speed of 400 r/min for 5 minutes, and after standing for 60 minutes for precipitation, the supernatant liquid is taken to measure various items. indicators, see Table 2 for the results.
- Example 1 Numbering COD, mg/L Chroma color Turbidity Example 1 2.5 6 colorless 7 Example 2 3.4 9 colorless 13 Example 3 7.1 16 colorless 10 Example 4 3.6 10 colorless 8 Example 5 8.9 11 colorless 12 Example 6 7.7 15 colorless 9 Example 7 10.4 13 colorless 11 Example 8 4.2 13 colorless 13
- composition of the present invention has the advantages of strong adsorption capacity, good decolorization effect, and good treatment effect on printing and dyeing wastewater.
- the decolorization rate reaches more than 98.8%, and the COD removal rate reaches 99.8%. above.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Hydrology & Water Resources (AREA)
- Engineering & Computer Science (AREA)
- Environmental & Geological Engineering (AREA)
- Water Supply & Treatment (AREA)
- Inorganic Chemistry (AREA)
- Analytical Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Water Treatment By Sorption (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Abstract
Disclosed is a waste water treatment composition for printing and dyeing wastewater. The composition contains, in percentage by weight, the following components: 40-60% of a flocculant, 30-50% of a modified nano-starch adsorbent, 5-10% of bentonite, 1-5% of a coagulant aid, and 1-5% of disodium ethylenediaminetetraacetate. The composition has a good treatment effect on printing and dyeing wastewater, the decolorization rate reaches 98.8% or more, and the COD removal rate reaches 99.8% or more.
Description
本发明属于污水处理领域,具体涉及一种用于印染废水的污水处理组合物及其制备方法。The invention belongs to the field of sewage treatment, and in particular relates to a sewage treatment composition for printing and dyeing wastewater and a preparation method thereof.
印染、纺织、染料和造纸等行业所排放的废水具有水量大、成分复杂、污染物浓度高、色度深等特点,且具有一定的抗氧化、抗生物降解性,已成为我国各大水域的重要污染源。这类高浓度高色度废水的脱色处理一直是各排放企业的难题之一,必须对其进行有效治理,减少对环境的污染和危害。The wastewater discharged from printing and dyeing, textile, dye and papermaking industries has the characteristics of large water volume, complex composition, high pollutant concentration, deep chromaticity, etc., and has certain anti-oxidation and anti-biodegradation properties. important source of pollution. The decolorization treatment of such high-concentration and high-chroma wastewater has always been one of the difficult problems of various discharge enterprises, and it must be effectively treated to reduce the pollution and harm to the environment.
例如,申请号为CN202010259781.1的中国发明专利公开了一种印染纺织业用污水处理剂及其制备方法,该污水处理剂由如下重量份原料制备而成:椰壳活性炭/壳聚糖复合物30-40份、聚合氯化铝5-10份、硝酸镍1-5份、气凝硅胶5-10份、聚合硫酸铁3-5份、聚丙烯酰胺5-8份、硝化细菌5-10份、混合助剂5-10份;该污水处理剂处理印染纺织污水效果良好,处理后的污水达到国家规定的排放标准,可循环利用,节约水资源,是一种高效的污水处理剂。For example, the Chinese invention patent with the application number CN202010259781.1 discloses a sewage treatment agent for printing and dyeing textile industry and a preparation method thereof. The sewage treatment agent is prepared from the following raw materials in parts by weight: coconut shell activated carbon/chitosan composite 30-40 parts, 5-10 parts of polyaluminum chloride, 1-5 parts of nickel nitrate, 5-10 parts of aerogel silica gel, 3-5 parts of polyferric sulfate, 5-8 parts of polyacrylamide, 5-10 parts of nitrifying bacteria The sewage treatment agent has a good effect on the treatment of printing and dyeing textile sewage, and the treated sewage meets the national discharge standard, can be recycled, and saves water resources. It is an efficient sewage treatment agent.
又如,申请号为CN201410503661.6的中国发明专利公开了一种印染废水处理剂的制备方法,包括以下步骤:(1)称取过100目筛粉煤灰10份,加入质量浓度为1.2%的壳聚糖类醋酸溶液50-150份,快速搅拌0.5h;(2)接着慢速搅拌,边搅拌边用5%的氢氧化钠溶液调和至中性得糊状物;(3)将上述糊状物熟化后抽滤,110℃恒温干燥后过80目筛即得所需印染废水处理剂。本发明的有益效果为:所述印染废水处理剂实现了废物利用,不会对环境造成污染,充分利用了粉煤灰的剩余价值;使用本印染废水处理剂,废水的脱色率可以达到98%以上,COD去除率可以达到95%以上。For another example, the Chinese invention patent with the application number CN201410503661.6 discloses a preparation method of a printing and dyeing wastewater treatment agent, comprising the following steps: (1) Weighing 10 parts of fly ash with a 100-mesh sieve, adding a mass concentration of 1.2% 50-150 parts of chitosan-based acetic acid solution of 50-150 parts of chitosan acetic acid solution, stirring rapidly for 0.5h; (2) then stirring at a slow speed, and mixing with 5% sodium hydroxide solution to neutrality while stirring to obtain a paste; (3) mixing the above After the paste is matured, it is filtered with suction, dried at a constant temperature of 110°C, and then passed through an 80-mesh sieve to obtain the desired printing and dyeing wastewater treatment agent. The beneficial effects of the invention are as follows: the printing and dyeing wastewater treatment agent realizes waste utilization, does not cause pollution to the environment, and fully utilizes the residual value of fly ash; using the printing and dyeing wastewater treatment agent, the decolorization rate of wastewater can reach 98% Above, the COD removal rate can reach more than 95%.
