CN1212258A - Method for preparation of water soluble sulfomethyl phenolic resin - Google Patents
Method for preparation of water soluble sulfomethyl phenolic resin Download PDFInfo
- Publication number
- CN1212258A CN1212258A CN 97116924 CN97116924A CN1212258A CN 1212258 A CN1212258 A CN 1212258A CN 97116924 CN97116924 CN 97116924 CN 97116924 A CN97116924 A CN 97116924A CN 1212258 A CN1212258 A CN 1212258A
- Authority
- CN
- China
- Prior art keywords
- preparation
- phenolic resin
- formaldehyde
- sulfomethyl
- water soluble
- 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.)
- Granted
Links
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract description 11
- -1 sulfomethyl phenolic resin Chemical compound 0.000 title claims abstract description 10
- 229920001568 phenolic resin Polymers 0.000 title claims abstract description 8
- 239000005011 phenolic resin Substances 0.000 title claims abstract description 8
- 238000000034 method Methods 0.000 title claims abstract description 7
- 238000002360 preparation method Methods 0.000 title abstract description 12
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims abstract description 30
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims abstract description 14
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims abstract description 9
- HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 claims abstract description 6
- 235000010262 sodium metabisulphite Nutrition 0.000 claims abstract description 6
- UOULCEYHQNCFFH-UHFFFAOYSA-M sodium;hydroxymethanesulfonate Chemical compound [Na+].OCS([O-])(=O)=O UOULCEYHQNCFFH-UHFFFAOYSA-M 0.000 claims abstract description 6
- 239000007864 aqueous solution Substances 0.000 claims abstract description 5
- 239000000243 solution Substances 0.000 claims abstract description 5
- 229920005989 resin Polymers 0.000 claims description 9
- 239000011347 resin Substances 0.000 claims description 9
- KWYUFKZDYYNOTN-UHFFFAOYSA-M potassium hydroxide Substances [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 7
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 claims description 6
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 claims description 6
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 claims description 6
- UJBCWFGVYCRSQB-UHFFFAOYSA-N [S].OC1=C(C=CC=C1)C Chemical compound [S].OC1=C(C=CC=C1)C UJBCWFGVYCRSQB-UHFFFAOYSA-N 0.000 claims description 3
- 238000010992 reflux Methods 0.000 abstract description 7
- 238000006068 polycondensation reaction Methods 0.000 abstract description 6
- DHKIVCMLYUCALN-UHFFFAOYSA-N (2-hydroxyphenyl)methanesulfonic acid Chemical compound OC1=CC=CC=C1CS(O)(=O)=O DHKIVCMLYUCALN-UHFFFAOYSA-N 0.000 abstract 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 abstract 1
- 239000008098 formaldehyde solution Substances 0.000 description 6
- 230000000630 rising effect Effects 0.000 description 6
- 238000003756 stirring Methods 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 238000010189 synthetic method Methods 0.000 description 2
- 206010044565 Tremor Diseases 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000004021 humic acid Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229920003987 resole Polymers 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
Landscapes
- Phenolic Resins Or Amino Resins (AREA)
Abstract
The preparation method of water-soluble sulfomethyl phenolic resin includes the following steps: using sodium pyrosulfite, formaldehyde and water to prepare sodium hydroxymethyl sulfonate aqueous solution, adding phenol and NaOH to obtain sulfomethyl phenol solution, then adding formaldehyde, through refluxing process, to obtain the sulfomethyl phenolic resin. Said preparation method is easy to control its end point, high in product purity, and solves the problem of mutual interference of sulfomethylation and phenolic polycondensation.
Description
The present invention is a kind of new synthetic method of preparation water soluble sulfomethyl phenolic resin.
United States Patent (USP) 3956140 is to be formed through polycondensation in the presence of S-WAT and sodium bisulfite by phenol, formaldehyde.Though this method is that sulfomethylation and polycondensation are finished simultaneously, but the bad control of reaction end, and the mutual interference problem that has sulfomethylation and phenolic aldehyde polycondensation, Chinese patent 85106524 are next the footwork copolycondensations of existence at sulfomethylation reagent and Sodium salts humic acids of phenol, formaldehyde.But this method can not be prepared pure sulfonated-pheno-formoldehyde resin.
The present invention is that the synthesis technique with sulfonated-pheno-formoldehyde resin was divided into for three steps and finishes: 1, the preparation of sodium hydroxymethane sulfonate; 2, the preparation of sulfomethylation phenol; 3, the preparation of sulfonated-pheno-formoldehyde resin, and in synthesis technique successful solution elder generation with the phenol sulfomethylation, but problem that can not polycondensation.
Synthetic method is as follows:
1, the preparation of sodium hydroxymethane sulfonate
Water is that solvent stirs the mixture of trembling down adding Sodium Pyrosulfite or S-WAT and sodium bisulfite, adds formaldehyde again and stirs, and is prepared into sodium hydroxymethane sulfonate.
