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Journal articles on the topic 'Polystyrene Latexes'

Author: Grafiati

Published: 6 September 2023

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1

Madaeni, Sayed Siavash, and Marziah Ghanbarian. "Characterization of polystyrene latexes." Polymer International 49, no. 11 (2000): 1356–64. http://dx.doi.org/10.1002/1097-0126(200011)49:11<1356::aid-pi493>3.0.co;2-a.

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2

Adjadj, Laurent P., Giuseppe Storti, and Massimo Morbidelli. "Ultrasound Attenuation in Polystyrene Latexes." Langmuir 19, no. 9 (April 2003): 3953–57. http://dx.doi.org/10.1021/la026893l.

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3

Lahmar, Hadjira, Ibrahim Badr, Chariya Kaewsaneha, Abdelhamid Elaissari, and Salima Saidi-Besbes. "1,2,3-triazole functionalized polystyrene and perdeuterated polystyrene chelating latexes." Colloid and Polymer Science 297, no. 7-8 (May 27, 2019): 1119–31. http://dx.doi.org/10.1007/s00396-019-04509-2.

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4

Donescu, Dan, Liana Fusulan, Stela Lungoci, Sever Serban, and Cristian Peteu. "Two-stage latexes of polystyrene acrylates." Journal of Dispersion Science and Technology 21, no. 5 (January 2000): 647–53. http://dx.doi.org/10.1080/01932690008913297.

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5

Xu, Zushun, and Warren T. Ford. "Polystyrene Latexes Containing Poly(propyleneimine) Dendrimers." Macromolecules 35, no. 20 (September 2002): 7662–68. http://dx.doi.org/10.1021/ma020312h.

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6

Xu, X. J., P. Y. Chow, and L. M. Gan. "Nanoparticles of Latexes from Commercial Polystyrene." Journal of Nanoscience and Nanotechnology 2, no. 1 (February 1, 2002): 61–65. http://dx.doi.org/10.1166/jnn.2002.066.

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7

Durrer, Carlo, Juan Manuel Irache, Dominique Duchene, and Gilles Ponchel. "Mucin Interactions with Functionalized Polystyrene Latexes." Journal of Colloid and Interface Science 170, no. 2 (March 1995): 555–61. http://dx.doi.org/10.1006/jcis.1995.1134.

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8

Pelton, R. H. "Polystyrene and polystyrene-butadiene latexes stabilized by poly(N-isopropylacrylamide)." Journal of Polymer Science Part A: Polymer Chemistry 26, no. 1 (January 1988): 9–18. http://dx.doi.org/10.1002/pola.1988.080260102.

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9

Barthet, Christelle, Steven P. Armes, Mohamed M. Chehimi, Carole Bilem, and Maria Omastova. "Surface Characterization of Polyaniline-Coated Polystyrene Latexes." Langmuir 14, no. 18 (September 1998): 5032–38. http://dx.doi.org/10.1021/la980102r.

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10

Rubio-Hernández, F. J., A. I. Gómez-Merino, E. Ruiz-Reina, and C. Carnero-Ruiz. "The primary electroviscous effect of polystyrene latexes." Colloids and Surfaces A: Physicochemical and Engineering Aspects 140, no. 1-3 (September 1998): 295–98. http://dx.doi.org/10.1016/s0927-7757(97)00286-0.

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11

Yang, Se-in, A. Klein, and L. H. Sperling. "Development of supermolecular structure in polystyrene latexes." Journal of Polymer Science Part B: Polymer Physics 27, no. 8 (July 1989): 1649–62. http://dx.doi.org/10.1002/polb.1989.090270805.

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12

Tian, Minmin, Zdeněk Tuzar, and Petr Munk. "Light Scattering of Particles Embedded in Soft Hydrogel." Collection of Czechoslovak Chemical Communications 60, no. 10 (1995): 1719–27. http://dx.doi.org/10.1135/cccc19951719.

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This study is concerned with soft polyacrylamide gels in which are embedded either polystyrene latexes or block copolymer micelles with polystyrene cores and poly(methacrylic acid) shells. We have found that light scattering provides useful structure information about the systems. For polystyrene latexes, both molar mass and radius of gyration do not change during the embedding in the hydrogel; for block copolymer micelles, molar mass does not change, while the size decreases upon immobilization. In all cases, the second virial coefficient is very small and overshadowed by the turbidity of the sample. For large particles with narrow particle size distribution, a combination of Guinier and Zimm plots has been used for obtaining the particle size and molar mass.

