欢迎登录材料期刊网

材料期刊网

高级检索

在3L的高压磁力搅拌釜中通过催化胺化三官能团聚醚多元醇,研究了活化后雷尼镍催化剂的组成对反应的影响。实验结果表明,端氨基聚醚合成反应催化剂的铝含量约为20%(质量分数)时活性较高,产品的总胺值可以达到340mg KOH/g,这与传统雷尼镍催化剂的铝含量(〈10%(质量分数))不同。应用X射线衍射(XRD)对催化剂进行了表征,其化学组成则用等离子体发射光谱仪(ICP-AES)进行分析。反应原料、中间产物、胺化产物用傅立叶变换红外光谱(FT-IR)进行分析,反应原料、产物和尾气用气相色谱(GC)进行分析,并推测了反应路线。

The effect of the activated Raney nickel catalyst composition on the catalytic amination was studied by preparation of trifunctional amine terminated polyether in a magnetically stirred stainless steel autoclave.The experiments indicated that the catalyst with 20% aluminium was more effective for the catalytic amination of polyether polyols,and the total amine of the product was up to 340mg KOH/g.X-ray diffraction(XRD) was employed to characterize the catalyst properties and the chemical composition was analyzed by inductively coupled plasma-atomic emission spectrometry(ICP-AES).The reaction route was deduced on the basis of the products and the off-gas analysis by gas chromatography(GC) and fourier transform infrared spectroscopy(FT-IR).

