CN1121998C - Emulsion type concrete curing agent - Google Patents

Emulsion type concrete curing agent Download PDF

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Publication number
CN1121998C
CN1121998C CN 99110818 CN99110818A CN1121998C CN 1121998 C CN1121998 C CN 1121998C CN 99110818 CN99110818 CN 99110818 CN 99110818 A CN99110818 A CN 99110818A CN 1121998 C CN1121998 C CN 1121998C
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China
Prior art keywords
curing agent
content
water
wax
described curing
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Expired - Lifetime
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CN 99110818
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Chinese (zh)
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CN1281834A (en
Inventor
彭朴
王福英
周勇
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Sinopec Research Institute of Petroleum Processing
China Petrochemical Corp
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Sinopec Research Institute of Petroleum Processing
China Petrochemical Corp
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Priority to CN 99110818 priority Critical patent/CN1121998C/en
Publication of CN1281834A publication Critical patent/CN1281834A/en
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Publication of CN1121998C publication Critical patent/CN1121998C/en
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Abstract

The present invention provides a concrete curing agent which comprises the following components by taking the total weight of the curing agent as a reference: 10 to 80% of mixed petroleum hydrocarbon, 0.5 to 15% of one or mixture of carboxylate type anionic surfactant, sulphonate type anionic surfactant and polyether class nonionic surfactant, and 10 to 80% of water, wherein the distillation range of the mixed petroleum hydrocarbon is from 350 to 520 DEG C, and the wax content is more than 70%. The curing agent has the advantages of simple formula, small dosage, high water retention rate and good combination property; the curing agent not only can be made into thin emulsion for direct use, but also can be made into concentrated emulsion which is diluted on the spot in use.

