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Journal articles on the topic 'Dibuty'

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Author: Grafiati

Published: 10 December 2022

Last updated: 28 January 2023

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1

Zhao, Zhao, Xue Gang Luo, and Xiao Yan Lin. "Photocatalytic Degradation of Methylene Blue by Modiflyed TiO₂ under Visible Light." Advanced Materials Research 197-198 (February 2011): 796–99. http://dx.doi.org/10.4028/www.scientific.net/amr.197-198.796.

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In this paper, we have studied the photocatalytic activity of TiO2which was modified by ferric stearate; ferrocene and nickel N,N-dibuty dithiocarbamate (NiDBC) , respectively. Innovatively, methylene blue (MB) was used as model pollutant. Under visible light irradiation, this paper studied the effect of the photocatalytic degradation of MB. The result shows that when the mass ratio is 5:1, the catalytic effect is C>B>A. When mass ratio is 1:1, the catalytic effect is B>C>A. Another result shows that with the increase of the amount TiO2, catalytic effect of TiO2modified by ferric stearate significantly increases, otherwise, TiO2modified by ferrocene and NiDBC were different.

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2

Zhao, Zhao, Xue Gang Luo, and Xiao Yan Lin. "Synergistic Effects of Ferric Stearate, Ferrocene and NiDBC." Materials Science Forum 658 (July 2010): 499–502. http://dx.doi.org/10.4028/www.scientific.net/msf.658.499.

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The synergistic effects of ferric stearate, ferrocene and nickel N,N-dibuty dithiocarbamate (NiDBC) on photocatalysis were studied. Absorption intensities and redox abilities of these pholocatalyst compounds were investigated by Diffuse Reflectance Spectroscopy (DRS) and cyclic voltammetry. The study indicated that adding Ferric stearate to either ferrocene or NiDBC reduced the absorption intensity at the range of 400-550nm. Mixed with NiDBC, the absorbance ranges of ferric stearate and ferrocene were both broadened from 200-550nm to 200-700nm. The results of cyclic voltammetry indicated that redox ability of ferrocene was inhibited by ferric stearate. Furthermore, accession of NiDBC may enhance the inhibition. NiDBC reduced the redox ability of ferric stearate as well.

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3

Zhao, Zhao, Xue Gang Luo, and Xiao Yan Lin. "Photocatalytic Decolorization of Methylene Blue by Ferric Stearate, Ferrocene and NiDBC under Sunlight Irradiation." Materials Science Forum 695 (July 2011): 133–36. http://dx.doi.org/10.4028/www.scientific.net/msf.695.133.

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In this work, ferric stearate, ferrocene and nickel N,N-dibuty dithiocarbamate (NiDBC) were utilized as photocatalyst for the decolorization of methylene blue (MB) aqueous solutions under sunlight irradiation. Pure MB solution was used as reference. Absorption intensities and surface morphology of these photocatalyst were investigated by Diffuse Reflectance Spectroscopy (DRS) and Scanning Electron Microscopy (SEM).The study indicated that ferric stearate had minimal promotion to the decolorization of MB aqueous solutions; and ferrocene exhibited better photocatalysis ability after had been irradiated 60 hours. In this study, NiDBC showed the best photocatalysis ability from the beginning. Furthermore, NiDBC enhanced the decolorization of MB after been irradiated for 31 hours. And after being irradiated 270 hours, the MB aqueous was completely decolorized by NiDBC.

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4

Boes, Evita. "PREPARASI CONTOH UJI PROFISIENSI UNTUK IDENTIFIKASI SENYAWA KIMIA BERBAHAYA." Jurnal Kimia Terapan Indonesia 17, no. 1 (June 10, 2015): 57–67. http://dx.doi.org/10.14203/jkti.v17i1.23.

