400-6699-117转1000
您好,欢迎您查看分析测试百科网,请问有什么帮助您的?
分析测试百科网 认证会员,请放心拨打!
诚信认证:
工商注册信息已核实!参考报价: | 面议 | 型号: | Impact Tester IT 100 XL (Bond Index) |
品牌: | 莱驰 | 产地: | 德国 |
关注度: | 16 | 信息完整度: | |
样本: | 典型用户: | 暂无 | |
供应商性质 | 行业代理 | 产地类别 | 进口 |
400-6699-117转1000
Abrasion Tester AT 100 XL (Bond Index)
功能和特性
资料下载
查询报价<
联系我们报价详情 目录下载 生成产品信息的PDF文档
The Bond Abrasion Index, devised by F.C. Bond in the 1940‘s, quantifies the abrasivity of ores and minerals. The index serves to calculate metal wear rates in crushers and ball consumption rates in ball mills.
The AT 100 XL consists of a rotating insert into which dry ore samples with a defined particle size are placed. An impact paddle mounted on a centre shaft, rotating at a higher speed than the insert, grinds the sample over a defined period of time.
Both insert and paddle rotate in the same direction. The paddle is made from standard alloy steel hardened to 500 Brinell. The Abrasion Index is calculated from the weight loss of the paddle under standard operating conditions.
优点
pre-set rotation speed and time
CE conform version
性能指标
应用 矿石和矿物的耐磨性量化
应用领域 地质 / 冶金, 建筑原料, 环境 / 资源回收利用
评估 利用拍子称重计算质量损失
进料粒度* < 19 mm
批次加料量* 400 g 每次
程序数量 4,每 400 g
耐磨性测试时间 4*15 min
旋转叶片 NO DATA FOUND (copySource=3" x 1" x ?" hardened to 500 Brinell)
转速 拍击 632 min-1 / 插入 70 min-1
电源数据: 230 V, 50 Hz
电源接头: 单相
机体尺寸 (宽x高x纵深) 700 x 1140 x 700 mm
净重 ~ 246 kg
标准 CE
Please note:
受样品材料性质和仪器配置/设定的影响
作用原理
The Bond Index Abrasion Tester AT 100 XL consists of a rotating insert into which a dry sample with a defined particle size is placed. An impact paddle mounted on a centre shaft rotating at a higher speed than the insert grinds the sample over a defined period of time.
Both insert and paddle rotate in the same direction. The paddle is made from standard alloy steel hardened to 500 Brinell. The Abrasion Index is calculated from the weight loss of the paddle under standard operating conditions.
根据技术改造和误差调整
德国retschTester AT 100 XL信息由北京谱飞科技有限公司为您提供,如您想了解更多关于德国retschTester AT 100 XL报价、型号、参数等信息,欢迎来电或留言咨询。
注:该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案,不可用于临床诊断或治疗等相关用途