用户名: 密码: 验证码:
基于间十五烷基酚聚酯型超分散剂研究
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
随着化石资源的日益枯竭,如何利用可再生资源已引起全世界的关注。腰果壳提取液的催化加氢产物是间十五烷基酚(PDP),能够替代石油类酚,属绿色可再生资源。基于PDP间位长链烷烃空间自由体积大的特性,本文将其作为超分散剂的溶剂化链段,能够提供较大的空间位阻效应,设计合成丙烯酸聚酯型和端氨基嵌段聚酯型超分散剂。研究分散剂制备方法和工艺条件,并对两种新型超分散剂的分散效果及吸附性能进行研究。
     以PDP和丙烯酰氯为原料,咪唑类离子液体为催化剂,三乙胺为敷酸剂,制备间十五烷基丙烯酸苯酯(PDPA)单体,通过红外、核磁、质谱和元素分析确认结构。利用响应面分析法对PDPA的合成工艺条件进行优化,得适宜工艺条件为:咪唑类离子液体用量2.02%,底物摩尔配比n(丙烯酰氯):n(PDP)=1.15:1,反应时间8.25h,反应温度57。C。在此工艺条件下,PDPA的收率可达87%。对PDP与丙烯酰氯的酯化反应进行动力学研究,得无催化剂和无缚酸剂条件下,酯化反应动力学方程为:在离子液体催化和三乙胺为缚酸剂下,酯化反应动力学方程为:
     测定PDPA在乙醇和甲醇混合溶剂以及甲苯等六种有机溶剂中273K-297K范围内的溶解度。利用Apelblat方程和λh方程模型对所测溶解度数据进行关联,结果显示Apelblat模型优于λh模型。采用Apelblat方程和范德霍夫方程对溶解过程的溶解熵和溶解焓进行计算,表明溶解过程都是熵驱动的自发过程。由基团贡献法估算PDPA的溶度参数,对不同溶剂中PDPA的溶解度大小进行比较。
     通过自由基无规共聚,合成PDPA、甲基丙烯酸(MAA)和丙烯酸丁酯(BA)三元聚酯型超分散剂,其制备适宜工艺条件为:偶氮二异丁腈(AIBN)用量为单体总质量2%;链转移剂用量为AIBN等摩尔比;反应温度70。C;反应时间8h。采用红外光谱和核磁氢谱对聚合物进行结构表征。研究PDPA/MAA/BA三元聚酯型超分散剂对钛白粉分散体系黏度和细度影响,结果表明:其适宜的重均分子量为6000左右;三种单体质量配比为PDPA:MAA:BA=1.2:1:10;钛白粉体系(固含量30%)黏度可降低到50mPa·s,细度可达20μm。
     在303K、313K、323K温度下,甲苯、异丙醇和乙酸乙酯三种溶剂中钛白粉对丙烯酸聚酯型超分散剂的等温吸附数据用四种常用模型进行拟合比较,结果表明Fritze-Schlunder模型拟合最好。钛白粉吸附超分散剂前后红外光谱无变化,说明钛白粉对丙烯酸聚酯型超分散剂在三种溶剂中的吸附主要为物理吸附。由Dubinin–Radushkevich方程计算结果表明,钛白粉在三种溶剂中对丙烯酸聚酯型超分散剂的平均自由吸附能在2.09~3.11kJ·mol-1之间,远小于化学吸附平均自由吸附能,证实吸附过程主要是物理吸附。
     碳黑是最难分散的颜料之一,为达到在溶剂体系中分散碳黑的目的,本课题结合PDP的分子结构特点,设计合成一种新型的嵌段聚酯型超分散剂。首先,以PDP引发己内酯开环聚合,制备端羟基聚酯,适宜工艺条件为:钛酸丁酯为催化剂,用量为5‰;反应温度110℃;反应时间16h。然后,马来酸酐与端羟基聚酯反应,制备端羧基聚酯,适宜工艺条件为:反应温度90℃,马来酸酐:端羟基聚酯=2.5:1(mol),反应时间10h。最后,端羧基聚酯与二乙烯三胺进行酰胺化反应,其适宜工艺条件为:反应温度120℃,反应时间12h。用红外光谱和核磁氢谱对嵌段聚酯分散剂进行结构表征。研究端氨基嵌段共聚物对碳黑分散体系黏度和细度影响,结果表明:其适宜的重均分子量为3000左右;胺值为20mgKOH/g;碳黑分散体系(固含量为30%)黏度可降低到30mPa·s,细度可达5μm。
     在303K、313K、323K温度下,甲苯、异丙醇和乙酸乙酯三种溶剂中碳黑对端氨基嵌段聚酯型超分散剂的等温吸附数据用四种常用模型进行拟合比较,结果表明Tempkin模型拟合最好。红外图谱间接证实碳黑对端氨基嵌段聚酯型超分散剂在三种溶剂中的吸附为物理吸附。由Dubinin–Radushkevich方程计算结果表明,碳黑在三种溶剂中对端氨基嵌段聚酯型超分散剂的平均自由吸附能在1.31~2.62kJ·mol-1之间,证实吸附过程主要是物理吸附。
     综合以上研究结果表明,以PDP制备丙烯酸聚酯型超分散剂和端氨基嵌段聚酯型超分散剂,在溶剂型体系中对钛白粉和碳黑均有较好的分散能力,对于拓展PDP在涂料行业的应用具有一定的指导意义。
While Petrochemical resources is drying up, how to make use of the renewable resources has attracted attentions of all the world.3-Pentadecylphenol(PDP) is the product of catalytic hydrogenation of cashew nut shell liquid, which could replace Petroleum phenol, so it's a kind of green renewable resources. Because of the Characteristics for PDP that the meta-position long-chain alkane has big free volume, in this paper, PDP is used as solvation segment of hyperdispersant, which will provide sufficient steric hindrance effect. The polyester acrylate type and amino terminal block polyester type of hyperdispersant were prepared to make a study on synthesis methods and synthesis techniques of the two hyperdispersants, which are used for the dispersion and adsorption research on titanium oxide and carbon black.
     Using PDP and acryloyl chloride as materials, imidazolium ionic liquids as catalyst, triethylamine as acid binding agent,3-pentadecylphenyl acrylate(PDPA) was prepared and its structure was characterized using FTIR, NMR, MS and EDS. Synthetic technological conditions of PDPA was optimized using Response Surface Methodology and the optimum conditions were as follows:usage of imidazolium ionic liquids2.02%(wt.%), molar ratio of acryloyl chloride to PDP1.15:1, reaction time8.25h, reaction temperature57℃. At this condition, the yield of PDPA can reach to87%. Kinetic study was made on the esterification reaction between acryloyl chloride and PDP, and when there were no catalyst and acid binding agent, kinetic equation of the esterification reaction was as follows: When ionic liquids as catalyst and triethylamine as acid binding agent exist, kinetic equation of the esterification reaction was as follows:
     The solubility of PDPA in mixed solvent of ethanol and methanol, toluene and other five organic solvents was measured at the temperature ranging from273K-297K, and Apelblat equation and λh equation model was used to correlate the solubility data and the results showed that Apelblat model is better than λh model. The dissolution enthalpy and entropy of PDPA were predicted with the solubility data using Apelblat equation and Van't Hoff equation, and the results showed that the dissolve process is an entropy-driven spontaneous process. Solubility parameter ofPDPA was got through group contribution method, and solubility data of PDPA indifferent solvent was compared.
     The acrylic polyester type of hyperdispersant including PDPA, methacrylicacid(MAA) and butyl acrylate(BA) was synthesized through free radicals randomcopolymer. The optimum conditions of preparation were as follows: usage ofazodiisobutyronitrile(AIBN) as initiator2%(wt.%), usage of chain transfer agent thesame molar as AIBN, reaction temperature70℃, reaction time8h. The structure ofthe polymer was characterized by FTIR and H-NMR. The influence of the acrylicpolyester type of hyperdispersant including PDPA, MAA and BA on the viscosity andfineness of titanium dioxide disperse system was also studied. The results indicatedthat: the optimum weight-average molecular weight6000, the quality ratio of PDPA:MAA:BA=1.2:1:10, viscosity of titanium dioxide disperse system (solid content30%) can reach50mPa·s, fineness can reach20μm.
