用户名: 密码: 验证码:
利用粉煤灰合成沸石技术与吸附性能研究
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
本论文目的是研究以粉煤灰为原料合成沸石,主要开展了从沸石制备工艺、材料品质表征、重金属及碱性染料吸附性能、吸附机理、沸石吸附剂再生这一较为系统的研究。论文探讨了由粉煤灰合成沸石的影响因素,从结构、性能和应用指标方面对比了采用两种方法(两步法和碱熔融—水热法)合成沸石的品质,并通过吸附等温线模型、动力学、热力学研究,深入解析了沸石吸附剂对重金属和染料的吸附机理。最后对粉煤灰合成沸石的新方法也进行了初步研究。
     首先,采用由粉煤灰制备沸石的两步法和碱熔融—水热法,重点探讨了NaOH溶液浓度、NaOH与粉煤灰质量比、Si/Al摩尔比和合成时间对沸石的种类和结晶度的影响,并从结构、性能及其应用指标三个方面对比研究了合成沸石的品质。结果表明,以除铁粉煤灰为原料,采用两步法分别合成了纯结构的NaA和八面沸石(NaX和NaY型沸石),在3种NaOH溶液浓度(1.67 mol·L~(-1),5 mol·L~(-1)和6.67 mol·L~(-1))条件下,由粉煤灰制备的硅铝凝胶在100℃下分别经过5.5 h,4h和3 h晶化后可得到纯结构NaA型沸石。通过激光粒度仪和透射电镜表征,在5 mol·L~(-1)和6.67 mol·L~(-1)NaOH溶液浓度的条件下首次合成了纯结构的亚微米NaA型沸石,平均粒径分别为450 nm和250 nm,粒度分布范围分别为3.84和2.44。在3.33 mol·L~(-1)NaOH溶液浓度条件下,通过调节硅铝凝胶的SiO_2/Al_2O_3摩尔比为7.36,晶化合成24 h后获得纯结构的NaX型沸石。通过晶胞参数(α)和X射线荧光两种手段计算的SiO_2/Al_2O_3摩尔比值说明,由除铁粉煤灰合成纯结构的NaY型高硅八面沸石。对于碱熔融—水热合成法,在NaOH与粉煤灰的质量比为1.3,由粉煤灰制备的硅铝凝胶在100℃下经过24 h晶化后可由粉煤灰得到单一、结晶度完好的NaX型沸石;在此基础上,通过添加铝源调节硅铝凝胶的SiO_2/Al_2O_3摩尔比,晶化合成5 h后可获得单一、结晶度完好的NaA型沸石矿物种类。
     对采用两种方法(两步法和碱熔融—水热法)制备的NaA和NaX型沸石的品质(结构、性能及其应用指标)进行了详细表征,并与相应商品沸石作了对比。IR光谱分析表明合成产物具有相应的沸石骨架结构红外谱峰;DTA分析表明了合成产物中沸石水的存在,且产物稳定性较好;通过比较化学组成表明,大规模应用合成产物不会对环境造成危害;比表面积、孔容和CEC的比较说明,合成产物的性能和各项应用指标均接近于商品沸石,具有良好的工业潜在应用价值。此外,除铁前后合成产物的CEC表明:粉煤灰除铁有利于沸石产物的合成。
     静态吸附条件下,两步法合成NaA型沸石吸附三种重金属(Cu(Ⅱ)、Cr(Ⅵ)和Zn(Ⅱ))的动边界模型研究表明,Cu(Ⅱ)和Zn(Ⅱ)离子的吸附过程主要由液膜扩散控制,而Cr(Ⅵ)离子的吸附过程主要由颗粒扩散控制,三种重金属离子的吸附过程都符合二级动力学速率方程。NaA型沸石对三种重金属离子的吸附等温线更加符合Langmuir模型,静态饱和吸附量分别为82.30,65.96和47.78 mg·g~(-1)。解吸与再生实验表明,Cu(Ⅱ)和Zn(Ⅱ)离子的解吸效果较好,有利于重金属的回收及沸石吸附剂的再生重复利用。NaA型沸石对Cu(Ⅱ)和Zn(Ⅱ)离子的吸附机理主要是金属氢氧化物沉淀和离子交换吸附,而对Cr(Ⅵ)离子的吸附机理主要是氢键作用和沸石吸附。
     静态吸附条件下,对于碱熔融—水热法合成NaA和NaX型沸石矿物吸附MB染料而言,MB染料的吸附过程主要由膜扩散和颗粒内扩散联合控制,一级、二级动力学速率方程吸附速率方程拟合结果显示,两种沸石吸附剂对MB染料的吸附则更符合二级动力学速率方程。在Langmuir和Freundlich模型中,它们对MB染料吸附的更符合Langmuir等温线模型,且MB染料在NaX型沸石上的静态饱和吸附量均大于NaA型沸石,热力学参数(焓ΔH、熵ΔS和ΔG)表明,一方面,它们对染料的吸附主要为吸热过程;另一方面,染料的吸附是一种自发过程。本文以初始pH值、温度和沸石用量为考察因素,研究了原始和再生吸附剂对MB染料去除率的影响,发现随着初始pH值、沸石用量和吸附温度的增大,MB染料的去除率增大,焙烧再生后的沸石矿物吸附剂对MB染料的吸附性能略低于原始吸附剂。NaA和NaX型沸石矿物对MB染料的吸附机理为,通过静电引力、氢键、n-π作用及范德华力吸附MB染料分子,其中,静电引力与氢键作用起主要作用。
     本文提出了新工艺及新方法以补充和发展由粉煤灰合成沸石的研究领域。主要包括:一是基于传统一步合成法,以熔融粉煤灰和脱硅粉煤灰为原料,考察NaOH溶液浓度和晶化时间对合成沸石矿物种类和结晶度的影响。结果显示,合成产物以NaA、NaP和HS型三种沸石矿物类型为主,另外有少量菱沸石生成。二是在F~-离子体系下的同步抽取法,采用NaOH溶液同步抽取脱硅粉煤灰中硅铝成分;而后利用HF酸调节溶液的pH值;最后在F~-和OH~-离子共存的体系中水热合成沸石。实验结果表明,应用此新方法,可由脱硅粉煤灰合成了纯结构的NaA-NaX-HS型混合沸石相。
The research objective of this dissertation is to investigate synthesis process of zeolites from fly ash(FA).The systemic investigations are performed about zeolites synthesis method,materials quality characterization,heavy metal ions/dye adsorption mechanism and adsorbents regeneration.The influential factors on zeolites synthesis were discussed and the qualities of zeolites synthesized from FA by two-step and alkaline fusion methods were compared from structure,performance and application target points of view.Based on adsorption isotherms,kinetic and thermodynamic studies,the adsorption mechanism of heavy metal ions and dye on synthetic zeolites was analyzed.Finally,the pilot study was performed for new process and method of FA synthesized zeolites in this dissertation.
