CN1058970C - 二(1,3-二卤-2-丙基)-2,2-二甲基-3-卤丙基磷酸酯 - Google Patents
二(1,3-二卤-2-丙基)-2,2-二甲基-3-卤丙基磷酸酯 Download PDFInfo
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- CN1058970C CN1058970C CN98101591A CN98101591A CN1058970C CN 1058970 C CN1058970 C CN 1058970C CN 98101591 A CN98101591 A CN 98101591A CN 98101591 A CN98101591 A CN 98101591A CN 1058970 C CN1058970 C CN 1058970C
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- halopropyl
- dihalo
- dimethyl
- phosphate
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- 229910019142 PO4 Inorganic materials 0.000 title claims abstract description 15
- 239000010452 phosphate Substances 0.000 title claims abstract description 15
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 title claims description 10
- 239000003063 flame retardant Substances 0.000 claims abstract description 27
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 10
- 238000006243 chemical reaction Methods 0.000 claims abstract description 9
- 150000002367 halogens Chemical class 0.000 claims abstract description 8
- LRWZZZWJMFNZIK-UHFFFAOYSA-N 2-chloro-3-methyloxirane Chemical compound CC1OC1Cl LRWZZZWJMFNZIK-UHFFFAOYSA-N 0.000 claims abstract description 4
- 239000002841 Lewis acid Substances 0.000 claims abstract description 4
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims abstract description 4
- 150000007517 lewis acids Chemical class 0.000 claims abstract description 4
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract description 4
- 239000011574 phosphorus Substances 0.000 claims abstract description 4
- 238000010189 synthetic method Methods 0.000 claims abstract description 3
- 125000005843 halogen group Chemical group 0.000 claims abstract 2
- 229920005830 Polyurethane Foam Polymers 0.000 claims description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 5
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical group ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 3
- 239000003513 alkali Substances 0.000 claims description 3
- 238000004140 cleaning Methods 0.000 claims description 3
- 238000004821 distillation Methods 0.000 claims description 3
- 238000001035 drying Methods 0.000 claims description 3
- 238000010792 warming Methods 0.000 claims description 3
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical group N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 abstract description 10
- -1 phosphate ester Chemical class 0.000 abstract description 7
- 239000006260 foam Substances 0.000 abstract description 6
- 229920002635 polyurethane Polymers 0.000 abstract description 3
- 239000004814 polyurethane Substances 0.000 abstract description 3
- 239000003054 catalyst Substances 0.000 abstract description 2
- 238000002485 combustion reaction Methods 0.000 abstract description 2
- 238000013459 approach Methods 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 238000004939 coking Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 150000003014 phosphoric acid esters Chemical class 0.000 description 2
- 239000011496 polyurethane foam Substances 0.000 description 2