基于上述现有技术,本发明人以从事此类产品多年丰富的实务经验及专业知识,并配合学理的运用,积极加以研究创新,以期创设一种用于印染废水的污水处理组合物及其制备方法,该组合物能够有效去除印染废水中的有害物质。Based on the above-mentioned prior art, the inventors actively conduct research and innovation with rich practical experience and professional knowledge engaged in such products for many years, and cooperate with the application of theory, in order to create a sewage treatment composition for printing and dyeing wastewater and its preparation The method, the composition can effectively remove harmful substances in printing and dyeing wastewater.
发明内容SUMMARY OF THE INVENTION
本发明的主要目的在于克服现有技术中的不足,提供一种用于印染废水的污水处理组合物及其制备方法。该组合物能够有效去除印染废水中的有害物质。The main purpose of the present invention is to overcome the deficiencies in the prior art, and to provide a sewage treatment composition for printing and dyeing wastewater and a preparation method thereof. The composition can effectively remove harmful substances in printing and dyeing wastewater.
本发明的目的及解决其技术问题是采用以下技术方案来实现。The purpose of the present invention and the technical problem to be solved are achieved by adopting the following technical solutions.
本发明提供了一种用于印染废水的污水处理组合物,按照重量百分比计,该组合物包括以下组分且各组分含量为:絮凝剂40~60%,改性纳米淀粉吸附剂30~50%,膨润土5~10%,助凝剂1~5%,乙二胺四乙酸二钠1~5%。The invention provides a sewage treatment composition for printing and dyeing wastewater. In terms of weight percentage, the composition includes the following components and the content of each component is: flocculant 40-60%, modified nano-starch adsorbent 30-60% 50%, bentonite 5-10%, coagulant aid 1-5%, disodium EDTA 1-5%.
前述的用于印染废水的污水处理组合物,其中,按照重量百分比计,该组合物包括以下组分且各组分含量为:絮凝剂50%,改性纳米淀粉吸附剂35%,膨润土8%,助凝剂3%,乙二胺四乙酸二钠4%。The aforementioned sewage treatment composition for printing and dyeing wastewater, wherein, in terms of weight percentage, the composition includes the following components and the content of each component is: flocculant 50%, modified nanostarch adsorbent 35%, bentonite 8% , 3% coagulant aid, 4% disodium EDTA.
前述的用于印染废水的污水处理组合物,其中,按照重量百分比计,该组合物包括以下组分且各组分含量为:絮凝剂50%,改性纳米淀粉吸附剂40%,膨润土5%,助凝剂3%,乙二胺四乙酸二钠2%。The aforementioned sewage treatment composition for printing and dyeing wastewater, wherein, in terms of weight percentage, the composition includes the following components and the content of each component is: flocculant 50%, modified nanostarch adsorbent 40%, bentonite 5% , 3% coagulant aid, 2% disodium EDTA.
前述的用于印染废水的污水处理组合物,其中,所述絮凝剂选自聚合硫酸氯化铁铝、聚合硫酸铁、聚丙烯酰胺、聚合氯化铝中的任一种。In the aforementioned sewage treatment composition for printing and dyeing wastewater, wherein the flocculant is selected from any one of polyferric sulfate aluminum chloride, polyferric sulfate, polyacrylamide, and polyaluminum chloride.
前述的用于印染废水的污水处理组合物,其中,所述助凝剂选自镧、铈、镨、钕、镥、铕、钆、铒、铥、钇的硝酸盐、硫酸盐中的一种或多种。The aforementioned sewage treatment composition for printing and dyeing wastewater, wherein the coagulant is selected from the nitrate and sulfate of lanthanum, cerium, praseodymium, neodymium, lutetium, europium, gadolinium, erbium, thulium, yttrium or more.
本发明的目的及解决其技术问题还通过采用以下技术方案来实现。The purpose of the present invention and the solution to its technical problems are also achieved by adopting the following technical solutions.
