新型纳米钒酸铋黄色颜料的制备与性能研究
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摘要
本文采用前驱体煅烧法和粉末煅烧法制备了纳米钒酸铋黄色颜料,并在前驱体煅烧法的基础上,添加CaCO_3、CaF_2、Al(OH)_3、MgO制备复合型钒酸铋颜料。通过X射线衍射分析(XRD)、热分析、傅立叶变换红外光谱(FT-IR)、电子显微分析等对纳米钒酸铋黄色颜料及复合型钒酸铋黄色颜料进行了表征。
     以Bi(NO_3)_3·5H_2O和NH_4VO_3为原料,利用前驱体煅烧法制备了BiVO_4黄色颜料,并系统地研究了不同反应条件如反应物浓度、溶液pH值、反应温度、反应时间、煅烧温度、煅烧时间对产物的影响,同时也研究了表面活性剂的种类和剂量对产物形貌、晶型结构、色相的影响。而在粉末煅烧法中主要研究了煅烧温度、煅烧时间、研磨、矿化剂的添加等制备工艺条件;并对两种方法制备的钒酸铋黄色颜料着色性能、热稳定性能和红外吸收性能进行了比较。研究结果表明:前驱体煅烧法可制备出颜色鲜亮、粒径分布均匀、平均粒径为15-30nm具有单斜晶系白钨矿结构的钒酸铋黄色颜料,加入表面活性剂DBS可改善颜料的分散性;粉末煅烧法制备的钒酸铋黄色颜料色泽偏暗,颗粒粒径要大,平均粒径大约在40-50nm左右,分散性较差。粉末煅烧法中CaF_2、H_3BO_3矿化剂的引入提高了产物的结晶度,产物的粒径也有所减小,颜料的色相也有所变化。两种方法制备的钒酸铋黄色颜料均有较好的热稳定性,红外吸收性能没有明显变化,但着色性能不同,前驱体煅烧法制备的钒酸铋黄色颜料着色力较强。
     在复合型钒酸铋颜料的研究中,通过添加CaCO_3、CaF_2、Al(OH)_3、MgO对钒酸铋黄色颜料改性,研究了不同物质及同种物质不同浓度对钒酸铋黄色颜料的晶体结构、热稳定性能、着色性能和红外吸收性能的影响。研究表明:复合型钒酸铋黄色颜料仍为单斜晶系白钨矿结构,具有比较好的热稳定性;添加不同物质可制备色相不同的钒酸铋黄色颜料,颜色可从黄相偏绿到黄相偏红,并且在添加同种物质条件下,随着添加量的增加,着色力有一定的变化。
In this paper,nano-BiVO_4 yellow pigments were prepared by the method of precursor calcined and the ceramic method.On the basis of the method of precursor calcined,composite BiVO_4 yellow pigments were prepared by doping CaCO_3,CaF_2,Al(OH)_3,MgO respectively. Additionally,nano-BiVO_4 yellow pigments and composite BiVO_4 yellow pigments were charactered by using XRD,thermal analysis technology,FT-IR and electron microscopy analysis and so on.
     Using Bi(NO_3)_3·5H_2O and NH_4VO_3 as raw materials,BiVO_4 yellow pigments were prepared by the method of precursor calcined.The influence of reaction concentration,the value of pH,reaction temperature,reaction time,calcining temperature and calcining time on the crystal morphology,particle size,color and distribution were investigated,including the kind of and the dose of surfactants.Furthermore,the preparation conditions of calcining temperature,calcining time,rubbing and mineralizations which including the categories and the dose were studied the ceramic method.For this two methods,the coloring,thermal stability and infrared absorption properties of BiVO_4 yellow pigments were discussed.The results show that the monoclinic BiVO_4 yellow pigments with bright color,uniform distribution and the average size between 15nm and 30nm were obtained by the method of precursor calcined.And the dispersion of BiVO_4 yellow pigments can be improved by adding surfactant DBS.However,the monoclinic BiVO_4 yellow pigments with dim color,poor distribution and the average size between 40nm and 50nm were obtained by the ceramic method.The degree of the monoclinic BiVO_4 yellow pigments' crystallization was improved, and the particle size was smaller,and the color was changed at a certain extent by adding the mineralizations such as CaF_2 and H_3BO_3 through the ceramic method.Compared to the ceramic method,the BiVO_4 yellow pigments which were prepared by the method of precursor calcined have a brighter color.The BiVO_4 yellow pigments which were prepared by the two methods have a better thermal stability and have unconspicuous change of infrared absorption. BiVO_4 yellow pigments were modified by doping CaCO_3,CaF_2,Al(OH)_3,and MgO.The effects of different substance and substance with different concentrations on the crystal structure,thermal stability,color performance and infrared absorption of BiVO_4 yellow pigments were investigated.The researches show that composite BiVO_4 yellow pigments have a monoclinic crystal structure and a better thermal stability.And the BiVO_4 yellow pigments with different hues were prepared by doping different substance.The pigment color can be changed from yellow with a little red to yellow with a little green.Moreover,with the doping dosage increasing,the color performance has changed under the condition of doping same substance.
