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Journal articles on the topic 'Polyhydric'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Sarsenov, A., V. K. Bishimbaev, B. A. Kapsalamov, K. K. Lepesov, K. M. Gapparova, and P. Grzesiak. "Chemical modification of cellulose for boron sorption from water solutions." Polish Journal of Chemical Technology 20, no. 4 (2018): 123–28. http://dx.doi.org/10.2478/pjct-2018-0064.

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Abstract It is shown that natural cellulose obtained from the walnut shell (Juglans regia) can be used for chemical modification of the selective boron sorbent. The modification was carried out by the coupling technique of chlorine derivatives of the polyhydric alcohols or polyols (mannitol, xylitol, sorbitol or glycerol). In this case new hybrid substances (sorbents) were obtained and they are represented by the formula: R-O-(CHOH)n-CH3, where R is a residue of the cellulose backbone, n is the number of functional (OH) groups of the polyhydric alcohols. The pulp mercerization was carried out

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2

Huang, Yuan Bo, Yun Wu Zheng, Hao Feng, Zhi Feng Zheng, and Ying Zi Jiang. "Study on Liquefaction of Corncob in Polyhydric Alcohols." Advanced Materials Research 183-185 (January 2011): 1110–13. http://dx.doi.org/10.4028/www.scientific.net/amr.183-185.1110.

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The liquefaction of corncob in polyhydric alcohols was investigated by using sulfuric acid as a catalyst. Results showed that the best liquefaction could be obtained with residue percent of 4.5% under the conditions with the corncob/polyhydric alcohols mass ratio of 1/5, reaction temperature of 150°C, reaction time of 60 min, catalyst amount of 3% (based on the weight of corncob), PEG 400/glycerin mass ratio of 7/3 in the polyhydric alcohols, respectively. The liquefied liquid products had acid number of 18.9 mg KOH/g and hydroxyl number of 616.3mg KOH/g, respectively.

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3

Uraki, Yasumitsu, and Yoshihiro Sano. "Polyhydric Alcohol Pulping at Atmospheric Pressure: An Effective Method for Organosolv Pulping of Softwoods." Holzforschung 53, no. 4 (1999): 411–15. http://dx.doi.org/10.1515/hf.1999.068.

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Summary Polyhydric alcohol pulping was developed to separate components of low-quality softwoods that are produced by thinning and improvement cutting as well as to establish a self-supporting pulping system. Propylene glycol (PG) was superior to ethylene glycol (EG) as solvent for polyhydric alcohol pulping at atmospheric pressure. PG pulping of fir, larch and cedar, with sulfuric acid as a catalyst, gave satisfactory pulps with few rejects and a very low level of residual lignin as compared with EG pulping. The PG pulps were readily bleached to approximately Kappa number 1 and 80% brightness

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4

Duan, Zhiqiang, Mengyuan Yin, Chuanxian Zhang, et al. "Polyhydric polymer-loaded pyrene composites as powerful adsorbents and fluorescent probes: highly efficient adsorption and test strips-based fluorimetric analysis of curcumin in urine and plant extracts." Analyst 143, no. 2 (2018): 392–95. http://dx.doi.org/10.1039/c7an01403a.

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5

COMBES, D., M. GRABER, and W. N. YE. "Stabilizing Effect of Polyhydric Alcohols." Annals of the New York Academy of Sciences 613, no. 1 Enzyme Engine (1990): 559–63. http://dx.doi.org/10.1111/j.1749-6632.1990.tb18220.x.

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6

Huba, Zachary J., and Everett E. Carpenter. "A versatile synthetic approach for the synthesis of CoO, CoxC, and Co based nanocomposites: tuning kinetics and crystal phase with different polyhydric alcohols." CrystEngComm 16, no. 34 (2014): 8000–8007. http://dx.doi.org/10.1039/c4ce00931b.

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7

Zhang, Jin Ping, Meng Hao Du, and Li Song Hu. "Microwave Liquefaction for Bamboo Powder Polyhydric Alcohols and Preparation of Polyether Glycol." Advanced Materials Research 726-731 (August 2013): 151–55. http://dx.doi.org/10.4028/www.scientific.net/amr.726-731.151.

