Citation: Wei-Guang Qiu, Fei-Long Zhang, Xu-Bao Jiang, Xiang-Zheng Kong. NMR Analysis to Identify Biuret Groups in Common Polyureas[J]. Chinese Journal of Polymer Science, ;2018, 36(10): 1150-1156. doi: 10.1007/s10118-018-2130-y shu

NMR Analysis to Identify Biuret Groups in Common Polyureas

  • Polyureas (PU) are well known as a class of high impact engineering materials, and widely used also in emerging advanced applications. As a general observation, most of them are only soluble in a very limited number of highly protonic solvents, which makes their chemical structure analysis a great challenge. Besides the presence of abundant hydrogen bonding, the poor solubility of PU in common organic solvents is often ascribed to the formation of biuret crosslinking in their molecular chains. To clarify the presence of biuret groups in PU has been of great interest. To this end, two samples, based on hexamethylene diisocyanate (HDI) and toluene diisocyanate (TDI) respectively, were synthesized by precipitation polymerization of each of these diisocyanates in water-acetone at 30 °C. Their chemical structures were analyzed by high resolution magic angle spinning (HR-MAS) NMR, and through comparison of their NMR spectra with those of specially prepared biuret-containing polyurea oligomers, it was concluded that biuret group was absent in all the PU prepared at 30 °C. In addition, this NMR analysis was also applied to a PU obtained by copolymerization of TDI with ethylene diamine (EDA) and water at 65 °C in EDA aqueous solution. It was confirmed that biuret unit was also absent in this PU and that EDA was more active than water towards TDI. The presence of EDA was crucial to the formation of uniform PU microspheres. This study provides therefore a reliable method for the analysis of PU chemical structure.
  • 加载中
    1. [1]

      Davidson, J. S.; Fisher, J. W.; Hammons, M. I.; Porter, J. R.; Dinan, R. J. Failure mechanisms of polymer-reinforced concrete masonry walls subjected to blast. J. Struct. Eng. 2005, 131(8), 1194−1205  doi: 10.1061/(ASCE)0733-9445(2005)131:8(1194)

    2. [2]

      Mohotti, D.; Ngo, T.; Mendis, P.; Raman, S. N. Polyurea coated composite aluminium plates subjected to high velocity projectile impact. Mater. Design 2013, 52(24), 1−16

    3. [3]

      Samiee, A.; Amirkhizi, A. V.; Nemat-Naser, S. Numerical study of the effect of polyurea on the performance of steel plates under blast loads. Mech. Mater. 2013, 64(9), 1−10

    4. [4]

      Ley, S. V.; Mitchell, C.; Pears, D.; Ramarao, C.; Yu, J. Q.; Zhou, W. Recyclable polyurea microencapsulated Pd nanoparticles: An efficient catalyst for hydrogenolysis of epoxides. Org. Lett. 2003, 5(24), 4665−4668  doi: 10.1021/ol0358509

    5. [5]

      Han, H.; Zhou, Y.; Li, S.; Wang, Y.; Kong, X. Z. Immobilization of lipase from pseudomon as fluorescens on porous polyurea and its application in kinetic resolution of racemic 1-phenylethanol. ACS Appl. Mater. Interfaces 2016, 8(39), 25714−25724  doi: 10.1021/acsami.6b07979

    6. [6]

      Jiang, X.; Yu, Y.; Li, X.; Kong, X. Z. High yield preparation of uniform polyurea microspheres through precipitation polymerization and their application as laccase immobilization support. Chem. Eng. J. 2017, 328, 1043−1050  doi: 10.1016/j.cej.2017.07.069

    7. [7]

      Jacquemond, M.; Jeckelmann, N.; Ouali, L.; Haefliger, O. P. Perfume-containing polyurea microcapsules with undetectable levels of free isocyanates. J. Appl. Polym. Sci. 2009, 114(5), 3074−3080  doi: 10.1002/app.v114:5

    8. [8]

