SIZING COMPOSITIONS FOR GLASS FIBER DIRECT ROVING FOR PRODUCING MULTIAXIAL FABRICS, AND PREPARATION METHODS AND APPLICATIONS THEREOF
20220306529 · 2022-09-29
Inventors
- Fenglin YE (Tongziang City, Zhejiang, CN)
- Qifeng Gei (Tongxiang City, Zhejiang, CN)
- Juan Liu (Tongxiang City, Zhejiang, CN)
- Hongya Zhou (Tongxiang City, Zhejiang, CN)
- Bilong Dai (Tongxiang City, Zhejiang, CN)
Cpc classification
C08L63/00
CHEMISTRY; METALLURGY
D10B2403/02412
TEXTILES; PAPER
C08L63/00
CHEMISTRY; METALLURGY
International classification
Abstract
A sizing composition for glass fiber direct roving for producing multiaxial fabrics is provided. The sizing composition includes, based on the total solids mass of the composition, 0.1 to 5.0% by solid mass of a first silane coupling agent, 2.5 to 11.0% by solid mass of a second silane coupling agent, 3.0 to 20.0% by solid mass of a first film former, 45.0 to 75.0% by solid mass of a second film former, 0 to 5.0% by solid mass of a plasticizer, 0.2 to 4.0% by solid mass of a first lubricant, 5.0 to 20.0% by solid mass of a second lubricant, and 0.01 to 3.0% by solid mass of a pH regulator. The first film former is a multifunctional epoxy emulsion, and the second film former is a low-molecular-weight liquid epoxy emulsion.
Claims
1. A sizing composition for glass fiber direct roving for producing multiaxial fabrics, characterized by comprising the following components, a solid mass of each of the following components accounting for a total solids mass of the sizing composition expressed in percentage by mass as follows: TABLE-US-00008 a first silane coupling agent 0.1[[~]]-5.0%; a second silane coupling agent 2.5[[~]]-11.0%; a first film former 3.0[[~]]-20.0%; a second film former 45.0[[~]]-75.0%; a plasticizer .sup. 0[[~]]-5.0%; a first lubricant 0.2[[~]]-4.0%; a second lubricant .sup. 5.0[[~]]-20.0%; and pH regulator 0.01[[~]]-3.0%; wherein the first film former is a multifunctional epoxy emulsion, and the multifunctional epoxy emulsion is at least one of a polyphenol epoxy emulsion or a glycidyl amine epoxy emulsion; and the second film former is a low-molecular-weight liquid epoxy emulsion; and a solids mass of the sizing composition accounts for 10-15% of the a total mass of the sizing composition, and a remainder of the sizing composition is deionized water.
2. The sizing composition according to claim 1, wherein, the sizing composition comprises the following components expressed in percentage by mass: TABLE-US-00009 the first silane coupling agent 0.5[[~]]-1.5%; the second silane coupling agent 3.5[[~]]-7.0%; the first film former 7.0[[~]]-16.0%; the second film former 50.0[[~]]-65.0%; the plasticizer .sup. 0[[~]]-3.0%; the first lubricant 0.5[[~]]-2.0%; the second lubricant .sup. 9.0[[~]]-16.0%; and pH regulator 0.01[[~]]-2.00%.
3. The sizing composition according to claim 1, wherein, the polyphenol epoxy emulsion is one or more of a 4,4′-diamino diphenyl methane tetrafunctional epoxy resin emulsion, a triglycidyl p-aminophenol trifunctional epoxy emulsion, and an epoxidized m-xylylenediamine tetrafunctional epoxy resin emulsion.
4. The sizing composition according to claim 1, wherein, the low-molecular-weight liquid epoxy emulsion is one or more of a glycidyl ester epoxy emulsion, an aliphatic glycidyl ether epoxy emulsion, a bisphenol A epoxy emulsion, a bisphenol F epoxy emulsion, a bisphenol AD epoxy emulsion, and a bisphenol S epoxy emulsion.
5. The sizing composition according to claim 1, wherein, the first silane coupling agent is one or more of a γ-aminopropyl triethoxy silane, a γ-aminopropyl trimethoxy silane, an N-β-(aminoethyl)-γ-aminopropyl trimethoxy silane, a γ-glycidyl etherpropyl trimethoxy silane, a 3-glycidyl propyl methoxydiethyloxy silane, and a γ-methacryloyloxypropyl trimethoxy silane.
