CN105037613A - Polymer dispersion - Google Patents
Polymer dispersion Download PDFInfo
- Publication number
- CN105037613A CN105037613A CN201510515581.7A CN201510515581A CN105037613A CN 105037613 A CN105037613 A CN 105037613A CN 201510515581 A CN201510515581 A CN 201510515581A CN 105037613 A CN105037613 A CN 105037613A
- Authority
- CN
- China
- Prior art keywords
- monomer
- sodium
- polymeric dispersions
- water
- dust
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Landscapes
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
The invention relates to a polymer dispersion. The polymer dispersion is prepared from the following raw materials by a soap-free emulsion copolymerization technique: 3-10 parts of anionic monomer, 10-25 parts of nonionic monomer, 0.3-1.0 part of pH buffering agent, 0.3-2 parts of initiator and 100 parts of water. The raw material also comprises an antalkali capable of regulating the pH value of the reaction system to 6.0-9.0. When being used as a dust suppressor, the polymer dispersion can form an effective shell on the fine dust surface, and has the advantages of higher construction safety and high application safety. When being used as a chemical dust suppressor, the polymer dispersion can be diluted with water and sprayed, and has the advantages of favorable comprehensive properties, high safety and environment friendliness.
Description
Technical field
The present invention relates to the chemical dust suppressant in urban road treating flour dust field, particularly polymeric dispersions.
Background technology
City size constantly expands, working-yard is in full flourish, and motor vehicle number increases fast, and material stockyard, concrete-agitating, gurry are stacked and be seen everywhere.City dust pollutes and becomes increasingly conspicuous, and haze weather is constant.In air, aerodynamic diameter is less than the fine particle (PM2.5) that the pellet (PM10) of 10 μm and aerodynamic diameter be less than 2.5 μm and is referred to as micronic dust in the present invention.Their easy enriching heavy metal ions, organic oxygen compound, bacterium and virus, PM2.5 particle directly enters bronchiole, alveolar because of nasal cavity and the unable stop of throat, and very big to harm, outstanding behaviours is teratogenesis, carcinogenic, mutagenesis.
The hydraulic dust-removing taking watering as form of construction work is simple, but because of the surface tension of water high, fine solid particle not easily soaks, and dust reduction rate generally only has 28%, and winter easily freezes, and evaporation in summer is fast, validity period is short.Dust, local depositing dust are just shifted in dust removal by ventilation, are not dust suppressions.It is effective that paulin hides, but fundamentally do not solve the problem of dust from flying, is not suitable for big area and uses.
In recent years, the dust Control effect of chemical dust suppressant is paid attention to gradually.According to action principle, chemical dust suppressant can be divided three classes: (1) humidity-preserving type.Sodium lauryl sulphate, fatty alcohol-polyoxyethylene ether, sodium alkyl benzene sulfonate, alkylphenol polyoxyethylene ether provide necessary wetting ability, and glycerol, ethylene glycol, glycol ether, calcium chloride and magnesium chloride etc. provide moisture absorption, humidity-holding effect.This dust-inhibitor often reduces the useful effect cycle because of volatilization and rain drop erosion.(2) binding type.Tiny dust granules is bonded to the larger particle of particle diameter, micronic dust can be suppressed to fly upward, reduce the chance that micronic dust enters lung.Main raw material is the waste liquid of papermaking and alcohol industry, waste residue and industrial slag wet goods, easily causes secondary pollution.(3) film-forming type.Natural polymer and synthesis polymer are soaking micronic dust, on the basis of adsorbing, and formed the shell with some strength by cohesion, its Film Morphology is similar to tarpaulin, and anti-dust effect is better than other types.
