TWM245953U - Breathable cloth-like film/nonwoven laminate - Google Patents

Breathable cloth-like film/nonwoven laminate

Info

Publication number
TWM245953U
TWM245953U TW92217538U TW92217538U TWM245953U TW M245953 U TWM245953 U TW M245953U TW 92217538 U TW92217538 U TW 92217538U TW 92217538 U TW92217538 U TW 92217538U TW M245953 U TWM245953 U TW M245953U
Authority
TW
Taiwan
Prior art keywords
film
woven
polymer
polyolefin
absorbent article
Prior art date
Application number
TW92217538U
Other languages
Chinese (zh)
Inventor
Ann Louise Mccormack
Original Assignee
Kimberly Clark Co
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 Kimberly Clark Co filed Critical Kimberly Clark Co
Priority to TW92217538U priority Critical patent/TWM245953U/en
Publication of TWM245953U publication Critical patent/TWM245953U/en

Links

Landscapes

  • Laminated Bodies (AREA)

Description

M245953 捌、新型說明: 【新型所屬之技術領域】 本創作有關透氣性薄膜和透氣的、似布的薄膜/非織物積層。尤其本創作有關 透氣性賴/賴物獅,其含有與麵之似械轉齡積層的透氣性薄膜。本 創作應用性相當廣,凡需要強度、舒適感、透氣性及不透液性的領域皆可。二個 具體的使闕域包含個人倾吸收物件及健_物品(射包含披布、袍子, 及相關的外科用品)。#人保護吸收物件的範例有尿布,衛生棉,失禁用衣服, 訓練褲,經帶等。本創作材料也可用來形成全部或部份的衣物物件。 【先前技術】 許多今日的產品包含人工合成組件的個人保護吸收物件,其中一例為尿布。 今日的尿布包含合成纖轉織物,其充#鄰接皮膚的人體側襯裡材料。尿布内有 -吸收芯材料’其可由天然木漿纖維製成,其中合併有合成纖維及超吸收體材 料。尿布的㈣或外罩,因為價袼之考量及不透雜之性f,f慣上由塑膠膜製 成0 雖然塑膠膜在使㈣能有效地收容雜及其他赫物,但基於穿著者健康之 觀點塑膠膜有觸摸敢不佳,不透水之缺點,因而傾於引起皮膚水合作用(版η hydration) ’使嬰兒絲尿布療。_個織麟法為:以透氣性瓣膜取代普通無 孔』膠膜為尿布$層材料。有許多種製造透氣性薄膜之方法,其巾包含打孔及使 用填充料。當使用填充料時,為了在聚合物與嵌人微粒之聚合物間產生小縫隙, 薄膜通吊在鋪間因壓碎填料而壓破,或被拉伸。這樣使膜上從某表面至另一表 面的通it扭曲’因而提供_條可讓水氣通過但仍可阻絕液體(如尿及水)之通道。M245953 新型 Description of the new type: [Technical field to which the new type belongs] This creation relates to breathable films and breathable, cloth-like films / non-woven laminates. In particular, this creation is related to breathable Lai / Laiwu Shi, which contains a breathable film that is mechanically aged. This application has a wide range of applications, and can be used in any field that requires strength, comfort, breathability, and liquid impermeability. The two specific implementation areas include personal absorption items and health items (the shots include drapes, robes, and related surgical supplies). Examples of human protection absorbent articles are diapers, sanitary napkins, incontinence clothes, training pants, warp belts, etc. This creative material can also be used to form all or part of clothing items. [Prior art] Many of today's products contain synthetic protective components for personal protection and absorption, one example being a diaper. Today's diapers contain synthetic fiber-to-fabrics that fill the human-side lining material that abuts the skin. The diaper has an -absorbent core material 'which may be made of natural wood pulp fibers, in which synthetic fibers and superabsorbent materials are combined. Diaphragm or outer cover, because of the consideration of price and impermeability, f, f is customarily made of plastic film. 0 Although plastic film can effectively contain sundries and other important things, it is based on the health of the wearer. Viewpoint Plastic film has the disadvantages of poor touch and impermeability, so it tends to cause skin hydration (version η hydration) to make baby silk diapers. The method of weaving is as follows: Replace the ordinary non-porous film with breathable valve as the material of the diaper. There are many ways to make breathable films, and the towels include perforations and the use of fillers. When using a filler, in order to create a small gap between the polymer and the polymer in which the particles are embedded, the film is hung in the shop to be crushed by crushing the filler, or stretched. This distorts the passage of the membrane from one surface to another ', thus providing a channel through which water vapor can pass but still block liquids such as urine and water.

5 C:\Etmice 2004\PK-007-02\PK-00^225\PKWl-0225-2.DOC 通常以聚_膜製造透氣膜。 填料之唆t生Ψ膝l· W、、财狀福為;討有齡/或無機 但日 w 1及/皿度可由透氣性材料降低。雖然如此, Γ”錢職贼制^相在表_«树,會有冷朗缺點。於 疋,另—個解決方法是利用非織物來作為尿布背層材料。 纖維非織物作成尿布背片時,減輕前述薄膜之問題但是這類纖維非織物提 雨的液峨絲)_。絲,满·撕《幅合做為背片 材料。某些纖維非織物材料比其他材料更能排水,尤其當他們含有—層纖細纖維 織物材料層時(如料層)。熔喷纖賴布是藉著觀熔化熱轉性材料通過 纖維的壓出板毛細孔’使之形成魏的線或長絲,再细高速氣流薄化而形成的 非織物。成品非織物的直徑很小,通常為10微米或更小;其被收集於形成表面 而為纖維雜物毛形式,其中具有不雜止倾通的小孔結構。例如,Buntin等 人之聰3,849,241。但《,即使利用熔喷層時,這類纖維非織物總是無法證明其 全部適用於充當個人保護產品之背片材料。 基於前述薄膜及纖維非織物的缺點,已嘗試將這二種材料結合,使二者截長 補短。結合透氣性膜及纖維非織物最佳性質的某一例子為結合含填充料線性聚烯 烴膜及聚丙烯或聚丙烯共聚物紡黏織布。為了讓二材料合作,他們必須稍微地彼 此連結或積層。有許多種連結膜及非織物的方法,其中包含熱及超音波黏合,膠 合,針刺,車縫。為了維持阻液性,針刺及車縫通常較為人們所不欲,因為在這 些加工時產生的孔較大而使液體滲漏。膠黏劑及膠合亦因為其本身會阻塞透氣性 膜孔並產生全部僵硬之積層,而較不受歡迎。膜及纖維非織物層則應較為完全。 ΓΛ Funirf 2Λ〇4\ ΡΚ-0Π1^)2\ ΡΚ4)01^)22ίι\ ΡΚ-/)〇ι, •02?^ ΠΠΓ M245953 就一般而§,為了良好地膠黏積層膜及非織物,必須在二材料整個内表面塗上均 勻之膜狀膠黏劑層,或者在分隔的區域上利用較大量,較局部的膠黏劑。膠黏劑 均勻施加時常會阻塞膜表面的孔,因而使先前的有孔膜變成無孔。這是吾人所不 欲的。在局部地區使用較大量之膠黏劑降低膜表面被膠黏劑阻塞之面積,但是其 膜/非織物積層因膠黏劑集中施加而有變硬的缺點。於是,較值得使用熱積層技術。 熱積層可利用加熱的式樣滾筒及超音波,以熱及壓力來完成,此二種技術均 非常適於連結由相同聚合物製成之膜及非織物。但是在某些例子中,用來製造膜 之聚合物不同於製造非織物者。這是由價格及物理性質所造成。線性低密度聚乙 烯膜(LLDPE)及聚丙稀非織物即是一例。這些聚合物在至少5克之黏合力下無法 彼此熱積層而為熱不相容的。而也有這種情況存在:當二層材料係相同時而相容 時,卻必須施加很大之壓力及熱來產生熱積層,使致膜上產生穿孔而積層通常也 太僵硬。結果,對於這類不相容及相容材料熱黏合之加工有一需求,以便能利用 此一材料及熱積層加工之優點。其成品亦有一需求。這些需求可被本創作滿足, 我們在下文終將詳細解釋。 【新型内容】 别述之缺點已被本創作解決。在本文中揭露透氣性薄膜及透氣、似布的膜/ 非織物積層吸收性册,歧祕㈣由透紐_與纖雜輯烴非織物熱黏 合而成。亦揭露前述材製法。 理想上,熱黏合係-種最受人所欲求之膜及非織物的積層法。熱黏合要求熱 相容性之材料。膜及非織物通常由提供所討論的材料之可企求特徵但彼此不易或 兀全不月b熱黏合之材料製成。在本創作的情況中,在膜上添加黏合劑,其僅須與5 C: \ Etmice 2004 \ PK-007-02 \ PK-00 ^ 225 \ PKWl-0225-2.DOC Breathable film is usually made of poly film. The fillers can be made into the shape of the knee l, W, and the wealth; for the age and / or inorganic, but the day w 1 and / can be reduced by the breathable material. Nonetheless, Γ ”qianzhizhe system ^ phase in the table _« tree, there will be a cold disadvantage. Yu Yi, another solution is to use non-woven fabrics as the backing material of diapers. When using fiber non-woven fabrics to make diaper backs , To alleviate the problems of the aforementioned film, but this kind of fiber non-woven fabrics carry rain). Silk, full · tear, "the web is used as a back sheet material. Some fiber non-woven materials can drain water more than other materials, especially when They contain a layer of fine fiber fabric material (such as a material layer). Meltblown fiber raisins are formed by melting the heat-converting material through the fiber's pores through the fiber's pressing pores to form Wei threads or filaments, and then Non-woven fabric formed by thin high-speed airflow. The diameter of the finished non-woven fabric is very small, usually 10 microns or less; it is collected in the form of fibrous debris hairs on the surface, which has a small non-stop pour. Porous structure. For example, Buntin et al., Satoshi 3,849,241. However, even when meltblown layers are used, such fibrous non-woven fabrics cannot always prove that they are all suitable for use as backsheet materials for personal protection products. Fabric Attempts have been made to combine these two materials to make them both longer and shorter. One example of the best properties of combining breathable films and fiber non-wovens is the combination of linear polyolefin films with fillers and polypropylene or polypropylene copolymerization Spunbond fabric. In order for the two materials to cooperate, they must be slightly joined or laminated to each other. There are many ways to join films and non-woven fabrics, including thermal and ultrasonic bonding, gluing, needle punching, sewing. In order to maintain Liquid resistance, acupuncture and sewing are usually less desirable, because the holes produced during these processes are large and cause liquid to leak. Adhesives and glues also block the breathable membrane holes and produce all of them. Stiff layers, which are less popular. Films and fibrous non-woven layers should be more complete. ΓΛ Funirf 2Λ〇4 \ ΡΚ-0Π1 ^) 2 \ ΡΚ4) 01 ^) 22ίι ΡΚ-/) 〇ι, • 02 ^ ΠΠΓ M245953 is general and §, in order to adhere the laminated film and the non-woven fabric well, the entire inner surface of the two materials must be coated with a uniform film-like adhesive layer, or a larger amount is used on the separated area, which is more local. Adhesive. Adhesive When applied evenly, it will often block the pores on the surface of the film, thus making the previous porous film non-porous. This is not what I want. Use a larger amount of adhesive in local areas to reduce the area of the film surface blocked by the adhesive. However, the film / non-woven laminate has the disadvantage of being hardened due to the concentrated application of the adhesive. Therefore, it is more worthwhile to use the thermal laminate technology. The thermal laminate can be completed by heat and pressure using a heated pattern roller and ultrasonic waves. Each of these techniques is well-suited for joining films and nonwovens made of the same polymer. But in some cases, the polymers used to make the film are different from those used to make the nonwoven. This is due to price and physical properties. One example is linear low-density polyethylene film (LLDPE) and polypropylene non-woven fabrics. These polymers cannot be thermally laminated with each other with a bonding force of at least 5 grams and are thermally incompatible. There is also a case where when the two layers of materials are the same and compatible at the same time, a great deal of pressure and heat must be applied to generate the heat build-up, which causes perforations on the film and the build-up is usually too stiff. As a result, there is a need for thermal bonding of such incompatible and compatible materials in order to take advantage of the advantages of such a material and thermal lamination. There is also a demand for its finished products. These needs can be met by this author, which we will explain in detail below. [New content] The shortcomings of other things have been solved by this creation. In this article, breathable films and breathable, cloth-like films / non-woven laminated absorbent books are disclosed, which are formed by thermal bonding of transparent fibers and non-woven fabrics. The aforementioned method of making materials is also disclosed. Ideally, the heat-bonding system is the most desirable lamination method for films and nonwovens. Thermal bonding requires thermally compatible materials. Films and nonwovens are usually made of materials that provide the desirable characteristics of the materials in question but are not easily or completely thermally bonded to each other. In the case of this creation, an adhesive is added to the film, which only has to be