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The bamboo powder is liquefied by microwave heating with polyethylene glycol (400), glycerin and EC as liquefiers and sulfuric acid as a catalyst. The microwave liquefaction process for bamboo powder polyhydric alcohols is studied with the single factor experiment to determine the optimal liquefaction conditions, which is: mass ratio of polyethylene glycol (400) and glycerin is 80:20; the liquefaction rate is 99% in the liquid-solid mass fraction at 4:1, sulfuric acid mass fraction at 3%, and microwave power at 800W for 15 minute reaction. Hydroxyl value for liquefied product of bamboo powder

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8

Sheila, Srivastava, Singh Sarika, and Kumar Sharma Rajendra. "Kinetics and mechanism of the ruthenium(III) catalyzed oxidation of some polyhydric alcohols by acid bromate." Journal of Indian Chemical Society Vol. 84, Nov 2007 (2007): 1109–13. https://doi.org/10.5281/zenodo.5824548.

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Chemical Laboratories, Feroze Gandhi College, Rae Bareli-229 001, Uttar Pradesh, India <em>E-mail </em>: sheila72@yahoo.com <em>Manuscript received 4 April 2007, revised 28 August 2007, accepted 29 August 2007</em> Ruthenium(lll) catalyzed oxidation of some polyhydric alcohols <em>d</em>-sorbitol and d-mannitol by acidic solution of potassium bromate in the presence of mercuric acetate as a scavenger for Br<sup>- </sup>ion have been made in the temperature range 30-45 •c. The reactions exhibit zero-order rate dependence with respect to each polyhydric alcohol and first order at low concen

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9

Zhuravlev, V. I., T. M. Usacheva, N. V. Lifanova, and E. P. Vydrina. "Dielectric properties of polyhydric alcohols: Butanediols." Russian Journal of General Chemistry 78, no. 6 (2008): 1189–96. http://dx.doi.org/10.1134/s1070363208060157.

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10

Rotger, M. Carmen, Antoni Costa, and Jose M. Saa. "Lithiation of polyhydric compounds. Salicylic acids." Journal of Organic Chemistry 58, no. 15 (1993): 4083–87. http://dx.doi.org/10.1021/jo00067a048.

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11

Hwang, Lydia L. Y., Nicholas Ronca, Nathan A. Solomon, and Joseph Steigman. "Complexes of technetium with polyhydric ligands." International Journal of Applied Radiation and Isotopes 36, no. 6 (1985): 475–80. http://dx.doi.org/10.1016/0020-708x(85)90212-1.

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12

J., SUNITHA, and K. SAIPRAKASH P. "Kinetic Study of Hydrolysis of Sucrose catalysed by Invertase in Aquo-polyhydric Alcohols." Journal of Indian Chemical Society Vol. 73, Apr-May 1996 (1996): 199–202. https://doi.org/10.5281/zenodo.5892557.

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Department of Chemistry, Osmania University, Hyderabad-500 007 <em>Manuscript received 28 February 1994, revised 13 July 1994, accepted 22 July 1994</em> Kinetic Study of Hydrolysis of Sucrose catalysed by Invertase in Aquo-polyhydric Alcohols.

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13

AMALENDU, BANERJEE, MANDAL DINABANDHU, PUTATUNDA ANUVA, and CHANDRA BANERJEE GOPAL. "Determination of Glykitols and other Polyhydric Alcohols by Vanadium(v) in Perchloric Acid." Journal of Indian Chemical Society Vol. 74, Aug 1997 (1997): 667–69. https://doi.org/10.5281/zenodo.5895321.

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Department of Chemistry, Jadavpur University, Calcutta-700 032 <em>Manuscript received 18 January 1996, revised 15 July 1996, accepted 2 August 1996</em> Determination of Glykitols and other Polyhydric Alcohols by Vanadium(v) in Perchloric Acid.

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14

S., N. BANERJEE, and R. GUHA B. "Study of Corrosion Inhibition Property of Polyhydric Alcohols in Relation to their Adsorption Properties." Journal of Indian Chemical Society Vol. 64, Sep 1987 (1987): 525–29. https://doi.org/10.5281/zenodo.6219170.

