CN106146402A - The preparation method of a kind of 2 imidazolidinones and formaldehyde scavenger - Google Patents

The preparation method of a kind of 2 imidazolidinones and formaldehyde scavenger Download PDF

Info

Publication number
CN106146402A
CN106146402A CN201610553057.3A CN201610553057A CN106146402A CN 106146402 A CN106146402 A CN 106146402A CN 201610553057 A CN201610553057 A CN 201610553057A CN 106146402 A CN106146402 A CN 106146402A
Authority
CN
China
Prior art keywords
formaldehyde
imidazolidinone
carbamide
formaldehyde scavenger
speed
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
Application number
CN201610553057.3A
Other languages
Chinese (zh)
Inventor
胡峰
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Guangdong Oudini Energy Technology Co Ltd
Original Assignee
Guangdong Oudini Energy Technology Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Guangdong Oudini Energy Technology Co Ltd filed Critical Guangdong Oudini Energy Technology Co Ltd
Priority to CN201610553057.3A priority Critical patent/CN106146402A/en
Publication of CN106146402A publication Critical patent/CN106146402A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/04Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D233/28Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/30Oxygen or sulfur atoms
    • C07D233/32One oxygen atom
    • C07D233/34Ethylene-urea
    • AHUMAN NECESSITIES
    • A62LIFE-SAVING; FIRE-FIGHTING
    • A62DCHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
    • A62D3/00Processes for making harmful chemical substances harmless or less harmful, by effecting a chemical change in the substances
    • A62D3/30Processes for making harmful chemical substances harmless or less harmful, by effecting a chemical change in the substances by reacting with chemical agents
    • A62D3/33Processes for making harmful chemical substances harmless or less harmful, by effecting a chemical change in the substances by reacting with chemical agents by chemical fixing the harmful substance, e.g. by chelation or complexation
    • AHUMAN NECESSITIES
    • A62LIFE-SAVING; FIRE-FIGHTING
    • A62DCHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
    • A62D2101/00Harmful chemical substances made harmless, or less harmful, by effecting chemical change
    • A62D2101/20Organic substances
    • A62D2101/28Organic substances containing oxygen, sulfur, selenium or tellurium, i.e. chalcogen

Abstract

Embodiment of the present invention discloses a kind of formaldehyde scavenger, it is applicable to spary and soft cloth brushing covers on the surface of furniture, door and window and leatherware, and can be the most internal, effectively stop and remove free formaldehyde, thus remove the formaldehyde in goods, improve the physical safety of user, including component: 2 imidazolidinones that Claims 1 to 5 is made, carbamide, wetting agent, auxiliary agent, water, mix.Embodiment of the present invention additionally provides the preparation method of a kind of 2 imidazolidinones, comprise the following steps: A, ethylenediamine, carbamide, ethylene glycol and water are added in reactor according to ratio that mol ratio is 1.4~1.5:1:0.5~0.8:1.5~2, it is stirred until homogeneous, be heated to 120~250 DEG C continuously stirred 2~4 hours, be cooled to 0 DEG C;B, filter after taking precipitate, described precipitate is used absolute ethanol washing, then through purification and be dried to obtain 2 imidazolidinones.

