CN112426619A - 一种量子能纤维改性离子感应基体材料 - Google Patents
一种量子能纤维改性离子感应基体材料 Download PDFInfo
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Abstract
本发明公开了一种量子能纤维改性离子感应基体材料,包括背衬层、粘贴层、离子堆积层、表面覆盖层以及剥离层,所述粘贴层置于背衬层和离子堆积层之间,在粘贴层的中间位置为离子堆积层,离子堆积层和剥离层之间为表面覆盖层,剥离层为最外层。离子堆积层为量子能纤维改性的聚酰亚胺薄膜经电晕充电制备而成。本发明设计合理,能够获得高比表面电压并生产微电流,电荷在产品的储存稳定,可最大限度地延长产品的持效期,并提高对腰椎和颈椎疼痛的治疗效果。
Description
技术领域
本发明涉及医用耗材技术领域,具体包含一种量子能纤维改性离子感应基体材料。
背景技术
近年来,随着生活方式的改变,电脑族、手机族和出租车司机等人群出现了越来赶工多的颈椎或腰椎病问题,这类人群由于工作或生活习惯的原因长时间保持颈椎和腰椎一个姿势,颈椎和腰椎的肌肉由于长期用力得不到休息,最后导致肌肉劳损,进一步诱发骨骼和间盘系统的腰颈椎病。而随着手机的便携化,腰椎或颈椎疾病的高发人群逐渐向低龄化发展。据统计,每10个颈椎不好的年轻人里,平均有5-6个是手机不离手的低头族。这类人中或多或少都伴随着腰颈椎疾病问题。
腰椎或颈椎疾病一个共同的特点就是伴随着难耐的疼痛,给患者带来极大的痛苦。目前用于消肿止痛、抗菌消炎的治疗,市面上存在形形色色的产品,但主要还是依靠药物的治疗方法,其中相当部分药物的疗效还难以令人满意,而且药物治疗伤痛时间长,存在一定的毒副作用。而市面上现有一些物理止痛治痛的产品,除了疗效作用一般外,还存在持效期短、需要频繁更换敷贴的不足。
发明内容
本发明的目的是为了解决现有产品在治疗腰颈椎疼痛等方面的不足,而提供一种可显著镇痛、止痛、并且疗效持久的离子感应基体材料。
为了实现上述目的,本发明提供的技术方案为:
一种量子能纤维改性离子感应基体材料,包括背衬层、粘贴层、离子堆积层、表面覆盖层以及剥离层,所述粘贴层置于背衬层和离子堆积层之间,在粘贴层的中间位置为离子堆积层,离子堆积层和剥离层之间为表面覆盖层,剥离层为最外层。其特征在于:所述的离子堆积层为量子能纤维改性的聚酰亚胺薄膜经电晕充电制备而成。
优选地,所述的量子能纤维改性的聚酰亚胺薄膜制备工艺如下:
S1:将重量份数为2~4份的N-(正丁基)-γ-氨丙基三乙氧基硅烷加入到80~100份的乙醇中,充分混合,加入5~10份的量子能纤维,在超声条件下低速搅拌1h,取出后用无水乙醇浸泡冲洗3次,80℃下烘干,得到偶联剂处理后的量子能纤维;
S2:在0℃~5℃,先将重量份数为100~150份的偶联剂处理后的量子能纤维加入到20~50 份的四氢呋喃中,搅拌至完全溶解后,然后将80~120份的均酐分批加入,进行原位聚合反应,加入完毕后,持续反应1-12h,得到聚酰胺酸溶液;
S3:将聚酰胺酸溶液用200目铜网过滤,使用自动涂膜机在玻璃板上进行涂膜,涂膜厚度为 0.5mm,在超净室中室温干燥24h后,放入150~250℃鼓风干燥箱进行热亚胺化2~3h,得到量子能纤维改性的聚酰亚胺薄膜。
优选地,所述的表面覆盖层为喷涂防辐射涂料层的金属箔,所述金属箔为铝箔、金箔、银箔或铜箔。
进一步地,所述的表面覆盖层的加工制备步骤包括:
S1:在低湿度条件下,按照重量份比称取甲苯二异氰酸酯5~10份、氧化铁红10-15份、硅胶粉40~60份、掺有30~40%TiAlC陶瓷粉的涂料粉20~30份,快速转入喷料筒中机械搅拌均匀,形成了混合涂料粉末;
