CN105199032A - Super-early-strength PCE (polycarboxylate ether) superplasticizer and preparation method thereof - Google Patents
Super-early-strength PCE (polycarboxylate ether) superplasticizer and preparation method thereof Download PDFInfo
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- CN105199032A CN105199032A CN201510666067.3A CN201510666067A CN105199032A CN 105199032 A CN105199032 A CN 105199032A CN 201510666067 A CN201510666067 A CN 201510666067A CN 105199032 A CN105199032 A CN 105199032A
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- 238000002360 preparation method Methods 0.000 title claims description 28
- 229920005646 polycarboxylate Polymers 0.000 title abstract description 16
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 title abstract description 8
- 239000008030 superplasticizer Substances 0.000 title abstract 9
- 150000001875 compounds Chemical class 0.000 claims abstract description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 73
- 239000003638 chemical reducing agent Substances 0.000 claims description 68
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 39
- JHUFGBSGINLPOW-UHFFFAOYSA-N 3-chloro-4-(trifluoromethoxy)benzoyl cyanide Chemical compound FC(F)(F)OC1=CC=C(C(=O)C#N)C=C1Cl JHUFGBSGINLPOW-UHFFFAOYSA-N 0.000 claims description 37
- 239000003999 initiator Substances 0.000 claims description 35
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 31
- LVHBHZANLOWSRM-UHFFFAOYSA-N itaconic acid Chemical compound OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims description 24
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 22
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 claims description 18
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims description 16
- 238000009413 insulation Methods 0.000 claims description 16
- 238000010792 warming Methods 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 14
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 13
- -1 sulfhydryl compound Chemical class 0.000 claims description 13
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinyl group Chemical group C1(O)=CC(O)=CC=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 9
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 9
- HMBNQNDUEFFFNZ-UHFFFAOYSA-N 4-ethenoxybutan-1-ol Chemical compound OCCCCOC=C HMBNQNDUEFFFNZ-UHFFFAOYSA-N 0.000 claims description 7
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 7
- ASUAYTHWZCLXAN-UHFFFAOYSA-N prenol Chemical compound CC(C)=CCO ASUAYTHWZCLXAN-UHFFFAOYSA-N 0.000 claims description 7
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical group [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 claims description 6
- 239000012312 sodium hydride Substances 0.000 claims description 6
- 229910000104 sodium hydride Inorganic materials 0.000 claims description 6
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 5
- 239000004160 Ammonium persulphate Substances 0.000 claims description 5
- 239000004342 Benzoyl peroxide Substances 0.000 claims description 5
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 claims description 5
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 claims description 5
- 235000019395 ammonium persulphate Nutrition 0.000 claims description 5
- 235000019400 benzoyl peroxide Nutrition 0.000 claims description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 4
- 239000004159 Potassium persulphate Substances 0.000 claims description 4
- XFCCROJBZHEHMS-UHFFFAOYSA-N methoxymethane;phenol Chemical compound COC.OC1=CC=CC=C1 XFCCROJBZHEHMS-UHFFFAOYSA-N 0.000 claims description 4
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 claims description 4
- 235000019394 potassium persulphate Nutrition 0.000 claims description 4
- 238000002791 soaking Methods 0.000 claims description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 3
- 239000011734 sodium Substances 0.000 claims description 3
- 229910052708 sodium Inorganic materials 0.000 claims description 3
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 claims description 2
- 101150065749 Churc1 gene Proteins 0.000 claims description 2
- 102100038239 Protein Churchill Human genes 0.000 claims description 2
- 150000001768 cations Chemical class 0.000 claims 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims 1
- 239000004568 cement Substances 0.000 abstract description 39
- 238000006243 chemical reaction Methods 0.000 abstract description 22
- 239000004567 concrete Substances 0.000 abstract description 19
- 230000000694 effects Effects 0.000 abstract description 7
- 150000002500 ions Chemical class 0.000 abstract description 7
- 239000000178 monomer Substances 0.000 abstract description 6
- 239000002994 raw material Substances 0.000 abstract description 5
- 238000009830 intercalation Methods 0.000 abstract description 3
- 230000002687 intercalation Effects 0.000 abstract description 3
- 238000001179 sorption measurement Methods 0.000 abstract description 2
- 239000000654 additive Substances 0.000 abstract 1
- 230000000996 additive effect Effects 0.000 abstract 1
- 230000036571 hydration Effects 0.000 abstract 1
- 238000006703 hydration reaction Methods 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 19
- 230000015572 biosynthetic process Effects 0.000 description 15
- 238000003786 synthesis reaction Methods 0.000 description 14
- 239000007864 aqueous solution Substances 0.000 description 10
- 238000009835 boiling Methods 0.000 description 9
- 239000008367 deionised water Substances 0.000 description 9
- 229910021641 deionized water Inorganic materials 0.000 description 9
- 239000002245 particle Substances 0.000 description 9
- 238000010992 reflux Methods 0.000 description 9
- 239000008187 granular material Substances 0.000 description 7
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 239000007795 chemical reaction product Substances 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- DNJIEGIFACGWOD-UHFFFAOYSA-N ethyl mercaptane Natural products CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 description 4
- 239000002002 slurry Substances 0.000 description 4
- 230000003335 steric effect Effects 0.000 description 4