     At the temperature of303K,313K and323K, the isothermal adsorption data oftitanium dioxide to the polyester acrylate type of hyperdispersant in the solvents oftoluene, isopropanol and ethyl acetate were fitted and compared using differentmodels, and the result showed that Fritze-Schlunder model was optimum. The FTIRdata also indicated that the adsorption of titanium dioxide to the polyester acrylatetype of hyperdispersant in the three solvents was mainly physical absorption. Theresult of Dubinin-Radushkevich equation showed that the average adsorption freeenergy of titanium dioxide to the polyester acrylate type of hyperdispersant in thethree solvents was2.09~3.11kJ·mol-1, which indicated that the adsorption wasmainly physical absorption.
     Carbon black was one of the hardest dispersed pigments, in order to disperse thecarbon black in the solvent system, a new block polyester type of hyperdispersant wasprepared in this paper combining with the structural character of PDP. Firstly, ring-opening polymerization of caprolactone was triggered by PDP to prepare hydroxyl-terminated polyester, and the optimum conditions of preparation were as follows:usage of butyl titanate as catalyst5‰, reaction temperature110℃, reaction time16h.Secondly, the carboxyl end group was got by the reaction between maleic anhydrideand hydroxyl-terminated polyester, and the optimum conditions were as follows:reaction temperature90℃, molar ratio of maleic anhydride to hydroxyl-terminatedpolyester2.5:1, reaction time10h. Finally, amidation occurred between the carboxyl end group and diethylenetriamine, and the optimum conditions were as follows:reaction temperature120℃, reaction time12h. The structure of the block polyestertype of hyperdispersant was characterized by FTIR and H-NMR, and the influence ofthe amino block copolymer on the viscosity and fineness of carbon black dispersesystem was also discussed. The results indicated that: the optimum weight-averagemolecular weight about3000, amine value20mgKOH/g, viscosity of carbon blackdisperse system (solid content30%) can reach30mPa·s, fineness can reach3μm.
     At the temperature of303K,313K and323K, the isothermal adsorption data ofcarbon black to amino terminal block polyester type of hyperdispersant in the solventsof toluene, isopropanol and ethyl acetate were fitted and compared using differentmodels, and the result showed that Tempkin model was optimum. The FTIR data alsoindicated that the adsorption of carbon black to amino terminal block polyester typeof hyperdispersant in the three solvents was mainly physical absorption. The result ofDubinin–Radushkevich equation showed that the average adsorption free energy ofcarbon black to amino terminal block polyester type of hyperdispersant in the threesolvents was1.31~2.62kJ·mol-1, which indicated that the adsorption was mainlyphysical absorption.
     Generally speaking, the above results suggest the polyester acrylate type andamino terminal block polyester type of hyperdispersant prepared by PDP both hadpreferable dispersive capacity to titanium dioxide and carbon black in solvent-bornesystem, which will has guiding sense to development of PDP in coating industry.
引文
[1] Alireza Aslani,Petri Helo,Marja Naaranoja.Role of renewable energy policies in energydependency in Finland:System dynamics approach[J].Applied Energy,2014,113:758~765
    [2] Juan C. Ronda,Gerard Lligadas,Marina,et al.A renewable approach to thermosettingresins[J].Reactive&Functional Polymers,2013,73:381~395
    [3] Gautam Dasa, Ranjan Dutta Kalita, Harekrishna Dekaa, et al. Biodegradation,cytocompatability and performance studies of vegetable oil based hyperbranchedpolyurethane modified biocompatible sulfonated epoxyresin/claynanocomposites[J].Progress in Organic Coatings,2013,76:1103~1111
    [4] Madeleine R. Yates Claire,Y. Barlow.Life cycle assessments of biodegradable,commercialbiopolymers—A critical review[J].Resources Conservation and Recycling,2013,78:54~66
    [5] Luc Eyraud, Benedict Clements, Abdoul Wane. Green investment: Trends anddeterminants[J].Energy Policy,2013,60:852~865
    [6] Benard Love,Charles R.Dawson.Cashew nut shell liquid.X.An investigation ofgeometrical configurations of the olefinic components of cardanol and some observationsconcerning ginkgol[J].Journal of The American Chemical Society,1958,80:643~645
    [7] V.J.Paul,Lourdu M.Yeddanopalli.On the olefinic nature of anacardic acid from Indiancashew nut shell liquid[J].Journal of The American Chemical Society1956,5:5675~5678
    [8] JohnH.Tyman.Determination of the component phenols in nature and technical cashewnut-shell liquid by gas-liquid chromatography[J].Analytical Chemistry,1976,48(1):30~34
    [9] Paramashivappa R,Kμmar PP.Novel method for isolation of major phenolic constituentsfrom cashew(Anacardiμmoccidentale L.) nut shell liquid[J].Journal of Agricultural andFood Chemistry,2001,49(5):2548~2551
    [10]刘国际,张勇,刘伟等.腰果酚的应用研究进展[J].材料导报,2012,26(5):90~94
    [11] Zhibo Mao,Tingliang Luo,Guoji Liu.Intrinsic Kinetics of Catalytic Hydrogenation ofCardanol[J].Ind. Eng. Chem. Res,2009,48(22):9910~9914
    [12]毛治博.腰果酚催化加氢研究[D].[博士学位论文].郑州:郑州大学,2010
    [13]胡立红,李书龙,刘欣等.腰果酚改性酚醛树脂的合成研究[J].生物质化学工程,2008,42(2):11~14
    [14]杨玮,殷荣忠,杨小云等.腰果酚/腰果壳油改性酚醛树脂的合成及其应用研究[J].热固性树脂,2010,25(5):21~26
    [15]金保宏,王柏臣,陈平等.BMI改性腰果壳油-酚醛树脂的热性能[J].合成树脂及塑料,2010,27(2):55~58
    [16]张洋,马榴强,李晓林等.硼酸、腰果油双改性酚醛树脂的合成[J].热固性树脂,1998,1:9~14
    [17] B.S.Rao,Aruna Palanisamy.Monofunctional benzoxazine from cardanol for bio-compositeapplications[J].Reactive&Functional Polymers,2011,71:148~154
    [18] Pornnapa Kasemsiri,Salim Hiziroglu,Sarawut Rimdusit.Effect of cashew nut shell liquidon gelation, cure kinetics, and thermomechanical properties of benzoxazineresin[J].Thermochimica Acta,2011,520:84~92
    [19] B.S.Rao,Aruna Palanisamy.A new thermo set system based on cardanol benzoxazine andhydroxy benzoxazoline with lower cure temperature[J].Progress in Organic Coatings,2012,74:427~434
    [20] Guomei Xu,Tiejun Shi,Jianhua,et al.Preparation of a liquid benzoxazine based oncardanol and the thermal stability of its graphene oxide composites[J].Journal of AppliedPolymer Science,2014,131(11):403~411
    [21] Shengfang Li, Tao Zou, Li Feng. Preparation and properties of cardanol-basedpolybenzoxazine/SiO2hybrids by sol-gel technique[J]. Journal of Applied PolymerScience,2013,128(6):4164~4171
    [22]戴志晟,郭铭.防腐性能优异的新型环氧树脂固化剂—腰果酚改性聚酰胺[J].现代涂料与涂装,2011,14(2):15~18