引文
[1]朱骥良,吴申年.颜料工艺学.第二版.北京:化学工业出版社,2002
    [2]杨宗志.新型无机黄色颜料—铋黄.化工新型材料,1996,8:23-25
    [3]王云燕,秦毅红.新型无机黄色颜料.涂料工业,1999,3:38-40
    [4]Bayer AG.Bismuth vanadate pigments,a process for their preparation and their use.US,5203917.1993
    [5]Reid,A.F.;Ringwood,A.E.Newly observed high pressure transformations in Mn_3O_4,CaAl_2O_4 and ZrSiO_4,Earth Planetary Lett.1969,6,205-208
    [6]Spear,J.A.Reviews in Minearlogy,vol.5,2nded.,Min.Soc.America,Washington,DC,1982,Chapter3.67-112
    [7]Leo J H Erkens et al.The Bulletin of the Bismuth Institute,1997,(70):1
    [8]Endriss H.Bismuth vanadata pigment in coating materials.Farbe Lack,1994,100(6):397-398
    [9]王云艳,秦毅红.新型黄色无机颜料——铋黄.涂料工业.1999(3):38-40
    [10]Smith,H.M.High Performance Pigments,Wiley-VCH Verlag-GmbH,Weinheim,Germany,2002
    [11]孙继红,范文浩,吴东等.溶胶-凝胶(sol-gel)化学及其应用.材料导报.2000,14(4):25
    [12]Yang C,Shih W Y.Effects of boehmite coating thickness on theconsolidation and rheological properties of boehmite coated SiC suspensions.J Am Ceram Soc.2001,84(12):2834-2840
    [13]邵庆辉,古国榜,张莉娟.微乳化技术在纳米材料制备中的应用研究.化工新型材料.2001,29(7):9
    [14]田玉明,黄平,冷叔炎.沉淀法的研究及其应用现状.材料导报.2000,14(2):48
    [15]Plaza R,Duran J,Quirantes et al.Surface chemical analysis and electrokinetic properties of spherical hematite particles coated with yttrium compounds.J Colloid Interface Sci,1997,194:398-407
    [16]张汝冰,刘宏英,李凤生.复合纳米材料制备研究Ⅱ.火炸药学报,2000,19(1):95
    [17]Alexandria,Virginia.DCMA Classification and Chemical Description of the Complex Inorganic Color Pigments.Dry Color Manufacturers'Association,1991,21(1):54-58
    [18]李凤生,宋洪昌,顾志明,等.超细粉体技术.第一版.北京:国防工业出版社,2000.128-129
    [19]Balducci,L.GE2940185
    [20]Ciba-Geigy A.G.EP443981.1991-08-28
    [21]Ciba-Geigy Corporation.Process for preparing bismuth vanadate pigments.US,5399335.1995
    [22]Schwochow Friedrich,Hill Rudolf Preparation of Yellow Bismuth Vanadate Pigment.德国专利,DE4119668.1992-12-17
    [23]Liedek,Knittel,Helmut et al.德国专利,DE200925
    [24]Vermoortebe,Frank.比利时专利,529653
    [25]杨南如.无机非金属材料测试方法.武汉:武汉理工大学出版社,2004.187-188
    [26]金伟其,胡威捷.辐射度、光度与色度及其测量.北京:北京理工大学出版社,2006:112-117
    [27]邓勃,王庚辰.分析仪器与仪器分析概论.北京:化学工业出版社,2005.84-85
    [28]邓芹英,刘岚,邓慧敏.波谱分析教程.第二版.北京:科学出版社,2007.45