S2:采用静电喷涂机将上述所制得的混合涂料粉末涂覆到金属箔表面,经150~180℃加热处理20~30min,冷却,得到喷涂有特殊涂料层的金属箔;
S3:将上述喷涂有特殊涂料层的金属箔浸泡于吸湿盐溶液中1~3h,浸泡完毕后取出,在 100~150℃的温度上烘干即得含防辐射涂料层的金属箔。
优选地,所述的吸湿性盐溶液为饱和氯化锂溶液、饱和氯化钙溶液中的任意一种。
优选地,所述的离子堆积层的加工过程如下:其通电电压范围为驻极电压正极选择 20~30KV,负极选择10~30KV,驻极距离为10~15cm,通电时间20~60min。
优选地,所述的表面覆盖层能完全覆盖离子堆积层,所述的剥离层为油光面托纸层,所述的剥离层能完全覆盖表面覆盖层,并且与背衬层、粘贴层的大小和尺寸完全相同。
量子能粉末来源于一种特殊的土层,该土壤经高温锻烧和研磨加工后得到亚微米级的粉末。该粉末为多组分颗粒,其主要成分为二氧化硅和硅铝酸盐,将该粉末与蒸馏水搅拌成糊状,放置在恒温恒湿室中,熟成90天后经过滤得到膏状量子能粉,再将膏状的量子能粉进行冷冻处理,并与聚酯树脂按照一定比例进行融合混合,熔融挤出呈球状或圆柱状的量子能涤纶母粒,最后高温熔融纺丝得到量子能纤维。
当稳定状态的量子能原子受到加热或光线照射后,会因外界赋予能量产生电子激发,此时电子由i=k轨道移动到i=L轨道,再移回i=k轨道,期间会以放射红外线形式释放出能量。由于其放射的远红外线与人体内细胞分子的振动频率接近,便引起人体细胞的原子和分子的共振,透过共鸣吸收,分子之间摩擦生热形成热反应,促使皮下深层温度上升,并使微血管扩张,加速血液循环,有利于清除血管囤积物及体内有害物质,将妨害新陈代谢的障碍清除,重新使组织复活,促进酵素生成,达到活化组织细胞、防止老化、强化免疫系统的目的。
本发明的有益效果为:本发明选取聚酰亚胺为离子堆积层的基体材料,通过量子能纤维对其进行改性,一方面有利于血液循环和新陈代谢,与离子贴作用于皮肤表面产生的微电流一道产生协同消痛止痛的作用,止痛效果显著;另一方面,量子能纤维中所含的无机化合物可提高离子贴基体材料的疏水性能,降低材料的电导性能,减少聚酰亚胺驻极体脱阱电荷的损失,从而使经离子堆积工艺的基体材料表面电荷更为稳定,止痛疗效更为持久。此外,采用喷涂有防辐射涂料层的金属箔作为表面覆盖层,可以进一步削弱聚酰亚胺膜材料表面附近耗散的离子对其电荷储存的影响,极大地抑制聚酰亚胺膜的极化,减少热效应,进一步减少聚酰亚胺膜的电荷衰减性,最大限度地延长产品使用的有效期。
具体实施例
下面结合实施例对本发明做进一步描述;以下实施例仅用于更加清楚地说明本发明的目的、技术方案及优点,并不能以此来限制本发明的保护范围。
实施例1:
一种量子能纤维改性离子感应基体材料,包括背衬层、粘贴层、离子堆积层、表面覆盖层以及剥离层,所述粘贴层置于背衬层和离子堆积层之间,在粘贴层的中间位置为离子堆积层,离子堆积层和剥离层之间为表面覆盖层,剥离层为最外层。所述的表面覆盖层能完全覆盖离子堆积层,所述的剥离层为油光面托纸层,所述的剥离层能完全覆盖表面覆盖层,并且与背衬层、粘贴层的大小和尺寸完全相同。
所述的离子堆积层由量子能纤维改性的聚酰亚胺薄膜经电晕充电制备而成,其通电电压范围为驻极电压正极选择20KV,负极选择10KV,驻极距离为12cm,通电时间50min。
所述的量子能纤维改性的聚酰亚胺薄膜制备工艺如下:
S1:将重量份数为2份的N-(正丁基)-γ-氨丙基三乙氧基硅烷加入到80份的乙醇中,充分混合,加入6份的量子能纤维,在超声条件下低速搅拌1h,取出后用无水乙醇浸泡冲洗3次,80℃下烘干,得到偶联剂处理后的量子能纤维;
