CN108822780B - Bonding material for cutting semiconductor silicon wafer - Google Patents

Bonding material for cutting semiconductor silicon wafer Download PDF

Info

Publication number
CN108822780B
CN108822780B CN201810337084.6A CN201810337084A CN108822780B CN 108822780 B CN108822780 B CN 108822780B CN 201810337084 A CN201810337084 A CN 201810337084A CN 108822780 B CN108822780 B CN 108822780B
Authority
CN
China
Prior art keywords
water
epoxy resin
absorbing
epoxy adhesive
resin
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
CN201810337084.6A
Other languages
Chinese (zh)
Other versions
CN108822780A (en
Inventor
袁求理
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hangzhou Dianzi University
Original Assignee
Hangzhou Dianzi University
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hangzhou Dianzi University filed Critical Hangzhou Dianzi University
Priority to CN201810337084.6A priority Critical patent/CN108822780B/en
Publication of CN108822780A publication Critical patent/CN108822780A/en
Application granted granted Critical
Publication of CN108822780B publication Critical patent/CN108822780B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J163/00Adhesives based on epoxy resins; Adhesives based on derivatives of epoxy resins
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J11/00Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/02Non-macromolecular additives
    • C09J11/04Non-macromolecular additives inorganic
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J11/00Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/02Non-macromolecular additives
    • C09J11/06Non-macromolecular additives organic
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J181/00Adhesives based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing sulfur, with or without nitrogen, oxygen, or carbon only; Adhesives based on polysulfones; Adhesives based on derivatives of such polymers
    • C09J181/02Polythioethers; Polythioether-ethers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • C08K2003/2206Oxides; Hydroxides of metals of calcium, strontium or barium
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

The invention discloses a bonding material for cutting a semiconductor silicon wafer. The components of the invention comprise epoxy resin, toughening agent, filler, coupling agent, water-absorbing material, polythiol, polyamide, filler and pigment. The invention adopts the water-absorbing and heat-releasing material calcium oxide to be added into the epoxy adhesive, when the resin plate and the steel workpiece plate bonded by the epoxy adhesive need to be soaked in water at normal temperature, the water-absorbing and heat-releasing material calcium oxide can absorb a large amount of water and release heat to cause the epoxy adhesive to lose efficacy, so that the resin plate and the steel workpiece plate can be easily separated in the water at normal temperature. The material is environment-friendly, and the harm to workers is greatly reduced; compared with the prior art, the epoxy adhesive can be rapidly disabled under normal temperature water.