    [23] Nilakshi V. Sadavarte,C.V. Avadhani,Parimal V. Naik,et al.Regularly alternatingpoly(amideimide)s containing pendent pentadecyl chains: Synthesis andcharacterization[J].European Polymer Journal,2010,46:1307~1315
    [24] Arvind S. More,Anandrao S. Patil,Prakash P. Wadgaonkar.Poly(amideimide)s containingpendant pentadecyl chains:Synthesis and characterization[J].Polymer Degradation andStability,2010,95:837~844
    [25] Santosh B.Mhaske,Radhika V.Bhingarkar,Madhukar B.Sabne, et al.Synthesis andcharacterization of end-capped polyimides and their gas permeability properties[J].Journalof Applied Polymer Science,2000,77:627~635
    [26] H.P. Bhunia,A. Basakb,T.K. Chakia,et al.Synthesis and characterization of polymersfrom cashewnut shell liquid: a renewable resource: V. Synthesis ofcopolyester[J].European Polymer Journal,2000,36:1157~1165
    [27] H.P.Bhunia,G.B.Nandoa,T.K.Chakia,et al.Synthesis and characterization of polymersfrom cashewnut shell liquid (CNSL): a renewable resource II. Synthesis ofpolyurethanes[J].European Polymer Journal,1999,35:1381~1391
    [28] Janne Ruokolainen,Mika Torkkeli,Ritva Serimaa,et al.Critical Interaction Strength forSurfactant-Induced Mesomorphic Structures in Polymer SurfactantSystems[J].Macromolecules,1996,29:6621~6628
    [29] Ian E.Bruce,Lina Mehta,Michael J. Porter,et al.Anionic Surfactants Synthesised fromReplenishable Phenolic Lipids[J].Journal of Surfactants and Detergents,2009,12(4):337~344
    [30] John H.P.Tyman, Ian E.Bruce. Synthesis and Characterization of PolyethoxylateSurfactants Derived from Phenolic Lipids[J].Journal of Surfactants and Detergents,2003,6(4):291~297
    [31] John H.P. Tyman, Ian E. Bruce. Surfactant Properties and Biodegradation ofPolyethoxylates from Phenolic Lipids[J].Journal of Surfactants and Detergents,2004,7(2):169~173
    [32] Graziella Tocco,Antonella Fais,Gabriele Meli.PEG-immobilization of cardol and solublepolymer-supported synthesis of some cardol–coμmarin derivatives: Preliminary evaluationof their inhibitory activity on mushroom tyrosinase[J].Bioorganic&Medicinal ChemistryLetters,2009,19:36~39
    [33] Isa G. J.de Avellar,Kênia Godoy,Gouvan C. Magalh es.New Quaternary AmmoniμmSalts Derived from Cardanol and their Use as Phase Transfer Catalyst[J].J. Braz. Chem.Soc,2000,11(1):22~26
    [34]张燕晓,徐丽,刘国际.一种新型季铵盐的合成与表征[J].河南化工,2010,27(8):51~54
    [35] Anita Swami,PR.Selvakannan,Renu Pasricha,Murali Sastry.One-Step Synthesis ofOrdered Two-Dimensional Assemblies of Silver Nanoparticles by the SpontaneousReduction of Silver Ions by Pentadecylphenol Langmuir Monolayers[J].Phys. Chem. B,2004,108:19269~19275
    [36] Ping Zhang,Junpeng Gao,Binyao Li,et al.Surface Morphology Evolution of a ThinPolymeric Supramolecular Film by Tuning Interactions[J]. Macromolecular RapidCommunications,2006,27:295~261
    [37] Amir W.Fahmi, Manfred Stamm. Spatially Correlated Metallic Nanostructures onSelf-Assembled Diblock Copolymer Templates[J].Langmuir,2005,21:1062~1066
    [38] Grofts PC,Ghahhary M,Tajbakhsh jadidi M.Aryl hydrogen phthalates[J].Org. ProcedInt,1990,22(4):538~540
    [39]贺丽鹏,燕方龙,曹勃阳等.苯胺和苯酚与环酐的酰胺化及酯化反应[J].吉林大学学报(理学版),2006,44(2):287~290
    [40] B.S.SITARAMAM, P.C.CHATTERJEE. Synthesis, Polymerization, and End-UseEvaluation of3-Pentadecylphenyl Acrylate and Methacrylate[J].Journal of AppliedPolymer Science,1989,37:33~37
    [41] H. E. Hoydonckx,D. Vos,S.Chavan.Esterification and Transesterification of RenewableChemicals[J].Chem. Mater Sci.2004,27(4):83~96
    [42] Wang W,Shao L,Cheng W.Bronsted acidic ionic liquids as novel catalysts for Prinsreaction[J].Cata. Com.,2008,9:337~341
    [43] Wu Q,Chen H,Han M,Wang D.Transesterification of Cottonseed Oil Catalyzed byBronsted Acidic Ionic Liquids[J].Ind. Eng. Chem. Res.,2007,46:7955~7960
    [44] Shi F,Zhang Q,Li D.Silica-Gel-Confined Ionic Liquids: A New Attempt for theDevelopment of Supported Nanoliquid Catalysis[J].Chem. Europ. J.,2005,11:5279~5288
    [45] Romero C,Baldelli S.Sμm Frequency Generation Study of the Room-Temperature IonicLiquids/Quartz Interface[J].J. Phys. Chem. B.,2006,110:6213~6223
    [46] Welton T.Ionic liquids in catalysis[J].Coordin Chem Rev.,2004,248:2459~2477
    [47] Brennecke JF, Maginn EJ. Ionic liquids: Innovative fluids for chemicalprocessing[J].AIChE J.,2001,47:2384~2389
    [48] Bourbiguo HO, Magna L. Ionic liquids: perspectives for organic and catalyticreactions[J].J Mol. Cat. A: Chem,2002,182:419~437
    [49] P. Vidya, Anju Chadha. Pseudomonas cepacia lipase catalyzed esterification andtransesterification of3-(furan-2-yl) propanoic acid/ethyl ester: A comparison in ionicliquids vs hexane[J].Journal of Molecular Catalysis B: Enzymatic,2010,65:68~72
    [50] Fang D,Zhou X,Ye Zh,Liu Z.Bronsted Acidic Ionic Liquids and Their Use as DualSolvent Catalysts for Fischer Esterifications[J].Ind. Eng. Chem. Res.,2006,45:7982~7984
    [51] Cole AC,Jensen JL,Ntai I,Tran KLT.Novel Br nsted Acidic Ionic Liquids and Their Useas Dual Solvent Catalysts[J].J. Am. Chem. Soc.,2002,24:5962~5963
    [52] Wei Z,Li F,Xing H.Reactivity of bronsted acid ionic liquids as dual solvent and catalystfor Fischer esterifications[J].Kor. j. Chem. Eng.,2009,26:666~672
    [53]闫海龙,李涛,吾满江.艾力.磺酸型离子液体的合成及其在酯化反应中的催化性能研究[J].化学与生物工程,2007,24(4):40~43
    [54]方东,刘祖亮,周新利.功能化离子液体室温催化合成乙酸苄酯[J].应用化学,2007,24:85~89
    [55]林文俊,钟丽娜,陈艳秋,林金清.季铵盐型离子液体催化合成乙酸正丁酯[J].化工学报,2011,62:74~79
    [56]贾俊英.离子液体催化合成氨基酸酯的工艺研究[M].[硕士学位论文].哈尔滨:哈尔滨理工大学,2010
    [57]蒋惠亮,姚伟杰.酸性离子液体催化合成三羟甲基丙烷三辛酸酯[J].精细化工,2011,28(7):726~728
    [58]李静,蒋剑春,徐俊明.酸性离子液体合成及其催化合成柠檬酸三乙酯的研究[J].生物质化学工程,2009,43(4):15~20
    [59] Krishna M.Deshmukh, Ziyauddin S.Qureshi, Kishor P.Dhake, BhalchandraM.Bhanage.Transesterification of dimethyl carbonate with phenol using Br nsted andLewis acidic ionic liquids[J].Catalysis Communications,2010,12:207~211
    [60] Scott A. Eastman,Alan J. Lesser,Thomas J. McCarth.Quantitative Poly(vinyl alcohol)Modification in Ionic Liquids: Esterification and Urethanation with Low SurfaceTension[J].Macromolecules,2010,43:4584~4588
    [61] Duanjian Tao,Xueming Lu,Jianfeng Lu,et al.Noncorrosive ionic liquids composed of[HSO4] as esterification catalysts[J].Chemical Engineering Journal,2011,171:1333~1339
    [62] Duanjian Tao,Youting Wu,Zheng Zhou.Kinetics for the Esterification Reaction ofn-Butanol with Acetic Acid Catalyzed by Noncorrosive Br nsted Acidic IonicLiquids[J].Ind. Eng. Chem. Res.,2011,50:1989~1996
    [63] Pandian Elavarasan,Kishore Kondamudi,Sreedevi Upadhyayula.Kinetics of phenolalkylation with tert-butyl alcohol using sulfonic acid functional ionic liquidcatalysts[J].Iternational journal of hydrogen energy,2007,32:1742~1748
