TW201912416A - Cutting substrate film - Google Patents
Cutting substrate film Download PDFInfo
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- TW201912416A TW201912416A TW107129168A TW107129168A TW201912416A TW 201912416 A TW201912416 A TW 201912416A TW 107129168 A TW107129168 A TW 107129168A TW 107129168 A TW107129168 A TW 107129168A TW 201912416 A TW201912416 A TW 201912416A
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- Taiwan
- Prior art keywords
- layer
- film
- dicing
- surface layer
- resin
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- 239000000758 substrate Substances 0.000 title claims abstract description 25
- 238000005520 cutting process Methods 0.000 title claims description 41
- 239000010410 layer Substances 0.000 claims abstract description 112
- 239000002344 surface layer Substances 0.000 claims abstract description 52
- 239000011342 resin composition Substances 0.000 claims abstract description 25
- 229920005989 resin Polymers 0.000 claims abstract description 22
- 239000011347 resin Substances 0.000 claims abstract description 22
- 239000005038 ethylene vinyl acetate Substances 0.000 claims description 24
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 24
- 229920013716 polyethylene resin Polymers 0.000 claims description 20
- 229920002803 thermoplastic polyurethane Polymers 0.000 claims description 16
- 239000013078 crystal Substances 0.000 claims description 14
- 229910000679 solder Inorganic materials 0.000 claims description 14
- 229920001684 low density polyethylene Polymers 0.000 claims description 13
- 239000004702 low-density polyethylene Substances 0.000 claims description 13
- 229920005749 polyurethane resin Polymers 0.000 claims description 10
- 239000002356 single layer Substances 0.000 claims description 10
- 239000012790 adhesive layer Substances 0.000 claims description 9
- 229920005648 ethylene methacrylic acid copolymer Polymers 0.000 claims description 9
- 239000004433 Thermoplastic polyurethane Substances 0.000 claims description 7
- 229920006225 ethylene-methyl acrylate Polymers 0.000 claims description 6
- 229920005680 ethylene-methyl methacrylate copolymer Polymers 0.000 claims description 6
- 229920010126 Linear Low Density Polyethylene (LLDPE) Polymers 0.000 claims description 4
- QYMGIIIPAFAFRX-UHFFFAOYSA-N butyl prop-2-enoate;ethene Chemical compound C=C.CCCCOC(=O)C=C QYMGIIIPAFAFRX-UHFFFAOYSA-N 0.000 claims description 3
- 229920006245 ethylene-butyl acrylate Polymers 0.000 claims description 3
- 229920006244 ethylene-ethyl acrylate Polymers 0.000 claims description 3
- 238000011084 recovery Methods 0.000 abstract description 13
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- 239000010408 film Substances 0.000 description 126
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- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000000498 cooling water Substances 0.000 description 2
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- 238000010438 heat treatment Methods 0.000 description 2
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 229920000554 ionomer Polymers 0.000 description 2
- 229920000092 linear low density polyethylene Polymers 0.000 description 2
- 239000004707 linear low-density polyethylene Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 229920000909 polytetrahydrofuran Polymers 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
- SBJCUZQNHOLYMD-UHFFFAOYSA-N 1,5-Naphthalene diisocyanate Chemical compound C1=CC=C2C(N=C=O)=CC=CC2=C1N=C=O SBJCUZQNHOLYMD-UHFFFAOYSA-N 0.000 description 1
- VOZKAJLKRJDJLL-UHFFFAOYSA-N 2,4-diaminotoluene Chemical compound CC1=CC=C(N)C=C1N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 description 1
- CTNICFBTUIFPOE-UHFFFAOYSA-N 2-(4-hydroxyphenoxy)ethane-1,1-diol Chemical compound OC(O)COC1=CC=C(O)C=C1 CTNICFBTUIFPOE-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- VEOIIOUWYNGYDA-UHFFFAOYSA-N 2-[2-(6-aminopurin-9-yl)ethoxy]ethylphosphonic acid Chemical compound NC1=NC=NC2=C1N=CN2CCOCCP(O)(O)=O VEOIIOUWYNGYDA-UHFFFAOYSA-N 0.000 description 1
- UPZFLZYXYGBAPL-UHFFFAOYSA-N 2-ethyl-2-methyl-1,3-dioxolane Chemical compound CCC1(C)OCCO1 UPZFLZYXYGBAPL-UHFFFAOYSA-N 0.000 description 1
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 1
- SPBDXSGPUHCETR-JFUDTMANSA-N 8883yp2r6d Chemical compound O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1[C@@H](OC)C[C@H](O[C@@H]2C(=C/C[C@@H]3C[C@@H](C[C@@]4(O[C@@H]([C@@H](C)CC4)C(C)C)O3)OC(=O)[C@@H]3C=C(C)[C@@H](O)[C@H]4OC\C([C@@]34O)=C/C=C/[C@@H]2C)/C)O[C@H]1C.C1C[C@H](C)[C@@H]([C@@H](C)CC)O[C@@]21O[C@H](C\C=C(C)\[C@@H](O[C@@H]1O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](OC)C3)[C@@H](OC)C1)[C@@H](C)\C=C\C=C/1[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\1)O)C[C@H]4C2 SPBDXSGPUHCETR-JFUDTMANSA-N 0.000 description 1
- 239000004970 Chain extender Substances 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 241000826860 Trapezium Species 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 229920006272 aromatic hydrocarbon resin Polymers 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical class C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 239000005043 ethylene-methyl acrylate Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- AYLRODJJLADBOB-QMMMGPOBSA-N methyl (2s)-2,6-diisocyanatohexanoate Chemical compound COC(=O)[C@@H](N=C=O)CCCCN=C=O AYLRODJJLADBOB-QMMMGPOBSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 238000005453 pelletization Methods 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920006146 polyetheresteramide block copolymer Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229920001935 styrene-ethylene-butadiene-styrene Polymers 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/40—Layered products comprising a layer of synthetic resin comprising polyurethanes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/20—Adhesives in the form of films or foils characterised by their carriers
- C09J7/29—Laminated material
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/67—Apparatus specially adapted for handling semiconductor or electric solid state devices during manufacture or treatment thereof; Apparatus specially adapted for handling wafers during manufacture or treatment of semiconductor or electric solid state devices or components ; Apparatus not specifically provided for elsewhere
- H01L21/683—Apparatus specially adapted for handling semiconductor or electric solid state devices during manufacture or treatment thereof; Apparatus specially adapted for handling wafers during manufacture or treatment of semiconductor or electric solid state devices or components ; Apparatus not specifically provided for elsewhere for supporting or gripping
- H01L21/6835—Apparatus specially adapted for handling semiconductor or electric solid state devices during manufacture or treatment thereof; Apparatus specially adapted for handling wafers during manufacture or treatment of semiconductor or electric solid state devices or components ; Apparatus not specifically provided for elsewhere for supporting or gripping using temporarily an auxiliary support
- H01L21/6836—Wafer tapes, e.g. grinding or dicing support tapes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2203/00—Applications of adhesives in processes or use of adhesives in the form of films or foils
- C09J2203/326—Applications of adhesives in processes or use of adhesives in the form of films or foils for bonding electronic components such as wafers, chips or semiconductors
Abstract
Description
本發明係關於一種切割用基體薄膜,其係在將半導體晶圓切割為晶片狀時,用於貼著半導體晶圓使其固定。 The present invention relates to a substrate film for dicing, which is used to attach and fix a semiconductor wafer when the semiconductor wafer is cut into a wafer shape.
製造半導體晶片之方法,有預先製造大面積之半導體晶圓,接著將其半導體晶圓切割(切斷分離)為晶片狀,最後將切割之晶片拾晶之方法。半導體晶圓之切斷方法,近年,習知係使用雷射加工裝置,不接觸半導體晶圓直接將半導體晶圓切斷(分斷)之隱形雷射晶圓切割。 The method for manufacturing a semiconductor wafer includes a method of manufacturing a large-area semiconductor wafer in advance, then cutting (cutting and separating) the semiconductor wafer into a wafer shape, and finally picking up the cut wafer. The cutting method of semiconductor wafers. In recent years, it has been known that the laser processing device uses a laser processing device, and does not contact the semiconductor wafer and directly cuts (breaks off) the semiconductor wafer.