S2:在4℃,先将重量份数为1500份的偶联剂处理后的量子能纤维加入到40份的四氢呋喃中,搅拌至完全溶解后,然后将80份的均酐分批加入,进行原位聚合反应,加入完毕后,持续反应8h,得到聚酰胺酸溶液;
S3:将聚酰胺酸溶液用200目铜网过滤,使用自动涂膜机在玻璃板上进行涂膜,涂膜厚度为 0.5mm,在超净室中室温干燥24h后,放入250℃鼓风干燥箱进行热亚胺化3h,得到量子能纤维改性的聚酰亚胺薄膜。
所述的表面覆盖层为喷涂防辐射涂料层的铝箔,其加工制备步骤包括:
S1:在低湿度条件下,按照重量份比称取甲苯二异氰酸酯5份、氧化铁红12份、硅胶粉40份、掺有40%TiAlC陶瓷粉的涂料粉20份,快速转入喷料筒中机械搅拌均匀,形成了混合涂料粉末;
S2:采用静电喷涂机将上述所制得的混合涂料粉末涂覆到铝箔表面,经160℃加热处理20min,冷却,得到喷涂有特殊涂料层的铝箔;
S3:将上述喷涂有特殊涂料层的铝箔浸泡于饱和氯化锂溶液溶液中1h,浸泡完毕后取出,在120℃的温度上烘干即得含防辐射涂料层的铝箔。
实施例2:
一种量子能纤维改性离子感应基体材料,包括背衬层、粘贴层、离子堆积层、表面覆盖层以及剥离层,所述粘贴层置于背衬层和离子堆积层之间,在粘贴层的中间位置为离子堆积层,离子堆积层和剥离层之间为表面覆盖层,剥离层为最外层。所述的表面覆盖层能完全覆盖离子堆积层,所述的剥离层为油光面托纸层,所述的剥离层能完全覆盖表面覆盖层,并且与背衬层、粘贴层的大小和尺寸完全相同。
所述的离子堆积层由量子能纤维改性的聚酰亚胺薄膜经电晕充电制备而成,其通电电压范围为驻极电压正极选择25KV,负极选择20KV,驻极距离为10cm,通电时间20min。所述的量子能纤维改性的聚酰亚胺薄膜制备工艺如下:
S1:将重量份数为3份的N-(正丁基)-γ-氨丙基三乙氧基硅烷加入到100份的乙醇中,充分混合,加入5份的量子能纤维,在超声条件下低速搅拌1h,取出后用无水乙醇浸泡冲洗3次,80℃下烘干,得到偶联剂处理后的量子能纤维;
S2:在0℃,先将重量份数为120份的偶联剂处理后的量子能纤维加入到20份的四氢呋喃中,搅拌至完全溶解后,然后将90份的均酐分批加入,进行原位聚合反应,加入完毕后,持续反应1h,得到聚酰胺酸溶液;
S3:将聚酰胺酸溶液用200目铜网过滤,使用自动涂膜机在玻璃板上进行涂膜,涂膜厚度为 0.5mm,在超净室中室温干燥24h后,放入150℃鼓风干燥箱进行热亚胺化2.5h,得到量子能纤维改性的聚酰亚胺薄膜。
所述的表面覆盖层为喷涂防辐射涂料层的金箔,其加工制备步骤包括:
S1:在低湿度条件下,按照重量份比称取甲苯二异氰酸酯6份、氧化铁红10份、硅胶粉60份、掺有30%TiAlC陶瓷粉的涂料粉28份,快速转入喷料筒中机械搅拌均匀,形成了混合涂料粉末;
S2:采用静电喷涂机将上述所制得的混合涂料粉末涂覆到金箔表面,经150℃加热处理25min,冷却,得到涂有特殊涂料层的金箔;
S3:将上述喷涂有特殊涂料层的金箔浸泡于饱和氯化锂溶液中2h,浸泡完毕后取出,在100℃的温度上烘干即得含防辐射涂料层的金箔。
实施例3:
一种量子能纤维改性离子感应基体材料,包括背衬层、粘贴层、离子堆积层、表面覆盖层以及剥离层,所述粘贴层置于背衬层和离子堆积层之间,在粘贴层的中间位置为离子堆积层,离子堆积层和剥离层之间为表面覆盖层,剥离层为最外层。所述的表面覆盖层能完全覆盖离子堆积层,所述的剥离层为油光面托纸层,所述的剥离层能完全覆盖表面覆盖层,并且与背衬层、粘贴层的大小和尺寸完全相同。
所述的离子堆积层由量子能纤维改性的聚酰亚胺薄膜经电晕充电制备而成,其通电电压范围为驻极电压正极选择30KV,负极选择30KV,驻极距离为14cm,通电时间30min。所述的量子能纤维改性的聚酰亚胺薄膜制备工艺如下:
S1:将重量份数为4份的N-(正丁基)-γ-氨丙基三乙氧基硅烷加入到95份的乙醇中,充分混合,加入10份的量子能纤维,在超声条件下低速搅拌1h,取出后用无水乙醇浸泡冲洗3次,80℃下烘干,得到偶联剂处理后的量子能纤维;
S2:在3℃,先将重量份数为130份的偶联剂处理后的量子能纤维加入到30份的四氢呋喃中,搅拌至完全溶解后,然后将120份的均酐分批加入,进行原位聚合反应,加入完毕后,
持续反应6h,得到聚酰胺酸溶液;
S3:将聚酰胺酸溶液用200目铜网过滤,使用自动涂膜机在玻璃板上进行涂膜,涂膜厚度为 0.5mm,在超净室中室温干燥24h后,放入180℃鼓风干燥箱进行热亚胺化2h,得到量子能纤维改性的聚酰亚胺薄膜。
所述的表面覆盖层为喷涂防辐射涂料层的银箔,其加工制备步骤包括:
S1:在低湿度条件下,按照重量份比称取甲苯二异氰酸酯8份、氧化铁红14份、硅胶粉50份、掺有35%TiAlC陶瓷粉的涂料粉25份,快速转入喷料筒中机械搅拌均匀,形成了混合涂料粉末;
S2:采用静电喷涂机将上述所制得的混合涂料粉末涂覆到银箔表面,经180℃加热处理30min,冷却,得到喷涂有特殊涂料层的银箔;
S3:将上述喷涂有特殊涂料层的银箔浸泡于饱和氯化钙溶液中1.5h,浸泡完毕后取出,在 130℃的温度上烘干即得含防辐射涂料层的银箔。
实施例4:
一种量子能纤维改性离子感应基体材料,包括背衬层、粘贴层、离子堆积层、表面覆盖层以及剥离层,所述粘贴层置于背衬层和离子堆积层之间,在粘贴层的中间位置为离子堆积层,离子堆积层和剥离层之间为表面覆盖层,剥离层为最外层。所述的表面覆盖层能完全覆盖离子堆积层,所述的剥离层为油光面托纸层,所述的剥离层能完全覆盖表面覆盖层,并且与背衬层、粘贴层的大小和尺寸完全相同。
所述的离子堆积层由量子能纤维改性的聚酰亚胺薄膜经电晕充电制备而成,其通电电压范围为驻极电压正极选择30KV,负极选择25KV,驻极距离为15cm,通电时间60min。
所述的量子能纤维改性的聚酰亚胺薄膜制备工艺如下:
S1:将重量份数为4份的N-(正丁基)-γ-氨丙基三乙氧基硅烷加入到90份的乙醇中,充分混合,加入8份的量子能纤维,在超声条件下低速搅拌1h,取出后用无水乙醇浸泡冲洗3次,80℃下烘干,得到偶联剂处理后的量子能纤维;
S2:在5℃,先将重量份数为100份的偶联剂处理后的量子能纤维加入到50份的四氢呋喃中,搅拌至完全溶解后,然后将100份的均酐分批加入,进行原位聚合反应,加入完毕后,
持续反应12h,得到聚酰胺酸溶液;
S3:将聚酰胺酸溶液用200目铜网过滤,使用自动涂膜机在玻璃板上进行涂膜,涂膜厚度为 0.5mm,在超净室中室温干燥24h后,放入200℃鼓风干燥箱进行热亚胺化3h,得到量子能纤维改性的聚酰亚胺薄膜。
所述的表面覆盖层为喷涂防辐射涂料层的铜箔,其加工制备步骤包括:
S1:在低湿度条件下,按照重量份比称取甲苯二异氰酸酯10份、氧化铁红15份、硅胶粉45份、掺有36%TiAlC陶瓷粉的涂料粉30份,快速转入喷料筒中机械搅拌均匀,形成了混合涂料粉末;
S2:采用静电喷涂机将上述所制得的混合涂料粉末涂覆到铜箔表面,经170℃加热处理30min,冷却,得到喷涂有特殊涂料层的铜箔;
S3:将上述喷涂有特殊涂料层的铜箔浸泡于饱和氯化钙溶液中3h,浸泡完毕后取出,在150℃的温度上烘干即得含防辐射涂料层的铜箔。
对比例1
仅将实施例1中的“量子能纤维”改为“活性炭纤维”,其余与实施例1的条件完全相同,形成对比例1。
对比例2