    [64] Dishun Zhao,Mengshuai Liu,Juan Zhang.Synthesis, characterization, and properties ofimidazole dicationic ionic liquids and their application in esterification[J].ChemicalEngineering Journal,2013,221:99~104
    [65]李明,包桂蓉,王华.高活性离子液体催化酯化反应的研究[J].应用化工,2010,39(4):480~483
    [66] Yingwei Zhao,Jinxing Long,Fanguo Deng.Catalytic amounts of Br nsted acidic ionicliquids promoted esterification: Study of acidity–activity relationship[J]. CatalysisCommunications,2009,10:732~736
    [67] Wanming Xiong,Manzhou Zhu,Li Deng,Yao Fu.Esterification of Organic Acid inBio-Oil using Acidic Ionic Liquid Catalysts[J].Energy&Fuels,2009,23:2278~2283
    [68] Stewart A. Forsyth,Douglas R. MacFarlane,Robin J.Thomson,et al.Rapid, clean, andmild O-acetylation of alcohols and carbohydrates in an ionic liquid[J].Chem. Commun.,2002,5:714~715
    [69]邹长军,粟松涛,左晓玲.1-甲基-3-丁基咪唑/AlCl3催化制备2-顺丁烯二酸二(2-乙基己)酯[J].化学试剂,2005,27(6):372~374
    [70]马卫华,俞马宏,钟秦.离子液体催化合成反丁烯二酸二乙酯[J].精细有机化工,2005,4:16~18
    [71] Dong Jiang,Yuan Yuan Wang,Li Yi Dai.Esterification of alcohols with acetic anhydridein br nsted acidic ionic liquids at room temperature[J].React.Kinet.Catal.Lett.,2008,93(2):257~263
    [72] Xinwen Peng,Junli Ren,Runcang Sun.Homogeneous Esterification of Xylan-RichHemicelluloses with Maleic anhydride in Ionic Liquid[J].Biomacromolecules,2010,11:3519~3524
    [73] J. S. HamPton.A review of hyperdispersant technology[J].American Chemical Society,1986,192:9~12
    [74] J.S. Hampton et al.Extending the boundaries of dispersant technology[J].Progress inOrganic Coating,2002,45(2):249~257
    [75] Faouzi Nsib,Naceur Ayed,Yves Chevalier.Selection of dispersants for the dispersion ofcarbon black in organic mediμm[J].Progress in Organic Coatings,2006,55:303~310
    [76] Darby Kozaka,David Moreton,Brian Vincent.The adsorption of non-ionic surfactants oncarbon black particles in hydrocarbon media[J].Colloids and Surfaces A: Physicochem.Eng. Aspects,2009,347:245~250
    [77] Saeed Farrokhpay. A review of polymeric dispersant stabilisation of titaniapigment[J].Advances in Colloid and Interface Science,2009,151:24~32
    [78] Mark A. Banash,Stuart G. Croll.A Quantitative study of polymeric dispersant adsorptiononto oxide-coated titania pigments[J].Progress in Organic Coatings,1999,35:37~44
    [79] J.A. Simms.A new graft polymer pigment dispersant synthesis[J].Progress in OrganicCoatings,1999,35:205~214
    [80] Harry J.Spinelli.Group transfer polymerization and its use in water basedpigment dispersants and emulsion stabilizers[J].Progress in Organic Coatings,1996,27:255~260
    [81] Ying Hu,Xugen Ying,J.M.Prausnitz.Continuous thermodynamics for polydispersepolymer solutions[J].Fluid Phase Equilibria,1995,104:229~252
    [82] Jie Wu,LiMin Wang,Ping Zhao,et al.New type of quaternary ammoniμm salt containingsiloxane group and used as favorable dispersant in the surface treatment of C.I. pigment red170[J].Progress in Organic Coatings,2008,63:189~194
    [83] Matthew F.Smiechowskia, Vadim F. Lvovicha. Characterization of non-aqueousdispersions of carbon black nanoparticles by electrochemical impedancespectroscopy[J].Journal of Electroanalytical Chemistry,2005,577:67~78
    [84] Faouzi Nsib,Naceur Ayed,Yves Chevalier.Selection of dispersants for the dispersion ofC.I. Pigment Violet23in organic medium[J].Dyes and Pigments,2007,74:133~140
    [85] H.J.W. van den Haak,L.L.M. Krutzea.Design of pigment dispersants for high-solids paintsystems[J].Progress in Organic Coatings,2001,43:56~63
    [86] Saeed Farrokhpay,Gayle E. Morris,Daniel Fornasiero,et al.Stabilisation of titaniapigment particles with anionic polymeric dispersants[J].Powder Technology,2010,202:143~150
    [87] Faouzi Nsib,Naceur Ayed,Yves Chevalier.Comparative study of the dispersion of threeoxide pigments with sodiμm polymethacrylate dispersants in alkaline mediμm[J].Progressin Organic Coatings,2007,60:267~280
    [88] F.L. Duivenvoorde,C.F. van Nostrμm,R. van der Lindea.The pigmentation of powdercoatings with the use of block copolymer dispersants[J].Progress in Organic Coatings,1999,36:225~230
    [89] C. Daescu.Dispersability of Organic Pigments[J].Dyes and Pigments,1998,38:173~180
    [90] Harald Frommelius,T. Svanholm,B. Kronberg,et al.A new concept for dispersing agentsin aqueous coatings[J].Progress in Organic Coatings,1996,35:191~196
    [91] Christian Kugge,Vincent S.J. Craig,John Daicic.A scanning electron microscope studyof the surface structure of mineral pigments, latices and thickeners used for paper coatingon non-absorbent substrates[J].Colloids and Surfaces A: Physicochem. Eng. Aspects,2004,238:1~11
    [92] F. Tiarks,T. Frechen,S. Kirsch,et al.Formulation effects on the distribution of pigmentparticles in paints[J].Progress in Organic Coatings,2003,48:140~152
    [93]武照强,冯开才,刘振兴.超分散剂[J].现代塑料加工应用,2001,13(5):45~49.
    [94]汪剑炜,王正东,胡黎明.超分散剂的分子结构设计[J].化工进展,1994,4:32~37
    [95] Frank Lux.Poly(2-hydroxyethylmethaerylate-co-styrene-4-sulfonic acid sodiμm salt) aversatile hyperdispersant system for controlling the size of conducting polymerparticles[J].Synthetic Metals,1999,102(1-3):1190~1193
    [96] Aijun Han,Mingquan Ye,Minchun Zhao,et al.Crystal structure, chromatic andnear-infrared reflective properties of iron doped YMnO3compounds as colored coolpigments[J].Dyes and Pigments,2013,99:527~530
    [97] Maryna G. Krivovaa,Dmitrij D. Grinshpana,Niklas Hedinb.Adsorption of CnTABrsurfactants on activated carbons[J].Colloids and Surfaces A: Physicochem. Eng. Aspects,2013,436:62~70
    [98] BV Derjaguin.Theory of the stability of strongly charged lyophobic sols and the adhesionof strongly charged particles in solutions of electrolytes[J].Acta Physicochim. USSR,1941,14:633~662
    [99] E.J.W. Verwey,J.T.G. Overbeek.Theory of the stability of lyophobic colloids[J].J.Physical Chemistry,1947,53(2):631~636
    [100] E.J.W.Verwey, J.T.G. Overbeek.Theory of the Stability of Lyophobic Colloids[M].NewYork:Elsevier,1999
    [101] Parfitt G. D.Dispersion of Powders in Liquids (3rd ed.)[M].London:Applied SciencePublishers,1981
    [102] Stuart Croll.DLVO theory applied to TiO2pigments and other materials in latexpaints[J].Progress in Organic Coatings,2002,44:131~146
    [103] Horn R. G.Surface forces and their action in ceramic materials[J].J.Am. Ceram. Soc.,1990,73:1117~1135
    [104] Fowkes F. M.,Pugh R. J.Steric and electrostatic contributions to the colloidal properties ofnonaqueous dispersions[J].ACS Symp. Ser.,1984,240:331~354.
