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Journal articles on the topic 'Degradation and stabilization of ruthenium'

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Published: 4 June 2021
Last updated: 8 February 2022

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1

Wilkie, Charles A. "Polymer Degradation and Stabilization." Polymer News 30, no. 4 (May 2005): 120–22. http://dx.doi.org/10.1080/00323910500458898.

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2

Billingham, N. C. "Polymer degradation and stabilization." Polymer 27, no. 9 (September 1986): 1478. http://dx.doi.org/10.1016/0032-3861(86)90057-1.

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3

Muheim, Andreas, Robert J. Todd, Danilo R. Casimiro, Harry B. Gray, and Frances H. Arnold. "Ruthenium-mediated protein cross-linking and stabilization." Journal of the American Chemical Society 115, no. 12 (June 1993): 5312–13. http://dx.doi.org/10.1021/ja00065a060.

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4

Giese, Ulrich, H. Hahn, and S. Thust. "Degradation and Stabilization of Elastomers." NIPPON GOMU KYOKAISHI 91, no. 7 (2018): 227–31. http://dx.doi.org/10.2324/gomu.91.227.

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5

Datta, R. N., N. M. Huntink, S. Datta, and A. G. Talma. "Rubber Vulcanizates Degradation and Stabilization." Rubber Chemistry and Technology 80, no. 3 (July 1, 2007): 436–80. http://dx.doi.org/10.5254/1.3548174.

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Abstract Degradation of rubber vulcanizates in the presence and absence of air as well as in presence of ozone is reviewed in this paper. The paper also outlines the means to overcome this undesirable phenomenon. Under anaerobic aging conditions, which is termed as reversion, the vulcanizates are exposed to elevated temperature in the absence of oxygen. The consequence of this process is reflected in a decline in physical properties and performance characteristics. These changes are directly related to modifications of the original crosslink structure. Decomposition reactions tend to predominate and thus leading to a reduction in crosslink density and physical properties as observed during extended cure or when using higher curing temperatures. The decrease in network density is common when vulcanizates are subject to an anaerobic aging process. However, in the presence of oxygen, the network density is increased with the main chain modifications playing a vital role. Over the years the rubber industry has developed several compounding approaches to address the changes in crosslink structure during thermal aging. This paper gives a review of these compounding approaches. As with many formulation changes in rubber compounding, there is a compromise that must be made when attempting to improve one performance characteristic. For example, improving the thermal stability of vulcanized natural rubber compounds by reducing the sulfur content of the crosslink through the use of the more efficient vulcanization systems will reduce dynamic performance properties such as fatigue resistance. The challenge is to define a way to improve thermal stability while maintaining dynamic performance characteristics. In the second part, the protection against aerobic ageing as well as in ozone environment is reviewed. The anti-degradant effects are summarized and means to counteract are outlined. The most commonly used antidegradants are N-isopropyl-N′-phenyl-p-phenylenediamine (IPPD) and N-(1,3-dimethylbutyl)-N′-phenyl-p-phenylenediamine (6PPD). Although conventional antidegradants such as IPPD and 6PPD are still the most widely used antidegradants in rubber, there is a trend and demand for longer-lasting and non-staining products. The relatively low molecular weight (MW) antioxidants have undergone an evolutionary change towards higher molecular weight products with the objective to achieve permanence in the rubber polymer, without loss of antioxidant activity. In the last two decades, several approaches have been evaluated in order to achieve this objective: attachment of hydrocarbon chains to conventional antioxidants in order to increase the MW and compatibility with the rubber matrix; oligomeric or polymeric antioxidants; and polymer bound or covulcanizable antioxidants. The disadvantage of polymer bound antioxidants was tackled by grafting antioxidants onto low MW polysiloxanes, which are compatible with many polymers. New developments on antiozonants have focused on non-staining and slow migrating products, which last longer in rubber compounds. Several new types of non-staining antiozonants have been developed, but none of them appeared to be as efficient as the chemically substituted p-phenylenediamines. The most prevalent approach to achieve non-staining ozone protection of rubber compounds is to use an inherently ozone-resistant, saturated backbone polymer in blends with a diene rubber. The disadvantage of this approach however, is the complicated mixing procedure needed to ensure that the required small polymer domain size is obtained
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6

Akers, Michael J. "Drug stabilization against oxidative degradation." Journal of Chemical Education 62, no. 4 (April 1985): 325. http://dx.doi.org/10.1021/ed062p325.

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7

Dimonie, M., A. Cornilescu, E. Nicolescu, S. Coca, M. Cuzmici, A. Ciupitoiu, F. Chiraleu, V. Drăgutan, S. Stoica, and M. Chipară. "Degradation and Stabilization of Polypentenamer." International Journal of Polymeric Materials 13, no. 1-4 (September 1990): 207–13. http://dx.doi.org/10.1080/00914039008039475.

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8

Golubeva, I. A., L. I. Tolstych, E. P. Gallyamova, and S. S. Zeldina. "Degradation and Stabilization of Polyacrylamide." International Journal of Polymeric Materials and Polymeric Biomaterials 16, no. 1-4 (February 1992): 131–37. http://dx.doi.org/10.1080/00914039208035415.

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9

Wilkie, Charles. "Column: Polymer Degradation and Stabilization." Polymer News 29, no. 3 (March 2004): 81–83. http://dx.doi.org/10.1080/00323910490980778.

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10

Robello, Douglas R., Teresa D. Eldridge, and Michael T. Swanson. "Degradation and stabilization of polycyanoacrylates." Journal of Polymer Science Part A: Polymer Chemistry 37, no. 24 (December 15, 1999): 4570–81. http://dx.doi.org/10.1002/(sici)1099-0518(19991215)37:24<4570::aid-pola14>3.0.co;2-#.

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11

Rivers, D. B., F. R. Frazer, D. W. Mason, and T. R. Tice. "Enzyme stabilization for pesticide degradation." Nuclear and Chemical Waste Management 8, no. 2 (January 1988): 157–63. http://dx.doi.org/10.1016/0191-815x(88)90074-5.

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12

TSUBOUCHI, Kenjiro. "Degradation and Stabilization of Polymer Coatings." Journal of the Japan Society of Colour Material 59, no. 5 (1986): 272–77. http://dx.doi.org/10.4011/shikizai1937.59.272.

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13

Xie, Fengwei, Tianlong Zhang, Peter Bryant, Valsala Kurusingal, John M. Colwell, and Bronwyn Laycock. "Degradation and stabilization of polyurethane elastomers." Progress in Polymer Science 90 (March 2019): 211–68. http://dx.doi.org/10.1016/j.progpolymsci.2018.12.003.

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14

Yang, Feng, Huilin Li, Liaoyuan Cai, Fan Lan, and Ming Xiang. "Degradation and Stabilization of Co-POM." Polymer-Plastics Technology and Engineering 48, no. 5 (May 6, 2009): 530–34. http://dx.doi.org/10.1080/03602550902824333.

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15

Waterman, Kenneth C., Roger C. Adami, Karen M. Alsante, Jinyang Hong, Margaret S. Landis, Franco Lombardo, and Christopher J. Roberts. "Stabilization of Pharmaceuticals to Oxidative Degradation." Pharmaceutical Development and Technology 7, no. 1 (January 2002): 1–32. http://dx.doi.org/10.1081/pdt-120002237.

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16

Corciovei, M., Floarea Taran, T. S[acaron]rbu, G. Ivan, Eva Dănilă, Maria Giurginca, and M. Chipară. "Degradation and Stabilization of Epichlorohydrin Elastomers." International Journal of Polymeric Materials 13, no. 1-4 (September 1990): 137–46. http://dx.doi.org/10.1080/00914039008039468.

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17

Glatzhofer, Daniel T., Yongwu Liang, Masood A. Khan, and Paul J. Fagan. "Stabilization of dibenzo-p-quinodimethane by (pentamethylcyclopentadienyl)ruthenium cation." Organometallics 10, no. 4 (April 1991): 833–34. http://dx.doi.org/10.1021/om00050a005.

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18

OHTANI, Hajime, and Shin TSUGE. "Degradation and Stabilization of Polymeric Materials. Thermal Degradation Behavior of Polymers." Kobunshi 46, no. 6 (1997): 394–97. http://dx.doi.org/10.1295/kobunshi.46.394.

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19

MORIGAKI, Masakazu. "Degradation and Stabilization of Color Photographic Dyes." Journal of the Japan Society of Colour Material 70, no. 12 (1997): 797–807. http://dx.doi.org/10.4011/shikizai1937.70.797.

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20

Yassin, Ahmady A., and Magdy W. Sabaa. "DEGRADATION AND STABILIZATION OF POLY(VINYL CHLORIDE)." Journal of Macromolecular Science, Part C 30, no. 3-4 (August 1990): 491–558. http://dx.doi.org/10.1080/07366579008050916.

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21

Liu, Baohua, Liban Chen, Min Zhang, and Aifang Yu. "Degradation and Stabilization of Poly(propylene carbonate)." Macromolecular Rapid Communications 23, no. 15 (October 1, 2002): 881–84. http://dx.doi.org/10.1002/1521-3927(20021001)23:15<881::aid-marc881>3.0.co;2-c.

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22

Billingham, N. C. "Degradation and stabilization of polymers: vol. 2." Polymer 31, no. 11 (November 1990): 2220. http://dx.doi.org/10.1016/0032-3861(90)90100-d.

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23

Grassie, Norman. "Degradation and stabilization of polymers. volume 2." Polymer Degradation and Stability 30, no. 3 (January 1990): 346–47. http://dx.doi.org/10.1016/0141-3910(90)90089-p.

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24

Potempa, Jan, Zofie Porwit-Bobr, and James Travis. "Stabilization vs. degradation of Staphylococcus aureus metalloproteinase." Biochimica et Biophysica Acta (BBA) - General Subjects 993, no. 2-3 (December 1989): 301–4. http://dx.doi.org/10.1016/0304-4165(89)90181-5.

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25

Pitt, Colin. "Chemical physics of polymer degradation and stabilization." Journal of Controlled Release 8, no. 3 (March 1989): 276. http://dx.doi.org/10.1016/0168-3659(89)90052-7.

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26

Rapp, Teresa L., Christopher B. Highley, Brian C. Manor, Jason A. Burdick, and Ivan J. Dmochowski. "Ruthenium-Crosslinked Hydrogels with Rapid, Visible-Light Degradation." Chemistry - A European Journal 24, no. 10 (January 10, 2018): 2328–33. http://dx.doi.org/10.1002/chem.201704580.

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27

He, Lei, Xiang Chen, Zhenyu Meng, Jintao Wang, Keyin Tian, Tianhu Li, and Fangwei Shao. "Octahedral ruthenium complexes selectively stabilize G-quadruplexes." Chemical Communications 52, no. 52 (2016): 8095–98. http://dx.doi.org/10.1039/c6cc03117j.

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Due to the unique three dimensional structures of Ru complexes, strong interactions such as H-bonds between the z-axial ligands and cation channels in G-quadruplexes enabled not only efficient stabilization of G-quadruplexes, but excellent binding resistance against duplex DNA.
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28

Bolton, Sarah L., Joseph E. Williams, and Michael B. Sponsler. "Stabilization of (Trialkylphosphine)ruthenium Alkylidene Metathesis Catalysts using Phosphine Exchange." Organometallics 26, no. 10 (May 2007): 2485–87. http://dx.doi.org/10.1021/om061098e.

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29

Esteruelas, Miguel A., Francisco J. Fernández-Alvarez, and Enrique Oñate. "Stabilization of NH Tautomers of Quinolines by Osmium and Ruthenium." Journal of the American Chemical Society 128, no. 40 (October 2006): 13044–45. http://dx.doi.org/10.1021/ja064979l.

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30

Yoshida, Jun, Kazunori Tateyama, Yasutoshi Kasahara, and Hidetaka Yuge. "Stabilization of oxidized ruthenium complexes by adsorption on clay minerals." Applied Clay Science 199 (December 2020): 105869. http://dx.doi.org/10.1016/j.clay.2020.105869.

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31

Liang, Z. X., T. S. Zhao, and J. B. Xu. "Stabilization of the platinum–ruthenium electrocatalyst against the dissolution of ruthenium with the incorporation of gold." Journal of Power Sources 185, no. 1 (October 2008): 166–70. http://dx.doi.org/10.1016/j.jpowsour.2008.06.009.

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32

Kohiyama, Mayumi F., and Sarita Lagalwar. "Stabilization and Degradation Mechanisms of Cytoplasmic Ataxin-1." Journal of Experimental Neuroscience 9s2 (January 2015): JEN.S25469. http://dx.doi.org/10.4137/jen.s25469.

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Aggregation-prone proteins in neurodegenerative disease disrupt cellular protein stabilization and degradation pathways. The neurodegenerative disease spinocerebellar ataxia type 1 (SCA1) is caused by a coding polyglutamine expansion in the Ataxin-1 gene ( ATXN1), which gives rise to the aggregation-prone mutant form of ATXN1 protein. Cerebellar Purkinje neurons, preferentially vulnerable in SCA1, produce ATXN1 protein in both cytoplasmic and nuclear compartments. Cytoplasmic stabilization of ATXN1 by phosphorylation and 14-3-3-mediated mechanisms ultimately drive translocation of the protein to the nucleus where aggregation may occur. However, experimental inhibition of phosphorylation and 14-3-3 binding results in rapid degradation of ATXN1, thus preventing nuclear translocation and cellular toxicity. The exact mechanism of cytoplasmic ATXN1 degradation is currently unknown; further investigation of degradation may provide future therapeutic targets. This review examines the present understanding of cytoplasmic ATXN1 stabilization and potential degradation mechanisms during normal and pathogenic states.
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33

Han, Seongok, Chongyoup Kim, and Dongsook Kwon. "Thermal/oxidative degradation and stabilization of polyethylene glycol." Polymer 38, no. 2 (January 1997): 317–23. http://dx.doi.org/10.1016/s0032-3861(97)88175-x.

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34

Vinhas, Glória M., Rosa M. Souto Maior, and Yêda M. B. de Almeida. "Radiolytic degradation and stabilization of poly(vinyl chloride)." Polymer Degradation and Stability 83, no. 3 (March 2004): 429–33. http://dx.doi.org/10.1016/j.polymdegradstab.2003.08.005.

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35

Pandit, Nivedita K., and Janet S. Hinderliter. "Degradation of Chlorthalidone in Methanol: Kinetics and Stabilization." Journal of Pharmaceutical Sciences 74, no. 8 (August 1985): 857–61. http://dx.doi.org/10.1002/jps.2600740811.

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36

Muller, P., R. Hrstka, D. Coomber, D. P. Lane, and B. Vojtesek. "Chaperone-dependent stabilization and degradation of p53 mutants." Oncogene 27, no. 24 (January 28, 2008): 3371–83. http://dx.doi.org/10.1038/sj.onc.1211010.

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37

Zaikov, G. Ye, and I. Ya Kalontarov. "Workshop on the degradation and stabilization of polymers." Polymer Science U.S.S.R. 27, no. 7 (January 1985): 1755–56. http://dx.doi.org/10.1016/0032-3950(85)90376-4.

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38

Allen, N. S. "Degradation and stabilization of vinyl chloride-based polymers." Polymer 30, no. 5 (May 1989): 956. http://dx.doi.org/10.1016/0032-3861(89)90201-2.

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39

Grassie, N. "Degradation and stabilization of vinyl chloride based polymers." Polymer Degradation and Stability 26, no. 2 (January 1989): 198–99. http://dx.doi.org/10.1016/0141-3910(89)90010-4.

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40

MIYAKE, Akira. "Degradation and Stabilization of Polymeric Materials. Chemical Recycling." Kobunshi 46, no. 6 (1997): 406–10. http://dx.doi.org/10.1295/kobunshi.46.406.

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41

Ouardad, Samira, and Frédéric Peruch. "Metathetic degradation of trans-1,4-polyisoprene with ruthenium catalysts." Polymer Degradation and Stability 99 (January 2014): 249–53. http://dx.doi.org/10.1016/j.polymdegradstab.2013.10.022.

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42

Brown, Douglas G., Phil A. Schauer, Javier Borau-Garcia, Brandon R. Fancy, and Curtis P. Berlinguette. "Stabilization of Ruthenium Sensitizers to TiO2 Surfaces through Cooperative Anchoring Groups." Journal of the American Chemical Society 135, no. 5 (January 23, 2013): 1692–95. http://dx.doi.org/10.1021/ja310965h.

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43

Abu Ahmad, Yamen, Avital Oknin-Vaisman, Eliya Bitman-Lotan, and Amir Orian. "From the Evasion of Degradation to Ubiquitin-Dependent Protein Stabilization." Cells 10, no. 9 (September 9, 2021): 2374. http://dx.doi.org/10.3390/cells10092374.

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A hallmark of cancer is dysregulated protein turnover (proteostasis), which involves pathologic ubiquitin-dependent degradation of tumor suppressor proteins, as well as increased oncoprotein stabilization. The latter is due, in part, to mutation within sequences, termed degrons, which are required for oncoprotein recognition by the substrate-recognition enzyme, E3 ubiquitin ligase. Stabilization may also result from the inactivation of the enzymatic machinery that mediates the degradation of oncoproteins. Importantly, inactivation in cancer of E3 enzymes that regulates the physiological degradation of oncoproteins, results in tumor cells that accumulate multiple active oncoproteins with prolonged half-lives, leading to the development of “degradation-resistant” cancer cells. In addition, specific sequences may enable ubiquitinated proteins to evade degradation at the 26S proteasome. While the ubiquitin-proteasome pathway was originally discovered as central for protein degradation, in cancer cells a ubiquitin-dependent protein stabilization pathway actively translates transient mitogenic signals into long-lasting protein stabilization and enhances the activity of key oncoproteins. A central enzyme in this pathway is the ubiquitin ligase RNF4. An intimate link connects protein stabilization with tumorigenesis in experimental models as well as in the clinic, suggesting that pharmacological inhibition of protein stabilization has potential for personalized medicine in cancer. In this review, we highlight old observations and recent advances in our knowledge regarding protein stabilization.
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44

Liu, Hailong, Xiang Luo, Xingyao Jiang, Chunyi Cui, and Zhen Huyan. "The Evaluation System of the Sustainable Development of Municipal Solid Waste Landfills and Its Application." Sustainability 13, no. 3 (January 22, 2021): 1150. http://dx.doi.org/10.3390/su13031150.

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Improving the understanding of the stabilization process is of great significance to guide the sustainable development of municipal solid waste (MSW) landfills. An evaluation system of the stabilization process of MSW landfills has been established. The indices of the evaluation system involve the degradation degree of MSW, the release of landfill gas production potential, and the settlement of landfills. Based on the biochemical-consolidation-solute migration coupled model, an evaluation method of the MSW landfill stabilization process is proposed by combining field tests with numerical simulation. The stabilization process of the Jiangcungou landfill in China is investigated by using the proposed method. The analyzed results show that the stabilization process of high kitchen waste content landfills can be divided into three stages, which is different from the stabilization process of landfills in developed countries. For the Jiangcungou landfill, the ratio of cellulose to lignin in MSW decreases rapidly during the fast degradation stage when obvious settlement occurs. During the slow degradation stage, the hydrolysis rate is slow and settlement develops slowly. When the landfill reaches the stabilization stage, the ratio of cellulose to lignin of MSW changes very slowly; most of the landfill gas potential has been released; the settlement stabilization is completed basically. The change processes of the three evaluation indices are different, of which the degradation stabilization index is the main one. According to the findings above, leachate recirculation is recommended to adjust the degradation environment in the landfill, which can be helpful to avoid acidification at the fast degradation stage. Temporary cover is suggested to improve landfill gas collection efficiency at the beginning of the stable methanogenic stage. The landfill site closure should be operated when the settlement rate is low.
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45

Lucarini, M. "Electron spin resonance imaging of polymer degradation and stabilization." Progress in Polymer Science 28, no. 2 (February 2003): 331–40. http://dx.doi.org/10.1016/s0079-6700(02)00031-x.

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46

Pfaendner, Rudolf. "(Photo)oxidative degradation and stabilization of flame retarded polymers." Polymer Degradation and Stability 98, no. 12 (December 2013): 2430–35. http://dx.doi.org/10.1016/j.polymdegradstab.2013.07.005.

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47

Georgousopoulou, Ioanna-Nektaria, Stamatina Vouyiouka, Patrice Dole, and Constantine D. Papaspyrides. "Thermo-mechanical degradation and stabilization of poly(butylene succinate)." Polymer Degradation and Stability 128 (June 2016): 182–92. http://dx.doi.org/10.1016/j.polymdegradstab.2016.03.012.

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48

Eusterhues, Karin, Cornelia Rumpel, and Ingrid Kögel-Knabner. "Stabilization of soil organic matter isolated via oxidative degradation." Organic Geochemistry 36, no. 11 (November 2005): 1567–75. http://dx.doi.org/10.1016/j.orggeochem.2005.06.010.

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49

Tolstikh, L. I., N. I. Akimov, I. A. Golubeva, and I. A. Shvetsov. "Degradation and Stabilization of Polyacrylamide in Polymer Flooding Conditions." International Journal of Polymeric Materials and Polymeric Biomaterials 17, no. 3-4 (August 1992): 177–93. http://dx.doi.org/10.1080/00914039208041113.

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50

Moroz, Ekaterina, Sean Carlin, Katerina Dyomina, Sean Burke, Howard T. Thaler, Ronald Blasberg, and Inna Serganova. "Real-Time Imaging of HIF-1α Stabilization and Degradation." PLoS ONE 4, no. 4 (April 4, 2009): e5077. http://dx.doi.org/10.1371/journal.pone.0005077.

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