仅将实施例1中的“量子能纤维”改为“藻酸盐纤维”,其余与实施例1的条件完全相同,形成对比例2。
对比例3
仅将实施例1中的“量子能纤维”改为“壳聚糖纤维”,其余与实施例1的条件完全相同,形成对比例3。
对比例4
仅将实施例2中的“甲苯二异氰酸酯6份、氧化铁红10份”去除,硅胶粉变为76份,其余与实施例2的条件完全相同,从而形成对比例4。
对比例5~6
仅将实施例3和实施例4中的“表面覆盖层为喷涂防辐射涂料层的银箔(铜箔)”改为“不喷涂任何防辐射涂料层的银箔(铜箔)”,其余与实施例3和实施例4的条件完全相同,从而形成对比例5~6。
实施例5表面电位测试
将实施例1~4、对比例1~6制得的离子堆积层立即进行表面电位测试,每组平行测定三次,取平均值,然后在产品自然的包装存储条件下放置60h后、离子堆积层裸露在外放置60h后,继续对不同试样进行离子堆积层表面电位值测试,其结果如下表所示:
表1不同试样在不同条件下表面电位值的变化
从上表中不同试样在不同条件下表面电位值变化的测试结果可知,本发明的试样在包装存储条件下经60h后,其表面电位值基本无衰减,从而能够推断出在产品保持期内长久不衰的效果,满足产品的存储要求;而对比例1~6中试样在在包装存储条件下经60h后,其表面电位值有一定程度的衰减。从不同试样的离子堆积层裸露放置的表面电位值变化的结果可知,本发明实施例的试样相对于对比例1~6的试样,有表面电位值的衰减比例有一个显著的降低。此外,对比例1~3相对于实施例1,其在相同的电晕充电条件下,其表面电位更低,说明本发明采用的量子能纤维对聚酰亚胺改性后,其捕获电荷的能力更强。
综合两组不同条件下电位衰减的数据可知,量子能纤维对聚酰亚胺改性,其本身所含的无机化合物可提高离子贴基体材料的疏水性能,降低材料的电导性能,减少聚酰亚胺驻极体脱阱电荷的损失,从而使经离子堆积工艺的基体材料表面电荷更为稳定(参见实施例1 和对比例1~3)。而“甲苯二异氰酸酯、氧化铁红”在含防辐射涂层的金属箔中对抗电荷衰减起着决定性的作用(参见实施例2和对比例4)。此外,金属箔中有无防辐射涂料层也对抵抗离子堆积层的电荷衰减起着显著的作用(参见实施例3~4和对比例5~6),采用喷涂有防辐射涂料层的金属箔作为表面覆盖层,可以进一步削弱聚酰亚胺膜材料表面附近耗散的离子对其电荷储存的影响,减少聚酰亚胺膜的电荷衰减性,最大限度地延长产品使用的有效期。
实施例6使用效果
将本发明实施例所加工制得的离子感应贴与对比例1~6用于临床上腰椎疼痛病的治疗。
(1)疗效标准
根据国家中医药管理局制定的《中国病症诊断疗效标准》:①治愈:疼痛等症状消失,关节活动正常,主要的理化检查指标正常。②显效:部分症状消除或主要症状消除,关节活动不受限,理化检查指标基本正常,X线显示明显好转。③有效:主要症状基本消除,关节活动轻度受限,主要理化检查指标有所改善,X线显示有好转。④无效:主要症状与关节活动无明显改善。
(2)结果
本临床应用中,共200例中,男94例,女106例,年龄38~77岁。使用上述产品或试样进行观察。使用前清洁患部皮肤,待干,取出产品,揭去剥离层和表面覆盖层,将贴膜均匀贴紧患处。每贴使用48小时后更换,1周为一疗程,连续治疗3个疗程。治疗期间不使用影响结果的其他相关治疗方法和药物。
表2不同产品或试样对颈椎病的治疗效果
从上述表中的结果可以明显地看出,本发明形成的离子感应贴产品,其对腰椎疼痛病的总有效率明显高于对比例的试样。这主要是由于本发明采用量子能纤维对聚酰亚胺的改性,有利于血液循环和新陈代谢,与离子贴作用于皮肤表面产生的微电流一道产生协同消痛止痛的作用,止痛效果显著。另一方面,量子能纤维中所含的无机化合物可提高离子贴基体材料的疏水性能,降低材料的电导性能,减少聚酰亚胺驻极体脱阱电荷的损失,从而使经离子堆积工艺的基体材料表面电荷更为稳定,止痛疗效更为持久。并且,采用含防辐射涂层的金属箔作为表面覆盖层,可进一步增强本发明离子堆积层的电荷稳定性,减少热效应导致的电荷衰减损失,最大限度地延长产品使用的有效期。
