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Journal articles on the topic 'Butylacrylate'

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1

Fares, Mohammad M., Adeeb S. El-faqeeh, Hasan Ghanem, Mohammad E. Osman, and Elfatih A. Hassan. "Hydrogels of starch-g-(tert-butylacrylate) and starch-g-(n-butylacrylate) copolymers." Journal of Thermal Analysis and Calorimetry 99, no. 2 (August 28, 2009): 659–66. http://dx.doi.org/10.1007/s10973-009-0213-2.

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2

Vainio, Tommi, Harri Jukarainen, and Jukka Sepp�l�. "Compatibilization of polypropylene/poly(n-butylacrylate) blend: Functionalization of the poly(n-butylacrylate) phase by copolymerization." Journal of Applied Polymer Science 59, no. 13 (March 28, 1996): 2095–105. http://dx.doi.org/10.1002/(sici)1097-4628(19960328)59:13<2095::aid-app14>3.0.co;2-z.

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3

Tonglairoum, Prasopchai, Ruairí P. Brannigan, Praneet Opanasopit, and Vitaliy V. Khutoryanskiy. "Maleimide-bearing nanogels as novel mucoadhesive materials for drug delivery." Journal of Materials Chemistry B 4, no. 40 (2016): 6581–87. http://dx.doi.org/10.1039/c6tb02124g.

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Novel class of mucoadhesive polymers has been developed via polymerisation of 2,5-dimethylfuran-protected 3-maleimidoethyl butylacrylate in the presence of presynthesised poly(N-vinylpyrrolidone) nanogel scaffolds. The resulting maleimide-bearing nanogels were capable of forming covalent linkages with mucosal membranes.
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4

KAWABE, Masayoshi, Keiji HAYASHI, and Shigeru KATAYAMA. "Interdiffusion in Poly (isobutylene) / Poly (butylacrylate) Interfaces." Journal of The Adhesion Society of Japan 36, no. 1 (2000): 17–22. http://dx.doi.org/10.11618/adhesion.36.17.

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5

Amouroux, Nicolas, Frédéric Restagno, and Liliane Léger. "Adhesion at Poly(Butylacrylate)–Poly(Dimethylsiloxane) Interfaces." Journal of Adhesion 83, no. 8 (September 27, 2007): 741–60. http://dx.doi.org/10.1080/00218460701585840.

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6

Shaffer, O. L., M. S. El-Aasser, and J. W. Vanderhoff. "TEM analysis of core/shell latex morphology." Proceedings, annual meeting, Electron Microscopy Society of America 45 (August 1987): 502–3. http://dx.doi.org/10.1017/s0424820100127153.

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Transmission electron microscopy is an excellent method to study particle size and particle morphology of latexes. Special sample techniques are utilized in the study of latexes and often more than one technique is needed to answer questions concerning the structure of the particle. If the latex is of a core/shell type the study becomes more complex. Sample preparation for studying latexes include staining with osmium tetroxide to crosslink and stain unsaturated polymers, cold stage if the latex is too soft to examine at room temperature, negative staining to increase contrast shadowing to determine the sag of the particle at room temperature, ultramicrotoming, cryoultramicrotoming or a combination of techniques such as staining and cold stage.The latex investigated was the first stage seed latex of poly (butylacrylate - butadiene) and the final latex a core-shell of poly(butylacrylate - butadiene)/poly(methyl methacrylate). Because of its unsaturation, poly(butadiene) can be preferentially stained with osmium tetroxide.
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7

Yue, Dongmei, Xinpeng Wei, Xunzhang Wang, Weimin Wang, and Liqun Zhang. "HYDROGENATED BUTADIENE-ACRYLONITRILE-BUTYLACRYLATE RUBBER AND ITS PROPERTIES." Rubber Chemistry and Technology 86, no. 2 (June 1, 2013): 165–74. http://dx.doi.org/10.5254/rct.13.88997.