C: \ Eunice 2004 \ ΡΚ-00Ί-02 \ PK-W1-0225\PK-<X)1^)225-2.DOC M245953 纖維非織物的輯烴聚合物部份可相容,而域層加工時充當熱及祕應的膠黏 劑。或者,黏合劑可併人纖維非織物之纖維中,以協助膜及織布之積層。為了維 寺、及纖維之整體性,而在積層加工時使針孔形成與強度損失之風險下降,用來 -層之值度應小於膜或纖維之聚稀烴聚合物的溶點。因此,膜及纖維均不得 到達其咖縣__當重制,俾錢品吸_物件包祕齡及隔雜 質。利用點合添加物與分離之黏合來“局部的“熱黏合,我們提供一個對透 氣膜多孔性損害最小,並_轉整個吸收性物件或積層的優良撓⑽徵的附著 方法。 在本創作中某實施例中,透氣膜/非織物積層的製法,由形成含下列吸收性 物質之膜’:佔10至68% (⑽之總乾重為基準)的主魏性聚烯烴聚合物, 約30至80%的填充料(微粒大小在〇 5至5微米間),約2至2〇%的黏合劑。然 後在滾筒間拉伸或壓破膜以造成透氣性。所製成之膜應有每24小時1〇〇克/平方 米的水汽輸送率 '然後在膜上熱積層聚烯烴非織物,而形成積層或吸收性物質。 積層應使積層二層材料的例大於5克。 薄膜層的合適材料包含(但非限制)優勢線性聚烯烴聚合物(如線性低密度 聚乙烯)及填充料(如碳酸鈣)。纖維非織物的合適材料包含(但非限制)聚丙 烯’聚烯烴混合物(聚丙烯纖維及線性低密度聚乙烯纖維)及複合纖維(其中聚 烤煙組件形成纖維外表面)。 加工首先牽涉前述聚合物之前擠出混合物的形成,然後將混合物擠成薄膜。 一旦薄膜被形成,其在低於膜之優勢線性聚合物之熔點的溫度下被拉伸,其中溫 度更值得低於黏合劑的軟化點。藉著拉伸薄膜,薄膜被薄化且變得多孔而且透C: \ Eunice 2004 \ ΡΚ-00Ί-02 \ PK-W1-0225 \ PK- < X) 1 ^) 225-2.DOC M245953 The hydrocarbon-containing polymer part of the fiber nonwoven is compatible, while the domain layer Acts as a heat and secretive adhesive during processing. Alternatively, the binder may be incorporated into the fibers of the fibrous non-woven fabric to assist the lamination of the film and the woven fabric. For the integrity of the temples and fibers, the risk of pinhole formation and loss of strength is reduced during lamination. The value of the layer should be less than the melting point of the polymer of the membrane or fiber. Therefore, neither the membrane nor the fiber can reach its county. When it is remanufactured. By using the bonding of point-bonding additives and separation to "local" thermal bonding, we provide an attachment method that minimizes the damage to the porosity of the air-permeable membrane and transfers the entire absorbent article or laminate. In one embodiment of the present invention, the method for producing a breathable film / non-woven laminate is formed by forming a film containing the following absorbent substance: 10 to 68% (based on the total dry weight of the main polyolefin polymer), About 30 to 80% of the filler (particle size between 05 and 5 microns), about 2 to 20% of the binder. The film is then stretched or crushed between rollers to create breathability. The produced film should have a water vapor transmission rate of 100 g / m2 per 24 hours, and then a polyolefin non-woven fabric is thermally laminated on the film to form a laminated or absorbent substance. The laminate should be made larger than 5 grams. Suitable materials for the film layer include, but are not limited to, advantageous linear polyolefin polymers (such as linear low density polyethylene) and fillers (such as calcium carbonate). Suitable materials for fibrous nonwovens include, but are not limited to, polypropylene ' polyolefin blends (polypropylene fibers and linear low-density polyethylene fibers) and composite fibers (wherein the components of flue-cured tobacco form the outer surface of the fibers). Processing first involves the formation of an extruded mixture before the aforementioned polymers, and then extruded the mixture into a film. Once the film is formed, it is stretched at a temperature below the melting point of the film's predominant linear polymer, where the temperature is more desirable than the softening point of the adhesive. By stretching the film, the film is thinned and becomes porous and transparent

〇\Eunice 2m\PK^2\PK^225\PK^225-2.DOC M245953 氣。拉伸後的膜依據有至少每24小時1〇〇克/平方米的水汽輸送率。然後薄膜在 溫度低於膜之優勢線性聚合物熔點的溫度下被黏在纖維聚烯烴非織物上以形成 積層。此外,需要的話,膜也可在與非織物黏合後被壓縮,然後引起整個複合物 收縮,產生波紋表面及膨鬆的複合物。 形成後的透氣性、似布膜/非織物積層吸收性物件具有多種用塗,而不止於個 人保護吸收物件的外罩。這類物件典型地包含體側裡及外罩,和夾於此二者間的 吸收芯材料。本創作的材料可作為外罩,其中纖維非織物層面對產品外表面而膜 層鄰接吸收芯材料。 或者,右熱黏合係吾人所欲但形成部份或全部之膜的聚合物與支持層為熱不 相容的,則黏合既可被添加到纖維非織物支持層中,而非或者也可添加入膜層 中。黏合劑可添加到形成纖維的聚合物混合物中,當纖維為單程份纖維時,黏合 劑可添加到整個纖維上。單成份纖維之外,也可用複合纖維來維持全部或部份之 非織物支持層。複合纖維之例子包含(但非限制)鞘/芯纖維,並列纖維及海島纖 維。此外,可使用雙成份纖維來形成纖維非織物支持層。在這類纖維所有構形中, 黏合劑應添加在形成纖維外表面至少一部份的纖維部份上,俾使黏合聚可與膜層 接觸並黏合之。纖維非織物支撐層形成後,可利用熱,壓力,與壓力且或超音波 將熱黏合於膜層上。 【實施方式】 本創作揭示一種改良的薄膜/非織物積層,其中利用優勢線性聚烯烴聚合物組 成的膜,填充料,熱黏合於聚烯烴基料之纖維非織物的黏合劑。由於習於線性低 选度聚乙烯膜及聚丙烯基料非織物的不相容性及膜與非織物層構成熔點,所以他〇 \ Eunice 2m \ PK ^ 2 \ PK ^ 225 \ PK ^ 225-2.DOC M245953 gas. The stretched film is based on a water vapor transport rate of at least 100 g / m2 per 24 hours. The film is then adhered to the fibrous polyolefin nonwoven at a temperature below the melting point of the film's dominant linear polymer to form a laminate. In addition, if desired, the film can be compressed after bonding to the non-woven fabric and then cause the entire composite to shrink, creating a corrugated surface and a bulky composite. The formed breathable, fabric-like / non-woven laminated absorbent article has a variety of coatings, not just the outer cover for personal protection of the absorbent article. Such articles typically include a bodyside and outer cover, and an absorbent core material sandwiched therebetween. The material created can be used as an outer cover, in which the fibrous non-woven layer faces the outer surface of the product and the film layer abuts the absorbent core material. Alternatively, the right thermal bonding is thermally incompatible with the polymer that forms part or all of the film that we want, but the bonding can be added to the fibrous non-woven support layer instead of or also Into the film layer. Binders can be added to the fiber-forming polymer mixture, and when the fiber is a single pass fiber, the binder can be added to the entire fiber. In addition to monocomponent fibers, composite fibers can also be used to maintain all or part of the non-woven support layer. Examples of composite fibers include, but are not limited to, sheath / core fibers, side-by-side fibers, and sea-island fibers. In addition, bicomponent fibers can be used to form a fibrous nonwoven support layer. In all configurations of such fibers, a binder should be added to the fiber portion that forms at least a portion of the outer surface of the fiber, so that the adhesive polymer can contact and adhere to the film layer. After the fibrous non-woven support layer is formed, heat, pressure, pressure, and / or ultrasound can be used to adhere heat to the film layer. [Embodiment] The present invention discloses an improved film / non-woven laminate, in which a film composed of an advantageous linear polyolefin polymer, a filler, and a fibrous non-woven adhesive that are thermally bonded to a polyolefin base are used. Due to the incompatibility of the linear low-selectivity polyethylene film and polypropylene-based nonwovens and the melting point of the film and the nonwoven layer, he

C:\ Eumce 2004\PK-001~02\PK-001^)225\PK-00i-0225-2.DOC M245953 們無法熱黏合。本創作提供-種透氣膜,職_特殊複合物及特殊之加工條 件,其可與輯織__物絲合。成品積層提供數種顧,包含外表面的 柔軟’似布觸感及可阻絕液體通過但仍具優良之水氣通透性。此外,因為線性低 密度聚乙賴的高㈣性聽充制緣故,縣魏,轉錄並具有很低的 “噪音“或“喝嚷聲“。結果,本創作的積層特別適合充當個人保護吸收產品(包 含尿布,衛生棉’訓練褲’失禁衣物,端帶等)之背片材料,但是不意味其僅於 本文中所述之用途。本創握的材料亦可用以形成衣物物件之全部或一部份。此 外,本創作得材料可用以形成全部或部份的醫療用品,如:外科披布,袍,擦布, 鞋罩,口罩,帽等。所以,這些用途亦被考慮在本創作之範圍内。 於另一實施例中,黏合劑可被添加在纖維非織物上,尤其是形成非織物之纖 維外表面的至少一部份上。結果,可以用另一裝置使無法熱相容之二層可被熱黏 合或積層。成品積層也適用於前文所述之用途。 參考第一圖,最基本形式的本創作吸收體或積層(ίο)包含彼此黏合之膜層 (12)以及纖維聚烯烴非織物舒適及支持層(14)。雖然此為本創作最基本之構 形,但需要時也可在複合物(10)上添加額外之材料層以形成多層複合物。例如, 第二纖維聚烯烴非織物(未示)可以黏在膜層(12)上香對於第一纖維聚烯烴非 織物(14)的一側上。 膜層(12)包含三個基本成份,首先為優勢線性聚烯烴聚合物(如線性低密 度聚乙烯),其次為填充料,第三為黏合或增黏劑。此三成份被混合,加熱之後 任何精於本項技術者所熟知之膜產生加工來擠成膜(鑄造及喷吹> 其他添加劑 或成份,若不嚴重影響膜之透氣能力及膜與纖維聚烯烴非織物舒適層(14)之熱C: \ Eumce 2004 \ PK-001 ~ 02 \ PK-001 ^) 225 \ PK-00i-0225-2.DOC M245953 They cannot be thermally bonded. This creation provides-a kind of breathable film, special _ special compound and special processing conditions, which can be combined with the woven __ material silk. The finished laminate provides several considerations, including the soft 'cloth-like feel of the outer surface and the ability to block liquids from passing but still have excellent water vapor permeability. In addition, because of the linear high-density hearing resistance of linear low-density polyethylene, the county Wei, transcribed and has a very low "noise" or "drinking sound." As a result, the laminate of this creation is particularly suitable for use as a backsheet material for personal protection absorbent products (including diapers, sanitary napkins 'training pants' incontinence clothing, end straps, etc.), but it is not meant to be used only for the purposes described herein. The material of this grip can also be used to form all or part of a clothing item. In addition, the materials created can be used to form all or part of medical supplies, such as surgical drapes, gowns, wipes, shoe covers, masks, caps, etc. Therefore, these uses are also considered within the scope of this creation. In another embodiment, a binder may be added to the fibrous nonwoven fabric, particularly to at least a portion of the outer surface of the fibrous nonwoven fabric. As a result, the two layers which are not thermally compatible can be thermally bonded or laminated with another device. Finished laminates are also suitable for the applications described above. Referring to the first figure, the most basic form of this creative absorbent body or laminate (ίο) includes a film layer (12) adhered to each other and a fiber polyolefin non-woven comfort and support layer (14). Although this is the most basic configuration of the creation, additional layers of material can be added to the composite (10) to form a multilayer composite if needed. For example, a second fiber polyolefin non-woven fabric (not shown) may be adhered to the film layer (12) on the side facing the first fiber polyolefin non-woven fabric (14). The film layer (12) contains three basic components. The first is a dominant linear polyolefin polymer (such as a linear low-density polyethylene), the second is a filler, and the third is an adhesive or tackifier. These three ingredients are mixed, and any film that is well-known to those skilled in the art is processed to extrude the film after heating (casting and blowing> other additives or ingredients, if it does not seriously affect the breathability of the film and the film and fiber polymerization Heat of olefin non-woven comfort layer (14)