    [29]王蕾,靖丽丽,高春香,张静.扫描电子显微镜在无机材料分析中的应用.当代化工,2007,(36)3:318-320
    [30]GB 5211.19-88
    [31]许秀莲,唐冠中.用氯氧化铋制备铋黄颜料的研究.南方冶金学院学报.1997.03:47-49
    [32]Li Y D,Li X L,Deng Z X,et al.Angew.Chem.Int.ED.,2002,41(2):333-335
    [33]Liu S W,Yue J,Gedanken A.Adv.Mater.,2001,13(9):656-558
    [34]Yu J Q,Kudo A.Chem.Lett.,2005,34(6):850-851
    [35]Zhang L,Chen D R,Jiao X L.J.Phys.Chem.B,2006,110(6):2668-2673
    [36]梁治齐,宗惠娟,李金华.功能性表面活性剂.北京:中国轻工业出版社,2002,107-113
    [37]肖进新,赵振国.表面活性剂应用原理.北京:化学工业出版社,2003,291-304
    [38]Wood P,Glasser F P.Ceramics International,2004,30:875
    [39]周学良.颜料.北京:化学工业出版社,2002,275-278
    [40]张克立.固相无机化学.第二版.湖北:武汉大学出版社,2006
    [41]李伟洲,李少波.钒酸铋颜料的研制.贵州化工,2003,28(1):21-26
    [42]孙蓓,高雅春.铬钇铝红色料中矿化剂的研究.陶瓷,2006,1:40~42
    [43]张萍,次立杰,张星辰等.钒酸铋黄色颜料的制备及其影响因素.石家庄学院学报,2006,8(6):9-11
    [44]魏坤,何地宝,翟建伟.沉淀法制备稀土氧化物纳米粉体的研究.稀土,1999,20(4):27-30
    [45]王春秀,李福利.纳米晶La_2O_3的制备及其红外吸收特性的研究.光谱学与光谱分 析,2006,26(5):846-849
    [46]陆佩文.硅酸盐物理化学.江苏:东南大学出版社,1991
    [47]US Patent 5,152,292.1992-10-06
    [48]US Patent 4,261,032.1981-04-07
    [49]朱振峰.Ce_(1-x)Pr_xO_2纳米晶粉体的制备及其结构与性能的研究.陕西科技大学,2007
    [50]贾锐军,彭同江,孙红娟,刘海峰.添加Ni~(2+)金红石型SnO_2纳米粒子的制备及表征.精细化工.2008,25(1):1-4
    [51]陈敬中.现在晶体化学--理论与方法.第一版.北京:高等教育出版社,2001
    [52]杨萍,赵家昱.硒化锌基颜料的研究.硅酸盐通报,1998,2:22-25
    [53]张阳.溶胶沉淀法合成硅酸锆包裹硫硒化镉颜料的研究.湘潭大学,2006
    [54]刘进,吴绍华,兰尧中.新型材料铋黄的研究进展.涂料技术与文摘,2004,6(25):6-9
    [55]邓芹英,刘岚,邓慧敏.波谱分析教程.第二版.北京:科学出版社,2007
    [56]黄继武.MDI Jade使用手册.湖南:中南大学,2006
    [57]Jobic Stephane.Synthesis methods and properties of Bi-V oxide pigment,I.M.N,France,1999,5:12
    [58]Mitsutake Oshikiri,Mauro Boero.Water Molecule Adsorption Properties On the BiVO_4(100) Surface.National Institute for Material Science.Japan,2006,9188-9194
    [59]Lin Zhou,Wenzhong Wang,Lisha Zhang et al.Single-Crystalline BiVO_4 Microtubes with Square Cross-Sections:Mierostrueture,Growth Mechanism,and Photoeatalytic Property.State Key Laboratory of High Performance Ceramics and Superfine Microstructure.China,2007,111,13659-13664
    [60]张立.纳米钒酸铋黄色颜料的制备与应用研究.山东大学,2006
    [61]高文元,孙俊才.类钙钛矿结构La_2Ni_(0.5)M_(0.5)O_(4+δ)(M=CO,Cu)材料的合成与电性能.电源技术,2005,29(3):160-163
    [62]王涵,黄志良,刘羽.掺钡钨矿型CAWO_4:Ba~(2+)荧光材料的制备与表征.武汉工程大学学报,2008,30(2):78-81

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