TWI224124B - Vinyl chloride paste resin composition and disposable gloves made therefrom - Google Patents
Vinyl chloride paste resin composition and disposable gloves made therefrom Download PDFInfo
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- TWI224124B TWI224124B TW90128310A TW90128310A TWI224124B TW I224124 B TWI224124 B TW I224124B TW 90128310 A TW90128310 A TW 90128310A TW 90128310 A TW90128310 A TW 90128310A TW I224124 B TWI224124 B TW I224124B
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技術領域·· 本發明係有關 型體。更詳細說明 即可丟棄的手套( 乙烯系糊狀樹脂組 習知技術: 於一種氯乙烯系糊狀樹脂組成物及其成 之,本發明係有關於一種適於在使用後 以下稱為用後可丟棄手套)之用等的氯 成物及用後可丟棄手套。 於食品、醫療領域等所使用的在 手掌部分中央的厚度約為80〜15〇 用後可丟棄手套係指 使用後即可丟棄的手套, Ain左右的手套。TECHNICAL FIELD ... This invention relates to a body. Gloves that can be discarded in more detail (the conventional technique of vinyl paste resin group: in a vinyl chloride paste resin composition and its formation, the present invention relates to a kind of Disposable gloves) and other chlorine products and disposable gloves. The thickness in the center of the palm used in food and medical fields is about 80 ~ 15. Disposable gloves after use refer to gloves that can be discarded after use, gloves around Ain.
糊妝上:’此種用後可丟棄手套之製造係由氯乙則 斑_ ί 成物所構成’藉由將陶瓷等的手模浸入50 °c合 I占度土70^00mPa.s左右的塑料溶膠(以下稱為溶膠) 旱上來之後,去掉多餘的溶膠,凝膠化,來加以製2 的加工方法。 以往,作為用後可丟棄手套用氣乙烯系糊狀樹脂組成 物,一般係使用鄰苯二曱酸酯系塑化劑,例如鄰苯二甲酸 一辛酯(DOP )、或鄰苯二曱酸二正丁酯(DBp )等。 然而,鄰本一曱酸二辛酯(D〇p)、鄰苯二甲酸丁〒 酯(BBP )、鄰苯二曱酸二正丁酯(DBp )、鄰苯二甲酸二 正戊酯(DPP )、鄰苯二甲酸二丙酯(DpRp )、鄰苯二甲 酉欠雙環己酉曰(DCHP)、或是鄰苯二曱酸二乙酯(ρΕρ)的 鄰笨二曱酸酯被懷疑是攪亂内分泌作用的物質(即所謂的 環境苛爾蒙)’在作為用後可丟棄手套用途的食品、醫療 領域,取代這些鄰苯二甲酸酯系塑化劑而改為衛生性優良On the make-up: 'The manufacturing of disposable gloves after use is made of chloroethene_ ί 成 物' By immersing a hand mold such as ceramics at 50 ° c and I occupying about 70 ^ 00mPa.s Plastisol (hereinafter referred to as sol) After drying up, remove the excess sol, gel, and then make the 2 processing method. In the past, phthalate plasticizers, such as monooctyl phthalate (DOP), or phthalic acid, have generally been used as disposable vinyl paste resin compositions for disposable gloves for disposable gloves. Di-n-butyl ester (DBp) and the like. However, dioctyl phthalate (DO), butyl phthalate (BBP), di-n-butyl phthalate (DBp), and di-n-pentyl phthalate (DPP) ), Dipropyl phthalate (DpRp), phthalate dihydrocyclohexyl (DCHP), or phthalate diethyl phthalate (ρΕρ) is suspected to be Substances that disturb endocrine action (so-called environmental hormones) are used in food and medical fields where disposable gloves can be discarded. They replace these phthalate-based plasticizers and are highly hygienic.
2066-4480-Pf.ptd 第5頁 1224124 五、發明說明(2) 的塑化劑較佳。 特開2〇⑽— 226482號公報記載著含有聚氯乙烯 =乙醯基檸檬酸三丁酯的溶膠組成物,然而 σ勿 (ATBC) ,,9|^D〇p 加熱時容易揮發,而有成型品的硬度(1〇〇%模量)弗择4低 乍為成型ασ的特性和觸感產生變化的情形,並不户 量500另以一pW,特開昭57-3846號公報記載著,添1分子 助用,,,例如含有己二酸二辛酿的組成物 的‘劑’ !,j如單獨調配己二酸二異壬’(dina) I y ;初期凝膠化比DOP慢,在凝膠熔融時,兩 :二量二時間,而有製品厚度多發生厚薄不均的情而形。 、,右大s調配,則有發生流出液汁之傾向的問題。 ^者,所謂初期凝膠化係表示,藉由加熱而增稠,至 >谷膠^止流動為止的速度。 捫至 糊狀Ϊί: Ϊ公平〇5 —13175號公報記載著,含有聚氯乙烯 ^ 二日二乍為硬化劑、例如過苯甲酸第三丁酯所形成的 ρ 然而作為苯甲酸酯系塑化劑,例如單獨使用 祕备 (旭電化工業株式會社製)的情形,由於與氣乙 夕了 Τ,树,的可混合性良好,初期凝膠化比D0P快很 二、^黏度隨著時間改變顯著地增加,故必須對溶膠的保 =財存條件加以調整,同時也容易產生加工上的問題。 ’’合膠很容易捲入氣泡,又由於捲入的氣泡難以脫 牙、,而有手套成型時容易產生針孔的傾向。2066-4480-Pf.ptd Page 5 1224124 V. Description of the invention (2) The plasticizer is better. Japanese Patent Application Laid-Open No. 20-226482 describes a sol composition containing polyvinyl chloride = tributyl citrate, but σ (ATBC), 9 | ^ D〇p is easy to volatilize when heated. The hardness (100% modulus) of the molded product is 4 low. This is because the characteristics and feel of the molding ασ are changed. The quantity is 500 and the pW is described in JP 57-3846. Add 1 molecule to help, for example, a 'agent' that contains adipic acid dicapryle! , j such as diisononyl adipate alone (dina) I y; initial gelation is slower than DOP, when the gel is melted, two: two times two times, and there are many cases of uneven thickness of the product Shape. If you mix the right and large s, there is a problem that the juice tends to flow out. The term "initial gelation" refers to a speed at which the thickener is thickened by heating and the gluten stops flowing.扪 to paste: ΪFair No. 05-13175 describes that it contains polyvinyl chloride ^ It is a hardener, such as tert-butyl perbenzoate, which is formed by ρ. However, it is a benzoate-based plastic. Chemical agents, such as the case of using Sebeki (manufactured by Asahi Denka Kogyo Co., Ltd.) alone, have good miscibility with Titanium and Titanium, and the initial gelation is much faster than DOP. Viscosity over time The change has increased significantly, so it is necessary to adjust the security conditions of the sol, and it is also prone to processing problems. ‘’ Glue is easily entangled with air bubbles, and because the air bubbles involved are difficult to remove teeth, pinholes tend to occur during glove molding.