Description

The preparation method of a kind of 2-imidazolidinone and formaldehyde scavenger
Technical field
The present invention relates to remove formaldehyde field, particularly relate to preparation method and the formaldehyde scavenger of a kind of 2-imidazolidinone.
Background technology
Formaldehyde chemical formula is HCHO, is colourless gas at normal temperatures, has special penetrating odor, due to the change that it is special Learn performance, chemical industry and fur coat industry use in a large number.
Industrially, as the binding agents such as urea-formaldehyde resin adhesive, melamine resin adehsive and phenolic resin glue all using formaldehyde as Primary raw material, and these binding agents are widely used in the production of the sheet materials such as plywood, Blockboard and density board.So Outward, the metope of building, ground, the finishing of furniture and auxiliary equipment will use this kind of binding agent.
In fur coat industry, formaldehyde tanning agent is a kind of widely used post-treatment agent, and the leather colour purity that can make leather is white, meets light Invariant color, and absorption of perspiration is strong, and in these products, the free formaldehyde of residual can slowly discharge, and release process is even up to more than ten Year.
Having many uses of formaldehyde is general, but harm is very big, and the especially harm to human body, formaldehyde in air content exceedes 0.1mg/m3Time, people just can smell a strange smell and not feel well, when content of formaldehyde is more than 0.5mg/m3Time, eyes can be felt to stimulate Sense, causes simultaneously and sheds tears, when concentration is higher, can cause headache, feel sick, cough, vomit, uncomfortable in chest and tachypnea etc., seriously can be instead Answer too drastic and cause death.Long Term Contact formaldehyde, human body constitution is easily deteriorated, and immunity degradation causes headache and insomnia etc., seriously Lesion tissue and cancer can be caused.
In the world, 2004 international cancer mechanism (IRAC) formaldehyde has been included in first kind carcinogen and teratogen Matter, it is indicated that nasopharyngeal carcinoma, tumor of nasal cavity, nasal sinus cancer and leukemia may be caused.
Summary of the invention
Embodiment of the present invention provides a kind of formaldehyde scavenger, it is adaptable to spary and soft cloth brushing cover at furniture, door Window and the surface of leatherware, and can be the most internal, effectively stop and remove free formaldehyde, thus removing the first in goods Aldehyde, improves the physical safety of user.
Embodiment of the present invention additionally provides the preparation method of a kind of 2-imidazolidinone.
For solving the problems referred to above, the preparation method of a kind of 2-imidazolidinone that the present invention provides, comprise the following steps:
A, by ethylenediamine, carbamide, ethylene glycol and water according to the ratio that mol ratio is 1.4~1.5:1:0.5~0.8:1.5~2 Example adds in reactor, is stirred until homogeneous, be heated to 120~250 DEG C continuously stirred 2~4 hours, be cooled to 0 DEG C;
B, filter after taking precipitate, described precipitate is used absolute ethanol washing, then through purification and be dried to obtain 2- Imidazolidinone.
Preferably, described in step A, the heating rate of heating is 6 DEG C/min.
Preferably, described in step A, the speed of stirring is 300~600rpm.
Preferably, the mol ratio described in step A be ethylenediamine, carbamide, ethylene glycol and water according to mol ratio be 1.4~ 1.5:1:0.5:1.5.
Preferably, in step A, described in be stirred until homogeneous, be heated to 120~250 DEG C continuously stirred 2~4 hours, be cooled to 0 DEG C, particularly as follows:
It is stirred at room temperature to uniformly with speed for 400rpm;
It is that 6 DEG C/min is heated to 150 DEG C with heating rate, continues to stir 50 minutes for 500rpm with speed;
It is that 6 DEG C/min is heated to 230 DEG C with heating rate.Continue to stir 140 minutes with speed for 400rpm;
Slowly cool to 0 DEG C.
The present invention also provides for a kind of formaldehyde scavenger, including component: the 2-imidazolidinone be made up of above-mentioned, carbamide, moistening Agent, auxiliary agent, water, mix.
Preferably, described 2-imidazolidinone, described carbamide, described wetting agent, described auxiliary agent, the weight ratio of described water For: 1~20 part: 1~20 part: 0.1~5 part: 0.1~10 part: 40~85 parts.
Preferably, described wetting agent is OP series emulsifying agent or NP series emulsifying agent.
Preferably, the mixture of one or more during described emulsifying agent is alkylphenol polyoxyethylene.
Preferably, one or more during described auxiliary agent is calcium chloride, barium chloride and magnesium chloride.
As can be seen from the above technical solutions, embodiment of the present invention has the advantage that 2-imidazolidinone has second two The advantage of amine, ethylene glycol and carbamide, utilize this 2-imidazolidinone and carbamide as the formaldehyde scavenger of effective ingredient, can be with free Formaldehyde produces chemical reaction, and 2-imidazolidinone and carbamide can react with formaldehyde, the polymer that production stability is high, prevent Back reaction, causes the spilling of formaldehyde, thus reaches to remove the effect of formaldehyde.
Further, this formaldehyde scavenger uses alkylphenol polyoxyethylene as emulsifying agent i.e. wetting agent so that this first The various compositions of aldehyde scavenger can form stable aqueous solvent by dispersing and dissolving in aqueous so that the cleaning agent of this formaldehyde is permissible It is fully contacted with furniture, door and window, leather etc., and penetrates into gap, remove and there is the free formaldehyde in gap.
Further, the 2-imidazolidinone of the present invention and the preparation process of formaldehyde scavenger are simple, and the response time is short, adopts Preparing 2-imidazolidinone with ethylenediamine, carbamide, ethylene glycol and water as raw material, 2-imidazolidinone and carbamide, wetting agent, auxiliary agent are molten In Xie Shui, form the aqueous solution of safety non-toxic, safe operation process, suitably promote the use of.
Detailed description of the invention
Embodiment of the present invention provides a kind of formaldehyde scavenger, it is adaptable to spary and soft cloth brushing cover at furniture, door Window and the surface of leatherware, and can be the most internal, effectively stop and remove free formaldehyde, thus removing the first in goods Aldehyde, improves the physical safety of user.
Embodiment of the present invention additionally provides the preparation method of a kind of 2-imidazolidinone.
The preparation method of a kind of 2-imidazolidinone that the present invention provides, comprises the following steps:
A, by ethylenediamine, carbamide, ethylene glycol and water according to the ratio that mol ratio is 1.4~1.5:1:0.5~0.8:1.5~2 Example adds in reactor, is stirred until homogeneous, be heated to 120~250 DEG C continuously stirred 2~4 hours, be cooled to 0 DEG C;
B, filter after taking precipitate, described precipitate is used absolute ethanol washing, then through purification and be dried to obtain 2- Imidazolidinone.
Wherein alleged continuously stirred, can be continuously stirred after raw material addition reactor, heating process is the most persistently stirred Mix.
Preferably, described in step A, the heating rate of heating is 6 DEG C/min.
Preferably, described in step A, the speed of stirring is 300~600rpm.
Preferably, the mol ratio described in step A be ethylenediamine, carbamide, ethylene glycol and water according to mol ratio be 1.4~ 1.5:1:0.5:1.5.
Preferably, in step A, described in be stirred until homogeneous, be heated to 120~250 DEG C continuously stirred 2~4 hours, be cooled to 0 DEG C, particularly as follows:
It is stirred at room temperature to uniformly with speed for 400rpm;
It is that 6 DEG C/min is heated to 150 DEG C with heating rate, continues to stir 50 minutes for 500rpm with speed;
It is that 6 DEG C/min is heated to 230 DEG C with heating rate.Continue to stir 140 minutes with speed for 400rpm;
Slowly cool to 0 DEG C.
The preparation method of this 2-imidazolidinone be briefly described below:
Take ethylenediamine, carbamide, ethylene glycol and water that mol ratio is 1.4~1.5:1:0.5~0.8:1.5~2 and add reaction In ware, after stirring with the speed of 300~600rpm, be heated up to 120~250 DEG C with the speed of 6 DEG C/min, and continue with The speed of 300~600rpm stirs 2~4 hours, is subsequently cooled to 0 DEG C.
Wherein, add the raw material in reaction utensil, after stirring with the speed of 400rpm, heat with the speed of 6 DEG C/min To 150 DEG C, continuously stirred, it is heated up to 230 DEG C with the speed of 6 DEG C/min the most again, continuously stirred.
The 2-imidazolidinone prepared by the method, it is ensured that the component of the formaldehyde scavenger then prepared is adaptive, only Use the material being beneficial to remove formaldehyde, such as carbamide, do not introduce other materials, in order to avoid destroying stablizing of formaldehyde scavenger of the present invention Property.
Present invention also offers a kind of formaldehyde scavenger formaldehyde scavenger, including component: by the above-mentioned 2-imidazolidine made Ketone, carbamide, wetting agent, auxiliary agent, water, mix.
Preferably, described 2-imidazolidinone, described carbamide, described wetting agent, described auxiliary agent, the weight ratio of described water For: 1~20 part: 1~20 part: 0.1~5 part: 0.1~10 part: 40~85 parts.
Preferably, described wetting agent is OP series emulsifying agent or NP series emulsifying agent.
Preferably, the mixture of one or more during described emulsifying agent is alkylphenol polyoxyethylene.
Preferably, one or more during described auxiliary agent is calcium chloride, barium chloride and magnesium chloride.
Formaldehyde scavenger of the present invention employs the 2-imidazolidinone being made up of ethylenediamine, carbamide, ethylene glycol, also uses breast The carbamide that agent, auxiliary agent and reinforcement use, is prepared by fully mixing, and wherein plays the mainly 2-imidazolidinone removing formaldehyde effect And carbamide.
Preferably, 2-imidazolidinone, carbamide, wetting agent, auxiliary agent, water weight ratio be preferably: 10~20 parts: 10~ 20 parts: 0.1~2 part: 0.1~2 part: 40~85 parts.
In general, the product such as furniture, leather is cleaned the chemical substance used, it is impossible to furniture and the surface of leather Cause damage, and the abutting relationship at furniture and leather products Present site and position, the more difficult removing of formaldehyde of closed position.
The 2-imidazolidinone of the present invention and carbamide have the strongest stability to free formaldehyde, when 2-imidazolidinone, carbamide with After formaldehyde contact, chemical reaction can be produced, reach to remove the effect of formaldehyde, and 2-imidazolidinone, carbamide and formaldehyde can be formed There is the polymer of superregulated property, prevent the generation of back reaction, so that the spilling of formaldehyde.
Furthermore, it is understood that this formaldehyde scavenger also uses the wetting agent with emulsification function--alkylphenol-polyethenoxy Ether so that in formaldehyde scavenger various compositions can dispersing and dissolving in aqueous, and form stable aqueous solution so that formaldehyde is clear Except agent can be fully contacted with furniture, door and window and leather etc., infiltrate through in their inside and the gap at position and position.
It should be noted that the formaldehyde removing that product is carried out by the present invention, the detection method of clearance rate is:
Take polylith test density plate, cut, take blank sample and spray formaldehyde scavenger test specimens, being placed in Laboratory Module, put After putting 6 hours, the air in sampling closed cabin, as sample, detects its concentration of formaldehyde, and the burst size of methanal of blank sample is C1, spray The burst size of methanal of the test specimens being coated with formaldehyde scavenger is C2, measures according to the mode of P=(C1-C2)/C1 × 100%.
Wherein, formula represents:
P: formaldehyde clearance, %;
C1: the burst size of methanal of blank sample, mg/m3
C2: the burst size of methanal of the test specimens of spraying formaldehyde scavenger, mg/m3
Below by embodiment, prepared by the present invention 2-imidazolidinone to be described in detail:
Embodiment 1
Taking mol ratio is: the ethylenediamine of 1.4:1:0.5:1.5, carbamide, ethylene glycol and water, is placed in reaction utensil, with 300rpm stirs, and is then heated to 180 DEG C with the speed of 6 DEG C/min and persistently keeps the speed of 300rpm to stir, Continue react for 3 hours, be cooled to 0 DEG C, filtration, after absolute ethanol washing, purification, obtain 2-imidazolidinone after drying.
Embodiment 2
Taking mol ratio is: the ethylenediamine of 1.4:1:0.5:1.5, carbamide, ethylene glycol and water, is placed in reaction utensil, with 300rpm stirs, and is then heated to 180 DEG C with the speed of 6 DEG C/min and persistently keeps the speed of 400rpm to stir, Continue react for 3 hours, be cooled to 0 DEG C, filtration, after absolute ethanol washing, purification, obtain 2-imidazolidinone after drying.
Embodiment 3
Taking mol ratio is: the ethylenediamine of 1.4:1:0.5:1.5, carbamide, ethylene glycol and water, is placed in reaction utensil, with 300rpm stirs, and is then heated to 180 DEG C with the speed of 6 DEG C/min and persistently keeps the speed of 500rpm to stir, Continue react for 3 hours, be cooled to 0 DEG C, filtration, after absolute ethanol washing, purification, obtain 2-imidazolidinone after drying.
Embodiment 4
Taking mol ratio is: the ethylenediamine of 1.4:1:0.5:1.5, carbamide, ethylene glycol and water, is placed in reaction utensil, with 300rpm stirs, and is then heated to 180 DEG C with the speed of 6 DEG C/min and persistently keeps the speed of 600rpm to stir, Continue react for 3 hours, be cooled to 0 DEG C, filtration, after absolute ethanol washing, purification, obtain 2-imidazolidinone after drying.
Example 1~the 2-imidazolidinone 5g of embodiment 4, put in a, b, c, d4 reaction utensil respectively, all adds: urine Element 1g, wetting agent 0.1g, auxiliary agent 0.1g, water 40g, obtain formaldehyde scavenger a, formaldehyde scavenger b, formaldehyde scavenger c, formaldehyde clear Except agent d.
The purpose taking a small amount of carbamide, wetting agent and auxiliary agent is to reduce the shadow that carbamide, wetting agent and auxiliary agent PARA FORMALDEHYDE PRILLS(91,95) absorb Ring, thus embody the dosage of 2-imidazolidinone more easily.
Taking one piece of density board, be divided into 4 fritters, and cut from centre, one-tenth 4 is little to density board test board, as Form aldehyde release Amount, is sprayed at 4 little in density board by formaldehyde scavenger a, formaldehyde scavenger b, formaldehyde scavenger c, formaldehyde scavenger d correspondence, Fountain height is identical, and after air-drying 24 hours, 4 to putting into different experiments cabin, takes out after 6 hours, and the formaldehyde testing each Laboratory Module is released High-volume.
Release result be embodiment 1 be 0.25mg/m3, embodiment 2 be 0.21mg/m3, embodiment 3 be 0.22mg/m3, real Execute example 4 for 0.27mg/m3
Visible, the effect of embodiment 2 and embodiment 3 is better than embodiment 1 and embodiment 4.
The 2-imidazolidinone that the preparation method of Example 2 obtains is as the basis of example below.
Below the embodiment of the formaldehyde scavenger of the present invention is described in detail:
Embodiment 5
Take 2-imidazolidinone 10g, carbamide 10g, alkylphenol polyoxyethylene (NP-10) 0.5g, calcium oxide 0.5g, water 79g, Stirring, to being completely dissolved, obtains formaldehyde scavenger e.
Carry out experimental verification:
Taking a length of 100cm, width is the vegetarian noodles density board of 50cm, cuts from centre, and cleaning is clean in the same way, The most numbered: plate e, plate i1.
Being sprayed on plate e by formaldehyde scavenger e, spray pattern is the two sides of plate and four limits are the most uniformly sprayed and covered Lid, quantity for spray is 30mL/m2;Plate i1 does not spray any material.
Plate e and plate i1 is placed in same environment and air-dries 24 hours, fetch the Form aldehyde release starting to test them Amount.
Plate e, plate i1 are respectively placed in the Laboratory Module of 21 cubic metre, close hatch door.After 6 hours, gather experiment Air sample in cabin, the concentration of formaldehyde of monitoring sample, the Laboratory Module residing for plate i1 obtains the burst size of methanal C1 of blank sample, spray It is coated with the burst size of methanal C2 of the test specimens of formaldehyde scavenger.
According to above-mentioned calculation P=(C1-C2)/C1 × 100%, calculate formaldehyde clearance, after result such as embodiment Shown in form 1.
Embodiment 6
Take 2-imidazolidinone 15g, carbamide 10g, alkylphenol polyoxyethylene (NP-10) 1g, calcium oxide 1g, water 73g, stirring To being completely dissolved, obtain formaldehyde scavenger f.
Carry out experimental verification:
Taking a length of 100cm, width is the vegetarian noodles density board of 50cm, cuts from centre, and cleaning is clean in the same way, The most numbered: plate f, plate i2.Being sprayed on plate f by formaldehyde scavenger f, spray pattern is two sides and four limits of plate All uniformly spraying covering, quantity for spray is 30mL/m2;Plate i2 does not spray any material.
Plate f and plate i2 is placed in same environment and air-dries 24 hours, fetch the Form aldehyde release starting to test them Amount.
Plate f, plate i2 are respectively placed in the Laboratory Module of 21 cubic metre, close hatch door.After 6 hours, gather experiment Air sample in cabin, the concentration of formaldehyde of monitoring sample, the Laboratory Module residing for plate i2 obtains the burst size of methanal C1 of blank sample, spray It is coated with the burst size of methanal C2 of the test specimens of formaldehyde scavenger.
According to above-mentioned calculation P=(C1-C2)/C1 × 100%, calculate formaldehyde clearance, after result such as embodiment Shown in form 1.
Embodiment 7
Take 2-imidazolidinone 10g, carbamide 20g, alkylphenol polyoxyethylene (NP-10) 1g, calcium oxide 0.5g, water 68.5g, Stirring, to being completely dissolved, obtains formaldehyde scavenger g.
Carry out experimental verification:
Taking a length of 100cm, width is the vegetarian noodles density board of 50cm, cuts from centre, and cleaning is clean in the same way, The most numbered: plate g, plate i3.Being sprayed on plate g by formaldehyde scavenger g, spray pattern is two sides and four limits of plate All uniformly spraying covering, quantity for spray is 30mL/m2;Plate i3 does not spray any material.
Plate g and plate i3 is placed in same environment and air-dries 24 hours, fetch the Form aldehyde release starting to test them Amount.
Plate g, plate i3 are respectively placed in the Laboratory Module of 21 cubic metre, close hatch door.After 6 hours, gather experiment Air sample in cabin, the concentration of formaldehyde of monitoring sample, the Laboratory Module residing for plate i3 obtains the burst size of methanal C1 of blank sample, spray It is coated with the burst size of methanal C2 of the test specimens of formaldehyde scavenger.
According to above-mentioned calculation P=(C1-C2)/C1 × 100%, calculate formaldehyde clearance, after result such as embodiment Shown in form 1.
Embodiment 8
Take 2-imidazolidinone 10g, carbamide 5g, alkylphenol polyoxyethylene (NP-10) 0.5, calcium oxide 1g, water 83.5g, stir Mix to being completely dissolved, obtain formaldehyde scavenger h.
