CN102718951B - 双酸一醇共聚改性pet-a及其单向热收缩膜制备工艺 - Google Patents

双酸一醇共聚改性pet-a及其单向热收缩膜制备工艺 Download PDF

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CN102718951B
CN102718951B CN2012101560232A CN201210156023A CN102718951B CN 102718951 B CN102718951 B CN 102718951B CN 2012101560232 A CN2012101560232 A CN 2012101560232A CN 201210156023 A CN201210156023 A CN 201210156023A CN 102718951 B CN102718951 B CN 102718951B
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cast strip
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杨小明
唐郁辉
严莜梅
姚榕楠
王傲忠
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Henan Yuanhong Polymer New Materials Co ltd
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唐郁辉
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
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    • B29C48/88Thermal treatment of the stream of extruded material, e.g. cooling
    • B29C48/911Cooling
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/001Combinations of extrusion moulding with other shaping operations
    • B29C48/0022Combinations of extrusion moulding with other shaping operations combined with cutting
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/022Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the choice of material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/03Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
    • B29C48/07Flat, e.g. panels
    • B29C48/08Flat, e.g. panels flexible, e.g. films
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25Component parts, details or accessories; Auxiliary operations
    • B29C48/88Thermal treatment of the stream of extruded material, e.g. cooling
    • B29C48/91Heating, e.g. for cross linking
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
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    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25Component parts, details or accessories; Auxiliary operations
