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Al-δ层状二硅酸钠晶体结构稳定性及α、β相层状二硅酸钠钙镁脱除机理的研究

Studies on the Crystal Structure Stability of Al-δ-Na2Si2O5 and Ca~(2+), Mg~(2+) Ion Binding Mechanism of α、β-Na2Si2O5

【作者】 李丽萍

【导师】 董晋湘;

【作者基本信息】 太原理工大学 , 工业催化, 2007, 硕士

【摘要】 层状二硅酸钠由于具有优良的阳离子脱除能力、良好的缓冲性能、与洗涤剂其它成分配伍性好、环境相容性等优点,被认为是一类具有广泛使用前景的新型无磷洗涤剂助洗剂。Al-δ层状二硅酸钠是δ层状二硅酸钠的同晶取代衍生物。Al-δ层状硅酸钠在热水中晶体结构稳定,有良好的钙、镁离子脱除能力、缓冲能力、去污能力,能够满足洗衣粉前配料工艺需要,解决了层状二硅酸钠应用研究中的重要技术难题。为了进一步详尽地掌握Al-δ层状二硅酸钠在使用中晶体结构的稳定性,为工业应用提供基础技术参数,本文重点考察了洗衣粉中主要组分表面活性剂、无机物对其稳定性的影响。同时,在四种不同水溶液(蒸馏水、自来水、钙离子溶液、镁离子溶液)中,通过考察α、β相层状二硅酸钠相的转变及固体保留率的变化,研究了它们的阳离子脱除机理。参照洗衣粉的基本组成配方,本文考察了表面活性剂(LAS、AOS、K12和AEO-9)对Al-δ-Na2Si2O5晶体结构稳定性的影响。采用XRD、FT-IR、TG分析和Ca2+脱除容量对Al-δ-Na2Si2O5及其与表面活性剂水浸后的样品进行了表征。实验结果表明:Al-δ-Na2Si2O5与LAS相互作用后,Al-δ-Na2Si2O5仍然可以保持δ相;LAS对Al-δ-Na2Si2O5晶体结构有保护作用。与K12(或AEO-9,AOS)相互作用后,物相转变成δ和kanemite的混合相。与K12相互作用后,尽管物相转变为混合相,但其对Al-δ-Na2Si2O5晶体结构有一定的保护作用。AEO-9对Al-δ-Na2Si2O5晶体结构没有明显的保护作用。AOS对Al-δ-Na2Si2O5晶体结构有破坏作用。参照洗衣粉的基本组成配方,考察了无机物(无水Na2SO4、NaCl、无水Na2CO3、水玻璃)对Al-δ-Na2Si2O5晶体结构稳定性的影响。采用XRD、FT-IR、TG分析和Ca2+脱除容量对Al-δ-Na2Si2O5及其与无机物水浸后的样品进行了表征。实验结果显示:Al-δ-Na2Si2O5与无机物混合水浸后,物相均由δ相转变成了δ和kanemite的混合相。Na2SO4、NaCl、Na2CO3对Al-δ-Na2Si2O5晶体结构都有一定的保护作用,而且NaCl对晶体结构的保护作用要比Na2S04更好。水玻璃在mH20/msolid<1时,对Al-δ-Na2Si2O5晶体结构有保护作用。当mH2O/msolid>1时,对Al-δ-Na2Si2O5晶体结构有破坏作用。本文通过考察α、β相层状二硅酸钠在四种不同水溶液(蒸馏水、自来水、钙离子溶液、镁离子溶液)中相的转变及固体保留率的变化,采用XRD、FT-IR、SEM现代仪器分析手段研究了它们的阳离子脱除过程。实验数据表明:在自来水中,β相层状二硅酸钠部分转化为有阳离子交换能力的层状硅酸钠kanemite,表现为离子交换特性:同时还有部分β相层状二硅酸钠会溶解进入水中,游离的硅酸根和氢氧根离子与钙离子和镁离子形成沉淀。证明β相层状二硅酸钠的阳离子脱除过程是具有离子交换和沉淀的双重特征。α相层状二硅酸钠在自来水中部分转化为未知相,其特性与其他层状材料的特性相似。同时部分α相层状二硅酸钠会溶解进入水中,游离的硅酸根和氢氧根离子与钙离子和镁离子形成沉淀。证明α相层状二硅酸钠的阳离子脱除过程也是具有离子交换和沉淀的双重特征。