Carry out experimental verification:
Taking a length of 100cm, width is the vegetarian noodles density board of 50cm, cuts from centre, and cleaning is clean in the same way, The most numbered: plate h, plate i4.Being sprayed on plate h by formaldehyde scavenger h, spray pattern is two sides and four limits of plate All uniformly spraying covering, quantity for spray is 30mL/m2;Plate i4 does not spray any material.
Plate h and plate i4 is placed in same environment and air-dries 24 hours, fetch the Form aldehyde release starting to test them Amount.
Plate h, plate i4 are respectively placed in the Laboratory Module of 21 cubic metre, close hatch door.After 6 hours, gather experiment Air sample in cabin, the concentration of formaldehyde of monitoring sample, the Laboratory Module residing for plate i4 obtains the burst size of methanal C1 of blank sample, spray It is coated with the burst size of methanal C2 of the test specimens of formaldehyde scavenger.
According to above-mentioned calculation P=(C1-C2)/C1 × 100%, calculate formaldehyde clearance, after result such as embodiment Shown in form 1.
Form 1
As can be seen from the above table, P optimal value is to occur in the formaldehyde scavenger f that embodiment 7 prepares, and embodiment 5 prepares Formaldehyde scavenger e takes second place.
By upper table it can also be seen that, the formaldehyde scavenger of the embodiment of the present invention 5~8 goes effect of formaldehyde very for sheet material Good.
Sprinkling, spary, the mode smeared is used to cover on furniture, door and window and leatherware surface, in the effect of wetting agent Under, launching rapidly at body surface, 2-imidazolidinone, carbamide can react rapidly with formaldehyde simultaneously, and under interacting, reaction The stability of thing is high, effectively prevents the generation of back reaction, is a kind of efficient and the formaldehyde scavenger removing formaldehyde of safety.
On the basis of embodiment 1~embodiment 8, study the optimum preparation side of 2-imidazolidinone of the present invention the most meticulously Case:
Embodiment 9
Consistent with the raw material quantity of embodiment 2, take mol ratio be the ethylenediamine of 1.4:1:0.5:1.5, carbamide, ethylene glycol and Water, is placed in reaction utensil, and difference is:
Stir with 300rpm, be then heated to 150 DEG C with the speed of 6 DEG C/min and persistently keep 400rpm's Speed stirs, and continues react for 190 minutes, is cooled to 0 DEG C, and filtration, after absolute ethanol washing, purification, obtains after drying 2-imidazolidinone.
Mix consistent with embodiment 7 content: 2-imidazolidinone 10g, carbamide 20g, alkylphenol polyoxyethylene (NP-10) 1g, calcium oxide 0.5g, water 68.5g, stirring, to being completely dissolved, obtains formaldehyde scavenger j.
Carry out experimental verification:
Taking a length of 100cm, width is the vegetarian noodles density board of 50cm, cuts from centre, and cleaning is clean in the same way, The most numbered: plate j, plate i5.Being sprayed on plate j by formaldehyde scavenger j, spray pattern is two sides and four limits of plate All uniformly spraying covering, quantity for spray is 30mL/m2;Plate i5 does not spray any material.
Plate j and plate i5 is placed in same environment and air-dries 24 hours, fetch the Form aldehyde release starting to test them Amount.
Plate j, plate i5 are respectively placed in the Laboratory Module of 21 cubic metre, close hatch door.After 6 hours, gather experiment Air sample in cabin, the concentration of formaldehyde of monitoring sample, the Laboratory Module residing for plate i5 obtains the burst size of methanal C1 of blank sample, spray It is coated with the burst size of methanal C2 of the test specimens of formaldehyde scavenger.
According to above-mentioned calculation P=(C1-C2)/C1 × 100%, calculate formaldehyde clearance, after result such as embodiment Shown in form 2.
Embodiment 10
Consistent with the raw material quantity of embodiment 2, take mol ratio be the ethylenediamine of 1.4:1:0.5:1.5, carbamide, ethylene glycol and Water, is placed in reaction utensil, and difference is:
It is stirred at room temperature to uniformly with speed for 400rpm;
It is that 6 DEG C/min is heated to 150 DEG C with heating rate, continues to stir 50 minutes for 500rpm with speed;
It is that 6 DEG C/min is heated to 230 DEG C with heating rate.Continue to stir 140 minutes with speed for 400rpm;
Slowly cool to 0 DEG C;
Filter, after absolute ethanol washing, purification, obtain 2-imidazolidinone after drying.
Mix consistent with embodiment 7 content: 2-imidazolidinone 10g, carbamide 20g, alkylphenol polyoxyethylene (NP-10) 1, calcium oxide 0.5g, water 68.5g, stirring, to being completely dissolved, obtains formaldehyde scavenger k.
Carry out experimental verification:
Taking a length of 100cm, width is the vegetarian noodles density board of 50cm, cuts from centre, and cleaning is clean in the same way, The most numbered: plate k, plate i6.Being sprayed on plate k by formaldehyde scavenger k, spray pattern is two sides and four limits of plate All uniformly spraying covering, quantity for spray is 30mL/m2;Plate i6 does not spray any material.
Plate k and plate i6 is placed in same environment and air-dries 24 hours, fetch the Form aldehyde release starting to test them Amount.
Plate k, plate i6 are respectively placed in the Laboratory Module of 21 cubic metre, close hatch door.After 6 hours, gather experiment Air sample in cabin, the concentration of formaldehyde of monitoring sample, the Laboratory Module residing for plate i6 obtains the burst size of methanal C1 of blank sample, spray It is coated with the burst size of methanal C2 of the test specimens of formaldehyde scavenger, owing to the difference that may relate to is less, therefore measures to arithmetic point Three.
According to above-mentioned calculation P=(C1-C2)/C1 × 100%, calculate formaldehyde clearance, after result such as embodiment Shown in form 2.
Form 2
Visible, the formaldehyde scavenger effect being worth by embodiment 10 is optimum.
The above, embodiment of above and embodiment only in order to technical scheme to be described, are not intended to limit; Although being described in detail the present invention with reference to aforementioned embodiments and embodiment, those of ordinary skill in the art should Understand: the technical scheme described in foregoing embodiments still can be modified by it, or to wherein portion of techniques feature Carry out equivalent;And these amendments or replacement, do not make the essence of appropriate technical solution depart from each embodiment of the present invention Spirit and scope with embodiment technical scheme.