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Chemistry Department, R. E. College, Durgapur-713 209 Central Mechanical Engineering Research Institute, Durgapur-713 209 <em>Manuscript received 8 May 1986, revised 3 June 1987, accepted 11 August 1987</em> Some polyhydric alcohols have been investigated as surface active and corrosion inhibitive species in mild steel —1 <em>N </em>sulphuric acid solution system at 25 ± 0.5°. The adsorption characteristics or these compounds have been determined by a capillary electrometer ; and dependence of the adsorption on structure and concentration of the adsorbate and on potential

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15

Bazunova, Marina V., Roman Yu Lazdin, Mariya R. Elinson, Lucia A. Sharafutdinova, Robert A. Mustakimov, and Elena I. Kulish. "On the possibility of obtaining the elastic and biocompatible film materials based on chitosan and N-succinyl chitosan." Chimica Techno Acta 9, no. 1 (2022): 20229108. http://dx.doi.org/10.15826/chimtech.2022.9.1.08.

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For the first time, the studies of polyhydric alcohols (glycerol, ethylene glycol and propylene glycol) impact on the structure, deformation–strength characteristics and hemocompatibility of the film materials based on chitosan and N-succinyl chitosan were carried out. It was shown that the introduction of polyhydric alcohols into molding solutions during the creation of the films based on chitosan and succinyl chitosan in the amount up to 0.05 mol/l is accompanied by the tensile elongation value increase by 2–2.5 times. The value of the breaking stress in this case decreases by 3–4 times. The

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16

Pavlik, Christopher, Amber Onorato, Steve Castro, Martha Morton, Mark Peczuh, and Michael B. Smith. "An Unexpectedly Facile Cyclization of Polyhydric Alcohols." Organic Letters 11, no. 16 (2009): 3722–25. http://dx.doi.org/10.1021/ol9013427.

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17

Kubo, Eiichiro, Ayumi Minoguchi, Hajime Sotokawa, and Ryusuke Nozaki. "Nearly constant dielectric loss of polyhydric alcohols." Journal of Non-Crystalline Solids 352, no. 42-49 (2006): 4724–28. http://dx.doi.org/10.1016/j.jnoncrysol.2006.01.107.

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18

Gurbanov, G. N., V. A. Kuli-zade, and M. A. Mamed’yarov. "Thermooxidative stability of cyclic polyhydric alcohol esters." Chemistry and Technology of Fuels and Oils 44, no. 1 (2008): 50–54. http://dx.doi.org/10.1007/s10553-008-0008-3.

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19

Bernier, Rene F., та Fred J. Stutzenberger. "Stabilization of β-glucosidase by polyhydric alcohols". Journal of Biotechnology 7, № 4 (1988): 293–98. http://dx.doi.org/10.1016/0168-1656(88)90041-7.

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20

Petrova, G. N., and O. N. Efimov. "Electrocatalytic reduction of polyhydric alcohols to hydrocarbons." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 40, no. 7 (1991): 1507–9. http://dx.doi.org/10.1007/bf00961270.

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21

Karatani, H. "An electrochemically triggered chemiluminescence from polyhydric alcohols." Journal of Photochemistry and Photobiology A: Chemistry 79, no. 1-2 (1994): 71–80. http://dx.doi.org/10.1016/1010-6030(93)03737-2.

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22

Makowska, Anna, Ewa Dyoniziak, Agnieszka Siporska, and Jerzy Szydłowski. "Miscibility of Ionic Liquids with Polyhydric Alcohols." Journal of Physical Chemistry B 114, no. 7 (2010): 2504–8. http://dx.doi.org/10.1021/jp911660a.

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23

Kojima, S., T. Koketsu, E. Takahashi, and M. Kanayasu. "Complex thermal effusivity of glassy polyhydric alcohols." Fluid Phase Equilibria 88 (August 1993): 209–18. http://dx.doi.org/10.1016/0378-3812(93)87112-e.

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24

Cai, Chiliu, Changhui Zhu, Haiyong Wang, et al. "Catalytic Hydrogenolysis of Biomass-derived Polyhydric Compounds to C2–C3 Small- Molecule Polyols: A Review." Current Organic Chemistry 23, no. 20 (2019): 2180–89. http://dx.doi.org/10.2174/1385272823666190913185618.

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Biomass energy has attracted much attention because of its clean and renewable characteristics. At present, C2–C3 polyols such as glycerol, 1,2-propanediol, and ethylene glycol, widely used as platforms for downstream chemicals or directly used as chemicals in diversified industries, mainly depend on the petrochemical industry. In terms of the feedstock for C2–C3 polyol production, the C3-derived glycerol is a side product during biodiesel synthesis, whereas the C5-derived xylitol and C6-derived sorbitol can be mainly obtained by hydrolysis–hydrogenation of hemicellulose and cellulose from lig

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25

Machneva, O. P., V. ,Ye Tsvetkov, and M. Yu Yekimova. "Polyhydric alcohols as modifiers of urea-formaldehyde resins." Adhesives. Sealants. Technologias, no. 12 (2018): 15–18. http://dx.doi.org/10.31044/1813-7008-2018-0-12-15-18.

