SU96335A1 - The method of obtaining dry resole resins from technical xylenols - Google Patents
The method of obtaining dry resole resins from technical xylenolsInfo
- Publication number
- SU96335A1 SU96335A1 SU446179A SU446179A SU96335A1 SU 96335 A1 SU96335 A1 SU 96335A1 SU 446179 A SU446179 A SU 446179A SU 446179 A SU446179 A SU 446179A SU 96335 A1 SU96335 A1 SU 96335A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- technical
- xylenols
- resole resins
- obtaining dry
- resin
- Prior art date
Links
- 229920005989 resin Polymers 0.000 title description 10
- 239000011347 resin Substances 0.000 title description 10
- 238000000034 method Methods 0.000 title description 5
- 150000003739 xylenols Chemical class 0.000 title description 5
- 229920003987 resole Polymers 0.000 title description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- 238000009833 condensation Methods 0.000 description 4
- 230000005494 condensation Effects 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000002253 acid Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 2
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000004312 hexamethylene tetramine Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
Landscapes
- Phenolic Resins Or Amino Resins (AREA)
Description
Примен е1 1ые обычно методы кондснсаци технических кснленолов привод т к образованню низкокачественных смол с мало в зкостью и низкой температурой каплепадени . Лишь добавка к техническому ксиленолу значительных количеств кристаллического фенола (60 вес. ч. на 40 вес. ч. к.силенола) позвол ет получать приемлемые ио своим качествам смолы.Applying the first commonly used methods of condensing technical xllenols leads to the formation of low-quality resins with low viscosity and low dropping point. Only the addition of significant quantities of crystalline phenol to the technical xylenol (60 parts by weight to 40 parts by weight of xylenol) gives acceptable resin properties.
Изменение рецептуры и конденсации по предлагаемому способу позвол ет получать прессматериал хорошего качества при одновременном значительном сокр;;цении расхода кристаллического фенола.Changing the formulation and condensation of the proposed method allows to obtain a press material of good quality with simultaneous significant reduction; consumption of crystalline phenol.
Сиособ состоит в применении щелочного катализатора с последуюнтей его нейтрализацией. Конденсаци с н;елочиым катализатором протекает при температуре 65-80 до достижени в зкости в 400- 700 сантипуазов, после чего щелочной катализатор не |трализуют фосфорной кислотой, ввод т жирные кислоты и смолу иеревод т па с шку . В конце сушки в котел вводитс 50 о-ньп водиый раствор уротроHiiHa в количестве 2,5 вес. ч.The method consists in the use of an alkaline catalyst followed by neutralization. Condensation with an alkaline catalyst occurs at a temperature of 65-80 to reach a viscosity of 400-700 centipoise, after which the alkaline catalyst is not neutralized with phosphoric acid, fatty acids and resin are introduced and dried. At the end of the drying, 50 o-hpp water solution of urotroHiiHa is introduced into the boiler in the amount of 2.5 weight. h
Пример. В котел емкостью ,5лг загружают 70 вес. ч. ксиленола , 30 вес. ч. фенола. 40 вес. ч. формальдегида , 0.9 вес. ч. окнсн магни и 0.3 вес. ч. 100%-цого едкого натрн . Смесь неремегливают 0 мин., после чего в рубашку даетс пар под давлением 0,2-0.5oT.i; и реакцнонна смеоь нагреваетс до . Затем, пар выключаетс , и дальнейшее нагревание реакционно) смеси происходит, благодар экзотермической реакции. При 60 к холодильник аппарата даетс полное охлаждение и выключаетс мешалка. При 85 начинаетс кипение. Через 5-7 мин. смесь охлаждаетс до 80. Дальне1 пца конденсаци ведетс при 75-80° до тех пор, пока в зкость смолы по Оствальду достигнет 200 сантипуазон. Температура снижаетс до 65 , и смесьExample. In the boiler, 5 lg load 70 weight. including xylenol, 30 wt. including phenol. 40 wt. including formaldehyde, 0.9 weight. including magnesium and 0.3 wt. including 100% caustic natrn. The mixture is not quenched for 0 minutes, after which steam is supplied to the jacket under a pressure of 0.2-0.5 ° T.i; and the reaction mixture is heated to. The steam is then turned off, and further heating of the reaction mixture occurs due to the exothermic reaction. At 60 k, a refrigerator of the apparatus is given complete cooling and the stirrer is turned off. At 85, boiling begins. In 5-7 minutes the mixture is cooled to 80. Farther condensation is carried out at 75-80 ° until the viscosity of the resin at Ostwald reaches 200 centipoise. The temperature drops to 65, and the mixture
№ 96335- 2 -No. 96335-2 -
, выдерживаетс при температуре 65-75 до в зкости 400-700 сантипуазов . Затем щелочной катализатор пейтрализуетс 25%-ным раствором фосфорной киедоты (,7вес. ч. на 100%-пую кислоту). После 5-is maintained at a temperature of 65-75 to a viscosity of 400-700 centipoise. Then the alkaline catalyst is neutralized with 25% phosphoric acid solution (, 7 weight parts per 100% acid). After 5
7мип. перемешивани ввод т жирные кислоты в количестве Звес. ч.7mip. mixing, the fatty acids in the amount of Zves are introduced. h
8течение 5 мин. производитс перемешивание с кислотами, и смола переводитс на сушку под вакуумом 500 мм. После отгона основной массы воды в котел ввод т 50%-ный водный раствор уротропина. Смола сушитс обычным способом и сливаетс в холодильные вагоны.8 course 5 min. mixing with acids is carried out, and the resin is transferred to drying under a vacuum of 500 mm. After the main mass of water is distilled off, a 50% aqueous solution of urotropin is introduced into the boiler. The resin is dried in the usual way and drained into refrigerated cars.