Claims (10)

1. the preparation method of a 2-imidazolidinone, it is characterised in that comprise the following steps:
A, ethylenediamine, carbamide, ethylene glycol and water are added according to the ratio that mol ratio is 1.4~1.5:1:0.5~0.8:1.5~2 Enter in reactor, be stirred until homogeneous, be heated to 120~250 DEG C continuously stirred 2~4 hours, be cooled to 0 DEG C;
B, filter after taking precipitate, described precipitate is used absolute ethanol washing, then through purification and be dried to obtain 2-imidazoles Alkanone.
The preparation method of 2-imidazolidinone the most according to claim 1, it is characterised in that the liter of heating described in step A Temperature speed is 6 DEG C/min.
The preparation method of 2-imidazolidinone the most according to claim 1, it is characterised in that the speed of stirring described in step A Rate is 300~600rpm.
4. according to the preparation method of the 2-imidazolidinone described in any one in claims 1 to 3, it is characterised in that in step A Described mol ratio be ethylenediamine, carbamide, ethylene glycol and water be 1.4~1.5:1:0.5:1.5 according to mol ratio.
5. according to the preparation method of the 2-imidazolidinone described in any one in claims 1 to 3, it is characterised in that step A In, described in be stirred until homogeneous, be heated to 120~250 DEG C continuously stirred 2~4 hours, be cooled to 0 DEG C, particularly as follows:
It is stirred at room temperature to uniformly with speed for 400rpm;
It is that 6 DEG C/min is heated to 150 DEG C with heating rate, continues to stir 50 minutes for 500rpm with speed;
It is that 6 DEG C/min is heated to 230 DEG C with heating rate.Continue to stir 140 minutes with speed for 400rpm;
Slowly cool to 0 DEG C.
6. a formaldehyde scavenger, it is characterised in that include component: the 2-imidazolidine being made up of Claims 1 to 5 any one Ketone, carbamide, wetting agent, auxiliary agent, water, mix.
Formaldehyde scavenger the most according to claim 6, it is characterised in that described 2-imidazolidinone, described carbamide, described profit Humectant, described auxiliary agent, the weight ratio of described water be: 1~20 part: 1~20 part: 0.1~5 part: 0.1~10 part: 40~85 Part.
Formaldehyde scavenger the most according to claim 6, it is characterised in that described wetting agent is OP series emulsifying agent or NP system Row emulsifying agent.
Formaldehyde scavenger the most according to claim 8, it is characterised in that described emulsifying agent is in alkylphenol polyoxyethylene The mixture of one or more.
10. according to the formaldehyde scavenger described in any one in claim 6~9, it is characterised in that described auxiliary agent is chlorination One or more in calcium, barium chloride and magnesium chloride.
CN201610553057.3A 2016-07-12 2016-07-12 The preparation method of a kind of 2 imidazolidinones and formaldehyde scavenger Pending CN106146402A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610553057.3A CN106146402A (en) 2016-07-12 2016-07-12 The preparation method of a kind of 2 imidazolidinones and formaldehyde scavenger