6. The sizing composition according to claim 1, wherein, the second silane coupling agent is one or more of an N-phenyl-N-aminoethyl-γ-aminopropyl trioxysilane hydrochloride, a cationic styrene aminotrimethoxy silane, and a polynitrogen amide silane.
7. The sizing composition according to claim 1, wherein, the plasticizer is one or more of a saturated polyester plasticizer, a polymeric benzoate ester plasticizer, a benzoate ester plasticizer, an adipate polymer plasticizer, and a polyol ester plasticizer.
8. The sizing composition according to claim 1, wherein, the first lubricant is one or more of a fatty acid amine, a fatty amide polycondensate, and an epoxy modified phenylsiloxane.
9. A method of preparing the sizing composition according to claim 1, characterized by comprising the following steps: 1) pre-dispersing the first silane coupling agent and the second silane coupling agent in the process as described below: adding deionized water and some pH regulator into a first vessel, and adding, under stirring, the first silane coupling agent into the first vessel; adding deionized water and more pH regulator into a second vessel, and adding, under stirring, the second silane coupling agent and deionized water with a mass of 15-30 times the mass of the second silane coupling agent; 2) pre-dissolving the first lubricant and the second lubricant in the process as described below: sequentially adding deionized water and the first lubricant into a third vessel, and stirring deionized water and the first lubricant till the first lubricant is fully dissolved; adding deionized water and the second lubricant into a fourth vessel, and stirring deionized water and the second lubricant till the second lubricant is fully dissolved; 3) pre-dissolving and diluting the first film former and the second film former in the process as described below: adding the first film former and deionized water into a fifth vessel, and stirring the first film former and deionized water till the first film former is dissolved; adding the second film former and deionized water into a sixth vessel, and stirring the second film former and deionized water till the second film former is dissolved; 4) adding into a preparation vessel successively the following: a) water accounting for 10%-30% of the total mass of the sizing composition to be prepared; b) a pre-dispersed first silane coupling agent and a pre-dispersed second silane coupling agent obtained in step 1); c) a pre-dissolved and diluted first film former and a pre-dissolved and diluted second film former obtained in step 3); d) a pre-dissolved first lubricant and a pre-dissolved second lubricant obtained in step 2); and e) the remainder of deionized water; and stirring and uniformly mixing to obtain the sizing composition for glass fiber direct roving for producing multiaxial fabrics.
10. An application of the sizing composition according to claim 1 for producing glass fiber multiaxial fabrics.
11. The sizing composition according to claim 1, wherein, the glycidyl amine epoxy emulsion is one or more of a dicyclopentadiene phenol glycidyl ester resin, an epoxidized m-xylylenediamine, a 1, 1, 1-tris (p-hydroxyphenyl) ethane glycidyl ether trifunctional epoxy emulsion, a tetra (4-hydroxyphenyl) ethane tetraglycidyl ether tetrafunctional epoxy emulsion, and a 1,3-bis (N, N-diglycidyl aminomethyl) cyclohexane tetrafunctional epoxy emulsion.
12. The sizing composition according to claim 1, wherein, the low-molecular-weight liquid epoxy emulsion has an epoxy equivalent of from 180 to 300 and an emulsion particle size of from 0.2 microns to 2.0 microns.
13. The sizing composition according to claim 1, wherein, the second lubricant is a polyethylene glycol (PEG) lubricant.
14. The sizing composition according to claim 1, wherein, the pH regulator is one or more of a citric acid, a boric acid, a formic acid, an acetic acid, and an organic amine.