    [105] Napper D. H.Polymeric Stabilisation of Colloidal Dispersions[M].London:AcademicPress,1983
    [106] Thomas Hahn. Chemical Engineering and Processing-Principles of Adsorption andReaction on Solid Surfaces(First Edition)[M].New York:Willy,1996
    [107] Ploehn H. J., Russel W. B., Hall C.K. Self-consistent field model of polymeradsorption—generalized formulation and ground-state solution[J].Macromolecules1988,21:1075~1085
    [108] Israelachvili J. N.Intermolecular and Surface Forces (2nd ed.)[M].London:AcademicPress,1992
    [109] Moreno R.The role of slip additives in tape-casting technology[J].Am. Ceram. Soc.,1992,71:1521~1531
    [110] Johnson S. B., Franks G. V., Scales P. J., et al.Surface chemistry–rheology relationships inconcentrated mineral suspensions[J].Int. J. Miner. Process.,2000,58:267~304
    [111] Lange F.F.Shape forming of ceramic powders by manipulating the interparticle pairpotential[J].Chem. Eng. Sci.,2001,56:3011~3020
    [112] Zhou Z., Scales P. J.Chemical and physical control of the rheology of concentrated metaloxide suspensions[J].Chem. Eng. Sci.,2001,56:2901~2920
    [113] Ellen Reuter,Stefan Silber,Christian Psiorz.The use of new blockcopolymeric dispersingagents for waterborne paints—theoretical and practical aspects[J].Progress in OrganicCoatings,1999,37:161~167
    [114] Jos Huybrechts,Paul Bruylants,Ken Kirshenbaμm,et al.New applications of catalyticchain transfer polymerization to waterborne binders for automotive paintsystems[J].Progress in Organic Coatings,2002,45:173~183
    [115] J. Philip Kaczmarski,Mingren Tang,J. Edward Glassa,et al.Development of and resultsfrom a chromatographic technique for the analysis of competitive adsorption on stabilizedTiO2surfaces[J].Progress in Organic Coatings,1997,30:15~23
    [116] Harry Podlesak,Lech Pawlowski,Jacky Laureyns,et al.Advanced microstructural studyof suspension plasma sprayed titanium oxide coatings[J].Surface&Coatings Technology,2008,202:3723~3731
    [117] Serge Creutz,Robert Jér me.Effectiveness of block copolymers as stabilizers for aqueoustitanium dioxide dispersions of a high solid content[J].Progress in Organic Coatings,2000,40:21~29
    [118] Frank Lux.Poly(2-hydroxyethylmethacrylate-co-styrene-4-sulfonic acid, sodiμm salt):A versatile hyperdispersant system for controlling the size of conducting polymerparticles[J].Synthetic Metals,1999,102:1190~1193
    [119] MohaMAAd Hossein Habibi,Mojtaba Nasr Esfahani.Preparation, characterization andphotocatalytic activity of a novel nanostructure composite film derived from nanopowderTiO2and solegel process using organic dispersant[J].Dyes and Pigments,2007,75:714~722
    [120] Yifen Lan,Jiangjen Lin.Clay-assisted dispersion of organic pigments in water[J].Dyesand Pigments,2011,90:21~27
    [121] D. T. Nguyen.Use of novel polyetheralkanolamine comb polymers as pigment dispersantsfor aqueous coating systemsa[J].J. Coat. Technol. Res.,2007,4(3):295~309
    [122] Sigmund W. M., Bell N. S., Bergstr m L.Novel powders-processing methods for advancedceramics[J].J. Am. Ceram.Soc.,2000,83:1557~1574
    [123] D.H Napper.Steric stabilization[J].Journal of Colloid and Interface Science,1977,58(2):390~407
    [124] D. H. Napper, Robert I Feigin. Depletion stabilization and depletionflocculation[J].Journal of Colloid and Interface Science,1980,75(2):525~541
    [125] D.H Napper.Flocculation studies of sterically stabilized dispersions[J].Journal of Colloidand Interface Science,1970,32(1):106~114
    [126] D.H Napper, A Netschey.Studies of the steric stabilization of colloidal particles[J].Journalof Colloid and Interface Science,1971,37(3):528~535
    [127] Hampton J.S.,Napper D.H.,Toyoda A.Contribution of Hyperdispersants to ModemDispersion Technology[J].American Ink Maker,1985,63(1):16~20
    [128] E.L Mackor.A theoretical approach of the colloid-chemical stability of dispersions inhydrocarbons[J].J.Colloid Interface Sci.,1951,6:492~499
    [129] E.L Mackor,J.H van der Waals.The statistics of the adsorption of rod-shaped molecules inconnection with the stability of certain colloidal dispersions[J].J.Colloid Interface Sci.,1952,7:535~550
    [130] E.W. Fisher.Elektronenmikroskopische Untersuchungen zur Stabilit t von Suspensionen inmakromolekularen L sungen[J].Colloid and Polymer Science,1958,160(2):120~141
    [131]王正东,胡黎明.超分散剂的作用机理及应用效果[J].精细石油化工,1996,11(6):59~62
    [132] Maxwell L D.Solsperse Hyperdispersant for Paints Ink[J].Paint Ink Int,1996,6:11~14
    [133]王正东.超分散剂的制备[D].[博士学位论文].上海:华东理工大学,1996
    [134] Francis L. Duivenvoorde,Jozua Laven, Rob van der Linde.Diblock copolymer dispersantsin polyester powder coatings[J].Progress in Organic Coatings,2002,45:127~137
    [135] Nsib F., Ayed N., Chevalier Y.Selection of dispersants for the dispersion of carbon black inorganic medium[J].Progr. Org. Coat,2006,55:303~310
    [136] Lin Y., Smith T. W., Alexandridis P.Adsorption of a Rake-Type Siloxane Surfactant ontoCarbon Black Nanoparticles Dispersed in Aqueous[J].MediaLangmuir,2002,18:6147~6158
    [137] Creutz S., Jerome R.Effectiveness of block copolymers as stabilizers for aqueous titaniumdioxide dispersions of a high solid content[J].Progr. Org. Coat,2000,40:21~29
    [138] Wang Z., Liu Q., Zhu H., Liu H., et al.Dispersing multi-walled carbon nanotubes withwater–soluble block copolymers and their use as supports for metalnanoparticles[J].Carbon,2007,45:285~92
    [139] Kahn M. G. C., Banerjee S., Wong S.S.Solubilization of Oxidized Single-Walled CarbonNanotubes in Organic and Aqueous Solvents through Organic Derivatization[J].NanoLett,2002,2:1215~218