in C: \ Ewnice 2004 \ ΡΚ-002*02 \ PK-001 »0225\ PK^OOl >0225-2, DOC M245953 黏合力,可被添加在膜中。就一般而言,膜層包含約10至68wt % (以膜總乾重 為基準)之優勢線性熱塑性聚合物,約2至20wt%之黏合劑,約30至80wt%的 填充料6於更具體實施例中,可額外地含〇至68wt%的其他聚烯烴(如聚丙稀)。 當與合適量之黏合劑混合時,已發現線性低密度聚乙稀是相當良好之薄膜基 料。但是一般咸信其他優勢線性聚稀烴聚合物亦可用於本創作。在本文中“線性 低密度聚乙烯“係指乙烯聚合物以及較高α烯烴共聚單體之聚合物,如:。 優勢線性“係指主聚合物鏈為線性的,其中每1〇〇〇個乙烯單元大約少於5個 長支鏈。長支鏈包含大於Q2的碳鏈。就非彈性的優勢線性聚烯烴聚合物而言。 短支鏈(cvc】2)因含共聚單體,將典型地被限制為每1000乙烯單元少於2〇個 短鏈,而彈性聚合物為20或更多。優勢線性聚烯烴聚合物的例子包含(但非限 制)線性聚烯烴,如:乙烯,丙烤,μ丁稀,冬甲基_戊烯,L己婦,卜辛烤及 較高級之烯烴和前述者之共聚戊。此外,乙烯與其他烯烴(包含戊烯,己烯,庚 烯,辛烯,壬烯,癸烯等)的共聚物亦為優勢線性熱塑性聚合物之例子。 本創作的主要目的是提供用以熱黏合透氣膜及纖維非織物的方法,其中該透 氣膜係由優勢線性聚烯烴聚合物製成,且該方法不會破壞個體層之整體性(尤其 是膜層)。藉著把黏合劑添加在依某種程度混合之膜聚合物中,可在較低溫且/或 壓力下,以較低的總黏合面積百分比來黏合膜及非織物。此外,不相容的膜及非 織物(如LLDPE膜及聚㈣非纖維)現在已經有效地積層。積層產生之後,仍 十为柔軟並且通常沒有因過絲合而造成之意外穿孔,以取得適合之積層。 就相容之LLDPE膜及聚㈣麵物而言,餅在傭鱗於LLDpE膜炼點 的皿度下’㈣15%之絲合面積來熱積層此二層,並且成品積層應足夠強而需in C: \ Ewnice 2004 \ ΡΚ-002 * 02 \ PK-001 »0225 \ PK ^ OOl > 0225-2, DOC M245953 Adhesive force can be added to the film. Generally speaking, the film layer contains about 10 to 68% by weight (based on the total dry weight of the film) of the advantageous linear thermoplastic polymer, about 2 to 20% by weight of the binder, and about 30 to 80% by weight of the filler. 6 More specifically In embodiments, it may additionally contain 0 to 68 wt% of other polyolefins (such as polypropylene). When mixed with a suitable amount of binder, linear low density polyethylene has been found to be a fairly good film base. But in general, other advantages of linear paraffin polymers can also be used in this work. As used herein, "linear low density polyethylene" refers to polymers of ethylene and higher alpha olefin comonomers, such as: "Dominant linear" means that the main polymer chain is linear, with approximately less than 5 long-chain branches per 1,000 ethylene units. The long-chain branches contain carbon chains greater than Q2. Non-elastic dominant linear polyolefin polymerization Short-chain branches (cvc) 2) will typically be limited to less than 20 short chains per 1,000 ethylene units due to the presence of comonomers, while elastic polymers are 20 or more. Advantages Linear Polyolefins Examples of polymers include, but are not limited to, linear polyolefins, such as: ethylene, propylene roast, μbutylene, winter methyl_pentene, L-Fife, bucin and higher olefins, and co-pentyl In addition, copolymers of ethylene with other olefins (including pentene, hexene, heptene, octene, nonene, decene, etc.) are also examples of advantageous linear thermoplastic polymers. The main purpose of this creation is to provide A method for thermally bonding a breathable film and a fibrous non-woven fabric, wherein the breathable film is made of a dominant linear polyolefin polymer, and the method does not damage the integrity of the individual layer (especially the film layer). By adding an adhesive In membrane polymers mixed to some extent, At lower temperatures and / or pressures, films and nonwovens are bonded with a lower percentage of total bonding area. In addition, incompatible films and nonwovens (such as LLDPE films and polyfluoride non-fibers) are now effectively laminated. After the layer is produced, it is still soft and there is usually no accidental perforation caused by over-threading, so as to obtain a suitable layer. For compatible LLDPE film and polymer surface, the cake is at the scale of the LLDpE film. The thickness of the wire is 15% of the combined area to heat build up the two layers, and the finished product should be strong enough to require

11 C:\Eunice2004\PK-001-02\PK-Wl-0225\PK-Wl-0225-2.DOC M245953 要至少5克之負荷來解積層該層物(以下文所樹枝黏合強度測試決定)。藉著添 加黏合覬覦膜聚合物混合物中,上述者可能的。在本文中“黏合劑“係一種添加 劑,其被添加入模聚合物混合物中時允許膜層級非織物曾在低於膜聚合物混合物 之主要優勢線性熱塑性聚合物成份之熔點至少5°C的情況下黏合(本例中“主要 “聚合物為線性低密度聚乙烯)。此外,成品積層之黏合或剝離強度應是少為5 克。 黏合劑亦係指增黏樹脂,其被討論於Kieffer等人USP4,789,699中,該專利 内容在本文中並供篸考。本創作黏合劑的目的在於允許麼及非織物曾在較低的溫 度下黏合。黏合劑的例子包含氫化的碳氫樹脂,如REGALREZ系列增黏劑及 ARKON 系列增黏劑。REGALREZ 樹脂可購自 Dalaware Wilmington 的 Hercules 〇 Regalrez增黏樹脂係高穩定、淡色、低分子量、無極性的樣脂。級數3102者據稱 具有102 R&B °C的軟化點,21°C下1·04的比重,149°C下100釐泊之溶化黏滯 度,51QC的玻璃轉位點(Tg)。REGALREZ 1094據稱具有94 °C的軟化點,21°C 下0·99的比重,126°C下100釐泊之溶化黏滯度,33°C的玻璃轉位點。級數1126 據稱具有126 °C的軟化點,21°C下0/97的比重,159°C下100釐泊之溶化黏滯 度,65。(:的玻璃轉位點。 ARKON系列樹脂係Illionis Chicago的Arakawa以石油碳氫樹脂製成之合成 增黏樹脂。例如,級數P-70者具70 °C的軟化點,而P-100者具1〇〇 °C的軟化點, P-125者具125°C之軟化點。 ZONATEC 501石樹脂是另一種增黏劑,其為軟化點150 °C的烯碳氫化物, 由 Panama City 的 Arizona Chemical 製造。EASTMAN 1023 PL 樹脂是非晶形聚丙11 C: \ Eunice2004 \ PK-001-02 \ PK-Wl-0225 \ PK-Wl-0225-2.DOC M245953 Delaminate the layer with a load of at least 5 grams (determined by the stick strength test of the branches below). The above is possible by adding a bonded rhenium membrane polymer mixture. "Adhesive" in this context is an additive that, when added to a mold polymer mixture, allows film-level non-wovens to be at least 5 ° C below the melting point of the linear polymer component, which is the main advantage of film polymer mixture Under-bonding (in this example, the "main" polymer is a linear low density polyethylene). In addition, the adhesive or peel strength of the finished laminate should be less than 5 grams. Binders also refer to tackifying resins, which are discussed in Kieffer et al. USP 4,789,699, which is incorporated herein by reference. The purpose of this adhesive is to allow non-woven fabrics to be bonded at lower temperatures. Examples of adhesives include hydrogenated hydrocarbon resins such as REGALREZ series tackifiers and ARKON series tackifiers. REGALREZ resins are available from Hercules of Dalaware Wilmington. Regalrez tackifying resins are highly stable, light-colored, low molecular weight, non-polar lipids. Grade 3102 is said to have a softening point of 102 R & B ° C, a specific gravity of 1.04 at 21 ° C, a melt viscosity of 100 centipoise at 149 ° C, and a glass transition point (Tg) of 51QC. REGALREZ 1094 is said to have a softening point of 94 ° C, a specific gravity of 0 · 99 at 21 ° C, a melt viscosity of 100 centipoise at 126 ° C, and a glass transition point of 33 ° C. Grade 1126 is said to have a softening point of 126 ° C, a specific gravity of 0/97 at 21 ° C, a melt viscosity of 100 centipoise at 159 ° C, and 65. (: Glass transition point. ARKON series resins are synthetic tackifying resins made of petroleum hydrocarbon resins by Arakawa of Illionis Chicago. For example, the grade P-70 has a softening point of 70 ° C, while the P-100 With a softening point of 100 ° C, P-125 has a softening point of 125 ° C. ZONATEC 501 stone resin is another tackifier, which is an olefinic hydrocarbon with a softening point of 150 ° C. Made by Arizona Chemical. EASTMAN 1023 PL resin is amorphous polypropylene