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13

Chakraborty, Saheli, and S. Ramakrishnan. "Surface-Functionalized Polystyrene Latexes Using Itaconate-Based Surfmers." Langmuir 34, no. 39 (September 7, 2018): 11729–37. http://dx.doi.org/10.1021/acs.langmuir.8b01708.

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14

Covolan, V. L., S. D'Antone, G. Ruggeri, and E. Chiellini. "Preparation of Aminated Polystyrene Latexes by Dispersion Polymerization." Macromolecules 33, no. 18 (September 2000): 6685–92. http://dx.doi.org/10.1021/ma0000430.

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15

Cho, Sun-Hee, Wan-Young Kim, Gu-Kwan Jeong, and Youn-Sik Lee. "Synthesis of nano-sized polypyrrole-coated polystyrene latexes." Colloids and Surfaces A: Physicochemical and Engineering Aspects 255, no. 1-3 (March 2005): 79–83. http://dx.doi.org/10.1016/j.colsurfa.2004.12.025.

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16

KUMAR, DHIRENDRA, and GEORGE B. BUTLER. "SYNTHESIS AND CHARACTERIZATION OF CONTROLLED SIZES: POLYSTYRENE LATEXES." Particulate Science and Technology 14, no. 4 (October 1996): 315–26. http://dx.doi.org/10.1080/02726359608906703.

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17

Cook, D. G., A. Rudin, and A. Plumtree. "Supermicron poly(butyl acrylate)/polystyrene core-shell latexes." Journal of Applied Polymer Science 46, no. 8 (November 15, 1992): 1387–93. http://dx.doi.org/10.1002/app.1992.070460808.

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18

Ronco, Ludmila Irene, Roque Javier Minari, and Luis Marcelino Gugliotta. "Hybrid Polystyrene/Polybutadiene Latexes With Low Environmental Impact." Macromolecular Reaction Engineering 10, no. 1 (October 12, 2015): 29–38. http://dx.doi.org/10.1002/mren.201500021.

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19

Lefay, Catherine, Maud Save, Bernadette Charleux, and Stéphanie Magnet. "Miniemulsion Polymerization Stabilized by a Well-Defined, Amphiphilic Gradient Poly(styrene-co-acrylic acid) Copolymer." Australian Journal of Chemistry 59, no. 8 (2006): 544. http://dx.doi.org/10.1071/ch06146.

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The nitroxide-mediated controlled free-radical copolymerization of styrene (St) and acrylic acid (AA) was used to synthesize a well-defined poly(St30%-co-AA70%) amphiphilic gradient copolymer. The latter proved to be an efficient stabilizer in the 45 wt.-% solids content, batch miniemulsion polymerizations of St and of mixtures of methyl methacrylate/n-butyl acrylate (35/65 w/w). With 2,2´-azobisisobutyronitrile as an oil-soluble initiator, polystyrene latexes with a very narrow particle distribution were obtained, whereas the water-soluble initiator, potassium persulfate, led to broad, multimodal particle size distributions. Such results were explained by the contribution of two nucleation mechanisms: droplet nucleation and homogeneous nucleation. In contrast, the poly(methyl methacrylate-co-n-butyl acrylate) latexes exhibited larger particle size and narrower particle size distributions with persulfate initiator, than the polystyrene latexes.

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20

de Macêdo Neto, José Costa, Bruno Mello de Freitas, Adalberto Gomes de Miranda, Reinaldo de Almeida Rodrigues, Gilberto Garcia Del Pino, Antônio Claudio Kieling, Marcos Dantas dos Santos, et al. "The Stability and Properties of Polystyrene/Kaolinite Nanocomposites during Synthesis via Emulsion Polymerization." Polymers 15, no. 9 (April 28, 2023): 2094. http://dx.doi.org/10.3390/polym15092094.

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The aim of this work was to study the stability and morphological properties of polystyrene latex containing kaolinite as a filler during the process of synthesis of nanocomposites viaemulsion polymerization. Nanocomposites with 1, 3, and 5 wt% of kaolinite were prepared. Latexes with 1 to 3 wt% of kaolinite were stable during the polymerization reaction. Hydrodynamic diameters of 93.68 and 82.11 nm were found for latexes with 1 and 3 wt% of kaolinite, respectively. The quantities of 1 to 3 wt% of kaolinite added during the reaction did not influence the reaction conversion curves or the number of particles. X-ray diffraction (XRD) and unconventional techniques of scanning electron microscopy (SEM) and high-resolution transmission electron microscopy (HRTEM) showed the presence of exfoliated and intercalated structures of the kaolinite.