    • B29C48/88Thermal treatment of the stream of extruded material, e.g. cooling
    • B29C48/911Cooling
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25Component parts, details or accessories; Auxiliary operations
    • B29C48/92Measuring, controlling or regulating
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C2948/00Indexing scheme relating to extrusion moulding
    • B29C2948/92Measuring, controlling or regulating
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    • B29C2948/92704Temperature
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    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C2948/00Indexing scheme relating to extrusion moulding
    • B29C2948/92Measuring, controlling or regulating
    • B29C2948/92819Location or phase of control
    • B29C2948/92857Extrusion unit
    • B29C2948/92876Feeding, melting, plasticising or pumping zones, e.g. the melt itself
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    • B29C2948/00Indexing scheme relating to extrusion moulding
    • B29C2948/92Measuring, controlling or regulating
    • B29C2948/92819Location or phase of control
    • B29C2948/92857Extrusion unit
    • B29C2948/92904Die; Nozzle zone

Abstract

本发明涉及一种化工产品的制备工艺,特别是一种双酸一醇共聚改性PET-A及其单向热收缩膜制备工艺。一种双酸一醇共聚改性PET-A的制备方法是以精对苯二甲酸(PTA)、间苯二甲酸(IPA)和乙二醇(MEG)为主要原料进行三元共聚改性制得PET-A聚酯,其单向热收缩膜制备工艺包括纵向和横向两种制备工艺,所得热收缩膜的各项性能相同。本发明原材料易得、制备工艺简单环保、产品透明度高,应用广泛,本发明的单向热收缩膜的制备工艺专用于食品包装热收缩薄膜材料,产品经纵向或横向拉伸后的成品透明度良好,热收缩率在95~130℃、2~3s内达45~80%,可替代有毒PVC热收缩食品包装袋及其他系列的热收缩包装材料。

Description

双酸一醇共聚改性PET-A及其单向热收缩膜制备工艺
技术领域
本发明涉及一种化工产品的制备工艺,特别是一种双酸一醇共聚改性PET-A及其单向热收缩膜制备工艺。
背景技术
聚酯(PET)热收缩薄膜是一种新型热收缩包装材料,它具有易于回收、无毒、无味、机械性能良好及环保的特点。在多数发达国家,PETG热收缩薄膜已成为取代聚氯乙烯(PVC)热收缩薄膜的理想替代品;中国已在2011年年底执行了关于禁用PVC食品包装材料的国务院文件。