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 4
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 4
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 0.000 description 4
- AGIBHMPYXXPGAX-UHFFFAOYSA-N 2-(iodomethyl)oxirane Chemical compound ICC1CO1 AGIBHMPYXXPGAX-UHFFFAOYSA-N 0.000 description 3
- DKIDEFUBRARXTE-UHFFFAOYSA-N 3-mercaptopropanoic acid Chemical compound OC(=O)CCS DKIDEFUBRARXTE-UHFFFAOYSA-N 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000000274 adsorptive effect Effects 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000010881 fly ash Substances 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 238000010189 synthetic method Methods 0.000 description 2
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 description 1
- LRWZZZWJMFNZIK-UHFFFAOYSA-N 2-chloro-3-methyloxirane Chemical compound CC1OC1Cl LRWZZZWJMFNZIK-UHFFFAOYSA-N 0.000 description 1
- CVEPFOUZABPRMK-UHFFFAOYSA-N 2-methylprop-2-enoic acid;styrene Chemical compound CC(=C)C(O)=O.C=CC1=CC=CC=C1 CVEPFOUZABPRMK-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000004873 anchoring Methods 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000001934 delay Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- GKIPXFAANLTWBM-UHFFFAOYSA-N epibromohydrin Chemical compound BrCC1CO1 GKIPXFAANLTWBM-UHFFFAOYSA-N 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 238000007306 functionalization reaction Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- QVDTXNVYSHVCGW-ONEGZZNKSA-N isopentenol Chemical compound CC(C)\C=C\O QVDTXNVYSHVCGW-ONEGZZNKSA-N 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 230000037048 polymerization activity Effects 0.000 description 1
- 229940051841 polyoxyethylene ether Drugs 0.000 description 1
- 229920000056 polyoxyethylene ether Polymers 0.000 description 1
- 229960002796 polystyrene sulfonate Drugs 0.000 description 1
- 239000011970 polystyrene sulfonate Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 230000000452 restraining effect Effects 0.000 description 1
- XWGJFPHUCFXLBL-UHFFFAOYSA-M rongalite Chemical compound [Na+].OCS([O-])=O XWGJFPHUCFXLBL-UHFFFAOYSA-M 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 125000002769 thiazolinyl group Chemical group 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Landscapes
- Macromonomer-Based Addition Polymer (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
Abstract
The invention provides a super-early-strength PCE (polycarboxylate ether) superplasticizer. The super-early-strength PCE superplasticizer is a compound shown in formula (I) and is synthesized with active macro-monomers used as raw materials, the space hindrance effect of the superplasticizer is further improved, and meanwhile, positive ions with good cement resistance are introduced in molecules, so that the superplasticizing rate, the cement resistance and the cement adaptability of the superplasticizer are increased. The superplasticizer has better tolerance and cannot have a continuous intercalation reaction with the cement. The positive ions of the super-early-strength PCE superplasticizer can inhibit expansion of the cement so as to reduce adsorption of the cement to an additive. The super-early-strength PCE superplasticizer can accelerate the hydration function of the cement and has the super-early-strength function. The super-early-strength PCE superplasticizer has super-early-strength and cement-resistant functions in common concrete.
Description
Technical field
The present invention relates to a kind of water reducer, be specifically related to a kind of ultra high early strength poly-carboxylic water reducer and preparation method thereof.
Background technology
In recent years, the R & D and manufacture of concrete admixture has tended to towards high-performance, pollution-free future development, and cement water reducing agent is that in concrete admixture, application surface is the widest, the one that usage quantity is maximum.Water reducer mixes in fresh concrete, can destroy the flucculation structure of cement granules, plays the effect of disperse cement particles and hydrated cementitious particle, thus discharges the free water in flucculation structure, increases the mobility of concrete mix.PCEs water reducer belongs to aniorfic surfactant, mixes in cement slurry, is adsorbed on cationic cement particle surface, and is dissociated into hydrophilic and organic anionic groups that is oleophilic function.
Water reducer molecular skeleton is made up of main chain and more side chain.Containing more active group on main chain, and polarity is stronger, rely on these active groups, main chain can " anchoring " on cement particle surface, and side chain has wetting ability, can stretch in the liquid phase, thus form larger three-dimensional adsorption structure at cement particle surface, produce space steric effect, thus cement granules is disperseed and stablizes.Carboxylic acid ion makes the negative charge on cement granules band produce electrostatic repulsion between cement granules, and cement granules is disperseed, and increases the contact of cement granules and water, makes the abundant aquation of cement.In the process of disperse cement particles, discharge the free water that aggregate comprises, improve workability, decrease and mix the water yield.
RCOO
-with Ca
2+ionization forms complex compound, reduces the Ca in solution
2+concentration, delays Ca (OH)
2form crystallization, reduce the formation of C-H-S gel, delayed the aquation of cement.
The polycarboxylate water-reducer (PCEs) with combed molecular structure is made up of to the main chain of negatively charged ion polyethoxye (PEO) side chain graft usually, PEO side chain produces space steric effect between the cement granules being suspended in aqueous phase, by adjusting the molecular structure of PCEs, different objects can be reached, as slump retaining is good, water-reducing rate is high, cohesiveness is good, resistance to mud is good, in addition low cost, the advantage such as pollution-free, the research of polycarboxylate water-reducer has become the focus of domestic and international concrete admixture research and development.