藉由隱形雷射晶圓切割提升半導體晶圓之切斷性(分斷性)之方法,係藉由在-15~5℃之低溫條件下實施膨脹,抑制設置在切割帶上之銲晶薄膜之延伸且增加應力之方法,被廣為人知係可良好地將半導體晶圓與銲晶薄膜一同切斷(分斷)之晶圓加工用帶(專利文獻1及2)。 The method of improving the cut-off (breakability) of semiconductor wafers by invisible laser wafer cutting is to suppress the solder crystal film provided on the dicing tape by expanding at a low temperature of -15 to 5 ° C. This method of extending and increasing the stress is widely known as a wafer processing tape (Patent Documents 1 and 2) which can well cut (break) a semiconductor wafer and a solder crystal film together.
【專利文獻1】日本特開2015-185584號公報 [Patent Document 1] Japanese Patent Laid-Open No. 2015-185584
【專利文獻2】日本特開2015-185591號公報 [Patent Document 2] Japanese Patent Laid-Open No. 2015-185591
本發明,目的在於提供一種切割用基體薄膜,其遇熱復原性高,機架回收性優異。 An object of the present invention is to provide a base film for cutting, which has high resilience to heat and excellent rack recoverability.
本發明,進一步,目的在於提供一種切割用基體薄膜,其即使在低溫條件下實施膨脹,仍可均勻延伸。 It is a further object of the present invention to provide a base film for cutting which can be uniformly stretched even if it is expanded under low temperature conditions.
本發明,進一步,目的在於提供一種切割用基體薄膜,其在隱形雷射晶圓切割(雷射切割)後,欲切斷(分斷)半導體晶圓與銲晶層時,即使在低溫條件(-15~5℃)及高速條件下實施膨脹,仍可良好地延伸。 The present invention further aims to provide a substrate film for dicing, which is used to cut (separate) the semiconductor wafer and the solder crystal layer after the invisible laser wafer dicing (laser dicing), even under low temperature conditions ( -15 ~ 5 ℃) and expansion under high speed conditions can still be well extended.
半導體生產線中,一般希望將膨脹步驟後之加工途中的製品所殘留之片材(含切割用基體薄膜之切割薄膜),暫時放在機架中受到保管。此時,若片材一直處於鬆弛狀態,則機架可能發生無法良好地收納、製品彼此會碰撞產生缺陷等之問題。該機架,係該業界所使用之名稱,其他亦被稱為拉鍊或外殼等。 In a semiconductor production line, it is generally desirable to temporarily store the sheet (including the dicing film of the dicing base film) remaining in the product during processing after the expansion step in a rack for temporary storage. At this time, if the sheet is always in a relaxed state, the rack may not be well stored, and products may collide with each other to cause defects. This rack is the name used by the industry, others are also called zipper or shell.
為了解決此問題,必須消除膨脹步驟後片材的鬆弛。其方法,目前存在熱收縮技術(加熱收縮復原技術)。此係對於膨脹步驟所生之鬆弛部加熱使該部分收縮,從而消除鬆弛者(亦即藉由加熱收縮之復原率高)。 To solve this problem, it is necessary to eliminate the slack of the sheet after the expansion step. As a method, a heat shrinkage technology (heat shrinkage recovery technology) currently exists. This is because the slack portion generated by the expansion step is heated to shrink the portion, thereby eliminating the slacker (that is, the recovery rate by heating and shrinking is high).
例如要求即使在-15~5℃之低溫條件下實施膨脹,切割薄膜 亦可均勻延伸,可良好地切斷半導體晶圓。 For example, it is required that even if the expansion is performed at a low temperature of -15 to 5 ° C, the dicing film can be stretched uniformly, and the semiconductor wafer can be cut well.
進一步,例如即使在隱形雷射晶圓切割後,除了前述低溫條件外,亦實施高速條件下之膨脹時,仍要求切割薄膜可均勻延伸,可良好地切斷(分斷)半導體晶圓與銲晶層。 Further, for example, even after the invisible laser wafer is diced, in addition to the aforementioned low temperature conditions, expansion is also performed under high speed conditions, the dicing film is required to be uniformly extended, and the semiconductor wafer and the solder can be well cut (divided).晶 层。 Crystal layer.
本發明者,為了解決上述課題而進行深入研究。 The present inventors have conducted intensive studies in order to solve the above problems.
發現切割用基體薄膜,包含下述之表層/中間層/裏層依序積層之構成,且因中間層使用聚胺基甲酸酯系樹脂,膨脹步驟後之片材(含切割用基體薄膜之切割薄膜)的鬆弛,可藉由熱收縮技術(加熱收縮復原技術)而良好地消除。 It was found that the substrate film for cutting includes the following surface layer / intermediate layer / inner layer laminated sequentially, and because the intermediate layer uses a polyurethane resin, the sheet after the expansion step (including the substrate film for cutting) The slack of the cutting film can be well eliminated by the heat shrinkage technology (heat shrinkage recovery technology).
發現前述切割用基體薄膜,即使在低溫條件下實施膨脹,切割薄膜仍可均勻延伸。發現前述切割用基體薄膜,除了低溫條件外,亦在高速條件下實施膨脹時,切割薄膜可良好地延伸。 It was found that the aforementioned dicing base film can be uniformly stretched even if it is expanded under low temperature conditions. It was found that, in addition to the low-temperature conditions, the aforementioned dicing base film can be stretched well when the expansion is performed under high-speed conditions.
項1. Item 1.
一種切割用基體薄膜,其係包含表層/中間層/裏層依序積層之構成之切割用基體薄膜,其特徵係表層及裏層係由含聚乙烯系樹脂之樹脂組成物所成;且中間層係由含聚胺基甲酸酯系樹脂之樹脂組成物所成。 A base film for cutting, which is a base film for cutting comprising a surface layer / intermediate layer / inner layer sequentially laminated, and is characterized in that the surface layer and the inner layer are made of a resin composition containing a polyethylene resin; The layer is made of a resin composition containing a polyurethane resin.
項2. Item 2.
如前述項1所記載之切割用基體薄膜,其中,前述表層及/或裏層,係單層或複數層。 The base film for dicing according to item 1, wherein the surface layer and / or the back layer are a single layer or a plurality of layers.
項3. Item 3.
如前述項1或2所記載之切割用基體薄膜,其中,前述聚乙烯系樹脂, 係選自支鏈狀低密度聚乙烯(LDPE)、直鏈狀低密度聚乙烯(LLDPE)、乙烯-乙酸乙烯酯共聚體(EVA)、乙烯-丙烯酸甲酯共聚體(EMA)、乙烯-丙烯酸乙酯共聚體、乙烯-丙烯酸丁酯共聚體、乙烯-甲基丙烯酸甲酯共聚體(EMMA)、乙烯-甲基丙烯酸共聚體(EMAA)、及離子體樹脂所成群中至少1種之樹脂。 The base film for dicing according to item 1 or 2, wherein the polyethylene-based resin is selected from branched low-density polyethylene (LDPE), linear low-density polyethylene (LLDPE), and ethylene-acetic acid. Vinyl ester copolymer (EVA), ethylene-methyl acrylate copolymer (EMA), ethylene-ethyl acrylate copolymer, ethylene-butyl acrylate copolymer, ethylene-methyl methacrylate copolymer (EMMA), ethylene- Resin of at least one of the group consisting of methacrylic acid interpolymer (EMAA) and ionomer resin.
項4. Item 4.
如前述項1~3中任一項所記載之切割用基體薄膜,其中,前述聚胺基甲酸酯系樹脂,係熱可塑性聚胺基甲酸酯樹脂(TPU)。 The base film for dicing according to any one of items 1 to 3, wherein the polyurethane resin is a thermoplastic polyurethane resin (TPU).
項5. Item 5.
一種切割薄膜,其特徵係於前述項1~4中任一項所記載之切割用基體薄膜之表層側,依序設置黏著劑層及銲晶層之切割薄膜。 A dicing film is characterized in that a dicing film in which an adhesive layer and a solder crystal layer are sequentially arranged on the surface layer side of the dicing base film according to any one of the foregoing items 1 to 4.