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21

Valić, S., M. Topić, M. Andreis, F. Ranogajec, Z. Veksli, and V. Šincek-Pećanić. "Polystyrene-Natural-Rubber Mixtures: Preparation and Properties." Rubber Chemistry and Technology 66, no. 1 (March 1, 1993): 14–18. http://dx.doi.org/10.5254/1.3538294.

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Abstract Thermoplastic elastomers were prepared from mixtures of polystyrene and natural-rubber latexes. The mechanical measurements, thermally stimulated depolarization current measurements, and NMR spin-spin relaxation measurements have shown that the properties of prepared thermoplastic elastomers depend on the composition and the interface created by changing the size of the accessible polystyrene surface.

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22

Li, Hong Yu, and Tian Xiao. "Polythiophene-Coated Polystyrene Core-Shell Nanoparticles with a Rod-Shaped Polythiophene Shell." Advanced Materials Research 712-715 (June 2013): 169–74. http://dx.doi.org/10.4028/www.scientific.net/amr.712-715.169.

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A core-shell nanocomposite particle with polystyrene sphere core and polythiophene overlayer shell was synthesized through thiophene chemical oxidative polymerization using uniquely structured polystyrene latexes template. The morphology of polythiophene shell, which has nanorods shaped or featureless surface morphology, can be simply controlled through varying the dosage and feeding methods of oxidizers.

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23

Prescott, James H., Shaw Ji Shiau, and Robert L. Rowell. "Characterization of polystyrene latexes by hydrodynamic and electrophoretic fingerprinting." Langmuir 9, no. 8 (August 1993): 2071–76. http://dx.doi.org/10.1021/la00032a027.

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24

Basinska, Teresa, Stanislaw Slomkowski, and Michel Delamar. "Synthesis and Characterization of Polystyrene Core/Polyacrolein Shell Latexes." Journal of Bioactive and Compatible Polymers 8, no. 3 (July 1993): 205–19. http://dx.doi.org/10.1177/088391159300800301.

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25

Hone, John H. E., Andrew M. Howe, and Thomas H. Whitesides. "Rheology of polystyrene latexes with adsorbed and free gelatin." Colloids and Surfaces A: Physicochemical and Engineering Aspects 161, no. 2 (January 2000): 283–306. http://dx.doi.org/10.1016/s0927-7757(99)00377-5.

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26

Sherman, Robert L., and Warren T. Ford. "Small Core/Thick Shell Polystyrene/Poly(methyl methacrylate) Latexes." Industrial & Engineering Chemistry Research 44, no. 23 (November 2005): 8538–41. http://dx.doi.org/10.1021/ie048867j.

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27

Delair, T., V. Marguet, C. Pichot, and B. Mandrand. "Synthesis and characterization of cationic amino functionalized polystyrene latexes." Colloid & Polymer Science 272, no. 8 (August 1994): 962–70. http://dx.doi.org/10.1007/bf00658894.

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28

Lascelles, Stuart F., and Steven P. Armes. "Synthesis and characterization of micrometersized polypyrrole-coated polystyrene latexes." Advanced Materials 7, no. 10 (October 1995): 864–66. http://dx.doi.org/10.1002/adma.19950071011.

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29

Jacobs, Jaco, Nicholas Gathergood, Johan P. A. Heuts, and Andreas Heise. "Amphiphilic glycosylated block copolypeptides as macromolecular surfactants in the emulsion polymerization of styrene." Polymer Chemistry 6, no. 25 (2015): 4634–40. http://dx.doi.org/10.1039/c5py00548e.

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Bio-inspired amphiphilic block copolymer surfactants fully derived from amino acids and sugars are synthesised. The materials are successfully employed in the synthesis of polystyrene latexes by emulsion polymerization.

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30

Lauterbach, Felix, and Volker Abetz. "An eco-friendly pathway to thermosensitive micellar nanoobjects via photoRAFT PISA: the full guide to poly(N-acryloylpyrrolidin)-block-polystyrene diblock copolymers." Soft Matter 16, no. 9 (2020): 2321–31. http://dx.doi.org/10.1039/c9sm02483b.

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Spherical macromolecular assemblies, so-called latexes, consisting of polystyrene (PS) resemble a relevant class of synthetic polymers used for a plethora of applications ranging from coatings or lubricants to biomedical applications.