本发明提供了一种用于印染废水的污水处理组合物的制备方法,该方法包括以下步骤:The invention provides a preparation method of a sewage treatment composition for printing and dyeing wastewater, which comprises the following steps:
(1)将纳米淀粉颗粒、柠檬酸及磷酸二氢钾加入水中至完全溶解,加热至130~150℃下反应3~5h;然后洗涤抽滤,干燥;将得到的产物和氯化铵溶液加入到水中,加热至70~90℃下搅拌0.5~1h配制成混合溶液;再加入丙烯酰胺溶液,继续搅拌3h,然后洗涤抽滤,并且干燥处理,得到改性纳米淀粉吸附剂;(1) Add nano-starch granules, citric acid and potassium dihydrogen phosphate into water to dissolve completely, then heat to 130~150℃ for 3~5h reaction; then wash, suction filter, and dry; add the obtained product and ammonium chloride solution into into water, heated to 70 to 90 °C and stirred for 0.5 to 1 h to prepare a mixed solution; then added acrylamide solution, continued to stir for 3 h, then washed, suction filtered, and dried to obtain a modified nanostarch adsorbent;
(2)将絮凝剂溶解在水中,在搅拌条件下加入膨润土和乙二胺四乙酸二钠,反应后得到混合溶液;(2) dissolving the flocculant in water, adding bentonite and disodium EDTA under stirring conditions, and obtaining a mixed solution after the reaction;
(3)在上述混合溶液中依次加入改性纳米淀粉吸附剂和助凝剂常温下搅拌均匀,然后真空干燥过夜,即得到污水处理组合物。(3) The modified nano-starch adsorbent and the coagulant aid are sequentially added to the above mixed solution, stirred evenly at room temperature, and then vacuum-dried overnight to obtain a sewage treatment composition.
前述的制备方法,其中,所述步骤(1)中所述纳米淀粉颗粒、柠檬酸及磷酸二氢钾的质量比为1:(0.1~0.5):(0.1~0.5)。In the aforementioned preparation method, the mass ratio of the nano-starch particles, citric acid and potassium dihydrogen phosphate in the step (1) is 1:(0.1-0.5):(0.1-0.5).
前述的制备方法,其中,所述步骤(1)中所述氯化铵溶液的浓度为0.1~0.5mol/L。In the aforementioned preparation method, the concentration of the ammonium chloride solution in the step (1) is 0.1-0.5 mol/L.
前述的制备方法,其中,所述步骤(1)中所述丙烯酰胺溶液的浓度为0.1~0.5mol/L。In the aforementioned preparation method, the concentration of the acrylamide solution in the step (1) is 0.1-0.5 mol/L.
前述的制备方法,其中,所述步骤(2)中所述反应条件为:温度20~40℃,时间1~3h。The aforementioned preparation method, wherein, the reaction conditions in the step (2) are: the temperature is 20-40° C., and the time is 1-3 hours.
借由上述技术方案,本发明至少具有下列优点:本发明的污水处理组合物稳定性好,适用于处理印染废水。本发明提供的污水处理组合物,采用纳米淀粉为基材,废水处理效果优异、无二次污染、经济环保,而且原料丰富可再生,具备巨大的应用前景。本发明的污水处理组合物对废水的处理效果好,在絮凝过程中可以产生较大的絮团,其脱色率达到98.8%以上,COD去除率达到99.8%以上。With the above technical solutions, the present invention has at least the following advantages: the sewage treatment composition of the present invention has good stability and is suitable for treating printing and dyeing wastewater. The sewage treatment composition provided by the invention adopts nano-starch as the base material, and has excellent wastewater treatment effect, no secondary pollution, economical and environmental protection, and abundant and renewable raw materials, and has a huge application prospect. The sewage treatment composition of the invention has good treatment effect on waste water, can generate larger flocs during the flocculation process, the decolorization rate reaches over 98.8%, and the COD removal rate reaches over 99.8%.
综上所述,本发明特殊的用于印染废水的污水处理组合物具有脱色效果好的优点。其具有上述诸多的优点及实用价值,并在同类产品和方法中未见有类似的设计公开发表或使用而确属创新,其不论在方法上或功能上皆有较大的改进,在技术上有较大的进步,并产生了好用及实用的效果,且较现有的产品具有增进的多项功效,从而更加适于实用,而具有产业的广泛利用价值,诚为一新颖、进步、实用的新设计。To sum up, the special sewage treatment composition for printing and dyeing wastewater of the present invention has the advantage of good decolorization effect. It has many of the above advantages and practical value, and there is no similar design published or used in similar products and methods, but it is indeed an innovation. It has great improvements in both methods and functions. It has made great progress, and has produced easy-to-use and practical effects. Compared with the existing products, it has improved many functions, so it is more suitable for practical use, and has the value of extensive use in the industry. It is a novel, progressive, and Practical new design.
上述说明仅是本发明技术方案的概述,为了能够更清楚了解本发明的技术手段,并可依照说明书的内容予以实施,以下以本发明的较佳实施例详细说明如后。The above description is only an overview of the technical solution of the present invention. In order to understand the technical means of the present invention more clearly, and to implement according to the content of the description, the preferred embodiments of the present invention are described in detail below.