Description

Bonding material for cutting semiconductor silicon wafer
Technical Field
The invention belongs to the technical field of material preparation, relates to preparation of a polymer composite material, and particularly relates to a bonding material for cutting a semiconductor silicon wafer.
Background
The development of semiconductors is continuously driven by the development of scientific technology. The development of automation and computers has reduced the cost of high technology products such as silicon wafers (integrated circuits) to a very low level. Particularly, photovoltaic energy has the advantages of no pollution, no noise, low maintenance cost, long service life and the like, and is rapidly developed in recent years, so that silicon wafers for constructing crystalline silicon solar cells are rapidly developed. In the process of cutting silicon wafers, silicon rods and resin plates must be fixed by silicon rod glue, and the resin plates and steel workpiece plates must be bonded by water boiling glue. The resin plate and the steel workpiece plate bonded by the boiled water glue can be degummed in hot water, so that the steel workpiece plate can be repeatedly used. Because the epoxy resin adhesive has the characteristics of high bonding strength, strong universality, relatively low price and the like, and has a series of excellent performances of excellent electrical insulation, stable chemical performance, good processing performance and the like, the silicon wafer cutting boiled water adhesive mainly adopts two-component epoxy resin adhesive at present. The invention discloses epoxy adhesive for silicon rod cutting and a preparation method thereof (application number: 201210258425.3), wherein powdery inorganic salts such as ammonium bicarbonate, sodium hydrosulfite or calcium hydrophosphate are adopted as degumming agents in epoxy resin adhesive, and the epoxy resin adhesive is decomposed and reacted in water at 50-60 ℃ to generate gas, so that a resin plate and a steel workpiece plate bonded by the epoxy adhesive can be degummed in hot water. However, these inorganic salts are decomposed in hot water to produce a small amount of gas, and thus the degumming time is long. A two-component epoxy adhesive and a preparation method thereof are invented by Shanghai Wei photovoltaic science and technology Limited company for a long time, and the application number is 201310016067. X.ammonium bicarbonate, ammonium carbonate, azodiisobutyronitrile, diethyl azodicarboxylate or p-toluenesulfonyl hydrazide are adopted as foaming agents and zinc oxide, urea and the like are adopted as foaming auxiliary agents in epoxy resin adhesive, and the epoxy resin adhesive is decomposed in hot water to react to generate gas, so that the resin plate and the steel workpiece plate bonded by the epoxy adhesive can be degummed in the hot water. However, these foaming agents can generate gas quickly only when the temperature is higher than 90 ℃, so that the epoxy resin plate and the steel workpiece plate bonded by the epoxy resin can be degummed in high-temperature hot water. Furthermore, epoxy adhesives typically use polysulfide rubber as a toughening agent, but polysulfide rubber has an unpleasant odor.
Disclosure of Invention
The invention aims to provide a bonding material for cutting a semiconductor silicon wafer aiming at the defects of the prior art, and the bonding material uses a water-absorbing heat-releasing material in an epoxy adhesive, so that the defect that the existing boiled epoxy adhesive needs high-temperature water degumming is overcome. Meanwhile, the synthetic plant ester chloro-methoxy fatty acid methyl ester is used as a toughening agent, so that the special toughening agent is special for toughening, is environment-friendly and odorless, and has a promoting effect on the adhesion of a metal material due to the chlorine.
The invention relates to a bonding material for cutting a semiconductor silicon wafer, which consists of A, B double components, wherein the components comprise the following raw materials in percentage by mass:
the component A comprises: 80-100 parts by weight of epoxy resin
10-30 parts of toughening agent
10-40 parts by weight of filler
0.5-1.0 part by weight of coupling agent
30-80 parts by weight of water-absorbing and heat-releasing material
And B component: 50-80 parts by weight of polythiol
30-40 parts by weight of polyamide
10-40 parts by weight of filler
1-4 parts by weight of pigment
The epoxy resin is one or a mixture of bisphenol A epoxy resin and bisphenol F epoxy resin;
the toughening agent is chloro-methoxy fatty acid methyl ester;
the filler is one or more of calcium carbonate, silicon dioxide, alumina and talcum powder;
the coupling agent is gamma-glycidol ether oxygen propyl trimethoxy silane;
the water-absorbing exothermal material is calcium oxide;
the pigment is phthalocyanine blue or phthalocyanine green.
When in use, A, B components are uniformly mixed, and the mixing ratio is that the mass ratio is 1: 1.
the invention also provides a preparation method of the material, which comprises the following steps:
the component A is prepared by adding the raw materials of epoxy resin, toughening agent, filler, coupling agent, water-absorbing material and the like into a stirrer according to a ratio, uniformly mixing by a high-speed dispersion machine under a vacuum condition, and then subpackaging.
And the component B is prepared by adding polythiol, polyamide, filler, pigment and other raw materials into a stirrer according to a ratio, uniformly mixing by a high-speed dispersion machine under a vacuum condition, and then subpackaging.