使用本發明之切割用基體薄膜,可更加迅速且簡便地將使用完畢之切割薄膜回收至機架。亦即,本發明之切割用基體薄膜,遇熱復原性高,即熱收縮性可良好地發揮,機架回收性優異。 By using the dicing base film of the present invention, the used dicing film can be recovered to the rack more quickly and easily. That is, the dicing base film of the present invention has high resilience when exposed to heat, that is, it exhibits good heat shrinkability, and has excellent rack recyclability.
使用本發明之切割用基體薄膜,即使在低溫條件下實施膨脹,仍可使切割薄膜均勻延伸。 With the dicing base film of the present invention, the dicing film can be uniformly stretched even if it is expanded under low temperature conditions.
使用本發明之切割用基體薄膜,例如在隱形雷射晶圓切割後,將半導體晶圓與銲晶層切斷(分斷)時,即使係在低溫條件及高速條件下實施膨脹之情形,切割薄膜亦可良好地延伸。 Using the dicing substrate film of the present invention, for example, when cutting a semiconductor wafer and a die bond layer after the invisible laser wafer is diced, the dicing is performed even if the expansion is performed under low temperature conditions and high speed conditions. The film also stretches well.
本發明係關於一種切割用基體薄膜。 The present invention relates to a base film for cutting.
進一步,本發明係關於一種切割薄膜,其係在切割用基體薄膜上依序設置黏著劑層及銲晶層。 Further, the present invention relates to a dicing film, in which an adhesive layer and a solder crystal layer are sequentially disposed on a dicing base film.
(1)切割用基體薄膜 (1) Cutting base film
本發明之切割用基體薄膜,特徵係包含:表層/中間層/裏層依序積層之構成。 The cutting base film of the present invention is characterized in that it comprises a structure in which a surface layer, an intermediate layer and an inner layer are sequentially laminated.
前述表層及/或裏層,單層或複數層為佳。 The surface layer and / or the back layer are preferably a single layer or a plurality of layers.
以下,詳細說明構成本發明之切割用基體薄膜之各層。 Hereinafter, each layer which comprises the dicing base film of this invention is demonstrated in detail.
(1-1)表層 (1-1) Surface layer
表層,係由含聚乙烯系樹脂之樹脂組成物所成。 The surface layer is made of a resin composition containing a polyethylene resin.
表層所含聚乙烯系樹脂,係使用選自支鏈狀低密度聚乙烯(LDPE)、直鏈狀低密度聚乙烯(LLDPE)、乙烯-乙酸乙烯酯共聚體(EVA)、乙烯-丙烯酸甲酯共聚體(EMA)、乙烯-丙烯酸乙酯共聚體、乙烯-丙烯酸丁酯共聚體、乙烯-甲基丙烯酸甲酯共聚體(EMMA)、乙烯-甲基丙烯酸共聚體(EMAA)、及離子體樹脂所成群中至少1種之成分為佳。 The polyethylene resin contained in the surface layer is selected from branched low-density polyethylene (LDPE), linear low-density polyethylene (LLDPE), ethylene-vinyl acetate copolymer (EVA), and ethylene-methyl acrylate. Interpolymer (EMA), ethylene-ethyl acrylate copolymer, ethylene-butyl acrylate copolymer, ethylene-methyl methacrylate copolymer (EMMA), ethylene-methacrylic acid copolymer (EMAA), and ionomer resin It is preferred that at least one of the constituents in the group is included.
表層,由於係由含此等中至少1種之成分之樹脂組成物所成,故切割用基體薄膜之膨脹性,亦即,基材之抗拉性優異。 Since the surface layer is made of a resin composition containing at least one of these components, the slicing of the base film for cutting, that is, the tensile strength of the base material is excellent.
其他,只要在不損及本發明之効果,亦可配合聚丙烯系樹脂。 In addition, as long as the effect of the present invention is not impaired, a polypropylene resin may be blended.
乙烯-乙酸乙烯酯共聚體(EVA)在190℃之熔體流動速率(MFR),約為30g/10分以下即可,約20g/10分以下為佳,約15g/10分以下較佳,約10g/10分以下更佳。藉由將上述MFR設定在10g/10分以下,可抑制與 中間層之黏度差,從而可安定地製膜。 The melt flow rate (MFR) of the ethylene-vinyl acetate copolymer (EVA) at 190 ° C is only about 30 g / 10 minutes or less, preferably about 20 g / 10 minutes or less, and more preferably about 15 g / 10 minutes or less. It is more preferably about 10 g / 10 minutes or less. By setting the MFR to 10 g / 10 minutes or less, it is possible to suppress a difference in viscosity from the intermediate layer and to form a film stably.
此外,EVA之MFR,為了易於進行樹脂的押出,約0.1g/10分以上為佳,約0.3g/10分以上較佳。 In addition, in order to facilitate the extrusion of the resin, the MFR of EVA is preferably about 0.1 g / 10 minutes or more, and more preferably about 0.3 g / 10 minutes or more.
EVA之密度,約0.9~0.96g/cm3為佳,約0.92~0.94g/cm3較佳。 The density of EVA is preferably about 0.9 to 0.96 g / cm 3, and more preferably about 0.92 to 0.94 g / cm 3 .
支鏈狀低密度聚乙烯(LDPE)在190℃之熔體流動速率(MFR),約10g/10分以下為佳,約6g/10分以下較佳。藉由將上述MFR設定在10g/10分以下,可抑制與中間層之黏度差,從而可安定地製膜。 The melt flow rate (MFR) of the branched low density polyethylene (LDPE) at 190 ° C is preferably about 10 g / 10 minutes or less, and more preferably about 6 g / 10 minutes or less. By setting the MFR to 10 g / 10 minutes or less, it is possible to suppress a difference in viscosity from the intermediate layer and to form a film stably.
此外,LDPE之MFR,為了易於進行樹脂的押出,約0.1g/10分以上為佳,約0.3g/10分以上較佳。 In addition, the MFR of LDPE is preferably about 0.1 g / 10 minutes or more, and more preferably about 0.3 g / 10 minutes or more in order to facilitate the extrusion of the resin.
LDPE之密度,約0.9~0.94g/cm3為佳,約0.91~0.93g/cm3較佳。 The density of LDPE is preferably about 0.9 to 0.94 g / cm 3, and more preferably about 0.91 to 0.93 g / cm 3 .
直鏈狀低密度聚乙烯(LLDPE)在190℃之熔體流動速率(MFR),約10g/10分以下為佳,約6g/10分以下較佳。藉由將上述MFR設定在10g/10分以下,可抑制與中間層之黏度差,從而可安定地製膜。 The melt flow rate (MFR) of the linear low-density polyethylene (LLDPE) at 190 ° C is preferably about 10 g / 10 minutes or less, and more preferably about 6 g / 10 minutes or less. By setting the MFR to 10 g / 10 minutes or less, it is possible to suppress a difference in viscosity from the intermediate layer and to form a film stably.
此外,LLDPE之MFR,為了易於進行樹脂的押出,約0.1g/10分以上為佳,約0.3g/10分以上較佳。 In addition, the MFR of LLDPE is preferably about 0.1 g / 10 minutes or more, and more preferably about 0.3 g / 10 minutes or more in order to facilitate the extrusion of the resin.
LLDPE之密度,約0.9~0.94g/cm3為佳,約0.91~0.93g/cm3較佳。 The density of LLDPE is preferably about 0.9 to 0.94 g / cm 3, and more preferably about 0.91 to 0.93 g / cm 3 .
在此,熔體流動速率(MFR)係根據ISO 1133所求得者,密度係根據ISO 1183-1:2004所求得者。 Here, the melt flow rate (MFR) is obtained according to ISO 1133, and the density is obtained according to ISO 1183-1: 2004.
表層,因應必要,亦可進一步含有抗靜電劑。前述表層可使用之抗靜電劑,表層中亦可使用。表層所使用之抗靜電劑,可從陰離子系、陽離子系、非離子系等之習知的界面活性劑中選擇,特別係根據持續性、 耐久性之觀點,PEEA樹脂、親水性PO樹脂等之非離子系界面活性劑為佳。 The surface layer may further contain an antistatic agent as necessary. The antistatic agent that can be used in the aforementioned surface layer can also be used in the surface layer. The antistatic agent used in the surface layer may be selected from conventional surfactants such as anionic, cationic, and nonionic, and is particularly based on the viewpoints of durability and durability, such as PEEA resin and hydrophilic PO resin. Nonionic surfactants are preferred.