     In the first,two-step and alkaline fusion methods were adopted to synthesize zeolites from fly ash.Emphasis was put on investigate the influential parameters such as concentrations of NaOH solution,NaOH/FA ration(g/g),Si/Al molar ratio and synthesis time on the type and degree of synthetic zeolites and qualities of synthetic zeolites from structure,performance and application target points of view. Experimental results demonstrated,for two-step method,pure-form LTA(NaA zeolite) and FAU type zeolites(NaX and NaY zeolite) were syhtesized from pretreated-FA, respectively.Generally,pure-form NaA zeolite could be synthesized form FA prepared aluminosilicate gel when following conditions were used:NaOH concentrations,1.67,5 and 6.67 mol·L~(-1);the synthesis temperature,100℃;the corresponding synthesis time,5.5,4 and 3 h.By analysis of particle size measurements and TEM,pure-form submicron-NaA zeolites are firstly synthesized at the condition of 5 and 6.67 mol·L~(-1) NaOH solution,respectively.The average crystal size and size span of the products are 450 nm and 250 nm,3.84 and 2.44,respectively; pure-form NaX zeolite could be synthesized form FA prepared aluminosilicate gel when following conditions were used:NaOH concentrations,3.33 mol·L~(-1); SiO_2/Al_2O_3 molar ratios,7.36;the synthesis temperature,100℃;the corresponding synthsis time,24 h.The SiO_2/Al_2O_3 molar ratios calculated using lattice parameters (a_0) and XRF explained pure-form NaY zeolite could be synthesized from pretreated-FA.For alkaline fusion method,single-phase and high-crystalline NaX zeolite could be synthesized form FA prepared aluminosilicate gel when following conditions were used:NaOH/FA ratio,1.3;the synthesis temperature,100℃;the corresponding synthesis time,24 h.Based on above studies,single-phase and high-crystalline NaA zeolite could be synthesized form FA after 5 h,and with the addition of Al source,to adjust SiO_2/Al_2O_3 molar ratios of prepared aluminosilicate gel.
     The qualities of NaA and NaX zeolites synthesized from FA by two-step and alkaline fusion methods were characterized detailedly from structure,performance and application target points of view.The corresponding commercial grade zeolites were also investigated for comparison.Analysis of IR spectra corresponds to peaks of corresponding zeolitic structural formation.DTA curves indicate the presence of zeolitic water in the products and the products have better stabilization.The elemental composition shows that the products do not pose any serious threat to the environment when compare with commercial zeolites.The data of the surface area,pore volume and CEC(CEC,Cation exchange capacity) values show that the qualities of synthetic zeolites are near to the corresponding commercial grade zeolites.FA synthesized zeolites have the potential value of industrial applications.In addition,CEC values clearly illustrated that acid-washing process demonstrated a benefit effect on synthesis.
     With the static method,the adsorption peoformance of NaA zeolite(two-step) to three heavy metal ions(Cu(Ⅱ),Cr(Ⅵ),Zn(Ⅱ)) and NaA and NaX zeolites(fusion) to MB dye in aqueous solution was studied and the adsorption mechanism was discussed, respectively.
     For two-step method,Moving Boundary Model analysis shows that the adsorption rate of Cu(Ⅱ) and Zn(Ⅱ) ions was mainly governed by liquid film diffusion, and intra-particle diffusion is important controlling factor for the adsorption rate of Cr(Ⅵ) ion.The adsorption processes of three heavy metal ions follow a pseudo-second-order kinetic model.The equilibrium adsorption data fitted to Langmuir isotherms and the greatest adsorption capacity of Cu(Ⅱ),Cr(Ⅵ) and Zn(Ⅱ) is 82.30 mg/g,65.96 mg/g and 47.78 mg/g,respectively.The desorption and regeneration experiments showed that excellent desorption effect of Cu(Ⅱ) and Zn(Ⅱ) ions favor to recover heavy metal ions and regenerate adsorbents.The adsorption mechanisms of Cu(Ⅱ) and Zn(Ⅱ) ions were proposed as:metal hydrate precipitation and cation exchange reaction while the adsorption mechanisms of Cr(Ⅵ) ion were the common effect of hydrogen bond and adsorption.
     For alkaline fusion method,the step of MB dye adsorption was governed by liquid film diffusion with the experimental data mathematically described using liquid film diffusion,intraparticle diffusion and chemical reaction equations and the adsorption process followed pseudo-second-order model.The adsorption data correlated well with Langmuir equation.Thermodynamic parameters(ΔH,ΔS andΔG) revealed that the adsorption of MB dye is endothermic in nature and spontaneous process.It showed the removal performance of MB on original and regenerative adsorbents was dependent on these parameters such as initial pH value of the solution, temperature and adsorbent dosage.Generally,the removal efficiency of MB increased with a rise of initial pH value of the solution,temperature and adsorbent dosage. Regenerative adsorbents exhibited lower adsorption capacity compared to original adsorbents.And the adsorption mechanisms of MB dye were concluded as:adsorption by an electrostatic force,hydrogen bond,n-πinteraction and Van der Waals force,of which the electrostatic force and hydrogen bond were the main effects.
     In order to supplement and develop the fields of FA synthesized zeolites,the new synthesis process and method were studied in this dissertation.On the basis of this idea,we proposed two synthesis routes:one was the modified one-step method.
     The influential parameters such as concentrations of NaOH solution and synthesis time were investigated on the type and degree of synthetic zeolites from fusion FA and desilicated FA.The results showed that the products contain mainly NaA、NaX and HS zeolites with the trace of chabazite.The other was simultaneous extraction method in F~- ion.This method contains three steps:(1) NaOH solution simultaneous extraction Si and Al from desilicated FA;(2) adjust pH value of the solution by HF acid;(3) hydrothermal synthesis zeolites in concomitan F~- and OH~- ions system.
引文
[1]杨效益,张高勇,李秋小,王峰.4A沸石的生产和应用.日用化学工业,2003,33(1):33-35.