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The sample of proficiency test for hazard chemical compounds in organic and water sample has been made to identify hazard chemical compounds. Here, various matrix was added to these hazard chemical compound. The organic sample derived from organic waste added with dichloromethane as the solvent, undecane 100 µl/mL, 1,2-dimethylbenzene 12 µl/mL, diesel 100 µl/mL and tributhyl phosphate 10,02 µg/mL, whereas water sample derived from water waste added with magnesium sulfate heptahydrate 120 µg/mL, sodium carbonate anhydrous 106 µg/mL, sodium sulfate anhydrous 284 µg/mL, calsium chloride dyhidrate 222 µg/mL, dikhloromethane 2,5 µl/mL, polyethylene glycol 505,4 µg/mL, 3,5 dihydroxytoluene 10,05 µg/mL and α methyl-α-propyl succinimide 10,01 µg/mL. Hazard chemical compounds that being added are Bis (3-methylbutyl) ethylphosphonate 10,04±0,31 µg/mL, Bis (2-chloroethyl) methylamine 20,59±0,14 µg/mL for organic sample and Pinacolyl methylphosphonate 9,80±0,18 µg/mL and Triethanolamine 14,84±0,10 µg/mL for water sample. Homogeneity and stability are determined quantitatively using GC-FPD (P-mode) and GC-FID with calibration curve using internal standard dibuty butylphosphonate, 2,6-dimethylphenol, dibutylphosphate and Bis (2-hydroxypropyl) aminoethanol with Relative Standard Deviation (RSD) 8,10 % and 12,40 µg/mL for Bis (3-methylbutyl) ethylphosphonate and 3,46 % and 14,19 µg/mL for Bis (2-chloroethyl) methylamine and 2,22 % and 11,28 µg/mL for Pinacolyl methylphosphonate and 2,70 % and 11,47 µg/mL for Triethanolamine. Relative Standard Deviation is a homogeneity value with requirements below 20 % and stability is a degradation result which value is less than 30 %.Keywords: hazard chemical compounds, proficiency test, homogeneity, stability, relative standard deviation

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5

Matsuoka, Takeshi, Kohta Kurohane, Wakana Suzuki, Erina Ogawa, Kamiyu Kobayashi, and Yasuyuki Imai. "Dibutyl Maleate and Dibutyl Fumarate Enhance Contact Sensitization to Fluorescein Isothiocyanate in Mice." Biological & Pharmaceutical Bulletin 39, no. 2 (2016): 272–77. http://dx.doi.org/10.1248/bpb.b15-00683.

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6

Lo Celso, Fabrizio, Bachir Aoun, Alessandro Triolo, and Olga Russina. "Liquid structure of dibutyl sulfoxide." Physical Chemistry Chemical Physics 18, no. 23 (2016): 15980–87. http://dx.doi.org/10.1039/c6cp02335e.

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7

Thormann, Jens, Ib Hansen, and Jens Misfeldt. "Occupational dermatitis from dibutyl maleinate." Contact Dermatitis 13, no. 5 (October 1985): 314–16. http://dx.doi.org/10.1111/j.1600-0536.1985.tb02585.x.

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8

English, J. S. C., C. R. Lovell, and R. J. G. Rycroft. "Contact dermatitis from dibutyl maleate." Contact Dermatitis 13, no. 5 (October 1985): 337–38. http://dx.doi.org/10.1111/j.1600-0536.1985.tb02594.x.

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9

Li, Qianli, Rufen Zhang, and Yang Shi. "Dibutyl 2,2′-bipyridine-4,4′-dicarboxylate." Acta Crystallographica Section E Structure Reports Online 65, no. 3 (February 6, 2009): o478. http://dx.doi.org/10.1107/s1600536809003997.

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10

Bowen, Richard D., Dennis Suh, and Johan K. Terlouw. "Reactions of ionized dibutyl ether." Organic Mass Spectrometry 29, no. 12 (December 1994): 791–805. http://dx.doi.org/10.1002/oms.1210291211.

