Biegaj Karolina W, Rowland Martin G, Lukas Tim M, Heng Jerry Y Y
Surfaces and Particle Engineering Laboratory, Department of Chemical Engineering, Imperial College London, South Kensington Campus, London SW7 2AZ, United Kingdom.
Pfizer Research and Development, Pfizer Ltd., Discovery Park House, Sandwich, Kent CT13 9NJ, United Kingdom.
ACS Omega. 2017 Apr 21;2(4):1576-1582. doi: 10.1021/acsomega.7b00125. eCollection 2017 Apr 30.
In the present study, the correlation between surface chemical groups and the electrostatic properties of particulate materials was studied. Glass beads were modified to produce OH-, NH-, CN-, and F-functionalized materials. The materials were charged separately both by friction and by conventional corona charging, and the results were compared. The results obtained from both methods indicated that the electrostatic properties are directly related to the surface functional group chemistry, with hydrophobic groups accumulating greater quantities of charge than hydrophilic groups. The fluorine-rich surface accumulated 5.89 times greater charge upon tribocharging with stainless steel than the hydroxyl-rich surface. However, in contrast to the tribocharging method, the charge polarity could not be determined when corona charging was used. Moreover, discharge profiles at different humidity levels (25% RH, 50% RH, and 75% RH) were obtained for each modified surface, which showed that higher humidity facilitates faster charge decay; however, this enhancement is surface chemistry-dependent. By increasing the humidity from 25% RH to 75% RH, the charge relaxation times can be accelerated 1.6 times for fluorine and 12.2 times for the cyano group. These data confirm that surface functional groups may dictate powder electrostatic behavior and account for observed charge accumulation and discharge phenomena.
在本研究中,研究了颗粒材料的表面化学基团与静电性能之间的相关性。对玻璃珠进行改性,以制备含羟基、氨基、氰基和氟官能团的材料。分别通过摩擦和传统电晕充电对材料进行充电,并对结果进行比较。两种方法得到的结果均表明,静电性能与表面官能团化学直接相关,疏水基团比亲水基团积累更多的电荷。与富含羟基的表面相比,富含氟的表面在与不锈钢摩擦起电时积累的电荷多5.89倍。然而,与摩擦起电方法不同,使用电晕充电时无法确定电荷极性。此外,还获得了每个改性表面在不同湿度水平(25%相对湿度、50%相对湿度和75%相对湿度)下的放电曲线,结果表明较高的湿度有助于更快的电荷衰减;然而,这种增强取决于表面化学性质。通过将湿度从25%相对湿度提高到75%相对湿度,氟官能团的电荷弛豫时间可加快1.6倍,氰基的电荷弛豫时间可加快12.2倍。这些数据证实,表面官能团可能决定粉末的静电行为,并解释观察到的电荷积累和放电现象。