Article(id=1320098778980406202, tenantId=1146029695717560320, journalId=1263187385517883426, issueId=1320098753533563467, articleNumber=null, orderNo=null, doi=10.14062/j.issn.0454-5648.20230873, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1699977600000, receivedDateStr=2023-11-15, revisedDate=1704729600000, revisedDateStr=2024-01-09, acceptedDate=null, acceptedDateStr=null, onlineDate=1792665675158, onlineDateStr=2026-10-22, pubDate=1732032000000, pubDateStr=2024-11-20, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1792665675158, onlineIssueDateStr=2026-10-22, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1792665675158, creator=13701087609, updateTime=1792665675158, updator=13701087609, issue=Issue{id=1320098753533563467, tenantId=1146029695717560320, journalId=1263187385517883426, year='2024', volume='52', issue='11', pageStart='3349', pageEnd='3662', issueExtLink='null', onlineDate='null', pubDate='1732032000000', pubDateStr='2024-11-20', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1792665669090, creator='13701087609', updateTime=1792666254807, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1320101210271626196, tenantId=1146029695717560320, journalId=1263187385517883426, issueId=1320098753533563467, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1320101210271626197, tenantId=1146029695717560320, journalId=1263187385517883426, issueId=1320098753533563467, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=3460, endPage=3469, ext={EN=ArticleExt(id=1320098779152372667, articleId=1320098778980406202, tenantId=1146029695717560320, journalId=1263187385517883426, language=EN, title=Evolution of Bonding Performance and Improvement Mechanism of Glass Fiber Reinforced Plastics-Concrete Based on Resin Matrix Modification, columnId=1321897857741861733, journalTitle=Journal of the Chinese Ceramic Society, columnName=Special Issue on Durability of High Performance Cement Concrete in Harsh Environment—Research Article, runingTitle=null, highlight=null, articleAbstract=
Introduction

The bonding properties of Fiber Reinforced Plastics (FRP) -concrete composites is directly related to the load carrying capacity and durability of FRP reinforced concrete structures. In addition, the study of bond properties can help us better understand how FRP bars behave in concrete and how they react under specific environmental conditions (e.g., high temperature, humidity, corrosion, etc.). This is valuable for predicting and improving the long-term performance of concrete structures. However, in offshore engineering, structures are exposed to strong corrosive environments all year round. Under the erosion of internal FRP bars by corrosive ions and the highly alkaline environment of the concrete pore solution, the matrix on the surface of FRP bars firstly suffers from deterioration phenomena such as dissolution, plasticization, and microcrack formation. Consequently, the bonding properties of the FRP-concrete interface are seriously affected, leading to the deterioration or failure of the concrete structure. Therefore, improving the corrosion resistance of FRP reinforcement is an important measure to ensure the long-term service of FRP-reinforced concrete structures. In this paper, the resin matrix modification of GFRP bars was realized by self-synthesized organosilicones and surface hydrophobic modification of nanofillers to obtain highly corrosion-resistant GFRP bars. To investigate the degradation of the interfacial adhesion between highly corrosion-resistant GFRP reinforcement and seawater-seasand concrete (SSC) in simulated pore solution of SSC at 60 ℃, and to reveal the mechanism of GFRP reinforcement-concrete adhesion enhancement through interfacial microstructure analysis.

Methods

Organosilicon synthesis: Hydrogen-containing silicone oil (PMHS) was mixed with γ-(2,3-epoxypropyloxy) propyltrimethoxysilane (KH560) in a mass ratio of 1∶1, with ethanol as the solvent, and reacted under the catalytic effect of NaOH for 8 h at ambient temperature using a magnetic stirrer (200 r/min), and then kept for spare.

CNT surface modification: 0.03% (mass fraction) of CNTs was stirred and dispersed into an ethanol and KOH organic solvent, and the CNT modifier was subsequently obtained by adding hydrogen-containing silicone oil (PMHS) and ethyl silicate (TEOS) after ultrasonic dispersion.