- 230000000979 retarding effect Effects 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- ANHAEBWRQNIPEV-UHFFFAOYSA-N 2-chloroethyl dihydrogen phosphate Chemical compound OP(O)(=O)OCCCl ANHAEBWRQNIPEV-UHFFFAOYSA-N 0.000 description 1
- 241000607142 Salmonella Species 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000000711 cancerogenic effect Effects 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000012757 flame retardant agent Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 230000002688 persistence Effects 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000012974 tin catalyst Substances 0.000 description 1
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- Fireproofing Substances (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
本发明涉及一种新型卤代烷基磷酸酯,具体地说是一种二(1,3-二卤-2-丙基)-2,2-二甲基-3-卤丙基磷酸酯,其结构式如下:X代表卤素。其合成方法:采用新戊二醇与三卤化磷反应,再加入卤素继续反应,然后加入催化剂Lewis酸,升温40~80℃时,开始加入稍过量的环氧氯丙烷。该成品是一种阻燃剂,特别适合于聚氨酯软泡的阻燃,与不含阻燃剂的相比,LOI值增加7~8个百分点,燃烧速率降低到0.52mm/s,机械性能与未阻燃产品基本接近。
Description
本发明涉及一种新型卤代烷基磷酸酯,具体地说是一种二(1,3-二卤-2-丙基)-2,2-二甲基-3-卤丙基磷酸酯。
目前常用于阻燃软质聚氨酯泡沫塑料的卤代磷酸酯类阻燃剂有:三(2-氯乙基)磷酸酯、三(1,3-二氯-2-丙基)磷酸酯及三(1-氯-2丙基)磷酸酯等,所含的卤族阻燃元素中只有氯,其理论氯的含量分别为37.25%、49.38%及33.0%,它们的阻燃效率仍不够理想,有时引起软泡“焦化”,对软泡机械性能的不利影响也仍需降低。
本发明的目的在于提供一种新型卤代烷基磷酸酯,同时含有两种阻燃卤素,卤素总含量达50%以上,阻燃效率有所提高,不引起软泡“焦化”,对软泡机械性能影响小,且通过了Ames试验。
本发明的目的是通过以下方案实现的。
X代表卤素。其合成方法:在反应器中,加入定量的三卤化磷,冷却到-10~10℃,加入新戊二醇溶于二氯甲烷形成的溶液,加料毕,升温至20~60℃,反应1-4h,再加入等摩尔量的卤素,同时控制反应温度在-10~10℃,再反应3~8h,然后加入催化剂Lewis酸,再升温40~80℃时,开始加入稍过量的环氧氯丙烷,反应完毕后,原液经碱洗、水洗至中性,减压蒸馏、干燥即得成品。该产品是一种阻燃剂,特别适用于聚氨酯软泡的阻燃剂。
本发明提供的二(1,3-二卤-2-丙基)-2,2-二甲基-3-卤丙基磷酸酯阻燃剂,同时含有(溴及氯)两种阻燃卤素,两者总含量达50%以上,没有致癌效应。在实际使用时,添加量为多元醇的12~15%时,与不含阻燃剂的聚氨酯软泡相比,不引起软泡“焦化”,LOI值增加7~8个百分点,燃烧速率由1.62mm/s,降低到0.52mm/s,机械性能与未加阻燃剂的产品基本接近。阻燃剂性能指际如下:酸度:0.20mg KOH/g,密度:1.460g/cm(25℃).折射率:1.4812(n25D),水含量:<0.2%。
本发明具有如下附图。
图1为二(1,3-二卤-2-丙基)-2,2-二甲基-3-卤丙基磷酸酯的IR图谱。
下面结合实施例对本发明详细说明。
实施例。
在一个三口烧瓶中,加入定量的三氯化磷,冷却至-10~10℃,逐滴加入新戊二醇溶于二氯甲烷形成的溶液,加料毕,撤去冰浴,升温到20~60°C,反应1-4h,再逐滴加入等摩尔量的溴素,在液溴滴加过程中,可以通过冰浴控制反应温度在-10~10℃,再反应3-8h,然后加入催化剂量的Lewis酸,搅拌均匀。当升温至40~80℃时,开始滴加稍过量的环氧氯丙烷。反应完毕后,将反应原液经碱洗、水洗至中性,减压蒸馏、干燥即得成品。其产品为A、B、C三者的混合物,其摩尔比为:1.0∶1.5∶1.0。
该产品的总收率约为89%,其IR图谱如图1所示:
元素分析结果如下:
C:26.21%(25.71%)
H:4.11%(3.90%)
Br:32.03%(31.16%)
Cl:21.54%(20.74%)(括号内数值为理论值)。
性能指标如下:
酸度:0.20mg KOH/g
密度:1.460g/cm2(25℃)
折射率:1.4812(n25D)
水含量:<0.2%。
由于该产品含磷量较高,分子量较大,具有挥发性低,热稳定性高,对水和碱溶液稳定,能和大多数有机聚合物互溶等特点,因此,是一种良好阻燃剂。采用此阻燃剂时,中密度聚醚型软质泡沫塑料一步法发泡工艺的基本配方如下:
(软泡的基本配方采用重量比,密度:29~35Kg/cm3
| 物料 | 聚醚 | TDI | 水 | 硅油 | 胺催化剂 | 锡催化剂 | 阻燃剂 |
| 含量 | 100 | 43.6 | 3.3 | 2.0 | 0.25 | 0.25 | 变量 |
从上述实验中发现,在聚氨酯软泡中使用时,加工性较好,对泡沫体的物理机械性能影响较小,不易焦烧,持久性好。在使用时的阻燃性能,氧指数LOI的测定结果见下表:
| 添加量% | 0 | 8 | 10 | 12 | 15 | 20 |
| LOI | 17.5 | 21.0 | 23.0 | 23.50 | 25.5 | 25.0 |
从上表看出,由于其自身的特点,特别适合于聚氨酯软泡的阻燃。在软泡中加入多元醇的12%的这种阻燃剂,就可以使氧指数大于23,泡沫体具有明显的自熄性。当聚氨酯发泡配方中该阻燃剂含量为15%时,氧指数达到最佳值。与不含阻燃剂的聚氨酯软泡相比,LOI值增加了7~8个百分点。因此,在聚氨酯软泡中,添加多元醇的12~15%的这种阻燃剂为最佳。
结果表明,阻燃聚氨酯软泡的阻燃性能和物理机械性能均为良好。
Claims (5)
2.一种二(1,3-二卤-2-丙基)-2,2-二甲基-3-卤丙基磷酸酯的合成方法,其特征在于反应器中,加入定量的三卤化磷,冷却到-10~10℃,加入新戊二醇溶于二氯甲烷形成的溶液,加料毕,升温至20~60℃,反应1-4h,再加入等摩尔量的卤素,同时控制反应温度在-10~10℃,再反应3~8h,然后加入催化剂Lewis酸,再升温40~80℃时,开始加入稍过量的环氧氯丙烷,反应完毕后,原液经碱洗、水洗至中性,减压蒸馏、干燥即得成品。
3.一种二(1,3-二卤-2-丙基)-2,2-二甲基-3-卤丙基磷酸酯的用途,其特征在于是一种阻燃剂。
