CN108070065A - A kind of self-hardening furan resin - Google Patents
A kind of self-hardening furan resin Download PDFInfo
- Publication number
- CN108070065A CN108070065A CN201610990485.2A CN201610990485A CN108070065A CN 108070065 A CN108070065 A CN 108070065A CN 201610990485 A CN201610990485 A CN 201610990485A CN 108070065 A CN108070065 A CN 108070065A
- Authority
- CN
- China
- Prior art keywords
- weight
- parts
- self
- furfuryl alcohol
- furan resin
- 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.)
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- 239000007849 furan resin Substances 0.000 title claims abstract description 18
- XPFVYQJUAUNWIW-UHFFFAOYSA-N furfuryl alcohol Chemical compound OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 claims abstract description 67
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims abstract description 15
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims abstract description 8
- 150000002989 phenols Chemical class 0.000 claims abstract description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000012744 reinforcing agent Substances 0.000 claims abstract description 7
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000004202 carbamide Substances 0.000 claims abstract description 5
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 claims abstract description 4
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 9
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 6
- 238000006243 chemical reaction Methods 0.000 claims description 6
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims description 6
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 5
- 239000006087 Silane Coupling Agent Substances 0.000 claims description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 3
- 150000002016 disaccharides Chemical class 0.000 claims description 3
- 150000004676 glycans Chemical class 0.000 claims description 3
- 229920001282 polysaccharide Polymers 0.000 claims description 3
- 239000005017 polysaccharide Substances 0.000 claims description 3
- 239000001384 succinic acid Substances 0.000 claims description 3
- 238000010792 warming Methods 0.000 claims description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 2
- BFSPAPKTIGPYOV-BQYQJAHWSA-N (e)-1-[4-(4-hydroxyphenyl)piperazin-1-yl]-3-thiophen-2-ylprop-2-en-1-one Chemical compound C1=CC(O)=CC=C1N1CCN(C(=O)\C=C\C=2SC=CC=2)CC1 BFSPAPKTIGPYOV-BQYQJAHWSA-N 0.000 claims 1
- 150000002576 ketones Chemical class 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 abstract description 8
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract description 6
- 239000011347 resin Substances 0.000 abstract description 6
- 229920005989 resin Polymers 0.000 abstract description 6
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 abstract description 3
- 239000007788 liquid Substances 0.000 abstract description 3
- 150000001720 carbohydrates Chemical class 0.000 abstract description 2
- 239000002994 raw material Substances 0.000 abstract description 2
- 239000002904 solvent Substances 0.000 abstract description 2
- 238000005266 casting Methods 0.000 description 8
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 6
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 3
- 239000004576 sand Substances 0.000 description 3
- 235000013399 edible fruits Nutrition 0.000 description 2
- 150000002972 pentoses Chemical class 0.000 description 2
- 238000007171 acid catalysis Methods 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 1
- 238000006210 cyclodehydration reaction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000002240 furans Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 230000001172 regenerating effect Effects 0.000 description 1
- 230000001932 seasonal effect Effects 0.000 description 1
- 239000010902 straw Substances 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000002912 waste gas Substances 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G16/00—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00
- C08G16/02—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes
- C08G16/025—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes with heterocyclic organic compounds
- C08G16/0256—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes with heterocyclic organic compounds containing oxygen in the ring
- C08G16/0262—Furfuryl alcohol
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G16/00—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00
- C08G16/02—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes
- C08G16/04—Chemically modified polycondensates
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
The present invention relates to a kind of self-hardening furan resins.Including following components and each component parts by weight:12 27 parts by weight of phenol, 0.5 20 parts by weight of urea, 30 105 parts by weight of furfuryl alcohol, 10 25 parts by weight of furfuryl alcohol substitute, 8 22 parts by weight of formaldehyde, 8 22 parts by weight of acetone, 0.1 0.5 parts by weight of reinforcing agent.Thick liquid is made by reacting using carbohydrate and phenols, formaldehyde using water as solvent, Modified Cast furane resins is used to prepare instead of furfuryl alcohol raw material, reduces manufacturing cost, and maintains original performance, production efficiency is high, reduces secondary pollution.
Description
Technical field
The present invention relates to a kind of furane resins more particularly to a kind of self-hardening furan resins.