Description

A kind of emulsion type concrete curing agent
The present invention relates to a kind of curing compound, thereby a kind ofly more precisely can form the emulsion type concrete curing agent that film prevents internal moisture evaporation at concrete surface,
Curing compound roughly can be divided into resin type, latex type, silicate-type and emulsion-type.Resin type need be used organic solvent diluting, and aromaticity content must not surpass 8% in the solvent of Japan's regulation curing agent, and volatile constituent should be nontoxic, nonflammable in the U.S. ASTM C-300 regulation curing agent.In fact curing agent with an organic solvent can't reach above-mentioned requirements.The latex type curing agent adopts the emulsion polymerization preparation, and cost is higher.After maintenance was finished, curing film was firm, was difficult to abolish, and subsequent handling is had disadvantageous effect.Silicate-type (aqueous silicate solution is commonly called as water glass) price is low, but water retention is also low, and summer weather can't satisfy the needs on curing concrete road surface when hot.
Kai Fa paraffin wax emulsions type curing agent water retention height in recent years, environmental sound, curing film also removes than being easier to, but the paraffin wax emulsions type curing agent of having developed is a raw material with the high-quality paraffin of high price mostly, and the consumption of emulsifying agent is higher, and compound emulsifying agent and wax amount ratio are substantially about 1: 1, emulsifiers formula is more complicated also, therefore production cost is higher, has limited applying of they, fails to replace in road construction the water glass type curing agent so far.As: CN85105219 has proposed a kind of concrete film curing agent, is made up of materials such as paraffin, stearic acid, aliphatics higher amines, levelling agent and Glacial acetic acid, and wherein the amount ratio of paraffin and emulsifying agent is 1: 1; CN 1047094 has proposed a kind of paraffin emulsifier, is made up of sodium alkyl benzene sulfonate, alkylol amide, tea saponin, cationic surfactant, hydrophilizing agent, anti-hard water agent, solubilizing agent etc., and wherein the amount ratio of paraffin and emulsifying agent is 0.2: 1.
The object of the present invention is to provide a kind of emulsion type concrete curing agent simple, that consumption is few, water retention is high of filling a prescription.
Curing compound provided by the invention comprises following component: with the curing agent gross weight is benchmark,
(1) boiling range is 350~520 ℃, wax content greater than 70% mixing petroleum hydrocarbon, and content is 10~80%;
(2) as the carboxylic acid type of emulsifying agent or a kind of or its mixture in sulfonate type anion surfactant or the polyethers nonionogenic tenside, content is 0.5~15%;
(3) water, content are 10~80%.
Said mixing petroleum hydrocarbon is the intermediates of lubricating oil processing process, i.e. sweat oil or soap wax etc. after decompressed wax oil, the dewaxing, and wax content is greater than 70%, and more preferably greater than 80%, boiling range is 350~520 ℃, preferred 380~450 ℃.Mix petroleum hydrocarbon and account for curing agent gross weight 10~80%, preferred 25~70%.
Said emulsifying agent can be anion surfactant or nonionogenic tenside.Said anion surfactant is selected from carboxylic acid type or sulfonate type anion surfactant, as oleate, stearate, ricinate or alkylbenzene sulfonate etc., can be oleic acid, the salt that stearic acid, ricinolic acid or alkyl benzene sulphonate (ABS) and trolamine, ammonium hydroxide, sodium hydroxide or potassium hydroxide etc. generate.Said nonionogenic tenside is selected from the polyethers nonionogenic tenside, as oleic acid polyoxyethylene, alkylphenol polyoxyethylene and polyacrylic acid polyoxyethylene ether-ester etc.Said emulsifying agent can be above-mentioned a kind of or two or more mixture wherein.The content of emulsifying agent accounts for curing agent gross weight 0.5~1 5%, preferred 2~10%.
The content of said water accounts for curing agent gross weight 10~80%, and preferred 25~70%.When water-content greater than the curing agent gross weight 50% the time, can directly use; For the ease of storing and transportation, also can be mixed with water-content less than 50% concentrated emulsion, being diluted to 50~80% during use at the scene can use.
Curing compound provided by the invention can prepare according to ordinary method, is about to petroleum hydrocarbon, emulsifying agent and water 60~80 ℃ of mixing, stirs to get final product in 10~60 minutes.
Curing compound provided by the invention has the following advantages:
(1) this curing agent replaces the film-forming components of finished product wax as curing agent with mixing petroleum hydrocarbon, replace complicated polycomponent emulsifying agent with 1~2 component emulsifying agent, and the emulsifying agent consumption is few, so production cost reduces greatly.
(2) this curing agent water retention can reach more than 85%, and water glass has only less than 20%.The wear resisting property of curing agent of the present invention, folding strength, ultimate compression strength are all apparently higher than the water glass type curing agent.
(3) the concentrated emulsion good stability of curing agent of the present invention is difficult for layering, adds behind the water just can form uniform dilute emulsion without any need for equipment, and atomize is good, can cover on the road surface equably.
In addition, curing agent of the present invention and water glass or polymer latex or the use of the two mixed together is not only cost-saved, also can further improve water retention.
Further specify the present invention below in conjunction with embodiment.
Embodiment 1~8 is the preparation of curing agent.
Embodiment 1