Starch, Mierocrystalline cellulose and vegetable polysaccharides and various deep processing product thereof belong to natural high moleculer eompound.The polymkeric substance of the monomers such as vinylformic acid, acrylate, vinyl acetate and isocyanic ester, and the cross-linking products of the oligopolymer such as epoxy resin and urea-formaldehyde resin all belongs to synthetic macromolecular compound.Macromolecular compound has the ability of film forming, can show weather-proof effect after crosslinked, solidification.CN103265990, CN102585770 and CN103305187 etc. disclose starch, derivatived cellulose, acrylic copolymer are the dust-inhibitor of main film forming substance, with the use of sodium-chlor, trisodium phosphate, copper sulfate, glycerine, sodium lauryl sulphate or alkylphenol polyoxyethylene, while improving use properties, also inherit the shortcoming such as the corrodibility of metal ion, the volatility of low molecule organic matter.
Invention polymeric dispersions.This dust-inhibitor is that starting monomer is prepared by soap-free silicone-acrylic emulsion technology by anionic monomers and non-ionic monomer, and working security and application security are better than traditional polymer emulsion system.Compared to water-soluble polymers dust-inhibitor, the shell that it is formed on dust particale surface has better resistance to erodible.
Summary of the invention
The object of the present invention is to provide polymeric dispersions.This polymeric dispersions with anionic monomers and non-ionic monomer for starting monomer is prepared by soap-free silicone-acrylic emulsion technology, first, the equal tool of the low molecule raw material selected is reactive, and final product containing volatility low molecule organic matter, does not have corrodibility high volence metal ion yet; Secondly, choose appropriate anionic monomers, nonionic starting monomer as reactive emulsifier, for system provides enough emulsification, stably dispersing effect, and by the selection of copolymerization temperature, thus make system need not use traditional low molecule emulsifying agent, the polymeric dispersions obtained as dust-inhibitor, can micronic dust surface formed effective shell, its working security and application security higher.Be applied as chemical dust suppressant, use can be sprayed, good combination property, safety and environmental protection by dilute with water.
Technical scheme of the present invention is:
Polymeric dispersions, this dispersion is prepared from by soap-free silicone-acrylic emulsion technology, and raw material comprises anionic monomers, non-ionic monomer, pH buffer reagent, initiator and water, and its proportioning raw materials is:
Described raw material also comprises alkaline neutraliser, and the amount of alkaline neutraliser is regulate the pH value of reaction system to 6.0-9.0.
Described anionic monomers is one or more in unsaturated carboxylic acid monomer and unsaturated sulfonic acid or its sodium salt anionoid monomer.Described unsaturated carboxylic acid monomer is specially vinylformic acid, methacrylic acid; Unsaturated sulfonic acid or its sodium salt anionoid monomer are specially sodium vinyl sulfonate, sodium allyl sulfonate, 2-acrylamide-2-methyl propane sulfonic.
Described non-ionic monomer is one or more in butyl acrylate, Isooctyl acrylate monomer, methyl methacrylate, hydroxyethyl methylacrylate, methoxy polyoxyethylene ether metacrylic acid ester and vinylbenzene.
Described pH buffer reagent is one or both in sodium bicarbonate, sodium carbonate and sodium-acetate.
Described initiator is one or both in Potassium Persulphate, ammonium persulphate and hydrogen peroxide/sulfuric acid ferrous iron, and add as an aqueous solution, the mass percentage concentration of solution is 5 ~ 10%.
Described alkaline neutraliser is one or both in ammoniacal liquor, 2-methylol Isopropylamine and 2-hydroxy ethoxy ethamine.
Described water is distilled water or tap water.