目前,国内已引进PET双向拉伸膜的大中型生产线100多条,年生产能力约为150万吨,该产品为一种结晶性非极性刚性高分子材料,其拉伸膜采用纵横双向高速高温结晶性细颈拉伸工艺,具体为从点开始逐渐延伸宽度到面的双向平衡膜,该种膜具有在高温(150℃)下不收缩的特点。普通PET是由一酸一醇合成的结晶型高聚物,其薄膜经过特殊工艺处理只能得到在150℃,5min内,30%以下的热收缩率,研究结果表明,若要获得高热收缩率的PET薄膜,必须进行改性。美国伊斯曼(EASFMAN)和韩国SK公司采用二醇(乙二醇MEG和1-4环己二甲醇CHDM)一酸共聚改性得到PETG热收缩材料,其热收缩性能良好,但价格昂贵,且CHDM在反应过程中易产生有害物质甲醇。签于此,寻求原材料易得,制备工艺简单,价格低廉,用途广泛的热收缩材料势在必行。
发明内容
本发明要解决的技术问题是:提供一种原材料易得、制备工艺简单、产品透明度高、用途广泛的环保型PET-A材料及一种拉伸工艺简单、热收缩率高、各项性能优异的单向拉伸热收缩膜。
本发明解决其技术问题所采用的技术方案是:一种双酸一醇共聚改性PET-A的制备方法,以精对苯二甲酸(PTA)、间苯二甲酸(IPA)和乙二醇(MEG)为主要原料进行三元共聚改性制得PET-A聚酯,具体制备步骤如下:
(1)初步聚合准备原料PTA、IPA、MEG、三氧化二锑、醋酸镁、醋酸锰、亚磷酸三苯酯和磷酸三苯酯,其中如下配比按摩尔比为:
PTA:IPA=(0.65~0.88):(0.12~0.35);
(PTA+IPA):MEG=1:(1.25~1.75);
如下配比按质量比为:
(PTA+IPA):三氧化二锑:醋酸镁:醋酸锰=
1:(0.03~0.05)%:(0.035~0.05)%:(0.02~0.03)%;
(PTA+IPA):亚磷酸三苯酯:磷酸三苯酯=1:0.02%:0.01%;
将准备好的物料按照MEG、PTA、IPA、三氧化二锑、醋酸镁、醋酸锰、亚磷酸三苯酯和磷酸三苯酯的顺序投入打浆釜中打浆0.5h得混合均匀的浆液,然后将浆液压入酯化釜中升温进行酯化反应,温度控制在190~250℃,酯化釜釜顶温度控制在95~110℃以下,常压酯化反应200~300min;以1molPTA酯化反应得2molH2O计算该酯化反应的理论出水量,当酯化釜釜顶出水量达到理论出水量的95%时,停止反应;
(2)进一步聚合将上述酯化反应结束后的浆液压入聚合反应器,温度控制在275~280℃,真空度控制在0.1MPa,反应时间为150~300min,当产物特性粘度为0.68~0.85,熔点为160~235℃时,停止反应;
(3)成品包装将上述进一步聚合得到的PET-A聚酯熔体冷却、切粒、检验,最后成品包装。
所述PTA:IPA=(0.65~0.88):(0.12~0.35)时,产物特性粘度可在0.68~0.85,熔点为160~235℃范围,上述PTA:IPA的摩尔比是本发明的关键所在,热收缩率为45~75%,具有热封粘结性,适用于各行各业的热收缩薄膜及其它用途的包装材料。
所述步骤(1)的酯化釜釜顶出水量达到理论出水量的95%时,釜顶温度下降至65℃以下,釜内温度上升至260℃。
所述三元共聚改性制得的产物为半结晶或非结晶PET-A聚酯。
一种PET-A的单向热收缩膜制备工艺,包括纵向和横向热收缩膜的两种制备工艺,两种制备工艺所得热收缩膜的各项性能相同,其中,纵向热收缩膜的制备工艺具有以下步骤:
(1)将干燥后的PETA聚酯原料加入双螺杆挤出机内熔融、挤出、铸带、冷却、成型,双螺杆挤出机温度控制在120~255℃,挤出铸带时模头温度控制在230~255℃,用低于30℃的铸带辊和冷风对铸带进行冷却;
(2)将铸带送入远红外拉伸区,在拉伸温度为65~120℃,拉伸倍数为1:3.5~4.5时对铸带进行纵向拉伸,纵向拉伸完毕后用65~100℃的温度对薄膜进行热处理;
(3)将上述成型薄膜在空气中冷却,然后收卷、检验,最后成品包装。
一种横向热收缩膜的制备工艺,具有以下步骤:
(1)将干燥后的PET-A聚酯原料加入双螺杆挤出机内熔融、挤出、铸带、冷却、成型,双螺杆挤出机温度控制在120~255℃,挤出铸带时模头温度控制在230~255℃,用低于30℃的铸带辊和冷风对铸带进行冷却;
(2)将铸带送入横向拉伸机组的预热段以75~90℃进行预热,然后在拉伸温度为65~120℃,拉伸倍数为1:3.5~4.5时进行横向拉伸,再用65~100℃的温度对薄膜进行热处理;
(3)将上述已成型的薄膜在空气中冷却,然后收卷、检验,最后成品包装。