而对比例中的试样,要么表面覆盖层所含防辐射涂层有缺陷不足以抵抗电荷的自然衰减,要么不含表面覆盖层的金属箔也会加速电荷自然衰减,要么采用其他纤维对聚酰亚胺的改性达不到使离子堆积层表面电荷稳定的效果,其结果很有可能每贴使用不到48h甚至不到24h就已经失效,因而治疗效果与本发明相比有显著的差别。
Claims (7)
1.一种量子能纤维改性离子感应基体材料,其特征在于:包括背衬层、粘贴层、离子堆积层、表面覆盖层以及剥离层,所述粘贴层置于背衬层和离子堆积层之间,在粘贴层的中间位置为离子堆积层,离子堆积层和剥离层之间为表面覆盖层,剥离层为最外层,所述的离子堆积层为量子能纤维改性的聚酰亚胺薄膜经电晕充电制备而成。
2.根据权利要求1所述的量子能纤维改性离子感应基体材料,其特征在于,所述的量子能纤维改性的聚酰亚胺薄膜制备工艺如下:
S1:将重量份数为2~4份的N-(正丁基)-γ-氨丙基三乙氧基硅烷加入到80~100份的乙醇中,充分混合,加入5~10份的量子能纤维,在超声条件下低速搅拌1h,取出后用无水乙醇浸泡冲洗3次,80℃下烘干,得到偶联剂处理后的量子能纤维;
S2:在0℃~5℃,先将重量份数为100~150份的偶联剂处理后的量子能纤维加入到20~50份的四氢呋喃中,搅拌至完全溶解后,然后将80~120份的均酐分批加入,进行原位聚合反应,加入完毕后,持续反应1~12h,得到聚酰胺酸溶液;
S3:将聚酰胺酸溶液用200目铜网过滤,使用自动涂膜机在玻璃板上进行涂膜,涂膜厚度为0.5mm,在超净室中室温干燥24h后,放入150~250℃鼓风干燥箱进行热亚胺化2~3h,得到量子能纤维改性的聚酰亚胺薄膜。
3.根据权利要求1所述的量子能纤维改性离子感应基体材料,其特征在于,所述的表面覆盖层为喷涂防辐射涂料层的金属箔,所述金属箔为铝箔、金箔、银箔或铜箔。
4.根据权利要求3所述的量子能纤维改性离子感应基体材料,其特征在于,所述的表面覆盖层的加工制备步骤包括:
S1:在低湿度条件下,按照重量份比称取甲苯二异氰酸酯5~10份、氧化铁红10~15份、硅胶粉40~60份、掺有30~40%TiAlC陶瓷粉的涂料粉20~30份,快速转入喷料筒中机械搅拌均匀,形成了混合涂料粉末;
S2:采用静电喷涂机将上述所制得的混合涂料粉末涂覆到金属箔表面,经150~180℃加热处理20~30min,冷却,得到喷涂有特殊涂料层的金属箔;
S3:将上述喷涂有特殊涂料层的金属箔浸泡于吸湿盐溶液中1~3h,浸泡完毕后取出,在100~150℃的温度上烘干即得含防辐射涂料层的金属箔。
5.根据权利要求4所述的量子能纤维改性离子感应基体材料,其特征在于,所述的吸湿性盐溶液为饱和氯化锂溶液、饱和氯化钙溶液中的任意一种。
6.根据权利要求1所述的量子能纤维改性离子感应基体材料,其特征在于,所述的离子堆积层的加工过程如下:其通电电压范围为驻极电压正极选择20~30KV,负极选择10~30KV,驻极距离为10~15cm,通电时间20~60min。
7.根据权利要求1所述的量子能纤维改性离子感应基体材料,其特征在于,所述的表面覆盖层能完全覆盖离子堆积层,所述的剥离层为油光面托纸层,所述的剥离层能完全覆盖表面覆盖层,并且与背衬层、粘贴层的大小和尺寸完全相同。
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