The main raw material of poly carboxylic acid series water reducer has unsaturated acid, as maleic anhydride, toxilic acid and the polymerisable carboxylic acid such as vinylformic acid, methacrylic acid, the thiazolinyl materials such as polyalkenyl hydrocarbon, ether, alcohol, poly styrene sulfonate or ester and acrylate, ester, dihydroxy-benzene, acrylamide etc., synthetic method has the direct copolymerization of polymerisable monomer, polymerization Post functionalization method, in-situ polymerization and grafting etc. substantially.
The direct copolymerization of polymerisable monomer: this synthetic method is generally first prepare the pendant reactive polymeric monomer (being generally methoxy polyethylene glycol methacrylate-styrene polymer) with polymerization activity, then the monomer of certain proportioning is mixed, directly adopt solution polymerization and obtain finished product.This polymerization process, technique is simple, but prerequisite wants composite reactive polymerizable surface-active macromonomer, and the performance of surface-active macromonomer directly determines and affect the performance of the finished product polycarboxylate water-reducer.
Current China market mainly contains for the production of the active polymeric monomer of PCEs water reducer:
MPEG: poly glycol monomethyl ether
VPEG:4-hydroxy butyl vinyl ether Soxylat A 25-7
APEG: allyl alcohol polyethenoxy ether
HPEG: isobutene alcohol Soxylat A 25-7
TPEG: isopentenol polyoxyethylene ether
APEG is bar-shaped rigid structure, high to cement adsorptive capacity, and TPEG microtexture is star-shape polymer, has soft segment microtexture, few to cement adsorptive capacity.
APEG is the main raw material of synthesizing polycarboxylic acid high-performance water reducing agent, the advantages such as PCEs water reducer has good dispersity, volume is low, and water-reducing rate is high, adaptability is good of synthesis; Shortcoming is inferior suitability, and Slump Time losing of Large is large.HPEG and TPEG is the water reducer of raw material production, and water-reducing rate is more or less the same, but summer uses, and slump retaining gap is comparatively large, and cement adaptability is slightly poor.Use the polycarboxylate water-reducer that TPEG is main material production, water-reducing rate is high, and slump retaining is good, strong to cement adaptability, and production process equipment is simple, and by polycarboxylate water-reducer, manufacturers is favored.But due to complicacy and the diversity of China's concrete raw material, especially when the earth content of sandstone is large, concrete slump-loss is large, the polycarboxylate water-reducer produced by TPEG, because PEG side chain and earth occur to connect intercalation, make its resistance to mud poor, can not meet the requirement of concrete construction performance.
Summary of the invention
The object of the invention is to overcome weak point that prior art exists and provide a kind of ultra high early strength poly-carboxylic water reducer and preparation method thereof, this water reducer has cationic charge in the molecular structure, due to both sexes structure and the space steric effect of its uniqueness, it is made to have unique dispersive ability, water-reducing rate is high, and resistance to earth is good.
For achieving the above object, the technical scheme taked: a kind of ultra high early strength poly-carboxylic water reducer, described ultra high early strength poly-carboxylic water reducer is the compound shown in formula I, and the structural formula of the compound shown in described formula I is as follows:
Wherein a is the integer of 1 ~ 80, and b is the integer of 1 ~ 80, and c is the integer of 1 ~ 50; L is the integer of 1 ~ 50;
A is
r is H or CH3;
B is
C is
M is
r
2, R
3and R
4be alone C respectively
1-3alkyl; X
-for Cl
-, Br
-or I
-; M is the integer of 5 ~ 200, and n is the integer of 0 ~ 50, and z is the integer of 1 ~ 150.
The invention provides the preparation method of ultra high early strength poly-carboxylic water reducer described above, said method comprising the steps of:
By surface-active macromonomer, one in methacrylic acid, vinylformic acid, methylene-succinic acid and maleic anhydride, the one in APEG, HPEG, VPEG and TPEG, sodium allyl sulfonate, water and molecular weight regulator mix, be warming up to 85 ~ 95 DEG C, drip initiator, time for adding is 1 ~ 10h, dropwises rear insulation, soaking time is 1 ~ 12h, then be cooled to 45 ~ 50 DEG C, add sodium hydroxide solution and regulate pH to 7.0-8.0, obtain ultra high early strength poly-carboxylic water reducer;
Described surface-active macromonomer is the compound shown in formula II, and the structural formula of the compound shown in described formula II is as follows:
Wherein R
1for H
2c==CH---O---CH
2cH
2cH
2cH
2---, H
2c==CHCH
2---,
or
r2, R3 and R4 are alone C1-3 alkyl respectively; X-is Cl-, Br-or I-;
M is the integer of 5 ~ 200, and n is the integer of 0 ~ 50, and z is the integer of 1 ~ 150.
Preferably, described m is the integer of 10 ~ 180, and described n is the integer of 0 ~ 40, and described z is the integer of 1 ~ 100.More preferably, described m is the integer of 12 ~ 100, and described n is the integer of 0 ~ 30, and described z is the integer of 1 ~ 80.