      Li, J.; Hughes, A. D.; Kalantar, T. H.; Drake, I. J.; Tucker, C. J.; Moore, J. S. Pickering-emulsion-templated encapsulation of a hydrophilic amine and its enhanced stability using poly(allyl amine). ACS Macro Lett. 2014, 3(10), 976−980  doi: 10.1021/mz500455j

    9. [9]

      Chen, L.; Xu, L.; Shang, H.; Zhang. Z. Microencapsulation of butyl stearate as a phase change material by interfacial polycondensation in a polyurea system. Energ. Convers. Manage. 2009, 50(3), 723−729  doi: 10.1016/j.enconman.2008.09.044

    10. [10]

      Ying, H.; Zhang, Y.; Cheng, J. Dynamic urea bond for the design of reversible and self-healing polymers. Nat. Commun. 2014, 5, 3218

    11. [11]

      Howarth, G. Polyurethanes, polyurethane dispersions and polyureas: Past, present and future. Surf. Coat. Int. Part B Coat. Trans. 2003, 86(2), 111−118  doi: 10.1007/BF02699621

    12. [12]

      Jiang, X.; Li, X.; Zhu, X.; Kong, X. Z. Preparation of highly uniform polyurea microspheres through precipitation polymerization and their characterization. Ind. Eng. Chem. Res. 2016, 55(44), 11528−11535  doi: 10.1021/acs.iecr.6b03526

    13. [13]

      Jiang, X.; Kong, X. Z.; Zhu, X. A Novel protocol for the preparation of uniform polymer microspheres with high yields through step polymerization of isophorone diisocyanate. J. Polym. Sci., Part A: Polym. Chem. 2011, 49(20), 4492−4497  doi: 10.1002/pola.v49.20

    14. [14]

      Sumi, M.; Chokki, Y.; Nakai, Y.; Nakabayashi, M.; Kanzawa, T. Studies on the structure of polyurethane elastomers. I. NMR spectra of the model compounds and some linear polyurethanes. Die Makromol. Chem. 1964, 78(1), 146−156  doi: 10.1002/macp.1964.020780112

    15. [15]

      Chattopadhyay, D. K.; Raju, K. V. S. N. Structural engineering of polyurethane coatings for high performance applications. Prog. Polym. Sci. 2007, 32(3), 352−418  doi: 10.1016/j.progpolymsci.2006.05.003

    16. [16]

      Suzuoki, K.; Kagawa, K.; Fukuma, K.; Uda, B.; Ohmura, J. The analysis of synthetic and side reactions of polyurethaneurea. Nippon Gomu Kyokaishi 1999, 72, 139−143  doi: 10.2324/gomu.72.139

    17. [17]

      Mathisen, R. J.; Yoo, J. K.; Sung, C. S. P. Dye labeling technique for monitoring the cure of polyimides and polyureas: Model compound studies. Macromolecules 1987, 20(6), 1414−1416  doi: 10.1021/ma00172a043

    18. [18]

      Okuto, H. Studies on the structure of polyurethane elastomers. II. High resolution NMR spectroscopic determination of allophanate and biuret linkages in the cured polyurethane elastomer: Degradation by amine. Die Makromol. Chem. 1966, 98(1), 148−163  doi: 10.1002/macp.1966.020980117

    19. [19]

      Delebecq, E.; Pascault, J.; Boutevin, B.; Ganachaud, F. On the Versatility of urethane/urea bonds: Reversibility, blocked isocyanate, and non-isocyanate polyurethane. Chem. Rev. 2013, 113(1), 80−118  doi: 10.1021/cr300195n

    20. [20]

      Zhang, X.; Zhang, X. Y.; He, Y.; Chen, H. Progress in synthesis and characterization of HDI biuret. Pain Coat. Ind. 2011, 41(10), 71−75

    21. [21]

      Lapprand, A.; Boisson, F.; Delolme, F.; Méchin, F.; Pascault, J. P. Reactivity of isocyanates with urethanes: conditions for allophanate formation. Polym. Degrad. Stab. 2005, 90(2), 363−373  doi: 10.1016/j.polymdegradstab.2005.01.045