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11

Romanov, G. V., �. P. Semkina, and A. N. Pudovik. "Dibutyl cyanophosphite and its properties." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 38, no. 3 (March 1989): 630–31. http://dx.doi.org/10.1007/bf00958064.

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12

Hoque, Md Ehtesham Ul, and Hai-Whang Lee. "Pyridinolysis of Dibutyl Chlorophosphate in Acetonitrile." Bulletin of the Korean Chemical Society 33, no. 3 (March 20, 2012): 1055–58. http://dx.doi.org/10.5012/bkcs.2012.33.3.1055.

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13

Hoque, Md Ehtesham Ul, and Hai-Whang Lee. "Pyridinolysis of Dibutyl Chlorothiophosphate in Acetonitrile." Bulletin of the Korean Chemical Society 33, no. 3 (March 20, 2012): 1085–88. http://dx.doi.org/10.5012/bkcs.2012.33.3.1085.

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14

Isobe, Hiroyuki, Taisuke Matsuno, Shunpei Hitosugi, and Waka Nakanishi. "2,11-Dibromo-5,8-dibutyl[4]helicene." Acta Crystallographica Section E Structure Reports Online 68, no. 4 (March 31, 2012): o1239. http://dx.doi.org/10.1107/s1600536812013141.

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A racemic mixture of the title compound, C26H26Br2, a brominated [4]helicene, crystallizes, forming columns of stacked molecules. There are two crystallographically unique molecules in the asymmetric unit, both with the same helical handedness. As is typical with helicene congeners, the unique molecules show short interatomic contacts between H atoms at the fjord region, with H...H distances of 1.87 and 1.94 Å. Molecules with the same helical handedness segregate in the crystal packing, forming homochiral columns. The stacked molecules are piled in a column with alternate orientations. The shortest C...C distance in the stacked molecules is 3.306 (4) Å.

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15

Zhao, Dong-dong, Peng Jiang, and Hong-Jun Zhu. "9,9-Dibutyl-9H-fluorene-2-carbonitrile." Acta Crystallographica Section E Structure Reports Online 68, no. 6 (May 26, 2012): o1903. http://dx.doi.org/10.1107/s1600536812022672.

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The fluorene fragment of the title compound, C22H25N, is essentially planar, with an r.m.s deviation of the five-membered ring of 0.005 (2) Å. The dihedral angle between this ring and the outer benzene rings are 1.5 (2) and 0.7 (2)° while that between the benzene rings is 2.1 (2)°. The cyano group makes an angle of 0.3 (2)° with the attached benzene ring.

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16

Yuan, Mao-Sen, Qi Fang, Lei Ji, and Wen-Tao Yu. "1,1′-Dibutyl-3,3′-biindolinylidene-2,2′-dione." Acta Crystallographica Section E Structure Reports Online 63, no. 11 (October 17, 2007): o4342. http://dx.doi.org/10.1107/s160053680705009x.

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The title molecule, C24H26N2O2, has its central C=C double bond placed on an inversion centre, and both indolin-2-one units are coplanar. The three terminal C atoms of the two butyl groups are disordered over two positions; the site occupancy factors are ca. 0.54 and 0.46. The central C=C bond exhibits an E configuration and is conjugated with the indole heterocycles. This aromatic character is related to the planarity of the isoindigo core and is reminiscent of that observed in stilbene.

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17

Maksimuk, Yu V., K. Ruzicka, and V. V. Diky. "Enthalpy of Formation of Dibutyl Phthalate." International Journal of Thermophysics 25, no. 2 (March 2004): 379–85. http://dx.doi.org/10.1023/b:ijot.0000028475.70749.d6.

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18

Cummings, A. M., and L. E. Gray. "Dibutyl phthalate: Maternal effects versus fetotoxicity." Toxicology Letters 39, no. 1 (November 1987): 43–50. http://dx.doi.org/10.1016/0378-4274(87)90255-4.

