聚甲醛塑料,俗称赛钢,为结晶性热可塑性塑料,具明显熔点165~175℃,性质zui接近金属。
产品说明 | |
Preliminary Datasheet Rapidly solidifying standard grade for injection molding. Ultraform® PRO offers a comprehensive service package, which supports customers in product development for the medical technology market. Ultraform® PRO is in compliance with Pharmacopoeia and Biocompatibility-Tests in Europe, United States and Japan as specified below. However, the biocompatibility tests were recorded on tests specimens of Ultraform PRO to show compatibility of the material in general. The biocompatibility-tests listed below are not part of any continuous production control. European Pharmacopoeia, Japanese Pharmacopoeia: The composition of the product complies with the requirements of the European Pharmacopoeia 7th Edition, Chap. 3.2.2. "Plastic Containers and Closures for Pharmaceutical Use" and with the requirements of the Japanese Pharmacopoeia, 15th Edition, General Information, "17. Plastic Containers for Pharmaceutical Products". However, suitability for the end application concerned including observation of given limitations and toxicological thresholds have to be ensured on the final article by the producer. US Pharmacopoeia: Biological Reactivity Tests, USP Plastic Class VI (USP VI) ISO 10993-5: Biological Evaluation of Medical Devices Part 5: Test for Cytotoxicity DMF: A Drug Master File (DMF) has been registered at FDA for Ultraform® PRO. Food Contact: Ultraform® PRO is in compliance with multiple regional food contact regulations, especially for Europe and United States. Additional compliances may also be available. Please contact your local representative or the Ultraplaste Infopoint (: ultraplaste.infopoint@basf.com, efon: +49 621-60-78780, +49 621-60-78730). For notice: However, BASF has not designed or tested its plastics with respect to all of the special requirements related to their use in medical devices (defined in risk classes I to III according to the European and US Medical Device legislation) and pharmaceutical applications. Therefore BASF makes no warranties, express or implied, concerning the suitability of any BASF plastics for use in any medical device and pharmaceutical applications. | |
总体 | |
材料状态 | 已商用:当前有效 |
资料 1 | Processing - Injection Molding Cooling Times (English)Technical Datasheet (English) |
搜索 UL 黄卡 | BASF CorporationUltraform® |
供货地区 | 北美洲欧洲亚太地区 |
性能特点 | 生物兼容性 |
用途 | 药物医疗/护理领域的应用 |
机构评级 | DMF 未评级EC 1907/2006 (REACH)EP Monograph 3.2.2ISO 10993 Part 5USP 第VI类 |
RoHS 合规性 | RoHS 合规 |
形式 | 颗粒 |
加工方法 | 注射成型 |
树脂ID (ISO 1043) | POM |
物理性能 | 额定值 | 单位制 | 测试方法 |
密度 | 1.40 | g/cm3 | ISO 1183 |
溶化体积流率(MVR) (190°C/2.16 kg) | 0.458 | in3/10min | ISO 1133 |
吸水率 | ISO 62 | ||
饱和, 73°F | 0.80 | % | |
平衡, 73°F, 50% RH | 0.20 | % | |
硬度 | 额定值 | 单位制 | 测试方法 |
球压硬度 (H 358/30) | 21000 | psi | ISO 2039-1 |
机械性能 | 额定值 | 单位制 | 测试方法 |
拉伸模量 (73°F) | 392000 | psi | ISO 527-2 |
拉伸应力 (屈服, 73°F) | 9430 | psi | ISO 527-2/50 |
拉伸应变 (屈服, 73°F) | 9.4 | % | ISO 527-2/50 |
断张率 (73°F) | 27 | % | ISO 527-2/50 |
拉伸蠕变模量 2 (1000 hr) | 203000 | psi | ISO 899-1 |
冲击性能 | 额定值 | 单位制 | 测试方法 |
简支梁缺口冲击强度 | ISO 179/1eA | ||
-22°F | 2.6 | ft·lb/in2 | |
73°F | 2.9 | ft·lb/in2 | |
简支梁缺口冲击强度 | ISO 179/1eU | ||
-22°F | 90 | ft·lb/in2 | |
73°F | 100 | ft·lb/in2 |
热性能 | 额定值 | 单位制 | 测试方法 |
热变形温度 (264 psi, 未退火) | 212 | °F | ISO 75-2/A |
熔融温度 | 333 | °F | ISO 11357-3 |
线形膨胀系数 - 流动 (73 到 131°F) | 0.000061 | in/in/°F | ISO 11359-2 |
zui高使用温度 - Short Cycle Operation | 212 | °F |
电气性能 | 额定值 | 单位制 | 测试方法 |
表面电阻率 | 1.0E+13 | ohm | IEC 60093 |
体积电阻率 | 1.0E+15 | ohm·cm | IEC 60093 |
相对电容率 (73°F, 1 MHz) | 3.80 | IEC 60250 | |
耗散因数 (73°F, 1 MHz) | 0.0050 | IEC 60250 | |
漏电起痕指数 (解决方案 A) | 600 | V | IEC 60112 |
可燃性 | 额定值 | 单位制 | 测试方法 |
UL 阻燃等级 (0.0630 in) | HB | UL 94 |
补充信息 | 额定值 | 测试方法 | |
Automotive Materials (> 39.4 mil) | + | FMVSS 302 | |
ISO Type | POM-K, M-GNR, 03-002 | ISO 9988-1 | |
Polymer Abbreviation | POM |
注射 | 额定值 | 单位制 | |
加工(熔体)温度 | 374 到 446 | °F | |
模具温度 | 140 到 248 | °F |
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