Sweat oil (wax content 87% reduces pressure 270g respectively, 48.3 ℃ of fusing points) and 18g oleic acid (Beijing Chemical Plant's product) mix, 200g distilled water and 15g trolamine (Beijing Chemical Plant's product) mix, after being preheated to 75 ℃ respectively again with the two mixing, stir 30min with mulser, make water-content and be 40% wax emulsion, under 25 ℃, measure emulsion viscosity according to the GB2794-81 method, measuring stability according to the GB6144-85 method is the breakdown of emulsion water-content, the results are shown in Table 1.
Embodiment 2
Respectively with 270g decompressed wax oil (wax content 70%, 40.2 ℃ of fusing points), 18g oleic acid and 3g alkylphenol polyoxyethylene (X-100, Union Carbide Corp's product) mixes, 294g distilled water and 15g trolamine mix, again with the two mixing, stir 20min after being preheated to 70 ℃ respectively, make water-content and be 60% wax emulsion with mulser, measure emulsion viscosity and stability down at 25 ℃, the results are shown in Table 1.
Embodiment 3
Respectively 270g decompressed wax oil (wax content 75%, 40.2 ℃ of fusing points) and 18g oleic acid are mixed, 200g distilled water and 15g trolamine mix, and preheating mixes respectively.Making water-content by embodiment 1 described method is 40% wax emulsion, measures emulsion viscosity and stability, the results are shown in Table 1.
Embodiment 4
Sweat oil (wax content 87 reduces pressure 270g respectively, 48.3 ℃ of fusing points), 18g oleic acid and 2g breast lark (auxiliary reagent factory, Tianjin product) mix, 300g distilled water and 9g trolamine mix, again with the two mixing, stir 30min after being preheated to 80 ℃ respectively, make water-content and be 50% wax emulsion with mulser, measure emulsion viscosity and stability down at 25 ℃, the results are shown in Table 1.
Embodiment 5
Sweat oil (wax content 87% reduces pressure 270g respectively, 48.3 ℃ of fusing points) and 18g ricinolic acid (Beijing Chemical Plant's product) mix, 131g distilled water and 18g trolamine mix, after being preheated to 75 ℃ respectively again with the two mixing, stir 35min with mulser, make water-content and be 30% wax emulsion, measure emulsion viscosities and stability down, the results are shown in Table 1 at 25 ℃.
Embodiment 6
Respectively with 270g soap wax (wax content 87,47.0 ℃ of fusing points) and 18g oleic acid mix, take by weighing 707g distilled water and 15g trolamine again, after being preheated to 80 ℃ respectively again with the two mixing, stir 20min with mulser, make water-content and be 70% wax emulsion, measure emulsion viscosities and stability down, the results are shown in Table 1 at 25 ℃.
Embodiment 7
Sweat oil (wax content 87% reduces pressure 270g earlier, 48.3 ℃ of fusing points) and 21g oleic acid polyoxyethylene (chemical plant, Lvshun product) mix, take by weighing 200g distilled water again, after being preheated to 75 ℃ respectively again with the two mixing, stir 30min with mulser, make water-content and be 40% wax emulsion, measure emulsion viscosities and stability down, the results are shown in Table 1 at 25 ℃.
Embodiment 8
Sweat oil (wax content 87% reduces pressure 135g respectively, 48.3 ℃ of fusing points) and 9g heavy alkylbenzene sulfonic acid (Jinzhou refinery product of petro-chemical corporation) mix, 7.5g trolamine and 350g distilled water mix, after being preheated to 80 ℃ respectively again with the two mixing, stir 30min with mulser, make water-content and be 30% wax emulsion, measure emulsion viscosities and stability down, the results are shown in Table 1 at 25 ℃.
Table 1
Curing agent Viscosity, mPa.s Breakdown of emulsion water-content (1 day), % One's water breaks content (60 days), %
Embodiment 1 360 0 0
Embodiment 2 280 0 0
Embodiment 3 260 0 0
Embodiment 4 280 0 0
Embodiment 5 490 0 0
Embodiment 6 190 0 0
Embodiment 7 330 0 0
Embodiment 8 190 0 0
Embodiment 9~11 is the use of curing agent
Embodiment 9
Get the emulsion 75g by embodiment 1 preparation, being diluted to the 125g water-content with tap water 50g is 64% curing agent.Press the method for ASTM C156 regulation and press 0.2kg/m 2Consumption be coated in mortar test block surface, after 72 hours the test test block water retention.Test result sees Table 2.
Embodiment 10
Get the emulsion 50g by embodiment 1 preparation, being diluted to the 100g water-content with tap water 50g is 70% curing agent.Press the method coating test block of embodiment 9, and the water retention of test test block.Test result sees Table 2.
Embodiment 11
The water-content of getting embodiment 6 preparations is 70% curing agent 100g, presses the method coating test block of embodiment 9, and the water retention of test test block.Test result sees Table 2.
Embodiment 12
Present embodiment is curing agent over-all properties evaluation of the present invention.
Get the curing agent 100g of embodiment 9 preparations, measure concrete abrasion resistance according to JTJ 053-94 method, weight loss is more little wear-resisting more.Measure concrete folding strength according to GB J81-85 method, the big more flexural capacity of ratio is strong more.Measure concrete ultimate compression strength according to GB J81-85 method, ratio is the bigger the better.Test result sees Table 3.
Comparative Examples 1
Water intaking glass mould curing agent (YM-84, water-content 70%) 100g presses the method for ASTM C156 regulation and presses 0.2kg/m 2Consumption be coated in mortar test block surface, test the water retention of test block after 72 hours respectively.Test result sees Table 2.Measure concrete abrasion resistance, folding strength and ultimate compression strength according to embodiment 12 described methods, test result sees Table 3.
Table 2 water retention test result
Prescription Water retention, %
Embodiment 9 84.3
Embodiment 10 80.6
Embodiment 11 83.0
Comparative Examples 1 19.7
Table 3
Curing agent The wear test weight loss, g The folding strength ratio, % Compressive strength rate, %
Embodiment 9 13.4 93.1 87.9
Comparative Examples 1 20.4 86.1 67.9