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19

Kuang, Q. J., W. Y. Zhao, and S. P. Cheng. "Toxicity of Dibutyl Phthalate to Algae." Bulletin of Environmental Contamination and Toxicology 71, no. 3 (September 1, 2003): 602–8. http://dx.doi.org/10.1007/s00128-003-8559-9.

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20

Chalabiyeva, A. Z., N. Ya Ishenko, D. R. Nurullayeva, and B. A. Mamedov. "WATER-DILUTING EPOXIDE TELOMER BASED ON DIBUTYL ETHER OF ADIPINIC ACID." Chemical Problems 18, no. 4 (2020): 451–56. http://dx.doi.org/10.32737/2221-8688-2020-4-451-456.

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A water-diluting epoxidetelomer was synthesized on the basis of allylglycidyl ether and dibutyl ether of adipinic acid under the effect of free radicals being generated during thermal decay of ditretbutyl peroxide. The reaction proceeds in one stage, the process is wasteless and fire-safe while the unreacted allylglycidyl ether returns to the reaction. The synthesized epoxytelomer is a low-viscous resin of lightyellow color, soluble in water, chloroform, acetone, M.w.=380-400 g.mol-1 , epoxide number –18-19%. The composition and structure of the obtained telomer were established due to physical and chemical investigations. The composition materials of hot and cold curing were developed on the basis of the obtained telomer. The curing process was studied by a method of differential-thermal analysis to show that the obtained materials were characterized by high heat-resistance and thermal stability. It revealed that the epoxide telomer has surface-active properties.

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21

Rapallo, Marcela. "Dibujo abierto." Revista Sonda: Investigación y Docencia en Artes y Letras 10 (December 31, 2021): 143–58. http://dx.doi.org/10.4995/sonda.2021.17822.

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Dibujo abierto es un concepto que abarca prácticas contemporáneas en las que el dibujo se presenta como un arte del tiempo, colectivo, relacional, e interdisciplinar. Toma el dibujo desde la idea de obra abierta y del concepto de código abierto desarrollado por la cultura del Software Libre. La apertura del dibujo hace referencia también a que al expandir su campo disciplinar pueda dialogar en vivo con las artes escénicas y pueda tomar de esas disciplinas métodos para desarrollar su propio lenguaje.La investigación se desarrolla a través de diferentes métodos para abordar el dibujo desde un enfoque transpersonal, deconstruyendo el lugar común que se le da de práctica individual. Apoyándose en la idea de que es una práctica accesible a cualquier persona, se busca contribuir a la reapropiación de los lenguajes artísticos por parte de la comunidad.

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22

Nie, Zhao Guang, Yan Fang Hu, Qian Xu, and Ji Ming Hu. "Study on Synthesis Technology of Dibutyl Phosphate." Advanced Materials Research 1052 (October 2014): 169–72. http://dx.doi.org/10.4028/www.scientific.net/amr.1052.169.

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The method of the synthesis of dibutyl phosphate from phosphorous acid and n-butanol has been explored. Effects of reaction conditions, such as the ratio of raw materials, reaction temperature, reaction time, catalyst type, and reaction time were investigated. The methods of analysis were studied. The composition of product was analyzed by titration method. The result showed: the best temperature was 125-135°C,the mole ratio of n-butanol / phosphorous acid was 3.6, the best reaction time without catalyst was 3h, the yield of dibutyl phosphate was 68%. The product can be separated by the agent of n-butanol/benzene 10:1 in TLC.

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23

Alsubaie, Aisha Manna, Yuko Arita, Matthew Atwater, Ali Mahfuz, and Morgan R. Peltier. "Enhancement of placental inflammation by Dibutyl Phthalate." Journal of Reproductive Immunology 147 (September 2021): 103368. http://dx.doi.org/10.1016/j.jri.2021.103368.