Предмет изобретени Subject invention
Способ получени сухих резольных смол из техничегких ксиленолов с добавкой 30% кристаллического фенола и в процессе сушки 2,5% уротропина, отличающийс тем, что конденсацию ведут при 65-80 с щелочным катализатором до в зкости смолы 400-700 сантипуазов, после чего нейтрализуют щелочь фосфорной кислотой и сушат смолу обычным способом.The method of obtaining dry resole resins from technical xylenols with the addition of 30% crystalline phenol and 2.5% hexamine during the drying process, characterized in that the condensation is carried out at 65-80 with an alkaline catalyst to a resin viscosity of 400-700 centipoise, after which the alkali is neutralized phosphoric acid and dried resin in the usual way.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU446179A SU96335A1 (en) | 1951-12-31 | 1951-12-31 | The method of obtaining dry resole resins from technical xylenols |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU446179A SU96335A1 (en) | 1951-12-31 | 1951-12-31 | The method of obtaining dry resole resins from technical xylenols |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU96335A1 true SU96335A1 (en) | 1952-11-30 |
Family
ID=48371216
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU446179A SU96335A1 (en) | 1951-12-31 | 1951-12-31 | The method of obtaining dry resole resins from technical xylenols |
Country Status (1)
| Country | Link |
|---|---|
| SU (1) | SU96335A1 (en) |
-
1951
- 1951-12-31 SU SU446179A patent/SU96335A1/en active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| SU96335A1 (en) | The method of obtaining dry resole resins from technical xylenols | |
| US1503984A (en) | Manufacture of 2.3-hydroxynaphthoic acid | |
| US2715114A (en) | Phenolic resins | |
| US1737121A (en) | Phenol-furfural resin and method of making same | |
| US1978821A (en) | Process of hardening condensation products from phenols and aldehydes | |
| US2837589A (en) | Active material for storage batteries | |
| SU65474A1 (en) | The method of obtaining phenol-aldehyde plastics | |
| US2289266A (en) | Method of making casting resins | |
| US2315432A (en) | Casting of phenolic resins | |
| SU37337A1 (en) | The method of obtaining complex resols with different catalysts | |
| SU973A1 (en) | The method of obtaining the condensation products of phenols with formaldehyde or its polymers | |
| SU86976A1 (en) | The method of obtaining phenol-alkyd and phenol-containing resins | |
| US2180981A (en) | Process of making phenol-aldehyde resins | |
| GB159494A (en) | A process for the manufacture of resinous phenol formaldehyde condensation products | |
| GB305468A (en) | Process for the preparation of artificial silk | |
| SU62771A1 (en) | The method of producing glue | |
| SU3096A1 (en) | The method of impregnation of wood | |
| US1500303A (en) | Process of making resinous material from paraldehyde | |
| US2379585A (en) | Sulphonation of benzene | |
| SU62995A1 (en) | The method of obtaining synthetic tanning agents | |
| DE672370C (en) | Process for the preparation of condensation products containing sulfuric acid residues | |
| US2047612A (en) | Preparation of sulphuric derivatives of higher aliphatic alcohols | |
| DE963905C (en) | Process for the production of synthetic resins, such as ion exchangers, in small pieces | |
| SU48305A1 (en) | The method of obtaining resinous condensation products | |
| SU9352A1 (en) | The method of obtaining aromatic hydrocarbons and their sulfonic acids with alkylated core |