15. The method of preparing the sizing composition according to claim 9, comprising the following steps: 1) pre-dispersing the first silane coupling agent and the second silane coupling agent in the process as described below: adding an amount of deionized water to a first disperser, the deionized water having a mass of 20-50 times the mass of the first silane coupling agent, using part of pH regulator to regulate a pH value of the deionized water to be 3.5-4.0, then slowly adding the first silane coupling agent to the deionized water being stirred at a rate of 50-200 r/min, and stirring for 15-30 minutes, and thus the first pre-dispersed silane coupling agent is obtained; adding an amount of deionized water to a second disperser, the deionized water havings a mass of 0.2-2.0 times the mass of the second silane coupling agent, adding the remaining pH regulator and the second silane coupling agent to the deionized water being stirred at a rate of 50-200 r/min, and stirring for 15-30 minutes, and then slowly adding deionized water with a mass of 15-30 times of the second silane coupling agent, and thus the second pre-dispersed silane coupling agent is obtained; 2) pre-dissolving the first lubricant and the second lubricant in the process as described below: adding an amount of deionized water to a third vessel, the deionized water having a mass of 5-10 times the mass of the first lubricant, then adding the first lubricant slowly and stirring mixture till the first lubricant is fully dissolved, thus the pre-dissolved first lubricant is obtained; adding an amount of deionized water to a fourth vessel, the deionized water having a temperature of 40-60° C. and a mass of 10-20 times the mass of the second lubricant, then slowly adding the second lubricant and stirring the mixture till the second lubricant is fully dissolved, thus the pre-dissolved second lubricant is obtained; 3) pre-dissolving and diluting the first film former and the second film former in the process as described below: successively adding the first film former and an amount of water to a fifth vessel, the water having a mass 1-2 times the mass of the first film former, stirring the mixture for 5-15 minutes till the first film former is fully dissolved, thus the pre-dissolved and diluted first film former is obtained; or alternatively, when a plasticizer is used, first adding the first film former to a fifth vessel, and then dripping the plasticizer into the fifth vessel at a rate of 2-12 g/min under stirring at a rate of 20-150 r/min, stirring the mixture for a period of 2-48 hours for plasticization, and then adding a mass of water that is 1-2 times the mass of the first film former, stirring the mixture for 5-15 minutes till it is fully homogenized, thus the pre-dissolved and diluted first film former is obtained; adding the second film former and an amount of water 1-2 times the mass of the second film former to a sixth vessel, stirring the mixture for a period of time till it is fully homogenized, thus the pre-dissolved and diluted second film former is obtained; 4) adding into a preparation vessel successively the following: a) an amount of water accounting for 10%-30% by mass of the total mass of the sizing composition to be prepared; b) the pre-dispersed first silane coupling agent and the pre-dispersed second silane coupling agent obtained in step 1); c) the pre-dissolved and diluted first film former and the pre-dissolved and diluted second film former obtained in step 3); d) the pre-dissolved and diluted first lubricant and the pre-dissolved and diluted second lubricant obtained in step 2); and e) the remainder of deionized water; and stirring the resulting mixture for 10-30 minutes, to obtain the sizing composition for glass fiber direct roving for producing multiaxial fabrics.
Description
DETAILED DESCRIPTION
[0065] The technical solutions according to the present application will be described clearly and completely below with reference to the specific embodiments of the present application. Apparently, the described embodiments are just some but not all of the embodiments of the present application. All other embodiments obtained by a person of ordinary skill in the art based on the embodiments of the present application without performing any creative work shall fall into the protection scope of the present application. It is to be noted that the embodiments in the present application and the features in the embodiments can be combined at will if not conflicted.
[0066] In the sizing composition for glass fiber direct roving for producing multiaxial fabrics according to the present application, the solids content of the sizing composition accounts for 10-15% of the total mass of the sizing composition, and the remainder is deionized water. The sizing composition comprises: 0.1-5.0% of a first silane coupling agent, 2.5-11.0% of a second silane coupling agent, 3.0-20.0% of a first film former, 45.0-75.0% of a second film former, 0-5.0% of a plasticizer, 0.2-4.0% of a first lubricant, 5.0-20.0% of a second lubricant, and 0.01-3.0% of a pH regulator, as expressed in solid mass percentage based on the total solids mass of the composition.
[0067] Preferably, the sizing composition comprises: 0.5-1.5% of the first silane coupling agent, 3.5-7.0% of the second silane coupling agent, 7.0-16.0% of the first film former, 50.0-65.0% of the second film former, 0-3.0% of the plasticizer, 0.5-2.0% of the first lubricant, 9.0-16.0% of the second lubricant, and 0.01-2.00% of the pH regulator, as expressed in solid mass percentage based on the total solids mass of the composition.