The preparation method of described polymeric dispersions, comprises the following steps:
(1) stock liquid is prepared: when anionic monomers is unsaturated carboxylic acid monomer, mixed with non-ionic monomer by unsaturated carboxylic acid monomer, for subsequent use as stock liquid; When anionic monomers be unsaturated sulfonic acid or its sodium salt anionoid monomer time, consisting of of stock liquid is only non-ionic monomer, adds in unsaturated sulfonic acid or its step of sodium salt anionoid monomer below (3); When anionic monomers be unsaturated carboxylic acid monomer and unsaturated sulfonic acid or its sodium salt anionoid monomer time, unsaturated carboxylic acid monomer is mixed with non-ionic monomer, for subsequent use as stock liquid, add in unsaturated sulfonic acid or its step of sodium salt anionoid monomer below (3);
(2) in the reactor that agitator, thermometer, dropping funnel and nitrogen conduit be housed, add pH buffer reagent and water, open and stir, nitrogen or argon replaces 10 ~ 30 minutes, heating in water bath heats up;
(3) when being warming up to 60-90 DEG C, when anionic monomers comprises unsaturated sulfonic acid or its sodium salt anionoid monomer, add initiator solution, unsaturated sulfonic acid or its sodium salt anionoid monomer, then add the stock liquid in step (1); Or, when anionic monomers does not comprise unsaturated sulfonic acid or its sodium salt anionoid monomer, add initiator solution, then add the stock liquid in step (1);
The feed postition of stock liquid is for adding or drip continuously in batches;
(4) after stock liquid adds completely, at 60-100 DEG C of insulation 0.5-2.5 hour;
(5) be cooled to room temperature, regulate the pH value of reaction system to 6.0-9.0 with alkaline neutraliser, discharging, is polymeric dispersions of the present invention.
In described step (3), the temperature of polyreaction, preferred 70-90 DEG C.
In described step (3), the time for adding of stock liquid is 2.0-4.0 hour.
In described step (4), the temperature of insulation, preferred 80-95 DEG C.
In described step (5), regulate the pH value of reaction system, preferred 7.0-9.0.
The application method of described polymeric dispersions, as chemical dust suppressant, according to quality than polymeric dispersions: water=1: the ratio mixing of 10-1000 injects sprinker or spraying vehicle, according to 1.0-2.5kg/m
2the consumption of road, sprays the surface uniform of this dust-inhibitor diluent to urban road, sidewalk.
Described be preferably polymeric dispersions with the blending ratio of water and dilute by 1: 20-500 and water.
The invention has the beneficial effects as follows:
(1) polymeric dispersions of the present invention is prepared by soap-free silicone-acrylic emulsion technology, and not containing volatility low molecule organic matters such as glycerine, ethylene glycol, residual oil, do not have secondary pollution, environmental safety is good; Copolymerization temperature is suitable, can avoid system gelation, prevent stability from declining, and can ensure that again the composition of multipolymer is stablized, contribute to stable system and weathering quality.
(2) polymeric dispersions of the present invention is prepared by soap-free silicone-acrylic emulsion technology, and not containing induced by alkyl hydroxybenzene emulsifying agent, working security and application security are better than traditional polymer emulsion system.
(3) polymeric dispersions of the present invention is not containing the high volence metal ion such as copper, calcium, aluminium, there is not etching problem to metal, vehicular traffic, working security and safety in utilization reliable.
(4) polymeric dispersions of the present invention forms shell on dust particale surface, and it is resistance to is erodiblely better than water-soluble polymers, can meet different application requiring better.
(5) polymeric dispersions of the present invention is used for urban road dust suppression, effectively can suppress dust from flying equally in places such as resident's rubbish district, construction site, mineral processing.
(6) preparation technology of the present invention is easy, does not relate to High Temperature High Pressure, does not have three waste discharge, is suitable for large-scale promotion and uses.
Embodiment
The present invention is further illustrated below in conjunction with embodiment:
Embodiment one
Mass fraction in gram, 3g vinylformic acid is as anionic monomers, and 18g butyl acrylate, 5g methyl methacrylate and 2g hydroxyethyl methylacrylate, as non-ionic monomer, mix rear for subsequent use as stock liquid.In the reactor that agitator, thermometer, dropping funnel and nitrogen conduit be housed, add 0.4g sodium bicarbonate and 100g distilled water, open and stir, with argon replaces 15 minutes.During heating in water bath to 80 DEG C, add persulfate aqueous solution and 4g sodium vinyl sulfonate that 8g mass concentration is 5%.After temperature-stable, drip aforesaid stock liquid continuously by dropping funnel, control rate of addition, dropwised in 3 hours.System is warming up to 85 DEG C, is incubated 1.5 hours, under the effect of stirring, system is down to room temperature.Alkaline neutraliser is made, regulation system pH value to 7.8 with ammoniacal liquor.Stir, discharging, be polymeric dispersions of the present invention.During onsite application, to dilute at 1: 50 in mass ratio with water, then inject sprinker, carry out sprinkling dust suppression.