    [140] Fernando K. A. S., Lin Y., Sun Y.P. Heigh aqueous solubility of functionalizedsingle-walled carbon nanotubes[J].Langmuir,2004,20:4777~4778
    [141] Bressy C., Hugues C., Bartolomeo P.Complexation of an acrylic resin by tertiary amines:synthesis and characterisation of new binders for antifouling paints[J].Eur. Poly. J.,2003,39:319~326
    [142] Dasgupta S.Adsorption behavior of macromolecules on colloidal magnetic oxide particles:interfacial interaction and dispersion characteristics[J].Progr. Org. Coat,1991,19:123~139
    [143] Xueli Zhang,Zhengdong Wang,Liming Hu.Adsorption of hyperdispersants having apoly-e-caprolactone solvatable chain on magnetic particles[J].Colloids and SurfacesA:Physicochemical and Engineering Aspects,1997,122:237~242
    [144]张雪莉,王正东,胡黎明.聚己内酯型超分散剂对磁浆流变行为和分散效果的影响[J].高等学校化学学报,1997,18(4):637~641
    [145]张雪莉,王正东,胡黎明.聚己内酯为溶剂化链的超分散剂在磁粉表面的吸附行为[J].华东理工大学学报,1997,23(3):292~297
    [146]冯开才,张胜寒,李谷,张黎明.聚酯型超分散剂对聚丙烯/无机填料复合材料力学性能的影响[J].塑料工业,2006,34:281~283
    [147] Qianping Ran, Min Qiao, Jiaping Liu, Changwen Miao.SMA-g-MPEG comb-like polymeras a dispersant for Al2O3suspensions[J].Applied Surface Science,2012,58:2447~2453
    [148]张清岑,刘小鹤,黄苏萍.超分散剂分子结构设计的研究[J].矿产综合利用,2002,4:15~19
    [149] Stephen Tanurdjaja,Carolina Tallon,Peter J. Scales,et al.Influence of dispersant size onrheology of non-aqueous ceramic particle suspensions[J].Advanced Powder Technology,2011,22:476~481
    [150]高毕亚,郑柏存,傅乐峰.聚丙烯酸钠超分散剂的合成及其分散性能研究[J].日用化学工业,2008,38(1):20~23
    [151] Bimal P. Singh,Sasmita Nayak,Samata Samal,et al.The role of poly(methacrylic acid)conformation on dispersion behavior of nanoTiO2powder[J].Applied Surface Science,2012,258:3524~3531
    [152]宋云华,范闯,王成忠.炭黑在聚酰胺6中的超分散性研究[J].中国塑料,2010,24(2):21~25
    [153]邢其毅,徐瑞秋,周政,裴伟伟.基础有机化学:下册.第2版[M].北京:高等教育出版社,2005.763~769
    [154] G.E.P.Box, K.B.Wilson. On the experimental attainment of optim μ mcondition[J].Breakthroughs in Statistics,1992,13:270~310
    [155] G.E.P.Box,N.R.Draper.A basis for the selection of a response surface design[J].Journalof american statistical association,1959,54:622~654
    [156] R.H.Myers,W.H.Carter.Response surface methodology[J].Technometrics,1989,31(2):1966~1988
    [157] R.H.Myers,D.C.Montgomery.Response surface methodology[M].New York:Wiley andSons,1995
    [158] Madamba PS. The Response Surface Methodology: An Application to OptimizeDehydration Operations of Selected Agricultural Crops[J].LWT-Food Sci Technol,2002,35:584~592
    [159] Sergio Luis Costa Ferreira, Roy Edward Bruns, Erik Galvao Paranhos da Silva, etal. Statistical designs and response surface techniques for the optimization ofchromatographic[J].J. Chromatograp A,2007,1158:2~14
    [160] Marcos Almeida Bezerra, Ricardo Erthal Santelli, Eliane Padua Oliveira, et al.Responsesurface methodology (RSM) as a tool for optimization in analytical chemistry[J].Talanta,2008,76:965~977
    [161] G. Kafuku, K. T. Tan, K. T. Lee, M. Mbarawa.Noncatalytic Biodiesel Fuel Production fromCroton megalocarpus[J].Oil Chem. Eng. Technol.,2011,34:1827~1834
    [162] Lucio C. Almeida, Luiz H. S. Gasparotto, Nerilso Bocchi, Romeu C. Rocha-Filho, etal.Galvanostatic Pb(II) removal from a simulated wastewater by using a stainless-steelwool cathode in a flow-through cell: a factorial-design study[J].J. Appl Electrochemistr,2008,38:167~173
    [163] Manuela E Pintado, F. Xavier Malcata.Optimization of modified atmosphere packagingwith respect to physicochemical characteristics of Requeijao[J].Food Res Interat,2000,33:821~832
    [164] Bahar Meryemo lua, Arif Hasano lu.Hydrogen production from aqueous-phase reformingof sorghμm biomass: An application of the response surface methodology[J].RenewableEnergy,2014,62:535~541
    [165] Sushma Thakur, D. C Saxena.Formulation of extruded snack food (gμm based cereal-pulse blend): optimization of ingredients levels using response surfacemethodology[J].LWT-Food Scienc Technolog,2000,33:354~361
    [166] I.A.W. Tan, A.L. Ahmad, B.H. Hameed.Optimization of preparation conditions foractivated carbons from coconut husk using response surface methodology[J].Chem. Eng.J.,2008,137:462~470
    [167] Guang Chena,Jun Lic,Zhiwei Sunc,et al.Rapid and sensitive ultrasonic-assistedderivatisation microextraction (UDME) technique for bitter taste-free amino acids (FAA)study by HPLC–FLD[J].Food Chemistry,2014,143:97~105
    [168] Shinkichi Shimizu, Nanao Watanabe, Toshiaki Kataoka, et al.Pyridine and PyridineDerivatives in Ullmann's Encyclopedia of Industrial Chemistry[M].New York:John Wiley&Sons,2007
    [169] Donald J Berry, Charles V Digiovanna, Stephanie S Metrick,et al. Catalysis by4-dialkylaminopyridines [J].Arkivoc.,2001,3:201~226
    [170] I.Held,P.von den Hoff,D. S. Stephenson,et al.Domino Catalysis in the DirectConversion of Carboxylic Acids to Esters[J].Adv. Synth. Cat.,2008,11:1891~1900
    [171] Ryan P. Wurz.Chiral.Dialkylamine Catalysts in Asymmetric Synthesis[J].Chem. Rev.,2007,107:5570~5595
    [172]蔡广乐.苯酚乙氧基化反应及乙醛酸合成方法的研究[硕士论文].沈阳:沈阳理工大学,2008
    [173]马德垺,顾树珍.用分子筛催化剂液相合成乙酸丁酯[J].石油化工,1989,18(7):431~436
    [174]蓝丽红,闫瑞一,李媚,等.阳离子交换膜催化合成乙酸丁酯动力学研究[J].离子交换与吸附,2006,22(2):168~174
    [175] Xing H B. Wang T. Zhou Z H, et al. Novel Bronsted-acidic ionic liquid for esterification[J].Industrial&Engineering Chemistry Research,2005,44:4147~4150
    [176]傅献彩,沈文霞,姚天扬,等.物理化学:下册.第5版[M].北京:高等教育出版社,2006.197~200
    [177] Smith. J.M..Chemical Engineering Kinetics.3rd edn[M].New York: McGraw-Hill,1981,82~91
    [178] H.Buchowski, A. Ksiazczak, K. Pietrzyk.Solvent activity along a saturation line andsolubility of hydrogen-bonding solids[J].J. Phys. Chem.,1980,84:975~979
    [179] A.Ksiazczak, J. Kosinski.Vapor pressure of binary three-phase (s-l-v) systems andsolubility[J].Fluid Phase Equilib,1988,44:211~219