[0068] Wherein, the first film former is a multifunctional epoxy emulsion, which is a polyphenol epoxy emulsion and/or a glycidyl amine epoxy emulsion. The polyphenol epoxy emulsion is one or more of a 4,4′-diamino diphenyl methane tetrafunctional epoxy resin emulsion, a triglycidyl p-aminophenol trifunctional epoxy emulsion, and an epoxidized m-xylylenediamine tetrafunctional epoxy resin emulsion; and the glycidyl amine epoxy emulsion is one or more of a dicyclopentadiene phenol glycidyl ester resin, an epoxidized m-xylylenediamine, a 1, 1, 1-tris (p-hydroxyphenyl) ethane glycidyl ether trifunctional epoxy emulsion, a tetra (4-hydroxyphenyl) ethane tetraglycidyl ether tetrafunctional epoxy emulsion, and a 1,3-bis (N, N-diglycidyl aminomethyl) cyclohexane tetrafunctional epoxy emulsion;
[0069] the second film former is a low-molecular-weight liquid epoxy emulsion, which is one or more of a glycidyl ester epoxy emulsion, an aliphatic glycidyl ether epoxy emulsion, a bisphenol A epoxy emulsion, a bisphenol F epoxy emulsion, a bisphenol AD epoxy emulsion, and a bisphenol S epoxy emulsion; and the low-molecular-weight liquid epoxy emulsion has an epoxy equivalent of 180-300 and an emulsion particle size of 0.2-2.0 microns;
[0070] the first silane coupling agent is one or more of a γ-aminopropyl triethoxy silane, a γ-aminopropyl trimethoxy silane, an N-β-(aminoethyl)-γ-aminopropyl trimethoxy silane, a γ-glycidyl etherpropyl trimethoxy silane, a 3-glycidyl propyl methoxydiethyloxy silane, and a γ-methacryloyloxypropyl trimethoxy silane;
[0071] the second silane coupling agent is one or more of an N-phenyl-N-aminoethyl-γ-aminopropyl trioxysilane hydrochloride, a cationic styrene aminotrimethoxy silane, and a polynitrogen amide silane;
[0072] the plasticizer is one or more of a saturated polyester plasticizer, a polymeric benzoate ester plasticizer, a benzoate ester plasticizer, an adipate polymer plasticizer, and a polyol ester plasticizer;
[0073] the first lubricant is one or more of a fatty acid amine, a fatty amide polycondensate, and an epoxy modified phenylsiloxane; the second lubricant is a PEG lubricant; and,
[0074] the pH regulator is one or more of a citric acid, a boric acid, a formic acid, an acetic acid, and an organic amine.
[0075] The method of preparing the sizing composition according to the present application comprises the following steps:
[0076] 1) an amount of deionized water is added to a first disperser, the deionized water has a mass of 20-50 times the mass of the first silane coupling agent, part of pH regulator is used to regulate the pH value of the deionized water to be 3.5-4.0, then the first silane coupling agent is added slowly to the deionized water being stirred at a rate of 50-200 r/min, and stirring for 15-30 minutes, and the first pre-dispersed silane coupling agent is obtained;
[0077] an amount of deionized water is added to a second disperser, the deionized water has a mass of 0.2-2.0 times the mass of the second silane coupling agent, the remaining pH regulator and the second silane coupling agent are added to the deionized water being stirred at a rate of 50-200 r/min, and stirring for 15-30 minutes, and then slowly add deionized water with a mass of 15-30 times of the second silane coupling agent, and the second pre-dispersed silane coupling agent is thus obtained;
[0078] 2) an amount of deionized water is added to a third vessel, the deionized water has a mass of 5-10 times the mass of the first lubricant, then add the first lubricant slowly and stir the mixture till the lubricant is fully dissolved, thus the pre-dissolved first lubricant is obtained;
[0079] an amount of deionized water is added to a fourth vessel, the deionized water has a temperature of 40-60° C. and a mass of 10-20 times the mass of the second lubricant, then slowly add the second lubricant and stir the mixture till the lubricant is fully dissolved, thus the pre-dissolved second lubricant is obtained;
[0080] 3) the first film former and an amount of water are successively added to a fifth vessel, the water has a mass 1-2 times the mass of the first film former, stir the mixture for 5-15 minutes till the film former is fully dissolved, and the pre-dissolved and diluted first film former is thus obtained;
[0081] or alternatively, when a plasticizer is used, the first film former is first added to a fifth vessel, and then the plasticizer is dripped into the fifth vessel at a rate of 2-12 g/min under stirring at a rate of 20-150 r/min, stir the mixture for a period of 2-48 hours for plasticization, and then add a mass of water that is 1-2 times the mass of the first film former, stir the mixture for 5-15 minutes till it is fully homogenized, and the pre-dissolved and diluted first film former is thus obtained;
[0082] the second film former and an amount of water 1-2 times the mass of the second film former are added to a sixth vessel, stir the mixture for a period of time till it is fully homogenized, and the pre-dissolved and diluted second film former is obtained;
[0083] 4) the following components are successively added to a preparation vessel:
[0084] a) an amount of water accounting for 10%-30% by mass of the total mass of the sizing composition to be prepared;
[0085] b) the pre-dispersed first silane coupling agent and the pre-dispersed second silane coupling agent obtained in step 1);
[0086] c) the pre-dissolved and diluted first film former and the pre-dissolved and diluted second film former obtained in step 3);
[0087] d) the pre-dissolved and diluted first lubricant and the pre-dissolved and diluted second lubricant obtained in step 2); and
[0088] e) the remainder of deionized water;
[0089] stir the resulting mixture for 10-30 minutes, and the sizing composition for glass fiber direct roving for producing multiaxial fabrics is obtained.