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ABSTRACT Butadiene-acrylonitrile-butylacrylate rubber (BNBR), which is synthesized by copolymerization of butadiene, acrylonitrile, and butyl acrylate, retains excellent properties of oil resistance and heat resistance because of the introduction of -CN, -COOR in the polymer. However, the presence of a lot of carbon-carbon double bonds (-C=C-) could lead to deterioration of material properties such as thermal stability and ozone resistance. To improve the properties of unsaturated elastomers, further chemical modification of diene-based polymers is very critical. Hydrogenation is a useful chemical modification method that can improve the thermal stability of diene-based polymer. BNBR was hydrogenated by homogenous hydrogenation using the Wilkinson catalyst RhCl(PPh3)3 in xylene. The effects of catalyst concentrations, reaction times, and hydrogen pressures on the conversion and product selectivity were discussed. The degree of hydrogenation was measured by proton nuclear magnetic resonance spectroscopy and Fourier transform infrared spectroscopy. The thermal stability of hydrogenated and nonhydrogenated copolymers was evaluated by thermogravimetric analysis (TGA). The CCD camera was used to characterize the ozone resistance of hydrogenated copolymer (HBNBR). The results obtained by TGA and the CCD camera show that the maximum saturation level is a critical factor for improvement of thermal stability and the ozone resistance of HBNBR.
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8

Sergeev, V. V., and Yu Ya Van-Chin-Syan. "Heats of mixing butylacrylate with certain organic solvents." Russian Journal of Applied Chemistry 85, no. 4 (April 2012): 689–91. http://dx.doi.org/10.1134/s1070427212040283.

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9

Encinar, Mario, Eduardo Guzmán, Margarita G. Prolongo, Ramón G. Rubio, Claudia Sandoval, Fernando González-Nilo, Ligia Gargallo, and Deodato Radić. "Dielectric and dynamic-mechanical study of the mobility of poly(t-butylacrylate) chains in diblock copolymers: Polystyrene-b-poly(t-butylacrylate)." Polymer 49, no. 26 (December 2008): 5650–58. http://dx.doi.org/10.1016/j.polymer.2008.10.023.

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10

Bedjaoui, L., T. Bouchaour, M. Benmouna, X. Coqueret, and U. Maschke. "Selective solubility of E7 components in poly (n-butylacrylate)." Physics Procedia 2, no. 3 (November 2009): 1475–79. http://dx.doi.org/10.1016/j.phpro.2009.11.119.

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11

Costa, L. C., M. E. Achour, M. P. F. Graça, M. El Hasnaoui, A. Outzourhit, and A. Oueriagli. "Dielectric properties of the ethylene butylacrylate/carbon black nanocomposites." Journal of Non-Crystalline Solids 356, no. 4-5 (February 2010): 270–74. http://dx.doi.org/10.1016/j.jnoncrysol.2009.11.008.

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12

Aizawa, Hidenobu, Shoji Kawashima, Shigeru Kurosawa, Kazutoshi Noda, Takayoshi Fujii, and Mitsuo Hirata. "Synthesis and characterization of plasma-polymerized tert-butylacrylate films." Thin Solid Films 515, no. 9 (March 2007): 4141–47. http://dx.doi.org/10.1016/j.tsf.2006.02.047.

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13

Bedjaoui, L., M. Benmouna, T. Bouchaour, X. Coqueret, and U. Maschke. "Selective Solubility of E7 Components in Poly(n-butylacrylate)." Molecular Crystals and Liquid Crystals 411, no. 1 (January 2004): 537–44. http://dx.doi.org/10.1080/15421400490436458.

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14

Cao, Gui-Ping, Zhong-Nan Zhu, Ming-Hua Zhang, and Wei-Kang Yuan. "Kinetics of butylacrylate polymerization in a starved feed reactor." Journal of Applied Polymer Science 93, no. 4 (2004): 1519–25. http://dx.doi.org/10.1002/app.20622.

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15

Bulatović, Vesna Ocelić, Vesna Rek, and Josipa Marković. "Rheological properties of bitumen modified with ethylene butylacrylate glycidylmethacrylate." Polymer Engineering & Science 54, no. 5 (July 5, 2013): 1056–65. http://dx.doi.org/10.1002/pen.23649.

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16

Schofield, W. C. E., and J. P. S. Badyal. "Pulsed Plasma Polymerisation of Butylacrylate for Pressure-Sensitive Adhesion." Plasma Chemistry and Plasma Processing 26, no. 4 (May 31, 2006): 361–69. http://dx.doi.org/10.1007/s11090-006-9013-7.

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17

Serkhacheva, N. S., E. V. Chernikova, N. I. Prokopov, M. S. Balashov, V. V. Ogay, and R. V. Toms. "Dispersion polymerization of n-butylacrylate under the action of acrylic acid and N-isopropylacrylamide copolymers." Plasticheskie massy, no. 9-10 (November 2, 2019): 34–38. http://dx.doi.org/10.35164/0554-2901-2019-9-10-34-38.

