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Zein-Based Materials: Effect of Nanocarbon Inclusion and Potential Applications

机译:基于ZEIN的材料:纳米碳包附和潜在应用的影响

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摘要

Zein-based materials were produced by dissolving zein water at pH 13, and subsequently congealing it with CaCl2. Biocarbon particles were produced with miscanthus biomass by pyrolization at 650 degrees C (M-L) and at 900 degrees C (M-H), followed by ball-milling. Increasing the pyrolization temperature caused the disappearance of functional groups on the particle surface and increased their hydrophobicity of the particles (as shown through Attenuated Total Reflection- Fourier Transform Infrared Spectroscopy, ATR-FTIR and by the preferential partitioning on the particles in toluene rather than water). Therefore, hydrophobic interactions were likely stronger between zein and M-H particles, than between zein and M-L particles. Measurements conducted using a zeta sizer showed that aggregates of zein and M-L particles were 1 mu m, and aggregates of zein and M-H particles were 1 mu m. M-H particles increased the shear viscous (G '') and elastic (G '') moduli of zein, and rendered the material elastic (G ' approximately equal to 6.6 x 10(4)Pa G '' approximately equal to 5.7 x 10(4) Pa with M-H and G ' approximately equal to 4.3 x 10(4) Pa and G '' approximately equal to 4.6 x 10(4) Pa without zein). M-H particles also increased the tensile strength of zein materials, potentially improving their usefulness as bioplastics. M-L particles increased the viscoelastic moduli of zein (G ' approximately equal to 6.7 x 10(4) Pa and G '' approximately equal to 7.3 x 10(4) Pa), but did not render the material elastic (i.e. G ' was not greater than G ''). Moreover, M-L particles stiffened zein at small elongational deformations, but rendered it brittle at larger deformations. M-H particles greatly reduced the permeability of zein barriers injected in sandy media, which can be for instance used to prevent the migration of subsurface contaminants. Flow reduction was 90% with zein and M-H, whereas it was 64% with zein only and 68% with zein and M-L particles and zein.[GRAPHICS].
机译:通过将玉米醇溶蛋白水溶解在pH13中并随后用CaCl 2施加来制备基于玉米蛋白的材料。通过在650℃(M-L)和900℃(M-H)以650℃(M-H)的溶解物,用烧焦产生生物羰基颗粒。增加溶解温度导致颗粒表面上的官能团的消失,并增加了颗粒的疏水性(如通过衰减的总反射 - 傅里叶变换红外光谱,ATR-FTIR和通过甲苯中的颗粒上的优先分配所示而不是水的疏水性)。因此,玉米醇溶蛋白和M-H颗粒之间的疏水相互作用可能较强,而不是玉米醇溶蛋白和M-L颗粒之间。使用Zeta Sizer进行的测量显示,玉米醇蛋白和M-L颗粒的聚集体>1μm,玉米醇蛋白和M-H颗粒的聚集体为<1μm。 MH颗粒增加了玉米醇蛋白的剪切粘性(g'')和弹性(g''),并使材料弹性(g'大约等于6.6×10(4)pa> g''大约等于5.7 x 10 (4)PA,MH和G'大约等于4.3×10(4)PA和G''大约等于4.6×10(4)PA,无ZEIN)。 M-H颗粒还增加了玉米醇料材料的拉伸强度,可能改善其作为生物塑料的有用性。 ml颗粒增加玉米醇溶蛋白的粘弹性模量(g'大约等于6.7×10(4)pa和g''大约等于7.3×10(4)pa),但没有使材料弹性(即g'不是大于g'')。此外,M-L颗粒在小的伸长变形下加强玉米蛋白,但在较大的变形下使其变脆。 M-H颗粒大大降低了在砂质介质中注入的玉米醇蛋白屏障的渗透性,这可以例如用于防止地下污染物的迁移。玉米醇蛋白和M-H的流量减少为90%,而玉米蛋白,玉米蛋白和玉米蛋白和M-L颗粒和玉米蛋白,68%为64%。[图形]。

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