印染助剂
印染助劑
인염조제
Textile Auxiliaries
2015年
9期
28-30
,共3页
吴彦彬%宋国全%吴正岭%闫广学%李永霞%杨素阁
吳彥彬%宋國全%吳正嶺%閆廣學%李永霞%楊素閣
오언빈%송국전%오정령%염엄학%리영하%양소각
1-辛基-2-吡咯烷酮%γ-丁内酯%辛胺%合成
1-辛基-2-吡咯烷酮%γ-丁內酯%辛胺%閤成
1-신기-2-필각완동%γ-정내지%신알%합성
1-octyl-2-pyrrolidone%γ-butyrolactone%octylamine%synthesis
以辛胺(C8H19N)、γ-丁内酯(C4H6O4)为原料,采用ZSM-5分子筛-铈复合催化剂,合成1-辛基-2-吡咯烷酮.在n(C8H19N):n(C4H6O4)=1.26:1.0,反应温度255~260℃,反应时间3.0~3.5 h,反应压力4.5~5.0 MPa,复合催化剂用量0.25%(对原料总质量)条件下,γ-丁内酯转化率大于98%,目标产物1-辛基-2-吡咯烷酮选择性大于97%.该方法解决了以磷酸作为催化剂的合成工艺对设备有腐蚀,后续分离提纯困难的缺点,具有工艺简单、操作方便、转化率及选择性高、成本低的特点.
以辛胺(C8H19N)、γ-丁內酯(C4H6O4)為原料,採用ZSM-5分子篩-鈰複閤催化劑,閤成1-辛基-2-吡咯烷酮.在n(C8H19N):n(C4H6O4)=1.26:1.0,反應溫度255~260℃,反應時間3.0~3.5 h,反應壓力4.5~5.0 MPa,複閤催化劑用量0.25%(對原料總質量)條件下,γ-丁內酯轉化率大于98%,目標產物1-辛基-2-吡咯烷酮選擇性大于97%.該方法解決瞭以燐痠作為催化劑的閤成工藝對設備有腐蝕,後續分離提純睏難的缺點,具有工藝簡單、操作方便、轉化率及選擇性高、成本低的特點.
이신알(C8H19N)、γ-정내지(C4H6O4)위원료,채용ZSM-5분자사-시복합최화제,합성1-신기-2-필각완동.재n(C8H19N):n(C4H6O4)=1.26:1.0,반응온도255~260℃,반응시간3.0~3.5 h,반응압력4.5~5.0 MPa,복합최화제용량0.25%(대원료총질량)조건하,γ-정내지전화솔대우98%,목표산물1-신기-2-필각완동선택성대우97%.해방법해결료이린산작위최화제적합성공예대설비유부식,후속분리제순곤난적결점,구유공예간단、조작방편、전화솔급선택성고、성본저적특점.
1-Octyl-2-pyrrolidone was prepared with γ-butyrolactone and octylamine as raw materials us?ing ZSM-5 zeolite-cerium composite as catalyst. The conversion of γ-butyrolactone was above 98%, and the selectivity of 1-octyl-2-pyrrolidone was above 97% under the fol owing process conditions: the molar ratio of octylamine and γ-butyrolactone was 1.26:1.0, reaction temperature was 255~260 ℃, reaction time was 3.0~3.5 h, reaction pressure was 4.5~5.0 MPa, and the catalyst dosage was 0.25% (on the mass of raw materi?als). The method solved the shortcomings of equipment corrosion and subsequent difficulties such as separa?tion and purification in synthesis process with phosphoric acid as catalyst. And this method had simple pro?cess, convenient operation, high conversion and selectivity, and low cost.