    [180] A.Ksiazczak, K. Moorthi, I. Nagata. Solid-solid transition and solubility of evenn-alkanes[J].Fluid Phase Equilib,1994,95:15~29
    [181] Y. Bao, J. Wang, Y. Wang, et al.The Measurement and Correlation of Solubility ofSpectinomycin Dihydrochloride in Pure Water and Acetone-water Mixture[J].J. Chem.Eng. Chin. Univ.,2003,17:457~461
    [182] J. Zi, B. Peng, W. Yan.Solubilities of rutin in eight solvents at T=283.15,298.15,313.15,323.15, and333.15K[J].Fluid Phase Equilib,2007,261:111~114
    [183] A.Apelblat, E.Manzurola. Solubilities of l-aspartic, dl-aspartic, dl-glutamicp-hydroxybenzoic, o-anistic, p-anisic, and Itaconic Acids in Water from T=278K to T=345K[J].J. Chem. Therm.,1997,29:1527~1533
    [184] A.Apelblat, E.Manzurola. Solubilities of o-acetylsalicylic,4-aminosalicylic,3,5-dinitrosalicylic, and p-toluic acid, and magnesiμm-DL-aspartate in water from T=(278to348) K[J].J. Chem. Therm.,1999,3l:85~91
    [185] E. Manzurola, A. Apelblat.Solubilities of L-glutamic acid,3-nitrobenzoic acid, p-toluicacid, calciμm-L-lactate, calciμm gluconate, magnesiμm-DL-aspartate, and magnesiμm-L-lactate in water[J].J. Chem. Therm.,2002,34:l127~l136
    [186] C.L. Zhang, F.A. Wang, Y. Wang. Solubilities of Sulfadiazine, Sulfamethazine,Sulfadimethoxine, Sulfamethoxydiazine, Sulfamonomethoxine, Sulfamethoxazole, andSulfachloropyrazine in Water from (298.15to333.15) K[J].J. Chem. Eng. Data,2007,52:1563~1566
    [187] Y.X. Mo, L. P. Dang, H. Y. Wei.Solubility of α-form and β-form of l-glutamic acid indifferent aqueous solvent mixtures[J].Fluid Phase Equilib,2011,300:105~109
    [188] P. Wang, J. K. Wang, J. B. Gong, M. J. Zhang.Determination of the solubility, dissolutionenthalpy and entropy of Deflazacort in different solvents[J].Fluid Phase Equilib,2011,306:171~174
    [189]何曼君,张红东,陈维孝,董西侠.高分子物理[M].上海:复旦大学出版社,2006
    [190] J.M.Prausnitz, R.N.Lichtenthaler, E.G. Azevedo. Molecular Thermodynamics ofFluid-Phase Equilibria.3rd ed[M].Prentice Hall:Upper Saddle River,1999.645~647
    [191] A.F.M. Barton. CRC Handbook of Solubility Parameters and Other CohesionParameters.2nd ed[M].Boca Raton:CRC Press,99~148
    [192] Tondeur, Carole, Riess. Polymers functionalized with amino acids or aminosynthesizing same, and use thereof as surfactants in cosmetic compositions, particularlynail varnishes[P].U S Patent,5958385,1999
    [193] Huybrechts, Jozef.Graft copolymer with a urea or imid functional group as pigmentdispersant[P].U S Patent,5852123,1998
    [194] Quednau P H.Dispersing agents, their use and solids coated therewith[P].U S Patent,5399294,1995
    [195] Campbell, Frederick, Schofield, at al. Surfactant products of poly (hydroxy-alkancarboxylic acid) phosphate esters[P].U S Patent,5300255,1994
    [196] Schofield, John D. Dispersion[P].U S Patent,4954177,1990
    [197] Haubennestel, Karlheinz, Kramp, et al.Addition compounds, suitable as dispersing agents,processes for their preparation, their use and solids coated therewith[P].U S Patent,4762752,1988
    [198] Hutchins, Clyde S, Shor, at al.Acrylic pigment dispersants made by group transferpolymerization[P].U S Patent,4656226,1987
    [199]贾振宇.分散剂丙烯酸丁酯/丙烯酸共聚物的制备和应用[J].精细石油化工进展,2006,7:1~4
    [200]公瑞煜,李建蓉,王洛礼等.聚羧酸型梳状共聚物超分散剂的构性关系[J].化工学报,2002,53(11):1143~1147
    [201] FrallkN.Jones.Polymeric materials with acid end groups[P].U S Patent,4070388,1978
    [202] Junfeng Zhua,Guanghua Zhang,Zhuo Miao et al.Synthesis and performance of acomblike amphoteric polycarboxylate dispersant for coal–water slurry[J].Colloids andSurfaces A: Physicochemical and Engineering Aspects,2012,42(5):101~107
    [203] F. Touaitia,P. Alama,R. Nilssonb,et al.Thermomechanical properties of CaCO3-latexpigment coatings: Impact of modified dispersing agents[J].Progress in Organic Coatings,2013,76(2):439~446
    [204] Jianzhong Ma,Yihong Liu,Yan Bao,et al.Research advances in polymer emulsion basedon “core–shell” structure particle design[J].Advances in Colloid and Interface Science,2013,197:118~131
    [205] S.M. Burkinshaw,G. Salihu.The wash-off of dyeings using interstitial water. Part4:Disperse and reactive dyes on polyester/cotton fabric[J].Dyes and Pigments,2013,99(3):548~560
    [206]潘祖仁等.高分子化学.第3版[M].北京:化学工业出版社,2003
    [207] Veronique M.B. Moloney, David Parris, Mohan J. Edirisinghe. Rheology of zirconiasuspensions in a nonpolar organic mediμm[J].J. AM. Ceram. Soc.,1995,78:3225~3232
    [208] Zaman A A, Tsuchiya R, Moudgil B M.Adsorption of a low-molecular-weight polyacrylicacid on silica, alμmina, and kaolin[J].J. Colloid Interf Sci.,2002,256:73~78
    [209] Marco P, Llorens J.Surface charge and rheological properties of raw porcelain gressuspension with acrylic copolymers bearing carboxylic groups[J].J. Eur Ceram Soc.,2009,29:559~564
    [210] Y.Y. Won, Steve P. Meeker, Veronique Trappe, David A. Weitz.Effect of Temperature onCarbon-Black Agglomeration in Hydrocarbon Liquid with AdsorbedDispersant[J].Langmuir,2005,21:924~932
    [211] Nojirl M, Hasegawa H, Ono T, et al.Influence of molecular structure of anionic polymerdispersants on dense silicon carbide suspension behavior and microstructures of greenbodies prepared by slip casting[J].J. Ceram. Soc. Jpn.,2003,111:327~332
    [212] Herbert Hommer.Interaction of polycarboxylate ether with silica fμme[J].J. Eur. Ceram.Soc.,2009,29:1847~1853
    [213] Ane M. Kjeldsen, Robert J. Flatt, Lennart Bergstr m.Relating the molecular structure ofcomb-type superplasticizers to the compression rheology of MgO suspensions[J].CementConcrete Res.,2006,36:1231~1239
    [214] Langmuir I. The adsorption, mica and platinμm[J].J. Am. Chem. Soc.,1918,40:1361~403.
