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Comparative Proteomics Based on 18O Labeling to Evaluate the Hepatotoxicity of Tris(2,3-dibromopropyl) Isocyanuratein Rats
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作者 Yu Li Xuefei Lü +1 位作者 Yuanzhan Yang Yulin Deng 《Journal of Beijing Institute of Technology》 EI CAS 2019年第3期659-666,共8页
Detecting protein expression levels in organisms exposed to environmental pollutants can help us understand the action mechanism of toxicity. In the present study, adult female Sprague-Dawley (SD) rats received a cons... Detecting protein expression levels in organisms exposed to environmental pollutants can help us understand the action mechanism of toxicity. In the present study, adult female Sprague-Dawley (SD) rats received a consecutive intraperitoneal injection of tris(2,3-dibromopropyl) isocyanurate (TBC) for seven days, and the ^16O/^18O labeling comparative proteomic approach was used to study the change of liver proteome in these rats. Thirty six differential proteins were identified between the control group and the high-dose-exposed group (8 mg/kg), of which, twenty eight proteins were down-regulated and eight proteins were up-regulated. Bioinformatics analysis revealed that most of the differential proteins were related with the metabolic and cellular processes. In addition, the contents of malondialdehyde (MDA), catalase (CAT), and glutathione (GSH) in liver were measured to evaluate the oxidative stress status induced by TBC exposure. Together, these findings showed that TBC might be toxic to liver by disrupting metabolic process and apoptosis. The results might provide a better insight into the mechanism of toxicity induced by TBC. 展开更多
关键词 comparative proteomic HEPATOTOXICITY ^18O LABELING oxidative stress tris(2 3-dibromopropyl) isocyanurate (TBC)
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Preparation of Macroporous Poly (vinyl alcohol-co-triallyl isocyanurate) Beads Bearing Aminocarboxylic Acid as Functional Groups by Suspension Polymerization
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作者 Hai Tao +4 位作者 LI Ke Yu SHI 《Chinese Chemical Letters》 SCIE CAS CSCD 2003年第3期267-269,共3页
Macroporous poly (vinyl acetate-co-triallyl isocyanurate) beads were prepared with suspension polymerization method. The copolymer beads were then transformed into poly (vinyl alcohol-co-triallyl isocyanurate) by est... Macroporous poly (vinyl acetate-co-triallyl isocyanurate) beads were prepared with suspension polymerization method. The copolymer beads were then transformed into poly (vinyl alcohol-co-triallyl isocyanurate) by ester exchange reaction. Aminocarboxylic acids were immobilized on the copolymer beads by the esterification of hydroxyl groups with diethyl-lenetriaminepentaacetic bisanhydride. The weak acid exchange capacities, specific surface areas and mean pore diameters of the resultant resin beads were measured. 展开更多
关键词 Macroporous adsorption resin suspension polymerization poly (vinyl alcohol-co-triallyl isocyanurate) aminocarboxylic acid.
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Formation of Hybrid Ring Structure of Cyanurate/Isocyanurate in the Reaction be-tween 2,4,6-Tris(4-Phenyl-Phenoxy)-1, 3,5-Triazine and Phenyl Glycidyl Ether
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作者 Daisuke Ohno Kazuya Zenyoji +2 位作者 Youji Kurihara Kazuyoshi Ueda Hitoshi Habuka 《International Journal of Organic Chemistry》 CAS 2016年第2期117-125,共9页
Reaction products of 2,4,6-tris(4-phenyl-phenoxy)-1,3,5-triazine derived from 4-phenylphenol cyanate ester and phenyl glycidyl ether were analyzed. In addition to an isocyanurate compound and an oxazolidone compound w... Reaction products of 2,4,6-tris(4-phenyl-phenoxy)-1,3,5-triazine derived from 4-phenylphenol cyanate ester and phenyl glycidyl ether were analyzed. In addition to an isocyanurate compound and an oxazolidone compound which were well known as reaction products of cyanate esters and epoxy resins, compounds with hybrid ring structure of cyanurate/isocyanurate were determined. Gibbs free energies of the compound having hybrid ring structure of cyanurate/isocyanurate with two isocyanurate moiety were found to be lower than that of the compound with cyanurate ring structure through calculations. Calculation data supported the existence of hybrid ring structure of cy-anurate/isocyanurate. It was revealed that isomerization from cyanurate to isocyanurate occurs via hybrid ring structure of cyanurate/isocyanurate in the reaction of aryl cyanurate and epoxy. 展开更多
关键词 Reaction products of 2 4 6-tris(4-phenyl-phenoxy)-1 3 5-triazine derived from 4-phenylphenol cya-nate ester and phenyl glycidyl ether were analyzed. In addition to an isocyanurate compound and an oxazolidone compound which were well known as reaction products of cyanate esters and epoxy resins compounds with hybrid ring structure of cyanurate/isocyanurate were determined. Gibbs free energies of the compound having hybrid ring structure of cyanurate/isocyanurate with two isocyanurate moiety were found to be lower than that of the compound with cyanurate ring struc-ture through calculations. Calculation data supported the existence of hybrid ring structure of cy-anurate/isocyanurate. It was revealed that isomerization from cyanurate to isocyanurate occurs via hybrid ring structure of cyanurate/isocyanurate in the reaction of aryl cyanurate and epoxy.