Surface modification of EG: EG was dripped onto the surface of expanded graphite in the mass ratio of TEOS∶PMHS=3∶1 in a vacuum environment; subsequently, the samples were placed in a microwave oven at 800 W for a rapid expansion for 10 s. The modified expanded graphite was placed in the organic solvents of KOH and anhydrous ethanol with heating and stirring until the mixture was homogeneous.

Preparation of modified epoxy resin hybrids: A bisphenol A-type epoxy resin (EGEBA), methyl tetrahydrophthalic anhydride curing agent (MeTHPA), and an accelerator (DMP-30) were mixed in a mass ratio of 100∶85∶5. Subsequently, 5% of the self-synthesized organosilicon was mixed with CNT and EG surface-modified nanofillers with a total solid content of 0.03% into the epoxy emulsion, and the mixed solution was stirred homogeneously using ultrasonication combined with triple-roller shear dispersion to obtain the modified epoxy resin mixture.

Preparation and testing of pull-out specimens: modified GFRP bars were embedded in the upper surface of concrete to a depth of 5 mm, and the size of the concrete was set to 100 mm × 100 mm × 300 mm. Hydraulic jacks were used to carry out single-end pull-out tests on the bonded specimens, and a digital CCD camera was used to capture the displacement and deformation of the interface throughout the entire process of de-bonding.

Microstructural characterization: the scaled-down specimens were prepared, and the microstructural changes at the FRP-concrete interface of the scaled-down specimens after corrosion were observed using scanning electron microscopy and X-ray computed tomography.

Results and discussion

From the pull-out damage pattern of the GFRP-concrete interface, it can be seen that after 120 d of corrosion, large areas of resin degradation on the surface of the N-GFRP reinforcement resulted in fiber exposure and carbon fiber rib detachment. Compared with N-GFRP, the corrosion degree of M-GFRP bar is less severe, and its surface only has speckled local yellowing and surface roughness phenomenon. Compared with the unmodified bars, the initial interfacial adhesion between corrosion-resistant GFRP bars and concrete was improved by 7.87%, and the interfacial adhesion was improved by about 15% in the 120 d-corrosion experiment. In addition, the maximum strain values at the interfaces of N-GFRP and M-GFRP with concrete decreased to 22.8×10-3、28.7×10-3, respectively in the 120 d-corrosion experiment. After the modification of the resin matrix of the FRP bars, the corrosion resistance of the bars is improved, which can better absorb and disperse the stress brought by the external load, making the stress distribution at the FRP-concrete interface more uniform and the deformation increased, thus slowing down the rate of loss of adhesive force.

Corrosion to 120 d, the interfacial spacing between N/M-GFRP and concrete reached 158.11 μm and 67.91 μm, respectively, which increased by about 100% and 60% compared to the uncorroded condition. The Vr value at the M-GFRP-concrete bonded interface (23.35%) was higher than that of N-GFRP (18.52%). The surface substrates at the N-GFRP reinforcement-concrete interface all were detached and a new layer was exposed. In contrast, the localized matrix spalling at the M-GFRP-concrete interface was less corrosive than that of the N-GFRP bars. Therefore, the debonding of GFRP-concrete mainly depends on the degradation degree of the matrix at the interface. The affinity between the resin matrix and the concrete was improved by matrix modification, and the introduction of hydrophobic network led to the improvement of the waterproofing performance of the bars, which effectively mitigated the degradation of the resin matrix of the bars, and then improved their bonding performance.

Conclusions

The main conclusions of this paper are summarized as following. Compared with the unmodified bars, the initial interfacial adhesion between corrosion-resistant GFRP bars and concrete was improved by 7.87%, and the interfacial adhesion was improved by about 15% in the 120 d-corrosion experiment. In addition, the maximum strain values at the interfaces of N-GFRP and M-GFRP with concrete decreased to 22.8×10-3、28.7×10-3, respectively in the 120 d-corrosion experiment. Compared with the two, the maximum strain at the interface increased by about 25.87% after modification. The damage modes of the debonding process were dominated by concrete cracking and GFRP bar pullout. The degradation rate of the interfacial matrix was mitigated by resin matrix modification, which improved the adhesive properties of the GFRP-concrete interface.