第6頁 1224124 ί、發明說明(3) 與用i::π ΐ在於提供-種氣乙烯系糊狀樹脂組成物 劑,保持著:π 2中係使用非鄰笨二甲酸ι系塑化 套具同等未:甲酸ι系塑化劑之用後可丢棄手 工條件來成型。 忐以習知的加工設備、方法與加 發明概述: 氯乙問胃’經不斷精心研究的結果發現,包括 化劑及苯甲由檸檬酸㈣塑化劑、己二酸醋系塑 播湖外制甲 塑化劑等3種塑化劑之中所選擇的至少2 種J化劑之虱乙烯系糊狀樹脂組成物, 的,完成本發明。 J仟从違成刚述目 輪’Π二本發明係有關於一種氣乙烯系糊狀樹脂组成 物,/、中匕括氣乙烯系糊狀樹脂及由擰 ⑴、己二酸I系塑化劑(B)及苯 二=劑 )43種塑化劑之中所選擇的2種以上的塑化劑。 對於適合的實施例係,前述塑化劑^ ^ ^ ^ ^ 與己二酸咖化劑⑴之氯乙稀 更進一步對於適合的實施例係,包括相對於 糊狀樹脂1 00重量分,由擰檬酸酯系塑化劑(A ) 5、 ’、 量%、與己二酸酯系塑化劑(B) 10〜50重量%所形〜0:t 劑5 0〜1 2 0重量分之氯乙烯系糊狀樹脂組成物。 、 對於適合的實施例係,前述塑化劑為擰檬酸 劑⑴與苯甲酸I系塑化劑(C)之氯乙稀系糊二=Page 6 1224124 ί, description of the invention (3) and the use of i :: π ΐ lies in providing-a kind of gas vinyl paste resin composition agent, maintaining: π 2 middle system uses non-ortho-benzyl dicarboxylic acid ι series plasticizing sleeve Equivalent: Formic acid ι plasticizer can be discarded by hand after molding.习 Summary of conventional processing equipment, methods, and inventions: Chloroethyl is asked by the stomach 'after careful research and found that it includes chemical agents and benzyl from citric acid, plasticizer, and adipic acid vinegar. The present invention has completed the vinyl-based paste-like resin composition of at least two types of plasticizers selected from three plasticizers such as nail plasticizers. J 仟 Congcheng Cheng's Eyeball 'II. The present invention relates to a gaseous vinyl paste resin composition, and / or a gaseous vinyl paste resin, and is plasticized by a screw, adipic acid I series. Agent (B) and Benzene = Agent) Two or more plasticizers selected from 43 plasticizers. For a suitable embodiment, the aforementioned plasticizer ^ ^ ^ ^ ^ and adipic acid chlorinating agent chloroethene is further. For a suitable embodiment, including 100 weight points with respect to the paste resin, Citric acid ester plasticizer (A) 5, ', amount%, and adipate plasticizer (B) 10 to 50% by weight ~ 0: t agent 5 0 to 1 2 0 parts by weight Vinyl chloride-based paste resin composition. For a suitable embodiment, the aforementioned plasticizer is citric acid paste ⑴ and benzoic acid I-based plasticizer (C).
1224124 五、發明說明(4) 成物。 f進#對於適合的實施例係,包括相對 糊狀树脂1GG重量分,由檸檬酸 ^氯乙烯系 量%、與苯甲酸醋系塑化劑(C) 10〜4。重〇〜90重 劑5 0〜1 2 0重量分之翕,咕/ U重里%所形成的塑化 斜於摘:二:烯系糊狀樹脂組成物。 ' σ的只軛例係,前述塑化劑為己- @ 劑⑴與苯甲酸,系塑化劑(c 广系塑化 成物。 氣乙沐糸糊狀樹脂組 更進一步對於適合的實施例係,包— ^ 量%、與苯甲酸酷系塑化劑(c)30,重 劑50~120重量分之氯乙浠系糊狀樹脂組成物。/成的』化 對於適合的實施例係’前述塑化劑為擰檬酸酯系塑化劑 (A )、己二酸S旨系塑化劑(B )、以及苯曱酸酿系塑二劑 (C )之氯乙烯系糊狀樹脂組成物。 更進一步對於適合的實施例係,包括相對於氣乙烯系 糊狀樹脂10 〇重量分,由檸檬酸酯系塑化劑(A )、己二酸 酯系塑化劑(B )、以及苯甲酸酯系塑化劑(c )所形成的 塑化劑5 0〜1 2 0重量分,至少包括此塑化劑之中的苯曱酸醋 系塑化劑(C ) 1〜40重量%之氯乙烯系糊狀樹脂組成物。 甚至,本發明係有關於一種對前述氯乙烯系糊狀樹脂 組成物施予成型所得到的用後可丟棄手套。 用以施行於本發明的最佳實施例: 本發明所使用的氯乙烯系糊狀樹脂可依照以下方法而 2066-4480-Pf.ptd 第8頁 丄々41241224124 V. Description of the invention (4) Product. f. For suitable embodiments, it includes 1 GG by weight relative to the pasty resin, 10% by weight of citric acid, vinyl chloride, and benzoate-based plasticizer (C). Weight: 0 to 90 weights; 50 to 120 weight percent; plasticization formed by g / U% by weight; oblique picking: two: olefinic paste resin composition. The σ is only a yoke example, and the aforementioned plasticizer is hexadecanol and benzoic acid, which is a plasticizer (c). It is a plasticized product. The gas resin group is further suitable for suitable embodiments. Including ^% by weight, and benzoic acid-based plasticizer (c) 30, heavy agent 50 ~ 120 parts by weight of chloroacetamidine paste resin composition. / "" For a suitable embodiment of the system " The plasticizer is composed of a citrate-based plasticizer (A), an adipic acid S-based plasticizer (B), and a phenylacetic acid-based plasticizer (C). Further, for a suitable embodiment, it includes 100 parts by weight based on 100% by weight of the gaseous vinyl-based paste resin, a citrate-based plasticizer (A), an adipate-based plasticizer (B), and The plasticizer formed by the benzoate plasticizer (c) is 50 to 120 weight percent, and at least includes the benzoate vinegar-based plasticizer (C) 1 to 40 weight. % Vinyl chloride-based paste resin composition. Furthermore, the present invention relates to a disposable glove which is obtained by subjecting the aforementioned vinyl chloride-based paste resin composition to molding. Purposes of a preferred embodiment of the present invention are: a vinyl chloride-based paste resin used in the present invention may 2066-4480-Pf.ptd 8 Shang 々 page 4124 according to the following method