C:\Eunice 2004\ΡΚ-00Ί-02\ΡΚ-ΌΟΊ-Ό225\PK-001-0225-2.DOC M245953 烯增黏劑’其軟化點為150-155125 QC ’可購自Longview的Eastman Chemical 其他黏合劑的例子一般包含(但非限制)··聚醯胺、乙烯共聚物(如··乙烯 醋酸乙烯酯(EVA)、乙烯丙烯酸乙酯(EEA)、乙烯丙烯酸(EAA)、乙稀丙稀 酸甲酯(EMA)、乙烯丙烯酸正-丁醋(ENBA)、木松香脂及其衍生物、碳氫樹脂、 聚烴婦樹脂、無規聚丙嫦及非結晶乙婦丙稀共聚物以及被稱為細化聚丙烤(Ττρ) 及烯烴熱塑性聚合物之類的材料,其中ERR藉由聚丙烯或聚丙稀/聚乙烯混合物 内的内反應氣多皆聚合作用,被機械分散或分子分散。 應瞭解前列之黏合或增黏劑僅係說明而已,並未意謂對本創作之範圍有所限 制。任何與其他膜且/或纖維聚合物可黏合的黏合劑,均能在低於膜或纖維混合物 之優勢線性熱塑性聚合物成分之熔點至少5。<:下,允許膜層與非纖維物層黏合; 並且任何能夠在層物間產生需5克負荷方能解開之鍵結者亦因本創作之緣故而被 認為是黏合劑黏合劑一般包括約2至20%之膜總重。雖然在此範圍之外的重量百 分比亦可利用,但是在較高之百分比時,薄膜的透氣性被折衷,就個人衛生吸收 物件而言,通常這是吾人不欲的。除了優勢線性聚烯烴聚合物及黏合劑之外。膜 層亦包含填充料。在本文中“填充料,,係指能被添加於膜聚合物擠壓混合物中的 材料’並且該材料舉出的膜不會有負面影響的化學干擾且能均勻地分散在膜中。 填充料一般為微粒狀且通常為圓形,其平均微粒尺寸約αι至〇·7微米。只要不 影響膜形成加工成品膜之透氣性及其對新為聚烯烴非織物或共形成之熱黏合能 力’則有機與無機填充黏鈞被認為在本創作之内。填充料的例子包含碳酸辦,多 種黏土,硅石,鋁,硫酸鋇,碳酸鈉,滑石,硫酸錢,二氧化鈦,沸泡石,硫酸 銘’纖維素類的粉末,硅藻土,硫酸鎂,碳酸鎂,碳酸鋇,高嶺土,雲母,碳, C:V£U„icc2004VPK^^2VpK^^225VpK^^225_2Dfx: M245953 氧簡,氧化鎂,氫氧化銘,木黎粉末,木材粉末,纖維素衍生物,幾丁質與幾 丁質衍生物。 如前文所述,膜可由熟悉形成者所知之"加卫來形成1前文所述的比例 將優勢線性聚烯烴聚合物,黏合劑,填充料混合在一起,然後加熱並擠出薄膜。 為了提供均勻的透氣性(可由膜之水汽輸送率表示),填充料應均勻地分散在聚 合物混合財,織均勻地分散麵巾。因摘作之毅,如果_水汽輸送率 至少為每24小時100克/平方米(利用與樣本相關之下文所述之測試方法來計 算),則其為“透氣性”。就-般而言,一旦膜被形成,則其將有小於約克/ 平方求的單㈣積重,並且在轉與薄倾,其單位面積重將小_ %克/平方 米’且更令人所欲地小於約18克/平方米。 在下文之例中所使用的膜為吹麵,但是其他種類的膜只要成形計數與填充 膜相容也被認為在本鑛範_。酬形鱗通常太厚且在獅咖於產生“嗔 嗔的噪音,且膜尚未有足夠之透氣性(以其水汽輸送率來測得)。結果,膜被 加熱至小於優勢線性熱塑性聚合物熔點5〇c,然後拉伸至少其原長的2.5倍,薄 化膜且造成㈣。在拉伸躺默更佳溫度係小雜合獻軟倾。某些黏合劑 的軟化點係在紐L因此,“絲化點之下加熱,,係指在該細最高溫度 之下的溫度0 薄化加工的額外特徵為膜不透明度的改變。膜形成時較為透明,但拉伸後變 得不透明。此外,雖然在拉伸加工期間膜變成有方向性的,但其亦變得較柔軟取 比拉伸刖i嚷聲”較低。若將所有之因子考慮進去,並想要至少每%小時議 克/平方米的水汽輪送率’職應該薄化至其單位面積重小於約35克/平方来(就C: \ Eunice 2004 \ ΡΚ-00Ί-02 \ ΡΚ-ΌΟΊ-Ό225 \ PK-001-0225-2.DOC M245953 ene tackifier 'its softening point is 150-155125 QC' Eastman Chemical available from Longview Other Examples of adhesives generally include, but are not limited to, polyamines, ethylene copolymers (such as ethylene ethylene acetate (EVA), ethylene ethyl acrylate (EEA), ethylene acrylic acid (EAA), ethylene propylene Ethyl Methyl Ester (EMA), Ethylene Acrylic N-Butyl Vinegar (ENBA), Wood Pine Balm and Its Derivatives, Hydrocarbon Resin, Polycarbonate Resin, Random Polyacrylamide and Amorphous Acrylic Copolymer In order to refine materials such as polypropylene baking (Tτρ) and olefin thermoplastic polymers, ERR is mostly polymerized by internal reaction gas in polypropylene or polypropylene / polyethylene mixture, and is mechanically or molecularly dispersed. The aforementioned adhesives or tackifiers are for illustration only and are not meant to limit the scope of this creation. Any adhesive that can be adhered to other films and / or fiber polymers can be lower than the film or fiber mixture. Advantageous linear thermoplastic polymer composition with a melting point of at least 5. <: below, allowing the film layer to be bonded to the non-fibrous layer; and anyone who can generate a bond between the layers that needs a 5 gram load to be able to be unlocked is also considered an adhesive for the sake of this creation Including about 2 to 20% of the total weight of the film. Although weight percentages outside this range can also be used, at higher percentages, the breathability of the film is compromised. For personal hygiene absorbent articles, this is usually I do n’t want it. In addition to the advantageous linear polyolefin polymers and adhesives. The film layer also contains fillers. In this article "fillers," means materials that can be added to the film polymer extrusion mixture 'and The film enumerated by this material does not have any negative chemical interference and can be uniformly dispersed in the film. The filler is generally particulate and usually circular, and its average particle size is about αι to 0.7 microns. As long as it does not affect The film permeability of the finished film and its thermal adhesive ability to newly formed polyolefin non-woven fabrics or co-formers are considered as organic and inorganic fillers. Examples of fillers include carbonic acid, a variety of Clay, silica, aluminum, barium sulfate, sodium carbonate, talc, sodium sulfate, titanium dioxide, zeolite, sulfate 'cellulose powder, diatomaceous earth, magnesium sulfate, magnesium carbonate, barium carbonate, kaolin, mica, carbon , C: V £ U „icc2004VPK ^^ 2VpK ^^ 225VpK ^^ 225_2Dfx: M245953 Oxygen, Magnesium Oxide, Hydroxide, Muli Powder, Wood Powder, Cellulose Derivatives, Chitin and Chitin Derivatives As mentioned previously, the film can be formed by the known " Carbon to be familiar to the former < 1 > to the ratios described above. The predominant linear polyolefin polymers, adhesives, fillers are mixed together, and then the film is heated and extruded. In order to provide uniform air permeability (which can be expressed by the water vapor transport rate of the film), the filler should be evenly dispersed in the polymer mixture, and the face towel should be uniformly dispersed. For the sake of abstraction, if the water vapor transmission rate is at least 100 g / m2 per 24 hours (calculated using the test method described below related to the sample), it is "breathable". In general, once the film is formed, it will have a unit weight of less than York / square, and it will be thinner and thinner, and its unit weight will be less than _% g / m2. Desirably less than about 18 grams / square meter. The film used in the examples below is a blown surface, but other types of films are considered to be in this category as long as the forming count is compatible with the filled film. The scales are usually too thick and produce a "noisy noise" in the lion coffee, and the membrane is not yet sufficiently breathable (as measured by its water vapor transport rate). As a result, the membrane is heated to a temperature below the melting point of the dominant linear thermoplastic polymer 50 ° C, and then stretch at least 2.5 times its original length, thinning the film and causing sluggishness. At the temperature of stretching and lying, a small hybrid provides a soft tilt. The softening point of some adhesives is at New L. Therefore "Heating below the silkening point" refers to the temperature below the thin maximum temperature. An additional feature of thinning is the change in film opacity. The film was more transparent when formed, but became opaque after stretching. In addition, although the film becomes directional during the stretching process, it also becomes softer and lower than the stretching 刖 i ”sound. If all factors are taken into account, and it is desired to discuss at least every% hours G / m2 water vapor delivery rate should be reduced to a unit area weight of less than about 35 g / m2 (just