    [215] Leechart P, Nakbanpote W, Thiravetyan P.Application of ‘waste’ woodshaving bottom ashfor adsorption of azo reactive dye[J].J. Envr. Mang.,2009,90:912~920
    [216] Freundlich H.M.F.Adsorption in L sungen. Zeitschrift für[J].Physikalische Chemie.,1906,57:385~470
    [217] Tsai, W.T., Lai, C.W., Hsien, K.J.Effect of particle size of activated clay on the adsorptionof paraquat from aqueous solution[J].J. Colloid Interf. Sci.,2003,263:29~34
    [218] Al Duri B, McKay G.Basic dye adsorption on carbon using a solid phase diffusionmodel[J].Chem. Eng. J.,1988,38:23~31
    [219] Treybal R. E.Mass transfer operations.Third Edition[M].New York:McGrawHill,1987
    [220] Gordon McKay.Use of adsorbents for the removal of pollutants from wastewaters[M].New York:CRC Press,1996.133~173
    [221] Wu CH.Adsorption of reactive dye onto carbon nanotubes: equilibriμm, kinetics andthermodynamics[J].J. Hazardous Materials,2007,144:93~100
    [222] Redlich O.,Peterson D.L.A useful adsorption isotherm[J].J. Phys. Chem.,1959,63:1024~1025
    [223] Altug Mert Sevim, Rustam Hojiyev, Ahmet Gül, Mehmet Sabri Celik.An investigation ofthe kinetics and thermodynamics of the adsorption of a cationic cobalt porphyrazine ontosepiolite[J].Dyes and Pigments,2011,88:25~38
    [224] Tempkin MJ, Pyzhev V.Kinetics of ammonia synthesis on promoted iron catalysts[J].Acta.Physiochimica USSR,1940,12:217~222
    [225] F. Molenaar.Adsorption studies of associative interactions between thickener and pigmentparticles[J].Progress in Organic Coatings,1997,30:167~171
    [226] W.K. Wijting,J.Laven,R.A.T.M. van Benthem,et al.Adsorption of ethoxylated styreneoxide and polyacrylic acid and mixtures there of on organic pigment[J].Journal of Colloidand Interface Science,2008,327:1~8
    [227] W.K. Wijting,J.Laven,R.A.T.M. van Benthem,et al.Adsorption of ethoxylated styreneoxide and polyacrylic acid and mixtures there of on organic pigment[J].J. Colloid andInterface Science,2008,327:1~8
    [228] Weihua Zou,Hongjuan Bai,Shuaipeng Gao.Characterization of modified sawdust, kineticand equilibriμm study about methylene blue adsorption in batch mode[J].Korean J. Chem.Eng.,2013,30(1):111~122
    [229] Weihua Zou,Lei Zhao,Lu Zhu.Efficient uraniμm(VI) biosorption on grapefruit peel:kinetic study and thermodynamic parameters[J].J. Radioanal Nucl Chem,2012,292:1303~1315
    [230] Helfferich. Ion exchange[M].New York:McGraw Hill,1962
    [231] M. Kara, H. Yuzer, E. Sabah, M.S. C elik.Adsorption of cobalt from aqueous solutionsonto sepiolite[J].Water Res.,2003,37:224~232
    [232] Y.S. Ho, G. McKay.Sorption of dyes and copper ions onto biosorbents[J].ProcessBiochem.,2003,38(7):1047~1061
    [233] Toshikatsu Kobayashi.Pigment dispersion in water-reducible paints[J].Progress in organiccoatings,1996,28(2):79~87
    [234] Donnet JB. Structure and reactivity of carbons: From carbon black to carboncomposites[J].Carbon,1982,20(4):267~282
    [235] Norio Tsubokawa. Functionalization of Carbon Material by Surface Grafting ofPolymers[J].Bulletin of the Chemical Society of Japan,2002,75(10):2115~2136
    [236] WB Ding,L Wang,Q Yang,et al.Recent Research Progress on Polymer Grafted CarbonBlack and Its Novel Applications[J].International Polymer Processing,2013,28(2):132~142
    [237] Kang Uk Lee,Kyung Ju Park,Oh Joong Kwon,et al.Preparation of the carbon spherecoated with iron oxide and its application for electronic paper[J].Deys and pigments,2014,102:22~28
    [238] L. Zhao,W.L. Liu,L.D. Zhang,et al.Fabrication of superhydrophobic and conductivesurface based on carbon nanotubes[J].Colloids and Surfaces A: Physicochemical andEngineering Aspects,2013,423:69~76
    [239] HayakawaM.,MitnaiM.,Yamada.T.Living ring-opening Polymerization of lactones usingcationic zirconocene complex catalysts[J].Macromol.Chem.Phys,1997,198:1305~1317
    [240] Kricheldorf H.R,Dennis Langanke.Polylactones54:ring-opening and ring-expansionpolymerizations of caprolactone initiated by germaniμm alkoxides[J].Poylmer,2002,43:1973~1977
    [241] Sanda.F,SanadaH.,Shibasaki Y,EndoT.Star polymer synthesis from epsilon-caprolactoneutilizing polyol/protonic acid initiator[J].Macromolecules,2002,35:680~683
    [242] LouX.D.,Detrembleur C.,Jerome R.Living cationic polymerization of delta-valerolactoneand synthesis of high molecular weihgt homopolymer and asymmetric telechelic and blockcopolymer[J].Macromolecules,2002,35:1190~1195
    [243] Shibaskai.Y,SandaF.,Endo.T.Acid-promoted living ring-opening polymerization of cycliccarbonates with B(OR)3[J].Macromolecules,2000,33:3630~3633
    [244] NomuraN.,Taira A.,Tomioka.T,Okada.A catalytic approach of cationic livingpolymerization:Sc(OTf)3-catalyzed ring-opening polymerization oflactones[J].Macromolecules,2000,33:1497~1499
    [245] YoshidaE.,Osagawa Y.Synthesis of poly(caprolactone) with a stable nitroxyl radical as anend-functional group and its application to a counter radical for living radicalpolymerization[J].Macromolecules,1998,31:1446~1453
    [246] BalsamoV,Von Gyldenfeldt F.,Stadler R.Synthesis of SBC,SC and BC block copolymersbased on polystyrene (S),Polybutadiene (B) and a crystallizable Poly(caprolactone)(C)block[J].Macromol.Chem.Phys.,1996,197:1159~1169
    [247] Sepulchre M., Dougres MA.NeblaiM. Nucleophile-initiated and thermal bulkpolymerizations of cyclic trimethylene carbonate in the absence of addedcatalysts[J].Macromol.Chem.Phys.,2000,201(13):1405~1414
    [248] Namekawa S., Suda S., Uyama H, Kobayashi S. Lipase-catalyzed ring-openingpolymerization of lactones to polyesters and its mechanisticaspects[J].Int.J.Biol.Macromol,1999,25:145~151
    [249] AL Azemi T.F.,Harmon J.P,Bisht K.S.Enzyme-catalyzed ring-opening copolymerizationof5-methyl-5-benzyloxycarbonyl-l,3-dioxan-2-one (MBC) with trimethylene carbonate(TMC):synthesis and characterization[J].Biomacromoleculesl,2000:1(3):493~500
    [250] Kricheldor H.R., Stricke A. Polymers of carbonic acid29. Bu2Sn(oct)2-initiatedpolymerizations of trimethylene carbonate (TMC,l,3-dioxanone-2)[J].Polymer,2000,41:7311~7320
    [251] Matsuda.T, Mizutani M., Arnold S.C. Molecular design of photocurable liuqidbiodegradable copolymers Synthesis and photocuring characteristics [J].Macromolecules,2000,33:795~800
    [252] Kumar A.,Garg K.,Gross R.A.Copolymerizations of pentadecalactone and trimehtylenecarbonate by chemical and lipase catalysis[J].Macromolecules,2001,34:3527~3533
    [253] Yasuda H.Organo-earth-metal initiated living polymerizations of polar and nonpolarmonomers[J].J.of Organomet.Chem.,2002,647:128~138
    [254] Ling J.,Shen Z.Q.Lanthanμm tis(2,6-di-tert-buytl-4-mehtylphenolate) as a novel,versatileinitiator for homo and copolymerization of cyclic carbonates and lactones[J].Macromol.Chem.phys.,2002,203:735~738
    [255] Albertsson A.C.,Varma I.K.Recent developments in ring opening polymerization oflactones for biomedical applications[J].Biomacromolecules,2003,4:1466~1486
    [256]胡合贵,戚国荣,李新华,等.马来酸酐与十八醇酯化反应研究[J].高校化学工程学报,1999,13(5):466~469
    [257] Mingjie Chen,Chaoyi Chen,Chuanfu Liu.Homogeneous modification of sugarcanebagasse with maleic anhydride in1-butyl-3-methylimidazoliμm chloride without anycatalysts[J].Industrial Crops and Products,2013,46:380~385
    [258] Paula Mazoa,Luis Rios,Diana Estenoz.Self-esterification of partially maleated castor oilusing conventional and microwave heating[J].Chemical Engineering Journal,2012,185-186:347~351
    [259] Smith P.G.Effect of surface hydrophilicity on charging mechanism of colloids inlow-permmittivity solvents[J].Journal of physical chemistry,2007,111(2):840~848
    [260] Green J.H.Stability of concentrated colloidal dispersions in apolar media[J].ParticulateScience and Technology,1987,5(3):289~299
    [261] Tabor R.F.Formation of surfactants-stabilized silica organosols[J].Langmuir,2008,24(22):12793~12797
    [262] Krishnakumar S.Adsorption of Aerosol-oT on graphite from aqueous and non-aqueousmedia[J].Collids and surface A Pysicochemical and Engineering Aspcects,1996,117(3):227~233

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700