TW202035163A - Packing sheet - Google Patents
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- TW202035163A TW202035163A TW109109804A TW109109804A TW202035163A TW 202035163 A TW202035163 A TW 202035163A TW 109109804 A TW109109804 A TW 109109804A TW 109109804 A TW109109804 A TW 109109804A TW 202035163 A TW202035163 A TW 202035163A
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/12—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
- C08J9/14—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent organic
- C08J9/141—Hydrocarbons
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B5/00—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts
- B32B5/18—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by features of a layer of foamed material
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- C—CHEMISTRY; METALLURGY
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- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0014—Use of organic additives
- C08J9/0028—Use of organic additives containing nitrogen
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0014—Use of organic additives
- C08J9/0047—Use of organic additives containing boron
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/0061—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof characterized by the use of several polymeric components
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2266/00—Composition of foam
- B32B2266/02—Organic
- B32B2266/0214—Materials belonging to B32B27/00
- B32B2266/025—Polyolefin
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/20—Properties of the layers or laminate having particular electrical or magnetic properties, e.g. piezoelectric
- B32B2307/21—Anti-static
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2203/00—Foams characterized by the expanding agent
- C08J2203/14—Saturated hydrocarbons, e.g. butane; Unspecified hydrocarbons
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2203/00—Foams characterized by the expanding agent
- C08J2203/18—Binary blends of expanding agents
- C08J2203/182—Binary blends of expanding agents of physical blowing agents, e.g. acetone and butane
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2323/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
- C08J2323/04—Homopolymers or copolymers of ethene
- C08J2323/06—Polyethene
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2323/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
- C08J2323/10—Homopolymers or copolymers of propene
- C08J2323/12—Polypropene
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2353/00—Characterised by the use of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives of such polymers
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- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
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Abstract
Description
本發明係關於包裝用片,其係關於具備聚烯烴系樹脂發泡片的包裝用片。 The present invention relates to a packaging sheet, and it relates to a packaging sheet provided with a polyolefin-based resin foamed sheet.
以往,相較於聚苯乙烯系樹脂發泡片及聚酯系樹脂發泡片等,聚烯烴系樹脂發泡片較為柔軟且緩衝性優良,因而廣泛用作包裝用片等。 In the past, compared with polystyrene-based resin foamed sheets, polyester-based resin foamed sheets, etc., polyolefin-based resin foamed sheets are softer and have excellent cushioning properties, and thus are widely used as packaging sheets and the like.
作為這種包裝用片,已知有聚烯烴系樹脂發泡片的單一片或在聚烯烴系樹脂發泡片上積層表面裝飾片而成的積層片等。 As such a packaging sheet, a single sheet of a polyolefin-based resin foamed sheet, a laminated sheet obtained by laminating a surface decorative sheet on a polyolefin-based resin foamed sheet, and the like are known.
作為以這種包裝用片所包裝的被包裝物,已知有電氣設備及電子設備或是構成此等的電氣設備用構件及電子設備用構件等。 As the object to be packaged with such a packaging sheet, electrical equipment and electronic equipment, or components for electrical equipment and electronic equipment, etc. are known.
該包裝用片之使用目的係保護被包裝物不受到保管中或運搬中的衝擊,亦在保管作為平面顯示器面板之基板的玻璃板、半導體基板、金屬板等的構件時,用作介設於構件之間的間隔紙等。 The purpose of the packaging sheet is to protect the packaged objects from shocks during storage or transportation. It is also used as an intermediary when storing components such as glass plates, semiconductor substrates, and metal plates that are the substrates of flat-panel display panels. Spacers between components, etc.
為了避免因為靜電而在包裝的對象物上產生附著物,而對於這樣的包裝用片要求抗靜電性。 In order to avoid the occurrence of adhesions on the packaging object due to static electricity, antistatic properties are required for such packaging sheets.
作為使聚烯烴系樹脂發泡片發揮抗靜電性的方法,已知有使聚烯烴系樹脂發泡片的形成材料中含有所謂高分子型抗靜電劑的聚合物型抗靜電劑或所謂低分子型抗靜電劑的界面活性劑的方法。 As a method for making a polyolefin resin foam sheet exhibit antistatic properties, there is known a polymer type antistatic agent called a polymer type antistatic agent or a so-called low molecular weight antistatic agent in the forming material of the polyolefin resin foam sheet. The method of surfactant type antistatic agent.
其中,關於界面活性劑,係藉由滲出至片表面來發揮抗靜電性,因此容易附著於保護對象物的表面(參照下述專利文獻1)。另一方面,聚合物型抗靜電劑在多數情況中包含金屬離子,而具有該金屬離子遷移至這種被包裝物而造成不良影響的疑慮。
Among them, the surfactant exhibits antistatic properties by exuding to the surface of the sheet, and therefore it is easy to adhere to the surface of the object to be protected (see
[先前技術文獻] [Prior Technical Literature]
[專利文獻] [Patent Literature]
[專利文獻1]日本特開2010-42556號公報 [Patent Document 1] JP 2010-42556 A
如上所述,要求包裝用片發揮抗靜電性,並且成分往包裝物的遷移少,但這樣的需求並未被滿足。 As described above, the packaging sheet is required to exhibit antistatic properties and have less migration of components to the packaging, but such a demand has not been met.
於是,本發明之課題係提供一種成分往被包裝物的遷移少且抗靜電性優良的包裝用片。 Therefore, the subject of the present invention is to provide a packaging sheet that has less migration of components to the packaging material and excellent antistatic properties.
為了解決上述課題而進行詳細研究的結果,本案發明人發現包含了施體/受體型抗靜電劑的聚烯烴系樹脂發泡片呈現優良的抗靜電性且難以發生金屬離子的遷移或滲出,進而完成本發明。 As a result of detailed studies to solve the above-mentioned problems, the inventors of the present case discovered that the polyolefin resin foamed sheet containing the donor/acceptor type antistatic agent exhibits excellent antistatic properties and is unlikely to cause migration or exudation of metal ions. Further completed the present invention.
亦即,為了解決上述課題,本發明提供一種包裝用片,其具備包含了施體/受體型抗靜電劑的聚烯烴系樹脂發泡片,而該聚烯烴系樹脂發泡片在至少一個表面上露出。 That is, in order to solve the above-mentioned problems, the present invention provides a packaging sheet comprising a polyolefin resin foamed sheet containing a donor/acceptor type antistatic agent, and the polyolefin resin foamed sheet has at least one Exposed on the surface.
在包含了施體/受體型抗靜電劑的聚烯烴系樹脂發泡片中,藉由使硼化物等施體與氮化物等受體共存而迅速進行電洞的擴散及電子的擴散,因此即使不利用鈉離子或鋰離子等金屬離子的作用亦可發揮良好的抗靜電性。 In the polyolefin-based resin foam sheet containing the donor/acceptor type antistatic agent, by coexisting donors such as borides and acceptors such as nitrides, the diffusion of holes and the diffusion of electrons proceed rapidly. Even if the action of metal ions such as sodium ion or lithium ion is not used, it can still exert good antistatic properties.
又,在包含了施體/受體型抗靜電劑的聚烯烴系樹脂發泡片中,即使不含有界面活性劑等成為滲出之原因的化合物,亦可發揮良好的抗靜電性。 In addition, the polyolefin-based resin foam sheet containing the donor/acceptor type antistatic agent can exhibit good antistatic properties even if it does not contain a compound that causes bleeding, such as a surfactant.
因此,以將這種聚烯烴系樹脂發泡片在至少一個表面露出的方式而具備的包裝用片,可一方面抑制成分往被包裝物遷移,一方面發揮優良的抗靜電性。 Therefore, the packaging sheet provided in such a way that the polyolefin resin foamed sheet is exposed on at least one surface can suppress the migration of components to the packaged object while exhibiting excellent antistatic properties.
1:聚烯烴系樹脂發泡片 1: Polyolefin resin foam sheet
1a:第1面
1a:
1b:第2面
1b:
2:玻璃板 2: glass plate
10:積層體 10: Laminated body
11、12:塗佈膜 11, 12: Coating film
100:包裝袋 100: Packing bag
100a:正面片 100a: front film
100b:反面片 100b: reverse sheet
101:密封部 101: Sealing part
102:開口部 102: opening
X1:印刷電路基板 X1: Printed circuit board
第1圖係顯示包裝用片的一使用型態的概略圖。 Figure 1 is a schematic diagram showing a usage pattern of the packaging sheet.
第2圖係本發明之一實施型態之包裝用片的概略剖面圖。 Figure 2 is a schematic cross-sectional view of a packaging sheet according to an embodiment of the present invention.
第3圖係顯示包裝用片的其他實施型態的概略圖。 Fig. 3 is a schematic diagram showing another embodiment of the packaging sheet.
說明本發明的包裝用片。 The packaging sheet of the present invention will be described.
以下以包裝用片為僅由聚烯烴系樹脂發泡片構成的單層片且正反兩面皆由聚烯烴系樹脂發泡片所構成的情況為例,說明本發明的實施型態。 Hereinafter, a case where the packaging sheet is a single-layer sheet composed only of a polyolefin-based resin foamed sheet and both the front and back sides are composed of a polyolefin-based resin foamed sheet is taken as an example to describe the embodiment of the present invention.