C:\Eunice 2004\PK-001^2\PK-001-0225\PK-001-022S-2.DOC M245953 個人保護衛生物件之應用而言),且更令人所欲地小於約15克/平方米。 纖維非織物舒適層(14)由聚婦烴纖維(如··聚丙烯)製成。在例子中,非 織物為聚丙烯紡黏織布,但其他聚烯烴纖維也可使用。纖維混合物亦可使用,其 中包含不同的聚烯烴纖維及聚烯烴,非聚烯烴纖維混合物(如:聚乙烯鞘/聚丙烯 芯複合纖維及聚酯纖維,纖維非織物重亦可包含天然纖維。具體的纖維種類包含 單組成纖維及複合纖維(如:並列,鞘/芯,海島複合纖維)。纖維可為直線形或 捲曲形,中空或實心。他們通常為圓或非圓形截面(包含雙肢,三肢,“χ,,截 面)。纖維長度可能是短的(如人短纖維)或長的(紡黏及熔喷纖維)。纖維之厚 度取決於所欲之性質。窄纖維提供較柔軟之非織物而較厚纖維將提供更大的強度 及彈性。或者,可利用多種纖維直徑之混合。就個人保護吸收物件之應用而言, 纖維直徑典型地約1至5丹尼。因本創作之緣故,“聚烯烴基料的纖維非織物,, 及纖維聚烯烴非織物”鈞指聚烯烴構成至少5〇%之纖維表面的纖維性非織物。 有多種非織物形成加工可應用於本創作。其例子包含(但非限制):氣流及 濕法成網法,人造短纖維梳理及黏合法,溶液紡絲法熔喷及紡黏加工。前述所有 之加工均為精於本項技術者所熟知。紡黏聚丙烯非織物特別適合本創作。紡黏非 織物可依照Appel之USP4,340,563的教示來製造,該專利在本文中併入以供參 考。紡黏材料係藉由將熱塑性材料擠過紡絲板之多數個喷絲孔來形成長絲,其中 被擠壓的長絲直徑被(例如)引射抽長或其他吾人熟悉的紡黏機制降低。 一旦纖維非織物舒適層(14)被形成,其可預先黏合以增加強度及整體性。 於例子所使用的聚丙烯紡黏織布係以黏合密度約1〇〇至3〇〇黏合點/平方英吋的黏 合式樣(黏合面積約15%)來預先黏合。黏合密度在此範圍之上及之下者,亦可 C:\Eunice 20°4\^^-001^2 \ΡΚ·0〇ιτ〇225\ρΚ^〇1^^ M245953 被利用,具體之密度係決定於個雜合點的大小。 為形成本創作之透氣,似布薄膜/非織物複合物(10),膜層(12)及纖維聚 稀^非織物層(14)被彼絲合,然後以第二®解馳合裝置(16)來熱黏在 起膜在併入複合物之前,典型地已被擠壓,拉伸及薄化,當為未拉伸狀態時, 餵入加工’再拉伸及薄化。此外,膜可在線上形成或拉伸。 纖維非織物亦可預先形成,從供給滾筒(22)解纏以進人黏合加工線。或者, 其亦能在線上形成。如果膜(12)及不織布(14)以_速度餵人黏合器(16), 則複合物(10)可做成較為雙向度的。或者,可引起複合物(1〇)收縮,以產生 有皺的,較厚的,較三向度的結構。引起收縮的的一個方法為加工期間將一或二 層置於張力下’如藉由加速且/或止動其中—層使其暫時拉伸彡脹而引起續折。 另-方面為使題縮狀態下的,在膜層巾有方向性的線性輯烴分子。在施加熱 於膜層(12)後,其通常造成收縮。於是,假使複合物(1〇)以小於複合物黏合 器(16)上的速度被收捲於收集滚筒(16)上,則膜將放鬆而引起縐折。 至少可利用二方法來完成二層的熱黏合。第一個為利用熱及壓力,如加熱的 式樣黏合滚筒。二個滾筒皆可有式樣,或一者有一者無。滚筒之二者可被加熱, 或可利用第一加熱源。如果條件指定’其中一滾筒也可被冷卻。無論如何,熱應 被調整俾使膜内的黏合劑變黏以黏合二層,同時維持溫度至少低於膜中主要優勢 線性聚烯烴聚合物的熔點5°C。“主要”一詞係指具有最高膜總重百分比的優勢 線性聚烯烴聚合物(如果在膜聚合物混合物中有超過一種的優勢線性聚稀煙聚合 物)。 黏合式樣及面積可隨特殊之最終使用來改變。合適的黏合式樣能包含點黏 M245953 合,連續線,裝飾»,以及前述者之結合。黏合面積取決於所欲之積層程度。 就個人保護吸收物件之應用而言,黏合應充足至少需5克負荷來轉積層此二層。 第二個黏合方法為超音波黏合,該法亦精於本項技術者所熟知。在此方法 中,砧滚筒也可被設計成任何前文所述之式樣。 複合物一旦形成,便可廣泛地應用,並不止於個人保護吸收物件之外罩。這 類的物件典型地包含體側襯裡,吸收芯材,背層或外罩。本創作之材料可充當為 外罩’其中纖維非織物層面向物件外部’膜層面對吸收芯材。於是膜層及體側襯 裡可藉黏合劑,以同於本創作二層之複合材料的式樣來熱封合。 在前文之討論中’黏合劑添加於膜層(12)中,使其與纖維非織物舒適及支 持層(14)相容。然而也能在支持層(14)之纖維上添加黏合劑。 如前文所述,纖維形成層(14)可為較短的人工短纖維或較長較連續纖維(如 紡黏與熔喷非織物)。在所有例子中可由單聚合物來製造纖維(如直線聚稀烴纖 維)或由多成分纖維來製造(如複合纖維)。在此二種纖維中,黏合劑必須在纖 維之外表面上,俾使膜及非織物層間形成黏合。就直線纖維而言(如聚乙烤纖 維),黏合劑可添加在聚乙烯前混合物中,並擠成纖維。就複合纖維來說,黏合 劑必須添加在將會結束於纖維露出表面上的聚合物中。在鞘/芯纖維例子中,其應 為勒部分’而就並排纖維來說,黏合劑可添加於聚合物之一或二者上,因為他們 均將露出纖維外表面。 黏合劑通常佔其添加之聚烯烴聚合物重的2至20%。(以用來形成纖維部分 之總聚合混合物重為基準)。因此在直線聚乙烯纖維中,聚合物混合物包含約2 至20wt%黏合劑及約80至89wt%之聚乙烯(無其他添加劑在纖維聚合物混合物C: \ Eunice 2004 \ PK-001 ^ 2 \ PK-001-0225 \ PK-001-022S-2.DOC M245953 for personal protection hygiene applications), and more desirable less than about 15 grams / Square meters. The fibrous non-woven comfort layer (14) is made of feminine fiber (such as polypropylene). In the example, the nonwoven is polypropylene spunbond, but other polyolefin fibers may be used. Fiber mixtures can also be used, which include different polyolefin fibers, polyolefins, and non-polyolefin fiber mixtures (such as polyethylene sheath / polypropylene core composite fibers and polyester fibers, and fiber non-woven fabrics can also include natural fibers. Specific The types of fibers include single-component fibers and composite fibers (such as: side-by-side, sheath / core, sea-island composite fibers). The fibers can be straight or curly, hollow or solid. They are usually round or non-circular cross-sections (including limbs) , Limbs, "χ ,, cross-section). Fiber length may be short (such as human short fibers) or long (spunbond and meltblown fibers). The thickness of the fibers depends on the desired properties. Narrow fibers provide softness Non-fabric and thicker fibers will provide greater strength and elasticity. Alternatively, a combination of multiple fiber diameters may be utilized. For personal protection absorbent applications, the fiber diameter is typically about 1 to 5 deniers. As a result of this creation For this reason, "polyolefin-based fibrous nonwoven fabrics, and fibrous polyolefin nonwoven fabrics" refer to fibrous nonwoven fabrics whose polyolefins constitute at least 50% of the fiber surface. Fabric formation processing can be applied to this creation. Examples include (but are not limited to): air-flow and wet-laying, artificial staple fiber carding and bonding, solution spinning, meltblowing and spunbonding. All of the foregoing processes are It is well known to those skilled in the art. Spunbond polypropylene non-woven fabrics are particularly suitable for this creation. Spunbond non-woven fabrics can be manufactured according to the teachings of USP 4,340,563 by Appel, which is incorporated herein by reference. Spunbond The material is formed by extruding a thermoplastic material through a plurality of spinnerets of a spinneret to form filaments, wherein the diameter of the extruded filaments is reduced by, for example, ejection or other spunbond mechanisms familiar to us. A fibrous non-woven comfort layer (14) is formed, which can be pre-bonded to increase strength and integrity. The polypropylene spunbond fabric used in the example has a bonding density of about 100 to 300 bonding points / square inch. Inch bonding pattern (bonding area is about 15%) to pre-bond. If the bonding density is above and below this range, C: \ Eunice 20 ° 4 \ ^^-001 ^ 2 \ ΡΚ · 0〇ιτ〇 225 \ ρΚ ^ 〇1 ^^ M245953 is used, the specific density is It depends on the size of the hybrid point. In order to form the breathability of this creation, the cloth-like film / non-woven composite (10), the film layer (12) and the fiber poly ^ non-woven layer (14) are joined together, and then The second ® decoupling device (16) is used to thermally bond the film before it is incorporated into the composite, which has typically been extruded, stretched and thinned. When it is in the unstretched state, it is fed into the process and re-stretched. And thinning. In addition, the film can be formed or stretched on the line. The fibrous non-woven fabric can also be formed in advance and unwound from the supply roller (22) to enter the bonding processing line. Alternatively, it can also be formed on the line. If the film ( 12) and non-woven fabric (14) feed the adhesive (16) to the person at a speed of _, the composite (10) can be made more bidirectional. Or, it can cause the composite (10) to shrink to produce wrinkles, Thicker, three-dimensional structure. One method of causing shrinkage is to place one or two layers under tension during processing ' such as by continuing and folding by accelerating and / or stopping them-the layers being temporarily stretched and swelled. On the other hand, it is a linear hydrocarbon-collecting molecule with a directional property in the film towel under the contracted state. After applying heat to the film layer (12), it usually causes shrinkage. Therefore, if the compound (10) is wound onto the collection drum (16) at a speed lower than that on the compound binder (16), the film will relax and cause creases. At least two methods can be used to complete the two-layer thermal bonding. The first is a bonding drum that uses heat and pressure, such as heating. Both rollers are available in style, or one or the other. Both of the drums may be heated, or a first heating source may be utilized. If conditions specify 'one of the drums can also be cooled. In any case, the heat should be adjusted to make the adhesive in the film sticky to adhere the two layers, while maintaining a temperature of at least 5 ° C below the melting point of the main linear polyolefin polymer in the film. The term "primary" refers to the dominant linear polyolefin polymer with the highest percentage of total film weight (if there is more than one dominant linear polysmoke polymer in the membrane polymer blend). Bonding style and area can be changed with special end use. Suitable bonding patterns can include point bonding M245953 bonding, continuous lines, decoration », and combinations of the foregoing. The bonding area depends on the desired degree of lamination. For the application of personal protective absorbent articles, adhesion should be sufficient to require at least a 5 gram load to transfer the two layers. The second bonding method is ultrasonic bonding, which is also well known to those skilled in the art. In this method, the anvil roller can also be designed in any of the manners previously described. Once the composite is formed, it can be used in a wide range of applications, not just for personal protective absorbent articles. Such articles typically include a bodyside liner, an absorbent core, a backing layer, or a cover. The material of this creation can be used as a cover ' wherein the fibrous nonwoven layer faces the exterior of the article ' Therefore, the film layer and the body-side lining can be heat-sealed by the adhesive in the same manner as the two-layer composite material of this creation. In the foregoing discussion, an 'adhesive' was added to the film layer (12) to make it compatible with the fibrous nonwoven comfort and support layer (14). However, it is also possible to add a binder to the fibers of the support layer (14). As mentioned above, the fiber-forming layer (14) may be a short artificial staple fiber or a longer and continuous fiber (such as a spunbond and meltblown nonwoven). In all cases, fibers can be made from a single polymer (such as a linear paraffin fiber) or from a multicomponent fiber (such as a composite fiber). In these two types of fibers, the binder must be on the outer surface of the fiber to cause adhesion between the film and the nonwoven layer. In the case of linear fibers (such as polyethylene baking fibers), the binder can be added to the polyethylene premix and extruded into fibers. For composite fibers, a binder must be added to the polymer that will end up on the exposed surface of the fiber. In the case of sheath / core fibers, it should be the Le 'portion, and in the case of side-by-side fibers, binders can be added to either or both of the polymers because they will all expose the fiber's outer surface. Binders usually make up 2 to 20% by weight of the polyolefin polymer to which they are added. (Based on the total polymer mixture weight used to form the fiber portion). Therefore, in a linear polyethylene fiber, the polymer mixture contains about 2 to 20% by weight of a binder and about 80 to 89% by weight of polyethylene (no other additives in the fiber polymer mixture

17 C: \ Eunice 2004 \ ΡΚ-ΟΟΊ-Ό2 \ PK-001-0225\PK-Wi-0225-2.DOC 中的情況下)。就複合或多成分纖維而言,百分率將以特殊纖維之混合物的總重 為基準。此外’,如果(例如)纖維為並列聚乙烯/聚丙烯纖維,黏合劑可在依相 同之重量百分率(相對於每一個體纖維而言)被添加在二個聚合物成分中,亦即 對於每一個體纖維聚合物成分為2至2〇wt%。 因為有可能在相同非織物中混合不同種類及組成的纖維,所以織布中並列非 全部之纖維必須具有存在於外表面上的黏合劑,只要膜及非織物層間能取得充足 之黏合’而使層彼此分離或解積層至少需要5克之負荷即可。如果纖維至少為5〇wt %之非織物層利用前述之方式黏合,則此將典型地發生。最後,在選擇黏合劑及 黏合條件時,應選擇一種黏合溫度可低於膜層中聚烯烴熔點的黏合劑。 為了說明本創作的熱黏合力,數個樣品一下文來製備。有許多樣本被限制測 试雙層間的黏合強度以膜的水汽輸送率(WVTR),(例四中為複合物計算 WVRT及黏合強度的測試方法如下文所述。 水汽輪送率 樣本材料的水汽輸送率(WVRT)係依ASTM標準E96-80來計算。直徑3 于的圓 ✓樣本疋一片位於 Sommerville,New Jersey 的 Hoechst Celanese17 C: \ Eunice 2004 \ ΡΚ-ΟΟΊ-Ό2 \ PK-001-0225 \ PK-Wi-0225-2.DOC). For composite or multicomponent fibers, the percentages will be based on the total weight of the blend of special fibers. In addition, if, for example, the fibers are side-by-side polyethylene / polypropylene fibers, the binder can be added to the two polymer components at the same weight percentage (relative to each individual fiber), that is, for each A bulk fiber polymer content is 2 to 20 wt%. Because it is possible to mix different types and compositions of fibers in the same non-woven fabric, not all of the fibers juxtaposed in the woven fabric must have a binder present on the outer surface, so long as sufficient adhesion can be achieved between the film and the non-woven layer, so that The layers need to be at least 5 grams to separate or deconstruct the layers. This will typically occur if the non-woven layer of fibers is at least 50 wt% bonded in the manner described above. Finally, when selecting the adhesive and the bonding conditions, a bonding agent whose bonding temperature can be lower than the melting point of the polyolefin in the film layer should be selected. To illustrate the thermal adhesion of this creation, several samples were prepared one after the other. There are many samples that are restricted to test the adhesive strength between the double layers based on the film's water vapor transport rate (WVTR). (The test method for calculating the WVRT and adhesive strength of the composite in Example 4 is as follows. Water Vapor Delivery Rate Sample Material Water Vapor Transmission Rate (WVRT) is calculated according to ASTM standard E96-80. A circle with a diameter of 3 mm ✓Sample: A piece of Hoechst Celanese in Sommerville, New Jersey

Corporation 的 CELGUARD (商標名)2500 膜。CELGUARA 2500 膜是微孔隙的 丙婦膜母材料製備5個樣品。測試盤是Thwing-Albert Instument Company 所售的揮發度計盤,編號6(M。每一揮發度計盤中倒入腦亳升的水及個別的帶 測材料樣本’控制材制橫跨盤之開口顧。麟邊盤扭緊,在盤緣形成密封, 使盤中待撕料或控制材料在直徑Μ公分的圓巾,暴露於周圍的大氣,該圓之 露出面積大約33,17平方公分。盤放人卿〇F(32〇c)的鼓風烘箱中丨小時,至平Corporation's CELGUARD (trade name) 2500 membrane. CELGUARA 2500 membrane is a microporous acrylic film master material prepared from 5 samples. The test discs are volatility meter discs sold by the Thwing-Albert Instument Company, number 6 (M. Each volatility meter disc is filled with brain-raised water and a separate sample of test material. The opening edge Gu. The edge edge disk is tightened tightly to form a seal at the edge of the disk, so that the material to be torn or controlled in the disk is a circular towel with a diameter of M cm and is exposed to the surrounding atmosphere. Put it in the blast oven of Renqing 0F (32〇c) for one hour, until flat