, authors=Yanan SUN1, Zuquan JIN1, Lin YANG2, authorsList=Yanan SUN, Zuquan JIN, Lin YANG, authorCompany=null, correspAuthors=Zuquan JIN, authorNote=

SU Yanan (1993-), female, Doctoral candidate. E-mail:

, correspAuthorsNote=
JIN Zuquan (1977-), male, Ph.D., Professor. E-mail:
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纤维增强复合材料(FRP)筋与混凝土粘结性能直接影响FRP筋增强混凝土结构承载力与耐久性。通过自合成有机硅与纳米填料表面疏水修饰实现玻璃纤维筋(GFRP筋)树脂基体改性,并实现高耐蚀GFRP筋制备。探究60 ℃海水海砂混凝土模拟孔溶液作用下高耐蚀GFRP筋与海水海砂混凝土界面粘结性能的退化规律,并通过界面微结构分析揭示GFRP筋-混凝土粘结性能提升机制。结果表明:相比未改性GFRP筋,高耐蚀GFRP筋与混凝土初始界面粘结力提升了7.87%,腐蚀120 d后界面粘结力提高了15%左右,界面处最大应变增加了约25.87%。GFRP筋与混凝土界面脱粘主要与GFRP筋基体降解有关。基体耐蚀性能的提升有效缓解了筋材的降解速率,进而改善GFRP筋-混凝土界面的粘结性能。

, authors=孙亚楠1, 金祖权1, 杨林2, authorsList=孙亚楠, 金祖权, 杨林, authorCompany=null, correspAuthors=金祖权, authorNote=

孙亚楠(1993—),女,博士研究生。

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金祖权(1977—),男,博士,教授。
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改性树脂基体玻璃纤维筋-混凝土界面粘结性能演化及提升机制
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孙亚楠 1 , 金祖权 1 , 杨林 2
硅酸盐学报 | 严酷环境下高性能水泥混凝土耐久性专题—研究论文 2024,52(11): 3460-3469
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硅酸盐学报 |严酷环境下高性能水泥混凝土耐久性专题—研究论文 2024 , 52 (11) : 3460 -3469
改性树脂基体玻璃纤维筋-混凝土界面粘结性能演化及提升机制
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孙亚楠1 , 金祖权1 , 杨林2
作者信息
  • 1.青岛理工大学,海洋环境混凝土技术教育部工程研究中心,山东 青岛 266520
  • 2.郑州大学,纤维复合建筑材料与结构教育部工程研究中心,郑州 450001
通讯作者:
金祖权(1977—),男,博士,教授。
作者简介:

孙亚楠(1993—),女,博士研究生。

Evolution of Bonding Performance and Improvement Mechanism of Glass Fiber Reinforced Plastics-Concrete Based on Resin Matrix Modification
Yanan SUN1 , Zuquan JIN1 , Lin YANG2
Affiliations
  • 1.Engineering Research Center of Concrete technology in marine environment, Ministry of Education, Qingdao University of Technology, Qingdao 266520, Shandong, China
  • 2.Engineering Research Center of the Ministry of Education for Fiber Reinforced Building Materials and Structures, Zhengzhou University, Zhengzhou 450001, China
  • Corresponding Author:
    JIN Zuquan (1977-), male, Ph.D., Professor. E-mail:

    SU Yanan (1993-), female, Doctoral candidate. E-mail:

出版时间: 2024-11-20 doi: 10.14062/j.issn.0454-5648.20230873
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纤维增强复合材料(FRP)筋与混凝土粘结性能直接影响FRP筋增强混凝土结构承载力与耐久性。通过自合成有机硅与纳米填料表面疏水修饰实现玻璃纤维筋(GFRP筋)树脂基体改性,并实现高耐蚀GFRP筋制备。探究60 ℃海水海砂混凝土模拟孔溶液作用下高耐蚀GFRP筋与海水海砂混凝土界面粘结性能的退化规律,并通过界面微结构分析揭示GFRP筋-混凝土粘结性能提升机制。结果表明:相比未改性GFRP筋,高耐蚀GFRP筋与混凝土初始界面粘结力提升了7.87%,腐蚀120 d后界面粘结力提高了15%左右,界面处最大应变增加了约25.87%。GFRP筋与混凝土界面脱粘主要与GFRP筋基体降解有关。基体耐蚀性能的提升有效缓解了筋材的降解速率,进而改善GFRP筋-混凝土界面的粘结性能。