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31

Fadil, Yasemin, Florent Jasinski, Tien Wing Guok, Stuart C. Thickett, Hideto Minami, and Per B. Zetterlund. "Pickering miniemulsion polymerization using graphene oxide: effect of addition of a conventional surfactant." Polymer Chemistry 9, no. 24 (2018): 3368–78. http://dx.doi.org/10.1039/c8py00667a.

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Polystyrene/graphene oxide (PSt/GO) nanocomposite latexes have been prepared by Pickering miniemulsion polymerization in the presence of the conventional surfactant sodium dodecyl sulfate (SDS) in order to investigate its influence on the polymerization mechanism.

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32

Barthet, Christelle, Steven P. Armes, Stuart F. Lascelles, Shen Y. Luk, and Heather M. E. Stanley. "Synthesis and Characterization of Micrometer-Sized, Polyaniline-Coated Polystyrene Latexes." Langmuir 14, no. 8 (April 1998): 2032–41. http://dx.doi.org/10.1021/la971064z.

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33

ASADA, Keisuke, Junji KIDO, Noriyuki KURAMOTO, and Katsutoshi NAGAI. "Adsorption of Poly(N-alkylsubstituted acrylamide)s onto Polystyrene Latexes." KOBUNSHI RONBUNSHU 52, no. 8 (1995): 504–11. http://dx.doi.org/10.1295/koron.52.504.

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34

Voegtli, L. P., and C. F. Zukoski. "Adsorption of ionic species to the surface of polystyrene latexes." Journal of Colloid and Interface Science 141, no. 1 (January 1991): 92–108. http://dx.doi.org/10.1016/0021-9797(91)90305-r.

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35

Charreyre, M. T., P. Boullanger, Th Delair, B. Mandrand, and C. Pichot. "Preparation and characterization of polystyrene latexes bearing disaccharide surface groups." Colloid & Polymer Science 271, no. 7 (July 1993): 668–79. http://dx.doi.org/10.1007/bf00652829.

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36

Lascelles, Stuart F., and Steven P. Armes. "Synthesis and characterization of micrometre-sized, polypyrrole-coated polystyrene latexes." Journal of Materials Chemistry 7, no. 8 (1997): 1339–47. http://dx.doi.org/10.1039/a700237h.

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37

Henry, F., C. Pichot, A. Kamel, and M. S. El Aasser. "Dielectric properties of cleaned and monodisperse polystyrene latexes in microwaves." Colloid and Polymer Science 267, no. 1 (January 1989): 48–58. http://dx.doi.org/10.1007/bf01410148.

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38

Yang, Ya Jiang, and Jan B. F. N. Engberts. "Preparation and stability of polystyrene latexes using polysoaps as emulsifiers." European Polymer Journal 28, no. 8 (August 1992): 881–86. http://dx.doi.org/10.1016/0014-3057(92)90314-r.

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39

Silverstein, M. S., and M. Narkis. "Rubber-modified polystyrene from multistage latexes: Rheological and physical properties." Journal of Applied Polymer Science 40, no. 910 (November 5, 1990): 1583–99. http://dx.doi.org/10.1002/app.1990.070400915.

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40

Choubal, Milind, and Warren T. Ford. "Crosslinked polystyrene latexes prepared with 12-(o-styryloxy)dodecyltrimethylammonium bromide." Journal of Polymer Science Part A: Polymer Chemistry 27, no. 6 (May 1989): 1873–82. http://dx.doi.org/10.1002/pola.1989.080270608.

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41

García-Salinas, María José, and F. Javier de las Nieves. "The primary electroviscous effect in polystyrene latexes with variable charge." Macromolecular Symposia 151, no. 1 (February 2000): 435–41. http://dx.doi.org/10.1002/1521-3900(200002)151:1<435::aid-masy435>3.0.co;2-0.

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42

Li, Liang, Na Guo, Xiao Zhang, Wen Ou, Shengcai Yang, Xin Su, and Yujun Feng. "Reversible Stability of Emulsion and Polymer Latex Controlled by Oligochitosan and CO2." Polymers 10, no. 12 (December 6, 2018): 1352. http://dx.doi.org/10.3390/polym10121352.