C: \ Eunice 2004\ PK-001-02 \ ΡΚ-001-0225 \ ΡΚ-00Ί -0225-2.DOC M245953 衡。烘箱為恒溫烘箱,外界空氣可從中循環,以避免水汽積聚於箱中。一合適的 鼓風烘箱為(例如)Blue Island的Blue M Electric c〇mpany所售之施e m Power-O-Matic 60烘箱。平衡完成時,從烘箱取出盤,稱重並立刻送入供箱中。 0.4小時之後,粗試水汽輸送率值以下文所述計算·· 測試TVWR= (24小時之損失重)χ 315·5克/平方公尺/24小時烘箱内的相 對溼度未具體地控制。 在預先没定之l〇〇°F (32°C)及大氣相對渔度的條件下,CELGUar〇 25〇〇 控制樣本的WVTR為5000克/平方公尺/24小時。 备然在每一個測試中均測試控制樣品,並且初試值利用下述公式來修正以設 定條件: WVTR=(測試WVTR/控制WVTR) X 500克/平方公尺/24小聘(克/平方公 尺/24小時)。 黏合強度 為測試膜層及纖維非織物舒適層間的黏合強度,在多種材料的樣本上進行解 積層或撕裂強度測試。切下2x約6英吋的樣本;然後用手解積層短端之一者, 產生能置入Sintech/2電腦整合測試系統的鉗鋏中,該系統由MTS Systems Corporation製造。鉗鋏隙被設定為100mm的幅距,且足以讓積狀態的材料停留 於其中,因此鉗鋏能移動65mm。樣本至於鉗鋏中,俾使鉗鋏展開1〇mm前,樣 本能開始解積層。十字頭速度設為300mm/分,資料記錄於i〇mm開始點及 65mmmm終點間。所記錄之資料指示出所需以分離二層的撕離強度或負荷(克), 以及最大、最小、平均值的標準指數(克)。 C:\Euniee 2Ω04\ΡΚ-00Ί-η2\ΡΚ·ϋ01-0225\ΡΚ4)0Ί-02?^.? M245953 例子 例一 置備二個透氣膜/非織物積層並評估之,以決定黏合劑之施加對水氣輸送率的 影響以及整個複合物之黏合強度。首先,置備三個多種聚合物混合物的透氣膜, 然後每一膜黏合於約2丹尼,0.5盎司(17gsm)聚丙烯紡黏非織物材料上,非織 物以15%黏合面預先黏合。每一膜成份含(以總重為基準)65wt%英中超塗層碳 酸妈,其具有1微米的平均微米尺寸以及7微米的頂截面。碳酸鈣購自Sylacaga 的ECCA鈣產品公司,其為ECC國際公司的支部。碳酸約與15-25wt%的線性低 密度聚乙稀混合,該聚合物係Dowlex 2517線性低密度聚乙烯及Dowlex 2532線 性低密度聚乙烯以1 : 4之重量比混合製成,因此混合物之熔化指數為10 M.I. (194°F 下/10 分)。Dowlex 聚合物購自 Midland 的 Dow Chemical,U.S.A·。其餘 10_20wt%的成份包括KS051P聚丙烯基料的聚合物,其購自Wilmington, Delaware之Himont,U.S.A.。KS051P聚合物為烯烴族熱塑性彈性或TPO多步反 應器產品,其中非晶形乙烯丙烯無規共聚物的分子分散在優勢半結晶的高聚丙烯 單體/低乙烯單體之連績基質中。非晶形成份在55°C左右開始軟化石,充當黏合 劑。如下文表1所示,樣本1含65%碳酸鈣,10%KSO51P聚合物,25%線性低 密度聚乙烯。樣本2含65%碳酸鈣,15%KS051P聚合物,20%線性低密度聚乙 烯。樣本3含65%碳酸的,20%KSO51P聚合物,15%線性低密度聚乙烯。三種 配方均在375°F (19ΓΟ下吹塑成薄膜,吹脹比約1.7,產生之膜的為拉伸規格 約1.25密爾(50gsm)。然後每一膜在機械方向的單元上,於i40°F (60°C)下拉 伸,拉伸率3倍。成品膜依表1所述之水氣輸送率之指示,可為透氣的,並且其 M245953 基重為14gsm。 表1 樣本 碳酸鈣 (wt %) LLDPE (wt %) KS051P (wt %) WVTR g/m2/ 24 hr 黏合強度 (克) 膜加工 MDO 強度 1 65 25 10 4530 24 優良 尚佳 2 65 20 15 4300 27 優良 優良 3 65 15 20 3710 26 優良 特優C: \ Eunice 2004 \ PK-001-02 \ ΡΚ-001-0225 \ ΡΚ-00Ί -0225-2.DOC M245953. The oven is a constant temperature oven, from which outside air can be circulated to prevent water vapor from accumulating in the oven. A suitable blast oven is, for example, the Schmid Power-O-Matic 60 oven sold by Blue M Electric Company of Blue Island. When the balance is complete, remove the pan from the oven, weigh it, and immediately place it in the supply bin. After 0.4 hours, the value of the crude test water vapor transmission rate is calculated as described below. Test TVWR = (24-hour weight loss) x 315 · 5 g / m² / 24-hour relative humidity in the oven is not specifically controlled. Under the conditions of 100 ° F (32 ° C) and relative relative fishery, the WVTR of the CELGUar 205 control sample was 5000 g / m2 / 24 hours. It is necessary to test the control sample in each test, and the initial test value is modified to set the conditions using the following formula: WVTR = (test WVTR / control WVTR) X 500 g / m² / 24 small employment (g / m²) Feet / 24 hours). Adhesive strength In order to test the adhesive strength between the film layer and the comfort layer of the fibrous non-woven fabric, delamination or tear strength tests were performed on samples of various materials. A 2x approximately 6-inch sample was cut out; then one of the short ends of the layer was deconvoluted by hand to produce a clamp that can be placed in a Sintech / 2 computer integrated test system made by MTS Systems Corporation. The jaw gap is set to a pitch of 100mm, which is enough to allow the material in the accumulated state to stay in it, so the jaw can move 65mm. As for the sample in the clamp, before the clamp is extended 10 mm, the sample can begin to deconstruct the layer. The crosshead speed was set to 300mm / min, and the data was recorded between the starting point of 10mm and the end point of 65mmmm. The recorded information indicates the tear strength or load (g) required to separate the two layers, and the standard index (g) of the maximum, minimum, and average values. C: \ Euniee 2Ω04 \ ΡΚ-00Ί-η2 \ ΡΚ · ϋ01-0225 \ ΡΚ4) 0Ί-02? ^.? M245953 Example Example 1 Two air-permeable membranes / non-woven laminates were prepared and evaluated to determine the application of the adhesive The effect on water vapor transport rate and the bonding strength of the whole composite. First, three air-permeable membranes with a mixture of multiple polymers were prepared, and then each membrane was bonded to about 2 deniers, 0.5 ounces (17 gsm) of polypropylene spunbond non-woven material, and the non-woven fabric was pre-bonded with a 15% bonding surface. Each film component contains (based on the total weight) 65% by weight of British and Chinese Super Coatings, which has an average micron size of 1 micron and a top cross section of 7 micron. Calcium carbonate was purchased from ECCA Calcium Products of Sylacaga, a division of ECC International. Carbonic acid is mixed with about 15-25wt% linear low-density polyethylene. The polymer is made of Dowlex 2517 linear low-density polyethylene and Dowlex 2532 linear low-density polyethylene at a weight ratio of 1: 4, so the mixture melts. The index is 10 MI (/ 10 points at 194 ° F). Dowlex polymer was purchased from Dow Chemical, U.S.A., Midland. The remaining 10-20% by weight of the composition includes a polymer of KS051P polypropylene base, which was purchased from Himont, U.S.A. of Wilmington, Delaware. KS051P polymer is an olefin-based thermoplastic elastomer or TPO multi-step reactor product, in which the molecules of amorphous ethylene propylene random copolymer are dispersed in a continuous matrix of dominant semi-crystalline high polypropylene monomer / low ethylene monomer. Amorphous components begin to soften around 55 ° C and act as a binder. As shown in Table 1 below, Sample 1 contains 65% calcium carbonate, 10% KSO51P polymer, and 25% linear low density polyethylene. Sample 2 contains 65% calcium carbonate, 15% KS051P polymer, and 20% linear low-density polyethylene. Sample 3 contains 65% carbonic acid, 20% KSO51P polymer, and 15% linear low density polyethylene. All three formulations are blown into a film at 375 ° F (19ΓΟ) with an inflation ratio of about 1.7. The resulting film is a stretch specification of about 1.25 mils (50gsm). Then each film is on a mechanically oriented unit at i40 Stretching at ° F (60 ° C), the stretching rate is 3 times. The finished film can be breathable according to the water vapor transmission rate indicated in Table 1, and its M245953 basis weight is 14gsm. Table 1 Sample calcium carbonate (wt%) LLDPE (wt%) KS051P (wt%) WVTR g / m2 / 24 hr Adhesive strength (g) MDO strength of film processing 1 65 25 10 4530 24 Excellent and good 2 65 20 15 4300 27 Excellent and good 3 65 15 20 3710 26 Excellent

從表1可見··隨著黏合劑量增加(本例中烯烴KS051P聚合物的非晶形乙稀 丙烯共聚物部份約在55°C開始軟化),水氣輸送率下降。然而,隨著增黏或黏合 劑之增加,樣本相反的顯示撕離強度增加,因此更能抗解積層。假使添加黏合劑, 則以肉眼觀察膜加工的難易及膜在機械方向的拉伸能力。表1指示:膜可加工性 為優良的,與添加至前擠壓混合物中的黏合劑無關。相反的,當黏合劑在膜中增 加時,可觀察到拉伸能力增加。在樣本1中,在機械方向拉伸膜的能力係尚佳, 而樣本3為特優。每一膜在1〇〇英尺/分(3〇·5米/分)之速度下與17gsm (〇·5盎 司)的聚丙稀紡黏不織布積層,層壓為20碎/平方英忖(ι·4ΐ公斤/平方公分), 其黏合式樣為黏合面積約15%的非連續黏合式樣。式樣滾筒的溫度維持於25〇〇F (121°C),同時與膜直接接觸之平滑的砧滾筒溫度為16〇〇F 從表1資料可得證:依照本創作的三個樣本均具有特優的水氣輸送率及特優 的黏合強度。樣本需要24至27克的負荷來拉離僅15%黏合面積的層物。此外, 膜層不具穿孔,此使本創作的材料作成個人保護吸收物件時提供隔離性質。It can be seen from Table 1 that as the adhesive amount increases (in this example, the amorphous ethylene propylene copolymer portion of the olefin KS051P polymer begins to soften at about 55 ° C), the water vapor transmission rate decreases. However, as tackifiers or adhesives were added, the samples on the contrary showed an increase in peel strength and were therefore more resistant to delamination. If an adhesive is added, the ease of film processing and the stretchability of the film in the mechanical direction are observed with the naked eye. Table 1 indicates that the film processability is excellent, regardless of the binder added to the pre-extrusion mixture. Conversely, as the adhesive was increased in the film, an increase in tensile ability was observed. In Sample 1, the ability to stretch the film in the mechanical direction is still good, while Sample 3 is particularly excellent. Each film was laminated with 17 gsm (0.5 ounces) of polypropylene spunbond non-woven fabric at a rate of 100 ft / min (30.5 m / min) and laminated to 20 pieces per square inch (ι · 4ΐkg / cm²), and its bonding pattern is a discontinuous bonding pattern with a bonding area of about 15%. The temperature of the model roller is maintained at 2500F (121 ° C), while the temperature of the smooth anvil roller that is in direct contact with the film is 1600F. From the information in Table 1, it can be proved that the three samples according to this creation all have special characteristics. Excellent water and gas transport rate and excellent bonding strength. The sample requires a load of 24 to 27 grams to pull away the layer with only 15% of the bonded area. In addition, the membrane is non-perforated, which allows the material of this creation to provide barrier properties when used as a personal protective absorbent article.