Measure film forming thickness: taking 150 gram particle degree is that to add to diameter be compacting in the culture dish of 12cm to 1500 object urban road micronic dusts.The tap water of the polymeric dispersions of embodiment by 50 times of quality is diluted, with 1.5kg/m
2consumption be sprayed to above-mentioned sample, 25 DEG C of freeze-day with constant temperature.Shell is peeled off, measures film forming layer thickness with slide calliper rule.
Evaluate performance of keeping humidity: taking 150 gram particle degree is that 1500 object urban road micronic dusts add to diameter and are compacting in the culture dish of 12cm, weigh.The tap water of the polymeric dispersions of embodiment by 50 times of quality is diluted, with 1.5kg/m
2consumption be sprayed to above-mentioned sample, weigh.Forced air drying in 40 DEG C of thermostat containers, evaluates insulated capacity with the forced air drying water retention of 3 hours.Moisture-retaining capacity strengthens, and the tap density of dust increases, and suppresses the ability of flying upward to improve.
Evaluate resistance to water erosion performance: sample preparation is identical with the method for mensuration film forming thickness with spray method.Sample is after 25 DEG C of freeze-day with constant temperature, and with the mode simulating nature precipitation sprayed, after soaking 12 hours, incline and excessive moisture, 25 DEG C of freeze-day with constant temperature 24 are little of sample surfaces substantially dry.Observe, record film-forming state now, using without visible crack as criterion up to standard.
Evaluate resistance to weathering: sample preparation is identical with the method for mensuration film forming thickness with spray method.Sample at 25 DEG C of freeze-day with constant temperature, weigh.The mass loss rate after 1.0h is closely purged continuously as weathering quality evaluation index to simulate strong breeze power.This index reflects the crust effect of dust-inhibitor, also embodies anti-dust effect.The shell that mass loss rate is low, compactness is strong, film-formation result is good, improve the sealing ability of dust-inhibitor to dust, anti-dust effect improves naturally.
Embodiment two
Implementation step is with embodiment one, and difference is: as non-ionic monomer, and 2g hydroxyethyl methylacrylate replaces with 2g methoxy polyoxyethylene ether metacrylic acid ester (pfpe molecule amount 500); Polymeric reaction temperature is 85 DEG C.
Method of evaluating performance is with embodiment one.
Embodiment three
Mass fraction in gram, it is for subsequent use 3g vinylformic acid, 16g butyl acrylate and 4g vinylbenzene to be mixed in proportion into stock liquid.In the reactor that agitator, thermometer, dropping funnel and nitrogen conduit be housed, add 0.3g sodium carbonate and 100g distilled water, open and stir, with nitrogen replacement 20 minutes.During heating in water bath to 80 DEG C, adding 10g mass concentration is 5% persulfate aqueous solution, 2g sodium allyl sulfonate and 2g2-acrylamide-2-methyl propane sulfonic.After temperature-stable, drip stock liquid continuously by dropping funnel, control rate of addition, dropwised in 3 hours.System is warming up to 85 DEG C, is incubated 1.5 hours, under the effect of stirring, system is down to room temperature.With 2-methylol Isopropylamine regulation system pH value.Stir further, discharging, is polymeric dispersions of the present invention.During onsite application, dilute by 1: 50 with water, then inject sprinker, carry out sprinkling dust suppression.
Above content is in conjunction with concrete preferred implementation further description made for the present invention; can not assert that the specific embodiment of the present invention is only limitted to this; for general technical staff of the technical field of the invention; without departing from the inventive concept of the premise; some simple deduction or replace can also be made, all should be considered as belonging to the present invention by submitted to claims determination scope of patent protection.