體之混烯單體、或可與氯乙埽單體共聚的單 合引發劑的存ϊΐί乳化劑等的水性介”,於水溶性聚 油溶性聚合引晶種乳化聚合、或是於 由對聚合後的乳职、# / ++進仃精細懸沣聚合。其次,藉 得到的前述糊狀订=乾燥等的方法而得到。如此所 此處,若平=脂;具有平均粒徑為〇.卜5"的粒子。 勢;若平均粒_ : : “ m小’則溶膠黏度有昇高的趨 趨勢。 上 V m大,則有凝膠化、熔融速度變慢的 於氣己可與氯乙烯單體共聚的單體,通常若伟使用 t 單體’則並未特別加以限定 醚二辛=丙Ϊ、異丁烯等的稀烴類;異丁基乙晞 -乂宁&乙烯醚等的乙烯醚類等。 鼻7二為土河述氯乙稀系糊狀樹脂的聚合度,最好使射值 〜80者較佳。κ值比7〇低的樹脂,則成型品的抗拉 有降低的趨勢。且κ值比8〇高的樹脂,則有聚合生產性降" 低而成本上昇的趨勢。 此處,樹脂的Κ值之測定係依據ISO 1 628-2。 前述氯乙烯系糊狀樹脂,可單獨以氯乙烯系糊狀樹 脂、或依其需要添加氯乙烯系摻合樹脂來加以使用。 前述氯乙烯系摻合樹脂可依照以下方法而得到。首 先’對氯乙烯單體、或可與氯乙烯單體共聚的單體之混合 物’在含有高分子系懸浮穩定劑等的水性介質中,於油^ 1224124 五、發明說明(6) 性聚合引發劑的存在下進行懸浮聚合。其次,藉由對聚合 後的漿料以離心脫水機等進行脫水後,再施行氣流乾燥、 或流動乾燥的方法等而得到。如此所得到的前述摻合樹 月曰’具有平均粒徑為1 〇〜7 m的粒子。此處,若平均粒徑 比10 小’則在工業生產上有困難的傾向;若平均粒徑 比7 0 // m大’則在低黏度溶膠中容易發生沈降,而有凝膠 化I溶融速度變慢的趨勢。如此所得到的前述氣乙烯系摻 合树月曰’以糊狀溶膠的流動性之改良等為目的,依需要合 併使用前述氣乙烯系糊狀樹脂。 作為氯乙烯系摻合樹脂的聚合度,最好使用K值為 〜7 0者較佳。若κ值比6 〇低,則抗拉強度有降低的趨勢; 右Κ值j;b70^高,則有凝膠化、熔融速度變慢的趨勢。 則述氯乙稀系糊狀樹脂與前述氯乙烯系摻合樹脂係, 自以往即廣為使用,各種等級的產品可從市場取得, 發明中可使用任一種。 — 八本發㈣塑㈣’相料前I氣乙料、糊狀樹 二旦 里刀,使用50〜120重量分較佳、而70〜100重量分 黏;而t I右Ϊ化劑量比5〇重量分少,則為了調整到加工 傾;。;此很多稀釋劑,甚至發生成型品有變硬的問題之 孔致不良率增: = 變薄、變$,由於製品產生針 1 20重量分,日則由於制有°口貝力化的傾向。相反地,若超過 有製品價值劣化的傾\品強度㈣和流出塑化劑液汁,而 對於本發明,作Α 下為則述塑化劑,由擰檬酸酯系塑化劑(ΑAqueous media such as mixed monomers or monomers that can be copolymerized with chloroacetin monomers, emulsifiers, etc., are used in emulsion polymerization of water-soluble poly-oil-soluble seed crystals, or After the polymerization, the lactate and # / ++ are finely suspended and polymerized. Secondly, it can be obtained by the method of the aforementioned paste preparation = drying, etc. So here, if flat = fat; it has an average particle size of 0. The particles of Bu 5 "potential; if the average particle _ :: "m is small," the viscosity of the sol tends to increase. If the upper V m is large, there are monomers that can be copolymerized with vinyl chloride monomers that gel and slow down the melting rate. Generally, if t monomers are used, the ether dioctane = propane is not particularly limited. , Isobutylene and other dilute hydrocarbons; isobutyl acetofluorene-pentin & vinyl ethers and other vinyl ethers. No. 72 is the degree of polymerization of Tuheshu's vinyl chloride paste resin. It is best to have a shot value of ~ 80. Resins having a lower κ value than 70 will tend to reduce the tensile strength of the molded product. In addition, resins with a higher κ value than 80 have a tendency to decrease polymerization productivity and increase costs. Here, the K value of the resin is measured in accordance with ISO 1 628-2. The vinyl chloride-based paste resin may be a vinyl chloride-based paste resin alone or a vinyl chloride-based blend resin may be added as needed. The vinyl chloride-based blend resin can be obtained by the following method. First, 'p-vinyl chloride monomer, or a mixture of monomers copolymerizable with vinyl chloride monomer', in an aqueous medium containing a polymer-based suspension stabilizer, etc., in oil ^ 1224124 V. Description of the invention (6) Initiation of sexual polymerization Suspension polymerization is performed in the presence of an agent. Next, it is obtained by dehydrating the polymerized slurry with a centrifugal dehydrator or the like, and then performing a method such as air drying or flow drying. The aforementioned blended tree obtained as described above has particles having an average particle diameter of 10 to 7 m. Here, if the average particle diameter is smaller than 10 ', it tends to be difficult in industrial production; if the average particle diameter is larger than 7 0 // m', sedimentation easily occurs in a low viscosity sol, and gelation I melts. Slower trend. The aforesaid gaseous vinyl-based blended tree is used in combination with the gaseous vinyl-based pasty resin as necessary for the purpose of improving the fluidity of the pasty sol. As the polymerization degree of the vinyl chloride-based blended resin, a K value of ~ 70 is preferably used. If the κ value is lower than 60, the tensile strength tends to decrease; the right K value j; b70 ^ higher, there is a tendency for gelation and slower melting speed. Then, the vinyl chloride-based paste resin and the vinyl chloride-based blended resin system have been widely used in the past. Various grades of products can be obtained from the market, and any of them can be used in the invention. — Babenfa ㈣ plastic ㈣ 相 相 I gas, B material, paste tree two denier knife, the use of 50 ~ 120 weight points is better, and 70 ~ 100 weight points are sticky; and t I the right belching dose ratio is 5 〇If the weight is small, it is tilted for processing. ; Many thinners, even the hardened holes of the molded product cause the defective rate to increase: = thinner and thinner, because the product produces needles of 20 weight points, and because of the tendency of the mouth to become forceful. . Conversely, if it exceeds the strength of the pour product with the deterioration of the value of the product and the outflow of the plasticizer juice, for the present invention, the plasticizer is described as A below, and the citric acid ester-based plasticizer (Α
