CN104290364B - 一种抗光老化的塑料丝及其制备方法 - Google Patents

一种抗光老化的塑料丝及其制备方法 Download PDF

Info

Publication number
CN104290364B
CN104290364B CN201410527371.5A CN201410527371A CN104290364B CN 104290364 B CN104290364 B CN 104290364B CN 201410527371 A CN201410527371 A CN 201410527371A CN 104290364 B CN104290364 B CN 104290364B
Authority
CN
China
Prior art keywords
parts
light aging
transition zone
plastic wire
flexible core
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
CN201410527371.5A
Other languages
English (en)
Other versions
CN104290364A (zh
Inventor
段海英
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
NINGXIA RUNLONG PACKAGING NEW MATERIAL Co Ltd
Original Assignee
NINGXIA RUNLONG PACKAGING NEW MATERIAL Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by NINGXIA RUNLONG PACKAGING NEW MATERIAL Co Ltd filed Critical NINGXIA RUNLONG PACKAGING NEW MATERIAL Co Ltd
Priority to CN201410527371.5A priority Critical patent/CN104290364B/zh
Publication of CN104290364A publication Critical patent/CN104290364A/zh
Application granted granted Critical
Publication of CN104290364B publication Critical patent/CN104290364B/zh
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B1/00Layered products having a non-planar shape
    • 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
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/06Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/18Layered products comprising a layer of synthetic resin characterised by the use of special additives
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/32Layered products comprising a layer of synthetic resin comprising polyolefins
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B37/00Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding
    • B32B37/06Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the heating method
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B37/00Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding
    • B32B37/14Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the properties of the layers
    • B32B37/15Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the properties of the layers with at least one layer being manufactured and immediately laminated before reaching its stable state, e.g. in which a layer is extruded and laminated while in semi-molten state
    • B32B37/153Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the properties of the layers with at least one layer being manufactured and immediately laminated before reaching its stable state, e.g. in which a layer is extruded and laminated while in semi-molten state at least one layer is extruded and immediately laminated while in semi-molten state
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/09Carboxylic acids; Metal salts thereof; Anhydrides thereof
    • C08K5/092Polycarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/10Esters; Ether-esters
    • C08K5/101Esters; Ether-esters of monocarboxylic acids
    • C08K5/103Esters; Ether-esters of monocarboxylic acids with polyalcohols
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/13Phenols; Phenolates
    • C08K5/136Phenols containing halogens
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/16Nitrogen-containing compounds
    • C08K5/20Carboxylic acid amides
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/16Nitrogen-containing compounds
    • C08K5/21Urea; Derivatives thereof, e.g. biuret
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/16Nitrogen-containing compounds
    • C08K5/22Compounds containing nitrogen bound to another nitrogen atom
    • C08K5/24Derivatives of hydrazine
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/16Nitrogen-containing compounds
    • C08K5/34Heterocyclic compounds having nitrogen in the ring
    • C08K5/3442Heterocyclic compounds having nitrogen in the ring having two nitrogen atoms in the ring
    • C08K5/3462Six-membered rings
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/16Nitrogen-containing compounds
    • C08K5/34Heterocyclic compounds having nitrogen in the ring
    • C08K5/3467Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
    • C08K5/3472Five-membered rings
    • C08K5/3475Five-membered rings condensed with carbocyclic rings
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/49Phosphorus-containing compounds
    • C08K5/51Phosphorus bound to oxygen
    • C08K5/52Phosphorus bound to oxygen only
    • C08K5/524Esters of phosphorous acids, e.g. of H3PO3
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/10Homopolymers or copolymers of propene
    • C08L23/12Polypropene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L55/00Compositions of homopolymers or copolymers, obtained by polymerisation reactions only involving carbon-to-carbon unsaturated bonds, not provided for in groups C08L23/00 - C08L53/00
    • C08L55/02ABS [Acrylonitrile-Butadiene-Styrene] polymers

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Extrusion Moulding Of Plastics Or The Like (AREA)
  • Laminated Bodies (AREA)

Abstract

本发明公开了一种抗光老化的塑料丝,包括内侧的柔性内芯和外侧的抗光老化表层,柔性内芯和抗光老化表层之间设置有过渡层。本发明还公开了一种抗光老化的塑料丝的制备方法,采用了分层制备的方式。本发明能够改进现有技术的不足,提高塑料丝的抗光老化性能。