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610553057.3A CN106146402A (en) 2016-07-12 2016-07-12 The preparation method of a kind of 2 imidazolidinones and formaldehyde scavenger

Publications (1)

Publication Number Publication Date
CN106146402A true CN106146402A (en) 2016-11-23

Family

ID=58062238

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610553057.3A Pending CN106146402A (en) 2016-07-12 2016-07-12 The preparation method of a kind of 2 imidazolidinones and formaldehyde scavenger

Country Status (1)

Country Link
CN (1) CN106146402A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106831593A (en) * 2017-03-22 2017-06-13 李其奎 A kind of synthetic method of ethylidene-urea
CN107551445A (en) * 2017-08-28 2018-01-09 广州市华之特奥因特种材料科技有限公司 Compound formaldehyde scavenger
CN110270045A (en) * 2019-07-12 2019-09-24 青岛爱家源环保科技有限公司 A kind of formaldehyde scavenger and preparation method thereof
CN111195410A (en) * 2018-11-16 2020-05-26 深圳市尤佳环境科技有限公司 Formaldehyde scavenger and preparation process thereof
CN114588767A (en) * 2022-03-16 2022-06-07 北京森态环保科技有限公司 Environment-friendly efficient formaldehyde removing agent and preparation method thereof
CN114849441A (en) * 2022-05-25 2022-08-05 李晓雅 Formaldehyde scavenging agent and formaldehyde scavenging method thereof

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104437388A (en) * 2014-11-26 2015-03-25 成都顺发消洗科技有限公司 Indoor methanol remover formula
CN104492379A (en) * 2014-11-26 2015-04-08 成都顺发消洗科技有限公司 Adsorption-reaction type solid formaldehyde elimination agent
CN104492380A (en) * 2014-11-26 2015-04-08 成都顺发消洗科技有限公司 Preparation method for indoor solid aldehyde removal agent
CN104874257A (en) * 2015-05-20 2015-09-02 上海韬鸿化工科技有限公司 Formaldehyde removing agent
CN105131862A (en) * 2015-09-18 2015-12-09 潘春尧 Formaldehyde elimination agent and preparation method thereof as well as adhesive, wooden product and artificial board