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Engineering sulfonated polymers for the removal of ultra-trace complexed Cr(Ⅲ)in tris(2-carboxyethyl)isocyanurate photoresist resin monomers
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作者 Huiyao Huang Shiquan Zhong +4 位作者 Yawen Chen Wangquan Gong Changshen Ye Ting Qiu Jie Chen 《Industrial Chemistry & Materials》 2025年第5期618-630,共13页
The semiconductor manufacturing industry imposes stringent requirements on the metal ion content of photoresist resin monomers.Tris(2-carboxyethyl)isocyanurate(H_(3)tci),a critical raw material for photoresist resin m... The semiconductor manufacturing industry imposes stringent requirements on the metal ion content of photoresist resin monomers.Tris(2-carboxyethyl)isocyanurate(H_(3)tci),a critical raw material for photoresist resin monomers,inevitably incorporates metal ions during production.However,its inherent carboxyethyl groups form stable coordination complexes with Cr(Ⅲ),hindering the semiconductor-grade resin monomer production.To achieve the ultra-deep removal of Cr(Ⅲ)at ultra-trace concentrations,inspired by the hard–soft-acid–base theory,we systematically modulated the electron-rich sulfonic acid group on polymers via controlled sulfonation conditions to achieve a novel series of adsorption materials(St)with ultra-high Cr(Ⅲ)adsorption affinity.The adsorption–recrystallization process using 6 g of St-V-15 could reduce the Cr(Ⅲ)concentration in a solution containing 1 g of H_(3)tci from 840 ppb to 27.5 ppb.Furthermore,St-V-15 exhibited a maximum adsorption capacity of 145 mg g^(−1)calculated using the Langmuir model and a rapid initial adsorption rate of 82.92 mg g^(−1)min^(−1)at 333 K.Additionally,St-V-15 demonstrated exceptional selectivity for Cr(Ⅲ)over competing ions(e.g.,K(Ⅰ),Mg(Ⅱ),Na(Ⅰ)and Zn(Ⅱ))and maintained stable performance over at least 10 adsorption–desorption cycles.The superior performance originated from the chelation between Cr(Ⅲ)and the sites of O atoms(S–O and S=O)combined with the electrostatic interaction between deprotonated sulfonic acid groups and Cr(Ⅲ).These results position St-V-15 as a promising adsorption material for ultra-trace Cr(Ⅲ)removal in H_(3)tci,offering a cost-effective solution for semiconductor-grade resin monomer production for the very first time. 展开更多
关键词 Tris(2-carboxyethyl)isocyanurate Complexed Cr(Ⅲ) ULTRA-TRACE Cr(Ⅲ)removal Sulfonated polymers
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Enhanced triallyl isocyanurate(TAIC)degradation through application of an 03/UV process:Performance optimization and degradation pathways 被引量:1
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作者 Yapeng Song Hui Gong +2 位作者 Jianbing Wang Fengmin Chang Kaijun Wang 《Frontiers of Environmental Science & Engineering》 SCIE EI CAS CSCD 2020年第4期103-113,共11页
Triallyl isocyanurate(TAIC,C12H15N3O3)has featured in wastewater treatment as a refractory organic compound due to the significant production capability and negative environmental impact.TAIC degradation was enhanced ... Triallyl isocyanurate(TAIC,C12H15N3O3)has featured in wastewater treatment as a refractory organic compound due to the significant production capability and negative environmental impact.TAIC degradation was enhanced when an ozone(O3)/ultraviolet(UV)process was applied compared with the application of an independent O3 process.Although 99%of TAIC could be degraded in 5 min during both processes,the O3/UV process had a 70%mineralization rate that was much higher than that of the independent O3 process(9%)in 30 min.Four possible degradation pathways were proposed based on the organic compounds of intermediate products identified during TAIC degradation through the application of independent 03 and O3/UV processes.pH impacted both the direct and indirect oxidation processes.Acidic and alkaline conditions preferred direct and indirect reactions respectively,with a pH of 9 achieving maximum Total Organic Carbon(TOC)removal.Both CO32-and HCO3-decreased TOC removal,however only CO32-negatively impacted TAIC degradation.Effects of Cl-as a radical scavenger became more marked only at high concentrations(over 500 mg/L Cl-).Particulate and suspended matter could hinder the transmission of ultraviolet light and reduce the production of HO·accordingly. 展开更多
关键词 Triallyl isocyanurate O3/UV Advanced oxidation processes(AOP) Degradation pathway
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Study on the condensation and crosslinking reactions of furfuryl alcohol and tris(2-hy-droxyethyl)isocyanurate by thermal methods