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24

Wang, Qiang, Zhi-dang Yang, Yang Wan, Jiao-yan Song, Chu Zhang, Meng-zu Sui, Zhi-jian Mu, and Shi-qiang Wei. "ADSORPTION OF DIBUTYL-PHTHALATE ON HUMIC ACID." Environmental Engineering and Management Journal 12, no. 9 (2013): 1791–95. http://dx.doi.org/10.30638/eemj.2013.216.

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25

ZHANG, ZiHui, XinYa XIE, Fan LI, NanPing WANG, and Lei XIAO. "Plasticizer dibutyl phthalate impairs vascular endothelial function." SCIENTIA SINICA Vitae 48, no. 5 (April 16, 2018): 535–43. http://dx.doi.org/10.1360/n052017-00247.

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26

Kwapniewski, Rachel, Sarah Kozaczka, Russ Hauser, Manori J. Silva, Antonia M. Calafat, and Susan M. Duty. "Occupational Exposure to Dibutyl Phthalate Among Manicurists." Journal of Occupational and Environmental Medicine 50, no. 6 (June 2008): 705–11. http://dx.doi.org/10.1097/jom.0b013e3181651571.

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27

Bomhard, E., and J. Ruf. "Acute Toxicologic Evaluation of Triethylamine Dibutyl Phosphate." Journal of the American College of Toxicology 15, no. 1_suppl (November 1996): S57. http://dx.doi.org/10.1177/10915818960150s129.

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28

Yuan, Mao-Sen, and Qi Fang. "(E)-1,1′-Dibutyl-3,3′-biindolinylidene-2,2′-dione." Acta Crystallographica Section E Structure Reports Online 67, no. 1 (December 8, 2010): o52. http://dx.doi.org/10.1107/s160053681005066x.

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29

Lin, H. K. "Extraction of zinc chloride with dibutyl butylphosphonate." Metallurgical Transactions B 24, no. 1 (February 1993): 11–15. http://dx.doi.org/10.1007/bf02657867.

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30

Comte, Olivier, Sylvie Genillard, and Céline Nkubana. "N,N-Dibutyl-2-p-tolyl-acetamide." Molecules 5, no. 12 (April 28, 2000): M161. http://dx.doi.org/10.3390/m161.

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31

Huang, G. L., H. W. Sun, and Z. H. Song. "Interactions Between Dibutyl Phthalate and Aquatic Organisms." Bulletin of Environmental Contamination and Toxicology 63, no. 6 (December 1, 1999): 759–65. http://dx.doi.org/10.1007/s001289901044.

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32

Mamat, Halidan. "Study of Cellulose-Dibutyl Sebacate Copolymer Synthesis and Characterization of Crosslinked Cellulose-Dibutyl Sebacate Copolymers for Oil Absorbency." Advanced Materials Research 311-313 (August 2011): 2075–83. http://dx.doi.org/10.4028/www.scientific.net/amr.311-313.2075.

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A novel cellulose-based oil absorbent crosslinked cellulose-dibutyl sebacate copolymers was prepared by the graft crosslinking polymerization of in situ synthesized dibutyl sebacate and cotton cellulose using potassium persulfate as an initiator. The copolymers were characterized by infrared spectroscopy, X-ray diffraction, scanning electron microscopy, thermogravimetry, differential scanning calorimetry, etc. The effects of reaction conditions, such as, ratio of reaction regents, reaction temperature, reaction time, etc, on the efficiency of oil absorbency were examined. The optimized reaction conditions for the synthesis of crosslinked cellulose-dibutyl sebacate copolymers were: m(cotton pulp):m(K2S2O8 initiator):m(dibutyl sebacate) = 1 0.025 2.0(W/W)，75°C，and 5-6 h. The resulting crosslinked cellulose-dibutyl sebacate copolymers were floppy and exhibited excellent oil absorbency efficiency.