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The regularities of dispersion radical polymerization of n-butylacrylate in water-alcohol medium under the action of polymer tritiocarbonates based on copolymers of acrylic acid and N-isopropylacrylamide have been investigated. The conditions for the formation of a block copolymer with controlled molecular weight and high yield have been found. The conditions of formation of stable suspensions of block copolymers with unimodal particle size distribution have been determined.
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18

Kosugi, Yuuki, Yoshiaki Matsuoka, and Kenji Urayama. "Yielding Behavior of Rubber-Particles Melts of Poly(n-butylacrylate)." Nihon Reoroji Gakkaishi 43, no. 3_4 (2015): 93–98. http://dx.doi.org/10.1678/rheology.43.93.

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19

Roy, Santanu, and Surekha Devi. "High solids content semicontinuous microemulsion copolymerization of methylmethacrylate and butylacrylate." Polymer 38, no. 13 (January 1997): 3325–31. http://dx.doi.org/10.1016/s0032-3861(96)00875-0.

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20

Khafagi, M. G., A. M. Salem, and H. A. Essawy. "Synthesis and optical characterization of poly(glycidylmethacrylate-co-butylacrylate) copolymers." Materials Letters 58, no. 29 (November 2004): 3674–80. http://dx.doi.org/10.1016/j.matlet.2004.06.054.

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21

Oh, Jung Kwon, Jun Wu, Mitchell A. Winnik, Gary P. Craun, Jude Rademacher, and Rajeev Farwaha. "Polymerizable benzophenone derivatives for labeling vinyl acetate-butylacrylate latex particles." Journal of Polymer Science Part A: Polymer Chemistry 40, no. 17 (July 24, 2002): 3001–11. http://dx.doi.org/10.1002/pola.10384.

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22

Zhu, Aiping, Aiyun Cai, Ziyi Yu, and Weidong Zhou. "Film characterization of poly(styrene-butylacrylate-acrylic acid)–silica nanocomposite." Journal of Colloid and Interface Science 322, no. 1 (June 2008): 51–58. http://dx.doi.org/10.1016/j.jcis.2008.02.014.

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23

Litmanovich, A. D., and V. O. Cherkezyan. "Intermolecular effects in the thermal degradation of poly-tert-butylacrylate." Polymer Science U.S.S.R. 27, no. 9 (January 1985): 2096–103. http://dx.doi.org/10.1016/0032-3950(85)90491-5.

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24

Lee, Hsun-Tsing, and Chee-Chan Wang. "Synthesis and Properties of Aqueous Polyurethane/Polytert-butylacrylate Hybrid Dispersions." Journal of Polymer Research 12, no. 4 (August 2005): 271–77. http://dx.doi.org/10.1007/s10965-004-4823-x.

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25

Tebaldi, M. L. D. S., T. C. Chaparro, and A. M. Santos. "Tri-Block Copolymers Obtained by RAFT Polymerization: A Promising Material for Drug-Delivery Systems." Materials Science Forum 636-637 (January 2010): 76–81. http://dx.doi.org/10.4028/www.scientific.net/msf.636-637.76.

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Tri-block copolymer with pH- and thermo-responsive consisting of poly(t-butylacrylate) and poly(vinylcaprolactam), (PtBA/PVCL) were prepared by RAFT polymerization and characterized by gel permeation chromatography (GPC) and 1H NMR. PtBA and PVCL were used as macro chain-transfer agents (MCTA) to synthesize PtBA-b-PVCL-b-PtBA and/or PVCL-b-PtBA-b-PVCL, which after partial hydrolysis led to amphiphilic tri-block copolymers P(tBA-co-AA)-b-PVCL-b-P(tBA-co-AA) and/or PVCL-b-P(tBA-co-AA)-b-PVCL.
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26

Pinheiro, Paula C., Sara Fateixa, Helena I. S. Nogueira, and Tito Trindade. "SERS study on adenine using a Ag/poly(t-butylacrylate) nanocomposite." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 101 (January 2013): 36–39. http://dx.doi.org/10.1016/j.saa.2012.09.079.

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27

El Hasnaoui, M., A. Triki, M. P. F. Graça, M. E. Achour, L. C. Costa, and M. Arous. "Electrical conductivity studies on carbon black loaded ethylene butylacrylate polymer composites." Journal of Non-Crystalline Solids 358, no. 20 (October 2012): 2810–15. http://dx.doi.org/10.1016/j.jnoncrysol.2012.07.008.

