JP2005133085A5 - - Google Patents
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- Publication number
- JP2005133085A5 JP2005133085A5 JP2004293979A JP2004293979A JP2005133085A5 JP 2005133085 A5 JP2005133085 A5 JP 2005133085A5 JP 2004293979 A JP2004293979 A JP 2004293979A JP 2004293979 A JP2004293979 A JP 2004293979A JP 2005133085 A5 JP2005133085 A5 JP 2005133085A5
- Authority
- JP
- Japan
- Prior art keywords
- resorcin
- formalin resin
- ketone
- organic solvent
- modified
- 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
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 41
- 239000011347 resin Substances 0.000 claims description 35
- 229920005989 resin Polymers 0.000 claims description 35
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims description 35
- KVBYPTUGEKVEIJ-UHFFFAOYSA-N benzene-1,3-diol;formaldehyde Chemical compound O=C.OC1=CC=CC(O)=C1 KVBYPTUGEKVEIJ-UHFFFAOYSA-N 0.000 claims description 33
- 229960001755 resorcinol Drugs 0.000 claims description 31
- 239000003960 organic solvent Substances 0.000 claims description 25
- 238000006243 chemical reaction Methods 0.000 claims description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 239000007788 liquid Substances 0.000 claims description 10
- 238000003756 stirring Methods 0.000 claims description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 6
- 229910017053 inorganic salt Inorganic materials 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 238000009835 boiling Methods 0.000 claims description 5
- 150000007522 mineralic acids Chemical class 0.000 claims description 5
- 150000007524 organic acids Chemical class 0.000 claims description 5
- 239000007795 chemical reaction product Substances 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- 238000004458 analytical method Methods 0.000 claims description 3
- 239000003125 aqueous solvent Substances 0.000 claims description 3
- 230000003197 catalytic effect Effects 0.000 claims description 3
- 238000005227 gel permeation chromatography Methods 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- 230000004048 modification Effects 0.000 claims description 3
- 238000012986 modification Methods 0.000 claims description 3
- 239000000178 monomer Substances 0.000 claims description 3
- 238000005580 one pot reaction Methods 0.000 claims description 3
- 239000007810 chemical reaction solvent Substances 0.000 claims description 2
- 238000000622 liquid--liquid extraction Methods 0.000 claims description 2
- 238000000034 method Methods 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- -1 nitrate ions Chemical class 0.000 claims 5
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
- 238000004821 distillation Methods 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 239000000243 solution Substances 0.000 claims 2
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 claims 1
- 229910002651 NO3 Inorganic materials 0.000 claims 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims 1
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 150000001340 alkali metals Chemical class 0.000 claims 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims 1
- 150000001342 alkaline earth metals Chemical class 0.000 claims 1
- 150000001450 anions Chemical class 0.000 claims 1
- 239000007864 aqueous solution Substances 0.000 claims 1
- 238000010533 azeotropic distillation Methods 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- 239000001110 calcium chloride Substances 0.000 claims 1
- 229910001628 calcium chloride Inorganic materials 0.000 claims 1
- 150000001768 cations Chemical class 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 238000001816 cooling Methods 0.000 claims 1
- 230000018044 dehydration Effects 0.000 claims 1
- 238000006297 dehydration reaction Methods 0.000 claims 1
- 238000010790 dilution Methods 0.000 claims 1
- 239000012895 dilution Substances 0.000 claims 1
- 238000001914 filtration Methods 0.000 claims 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 claims 1
- 229910052740 iodine Inorganic materials 0.000 claims 1
- 239000011630 iodine Substances 0.000 claims 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 238000000926 separation method Methods 0.000 claims 1
- 239000008346 aqueous phase Substances 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000012074 organic phase Substances 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 1
- 108010039491 Ricin Proteins 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
- 229940092714 benzenesulfonic acid Drugs 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2004293979A JP4256828B2 (ja) | 2003-10-07 | 2004-10-06 | ケトン変性レゾルシンホルマリン樹脂 |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2003348496 | 2003-10-07 | ||
| JP2004293979A JP4256828B2 (ja) | 2003-10-07 | 2004-10-06 | ケトン変性レゾルシンホルマリン樹脂 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007262325A Division JP4885104B2 (ja) | 2003-10-07 | 2007-10-05 | ケトン変性レゾルシンホルマリン樹脂の製造方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2005133085A JP2005133085A (ja) | 2005-05-26 |
| JP2005133085A5 true JP2005133085A5 (enrdf_load_stackoverflow) | 2007-12-27 |
| JP4256828B2 JP4256828B2 (ja) | 2009-04-22 |
Family
ID=34655973
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004293979A Expired - Fee Related JP4256828B2 (ja) | 2003-10-07 | 2004-10-06 | ケトン変性レゾルシンホルマリン樹脂 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP4256828B2 (enrdf_load_stackoverflow) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4885828B2 (ja) * | 2003-10-07 | 2012-02-29 | 保土谷化学工業株式会社 | レゾルシンホルマリン樹脂 |
| JP5310329B2 (ja) * | 2004-03-02 | 2013-10-09 | 住友化学株式会社 | レゾルシン／ホルムアルデヒド／脂肪族ケトン樹脂の製造方法 |
| US7834124B2 (en) * | 2005-01-25 | 2010-11-16 | Hodogaya Chemical Co., Ltd. | Ketone-modified resorcinol-formalin resin |
| JP4983187B2 (ja) * | 2006-07-24 | 2012-07-25 | 住友化学株式会社 | レゾルシン／ホルムアルデヒド樹脂の製造方法 |
| JP2008133427A (ja) * | 2006-10-26 | 2008-06-12 | Sumitomo Chemical Co Ltd | レゾルシン／ホルムアルデヒド樹脂の製造方法 |
| JP5387299B2 (ja) * | 2009-09-30 | 2014-01-15 | Ｄｉｃ株式会社 | フェノール樹脂の製造方法 |
| CN115594277B (zh) * | 2022-11-11 | 2024-08-09 | 扬州大学 | 一种胶体间苯二酚-甲醛树脂在处理含溴废水中的应用 |
-
2004
- 2004-10-06 JP JP2004293979A patent/JP4256828B2/ja not_active Expired - Fee Related
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