CN102516676B - 药用合成垫片及其制备方法 - Google Patents
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- B29C48/25—Component parts, details or accessories; Auxiliary operations
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
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- B29C2948/92—Measuring, controlling or regulating
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- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
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- B29C2948/00—Indexing scheme relating to extrusion moulding
- B29C2948/92—Measuring, controlling or regulating
- B29C2948/92504—Controlled parameter
- B29C2948/92704—Temperature
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2948/00—Indexing scheme relating to extrusion moulding
- B29C2948/92—Measuring, controlling or regulating
- B29C2948/92819—Location or phase of control
- B29C2948/92857—Extrusion unit
- B29C2948/92876—Feeding, melting, plasticising or pumping zones, e.g. the melt itself
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C2948/00—Indexing scheme relating to extrusion moulding
- B29C2948/92—Measuring, controlling or regulating
- B29C2948/92819—Location or phase of control
- B29C2948/92923—Calibration, after-treatment or cooling zone
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Abstract
本发明涉及一种药用包装材料,具体涉及一种药用合成垫片及其制备方法,其特征在于由以下原料制成:氯化丁基橡胶、煅烧高岭土、叔辛基苯酚甲醛树脂、硬脂酸、氧化锌、改性聚乙烯、钛白粉、半补强炉法炭黑和氧化镁。本发明的优点在于:(1)以医用弹性体为主要原料,在保证垫片所需物理机械性能的同时,极大地降低了生产成本;(2)配方中所用的各种原料,均无任何毒副作用,并且完全符合医用原材料的标准,完全环保、无环境污染;(3)生产工艺简单,极大地减少了能耗,提高了生产效率;(4)工序的减少使人为出错的因素大大降低,保证了质量的稳定性;(5)产品性能佳,无落屑现象。
Description
技术领域
本发明涉及一种药用包装材料,具体涉及一种药用合成垫片及其制备方法。
背景技术
药用垫片是药用包材领域最常用的一种密封元件,用于防止流体泄露等。传统的药用合成垫片是由聚异戊二烯橡胶及其相关辅料,经炼胶、硫化、压片、切片、冷冲、硅化、制冷等二十多道工序生产而成,生产工艺繁琐、耗能耗时、并对环境有一定的污染,不但生产成本居高不下,而且产品质量得不到保障,针刺落屑的现象时有发生。一种成本低廉、工艺简单、安全环保、品质优良的药用合成聚异戊二烯垫片的替代品亟待出现。
发明内容
本发明的目的是提供一种药用合成垫片及其制备方法,能够具有成本低、工艺简单、安全环保并且品质优良,不会有落屑现象的发生。
本发明所述的一种药用合成垫片,由以下重量份数的原料制成:氯化丁基橡胶45000份、煅烧高岭土40500份、叔辛基苯酚甲醛树脂675份、硬脂酸450份、氧化锌2250份、改性聚乙烯900份、钛白粉1350份、半补强炉法炭黑166份和氧化镁60份。
本发明所述的药用合成垫片的制备方法,包括以下步骤:
(1)配料、密炼:将各种原料均匀的混合在一起,在密炼机中密炼操作8-10min,排胶温度为95-105℃,然后加入到XKY-550橡胶开放式炼胶机中进行开炼,开炼操作8-10min,前、后辊温度分别为60±5℃和65±5℃,最后通过挂架式冷却装置进行冷却,冷却至40℃以下,经冷却后的胶片进行卷取、停放,停放时间在1天~10天内;
(2)预成型:将胶片经过导向辊进入冷喂料挤出机的喂料口,开始挤出,挤出的胶料被机头刀片割开,由圆筒变成片状,其中,加压、塑化温度为35℃,挤出温度为30℃,挤出的胶片送往三辊压延机,通入蒸汽加热三辊压延机的辊筒,三辊压延机上辊温度为60±5℃,经压延后的胶片直接送到八辊冷却装置,打开的八辊冷却装置的冷却水,使胶片冷却到40℃以下,冷却好之后定长裁片装置,通过调整编码器参数,使胶片裁断的长度达到683~700mm,将胶片放入不锈钢盘,再放进胶盘存放架上,停放,停放时间在8小时~10天内;
(3)硫化:采用抽真空模塑成型机对胶片进行硫化,硫化温度193±2℃,硫化时间280~320s,硫化压力≥3100KN,硫化结束后,垫片成型;
(4)除边:采用除边机对垫片进行除边,除边机的空气压力表控制在0.55-0.75MPa;