Claims (5)
1. polymeric dispersions, be is characterized by this dispersion and is prepared from by soap-free silicone-acrylic emulsion technology, and raw material comprises anionic monomers, non-ionic monomer, pH buffer reagent, initiator and water, and its proportioning raw materials is:
Described raw material also comprises alkaline neutraliser, and the amount of alkaline neutraliser is regulate the pH value of reaction system to 6.0-9.0;
Described anionic monomers is one or more in unsaturated carboxylic acid monomer and unsaturated sulfonic acid or its sodium salt anionoid monomer;
Described water is distilled water or tap water;
Described non-ionic monomer is one or more in butyl acrylate, Isooctyl acrylate monomer, methyl methacrylate, hydroxyethyl methylacrylate, methoxy polyoxyethylene ether metacrylic acid ester and vinylbenzene.
2. polymeric dispersions as claimed in claim 1, is characterized by described unsaturated carboxylic acid monomer and is specially vinylformic acid, methacrylic acid; Unsaturated sulfonic acid or its sodium salt anionoid monomer are specially sodium vinyl sulfonate, sodium allyl sulfonate, 2-acrylamide-2-methyl propane sulfonic.
3. polymeric dispersions as claimed in claim 1, it is characterized by described pH buffer reagent is one or both in sodium bicarbonate, sodium carbonate and sodium-acetate.
4. polymeric dispersions as claimed in claim 1, it is characterized by described initiator is one or both in Potassium Persulphate, ammonium persulphate and hydrogen peroxide/sulfuric acid ferrous iron, and add as an aqueous solution, the mass percentage concentration of solution is 5 ~ 10%.
5. polymeric dispersions as claimed in claim 1, it is characterized by described alkaline neutraliser is one or both in ammoniacal liquor, 2-methylol Isopropylamine and 2-hydroxy ethoxy ethamine.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201510515581.7A CN105037613A (en) | 2015-08-20 | 2015-08-20 | Polymer dispersion |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201510515581.7A CN105037613A (en) | 2015-08-20 | 2015-08-20 | Polymer dispersion |
Publications (1)
Publication Number | Publication Date |
---|---|
CN105037613A true CN105037613A (en) | 2015-11-11 |
Family
ID=54444616
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201510515581.7A Pending CN105037613A (en) | 2015-08-20 | 2015-08-20 | Polymer dispersion |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN105037613A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107936167A (en) * | 2017-12-21 | 2018-04-20 | 苏州希尔盖森新材料有限公司 | One kind has hydrophilic polystyrene microsphere |
CN108795403A (en) * | 2017-04-27 | 2018-11-13 | 中国石油天然气股份有限公司 | Change for alcohol radical acid solution sticks agent and preparation method thereof |
CN109384891A (en) * | 2018-09-21 | 2019-02-26 | 深圳市益达兴科技股份有限公司 | A kind of aqueous adhesives preparation method and aqueous adhesives obtained |
CN109731517A (en) * | 2019-01-31 | 2019-05-10 | 陕西延长石油(集团)有限责任公司 | A kind of device and method of recirculating fluidized bed ash discharge depositing dust |
CN114133150A (en) * | 2021-12-31 | 2022-03-04 | 广州富思德化工科技有限公司 | High-flash-point environment-friendly emulsified oil and preparation method thereof |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102977856A (en) * | 2012-11-21 | 2013-03-20 | 青岛文创科技有限公司 | Acrylic ester dust suppressant |
CN104693339A (en) * | 2015-03-30 | 2015-06-10 | 河北工业大学 | Water-based dust depressor and preparation method thereof |
CN104693345A (en) * | 2015-03-30 | 2015-06-10 | 河北工业大学 | Polymer dispersion and preparation method thereof |
-
2015
- 2015-08-20 CN CN201510515581.7A patent/CN105037613A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102977856A (en) * | 2012-11-21 | 2013-03-20 | 青岛文创科技有限公司 | Acrylic ester dust suppressant |
CN104693339A (en) * | 2015-03-30 | 2015-06-10 | 河北工业大学 | Water-based dust depressor and preparation method thereof |
