功能材料
功能材料
공능재료
JOURNAL OF FUNCTIONAL MATERIALS
2014年
2期
2059-2062
,共4页
王彩%侯朝霞%王美涵%王浩%夏建国%关玉峒%王少洪
王綵%侯朝霞%王美涵%王浩%夏建國%關玉峒%王少洪
왕채%후조하%왕미함%왕호%하건국%관옥동%왕소홍
聚丙烯酰胺%改性%羟基磷灰石%Cu2+%吸附
聚丙烯酰胺%改性%羥基燐灰石%Cu2+%吸附
취병희선알%개성%간기린회석%Cu2+%흡부
PAM%modified%HA%Cu2+%adsorption
用聚丙烯酰胺(PAM)对用微乳液法合成的纳米羟基磷灰石(HA)粉体进行有机改性制备。通过用X射线衍射(XRD)、扫描电镜(SEM)、傅立叶转换红外光谱(FT-IR)等测试手段对合成的粉体的化学组分、粒度大小、表面形态进行表征分析。实验结果表明,PAM使 HA 晶体发生相转变,有 CaHPO4的生成。PAM 改性后 HA 杆状颗粒由80 nm 变为120 nm。1635.6 cm-1特征峰表明 PAM与 HA 中的Ca2+发生络合,使PAM接枝在HA表面。另外,探讨了不同质量分数的 PAM-HA 改性粉体水中分散性及吸附重金属离子(Cu2+)性能研究。
用聚丙烯酰胺(PAM)對用微乳液法閤成的納米羥基燐灰石(HA)粉體進行有機改性製備。通過用X射線衍射(XRD)、掃描電鏡(SEM)、傅立葉轉換紅外光譜(FT-IR)等測試手段對閤成的粉體的化學組分、粒度大小、錶麵形態進行錶徵分析。實驗結果錶明,PAM使 HA 晶體髮生相轉變,有 CaHPO4的生成。PAM 改性後 HA 桿狀顆粒由80 nm 變為120 nm。1635.6 cm-1特徵峰錶明 PAM與 HA 中的Ca2+髮生絡閤,使PAM接枝在HA錶麵。另外,探討瞭不同質量分數的 PAM-HA 改性粉體水中分散性及吸附重金屬離子(Cu2+)性能研究。
용취병희선알(PAM)대용미유액법합성적납미간기린회석(HA)분체진행유궤개성제비。통과용X사선연사(XRD)、소묘전경(SEM)、부립협전환홍외광보(FT-IR)등측시수단대합성적분체적화학조분、립도대소、표면형태진행표정분석。실험결과표명,PAM사 HA 정체발생상전변,유 CaHPO4적생성。PAM 개성후 HA 간상과립유80 nm 변위120 nm。1635.6 cm-1특정봉표명 PAM여 HA 중적Ca2+발생락합,사PAM접지재HA표면。령외,탐토료불동질량분수적 PAM-HA 개성분체수중분산성급흡부중금속리자(Cu2+)성능연구。
Hydroxyapatite nanoparticles were synthesized via a W/O process with Ca(NO3 )2 ·4H2 O and H3 PO4 as raw material.PAM-HA particles were obtained by PAM modification HA in water solution.The morpholo-gy,size,phase structure and FT-IR spectrum of HA and PAM-HA were characterized by transmission electron microscopy,X-ray diffraction,FT-IR spectrograph.The experimental results showed that PAM played a role in crystal transformed of HA,CaHPO4 crystalline phase appeared.The size of PAM modified rod-shaped HA particles were from 80 to 120 nm.Characteristic peak in the 1 635.6 cm-1 showed that PAM and Ca2 + in the HA complexation,PAM grafted on the surface of HA.In addition,the dispersion and adsorption performance (Cu2 +)of PAM-HA were improved.