本发明采用双酸一醇共聚改性PET-A聚酯,原材料易得、制备工艺简单环保、产品透明度高、加工性能优异,可广泛用于挤出、吹塑、注塑及流延等领域;本发明的单向热收缩膜的制备工艺专用于食品包装热收缩薄膜材料,产品经纵向或横向拉伸后的成品透明度良好,热收缩率在95~130℃、2~3s内达45~80%,可替代有毒PVC热收缩食品包装袋及其他系列的热收缩包装材料。
附图说明
下面结合附图和实施例对本发明进一步说明;
图1是本发明的纵向热收缩膜的制备工艺示意图;
图2是本发明的横向热收缩膜的制备工艺示意图;
1.挤出区,2.铸带区,3.远红外拉伸区,4.热处理区,5.收卷,6.预热段,7.拉伸区。
具体实施方式
实例一
一种双酸一醇共聚改性PETA的制备方法,以精对苯二甲酸(PTA)、间苯二甲酸(IPA)和乙二醇(MEG)为主要原料进行三元共聚改性制得PET-A聚酯,具体工艺步骤如下:
(1)初步聚合准备原料PTA 6kg、IPA 1.38kg、MEG 3.8kg、三氧化二锑3.5g、醋酸镁2.6g、醋酸锰2.0g、亚磷酸三苯酯1.47g和磷酸三苯酯0.38g;
将准备好的物料按照MEG、PTA、IPA、三氧化二锑、醋酸镁、醋酸锰、亚磷酸三苯酯和磷酸三苯酯的加入顺序,投入打浆釜中打浆0.5h得混合均匀的浆液,然后将浆液压入酯化釜中升温进行酯化反应,温度控制在190~250℃,酯化釜釜顶温度控制在95~110℃以下,常压酯化反应200~300min;以1molPTA酯化反应得2molH2O计算该酯化反应得理论出水量,当酯化釜釜顶出水量达到理论出水量的95%时,停止反应;
(2)进一步聚合将上述酯化反应结束后的浆液压入聚合反应器,温度控制在275~280℃,真空度控制在0.1MPa,反应时间为150~300min,当产物特性粘度为0.68~0.85,熔点为210~235℃时,停止反应;
(3)成品包装将上述进一步聚合得到的PETA聚酯熔体冷却、切粒、检验,最后成品包装。
本实施例所得成品的热收缩率为45~60%。
实例二
一种双酸一醇共聚改性PET-A的制备方法,以精对苯二甲酸(PTA)、间苯二甲酸(IPA)和乙二醇(MEG)为主要原料进行三元共聚改性制得PET-A聚酯,具体工艺步骤如下:
(1)初步聚合准备原料PTA 6kg、IPA 3.9kg、MEG 6.1kg、三氧化二锑3.5g、醋酸镁3.5g、醋酸锰2g、亚磷酸三苯酯1.8g和磷酸三苯酯1g;
将准备好的物料按照MEG、PTA、IPA、三氧化二锑、醋酸镁、醋酸锰、亚磷酸三苯酯和磷酸三苯酯的加入顺序,投入打浆釜中打浆0.5h得混合均匀的浆液,然后将浆液压入酯化釜中升温进行酯化反应,温度控制在190~250℃,酯化釜釜顶温度控制在95~110℃以下,常压酯化反应200~300min;以1molPTA酯化反应得2molH2O计算该酯化反应得理论出水量,当酯化釜釜顶出水量达到理论出水量的95%时,停止反应;
(2)进一步聚合将上述酯化反应结束后的浆液压入聚合反应器,温度控制在275~280℃,真空度控制在0.1MPa,反应时间为150~300min,当产物特性粘度为0.68~0.85,熔点为170~185℃时,停止反应;
(3)成品包装将上述进一步聚合得到的PET-A聚酯熔体冷却、切粒、检验,最后成品包装。
本实施例所得成品的热收缩率为65~80%。
实例三
将上述实例一和实例二所得PET-A聚酯制备一种纵向热收缩膜,其制备工艺具有如下步骤:
(1)将干燥后的PET-A聚酯原料加入双螺杆挤出机内熔融、挤出、铸带、冷却、成型,挤出区1一区到五区的温度分别190℃,220℃,245℃,255℃,255℃,挤出铸带区2六区模头温度分别控制在245℃,245℃,255℃,255℃,245℃,245℃,用低于30℃的铸带辊和冷风对铸带进行冷却;
(2)将铸带送入远红外拉伸区3,在拉伸温度为85~90℃,拉伸倍数为1:4时对铸带进行纵向拉伸,纵向拉伸完毕后在热处理区4用五区温度分别为65℃,70℃,70℃,70℃,65℃的温度对薄膜进行热处理;
(3)将上述成型薄膜在空气中冷却,然后收卷5、检验,最后成品包装。
实例四
将上述实例一和实例二所得PET-A聚酯制备一种横向热收缩膜,其制备工艺具有如下步骤:
(1)将干燥后的PET-A聚酯原料加入双螺杆挤出机内熔融、挤出、铸带、冷却、成型,挤出机一区到五区的温度分别190℃,220℃,245℃,255℃,255℃,挤出铸带时六区模头温度分别控制在245℃,245℃,255℃,255℃,245℃,245℃,用低于30℃的铸带辊和冷风对铸带进行冷却;