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26

Jimoh, Simiat, Lawal Olajumoke, Ashorobi Adisa, et al. "Microbial Synthesis of Polyhydric Alcohol by Saccharomyces cerevisiae." Microbiology Research Journal International 23, no. 1 (2018): 1–6. http://dx.doi.org/10.9734/mrji/2018/34852.

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27

Uyama, Makoto, Makoto Harada, Takehiko Tsukahara, and Tetsuo Okada. "Behavior of Polyhydric Alcohols at Ice/Liquid Interface." Journal of Physical Chemistry C 117, no. 47 (2013): 24873–82. http://dx.doi.org/10.1021/jp408722x.

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28

Kireev, V. V., K. S. Khitrin, and A. A. Alalykin. "Oligomeric Phosphites Based on Polyhydric Phenols and Triarylphosphites." International Polymer Science and Technology 34, no. 10 (2007): 45–49. http://dx.doi.org/10.1177/0307174x0703401009.

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29

Grineva, O. V., V. I. Zhuravlev, and N. V. Lifanova. "Densities and Dielectric Permittivities of Four Polyhydric Alcohols." Journal of Chemical & Engineering Data 41, no. 2 (1996): 155–57. http://dx.doi.org/10.1021/je950076o.

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30

Kojima, Seiji. "Thermal and dielectric dispersions of supercooled polyhydric alcohols." Ferroelectrics 137, no. 1 (1992): 315–23. http://dx.doi.org/10.1080/00150199208015962.

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31

Kurimoto, Yasuji, Shuichi Doi, and Yasuo Tamura. "Species Effects on Wood-Liquefaction in Polyhydric Alcohols." Holzforschung 53, no. 6 (1999): 617–22. http://dx.doi.org/10.1515/hf.1999.102.

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Summary Four softwood and three hardwood species were liquefied using polyethylene glycol (PEG) or glycerol-containing PEG solvent systems as liquefaction reagents under defined reaction conditions: wood / liquefaction reagent / sulfuric acid = 3.00/9.00/0.27 gram, at 150 °C. The percentage residues and hydroxyl numbers were determined as an estimate of polyol value of the solution. The PEG system yielded 10–30% residual materials even under the best reaction conditions since low -OH group content resulted to re-condensation of liquefied wood (LW). The hydroxyl numbers linearly decreased from

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32

Cioci, Federico. "Thermostabilization of erythrocyte carbonic anhydrase by polyhydric additives." Enzyme and Microbial Technology 17, no. 7 (1995): 592–600. http://dx.doi.org/10.1016/0141-0229(94)00079-7.

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33

Hassan, El-barbary M., and Nadia Shukry. "Polyhydric alcohol liquefaction of some lignocellulosic agricultural residues." Industrial Crops and Products 27, no. 1 (2008): 33–38. http://dx.doi.org/10.1016/j.indcrop.2007.07.004.

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34

Slushkov, A. M., B. I. Petrov, and G. A. Domrachev. "Reactions of bisarene organochromium compounds with polyhydric alcohols." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 34, no. 6 (1985): 1295–97. http://dx.doi.org/10.1007/bf00956106.

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35

ROTGER, M. C., A. COSTA, and J. M. SAA. "ChemInform Abstract: Lithiation of Polyhydric Compounds. Salicylic Acids." ChemInform 24, no. 45 (2010): no. http://dx.doi.org/10.1002/chin.199345149.

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36

Zheng, Zhi Feng, Hui Pan, Yuan Bo Huang, and Y. Hse Chung. "Bio-Based Rigid Polyurethane Foam from Liquefied Products of Wood in the Presence of Polyhydric Alcohols." Advanced Materials Research 168-170 (December 2010): 1281–84. http://dx.doi.org/10.4028/www.scientific.net/amr.168-170.1281.

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Rigid polyurethane foams were prepared from the liquefied wood polyols, which was obtained by the liquefaction of southern pine wood in the presence of polyhydric alcohols with sulfuric acid catalyst by using microwave-assistant as an energy source. The properties of liquefied biomass-based polyols and the rigid polyurethane foams were investigated. The results indicated that the foams exhibited excellent mechanical properties.

