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Chemistry of proton track registration in cellulose nitrate polymers

机译:硝酸纤维素聚合物中质子轨迹配准的化学

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Changes in the intensities of the functional groups within the surface region(upper 500 nm)of cellulose nitrate films,exposed to 0.5 MeV protons and processed chemically to visualize proton tracks,have been determined quantitatively by attenuated total reflectance(ATR)infrared spectrometry.Within the penetration depth of protons resulting from the thermal neutron reaction,14N(n,p)14C at a neutron fluence of 2 x 10~(11),absorption intensities of nitrate(-ONO2)and ether(-C-O-C-)are depleted by up to 37% and 12% at respective characteristic vibrational frequencies.The observed cleavage of the ether linkages(C-O-C at 1060 cm~(-1))in the main cellulose chain creates lower molecular weight polymer fragments,and also causes depolymerization.Both reactions increase the accessibility of the polymer to chemical attack by the NaOH etchant at the chemically altered sites.The unique track registration of low energy protons(0.5-0.3 MeV)in cellulose nitrate primarily results from selective chemical induced damage from energy deposition interactions at bonded nitrate group sites.
机译:通过衰减全反射率(ATR)红外光谱法定量确定了硝酸纤维素膜表面区域(高于500 nm)内暴露于0.5 MeV质子并进行化学处理以可视化质子迹线的官能团强度的变化。热中子反应产生的质子穿透深度,中子注量为2 x 10〜(11)时的14N(n,p)14C,硝酸盐(-ONO2)和醚(-COC-)的吸收强度被耗尽在各自的特征振动频率下分别高达37%和12%。观察到的主纤维素链中醚键(COC在1060 cm〜(-1)处)的裂解产生了较低分子量的聚合物片段,并引起了解聚。增加了聚合物在化学变化位点上受到NaOH蚀刻剂化学侵蚀的可及性。硝酸纤维素中低能质子(0.5-0.3 MeV)的独特轨迹记录主要来自选择性化学反应在键合硝酸盐基团位点上的能量沉积相互作用引起了破坏。

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