2, the preparation of sulfomethylation phenol
In the aqueous solution of above-mentioned sodium hydroxymethane sulfonate, add phenol, add oxyhydroxide again, be prepared into the sulphur methylphenol in temperature rising reflux 0.5-1 hour.
3, the preparation of sulfonated-pheno-formoldehyde resin
Add formaldehyde backflow 1-3 hour until being prepared into sulfonated-pheno-formoldehyde resin at the solution of sulfomethylation phenol.
The component of sulfonated-pheno-formoldehyde resin and content (weight percentage)
Component content
Sodium Pyrosulfite 26-42
(S-WAT and sodium bisulfite)
Oxyhydroxide 5-12
Formaldehyde 18-34
Phenol 30-45
The water soluble sulfomethyl phenolic resin purity height of the present invention's preparation, terminal point is easy to control, has overcome the mutual interference problem of sulfomethylation and phenolic aldehyde polycondensation.
Embodiment 1,
In 1000 liter retort, add 350kg water, add Sodium Pyrosulfite 40kg, add formaldehyde solution (36%) 30kg again, 25 ℃ are stirred adding phenol 55kg after 30 minutes down, potassium hydroxide 10kg, temperature rising reflux adds formaldehyde solution 100kg again and refluxed 1.5 hours after 1 hour, be prepared into sulfonated-pheno-formoldehyde resin.
Embodiment 2,
In 500 liter retort, add people's water 160kg S-WAT 25kg, sodium bisulfite 15kg, add formaldehyde solution (36%) 30kg again, stir under the room temperature and add phenol 53kg after 40 minutes, potassium hydroxide 12kg, temperature rising reflux adds formaldehyde solution 110kg again after 0.5 hour, temperature rising reflux was prepared into the sulfonated-pheno-formoldehyde resin aqueous solution in 120 minutes, and (but also drying is prepared into solid powder.Embodiment 3,
Embodiment 3,
In the retort of 1000 liters, add entry 350kg, Sodium Pyrosulfite 40kg, S-WAT 10kg, sodium bisulfite 8kg, formaldehyde solution 60kg stirs adding phenol 60kg after 60 minutes, sodium hydroxide 22kg under the room temperature, temperature rising reflux added formaldehyde solution 180kg temperature rising reflux 90-150 minute again after 60 minutes, be prepared into sulfomethylation resol.(also but drying is prepared into solid powder).
Claims (2)
1, a kind of method for making of water soluble sulfomethyl phenolic resin is characterized in that step is carried out in the following order:
(1) add Sodium Pyrosulfite or S-WAT and sodium bisulfite 26-42% in water, formaldehyde 18-34% makes the sodium hydroxymethane sulfonate aqueous solution,
(2) add people's phenol 30-40% in the above-mentioned aqueous solution, oxyhydroxide 5-12% made sulphur methylphenol solution through backflow 0.5-1 hour,
(3) in above-mentioned sulphur methylphenol solution, add formaldehyde 18-34% backflow 1-3 hour, make sulfonated-pheno-formoldehyde resin.
2, a kind of water soluble sulfomethyl phenolic resin according to claim 1 is characterized in that described oxyhydroxide is NaOH or KOH.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 97116924 CN1073578C (en) | 1997-09-25 | 1997-09-25 | Method for preparation of water soluble sulfomethyl phenolic resin |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 97116924 CN1073578C (en) | 1997-09-25 | 1997-09-25 | Method for preparation of water soluble sulfomethyl phenolic resin |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1212258A true CN1212258A (en) | 1999-03-31 |
| CN1073578C CN1073578C (en) | 2001-10-24 |
Family
ID=5174209
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 97116924 Expired - Fee Related CN1073578C (en) | 1997-09-25 | 1997-09-25 | Method for preparation of water soluble sulfomethyl phenolic resin |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1073578C (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101798914A (en) * | 2010-04-08 | 2010-08-11 | 中国石油大学(华东) | Method for improving high-temperature stability of sulfonated drilling fluid |
| CN113045719A (en) * | 2021-03-23 | 2021-06-29 | 中国石油大学(华东) | Plugging agent suitable for water plugging of high-temperature high-salinity clastic rock oil reservoir and preparation method thereof |
| CN115341398A (en) * | 2021-12-29 | 2022-11-15 | 广东宏昊化工有限公司 | Acidic color fixing agent, preparation method and application method thereof |
| CN117024908A (en) * | 2023-10-10 | 2023-11-10 | 季华实验室 | Phenolic resin-based water-lubricated bearing material and preparation method thereof |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102533231A (en) * | 2011-12-02 | 2012-07-04 | 新疆德蓝股份有限公司 | fluid-loss reducing additive for ultra-high temperature drilling |
-
1997
- 1997-09-25 CN CN 97116924 patent/CN1073578C/en not_active Expired - Fee Related
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101798914A (en) * | 2010-04-08 | 2010-08-11 | 中国石油大学(华东) | Method for improving high-temperature stability of sulfonated drilling fluid |