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37

A., K. Nugmanov, and K. Dashdiyeva T. "INFLUENCE WETTABILITY OF THE SURFACTANTS ON THE EFFICIENCY OF "IKHLAS" NANODEMULSIFIERS FOR CLEANING OF PRODUCED WATERS FROM THE HYDROCARBONS IN THE CONDITIONS PRIMARY PREPARATION OF OIL." International Journal of Advanced Trends in Engineering and Technology 4, no. 1 (2019): 11–17. https://doi.org/10.5281/zenodo.2923865.

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The article discusses the features of the synergistic effect of the compositions of nanodemulsifiers in the purification of oil from water and water from oil. Synergy is caused by the composition of non-ionic surfactants of ethoxylated esters of n-aliphatic acids and the block of copolymers of oxyalkylene esters with polyhydric alcohols. Theoretical predictions for synergistic compositions were confirmed by laboratory results.

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38

Elbrus Mammadov, Sevinj Guliyeva, Elbrus Mammadov, Sevinj Guliyeva. "UNUSUAL TRANSFORMATIONS OF 2,3- AND 1,3- BUTHANEDIOL MONOPROPARGYL ETHERS." PAHTEI-Procedings of Azerbaijan High Technical Educational Institutions 46, no. 11 (2024): 94–102. https://doi.org/10.36962/pahtei46112024-11.

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Research in the field of chemistry of oxygen-containing derivatives of acetylene has acquired considerable interest. Of the simple ethers containing a triple carbon-carbon bond, ethynyl and propargyl ethers of monohydric alcohols and phenols, as well as alkyl and aryl ethers of acetylene glycols have been studied in most detail. Alkynyl, especially propargyl mono- and diesters of polyhydric alcohols have not been studied extensively. Due to the presence of highly reactive centers, ethers occupy a special place in the field of chemistry of oxygen-containing derivatives of acetylenes. Acetylene

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39

Glazunov, A. M., A. G. Mozyrev, S. P. Semuhin, and E. O. Zemlyanskiy. "Etheropoliamide depressor additives for oil fuel fractions." Oil and Gas Studies, no. 5 (November 17, 2019): 153–59. http://dx.doi.org/10.31660/0445-0108-2019-5-153-159.

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Improving the low-temperature properties of oil fractions, in particular diesel fuels using depressant additives, is one of the simplest and most effective methods. The synthesis of additives based on the use of domestic industrial raw materials. The article presents the data on the development of polyamide depressant additives; we used pyromellitic dianhydride (it is a product derived from polyhydric acid) as a base.

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40

Yang, Xin Hui, Yuan Bo Huang, Zhi Feng Zheng, and Ya Dong Zhang. "Liquefaction of Cornstalk in the Presence of Polyhydric Alcohols." Advanced Materials Research 236-238 (May 2011): 341–45. http://dx.doi.org/10.4028/www.scientific.net/amr.236-238.341.

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The liquefaction of cornstalk in the presence of polyhydric alcohols with sulfuric acid as catalyst was investigated. Effects of various liquefaction condition parameters on the liquefaction and its liquefied products were mainly investigated. Results showed that the liquefaction parameters had an obvious effect on the residue percent and the viscosity, acid and hydroxyl number of its liquefied products. The efficient liquefaction of cornstalk with low residue percent of 9.4% was obtained under the mild condition of a PEG #400/glycerin ratio of 7/3, a cornstalk/liquefaction reagent ratio of 1/

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41

Zhuravlev, V. I., and T. M. Usacheva. "Novel approach to relaxation data analysis in polyhydric alcohols." Moscow University Chemistry Bulletin 66, no. 6 (2011): 333–39. http://dx.doi.org/10.3103/s0027131411060113.

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42

Toniolo, C., G. M. Bonora, and A. Fontana. "POLYHYDRIC ALCOHOLS: STUCTURE-SUPPORTING SOLVENTS FOR POLYPEPTIDES AND PROTEINS." International Journal of Peptide and Protein Research 6, no. 5 (2009): 283–85. http://dx.doi.org/10.1111/j.1399-3011.1974.tb02386.x.