参考文献

[1] 张翔宇,刘明辉,李荣光,范晓东,俞国星,田威,孙乐.喷涂聚脲弹性体用端氨基聚醚的合成与表征[J].高分子材料科学与工程,2007(04):67-70.
[2] Richard J G;Doris M;Rodney F .Reaction injection molden elastomer containining an internal mold release made by a two-stream system[P].US:4396729,1983.
[3] Aradi A;Colueci W J;Copley K et al.Use of detergentadditives in high-ethanol fuels for deposit control[P].US:20050034360,2005.
[4] 华峰君,胡春圃.聚氧化丙烯多胺的合成、表征及对环氧树脂的增韧效应[J].高分子材料科学与工程,1999(02):21-23.
[5] 谭家顶,程珏,郭晶,张军营.几种胺类固化剂对环氧树脂固化行为及固化物性能的影响[J].化工学报,2011(06):1723-1729.
[6] Roundhill D M .Transition metal and enzyme catalyzed reactions involving reactions with ammonia and amines[J].Chemical Reviews,1992,92:1-27.
[7] A. Fischer;M. Maciejewski;T. Burgi;T. Mallat;A. Baiker .Cobalt-Catalyzed Amination of 1, 3-Propanediol: Effects of Catalyst Promotion and Use of Supercritical Ammonia as Solvent and Reactant[J].Journal of Catalysis,1999(2):373-383.
[8] Baiker A;Kijenski J .Catalytic synthesis of higher ali-phatic amines from the corresponding alcohols[J].Ca-talysis Reviews:Science and Engineering,1985,27:653-697.
[9] 郁维铭.端氨基聚醚的合成方法及其应用[J].聚氨酯工业,2002(01):1-5.
[10] 白国义,陈立功.双官能团醇类化合物催化胺化反应的研究进展[J].化学进展,2005(02):293-298.
[11] 李秋小,张高勇.脂肪醇催化胺化制叔胺工艺技术现状及前景[J].日用化学工业,2001(04):21-25.
[12] Sewell GS.;Vansteen E.;Oconnor CT. .EFFECT OF ACTIVATION PROCEDURE AND SUPPORT ON THE REDUCTIVE AMINATION OF ETHANOL USING SUPPORTED COBALT CATALYSTS[J].Journal of Catalysis,1997(2):513-521.
[13] Ruming Feng;Deju Wang;Zhongneng Liu .Shape-selective amination of EO over HZSM-5 for MEA and DEA[J].Catalysis Communications,2010(15):1220-1223.
[14] Jobson E;Balker A;Wokaun A .Copper-catalyzed de-hydroamination of 1-hexanol with dimethylamine:an in situ FT-IR study[J].Jouranal of Molecular Catalysis,1990,60:399-416.
[15] Sirokm6n G;MolncirA;Bartok M .Studies on the con-versions of diols and cyclic ethers.Part LI.Effect of di-ethylamine on the copper-catalysed transformation of 1,3-butanediol[J].Jouranal of Molecular Catalysis,1983,19:35-40.
[16] Kijenski J;Niedzielski P J;Balker A .Synthesis of cyclic amines and their alkyl derivatives from amino alcohols over supported copper catalysts[J].Applied Catalysis,1989,53:107-112.
[17] Fischer A;Mallat T;Baiker A .Amination of diols and polyols to acyclic amines[J].Catalysis Today,1997,37:167-189.
[18] Hu H;Xie F;Pei Y et al.Skeletal Ni catalysts pre-pared from Ni-AI alloys rapidly quenched at different rates:texture,structure and catalytic performance in chemoselective hydrogenation of 2-ethylanthraquinone[J].Journal of Catalysis,2006,237:143-151.
[19] Hu H;Qiao M;Wang S et al.Structural and catalytic properties of skeletal Ni catalyst prepared from the rap-idly quenched Nis0 Als0 alloy[J].Journal of Catalysis,2004,221:612-618.
[20] Raney M .Method of preparing catalytic material[P].US:1563787,1925.
[21] Hoffer B W;Crezee E F;Devred P R M et al.The role of the active phase of Raney-type Ni catalysts in the se- lective hydrogenation of d-glucose to d-sorhitol[J].Ap- plied Catalysis A General,2003,253:437-452.
[22] Xufeng Ye;Yue An;Guohua Xu .Kinetics of 9-ethylcarbazole hydrogenation over Raney-Ni catalyst for hydrogen storage[J].Journal of Alloys and Compounds: An Interdisciplinary Journal of Materials Science and Solid-state Chemistry and Physics,2011(1):152-156.
[23] Alvise Perosa;Pietro Tundo .Selective Hydrogenolysis of Glycerol with Raney Nickel[J].Industrial & Engineering Chemistry Research,2005(23):8535-8537.
[24] Bram W.Hoffer;Jacob A.Moulijn .Hydrogenation of dinitriles on Raney-type Ni catalysts:kinetic and mechanistic aspects[J].Applied Catalysis, A. General: An International Journal Devoted to Catalytic Science and Its Applications,2009(1/2):193-201.
[25] Devred F;Hoffer B W;Sloof W G et al.Hydrogena-tion of dinitriles on Raney-type Ni catalysts:kinetic and mechanistic aspects[J].Applied Catalysis A:General,2003,244:291-300.
[26] Lee J M;Winfrey J C;Jackson L .Polyoxyalkylene-polyamines[P].US:3236895,1966.
[27] Larkin J M;Renken T L .Process for the preparation of polyoxyalkylene polyamines[P].US:4766245,1988.
[28] Bakker M L;Young D J;Wainwright M S .Selective le-acing of nickel-aluminium(NiAla and Ni2 Ala)interme-tallies to form Raney niekels[J].Journal of Material Sci-ence,1988,23:3921-3926.
[29] Warg R;Chen H;Lu Z et al.Structural transitions during aluminum leaching of NiAIa Phase in a Raney Ni-A1 alloy[J].Journal of Materials Science,2008,43:5712-5719.
[30] Cristiane B. Rodella;Guinther Kellermann;Maria Suzana P. Francisco .Textural and Structural Analyses of Industrial Raney Nickel Catalyst[J].Industrial & Engineering Chemistry Research,2008(22):8612-8618.
[31] 肖慧明,王建明,陈惠,潘滔,张鉴清.Al取代α-Ni(OH)2 的有机溶剂法合成及其电化学性能[J].功能材料,2003(05):553-555.
[32] Devred F;Gieske A H;Adkins N et al.Influence of phase composition and particle size of atomised Ni-A1 al-loy samples on the catalytic performance of Raney type nickel catalysts[J].Applied Catalysis A:General,2009,356:154-161.
[33] 杨志禄,王进,孙鸿,陈俊英,黄楠.等离子体聚合沉积聚烯丙胺薄膜改性聚酯及体外血小板粘附研究[J].功能材料,2008(09):1559-1561,1566.
上一张 下一张
上一张 下一张
计量
  • 下载量()
  • 访问量()
文章评分
  • 您的评分:
  • 1
    0%
  • 2
    0%
  • 3
    0%
  • 4
    0%
  • 5
    0%