The invention adopts the water-absorbing and heat-releasing material calcium oxide to be added into the epoxy adhesive, when the resin plate and the steel workpiece plate bonded by the epoxy adhesive need to be soaked in water at normal temperature, the water-absorbing and heat-releasing material calcium oxide can absorb a large amount of water and release heat to cause the epoxy adhesive to lose efficacy, so that the resin plate and the steel workpiece plate can be easily separated in the water at normal temperature. The material is environment-friendly, and the harm to workers is greatly reduced; compared with the prior art, the epoxy adhesive can be rapidly disabled under normal temperature water.
Detailed Description
The present invention is further analyzed with reference to the following specific examples.
Example 1:
(1) the component A is prepared by adding raw materials of 80 kg of bisphenol A epoxy resin, 10 kg of chloromethoxy fatty acid methyl ester, 12 kg of calcium carbonate, 0.8 kg of gamma-glycidyl ether oxypropyl trimethoxy silane, 30 kg of calcium oxide and the like into a stirrer, uniformly mixing by a high-speed dispersion machine under a vacuum condition, and then subpackaging.
(2) And the component B is prepared by adding 50 kg of polythiol, 30 kg of polyamide, 20 kg of calcium carbonate, 2 kg of phthalocyanine blue and the like into a stirrer, uniformly mixing by using a high-speed disperser under a vacuum condition, and subpackaging.
When in use, A, B components are required to be uniformly mixed, and the mixing ratio is that the mass ratio is 1: 1, bonding the resin plate and the steel workpiece plate.
Example 2:
(1) the component A is prepared by adding 100 kg of bisphenol F epoxy resin, 25 kg of chloromethoxy fatty acid methyl ester, 10 kg of silicon dioxide, 1 kg of gamma-glycidyl ether oxypropyl trimethoxy silane, 30 kg of calcium oxide and the like into a stirrer, uniformly mixing by a high-speed dispersion machine under a vacuum condition, and then subpackaging.
(2) And the component B is prepared by adding 80 kg of polythiol, 40 kg of polyamide, 10 kg of silicon dioxide, 4 kg of phthalocyanine green and the like into a stirrer, uniformly mixing by using a high-speed dispersion machine under a vacuum condition, and subpackaging.
When in use, A, B components are required to be uniformly mixed, and the mixing ratio is that the mass ratio is 1: 1, bonding the resin plate and the steel workpiece plate.
Example 3:
(1) the component A is prepared by adding raw materials of 45 kg of bisphenol A epoxy resin, 45 kg of bisphenol F epoxy resin, 30 kg of chloromethoxy fatty acid methyl ester, 40 kg of alumina, 0.5 kg of gamma-glycidyl ether oxypropyl trimethoxysilane, 80 kg of calcium oxide and the like into a stirrer, uniformly mixing by a high-speed dispersion machine under a vacuum condition, and then subpackaging.
(2) And the component B is prepared by adding 60 kg of polythiol, 30 kg of polyamide, 40 kg of alumina, 1 kg of phthalocyanine blue and the like into a stirrer, uniformly mixing by using a high-speed dispersion machine under a vacuum condition, and then subpackaging.
When in use, A, B components are required to be uniformly mixed, and the mixing ratio is that the mass ratio is 1: 1, bonding the resin plate and the steel workpiece plate.
Example 4:
(1) the component A is prepared by adding 85 kg of bisphenol A epoxy resin, 15 kg of chloromethoxy fatty acid methyl ester, 30 kg of talcum powder, 0.6 kg of gamma-glycidyl ether oxypropyl trimethoxy silane, 80 kg of calcium oxide and the like into a stirrer, uniformly mixing by a high-speed dispersion machine under a vacuum condition, and then subpackaging.
(2) And the component B is prepared by adding 70 kg of polythiol, 30 kg of polyamide, 25 kg of talcum powder, 2 kg of phthalocyanine green and the like into a stirrer, uniformly mixing by using a high-speed dispersion machine under a vacuum condition, and subpackaging.
When in use, A, B components are required to be uniformly mixed, and the mixing ratio is that the mass ratio is 1: 1, bonding the resin plate and the steel workpiece plate.
Example 5:
(1) the component A is prepared by adding raw materials of 95 kg of bisphenol F epoxy resin, 15 kg of chloromethoxy fatty acid methyl ester, 10 kg of calcium carbonate, 10 kg of silicon dioxide, 0.9 kg of gamma-glycidyl ether oxypropyl trimethoxy silane, 60 kg of calcium oxide and the like into a stirrer, uniformly mixing by a high-speed dispersion machine under a vacuum condition, and then subpackaging.
(2) B, preparation of a component: adding 65 kg of polythiol, 35 kg of polyamide, 10 kg of silicon dioxide, 10 kg of alumina, 4 kg of phthalocyanine blue and the like into a stirrer, uniformly mixing by a high-speed disperser under a vacuum condition, and subpackaging.
When in use, A, B components are required to be uniformly mixed, and the mixing ratio is that the mass ratio is 1: 1, bonding the resin plate and the steel workpiece plate.
Performance test of the bonding material for cutting the semiconductor silicon wafer:
1. shear and tensile strength were determined according to GB7124-86 [ method for determining adhesive tensile shear strength (metal-metal) ].
2. And (3) determining the degumming time in water: and (3) bonding the resin sheet and a stainless steel sheet (with the length of 10cm and the width of 1 cm) with the bonding area of 8cm and 1cm, suspending the resin sheet and the stainless steel sheet in normal-temperature water at 25 ℃ after the resin sheet and the stainless steel sheet are completely cured, and recording the time for separating and releasing the resin sheet and the steel workpiece plate.
TABLE 1 Properties of Binder for semiconductor silicon wafer dicing
Sample (I) Shear strength (MPa) Tensile Strength (MPa) Degumming time (min/25 ℃ C.)
Example 1 19.2 20.5 17
Example 2 17.8 19.7 18
Example 3 18.6 20.3 18
Example 4 16.7 18.8 19
Example 5 18.9 19.1 17