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33

Chaudhary, Rakesh Singh, Tejas Patel, Job Richard Kumar, and Mohamed Chan. "Effect of substitution of plasticizer dibutyl phthalate with dibutyl sebacate on Eudragit® RS30D drug release rate control." Pharmaceutical Development and Technology 24, no. 3 (May 8, 2018): 276–82. http://dx.doi.org/10.1080/10837450.2018.1469151.

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34

Andie, Andie. "SISTEM INFORMASI DAN ADMINISTRASI RT (SIPAKRT) BERBASIS WEB." Technologia: Jurnal Ilmiah 10, no. 3 (July 11, 2019): 140. http://dx.doi.org/10.31602/tji.v10i3.2120.

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Sistem Informasi Pak RT (SIPAK RT) merupakan aplikasi yang akan dirancang dan dibuat untuk mempermudah pekerjaan Ketua Rukun Tetangga (RT), template dibuat berdasarkan surat yang dibutuhkan, warga bisa mengisi form pembuatan surat berdasarkan data dirinya dirumah, setelah data berhasil masuk Ketua RT akan mendapatkan pemberitahuan dan dapat segera memvalidasi data dan memprint surat langsung dan segera menandatanganinya. Apabila surat sudah selesai, akan ada pemberitahuan ke warga bahwa surat sudah dapat diambil. Aplikasi SIPAK RT berbasis online dan dapat digunakan dimana pun dan kapan pun. Masing-masing kepala keluarga akan mendapatkan Username dan password. Aplikasi juga dapat dibuka menggunakan berbagai device termasuk handphone warga masing-masing.Keyword : sistem, informasi, rt, online, handphone.

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35

Vives, María Rosa. "Un dibujo inédito de Rogelio de Egusquiza, copia del dibujo preparatorio de la Sibila Líbica de Miguel Ángel." Archivo Español de Arte 80, no. 317 (March 30, 2007): 103–6. http://dx.doi.org/10.3989/aearte.2007.v80.i317.71.

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36

Medina, Ainhoa. "Dibuja una programadora." UMH Sapiens Divulgación Científica, no. 28 (September 2020): 4–7. http://dx.doi.org/10.21134/22553568.2020.28.dp.

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37

Kolef Osorio, Sergio. "Notas sobre dibujo." Revista Sonda: Investigación y Docencia en Artes y Letras 6 (December 31, 2017): 19–28. http://dx.doi.org/10.4995/sonda.2017.18352.

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El presente ensayo aborda dos procesos de pensamiento y construcción de dibujos. El primero asume la ceguera como un encuentro con la reflexión sobre la decisión propia de nulificar la visión binocular. El otro permite tocar algunas disyuntivas contemporáneas sobre la pintura y el dibujo, en relación a los conceptos de gravedad en el espacio compositivo, la luz y los procesos gráficos que incluyen materiales en los que se revisa algo sobre su historia material y cualidades constructivas para el dibujo.

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38

Jooris, Roland, Marco Antonio Campos, Stefaan van den Bremt, and John Irons. "Tekening / Dibujo / Drawing." Sirena: poesia, arte y critica 2007, no. 1 (2007): 154–55. http://dx.doi.org/10.1353/sir.2007.0068.

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39

Saikova, Svetlana V., Dmitriy I. Chistyakov, Diana I. Saykova, Yury L. Mikhlin, and Dmitriy V. Kuzmin. "Synthesis and Characterization of Lead Dibutyl Dithiophosphate Nanoparticles." Journal of Siberian Federal University. Chemistry 14, no. 3 (September 2021): 350–59. http://dx.doi.org/10.17516/1998-2836-0243.