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作者 CHEN,Xue-Si ZHENG,Guo-Dong LIU,Zhen-Hai XU,Ji-Ping Changchun Institute of Applied Chemistry,Academia Sinica,Changchun 130022 《Chinese Journal of Chemistry》 SCIE CAS CSCD 1991年第3期193-198,共0页
Condensation and crosslinking reactions of furfuryl alcohol(FA)and FA with tris(2-hydro- xyethyl)isocyanurate(THEIC)are studied by means of DSC,TG,TBA,NMR and elemental analysis. Four exothermic peaks are observed on ... Condensation and crosslinking reactions of furfuryl alcohol(FA)and FA with tris(2-hydro- xyethyl)isocyanurate(THEIC)are studied by means of DSC,TG,TBA,NMR and elemental analysis. Four exothermic peaks are observed on the DSC curves of thermal condensation of FA and FA with THEIC in the presence of sulfuric acid.The peaks Ⅰ,Ⅱ(50—80℃),Ⅲ(110—130℃)and Ⅳ(150— 190℃)correspond to linear polycondensation of FA through head-to-tail condensation,head-to-head etherification,crosslinking dehydration reaction between methylene group and terminal hydroxy group of FA polymeric chain and to further crosslinking reaction at higher temperature,respectively.The reactivity of FA and THEIC increases sharply at 130—150℃ and THEIC is reacted completely at 150℃.Addition of THEIC raises the initial decomposition temperature of FA polymer by 60℃. 展开更多
关键词 FA Study on the condensation and crosslinking reactions of furfuryl alcohol and tris hy-droxyethyl)isocyanurate by thermal methods
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Synthesis and Thermal Properties of a Novel Nitrogen-containing Epoxy Resin 被引量:3
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作者 XingHongZHANC HongMeiWAN YuQinMIN ZuoFANC GuoRongQI 《Chinese Chemical Letters》 SCIE CAS CSCD 2005年第4期547-550,共4页
A new nitrogen-containing epoxy resin (XT resin) was synthesized from chain extension of xylenephenolformaldehyde resin (XPF) and triglycidyl isocyanurate (TGIC) in the presence of base catalyst. FT-IR and H-NMR ana... A new nitrogen-containing epoxy resin (XT resin) was synthesized from chain extension of xylenephenolformaldehyde resin (XPF) and triglycidyl isocyanurate (TGIC) in the presence of base catalyst. FT-IR and H-NMR analysis confirmed the chemical structure of XT resin. It was 1 cured with dicyandiamide (DICY) and diaminodiphenyl sulfone (DDS). Dynamic mechanical analysis (DMA) results showed that the introduction of triazine ring provides epoxy polymer with good thermal stability. Furthermore, high char yields at 800℃ in thermogravimetric (TGA) analysis indicated that XT resin had potential flame retardance. 展开更多
关键词 Nitrogen-containing epoxy resin xylenephenolformaldehyde resin (XPF) triglycidyl isocyanurate (TGIC) thermal stability.
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Polyisocyanuratoesters:Renewable Linear Polyesters with High Flame Retardancy
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作者 Zijian Chen Rui Hou +3 位作者 Jianbing Cheng Fengjie Fang Donglin Tang Guangzhao Zhang 《Journal of Renewable Materials》 SCIE 2018年第6期584-590,共7页
Biobased urea nowadays attracts increasing attention as a biomass resource with giant potential,which benefits from the development of biobased ammonia and ecological sanitation system.Urea is an ideal feedstock for c... Biobased urea nowadays attracts increasing attention as a biomass resource with giant potential,which benefits from the development of biobased ammonia and ecological sanitation system.Urea is an ideal feedstock for chemical industry and developing new urea-based polymer materials can take advantage of the urea resource.In this work,a class of renewable linear polyesters,namely polyisocyanuratoesters(PICEs)were synthesized from a urea-based monomer bis(2-carbomethoxyethyl)isocyanurate and biobased aliphatic diols.Compared with conventional aliphatic polyesters,PICEs containing isocyanurate rings in the polymer chain backbone exhibit outstanding flame retardancy that both PICE-4(the number‘4’refers to the number of methylene in diols,e.g.4 for butylene and 6 for hexylene)and PICE-6 have high limiting oxygen index values over 30%.In the UL 94 tests,PICE-6 reaches V-1 rating;while V-2 is found for PICE-10.All PICEs exhibit similar pyrolysis behavior that the temperatures of 5%weight loss are around 320°C.PICEs are found to have glass transition among 20°C-45°C.No crystallization behavior is observed without annealing except for PICE-10,which can crystallize even at room temperature. 展开更多
关键词 UREA isocyanurate ring aliphatic diol linear polyester flame retardancy
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