表層含有抗靜電劑時,抗靜電劑之含量,在表層之樹脂組成物中,抗靜電劑係約5~25重量%為佳,約7~22重量%較佳。藉由在前述範圍內配合抗靜電劑,即使接觸膨脹環而產生相同之膨脹,亦可不損及表層之滑動性。 When the surface layer contains an antistatic agent, the content of the antistatic agent is preferably about 5 to 25% by weight, and more preferably about 7 to 22% by weight in the resin composition of the surface layer. By blending the antistatic agent within the aforementioned range, even if the same expansion occurs due to contact with the expansion ring, the sliding properties of the surface layer are not impaired.
此外,由於可有効地賦予半導電性,故可迅速地將所產生之静電進行除電。例如,含有上述範圍之抗靜電劑之本發明之切割用基體薄膜,因其裏面之表面電阻率係約107~1012Ω/□故為佳。 In addition, since semiconductivity can be effectively provided, the generated static electricity can be quickly removed. For example, the substrate film for cutting of the present invention containing the antistatic agent in the above range has a surface resistivity of about 10 7 to 10 12 Ω / □.
表層,亦可進一步添加抗黏著劑等。藉由添加抗黏著劑,可抑制切割用基體薄膜捲成滾輪狀時之黏著,故為佳。抗黏著劑,可示例如無機系或有機系之微粒子。 An anti-adhesive agent may be further added to the surface layer. The addition of an anti-adhesive agent is preferable because it can suppress the adhesion when the base film for cutting is rolled into a roller shape. Examples of the anti-adhesive agent include inorganic or organic fine particles.
(1-2)裏層 (1-2) Inside
裏層,與表層相同,係由含聚乙烯系樹脂之樹脂組成物所成。 The inner layer, like the surface layer, is made of a resin composition containing a polyethylene resin.
可使用表層所使用之聚乙烯系樹脂,亦可使用與表層不同之聚乙烯系樹脂。 The polyethylene resin used in the surface layer may be used, or a polyethylene resin different from the surface layer may be used.
此外,因應必要,亦可與表層相同,含有抗靜電劑或抗黏著劑。 In addition, if necessary, the surface layer may contain an antistatic agent or an anti-adhesive agent.
本發明之切割用基體薄膜中,前述表層及/或裏層,可係單層,亦可係複數層。本發明之切割用基體薄膜,因應必要,可設置複數層表層及/或裏層。 In the dicing base film of the present invention, the surface layer and / or the back layer may be a single layer or a plurality of layers. The cutting base film of the present invention may be provided with a plurality of surface layers and / or back layers as necessary.
表層及/或裏層為複數層時,從最表層側依序以表層-1、表層-2、表層-3、...表示,此外,從最裏層側依序以裏層-1、裏層-2、裏層-3、 ...表示。 When the surface layer and / or the inner layer are plural layers, the surface layer-1, the surface layer-2, the surface layer-3, and . . Indicates, in addition, from the innermost layer side, the inner layer-1, the inner layer-2, the inner layer-3, and. . . Means.
(1-3)中間層 (1-3) middle layer
中間層,係由含有聚胺基甲酸酯系樹脂(PU)之樹脂組成物所成。 The intermediate layer is made of a resin composition containing a polyurethane resin (PU).
前述PU,係熱可塑性聚胺基甲酸酯樹脂(TPU)為佳。 The PU is preferably a thermoplastic polyurethane resin (TPU).
切割用基體薄膜,藉由具有含聚胺基甲酸酯系樹脂(PU)之樹脂組成物所成中間層,從而可提升膨脹性。 The base film for dicing has an intermediate layer formed of a resin composition containing a polyurethane resin (PU), thereby improving the swellability.
切割用基體薄膜,藉由具有含聚胺基甲酸酯系樹脂(PU)之樹脂組成物所成中間層,例如在隱形雷射晶圓切割後,將半導體晶圓與銲晶層切斷(分斷)時,即使在低溫條件及高速條件下實施膨脹之情形,切割薄膜亦可良好地延伸。 The substrate film for dicing has an intermediate layer formed of a resin composition containing a polyurethane resin (PU). In the case of breaking), the dicing film can be stretched well even when the expansion is performed under low temperature conditions and high speed conditions.
(i)聚胺基甲酸酯系樹脂(PU) (i) Polyurethane resin (PU)
聚胺基甲酸酯系樹脂(PU),係使用熱可塑性聚胺基甲酸酯樹脂(TPU)為佳。TPU,係將聚異氰酸酯、多元醇及鏈伸長劑進行反應而得,係由多元醇與聚異氰酸酯反應而成之軟質段與鏈伸長劑及聚異氰酸酯反應而成之硬質段所成之嵌段聚合物。 The polyurethane resin (PU) is preferably a thermoplastic polyurethane resin (TPU). TPU is obtained by reacting polyisocyanate, polyol and chain elongation agent. It is a block polymerization of the soft segment formed by the reaction of polyol and polyisocyanate and the hard segment formed by the reaction of chain extender and polyisocyanate Thing.
聚異氰酸酯,可列舉例如:二苯甲烷二異氰酸酯、六亞甲基二異氰酸酯、離胺酸二異氰酸酯、1,5-萘二異氰酸酯、二異氰酸異佛爾酮、苯二亞甲基二異氰酸酯等。此等之中,二苯甲烷二異氰酸酯及/或六亞甲基二異氰酸酯,根據熱可塑性聚胺基甲酸酯樹脂之耐磨性之觀點為佳。 Examples of the polyisocyanate include: diphenylmethane diisocyanate, hexamethylene diisocyanate, lysine diisocyanate, 1,5-naphthalene diisocyanate, isophorone diisocyanate, and benzenedimethylene diisocyanate. Wait. Among these, diphenylmethane diisocyanate and / or hexamethylene diisocyanate are preferred from the viewpoint of abrasion resistance of a thermoplastic polyurethane resin.
多元醇,可列舉例如:聚四亞甲基醚二醇、聚酯多元醇、內酯系聚酯多元醇等。聚酯多元醇,係藉由二羧酸與二醇之聚縮合反應而得。 Examples of the polyol include polytetramethylene ether glycol, polyester polyol, and lactone-based polyester polyol. Polyester polyols are obtained by the polycondensation reaction of a dicarboxylic acid and a diol.
聚酯多元醇之製造所使用之二醇,具體可列舉例如:乙二 醇、1,3-丙二醇、1,4-丁二醇、1,5-戊二醇、1,6-己二醇等,將此等單獨或併用者。 Specific examples of diols used in the production of polyester polyols include ethylene glycol, 1,3-propanediol, 1,4-butanediol, 1,5-pentanediol, and 1,6-hexanediol. Etc., these alone or in combination.
此外,本發明所使用之二羧酸,可列舉例如:己二酸、癸二酸等,將此等單獨或併用者。 Examples of the dicarboxylic acid used in the present invention include adipic acid, sebacic acid, and the like, and these may be used alone or in combination.
此等多元醇之中,根據熱可塑性聚胺基甲酸酯樹脂可得高抗衝擊性之觀點,係聚四亞甲基醚二醇為佳。此外,相關多元醇之數平均分子量,係1,000~4,000為佳,數平均分子量係2,000~3,000特佳。 Among these polyols, polytetramethylene ether glycol is preferred from the viewpoint that a thermoplastic polyurethane resin can obtain high impact resistance. The number average molecular weight of the related polyol is preferably 1,000 to 4,000, and the number average molecular weight is particularly preferably 2,000 to 3,000.
此外,鏈伸長劑,可列舉例如:乙二醇、1,4-丁二醇、1,6-己二醇等之碳原子數為2~6之脂肪族直鏈二醇;對苯二酚二羥乙基醚等。亦可與己二胺、異佛爾酮二胺、甲苯二胺、單乙醇胺等之胺類部分併用。此等中,根據熱可塑性聚胺基甲酸酯樹脂之耐磨性之觀點,碳原子數為2~6之脂肪族直鏈二醇為佳。 Examples of the chain elongating agent include aliphatic linear diols having 2 to 6 carbon atoms, such as ethylene glycol, 1,4-butanediol, and 1,6-hexanediol; and hydroquinone Dihydroxyethyl ether and so on. It can also be used in combination with amines such as hexamethylenediamine, isophoronediamine, toluenediamine, and monoethanolamine. Among these, from the viewpoint of the abrasion resistance of the thermoplastic polyurethane resin, an aliphatic linear diol having 2 to 6 carbon atoms is preferred.
