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为了提高生物惰性材料C/C的生物活性以及C/C基体与生物活性材料羟基磷灰石(HAp)的结合强度,以丙烯酰胺单体(AM)和声化学制备的纳米HAp为原料,异丙醇为分散介质,采用水热电泳聚合沉积法在C/C复合材料表面制备了羟基磷灰石-聚丙烯酰胺(HAp-PAM)生物复合涂层.用XRD、TEM、SEM、FTIR、力学性能测试等手段对涂层的相组成、官能团、断面的微观形貌及结合强度进行了测试和表征,研究了水热沉积电压对复合涂层结构和性能的影响.结果表明:随着沉积电压的升高,涂层中HAp的衍射峰呈现先增强后减小的趋势,PAM的衍射峰逐渐消失;涂层的结合强度随着电压的升高先增强后减小.沉积电压为150 V时,涂层的致密性和均匀性达到最佳,涂层的厚度以及涂层与基体的结合强度分别达到最大值25μm和19 MPa.

参考文献

[1] 朱广艳,黄剑锋,曹丽云,等.沉积电压对碳/碳复合材料表面羟基磷灰石涂层相组成及显微结构的影响[J].硅酸盐学报,2008,36(2):154-158.Zhu Guangyan,Huang Jianfeng,Cao Liyun,et al.Influence of deposition voltage on the phase composition and microstructure of the hydroxyapatite coatings on C/Ccomposites[J].Journal of the Chinese Ceramic Society,2008,36(2):154-158.
[2] 谭延斌,杨庆铭,王毅.纳米级经基磷灰石骨科材料研究进展[J].国外医学:骨科学分册,2004,25(3):164-165.Tan Yanbin,Yang Qingming,Wang Yi.Research progress of nanophase hydroxyapatite bone material[J].Foreign Medical Sciences:Section of Orthopaedics,2004,25(3):164-165.
[3] 张春华,王丹,张松,等.钛合金表面激光气体氮化及其HA复合涂层的制备[J].沈阳工业大学学报,2008,30(6):653-657.Zhang Chunhua,Wang Dan,Zhang Song,et al.Laser gas nitriding and hydroxyapatite deposit on substrate of titanium alloy[J].Journal of Shenyang University of Technology,2008,30(6):653-657.
[4] 张春艳,曾荣昌,陈君,等.镁合金AZ31表面液相沉积Ca-P生物陶瓷涂层的研究[J].稀有金属材料与工程,2009,38(8):1363-1367.Zhang Chunyan,Zeng Rongchang,Chen Jun,et al.Study on chemical deposition of calcium-phosphate bioceramic coating on AZ31 magnesium alloy surface[J].Rare Metal Materials and Engineering,2009,38(8):1363-1367.
[5] 付涛,憨勇,宋忠孝,等.碳/碳复合材料表面诱导沉积生理磷灰石层[J].无机材料学报,2002,17(1):189-192.Fu Tao,Han Yong,Song Zhongxiao,et al.Induction of biological apatite layer on the surface of carbon/carbon composite[J].Journal of Inorganic Materials,2002,17 (1):189-192.
[6] 李慕勤,尚大山,刘冬梅,等.电结晶羟基磷灰石涂层结构的研究[J].中国表面工程,2003(1):31-33.Li Muqin,Shang Dashan,Liu Dongmei,et al.Study on structure of the hydroxyapatite coating prepared by electrodeposition[J].Chinese Surface Engineering,2003 (1):31-33.
[7] 宁成云,王迎军,赵娜如,等.HA/ZrO2功能梯度涂层中羟基磷灰石的超微结构分析[J].中国材料科技与设备,2007(3):61-64.Ning Chengyun,Wang Yingjun,Zhao Naru,et al.Supermicrostructural characteristics of hydroxyapatite of HA/ZrO2functional gradient coating[J].Chinese Materials Science Technology & Equipment,2007(3):61-64.
[8] Toch A,Brozeka A,Blazewicz S,et al.FTIR study of electrochemically deposited hydroxyapatite coatings on carbon materials[J].J Mol Struck,2003,651/653:389-390.
[9] 熊信柏,李贺军,黄剑锋,等.一种制备仿生生物活性钙磷涂层的新方法[J].稀有金属材料与工程,2004,33(3):313-314.Xiong Xinbo,Li Hejun,Huang Jianfeng,et al.A novel method for preparing biomimetic bioactive calcium phosphate coatings[J].Metal Materials and Engineering,2004,33(3):313-314.
[10] 李颖华,曹丽云,黄剑锋,等.碳/碳复合材料表面纳米HAp/壳聚糖生物复合涂层的制备[J].航空材料学报,2009,29(4):81-84.Li Yinghua,Cao Liyun,Huang Jianfeng,et al.Preparation of nano-hydroxyapatite/chitosan bio-coatings on carbon/carbon composites[J].Journal of Aeronautical Materials,2009,29(4):81-84.
[11] 廖建国,李玉宝,王学江,等.纳米羟基磷灰石/聚碳酸酯复合生物材料I:制备及表征[J].复合材料学报,2008,25(3):63-67.Liao Jianguo,Li Yubao,Wang Xuejiang,et al.Nanohydroxyapatite/polycarbonate composites I:Preparation and characterization[J].Acta Materiae Compositae Sinica,2008,25(3):63-67.
[12] 方道斌,郭睿威,哈润华,等.丙烯酰胺聚合物[M].北京:化学工业出版社,2006:6.
[13] Cao L Y,Zhang C B,Huang J F.Influence of temperature,[Ca2+],Ca/P ratio and ultrasonic power on the crystallinity and morphology of hydroxyapatite nanoparticles prepared with a novel ultrasonic precipitation method[J].Materials Letter,2005,59:1902-1906.
[14] 熊信柏,李贺军,黄剑锋,等.碳/碳复合材料表面声电沉积/碱热处理复合工艺制备羟基磷灰石生物活性涂层的研究[J].稀有金属材料与工程,2005,34(9):1489-1492.Xiong Xinbo,Li Hejun,Huang Jianfeng,et al.Bioactive hydroxyapatite coating on carbon/carbon composite prepared by sonoelectrodeposition and alkaline-heat treatment[J].Rare Metal Materials and Engineering,2005,34(9):1489-1492.
[15] 倪军,刘榕芳,肖秀峰,等.电泳沉积HA/Ti复合涂层的结合强度和热稳定性[J].稀有金属材料与工程,2006,35(1):119-122.Ni Jun,Liu Rongfang,Xiao Xiufeng,et al.Study on bonding strength and thermal stability of electrophoretic deposition HA/Ti composite coatings[J].Rare Metal Materials and Engineering,2006,35(1):119-122.
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