Preferably, described surface-active macromonomer, one in methacrylic acid, vinylformic acid, methylene-succinic acid and maleic anhydride, the mol ratio of a kind of and sodium allyl sulfonate in APEG, HPEG, VPEG and TPEG is described surface-active macromonomer: the one in methacrylic acid, vinylformic acid, methylene-succinic acid and maleic anhydride: the one in APEG, HPEG, VPEG and TPEG: sodium allyl sulfonate=1.0 ~ 3.0:1 ~ 6.0:1:0.2 ~ 6.0.
Preferably, described molecular weight regulator is at least one in sulfhydryl compound and Virahol, the consumption of described molecular weight regulator is described surface-active macromonomer, one in methacrylic acid, vinylformic acid, methylene-succinic acid and maleic anhydride, 0.005 ~ 5% of a kind of and acrylamide in APEG, HPEG, VPEG and TPEG and the total mole number of sodium allyl sulfonate.More preferably, described molecular weight regulator is at least one in 3-thiohydracrylic acid, Thiovanic acid, mercaptoethanol, rongalite and Virahol, the consumption of described molecular weight regulator is described surface-active macromonomer, a kind of and 1 ~ 3.5% of a kind of total mole number in APEG, HPEG, VPEG and TPEG in methacrylic acid, vinylformic acid, methylene-succinic acid and maleic anhydride.Most preferably, the consumption of described molecular weight regulator is described surface-active macromonomer, a kind of and 1.2 ~ 2.5% of a kind of total mole number in APEG, HPEG, VPEG and TPEG in methacrylic acid, vinylformic acid, methylene-succinic acid and maleic anhydride.
Preferably, the time for adding of described initiator is 2 ~ 3h; Described soaking time is 2 ~ 4h.
Preferably, the mass concentration of described sodium hydroxide solution is 30%; Described initiator is the one in the aqueous solution of Potassium Persulphate, ammonium persulphate, hydrogen peroxide and benzoyl peroxide, the consumption of described initiator is described surface-active macromonomer, one in methacrylic acid, vinylformic acid, methylene-succinic acid and maleic anhydride, 0.05% ~ 5% of a kind of and acrylamide in APEG, HPEG, VPEG and TPEG and the total mole number of sodium allyl sulfonate.
Preferably, described cation quaternary ammonium salt PEO surface-active macromonomer is prepared from by following methods:
(1) by the one in vinyl carbinol, isobutene alcohol, 4-hydroxy butyl vinyl ether and prenol, one in the mixture of oxyethane and oxyethane and propylene oxide, mix with epoxyhalopropane, add catalyzer, react 2 ~ 10 hours under temperature is 80 ~ 150 DEG C of conditions, obtain active intermediate; Its reaction equation is as follows:
(2) quarternary ammonium salt compound is mixed with stopper, slowly add the active intermediate that step (1) synthesizes and react 1 ~ 10h under temperature is 10 ~ 80 DEG C of conditions, obtain described surface-active macromonomer; Its reaction equation is as follows:
Described quarternary ammonium salt compound is N (R
2r
3r
4), wherein R
2, R
3and R
4be alone C respectively
1-3alkyl.
Preferably, one in described step (1) in vinyl carbinol, isobutene alcohol, 4-hydroxy butyl vinyl ether and prenol, one in the mixture of oxyethane and oxyethane and propylene oxide is the one in vinyl carbinol, isobutene alcohol, 4-hydroxy butyl vinyl ether and prenol with the mol ratio of epoxyhalopropane: the one in the mixture of oxyethane and oxyethane and propylene oxide: epoxyhalopropane=1:5 ~ 250:1 ~ 150.
Preferably, in described step (2), the mol ratio of quarternary ammonium salt compound and active intermediate is 0.2:1 ~ 2:1.
Preferably, in described step (1), catalyzer is sodium hydride or sodium; Stopper is Resorcinol or to methyl ether phenol, the consumption of described stopper is 0.02% ~ 0.08% of described active intermediate mole number in described step (2).
Beneficial effect of the present invention is: the invention provides a kind of ultra high early strength poly-carboxylic water reducer, and relative to prior art, its advantage is:
Ultra high early strength poly-carboxylic water reducer of the present invention with cation quaternary ammonium salt PEO surface-active macromonomer for Material synthesis, while the space steric effect improving water reducer further, introduce positively charged ion in the molecule, and positively charged ion has good anti-mud, thus improve water-reducing rate, resistance to mud and the adaptability to cement of water reducer.To earth, there is better tolerance, do not occur to connect intercalation with earth.
The positively charged ion of ultra high early strength poly-carboxylic water reducer of the present invention can suppress the expansion of earth, thus reduces earth to the absorption of admixture.When ultra high early strength poly-carboxylic water reducer of the present invention joins in cement slurry, the anionic charge of main chain is adsorbed on positively charged cement particle surface, and the positive charge of side chain end group is then adsorbed on electronegative cement particle surface, disperse cement particles.Because poly-hydroxy becomes hydrogen bond with water, add the viscosity of cement slurry, improve mobility and the cohesiveness of concrete mix.
Ultra high early strength poly-carboxylic water reducer of the present invention can accelerate the water of cement and turn use into, has super hardening effect.Ultra high early strength poly-carboxylic water reducer of the present invention, in normal concrete, has resistance to mud effect, is used in pipe pile body concrete, have super hardening effect, can realize singly exempting from and twoly exempting from technique of pile tube, and not need to add any active mineral admixture.