翌化劑之中所選擇的至 人^现阳尔塑化劑(c J塑化劑之中,僅調配任“重^其ti種來加以使用。這 去達到所預期的目的。 虱乙烯系糊狀樹脂,並無 作為前述檸檬酸酯系塑化_ , 1出:例如,檸檬酸三乙5旨1 °並未特別限定。可 -夂一乙酯、乙醯基擰檬酸三豕s夂一丁 s日、乙醯基檸檬 基己酯、乙醯基擰檬酸—正其曰、乙醯基檸檬酸三-2-乙 酯、或檸檬酸三硬脂醯酯等。土六酯、檸檬酸二硬脂醯 低揮發性及適度的凝膠化、卜^ f ’以顯不加熱加工時的 用乙醯基檸檬酸三丁酯(ATB^ 2特性的觀點看來,適於使 作為前述己二酸酯♦朔 可 舉出:例如,己二酸雙二2—背彳(B)並未特別限定 壬酯(DINA)、己二酸二異八\己酯(D0A)、己二酸二 辛酯正癸酯(N〇DA)等。^酉曰、(DID一A)、或己二酸一 j 發性及適度的凝膠化、炫上:’以顯示加熱加工時的低 二酸二異壬酯(DINA )。田、性的觀點看來,適於使用 作為前述苯甲酸酯系塑化 舉出:例如,一裣-系f d d )並未特別限定。刁 酷、或」甘醇二Ϊ;::醇:Γ”、,甘醇二苯甲 化較小的觀點看來,單獨使用’、以:膠的黏度隨時間 土口口車二佳#為則述—縮二丙二醇二苯甲酸醋,具體而 a ,有ΡΝ-6120 (旭電化工業製)、Benz〇fiex9^ (Velsicol 社製)等。 、發明說明⑻ (这使用擰檬酸酯系塑化劑(A )、及己二酸酯系塑化1 套)作為前述塑化劑,顯示與使用DOP的用後可丟棄手" 迷斤於製造時具同樣的溶膠黏度隨時間變化、初期凝膠 、X、及物性的特點,故較佳。 > 匕 (A作為這些塑化劑的調配比,係前述擰檬酸酯系塑化 量% 5 〇〜9 〇重量%、前述己二酸酯系塑化劑(B ) 1 0〜5 0重" 重量。而塑化劑(A) 60〜70重量%、塑化劑(B) 3〇〜4〇 少,°目則、更佳。若前述擰檬酸酯系塑化劑U )比50重旦0/ 則溶m初期凝膠化有變慢的傾向。並且若超過90重量°Γ,0 己- I黏度隨時間變化有增大,製品變硬的傾向。甚& ‘以塑r"B)比㈣量”,則溶膠:度;= 初期;::有= 傾向。並且若超™": 化劑^者),作使:」寧檬酸咖化劑(A)、苯⑷^ 快、且牟Λ :述塑化劑,則從可得到初期凝膠化較 配比,| =品之觀點看來較佳μ乍為這些塑化劑的, 本甲酸I系塑化劑(c) 10〜40重旦二ϋ 90重“、前述 70,重《、塑化劑(C)20〜3〇r量^更:塑化劑(Α) 檬酸I系塑化劑(Α)比6。重 ,則二佳。若前述檸 化有增大的趨勢。並且若超過9〇ί量;隨時間變 傾向。若前述笨甲酸I系塑化劑(則有2品變硬的 製品變硬的傾向。並且若超過里/:少,則有 較快、黏度隨時間變化有稍微增大二勢則有順膝化Among the plasticizers, the most suitable plasticizer (cJ plasticizers, only the "heavy ti species" are used. This will achieve the intended purpose. Vinyl lice Pasty resin, not as the aforementioned citrate-based plasticization, 1 output: For example, triethyl citrate is not specifically limited to 1 °. May be-ethyl acetate, ethyl ethyl triacetate N-butanes, Ethyl-Limonylhexyl, Ethyl-L-Citrate—Ortho-Ethyl, Tri-2-Ethyl-Ethyl Citrate, or Tristearyl Citrate, etc. , Low volatility and moderate gelation of distearyl citrate, and ^ f 'from the point of view of the characteristics of using butyl ethyl tributyl citrate (ATB ^ 2 when showing no heat processing), suitable for Examples of the aforementioned adipic acid ester include, for example, adipic acid di-di-2-dipicium (B) is not particularly limited to nonyl ester (DINA), diisooctadecyl adipate (DOA), Dioctyl dioctyl n-decyl ester (NODA), etc. ^ 酉, (DID-A), or adipic acid-j hair and moderate gelation, dazzling: 'to show the heat processing Diisononyl disorate (DINA). From the viewpoint of Tian and Xing, it is suitable to use as the aforementioned benzoate-based plasticizing. For example, mono-fd) is not particularly limited. Diaoku, or "Glycol Di:;: Alcohol: Γ ”, from the standpoint of small glycol dibenzoylation, the use of alone, to: the viscosity of the glue over time Tukoukouche Erjia # is described as dipropylene glycol dibenzoate, specifically a There are PN-6120 (manufactured by Asahi Denka Kogyo Co., Ltd.), Benzofiex 9 ^ (manufactured by Velsicol), etc., description of the invention (this uses citrate plasticizer (A), and adipate plasticization 1 set) As the aforementioned plasticizer, it is better to display the same sol viscosity change with time, initial gel, X, and physical properties as the plasticizer that can be discarded after use with DOP. > D (A is the blending ratio of these plasticizers, based on the above-mentioned citrate-based plasticizing amount% 50 to 90% by weight, and the aforementioned adipate-based plasticizer (B) 1 0 to 50. Weight " Weight. While the plasticizer (A) is 60 to 70% by weight and the plasticizer (B) is 30 to 40% less, it is even better. If the aforementioned citrate plasticizer U ) Than 50 / denier than 0 /, the initial gelation tends to slow down. If it exceeds 90 weight ° Γ, the viscosity of 0H-I increases with time, and the product tends to become hard. Even & ' In order to measure the ratio of r " B), the sol: degree; = initial stage; ::: have = tendency. And if Ultra ™ ": 化 剂 ^ 者), make: "Limonate (A), Benzene ^ ^ fast, and Mou: said plasticizer, from the initial gelation can be obtained from From the point of view of the ratio, it is better that μ is for these plasticizers. The formic acid I-based plasticizer (c) 10 ~ 40 dwt. 90% d, 70 d. The amount of the agent (C) is 20 ~ 30r. More: the plasticizer (A) citric acid I-based plasticizer (A) is heavier than 6. The second best. If the aforementioned citration has a tendency to increase. And Over 9〇ί amount; tends to change with time. If the aforementioned stearic acid I-based plasticizer (there are 2 products that become hard, the product tends to become hard. And if it exceeds lin /: less, it has a faster, viscosity with time The change is slightly increased and the second trend is smooth
