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首页> 外文期刊>Journal of Applied Polymer Science >Relationship Between Pore Sructure and ~H-NMR Relaxation Times in TiO_2/Poly(dimethylsiloxane) and CaCO_3/Poly(dimethylsiloxane) Composite Powders
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Relationship Between Pore Sructure and ~H-NMR Relaxation Times in TiO_2/Poly(dimethylsiloxane) and CaCO_3/Poly(dimethylsiloxane) Composite Powders

机译:TiO_2 /聚(二甲基硅氧烷)和CaCO_3 /聚(二甲基硅氧烷)复合粉体的孔结构与〜H-NMR弛豫时间的关系

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Titanium(IV) oxide/polydimethylsiloxane (PDMS) and calcium carbonate/PDMS composite powders were obtained by adsorption of the polymer from a chloroform solution onto the inorganic particles followed by a thermal treatment.The composites were characterized by ~1H-NMR relaxation and porosimetry.The composites present shorter spin-lattice (T_1) and spin-spin (T_2) proton relaxation times than silica-reinformced PDMS,and the activation energies for the motions that cause spinlattice relaxation are 5.8,4.9,and 0.72 kJ mol~(-1) for TiO_2/PDMS,CaCO-3/PDMS,and neat PDMS,respectively,respectively,revealing the greater rigidity of the polymer chains within the composite.Spin-spin relaxation 9T_2) measurements of the composites showed a major component with a shorter T_2 and a minor component with a longer T_2.The intensity ratio of these two components is very close to the ratio between the amount of polymer that remains between the particles and that penctrating the particle pores as measured by Hg intrusion porosimetry.The shorter T_2 component was thus assigned to polymer interspersed among the particles,while the longer T_2 component was assigned to polymer within the particle pores.
机译:通过将聚合物从氯仿溶液中吸附到无机颗粒上并进行热处理,制得氧化钛(IV)/聚二甲基硅氧烷(PDMS)和碳酸钙/ PDMS复合粉末,并通过〜1H-NMR弛豫和孔隙率法对其进行了表征复合材料的自旋晶格(T_1)和自旋旋(T_2)质子弛豫时间比二氧化硅增强的PDMS短,引起自旋晶格弛豫的运动的活化能为5.8、4.9和0.72 kJ mol〜(- 1)分别针对TiO_2 / PDMS,CaCO-3 / PDMS和纯PDMS,揭示了复合材料中聚合物链的刚性更高。自旋-旋转弛豫9T_2)测量表明,复合材料的主要成分较短T_2和T_2较长的次要组分。这两个组分的强度比非常接近颗粒之间残留的聚合物量与贯穿颗粒孔的聚合物之间的比率。通过Hg侵入孔隙率法,较短的T_2组分被分配给散布在颗粒之间的聚合物,而较长的T_2组分被分配给颗粒孔内的聚合物。

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