Embodiment
For better the object, technical solutions and advantages of the present invention being described, below in conjunction with specific embodiment, the invention will be further described.
Embodiment 1
A kind of embodiment of the preparation method of surface-active macromonomer of the present invention:
1), the synthesis of active intermediate
5mol prenol is injected, 5g sodium hydride, 25mol oxyethane in the autoclave closed, and 5mol epoxy chloropropane, stir, 80 DEG C of reaction 10h, obtain reaction product active intermediate.
2) synthesis of surface-active macromonomer
1mol triethylamine and 0.001mol Resorcinol are added in flask, is warming up to 10 DEG C, slowly drip the triethylamine solution of the active intermediate synthesized containing 5mol step (1), after dropwising, under 10 DEG C of conditions, continue insulation reaction 10h, obtain surface-active macromonomer.
Embodiment 2
A kind of embodiment of the preparation method of cation quaternary ammonium salt PEO surface-active macromonomer of the present invention:
1), the synthesis of active intermediate
5mol isobutene alcohol is injected, 20g sodium hydride, 500mol oxyethane, 250mol propylene oxide in the autoclave closed, and 750mol epoxy bromopropane, stir, 150 DEG C of reaction 2h, obtain reaction product active intermediate.
2) synthesis of surface-active macromonomer
3mol Trimethylamine 99 and 0.004mol Resorcinol are added in flask, is warming up to 30 DEG C, slowly drip the trimethylamine solution of the active intermediate synthesized containing 5mol step (1), after dropwising, under 30 DEG C of conditions, continue insulation reaction 10h, obtain surface-active macromonomer.
Embodiment 3
A kind of embodiment of the preparation method of surface-active macromonomer of the present invention:
1), the synthesis of active intermediate
5mol vinyl carbinol is injected, 10g sodium hydride, 1000mol oxyethane in the autoclave closed, and 400mol Epiiodohydrin, stir, 100 DEG C of reaction 6h, obtain reaction product active intermediate.
2) synthesis of surface-active macromonomer
5mol tripropyl amine and 0.0015mol Resorcinol are added in flask, is warming up to 50 DEG C, slowly drip the tripropyl amine solution of the active intermediate synthesized containing 5mol step (1), after dropwising, under 50 DEG C of conditions, continue insulation reaction 8h, obtain surface-active macromonomer.
Embodiment 4
A kind of embodiment of the preparation method of surface-active macromonomer of the present invention:
1), the synthesis of active intermediate
In the autoclave closed, inject 5mol4-hydroxy butyl vinyl ether, 10g sodium hydride, 50mol oxyethane, 5mol propylene oxide and 500mol Epiiodohydrin, stir 120 DEG C of reaction 5h, obtain reaction product active intermediate.
2) synthesis of surface-active macromonomer
By 7molN, N-dimethyl amine and 0.0025mol add in flask to methyl ether phenol, be warming up to 70 DEG C, slow dropping contains the N of the active intermediate that 5mol step (1) is synthesized, N-dimethyl amine solution, after dropwising, under 70 DEG C of conditions, continue insulation reaction 4h, obtain surface-active macromonomer.
Embodiment 5
A kind of embodiment of the preparation method of surface-active macromonomer of the present invention:
1), the synthesis of active intermediate
5mol vinyl carbinol is injected, 10g sodium, 900mol oxyethane, 150mol propylene oxide in the autoclave closed, and 250mol Epiiodohydrin, stir, 120 DEG C of reaction 5h, obtain reaction product active intermediate.
2) synthesis of surface-active macromonomer
By 10molN, N-diethyl methyl amine and 0.002mol add in flask to methyl ether phenol, be warming up to 80 DEG C, slow dropping contains the N of the active intermediate that 5mol step (1) is synthesized, N-diethyl methyl amine solution, after dropwising, under 80 DEG C of conditions, continue insulation reaction 1h, obtain surface-active macromonomer.
Embodiment 6
A kind of embodiment of the preparation method of ultra high early strength poly-carboxylic water reducer of the present invention:
Agitator is being housed, in the 1000ml four-hole boiling flask of thermometer and reflux condensing tube, add molecular weight regulator, surface-active macromonomer described in 1.0mol embodiment 1, 1mol methacrylic acid, 1.0molAPEG, 0.2mol sodium allyl sulfonate and 400ml deionized water, described molecular weight regulator is 3-thiohydracrylic acid, the consumption of described molecular weight regulator is described surface-active macromonomer, methacrylic acid, 0.005% of sodium allyl sulfonate and APEG total mole number, be warming up to 85 DEG C, drip the aqueous solution of initiator, described initiator is Potassium Persulphate, the consumption of described initiator is described surface-active macromonomer, methacrylic acid, 0.05% of sodium allyl sulfonate and APEG total mole number, time for adding is 1h, after dropwising, insulation reaction 1h, at being cooled to 50 DEG C, add the NaOH solution that mass concentration is 30%, regulate pH=7.0, obtain ultra high early strength poly-carboxylic water reducer.