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28

Hebeish, A., A. El Shafei, and S. Shaarawy. "Synthesis and Characterization of Multifunctional Cotton Containing Cyclodextrin and Butylacrylate Moieties." Polymer-Plastics Technology and Engineering 48, no. 8 (July 21, 2009): 839–50. http://dx.doi.org/10.1080/03602550902994904.

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29

Yang, Wenqing, Xuan‐Lun Wang, Jianfeng Li, Xingru Yan, Shengsong Ge, Sruthi Tadakamalla, and Zhanhu Guo. "Polyoxymethylene/ethylene butylacrylate copolymer/ethylene‐methyl acrylate‐glycidyl methacrylate ternary blends." Polymer Engineering & Science 58, no. 7 (August 2017): 1127–34. http://dx.doi.org/10.1002/pen.24675.

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30

Xiong, Mingna, Guangxin Gu, Bo You, and Limin Wu. "Preparation and characterization of poly(styrene butylacrylate) latex/nano-ZnO nanocomposites." Journal of Applied Polymer Science 90, no. 7 (September 22, 2003): 1923–31. http://dx.doi.org/10.1002/app.12869.

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31

Wang, Kun Yan. "Morphology and Crystallization Behavior of PTT Blends with PTW." Key Engineering Materials 777 (August 2018): 90–94. http://dx.doi.org/10.4028/www.scientific.net/kem.777.90.

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Poly (trimethylene terephthalate) (PTT)/Poly (ethylene-butylacrylate-glyciyl methacrylate) (PTW) blends have been prepared in composition by weight 95/5, 90/10, 80/20 and 70/30 using the twin screw extruder approach. Their morphologies, crystallization behavior and mechanical properties were investigated. Scanning electron microscopy observation shows the uniform dispersion of PTW in PTT matrix with weight-average particle size from 0.98 to 3.64μm when the PTW content increases from 5wt% to 30wt% in the blends. The presence of the PTW increased the crystallinity of PTT matrix in PTT/PTW blends. A nucleation activity of the PTW appears in PTT/PTW blends.
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32

Chen, Jian, Fu Jie Yang, Hong Xiang Zhu, Yong Hong Li, and Shuang Fei Wang. "Study on Synthesis of High Performance Emulsion of Paper Sizing Agent under Microwave Radiation." Advanced Materials Research 602-604 (December 2012): 1304–8. http://dx.doi.org/10.4028/www.scientific.net/amr.602-604.1304.

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After the treatment of the ultrasound, the paper sizing agent preparation process with emulsion copolymerization of methyl methl acrylate and butylacrylate under microwave irradiation is discussed. To research the synthesis of sizing agent, the change of emulsion polymerization products of monomer conversion, particle size, and centrifugal stability were observed under types of conditions such as microwave power and dosage of emulsifiers. This synthetic method is due to use the microwave irradiation so that its response is very fast, and it can provide a new approach to prepare efficiently a paper sizing agent in the paper making.
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33

Zhao, Chen Yang, Ju Jie Ren, Shao Ying Li, and Jin Song Ma. "Optimization of Technology of Emulsion Polymerization with High Solid Content and SAS Regression Procedure." Advanced Materials Research 554-556 (July 2012): 161–67. http://dx.doi.org/10.4028/www.scientific.net/amr.554-556.161.

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A random-arranged experimental design method was employed to optimize the technology of styrene/butylacrylate/acrylic acid (St/BA/AA) emulsion polymerization with high solid content. The random-designed experimental results were analyzed with regression analysis by using statistical analysis system (SAS), and the optimal regression equations between the principal factors and the emulsion properties were in turn established. It is shown that the viscosity of emulsions is greatly affected by the following factors: solid content, the interaction between the emulsifier content and solid content, the interaction between the initiator concentration and reaction temperature, the interaction between functional monomer and reaction temperature.
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34

Wang, Xiaoping, Qinwei Shi, and Hailong Hu. "Load dependence and scanning size effect on friction of Polytert-butylacrylate film." Thin Solid Films 466, no. 1-2 (November 2004): 183–88. http://dx.doi.org/10.1016/j.tsf.2004.03.029.