[0090] The examples below illustrate some exemplary embodiments of the present application.
EXAMPLES
[0091]
TABLE-US-00003 TABLE 1 Examples Illustrating the Sizing Compositions of the Present Application Component/% Example Example Example Example Example Example Example Example Example Example (and LOI) 1 2 3 4 5 6 7 8 9 10 First silane 0.5 0.6 0.7 0.8 0.8 1.2 1 1.4 4.5 3 coupling agent Second silane 7 7 5.6 6 5 5 6 4 3 10 coupling agent First film former 7 12 9 16 12 11 14 16 20 4 Second film former 64.92 63.4 65 60 62.3 63.2 61 63.4 46 70 Plasticizer — 0.2 0.5 0.4 2 1 2 3 3.5 5 First lubricant 0.5 0.6 1 1.2 1.5 1.5 1.5 2 4 0.2 Second lubricant 20 16 18 15 16 17 14.2 10 16 5 Citric acid 0.08 0.2 0.2 0.6 0.4 0.1 0.3 0.2 3 2.8 LOI (%) 0.54 0.56 0.55 0.53 0.56 0.54 0.57 0.53 0.55 0.53
[0092] The components in the sizing compositions respectively under Examples 1-10 of Table 1 are as follows:
[0093] the first silane coupling agent: A-187, available from Momentive, γ-glycidyl etherpropyl trimethoxy silane;
[0094] the second silane coupling agent: OFS-6032, available from Dow Corning, cationic styrene aminotrimethoxy silane;
[0095] the first film former: TX-612, available from Jushi Group, triglycidyl p-aminophenol emulsion;
[0096] the second film former: EPI-REZ 3510-W-60, available from HEXION, bisphenol A epoxy emulsion;
[0097] the first lubricant: epoxy modified phenyl siloxane emulsion, available from Shanghai Shinchem Chemical Products;
[0098] the second lubricant: PEG400MO, available from Toho Chemical Industry;
[0099] the plasticizer: Neoxil 9166, available from AOC, saturated polyester; and
[0100] the pH regulator: citric acid, available from SINOPEC.
[0101] It is to be noted that the specific types and contents of the above-mentioned components do not constitute a limitation of the protection scope of the present application.
TABLE-US-00004 TABLE 2 Examples Illustrating the Sizing Compositions of the Present Application (continued) Component/% Example Example Example Example Example Example Example Example Example Example (and LOI) 11 12 13 14 15 16 17 18 19 20 First silane 0.2 5 1.4 1.5 0.5 1.2 4 2.5 3.5 0.8 coupling agent Second silane 10.5 3.5 6.5 4 7 6.5 2.5 8 6 11 coupling agent First film A 4 3 9 13 11 — 20 — 1 5 former B 1.5 7.3 — 3 2 14 — 3 6 4 Second film former 71.45 75 64 56 61.6 65 46 67 61.2 68 Plasticizer 2 — 2.5 2.5 1 3 1.5 3.3 5 0.5 First lubricant 0.2 1 1.8 2 1 0.5 4 2 0.8 3.5 Second lubricant 10.1 5 14.3 16 15.5 9 20 14 15 4.2 Acetic acid 0.05 0.2 0.5 2 0.4 0.8 2 0.2 1.5 3 LOI (%) 0.56 0.55 0.55 0.53 0.54 0.54 0.57 0.54 0.55 0.56
[0102] The components in the sizing compositions respectively under Examples 11-20 of Table 2 are as follows:
[0103] the first silane coupling agent: A-174, available from Momentive, γ-methacryloyloxypropyl trimethoxy silane;
[0104] the second silane coupling agent: A-1387, available from Jushi Group, polynitrogen amide silane;
[0105] the first film former: A: TX-686, available from Jushi Group, epoxidized m-xylylenediamine tetrafunctional epoxy resin; and B: TX-688, available from Jushi Group, dicyclopentadiene phenol glycidyl ester resin;
[0106] the second film former: TX-613, available from Jushi Group, bisphenol F epoxy emulsion;
[0107] the first lubricant: CATIONIC Softener Conc. Flake, available from EVONIK INDUSTRIES, fatty acid amine;
[0108] the second lubricant: PEG400 Monopelargonate, available from Pulcra Chemicals;
[0109] the plasticizer: BENZOFLEX 50, available from Eastman Specialties Wuhan Youji Chemical, polymeric benzoate ester plasticizer; and
[0110] the pH regulator: acetic acid, available from SINOPEC.