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43

Lee, Choon Guen, Jisun Lee, Da Gyung Lee, et al. "Immunostimulating activity of polyhydric alcohol isolated from Taxus cuspidata." International Journal of Biological Macromolecules 85 (April 2016): 505–13. http://dx.doi.org/10.1016/j.ijbiomac.2016.01.027.

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44

Li, Xiao Xing, Jie Chen, and Ji Zhang Jia. "Synthesis of Hyperbranched Polymeric Bactericides." Applied Mechanics and Materials 273 (January 2013): 488–91. http://dx.doi.org/10.4028/www.scientific.net/amm.273.488.

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This paper studied a kind of new bactericides material. We synthesized a kind of hyperbranched polymer. It had bactericidal performance. Cyanuric chloride reacted with 1,3,5-trihydroxybenzene. Then got a kind of polyhydric of hyperbranched polymer. This hyperbranched polymer reacted with hydrobromic acid, diethylenetriamine, chloroacetic acid in deferent steps. And finally we got a new kind of hyperbranched polymer bactericides.The relevant key factors to influence those reaction was studied. This paper created a new direction of bactericides material development.

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45

Manaenkov, Oleg, and Olga Kislitsa. "Synthesis of Polymeric Sorbents with Magnetic Properties." International Journal of Chemical Engineering and Materials 1 (December 31, 2022): 25–29. http://dx.doi.org/10.37394/232031.2022.1.5.

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In this work, a procedure for the synthesis of polymeric sorbents based on hypercrosslinked polystyrene (HPS) with magnetic properties was developed. The technique is based on the reduction of iron salts with polyhydric alcohols at high temperature in an inert atmosphere. The resulting sorbents retain their original characteristics: an extended specific surface area, micro-mesoporous structure, acquiring magnetic properties, which makes it possible to use them as magnetically separable sorbents, supports for the active phase of heterogeneous catalytic systems etc.

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46

Niu, Min, Guang-jie Zhao, and Mehmet Hakki Alma. "Thermogravimetric studies on condensed wood residues in polyhydric alcohols liquefaction." BioResources 6, no. 1 (2011): 615–30. http://dx.doi.org/10.15376/biores.6.1.615-630.

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To further clarify reasons for formation of condensed residues during the last stage of wood liquefaction in the medium of polyhydric alcohols and sulfuric acid catalyst, the weight loss behaviors and thermal reaction kinetics of condensed residues were studied by thermogravimetric analysis (TGA). Simultaneously, chemical methods were used to analyze the contents of lignin, cellulose, and holocellulose in the condensed residues. For all the unliquefied wood residues, the contents of cellulose decreased, and the residual ratios after TGA pyrolysis and the contents of lignin increased as a funct

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47

Chen, Qiu Ling, Ke Wei Sun, and Chun Hong Zhang. "The Liquefaction Mechanism Research of Straw Fiber in Polyhydric Alcohol." Advanced Materials Research 518-523 (May 2012): 3546–51. http://dx.doi.org/10.4028/www.scientific.net/amr.518-523.3546.

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Two key products were isolated and purified from liquid mixture composition of wheat straw, by means of a combination of organic solvent extraction and column chromatography. Their structures were identified on basis of nuclear magnetic resonance (1H-NMR, 13C-NMR, DEPT), mass spectrometry (MS), and infrared (IR). The mechanism of liquefaction of straw was inferred from the structures of products and changes of hydroxyl value and liquefaction residue, which make up the lack of mechanistic studies of overall utilization of plant fibers.

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48

Xiyuan, Hua, Song Hongyan, and Hu Guanjian. "THE EFFECT OF POLYHYDRIC ALCOHOLS ON O/W TYPE MICROEMULSION." Acta Physico-Chimica Sinica 1, no. 05 (1985): 482–86. http://dx.doi.org/10.3866/pku.whxb19850514.

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49

Isaeva, E. I., S. N. Kiryukhina, and V. V. Gorbunova. "Photochemical synthesis of silver and gold nanoparticles in polyhydric alcohols." Russian Journal of General Chemistry 83, no. 4 (2013): 619–23. http://dx.doi.org/10.1134/s1070363213040014.

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50

Minoguchi, Ayumi, Toshiya Kaneko, Hajime Sotokawa, and Ryusuke Nozaki. "Dielectric relaxation processes in supercooled polyhydric alcohols and their mixtures." Journal of Non-Crystalline Solids 352, no. 42-49 (2006): 4742–45. http://dx.doi.org/10.1016/j.jnoncrysol.2006.04.026.

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