为了使本发明实现的技术手段、创作特征、达成目的与功效易于明白了解,下面将 结合本发明实施例,对本发明实施例中的技术方案进行清楚、完整地描述,显然,所描述的实施例仅仅是本发明一部分实施例,而不是全部的实施例。基于本发明中的实施例,本领域普通技术人员在没有作出创造性劳动前提下所获得的所有其它实施例,都属于本发明保护的范围。In order to make it easy to understand the technical means, creative features, goals and effects realized by the present invention, the technical solutions in the embodiments of the present invention will be clearly and completely described below in conjunction with the embodiments of the present invention. Obviously, the described embodiments It is only a part of the embodiments of the present invention, but not all of the embodiments. Based on the embodiments of the present invention, all other embodiments obtained by those of ordinary skill in the art without creative efforts shall fall within the protection scope of the present invention.
实施例1Example 1
将纳米淀粉颗粒、柠檬酸及磷酸二氢钾按照质量比为1:0.3:0.3的量加入水中至完全溶解,加热至140℃下反应4h;然后洗涤抽滤,干燥;将得到的产物和浓度为0.3mol/L的氯化铵溶液加入到水中,加热至80℃下搅拌0.5h配制成混合溶液;再加入浓度为0.3mol/L的丙烯酰胺溶液,继续搅拌3h,然后洗涤抽滤,并且干燥处理,得到改性纳米淀粉吸附剂。将50份聚合硫酸氯化铁铝溶解在100份水中,在搅拌条件下加入8份膨润土和4份乙二胺四乙酸二钠,在30℃下反应2h后,得到混合溶液。在上述混合溶液中依次加入35份改性纳米淀粉吸附剂和3份硝酸铈常温下搅拌均匀,然后真空干燥过夜,即得到污水处理组合物。Add nano-starch granules, citric acid and potassium dihydrogen phosphate in a mass ratio of 1:0.3:0.3 into water to dissolve completely, then heat to 140°C for 4 hours of reaction; then wash, filter, and dry; the obtained product and concentration A 0.3 mol/L ammonium chloride solution was added to the water, heated to 80 °C and stirred for 0.5 h to prepare a mixed solution; then a 0.3 mol/L acrylamide solution was added, stirring continued for 3 h, then washing and suction filtration, and After drying, the modified nano-starch adsorbent is obtained. Dissolve 50 parts of polyferric sulfate aluminum chloride in 100 parts of water, add 8 parts of bentonite and 4 parts of disodium EDTA under stirring conditions, and react at 30° C. for 2 hours to obtain a mixed solution. 35 parts of modified nano-starch adsorbent and 3 parts of cerium nitrate were sequentially added to the above mixed solution, stirred evenly at room temperature, and then vacuum-dried overnight to obtain a sewage treatment composition.
实施例2Example 2
将纳米淀粉颗粒、柠檬酸及磷酸二氢钾按照质量比为1:0.1:0.5的量加入水中至完全溶解,加热至140℃下反应4h;然后洗涤抽滤,干燥;将得到的产物和浓度为0.1mol/L的氯化铵溶液加入到水中,加热至80℃下搅拌0.5h配制成混合溶液;再加入浓度为0.5mol/L的丙烯酰胺溶液,继续搅拌3h,然后洗涤抽滤,并且干燥处理,得到改性纳米淀粉吸附剂。将50份聚合硫酸铁溶解在100份水中,在搅拌条件下加入5份膨润土和2份乙二胺四乙酸二钠,在30℃下反应2h后,得到混合溶液。在上述混合溶液中依次加入40份改性纳米淀粉吸附剂和3份硝酸镨常温下搅拌均匀,然后真空干燥过夜,即得到污水处理组合物。Add nano-starch particles, citric acid and potassium dihydrogen phosphate into water in a mass ratio of 1:0.1:0.5 to complete dissolution, then heat to 140 °C for reaction for 4 hours; then wash, suction, filter, and dry; A 0.1 mol/L ammonium chloride solution was added to the water, heated to 80 °C and stirred for 0.5 h to prepare a mixed solution; then a 0.5 mol/L acrylamide solution was added, stirring continued for 3 h, then washing and suction filtration, and After drying, the modified nano-starch adsorbent is obtained. Dissolve 50 parts of polymeric ferric sulfate in 100 parts of water, add 5 parts of bentonite and 2 parts of disodium EDTA under stirring conditions, and react at 30° C. for 2 hours to obtain a mixed solution. 40 parts of modified nano-starch adsorbent and 3 parts of praseodymium nitrate were sequentially added to the above mixed solution, stirred evenly at room temperature, and then vacuum-dried overnight to obtain a sewage treatment composition.