[0111] In order to further demonstrate the beneficial effects of the present application, comparisons are made between the sizing compositions of the present application and the sizing compositions of reference examples by testing the properties of these compositions and the properties of reinforced composites containing these compositions. The specific test results are given below in Tables 3-5. The sizing composition of each of the reference examples 1-4 comprises the following components expressed in solid mass percentage based on the total solids mass of the corresponding composition.
Reference Example 1
[0112] a first silane coupling agent: 10% of A-187, available from Momentive, γ-glycidyl etherpropyl trimethoxy silane;
[0113] a second silane coupling agent: 15% of OFS-6032, available from Dow Corning, cationic styrene aminotrimethoxy silane;
[0114] a first film former: 25% of TX-612, available from Jushi Group, multifunctional triglycidyl p-aminophenol emulsion;
[0115] a second film former: 40.97% of EPI-REZ 3510-W-60, available from HEXION, bisphenol A epoxy emulsion;
[0116] a first lubricant: 6% of epoxy modified phenyl siloxane emulsion, available from Shanghai Shinchem Chemical Products;
[0117] a second lubricant: 0.02% of PEG400MO, available from Toho Chemical Industry;
[0118] a plasticizer: 3% of Neoxil 9166, available from AOC, saturated polyester; and
[0119] pH regulator: 0.01% of citric acid, available from SINOPEC.
Reference Example 2
[0120] coupling agent: 15% of A-187, available from Momentive, γ-glycidyl etherpropyl trimethoxy silane;
[0121] lubricant: 15% of epoxy modified phenyl siloxane emulsion, available from Shanghai Shinchem Chemical Products; and 9% of Katex6760, available from Pulcra Chemicals, polyethyleneimine salt;
[0122] film former: 60.9% of EPI-REZ 3510-W-60, available from HEXION, bisphenol A epoxy emulsion;
[0123] pH regulator: 0.1% of citric acid, available from SINOPEC.
Reference Example 3
[0124] coupling agent: 15% of A-187, available from Momentive, γ-glycidyl etherpropyl trimethoxy silane;
[0125] lubricant: 5% of Katex8760, available from Pulcra Specialty Chemicals (Shanghai); and 15% of PEG400MO, available from Toho Chemical Industry;
[0126] film former: 64.9% of EPI-REZ 3510-W-60, available from HEXION, bisphenol A epoxy emulsion;
[0127] pH regulator: 0.1% of acetic acid, available from SINOPEC.
Reference Example 4
[0128] coupling agent: 10% of A-174, available from Momentive, γ-methacryloyloxypropyl trimethoxy silane; and 5% of A-1100, available from Momentive, γ-aminopropyl triethoxysilane;
[0129] lubricant: 10% of Katex8760, available from Pulcra Specialty Chemicals (Shanghai); and 15% of PEG400MO, available from Toho Chemical Industry;
[0130] film former: 58% of EPI-REZ 3510-W-60, available from HEXION, bisphenol A epoxy emulsion;
[0131] pH regulator: 2% of acetic acid, available from SINOPEC.