2066-4480-Pf.ptd 第12頁 1224124 五、發明說明(9) 並且,使用己二酸酯系塑化劑⑴、苯甲酸 化劑(c)作為塑化劑,顯示與使用D0P的用後可丟棄手 套,於製造時具同樣的溶膠黏度隨時間變凝 速度、雜的特點,故較佳。作為這些塑化;=化 比,係刖述己一酸酯系塑化劑(B) i 0〜7〇重量%、 甲酸酯系塑化劑(C ) 30〜90重量%較佳。而塑化' 30〜60重量%、塑化劑(c)4〇〜7〇重量%則更佳。二/ (B)比1〇重量%少,則溶膠黏度隨刖時間變 化有增大的趨勢。並且,若超過7〇重量%,則初 有變慢的傾向。若前述苯曱酸醋系塑化劑(c)比3〇請 少二貝:“刀期ΐ t化有變慢的傾向。並且若超過9〇重量%, 則溶膠黏度隨時間變化有增大的趨勢。 同時,使用檸檬酸酯系塑化劑(A )、己二酸酯系塑 =用(=的:ΐ甲酸醋系塑化劑(C)作為塑化劑,顯示 度隨時間變化、,時具同樣的溶膠黏 α) Iρ - ^ /的凋比,係刖述檸檬酸酯系塑化劑 二=一二=二,◦一、苯甲 )—的合計…量%、塑化劑= 的口口卞比6 〇重1 % /丨、 目|、、众柳 丁 墊。甘0 則,合膠黏度隨時間變化有增大的趨 度較:且=:9;巧V:1有無法得到初期凝 、、製13口之傾向。若前述苯甲酸酯系塑化劑2066-4480-Pf.ptd Page 12 1224124 V. Description of the invention (9) In addition, the adipate-based plasticizer ⑴ and benzoate (c) are used as plasticizers to show and use DOP after use. Disposable gloves are preferred because they have the same sol viscosity and time-varying variability during manufacturing. As these plasticization ratios, the adipate-based plasticizer (B) i is 0 to 70% by weight, and the formate-based plasticizer (C) is preferably 30 to 90% by weight. On the other hand, it is more preferable that the plasticizing agent is 30 to 60% by weight and the plasticizer (c) is 40 to 70% by weight. If (b) is less than 10% by weight, the sol viscosity tends to increase with time. In addition, if it exceeds 70% by weight, it tends to be slow at first. If the phenyl acetic acid vinegar-based plasticizer (c) is less than 30, please say: "The blade period tends to become slower. If it exceeds 90% by weight, the sol viscosity will increase with time. At the same time, the use of citrate-based plasticizer (A), adipate-based plastic = = (=: acetic acid-based vinegar-based plasticizer (C) as plasticizer, the degree of display changes with time, , With the same sol viscosity α) Iρ-^ / withering ratio, which is the citrate plasticizer two = one two = two, ◦ one, benzyl)-total amount, plasticizer = 口 口 卞 1% heavier than 6 〇 / 丨, mesh | ,, zhongliutian pads. Gan 0, the glue viscosity tends to increase with time compared with: and =: 9; Q V: 1 There is a tendency that the initial coagulation cannot be obtained, and 13 mouths are prepared. If the benzoate plasticizer is used
12241241224124
五、發明說明(10) (C ) 比1重量%低,則右| & _ 、有…去侍到初期凝膠化速度較快、 且柔軟的製品之傾向。祐η 4 1 間變化有稍獨大的趨勢。右超過40重量°/°,則黏度隨時 後可ii手ί:Γ: 2稀“則脂組成物能夠作為用 糊狀樹脂、與前述塑化巧之^種情形,除了前述氯乙缚系 的^疋劑、稀釋劑、及苴仙 丨尺用 疋这樣的调配則無特別的限制。 要 =稀釋劑並未特別限定。例如,能夠使用4_: 或正烷烴等 甲基1,3戊一醇一異丁酸酯(τ $ I b / 、寸。 同時」前述穩定劑並未特別限定\例^如—能y·使用 Ca-ZMt疋劑Ba_Zn穩定劑、以穩定劑等。 氧化ίί,=加劑並未特別限定。例>,能夠使用環 對於* ^乳亞麻仁油、或環氧化脂肪酸烷基酯等。 所傕用的^明的氯乙烯系糊狀樹脂組成4勿,添加本發明 =力:述塑化劑’…本發明的效果所發現的範圍 :的塑化劑來使用。而使用其他塑化劑的情 為30重:乙烯系糊狀樹脂100重量/分,該添加量 下:而20重量分以下較佳,10重量分以下則 脂100重W、他塑化劑的添加量,相對於氯乙烯系糊狀樹 & 0 .θ Α里/,若超過30重量分,則有無法保持具較佳特 性的混t塑化劑系的平衡之傾向。 住特 菸明ΐ ΐ:雖基於實施例來對本發明加以詳細說明,作本 發明並不党限於以下實施例。 彳-本5. Description of the invention (10) (C) is lower than 1% by weight, then the right | & _, there is a tendency to ... wait for the initial gelation speed and soft products. You η 4 1 has a slightly dominant change. If the weight is more than 40 °° / °, the viscosity can be used at any time. Γ: 2: Dilute "The lipid composition can be used as a paste resin and plasticized with the above-mentioned cases. ^ Elixir, diluent, and blending agents are not particularly limited. It is not limited. For example, diluents are not particularly limited. For example, methyl 1,3 pentane, such as 4_: or n-alkane can be used. Alcohol-isobutyrate (τ $ I b /, inch. At the same time, the aforementioned stabilizer is not particularly limited. For example ^ can use Ca-ZMt tincture Ba_Zn stabilizer, stabilizer, etc. Oxidation, = Additives are not particularly limited. Examples > Rings can be used. ^ Milk linseed oil, or epoxidized fatty acid alkyl esters, etc. The used vinyl chloride-based paste resin composition 4 does not need to be added. The present invention = force: the plasticizer '... The scope of the effect of the present invention: the use of plasticizers. The use of other plasticizers is 30 weight: vinyl paste resin 100 weight / minute, the Under the amount of addition: 20 weight points or less is preferred, fat weight is less than 100 weight W, the amount of other plasticizers, relative to ethyl chloride It is a paste-like tree & 0 .θ Α /, and if it exceeds 30% by weight, there is a tendency that the balance of a mixed plasticizer system with better characteristics cannot be maintained. The present invention will be described in detail, and the present invention is not limited to the following embodiments.