熱可塑性聚胺基甲酸酯樹脂之密度,係約1.1~1.5g/cm3為佳,約1.1~1.3g/cm3較佳。 The density of the thermoplastic polyurethane resin is preferably about 1.1 to 1.5 g / cm 3, and more preferably about 1.1 to 1.3 g / cm 3 .
熱可塑性聚胺基甲酸酯樹脂,可藉由將上述原料進行一步法、預聚物法等之習知的方法而製造。 The thermoplastic polyurethane resin can be produced by a known method such as a one-step method or a prepolymer method of the aforementioned raw materials.
PU,可列舉例如:DIC科思創股份有限公司製(DIC Covestro Polymer Ltd.)之PANDEX,日本米拉克特朗股份有限公司(Nippon Miractran Co,Ltd.)製之Miractran等。 Examples of PU include PANDEX manufactured by DIC Covestro Polymer Ltd., Miractran manufactured by Nippon Miractran Co, Ltd., and the like.
中間層,構成其之樹脂組成物,除了前述(i)PU外,亦可包含(ii)聚乙烯系樹脂。 The intermediate layer and the resin composition constituting the intermediate layer may include (ii) a polyethylene-based resin in addition to the (i) PU described above.
(ii)聚乙烯系樹脂 (ii) Polyethylene resin
聚乙烯系樹脂,可使用表層可以使用之樹脂。 As the polyethylene resin, a resin that can be used for the surface layer can be used.
亦可將與表層所使用之聚乙烯系樹脂相同之樹脂用於中間層,亦可使用與表層所使用之聚乙烯系樹脂不同之樹脂。聚乙烯系樹脂,係使用上述PU加上乙烯-甲基丙烯酸共聚體(EMAA)為佳。 The same resin as the polyethylene resin used in the surface layer may be used for the intermediate layer, and a resin different from the polyethylene resin used in the surface layer may be used. As the polyethylene resin, it is preferable to use the above-mentioned PU plus an ethylene-methacrylic acid copolymer (EMAA).
中間層含有聚乙烯系樹脂時之含有比例,係0~80重量%為佳,0~70重量%較佳。 The content ratio when the intermediate layer contains a polyethylene resin is preferably 0 to 80% by weight, and more preferably 0 to 70% by weight.
聚乙烯系樹脂只要在0~80重量%之範圍內,則有良好之切割用基體薄膜之膨脹性,亦即抗拉性。 As long as the polyethylene-based resin is in the range of 0 to 80% by weight, it has good swellability, that is, tensile properties, of the base film for cutting.
(1-4)切割用基體薄膜之層構成 (1-4) Layer structure of base film for cutting
本發明之切割用基體薄膜,係包含表層/中間層/裏層依序積層之構成。 The dicing base film of the present invention includes a surface layer, an intermediate layer, and an inner layer which are sequentially laminated.
表層,係位於晶圓接觸側,與黏著層相接之層。 The surface layer is a layer located on the contact side of the wafer and in contact with the adhesive layer.
中間層,可由各樹脂單獨形成層(單層),亦可由樹脂之混合物形成層(單層),亦可由各樹脂形成各層(多層)。 The intermediate layer may be formed of a single layer (single layer) by each resin, or a layer (single layer) of a resin mixture, or each layer (multilayer) of each resin.
本發明之切割用基體薄膜中,前述表層及/或裏層,係單層或複數層為佳。表裏層,LDPE、EVA等,可由各樹脂形成層(單層),亦可由樹脂之混合物形成層(單層),亦可由各樹脂形成各層(多層)。 In the dicing base film of the present invention, the surface layer and / or the back layer are preferably a single layer or a plurality of layers. The front and back layers, LDPE, EVA, etc., can be formed from each resin (single layer), or a mixture of resins (single layer), and each layer (multilayer) from each resin.
本發明之切割用基體薄膜之整體之厚度,係約50~300μm為佳,約70~200μm較佳,約80~150μm更佳。藉由將切割用基體薄膜之整體之厚度設定在50μm以上,在切割半導體晶圓時,可保護半導體晶圓不受到衝撃。 The overall thickness of the substrate film for cutting of the present invention is preferably about 50 to 300 μm, more preferably about 70 to 200 μm, and even more preferably about 80 to 150 μm. By setting the entire thickness of the dicing base film to 50 μm or more, the semiconductor wafer can be protected from being washed out when the semiconductor wafer is cut.
相對於切割用基體薄膜之全厚度,表層及裏層之厚度之比例係約4~80%為佳,約10~60%較佳。 Relative to the full thickness of the substrate film for cutting, the thickness ratio of the surface layer and the back layer is preferably about 4 to 80%, and more preferably about 10 to 60%.
相對於切割用基體薄膜之全厚度,中間層之厚度之比例係約20~96%為佳,約40~90%較佳。 The ratio of the thickness of the intermediate layer to the full thickness of the substrate film for cutting is preferably about 20 to 96%, and more preferably about 40 to 90%.
切割用基體薄膜之具體例,說明切割用基體薄膜之全厚度為60~100μm之情形。 A specific example of the base film for dicing is a case where the full thickness of the base film for dicing is 60 to 100 μm.
表層及裏層之厚度,各約2~44μm為佳,各約10~38μm較佳。表層及裏層為複數層時,總厚度,只要在上述之厚度範圍內形成各層即可。 The thickness of the surface layer and the back layer is preferably about 2 to 44 μm each, and more preferably about 10 to 38 μm each. When the surface layer and the back layer are plural layers, the total thickness may be formed by forming each layer within the above-mentioned thickness range.
中間層之厚度係約12~96μm為佳,約24~80μm較佳。中間層為複數層時,總厚度,只要在上述之厚度範圍內形成各層即可。 The thickness of the intermediate layer is preferably about 12 to 96 μm, and more preferably about 24 to 80 μm. When the intermediate layer is a plurality of layers, the total thickness may be formed by forming each layer within the thickness range described above.
3種5層之例(表層-1/表層-2/中間層/裏層-2/裏層-1) Example of 3 types and 5 layers (Surface-1 / Surface-2 / Intermediate / Inner-2 / Inner-1)
3種5層之例,如上述,表層-1與表層-2之總厚度係在上述表層之厚度之範圍內,相同地,裏層-1與裏層-2之總厚度係在上述裏層之厚度之範圍內。 Examples of three types of five layers. As mentioned above, the total thickness of surface layer-1 and surface layer-2 is within the thickness of the surface layer. Similarly, the total thickness of inner layer-1 and inner layer-2 is in the inner layer. Range of thickness.
表層-1與表層-2,可使用相同種類之聚乙烯系樹脂,亦可使用不同種類之聚乙烯系樹脂。 As the surface layer-1 and the surface layer-2, the same type of polyethylene resin can be used, and different types of polyethylene resin can also be used.
裏層-1與裏層-2,可使用相同種類之聚乙烯系樹脂,亦可使用不同種類之聚乙烯系樹脂。 The inner layer-1 and the inner layer-2 can use the same kind of polyethylene resin, and different kinds of polyethylene resin can also be used.
使用相同種類之聚乙烯系樹脂之情形,例如,使用EVA時,表層-2及裏層-2所使用之EVA,與表層-1及裏層-1所使用之EVA相比,係使用乙烯基之含量(VA含量)較高之EVA為佳。 When the same type of polyethylene resin is used, for example, when EVA is used, the EVA used for the surface layer-2 and the inner layer-2 is compared with the EVA used for the surface layer-1 and the inner layer-1. EVA with a higher content (VA content) is preferred.
表層-1及裏層-1,使用VA含量約5~15重量%之EVA為佳,使用約7~13重量%之EVA較佳。 For the surface layer-1 and the inner layer-1, it is better to use EVA with a VA content of about 5 to 15% by weight, and it is better to use about 7 to 13% by weight of EVA.
表層-2及裏層-2,使用VA含量約15~33重量%之EVA為佳,使用約28~33重量%之EVA較佳。 For surface layer-2 and inner layer-2, it is better to use EVA with a VA content of about 15 to 33% by weight, and it is better to use about 28 to 33% by weight of EVA.
此外,根據MFR之觀點,表層-2及裏層-2所使用之EVA,與表層-1及裏層-1相比,係使用熔體流動速率(MFR)較高之EVA為佳。 In addition, from the viewpoint of MFR, the EVA used for the surface layer-2 and the inner layer-2 is better than the surface layer-1 and the inner layer-1, which uses EVA with a higher melt flow rate (MFR).
表層-1及裏層-1,EVA在190℃之MFR,約0.1g/10分~10g/10分為佳,約5g/10分~10g/10分較佳。 For the surface layer-1 and the inner layer-1, the MFR of EVA at 190 ° C is preferably about 0.1g / 10 minutes to 10g / 10 minutes, and preferably about 5g / 10 minutes to 10g / 10 minutes.
表層-2及裏層-2,EVA在190℃之MFR,約10g/10分~40g/10分為佳,約12g/10分~35g/10分較佳。 For the surface layer-2 and the inner layer-2, the MFR of EVA at 190 ° C is preferably about 10g / 10 minutes to 40g / 10 minutes, and preferably about 12g / 10 minutes to 35g / 10 minutes.
(2)切割用基體薄膜之製法 (2) Manufacturing method of substrate film for cutting
表層/中間層/裏層之切割用基體薄膜,可藉由將表層、中間層、及裏層用之樹脂組成物進行多層共押出成形而製造。具體而言,可藉由將前述表層用樹脂組成物、中間層用樹脂組成物、及裏層用樹脂組成物,作為表層/中間層/裏層依序積層進行共押出成形而製造。 The substrate film for cutting the surface layer / intermediate layer / inner layer can be produced by multi-layer co-extrusion molding of the resin composition for the surface layer, the intermediate layer, and the inner layer. Specifically, the resin composition for the surface layer, the resin composition for the intermediate layer, and the resin composition for the back layer can be produced by co-extrusion molding as a surface layer / intermediate layer / back layer in order.
進一步,表層及裏層為複數層構成時,可將各表層及裏層用之樹脂組成物分別投入押出機,例如,可藉由將表層-1/表層-2/中間層/裏層-2/裏層-1依序積層共押出成形而製造。 Further, when the surface layer and the inner layer are composed of a plurality of layers, the resin composition for each surface layer and the inner layer may be separately charged into the extruder. For example, the surface layer-1 / surface layer-2 / intermediate layer / inner layer-2 may be used. / Inner layer-1 is sequentially laminated and co-extruded.
構成表層之樹脂組成物,可因應必要進一步添加抗靜電劑。裏層亦相同。 The resin composition constituting the surface layer may further be added with an antistatic agent as necessary. The same goes for the inner layer.
將上述之各層用樹脂分別依序向螺絲式押出機供給,在180~240℃下從多層T模押出薄膜狀,使其通過30~70℃之冷卻輥進行冷卻後在實質無延伸之狀態下取出。抑或,亦可取得各層用樹脂之暫時性之製粒後,如上述進行押出成形。 The above-mentioned resins for each layer are sequentially supplied to the screw extruder, and the film is extruded from the multilayer T die at 180 to 240 ° C, and cooled by a cooling roller at 30 to 70 ° C in a substantially non-extended state. take out. Alternatively, after temporarily pelletizing the resin for each layer, extrusion molding may be performed as described above.
取出時實質無延伸,係為了有效地進行切割後的薄膜擴張。此實質無延伸,係包含無延伸,抑或,對於切割薄膜之擴張不會產生壞影 響的些微之延伸。通常,取出薄膜時,只要拉伸不產生鬆弛即可。 There is virtually no elongation at the time of taking out, in order to effectively expand the film after cutting. This substantial non-elongation includes no elongation, or a slight extension that does not adversely affect the expansion of the dicing film. Generally, when the film is taken out, it is sufficient as long as it does not cause slack in stretching.
(3)切割薄膜之製造 (3) Manufacturing of cutting film
本發明之切割薄膜,可根據習知技術而製造。例如,以有機溶劑等之溶劑將構成黏著劑層之黏著劑溶解,塗佈在切割用基體薄膜上,去除溶劑,從而可得到基體薄膜/黏著劑層之構成之薄膜。 The dicing film of the present invention can be produced according to a conventional technique. For example, a solvent such as an organic solvent is used to dissolve the adhesive constituting the adhesive layer, and apply the solvent to the substrate film for dicing, and remove the solvent to obtain a film composed of the substrate film / adhesive layer.
構成銲晶層之樹脂組成物,以有機溶劑等之溶劑將其溶解,塗佈在其他之薄膜(剝離薄膜)上,去除溶劑,從而製作銲晶薄膜。 The resin composition constituting the solder crystal layer is dissolved in a solvent such as an organic solvent, applied to another film (peeling film), and the solvent is removed to prepare a solder crystal film.
進一步,藉由將前述黏著劑層與銲晶層對向重合,從而製作切割薄膜。藉此,可得到基體薄膜/黏著劑層/銲晶層之構成之薄膜。此階段之銲晶層,與半導體晶圓及黏著層在微弱(擬似)接著之狀態下貼合。 Further, the adhesive layer and the solder crystal layer are oppositely overlapped to form a dicing film. Thereby, a thin film composed of a base film, an adhesive layer, and a solder crystal layer can be obtained. The solder crystal layer at this stage is bonded to the semiconductor wafer and the adhesive layer in a weak (pseudo-) adhesive state.
膨脹後,將分斷之半導體晶片與銲晶層,與所定之封裝或半導體晶片積層,過熱至銲晶層強接著為止之溫度,從而接著。 After the expansion, the separated semiconductor wafer and solder crystal layer are laminated with a predetermined package or semiconductor wafer, and overheated to a temperature where the solder crystal layer is strongly adhered, thereby continuing.
以下,藉由實施例詳細說明本發明,惟本發明並非限定為此等實施例。 Hereinafter, the present invention is described in detail by examples, but the present invention is not limited to these examples.
(1)切割用基體薄膜之原料 (1) Raw material for cutting substrate film
表1表示切割用基體薄膜之原料。 Table 1 shows the raw materials of the base film for cutting.
[簡稱之說明] [Description of abbreviation]
PE-1~9:聚乙烯系樹脂1~9 PE-1 ~ 9: Polyethylene resins 1 ~ 9
SEBS:氫化苯乙烯-丁二烯共聚體 SEBS: hydrogenated styrene-butadiene interpolymer
(苯乙烯-乙烯-丁烯-苯乙烯共聚體) (Styrene-ethylene-butene-styrene copolymer)
TPU:熱可塑性聚胺基甲酸酯(PU) TPU: Thermoplastic Polyurethane (PU)
非晶性PO:非晶性聚烯烴 Amorphous PO: Amorphous polyolefin
LDPE:支鏈狀低密度聚乙烯 LDPE: branched low density polyethylene
EVA:乙烯-乙酸乙烯酯共聚體 EVA: ethylene-vinyl acetate copolymer
VA含量:乙酸乙烯酯含有比例 VA content: the proportion of vinyl acetate
EMAA:乙烯-甲基丙烯酸共聚體 EMAA: ethylene-methacrylic acid copolymer
MAA含量:甲基丙烯酸含量 MAA content: methacrylic acid content
St含量:苯乙烯含有比例 St content: the proportion of styrene
(乙烯基芳烴系樹脂中之乙烯基芳烴(St)成分之含量) (Content of vinyl aromatic hydrocarbon (St) component in vinyl aromatic hydrocarbon resin)
(2)表層/中間層/裏層之切割用基體薄膜之製造 (2) Manufacture of base film for cutting of surface layer / intermediate layer / inner layer
根據表2所記載之表層/中間層/裏層(3層),以各成分及組成配合樹脂組成物,從而製作切割用基體薄膜。 Based on the surface layer / intermediate layer / back layer (three layers) described in Table 2, the resin composition was blended with each component and composition to produce a base film for cutting.
將構成各層之樹脂組成物,分別投入調整至220℃之押出機,表層/中間層/裏層依序以220℃之T模押出並積層,在有30℃之冷卻水循環之冷卻輥上共押出,從而得到片材狀之3層薄膜。 The resin composition constituting each layer is respectively put into an extruder adjusted to 220 ° C, and the surface layer / intermediate layer / inner layer is sequentially extruded and laminated in a T mold of 220 ° C, and extruded on a cooling roll having a cooling water circulation of 30 ° C Thus, a sheet-like three-layer film was obtained.