Claims (9)

1. emulsion type concrete curing agent, it is characterized in that comprising following component: with the curing agent gross weight is benchmark,
(1) 10~80% boiling range is 350~520 ℃, wax content greater than 70% the mixing petroleum hydrocarbon of being made up of sweat oil after decompressed wax oil, the dewaxing or soap wax;
(2) 0.5~15% the emulsifying agent that is selected from a kind of or its mixture in carboxylic acid type or sulfonate type anion surfactant or the polyethers nonionogenic tenside;
(3) 10~80% water.
2. according to the described curing agent of claim 1, it is characterized in that the boiling range of said mixing petroleum hydrocarbon is 380~450 ℃.
3. according to the described curing agent of claim 1, it is characterized in that the wax content of said mixing petroleum hydrocarbon is greater than 80%.
4. according to the described curing agent of claim 1, it is characterized in that the content of said mixing petroleum hydrocarbon in curing agent is 25~70%.
5. according to the described curing agent of claim 1, it is characterized in that the content of said emulsifying agent is 2~10%.
6. according to the described curing agent of claim 1, it is characterized in that the content of said water is 25~70%.
7. according to the described curing agent of claim 1, it is characterized in that said carboxylic acid type or sulfonate type anion surfactant are selected from oleate, stearate, ricinate or alkyl benzene sulphonate (ABS) salt anionic surfactant.
8. according to claim 1 or 8 described curing agents, it is characterized in that said carboxylic acid type or sulfonate type anion surfactant are the salt that oleic acid, stearic acid, ricinolic acid or alkyl benzene sulphonate (ABS) and trolamine, ammonium hydroxide, sodium hydroxide or potassium hydroxide generate.
9. according to the described curing agent of claim 1, it is characterized in that said nonionogenic tenside is selected from oleic acid polyoxyethylene, alkylphenol polyoxyethylene or polyacrylic acid polyoxyethylene ether-ester.
CN 99110818 1999-07-22 1999-07-22 Emulsion type concrete curing agent Expired - Lifetime CN1121998C (en)

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Application Number Priority Date Filing Date Title
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Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1317217C (en) * 2005-04-05 2007-05-23 蒋发学 Multifunctional assistant for cement concrete
CN1328200C (en) * 2005-07-26 2007-07-25 李全堂 Concrete curing agent
EP1935862A1 (en) * 2006-12-22 2008-06-25 Rohm and Haas France SAS Method for treating concrete
CN101805145B (en) * 2010-03-12 2012-11-21 江苏省建筑科学研究院有限公司 Plastic concrete water evaporation inhibitor and preparation method thereof

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