4.如权利要求3所述的用途,其特征在于特别适用于聚氨酯软泡的阻燃剂。
5.如权利要求3或4所述的用途,其特征在于在聚氨酯软泡中加入为多元醇的12%~15%的二(1,3-二卤-2-丙基)-2,2-二甲基-3-卤丙基磷酸酯。
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN98101591A CN1058970C (zh) | 1998-04-27 | 1998-04-27 | 二(1,3-二卤-2-丙基)-2,2-二甲基-3-卤丙基磷酸酯 |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN98101591A CN1058970C (zh) | 1998-04-27 | 1998-04-27 | 二(1,3-二卤-2-丙基)-2,2-二甲基-3-卤丙基磷酸酯 |
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| Publication Number | Publication Date |
|---|---|
| CN1203236A CN1203236A (zh) | 1998-12-30 |
| CN1058970C true CN1058970C (zh) | 2000-11-29 |
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| CN98101591A Expired - Fee Related CN1058970C (zh) | 1998-04-27 | 1998-04-27 | 二(1,3-二卤-2-丙基)-2,2-二甲基-3-卤丙基磷酸酯 |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CN111518133A (zh) * | 2020-04-24 | 2020-08-11 | 南京聚发新材料有限公司 | 反应型阻燃剂、包含该阻燃剂双组份聚氨酯树脂和制备该阻燃剂的方法 |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3509076A (en) * | 1968-09-23 | 1970-04-28 | Mobil Oil Corp | Polymers and process for making same |
| US3840488A (en) * | 1972-08-28 | 1974-10-08 | Union Oil Co | Latex with improved flame resistance and stability |
| US3943196A (en) * | 1974-06-19 | 1976-03-09 | The United States Of America As Represented By The Secretary Of The Navy | Alkoxy derivatives of the adduct from phosphorus oxychloride and hexamethylphosphoramide |
| US4086303A (en) * | 1977-04-04 | 1978-04-25 | Stauffer Chemical Company | Copolycondensation products of β-haloalkyl phosphates and dialkyl phosphonates |
| US4152371A (en) * | 1973-11-12 | 1979-05-01 | Stauffer Chemical Company | Copolycondensation products of β-haloalkyl phosphates and dialkyl phosphonates |
| US4225522A (en) * | 1979-01-02 | 1980-09-30 | Stauffer Chemical Company | Copolycondensation products of β-haloalkyl phosphates and dialkyl phosphonates |
-
1998
- 1998-04-27 CN CN98101591A patent/CN1058970C/zh not_active Expired - Fee Related
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3509076A (en) * | 1968-09-23 | 1970-04-28 | Mobil Oil Corp | Polymers and process for making same |
| US3840488A (en) * | 1972-08-28 | 1974-10-08 | Union Oil Co | Latex with improved flame resistance and stability |
| US4152371A (en) * | 1973-11-12 | 1979-05-01 | Stauffer Chemical Company | Copolycondensation products of β-haloalkyl phosphates and dialkyl phosphonates |
| US3943196A (en) * | 1974-06-19 | 1976-03-09 | The United States Of America As Represented By The Secretary Of The Navy | Alkoxy derivatives of the adduct from phosphorus oxychloride and hexamethylphosphoramide |
| US4086303A (en) * | 1977-04-04 | 1978-04-25 | Stauffer Chemical Company | Copolycondensation products of β-haloalkyl phosphates and dialkyl phosphonates |
| US4225522A (en) * | 1979-01-02 | 1980-09-30 | Stauffer Chemical Company | Copolycondensation products of β-haloalkyl phosphates and dialkyl phosphonates |
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| Publication number | Publication date |
|---|---|
| CN1203236A (zh) | 1998-12-30 |
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