[1] Mo Ping, Huang Yuming. A high performance liquid chromatography-UV detection method for determination of sodium dodecylbenzene sulfonate in wasterwater [J]. Journal of Southwest University, 2007, 29(1): 65-68.
[2] X Y Ma, X C Wang. Ecotoxicity comparison of organic contaminants and heavy metals using vibrio-qinghaiensis sp.-Q67 [J]. Water Sci Technol, 2013, 67(10): 2221-2227.
[3] Yang Lili, Wang Yutian, Lu Xinqiong. Identification and measurement of petroleum pollution by three-dimensional matrix fluorescence with second-order calibration methods [J]. Chinese J Lasers, 2013, 40(6): 0615002.
[4] Yin Gaofang, Zhao Nanjing, Hu Li, et al.. Classified measurement of phytoplankton based on characteristic fluorescence of photosynthetic pigments [J]. Acta Optica Sinica, 2014, 34(9): 0930005.
[5] C Bengoechea, C A Samuel. Analysis of linear alkylbenzene sulfonate in waste water and sludge by high performance liquid chromatography: An exercise of validation [J]. J Surfactants Deterg, 2009, 12(1): 21-29.
[6] J Sima, M Pazdernik, J Triska，et al.. Degradation of surface-active compounds in a constructed wetland determined using high performance liquid chromatography and extraction spectrophotometry [J]. J Environ Sci Heal A, 2013, 48(5): 559-567.
[7] K Fischer, E Fries, W Korner, et al.. New developments in the trace analysis of organic water pollutants [J]. Microbiol Biot, 2012, 94(1):11-28.
[8] J E Heinze. Comment on“degradation of two persistent surfactants by UV-enhanced ozonation”[J]. J Surfactants Deterg, 2012, 15(6): 815-818.
[9] X B He, O Guvench, A D Jr Mackerell, et al.. Atomistic simulation study of linear alkylbenzene sulfonates at the water/air interface [J]. J Phys Chem B, 2010, 114 (30): 9787-9794.
[10] T Cheng, Q Chen, F Li, et al.. Classic force field for predicting surface tension and interfacial properties of sodium dodecyl sulfate [J]. J Phys Chem B, 2010, 114 (43): 13736-13744.
[11] G Lashermes, Y Zhang, S Houot, et al.. Simulation of organic matter and pollutant evolution during composting: The cop-compost model [J]. J Environ Qual, 2013, 42(2): 361-372.
[12] S Devi, M C Chattopadhyaya. Determination of sodium dodecyl sulfate in toothpastes by a PVC matrix membrane sensor [J]. J Surfactants Deterg, 2013, 16(3): 391-396.
[13] Z G Chen, Y R Peng, F Xie, et al.. Determination of anionic surfactant in surface water by resonance light-scattering technology [J]. Int J Environ An Ch, 2010, 90(7): 573-585.
[14] M Hampel, A Mauffret, K Pazdro, et al.. Anionic surfactant linear alkylbenzene sulfonates (LAS) in sediments from the Gulf of Gdańsk (southern Baltic Sea, Poland) and its environmental implications [J]. Environ Monit Assess, 2012, 184(10): 6013-6023.
[15] A K Asok, M S Jisha. Biodegradation of the anionic surfactant linear alkylbenzene sulfonate (LAS) by autochthonous Pseudomonas sp. [J]. Water Air Soil Poll, 2012, 223(8): 5039-5048.
[16] M Arvand, E Bozorgzadeh, S Shariati, et al.. Trace determination of linear alkylbenzene sulfonates using ionic liquid based ultrasoundassisted dispersive liquid-liquid microextraction and response surface methodology [J]. Anal Methods, 2012, 4(8): 2272-2277.
[17] Yang Dawei, Fan Xiaolei, Kind Tobias, et al.. Analysis of polar lipids in Chlamydomonas reinhardtii using nanoelectrospray direct infusion method and gas chromatography and mass spectrometric detection [J]. Acta Chimica Sinica, 2013, 71(4): 663-669.
[18] Wang Xiaojing, Wu Yan, Wang Liming. Determination of betaine in fruits of Lycium barbarum L. by solid phase extraction and high-performance liquid chromatography [J]. Food Science, 2010, 31(8): 199-201.
[19] Zhao Peng, Xu Jilin, Liu Xuemei, et al.. Determination of betaines in four marine algae by liquid chromatography - mass spectrometry[J]. Chinese Pharmaceutical Journal, 2011, 46(24): 1886-1889.
[20] Z H Ren, Y Luo, Y C Zheng, et al.. Interaction behavior between an amino sulfonate surfactant and octylphenol polyoxyethylene ether (10) in aqueous solution [J]. J Solution Chem, 2014, 43(5): 853-869.
[21] Zhao Haina, Cheng Xinhao, Zhao Oudi, et al.. Mixed cationic and anionic surfactant systems achieve ultra-low interfacial tension in the Karamay oil field [J]. Acta Physico-Chimica Sinica, 2014, 30(4): 693-698.
[22] T L Neoh, C Yamamoto, S Ikefuji, et al.. Heat stability of allyl isothiocyanate and phenyl isothiocyanate complexed with randomly methylated β-cyclodextrin [J]. Food Chem, 2012, 131(4): 1123-1131.
[24] A Chmielewska, T Baczek. Comparative analysis of chiral drugs in view of chemometrics [J]. J AOAC Int, 2012, 95 (3): 624-635.
[25] Wang Chunmiao, Hou Huaxin, Li Danrong, et al.. Observation of emodin-β-CD inclusion complex′s transmembrane transport in nasopharyngeal carcinoma cells and its distribution by the laser scanning confocal microscope [J]. Chinese J Lasers, 2014, 41(5): 0504001.
[26] Yu Rong, Jiang Yuesong. Photoacoustic spectroscopy system with amplitude spectrum and phase spectrum measurement functions [J]. Acta Optica Sinica, 2014, 34(2): 0230001.
[27] F Belal, M S El- Din, F Aly, et al.. Fluorometric determination of bopindolol and celiprolol in pharmaceutical preparations and biological fluids [J]. J Fluoresc, 2012, 22(4): 1141-1150.
[28] A Mendez-Ardoy, T Steentjes, T Kudernac, et al.. Self-assembled monolayers on gold of β-cyclodextrin adsorbates with different anchoring groups [J]. Langmuir, 2014, 30(12): 3467-3476.
[29] C Jullian, V Brossard, I Gonzalez, et al.. Cyclodextrins-kaempferol inclusion complexes: Spectroscopic and reactivity studies [J]. J Solution Chem, 2011, 40(4): 727-739.