二叶丄厶1Two-leaf cormorant 1
用後可丢畢丰;^ / 入由氯乙烯系糊狀樹脂組成=:由將陶兗等的手模浸 後,去掉多餘的溶膠,凝膠化=的溶膠中,拿上來之 以f诰。而斟士政Q " b 基於此製造加工方法來加 法來製造。此時,t述、容豚的:f手#,也可猎由前述方 70~ 3 0 0mPa ^ 膠的黏度係,在5 0 t:的黏度為 掇的〜跌右代工 若黏度比7〇mPa. s低,則附著於手 : = 少的傾向。同時,若超過3〇〇mPa.s,則附著 於手极的浴膠有過多的傾向。 「塑料溶膠之製作方法」 對於以稀釋劑作黏 進行減壓下靜置脫 所使用的塑化劑顯 對顯示於第1表的調配進行混煉, 度調整,大約作成同樣黏度的試樣, 泡,破泡後5分鐘,得到溶膠。再者, 示於第2表。 於IS02555的布魯克菲 添加稀釋劑以使實施例 再者’初期黏度的調整係,基 爾德型旋轉黏度計的表觀黏度值, 與比較例都在1 8 0〜2 1 0的範圍内。Bi Feng can be thrown after use; ^ / Composed of vinyl chloride-based paste resin =: After dipping a hand mold such as Tao Yan, remove excess sol, gel = = sol, take it as f 诰. And Qushizheng Q " b based on this manufacturing processing method to add manufacturing. At this time, the following description and the content of the dolphin: f 手 # can also be used to calculate the viscosity of the aforementioned 70 ~ 300 mPa ^ glue, at 50 t: the viscosity is 〜 ~~ if the viscosity is lower than 7 〇mPa. S is low, then adhere to the hand: = tendency to less. At the same time, if it exceeds 300 mPa.s, the bath gel adhered to the hand electrode tends to be excessive. "Production method of plastisol" For the plasticizer used under the reduced pressure to stand and remove under reduced pressure, the blending shown in Table 1 is kneaded, and the degree is adjusted to make a sample of approximately the same viscosity. After foaming, 5 minutes after foam breaking, a sol was obtained. The results are shown in Table 2. In Brookfield, IS02555, a diluent was added to adjust the initial viscosity of the examples. The apparent viscosity values of the Kildell type viscometer and the comparative examples are all in the range of 180 to 210.
2066-4480-Pf.ptd 第15頁 1224124 五、發明說明(12) 第1表 氯乙唏糊狀樹脂 C鐘淵化學工業株式會社製,PSM-71 CK值= 72)〕 100重量分 塑化劑 C參照第2表〕 9〇重量分 Ca-Zn穩定劑 (旭電化工業株式會社絜,AC-311〕 3重量分 環氡化豆油 C旭電化工業株式會社絜,〇·13〇Ρ〕 3重量分 稀釋劑(ΤΧΙΒ) (協和發酵工業株式舍社製,牛3 —y —儿D〕 記載於各表中 第2表 DOP 鄰苯二甲酸二辛酯 協和發酵工業株式會社製 ATBC (檸檬酸系) 乙醯基檸檬酸三丁酯 三建化工株式會社製 DINA (已二酸系) 已二酸二異壬酯 三建化工株式會社絜 PN-6120 (苯曱酸系) 一縮二丙二醇二苯甲酸酯 ------------ ^一 旭電化工業株式會社絜 ———__^^2066-4480-Pf.ptd Page 15 1224124 V. Description of the invention (12) Table 1 Chloroacetam paste resin C Zhongyuan Chemical Industry Co., Ltd., PSM-71 CK value = 72)] Plasticized by 100 parts by weight For agent C, refer to Table 2.] 90% by weight Ca-Zn stabilizer (Asahi Denka Kogyo Co., Ltd., AC-311) 3% by weight Cyclofluorinated soybean oil C Asahi Kagaku Kogyo Co., Ltd., 0.13P] 3 Weight Diluent (TXIB) (produced by Kyowa Fermentation Co., Ltd., cattle 3 — y — er D) is described in Table 2 of each table. DOP Dioctyl phthalate Kyowa Fermentation Co., Ltd. ATBC (Citric acid System) Diethyl Acetyl Tributyl Citrate Sanjian Chemical Co., Ltd. (Adipic acid) Diisononyl adipate Sanjian Chemical Co., Ltd. 絜 PN-6120 (Phenylacetic acid) Dipropylene glycol two Benzoate ------------ ^ Yi Asahi Chemical Industry Co., Ltd. 絜 ————__ ^^
「黏度測定方法 塑料溶膠的黏度係基於IS025 5 5的布魯克菲爾德絮旋 轉黏度計的表觀黏度之測定方法。測定溫度係以用後 < 委"Viscosity measurement method The viscosity of plastisol is based on the apparent viscosity of a Brookfield flocculation viscometer based on IS025 5 5. The temperature is measured after use <
2066-4480-Pf.ptd 第16頁 山4124 五、發明說明(13) 棄手套的平均實際加工溶膠溫度501來加以實施,測定i =時後、24小時後、及48小時後轉速12rpm的值,算出表 觀黏度(mPa.s)。 「抗拉強度測定方法」 將前述所調整的溶膠塗布約20 0 /^m的厚度於2mm厚的 ^板上。其次’用烘箱於2()(rc進行5分鐘凝膠化,以傳 j方法製作薄片。使用前述薄片依照JIS〖7113的規定製 :::形jis 3號試片’使用高壓爸,以20 0mm/分的測試 (' %、) ?則定1 〇 〇%模量(Mpa )、抗拉強度(Mpa )及拉伸率 「初期凝膠化性測定方法」 —eome t er AR5 Ο Ο (ΤΑ Instruments社製)來 ,二同/皿(9 5 C )時的黏度變化,評估初期凝膠化的逮 慢)。 · 塑化劑單獨調配的特性如第3表所示。2066-4480-Pf.ptd Page 16 Mt. 4124 V. Description of the invention (13) The average actual processed sol temperature 501 for discarded gloves is implemented. Measure i = 12 hours, 24 hours, and 48 rpm after 48 hours. , Calculate the apparent viscosity (mPa.s). "Tensile strength measurement method" The adjusted sol was coated with a thickness of about 20 0 / ^ m on a 2mm thick plate. Next, 'use gel in 2 () (rc for 5 minutes to gelate, and use the method described in JIS [7113 ::: shape jis No. 3 test piece] to make sheets using the aforementioned sheet. Test at 0mm / min ('%,)? Set 100% modulus (Mpa), tensile strength (Mpa), and elongation "evaluation method of initial gelation" —eome t er AR5 Ο Ο (ΤΑ (Produced by Instruments), the viscosity change at the same time (95 C), to evaluate the slowness of the initial gelation). · The characteristics of the plasticizer alone are shown in Table 3.