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We examined the interaction of aqueous solutions of lead nitrate and sodium dibutyl dithiophosphate and showed the formation nanoparticles of lead dibutyl dithiophosphate. The effect of reaction parameters on the synthesis of nanoparticles was studied and the optimal conditions for the formation of their stable hydrosols were determined. The obtained products were investigated by methods of optical spectroscopy, dynamic light scattering. The average size of 15–20 nm, but due to the low surface charge, they are combined into larger aggregates. The UV‑vis spectra has absorption maximum at about 320 nm. TEM micrographs and Pb 2p, S2p XAS spectra revealed a composition and structure of the particles. These nanoparticles can play an important role in the flotation of sulfide minerals of nonferrous metals

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40

Jackson, E. M. "Subungual Penetration of Dibutyl Phthalate in Human Fingernails." Skin Pharmacology and Physiology 21, no. 1 (2008): 10–14. http://dx.doi.org/10.1159/000109083.

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41

Huang, Yao-Zeng, Li-Lan Shi, Sao-Wei Li, and Xue-Qing Wen. "An efficient olefination method catalysed by dibutyl telluride." Journal of the Chemical Society, Perkin Transactions 1, no. 12 (1989): 2397. http://dx.doi.org/10.1039/p19890002397.

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42

Kraicheva, I. "Addition Products of Dibutyl Phosphite to Schiff Bases." Phosphorus, Sulfur, and Silicon and the Related Elements 134, no. 1 (February 1, 1998): 287–94. http://dx.doi.org/10.1080/10426509808545469.

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43

Liu, Lei, Na Liu, Wei Xu, and Dao-Ben Zhu. "4,4′-Bis[2-(3,4-dibutyl-2-thienylethynyl)]biphenyl." Acta Crystallographica Section E Structure Reports Online 64, no. 12 (November 13, 2008): o2306. http://dx.doi.org/10.1107/s1600536808036143.

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44

Li, Laisheng, Wanpeng Zhu, Le Chen, Pengyi Zhang, and Zhongyin Chen. "Photocatalytic ozonation of dibutyl phthalate over TiO2 film." Journal of Photochemistry and Photobiology A: Chemistry 175, no. 2-3 (October 2005): 172–77. http://dx.doi.org/10.1016/j.jphotochem.2005.01.020.

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45

Svatikov, M. Yu, E. A. Gruzinova, and G. V. Kotrelev. "Reaction of dibutyl phenylborate with hexamethyldisilazane and hexamethylcyclotrisilazane." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 40, no. 7 (July 1991): 1494–96. http://dx.doi.org/10.1007/bf00961265.

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46

Farzanehfar, Vahid, Nima Naderi, Farzad Kobarfard, and Mehrdad Faizi. "Determination of dibutyl phthalate neurobehavioral toxicity in mice." Food and Chemical Toxicology 94 (August 2016): 221–26. http://dx.doi.org/10.1016/j.fct.2016.05.006.

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Xu, Xiang-Rong, and Xiao-Yan Li. "Adsorption behaviour of dibutyl phthalate on marine sediments." Marine Pollution Bulletin 57, no. 6-12 (January 2008): 403–8. http://dx.doi.org/10.1016/j.marpolbul.2008.01.023.

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Ruikar, A. D., T. V. Gadkari, U. D. Phalgune, V. G. Puranik, and N. R. Deshpande. "Dibutyl phthalate, a secondary metabolite from Mimusops elengi." Chemistry of Natural Compounds 46, no. 6 (January 2011): 955–56. http://dx.doi.org/10.1007/s10600-011-9793-8.

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Tang, Jie, Tohru Kamo, Muneyoshi Yamada, Yozo Ohshima, and Akira Amano. "The Reaction of Dibutyl Disulfide with Hydrogen Atom." Bulletin of the Chemical Society of Japan 60, no. 6 (June 1987): 2019–22. http://dx.doi.org/10.1246/bcsj.60.2019.

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Liu, Ying, Xianxi Zhang, Zechun Xue, and Jian Sheng. "Dibutyl 5-[(4-ethoxycarbonylphenyl)diazenyl]benzene-1,3-dicarboxylate." Acta Crystallographica Section E Structure Reports Online 66, no. 7 (June 23, 2010): o1730. http://dx.doi.org/10.1107/s1600536810022762.

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