实施例3Example 3
将纳米淀粉颗粒、柠檬酸及磷酸二氢钾按照质量比为1:0.1:0.5的量加入水中至完全溶解,加热至140℃下反应4h;然后洗涤抽滤,干燥;将得到的产物和浓度为0.1mol/L的氯化铵溶液加入到水中,加热至80℃下搅拌0.5h配制成混合溶液;再加入浓度为0.5mol/L的丙烯酰胺溶液,继续搅拌3h,然后洗涤抽滤,并且干燥处理,得到改性 纳米淀粉吸附剂。将50份聚丙烯酰胺溶解在100份水中,在搅拌条件下加入8份膨润土和1份乙二胺四乙酸二钠,在30℃下反应2h后,得到混合溶液。在上述混合溶液中依次加入40份改性纳米淀粉吸附剂和1份硫酸钕常温下搅拌均匀,然后真空干燥过夜,即得到污水处理组合物。Add nano-starch particles, citric acid and potassium dihydrogen phosphate into water in a mass ratio of 1:0.1:0.5 to complete dissolution, then heat to 140 °C for reaction for 4 hours; then wash, suction, filter, and dry; A 0.1 mol/L ammonium chloride solution was added to the water, heated to 80 °C and stirred for 0.5 h to prepare a mixed solution; then a 0.5 mol/L acrylamide solution was added, stirring continued for 3 h, then washing and suction filtration, and After drying, the modified nano-starch adsorbent is obtained. 50 parts of polyacrylamide were dissolved in 100 parts of water, 8 parts of bentonite and 1 part of disodium EDTA were added under stirring conditions, and a mixed solution was obtained after reacting at 30° C. for 2 hours. 40 parts of modified nano-starch adsorbent and 1 part of neodymium sulfate were sequentially added to the above mixed solution, stirred evenly at room temperature, and then vacuum-dried overnight to obtain a sewage treatment composition.
实施例4Example 4
将纳米淀粉颗粒、柠檬酸及磷酸二氢钾按照质量比为1:0.3:0.3的量加入水中至完全溶解,加热至150℃下反应3h;然后洗涤抽滤,干燥;将得到的产物和浓度为0.5mol/L的氯化铵溶液加入到水中,加热至90℃下搅拌0.1h配制成混合溶液;再加入浓度为0.5mol/L的丙烯酰胺溶液,继续搅拌3h,然后洗涤抽滤,并且干燥处理,得到改性纳米淀粉吸附剂。将50份聚合氯化铝溶解在100份水中,在搅拌条件下加入8份膨润土和1份乙二胺四乙酸二钠,在30℃下反应2h后,得到混合溶液。在上述混合溶液中依次加入40份改性纳米淀粉吸附剂和1份硝酸钕常温下搅拌均匀,然后真空干燥过夜,即得到污水处理组合物。Add nano-starch granules, citric acid and potassium dihydrogen phosphate in a mass ratio of 1:0.3:0.3 into water to dissolve completely, then heat to 150°C for reaction for 3 hours; then wash and suction filter, and dry; the obtained product and concentration A 0.5 mol/L ammonium chloride solution was added to water, heated to 90°C and stirred for 0.1 h to prepare a mixed solution; then a 0.5 mol/L acrylamide solution was added, stirring continued for 3 h, then washing and suction filtration, and After drying, the modified nano-starch adsorbent is obtained. Dissolve 50 parts of polyaluminum chloride in 100 parts of water, add 8 parts of bentonite and 1 part of disodium EDTA under stirring conditions, and react at 30° C. for 2 hours to obtain a mixed solution. 40 parts of modified nano-starch adsorbent and 1 part of neodymium nitrate were sequentially added to the above mixed solution, stirred evenly at room temperature, and then vacuum-dried overnight to obtain a sewage treatment composition.
实施例5Example 5
将纳米淀粉颗粒、柠檬酸及磷酸二氢钾按照质量比为1:0.2:0.3的量加入水中至完全溶解,加热至150℃下反应3h;然后洗涤抽滤,干燥;将得到的产物和浓度为0.1mol/L的氯化铵溶液加入到水中,加热至70℃下搅拌1h配制成混合溶液;再加入浓度为0.3mol/L的丙烯酰胺溶液,继续搅拌3h,然后洗涤抽滤,并且干燥处理,得到改性纳米淀粉吸附剂。将50份聚合氯化铝溶解在100份水中,在搅拌条件下加入5份膨润土和2份乙二胺四乙酸二钠,在40℃下反应2h后,得到混合溶液。在上述混合溶液中依次加入40份改性纳米淀粉吸附剂和3份硫酸镥常温下搅拌均匀,然后真空干燥过夜,即得到污水处理组合物。Add nano-starch particles, citric acid and potassium dihydrogen phosphate into water in a mass ratio of 1:0.2:0.3 to complete dissolution, then heat to 150 °C for reaction for 3 hours; then wash, suction, filter, and dry; A 0.1 mol/L ammonium chloride solution was added to water, heated to 70°C and stirred for 1 h to prepare a mixed solution; then a 0.3 mol/L acrylamide solution was added, stirring continued for 3 h, then washed and suction filtered, and dried treatment to obtain a modified nano-starch adsorbent. Dissolve 50 parts of polyaluminum chloride in 100 parts of water, add 5 parts of bentonite and 2 parts of disodium EDTA under stirring conditions, and react at 40° C. for 2 hours to obtain a mixed solution. 40 parts of modified nano-starch adsorbent and 3 parts of lutetium sulfate were sequentially added to the above mixed solution, stirred evenly at room temperature, and then vacuum-dried overnight to obtain a sewage treatment composition.