    22. [22]

      Jiang, X.; Zhu, X.; Arnold, A. A.; Kong, X. Z.; Claverie, J. P. Polyurea structure characterization by HR-MAS NMR spectroscopy. Ind. Eng. Chem. Res. 2017, 56(11), 2993−2998  doi: 10.1021/acs.iecr.7b00192

    23. [23]

      Han, H.; Li, S.; Zhu, X.; Jiang, X.; Kong, X. Z. One step preparation of porous polyurea by reaction of toluene diisocyanate with water and its characterization. RSC Adv. 2014, 4(63), 33520−33529  doi: 10.1039/C4RA06383J

    24. [24]

      Jiang, X.; Zhu, X.; Kong, X. Z. A facile route to preparation of uniform polymer microspheres by quiescent polymerization with reactor standing still without any stirring. Chem. Eng. J. 2012, 213(12), 214−217

    25. [25]

      Kong, X. Z.; Jiang, W.; Jiang, X.; Zhu, X. Preparation of core-shell and hollow polyurea microspheres via precipitation polymerization using polyamine as crosslinker monomer. Polym. Chem. 2013, 4(24), 5776−5784  doi: 10.1039/c3py00809f

    26. [26]

      Li, S. S.; Han, H.; Zhu, X.; Jiang, X.; Kong, X. Z. Preparation and formation mechanism of porous polyurea by reaction of toluene diisocyanate with water and its Application as adsorbent for anionic dye removal. Chinese J. Polym. Sci. 2015, 33(8), 1196−1210  doi: 10.1007/s10118-015-1670-7

    27. [27]

      Li, S.; Zhu, X.; Kong, X. Z.; Jiang, X. One step synthesis of porous polyurea by using TDI and EDA and its characterization. Acta Polymerica Sinica (in Chinese) 2016, (3), 391−398

    28. [28]

      Yang, Y.; Jiang, X.; Zhu, X.; Kong, X. Z. A facile pathway to polyurea nanofiber fabrication and polymer morphology control in copolymerization of oxydianiline and toluene diisocyanate in acetone. RSC Adv. 2015, 5(10), 7426−7432  doi: 10.1039/C4RA15309J

    29. [29]

      Alam, T. M.; Jenkins, J. E. " Advanced Aspects of Spectroscopy”, Intech, Croatia, 2012, p. 279–301.

    30. [30]

      Li, S.; Zhao, J.; Zhang, Z.; Zhang, J.; Yang, W. Aliphatic thermoplastic polyurethane-ureas and polyureas synthesized through a non-isocyanate route. RSC Adv. 2015, 5(9), 6843−6852  doi: 10.1039/C4RA12195C

    31. [31]

      Harris, R. F.; Kinney, J. E.; Savina, M. R.; Jeor, V. L. S.; Bicerano, J.; Durvasula, V. R.; Moreno, L. N. Synthesis and characterization of urea-based polyureas: 1. Urea-terminated poly(1,6-hexamethyleneurea) polyol dispersions. Polymer 1995, 36(22), 4275−4285

    32. [32]

      Edwards, P. A.; Striemer, G.; Webster, D. C. Synthesis, characterization and self-crosslinking of glycidyl carbamate functional resins. Prog. Org. Coat. 2006, 57(2), 128−139  doi: 10.1016/j.porgcoat.2006.08.002

    33. [33]

      Wendisch, D.; Reiff, H.; Dieterich, D. Kernresonanzspektroskopische beiträge zur struktur und stereochemie von (cyclo)aliphatischen isocyanaten und deren folgeprodukten. Angew. Makromol. Chem. 1986, 141(1), 173−183  doi: 10.1002/apmc.1986.051410117

    34. [34]

      Zhang, F.; Jiang, X.; Zhu, X.; Chen, Z.; Kong, X. Z. Preparation of uniform and porous polyurea microspheres of large size through interfacial polymerization of toluene diisocyanate in water solution of ethylene diamine. Chem. Eng. J. 2016, 303, 48−55  doi: 10.1016/j.cej.2016.05.145