1224124 五、發明說明(14) 第3表 _^ 比較例 1 2 3 4 調 DOP 90 _ _ — 配 ATBC〔檸檬酸系〕 —— 90 — 一 重 量 分 DINA〔已二酸系) — _ 90 一 PN-6120 (苯甲酸系〕 — _ — 90 〔稀釋劑) 20 7 0 25 黏 1小時 180 190 180 200 度 24小時 270 370 190 1020 牝小時 340 520 200 無法測定 初期凝膠化 Δ 〇 X ◎ 物 100〇罐量 4.4 6.7 4.6 4.5 性 抗拉強度 16.0 19.7 13.3 18.8 拉伸率 445 359 414 393 若與比較例1的DOP調配相比較,則比較例2的^队單 獨調配具有用以調整黏度的稀釋劑量較少、初期凝膠化亦 較快的優點;但1 00%模量物性較高,而成為硬薄片。比較 例3的D I N A單獨調配也是同樣地,具有用以調整黏度的稀 釋劑量較少、且黏度隨時間變化較小的優點,但初期凝膠 化非常慢,且抗拉強度降低。同時,比較例4的pN_612〇單 獨凋配具有初期凝膠化非常快、抗拉強度較高的優點, 黏度隨時間變化非常大。 ATBC與DINA的混合調配系的特性如第4表所示。1224124 V. Description of the invention (14) Table 3 _ ^ Comparative Example 1 2 3 4 Adjust DOP 90 _ _ — With ATBC [Citric acid system] —— 90 — One weight cent DINA [Adipic acid system] — _ 90 A PN-6120 (benzoic acid series) — _ — 90 [thinner] 20 7 0 25 Sticky for 1 hour 180 190 180 200 Degree 24 hours 270 370 190 1020 Hour 340 520 200 Unable to measure initial gelation Δ 〇X ◎ 100 OO tanks 4.4 6.7 4.6 4.5 Tensile strength 16.0 19.7 13.3 18.8 Elongation 445 359 414 393 If compared with the DOP formulation of Comparative Example 1, the ^ team of Comparative Example 2 alone has a dilution for adjusting viscosity It has the advantages of less dosage and faster initial gelation; however, its 100% modulus has higher physical properties and becomes a hard sheet. The same formulation of D I N A in Comparative Example 3 also has the advantages of less diluent for adjusting viscosity and less change in viscosity with time. However, the initial gelation is very slow and the tensile strength decreases. At the same time, pN_612 of Comparative Example 4 alone has the advantages of very fast initial gelation and high tensile strength, and the viscosity changes greatly with time. The characteristics of the mixed deployment system of ATBC and DINA are shown in Table 4.
2066-4480-Pf.ptd 第18頁 1224124 五、發明說明(15) 第4表 實施例 1 2 3 調 配 重 量 分 ATBC (檸檬酸系〕 60 45 30 DINA〔已二酸系〕 30 45 60 ΡΝ·612〇〔苯甲酸系〕 — — 一 ΤΧΙΒ (稀釋劑〕 1 1 0 黏 度 1小時 210 210 200 24小時 310 280 260 48小時 380 330 290 初期凝膠化 〇 〇 Δ 物 性 100%^ 量 4.6 4.5 4.4 抗拉強度 15.9 15.2 14.6 拉伸率 407 403 412 實施例1、2具有與DOP單獨調配同等程度的物性、且 初期凝膠化快。並且,如實施例3,若D I NA的比率增加, 則初期凝膠化比DOP單獨調配有稍微變慢的傾向。然而, 與比較例相比,則改善效果相當顯著。 ATBC與PN-6120的混合調配系的特性如第5表所示。2066-4480-Pf.ptd Page 18 1224124 V. Description of the invention (15) Example of Table 4 1 2 3 Formulation weight ATBC (Citric acid) 60 45 30 DINA [Adipic acid] 30 45 60 PN · 612〇 [benzoic acid type] — — TTXIB (diluent) 1 1 0 viscosity 1 hour 210 210 200 24 hours 310 280 260 48 hours 380 330 290 initial gelation 〇〇Δ physical properties 100% ^ amount 4.6 4.5 4.4 anti Tensile strength 15.9 15.2 14.6 Elongation 407 403 412 Examples 1 and 2 have the same physical properties as DOP alone, and the initial gelation is fast. Also, as in Example 3, if the ratio of DI NA increases, the initial setting The gelation tends to be slightly slower than the DOP formulation alone. However, the improvement effect is quite significant compared to the comparative example. The characteristics of the mixed formulation system of ATBC and PN-6120 are shown in Table 5.
2066-4480-Pf.ptd 第19頁 1224124 五、發明說明(16) 第5表 實施例 4 5 6 調 配 重 量 分 ATBC〔檸檬酸系〕 60 70 45 DINA (已二酸系〕 — — — ΡΝ-όΠΟ〔苯曱酸系〕 30 20 45 ΤΧΙΒ (稀釋劑〕 12 10 20 黏 度 1小時 180 190 190 24小時 390 360 450 48小時 570 500 690 初期凝膠化 ◎ ◎ ◎ 物 性 100贿量 5.0 5.1 4.3 抗拉強度 16.7 17.8 16.0 拉伸率 404 429 409 實施例4、5也具有與DOP單獨調配同等程度的物性、 且初期凝膠化快。並且,如實施例6,若PN-6120的比率增 加,則初期凝膠化快而黏度的隨時間變化有稍微增大的傾 向。然而,與比較例、特別是比較例3、4相比,則改善效 果相當顯著。 DINA與PN-6 120的混合調酉己系的特性如第6表所示。2066-4480-Pf.ptd Page 19 1224124 V. Description of the invention (16) Example 5 of Table 4 5 6 Formulation weight ATBC [Citric acid] 60 70 45 DINA (Adipic acid) — — — PN- όΠΟ [Benzene acid system] 30 20 45 ΤΙΙΒ (thinner) 12 10 20 Viscosity for 1 hour 180 190 190 24 hours 390 360 450 48 hours 570 500 690 Initial gelation ◎ ◎ ◎ Physical properties 100 5.1 5.0 4.3 Strength 16.7 17.8 16.0 Elongation 404 429 409 Examples 4 and 5 also have the same physical properties as the DOP alone, and the initial gelation is fast. As in Example 6, if the ratio of PN-6120 increases, the initial The gelation is fast and the viscosity tends to increase slightly with time. However, compared with Comparative Examples, especially Comparative Examples 3 and 4, the improvement effect is quite significant. DINA mixed with PN-6 120 The characteristics of the system are shown in Table 6.
