Department of Materials Science & Engineering, Northwestern University, Evanston, IL 60208, USA.
Acta Biomater. 2012 Jan;8(1):253-61. doi: 10.1016/j.actbio.2011.08.014. Epub 2011 Aug 22.
While the matrix/reinforcement load-transfer occurring at the micro- and nanoscale in nonbiological composites subjected to creep deformation is well understood, this topic has been little studied in biological composites such as bone. Here, for the first time in bone, the mechanisms of time-dependent load transfer occurring at the nanoscale between the collagen phase and the hydroxyapatite (HAP) platelets are studied. Bovine cortical bone samples are subjected to synchrotron X-ray diffraction to measure in situ the evolution of elastic strains in the crystalline HAP phase and the evolution of viscoelastic strains accumulating in the mineralized collagen fibrils under creep conditions at body temperature. For a constant compressive stress, both types of strains increase linearly with time. This suggests that bone, as it deforms macroscopically, is behaving as a traditional composite, shedding load from the more compliant, viscoelastic collagen matrix to the reinforcing elastic HAP platelets. This behavior is modeled by finite-element simulation carried out at the fibrillar level.
虽然在经受蠕变变形的非生物复合材料中,微观和纳米尺度上的基质/增强体的载荷传递机制已经得到很好的理解,但在骨骼等生物复合材料中,这一课题的研究还很少。在这里,首次在骨骼中研究了在纳米尺度上,胶原蛋白相与羟基磷灰石(HAP)板之间的时变载荷传递机制。对牛皮质骨样品进行同步加速器 X 射线衍射,以原位测量在体温下蠕变条件下,结晶 HAP 相中的弹性应变演变和矿化胶原原纤维中积累的粘弹性应变的演变。对于恒定的压缩应力,两种类型的应变都随时间呈线性增加。这表明,骨骼在宏观变形时,表现得像一种传统的复合材料,将载荷从更具弹性的粘弹性胶原基质传递到增强弹性的 HAP 板上。这种行为是通过在纤维水平上进行的有限元模拟来建模的。