TH7915B - A new end-to-end process for polyethylene with hydroxyl functional group - Google Patents
A new end-to-end process for polyethylene with hydroxyl functional groupInfo
- Publication number
- TH7915B TH7915B TH9301000483A TH9301000483A TH7915B TH 7915 B TH7915 B TH 7915B TH 9301000483 A TH9301000483 A TH 9301000483A TH 9301000483 A TH9301000483 A TH 9301000483A TH 7915 B TH7915 B TH 7915B
- Authority
- TH
- Thailand
- Prior art keywords
- polyether
- hydroxyl functional
- group
- sulfonic
- functional groups
- Prior art date
Links
- 125000002887 hydroxy group Chemical group [H]O* 0.000 title claims abstract 11
- 238000000034 method Methods 0.000 title claims abstract 9
- -1 polyethylene Polymers 0.000 title claims 4
- 239000004698 Polyethylene Substances 0.000 title claims 3
- 229920000573 polyethylene Polymers 0.000 title claims 3
- 229920000570 polyether Polymers 0.000 claims abstract 11
- 239000004721 Polyphenylene oxide Substances 0.000 claims abstract 8
- 239000002253 acid Substances 0.000 claims abstract 8
- 150000007513 acids Chemical class 0.000 claims abstract 4
- 238000006243 chemical reaction Methods 0.000 claims abstract 3
- 150000003839 salts Chemical class 0.000 claims abstract 3
- 239000003054 catalyst Substances 0.000 claims abstract 2
- 150000002500 ions Chemical class 0.000 claims abstract 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims 3
- 239000000203 mixture Substances 0.000 claims 3
- 239000000725 suspension Substances 0.000 claims 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 2
- COVZYZSDYWQREU-UHFFFAOYSA-N Busulfan Chemical compound CS(=O)(=O)OCCCCOS(C)(=O)=O COVZYZSDYWQREU-UHFFFAOYSA-N 0.000 claims 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims 2
- 229910021645 metal ion Inorganic materials 0.000 claims 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 claims 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims 1
- 229910052788 barium Inorganic materials 0.000 claims 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims 1
- LPTWEDZIPSKWDG-UHFFFAOYSA-N benzenesulfonic acid;dodecane Chemical compound OS(=O)(=O)C1=CC=CC=C1.CCCCCCCCCCCC LPTWEDZIPSKWDG-UHFFFAOYSA-N 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 150000001913 cyanates Chemical class 0.000 claims 1
- 238000000354 decomposition reaction Methods 0.000 claims 1
- 238000004090 dissolution Methods 0.000 claims 1
- KWKXNDCHNDYVRT-UHFFFAOYSA-N dodecylbenzene Chemical compound CCCCCCCCCCCCC1=CC=CC=C1 KWKXNDCHNDYVRT-UHFFFAOYSA-N 0.000 claims 1
- BDAGIHXWWSANSR-UHFFFAOYSA-N formic acid Substances OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims 1
- 235000019253 formic acid Nutrition 0.000 claims 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid group Chemical group C(CCCCC)(=O)O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 claims 1
- AFVFQIVMOAPDHO-UHFFFAOYSA-N methanesulfonic acid Substances CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 229910052700 potassium Inorganic materials 0.000 claims 1
- 239000011591 potassium Substances 0.000 claims 1
- 229910052708 sodium Inorganic materials 0.000 claims 1
- 239000011734 sodium Substances 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 239000013638 trimer Substances 0.000 claims 1
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 abstract 2
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 abstract 1
- 150000002009 diols Chemical class 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 150000002739 metals Chemical class 0.000 abstract 1
- 229920002635 polyurethane Polymers 0.000 abstract 1
- 239000004814 polyurethane Substances 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
Abstract
วิธีเตรียมพอลิอีเธอร์ที่มีหมู่ฟังก์ชั่นไฮดรอกซิอยู่ด้วยซึ่งประกอบด้วยตัวอย่างเช่นทำ (a) พอลิอีเธอร์ที่มีหมู่ฟังก์ชั่นไฮดรอกซิอยู่ด้วยซึ่งมีไอออนของโลหะหมู่ IA หรือหมู่ IIA อยู่ด้วยน้อยกว่าหรือเท่ากับ 200 ppm และ (b) กรดชนิดหนึ่งให้สัมผัสกัน การทำให้สัมผัสนี้ควรปฏิบัติให้สำเร็จภายใต้สภาวะทำปฏิกริยาในลักษณะที่ทำให้เกิดเกลือขึ้นมาซึ่งไม่เหมาะสมต่อการสนับสนุนปฏิกิริยาการเกิดไทรเมอร์อย่างมีนัยสำคัญถ้าให้พอลิอีเธอร์ที่มีหมู่ไฮดรอกซิอยู่ด้วยนี้ทำปฏิกิริยากับสารประกอบไอโซไซแอเนตปริมาณของกรดนี้เพียงพอเพื่อทำตัวเร่งปฏิกิริยาชนิดเบสให้เป็นกลางโดยส่วนใหญ่โดยปราศจากความต้องการขั้นตอนเพิ่มเติมเพื่อเอาของcข็งออกไปก่อนนำพอลิอีเธอร์ที่มีหมู่ฟังก์ชั่นไฮดรอกซิอยู่ด้วยไปใช้งานด้านต่าง ๆ เช่นการผลิตพอลิยูรีเธอและผลิตภัณฑ์ที่เกี่ยวข้องกันซึ่งอาจจะไม่ปรารถนาการเกิดการไทรเมอร์ที่สูงขึ้น อาจจะเติมกรดเพิ่มเติมได้ด้วยเหมือนกันเพื่อนเปลี่ยนหน่วยโทรพินิลอีเธอร์ที่มีอยู่ในโครงร่างของพอลิอีเธอร์ให้เป็นโพรพิโอแนลดิไฮด์และไดออลที่สมกันนี้ Methods for preparing polyethers with hydroxyl functional groups, for example, make (a) polyethers with hydroxyl functional groups in which ions of Group IA or Group IIA metals present less than or equal to 200 ppm and (b) some acids come into contact. This exposure should be accomplished under reaction conditions in such a way as to produce salts which are unsuitable to support a significant trimmer reaction if a polyether containing polyether is given. The amount of this acid is sufficient to neutralize most of the base catalysts without the need for additional steps to remove the solids first. Polyethers containing hydroxyl functional groups are used in areas such as the production of polyurethanes and related products where trimmerization may not be desired. higher Additional acids may also be added to convert the tropinylether units present in the polyether structure to propionaldehyde and diols.
Claims (8)
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TH13815A TH13815A (en) | 1994-04-15 |
| TH7915B true TH7915B (en) | 1998-04-02 |
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