Embodiment 7
A kind of embodiment of the preparation method of ultra high early strength poly-carboxylic water reducer of the present invention:
Agitator is being housed, in the 1000ml four-hole boiling flask of thermometer and reflux condensing tube, add molecular weight regulator, surface-active macromonomer described in 2mol embodiment 2, 2mol vinylformic acid, , 1molHPEG, 1mol sodium allyl sulfonate and 600ml deionized water, described molecular weight regulator is Thiovanic acid, the consumption of described molecular weight regulator is described surface-active macromonomer, vinylformic acid, 5% of sodium allyl sulfonate and HPEG total mole number, be warming up to 95 DEG C, drip the aqueous solution of initiator, described initiator is ammonium persulphate, the consumption of described initiator is described surface-active macromonomer, vinylformic acid, 5% of sodium allyl sulfonate and HPEG total mole number, time for adding is 10h, after dropwising, insulation reaction 12h, at being cooled to 45 DEG C, add the NaOH solution that mass concentration is 30%, regulate pH=8.0, obtain ultra high early strength poly-carboxylic water reducer.
Embodiment 8
A kind of embodiment of the preparation method of ultra high early strength poly-carboxylic water reducer of the present invention:
Agitator is being housed, in the 1000ml four-hole boiling flask of thermometer and reflux condensing tube, add molecular weight regulator, surface-active macromonomer described in 3mol embodiment 3, 6mol vinylformic acid, 1molTPEG, 6mol sodium allyl sulfonate and 500ml deionized water, described molecular weight regulator is mercaptoethanol, the consumption of described molecular weight regulator is described surface-active macromonomer, vinylformic acid, 1% of sodium allyl sulfonate and TPEG total mole number, be warming up to 90 DEG C, drip the aqueous solution of initiator, described initiator is benzoyl peroxide, the consumption of described initiator is described surface-active macromonomer, vinylformic acid, 0.1% of sodium allyl sulfonate and TPEG total mole number, time for adding is 5h, after dropwising, insulation reaction 6h, at being cooled to 50 DEG C, add the NaOH solution that mass concentration is 30%, regulate pH=7.5, obtain ultra high early strength poly-carboxylic water reducer.
Embodiment 9
A kind of embodiment of the preparation method of ultra high early strength poly-carboxylic water reducer of the present invention:
Agitator is being housed, in the 1000ml four-hole boiling flask of thermometer and reflux condensing tube, add molecular weight regulator, surface-active macromonomer described in 3mol embodiment 4, 3mol methacrylic acid, 1.0molVPEG, 3mol sodium allyl sulfonate and 400ml deionized water, described molecular weight regulator is Virahol, the consumption of described molecular weight regulator is described surface-active macromonomer, methacrylic acid, 3.5% of sodium allyl sulfonate and VPEG total mole number, be warming up to 85 DEG C, drip the aqueous solution of initiator, described initiator is hydrogen peroxide, the consumption of described initiator is described surface-active macromonomer, methacrylic acid, 3% of sodium allyl sulfonate and VPEG total mole number, time for adding is 2h, after dropwising, insulation reaction 2h, at being cooled to 50 DEG C, add the NaOH solution that mass concentration is 30%, regulate pH=7.0, obtain ultra high early strength poly-carboxylic water reducer.
Embodiment 10
A kind of embodiment of the preparation method of ultra high early strength poly-carboxylic water reducer of the present invention:
Agitator is being housed, in the 1000ml four-hole boiling flask of thermometer and reflux condensing tube, add molecular weight regulator, surface-active macromonomer described in 3mol embodiment 5, 1mol vinylformic acid, 1molHPEG, 3mol sodium allyl sulfonate and 600ml deionized water, described molecular weight regulator is Thiovanic acid, the consumption of described molecular weight regulator is described surface-active macromonomer, vinylformic acid, 1.2% of sodium allyl sulfonate and HPEG total mole number, be warming up to 95 DEG C, drip the aqueous solution of initiator, described initiator is ammonium persulphate, the consumption of described initiator is described surface-active macromonomer, vinylformic acid, 2% of sodium allyl sulfonate and HPEG total mole number, time for adding is 3h, after dropwising, insulation reaction 4h, at being cooled to 45 DEG C, add the NaOH solution that mass concentration is 30%, regulate pH=8.0, obtain ultra high early strength poly-carboxylic water reducer.
Embodiment 11
A kind of embodiment of the preparation method of ultra high early strength poly-carboxylic water reducer of the present invention:
Agitator is being housed, in the 1000ml four-hole boiling flask of thermometer and reflux condensing tube, add molecular weight regulator, surface-active macromonomer described in 1mol embodiment 1, 4mol vinylformic acid, 1molTPEG, 4mol sodium allyl sulfonate and 500ml deionized water, described molecular weight regulator is mercaptoethanol, the consumption of described molecular weight regulator is described surface-active macromonomer, vinylformic acid, 2.5% of sodium allyl sulfonate and TPEG total mole number, be warming up to 90 DEG C, drip the aqueous solution of initiator, described initiator is benzoyl peroxide, the consumption of described initiator is described surface-active macromonomer, vinylformic acid, 1% of sodium allyl sulfonate and TPEG total mole number, time for adding is 7h, after dropwising, insulation reaction 8h, at being cooled to 50 DEG C, add the NaOH solution that mass concentration is 30%, regulate pH=7.5, obtain ultra high early strength poly-carboxylic water reducer.
