Alkyl ketene dimer

structure of the AKD derived from palmitic acid.

Alkyl ketene dimers (AKDs) are a family of organic compounds based on the 4-membered ring system of 2-oxetanone, which is also the central structural element of propiolactone and diketene. Attached to the oxetane ring of technically relevant alkyl ketene dimers there is a C12 – C16 alkyl group in the 3-position and a C13 – C17 in the 4-position.

The main application of alkylated ketene dimers is in the sizing of paper and cardboard, as well as in the hydrophobation of cellulose fibers. The products thus modified are distinguished by higher mechanical strengths and less penetration of water, inks or printing inks.[1]

AKD's feature hydrophobic alkyl groups extending from a propiolactone ring. A specific example is derived from the dimerization of the ketene of stearic acid. This ketene is generated by pyrolysis of stearoyl chloride.[2] AKD's react with the hydroxyl groups on the celluose via esterification reaction. The esterification is competitive with hydrolysis of the AKD. Prior to the development of AKD's, hydrophobicity was imparted by incorporating rosin into the paper.[3]

Related to AKDs, is alkenylsuccinic anhydride (ASA). As for AKDs, ASA reacts with hydroxy groups of the cellulose to form an ester, anchoring the hydrophobic group to the surface. ASA is prepared by the ene reaction of unsaturated hydrocarbons with maleic anhydride.[4]

History

As early as 1901, published the synthesis of alkyl ketene dimers by the reaction of carboxylic acid chlorides with tertiary amines,[5] the reaction products for polymers.[6]

Synthese von Alkylketendimeren (AKD)

The molecular weight determined by the early researchers did indicate a multiple of the group R1R2CH=C=O. Therefore, a so-called pyronone (a diketone structure with a cyclobutane ring) was proposed[7] as reaction product, e. g. from the reaction of isobutyryl chloride and triethylamine.[8][9]

Alternative Strukturen von Dimerisierungsprodukten

The primary reaction products of carboxylic acid chlorides with hydrogen atoms in α-position and tertiary amines were identified by Hermann Staudinger[10][11] and Norman Thomas Mortimer Wilsmore[12] as highly reactive ketenes (ethenones) which form 2-oxetanones with an alkylidene group when dimerizing in a [2 + 2] photocycloadditions. This gradually brought clarity about the constitution of alkylated ketene dimers.

The clarification of the constitution was complicated by different dimerization products of the ketenes. For example, the simple ketene (H2C=C=O) dimerizes to diketene (4-methylen 2-oxetanone), while substituted ketenes, such as dimethyl ketene (Me2C=C=O, formed from isobutyryl chloride with triethylamine) dimerize in a head-to-tail addition to 2,2,4,4-tetramethylcyclobutanedione.[7][13]

Dimerisierung von Dimethylketen zum Tetramethyl-1,3-cyclobutandion

The 2,2,4,4,4-tetramethylcyclobutanedione can easily be isomerized to dimethyl ketene dimer (4-isopropylidene-3,3-dimethyl-2-oxetanone).[14]

Isomerisierung von Tetramethyl-1,3-cyclobutandion zum Dimethylketendimer

The synthesis and characterization of hexadecyl ketene dimer, a key substance for alkylated ketene dimers used in the paper industry, was first described in a patent[15] in 1945 and in a publication[16] in 1947.

A quantum-chemical study rejected the formation of a cyclobutanedione during the dimerization of n-alkylketene R-CH=C=O in favour of the formation of the thermodynamically more stable 2-oxetanone structure.[17]

Preparation

The industrial synthesis of alkylated ketenedimers (at that time still called ketoethenones) was patented in 1945 from long-chain carboxylic acid chlorides in inert solvents (such as e. g. B. diethyl ether or benzene) with triethylamine as tertiary amine under anhydrous conditions. After filtration of the insoluble triethylamine hydrochloride and evaporation of the solvent, long-chain alkyl chain dimers are obtained in yields of more than 90%.[15]

Synthese von C18-AKD aus Stearoylchlorid

The use of other solvents, such as carboxylic acid esters or ketones for easier separation of trialkylamine hydrochlorides or other amines, such as N,N,N',N'-tetramethyl-1,6-hexane diamine[18] does not provide any significant advantages.