| CN101798914B (en) * | 2010-04-08 | 2013-01-02 | 中国石油大学(华东) | Method for improving high-temperature stability of sulfonated drilling fluid |
| CN113045719A (en) * | 2021-03-23 | 2021-06-29 | 中国石油大学(华东) | Plugging agent suitable for water plugging of high-temperature high-salinity clastic rock oil reservoir and preparation method thereof |
| CN113045719B (en) * | 2021-03-23 | 2022-11-08 | 中国石油大学(华东) | Plugging agent suitable for water plugging of high-temperature high-salinity clastic rock oil reservoir and preparation method thereof |
| CN115341398A (en) * | 2021-12-29 | 2022-11-15 | 广东宏昊化工有限公司 | Acidic color fixing agent, preparation method and application method thereof |
| CN117024908A (en) * | 2023-10-10 | 2023-11-10 | 季华实验室 | Phenolic resin-based water-lubricated bearing material and preparation method thereof |
| CN117024908B (en) * | 2023-10-10 | 2023-12-12 | 季华实验室 | Phenolic resin-based water-lubricated bearing material and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1073578C (en) | 2001-10-24 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN100355691C (en) | Process for preparing sodium lignosulfonate water-reducing agent by using pulping black liquid | |
| US20110124847A1 (en) | Method for preparing concrete water reducer by grafting of lignosulfonate with carbonyl aliphatics | |
| CN1073578C (en) | Method for preparation of water soluble sulfomethyl phenolic resin | |
| CN111646881B (en) | Synthetic method of m-trifluoromethyl phenol | |
| CN111848978B (en) | Modified bagasse retarder and preparation method thereof | |
| CN113698166A (en) | High-strength fly ash brick and preparation method thereof | |
| CN114369435B (en) | Preparation method of biomass-based adhesive and adhesive | |
| CN105753358A (en) | Method for synthesizing modified sulfamate water reducer by utilizing wastewater generated in J acid production process | |
| CN1131651A (en) | Cement waterproof agent and its preparation method | |
| CN105800988A (en) | Method for synthesizing modified sulfamate water reducer by utilizing wastewater generated in H acid production process | |
| CN110255950B (en) | Process for producing water reducing agent by using H acid mother liquor | |
| CN105753357A (en) | Method for synthesizing modified sulfamate water reducer by utilizing wastewater generated in tobias acid production process | |
| CN106830977B (en) | Production method for non-autoclaved self-insulation lightweight concrete building block | |
| CN102010148B (en) | Method for producing naphthalene series water reducing agent and aliphatic water reducing agent | |
| CN114570375B (en) | Hydrotalcite-based catalyst, preparation method thereof and application of hydrotalcite-based catalyst in efficient catalytic preparation of vanillin | |
| CN1127298C (en) | Comprehensive utilization method of brown coal | |
| CN105645819A (en) | Method for synthesizing modified aminosulfonate superplasticizer from wastewater produced in K acid production process | |
| CN105731858A (en) | Method for synthesizing a modified amino sulfonate water-reducing agent by utilizing wastewater generated in dye intermediate production process | |
| CN1109020C (en) | Method for separating ammonium sulfate and ammonium hydrogen sulfate and method for producing 2-hydroxyl-4-methyl-thiobutanoic acid using said method | |
| CN1057521C (en) | Improved process for prodn. of 1-amino-8 naphthol-3,6-disulfonate of mono-sodium | |
| CN100355719C (en) | Salicylic acid preparing process | |
| CN106279562B (en) | A kind of synthesis technology of polycarboxylate water-reducer | |
| CN103739804A (en) | Scavenger for free formaldehyde in etherified amino resin and using method thereof | |
| CN1600734A (en) | Method for preparing water reducing agent for cement | |
| CN1071152A (en) | Utilize spent pulping liquor to make cement water reducing agent |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| ASS | Succession or assignment of patent right |
Owner name: PHYSICAL CHEMISTRY TECHNOLOGY INST., CHINESE ACAD Free format text: FORMER OWNER: CHEMISTRY INSTITUTE, CHINESE ACADEMY OF SCIENCES Effective date: 20030718 |
|
| C41 | Transfer of patent application or patent right or utility model | ||
| TR01 | Transfer of patent right |
Effective date of registration: 20030718 Address after: 100101 Beijing city Chaoyang District Datun Road No. 3 Patentee after: Technical Institute of Physics and Chemistry Chinese Academy of Sciences Address before: 100080,, 2 North 1 Street, Beijing, Haidian District, Guan Jiayu Patentee before: Institute of Chemistry, Chinese Academy of Sciences |
|
| C19 | Lapse of patent right due to non-payment of the annual fee | ||
| CF01 | Termination of patent right due to non-payment of annual fee |