实施例6Example 6
将纳米淀粉颗粒、柠檬酸及磷酸二氢钾按照质量比为1:0.2:0.3的量加入水中至完全溶解,加热至150℃下反应3h;然后洗涤抽滤,干燥;将得到的产物和浓度为0.1mol/L的氯化铵溶液加入到水中,加热至70℃下搅拌1h配制成混合溶液;再加入浓度为0.3mol/L的丙烯酰胺溶液,继续搅拌3h,然后洗涤抽滤,并且干燥处理,得到改性 纳米淀粉吸附剂。将40份聚丙烯酰胺溶解在100份水中,在搅拌条件下加入10份膨润土和5份乙二胺四乙酸二钠,在40℃下反应2h后,得到混合溶液。在上述混合溶液中依次加入40份改性纳米淀粉吸附剂和5份硫酸镧常温下搅拌均匀,然后真空干燥过夜,即得到污水处理组合物。Add nano-starch particles, citric acid and potassium dihydrogen phosphate into water in a mass ratio of 1:0.2:0.3 to complete dissolution, then heat to 150 °C for reaction for 3 hours; then wash, suction, filter, and dry; A 0.1 mol/L ammonium chloride solution was added to water, heated to 70°C and stirred for 1 h to prepare a mixed solution; then a 0.3 mol/L acrylamide solution was added, stirring continued for 3 h, then washed and suction filtered, and dried treatment to obtain a modified nano-starch adsorbent. 40 parts of polyacrylamide were dissolved in 100 parts of water, 10 parts of bentonite and 5 parts of disodium EDTA were added under stirring conditions, and the mixed solution was obtained after reacting at 40° C. for 2 hours. 40 parts of modified nano-starch adsorbent and 5 parts of lanthanum sulfate were sequentially added to the above mixed solution, stirred evenly at room temperature, and then vacuum-dried overnight to obtain a sewage treatment composition.
实施例7Example 7
将纳米淀粉颗粒、柠檬酸及磷酸二氢钾按照质量比为1:0.3:0.1的量加入水中至完全溶解,加热至140℃下反应3h;然后洗涤抽滤,干燥;将得到的产物和浓度为0.3mol/L的氯化铵溶液加入到水中,加热至80℃下搅拌1h配制成混合溶液;再加入浓度为0.3mol/L的丙烯酰胺溶液,继续搅拌3h,然后洗涤抽滤,并且干燥处理,得到改性纳米淀粉吸附剂。将60份聚合硫酸氯化铁铝溶解在100份水中,在搅拌条件下加入5份膨润土和3份乙二胺四乙酸二钠,在40℃下反应2h后,得到混合溶液。在上述混合溶液中依次加入30份改性纳米淀粉吸附剂和2份硝酸镧常温下搅拌均匀,然后真空干燥过夜,即得到污水处理组合物。Add nano-starch particles, citric acid and potassium dihydrogen phosphate into water in a mass ratio of 1:0.3:0.1 to complete dissolution, then heat to 140 °C for reaction for 3 hours; then wash, suction, filter, and dry; A 0.3mol/L ammonium chloride solution was added to water, heated to 80°C and stirred for 1 h to prepare a mixed solution; then a 0.3mol/L acrylamide solution was added, stirring continued for 3h, then washing, suction filtration, and drying treatment to obtain a modified nano-starch adsorbent. Dissolve 60 parts of polyferric sulfate aluminum chloride in 100 parts of water, add 5 parts of bentonite and 3 parts of disodium EDTA under stirring conditions, and react at 40° C. for 2 hours to obtain a mixed solution. 30 parts of modified nano-starch adsorbent and 2 parts of lanthanum nitrate were sequentially added to the above mixed solution, stirred evenly at room temperature, and then vacuum-dried overnight to obtain a sewage treatment composition.
实施例8Example 8
将纳米淀粉颗粒、柠檬酸及磷酸二氢钾按照质量比为1:0.2:0.3的量加入水中至完全溶解,加热至140℃下反应3h;然后洗涤抽滤,干燥;将得到的产物和浓度为0.3mol/L的氯化铵溶液加入到水中,加热至80℃下搅拌1h配制成混合溶液;再加入浓度为0.3mol/L的丙烯酰胺溶液,继续搅拌3h,然后洗涤抽滤,并且干燥处理,得到改性纳米淀粉吸附剂。将40份聚合硫酸铁溶解在100份水中,在搅拌条件下加入5份膨润土和3份乙二胺四乙酸二钠,在30℃下反应2h后,得到混合溶液。在上述混合溶液中依次加入50份改性纳米淀粉吸附剂和2份硝酸镧常温下搅拌均匀,然后真空干燥过夜,即得到污水处理组合物。Add nano-starch particles, citric acid and potassium dihydrogen phosphate into water in a mass ratio of 1:0.2:0.3 to complete dissolution, and heat to 140 °C for reaction for 3 hours; then wash, suction, filter, and dry; A 0.3mol/L ammonium chloride solution was added to water, heated to 80°C and stirred for 1 h to prepare a mixed solution; then a 0.3mol/L acrylamide solution was added, stirring continued for 3h, then washing, suction filtration, and drying treatment to obtain a modified nano-starch adsorbent. Dissolve 40 parts of polymeric ferric sulfate in 100 parts of water, add 5 parts of bentonite and 3 parts of disodium EDTA under stirring conditions, and react at 30° C. for 2 hours to obtain a mixed solution. 50 parts of modified nano-starch adsorbent and 2 parts of lanthanum nitrate were sequentially added to the above mixed solution, stirred evenly at room temperature, and then vacuum-dried overnight to obtain a sewage treatment composition.
