Carbamate-functional, biobased surfactants derived from cardanol, carbon dioxide, and amino acids: Their synthesis and properties

被引:3
作者
Zhu, Tianyu [1 ]
Qian, Dong [1 ]
Duan, Tong [1 ]
Li, Jinlan [1 ]
Yu, Hui [1 ]
Huang, Weizhou [1 ]
Zhou, Yi [1 ]
Zhang, Zhen [1 ]
Sun, Jie [2 ,3 ]
机构
[1] Nanjing Tech Univ, Coll Biotechnol & Pharmaceut Engn, Nanjing, Peoples R China
[2] Nanjing Tech Univ, Coll Food Sci & Light Ind, Nanjing, Peoples R China
[3] Nanjing Tech Univ, Coll Food Sci & Light Ind, 30 Puzhu Rd South, Nanjing 211816, Peoples R China
关键词
amino acid; carbamate group; cardanol; CO2; fully-biobased; surfactants; AMPHOTERIC SURFACTANTS; ANIONIC SURFACTANTS; BEHAVIOR; SERIES; HEADGROUPS; KINETICS;
D O I
10.1002/jsde.12707
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Three biobased, CO2-consuming, and carbamate-groups-containing surfactants (CC-G, CC-T, CC-L) were synthesized separately by combination of Cardanol, CO2, Glycine sodium salt (G), Taurine sodium salt (T), and Lysine sodium salt (L). The chemical structures of CC-G, CC-T, CC-L were confirmed by H-1 NMR and IR spectra. Thermal properties of these surfactants were studied with TGA and DSC. Their critical micelle concentration (CMC) and surface tension at CMC (?CMC) in aqueous solution were obtained by surface tension and conductivity methods, respectively. The amount of excess concentration (G(max)) and the average occupied surface area (Amin) of three surfactants were calculated. Gmax of CC-G, CC-T and CC-L was 2.35 x 10(-7) mmol/m(2), 2.23 x 10(-7) mmol/ m(2), and 6.16 x 10(-7) mmol/m(2), separately. Amin of CC-G was 0.71 nm(2)/mmol, CC-T 0.74 nm(2)/mmol, CC-L 2.70 nm(2)/mmol. The Krafft point, emulsification, and foaming power of these surfactants were investigated as well. The Krafft points were 0 degrees C (CC-G), 5 degrees C (CC-T) and 20 degrees C (CC-T). For CC-G, the separa-tion time of 10 mL double distilled water (DDW) was 43 min, CC-T 40 min, and CC-L 37 min. It was inferred from the calculated packing parameters that shape of the micelle of CC-G, CC-T were cylindrical in aqueous media, while CC-L was spheroidal in aqueous media.
引用
收藏
页码:103 / 113
页数:11
相关论文
共 62 条
  • [51] [王俊 Wang Jun], 2010, [应用化学, Chinese Journal of Applied Chemistry], V27, P866
  • [52] Wei Y., 2003, DETERGENT COSMETICS, V26, P20
  • [53] Crystalline structures and mesomorphic properties of gemini diammonium surfactants with a pendant hydroxyl group
    Wei, Zengbin
    Wei, Xilian
    Sun, Dezhi
    Liu, Jiuqiang
    Tang, Xiaojuan
    [J]. JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2011, 354 (02) : 677 - 685
  • [54] Xie WL., 2001, CHEM IND FOR PROD, V21, P83
  • [55] Limitations in the Application of the Gibbs Equation to Anionic Surfactants at the Air/Water Surface: Sodium Dodecylsulfate and Sodium Dodecylmonooxyethylenesulfate Above and Below the CMC
    Xu, Hui
    Li, Pei Xun
    Ma, Kun
    Thomas, Robert K.
    Penfold, Jeffrey
    Lu, Jian Ren
    [J]. LANGMUIR, 2013, 29 (30) : 9335 - 9351
  • [56] [徐丽 Xu Li], 2013, [精细石油化工, Speciality Petrochemicals], V30, P1
  • [57] Synthesis and properties of novel alkylbetaine zwitterionic gemini surfactants derived from cyanuric chloride
    Xue, Chunli
    Zhu, Hailin
    Zhang, Tingting
    Cao, Duanlin
    Hu, Zhiyong
    [J]. COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS, 2011, 375 (1-3) : 141 - 146
  • [58] Carbon dioxide cycle via electrocatalysis: Electrochemical carboxylation of CO2 and decarboxylative functionalization of carboxylic acids
    Yang, Zixin
    Yu, Yi
    Lai, Liangchuan
    Zhou, Ledan
    Ye, Keyin
    Chen, Fen-Er
    [J]. GREEN SYNTHESIS AND CATALYSIS, 2021, 2 (01): : 19 - 26
  • [59] Comparison of hydrogen bonding in polydimethylsiloxane and polyether based urethane and urea copolymers
    Yilgör, E
    Burgaz, E
    Yurtsever, E
    Yilgör, I
    [J]. POLYMER, 2000, 41 (03) : 849 - 857
  • [60] NEW AMPHOTERIC SURFACTANTS DERIVED FROM LYSINE .1. PREPARATION AND PROPERTIES OF N-EPSILON-ACYLLYSINE DERIVATIVES
    YOKOTA, H
    SAGAWA, K
    EGUCHI, C
    TAKEHARA, M
    OGINO, K
    SHIBAYAMA, T
    [J]. JOURNAL OF THE AMERICAN OIL CHEMISTS SOCIETY, 1985, 62 (12) : 1716 - 1719