炭素技术
炭素技術
탄소기술
CARBON TECHNIQUES
2009年
6期
1-5
,共5页
石墨微粉%粒度分布特性%激光法%分散剂%单宁酸
石墨微粉%粒度分佈特性%激光法%分散劑%單寧痠
석묵미분%립도분포특성%격광법%분산제%단저산
Graphite powder%granularity distribution characteristics%laser method%dispersant%tannic acid
以水为分散介质,用激光法测定了球形天然石墨炭包覆(C-NG)试样和人造石墨(AG)试样的粒度分布特性.实验结果表明:由于石墨表面的疏水性,其颗粒在水中会聚集成团,因此不可能准确地测定试样的粒度分布特性.在水中添加具有复极性分子结构的单宁酸后,由于其非极性端定向吸附于石墨颗粒表面,极性端面向水,与水分子结合形成水分子层,从而阻挡了石墨颗粒的团聚,起到了分散(隔离)作用;单宁酸的添加量必须适当,过量时将使石墨颗粒表面的饱和单分子层叠加为双分子层,使石墨颗粒表面又逐渐转变为疏水性,从而使石墨颗粒之间再次发生团聚;测试时增加分散(搅拌)时间有利于石墨颗粒的分散,但影响甚微.
以水為分散介質,用激光法測定瞭毬形天然石墨炭包覆(C-NG)試樣和人造石墨(AG)試樣的粒度分佈特性.實驗結果錶明:由于石墨錶麵的疏水性,其顆粒在水中會聚集成糰,因此不可能準確地測定試樣的粒度分佈特性.在水中添加具有複極性分子結構的單寧痠後,由于其非極性耑定嚮吸附于石墨顆粒錶麵,極性耑麵嚮水,與水分子結閤形成水分子層,從而阻擋瞭石墨顆粒的糰聚,起到瞭分散(隔離)作用;單寧痠的添加量必鬚適噹,過量時將使石墨顆粒錶麵的飽和單分子層疊加為雙分子層,使石墨顆粒錶麵又逐漸轉變為疏水性,從而使石墨顆粒之間再次髮生糰聚;測試時增加分散(攪拌)時間有利于石墨顆粒的分散,但影響甚微.
이수위분산개질,용격광법측정료구형천연석묵탄포복(C-NG)시양화인조석묵(AG)시양적립도분포특성.실험결과표명:유우석묵표면적소수성,기과립재수중회취집성단,인차불가능준학지측정시양적립도분포특성.재수중첨가구유복겁성분자결구적단저산후,유우기비겁성단정향흡부우석묵과립표면,겁성단면향수,여수분자결합형성수분자층,종이조당료석묵과립적단취,기도료분산(격리)작용;단저산적첨가량필수괄당,과량시장사석묵과립표면적포화단분자층첩가위쌍분자층,사석묵과립표면우축점전변위소수성,종이사석묵과립지간재차발생단취;측시시증가분산(교반)시간유리우석묵과립적분산,단영향심미.
The granularity distribution characteristics of carbon sample coated natural graphite (C-NG) and artificial graphite (AG) sample were determined by laser method in the medium of water. The experimental results show that the graphite particles aggregate in water due to their hydrophobic surfaces. Therefore the granularity distributions characteristics cannot be determined correctly. Tannic acid possesses the molecular structure of complex polarity. After adding it into water, its molecules will adsorb on the surfaces of graphite particles with their nonpolar ends. The polar ends will face to the water and combine with water molecules to form a layer of water, which will hinder the aggregation of graphite particles and produce the dispersing (separating) action. The addition of tannic acid must be appropriate. Excess of it will transform the surfaces of graphite particles from saturated monomolecular layers to bimolecular layers. The surfaces of graphite particles will become hydrophobic gradually and the graphite particles will aggregate again. Increasing the dispersing (stirring ) time will be benefit to disper graphite particles in water, but the influences is very little.