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104437388A (en) * 2014-11-26 2015-03-25 成都顺发消洗科技有限公司 Indoor methanol remover formula
CN104492379A (en) * 2014-11-26 2015-04-08 成都顺发消洗科技有限公司 Adsorption-reaction type solid formaldehyde elimination agent
CN104492380A (en) * 2014-11-26 2015-04-08 成都顺发消洗科技有限公司 Preparation method for indoor solid aldehyde removal agent
CN104874257A (en) * 2015-05-20 2015-09-02 上海韬鸿化工科技有限公司 Formaldehyde removing agent
CN105131862A (en) * 2015-09-18 2015-12-09 潘春尧 Formaldehyde elimination agent and preparation method thereof as well as adhesive, wooden product and artificial board

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
姚转乐等: "1,3-二甲基-2-咪唑啉酮的制备", 《应用化工》 *
徐凯等: "溶剂对2-咪唑烷酮合成的影响", 《精细与专用化学品》 *

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106831593A (en) * 2017-03-22 2017-06-13 李其奎 A kind of synthetic method of ethylidene-urea
CN107551445A (en) * 2017-08-28 2018-01-09 广州市华之特奥因特种材料科技有限公司 Compound formaldehyde scavenger
CN111195410A (en) * 2018-11-16 2020-05-26 深圳市尤佳环境科技有限公司 Formaldehyde scavenger and preparation process thereof
CN110270045A (en) * 2019-07-12 2019-09-24 青岛爱家源环保科技有限公司 A kind of formaldehyde scavenger and preparation method thereof
CN114588767A (en) * 2022-03-16 2022-06-07 北京森态环保科技有限公司 Environment-friendly efficient formaldehyde removing agent and preparation method thereof
CN114849441A (en) * 2022-05-25 2022-08-05 李晓雅 Formaldehyde scavenging agent and formaldehyde scavenging method thereof

Similar Documents

Publication Publication Date Title
CN106146402A (en) The preparation method of a kind of 2 imidazolidinones and formaldehyde scavenger
Sheikh et al. Multifunctional modification of linen fabric using chitosan-based formulations
CN106267677A (en) A kind of deodouring agent for removing formaldehyde and preparation method thereof
CN104387871B (en) Interior wall latex paint containing sticky rice glue and preparation method of interior wall latex paint
CN102343134A (en) Formaldehyde scavenging agent and preparation method thereof
CN102182058A (en) Method for manufacturing halogen-free, washing-resistant and flame retardant polyamide hook and loop fastener
CN104623855A (en) Plant type formaldehyde removing agent and preparation method
CN107158927A (en) A kind of zein formaldehyde scavenger and preparation method thereof
CN103358374A (en) Method for bleaching liriodendron tulipifera wood for furniture
CN105155291B (en) A kind of preparation method of environment-friendly type antifouling synthetic leather
KR100829316B1 (en) Method of Genuine Leather
CN103015221B (en) Production method of waterborne polyurethane synthetic leather based on steam solidification
JP5379375B2 (en) Antiviral imparting composition and method for producing antiviral product using the same
CN109501693A (en) Antibacterial roof of the vehicle and preparation method thereof
CN105778763A (en) Preparation process of anion decoration plate
CN104862973B (en) Fabric ultraviolet shielding coating material and preparation method
CN107189532A (en) A kind of graphene formaldehyde-removing wallpaper, wall paper and preparation method
CN106732386A (en) A kind of preparation method with polyethylene glycol and organic quick lime composite drying agent
CN106342877A (en) Mildew-proof antibacterial solvent and preparation process thereof
CN102154825B (en) Formaldehyde exterminator for textile fabrics and preparation and application methods thereof
CN111841313A (en) Formaldehyde purifying agent and use method thereof
CN105194832A (en) Air-purifying nanometer wet tissue
CN107858837A (en) A kind of artificial leather microcapsules perfumed finishing agent and preparation method thereof
CN107597194A (en) A kind of preparation method of new ZnO/ fungies fiber optic catalytic composite material
CN110845899A (en) Negative ion formaldehyde-removing paint and preparation method thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
CB02 Change of applicant information

Address after: 510000 No. 8 Industrial Park, South Fuyuan Third Road, Jinghu Avenue, Huadu District, Guangzhou City, Guangdong Province, self-compiled 4 second floor F206 buildings (i.e. factory building D)

Applicant after: Guangdong Zhong Ke Le Living Environmental Technology Co., Ltd.

Address before: Room 806, Room 3, Fengshang Business Building, 10 Fenghuangbei Road, Xinhua Street, Huadu District, Guangzhou City, Guangdong 510000

Applicant before: Guangdong Oudini Energy Technology Co. Ltd.

CB02 Change of applicant information
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20161123

WD01 Invention patent application deemed withdrawn after publication