(5)筛屑、清洗、包装:是采用震动筛和转鼓筛对垫片进行筛屑,筛屑完成后在清洗机里对垫片完成清洗、漂洗、硅化、干燥和冷却的一体化操作,最后得到产品,包装即可。
其中,步骤(5)中的清洗机优选按照以下标准设置:转速控制在1转/分钟、硅化时间控制在5~30分钟、干燥时间控制在60~90分钟。
本发明的优点在于:(1)以医用弹性体为主要原料,在保证垫片所需物理机械性能的同时,极大地降低了生产成本;(2)配方中所用的各种原料,均无任何毒副作用,并且完全符合医用原材料的标准,完全环保、无环境污染;(3)生产工艺简单,极大地减少了能耗,提高了生产效率;(4)工序的减少使人为出错的因素大大降低,保证了质量的稳定性;(5)产品性能佳,无落屑现象。
具体实施方式
以下结合实施例对本发明做进一步说明。
实施例1:
本实施例的原料配方为:氯化丁基橡胶45000g、煅烧高岭土40500g、叔辛基苯酚甲醛树脂675g、硬脂酸450g、氧化锌2250g、改性聚乙烯900g、钛白粉1350g、半补强炉法炭黑166g和氧化镁60g。
本实施例按照以下步骤制备产品:
(1)配料、密炼:将各种原料均匀的混合在一起,在密炼机中密炼操作10min,排胶温度为100℃,然后加入到XKY-550橡胶开放式炼胶机中进行开炼,开炼操作10min,前、后辊温度分别为60±5℃和65±5℃,最后通过挂架式冷却装置进行冷却,冷却至25℃,经冷却后的胶片进行卷取、停放5天;
(2)预成型:将胶片经过导向辊进入冷喂料挤出机的喂料口,开始挤出,挤出的胶料被机头刀片割开,由圆筒变成片状,其中,加压、塑化温度为35℃,挤出温度为30℃,挤出的胶片送往三辊压延机,通入蒸汽加热三辊压延机的辊筒,三辊压延机上辊温度为60±5℃,经压延后的胶片直接送到八辊冷却装置,打开的八辊冷却装置的冷却水,使胶片冷却到40℃以下,冷却好之后定长裁片装置,通过调整编码器参数,使胶片裁断的长度达到700mm,将胶片放入不锈钢盘,再放进胶盘存放架上,停放5天;
(3)硫化:采用抽真空模塑成型机对胶片进行硫化,硫化温度193±2℃,硫化时间300s,硫化压力≥3100KN,硫化结束后,垫片成型;
(4)除边:采用除边机对垫片进行除边,除边机的空气压力表控制在0.70MPa;
(5)筛屑、清洗、包装:是采用震动筛和转鼓筛对垫片进行筛屑,筛屑完成后在清洗机里对垫片完成清洗、漂洗、硅化、干燥和冷却的一体化操作,最后得到产品,包装即可。
其中,步骤(5)中的清洗机按照以下标准设置:转速控制在1转/分钟、硅化时间控制在20分钟、干燥时间控制在60分钟。
实施例2:
将硫化时间改为280s,其它制备步骤同实施例1一样。
实施例3:
将硫化时间改为320s,其它制备步骤同实施例1一样。
实施例1的物理机械性能测试:
将垫片夹入电子拉力试验机两夹具(标距为25mm),力量归零、伸长量归零,然后启动测试,进行拉力测试。将拉伸强度、扯断伸长率、300%定伸应力值记录于原始记录上。如果垫片扯断时断裂面不在标距范围内,则此数据不作为有效结果。下表为实施例1物理性能所达到的技术指标:
扯断伸长率(Mpa) | 300%定伸强力(Mpa) | 拉伸强度(Mpa) |
≥550 | ≥1.2 | ≥4.0 |
实施例1~实施例3的快速性能项目检测及指标:
硫化阶段对应的指标说明:
T10 | 【ML+(MH-ML)×10%】时扭矩所对应的时间 |
T90 | 【ML+(MH-ML)×90%】时扭矩所对应的时间 |
ML | 胶料流动过程中的最低扭矩值,它反应胶料在一定条件(温度)下的冲模流动性 |
MH | 胶料流动过程中的最高扭矩值,它反应胶料的物性 |
下表为实施例1~实施例3的产品的密度、硬度及T10和T90的技术指标:
密度 | 硬度(邵尔A) | T10(Sec) | T90(Sec) | |
实施例1 | 1.38±0.03 | 54±5 | ≥35 | ≤240 |
实施例2 | 1.38±0.03 | 58±5 | ≥40 | ≤260 |
实施例3 | 1.26±0.03 | 48±5 | ≥30 | ≤350 |
Claims (2)
1.一种药用合成垫片,其特征在于由以下重量份数的原料制成:氯化丁基橡胶45000份、煅烧高岭土40500份、叔辛基苯酚甲醛树脂675份、硬脂酸450份、氧化锌2250份、改性聚乙烯900份、钛白粉1350份、半补强炉法炭黑166份和氧化镁60份;
制备方法包括以下步骤:
(1)配料、密炼:将各种原料均匀的混合在一起,在密炼机中密炼操作8-10min,排胶温度为95-105℃,然后加入到XKY-550橡胶开放式炼胶机中进行开炼,开炼操作8-10min,前、后辊温度分别为60±5℃和65±5℃,最后通过挂架式冷却装置进行冷却,冷却至40℃以下,经冷却后的胶片进行卷取、停放,停放时间在1天~10天内;
(2)预成型:将胶片经过导向辊进入冷喂料挤出机的喂料口,开始挤出,挤出的胶料被机头刀片割开,由圆筒变成片状,其中,加压、塑化温度为35℃,挤出温度为30℃,挤出的胶片送往三辊压延机,通入蒸汽加热三辊压延机的辊筒,三辊压延机上辊温度为60±5℃,经压延后的胶片直接送到八辊冷却装置,打开的八辊冷却装置的冷却水,使胶片冷却到40℃以下,冷却好之后定长裁片装置,通过调整编码器参数,使胶片裁断的长度达到683~700mm,将胶片放入不锈钢盘,再放进胶盘存放架上,停放,停放时间在8小时~10天内;
(3)硫化:采用抽真空模塑成型机对胶片进行硫化,硫化温度193±2℃,硫化时间280~320s,硫化压力≥3100KN,硫化结束后,垫片成型;
(4)除边:采用除边机对垫片进行除边,除边机的空气压力表控制在0.55-0.75MPa;
(5)筛屑、清洗、包装:采用震动筛和转鼓筛对垫片进行筛屑,筛屑完成后在清洗机里对垫片完成清洗、漂洗、硅化、干燥和冷却的一体化操作,最后得到产品,包装即可。
2.根据权利要求1所述的药用合成垫片,其特征在于步骤(5)中清洗机转速控制在1转/分钟、硅化时间控制在5~30分钟、干燥时间控制在60~90分钟。
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