CN107841269A - The preparation method of low burst size of methanal adhesive - Google Patents

The preparation method of low burst size of methanal adhesive Download PDF

Info

Publication number
CN107841269A
CN107841269A CN201711229946.5A CN201711229946A CN107841269A CN 107841269 A CN107841269 A CN 107841269A CN 201711229946 A CN201711229946 A CN 201711229946A CN 107841269 A CN107841269 A CN 107841269A
Authority
CN
China
Prior art keywords
parts
methanal
burst size
titanium dioxide
powder
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.)
Withdrawn
Application number
CN201711229946.5A
Other languages
Chinese (zh)
Inventor
戴福成
叶佐林
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.)
Liuzhou Honglian Wood Industry Co Ltd
Original Assignee
Liuzhou Honglian Wood Industry 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 Liuzhou Honglian Wood Industry Co Ltd filed Critical Liuzhou Honglian Wood Industry Co Ltd
Priority to CN201711229946.5A priority Critical patent/CN107841269A/en
Publication of CN107841269A publication Critical patent/CN107841269A/en
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J161/00Adhesives based on condensation polymers of aldehydes or ketones; Adhesives based on derivatives of such polymers
    • C09J161/04Condensation polymers of aldehydes or ketones with phenols only
    • C09J161/06Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J11/00Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/02Non-macromolecular additives
    • C09J11/04Non-macromolecular additives inorganic
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J11/00Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/08Macromolecular additives
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • C08K2003/2237Oxides; Hydroxides of metals of titanium
    • C08K2003/2241Titanium dioxide
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00Specific properties of additives
    • C08K2201/011Nanostructured additives
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend
    • C08L2205/035Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend

Abstract

The present invention discloses a kind of preparation method of low burst size of methanal adhesive, belongs to organic adhesion agent technical field.The present invention includes the particle into particle diameter for Nano grade by titanium dioxide, activated carbon, Silica abrasive, is then put into together with phenolic resin in reactor, and is heated to 80 DEG C~110 DEG C, stirs;Then, methylcellulose, turpentine oil, flake asbestos, acetone, ethanol, polyvinyl alcohol are added into the reactor, and is heated to 250 DEG C~260 DEG C, is reacted 1 hour~3 hours.The present invention is mainly by adding titanium dioxide, activated carbon, silica, there is redox and absorption transformation using it to free formaldehyde, so as to reduce the burst size of methanal of product adhesive, reach and solve the purpose that traditional phenolic resin glue has the high problem of burst size of methanal.

Description

The preparation method of low burst size of methanal adhesive
Technical field
The invention belongs to organic adhesion agent technical field, more particularly to a kind of preparation side of low burst size of methanal adhesive Method.
Background technology
Can be by of the same race or two or more homogeneities or heterogeneous product(Or material)Link together, have after solidification sufficiently strong Organic or inorganic, natural or synthetic a kind of material of degree, it is referred to as adhesive or bonding agent, traditionally adhesive, abbreviation For glue.
Although the application of adhesive is very extensive, all there is dirty to environment to some extent for the adhesive of market sale The latency of dye.Harmful substance in adhesive is mainly benzene, toluene, formaldehyde, methanol, styrene, chloroform, four chlorinations Carbon, 1, it is 2 one dichloroethanes, toluene di-isocyanate(TDI), m-phenylene diamine (MPD), tricresyl phosphate, ethylenediamine, dimethylaniline, anti-old Agent D, coal tar, flake asbestos, silica flour etc..
Wherein, on formaldehyde, as the improvement of people's living standards, substantial amounts of woodworking article is applied to indoor dress Repair, and it is conventional that adhesive --- phenolic resin glue is during glue and pressing plate, and the people made of phenolic resin glue Plate is made during long-term use, can continue largely to discharge free formaldehyde, have a strong impact on the health of the mankind.Therefore, people Wish to search out one kind and can replace traditional phenolic resin glue and the low-down substitute of burst size of methanal.
The content of the invention
The present invention provides a kind of preparation method of low burst size of methanal adhesive, is deposited so as to solve traditional phenolic resin glue Burst size of methanal is high the problem of.
In order to solve the above-mentioned technical problem, the technical solution adopted in the present invention is:
It uses the raw material of following parts by weight:
100 parts~200 parts of phenolic resin, 50 parts~60 parts of carboxymethyl cellulose, 15 parts~20 parts of turpentine oil, 10 parts of flake asbestos~ 15 parts, 5 parts~8 parts of acetone, 2 parts~4 parts of ethanol, 0.1 part~0.5 part of polyvinyl alcohol, 1 part~5 parts of titanium dioxide, activated carbon 4 Part~8 parts, 3 parts~7 parts of silica;
Its preparation method comprises the following steps:
A. according to the above ratio, first respectively by titanium dioxide, activated carbon, Silica abrasive into particle diameter be Nano grade particle, Nano titanium dioxide powder, nano level active carbon powder and nanometer grade silica powder are obtained, it is standby;
B. by Nano titanium dioxide powder, nano level active carbon powder and nanoscale made from phenolic resin and step A SiO 2 powder is put into reactor, and is heated to 80 DEG C~110 DEG C, is stirred;
C. then, methylcellulose, turpentine oil, flake asbestos, acetone, ethanol, polyvinyl alcohol are added into the reactor, and is added Heat is reacted 1 hour~3 hours to 250 DEG C~260 DEG C.
In above-mentioned technical proposal, more specifically technical scheme can also be:160 parts of the phenolic resin, carboxymethyl cellulose 54 parts of element, 18 parts of turpentine oil, 11 parts of flake asbestos, 7 parts of acetone, 3 parts of ethanol, 0.4 part of polyvinyl alcohol, 3 parts of titanium dioxide, activated carbon 6 parts, 5 parts of silica.
Due to being had the advantages that using above-mentioned technical proposal, the present invention:
The present invention has redox work to free formaldehyde mainly by adding titanium dioxide, activated carbon, silica using it With and absorption transformation, so as to reduce the burst size of methanal of product adhesive, reach and solve traditional phenolic resin glue and exist The purpose of the high problem of burst size of methanal.
Embodiment
Below in conjunction with instantiation, the invention will be further described:
Embodiment 1 --- the preparation method of low burst size of methanal adhesive
Using following raw material:
Phenolic resin 160kg, carboxymethyl cellulose 54kg, turpentine oil 18kg, flake asbestos 11kg, acetone 7kg, ethanol 3kg, poly- second Enol 0.4kg, titanium dioxide 3kg, activated carbon 6kg, silica 5kg;
Its preparation method comprises the following steps:
A. according to the above ratio, first respectively by titanium dioxide, activated carbon, Silica abrasive into particle diameter be Nano grade particle, Nano titanium dioxide powder, nano level active carbon powder and nanometer grade silica powder are obtained, it is standby;
B. by Nano titanium dioxide powder, nano level active carbon powder and nanoscale made from phenolic resin and step A SiO 2 powder is put into reactor, and is heated to 80 DEG C, is stirred;
C. then, methylcellulose, turpentine oil, flake asbestos, acetone, ethanol, polyvinyl alcohol are added into the reactor, and is added Heat is reacted 3 hours to 250 DEG C.
The present embodiment system is used to wood-based plate be made, and to the wood-based plate according to GB18580-2001《Indoor decorating Burst size of methanal in material wood-based plate and its product》Climate box method carries out burst size of methanal detection, and its result is shown, Form aldehyde release Measure as 0.005mg/m3
Embodiment 2 --- the preparation method of low burst size of methanal adhesive
Using following raw material:
Phenolic resin 200kg, carboxymethyl cellulose 60kg, turpentine oil 20kg, flake asbestos 15kg, acetone 8kg, ethanol 4kg, poly- second Enol 0.5kg, titanium dioxide 5kg, activated carbon 8kg, silica 7kg;
Its preparation method comprises the following steps:
A. according to the above ratio, first respectively by titanium dioxide, activated carbon, Silica abrasive into particle diameter be Nano grade particle, Nano titanium dioxide powder, nano level active carbon powder and nanometer grade silica powder are obtained, it is standby;
B. by Nano titanium dioxide powder, nano level active carbon powder and nanoscale made from phenolic resin and step A SiO 2 powder is put into reactor, and is heated to 110 DEG C, is stirred;
C. then, methylcellulose, turpentine oil, flake asbestos, acetone, ethanol, polyvinyl alcohol are added into the reactor, and is added Heat is reacted 1 hour to 260 DEG C.
The present embodiment system is used to wood-based plate be made, and to the wood-based plate according to GB18580-2001《Indoor decorating Burst size of methanal in material wood-based plate and its product》Climate box method carries out burst size of methanal detection, and its result is shown, Form aldehyde release Measure as 0.006mg/m3
Embodiment 3 --- the preparation method of low burst size of methanal adhesive
Using following raw material:
Phenolic resin 100kg, carboxymethyl cellulose 50kg, turpentine oil 15kg, flake asbestos 10kg, acetone 5kg, ethanol 2kg, poly- second Enol 0.1kg, titanium dioxide 1kg, activated carbon 4kg, silica 3kg;
Its preparation method comprises the following steps:
A. according to the above ratio, first respectively by titanium dioxide, activated carbon, Silica abrasive into particle diameter be Nano grade particle, Nano titanium dioxide powder, nano level active carbon powder and nanometer grade silica powder are obtained, it is standby;
B. by Nano titanium dioxide powder, nano level active carbon powder and nanoscale made from phenolic resin and step A SiO 2 powder is put into reactor, and is heated to 105 DEG C, is stirred;
C. then, methylcellulose, turpentine oil, flake asbestos, acetone, ethanol, polyvinyl alcohol are added into the reactor, and is added Heat is reacted 2 hours to 255 DEG C.
The present embodiment system is used to wood-based plate be made, and to the wood-based plate according to GB18580-2001《Indoor decorating Burst size of methanal in material wood-based plate and its product》Climate box method carries out burst size of methanal detection, and its result is shown, Form aldehyde release Measure as 0.004mg/m3
Comparative example 1 --- the preparation method of low burst size of methanal adhesive
Using following raw material:
Phenolic resin 160kg, carboxymethyl cellulose 54kg, turpentine oil 18kg, flake asbestos 11kg, acetone 7kg, ethanol 3kg, poly- second Enol 0.4kg;
Its preparation method comprises the following steps:
Phenolic resin, methylcellulose, turpentine oil, flake asbestos, acetone, ethanol, polyvinyl alcohol are put into reactor and stirred It is even, 250 DEG C are then heated to, is reacted 3 hours.
This comparative example system is used to wood-based plate be made, and to the wood-based plate according to GB18580-2001《Indoor decorating Burst size of methanal in material wood-based plate and its product》Climate box method carries out burst size of methanal detection, and its result is shown, Form aldehyde release Measure as 0.10mg/m3
Comparative example 2 --- the preparation method of low burst size of methanal adhesive
Using following raw material:
Phenolic resin 200kg, carboxymethyl cellulose 60kg, turpentine oil 20kg, flake asbestos 15kg, acetone 8kg, ethanol 4kg, poly- second Enol 0.5kg, activated carbon 8kg, silica 7kg;
Its preparation method comprises the following steps:
A. according to the above ratio, first nanometer is obtained respectively by activated carbon, Silica abrasive into the particle that particle diameter is Nano grade Level active carbon powder and nanometer grade silica powder, it is standby;
B. nano level active carbon powder made from phenolic resin and step A and nanometer grade silica powder are put into instead Answer in kettle, and be heated to 110 DEG C, stir;
C. then, methylcellulose, turpentine oil, flake asbestos, acetone, ethanol, polyvinyl alcohol are added into the reactor, and is added Heat is reacted 1 hour to 260 DEG C.
This comparative example system is used to wood-based plate be made, and to the wood-based plate according to GB18580-2001《Indoor decorating Burst size of methanal in material wood-based plate and its product》Climate box method carries out burst size of methanal detection, and its result is shown, Form aldehyde release Measure as 0.05mg/m3
Comparative example 3 --- the preparation method of low burst size of methanal adhesive
Using following raw material:
Phenolic resin 100kg, carboxymethyl cellulose 50kg, turpentine oil 15kg, flake asbestos 10kg, acetone 5kg, ethanol 2kg, poly- second Enol 0.1kg, titanium dioxide 1kg, silica 3kg;
Its preparation method comprises the following steps:
A. according to the above ratio, first received respectively by titanium dioxide, Silica abrasive into the particle that particle diameter is Nano grade Meter level titania powder and nanometer grade silica powder, it is standby;
B. Nano titanium dioxide powder made from phenolic resin and step A and nanometer grade silica powder are put into In reactor, and 105 DEG C are heated to, stirred;
C. then, methylcellulose, turpentine oil, flake asbestos, acetone, ethanol, polyvinyl alcohol are added into the reactor, and is added Heat is reacted 2 hours to 255 DEG C.
This comparative example system is used to wood-based plate be made, and to the wood-based plate according to GB18580-2001《Indoor decorating Burst size of methanal in material wood-based plate and its product》Climate box method carries out burst size of methanal detection, and its result is shown, Form aldehyde release Measure as 0.06mg/m3
Comparative example 4 --- the preparation method of low burst size of methanal adhesive
Using following raw material:
Phenolic resin 100kg, carboxymethyl cellulose 50kg, turpentine oil 15kg, flake asbestos 10kg, acetone 5kg, ethanol 2kg, poly- second Enol 0.1kg, titanium dioxide 1kg, activated carbon 4kg;
Its preparation method comprises the following steps:
A. according to the above ratio, titanium dioxide, activated carbon are first ground into the particle that particle diameter is Nano grade respectively, obtain nanometer Grade titanium dioxide powder, nano level active carbon powder, it is standby;
B. Nano titanium dioxide powder, nano level active carbon powder made from phenolic resin and step A are put into reactor In, and 105 DEG C are heated to, stir;
C. then, methylcellulose, turpentine oil, flake asbestos, acetone, ethanol, polyvinyl alcohol are added into the reactor, and is added Heat is reacted 2 hours to 255 DEG C.
This comparative example system is used to wood-based plate be made, and to the wood-based plate according to GB18580-2001《Indoor decorating Burst size of methanal in material wood-based plate and its product》Climate box method carries out burst size of methanal detection, and its result is shown, Form aldehyde release Measure as 0.070mg/m3