基体改性  /  界面粘结性能  /  数字图像相关技术  /  分子模拟  /  微结构演变
Introduction

The bonding properties of Fiber Reinforced Plastics (FRP) -concrete composites is directly related to the load carrying capacity and durability of FRP reinforced concrete structures. In addition, the study of bond properties can help us better understand how FRP bars behave in concrete and how they react under specific environmental conditions (e.g., high temperature, humidity, corrosion, etc.). This is valuable for predicting and improving the long-term performance of concrete structures. However, in offshore engineering, structures are exposed to strong corrosive environments all year round. Under the erosion of internal FRP bars by corrosive ions and the highly alkaline environment of the concrete pore solution, the matrix on the surface of FRP bars firstly suffers from deterioration phenomena such as dissolution, plasticization, and microcrack formation. Consequently, the bonding properties of the FRP-concrete interface are seriously affected, leading to the deterioration or failure of the concrete structure. Therefore, improving the corrosion resistance of FRP reinforcement is an important measure to ensure the long-term service of FRP-reinforced concrete structures. In this paper, the resin matrix modification of GFRP bars was realized by self-synthesized organosilicones and surface hydrophobic modification of nanofillers to obtain highly corrosion-resistant GFRP bars. To investigate the degradation of the interfacial adhesion between highly corrosion-resistant GFRP reinforcement and seawater-seasand concrete (SSC) in simulated pore solution of SSC at 60 ℃, and to reveal the mechanism of GFRP reinforcement-concrete adhesion enhancement through interfacial microstructure analysis.

Methods

Organosilicon synthesis: Hydrogen-containing silicone oil (PMHS) was mixed with γ-(2,3-epoxypropyloxy) propyltrimethoxysilane (KH560) in a mass ratio of 1∶1, with ethanol as the solvent, and reacted under the catalytic effect of NaOH for 8 h at ambient temperature using a magnetic stirrer (200 r/min), and then kept for spare.

CNT surface modification: 0.03% (mass fraction) of CNTs was stirred and dispersed into an ethanol and KOH organic solvent, and the CNT modifier was subsequently obtained by adding hydrogen-containing silicone oil (PMHS) and ethyl silicate (TEOS) after ultrasonic dispersion.

Surface modification of EG: EG was dripped onto the surface of expanded graphite in the mass ratio of TEOS∶PMHS=3∶1 in a vacuum environment; subsequently, the samples were placed in a microwave oven at 800 W for a rapid expansion for 10 s. The modified expanded graphite was placed in the organic solvents of KOH and anhydrous ethanol with heating and stirring until the mixture was homogeneous.

Preparation of modified epoxy resin hybrids: A bisphenol A-type epoxy resin (EGEBA), methyl tetrahydrophthalic anhydride curing agent (MeTHPA), and an accelerator (DMP-30) were mixed in a mass ratio of 100∶85∶5. Subsequently, 5% of the self-synthesized organosilicon was mixed with CNT and EG surface-modified nanofillers with a total solid content of 0.03% into the epoxy emulsion, and the mixed solution was stirred homogeneously using ultrasonication combined with triple-roller shear dispersion to obtain the modified epoxy resin mixture.

Preparation and testing of pull-out specimens: modified GFRP bars were embedded in the upper surface of concrete to a depth of 5 mm, and the size of the concrete was set to 100 mm × 100 mm × 300 mm. Hydraulic jacks were used to carry out single-end pull-out tests on the bonded specimens, and a digital CCD camera was used to capture the displacement and deformation of the interface throughout the entire process of de-bonding.

Microstructural characterization: the scaled-down specimens were prepared, and the microstructural changes at the FRP-concrete interface of the scaled-down specimens after corrosion were observed using scanning electron microscopy and X-ray computed tomography.