【Abstract】 Layered sodium disilicates(Na2Si2O5) have good ion binding capacity, finealkaline buffer capacity, cooperation with other composition in good method,harmony with enviroment and so on. They were considered as efficientnon-phosphate detergent builder with excellent prospect. Al-δ-Na2Si2O5 is thesame crystal ramification ofδ-Na2Si2O5. Al-δ-Na2Si2O5 has high frameworkstability in hot water, it also has better Ca2+ and Mg2+ binding capacity, alkalinebuffer capacity and cleaning capacity. Therefore it met the requirements of thespray drying process and solved important technology problem in applicationfield of Na2Si2O5. For further review the crystal structure stability ofAl-δ-Na2Si2O5 and provide basic technical parameter for industrial application.This paper mainly investigated interactional effect of surfactants and inorganicchemicals (main components in detergents) on crystal structure stability ofAl-δ-Na2Si2O5. Ion binding capacity ofα-Na2Si2O5 andβ-Na2Si2O5 was investigated by phase transformation and the residual solid yield in differentsolution (distilled water, tap water, water with Ca2+, water with Mg2+).According to basic component of detergents, this paper investigated effectof surfactants (LAS, AOS, K12 and AEO-9) on Al-δ-Na2Si2O5 under thecondition near detergent spray drying process. Typical samples werecharacterized by XRD, TG, FT-IR and Ca2+ ion binding capacity. Theexperimental results showed that Al-δ-Na2Si2O5 might keep asδphase afterinteracted with LAS. LAS had better protective function to Al-δ-Na2Si2O5.Al-δ-Na2Si2O5 had changed to a mixed phase ofδphase and kanemite afterinteracted with K12 (or AEO-9, AOS). K12 also had better protective functionto the crystal structure stability of Al-δ-Na2Si2O5 though it had changed to amixed phase. AEO-9 had not obviously protective function to the crystalstructure stability of Al-δ-Na2Si2O5. But AOS had destructive function to crystalstructure of Al-δ-Na2Si2O5.According to basic component of detergents, this paper investigated effectof inorganic chemicals on the crystal structure stability of Al-δ-Na2Si2O5.Typical samples were characterized by XRD, TG, FT-IR and Ca2+ ion bindingcapacity. The experimental results showed that Al-δ-Na2Si2O5 had changed to amixed phase ofδphase and kanemite after marinating with inorganic chemicals.Na2SO4, NaCl and Na2CO3 have definite protective function to the crystalstructure stability of Al-δ-Na2Si2O5, NaCl had better protective function toAl-δ-Na2Si2O5 than Na2SO4. Water glass had protective function to crystal structure of Al-δ-Na2Si2O5 at mH2O/msolid<1. But water glass had negative effecton the stability of Al-δ-Na2Si2O5 at mH2O/msolid>1.To investigate the mechanism of cation binding, the phase change andresidual solid yield after the hydrolysis ofα,β-Na2Si2O5 in different watersolution (distilled water, tap water, water with Ca2+ and water with Mg2+) werecharacterized by XRD, FT-IR and SEM. The experimental data showed that apart ofβ-Na2Si2O5 transformed into kanemite with ion exchange ability in tapwater, the other part ofβ-Na2Si2O5 dissolved in water and formed precipitationthrough bonding with Ca2+ and Mg2+. The data proved that ion bindingmechanism ofβ-Na2Si2O5 has the characteristic of ion exchange and sediment.In distilled water, a part ofα-Na2Si2O5 transformed into an unknown phase,which was similar to other layered material, the other part ofα-Na2Si2O5dissolved in water and formed precipitation through bonding with Ca2+ and Mg2+.The data proved that ion binding mechanism ofα-Na2Si2O5 has the characteristicof ion exchange and sediment.

  • 【分类号】TQ649.1
  • 【被引频次】2
  • 【下载频次】247
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