Helminger Maria, Wu Baohu, Kollmann Tina, Benke Dominik, Schwahn Dietmar, Pipich Vitaliy, Faivre Damien, Zahn Dirk, Cölfen Helmut
Physical Chemistry, University of Konstanz Universitätsstrasse 10, D-78457, Konstanz, Germany.
Physical Chemistry, University of Konstanz Universitätsstrasse 10, D-78457, Konstanz, Germany ; Jülich Centre for Neutron Science JCNS-MLZ, Outstation at MLZ Lichtenbergstrasse 1, D-85747, Garching, Germany.
Adv Funct Mater. 2014 Jun;24(21):3187-3196. doi: 10.1002/adfm.201303547. Epub 2014 Feb 12.
A simple preparation of thermoreversible gelatin-based ferrogels in water provides a constant structure defined by the crosslinking degree for gelatin contents between 6 and 18 wt%. The possibility of varying magnetite nanoparticle concentration between 20 and 70 wt% is also reported. Simulation studies hint at the suitability of collagen to bind iron and hydroxide ions, suggesting that collagen acts as a nucleation seed to iron hydroxide aggregation, and thus the intergrowth of collagen and magnetite nanoparticles already at the precursor stage. The detailed structure of the individual ferrogel components is characterized by small-angle neutron scattering (SANS) using contrast matching. The magnetite structure characterization is supplemented by small-angle X-ray scattering and microscopy only visualizing magnetite. SANS shows an unchanged gelatin structure of average mesh size larger than the nanoparticles with respect to gel concentration while the magnetite nanoparticles size of around 10 nm seems to be limited by the gel mesh size. Swelling measurements underline that magnetite acts as additional crosslinker and therefore varying the magnetic and mechanical properties of the ferrogels. Overall, the simple and variable synthesis protocol, the cheap and easy accessibility of the components as well as the biocompatibility of the gelatin-based materials suggest them for a number of applications including actuators.
在水中简单制备基于明胶的热可逆铁凝胶,可得到一种由明胶含量在6至18 wt%之间的交联度所定义的恒定结构。文中还报道了在20至70 wt%之间改变磁铁矿纳米颗粒浓度的可能性。模拟研究暗示胶原蛋白适合结合铁离子和氢氧根离子,这表明胶原蛋白作为氢氧化铁聚集的成核种子,因此在前驱体阶段胶原蛋白和磁铁矿纳米颗粒就已共生。使用对比匹配的小角中子散射(SANS)对单个铁凝胶组分的详细结构进行了表征。仅通过小角X射线散射和显微镜观察磁铁矿对磁铁矿结构进行表征。SANS显示,相对于凝胶浓度,平均网孔尺寸大于纳米颗粒的明胶结构不变,而尺寸约为10 nm的磁铁矿纳米颗粒似乎受凝胶网孔尺寸限制。溶胀测量结果强调,磁铁矿起到额外交联剂的作用,因此改变了铁凝胶的磁性和机械性能。总体而言,简单且可变的合成方案、组分廉价且易于获取以及基于明胶材料的生物相容性表明它们可用于包括致动器在内的多种应用。