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The addition of salt to a colloid solution ensures that emulsions can be easily separated into two phases and that polymer latexes can be coagulated. The switchable stability of emulsions and polymer latexes would improve the properties for their current applications. A switchable process of salt addition can be achieved using CO2 and switchable water, and it is a novel, benign approach to achieving a switchable ionic strength in an aqueous solution. However, the problem associated with switchable water is that its additives are all synthetic tertiary amines, most of which are harmful to human beings and the environment. Oligochitosan, as a natural product, can also be used as a switchable water additive. In this paper, a new switchable water system using oligochitosan to change the ionic strength was explored for use in several potential industrial applications. The conductivity of the aqueous solution of oligochitosan (0.2 wt.%) was switched from 0.2 to 331 μS/cm through the addition and removal of CO2. Oligochitosan and CO2 were successfully utilized to reversibly break a crude oil emulsion. Polystyrene (PS) latexes could also be reversibly destabilized; the zeta potential of the PS latex changed between −5.8 and −45.2 mV in the absence and presence of CO2 after oligochitosan was dissolved in the PS latex. The use of oligochitosan is a more environmentally friendly means for reversibly separating colloid solutions.

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43

Graillat, C., B. Dumont, P. Depraetere, V. Vintenon, and C. Pichot. "Stability behavior of polystyrene latexes covered with zwitterionic sulfobetaine-type emulsifiers." Langmuir 7, no. 5 (May 22, 1991): 872–77. http://dx.doi.org/10.1021/la00053a010.

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44

Ford, Warren T., Hui Yu, Jeng Jong Lee, and Hany El-Hamshary. "Synthesis of monodisperse crosslinked polystyrene latexes containing (vinylbenzyl)trimethylammonium chloride units." Langmuir 9, no. 7 (July 1993): 1698–703. http://dx.doi.org/10.1021/la00031a016.

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45

Xu, Xiao-Jun, Pei-Yong Chow, Chai-Hoon Quek, Huey-Hoon Hng, and Leong-Ming Gan. "Nanoparticles of Polystyrene Latexes by Semicontinuous Microemulsion Polymerization Using Mixed Surfactants." Journal of Nanoscience and Nanotechnology 3, no. 3 (June 1, 2003): 235–40. http://dx.doi.org/10.1166/jnn.2003.170.

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46

Weng, L. T., P. Bertrand, J. H. Stone-Masui, and W. E. E. Stone. "ToF SIMS study of the desorption of emulsifiers from polystyrene latexes." Surface and Interface Analysis 21, no. 6-7 (June 1994): 387–94. http://dx.doi.org/10.1002/sia.740210611.

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47

Keerthika, Nagarajan, Arumugam Jayalakshmi, and S. G. Ramkumar. "Anchored block‐copolymer surfactants for the synthesis of redispersible polystyrene latexes." Journal of Applied Polymer Science 137, no. 29 (December 24, 2019): 48875. http://dx.doi.org/10.1002/app.48875.

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48

Sun, Peiqin, Yao Li, Dazhuang Liu, Shaohui Sun, and Ke Zhao. "Effect of initiator on morphology in poly(vinyl acetate)/polystyrene and poly(butyl acrylate)/polystyrene composite latexes." Polymer Bulletin 55, no. 5 (September 23, 2005): 323–32. http://dx.doi.org/10.1007/s00289-005-0443-9.

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49

Geng, Xiang, Myra Xuemei Zhai, Tong Sun, and Greg Meyers. "Morphology Observation of Latex Particles with Scanning Transmission Electron Microscopy by a Hydroxyethyl Cellulose Embedding Combined with RuO4 Staining Method." Microscopy and Microanalysis 19, no. 2 (February 26, 2013): 319–26. http://dx.doi.org/10.1017/s1431927612014377.

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AbstractImaging of latex particles, especially those with low glass transition temperature (Tg) has been a challenging issue. Different sample preparation methods for characterization of the morphology of a poly(n-butyl acrylate)/polystyrene two-phase latex are discussed and compared in this study. A method via hydroxyethyl cellulose embedding combined with ruthenium tetraoxide (RuO4) staining for scanning transmission electron microscope (STEM) observation is developed. By using this method, the spherical shape of latex particles can be maintained without deformation. The degree of incorporation of RuO4 into latex particles and cellulose matrix is different, which makes latex particles readily identifiable from cellulose matrix under STEM. A series of latexes with different structures such as copolymer latex and organic-inorganic hybrid latex were also successfully investigated by this method. The results indicate this specimen preparation method can be applied to study the morphology of a wide range of latex systems.

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50

Poyarkova, T. N., S. V. Zhdanova, I. N. Pugacheva, and S. S. Nikulin. "Coagulating effect of alkali metal chlorides on polystyrene and butadiene-styrene latexes." Russian Journal of Applied Chemistry 85, no. 9 (September 2012): 1444–46. http://dx.doi.org/10.1134/s1070427212090236.

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