试验例1污水处理组合物的废水处理效果评价Test Example 1 Evaluation of Wastewater Treatment Effect of Wastewater Treatment Composition
试验方法:将实施例1-8制得的组合物应用于印染废水的废水处理试验中,原始印染废水主要水质指标见表1。具体方法为:在处理过程中,将组合物按照每升水20mL的投料比例直接加入到废水中,先以400r/min的速度进行搅拌5min,,静置沉淀60min 后,取上清液测各项指标,结果参见表2。Test method: The compositions prepared in Examples 1-8 were applied to the wastewater treatment test of printing and dyeing wastewater. The main water quality indicators of the original printing and dyeing wastewater are shown in Table 1. The specific method is as follows: in the treatment process, the composition is directly added to the waste water according to the feeding ratio of 20 mL per liter of water, first stirred at a speed of 400 r/min for 5 minutes, and after standing for 60 minutes for precipitation, the supernatant liquid is taken to measure various items. indicators, see Table 2 for the results.
表1印染废水水质指标Table 1 Water Quality Index of Printing and Dyeing Wastewater
指标index | COD,mg/LCOD, mg/L | 色度Chroma | 颜色color | 浊度Turbidity |
印染废水Dyeing Wastewater | 12501250 | 500500 | 深黄色dark yellow | 150150 |
表2处理后的指标测定Table 2 Determination of indicators after treatment
编号Numbering | COD,mg/LCOD, mg/L | 色度Chroma | 颜色color | 浊度Turbidity |
实施例1Example 1 | 2.52.5 | 66 | 无色colorless | 77 |
实施例2Example 2 | 3.43.4 | 99 | 无色colorless | 1313 |
实施例3Example 3 | 7.17.1 | 1616 | 无色colorless | 1010 |
实施例4Example 4 | 3.63.6 | 1010 | 无色colorless | 88 |
实施例5Example 5 | 8.98.9 | 1111 | 无色colorless | 1212 |
实施例6Example 6 | 7.77.7 | 1515 | 无色colorless | 99 |
实施例7Example 7 | 10.410.4 | 1313 | 无色colorless | 1111 |
实施例8Example 8 | 4.24.2 | 1313 | 无色colorless | 1313 |
由上表1和2的结果可以看出,本发明的组合物具有吸附能力强、脱色效果好的优点,对印染废水的处理效果好,其脱色率达到98.8%以上,COD去除率达到99.8%以上。It can be seen from the results in Tables 1 and 2 that the composition of the present invention has the advantages of strong adsorption capacity, good decolorization effect, and good treatment effect on printing and dyeing wastewater. The decolorization rate reaches more than 98.8%, and the COD removal rate reaches 99.8%. above.
以上所述,仅是本发明的较佳实施例而已,并非对本发明作任何形式上的限制,虽然本发明已以较佳实施例揭露如上,然而并非用以限定本发明,任何熟悉本专业的技术人员,在不脱离本发明技术方案范围内,当可利用上述揭示的方法及技术内容作出些许的更动或修饰为等同变化的等效实施例,但凡是未脱离本发明技术方案的内容,依据本发明的技术实质对以上实施例所作的任何简单修改、等同变化与修饰,均仍属于本发明 技术方案的范围内。The above are only preferred embodiments of the present invention, and do not limit the present invention in any form. Although the present invention has been disclosed above with preferred embodiments, it is not intended to limit the present invention. The skilled person, within the scope of the technical solution of the present invention, can make some changes or modifications to equivalent examples of equivalent changes by using the methods and technical contents disclosed above, but not departing from the content of the technical solution of the present invention, Any simple modifications, equivalent changes and modifications made to the above embodiments according to the technical essence of the present invention still fall within the scope of the technical solutions of the present invention.
Claims (10)
- 一种用于印染废水的污水处理组合物,按照重量百分比计,该组合物包括以下组分且各组分含量为:絮凝剂40~60%,改性纳米淀粉吸附剂30~50%,膨润土5~10%,助凝剂1~5%,乙二胺四乙酸二钠1~5%。A sewage treatment composition for printing and dyeing wastewater, in terms of percentage by weight, the composition comprises the following components and the contents of each component are: flocculant 40-60%, modified nano-starch adsorbent 30-50%, bentonite 5~10%, coagulation aid 1~5%, disodium EDTA 1~5%.