    35. [35]

      Entelis, S. G.; Nesterov, O. V. Kinetics and mechanism of the reactions of isocyanates with compounds containing " active” hydrogen. Russ. Chem. Rev. 1966, 35(12), 917−930  doi: 10.1070/RC1966v035n12ABEH001555

    36. [36]

      Lu, X.; Wang, Y.; Wu, X. Molecular interactions in polyurea by 1-D and 2-D NMR. Polymer 1993, 34(1), 56−60  doi: 10.1016/0032-3861(93)90283-G

  • 加载中
    1. [1]

      Zhigang ZengChangzhou LiaoLei Yu . Molecules for COVID-19 treatment. Chinese Chemical Letters, 2024, 35(7): 109349-. doi: 10.1016/j.cclet.2023.109349

    2. [2]

      Hong Lu Yidie Zhai Xingxing Cheng Yujia Gao Qing Wei Hao Wei . Advancements and Expansions in the Proline-Catalyzed Asymmetric Aldol Reaction. University Chemistry, 2024, 39(5): 154-162. doi: 10.3866/PKU.DXHX202310074

    3. [3]

      Haolin Zhan Qiyuan Fang Jiawei Liu Xiaoqi Shi Xinyu Chen Yuqing Huang Zhong Chen . Noise Reduction of Nuclear Magnetic Resonance Spectroscopy Using Lightweight Deep Neural Networ. Acta Physico-Chimica Sinica, 2025, 41(2): 100017-. doi: 10.3866/PKU.WHXB202310045

    4. [4]

      Ling-Hao ZhaoHai-Wei YanJian-Shuang JiangXu ZhangXiang YuanYa-Nan YangPei-Cheng Zhang . Effective assignment of positional isomers in dimeric shikonin and its analogs by 1H NMR spectroscopy. Chinese Chemical Letters, 2024, 35(5): 108863-. doi: 10.1016/j.cclet.2023.108863

    5. [5]

      Xinzhi Ding Chong Liu Jing Niu Nan Chen Shutao Xu Yingxu Wei Zhongmin Liu . Solid-state NMR study of the stability of MOR framework aluminum. Chinese Journal of Structural Chemistry, 2024, 43(4): 100247-100247. doi: 10.1016/j.cjsc.2024.100247

    6. [6]

      Chengde WangLiping HuangShanshan WangLihao WuYi WangJun Dong . A distinction of gliomas at cellular and tissue level by surface-enhanced Raman scattering spectroscopy. Chinese Chemical Letters, 2024, 35(5): 109383-. doi: 10.1016/j.cclet.2023.109383

    7. [7]

      Manyu ZhuFei LiangLie WuZihao LiChen WangShule LiuXiue Jiang . Revealing the difference of Stark tuning rate between interface and bulk by surface-enhanced infrared absorption spectroscopy. Chinese Chemical Letters, 2025, 36(2): 109962-. doi: 10.1016/j.cclet.2024.109962

    8. [8]

      Honglin Gao Chunlin Yuan Hongyu Chen Aiyi Dong Pan Gao Guangjin Hou . Surface gallium hydride on Ga2O3 polymorphs: A comparative solid-state NMR study. Chinese Journal of Structural Chemistry, 2025, 44(4): 100561-100561. doi: 10.1016/j.cjsc.2025.100561

    9. [9]

      Xueling YuLixing FuTong WangZhixin LiuNa NiuLigang Chen . Multivariate chemical analysis: From sensors to sensor arrays. Chinese Chemical Letters, 2024, 35(7): 109167-. doi: 10.1016/j.cclet.2023.109167

    10. [10]

      Tiantian LongHongmei LuoJingbo SunFengniu LuYi ChenDong XuZhiqin Yuan . Carbonization-engineered ultrafast chemical reaction on nanointerface. Chinese Chemical Letters, 2025, 36(3): 109728-. doi: 10.1016/j.cclet.2024.109728