(2)将铸带送入横向拉伸机组的预热段6四区温度分别为90℃,75℃,80℃,80℃进行预热,然后在拉伸区7四区温度分别为80℃,85℃,90℃,90℃进行拉伸,拉伸倍数为1:4时进行横向拉伸,再用热处理区4四区温度为85℃,90℃,90℃,90℃对薄膜进行热处理;
(3)将上述已成型的薄膜在空气中冷却,然后收卷、检验,最后成品包装。上述实例四所得热收缩膜的相关性能如下表所示:
Figure BDA00001650772000081
由上表可知,本实施例所得PET-A聚酯经纵向或横向拉伸后的成品透光率良好,热收缩率在100℃、2-3s内达73%,可替代有毒PVC热收缩食品包装袋及其他系列的热收缩包装材料。

Claims (5)

1.一种双酸一醇共聚改性PET-A的制备方法,其特征是:具体制备步骤如下:
(1)初步聚合 准备原料PTA、IPA、MEG、三氧化二锑、醋酸镁、醋酸锰、亚磷酸三苯酯和磷酸三苯酯,其中如下配比按摩尔比为:
PTA:IPA=(0.65~0.88):(0.12~0.35);
(PTA+IPA):MEG=1:(1.25~1.75);
如下配比按质量比为:
(PTA+IPA):三氧化二锑:醋酸镁:醋酸锰=
1:(0.03~0.05)%:(0.035~0.05)%:(0.02~0.03)%;
(PTA+IPA):亚磷酸三苯酯:磷酸三苯酯=1:0.02%:0.01%;
将准备好的物料按照MEG、PTA、IPA、三氧化二锑、醋酸镁、醋酸锰、亚磷酸三苯酯和磷酸三苯酯的顺序投入打浆釜中打浆0.5h得混合均匀的浆液,然后将浆液压入酯化釜中升温进行酯化反应,温度控制在190~250℃,酯化釜釜顶温度控制在95~110℃以下,常压酯化反应200~300min;以1molPTA酯化反应得2molH2O计算该酯化反应的理论出水量,当酯化釜釜顶出水量达到理论出水量的95%时,停止反应;
(2)进一步聚合 将上述酯化反应结束后的浆液压入聚合反应器,温度控制在275~280℃,真空度控制在0.1MPa,反应时间为150~300min,根据用户需求的特性粘度0.68~0.85和熔点为160~235℃范围内控制,停止反应;
(3)成品包装 将上述进一步聚合得到的PET-A聚酯熔体冷却、切粒、检验,最后成品包装;
所述PTA:IPA=(0.65~0.88):(0.12~0.35)时,产物特性粘度可在0.68~0.85,熔点为160~235℃范围,根据权利要求,上述PTA:IPA的摩尔比是关键所在,热收缩率为45~75%,具有热封粘结性,适用于各行各业的热收缩薄膜及其它用途的包装材料。
2.如权利要求1所述的双酸一醇共聚改性PET-A的制备方法,其特征是:所述步骤(1)中的酯化釜釜顶出水量达到理论出水量的95%时,釜顶温度下降至65℃以下,釜内温度上升至260℃。
3.如权利要求1所述的双酸一醇共聚改性PET-A的制备方法,其特征是:所述步骤(3)中的成品为半结晶或非结晶PET-A聚酯。
4.如权利要求1所述的双酸一醇共聚改性PET-A的制备方法,其特征是:该PET-A的一种纵向热收缩膜的制备工艺具有以下步骤:
(1)将干燥后的PET-A聚酯原料加入双螺杆挤出机内熔融、挤出、铸带、冷却、成型,双螺杆挤出机温度控制在120~255℃,挤出铸带时模头温度控制在230~255℃,用低于30℃的铸带辊和冷风对铸带进行冷却;
(2)将铸带送入远红外拉伸区,在拉伸温度为65~120℃,拉伸倍数为1:3.5~4.5时对铸带进行纵向拉伸,纵向拉伸完毕后用65~100℃的温度对薄膜进行热处理;
(3)将上述成型薄膜在空气中冷却,然后收卷、检验,最后成品包装。
5.如权利要求1所述的双酸一醇共聚改性PET-A的制备方法,其特征是:该PET-A的一种横向热收缩膜的制备工艺具有以下步骤:
(1)将干燥后的PET-A聚酯原料加入双螺杆挤出机内熔融、挤出、铸带、冷却、成型,双螺杆挤出机温度控制在120~255℃,挤出铸带时模头温度控制在230~255℃,用低于30℃的铸带辊和冷风对铸带进行冷却;
(2)将铸带送入横向拉伸机组的预热段以75~90℃进行预热,然后在拉伸温度为65~120℃,拉伸倍数为1:3.5~4.5时进行横向拉伸,再用65~100℃的温度对薄膜进行热处理;
(3)将上述已成型的薄膜在空气中冷却,然后收卷、检验,最后成品包装。
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