TABLE-US-00005 TABLE 3 Tested Properties and Their Comparison Example Example Example Example Example Example Example Example Tested property 1 2 3 4 5 6 7 8 Fuzz amount (mg/1000 m) 12 13 6 11 8 15 14 6 Dissolution rate in 83 78 85 70 79 81 78 73 acetone (%) 90° Tensile strength (MPa) 58 64 59 63 65 61 63 62 Shear strength (MPa) 72.4 78.2 71.7 70.1 78.9 70.5 73.3 75.1 Glass fiber content (%) 75.2 75.0 74.9 75.3 75.1 75.4 74.8 74.8 LOI (%) 0.54 0.56 0.55 0.53 0.56 0.54 0.57 0.53
TABLE-US-00006 TABLE 4 Tested Properties and Their Comparison (continued) Example Example Example Example Example Example Example Example Tested property 9 10 11 12 13 14 15 16 Fuzz amount (mg/1000 m) 9 11 12 12 10 11 12 8 Dissolution rate in 73 81 76 74 72 73 74 74 acetone (%) 90° Tensile strength (MPa) 60 61 61 62 65 63 63 64 Shear strength (MPa) 70.3 71.2 70.9 70.9 74.8 72.8 73.8 74.3 Glass fiber content (%) 74.9 75.0 74.7 74.9 75.0 75.2 74.9 75.1 LOI (%) 0.55 0.56 0.56 0.55 0.55 0.53 0.54 0.54
TABLE-US-00007 TABLE 5 Tested Properties and Their Comparison (continued) Example Example Example Example Ref. Ref. Ref. Ref. Tested property 17 18 19 20 example 1 example 2 example 3 example 4 Fuzz amount (mg/1000 m) 9 10 9 11 17 18 10 20 Dissolution rate in 75.2 77.8 79 80 68 92 93 89 acetone (%) 90° Tensile strength (MPa) 60 61 62 60 54 46 41 48 Shear strength (MPa) 70.2 72.3 72.1 70.1 68 66 60 67 Glass fiber content (%) 74.9 74.8 75.0 74.7 74. 75.1 74.9 75.0 LOI (%) 0.57 0.54 0.55 0.56 0.57 0.56 0.55 0.58
[0132] The above test data are obtained by using the commonly available methods of testing glass fiber products, which belong to the common general knowledge in the art. A comparison of the test data for the examples 1-20 of the present application and for the reference examples show that the values of the fuzz amount, dissolution rate in acetone, 90° tensile strength, and shear strength in the exemplary examples of the present application are all significantly better than those in the reference examples. This means the exemplary examples of the present application have the advantages of low fuzz, appropriate acetone dissolution rate, and excellent tensile strength and shear strength. The content of each component in the sizing compositions respectively under examples 1-20 is appropriate and reasonable, and the mechanical strength rendered by each composition is high, which meets the process requirements for producing multiaxial fabrics.
[0133] In conclusion, the sizing composition according to the present application has good compatibility with the matrix epoxy resin. In addition, the film former in the sizing composition can react with the matrix epoxy resin, which helps to improve the mechanical strength and stability of the composite materials. When applied on the surface of glass fiber, the sizing composition can ensure that the coating of the sizing in the glass fiber multiaxial fabrics to be made has a moderate and suitable dissolution rate in the resin, the dissolution rate being neither too fast nor too slow, so that a full wet-out of the fabrics by the resin will be guaranteed; what's more, the coated glass fiber in the fabrics has good bonding with the resin. The sizing composition also enables the sized glass fiber to have low fuzz and smooth weaving performance in the subsequent process.
[0134] The contents described above can be implemented independently or in combination in various ways, and these transformations shall fall into the protection scope of the present application.
[0135] Finally, it is to be noted that the foregoing exemplary embodiments are used merely for the purpose of describing the technical solutions of the present application and not intended to constitute any limitations thereto. Although the present application has been specifically described with reference to the foregoing embodiments, it should be understood by a person of ordinary skill in the art that modifications can be made to the technical solutions described in the embodiments, and equivalent replacements can be made to some technical features of the solutions; and these modifications or equivalent replacements shall not make the essence of corresponding technical solutions depart from the spirit and scope of the technical solutions described in the embodiments of the present application.
INDUSTRIAL APPLICABILITY
[0136] The sizing composition for glass fiber direct roving for producing multiaxial fabrics according to the present application has a suitable dissolution rate in the resin, and has good compatibility with the resin. It can modify the physical and chemical properties of the surface of glass fiber, improve various performances of glass fiber, and thus meet the process requirements for producing glass fiber multiaxial fabrics. The wind turbine blades made from the glass fiber multiaxial fabrics containing the sizing composition according to the present application have such advantages as stable mechanical strength, excellent fatigue resistance, and longer service life.