Background technology
Furane resins are made of in a kind of structure containing furan nucleus, are modified furfuryl alcohol by furfuryl alcohol and phenol, urea or various aldehyde
Thermosetting resin, casting is exactly one kind therein with self-hardening furan resin, and casting under normal circumstances is with self-hardening furan resin
It is faint yellow to amber transparent or translucent uniform liquid.Casting self-hardening furan resin can make sand by acid catalysis at room temperature
Type hardens, and is a kind of binding agent that casting industry is the most frequently used, application amount is maximum, its main feature is that moulding is simple, sand mold collapsibility is good,
Regenerating used reclamation rate is high, resin sand intensity is high, smell is small.At present, the preparation of casting self-hardening furan resin, is primarily present chaff
A series of problems, such as alcohol addition height, low production efficiency, secondary pollution.Therefore the cost of resin is influenced very big by furfuryl alcohol.System
The step of standby furfuryl alcohol, mainly hydrolyzes the renewable agricultural and sideline product such as corncob and crop straw under catalyst action, is converted into
Pentose;Pentose generates furfural through cyclodehydration;Furfural obtains furfuryl alcohol after catalytic hydrogenation again.Since preparation method is cumbersome, so
The manufacturing cost of furfuryl alcohol is higher.In addition, corncob and crop material are seasonal agricultural product, cause the price fluctuation in furfuryl alcohol market
Property is larger.On the other hand, there are the problems such as yield is low, waste water and gas is seriously polluted by the preparation process of furfural.Therefore there is an urgent need for prepare
Suitable furfuryl alcohol substitute is used to prepare furan resin for casting, is allowed to that original performance can not only be kept, and can significantly drop
The cost and environmental protection of low furan resin for casting.
The content of the invention
In view of the foregoing drawbacks, it is an object of the invention to provide a kind of manufacturing cost is cheap, original performance, production effect are kept
Rate is high, reduces a kind of self-hardening furan resin of secondary pollution.
The technical solution adopted in the present invention is therefore:
Including following components and each component parts by weight:Phenol 12-27 parts by weight, urea 0.5-20 parts by weight, furfuryl alcohol 30-105
Parts by weight, furfuryl alcohol substitute 10-25 parts by weight, formaldehyde 8-22 parts by weight, acetone 8-22 parts by weight, reinforcing agent 0.1-0.5 weight
Part.
As being further improved for above-mentioned technical proposal, the furfuryl alcohol substitute is made by following steps:By 50 weight
Any combination more than one or both of part six-carbon monosaccharide and disaccharides containing six-carbon monosaccharide structural unit, polysaccharide is dissolved in 15
In~90 parts by weight water, 0.1~26 parts by weight phenols and 5~20 parts by weight acid are then added in, in 60~95 DEG C of temperature conditionss
It is lower reaction 0.5~8 it is small when after, after pH value is adjusted to 7.5~9.5 after being cooled to 25~85 DEG C add in 0.1~15 parts by weight of formaldehyde,
Be warming up to 50~90 DEG C reaction 0.5~5 it is small when, then remove 5~140 parts by weight water, obtain furfuryl alcohol substitute.
As being further improved for above-mentioned technical proposal, the reinforcing agent is silane coupling agent KH602.
As being further improved for above-mentioned technical proposal, the phenols is resorcinol, p-cresol, hydroquinone and waist
One or more combinations of fruit phenol.
As being further improved for above-mentioned technical proposal, the acid is phosphoric acid, sulfuric acid, citric acid and succinic acid one kind or
Multiple combinations.
It is an advantage of the invention that:
Thick liquid is made by reacting using carbohydrate and phenols, formaldehyde using water as solvent, is used to prepare and changes instead of furfuryl alcohol raw material
Property furan resin for casting, reduce manufacturing cost, and maintain original performance, production efficiency is high, reduces secondary pollution.
Specific embodiment
A kind of self-hardening furan resin, including following components and each component parts by weight:Phenol 12-27 parts by weight, urea
0.5-20 parts by weight, furfuryl alcohol 30-105 parts by weight, furfuryl alcohol substitute 10-25 parts by weight, formaldehyde 8-22 parts by weight, acetone 8-22 weights
Measure part, reinforcing agent 0.1-0.5 parts by weight.
As being further improved for above-mentioned technical proposal, the furfuryl alcohol substitute is made by following steps:By 50 weight
Any combination more than one or both of part six-carbon monosaccharide and disaccharides containing six-carbon monosaccharide structural unit, polysaccharide is dissolved in 15
In~90 parts by weight water, 0.1~26 parts by weight phenols and 5~20 parts by weight acid are then added in, in 60~95 DEG C of temperature conditionss
It is lower reaction 0.5~8 it is small when after, after pH value is adjusted to 7.5~9.5 after being cooled to 25~85 DEG C add in 0.1~15 parts by weight of formaldehyde,
Be warming up to 50~90 DEG C reaction 0.5~5 it is small when, then remove 5~140 parts by weight water, obtain furfuryl alcohol substitute.
As being further improved for above-mentioned technical proposal, the reinforcing agent is silane coupling agent KH602.
As being further improved for above-mentioned technical proposal, the phenols is resorcinol, p-cresol, hydroquinone and waist
One or more combinations of fruit phenol.
As being further improved for above-mentioned technical proposal, the acid is phosphoric acid, sulfuric acid, citric acid and succinic acid one kind or
Multiple combinations.
Claims (5)
1. a kind of self-hardening furan resin, which is characterized in that including following components and each component parts by weight:Phenol 12-27 weight
Part, urea 0.5-20 parts by weight, furfuryl alcohol 30-105 parts by weight, furfuryl alcohol substitute 10-25 parts by weight, formaldehyde 8-22 parts by weight, third
Ketone 8-22 parts by weight, reinforcing agent 0.1-0.5 parts by weight.
2. a kind of self-hardening furan resin according to claim 1, which is characterized in that the furfuryl alcohol substitute passes through following step
It is rapid to be made:More than one or both of 50 parts by weight six-carbon monosaccharides and disaccharides containing six-carbon monosaccharide structural unit, polysaccharide
Any combination be dissolved in 15~90 parts by weight water, then add in 0.1~26 parts by weight phenols and 5~20 parts by weight acid, 60
After when reaction 0.5~8 is small under~95 DEG C of temperature conditionss, added in after pH value is adjusted to 7.5~9.5 after being cooled to 25~85 DEG C
0.1~15 parts by weight of formaldehyde, be warming up to 50~90 DEG C reaction 0.5~5 it is small when, then remove 5~140 parts by weight water, obtain chaff
Alcohol substitute.
3. a kind of self-hardening furan resin according to claim 1, which is characterized in that the reinforcing agent is silane coupling agent
KH602。
4. a kind of self-hardening furan resin according to claim 2, which is characterized in that the phenols is resorcinol, to first
One or more combinations of phenol, hydroquinone and anacardol.
5. a kind of self-hardening furan resin according to claim 2, which is characterized in that the acid is phosphoric acid, sulfuric acid, citric acid
With the one or more combination of succinic acid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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CN201610990485.2A CN108070065A (en) | 2016-11-10 | 2016-11-10 | A kind of self-hardening furan resin |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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CN201610990485.2A CN108070065A (en) | 2016-11-10 | 2016-11-10 | A kind of self-hardening furan resin |
Publications (1)
Publication Number | Publication Date |
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CN108070065A true CN108070065A (en) | 2018-05-25 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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CN201610990485.2A Pending CN108070065A (en) | 2016-11-10 | 2016-11-10 | A kind of self-hardening furan resin |
Country Status (1)
Country | Link |
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CN (1) | CN108070065A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110776612A (en) * | 2019-10-23 | 2020-02-11 | 广东省铸力铸材科技有限公司 | Furan resin and preparation method thereof |
CN111531119A (en) * | 2020-04-29 | 2020-08-14 | 宁夏共享化工有限公司 | Fructose modified furan resin for casting and preparation method thereof |
CN112512722A (en) * | 2018-08-24 | 2021-03-16 | 花王株式会社 | Binder composition for mold making |
CN112778478A (en) * | 2020-12-30 | 2021-05-11 | 广东省铸力铸材科技有限公司 | Furan resin and preparation method and application thereof |
-
2016
- 2016-11-10 CN CN201610990485.2A patent/CN108070065A/en active Pending
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112512722A (en) * | 2018-08-24 | 2021-03-16 | 花王株式会社 | Binder composition for mold making |
CN112512722B (en) * | 2018-08-24 | 2023-02-28 | 花王株式会社 | Binder composition for mold making |
CN110776612A (en) * | 2019-10-23 | 2020-02-11 | 广东省铸力铸材科技有限公司 | Furan resin and preparation method thereof |
CN111531119A (en) * | 2020-04-29 | 2020-08-14 | 宁夏共享化工有限公司 | Fructose modified furan resin for casting and preparation method thereof |
CN111531119B (en) * | 2020-04-29 | 2021-10-08 | 宁夏共享化工有限公司 | Fructose modified furan resin for casting and preparation method thereof |
CN112778478A (en) * | 2020-12-30 | 2021-05-11 | 广东省铸力铸材科技有限公司 | Furan resin and preparation method and application thereof |
CN112778478B (en) * | 2020-12-30 | 2023-09-29 | 广东省铸力铸材科技有限公司 | Furan resin and preparation method and application thereof |
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Legal Events
Date | Code | Title | Description |
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PB01 | Publication | ||
PB01 | Publication | ||
WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20180525 |
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WD01 | Invention patent application deemed withdrawn after publication |