(3)表層-1/表層-2/中間層/裏層-2/裏層-1之切割用基體薄膜之製造 (3) Manufacture of base film for cutting of surface layer-1 / surface layer-2 / intermediate layer / inner layer-2 / inner layer-1
根據表3及4所記載之表層-1/表層-2/中間層/裏層-2/裏層-1(5層),以各 成分及組成配合樹脂組成物,從而製作切割用基體薄膜。 Based on the surface layer-1 / surface layer-2 / intermediate layer / inner layer-2 / inner layer-1 (5 layers) described in Tables 3 and 4, the resin composition was compounded with each component and composition to produce a substrate film for cutting.
將構成各層之樹脂組成物,分別投入調整至220℃之押出機,表層-1/表層-2/中間層/裏層-2/裏層-1依序以220℃之T模押出並積層,在有30℃之冷卻水循環之冷卻輥上共押出,從而得到片材狀之5層薄膜。 Put the resin composition constituting each layer into an extruder adjusted to 220 ° C, and the surface layer-1 / surface layer-2 / intermediate layer / inner layer-2 / inner layer-1 are sequentially extruded and laminated at 220 ℃ T, It was co-extruded on a cooling roll with 30 ° C cooling water circulation to obtain a sheet-like five-layer film.
(4)切割用基體薄膜之評估 (4) Evaluation of substrate film for cutting
(4-1)低溫膨脹性(Ex性) (4-1) Low temperature expansion (Ex)
<評估方法> <Evaluation method>
(拉伸伸度之測量) (Measurement of tensile elongation)
薄膜之MD方向(薄膜成形之押出方向)及TD方向(藉由薄膜成形而成形之薄膜之寬方向),係在200mm/min之拉伸速度下,使用加工為寬10mm且夾盤間距離為40mm之薄膜樣品進行薄膜之拉伸伸度測量。 The MD direction of the film (extrusion direction of film forming) and TD direction (width direction of the film formed by film forming) are processed at a stretching speed of 200 mm / min, and the processing is 10 mm wide and the distance between the chucks is A film sample of 40 mm was used to measure the tensile elongation of the film.
(25%模量之測量) (Measurement of 25% modulus)
薄膜之MD方向(薄膜成形之押出方向)及TD方向(藉由薄膜成形而成形之薄膜之寬方向),係在200mm/min之拉伸速度下,使用加工為寬10mm且夾盤間距離為40mm之薄膜樣品,得到SS曲線(應力-應變曲線)。 The MD direction of the film (extrusion direction for film formation) and TD direction (width direction of the film formed by film formation) are processed at a stretching speed of 200 mm / min, using a 10 mm width and a distance between the chucks of For a 40 mm film sample, an SS curve (stress-strain curve) was obtained.
分別讀取所得SS曲線在延伸率25%的應力值。 Read the stress values of the obtained SS curves at 25% elongation.
<評估基準> <Evaluation Criteria>
(一)低溫膨脹性(低溫Ex性) (I) Low temperature expansion (low temperature Ex)
○:進行拉伸試驗時,延伸率為100%以上。 ○: When a tensile test is performed, the elongation is 100% or more.
×:進行拉伸試驗時,薄膜延伸率未達100%。 ×: When the tensile test was performed, the film elongation did not reach 100%.
(二)均勻膨脹性(均勻Ex性) (Two) uniform expansion (uniform Ex)
求得MD方向在延伸率25%的應力值與TD方向在延伸率25%的應力值之比,作為模量比(MD/TD)。 The ratio of the stress value at 25% elongation in the MD direction to the stress value at 25% elongation in the TD direction was determined as the modulus ratio (MD / TD).
○:模量比(MD/TD)未達1.5。 :: The modulus ratio (MD / TD) is less than 1.5.
×:模量比(MD/TD)為1.5以上。 ×: The modulus ratio (MD / TD) is 1.5 or more.
藉由使模量比(MD/TD)在前述範圍中,切割用基體薄膜,在-15~5℃之低溫條件下,可發揮良好的均勻膨脹性(均勻Ex性)。 When the modulus ratio (MD / TD) is in the aforementioned range, the substrate film for cutting can exhibit good uniform expansion property (uniform ex property) under a low temperature condition of -15 to 5 ° C.
(4-2)低溫高速膨脹性(低溫高速Ex性) (4-2) Low temperature and high speed expansion (low temperature and high speed Ex)
<評估方法> <Evaluation method>
(斷裂延伸(最大延伸)(%)之測量) (Measurement of fracture extension (maximum extension) (%))
拉伸試驗:使用島津製作所股份有限公司製「HYDROSHOT.HITS-T10」,在-15±2℃環境下,以250mm/sec之拉伸速度,將薄膜樣品之MD方向及TD方向延伸至斷裂為止,該薄膜樣品係加工為寬25mm且夾盤間距離為10mm。 Tensile test: "HYDROSHOT.HITS-T10" manufactured by Shimadzu Corporation was used to extend the MD direction and TD direction of the film sample to break at -15 ± 2 ° C at a tensile speed of 250 mm / sec. The film sample was processed to a width of 25 mm and a distance between the chucks of 10 mm.
藉由負荷與延伸之數據圖,作成SS曲線(應力-應變曲線),從而算出斷裂延伸(最大延伸)。 Based on the data graph of load and extension, the SS curve (stress-strain curve) was made to calculate the fracture extension (maximum extension).
<評估基準> <Evaluation Criteria>
(高速拉伸試驗評估(機械特性)) (Evaluation of high-speed tensile test (mechanical characteristics))
○:MD及TD方向之斷裂拉伸延伸為120%以上。 ○: The tensile elongation at break in the MD and TD directions is 120% or more.
×:MD及TD方向之斷裂拉伸延伸未達120%。 ×: The tensile elongation at break in the MD and TD directions did not reach 120%.
此評估方法,係藉由將拉伸速度設定為250mm/sec,進行拉伸試驗,除了低溫條件,亦評估高速條件下之膨脹性。並且,藉由使薄膜之MD及TD方向之斷裂拉伸延伸為120%以上,例如隱形雷射晶圓切割後,實施低溫條件(-15~5℃)及高速條件下之膨脹時,薄膜可良好地延伸。 In this evaluation method, a tensile test is performed by setting the tensile speed to 250 mm / sec. In addition to the low temperature conditions, the swellability under high speed conditions is also evaluated. In addition, the film can be stretched to 120% or more in the MD and TD directions. For example, after the invisible laser wafer is diced, the film can be expanded under low temperature conditions (-15 to 5 ° C) and high speed conditions. Extends well.
(4-3)熱收縮性(HS性) (4-3) Heat shrinkability (HS properties)
條件1-拉伸試驗:使用島津製作所股份有限公司製「AUTOGRAPH AG-500NX TRAPEZIUM X」,在-15±2℃環境下,以200mm/min之拉伸速度,將薄膜樣品之MD方向及TD方向分別延伸200%,該薄膜樣品係加工為寬10mm且夾盤間距離為40mm。 Condition 1-Tensile test: "AUTOGRAPH AG-500NX TRAPEZIUM X" manufactured by Shimadzu Corporation was used, under the environment of -15 ± 2 ° C, at a tensile speed of 200 mm / min, the MD direction and TD direction of the film sample The film samples were stretched by 200%, and the film samples were processed to a width of 10 mm and a distance between the chucks of 40 mm.
條件2-收縮試驗:使用三菱重工冷熱股份有限公司製「恆濕器TBP105DA」,設定溫度80℃將樣品加熱5秒。 Condition 2-Shrinkage test: A "hygrostat TBP105DA" manufactured by Mitsubishi Heavy Industries Co., Ltd. was used, and the sample was heated for 5 seconds at a set temperature of 80 ° C.
<評估方法> <Evaluation method>
作成尺寸為長100mm(標線間隔40mm+端部(上下各30mm)),寬10mm之長條形薄膜樣品,以上述條件1進行伸長。 A strip-shaped film sample having a length of 100 mm (a space between the marking lines + an end portion (30 mm above and below)) and a width of 10 mm was prepared and stretched under the conditions 1 described above.