    [2]Grubb D G,Guimaraes M S,Valencia R.Phosphate immobilization using an acidic type F fly ash.J.Hazard.Mater.,2000,76(2-3):217-436.
    [3]Querol X,Moreno N,Uma(?)a J C,Alastuey A,Hern(?)ndez E,L(?)pez-Soler A.Synthesis of zeolites from coal fly ash:an overview.Int.J.Coal.Geol.,2002,50(1-4):413-423.
    [4]庆承松,任升莲,宋传中.电厂粉煤灰的特征及其综合利用.合肥工业大学学报,2003,26(4):39-43.
    [5]H(o|¨)ller H,Wirsching U.Zeolite formation from fly ash.Forchr.Miner.,1985,63:21-43.
    [6]竹蕾,卢升高,何黎平.火电厂粉煤灰的矿物学、形态与物理性质.科技通报,2004,20(4):359-362.
    [7]Qian J C.Glasser F P.Bulk composition of the glassy phase in some commercial PFA's.In:Mat Res Soc Symp Proc.2000,Vol113,p39-44.
    [8]庆承松,任升莲,宋传中.粉煤灰合成沸石中间体的表征与性质.合肥工业大学学报(自然科学版),2005,25(1):530-533.
    [9]Iyer R S,Scott J A.Power station fly ash-a review of value-added utilization outside of the construction industry.Resour.Conserv.Recy.,2001,31(3):217-228.
    [10]Shen D S,Zheng Y J.The use of ground fly ash for the production of cement or concrete.London:International Symposium.The use of PFA in Concrete.,1982,156-157.
    [11]陈昭宜.飞灰性质和它对环境的影响.上海环境科学,1982,(2):16-18.
    [12]http://www.solidwaste.com.cn.
    [13]Davis R E.Historial Acconnts of Mass Concrete.Symposium on Mass Concrete.1963,Indiana.
    [14]赵秀岩.石安高速路吃灰千万吨.中国环境报,1995.
    [15]Atis C D.Heat evolution of high-volume fly ash concrete.Cement.Concrete.Res.,2002,32(5):751-756.
    [16]Atis C D.High volume fly ash abrasion resistant concrete.J.Mater.Civ.Eng.,2002,14(3):274-277.
    [17]Atis C D,Celik O N.Relation between abrasion resistance and flexural strength of hing volume fly ash concrete.Mater.Struct.,2002,248(35):257-260.
    [18]Atis C D,Kilic A,Sevim U K.Strength and shrinkage properties of mortar containing a nonstandard high-calcium fly ash.Cement.Concrete.Res.,2004,34(1):99-102.
    [19]Demirbog R,Gul R.The effects of expanded perlite aggregate,silica fume and fly ash on the thermal conductivity of lightweight concrete.Cement.Concrete.Res.,2003,33(5):723-727.
    [20]Bouzoubaa N,Zhang M H,Malhotra V M.Mechanical properties and durability of concrete made with high-volume fly ash blended cements using a coarse fly ash.Cement.Concrete.Res.,2001,31(10):1393-1402.
    [21]Park H C,Park Y J,Stevens R.Synthesis of alumina from high purity alum derived from coal fly ash.Mat.Sci.Eng A-Struct.,2004,367(1-2):166-170.
    [22]Wang H J,Wang Y L.SiC powders prepared from fly ash.J.Mater.Process.Tech.,2001,117(1-2):52-57.
    [23]Cheng T W,Ueng T H,Chen Y S,Chiu J P.Production of glass-ceramic from incinerator fly ash.Ceram.Int.2002,28(7):779-783.
    [24]Park Y J,Moon S O,Heo J.Crystalline phase control of glass ceramics obtained from sewage sludge fly ash.Ceram.Int.,2003,29(2):223-227.
    [25]Panday K K,Prasad G,Singh V N.Copper(Ⅱ) removal from aqueous solutions by fly ash.Water.Res.,1985,19(7):869-873.
    [26]Apak R,Tutem E,Hugul M,Hizal J.Heavy metal cation retention by unconventional sorbents(red muds and fly ashes).Water.Res.,1998,32(2):430-440.
    [27]Shawabkeh R,Al-Harahsbeh A,Hami M,Khlaifat A.Conversion of oil shale ash into zeolite for cadmium and lead removal from wastewater.Fuel.,2004,83(7-8):981-985.
    [28]Ayala J,Blanco F,Garcia P,Rodriguez P,Sancho J.Asturian fly ash as a heavy metals removal material.Fuel.,1998,77(11):1147-1154.
    [29]Banerjee S S,Jayaram R V,Joshi M V,Removal of nickel(Ⅱ) and zinc(Ⅱ) from wastewater using fly ash and impregnated fly ash.Sep.Sci.Technol.,2003,38:1015-1032.
    [30]Bayat B.Combined removal of zinc(Ⅱ) and cadmium(Ⅱ) from aqueous solutions by adsorption onto high-calcium Turkish fly ash.Water.Air.Soil.Poll.,2002,136:69-92.
    [31]Banerjee S S,Joshi M V,Jayaram R V.Removal of Cr(Ⅵ) and Hg(Ⅱ) from aqueous solutions using fly ash and impregnated fly ash.Sep.Sci.Technol.,2004,39:1611-1629.
    [32]SenA K,De A K.Adsorption of mercury(Ⅱ) by coal fly ash.Water.Res.,1987,21(8):885-888.
    [33]Diamadopoulos E,Ioannidis S,Sakellaropoulos G.P.As(Ⅴ) removal from aqueous solutions by fly ash.Water.Res.,1993,27(12):1773-1777.
    [34]Pattanayak J,Mondal K,Mathew S,Lalvani S B.A parametric evaluation of the removal of As(Ⅴ) and As(Ⅲ) by carbon-based adsorbents.Carbon.,2000,38(4):589-596.
    [35]Viraraghavan T,Ramakrishna K R,Fly ash for color removal from synthetic dye solutions.Water.Qual.Res.J.Can.,1999,34:505-517.
    [36]Janos P,Buchtova H,Ryznarova M,Sorption of dyes from aqueous solutions onto fly ash.Water.Res.,2003,37(20):4938-4944.
    [37]Woolard C D,Strong J,Erasmus C R,Evaluation of the use of modified coal ash as a potential sorbent for organic waste streams.Appl.Geochem.,2002,17(8):1159-1164.
    [38]Wang S,Boyjoo Y,Cboueib A,Zhu Z H,Removal of dyes from aqueous solution using fly ash and red mud.Water.Res.,2005,39(1):129-138.