Claims (2)

  1. A kind of 1. preparation method of low burst size of methanal adhesive, it is characterised in that:
    Using the raw material of following parts by weight:
    100 parts~200 parts of phenolic resin, 50 parts~60 parts of carboxymethyl cellulose, 15 parts~20 parts of turpentine oil, 10 parts of flake asbestos~ 15 parts, 5 parts~8 parts of acetone, 2 parts~4 parts of ethanol, 0.1 part~0.5 part of polyvinyl alcohol, 1 part~5 parts of titanium dioxide, activated carbon 4 Part~8 parts, 3 parts~7 parts of silica;
    Its preparation method comprises the following steps:
    A. according to the above ratio, first respectively by titanium dioxide, activated carbon, Silica abrasive into particle diameter be Nano grade particle, Nano titanium dioxide powder, nano level active carbon powder and nanometer grade silica powder are obtained, it is standby;
    B. by Nano titanium dioxide powder, nano level active carbon powder and nanoscale made from phenolic resin and step A SiO 2 powder is put into reactor, and is heated to 80 DEG C~110 DEG C, is stirred;
    C. then, methylcellulose, turpentine oil, flake asbestos, acetone, ethanol, polyvinyl alcohol are added into the reactor, and is added Heat is reacted 1 hour~3 hours to 250 DEG C~260 DEG C.
  2. 2. the preparation method of low burst size of methanal adhesive according to claim 1, it is characterised in that:The phenolic resin 160 parts, 54 parts of carboxymethyl cellulose, 18 parts of turpentine oil, 11 parts of flake asbestos, 7 parts of acetone, 3 parts of ethanol, 0.4 part of polyvinyl alcohol, two 3 parts of titanium oxide, 6 parts of activated carbon, 5 parts of silica.
CN201711229946.5A 2017-11-29 2017-11-29 The preparation method of low burst size of methanal adhesive Withdrawn CN107841269A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201711229946.5A CN107841269A (en) 2017-11-29 2017-11-29 The preparation method of low burst size of methanal adhesive