Ml 在本例中,拉伸溫度之作用係以前文例1之樣本1有關的膜配方來評估。當Ml In this example, the effect of the stretching temperature was evaluated on the film formulation related to sample 1 of the previous example 1. when

21 C: \ Eunice 2004 \ ΡΚ-ΟΟΊ-02 \ ΡΚ-ΟΟΊ-0225 \ ΡΚ-00ί·0225-2. DOC M245953 KS051P聚合物非晶狀成份在本質上變得更似黏合劑時,其逐漸的軟化被認為會 妨礙碳酸鈣微粒及樹脂基質之界面上的聚合物混合物完全斷裂。為確定此觀點, 在140°F (63°C )至186〇F (86°C )下,膜樣本拉伸3倍(亦即〗米的樣本拉伸至 3米)。當拉伸溫度增加,水氣輸送率下降,很可能因為膜中碳酸舞微粒周圍形成 較少或較小的孔隙。如表2中所示,拉伸溫增加的確能增加線性低密度聚乙烯分 子的流動性,因而改良拉伸的容易度。當溫度由146°F (63°C)增加至186°F (86 °C)時,拉伸容易度增加。177$ (81°C)及186°F (86。〇間,膜之分子中顯示 極端的取向,因此,在機械方向上展現更多的分裂及更易於撕破。結果,可藉著 合適之拉伸溫度擇來最大化膜之WVTR,可加工性,機械性質之平衡。拉伸在溫 度小於膜混合物主要優勢線性聚烯烴聚合物之熔點並在黏合劑軟化點左右時,可 取得最佳的拉伸及透氣性。 表2 拉伸溫度 °F / °C WVTR g / m2 / 24 hr 拉 MDO 伸 146/63 4300 尚 佳 157/69 4100 優 良 167/75 3960 優 良 177/81 3730 裂 開 186/86 3515 裂 開更多 例3 在例1及2中,所有的樣本(以乾重為基準)包含65%的碳酸鈣,15至25 %線性低密度聚乙烯及10至20%烯蒙KS051P聚丙烯基料的聚合物樹脂,該樹 脂包含可充當增黏劑或黏合記得非晶狀乙烯丙烯無規共聚物。於例3中,65wt% 的碳酸約及30wt%線性低密度聚乙烯被混合。如表三所示,在基本混合物中添加21 C: \ Eunice 2004 \ ΡΚ-ΟΟΊ-02 \ ΡΚ-ΟΟΊ-0225 \ ΡΚ-00ί · 0225-2. DOC M245953 KS051P When the amorphous component of the polymer becomes more adhesive-like in nature, its gradually Softening is believed to prevent complete fracture of the polymer mixture at the interface of the calcium carbonate particles and the resin matrix. To determine this point, film samples were stretched 3 times (that is, samples of 1 meter were stretched to 3 meters) at 140 ° F (63 ° C) to 186 ° F (86 ° C). As the stretching temperature increases, the water vapor transport rate decreases, probably because fewer or smaller pores are formed around the carbonic acid dance particles in the film. As shown in Table 2, an increase in the stretching temperature does increase the fluidity of the linear low-density polyethylene molecules, thereby improving the ease of stretching. As the temperature increases from 146 ° F (63 ° C) to 186 ° F (86 ° C), the ease of stretching increases. Between 177 $ (81 ° C) and 186 ° F (86 °), the molecules of the film show extreme orientation, so they show more splitting and easier tearing in the mechanical direction. As a result, the Stretching temperature is selected to maximize the balance of WVTR, processability, and mechanical properties of the film. Stretching can achieve the best when the temperature is lower than the melting point of the film mixture's main advantage, the linear polyolefin polymer, and around the softening point of the adhesive. Tensile and air permeability. Table 2 Tensile temperature ° F / ° C WVTR g / m2 / 24 hr Pull MDO extension 146/63 4300 Fair 157/69 4100 Excellent 167/75 3960 Excellent 177/81 3730 Rip 186 / 86 3515 Cracking more Example 3 In Examples 1 and 2, all samples (based on dry weight) contained 65% calcium carbonate, 15 to 25% linear low density polyethylene, and 10 to 20% olefin KS051P polymer. A propylene-based polymer resin containing an amorphous ethylene propylene random copolymer that can act as a tackifier or adhesive. In Example 3, 65% by weight of carbonic acid and 30% by weight of linear low density polyethylene were mixed. As shown in Table III, add to the basic mixture

r \ F.unicp 20M\PKJ)0i-02\PK-O0^225\PK^0i-022S-2.D〇C M245953 5wt% —系列已知的增黏劑及黏合劑。黏合劑包含以职化没1〇94<31〇2及1126黏 合劑及Zonatac 5〇lL與Eastman 1〇22肌黏合劑。此外,例】樣本2之膜配方亦 依例1所述被形成膜。每一個膜以1/7的吹增比率被吹塑成約15㈣(6〇gsm) 的規格。膜在機械方向,於146〇F (63<t )下,被拉伸成原長之3倍。此拉伸溫 度低於優躲錄驗聚合之熔點⑽加听卜麟本接著在酸⑴之條 件下,與例1所述之聚丙烯非織物積層,全部之黏合面積約15%。式樣滾筒的溫 度保持於250°F (121°C),與膜直接接觸之平滑的砧滾筒為16〇〇F (71。〇, 175〇F (79C) ’ 185 F (85°C)及195°F (91°C)。四個黏合溫度之膜/不織布積層均測試 黏合強度。此外,母一膜均測水氣輸送率,膜加工性的容易度可由視覺觀察。結 果呈現於表3。 表3 黏合前wt% 碳酸鈣LLDPE (wt%) (wt%) WVTR g/m2/ 24 hr 160°F 黏合強度(克) 175〇F 185〇F 195〇F 膜加工 MDO 拉伸 65% 20% 4300 41 ♦ 本 * 優良 尚佳 65% 30% 2300 3 5 6 10 特優 特優 65% 30% 3840 3 3 7 5 特優 特優 65% 30% 3198 3 3 5 7 優良 優良 65% 30% 2990 4 4 10 9 特優 特優 65% 30% 4900 8 7 10 7 優良 優良 KSO50 15%r \ F.unicp 20M \ PKJ) 0i-02 \ PK-O0 ^ 225 \ PK ^ 0i-022S-2.D0C M245953 5wt% —A series of known tackifiers and adhesives. Adhesives include Chem 1094 < 3102 and 1126 adhesives and Zonatac 50L and Eastman 1022 muscle adhesives. In addition, Example] The film formulation of Sample 2 was also formed into a film as described in Example 1. Each film was blow-molded to a size of about 15 ㈣ (60 gsm) at a blow-up ratio of 1/7. The film was stretched to 3 times its original length at 1460F (63 < t) in the mechanical direction. The tensile temperature is lower than the melting point of the best-in-class polymer. Then, under the condition of acidic acid, laminated with the polypropylene non-woven fabric described in Example 1, the total bonding area is about 15%. The temperature of the pattern roller is maintained at 250 ° F (121 ° C), and the smooth anvil roller in direct contact with the film is 1600F (71.0, 175F (79C) '185F (85 ° C) and 195 ° F (91 ° C). The film / non-woven laminates at all four bonding temperatures were tested for bonding strength. In addition, the mother and film were tested for water vapor transmission rate, and the ease of film processability was visually observed. The results are shown in Table 3. Table 3 wt% calcium carbonate LLDPE (wt%) (wt%) WVTR g / m2 / 24 hr 160 ° F Adhesive strength (g) 175〇F 185〇F 195〇F Film processing MDO Stretch 65% 20% 4300 41 ♦ Original * Excellent 65% 30% 2300 3 5 6 10 Premium 65% 30% 3840 3 3 7 5 Premium 65% 30% 3198 3 3 5 7 Excellent 65% 30% 2990 4 4 10 9 Special Excellent 65% 30% 4900 8 7 10 7 Excellent Excellent KSO50 15%

Regalrez 1094 5%Regalrez 1094 5%

Regalrez 3102 5%Regalrez 3102 5%

Regalrez 1126 5%Regalrez 1126 5%

Zonatac 501L 5% 1023PL 5% *不能分離(黏合良好) 烯蒙KSO50黏合劑提供最好的二層物間黏合強度,但要記住:其在膜中佔Zonatac 501L 5% 1023PL 5% * Cannot be separated (good adhesion) The olefin KSO50 adhesive provides the best two-layer adhesion strength, but keep in mind that it occupies in the film

23 C:\EMmce 2004\PK-001-02\PK-001-0225\PK-001-0225-2.DOC M245953 15wt%,而其他黏合劑為5wt%。大多數的黏合劑在黏合溫度增加時似乎增加黏 合’但某些黏合劑的最高峰為185°F ’ ‘然後在195〇F時黏合強度開始下降。所有 黏合劑顏加工性在優良及特優之間,但仙_ Ks⑽黏合躺膜在機械方 向的拉伸僅尚佳。所有膜均顯示良好的水氣輸送率。 例4 於例4中,以本創狀透氣似布物複合婦代普通的聚乙觸(控 制組),作為尿布外罩,進行臨床研究,以決定其降低皮膚水合作用的效率。所 製之尿布包含控料罩及侧1樣本2之膜/_物積層。複合物之膜層具每24 小時4300克/平方米的水氣輸送率,複合物的水氣輸送率為每%小時41⑻克/ 平方米。控制尿布單層L2密爾厚的聚乙烯膜之wvtr約每24小時4〇至5〇克/ 平方米。 每一尿布沖入60毫升的合成尿,然後包住測試者前臂。在預定的間隔時間 中,測量WVTR,決定皮膚水合作用之程度。基於測試結果,使用本創作複合物 之尿布下方使用者皮膚之皮膚水合作用,很明顯地小於控制組尿布,因而證明在 維持透氣性並降低皮廣水合作用的同時,可在二層物中取得有效之黏合。 如前述例子可見到者,本創作的材料提供透氣性似布的膜/非織物複合物,而 層物間具優良的黏合。非織物層用以強固透氣的膜層,並且在複合物充當個人保 護吸收物件(如尿布)時,非織物層有助於克服透氣膜之溼冷本性。此外,由於 在膜及/或纖維聚合物混合物中併入黏合劑,不相容的聚合物/層可彼此熱積層。 如此詳細地描述本創作之後,一般皆知在不離開本創作精神及後序申請專利 範圍下,可製成許多修飾及改變。23 C: \ EMmce 2004 \ PK-001-02 \ PK-001-0225 \ PK-001-0225-2.DOC M245953 15wt%, while other adhesives are 5wt%. Most adhesives appear to increase adhesion as the adhesion temperature increases ', but the highest peak of some adhesives is 185 ° F' and then the adhesive strength begins to decrease at 1950F. All adhesives have good workability between excellent and special, but the _Ks⑽ adhesive lay-up film only stretches in the mechanical direction. All films showed good water vapor transport rates. Example 4 In Example 4, the original wound-like, breathable cloth-like compound with ordinary female polyethene (control group) was used as a diaper cover for clinical research to determine its efficiency of reducing skin hydration. The manufactured diaper includes a material control cover and a film / material layer of sample 1 on side 1. The composite film has a water vapor transport rate of 4300 g / m 2 per 24 hours, and the water vapor transport rate of the composite is 41 g / m 2 per hour. The wvtr of a single-layer L2 mil-thick polyethylene film for controlling a diaper is about 40 to 50 grams per square meter per 24 hours. Each diaper was flushed with 60 ml of synthetic urine and then wrapped around the subject's forearm. At predetermined intervals, the WVTR is measured to determine the degree of skin hydration. Based on the test results, the skin hydration of the user's skin under the diaper using this creative compound is significantly smaller than that of the control group. Therefore, it can be proved that it can be used in the second layer while maintaining breathability and reducing skin hydration. To obtain effective bonding. As can be seen from the foregoing examples, the material of this creation provides a breathable cloth-like film / non-woven composite with excellent adhesion between the layers. The non-woven layer is used to strengthen the breathable film layer, and the non-woven layer helps to overcome the wet and cold nature of the breathable film when the composite acts as a personal protective absorbent article, such as a diaper. In addition, incompatible polymers / layers can be thermally laminated to each other due to the incorporation of a binder into the film and / or fiber polymer mixture. After describing this creation in such detail, it is generally known that many modifications and changes can be made without departing from the spirit of this creation and the scope of subsequent patent applications.

24 C:\Eunice2004\PK-001-02\PK-001-O225\PK-001^225-2.DOC 圖式元件說明 10 composite 積層 12 film layer 膜層 14 support layer 支持層 16 bonder 黏合劑 18 take up roll 起始滚轴 M245953 【圖式簡單說明】 第一圖為本創作之透氣、似布薄膜/非織物複合物橫斷面視圖。 第二圖為本創作之透氣、似布薄膜/非織物複合物之加工圖示。24 C: \ Eunice2004 \ PK-001-02 \ PK-001-O225 \ PK-001 ^ 225-2.DOC Graphic element description 10 composite laminated 12 film layer film layer 14 support layer 16 bonder adhesive 18 take up roll Starting roller M245953 [Schematic description] The first picture is a cross-sectional view of the breathable, cloth-like film / non-woven composite of the creation. The second picture is the processing diagram of the breathable, cloth-like film / non-woven composite created.