    [39]Mohan D,Singh K P,Singh G,Kumar K,Removal of dyes from wastewater using flyash,a low-cost adsorbent.Ind.Eng.Chem.Res.,2002,41(15):3688-3695.
    [40]Acemioglu B,Adsorption of Congo red from aqueous solution onto calcium-rich fly ash.J.Colloid.Interface.Sci.,2004,274(2):371-379.
    [41]Akgerman A,Zardkoohi M,Adsorption of phenolic compounds on fly ash,J.Chem.Eng.Data.,1996,41(2):185-187.
    [42]Viraraghavan T F,Alfaro D M,Adsorption of phenol from wastewater by peat,fly ash and bentonite.J.Hazard.Mater.,1995,57(1-3):59-70.
    [43]Aksu Z,Yener J,A comparative adsorption/biosorption study of mono-chlorinated phenols onto various sorbents.Waste.Manage.,2001,21(8):695-702.
    [44]Singh B K,Nayak P S,Sorption equilibrium studies of toxic nitrosubstituted phenols on fly ash.Adsorpt.Sci.Technol.,2004,22:295-310.
    [45]Dutta B,Basu J K,DasGupta S,Removal of cresol from aqueous solution using fly ash as adsorbent:experiments and modeling.Sep.Sci.Techuol.,2003,38:1345-1360.
    [46]Davini P,Investigation of flue gas desulphurization by fly ash and calcium hydroxide mixtures.Resour.Conserv.Recy.,1995,15(3-4):193-201.
    [47]Davini P,Investigation of the SO2 adsorption properties of Ca(OH)_2-fly ash systems.Fuel.,1996,75(6):713-716.
    [48]Davini P,Flue gas treatment by activated carbon obtained from oilfired fly ash.Carbon.,2002,40(11):1973-1979.
    [49]Rubel A,Andrews R,Gonzalez R,Groppo J,Robl T,Adsorption of Hg and NOx on coal by-products.Fuel.,2005,84(7-8):911-916.
    [50]徐如人,庞文琴,于吉红.分子筛与多孔材料化学(21世纪科学版化学专著系列).北京:科学出版社,2004.
    [51]Lahav O,Green M,Ammonium Removal Using Ion Exchange and Biological Regeneration.Water.Res.,1998,32(7):2019-2028.
    [52]Rozic M,Cerjan S S,Ammonium removal from water by treatment with clays and zeolite.Water.Res.,2000,34(14):3675-3681.
    [53]张兰泉,崔金贵,肖举强.沸石复合吸附剂除磷性能研究.兰州铁道学院院报,1999,18(2):116-120.
    [54]Murayama N,Yamamoto H,Shibata J.Mechanism of zeolite synthesis from coal fly ash by alkai hydrothermal reaction.Int.J.Miner.Process.,2002,64(1):1-7.
    [55]Mondragon R F.New perspectives for coal ash utilization:synthesis of zeolitic materials.Fuel.,1990,69(2):263-266.
    [56]Querol X,Alastuey A,Lopez-Soler A.A fast method for recycling fly ash:microwave-assisted zeolite synthesis.Environ.Sci.Technol.,1997,31(9):2527-2533.
    [57]Steenbruggen G,Hollman G G.The synthesis of zeolites from fly ash and the properties of the zeolite products.J.Geochem.Explor.,1998,62(1-3):305-309.
    [58]Chareonpanich M,Namto T,Kongkachuichay P.Synthesis of ZSM-5 zeolite from lignite fly ash and rice husk ash.Fuel.Process.Technol.,2004,85(15):1623-1634.
    [59]Hollman G G,Steenbruggen G,Janssen-Jurkovicova M.A two-step process for the synthesis of zeolites from coal fly ash.Fuel.,1999,78(10):1225-1230.
    [60]Diamond S.On the glass present in low calcium and in high calcium fly ashes.Cement.Concrete.Res.,1984,14(1):459-464.
    [61]王华,张强,宋存义.莫来石在粉煤灰碱性溶液中的反应行为.粉煤灰综合利用,2001,(5):24-27.
    [62]Shigemoto N,Hayshi H,Miyuaura K.Selective formation of Na-X zeolite from coal fly ash by fusion with sodium prior to hydrothermal reaction.J.Mater.Sci.,1993,28(3):4781-4786.
    [63]Shigemoto N,Sugiyama S,Hayshi H.Characterization of Na-X,Na-A and their amorphous precursors by IR,MAS,NMR and XPS.Fuel.Energy.,1996,37(3):231.
    [64]Bergaut V,Singer A.High capacity cation exchanger by hydrothermal zeolitization of coal fly ash.Appl.Clay.Sci.,1996,10(5):369-378.
    [65]Chang H L,Shih W H.Synthesis of zeolites A and X from fly ashes and their ion-exchange behavior with cobalt ions.Ind.Eng.Chem.Res.,2000,39(11):4185-4191.
    [66]焦庆祝,庞文琴,霍启升.用英安岩和粉煤灰合成ZSM-5分子筛研究.硅酸盐通报,1996,(4):29-31.
    [67]Molina A,Poole C.A comparative study using two methods to produce zeolites from fly ash.Miner.Eng.,2004,17(2):167-173.
    [68]Park M,Choi C L.Lim W.Molten-Salt method for the synthesis of zeolitic materials I,zeolite formation in alkaline Molten-Salt system.Micropor.Mesopor.Mat.,2000,37(1-2):81-89.
    [69]Park M,Choi C L,Lee D H.Salt-Thermal zeolitization of fly ash.Environ.Sci.Technol.,2001,35(13):2812-2816.
    [70]王德举.利用粉煤灰合成沸石的研究进展.粉煤灰综合利用,2002(6):32-33.
    [71]Al-Degs Y,Khraisheh M A M,Allen S J.Effect of Carbon Surface Chemistry on the Removal of Reactive Dye from Textile Effluence.Water.Res.,2000,34(3):927-933.
    [72]冯栩,廖银章,李旭东.印染废水生物处理技术的进展.印染,2006,(15):48-51.
    [73]Zamora R M R,Schouwenaars R A.Moreno D and Bultron G.Production of ctivated carbon from petroleum coke and its application in water treatment for removal of metals and phenel. Water.Sci.Technol.,2000,42(5-6):119-126.
    [74]Scott J A.Karanjkar A M.Immobilized biofilms on granular activated carbon for removal and accumulation of heavy metals from contaminated streams.Water.Sci.Technol.,1998,38(8-9):197-204.
    [75]Felix H R.Kasak L J.Phytoremediation of heavy metals contaminated wastewater,case studies.Proceeding of 99'R Congress(Recovery,Recycling,Reintegration).1999.
    [76]Chien L,Chang J E,Lu M C.Application of fly ashes in the removal of metal ions from wastewater.Proceeding of 99'R Congress(Recovery,Recycling,Reintegration).1999.
    [77]王绍文,姜凤有.重金属废水治理技术,北京:冶金工业出版社,1993,p20-118.
    [78]巴音,王蓝.用腐植酸树脂处理工业废水,环境保护十年选编,环境保护杂志社,1984.
    [79]蓝淑澄.活性炭载水处理上的应用.环境保护十年选编,环境保护杂志社,1984.
    [80]Qian Y.Appropriate process and technology for wastwater treatment and reclamation in China.Water.Sci.Technol.,2000,42(12):107-114.
    [81]Forgacs E,Cserha T,Oros G.Removal of synthetic dyes from wastewaters:a review.Environ.Int.,2004,30(7):953-971.
    [82]张宇峰,滕洁,张雪英.印染废水处理技术的研究进展.工业水处理,2003,23(4):23-27.
    [83]李风亭,陆雪非,张冰如.印染废水脱色方法.水处理技术,2003,29(1):12-14.
    [84]Slokar Y M,Marechal L.Methods of decoloration of textile wastewaters.Dyes.Pigments.,1997,37(4),335-356.
    [85]Raghavacharya C.Colour removal from industrial effluents-a comparative review of available technologies.Chem.Eng.,1997,32:53-54.
    [86]Robinson T,McMullan G,Marchant R.Remediation of dyes in textile effluent:a critical review on current treatment technologies with a proposed alternative.Bioresource.Technol.,2001,77(3):247-255.
    [87]Chang H L,Shih W H.Sythesis of zeolites A and X from fly ashes and their ion-exchange behavior with cobalt ions.Ind.Eng.Chem.Res.,2000,39(11):4185-4191.
    [88]Shih W H,Chang H L.Conversion of fly ash into zeolites for ion-exchange applications.Mater.Lett.,1996,28(4-6):263-268.
    [89]Moreno N,Querol X,Alora C.Utilisation of zeolites synthesized from coal fly ash for the purification of acid mine waters.Environ.Sci.Technol.,2001,35(17):3526-3534.
    [90]Hui K S,Chao C Y H,Kot S C.Removal of mixed heavy metal ions in wastewater by zeolite 4A and residual products from recycled coal fly ash.J.Hazard.Mater.,2005,B127(1-3):89-101.
    [91]Li L,Wang S B,Zhu Z G.Geopolymeric adsorbents from fly ash for dye removal aqueous solution.J.Colloid.Interf.Sci.,2006,300(1):52-59.
    [92]Acemioglu B.Adsorption of Congo red from aqueous solutin onto calcium-rich fly ash.J.Colloid.Interf.Sci.,2004,274(2):371-379.
    [93]Wang S B,Soudi M,Li L,Zhu Z H.Coal ash conversion into effective adsorbents for removal of beavy metals and dyes from wastewater.J.Hazard.Mater.,2006,B133(1):243-251.
    [1]Brown G E.How minerals react with water.Science.,2001,294:69-70.
    [2]Frost R L,Kristof J,Paroz G N.Raman microscope of dickete,kaolinite and their interface Analyst,1998,123(4):611-616.
    [3]吴大清,刁桂仪,袁鹏.矿物表面活性及其量度.矿物学报,2001,21(3):307-311.
    [4]Brady P V.Physics and Chemistry of Mineral surface.Florida:CRC press,1996,p1-61.
    [5]吴大清,刁桂仪,魏俊峰.矿物表面基团与表面作用.高校地质学报,2000,6(2):225-232.
    [6]Koretsky C M,Sverjensky D A,Sahai N.A model of surface site types on oxide and silicate minerals based on crystal chemistry:Implications for site types and densities,multi-site adsorption,surface infrared spectroscopy,and dissolution kinetics.Amer.J.Science.,1998,295(5):349-438.
    [7]Davis J A,Kent D B.Surface complexation modeling in aqueous geochemistry,In:Hochella MF,White AF.,Mineral-water Interface Geochemistry:Reviews in Mineralogy,Vol23.Washington,D C:Miner Soc Am.1990,177-259.
    [8]窦涛.分子筛合成中的固体化学及分子筛新材料.太原:中国科学院山西煤炭化学研究所,1998.
    [9]Molina A,Poole C.A comparative study using two methods to produce zeolite from fly ash.Miner.Eng.,2004,17(2):167-173.
    [10]王华,宋存义,张强.国外利用粉煤灰合成沸石的研究现状.化工矿物与加工,2007,(7):1-8.
    [11]Hui K S,Chao C Y H.Effects of step-change of synthesis temperature on synthesis of zeolite 4A from coal fly ash.Micropor.Mesopor.Mat.,2006,88(1-3):145-151.
    [12]国家环境保护局《水和废水监测分析》编委会.水和废水监测分析方法.北京:中国环境科学出版社,2002.
    [1]Hollman G G,Steenbruggen G,Janssen-Jurkovicova M.A two-step process for the synthesis of zeolites from coal fly ash.Fuel.,1999,78(10):1225-1230.
    [2]Hui K S,Chao C Y H.Effects of step-change of synthesis temperature on synthesis of zeolite 4A from coal fly ash.Micropor.Mesopor.Mat.,2006,88(1-3):145-151.
    [3]Tanaka H,Miyagawa A,Eguchi H,Hino R.Synthesis of a pure-form Zeolite A from coal Fly ash by dialysis.Ind.Eng.Chem.Res.,2004,43(19):6090-6094.
    [4]Murayama N,Yamamoto H,Shibata J.Mechanism of zeolite synthesis from coal fly ash by alkai hydrothermal reaction.Int.J.Miner.Process.,2002,64(1):1-7.
    [5]Inada M,Egnchi Y.Synthesis of zeolite from coal fly ashes with different silica-alumina composition.Fuel.,2005,84(2-3):299-304.
    [6]黄渭澄.电镀三废处理.成都:四川科学技术出版社.1983.
    [7]佟玉衡.实用废水处理技术.北京:华学工业出版社.1998.
    [8]唐受印,汪大辜.废水处理工程.北京:华学工业出版社.1999.
    [9]甘光奉,甘莉.高分子絮凝剂研究的进展.工业水处理,1999,19(2):14-18.
    [10]盛桂浓.国外处理重金属矿上废水的几种方法.冶金环保情报资料.1985.
    [11]Hui K S,Chao C Y H,Kot S C.Removal of mixed heavy metal ions in wastewater by zeolite 4A and residual products from recycled coal fly ash.J.Hazard.Mater.,2005,B127(1-3):89-101.
    [12]Tanaha H,Sakai Y,Hino R.Formation of Na-A and Na-X zeolites from waste solutions in conversion of coal fly ash to zeolites.Mater.Res.Bull.,2002,37(11):1873-1884.
    [13]徐如人,庞文琴,于吉红.分子筛与多孔材料化学(21世纪科学版化学专著系列).北京:科学出版社,2004.211-213.
    [14]Chang H L,Shih W H.Sythesis of zeolites A and X from fly ashes and their ion-exchange behavior with cobalt ions.Ind.Eng.Chem.Res.,2000,39(11):4185-4191.
    [15]Petrovic I,Navrotsky A,Davis M E.Thermochemical study of the stability of frameworks in high silica zeolites.Chem.Mater.,1993,5(12):1805-1813.
    [16]Barrer R M.Hydrothermal chemistry of zeolites.Academic Press,1982.
    [17]Barrer R M,Denny P J.Hydrothermal chemistry of the silicates.Part Ⅸ:Nitrogenous Aluminosilicates.J.Chem.Soc.,196,16(16):971-982.
    [18]Wang C-F,Li J-S,Wang L-J,Sun X-Y.Influence of NaOH concentrations on synthesis of pure-form zeolite A from fly ash using two-stage method.J.Hazard.Mater.,2008,127(1-3):89-101.
    [19]Adnadjevic B,Vuldcevic J,Filipovic-Rojka Z.The influence of NaX zeolite particle size on crystallinity measured by the XRD method.Zeolites.,1990,10(7):699-702.
    [20]Tanaka H,Eguchi H,Fujimoto S,Hino R.Two-step process for synthesis of a single phase Na-A zeolite from coal fly ash by dialysis.Fuel.,2006,85(10-11):1329-1334.
    [21]Kacirek H,Lechert H.Rates of crystallization and a model for the growth of sodium-Y zeolites.J.Phys.Chem.A.,1976,80(12):1291-1296.
    [22]Kuehl G H,Olson D H,Dempsy E.Variation of the lattice parameter with aluminum content in synthetic sodium faujasites-a evidence for ordering of the framework ions.J.Phys.Chem.A.,1969,73(2):387-390.
    [23]Chang H-L,Shih W-H.A general method for the conversion of fly ash into zeolites as ion exchanger for cesium.Ind.Eng.Chem.Res.,1998,37(1):71-78.
    [24]Semmens M J,Seyfarth M.The selectivity of clinoptilolite for certain heavy metals.Pergamon Press Ltd:Oxford.1978.
    [25]Breck D W.Zeolite molecular Sieves,Chemistry,and Use.John Wiley & Sons:New York.1974.
    [26]Panayotova M L.Kinetics and therdynamies of copper ions removal from wasterwater by use of zeolite.Waste.Manage.,2001,21(7):671-676.
    [27]Alvarez-Ayuso E,Garcia-Sanchez A,Querol X.Purification of metal electroplating waste water using zeolites.Water.Res.,2003,37(20):4855-4862.
    [28]Filippidis A,Godelitsas A,Charistos D,Misaelides P,Kassoli-Fournarak A.The chemical behavior of natural zeolites in aqueous environments:Interactions between low-silica zeolites and 1M NaCl solutions of different initial pH-values.Appl.Clay.Sci.,1996,11(2-4):199-209.
    [29]顾翼东,谢高阳.无机化学丛书(第8卷).北京:科学出版社,1998,p51-52.
    [30]马红梅,朱志良,张荣华.弱碱性环氧阴离子交换树脂去除水中铜的动力学研究.离子交换与吸附,2006,22(6):519-526.
    [31]Lagergren,S.About the theory of so-called adsorption of soluble substances.Kung.Sven.Veten.Hand.,1898,24,1-39.
    [32]Ho Y S,McKay G.Pseudo-second order model for sorption processes.Process.Biochem.,1999,34(5):451-465.
    [33]丁世敏,封享华,汪玉庭.交联壳聚糖多孔微球对染料的吸附平衡及吸附动力学分析. 分析科学学报,2005,21(2):127-130.
    [34]Chang M Y,Juang R S.Adsorption of tannic acid,humic acid,and dyes from water using the composite of chitosan and activated clay.J.Colloid.Interface.Sci.,2004,278(1):18-25.
    [35]靳昕,王英滨,林智辉.MCM-41中孔分子筛净化含Cr(Ⅵ)废水的实验研究.离子交换与吸附,2006,22(6):536-543.
    [36]Shriver D F,Atkins P W,Langford C H.Inorganic Chemistry.Freeman:New York.1990.
    [37]Langmuir I.Adsorption of gases on plain surface of glass micaplatium.J.Am.Chem.Soc.,1918,40(9):1361-1403.
    [38]Namasivayam C,Jeyakumar R,Yamuna R T.Dye removal from waste-water by adsorption on waste Fe(Ⅲ)/Cr(Ⅲ) hydroxide.Waste.Manage.,1994,14(7):643-648.
    [39]Namasivayam C,Yamuna R T,Jayanthi J.Removal of methylene blue from wastewater by adsorption on cellulosic waste,orange peel,Cell.Chem.Technol.,2003,37(7):333-339.
    [1]Hollman G G,Steenbruggen G,Janssen-Jurkovicova M.A two-step process for the synthesis of zeolites from coal fly ash.Fuel.,1999,78(10):1225-1230.
    [2]Hui K S,Chao C Y H.Effects of step-change of synthesis temperature on synthesis of zeolite 4A from coal fly ash.Micropor.Mesopor.Mat.,2006,88(1-3):145-151.
    [3]Tanaka H,Miyagawa A,Eguchi H,Hino R.Synthesis of a pure-form Zeolite A from coal Fly ash by dialysis.Ind.Eng.Chem.Res.,2004,43(19):6090-6094.
    [4]Tanaha H,Sakai Y,Hino R.Formation of Na-A and Na-X zeolites from waste solutions in conversion of coal fly ash to zeolites.Mater.Res.Bull.,2002,37(11):1873-1884.
    [5]李方文,魏先勋,马淞江.煅烧对粉煤灰合4A沸石的作用.环境科学与技术,2003,26(4):13-17.
    [6]Shigemoto N,Hayshi H,Miyuaura K.Selective formation of Na-X zeolite from coal fly ash by fusion with sodium prior to hydrothermal reaction.J.Mater.Sci.,1993,28(3):4781-4786.
    [7]Shigemoto N,Sugiyama S,Hayshi H.Characterization of Na-X,Na-A,and their amorphous precursors by IR,MAS,NMR and XPS.Fuel.Energy.,1996,37(3):231.
    [8]Molina A,Poole C.A comparative study using two methods to produce zeolite from fly ash.Miner.Eng,2004,17(2):167-173.
    [9]Chang H-L,Shih W-H.Sythesis of zeolites A and X from fly ashes and their ion-exchange behavior with cobalt ions.Ind.Eng.Chem.Res.,2000,39(11):4185-4191.
    [10]Chang H-L,Shih W-H.A general method for the conversion of fly ash into zeolites as ion exchanger for cesium.Ind.Eng.Chem.Res.,1998,37(1):71-78.
    [11]Frost R L,Kristof J,Paroz G N.Raman microscope of dickete,kaolinite and their interface Analyst.1998,123(4):611-616.
    [12]吴大清,刁桂仪,袁鹏.矿物表面活性及其量度.矿物学报,2001,21(3):307-311.
    [13]Brady P V.Physics and Chemistry of Mineral surface.Florida:CRC press,1996,p1-61.
    [14]吴大清,刁桂仪,魏俊峰.矿物表面基团与表面作用.高校地质学报,2000,6(2):225-232.
    [15]Koretsky C M,Sverjensky D A,Sahai N.A model of surface site types on oxide and silicate minerals based on crystal chemistry.Implications for site types and densities,multi-site adsorption,surface infrared spectroscopy,and dissolution kinetics.Amer.J.Science.,1998,295(5):349-438.
    [16]Estevez M J T,Arbeloa F L,Arbeloa T L.Characterization of rhodamine 6G adsorbed onto hectorite by electric spectroscopy.J.Colloid.Interf.Sci.,1995,171(2):439-445.
    [17]Rytwo G.,Tropp D,Serhan C.Adsorption of diquat,paraquat and methyl green on sepiolite:experimental results and model calculation.Appl.Clay.Sci.,2002,20(6):273-282.
    [18]Barrer R M.Hydrothermal chemistry of zeolites.Academic Press,1982.
    [19]赵世永.粉煤灰合成4A沸石及应用研究.西安科技大学硕士论文,2005.
    [20]Flanigen E M,Khatami H,Szymanski H A.Molecular sieve zeolite Ⅰ.Academic,Prague,1971,p201.
    [21]中国科学院大连化学物理研究所分子筛组.沸石分子筛.北京:科学出版社,1978.
    [22]徐如人,庞文琴,于吉红.分子筛与多孔材料化学(21世纪科学版化学专著系列).北京:科学出版社,2004.
    [23]国家环境保护局《水和废水监测分析》编委会.水和废水监测分析方法.北京:中国环境科学出版社,2002.
    [24]Rayalu S S,Udhoji J S,Munshi K N,Hasan M Z.Highly crystalline zeolite-a from fly ash of bituminous and lignite coal combustion.J.Hazard.Mater.,2001,88(1):107-201.
    [25]Weitkamp J,Puppe L.Catalysis and Zeolite,Fundamentals and Applications.Springer,Germany,1999,Chapters 1-2.
    [26]王华,宋存义,张强.国外利用粉煤灰合成沸石的研究现状.化工矿物与加工,2007,(7):1-8.
    [27]Christophliemk P,Gerike P.Potokar M.Handbook of environmental chemistry,1st ed.,Springer-Verlag,Berlin,1992.
    [28]Gloxhuber C,Potokar M,Pittermann W.Zeolite A-a phosphate substitute for detergents-toxicological investigation.Food.Chem.Toxicol.,1983,21(3):209-220.
    [29]马红梅,朱志良,张荣华.弱碱性环氧阴离子交换树脂去除水中铜的动力学研究.离子交换与吸附,2006,22(6):519-526.
    [30]林俊雄.硅藻土基吸附剂的制备、表征及其染料吸附特性研究.浙江大学博士论文,2007.
    [31]Al-Ghouti M,Khraisheh M A M,Abmad M N M.Thermodynamic behaviour and the effect of temperature on the removal of dyes from aqueous solution using modified diatomite:A kinetic study.J.Colloid.Interf.Sci.,2005,287(1):6-13.
    [32]Weber W J,Morris J C.Kinetics of adsorption on carbon from solution.J.Sanitary.Eng.Div.Am.Soc.Civ.Eng.,1963,89:31-60.
    [33]Lagergren,S.About the theory of so-called adsorption of soluble substances.Kung.Sven.Veten.Hand.,1898,24:1-39.
    [34]Ho Y S,McKay G.Pseudo-second order model for sorption processes.Process.Biocbem.,1999,34(5):451-465.
    [35]Langmuir I.Adsorption of gases on plain surface of glass micaplatium.J.Am.Chem.Soc.,1918,40(9):1361-1403.
    [36]Namasivayam C,Jeyakumar R,Yamuna R T.Dye removal from waste-water by adsorption on waste Fe(Ⅲ)/Cr(Ⅲ) hydroxide.Waste Manage.,1994,14(7):643-648.
    [37]Namasivayam C,Yamuna R T,Jayanthi J.Removal of methylene blue from wastewater by adsorption on cellulosic waste,orange peel,Cell.Chem.Technol.,2003,37(7):333-339.
    [38]Wang S,Boyjoo Y,Choueib A,Zhu Z H.Removal of dyes from aqueous solution using fly ash and red mud.Water.Res.,2005,39(1):129-138.
    [39]Wang S,Soudi M,Li L,Zhu Z H.Coal ash conversion into effective adsorbents for removal of heavy metals and dyes from wastewater.J.Hazard.Mater.,2006,B133(1-3):243-251.
    [40]Woolard C D,Strong J.and Erasmus C R.Evaluation of the use of modified coal ash as a potential sorbent for organic waste streams.Appl.Geochem.,2002,17(9):1159-1164.
    [41]Breck D W.Zeolite molecular Sieves,Chemistry,and Use,John Wiley & Sons.New York.1974.
    [42]Wang S,Boyjoo Y,Choueib A,Zhu Z H.Removal of dyes from aqueous solution using fly ash and red mud.Water.Res.,2005,39(1):129-138.
    [43]Das S K,Bhowal J,Das A R.Adsorption behavior of rhodamine B on Rhizopus oryzae Biomass.Langmuir.,2006,22(17):7265-7272.
    [44]Ghosh D,Bhattacharyya K.Adsorption of methylene blue on kaolinite.Appl.Clay.Sci.,2002,20(6):295-300.
    [45]Gupta V K,Mohan D,Sharma S.Removal of basic dyes(rhodamine B and methylene blue) from aqueous solutions using bagasse fly ash.Sep.Sci.Tech.,2000,35:2097-2113.
    [46]Al-Ghouti M A,Khraisheh M A M,Allen S J.The removal of dyes from textile wastewater:a study of the physical characteristics and adsorption mechanisms of diatomaceous earth.J.Environ.Manage.,2003,69(3):229-238.
    [47]Al-Qodah,Z.Adsorption of dyes using shale oil ash.Water.Res.,2000,34(17):4295-4303.
    [48]Shriver D F,Atkins P W,Langford C H,.Inorganic Chemistry.Freeman:New York.1990.
    [49]Cooney D O.Adsorption design for wastewater treatment.Lewis Publishers,CRC Press LLCBoca Ration,Florida,U.S.A.,1999.
    [50]Fu Y Z.Removal of dyes from aqueous solution by the fungus aspergillus niger.Ph.D.thesis,Engineering University of Regina,Saskatchewan:2002.
    [51]Karickhoff W S,Brown D S,Scott T A.Sorption of hydrophobic pollutants on natural sediments.Water Res.,1979,13(3):241-248.
    [52]Ei-Nahhal Y Z,Safi J M.Adsorption of phenanthrene on organoclays from distilled and saline water.J.Colloid.Interf.Sci.,2004,269(2):265-273.
    [53]Palheiros L B,Duarte A C,Oliveira J P,Hall A.The influence of pH,ionic strength and chloride concentration on the adsorption of cadmium by sediment.Water.Sci.Technol.,1989,21:1873-1876.
    [54]王淑荣.染整废水处理.北京:中国纺织出版社,2005.
    [55]Nollet H,Roels M,Lutgen P,Van D M P,Verstraete W.Removal of PCBs from wastewater using fly ash.Chemosphere.,2003,53(6):655-665.
    [1]Murayama N,Yamamoto H,Shibata J.Mechanism of zeolite synthesis from coal fly ash by alkai hydrothermal reaction.Int.J.Miner.Process.,2002,64(1):1-7.
    [2]Mondragon R F.New perspectives for coal ash utilization:synthesis of zeolitic materials.Fuel.,1990,69(2):263-266.
    [3]Querol X,Alastuey A,Lopez-Soler A.A fast method for recycling fly ash:microwave-assisted zeolite synthesis.Environ.Sci.Technol.,1997,31(9):2527-2533.
    [4]Steenbruggen G,Hollman G G.The synthesis of zeolites from fly ash and the properties of the zeolite products.J.Geochem.Explor.,1998,62(1-3):305-309.
    [5]Chareonpanich M,Namto T,Kongkachuichay P.Synthesis of ZSM-5 zeolite from lignite fly ash and rice husk ash.Fuel.Process.Technol.,2004,85(15):1623-1634.
    [6]Park M,Choi C L.Lim W.Molten-Salt method for the synthesis of zeolitic materials I,zeolite formation in alkaline Molten-Salt system.Micropor.Mesopor.Mat.,2000,37(1-2):81-89.
    [7]Park M,Choi C L,Lee D H.Salt-Thermal zeolitization of fly ash.Environ.Sci.Techmol.,2001,35(13):2812-2816.
    [8]Diamond S.On the glass present in low calcium and in high calcium fly ashes.Cement.Concrete.Res.,1984,14(1):459-464.
    [9]王华,张强,宋存义.莫来石在粉煤灰碱性溶液中的反应行为.粉煤灰综合利用,2001,(5):24-27.
    [10]Shigemoto N,Hayshi H,Miyuaura K.Selective formation of Na-X zeolite from coal fly ash by fusion with sodium prior to hydrothermal reaction.J.Mater.Sci.,1993,28(3):4781-4786.
    [11]Shigemoto N,Sugiyama S,Hayshi H.Characterization of Na-X,Na-A and their amorphous precursors by IR,MAS,NMR and XPS.Fuel.Energy.,1996,37(3):231.
    [12]Bergaut V,Singer A.High capacity cation exchanger by hydrothermal zeolitization of coal fly ash.Appl.Clay.Sci.,1996,10(5):369-378.
    [13]Chang H-L,Shih W-H.Synthesis of zeolites A and X from fly ashes and their ion-exchange behavior with cobaltions.Ind.Eng.Chem.Res.,2000,39(11):4185-4191.
    [14]焦庆祝,庞文琴,霍启升.用英安岩和粉煤灰合成ZSM-5分子筛研究.硅酸盐通报,1996,(4):29-31.
    [15]Molina A,Poole C.A comparative study using two methods to produce zeolites from fly ash.Miner.Eng.,2004,17(2):167-173.
    [16]Hollman G G,Steenbruggen G,Janssen-Jurkovicova M.A two-step process for the synthesis of zeolites from coal fly ash.Fuel.,1999,78(10):1225-1230.
    [17]国家环境保护局《水和废水监测分析》编委会.水和废水监测分析方法.北京:中国环境科学出版社,2002.
    [18]Querol X,Moreno N,Uma(?)a J C,Alastuey A,Hern(?)ndez E,L(?)pez-Soler A.Synthesis of zeolites from coal fly ash:an overview.Int.J.Coal.Geol.,2002,50(1-4):413-423.
    [19]陈连璋.沸石分子筛催化.大连:大连理工大学出版社,1990.
    [20]Barrer R M.Hydrothermal chemistry of zeolites,Academic Press,1982.
    [21]Barrer R M,Denny P J.Hydrothermal chemistry of the silicates.Part Ⅸ.Nitrogenous Aluminosilicates.J.Chem.Soc.,1961,45:971-982.
    [22]Flanigen E M.A review and new perspectives in zeolite crystallization.Adv.Chem.Ser.,1973,121:119-139.
    [23]Kessler H,Patarin J,Schott-Darie C,Guth J L.Synthesis of high-silica zeolites and phosphate-based materials in the presence of Fluoride.Stud.Surf.Sci.Catal.,1994,85:75-113.

© 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