Claims (1)

1. A bonding material for cutting semiconductor silicon wafers consists of A, B double components and is characterized in that the components comprise the following raw materials in percentage by weight:
Figure FDA0003018231770000011
Figure FDA0003018231770000012
the epoxy resin is one or a mixture of bisphenol A epoxy resin and bisphenol F epoxy resin;
the toughening agent is chloro-methoxy fatty acid methyl ester;
the filler is one or more of calcium carbonate, silicon dioxide, alumina and talcum powder;
the coupling agent is gamma-glycidol ether oxygen propyl trimethoxy silane;
the water-absorbing exothermal material is calcium oxide;
the pigment is phthalocyanine blue or phthalocyanine green;
when in use, the A, B components are mixed in a mass ratio of 1: 1.
CN201810337084.6A 2018-04-16 2018-04-16 Bonding material for cutting semiconductor silicon wafer Active CN108822780B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810337084.6A CN108822780B (en) 2018-04-16 2018-04-16 Bonding material for cutting semiconductor silicon wafer

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810337084.6A CN108822780B (en) 2018-04-16 2018-04-16 Bonding material for cutting semiconductor silicon wafer

Publications (2)

Publication Number Publication Date
CN108822780A CN108822780A (en) 2018-11-16
CN108822780B true CN108822780B (en) 2021-06-01

Family

ID=64154059

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810337084.6A Active CN108822780B (en) 2018-04-16 2018-04-16 Bonding material for cutting semiconductor silicon wafer

Country Status (1)

Country Link
CN (1) CN108822780B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111873200B (en) * 2020-07-15 2022-04-22 中锗科技有限公司 Method for improving yield of rounding of germanium/silicon infrared crystal

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE374759B (en) * 1969-03-24 1975-03-17 Litton Business Systems Inc
CN102786904B (en) * 2012-07-30 2014-02-19 东莞市永固绝缘材料有限公司 Fixing glue for cutting crystalline materials and preparation method thereof
EP3170860B1 (en) * 2015-11-19 2020-07-29 3M Innovative Properties Company Structural adhesive with improved corrosion resistance

Also Published As

Publication number Publication date
CN108822780A (en) 2018-11-16

Similar Documents

Publication Publication Date Title
CN102925088B (en) Solar crystalline silicon wafer temporary adhesive and its preparation method
CN102390094A (en) Solar-grade silicon wafer being cut by diamond wire and cutting method thereof
CN102627931B (en) Pre-catalytic bonding glue and preparation method thereof
CN108822780B (en) Bonding material for cutting semiconductor silicon wafer
CN105633341B (en) A kind of high-termal conductivity based lithium-ion battery positive plate and preparation method thereof
CN109321185B (en) Water-boiling degumming viscose glue and preparation method thereof
CN108624268B (en) Composite material for manufacturing solar silicon wafer
CN108676532B (en) Epoxy resin bonding material
CN115028386A (en) Compound cement grinding aid containing monoethanol diisopropanolamine and preparation method thereof
CN102659324B (en) Gluing and degluing method for metal part and glass part
CN111171284A (en) Epoxy modified aliphatic amine curing agent and application thereof in silicon ingot cutting fixing glue
CN108822781B (en) High-molecular adhesive material
CN107902990B (en) Method for preparing polymer cement waterproof mortar by using quartz sand dust
CN102181042A (en) Method for preparing epoxy resin curing agent
CN102786904A (en) Fixing glue for cutting crystalline materials and preparation method thereof
CN112250410A (en) Antistatic plate using industrial byproduct gypsum as raw material and preparation method thereof
CN102190857B (en) Solvent-free double-component epoxy moisture-proof film
CN115093819B (en) Adhesive for connecting composite boards and application method thereof
CN106363759B (en) A kind of wood-based plate
CN102229792A (en) Solar silicon wafer cutting mortar
CN108359404A (en) A kind of solar photovoltaic cell backplane adhesive and preparation method
CN115558452A (en) Bi-component structural adhesive for bonding power battery and preparation method thereof
CN108864849A (en) A kind of high-temperature resistant anti-corrosive switchgear
CN115340662A (en) Polyether modified epoxy curing agent and application thereof in silicon rod cutting
CN115232588B (en) Water boiling glue applied to large-size 210 silicon rod cutting and preparation method thereof

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant