欢迎登录材料期刊网

材料期刊网

高级检索

在采用阳离子型双子( gemini)表面活性剂作为乳化剂,不使用任何助乳化剂的条件下,通过改进微乳液聚合工艺制备了窄分布粒径可控的阳离子型聚苯乙烯(PS)纳米乳液.改进微乳液聚合的主要特点是:大部分苯乙烯以预乳液的形式恒速滴入引发聚合的微乳液中,使用具有高乳化性能的gemini表面活性剂作为乳化剂能明显降低乳胶粒粒径.实验结果表明,少量阳离子单体三甲基烯丙基氯化铵作为共聚单体能够明显减小Z均粒径、降低粒度分布,乳化剂用量、引发剂用量和反应温度均能影响制备乳胶粒的粒径及其粒度分布.乳化剂和引发剂用量分别为苯乙烯质量的5% ~ 10%和1.0% ~1.5%、反应温度为70~75℃时,能够制备粒径小分布窄的阳离子型聚苯乙烯纳米粒子.Z均粒径与苯乙烯质量之间的线性关系表明,Z均粒径可以通过苯乙烯用量来控制.不同聚合工艺下制备的聚合物粒度分布曲线表明,改进微乳液聚合工艺(半连续预乳化工艺)在制备窄分布的聚合物纳米粒子方面具有很强的优越性.

参考文献

[1] Pathak S,Greci M T,Kwong R C,et al.Synthesis and Applications of Palladium-Coated Poly(vinylpyridine) Nanospheres[J].Chem Mater,2000,12(7):1985-1989.
[2] Chae W S,Braun P V.Templated Mesoporous Silica Colloids with Controlled Internal Structures[J].Chem Mater,2007,19(23):5593-5597.
[3] Doherty C M,Caruso R A,Smarsly B M,et al.Colloidal Crystal Templating to Produce Hierarchically Porous LiFePO4 Electrode Materials for High Power Lithium Ion Batteries[J].Chem Mater,2009,21 (13):2895-2903.
[4] Kallinteri P,Higgins S,Hutcheon G A,et al.Novel Functionalized Biodegradable Polymers for Nanoparticle Drug Delivery Systems[J].Biomacromolecules,2005,6(4):1885-1894.
[5] Wang Y,Gao S,Ye W H,et al.Co-delivery of Drugs and DNA from Cationic Core-shell Nanoparticles Self-assembled from a Biodegradable Copolymer[J].Nat Mater,2006,5 (10):791-796.
[6] Dez S,Miguliz I,Tros de Ilarduya C.Targeted Cationic Poly(D,L-lactic-co-glycolic acid) Nanoparticles for Gene Delivery to Cultured Cells[J].Cell Mol Biol Lett,2009,14(2):347-362.
[7] Chen J,Tian B,Yin X,et al. Preparation,Characterization and Transfection Efficiency of Cationic PEGylated PLA Nanoparticles as Gene Delivery Systems[J].J Biotechnol,2007,130(2):107-113.
[8] Zhang K,Fang H,Wang Z,et al.Cationic Shell-crosslinked Knedel-like Nanoparticles for Highly Efficient Gene and Oligonucleotide Transfection of Mammalian Cells[J].Biomaterials,2009,30(5):968-977.
[9] Zou Q C,Yan Q J,Song G W,et al.Detection of DNA Using Cationic Polyhedral Oligomeric Silsesquioxane Nanoparticles as the Probe by Resonance Light Scattering Technique[J].Biosens Bioelectron,2007,22(7):1461-1465.
[10] Kong X,Wu Q,Hu W,et al.Monodisperse Ultrafine Polystyrene Nanoparticles Prepared by a Semicontinuous Microemulsion Polymerization[J].J Polym Sci,Part A:Polym Chem,2008,46(13):4522-4528.
[11] Harding I H.Amphoteric Polystyrene Latex Colloids:Polymerization Pathway and the Control of Particle Size and Potential[J].Colloid Polym Sci,1985,263(1):58-66.
[12] Zheng L Q,Zhu W Z,Shen Q,et al.Kinetic and Size Control of Polystyrene and Polyacrylic Octadecyl Ester Lattices via Polymerization in O/W Microemulsions[J].Colloid Surf A,2002,201 (1/3):111-121.
[13] Antonietti M,Bremser W,Mschenbom D,et al.Synthesis and Size Control of Polystyrene Latices via Polymerization in Microemulsion[J].Macromolecules,1991,24(25):6636-6643.
[14] He G,Pan Q,Rempel G L.Synthesis of Poly(methyl methacrylate) Nanosize Particles by Differential Microemulsion Polymerization[J].Macromol Rapid Comm,2003,24(9):585-588.
[15] Xu X J,Gan L M.Recent Advances in the Synthesis of Nanoparticles of Polymer Latexes with High Polymer-to-surfactant Ratios by M icroemulsion Polymerization[J].Curr Opin Colloid Interface Sci,2005,10(5/6):239-244.
[16] Xu X J,Chew C H,Siow K S,et al.Microemulsion Polymerization of Styrene for Obtaining High Ratios of Polystyrene/surfactant[J].Langmuir,1999,15 (23):8067-8071.
[17] Yildiz U,Capek I.Microemulsion Polymerization of Styrene in the Presence of Macroinimer[J].Polymer,2003,44(8):2193-2200.
[18] Tehrani Bagha A R,Bahrami H,Movassagh B,et al.Interactions of Gemini Cationic Surfactants with Anionic Azo Dyes and Their Inhibited Effects on Dyeability of Cotton Fabric[J].Dyes Pigm,2007,72(3):331-338.
[19] Antonietti M,Lohmann S,Van Niel C. Polymerization in Microemulsion.2.Surface Control and Functionalization of Microparticles[J].Macromolecules,1992,25 (3):1139-1143.
[20] Xu X J,Siow K S,Wong M K,et al.M icroemulsion Polymerization via Hollow-fiber Feeding of Monomer[J].Langmuir,2001,17(15):4519-4524.
[21] Rabelero M,Zacarias M,Mendizabal E,et al.High-content Polystyrene Latex by Microemulsion Polymerization[J].Polym Bull,1997,38(6):695-700.
[22] Prez-Luna V H,Puig J E,Castao V M,et al.Styrene Polymerization in Three-component Cationic Microemulsions[J].Langmuir,1990,6(6):1040-1044.
[23] Gan L M,Chew C H,Lim J H,et al.Styrene Polymerization in Ternary Microemulsions:Effects of Water-soluble and Oilsoluble Initiators[J].Colloid Polym Sci,1994,272(9):1082-1089.
[24] Gan L M,Chew C H,Lee K C,et al.Formation of Polystyrene Nanoparticles in Ternary Cationic Microemulsions[J].Polymer,1994,35 (12):2659-2664.
[25] Dreja M,Tieke B.Polymerization of Styrene in Ternary Microemulsion Using Cationic Gemini Surfactants[J].Langmuir,1998,14(4):800-807.
[26] Liu L J,Krieger I M.Emulsifier-free Emulsion Polymerization with Cationic Comonomer[J].J Polym Sci:Polym Chem Ed,1981,19(11):3013-3026.
[27] Guillaume J L,Pichot C,Guillot J.Emulsifier-free Emulsion Copolymerization of Styrene and Butyl Acrylate. Ⅱ.Kinetic Studies in the Presence of Ionogenic Comonomers[J].J Polym Sci:Polym Chem Ed,1988,26 (7):1937-1959.
[28] Dam T,Engberts J B F N,Karthser J,et al.Synthesis,Surface Properties and Oil Solubilisation Capacity of Catiortic Gemini Surfactants[J].Colloid Surf A,1996,118(1/2):41-49.
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%