Embodiment 12
A kind of embodiment of the preparation method of ultra high early strength poly-carboxylic water reducer of the present invention:
Agitator is being housed, in the 1000ml four-hole boiling flask of thermometer and reflux condensing tube, add molecular weight regulator, surface-active macromonomer described in 1.6mol embodiment 2, 1.2mol methacrylic acid, 1.0molAPEG, 1.6mol sodium allyl sulfonate and 400ml deionized water, described molecular weight regulator is 3-thiohydracrylic acid, , the consumption of described molecular weight regulator is described surface-active macromonomer, methacrylic acid, 2% of sodium allyl sulfonate and APEG total mole number, be warming up to 85 DEG C, drip the aqueous solution of initiator, described initiator is Potassium Persulphate, the consumption of described initiator is described surface-active macromonomer, methacrylic acid, 1.5% of sodium allyl sulfonate and APEG total mole number, time for adding is 9h, after dropwising, insulation reaction 10h, at being cooled to 50 DEG C, add the NaOH solution that mass concentration is 30%, regulate pH=7.0, obtain ultra high early strength poly-carboxylic water reducer.
Embodiment 13
A kind of embodiment of the preparation method of ultra high early strength poly-carboxylic water reducer of the present invention:
Agitator is being housed, in the 1000ml four-hole boiling flask of thermometer and reflux condensing tube, add molecular weight regulator, surface-active macromonomer described in 1.0mol embodiment 3, 2mol vinylformic acid, , 1molHPEG, 2.0mol sodium allyl sulfonate and 600ml deionized water, described molecular weight regulator is Thiovanic acid, the consumption of described molecular weight regulator is described surface-active macromonomer, vinylformic acid, 0.1% of sodium allyl sulfonate and HPEG total mole number, be warming up to 95 DEG C, drip the aqueous solution of initiator, described initiator is ammonium persulphate, the consumption of described initiator is described surface-active macromonomer, vinylformic acid, 0.5% of sodium allyl sulfonate and HPEG total mole number, time for adding is 3h, after dropwising, insulation reaction 4h, at being cooled to 45 DEG C, add the NaOH solution that mass concentration is 30%, regulate pH=8.0, obtain ultra high early strength poly-carboxylic water reducer.
Embodiment 14
A kind of embodiment of the preparation method of ultra high early strength poly-carboxylic water reducer of the present invention:
Agitator is being housed, in the 1000ml four-hole boiling flask of thermometer and reflux condensing tube, add molecular weight regulator, surface-active macromonomer described in 1mol embodiment 4, 1mol vinylformic acid, , 1molTPEG, 1mol sodium allyl sulfonate and 500ml deionized water, described molecular weight regulator is mercaptoethanol, , the consumption of described molecular weight regulator is described surface-active macromonomer, vinylformic acid, 0.01% of sodium allyl sulfonate and TPEG total mole number, be warming up to 90 DEG C, drip the aqueous solution of initiator, described initiator is benzoyl peroxide, the consumption of described initiator is described surface-active macromonomer, vinylformic acid, 4% of sodium allyl sulfonate and TPEG total mole number, time for adding is 1h, after dropwising, insulation reaction 12h, at being cooled to 50 DEG C, add the NaOH solution that mass concentration is 30%, regulate pH=7.5, obtain ultra high early strength poly-carboxylic water reducer.
Embodiment 15: the practical application technique effect of ultra high early strength poly-carboxylic water reducer of the present invention in concrete
Adopt the ultra high early strength poly-carboxylic water reducer of synthesis in the embodiment of the present invention 6 ~ 14 to prepare concrete, with common polycarboxylate water-reducer as a comparison, common polycarboxylate water-reducer is the polycarboxylate water-reducer of not cation quaternary ammonium salt.First the ultra high early strength poly-carboxylic water reducer of synthesis and the water-reducing rate of common polycarboxylate water-reducer in the embodiment of the present invention 6 ~ 14 is measured, then prepare concrete by following proportioning, measure the performances such as concrete time of coagulation, 2h slump-loss and maturing strength development.
The proportioning of normal concrete is as follows:
Cement: flyash: breeze: river sand: rubble: water: common polycarboxylate water-reducer=200:90:60:800:1080:165:8.5;
The mix proportion that the embodiment of the present invention 6 ~ 14 ultra high early strength poly-carboxylic water reducer obtains is as follows:
Cement: flyash: breeze: river sand: rubble: water: polycarboxylate water-reducer=200:9:60:800:1080:165:7.0 of the present invention.
The concrete effectiveness comparison prepared by the embodiment of the present invention 6 ~ 14 ultra high early strength poly-carboxylic water reducer and common polycarboxylate water-reducer is as follows:
As can be seen here, ultra high early strength poly-carboxylic water reducer of the present invention is used in concrete, compared with common polycarboxylate water-reducer, better dispersiveness is had to cement slurry, water-reducing rate improves, and simultaneously because the positively charged ion of side chain is adsorbed with restraining effect to clay, resistance to mud is good; There is super hardening effect simultaneously, can promote that cement hydrationization is reacted, the strength development of maturing is played a driving role.
Finally to should be noted that; above embodiment is only in order to illustrate technical scheme of the present invention but not limiting the scope of the invention; although be explained in detail the present invention with reference to preferred embodiment; those of ordinary skill in the art is to be understood that; can modify to technical scheme of the present invention or equivalent replacement, and not depart from essence and the scope of technical solution of the present invention.