又,以下例示該聚烯烴系樹脂發泡片為擠製發泡體的情況。 In addition, the case where the polyolefin resin foamed sheet is an extruded foam is exemplified below.
更詳細而言,以下一方面例示將具備「藉由使包含聚烯烴系樹脂的聚烯烴系樹脂組成物擠製發泡所形成之聚烯烴系樹脂發泡片」的包裝用片作為電子零件的袋子或玻璃板的間隔紙使用的情況,一方面說明本發明的實施型態。 In more detail, the following exemplifies a packaging sheet comprising a "polyolefin resin foam sheet formed by extrusion foaming a polyolefin resin composition containing a polyolefin resin" as an electronic component The use of the spacer paper for the bag or the glass plate, on the one hand, illustrates the embodiment of the present invention.
第1圖係顯示使用本實施型態之包裝用片作為用以收納印刷電路基板X1之包裝袋100的構成材料的樣子者。
Fig. 1 shows a state in which the packaging sheet of the present embodiment is used as a constituent material of the
本實施型態的前述包裝袋100,係由面積比印刷電路基板X1更大的矩形之正面片100a與反面片100b的2片包裝用片所構成。
The
本實施型態的前述包裝袋100,係對於將前述正面片100a與前述反面片100b以使輪廓對齊的方式重疊的積層品實施3邊密封而成者。
The
亦即,前述包裝袋100具有沿著正面片100a及反面片100b的4邊之中的3邊使其互相接著的密封部101,而沿著剩餘一邊的部分並未接著,其構成用以取放前述印刷電路基板X1的開口部102。
That is, the
前述包裝袋100中,正面片100a與反面片100b,可由彼此相同的片構成,亦可由分別不同的片所構成。
In the
本實施型態的前述包裝袋100,正面片100a與反面片100b兩者係藉由相同的聚烯烴系樹脂發泡片1所構成。
In the
第2圖係顯示本實施型態中採用作正面片100a及反面片100b的聚烯烴系樹脂發泡片的剖面形狀者。
Fig. 2 shows the cross-sectional shape of the polyolefin resin foamed sheet used as the
如圖所示,本實施型態的聚烯烴系樹脂發泡片1具備構成包裝袋100之內側面而與前述印刷電路基板X1相接的第1面1a、與構成包裝袋100之外側面的第2面1b。
As shown in the figure, the polyolefin-based
本實施型態的聚烯烴系樹脂發泡片1係由作為基質聚合物的聚烯烴系樹脂與包含抗靜電劑的聚烯烴系樹脂組成物所構成。
The polyolefin resin foamed
作為本實施型態的聚烯烴系樹脂發泡片1所含有的前述聚烯烴系樹脂,可列舉例如:聚乙烯系樹脂、聚丙烯系樹脂、乙烯-α烯烴樹脂等。
Examples of the polyolefin resin contained in the polyolefin
構成聚烯烴系樹脂發泡片的聚烯烴系樹脂組成物中,不需要單獨含有1種聚烯烴系樹脂,亦可含有2種以上。 The polyolefin-based resin composition constituting the polyolefin-based resin foamed sheet does not need to contain one type of polyolefin-based resin alone, and may contain two or more types.
作為聚烯烴系樹脂組成物所含有的聚烯烴系樹脂,較佳為聚丙烯系樹脂。 The polyolefin resin contained in the polyolefin resin composition is preferably a polypropylene resin.
前述聚丙烯系樹脂可為屬於丙烯之單獨聚合物的均聚丙烯(hPP),亦可為除了丙烯之外亦包含少量乙烯或丁烯-1等的共聚物。 The aforementioned polypropylene resin may be a homopolypropylene (hPP) which is a single polymer of propylene, or a copolymer containing a small amount of ethylene or butene-1 in addition to propylene.
前述聚丙烯系樹脂之立體構造規整性並未特別做限定,亦可為同排聚丙烯(iPP)、對排聚丙烯(sPP)、雜排聚丙烯(aPP)等的任一者。 The three-dimensional structure regularity of the polypropylene resin is not particularly limited, and it may be any of in-line polypropylene (iPP), para-propylene (sPP), hetero-polypropylene (aPP), and the like.
前述共聚物亦可為使丙烯與乙烯進行無規共聚合而成的無規聚丙烯(rPP)。 The aforementioned copolymer may also be random polypropylene (rPP) obtained by random copolymerization of propylene and ethylene.
前述共聚物亦可為下述的嵌段聚丙烯(bPP):在丙烯之聚合反應的後期導入乙烯,藉此使丙烯-乙烯共聚物以構成區域相(domain phase)的方式分散於均聚丙烯的基材相(matrix phase)之中。 The aforementioned copolymer may also be the following block polypropylene (bPP): ethylene is introduced in the late stage of the polymerization reaction of propylene, whereby the propylene-ethylene copolymer is dispersed in the homopolypropylene in a domain phase. In the matrix phase.
前述嵌段聚丙烯可為以含量40質量%以上的比例含有丙烯-乙烯共聚物的彈性物質者,亦可為所謂的烯烴系熱塑性彈性體(TPO)等。 The aforementioned block polypropylene may be an elastic substance containing a propylene-ethylene copolymer in a content of 40% by mass or more, or may be a so-called olefin-based thermoplastic elastomer (TPO) or the like.
前述聚丙烯系樹脂可為以化學交聯或電子束交聯等而形成長鏈分支者,亦可為所謂的高熔融張力聚丙烯(HMS-PP)等。 The above-mentioned polypropylene resin may be a long-chain branch formed by chemical crosslinking or electron beam crosslinking, or so-called high melt tension polypropylene (HMS-PP) or the like.
作為聚烯烴系樹脂發泡片1所含有的聚丙烯系樹脂,較佳為嵌段聚丙烯(bPP)或高熔融張力聚丙烯(HMS-PP),較佳係將兩者混合使用。
The polypropylene resin contained in the polyolefin
嵌段聚丙烯(bPP)相對於高熔融張力聚丙烯(HMS-PP)的質量比例(bPP/(bPP+HMS-PP))較佳為20質量%以上,更佳為30質量%以上,特佳為40質量%以上。 The mass ratio of block polypropylene (bPP) to high melt tension polypropylene (HMS-PP) (bPP/(bPP+HMS-PP)) is preferably 20% by mass or more, more preferably 30% by mass or more. Preferably, it is 40% by mass or more.
前述質量比例(bPP/(bPP+HMS-PP))較佳為80質量%以下,更佳為70質量%以下,特佳為60質量%以下。 The aforementioned mass ratio (bPP/(bPP+HMS-PP)) is preferably 80% by mass or less, more preferably 70% by mass or less, and particularly preferably 60% by mass or less.
高熔融張力聚丙烯較佳係於230℃中呈現3cN以上之熔融張力者。前述熔融張力較佳為4cN以上,特佳為5cN以上。前述熔融張力較佳為30cN以下,更佳為28cN以下。 The high melt tension polypropylene preferably exhibits a melt tension of 3 cN or more at 230°C. The aforementioned melt tension is preferably 4 cN or more, particularly preferably 5 cN or more. The aforementioned melt tension is preferably 30 cN or less, more preferably 28 cN or less.
前述熔融張力例如可以下述方法求得。 The aforementioned melt tension can be obtained, for example, by the following method.
(熔融張力測量方法) (Melting tension measurement method)
試樣在測量對象為顆粒的情況下直接使用,在測量對象為聚烯烴系樹脂發泡片等片狀的情況,則係使用造粒機(例如,東洋精機製作所股份有限公司製的「HAND TRUDER型PM-1」)以汽缸溫度220℃、從填充試樣到擠製開始的待機時間為2.5分鐘的條件將該聚烯烴系樹脂發泡片顆粒化而成者。 The sample is used as it is when the measurement object is pellets, and when the measurement object is a polyolefin resin foamed sheet, etc., a pelletizer (for example, "HAND TRUDER" manufactured by Toyo Seiki Seisakusho Co., Ltd. Type PM-1") The polyolefin-based resin foamed sheet was pelletized under the conditions of a cylinder temperature of 220°C and a standby time of 2.5 minutes from filling the sample to the start of extrusion.
熔融張力係使用雙孔毛細管流變計Twin-bore Capillary Rheometer Rheologic5000T(義大利Chiast公司製)進行測量。 The melt tension was measured using a Twin-bore Capillary Rheometer Rheologic 5000T (manufactured by Chiast, Italy).
具體而言,在加熱至試驗溫度的徑長15mm的筒中填充測量試樣樹脂後,預熱5分鐘之後,從上述測量裝置的毛細管模(口徑2.0mm,長度20mm,流入角度平坦),使活塞下降速度(0.1546mm/s)保持固定,一邊擠製為帶狀, 一邊使該帶狀物通過位於上述毛細管模下方27cm的張力檢測滑輪之後,使用捲繞輥,一邊以初速8.7mm/s、加速度12mm/s2逐漸增加其捲繞速度,一邊進行捲繞,將帶狀物即將切斷之前的極大值與極小值的平均作為試樣的熔融張力。 Specifically, a 15mm diameter cylinder heated to the test temperature is filled with the measurement sample resin, and after preheating for 5 minutes, from the capillary die of the measuring device (bore diameter 2.0mm, length 20mm, flat inflow angle), make the piston The descending speed (0.1546mm/s) is kept constant, while extruding into a ribbon shape, the ribbon is passed through a tension detection pulley 27cm below the capillary mold, and then a winding roller is used to set the initial speed at 8.7mm/s. The acceleration of 12mm/s 2 gradually increases the winding speed while winding, and the average of the maximum value and the minimum value immediately before the ribbon is cut is used as the melt tension of the sample.
另外,在張力描圖中只有1個極大點的情況下,則將該極大值作為熔融張力。 In addition, when there is only one maximum point in the tension trace, the maximum value is used as the melt tension.
作為聚烯烴系樹脂組成物所含有的較佳聚烯烴系樹脂,除了如上述之聚丙烯系樹脂以外,可列舉低密度聚乙烯樹脂。 As a preferable polyolefin resin contained in the polyolefin resin composition, in addition to the above-mentioned polypropylene resin, a low density polyethylene resin can be cited.
作為前述低密度聚乙烯樹脂,可列舉例如:藉由中低壓法聚合的直鏈低密度聚乙烯樹脂(LLDPE)、或藉由高壓法而在分子結構中形成有長鏈分支的低密度聚乙烯樹脂(LDPE)。 Examples of the aforementioned low-density polyethylene resin include linear low-density polyethylene resin (LLDPE) polymerized by a medium-low pressure method, or low-density polyethylene having long-chain branches formed in a molecular structure by a high-pressure method. Resin (LDPE).
作為前述低密度聚乙烯樹脂(LDPE),較佳為樹脂密度在910kg/m3以上、930kg/m3以下者。 The low-density polyethylene resin (LDPE) preferably has a resin density of 910 kg/m 3 or more and 930 kg/m 3 or less.
作為前述直鏈低密度聚乙烯樹脂(LLDPE),較佳為樹脂密度在910kg/m3以上、925kg/m3以下者。 The linear low-density polyethylene resin (LLDPE) preferably has a resin density of 910 kg/m 3 or more and 925 kg/m 3 or less.
前述低密度聚乙烯樹脂(LDPE)或前述直鏈低密度聚乙烯樹脂(LLDPE),熔融流動速率(以下稱為「MFR」)較佳為1g/10min以上10g/10min以下。 The low density polyethylene resin (LDPE) or the linear low density polyethylene resin (LLDPE) preferably has a melt flow rate (hereinafter referred to as "MFR") of 1 g/10 min or more and 10 g/10 min or less.
上述熔融流動速率,只要本說明書中未特別說明,則針對後述高分子型抗靜電劑的MFR,意指根據JIS K 7210:1999「塑膠-熱塑性塑膠的熔融流動速率(MFR)」及熔融體積流動速率(MVR)的試驗方法」B法記載的方法(但,試驗溫度為190℃,載重為21.18N)所測量的值。 The above-mentioned melt flow rate, unless otherwise specified in this specification, refers to the MFR of the polymer antistatic agent mentioned later, which is based on JIS K 7210: 1999 "Plastic-thermoplastic melt flow rate (MFR)" and melt volume flow Test method of rate (MVR)" The value measured by the method described in Method B (however, the test temperature is 190°C and the load is 21.18N).
與上述聚烯烴系樹脂同時含有於聚烯烴系樹脂組成物之中的前述施體/受體型抗靜電劑,例如,可採用由有機硼化物與鹼性氮化物的組合所構成者。 The donor/acceptor type antistatic agent contained in the polyolefin resin composition together with the polyolefin resin may be, for example, a combination of an organic boride and a basic nitride.
作為前述施體/受體型抗靜電劑,較佳為與聚烯烴系樹脂之相容性優良者,較佳係具有一定程度之長度的烷基鏈。 As the aforementioned donor/acceptor type antistatic agent, one having excellent compatibility with polyolefin resin is preferred, and an alkyl chain having a certain length is preferred.
前述施體/受體型抗靜電劑較佳為以下述通式(1)所示者。 The aforementioned donor/acceptor type antistatic agent is preferably one represented by the following general formula (1).
另外,上述式(1)中的「R1」及「R2」分別獨立為「R7CO-OCH2-」或「HOCH2-」,且至少一者為「R7CO-OCH2-」。上述式(1)中的「R3」及「R4」分別獨立為「CH3-」、「C2H5-」、「HOCH2-」、「HOC2H4-」或「HOCH2CH(CH3)-」。上述式(1)中的「R5」為「-C2H4-」或「-C3H6-」。上述式(1)中的「R6」及「R7」分別獨立為碳數11至21的烷基。 In addition, "R 1 "and "R 2 " in the above formula (1) are independently "R 7 CO-OCH 2 -" or "HOCH 2 -", and at least one of them is "R 7 CO-OCH 2 -""."R 3 "and "R 4 " in the above formula (1) are independently "CH 3 -", "C 2 H 5 -", "HOCH 2 -", "HOC 2 H 4 -" or "HOCH 2 CH(CH 3 ) - ". "R 5 "in the above formula (1) is "-C 2 H 4 -" or "-C 3 H 6 -". "R 6 "and "R 7 " in the above formula (1) are each independently an alkyl group having 11 to 21 carbon atoms.
又,作為前述施體/受體型的抗靜電劑,亦可為下述通式(2)所示者。 In addition, as the aforementioned donor/acceptor type antistatic agent, one represented by the following general formula (2) may also be used.
另外,上述式(2)中的「R1」及「R2」分別獨立為「R7CO-OCH2-」或「HOCH2-」,且至少一者為「R7CO-OCH2-」。上述式(2)中的「R3」及「R4」分別獨立為「CH3-」、「C2H5-」、「HOCH2-」、「HOC2H4-」或「HOCH2CH(CH3)-」。上述式(2)中的「R5」為「-C2H4-」或「-C3H6-」。上述式(2)中的「R6」及「R7」分別獨立為碳數11至21的烷基。 In addition, "R 1 "and "R 2 " in the above formula (2) are independently "R 7 CO-OCH 2 -" or "HOCH 2 -", and at least one of them is "R 7 CO-OCH 2 -""."R 3 "and "R 4 " in the above formula (2) are independently "CH 3 -", "C 2 H 5 -", "HOCH 2 -", "HOC 2 H 4 -" or "HOCH 2 CH(CH 3 )-". "R 5 "in the above formula (2) is "-C 2 H 4 -" or "-C 3 H 6 -". "R 6 "and "R 7 " in the above formula (2) are each independently an alkyl group having 11 to 21 carbon atoms.
前述通式(1)及(2)中,上段的有機硼化物的部分成為施體,下段的鹼性氮成為受體。 In the aforementioned general formulas (1) and (2), the organoboride portion in the upper stage becomes the donor, and the basic nitrogen in the lower stage becomes the acceptor.
另外,前述施體中的「(-)」表示硼原子的吸電子性變強、「(+)」表示氧原子的供電子性變強。 In addition, "(-)" in the aforementioned donor means that the electron withdrawing property of the boron atom becomes stronger, and "(+)" means that the electron donating property of the oxygen atom becomes stronger.
又,前述施體中的「→」表示電子被吸附的路徑、「---」表示原子間鍵結力變弱的狀態。 In addition, "→" in the aforementioned donor body indicates a path through which electrons are adsorbed, and "---" indicates a state where the bonding force between atoms is weakened.
再者,「δ+」表示共價鍵存在極性。 Furthermore, "δ+" indicates that the covalent bond has polarity.
又,如上述以通式(1)及(2)表示者之中,作為本實施型態中的該施體/受體型的抗靜電劑,較佳為以分子式「C42H81O8B」表示的有機硼化物與以分子式「C23H48ON2」表示的鹼性氮化物的組合,或以分子式 「C42H81O8B」表示的有機硼化物與分子式「C23H47O2N」表示的鹼性氮化物的組合。 In addition, as the above-mentioned general formulas (1) and (2), as the donor/acceptor type antistatic agent in this embodiment, it is preferable to use the molecular formula "C 42 H 81 O 8 B The combination of the organic boride represented by "" and the basic nitride represented by the molecular formula "C 23 H 48 ON 2 ", or the organic boride represented by the molecular formula "C 42 H 81 O 8 B" and the molecular formula "C 23 H 47 A combination of basic nitrides represented by "O 2 N".
就前述聚烯烴系樹脂組成物中的前述施體/受體型抗靜電劑的含量而言,在將聚烯烴系樹脂組成物所包含之所有聚烯烴系樹脂的總量設為100質量份時,較佳為0.1質量份以上,更佳為0.2質量份以上,再佳為0.3質量份以上。 Regarding the content of the donor/acceptor type antistatic agent in the polyolefin resin composition, when the total amount of all polyolefin resins contained in the polyolefin resin composition is 100 parts by mass , Preferably 0.1 parts by mass or more, more preferably 0.2 parts by mass or more, and still more preferably 0.3 parts by mass or more.
就前述聚烯烴系樹脂組成物中的前述施體/受體型抗靜電劑的含量而言,在將聚烯烴系樹脂組成物所包含之所有聚烯烴系樹脂的總量設為100質量份時,較佳為3.0質量份以下,更佳為2.8質量份以下,再佳為2.6質量份以下。 Regarding the content of the donor/acceptor type antistatic agent in the polyolefin resin composition, when the total amount of all polyolefin resins contained in the polyolefin resin composition is 100 parts by mass , Preferably 3.0 parts by mass or less, more preferably 2.8 parts by mass or less, and still more preferably 2.6 parts by mass or less.
本實施型態的聚烯烴系樹脂發泡片1,因為藉由擠製發泡法所製造,因此在該擠製發泡法中所使用的前述聚烯烴系樹脂組成物中,除了目前為止所述之成分以外,可更含有發泡所需之成分。
The polyolefin
作為用於此發泡的成分,可列舉發泡劑及氣泡調整劑。 Examples of components used for this foaming include foaming agents and bubble regulators.
作為前述發泡劑,可列舉異丁烷、正丁烷、丙烷、戊烷、己烷、環丁烷、環戊烷等烴、二氧化碳、氮等無機氣體。 Examples of the blowing agent include hydrocarbons such as isobutane, n-butane, propane, pentane, hexane, cyclobutane, and cyclopentane, and inorganic gases such as carbon dioxide and nitrogen.
其中,作為前述發泡劑,較佳為異丁烷與正丁烷的混合丁烷。 Among them, as the aforementioned blowing agent, a mixed butane of isobutane and n-butane is preferred.
如此,若使用異丁烷/正丁烷的混合丁烷,則係藉由異丁烷抑制擠製步驟中發泡劑急遽逸散。 In this way, if a mixed butane of isobutane/n-butane is used, isobutane is used to suppress the rapid escape of the blowing agent during the extrusion step.
另一方面,與聚烯烴系樹脂的相容性優異的正丁烷,抑制連續氣泡率增加,因此可得到收縮少且連續氣泡率低而緩衝性優良的聚烯烴系樹脂發泡片1。
On the other hand, n-butane, which is excellent in compatibility with polyolefin-based resins, suppresses an increase in the open cell ratio, and therefore can obtain a polyolefin-based resin foamed
另外,擠製發泡時使用的發泡劑的量,雖亦與要求之發泡程度相關,但相對於聚烯烴系樹脂100質量份,通常為5質量份以上,25質量份以下。 In addition, although the amount of foaming agent used in extrusion foaming is also related to the required degree of foaming, it is usually 5 parts by mass or more and 25 parts by mass or less with respect to 100 parts by mass of the polyolefin resin.
通常使發泡劑的添加比例在這樣的範圍,是因為若發泡劑未達5質量份則可能難以得到充分的發泡,若超過25質量份則可能導致氣泡膜破裂而無法得到良好的聚烯烴系樹脂發泡片。 Generally, the addition ratio of the blowing agent is set in such a range, because if the blowing agent is less than 5 parts by mass, it may be difficult to obtain sufficient foaming, and if it exceeds 25 parts by mass, the bubble film may burst and a good polymerization may not be obtained. Olefin resin foam sheet.
又,作為用於調整由發泡劑所形成之氣泡的前述氣泡調整劑,可列舉滑石、二氧化矽等無機粉末等。亦可將用作分解型發泡劑的多價羧酸與碳酸鈉或小蘇打(碳酸氫鈉)的混合物、偶氮二羧酸醯胺等作為前述氣泡調整劑使用。 In addition, as the aforementioned bubble regulator for regulating the bubbles formed by the foaming agent, inorganic powders such as talc and silica can be cited. A mixture of polyvalent carboxylic acid and sodium carbonate or sodium bicarbonate (sodium bicarbonate), azodicarboxylate, etc., used as a decomposable blowing agent can also be used as the aforementioned bubble regulator.
此等可單獨使用,亦可併用複數種。此氣泡調整劑的添加量,在聚烯烴系樹脂每100質量份中,較佳為0.5質量份以下。 These can be used singly or in combination. The addition amount of this air bubble regulator is preferably 0.5 parts by mass or less per 100 parts by mass of the polyolefin resin.
本實施型態的聚烯烴系樹脂發泡片1中,除了上述成分以外,亦可因應需求含有熱穩定劑、紫外線吸收劑、抗氧化劑、著色劑等的添加劑。
In addition to the above-mentioned components, the polyolefin-based resin foamed
另外,除了聚烯烴系樹脂與施體/受體型抗靜電劑以外,聚烯烴系樹脂發泡片1所含有的其他成分的比例,較佳為10質量%以下,更佳為5質量%以下。
In addition to the polyolefin resin and the donor/acceptor type antistatic agent, the ratio of other components contained in the polyolefin
亦即,構成聚烯烴系樹脂發泡片1的聚烯烴系樹脂組成物中的聚烯烴系樹脂與施體/受體型抗靜電劑的總比例較佳為90質量%以上,更佳為95質量%以上。
That is, the total ratio of the polyolefin resin and the donor/acceptor type antistatic agent in the polyolefin resin composition constituting the polyolefin
由上述聚烯烴系樹脂組成物所構成之聚烯烴系樹脂發泡片1的密度(視密度)並未特別限定,只要可發揮一般要求之緩衝性的程度即可,通常未達150kg/m3,較佳為100kg/m3以下,特佳為70kg/m3以下。
The density (apparent density) of the polyolefin-based resin foamed
選擇這樣的密度較佳,是因為藉由使密度在上限以下,可確實賦予聚烯烴系樹脂發泡片1優良的柔軟性與緩衝性,藉由使密度在下限以上,可使聚烯烴系樹脂發泡片1發揮優良的強度。
Such a density is preferably selected because by making the density below the upper limit, the polyolefin resin foamed
從此點來看,聚烯烴系樹脂發泡片1的密度較佳為10kg/m3以上,更佳為15kg/m3以上。
From this point of view, the density of the polyolefin-based resin foamed
聚烯烴系樹脂發泡片1的密度,係根據JIS K7222:1999「發泡塑膠及橡膠-視密度的測量」記載之方法測量,具體係以下述方法測量。
The density of the polyolefin
(密度測量方法) (Density measurement method)
從聚烯烴系樹脂發泡片,製作100cm3以上的試樣,在JIS K7100:1999的記號23/50、2級環境下,對於此試樣進行狀態調整16小時後,測量其尺寸、質量,以下式算出視密度。
From the polyolefin-based resin foam sheet, a sample of 100 cm 3 or more is prepared, and the size and mass of the sample are measured after the state is adjusted for 16 hours under the 23/50 of JIS K7100: 1999 and
視密度(g/cm3)=試樣的質量(g)/試樣的體積(cm3) Apparent density (g/cm 3 ) = sample mass (g) / sample volume (cm 3 )
另外,關於試樣的尺寸測量,例如,可使用Mitutoyo Corporation公司製「DIGIMATIC」CD-15型。 In addition, regarding the size measurement of the sample, for example, the "DIGIMATIC" CD-15 type manufactured by Mitutoyo Corporation can be used.
前述聚烯烴系樹脂發泡片的厚度較佳為0.1mm以上,更佳為0.15mm以上,再佳為0.3mm以上。 The thickness of the aforementioned polyolefin resin foamed sheet is preferably 0.1 mm or more, more preferably 0.15 mm or more, and still more preferably 0.3 mm or more.
前述聚烯烴系樹脂發泡片的厚度較佳為6mm以下,更佳為5mm以下,再佳為4mm以下。 The thickness of the aforementioned polyolefin resin foamed sheet is preferably 6 mm or less, more preferably 5 mm or less, and still more preferably 4 mm or less.
聚烯烴系樹脂發泡片1的厚度,例如,可設為在隨機選擇的10處以上之測量點中所測量之厚度的平均值而求得者。
The thickness of the polyolefin-based resin foamed
前述聚烯烴系樹脂發泡片之基重較佳為10g/m2以上,更佳為15g/m2以上,再佳為25g/m2以上。 The basis weight of the aforementioned polyolefin resin foamed sheet is preferably 10 g/m 2 or more, more preferably 15 g/m 2 or more, and still more preferably 25 g/m 2 or more.
前述聚烯烴系樹脂發泡片的基重較佳為600g/m2以下,更佳為500g/m2以下,再佳為400g/m2以下。 The basis weight of the aforementioned polyolefin resin foamed sheet is preferably 600 g/m 2 or less, more preferably 500 g/m 2 or less, and still more preferably 400 g/m 2 or less.
前述聚烯烴系樹脂發泡片的基重,可根據JIS P8124:2011「紙及卡紙-基重測量方法」記載的方法來進行測量。 The basis weight of the aforementioned polyolefin resin foamed sheet can be measured according to the method described in JIS P8124:2011 "Paper and Cardboard-Basis Weight Measurement Method".
具體而言,可裁切出10片100cm2以上的樣本,測量各質量與面積,以下式求得。 Specifically, 10 pieces of 100 cm 2 or more samples can be cut out, and each mass and area can be measured, and the following formula can be used to obtain.
基重(g/m2)=10000×試驗片質量(g)/試驗單面積(cm2) Basis weight (g/m 2 )=10000×test piece mass (g)/test single area (cm 2 )
關於前述聚烯烴系樹脂發泡片,至少前述第1面1a(與被包裝物相接的表面)中的滲出量較佳為0.3質量%以下,滲出量更佳係在0.2質量%以下,滲出量再佳係在0.1質量%以下。
Regarding the aforementioned polyolefin resin foamed sheet, the amount of exudation in at least the
前述聚烯烴系樹脂發泡片的滲出量可以下述方法求得。 The amount of exudation of the aforementioned polyolefin resin foamed sheet can be obtained by the following method.
將試樣裁切為100mm×100mm的尺寸,將試樣放入120mm×170mm的較厚的附夾鏈密封袋。 Cut the sample into a size of 100mm×100mm, and put the sample into a thicker sealed bag with a chain of 120mm×170mm.
在此密封袋中加入20ml的甲醇,盡量排出空氣並封閉夾鏈,以手搖晃密封袋約100次。 Add 20ml of methanol into this sealed bag, try to exhaust air and close the zipper, shake the sealed bag about 100 times by hand.
搖晃之後打開夾鏈,將密封袋之中的甲醇取出至燒杯,在105℃的恆溫槽加熱24小時使甲醇蒸發而得到乾燥固體。 After shaking, the zipper was opened, the methanol in the sealed bag was taken out to a beaker, and heated in a constant temperature bath at 105°C for 24 hours to evaporate the methanol to obtain a dry solid.
之後,將燒杯放入乾燥器,在乾燥器中放冷,測量回到常溫後的蒸發乾燥固體的質量。 After that, put the beaker into a desiccator, let it cool in the desiccator, and measure the mass of the evaporated and dried solid after returning to normal temperature.
另外,測量原則上係使用分別從不同處裁切出來的3個試樣而實施3次。 In addition, the measurement is carried out three times in principle using three samples cut out from different places.
然後,將3次測量的平均值作為前述聚烯烴系樹脂發泡片的滲出量。 Then, the average value of 3 measurements was taken as the amount of exudation of the aforementioned polyolefin resin foamed sheet.
前述聚烯烴系樹脂發泡片中,至少前述第1面1a(與被包裝物相接的表面)中的鹼金屬離子及鹼土金屬離子的量(總量)較佳為2mg/m2以下。
In the polyolefin resin foamed sheet, the amount (total amount) of alkali metal ions and alkaline earth metal ions in at least the
前述第1面1a中的鹼金屬離子及鹼土金屬離子量更佳為1mg/m2以下,再佳為0.5mg/m2以下。
The amount of alkali metal ions and alkaline earth metal ions in the
前述聚烯烴系樹脂發泡片的鹼金屬離子及鹼土金屬離子的量,可由下述方法求得。 The amount of alkali metal ions and alkaline earth metal ions in the aforementioned polyolefin resin foamed sheet can be obtained by the following method.
將試樣裁切為100mm×100mm的尺寸,將試樣放入120mm×170mm的較厚的附夾鏈密封袋。 Cut the sample into a size of 100mm×100mm, and put the sample into a thicker sealed bag with a chain of 120mm×170mm.
在此密封袋中加入20ml的離子交換水,盡量排除空氣並封閉夾鏈,保持於60℃的恆溫槽內,經過30分鐘後,以手搖晃此密封袋10次。
Add 20ml of ion-exchange water to this sealed bag, try to remove air and close the zipper, keep it in a constant temperature bath at 60°C, after 30 minutes, shake the sealed
再30分鐘後相同地以手搖晃密封袋10次後,打開密封袋取出其中的離子交換水。然後,使用多功能型ICP發光分光分析裝置(商品名稱「ICPE-9000」,島津製作所(股)製),以下述測量條件測量離子交換水所包含的鹼金屬離子及鹼土金屬離子的量。
After another 30 minutes, the sealed bag was shaken by
(測量條件) (Measurement conditions)
觀測方向:軸向 Observation direction: axial
曝光時間:30秒 Exposure time: 30 seconds
高頻輸出:1.20kW High frequency output: 1.20kW
載體流量:0.7mL/min Carrier flow rate: 0.7mL/min
電漿流量:10.0mL/min Plasma flow rate: 10.0mL/min
輔助流量:0.6mL/min Auxiliary flow rate: 0.6mL/min
前述聚烯烴系樹脂發泡片中,至少前述第1面1a(與被包裝物相接的表面)中的表面電阻率,較佳係在以乙醇擦拭後仍呈現既定值。
In the polyolefin-based resin foam sheet, at least the surface resistivity of the
具體而言,以乙醇擦拭後,在溫度20℃、相對濕度60%RH的條件下所測量之前述聚烯烴系樹脂發泡片的前述表面電阻率較佳為1×108Ω以上,更佳為1×109Ω以上,特佳為1×1010Ω以上。 Specifically, after wiping with ethanol, the surface resistivity of the polyolefin-based resin foamed sheet measured under the conditions of a temperature of 20°C and a relative humidity of 60%RH is preferably 1×10 8 Ω or more, more preferably It is 1×10 9 Ω or more, particularly preferably 1×10 10 Ω or more.
前述表面電阻率較佳為1×1012Ω以下,更佳為1×1011Ω以下。 The aforementioned surface resistivity is preferably 1×10 12 Ω or less, more preferably 1×10 11 Ω or less.
表面電阻率,可根據JIS K6911:1995「熱硬化性塑膠一般試驗方法」記載的方法進行測量。 The surface resistivity can be measured according to the method described in JIS K6911: 1995 "General Test Methods for Thermosetting Plastics".
可使用試驗裝置(Advantest(股)製的數位超高電阻/微少電流計,型號「R3840」及RESISTIVITY CHAMBER,型號「R12702A」)測量表面電阻率。表面電阻率係以約30N的載重將電極壓附於從聚烯烴系樹脂發泡片採取的試樣上,並以500V充電1分鐘之後,測量其電阻值,再藉由下式算出者。 The test device (Advantest (stock) digital ultra-high resistance/micro current meter, model "R3840" and RESISTIVITY CHAMBER, model "R12702A") can be used to measure surface resistivity. The surface resistivity is calculated by pressing the electrode on a sample taken from a polyolefin resin foam sheet with a load of about 30N, charging it at 500V for 1 minute, measuring its resistance value, and calculating it by the following formula.
另外,試樣為寬度100mm×長度100mm×厚度(聚烯烴系樹脂發泡片本身的厚度)。 In addition, the sample has a width of 100 mm × a length of 100 mm × thickness (thickness of the polyolefin resin foam sheet itself).
測量係在溫度20±2℃、相對濕度65±5%RH的環境下調整狀態24小時以上後實施,試驗環境為溫度20±2℃、相對濕度65±5%RH。 The measurement is carried out after adjusting the state for more than 24 hours in an environment with a temperature of 20±2°C and a relative humidity of 65±5%RH. The test environment is a temperature of 20±2°C and a relative humidity of 65±5%RH.
試樣數(n數)為5個,原則上係分別測量正反兩面。 The number of samples (n number) is 5, and in principle the front and back sides are measured separately.
另外,試樣在調整狀態後以乙醇擦拭表面。 In addition, the surface of the sample was wiped with ethanol after conditioning.
以乙醇所進行的擦拭係以下述方式實施。 The wiping with ethanol was implemented in the following manner.
使用以沾附少量乙醇的紙巾(例如,商品名稱「KimWipes」)數次擦拭經過調整狀態之後的100mm見方之試樣的整個測量面。 Wipe the entire measuring surface of the 100mm square sample after adjustment with a paper towel (for example, the product name "KimWipes") with a small amount of ethanol.
表面電阻率,在該擦拭之後,於試驗環境下保持1小時後實施。 After the wiping, the surface resistivity was kept in a test environment for 1 hour and then implemented.
另外,各試樣的表面電阻率係以下式求得,針對所有試樣算出測量值並進行平均,將其平均值作為聚烯烴系樹脂發泡片的表面電阻率。 In addition, the surface resistivity of each sample was calculated by the following formula, and the measured values were calculated and averaged for all samples, and the average value was used as the surface resistivity of the polyolefin-based resin foamed sheet.
ρs=(π(D+d)/(D-d))×Rs ρs=(π(D+d)/(D-d))×Rs
ρs:表面電阻率(MΩ) ρs: Surface resistivity (MΩ)
D:表面的環狀電極之內徑(cm) D: The inner diameter of the ring electrode on the surface (cm)
d:表面電極的內圓之外徑(cm) d: The outer diameter of the inner circle of the surface electrode (cm)
Rs:表面電阻(MΩ) Rs: Surface resistance (MΩ)
本實施型態中的聚烯烴系樹脂發泡片1,在發揮上述表面性狀的範圍內,亦可含有少量的高分子型抗靜電劑及少量的界面活性劑。
The polyolefin-based resin foamed
作為前述高分子型抗靜電劑,可列舉:聚環氧乙烷、聚環氧丙烷、聚乙二醇、聚酯醯胺、聚醚酯醯胺、乙烯-甲基丙烯酸共聚物等的離子聚合物、聚乙二醇甲基丙烯酸酯系共聚物等的四級銨鹽,日本特開2001-278985號公報記載之烯烴系嵌段與親水性嵌段的共聚物等。 Examples of the aforementioned polymer type antistatic agent include: ionic polymerization of polyethylene oxide, polypropylene oxide, polyethylene glycol, polyester amide, polyether ester amide, ethylene-methacrylic acid copolymer, etc. Quaternary ammonium salts such as polyethylene glycol methacrylate copolymers, copolymers of olefin-based blocks and hydrophilic blocks described in JP 2001-278985 A, etc.
聚烯烴系樹脂發泡片中的高分子型抗靜電劑的含量較佳為1質量%以下,更佳為0.5質量%以下,特佳為0.1質量%以下。 The content of the polymer antistatic agent in the polyolefin-based resin foam sheet is preferably 1% by mass or less, more preferably 0.5% by mass or less, and particularly preferably 0.1% by mass or less.
本實施型態的聚烯烴系樹脂發泡片,不含有高分子型抗靜電劑而尤佳。 The polyolefin resin foamed sheet of this embodiment does not contain a polymer antistatic agent and is particularly preferred.
作為前述界面活性劑,可列舉:非離子系界面活性劑、陰離子系界面活性劑、陽離子系界面活性劑、兩性界面活性劑等。 Examples of the aforementioned surfactant include nonionic surfactants, anionic surfactants, cationic surfactants, and amphoteric surfactants.
聚烯烴系樹脂發泡片中的界面活性劑的含量較佳為1質量%以下,更佳為0.5質量%以下,特佳為0.1質量%以下。 The content of the surfactant in the polyolefin-based resin foam sheet is preferably 1% by mass or less, more preferably 0.5% by mass or less, and particularly preferably 0.1% by mass or less.
本實施型態的聚烯烴系樹脂發泡片以不含有界面活性劑者尤佳。 The polyolefin-based resin foamed sheet of the present embodiment preferably does not contain a surfactant.
本實施型態中的聚烯烴系樹脂發泡片1中,就可不區分正反面而使用之點中,不僅前述第1面1a,前述第2面1b亦具有如前述的表面性狀者較佳。
In the polyolefin-based resin foamed
然而,前述第2面1b因為未與作為被包裝物的印刷電路基板X1相接,因此本實施型態的包裝用片(正面片100a、反面片100b),亦可為在聚烯烴系樹脂發泡片1的單面上積層纖維片(紙、布帛等)、膜(樹脂膜、金屬
膜、複合膜等)及不包含施體/受體型抗靜電劑的樹脂發泡片等任一者的多層結構。
However, since the aforementioned
亦即,本實施型態中的包裝用片,只要以使揉合有施體/受體型抗靜電劑的聚烯烴系樹脂發泡片在至少一個表面上露出的方式具備即可。 That is, the packaging sheet in this embodiment mode may be provided so as to expose the polyolefin resin foam sheet kneaded with the donor/acceptor type antistatic agent on at least one surface.
以上的說明中,雖例示包裝袋100作為包裝用片的使用型態,但本實施型態中的包裝用片,亦可用於其他用途。
In the above description, although the use type of the
以第3圖為例說明本實施型態中的包裝用片的其他實施型態。 Taking Fig. 3 as an example, another embodiment of the packaging sheet in this embodiment is described.
第3圖所示的包裝用片,係僅以聚烯烴系樹脂發泡片1構成的單層片,其在將玻璃板2於上下方向積層複數片而形成積層體10時,作為介在相鄰玻璃板2之間的間隔紙使用。
The packaging sheet shown in Figure 3 is a single-layer sheet composed of only the polyolefin-based
本實施型態中的前述玻璃板2,係電漿顯示器面板或液晶顯示器面板等的平面顯示器面板用的玻璃板。
The
構成包裝袋100的包裝用片,係以僅使兩表面之中的一面側(第1面1a)與作為被包裝物的印刷電路基板X1相接的方式使用,但第3圖所示的包裝用片,係聚烯烴系樹脂發泡片1的第1面1a與第2面1b雙方皆為抵接於作為被包裝物之玻璃板2的抵接面。
The packaging sheet constituting the
因此,此實施型態中所使用的包裝用片,較佳係以使揉合有施體/受體型抗靜電劑的聚烯烴系樹脂發泡片在兩表面露出的方式而具備聚烯烴系樹脂發泡片。 Therefore, the packaging sheet used in this embodiment preferably has a polyolefin-based resin foam sheet so that the polyolefin-based resin foam sheet kneaded with the donor/acceptor type antistatic agent is exposed on both surfaces. Resin foam sheet.
要求聚烯烴系樹脂發泡片於兩表面露出的情況,包裝用片無須以單一的聚烯烴系樹脂發泡片1構成,亦可為將2片的聚烯烴系樹脂發泡片1直接或經介其他片的狀態進行積層的積層片。
When the polyolefin-based resin foamed sheet is required to be exposed on both surfaces, the packaging sheet does not need to be composed of a single polyolefin-based resin foamed
亦即,包裝用片可為具有設於一面側的第1表面層與設於其他面側的第2表面層分別由含有施體/受體型抗靜電劑之聚烯烴系樹脂發泡片所構成 的2層結構者,亦可為具有前述第1表面層與前述第2表面層與之間具備1層或2層以上之中間層的3層以上之積層結構、且前述第1表面層與前述第2表面層分別由包含施體/受體型抗靜電劑之聚烯烴系樹脂發泡片所構成者。 That is, the packaging sheet may have a first surface layer provided on one side and a second surface layer provided on the other side, each made of a polyolefin resin foam sheet containing a donor/acceptor type antistatic agent. constitute The two-layer structure may also have a three-layer or more-layer structure with one or more intermediate layers between the first surface layer and the second surface layer, and the first surface layer and the The second surface layer is each composed of a polyolefin-based resin foam sheet containing a donor/acceptor type antistatic agent.
如上所述,包裝用片具備複數片聚烯烴系樹脂發泡片的情況,一聚烯烴系樹脂發泡片與其他聚烯烴系樹脂發泡片之厚度及施體/受體型抗靜電劑的含量等可相同亦可不同。 As mentioned above, when the packaging sheet has a plurality of polyolefin resin foam sheets, the thickness of a polyolefin resin foam sheet and other polyolefin resin foam sheets and the difference between the donor/acceptor type antistatic agent The content etc. may be the same or different.
如上述之聚烯烴系樹脂發泡片1,如前所述,本實施型態中,係由擠製發泡法所製造。
As mentioned above, the polyolefin resin foamed
具體而言,可進行下述擠製步驟來製造聚烯烴系樹脂發泡片1:從裝設於擠製機之前端的圓模(Circular die)等,將前述聚烯烴系樹脂組成物連續地擠製發泡為片狀,以製作擠製發泡片。 Specifically, the following extrusion steps can be carried out to produce the polyolefin resin foam sheet 1: from a circular die (Circular die) installed at the front end of the extruder, the aforementioned polyolefin resin composition is continuously extruded Make foam into a sheet to make extruded foam sheet.
該擠製步驟中,因為施體/受體型抗靜電劑對於聚烯烴系樹脂顯示親和性,因此該施體/受體型抗靜電劑成為以良好的分散狀態包含於聚烯烴系樹脂發泡片中的狀態。 In the extrusion step, since the donor/acceptor type antistatic agent shows affinity for the polyolefin resin, the donor/acceptor type antistatic agent becomes contained in the polyolefin resin foam sheet in a good dispersion state In the state.
抗靜電劑已知有塗佈於樹脂產品等的表面而使用的塗佈型者、與揉合至樹脂產品中而使用的揉合型者。 Known antistatic agents include a coating type used for coating on the surface of a resin product, and a kneading type used for kneading the resin product.
如上所述,本實施型態中,施體/受體型抗靜電劑係作為揉合型抗靜電劑使用。 As described above, in this embodiment, the donor/acceptor type antistatic agent is used as a kneading type antistatic agent.
揉合有施體/受體型抗靜電劑的聚烯烴系樹脂發泡片1,不僅發揮優良的抗靜電性,且其成分相對於相接之對象材料的遷移少。
The polyolefin-based
然後,在該擠製步驟中,抑制施體/受體型抗靜電劑滲出至聚烯烴系樹脂發泡片1的表面。
Then, in this extrusion step, the donor/acceptor type antistatic agent is prevented from oozing out to the surface of the polyolefin resin foamed
本實施型態中的前述擠製步驟中,對於從圓模連續擠製的筒狀發泡體進行第1次冷卻及第2次冷卻,該第1次冷卻係在擠製後立即從內外吹附冷卻空氣以進行空冷,該第2次冷卻係以冷卻用芯軸將空冷後的發泡體進一步冷卻。 In the aforementioned extrusion step in this embodiment, the cylindrical foam continuously extruded from the circular mold is subjected to the first cooling and the second cooling. The first cooling is to blow from the inside and outside immediately after the extrusion. Cooling air is added for air cooling, and the second cooling system uses a cooling mandrel to further cool the air-cooled foam.
前述擠製步驟中,一邊以設於冷卻用芯軸之下游側的刀具將筒狀發泡體在擠製方向上切斷,一邊將其取出。 In the aforementioned extrusion step, the cylindrical foam is cut in the extrusion direction with a cutter provided on the downstream side of the cooling mandrel and taken out.
本實施型態中的前述擠製步驟中,使用外徑大於圓模直徑的冷卻用芯軸進行第2次冷卻。 In the aforementioned extrusion step in this embodiment, a cooling mandrel with an outer diameter larger than the diameter of the circular mold is used for the second cooling.
因此,該第2次冷卻,係藉由使冷卻用芯軸的外周面滑接於經過第1次冷卻的筒狀發泡體之內周面而實施。 Therefore, this second cooling is performed by sliding the outer peripheral surface of the cooling mandrel to the inner peripheral surface of the cylindrical foam that has undergone the first cooling.
該第2次冷卻中,一邊將經過第1次冷卻的筒狀發泡體冷卻,一邊亦同時以冷卻用芯軸進行擴徑。 In this second cooling, while cooling the cylindrical foam after the first cooling, the diameter is also expanded with the cooling mandrel at the same time.
如前述在擠製方向上以刀具所切斷的發泡體,經過展開而成為帶狀後,進行捲繞而構成前述原料捲筒。 As described above, the foam cut by a cutter in the extrusion direction is unrolled into a strip shape, and then wound to form the raw material roll.
本實施型態中,為了使聚烯烴系樹脂發泡片1發揮優良的緩衝性,作為聚烯烴系樹脂組成物所含有的聚烯烴系樹脂,係採用前述高熔融張力聚丙烯(HMS-PP)與嵌段聚丙烯(bPP)中的至少一者,較佳係採用兩者,較佳係使聚烯烴系樹脂組成物成為結晶性低於均聚丙烯(hPP)等的狀態。
In this embodiment, in order for the polyolefin resin foamed
聚丙烯的理想結晶之結晶熔解熱量為209J/g,均聚丙烯(hPP)的結晶化度通常為50%至70%。 The ideal crystallization of polypropylene has a heat of fusion of 209J/g, and the degree of crystallinity of homopolypropylene (hPP) is usually 50% to 70%.
從上述來看,前述聚烯烴系樹脂組成物之結晶化度較佳為40%以下,更佳為30%以下。 In view of the above, the degree of crystallinity of the aforementioned polyolefin resin composition is preferably 40% or less, more preferably 30% or less.
亦即,聚烯烴系樹脂組成物的結晶化熱量較佳為83J/g以下,更佳為62J/g以下。 That is, the heat of crystallization of the polyolefin-based resin composition is preferably 83 J/g or less, more preferably 62 J/g or less.
聚烯烴系樹脂組成物的結晶化熱量,可以JIS K7122:2012「塑膠的轉移熱測量方法」記載之方法測量。 The heat of crystallization of the polyolefin resin composition can be measured by the method described in JIS K7122: 2012 "Measuring Method of Heat of Transfer of Plastics".
具體而言,可以下述方法求得。 Specifically, it can be obtained by the following method.
(求得結晶化熱量的方法) (Method for obtaining heat of crystallization)
使用示差掃描熱量計裝置(例如,SII nanotechnology公司製,型號「DSC6220」),以無間隙的方式將約6mg的試樣填入鋁製測量容器的底部,在氮氣流量20mL/min之下,從30℃降溫至-40℃後,保持10分鐘,從-40℃升溫至220℃(第一次加熱),保持10分鐘後從220℃降溫至-40℃(冷卻),保持10分鐘後,從-40℃升溫至220℃(第二次加熱),得到DSC曲線。 Using a differential scanning calorimeter device (for example, manufactured by SII nanotechnology, model "DSC6220"), about 6 mg of sample is filled into the bottom of the aluminum measuring container in a gapless manner, and the nitrogen flow rate is 20 mL/min. After cooling from 30°C to -40°C, keep it for 10 minutes, increase from -40°C to 220°C (first heating), keep it for 10 minutes and then lower the temperature from 220°C to -40°C (cooling), keep it for 10 minutes, The temperature was increased from -40°C to 220°C (the second heating) to obtain the DSC curve.
另外,所有的升溫及降溫,係以速度10℃/min進行,基準物質係使用氧化鋁。 In addition, all heating and cooling were performed at a rate of 10°C/min, and alumina was used as the reference material.
前述結晶化熱量,係從冷卻過程中所觀察到的結晶化峰值之面積求得。 The aforementioned heat of crystallization is obtained from the area of the crystallization peak observed during the cooling process.
結晶化熱量,可使用裝置附屬的解析軟體,由將DSC曲線從高溫側的基準線離開的點與該DSC曲線再次回到低溫側之基準線的點連結的直線與DSC曲線所圍住之部分的面積算出。 The heat of crystallization can be obtained by using the analysis software attached to the device. The part enclosed by the straight line connecting the point where the DSC curve departs from the reference line on the high temperature side and the point where the DSC curve returns to the reference line on the low temperature side and the DSC curve The area is calculated.
本實施型態中,為了使聚烯烴系樹脂發泡片1發揮優良的緩衝性,亦可藉由上述冷卻空氣或以冷卻用芯軸所進行之冷卻,使聚烯烴系樹脂發泡片快速冷卻至結晶化溫度以下,而抑制內部形成聚丙烯的結晶。
In this embodiment, in order to make the polyolefin
另外,聚烯烴系樹脂發泡片1的結晶化被抑制,此點可由在求取結晶化熱量之操作中的「第一次加熱」中的熔解熱量其值低於「第二次加熱」中所求得之熔解熱量來確認。
In addition, the crystallization of the polyolefin-based resin foamed
「第一次加熱」中的熔解熱量(Qm1)相對於聚烯烴系樹脂發泡片1的「第二次加熱」中的熔解熱量(Qm2)的比例(Qm1/Qm2)較佳為0.9以下。
The ratio (Qm1/Qm2) of the heat of fusion (Qm1) in the "first heating" to the heat of fusion (Qm2) in the "second heating" of the polyolefin-based
前述比例(Qm1/Qm2)更佳為0.8以下。 The aforementioned ratio (Qm1/Qm2) is more preferably 0.8 or less.
聚烯烴系樹脂發泡片的熔解熱量,與結晶化熱量相同,可使用裝置附屬的解析軟體求得,可由將DSC曲線從低溫側之基準線遠離的點與該DSC曲線再次回到高溫側之基準線的點連結的直線與DSC曲線所圍住之部分的面積算出。 The heat of fusion of the polyolefin-based resin foam sheet is the same as the heat of crystallization. It can be obtained using the analysis software attached to the device. It can be calculated from the point where the DSC curve is far from the reference line on the low temperature side and the DSC curve back to the high temperature side Calculate the area of the part enclosed by the straight line connecting the points of the reference line and the DSC curve.
本實施型態中,如上所述,例示了就將聚烯烴系樹脂發泡片輕易調整成理想狀態而作為包裝用片之點中,藉由擠製發泡製造該聚烯烴系樹脂發泡片的情況,但本發明的包裝用片所具備的聚烯烴系樹脂發泡片,亦可由其他製法製作。 In this embodiment, as described above, it is illustrated that the polyolefin-based resin foamed sheet can be easily adjusted to an ideal state as a packaging sheet, and the polyolefin-based resin foamed sheet is produced by extrusion foaming. However, the polyolefin-based resin foam sheet included in the packaging sheet of the present invention may be produced by other manufacturing methods.
本實施型態中,雖舉出印刷電路基板及玻璃板作為以包裝用片包裝的被包裝物,但作為前述被包裝物,例如,係以矽晶片、硬碟、微處理器、發光二極體、藍寶石晶片、碟片基板、IC晶片、磁光碟(MO)、DVD、BD、各種記憶體、液晶濾波器、硬碟用磁電阻頭、CCD、標線片(Reticle)等的電氣設備用構件及電子設備用構件較為理想。 In this embodiment, although the printed circuit board and glass plate are cited as the packaged objects packaged by the packaging sheet, as the aforementioned packaged objects, for example, silicon chips, hard disks, microprocessors, light-emitting diodes For electrical equipment such as body, sapphire chip, disc substrate, IC chip, magneto-optical disc (MO), DVD, BD, various memories, liquid crystal filter, magnetic resistance head for hard disc, CCD, reticle, etc. Components and components for electronic equipment are ideal.
又,前述被包裝物,亦可為組裝有此等構件的電腦、螢幕、錄影機、智慧型手機、平板電腦等所謂的電氣設備及電子設備。 In addition, the aforementioned packaged objects may also be so-called electrical equipment and electronic equipment such as computers, screens, video recorders, smartphones, and tablet computers in which these components are assembled.
亦即,本發明的包裝用片,其用途並未特別限定。 That is, the use of the packaging sheet of the present invention is not particularly limited.
又,本發明的包裝用片,關於用途以外的事項亦不因為上述例示而有任何限定。 In addition, the packaging sheet of the present invention is not limited in any way with regard to matters other than the use due to the above-mentioned examples.
[實施例] [Example]
接著舉出實施例更詳細說明本發明,但本發明不限於此等。 Next, examples are given to explain the present invention in more detail, but the present invention is not limited to these.
(實施例1) (Example 1)
使用第一段(上游側)的擠製機為口徑90mm之單軸擠製機、第二段(下游側)的擠製機為口徑115mm之單軸擠製機所構成的串列式擠製機作為擠製機,而製作聚丙烯系樹脂發泡片。 The first stage (upstream side) extruder is a single-shaft extruder with a diameter of 90mm, and the second stage (downstream side) is a single-axis extruder with a diameter of 115mm. The machine was used as an extruder to produce a polypropylene resin foam sheet.
準備下述調配物:對於以50:50的質量比例包含高熔融張力聚丙烯(HMS-PP)與嵌段聚丙烯(bPP)的混合聚丙烯系樹脂100質量份,以成為0.5質量份的比例添加施體/受體型抗靜電劑(有機硼化物與鹼性氮化物的混和物),並以成為0.2質量份的比例添加氣泡調整劑(滑石系氣泡調整劑)。 The following formulation was prepared: 100 parts by mass of a mixed polypropylene resin containing high melt tension polypropylene (HMS-PP) and block polypropylene (bPP) in a mass ratio of 50:50 to 0.5 parts by mass A donor/acceptor type antistatic agent (a mixture of an organic boride and a basic nitride) is added, and a bubble regulator (talc-based bubble regulator) is added at a ratio of 0.2 parts by mass.
將此調配物供給至第一段的口徑90mm的擠製機的進料斗,於200℃加熱熔融後,以相對於此熔融樹脂100質量份的比例成為4質量份的方式,從第一段的擠製機的途中壓入作為發泡劑的丁烷(異丁烷/正丁烷=35/65),以該擠製機進行熔融揉合。 This formulation was fed to the hopper of the extruder with a caliber of 90 mm in the first stage, heated and melted at 200°C, and then 4 parts by mass relative to 100 parts by mass of the molten resin. In the middle of the extruder, butane (isobutane/n-butane=35/65) as a blowing agent was pressed in, and the extruder was used for melt kneading.
將由熔融揉合所得到的揉合物通過連接管供給至第二段的擠製機,在該擠製機的內部一邊繼續前述揉合物的揉合一邊使前述揉合物的溫度降低至170℃。 The kneaded mixture obtained by the melt kneading was supplied to the extruder in the second stage through the connecting pipe, and the temperature of the kneaded mixture was lowered to 170 while continuing the kneading inside the extruder. ℃.
如此,以成為擠製量98.5kg/小時的方式,從與擠製機前端連接的口徑140mm、狹縫間隙0.95mm的圓模之圓環狀狹縫,將經過降溫的揉合物擠製於大氣中而使其成為筒狀,以使前述揉合物發泡而形成筒狀發泡體。 In this way, the reduced temperature kneaded mixture was extruded from the circular slit of a circular die with a diameter of 140 mm and a slit gap of 0.95 mm connected to the tip of the extruder so that the extrusion volume was 98.5 kg/hour. It is made into a cylindrical shape in the atmosphere to foam the aforementioned kneaded product to form a cylindrical foam.
藉由經過冷卻之芯軸(芯軸徑:φ414mm,長度:500mm),一邊將該發泡體擴徑一邊進行抽取,使用空氣冷卻環對於該發泡體的外側面吹附空氣以使該發泡體冷卻,使用刀具將該經過冷卻的發泡體切開,製作聚烯烴系樹脂發泡片。 With the cooled mandrel (mandrel diameter: φ414mm, length: 500mm), the foam is drawn while expanding the diameter, and an air cooling ring is used to blow air on the outer surface of the foam to make the foam The foam was cooled, and the cooled foam was cut with a knife to produce a polyolefin resin foam sheet.
(實施例2) (Example 2)
使用低密度聚乙烯(LDPE)取代混合聚丙烯系樹脂,將施體/受體型抗靜電劑的量從0.5質量份變更為0.3質量份以及變更擠製條件,除此之外,與實施例1相同地製作聚烯烴系樹脂發泡片。 Use low density polyethylene (LDPE) instead of mixed polypropylene resin, change the amount of donor/acceptor type antistatic agent from 0.5 parts by mass to 0.3 parts by mass, and change the extrusion conditions. 1 In the same manner, a polyolefin resin foamed sheet was produced.
(實施例3) (Example 3)
將施體/受體型抗靜電劑的量從0.3質量份變更為2.0質量份,除此之外,與實施例2相同地製作聚烯烴系樹脂發泡片。 Except having changed the amount of the donor/acceptor type antistatic agent from 0.3 parts by mass to 2.0 parts by mass, the same procedure as in Example 2 was carried out to produce a polyolefin-based resin foam sheet.
(比較例1) (Comparative example 1)
使用高分子型抗靜電劑取代施體/受體型抗靜電劑,相對於混合聚丙烯系樹脂100質量份,使高分子型抗靜電劑的添加量為8質量份,除此之外,與實施例1相同地製作聚烯烴系樹脂發泡片。 Use a polymer type antistatic agent instead of the donor/acceptor type antistatic agent, and make the addition amount of the polymer type antistatic agent 8 parts by mass relative to 100 parts by mass of the mixed polypropylene resin. In addition, In the same manner as in Example 1, a polyolefin resin foamed sheet was produced.
(比較例2) (Comparative example 2)
使用界面活性劑(單硬脂酸甘油酯)取代施體/受體型抗靜電劑,相對於低密度聚乙烯(LDPE)100質量份,使界面活性劑的量為1.5質量份,除此之外,與實施例2相同地製作聚烯烴系樹脂發泡片。 Use surfactant (glyceryl monostearate) instead of donor/acceptor type antistatic agent, and make the amount of surfactant 1.5 parts by mass relative to 100 parts by mass of low-density polyethylene (LDPE). Except that, in the same manner as in Example 2, a polyolefin-based resin foam sheet was produced.
(比較例3) (Comparative example 3)
將界面活性劑由單硬脂酸甘油酯變更為烷基二乙醇醯胺,相對於低密度聚乙烯(LDPE)100質量份,將界面活性劑的量從1.5質量份變更為3.4質量份,除此之外,與比較例2相同地製作聚烯烴系樹脂發泡片。 The surfactant was changed from glyceryl monostearate to alkyl diethanolamide, and the amount of surfactant was changed from 1.5 parts by mass to 3.4 parts by mass relative to 100 parts by mass of low-density polyethylene (LDPE). Otherwise, a polyolefin-based resin foam sheet was produced in the same manner as in Comparative Example 2.
所得之聚烯烴系樹脂發泡片的物性如表所述。 The physical properties of the obtained polyolefin resin foamed sheet are as shown in the table.
(物性評估項目) (Property Evaluation Project)
厚度:聚烯烴系樹脂發泡片的厚度 Thickness: the thickness of the polyolefin resin foam sheet
基重:聚烯烴系樹脂發泡片的基重 Basis weight: Basis weight of polyolefin resin foamed sheet
表面電阻率:以乙醇擦拭聚烯烴系樹脂發泡片的表面後,於溫度20℃、相對濕度60%RH的條件下測量的表面電阻率 Surface resistivity: The surface resistivity measured under the conditions of a temperature of 20°C and a relative humidity of 60%RH after wiping the surface of the polyolefin resin foam sheet with ethanol
滲出量:在聚烯烴系樹脂發泡片表面的滲出量 Exudation amount: the amount of exudation on the surface of the polyolefin resin foamed sheet
金屬離子量:在聚烯烴系樹脂發泡片表面的鹼金屬離子及鹼土金屬離子的總量 Metal ion amount: the total amount of alkali metal ions and alkaline earth metal ions on the surface of the polyolefin resin foamed sheet
[表1]
從上述結果可知,使包裝用片具備包含施體/受體型抗靜電劑的聚烯烴系樹脂發泡片,可有效減少成分往被包裝物的遷移。 From the above results, it can be seen that providing the packaging sheet with a polyolefin-based resin foam sheet containing a donor/acceptor type antistatic agent can effectively reduce the migration of components to the packaged object.
亦即,如上所述可知,本發明的包裝用片,成分往被包裝物的遷移少且抗靜電性優良。 That is, as described above, it can be seen that the packaging sheet of the present invention has little migration of components to the packaged object and has excellent antistatic properties.
1:聚烯烴系樹脂發泡片 1: Polyolefin resin foam sheet
1a:第1面
1a:
1b:第2面
1b:
100:包裝袋 100: Packing bag
100a:正面片 100a: front film
100b:反面片 100b: reverse sheet
101:密封部 101: Sealing part
102:開口部 102: opening
X1:印刷電路基板 X1: Printed circuit board
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