CN104693345A (en) * | 2015-03-30 | 2015-06-10 | 河北工业大学 | Polymer dispersion and preparation method thereof |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108795403A (en) * | 2017-04-27 | 2018-11-13 | 中国石油天然气股份有限公司 | Change for alcohol radical acid solution sticks agent and preparation method thereof |
CN108795403B (en) * | 2017-04-27 | 2021-03-30 | 中国石油天然气股份有限公司 | Viscosity modifier for alcohol-based acid solution and preparation method thereof |
CN107936167A (en) * | 2017-12-21 | 2018-04-20 | 苏州希尔盖森新材料有限公司 | One kind has hydrophilic polystyrene microsphere |
CN109384891A (en) * | 2018-09-21 | 2019-02-26 | 深圳市益达兴科技股份有限公司 | A kind of aqueous adhesives preparation method and aqueous adhesives obtained |
CN109731517A (en) * | 2019-01-31 | 2019-05-10 | 陕西延长石油(集团)有限责任公司 | A kind of device and method of recirculating fluidized bed ash discharge depositing dust |
CN109731517B (en) * | 2019-01-31 | 2021-08-24 | 陕西延长石油(集团)有限责任公司 | Device and method for discharging ash and reducing dust of circulating fluidized bed |
CN114133150A (en) * | 2021-12-31 | 2022-03-04 | 广州富思德化工科技有限公司 | High-flash-point environment-friendly emulsified oil and preparation method thereof |
CN114133150B (en) * | 2021-12-31 | 2023-12-08 | 广州富思德化工科技有限公司 | High-flash-point environment-friendly emulsified oil and preparation method thereof |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN104693345B (en) | A kind of polymeric dispersions and preparation method thereof | |
CN105037613A (en) | Polymer dispersion | |
CN111662679B (en) | Composite ecological visual dust suppressant and preparation method and application thereof | |
CN109415618B (en) | Efficient environment-friendly dust suppressant and preparation method and application thereof | |
JP6603339B2 (en) | Highly efficient and environmentally compatible dust suppressant, its blending method and its use | |
CN104693339A (en) | Water-based dust depressor and preparation method thereof | |
CN111117568B (en) | Ecological dust suppressant for surface mine dust control and preparation method thereof | |
CN103059681B (en) | Water-based quick-drying external crosslinking functional paint and preparation method thereof | |
CN102432730B (en) | Method for producing resin emulsion used for water-based metallic paint and produced resin emulsion thereof | |
CN108559449B (en) | High-dilution-ratio aqueous liquid dust suppressant and preparation and use methods thereof | |
CN103305187B (en) | Compound chemical coal dust suppressant and preparation method thereof | |
CN105504130A (en) | Compound type dust inhibiting and sand solidifying agent and preparation method thereof | |
CN110172331B (en) | Moistening bonding type grafting modification inhibitor for dust control and preparation method thereof | |
CN102675521A (en) | Water-soluble macromolecular sand fixing agent and preparation method | |
CN106008851B (en) | A kind of construction dust suppressant and preparation method thereof | |
CN103601404A (en) | Concrete curing agent and preparation method thereof | |
CN109320663B (en) | Dust suppressant for road construction and preparation method thereof | |
CN109456734A (en) | A kind of soil-rock mixture structure road dust solidification dust suppressant and preparation method thereof | |
CN114561189B (en) | Lignin phenolic resin dust suppressant and preparation method thereof | |
CN106008791A (en) | Mineral powder suppressant and preparing method thereof | |
CN114479764B (en) | Polycarboxylic acid high-efficiency dust suppressant and preparation method and application thereof | |
CN104086686A (en) | Styrene-acrylic emulsion with excellent freeze-thaw stability as well as preparation method and application thereof | |
CN107057644B (en) | A kind of preparation method of natural environmental-protective dust suppressant | |
CN108929657A (en) | A kind of miberal powder dust suppressant and preparation method thereof | |
CN109181644A (en) | A kind of Road dust suppressant and preparation method thereof and usage mode |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
WD01 | Invention patent application deemed withdrawn after publication | ||
WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20151111 |