Claims (10)
1. a ultra high early strength poly-carboxylic water reducer, is characterized in that, described ultra high early strength poly-carboxylic water reducer is the compound shown in formula I, and the structural formula of the compound shown in described formula I is as follows:
Wherein a is the integer of 1 ~ 80, and b is the integer of 1 ~ 80, and c is the integer of 1 ~ 50; L is the integer of 1 ~ 50;
A is
r is H or CH3;
B is
C is
M is
r
2, R
3and R
4be alone C respectively
1-3alkyl; X
-be Cl
-, Br
-or I
-; M is the integer of 5 ~ 200, and n is the integer of 0 ~ 50, and z is the integer of 1 ~ 150.
2. a preparation method for ultra high early strength poly-carboxylic water reducer as claimed in claim 1, is characterized in that, said method comprising the steps of:
By surface-active macromonomer, one in methacrylic acid, vinylformic acid, methylene-succinic acid and maleic anhydride, the one in APEG, HPEG, VPEG and TPEG, sodium allyl sulfonate, water and molecular weight regulator mix, be warming up to 85 ~ 95 DEG C, drip initiator, time for adding is 1 ~ 10h, dropwises rear insulation, soaking time is 1 ~ 12h, then be cooled to 45 ~ 50 DEG C, add sodium hydroxide solution and regulate pH to 7.0-8.0, obtain ultra high early strength poly-carboxylic water reducer;
Described surface-active macromonomer is the compound shown in formula II, and the structural formula of the compound shown in described formula II is as follows:
Wherein R
1for H
2c=CH-O-CH
2cH
2cH
2cH
2-, H
2c=CHCH
2-,
or
r
2, R
3and R
4be alone C respectively
1-3alkyl; X
-for Cl
-, Br
-or I
-;
M is the integer of 5 ~ 200, and n is the integer of 0 ~ 50, and z is the integer of 1 ~ 150.
3. preparation method according to claim 2, it is characterized in that, described surface-active macromonomer, one in methacrylic acid, vinylformic acid, methylene-succinic acid and maleic anhydride, the mol ratio of a kind of and sodium allyl sulfonate in APEG, HPEG, VPEG and TPEG is described surface-active macromonomer: the one in methacrylic acid, vinylformic acid, methylene-succinic acid and maleic anhydride: the one in APEG, HPEG, VPEG and TPEG: sodium allyl sulfonate=1.0 ~ 3.0:1 ~ 6.0:1:0.2 ~ 6.0.
4. preparation method according to claim 2, it is characterized in that, described molecular weight regulator is at least one in sulfhydryl compound and Virahol, the consumption of described molecular weight regulator is described surface-active macromonomer, one in methacrylic acid, vinylformic acid, methylene-succinic acid and maleic anhydride, 0.005 ~ 5% of a kind of and acrylamide in APEG, HPEG, VPEG and TPEG and the total mole number of sodium allyl sulfonate.
5. preparation method according to claim 2, is characterized in that, the time for adding of described initiator is 2 ~ 3h; Described soaking time is 2 ~ 4h.
6. preparation method according to claim 2, is characterized in that, the mass concentration of described sodium hydroxide solution is 30%; Described initiator is the one in Potassium Persulphate, ammonium persulphate, hydrogen peroxide and benzoyl peroxide, the consumption of described initiator is described surface-active macromonomer, one in methacrylic acid, vinylformic acid, methylene-succinic acid and maleic anhydride, 0.05% ~ 5% of a kind of and acrylamide in APEG, HPEG, VPEG and TPEG and the total mole number of sodium allyl sulfonate.
7. preparation method according to claim 2, is characterized in that, described cation quaternary ammonium salt PEO surface-active macromonomer is prepared from by following methods:
(1) by the one in vinyl carbinol, isobutene alcohol, 4-hydroxy butyl vinyl ether and prenol, one in the mixture of oxyethane and oxyethane and propylene oxide, mix with epoxyhalopropane, add catalyzer, react 2 ~ 10 hours under temperature is 80 ~ 150 DEG C of conditions, obtain active intermediate;
(2) quarternary ammonium salt compound is mixed with stopper, slowly add the active intermediate that step (1) synthesizes and react 1 ~ 10h under temperature is 10 ~ 80 DEG C of conditions, obtain described surface-active macromonomer;
Described quarternary ammonium salt compound is N (R
2r
3r
4), wherein R
2, R
3and R
4be alone C respectively
1-3alkyl.
8. preparation method according to claim 7, it is characterized in that, one in described step (1) in vinyl carbinol, isobutene alcohol, 4-hydroxy butyl vinyl ether and prenol, one in the mixture of oxyethane and oxyethane and propylene oxide is the one in vinyl carbinol, isobutene alcohol, 4-hydroxy butyl vinyl ether and prenol with the mol ratio of epoxyhalopropane: the one in the mixture of oxyethane and oxyethane and propylene oxide: epoxyhalopropane=1:5 ~ 250:1 ~ 150.
9. preparation method according to claim 7, is characterized in that, in described step (2), the mol ratio of quarternary ammonium salt compound and active intermediate is 0.2:1 ~ 2:1.
10. preparation method according to claim 7, is characterized in that, in described step (1), catalyzer is sodium hydride or sodium; Stopper is Resorcinol or to methyl ether phenol, the consumption of described stopper is 0.02% ~ 0.08% of described active intermediate mole number in described step (2).
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