- 根据权利要求1所述的用于印染废水的污水处理组合物,其中,按照重量百分比计,该组合物包括以下组分且各组分含量为:絮凝剂50%,改性纳米淀粉吸附剂35%,膨润土8%,助凝剂3%,乙二胺四乙酸二钠4%。The sewage treatment composition for printing and dyeing wastewater according to claim 1, wherein, by weight percentage, the composition comprises the following components and the content of each component is: flocculant 50%, modified nano-starch adsorbent 35% %, bentonite 8%, coagulant aid 3%, disodium EDTA 4%.
- 根据权利要求1所述的用于印染废水的污水处理组合物,其中,按照重量百分比计,该组合物包括以下组分且各组分含量为:絮凝剂50%,改性纳米淀粉吸附剂40%,膨润土5%,助凝剂3%,乙二胺四乙酸二钠2%。The sewage treatment composition for printing and dyeing wastewater according to claim 1, wherein, in terms of weight percentage, the composition comprises the following components and the content of each component is: flocculant 50%, modified nano-starch adsorbent 40% %, bentonite 5%, coagulant aid 3%, disodium EDTA 2%.
- 根据权利要求1所述的用于印染废水的污水处理组合物,其中,所述絮凝剂选自聚合硫酸氯化铁铝、聚合硫酸铁、聚丙烯酰胺、聚合氯化铝中的任一种。The sewage treatment composition for printing and dyeing wastewater according to claim 1, wherein the flocculant is selected from any one of polyferric sulfate aluminum chloride, polyferric sulfate, polyacrylamide, and polyaluminum chloride.
- 根据权利要求1所述的用于印染废水的污水处理组合物,其中,所述助凝剂选自镧、铈、镨、钕、镥、铕、钆、铒、铥、钇的硝酸盐、硫酸盐中的一种或多种。The sewage treatment composition for printing and dyeing wastewater according to claim 1, wherein the coagulant is selected from the group consisting of lanthanum, cerium, praseodymium, neodymium, lutetium, europium, gadolinium, erbium, thulium, yttrium nitrate, sulfuric acid one or more of the salts.
- 一种用于印染废水的污水处理组合物的制备方法,该方法包括以下步骤:A preparation method of a sewage treatment composition for printing and dyeing wastewater, the method comprising the following steps:(1)将纳米淀粉颗粒、柠檬酸及磷酸二氢钾加入水中至完全溶解,加热至130~150℃下反应3~5h;然后洗涤抽滤,干燥;将得到的产物和氯化铵溶液加入到水中,加热至70~90℃下搅拌0.5~1h配制成混合溶液;再加入丙烯酰胺溶液,继续搅拌3h,然后洗涤抽滤,并且干燥处理,得到改性纳米淀粉吸附剂;(1) Add nano-starch granules, citric acid and potassium dihydrogen phosphate into water to dissolve completely, then heat to 130~150℃ for 3~5h reaction; then wash, suction filter, and dry; add the obtained product and ammonium chloride solution into into water, heated to 70 to 90 °C and stirred for 0.5 to 1 h to prepare a mixed solution; then added acrylamide solution, continued to stir for 3 h, then washed, suction filtered, and dried to obtain a modified nanostarch adsorbent;(2)将絮凝剂溶解在水中,在搅拌条件下加入膨润土和乙二胺四乙酸二钠,反应后得到混合溶液;(2) dissolving the flocculant in water, adding bentonite and disodium EDTA under stirring conditions, and obtaining a mixed solution after the reaction;(3)在上述混合溶液中依次加入改性纳米淀粉吸附剂和助凝剂常温下搅拌均匀,然后真空干燥过夜,即得到污水处理组合物。(3) The modified nano-starch adsorbent and the coagulant aid are sequentially added to the above mixed solution, stirred evenly at room temperature, and then vacuum-dried overnight to obtain a sewage treatment composition.
- 根据权利要求6所述的制备方法,其中,所述步骤(1)中所述纳米淀粉颗粒、柠檬酸及磷酸二氢钾的质量比为1:(0.1~0.5):(0.1~0.5)。The preparation method according to claim 6, wherein the mass ratio of the nano-starch particles, citric acid and potassium dihydrogen phosphate in the step (1) is 1:(0.1-0.5):(0.1-0.5).
- 根据权利要求6所述的制备方法,其中,所述步骤(1)中所述氯化铵溶液的浓度为0.1~0.5mol/L。The preparation method according to claim 6, wherein the concentration of the ammonium chloride solution in the step (1) is 0.1-0.5 mol/L.
- 根据权利要求6所述的制备方法,其中,所述步骤(1)中所述丙烯酰胺溶液的浓度为0.1~0.5mol/L。The preparation method according to claim 6, wherein the concentration of the acrylamide solution in the step (1) is 0.1-0.5 mol/L.
- 根据权利要求6所述的制备方法,其中,所述步骤(2)中所述反应条件为:温度20~40℃,时间1~3h。The preparation method according to claim 6, wherein the reaction conditions in the step (2) are: a temperature of 20-40° C. and a time of 1-3 hours.
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