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35

Natalia, Becerra, Andrade Henry, López Betty, Restrepo Luz Marina, and Raiteri Roberto. "Probing poly(N-isopropylacrylamide-co-butylacrylate)/cell interactions by atomic force microscopy." Journal of Biomedical Materials Research Part A 103, no. 1 (March 21, 2014): 145–53. http://dx.doi.org/10.1002/jbm.a.35163.

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36

Mishra, Anuradha, and Swati Daswal. "Copolymerization ofn-butylacrylate with styrene by a novel photoinitiator, 1-(bromoacetyl)pyrene." Journal of Applied Polymer Science 102, no. 4 (2006): 3233–39. http://dx.doi.org/10.1002/app.24596.

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37

Mishra, Anuradha, and Swati Daswal. "Copolymerization ofn-butylacrylate with methylmethacrylate by a novel photoinitiator, 1-(bromoacetyl)pyrene." International Journal of Chemical Kinetics 39, no. 5 (2007): 261–67. http://dx.doi.org/10.1002/kin.20234.

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38

Naghash, Hamid Javaherian, Akram Karimzadeh, and Ahmad Reza Massah. "Synthesis and properties of styrene-butylacrylate emulsion copolymers modified by silane compounds." Journal of Applied Polymer Science 112, no. 2 (April 15, 2009): 1037–44. http://dx.doi.org/10.1002/app.29555.

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39

Rouhallah, Bagheri, and Mohsenipour Ali-Asghar. "Synthesis of methyl methacrylate-n-butylacrylate copolymers: Study of the paint properties." Journal of Applied Polymer Science 70, no. 2 (October 10, 1998): 367–72. http://dx.doi.org/10.1002/(sici)1097-4628(19981003)70:2<367::aid-app17>3.0.co;2-1.

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40

C�rdenas T., Galo, Elizabeth Salgado C., Juan Morales, and Hugo Soto Z. "Synthesis and properties of poly(butylacrylate-co-butylmethacrylate) doped with metal clusters." Journal of Applied Polymer Science 73, no. 7 (August 15, 1999): 1239–45. http://dx.doi.org/10.1002/(sici)1097-4628(19990815)73:7<1239::aid-app18>3.0.co;2-j.

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41

Wang, Kun Yan. "Toughened Poly(Trimethylene Terephthalate) by Reactive Blending with PTW." Key Engineering Materials 777 (August 2018): 70–74. http://dx.doi.org/10.4028/www.scientific.net/kem.777.70.

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New toughened poly (trimethylene terephthalate) (PTT) materials were obtained by reactive blending with poly (ethylene-butylacrylate-glycidyl methacrylate) (PTW). Morphology observation showed the well-dispersed domains of PTW in PTT matrix. The notched impact strength of the blends with 30wt% PTW is obviously higher than that of pure PTT. PTT-g-PTW copolymer as compatibilizer was formed by the interfacial reaction between the end epoxy group of PTW and the carboxylic or hydroxyl groups at the chain ends of PTT in the blends. Large number of stretched polymeric fibrils are uniformly distributed on the Izod impact fractured surface, which leads to an improvement in fracture toughness due to the consumption of fracture energy.
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42

Motsoane, Nthabiseng M., Ilia A. Guzei, and James Darkwa. "Poly(pyrazol-1-ylmethyl)benzene Palladium Complexes: Synthesis, Characterisation and Evaluation as Heck Coupling Catalysts." Zeitschrift für Naturforschung B 62, no. 3 (March 1, 2007): 323–30. http://dx.doi.org/10.1515/znb-2007-0304.

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The poly(pyrazol-1-ylmethyl)benzenes L1 - L5 react with [PdCl2(NCMe)2] or [PdClMe(COD)] to form dinuclear palladium complexes [{PdClX(3,5-Me2pzCH2)2-1,2-C6H4}2] (X = Cl (1), Me (2)), [{PdCl2(3,5-Me2pzCH2)2-1,3-C6H4}2] (3), palladium complexes [{Pd2(μ-Cl)2Me2(3,5- Me2pzCH2)2-1,3-C6H4}] (4), [{Pd2(μ-Cl)2X2(3,5-Me2pzCH2)2-1,4-C6H4}] (X = Cl (5), Me (6)), [{Pd2(μ-Cl)2Cl2(3,5-tBu2pzCH2)2-1,4-C6H4}] (7), and tetranuclear [{Pd2(μ-Cl)2Cl2(3,5- Me2pzCH2)2}2-1,4-C6H4] (8). The structures of 1, 2 and 8 were confirmed by X-ray structure analysis. The complexes efficiently catalyse the coupling reaction of iodobenzene and butylacrylate at 80 °C.
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43

Bouchaour, T., M. Benmouna, X. Coqueret, and U. Maschke. "Swelling and Deswelling of Poly (n-butylacrylate) Networks in Isotropic and Nematic Solvents." Molecular Crystals and Liquid Crystals 411, no. 1 (January 2004): 553–59. http://dx.doi.org/10.1080/15421400490436494.