    11. [11]

      Ruotong WeiAokun LiuJian KuangZhiwen WangLu YuChanglin Tian . Probing the dynamic properties in the LLPS process via site-directed spin labeling-electron paramagnetic resonance (SDSL-EPR) spectroscopy. Chinese Chemical Letters, 2025, 36(4): 110029-. doi: 10.1016/j.cclet.2024.110029

    12. [12]

      Min FuPan HeSen ZhouWenqiang LiuBo MaShiying ShangYaohao LiRuihan WangZhongping Tan . An unexpected stereochemical effect of thio-substituted Asp in native chemical ligation. Chinese Chemical Letters, 2024, 35(8): 109434-. doi: 10.1016/j.cclet.2023.109434

    13. [13]

      Xianxu ChuLu WangJunru LiHui Xu . Surface chemical microenvironment engineering of catalysts by organic molecules for boosting electrocatalytic reaction. Chinese Chemical Letters, 2024, 35(8): 109105-. doi: 10.1016/j.cclet.2023.109105

    14. [14]

      Xu-Hui YueXiang-Wen ZhangHui-Min HeLei QiaoZhong-Ming Sun . Synthesis, chemical bonding and reactivity of new medium-sized polyarsenides. Chinese Chemical Letters, 2024, 35(7): 108907-. doi: 10.1016/j.cclet.2023.108907

    15. [15]

      Ali DaiZhiguo ZhengLiusheng DuanJian WuWeiming Tan . Small molecule chemical scaffolds in plant growth regulators for the development of agrochemicals. Chinese Chemical Letters, 2025, 36(4): 110462-. doi: 10.1016/j.cclet.2024.110462

    16. [16]

      Runze Liu Yankai Bian Weili Dai . Qualitative and quantitative analysis of Brønsted and Lewis acid sites in zeolites: A combined probe-assisted 1H MAS NMR and NH3-TPD investigation. Chinese Journal of Structural Chemistry, 2024, 43(4): 100250-100250. doi: 10.1016/j.cjsc.2024.100250

    17. [17]

      Ying LiLong-Jie WangYong-Kang ZhouJun LiangBin XiaoJi-Shen Zheng . An improved installation of 2-hydroxy-4-methoxybenzyl (iHmb) method for chemical protein synthesis. Chinese Chemical Letters, 2024, 35(5): 109033-. doi: 10.1016/j.cclet.2023.109033

    18. [18]

      Min HuangRu ChengShuai WenLiangtong LiJie GaoXiaohui ZhaoChunmei LiHongyan ZouJian Wang . Ultrasensitive detection of microRNA-21 in human serum based on the confinement effect enhanced chemical etching of gold nanorods. Chinese Chemical Letters, 2024, 35(9): 109379-. doi: 10.1016/j.cclet.2023.109379

    19. [19]

      Lian SunHonglei WangMing MaTingting CaoLeilei ZhangXingui Zhou . Shape and composition evolution of Pt and Pt3M nanocrystals under HCl chemical etching. Chinese Chemical Letters, 2024, 35(9): 109188-. doi: 10.1016/j.cclet.2023.109188

    20. [20]

      Yongjian LiXinyu ZhuChenxi WeiYouyou FangXinyu WangYizhi ZhaiWenlong KangLai ChenDuanyun CaoMeng WangYun LuQing HuangYuefeng SuHong YuanNing LiFeng Wu . Unraveling the chemical and structural evolution of novel Li-rich layered/rocksalt intergrown cathode for Li-ion batteries. Chinese Chemical Letters, 2024, 35(12): 109536-. doi: 10.1016/j.cclet.2024.109536

Metrics
  • PDF Downloads(0)
  • Abstract views(949)
  • HTML views(57)

通讯作者: 陈斌, bchen63@163.com
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索
Address:Zhongguancun North First Street 2,100190 Beijing, PR China Tel: +86-010-82449177-888
Powered By info@rhhz.net

/

DownLoad:  Full-Size Img  PowerPoint
Return