2066-4480-Pf.ptd 第20頁 1224124 五、發明說明(17) 第6表 實施例 7 8 9 調 配 重 量 分 ATBC〔檸檬酸系〕 — — — DINA〔已二酸系〕 50 60 70 PN —6120〔苯甲酸系〕 40 30 20 TXIB (稀釋劑〕 8 5 3 黏 度 1小時 190 200 200 24小時 340 290 250 48小時 400 320 280 初期凝膠化 〇 Δ Δ 物 性 100〇嫌量 4.5 4.3 4.4 抗拉強度 15.5 15.0 14.0 拉伸率 419 413 416 實施例7、8係黏度隨時間變化較小,物性也與DOP具 同等程度。並且,如實施例9,若D I NA的比率增加,則初 期凝膠化比DOP單獨調配有稍微變慢的傾向。然而,與比 較例相比,則改善效果相當顯著。 ATBC、 DINA、PN-6120的三種混合調配系的特性如第 7表所示。2066-4480-Pf.ptd Page 20 1224124 V. Description of the invention (17) Example of Table 6 7 8 9 Formulation weight ATBC [Citric acid system] — — — DINA [Adipic acid system] 50 60 70 PN — 6120 [benzoic acid type] 40 30 20 TXIB (diluent) 8 5 3 Viscosity 1 hour 190 200 200 24 hours 340 290 250 48 hours 400 320 280 Initial gelation 〇Δ Δ Physical properties 100 〇Amount 4.5 4.3 4.4 Tensile resistance Strength 15.5 15.0 14.0 Elongation 419 413 416 The viscosity changes of Example 7 and 8 with time are small, and the physical properties are similar to DOP. Also, as in Example 9, if the ratio of DI NA is increased, the initial gelation It tends to be slightly slower than the DOP alone. However, compared with the comparative example, the improvement effect is quite significant. The characteristics of the three mixed deployment systems of ATBC, DINA, and PN-6120 are shown in Table 7.
2066-4480-Pf.ptd 第21頁 1224124 五 、發明說明(18) 第7表 調配$15黏度2066-4480-Pf.ptd Page 21 1224124 V. Description of the invention (18) Table 7 Blend $ 15 viscosity
ATBC〔檸檬酸系〕 -------- DINA (已二酸系〕 PN —6U0〔苯甲酸系1 ΐ™〔稀釋劑〕 ~ 1小時 24小時 48小時 初期凝膠化 100%^ 量 40 620 性 抗拉強度 拉伸率 404 425 421 物性實=也具有與_單獨調配同等程度的 的比率增加,則黏产隨日,門你仆古=知例12,若PN—6120 干曰 〜柘度W日守間變化有稍微增大的傾向。麸 :著與比較例、特別是比較例3、4相比,則=果;目當 因而’使用如實施例所示的調酉 狀樹脂組成物的情形,不♦ I 4仟至]的虱乙烯糸糊 變,而η二對加工條件等作大幅的改 ί紫:=:件具有與,調配同等品質的製品。 產業上的可利用性: V衣口 第22頁 2066-4480-Pf.ptd 1224124 五、發明說明(19) 本發明的氯乙烯系糊狀樹脂組成物係,使用衛生性優 良的非鄰苯二甲酸酯系塑化劑、具有與使用鄰苯二甲酸酯 系塑化劑的用後可丟棄手套同等的物性、且能夠在習知的 加工條件下成型者。ATBC 〔Citric acid type〕 -------- DINA (Adipic acid type) PN — 6U0 [Benzoic acid type 1 ΐ ™ [Diluent] ~ 1 hour 24 hours 48 hours Initial gelation 100% ^ Amount 40 620 Tensile strength tensile elongation rate 404 425 421 Physical property = also has the same increase in the ratio of _ alone deployment, then the viscous yield with the day, the door you serve = = Example 12, if PN-6120 dry ~ The degree of change in temperature between W and S tends to increase slightly. Bran: Compared with the comparative examples, especially comparative examples 3 and 4, then = = fruit; therefore, the use of the spoon-like resin as shown in the examples In the case of the composition, the vinyl acetate paste does not change, but η2 greatly changes the processing conditions, etc .: =: The product has the same quality as that of the product. Industrially available Properties: V clothing port Page 22 2066-4480-Pf.ptd 1224124 V. Description of the invention (19) The vinyl chloride-based paste resin composition of the present invention uses a non-phthalate plastic with excellent hygiene. Chemical agent, has physical properties equivalent to disposable gloves using phthalate plasticizer, and can be used under known processing conditions Type person.
2066-4480-Pf.ptd 第23頁2066-4480-Pf.ptd Page 23
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JP2005290022A (en) * | 2004-03-31 | 2005-10-20 | Kanto Leather Co Ltd | Vinyl chloride-based resin paste for decorative sheet |
CN1810884B (en) * | 2006-02-20 | 2010-05-12 | 佛山市南海区黄歧顺隆化工塑料有限公司 | Enviroment friendly plasticizer |
JP4832131B2 (en) * | 2006-03-23 | 2011-12-07 | オカモト株式会社 | PVC gloves |
JP4908888B2 (en) * | 2006-03-23 | 2012-04-04 | オカモト株式会社 | PVC gloves |
CN101376731B (en) * | 2008-10-08 | 2011-04-06 | 郑建明 | PVC gloves production method using non-o-benzene plasticiser |
JP5487802B2 (en) * | 2009-08-21 | 2014-05-14 | 横浜ゴム株式会社 | Pneumatic tire |
EP2354172B1 (en) * | 2010-02-08 | 2012-11-21 | LANXESS Deutschland GmbH | Phthalate-free isocyanurate preparations |
CN102417675A (en) * | 2011-09-23 | 2012-04-18 | 安徽万朗磁塑集团有限公司 | Novel green environmental protection antibacterial door gasket rubber jacket material formula and preparation method |
CN104704077A (en) * | 2012-02-14 | 2015-06-10 | 艾黙罗德卡拉玛化学品公司 | Monobenzoate useful as a plasticizer in adhesive preparations |
JP6148563B2 (en) * | 2013-07-31 | 2017-06-14 | リケンテクノス株式会社 | Medical radiation sterilized vinyl chloride resin composition and medical device comprising the same |
JP6148564B2 (en) * | 2013-07-31 | 2017-06-14 | リケンテクノス株式会社 | Medical radiation sterilized vinyl chloride resin composition and medical device comprising the same |
JP6148566B2 (en) * | 2013-08-01 | 2017-06-14 | リケンテクノス株式会社 | Medical radiation sterilized vinyl chloride resin composition and medical device comprising the same |
JP6148565B2 (en) * | 2013-08-01 | 2017-06-14 | リケンテクノス株式会社 | Medical radiation sterilized vinyl chloride resin composition and medical device comprising the same |
US10407559B2 (en) | 2014-03-27 | 2019-09-10 | New Japan Chemical Co., Ltd. | Plasticizer for vinyl chloride resin containing non-phthalate ester and vinyl chloride resin composition containing such plasticizer |
JP6343473B2 (en) * | 2014-03-31 | 2018-06-13 | パーカーアサヒ株式会社 | Sealant composition |
CN107614492A (en) | 2015-05-27 | 2018-01-19 | 新日本理化株式会社 | 7-oxa-bicyclo[4.1.0 dicarboxylic diester, plasticiser, stabilizer and resin combination |
CN110305343B (en) * | 2019-07-26 | 2022-08-23 | 山东蓝帆新材料有限公司 | PVC gloves and preparation method thereof |
CN110372894B (en) * | 2019-07-26 | 2022-08-26 | 山东蓝帆新材料有限公司 | PVC gloves and preparation method thereof |
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