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201711229946.5A CN107841269A (en) 2017-11-29 2017-11-29 The preparation method of low burst size of methanal adhesive

Publications (1)

Publication Number Publication Date
CN107841269A true CN107841269A (en) 2018-03-27

Family

ID=61679347

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201711229946.5A Withdrawn CN107841269A (en) 2017-11-29 2017-11-29 The preparation method of low burst size of methanal adhesive

Country Status (1)

Country Link
CN (1) CN107841269A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113389082A (en) * 2021-07-19 2021-09-14 广东福美新材料科技有限公司 Long-acting low-formaldehyde impregnated paper and preparation method thereof

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104513641A (en) * 2013-12-15 2015-04-15 广西鹿寨通用人造板有限公司 Preparation method of low formaldehyde emission adhesive
CN104877609A (en) * 2015-05-19 2015-09-02 广西众昌树脂有限公司 Phenol-formaldehyde resin adhesive
CN107175074A (en) * 2017-07-12 2017-09-19 河南西超实业有限公司 One kind is except modified formaldehyde activated carbon and preparation method thereof

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104513641A (en) * 2013-12-15 2015-04-15 广西鹿寨通用人造板有限公司 Preparation method of low formaldehyde emission adhesive
CN104877609A (en) * 2015-05-19 2015-09-02 广西众昌树脂有限公司 Phenol-formaldehyde resin adhesive
CN107175074A (en) * 2017-07-12 2017-09-19 河南西超实业有限公司 One kind is except modified formaldehyde activated carbon and preparation method thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113389082A (en) * 2021-07-19 2021-09-14 广东福美新材料科技有限公司 Long-acting low-formaldehyde impregnated paper and preparation method thereof

Similar Documents

Publication Publication Date Title
CN105345911A (en) Flame-retardant straw shaving board and manufacturing method thereof
CN100587020C (en) Adhesive for artificial plate and preparation method thereof
CN101200624A (en) Lumber adhesive agent additives and preparation technique
CN100382947C (en) Bamboo carbon plate and its manufacturing technology
CN103254842A (en) Modified starch wood adhesive, and preparation method and application thereof
CN103205218B (en) Special filler for plywood glue
CN105199465A (en) Novel outer wall waterproof putty powder as well as preparation and using method thereof
CN107841269A (en) The preparation method of low burst size of methanal adhesive
CN104927419A (en) Reaction film formation inorganic dry powder coating material and production method thereof
CN105602302B (en) A kind of aqueous inorganic negative ion paint and preparation method thereof
CN104276790B (en) A kind of mildew-resistant heat-insulation wall plate and preparation method thereof
CN102994003A (en) Urea-formaldehyde resin additive and application thereof
CN102585129B (en) Urea-formaldehyde resin for artificial board and modification modulation method thereof
CN104513641B (en) The preparation method of low burst size of methanal adhesive
CN104497937A (en) Low-molar ratio modified adhesive for laminate flooring base material and preparation method thereof
CN101955748A (en) Formaldehyde-free corn protein powder wood adhesive and preparation method thereof
CN102619914B (en) Disc type brake block of petroleum and preparation method thereof
CN106542773A (en) A kind of polyester fiber strengthens resistance and splits type diatom mud material and preparation method thereof
CN103692532B (en) A kind of method of preparing floor base material with reed rod
CN103275661B (en) Carbon nano-tube modification urea-formaldehyde resin adhesive
CN101205348A (en) Urea-formaldehyde resin additive, urea-formaldehyde resin containing the same and preparation method thereof
CN104789153A (en) Filler for high-water-resistant urea-formaldehyde resin and preparation method of filler
CN103275660B (en) The preparation method of carbon nano-tube modification urea-formaldehyde resin adhesive
CN104046210B (en) Method for preparing soybean-oil-based dual-component low-temperature curing adhesive
CN101177505B (en) Phenolic resin additive, phenolic resin containing the same and preparation method thereof

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
WW01 Invention patent application withdrawn after publication

Application publication date: 20180327

WW01 Invention patent application withdrawn after publication