Results and discussion

From the pull-out damage pattern of the GFRP-concrete interface, it can be seen that after 120 d of corrosion, large areas of resin degradation on the surface of the N-GFRP reinforcement resulted in fiber exposure and carbon fiber rib detachment. Compared with N-GFRP, the corrosion degree of M-GFRP bar is less severe, and its surface only has speckled local yellowing and surface roughness phenomenon. Compared with the unmodified bars, the initial interfacial adhesion between corrosion-resistant GFRP bars and concrete was improved by 7.87%, and the interfacial adhesion was improved by about 15% in the 120 d-corrosion experiment. In addition, the maximum strain values at the interfaces of N-GFRP and M-GFRP with concrete decreased to 22.8×10-3、28.7×10-3, respectively in the 120 d-corrosion experiment. After the modification of the resin matrix of the FRP bars, the corrosion resistance of the bars is improved, which can better absorb and disperse the stress brought by the external load, making the stress distribution at the FRP-concrete interface more uniform and the deformation increased, thus slowing down the rate of loss of adhesive force.

Corrosion to 120 d, the interfacial spacing between N/M-GFRP and concrete reached 158.11 μm and 67.91 μm, respectively, which increased by about 100% and 60% compared to the uncorroded condition. The Vr value at the M-GFRP-concrete bonded interface (23.35%) was higher than that of N-GFRP (18.52%). The surface substrates at the N-GFRP reinforcement-concrete interface all were detached and a new layer was exposed. In contrast, the localized matrix spalling at the M-GFRP-concrete interface was less corrosive than that of the N-GFRP bars. Therefore, the debonding of GFRP-concrete mainly depends on the degradation degree of the matrix at the interface. The affinity between the resin matrix and the concrete was improved by matrix modification, and the introduction of hydrophobic network led to the improvement of the waterproofing performance of the bars, which effectively mitigated the degradation of the resin matrix of the bars, and then improved their bonding performance.

Conclusions

The main conclusions of this paper are summarized as following. Compared with the unmodified bars, the initial interfacial adhesion between corrosion-resistant GFRP bars and concrete was improved by 7.87%, and the interfacial adhesion was improved by about 15% in the 120 d-corrosion experiment. In addition, the maximum strain values at the interfaces of N-GFRP and M-GFRP with concrete decreased to 22.8×10-3、28.7×10-3, respectively in the 120 d-corrosion experiment. Compared with the two, the maximum strain at the interface increased by about 25.87% after modification. The damage modes of the debonding process were dominated by concrete cracking and GFRP bar pullout. The degradation rate of the interfacial matrix was mitigated by resin matrix modification, which improved the adhesive properties of the GFRP-concrete interface.

matrix modification  /  interfacial bonding  /  digital image correlated technologies  /  molecular simulation  /  microstructural evolution
孙亚楠, 金祖权, 杨林. 改性树脂基体玻璃纤维筋-混凝土界面粘结性能演化及提升机制. 硅酸盐学报, 2024 , 52 (11) : 3460 -3469 . DOI: 10.14062/j.issn.0454-5648.20230873
Yanan SUN, Zuquan JIN, Lin YANG. Evolution of Bonding Performance and Improvement Mechanism of Glass Fiber Reinforced Plastics-Concrete Based on Resin Matrix Modification[J]. Journal of the Chinese Ceramic Society, 2024 , 52 (11) : 3460 -3469 . DOI: 10.14062/j.issn.0454-5648.20230873
  • 国家自然科学基金(52225905; U2106221)
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2024年第52卷第11期
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doi: 10.14062/j.issn.0454-5648.20230873
  • 接收时间:2023-11-15
  • 首发时间:2026-10-22
  • 出版时间:2024-11-20
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  • 收稿日期:2023-11-15
  • 修回日期:2024-01-09
基金
国家自然科学基金(52225905; U2106221)
作者信息
    1.青岛理工大学,海洋环境混凝土技术教育部工程研究中心,山东 青岛 266520
    2.郑州大学,纤维复合建筑材料与结构教育部工程研究中心,郑州 450001

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金祖权(1977—),男,博士,教授。
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2种不同金属材料的力学参数
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属
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种数
Number of
species
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鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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