25 C: \ Eunice 2004 \ PK-001-02 \ ΡΚ-ΟΟΊ -0225\ ΡΚ-ΟΟΊ -0225-2. DOC25 C: \ Eunice 2004 \ PK-001-02 \ ΡΚ-ΟΟΊ -0225 \ ΡΚ-ΟΟΊ -0225-2. DOC

Claims (1)

M245953 玖、申請專利範圍: 1、 一種透氣性似布薄膜/非織物積層吸收性物件,其中積層包含: 一膜’其由包含下列之混合物形成,含1〇至68% (以膜的乾總重為基準)的 優勢線性聚烯烴聚合物,30至80%的填充料,2至2〇%的黏合劑,該膜的水 汽輸送率至少為每24小時100克/平方米,以及 一纖維性聚烯烴非織物,其與該膜直接地黏合而形成一積層,該積層至少具 有24克的撕離強度。 2、 如申請專利範圍第1項的吸收性物件,其中該優勢線性聚烯烴聚合物為線性低 密度聚乙烯。 3、 如申請專利範圍第1項的吸收性物件,其巾該填充料為碳酸約。 4、 如申請專纖圍第1項的吸收性物件,其巾顏為每單位面積重量大於〇克/平 方米小於35克/平方米的被拉伸膜。 5、 如申凊專利範圍第1項的吸收性物件,其中該膜為每單位面積重量大於〇克坪 方米小於18克/平方米的被拉伸膜。 6、 如申請專利範賺項的吸收性物件,其中該纖維輯烴非織物為聚丙稀非織 物。 7、 如申請專利範圍第i項的吸收性物件,其中該纖維聚稀烴非織物包含複合纖維, 該複合纖維具有一聚烯烴成分。 々申吻專她圍第1獅吸倾物件,其巾賴減於纖維料烴非織物的 一側上黏有第二纖維性聚烯烴非織物。 9、-種透氣性似布薄膜/非織物積層缝性物件,其中個人保護吸收性物件包含: 26 C:⑽-綱:彻卿⑽侧㈣咖 M245953 一體側襯裡及一外罩和夾於此二者間的吸收芯材,該外罩包括一膜,該膜甴 含下列成分的混合物形成,含1〇至68% (以膜的乾總重為基準)的優勢線性 聚烯烴聚合物,30至80%的填充料,2至20%的黏合劑,該膜具有至少每24 小時100克/平方米的水汽輸送率,以及 一纖維性聚稀煙非織物直接黏合該膜而形成之積層,該積層具有至少24克的 撕離強度。 10、 一種透氣性似布薄膜/非織物積層吸收性物件,其中積層包含: 一膜,其由包含下列成分的混合物形成,(以膜的乾總重為基準)含1〇至68 %的優勢線性聚烯烴聚合物,30至80%的填充料,2至20%的黏合劑,該膜 具有至少每24小時100克/平方米的水汽輸送率,以及 一纖維性聚稀煙非織物直接黏合該膜而形成之積層,該積層具有至少24克的 撕離強度。 11、 一種透氣性似布薄膜/非織物積層吸收性物件,其中積層包含·· 形成前擠壓混合物,混合物包含(以膜乾總重為基準)1〇至68%的優勢線性 聚烯烴聚合物,30至80%的填充料,2至20%的黏合劑; 一由别擠壓混合物形成的膜;在溫度低於該優勢線性熱塑性聚合物的炼點下 拉伸該膜;以及 一由該膜與一纖維性聚烯烴非織物直接粘合形成的積層,其是在溫度低於該 膜中該優勢線性熱塑性聚合物的熔點下粘合而成,該積層具有至少24克的撕 離強度。 12、 如申請專利範圍第η項的非織物吸收性物件,其中該積層上方更進一步包括 27 C: \ Eunice 2004 \ΡΚ-ΌΟΊ-ΟΖ \PK-00J-0225 \ΡΚ-00Ί-0225-2.DOC M245953 波紋表面。 、如申請專利範M11項的非織物吸收性物件,其中該膜的拉伸係在溫度為該 黏合劑軟化點時完成。 14、 一種透氣性似布薄膜/非織物積層吸收性物件,其中積層包含: 形成膜層,其包含(以膜的乾總重為基準)3〇至轉的填充料以及2〇至7〇% 的聚烯烴聚合物;拉伸該膜層; 利用含聚烯烴聚合物及黏合劑之纖維性非織物内多數的纖維,將該纖維性非 織物直接黏合該膜層,該聚烯烴聚合物及該黏合劑係至少形成該纖維外表面 的一部分,以產生一至少24克的撕離強度。 15、 一種透氣性似布薄膜/非織物積層吸收性物件,其中積層包含: 一膜層,其包含(以膜之乾總重為基準)30至80%的填充料以及20至70%的 聚烯烴聚合物;以及 一纖維性非織物,該纖維性非織物含聚烯烴聚合物以及黏合劑,藉由其内部 的多數纖維與前述膜直接地黏合,該聚烯烴聚合物及該黏合劑至少形成該纖 維外表面的一部分,以產生一介於前述膜層與前述纖維性非織物之間的撕離 強度至少為24克。 28 C: \ Eunice 2004\ PK-001-02\ PK-001-022S \PK-001-0225-2. DOCM245953 范围 Application scope: 1. A breathable cloth-like film / non-woven laminated absorbent article, wherein the laminated layer comprises: a film 'formed of a mixture containing the following, containing 10 to 68% (based on the dry total of the film Weight basis) Advantages of linear polyolefin polymers, 30 to 80% filler, 2 to 20% binder, the film has a water vapor transmission rate of at least 100 g / m2 per 24 hours, and a fiber property Polyolefin non-woven fabric, which is directly bonded to the film to form a laminate, the laminate having a tear strength of at least 24 grams. 2. The absorbent article according to item 1 of the patent application, wherein the advantageous linear polyolefin polymer is a linear low-density polyethylene. 3. If the absorbent article in item 1 of the patent application scope, the filling material of the towel is carbonic acid. 4. If applying for the absorbent article of the special fiber enveloping item 1, the towel face is a stretched film with a weight per unit area of greater than 0 g / m2 and less than 35 g / m2. 5. The absorptive article according to item 1 of the patent application scope, wherein the film is a stretched film with a weight per unit area of more than 0 grams square meters and less than 18 grams per square meter. 6. For an absorbent article such as a patent application, the fiber-containing hydrocarbon non-woven fabric is a polypropylene non-woven fabric. 7. The absorbent article according to item i of the patent application scope, wherein the fiber polyolefin non-woven fabric comprises composite fibers, and the composite fibers have a polyolefin component. Tong Shen kissed her about the 1st lion sucking object, and the towel was reduced to the side of the fibrous hydrocarbon non-woven fabric with a second fibrous polyolefin non-woven fabric. 9. A kind of breathable cloth-like film / non-woven laminated seam-like articles, among which the personal protection and absorbent articles include: 26 C: ⑽- 纲: ⑽ 卿 ⑽ 面 ㈣㈣ M245953 Integrated side lining and a cover and sandwiched between the two An absorbent core material for the user, the cover includes a film formed by a mixture of the following ingredients, containing 10 to 68% (based on the total dry weight of the film) of the advantageous linear polyolefin polymer, 30 to 80 % Filling material, 2 to 20% adhesive, the film has a water vapor transmission rate of at least 100 g / m 2 per 24 hours, and a fibrous polysmoky non-woven fabric directly bonded to the film to form a laminate, the laminate Has a tear strength of at least 24 grams. 10. A breathable cloth-like film / non-woven laminated absorbent article, wherein the laminated layer comprises: a film formed of a mixture containing the following ingredients (based on the total dry weight of the film) with an advantage of 10 to 68% Linear polyolefin polymer, 30 to 80% filler, 2 to 20% binder, the film has a water vapor transmission rate of at least 100 g / m2 per 24 hours, and a fibrous polysmoky non-woven fabric directly bonded The film is formed into a laminate having a peel strength of at least 24 grams. 11. A breathable cloth-like film / non-woven laminated absorbent article, wherein the laminated layer contains an extruded mixture before formation, and the mixture contains (based on the total dry weight of the film) 10 to 68% of the advantageous linear polyolefin polymer 30 to 80% of filler, 2 to 20% of binder; a film formed from an extruded mixture; the film is stretched at a temperature lower than the refining point of the advantageous linear thermoplastic polymer; and The laminate formed by directly bonding the film to a fibrous polyolefin non-woven is bonded at a temperature lower than the melting point of the dominant linear thermoplastic polymer in the film, and the laminate has a tear strength of at least 24 grams. 12. If the non-woven absorbent article of item η in the scope of patent application, the layer further includes 27 C: \ Eunice 2004 \ ΡΚ-ΌΟΊ-ΟZ \ PK-00J-0225 \ ΡΚ-00Ί-0225-2. DOC M245953 Corrugated surface. For example, the non-woven absorbent article of the patent application No. M11, wherein the stretching of the film is completed when the temperature is the softening point of the adhesive. 14. A breathable cloth-like film / non-woven laminated absorbent article, wherein the laminated layer comprises: forming a film layer, which (based on the total dry weight of the film) of 30 to 70% of the filler and 20 to 70% A polyolefin polymer; stretching the film layer; using the majority of fibers in a fibrous nonwoven fabric containing a polyolefin polymer and an adhesive, directly bonding the fibrous nonwoven fabric to the film layer, the polyolefin polymer and the The adhesive forms at least a portion of the outer surface of the fiber to produce a tear strength of at least 24 grams. 15. A breathable cloth-like film / non-woven laminated absorbent article, wherein the laminated layer comprises: a film layer containing (based on the total dry weight of the film) 30 to 80% of the filler and 20 to 70% of the polymer An olefin polymer; and a fibrous non-woven fabric containing a polyolefin polymer and a binder, and through the majority of the fibers in the fibrous non-woven fabric are directly bonded to the aforementioned film, the polyolefin polymer and the binder form at least A portion of the outer surface of the fiber to produce a tear strength between the film layer and the fibrous nonwoven of at least 24 grams. 28 C: \ Eunice 2004 \ PK-001-02 \ PK-001-022S \ PK-001-0225-2. DOC
TW92217538U 2003-09-30 2003-09-30 Breathable cloth-like film/nonwoven laminate TWM245953U (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
TW92217538U TWM245953U (en) 2003-09-30 2003-09-30 Breathable cloth-like film/nonwoven laminate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
TW92217538U TWM245953U (en) 2003-09-30 2003-09-30 Breathable cloth-like film/nonwoven laminate

Publications (1)

Publication Number Publication Date
TWM245953U true TWM245953U (en) 2004-10-11

Family

ID=34433493

Family Applications (1)

Application Number Title Priority Date Filing Date
TW92217538U TWM245953U (en) 2003-09-30 2003-09-30 Breathable cloth-like film/nonwoven laminate

Country Status (1)

Country Link
TW (1) TWM245953U (en)

Similar Documents

Publication Publication Date Title
JP3373211B2 (en) Breathable cloth film / nonwoven fabric composite
JP7080251B2 (en) Airlaid composite sheet material
KR100723553B1 (en) Styrenic block copolymer breathable elastomeric films
JP4837681B2 (en) Nonwoven fabric laminate, moisture-permeable nonwoven fabric laminate sheet using nonwoven fabric laminate, and hygiene article using them
JP6235589B2 (en) Method for producing stretchable web laminate
CN1092563C (en) Low gauge films and film/nonwoven laminates
KR101321215B1 (en) Filament-meltblown composite materials, and methods of making same
AU2009247715B2 (en) Latent elastic composite formed from a multi-layered film
MXPA02004367A (en) Coextruded, elastomeric breathable films and process for making same.
MX2010013820A (en) Elastic composite formed from multiple laminate structures.
JP2003515619A (en) Breathable elastomer film of styrenic block copolymer
KR20020062335A (en) Breathable Laminate Permanently Conformable to the Contours of a Wearer
JP2006506245A (en) Breathable elastic multilayer film and method for producing breathable elastic multilayer film
JP2007530310A (en) Single-sided surface material stretch bonded laminate and method for producing the same
KR20120123658A (en) Nonwoven composite including an apertured elastic film and method of making
JP2003523842A (en) Breathable laminate for permanent fit to the wearer's body
WO1997049853A1 (en) Nonwoven fabric of long fibers and absorbent article made therefrom
JP3883220B2 (en) Moisture permeable sheet and absorbent article using the same
RU2630146C1 (en) Multi-layer elastic layer materials with high strength and elasticity and methods of their obtaining
TW513344B (en) Film-nonwoven laminate containing an adhesively-reinforced stretch-thinned film
TWM245953U (en) Breathable cloth-like film/nonwoven laminate
WO2024128229A1 (en) Nonwoven fabric laminate, stretchable nonwoven fabric laminate, fiber product, absorbent article, mask, and poultice
JP2003512193A (en) Liquid transport material for laminates of inelastic sheet layers, necked for lateral expansion and contraction
JP2001057992A (en) Fastening tape for paper diaper
CN115135498A (en) Non-blocking multilayer elastomeric compositions

Legal Events

Date Code Title Description
MM4K Annulment or lapse of a utility model due to non-payment of fees