200%伸長之狀態下保持10秒後,將夾盤回復至原來位置,放開夾盤,使樣品以上述條件2進行收縮。 After holding at 200% elongation for 10 seconds, return the chuck to its original position, release the chuck, and shrink the sample under Condition 2 above.
測量收縮後之標線間隔L[mm],藉由下述算式,算出回復率。 The interval L [mm] after the shrinkage was measured, and the recovery rate was calculated by the following formula.
回復率[%]={(120-L)/80}×100 Response rate [%] = {(120-L) / 80} × 100
MD方向及TD方向一同測量回復率,將此標示為熱收縮性(HS性)。 The MD and TD directions were used to measure the recovery rate, and this was designated as heat shrinkage (HS).
<評估基準> <Evaluation Criteria>
(一)熱收縮性(HS性) (A) heat shrinkability (HS)
○:經過熱收縮,回復率為70%以上。 ○: After heat shrinkage, the recovery rate was 70% or more.
回復率,較佳係90~110%。 The response rate is preferably 90 ~ 110%.
×:經過熱收縮,回復率未達70%。 ×: After heat shrinkage, the recovery rate was less than 70%.
藉由使MD及TD方向之回復率在前述範圍中,切割用基體薄膜,在80℃環境下,可發揮良好的熱收縮性(HS性)。 When the recovery rates in the MD and TD directions are within the aforementioned ranges, the base film for dicing can exhibit good heat shrinkability (HS properties) in an environment of 80 ° C.
(二)均勻熱收縮性(均勻HS性) (Two) uniform heat shrinkability (uniform HS)
○:MD方向之回復率與TD方向之回復率之比(MD/TD)未達1.2。 ○: The ratio of the recovery rate in the MD direction to the recovery rate in the TD direction (MD / TD) is less than 1.2.
回復率之比(MD/TD),較佳係0.9~1.15。 The response rate ratio (MD / TD) is preferably 0.9 to 1.15.
×:回復率之比(MD/TD)為1.2以上。 ×: The ratio of response rate (MD / TD) is 1.2 or more.
藉由使回復率之比(MD/TD)在前述範圍中,切割用基體薄膜,在80℃之條件下,可發揮良好的均勻熱收縮性(均勻HS性)。 When the recovery ratio (MD / TD) is within the aforementioned range, the base film for dicing can exhibit good uniform heat shrinkability (uniform HS property) under the condition of 80 ° C.
本發明之切割用基體薄膜(實施例1~12),即使在低溫條件下實施膨脹,切割薄膜亦可均勻延伸。 The dicing base film (Examples 1 to 12) of the present invention can be uniformly stretched even if it is expanded under low temperature conditions.
本發明(實施例)之切割用基體薄膜,與比較例相比,熱收縮 性(HS性)之數值顯著係較大之值。亦即,本發明之切割用基體薄膜,熱收縮性較良好。 Compared with the comparative example, the value of the heat shrinkability (HS property) of the base film for dicing of the present invention (Example) is significantly larger. That is, the base film for dicing of the present invention has good heat shrinkability.
低溫膨脹性(Ex性),本發明(實施例)及比較例之切割用基體薄膜,任一者皆在容許範圍內。 Any of the low-temperature expansion properties (Ex properties), the dicing base film of the present invention (examples) and the comparative examples is within an allowable range.
本發明(實施例)之切割用基體薄膜,與比較例相比,低溫高速膨脹性(低溫高速Ex性)良好。 Compared with the comparative example, the base film for dicing of this invention (Example) has a low-temperature high-speed expansion property (low-temperature high-speed Ex property).
(5)考察 (5) Inspection
熱收縮性 Heat shrinkability
使用本發明之切割用基體薄膜,即使切割薄膜(片材)經過膨脹步驟後,只要對所生鬆弛部加熱即可使該部分收縮,從而消除鬆弛。 With the dicing base film of the present invention, even if the dicing film (sheet) is subjected to the expansion step, the generated slack portion can be contracted by heating the slack portion, thereby eliminating slack.
使用本發明之切割用基體薄膜,特別係切割薄膜(片材),藉由加熱收縮之復原率高。 The dicing base film of the present invention, particularly a dicing film (sheet), has a high recovery rate by heat shrinkage.
使用本發明之切割用基體薄膜,可更迅速且簡便地將使用完之切割薄膜回收至機架。亦即,本發明之切割用基體薄膜,遇熱復原性高,且切割薄膜可均勻地回復。即熱收縮性被良好地發揮,機架回收性優異。此外,使用本發明之切割用基體薄膜之製品彼此不會衝突亦不會產生缺陷。 By using the dicing base film of the present invention, the used dicing film can be recovered to the rack more quickly and easily. That is, the dicing base film of the present invention has high resilience to heat, and the dicing film can be recovered uniformly. That is, the heat shrinkability is exhibited well, and the rack recyclability is excellent. In addition, products using the dicing base film of the present invention do not conflict with each other and do not cause defects.
膨脹性 Expansive
使用本發明之切割用基體薄膜,即使在低溫條件下實施膨脹,膨脹性仍良好,且切割薄膜可均勻延伸。使用本發明之切割用基體薄膜,在低溫條件下實施膨脹,可將半導體晶圓與銲晶層一同良好地切斷(分斷)。 Using the dicing base film of the present invention, even if expansion is performed under low temperature conditions, the swellability is good, and the dicing film can be uniformly stretched. By using the dicing base film of the present invention and performing expansion under a low temperature condition, the semiconductor wafer and the die bond layer can be well cut (divided) together.
使用本發明之切割用基體薄膜,特別係,隱形雷射晶圓切割後,切斷(分斷)半導體晶圓與銲晶層時,即使在低溫條件及高速條件下實施 膨脹,膨脹性亦良好,切割薄膜可良好地延伸。使用本發明之切割用基體薄膜,即使在低溫條件及高速條件下實施膨脹,可將半導體晶圓與銲晶層一同良好地切斷(分斷)。 When the substrate film for dicing of the present invention is used, in particular, after the invisible laser wafer is diced, the semiconductor wafer and the die bond layer are cut (separated), the expansion is good even when the expansion is performed at low temperature and high speed The cutting film can be extended well. By using the dicing base film of the present invention, even if expansion is performed under low-temperature conditions and high-speed conditions, the semiconductor wafer and the die bond layer can be well cut (separated) together.
使用本發明之切割用基體薄膜,在半導體製品持續小型化,片材追求再擴張(膨脹性)之中,可成為擴張性.收縮性更高之片材。 The use of the dicing base film of the present invention can be expanded while the semiconductor products continue to be miniaturized, and the sheet is being re-expanded (expandable). Higher shrinkage sheet.
Claims (5)
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CN113122160A (en) * | 2021-04-29 | 2021-07-16 | 东莞市金恒晟新材料科技有限公司 | Preparation method of novel thermal tackifying protective film |
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JP4510954B2 (en) * | 1998-08-10 | 2010-07-28 | リンテック株式会社 | Dicing tape and dicing method |
JP4780828B2 (en) * | 2000-11-22 | 2011-09-28 | 三井化学株式会社 | Adhesive tape for wafer processing, method for producing the same and method for using the same |
JP4195646B2 (en) * | 2002-07-26 | 2008-12-10 | 日東電工株式会社 | MULTILAYER SHEET, ITS MANUFACTURING METHOD, AND ADHESIVE SHEET USING THE MULTILAYER SHEET |
CN101157406B (en) * | 2007-10-30 | 2010-12-29 | 中国石化扬子石油化工有限公司 | A packaging elastic contraction film and preparing method |
JP5314308B2 (en) * | 2008-03-25 | 2013-10-16 | リンテック株式会社 | Laser dicing / die-bonding sheet and chip composite manufacturing method |
JP6264126B2 (en) | 2014-03-20 | 2018-01-24 | 日立化成株式会社 | Wafer processing tape |
JP6299315B2 (en) | 2014-03-20 | 2018-03-28 | 日立化成株式会社 | Wafer processing tape |
WO2016052444A1 (en) | 2014-09-29 | 2016-04-07 | リンテック株式会社 | Base for sheets for semiconductor wafer processing, sheet for semiconductor wafer processing, and method for manufacturing semiconductor device |
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JP2024008947A (en) | 2024-01-19 |
JP7421339B2 (en) | 2024-01-24 |
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WO2019039253A1 (en) | 2019-02-28 |
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