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44

JEONG, Min-Yeong, Byung-Yoon AHN, Sang-Koul LEE, Won-Ki LEE, and Nam-Ju JO. "Antistatic coating material consisting of poly (butylacrylate-co-styrene) core-nickel shell particle." Transactions of Nonferrous Metals Society of China 19 (September 2009): s119—s123. http://dx.doi.org/10.1016/s1003-6326(10)60258-0.

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45

Chitta, Rajesh, Robert Brüll, Tibor Macko, Vincent Monteil, Christophe Boisson, Etienne Grau, and Alexandra Leblanc. "Characterization of Ethylene methyl methacrylate and Ethylene butylacrylate Copolymers with Interactive Liquid Chromatography." Macromolecular Symposia 298, no. 1 (December 2010): 191–99. http://dx.doi.org/10.1002/masy.201000039.

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46

Yurekli, Yilmaz, Sacide Alsoy Altinkaya, and John M. Zielinski. "Solubility and diffusivity of methylmethacrylate and butylacrylate monomers in a MMA–BA copolymer." Journal of Polymer Science Part B: Polymer Physics 45, no. 15 (2007): 1996–2006. http://dx.doi.org/10.1002/polb.21189.

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47

Boujioui, Fadoi, Helen Damerow, Flanco Zhuge, and Jean‐François Gohy. "Solid Polymer Electrolytes Based on Copolymers of Cyclic Carbonate Acrylate and n ‐Butylacrylate." Macromolecular Chemistry and Physics 221, no. 6 (February 24, 2020): 1900556. http://dx.doi.org/10.1002/macp.201900556.

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48

Mokhtar, S. M., E. M. Youssef, and M. A. Abd El-Ghaffar. "CHARACTERIZATION AND ELECTRICAL PROPERTIES OF ITACONIC ACID/BUTYLACRYLATE COPOLYMERS AND THEIR METAL COMPLEXES." Journal of Macromolecular Science, Part A 38, no. 1 (February 27, 2001): 19–32. http://dx.doi.org/10.1081/ma-100000357.

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49

Liu, Jing, Kun Cui, Qiao-Ling Zhao, Jin Huang, Tao Jiang, and Zhi Ma. "New ABA tri-block copolymers of poly(tert-butylacrylate)-b-poly(2,2,2-trifluoroethyl acrylate)-b-poly(tert-butylacrylate): Synthesis, self-assembly and fabrication of their porous films, spheres, and fibers." European Polymer Journal 113 (April 2019): 52–59. http://dx.doi.org/10.1016/j.eurpolymj.2019.01.037.

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50

Zheng, Huaili, Yongjun Sun, Xiaomin Tang, Mingzhuo Tan, Jiangya Ma, Wei Chen, and Yong Liao. "UV-Initiated Polymerization of Cationic Polyacrylamide: Synthesis, Characterization, and Sludge Dewatering Performance." Scientific World Journal 2013 (2013): 1–7. http://dx.doi.org/10.1155/2013/937937.

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Abstract:
P(AM-DAC-BA) was synthesized through copolymerization of acrylamide (AM), acryloyloxyethyl trimethyl ammonium chloride (DAC), and butylacrylate (BA) under ultraviolet (UV) initiation using response surface methodology (RSM). The influences of light intensity, illumination time, and photoinitiator concentration on the intrinsic viscosity[η]of P(AM-DAC-BA) were investigated. RSM model based on the influencing data was established for optimizing synthetic conditions. It was found that, at light intensity 1491.67 μw·cm−2, illumination time 117.89 min, and photoinitiator concentration 0.60‰, there was a better material performance achieved. Thus P(AM-DAC-BA) prepared under the above conditions showed excellent dewatering performance that, with 40 mg·L−1P(AM-DAC-BA) at pH 7, the residual turbidity of supernatant and the dry solid content were up to 38 NTU, 28.5%, respectively.
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