Description

一种抗光老化的塑料丝及其制备方法
技术领域
本发明涉及塑料制程技术领域,尤其是一种抗光老化的塑料丝及其制备方法。
背景技术
塑料丝广泛应用在产品包装、交通运输、工农业生产等多个领域。塑料丝在长时间强光照射下会发生快速老化,究其原因是因为紫外线的照射作用。现有技术中通过添加系外线吸收剂,对紫外线进行吸收。但是,由于为了保证塑料丝本身的韧性和强度,紫外线吸收剂可添加的量极少,这就限制了塑料丝对于光照的抗老化性能。
发明内容
本发明要解决的技术问题是提供一种抗光老化的塑料丝及其制备方法,能够解决现有技术的不足,提高塑料丝的抗光老化性能。
为解决上述技术问题,本发明所采取的技术方案如下。
一种抗光老化的塑料丝,包括内侧的柔性内芯和外侧的抗光老化表层,柔性内芯和抗光老化表层之间设置有过渡层。
作为优选,所述柔性内芯包括下述重量份数的组分,ABS树脂250~400份,2-酮戊二酸10~20份,2,4-二硝苯肼10~20份,豆蔻酸甘油酯50~70份,4-甲基乙酰苯胺30~60份。
作为优选,所述抗光老化表层包括下述重量份数的组分,聚丙烯100~150份,三亚磷酸酯20~25份,苯并三氮唑10~15份,3-氨基甲酰甲基-5-甲基-己酸15~20份,2,4,6-三氯酚10~15份,安息香甲基醚25~35份。
作为优选,所述过渡层包括ABS树脂110~150份,聚丙烯60~80份,二苯氨基脲3~5份,帕潘立酮10~20份,5-氨基-2-甲基嘧啶40~65份,5-氯代苯并三唑20~30份。
上述抗光老化的塑料丝的制备方法,包括以下步骤:
A、将柔性内芯的原料加热熔化,注入搅拌机搅拌均匀,然后通过挤出机挤出成型;挤出的压力为2~3bar,挤出速度为30~70mL/s,挤出后的成型温度保持在50℃~55℃,成型时间持续3小时,然后降至室温冷却;
B、将过渡层的原料加热熔化,注入搅拌机搅拌均匀,然后将过渡层的原料分三次均匀喷涂在成型的柔性内芯外侧;第一次喷涂时,使用过渡层原料的10%,喷涂时柔性内芯的温度保持在40℃~45℃;第二次喷涂时,使用过渡层原料的60%,第三次喷涂时,使用过渡层原料的30%,进行第二次喷涂和第三次喷涂时,柔性内芯保持室温;
C、将过渡层的表面进行打磨,使其粗糙度Ra的值保持在150~200之间。
D、将抗光老化表层的原料加热熔化,注入搅拌机搅拌均匀,然后使用挤出机挤出成型;挤出的压力为4~4.5bar,挤出速度为120~150mL/s,挤出成型时,柔性内芯和过渡层保持室温。
采用上述技术方案所带来的有益效果在于:本发明通过改进塑料丝的成分组成,将整个塑料丝分成三部分进行制备,柔性内芯可以保证塑料丝拥有良好的韧性和抗拉强度,抗光老化表层通过在原有塑料材料基础上的改性,提高了紫外线吸收能力,过渡层通过与柔性内芯和抗光老化表层的交联作用,提高了整个塑料丝的一体性。
附图说明
图1是本发明一个具体实施方式的结构图。
图中:1、柔性内芯;2、抗光老化表层;3、过渡层。
具体实施方式
参照图1,本发明提供的抗光老化塑料丝的结构包括内侧的柔性内芯1和外侧的抗光老化表层2,柔性内芯1和抗光老化表层2之间设置有过渡层3。
实施例1
所述柔性内芯1包括下述重量份数的组分,ABS树脂330份,2-酮戊二酸11份,2,4-二硝苯肼16份,豆蔻酸甘油酯65份,4-甲基乙酰苯胺35份。抗光老化表层2包括下述重量份数的组分,聚丙烯140份,三亚磷酸酯22份,苯并三氮唑12份,3-氨基甲酰甲基-5-甲基-己酸18份,2,4,6-三氯酚14份,安息香甲基醚33份。过渡层3包括ABS树脂120份,聚丙烯76份,二苯氨基脲3份,帕潘立酮11份,5-氨基-2-甲基嘧啶48份,5-氯代苯并三唑26份。
制备方法为:
A、将ABS树脂加热熔化,然后加入8份2,4-二硝苯肼,搅拌均匀,然后加入2-酮戊二酸和豆蔻酸甘油酯,搅拌均匀,最后再加入注入8份2,4-二硝苯肼,搅拌均匀,静置15min使原料组分充分融合,然后通过挤出机挤出成型;挤出的压力为2.3bar,挤出速度为55mL/s,挤出后的成型温度保持在50℃,成型时间持续3小时,然后降至室温冷却;
B、将ABS树脂和聚丙烯加热熔化,搅拌均匀,然后加入1份二苯氨基脲和5份5-氯代苯并三唑,搅拌10min,然后加入1份二苯氨基脲、11份帕潘立酮和20份5-氨基-2-甲基嘧啶,搅拌20min,最后加入1份二苯氨基脲、28份5-氨基-2-甲基嘧啶和21份5-氯代苯并三唑,搅拌10min,然后将过渡层3的原料分三次均匀喷涂在成型的柔性内芯1外侧;第一次喷涂时,使用过渡层3原料的10%,喷涂时柔性内芯1的温度保持在40℃;第二次喷涂时,使用过渡层3原料的60%,第三次喷涂时,使用过渡层3原料的30%,进行第二次喷涂和第三次喷涂时,柔性内芯1保持室温;喷涂过程中过渡层3原料保持持续搅拌;
C、将过渡层3的表面进行打磨,使其粗糙度Ra的值保持在160。
D、将聚丙烯加热熔化,然后将剩余原料组份平均分为三次注入搅拌机搅拌,每次搅拌20min,然后使用挤出机挤出成型;挤出的压力为4.2bar,挤出速度为130mL/s,挤出成型时,柔性内芯1和过渡层3保持室温。
实施例2
所述柔性内芯1包括下述重量份数的组分,ABS树脂260份,2-酮戊二酸19份,2,4-二硝苯肼18份,豆蔻酸甘油酯55份,4-甲基乙酰苯胺43份。抗光老化表层2包括下述重量份数的组分,聚丙烯110份,三亚磷酸酯25份,苯并三氮唑14份,3-氨基甲酰甲基-5-甲基-己酸13份,2,4,6-三氯酚11份,安息香甲基醚25份。过渡层3包括ABS树脂145份,聚丙烯62份,二苯氨基脲4份,帕潘立酮15份,5-氨基-2-甲基嘧啶55份,5-氯代苯并三唑21份。
制备方法为:
A、将ABS树脂加热熔化,然后加入9份2,4-二硝苯肼,搅拌均匀,然后加入2-酮戊二酸和豆蔻酸甘油酯,搅拌均匀,最后再加入注入9份2,4-二硝苯肼,搅拌均匀,静置15min使原料组分充分融合,然后通过挤出机挤出成型;挤出的压力为2.1bar,挤出速度为35mL/s,挤出后的成型温度保持在50℃,成型时间持续3小时,然后降至室温冷却;
B、将ABS树脂和聚丙烯加热熔化,搅拌均匀,然后加入1份二苯氨基脲和10份5-氯代苯并三唑,搅拌10min,然后加入2份二苯氨基脲、5份帕潘立酮和20份5-氨基-2-甲基嘧啶,搅拌20min,最后加入1份二苯氨基脲、35份5-氨基-2-甲基嘧啶、11份5-氯代苯并三唑和10份帕潘立酮,搅拌10min,然后将过渡层3的原料分三次均匀喷涂在成型的柔性内芯1外侧;第一次喷涂时,使用过渡层3原料的20%,喷涂时柔性内芯1的温度保持在40℃;第二次喷涂时,使用过渡层3原料的60%,第三次喷涂时,使用过渡层3原料的20%,进行第二次喷涂和第三次喷涂时,柔性内芯1保持室温;喷涂过程中过渡层3原料保持持续搅拌;
C、将过渡层3的表面进行打磨,使其粗糙度Ra的值保持在175。
D、将聚丙烯加热熔化,然后将剩余原料组份平均分为三次注入搅拌机搅拌,每次搅拌20min,然后使用挤出机挤出成型;挤出的压力为4.1bar,挤出速度为140mL/s,挤出成型时,柔性内芯1和过渡层3保持室温。
实施例3
柔性内芯1包括下述重量份数的组分,ABS树脂390份,2-酮戊二酸15份,2,4-二硝苯肼11份,豆蔻酸甘油酯50份,4-甲基乙酰苯胺57份。抗光老化表层2包括下述重量份数的组分,聚丙烯120份,三亚磷酸酯21份,苯并三氮唑10份,3-氨基甲酰甲基-5-甲基-己酸16份,2,4,6-三氯酚13份,安息香甲基醚30份。过渡层3包括ABS树脂125份,聚丙烯70份,二苯氨基脲5份,帕潘立酮19份,5-氨基-2-甲基嘧啶62份,5-氯代苯并三唑28份。
制备方法为:
A、将ABS树脂加热熔化,然后加入5份2,4-二硝苯肼,搅拌均匀,然后加入2-酮戊二酸和豆蔻酸甘油酯,搅拌均匀,最后再加入注入6份2,4-二硝苯肼,搅拌均匀,静置15min使原料组分充分融合,然后通过挤出机挤出成型;挤出的压力为2.85bar,挤出速度为70mL/s,挤出后的成型温度保持在50℃,成型时间持续3小时,然后降至室温冷却;
B、将ABS树脂和聚丙烯加热熔化,搅拌均匀,然后加入2份二苯氨基脲,搅拌10min,然后加入全部5-氯代苯并三唑,搅拌20min,然后加入2份二苯氨基脲、10份帕潘立酮和30份5-氨基-2-甲基嘧啶,搅拌20min,最后加入1份二苯氨基脲、32份5-氨基-2-甲基嘧啶和9份帕潘立酮,搅拌10min,然后将过渡层3的原料分三次均匀喷涂在成型的柔性内芯1外侧;第一次喷涂时,使用过渡层3原料的20%,喷涂时柔性内芯1的温度保持在40℃;第二次喷涂时,使用过渡层3原料的60%,第三次喷涂时,使用过渡层3原料的20%,进行第二次喷涂和第三次喷涂时,柔性内芯1保持室温;喷涂过程中过渡层3原料保持持续搅拌;
C、将过渡层3的表面进行打磨,使其粗糙度Ra的值保持在190。
D、将聚丙烯加热熔化,然后将剩余原料组份平均分为三次注入搅拌机搅拌,每次搅拌20min,然后使用挤出机挤出成型;挤出的压力为4.4bar,挤出速度为150mL/s,挤出成型时,柔性内芯1和过渡层3保持室温。
本发明使用2,4-二硝苯肼对ABS树脂进行改性,提高其抗拉强度,2-酮戊二酸可以提高ABS树脂的抗氧化性,豆蔻酸甘油酯作为相容剂提高了整个柔性内芯的均匀度。聚丙烯具有较高的强度,在外表面可以提高塑料丝的耐磨度,三亚磷酸酯和苯并三氮唑作为紫外线吸收剂,可以对紫外线进行吸收,三氯酚可以提高三亚磷酸酯和苯并三氮唑在聚丙烯内的相容度,减小三亚磷酸酯和苯并三氮唑对聚丙烯本身强度的削弱。3-氨基甲酰甲基-5-甲基-己酸可提高表层的斥水性,安息香甲基醚可以使三亚磷酸酯和苯并三氮唑在挤出成型时与过渡层形成相容区,提高三亚磷酸酯和苯并三氮唑在整个塑料丝内的分布深度,从而提高紫外线的吸收强度。过渡层使用ABS树脂和聚丙烯的混合组分,可以实现与柔性内芯和抗光老化表层的相互连接强度,帕潘立酮可以是过渡层具有良好的热稳定性,5-氨基-2-甲基嘧啶与豆蔻酸甘油酯可相互交联,提高过度层与柔性内芯的连接力,二苯氨基脲和5-氯代苯并三唑可提高ABS树脂和聚丙烯的相容度。
其中,ABS树脂采购自北京恒业中远化工有限公司,2-酮戊二酸和2,4-二硝苯肼采购自上海迈瑞尔化学技术有限公司,豆蔻酸甘油酯采购自上海同田生物技术有限公司,4-甲基乙酰苯胺和聚丙烯采购自北京华威锐化工有限公司,三亚磷酸酯采购自上海浦东润路化工厂,苯并三氮唑采购自天津中信凯泰化工有限公司,3-氨基甲酰甲基-5-甲基-己酸采购自浙江省三门腾龙化工有限公司,2,4,6-三氯酚采购自赛默飞世尔科技(中国)有限公司,安息香甲基醚采购自百灵威科技有限公司,二苯氨基脲采购自大连美仑生物技术有限公司,帕潘立酮采购自孝感深远化工有限公司,5-氨基-2-甲基嘧啶采购自北京偶合科技有限公司,5-氯代苯并三唑采购自阿达玛斯试剂有限公司。
将现有技术中仅添加紫外线吸收剂的ABS树脂塑料丝与本发明中三个实施例的塑料丝进行光老化试验(紫外线强度500μW/cm,2照射时间100h,试验样品数均为100个,试验结构取平均值),对实验前后的抗拉强度进行对比:
组别 试验前抗拉强度(N/mm2) 试验后抗拉强度(N/mm2)
现有技术 3500 1235
实施例1 4200 3880
实施例2 4500 4200
实施例3 4500 4250
以上显示和描述了本发明的基本原理和主要特征和本发明的优点。本行业的技术人员应该了解,本发明不受上述实施例的限制,上述实施例和说明书中描述的只是说明本发明的原理,在不脱离本发明精神和范围的前提下,本发明还会有各种变化和改进,这些变化和改进都落入要求保护的本发明范围内。本发明要求保护范围由所附的权利要求书及其等效物界定。

Claims (3)

1.一种抗光老化的塑料丝,其特征在于:包括内侧的柔性内芯(1)和外侧的抗光老化表层(2),柔性内芯(1)和抗光老化表层(2)之间设置有过渡层(3),所述柔性内芯(1)包括下述重量份数的组分,ABS树脂250~400份,2-酮戊二酸10~20份,2,4-二硝苯肼10~20份,豆蔻酸甘油酯50~70份,4-甲基乙酰苯胺30~60份。
2.根据权利要求1所述的抗光老化的塑料丝,其特征在于:所述抗光老化表层(2)包括下述重量份数的组分,聚丙烯100~150份,三亚磷酸酯20~25份,苯并三氮唑10~15份,3-氨基甲酰甲基-5-甲基-己酸15~20份,2,4,6-三氯酚10~15份,安息香甲基醚25~35份。
3.根据权利要求1所述的抗光老化的塑料丝,其特征在于:所述过渡层(3)包括ABS树脂110~150份,聚丙烯60~80份,二苯氨基脲3~5份,帕潘立酮10~20份,5-氨基-2-甲基嘧啶40~65份,5-氯代苯并三唑20~30份。
CN201410527371.5A 2014-10-09 2014-10-09 一种抗光老化的塑料丝及其制备方法 Active CN104290364B (zh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201410527371.5A CN104290364B (zh) 2014-10-09 2014-10-09 一种抗光老化的塑料丝及其制备方法

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201410527371.5A CN104290364B (zh) 2014-10-09 2014-10-09 一种抗光老化的塑料丝及其制备方法

Publications (2)

Publication Number Publication Date
CN104290364A CN104290364A (zh) 2015-01-21
CN104290364B true CN104290364B (zh) 2016-03-02

Family

ID=52310426

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201410527371.5A Active CN104290364B (zh) 2014-10-09 2014-10-09 一种抗光老化的塑料丝及其制备方法

Country Status (1)

Country Link
CN (1) CN104290364B (zh)

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE29807472U1 (de) * 1998-04-24 1998-07-23 Recytex Textilaufbereitung Gmb Effektgarn
CN101067221A (zh) * 2007-06-12 2007-11-07 江苏盛虹化纤有限公司 芯皮型抗老化聚脂长丝
CN101210097A (zh) * 2006-12-30 2008-07-02 上海普利特复合材料有限公司 一种具有优异耐光老化性能的abs材料及其制备方法
CN103874793A (zh) * 2011-09-21 2014-06-18 唐纳森公司 由用树脂质醛组合物交联聚合物制成的细纤维

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0673607A (ja) * 1992-08-27 1994-03-15 Asahi Chem Ind Co Ltd 鞘芯型アクリル系合成繊維及びその製造法

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE29807472U1 (de) * 1998-04-24 1998-07-23 Recytex Textilaufbereitung Gmb Effektgarn
CN101210097A (zh) * 2006-12-30 2008-07-02 上海普利特复合材料有限公司 一种具有优异耐光老化性能的abs材料及其制备方法
CN101067221A (zh) * 2007-06-12 2007-11-07 江苏盛虹化纤有限公司 芯皮型抗老化聚脂长丝
CN103874793A (zh) * 2011-09-21 2014-06-18 唐纳森公司 由用树脂质醛组合物交联聚合物制成的细纤维

Also Published As

Publication number Publication date
CN104290364A (zh) 2015-01-21

Similar Documents

Publication Publication Date Title
CN102732200B (zh) 植物油基胶粘剂、复合人造板的制造方法以及复合人造板
JP2015510027A5 (zh)
CN103214985B (zh) 一种含有改性硅藻土的热熔胶及其制备方法
ES2933100T3 (es) Método para preparar un producto de elastómero de poliuretano termoplástico espumado
MX2018000002A (es) Tereftalato de polietileno reforzado con grafeno.
MY173821A (en) Resin-soluble veils for composite article fabrication and methods of manufacturing the same
CN104558687B (zh) 一种石头纸专用球形碳酸钙及其制备方法
CN104290364B (zh) 一种抗光老化的塑料丝及其制备方法
CN103895202A (zh) 一种用物理发泡工艺一次性挤出成型生产xps装饰条异型材檐板的方法
CN103965647A (zh) 一种发光工程塑料
CN109485974A (zh) 一种紫外光辐照交联聚乙烯绝缘料
CN102408725A (zh) 一种适用于微波硫化的硅橡胶及制备方法
CN104166199A (zh) 发泡填充绳的制造方法
CN107298780B (zh) 一种废旧胶粉车用挡泥板及其制备方法
CN104497395A (zh) 一种原位自增强的聚甲醛/聚乙烯复合材料及制备方法
CN106905600A (zh) 一种3d打印用改性聚丙烯复合材料及其制备方法
CN104761862A (zh) 一种高分子包装材料的制备方法
CN104877222A (zh) 一种新型轻质高强低密度光电缆护套料及其制备方法
CN105034306A (zh) 一种灌溉用高强度耐热双层薄壁pe软管及其制造方法
CN103467948B (zh) 棉纤维与聚乳酸共混的可降解塑料
CN104262943A (zh) 一种高硬度塑胶
CN111605276A (zh) 一种熔融共挤多层透明的紫外近红外屏蔽高分子材料、制备方法及其应用
CN105269829A (zh) 一种玻璃纤维树脂滑道的成型方法
KR101588795B1 (ko) 친환경 천연재료를 이용한 파이프의 제조방법
CN105646795A (zh) 一种用于立体光固化成型技术的树脂及其制备方法

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
PE01 Entry into force of the registration of the contract for pledge of patent right
PE01 Entry into force of the registration of the contract for pledge of patent right

Denomination of invention: A kind of anti light aging plastic wire and its preparation method

Effective date of registration: 20221206

Granted publication date: 20160302

Pledgee: Shizuishan Xinhui Financing Guarantee Co.,Ltd.

Pledgor: NINGXIA RUNLONG PACKAGING NEW MATERIAL Co.,Ltd.

Registration number: Y2022980025438

PC01 Cancellation of the registration of the contract for pledge of patent right
PC01 Cancellation of the registration of the contract for pledge of patent right

Date of cancellation: 20231206

Granted publication date: 20160302

Pledgee: Shizuishan Xinhui Financing Guarantee Co.,Ltd.

Pledgor: NINGXIA RUNLONG PACKAGING NEW MATERIAL Co.,Ltd.

Registration number: Y2022980025438

PE01 Entry into force of the registration of the contract for pledge of patent right
PE01 Entry into force of the registration of the contract for pledge of patent right

Denomination of invention: A plastic wire with photo aging resistance and its preparation method

Effective date of registration: 20231222

Granted publication date: 20160302

Pledgee: Shizuishan Xinhui Financing Guarantee Co.,Ltd.

Pledgor: NINGXIA RUNLONG PACKAGING NEW MATERIAL Co.,Ltd.

Registration number: Y2023980073377