Also processes without the solvent use are described, in which the resulting amine hydrochloride is either filtered off or extracted with diluted aqueous acids.[19]

A continuous process in which long-chain carboxylic acid chloride and tertiary amine (e. g. dimethyl isopropylamine, dimethylcyclohexylamine or triethylamine) is supplied separately without solvents to a tube reactor, kneader or preferably a twin-screw extruder or planetary roller extruder and reacted at temperatures between 90 and 110 °C, delivers lactone contents of over 90% at short reaction times. Processing is carried out by phase separation or acidic extraction.[20]

Use

Alkylated ketene dimers as paper sizing agents

The problems with the acidic (aluminum sulfate-mediated) mass sizing of paper with alkaline-digested colophony resins introduced since the early 19th century led besides the use of alkaline flocculants (such as chalk or calcium carbonate as the so-called alkali reserve) to the search for alternative materials for sizing in a neutral or alkaline environment. In addition to the significantly more reactive alkenylsuccinic anhydrides (which do also hydrolyze rapidly in the presence of water) alkylated ketene dimers have begun to be preferred surface and mass sizes in the paper industry from the 1960s onwards, beginning in the 1950s.[21]

Strukturformel von C18-Alkenylbernsteinsäureanhydrid (ASA)

Industrially applied AKDs are derived from fatty acids with chain lengths between C14 (myristic acid) to C22 (behenic acid); palmityl (C16) diketene and stearyl (C18) ketene and mixtures thereof are preferably used, as well as fatty acid mixtures from the hydrolysis of animal and vegetable fats. Because of the chain length of the original fatty acids, AKD are waxy solids with melting points between 42 and about 70 °C. Mixtures of alkylated ketene dimers and water are dispersions at temperatures below 40 °C or emulsions at temperatures above 45 °C. Liquid AKD are not widely used, they are based on unsaturated fatty acids like oleic acid or branched fatty acids, like isostearic acid.

Aqueous alkyldiketene dispersions generally contain 10-20 wt% of AKD, as well as active protective colloids (particularly polycations such as cationic starch, copolymers of N-vinylpyrrolidone and quaternized N-vinylimidazole, acylated polyethyleneimines or cationic high molecular weight polyacrylamides with an average molar mass up to 7 million g/mol) and other stabilizers (usually anionic surfactants, for example ligninsulfonates or condensation products of naphthalenesulfonic acid sodium salt and formaldehyde).[22] Such stabilized AKD dispersions are active and stable at room temperature for up to three months and also tolerate the addition of different fillers for paper or cardboard (e.g. kaolin, chalk, talc, titanium dioxide, calcium sulfate, aluminum oxide, etc.) from 5 to 25%. The amounts of alkyl ketene dimers used for the sizing of paper and paper products are preferably in the range from 0.15 to 0.8 wt%, sometimes from 0.05 to 0.2 wt%,[20] based on the dry paper stock.

Paper sizing with alkylated ketene dimers

For paper sizing with AKD, a three-step process was proposed which, despite controversial discussions in the 1990s, seems to describe the processes that are taking place best and explains the results achieved.[23] Decisive criteria for the quality of the hydrophobing of papers are

  1. the retention of the AKD particles on the wet paper mass on the paper screen
  2. the spreading of the AKD particles on the surface and the penetration in the paper mass
  3. the chemical reaction of the hydroxyl groups of the cellulose (esterification) with the alkylated ketene dimers to form beta-ketocarboxylic esters.
Reaktion von Alkylketendimeren (AKD) mit Cellulose

The molecular structure (i.e. molar mass and cross-linking degree), the molar charge density of cationic groups, the exact dosage of the cationic polymer as a dispersion stabilizer and retention aid as well as keeping the other process parameters such as temperature, pH and residence times is crucial.

After removal of excess water - also to avoid hydrolysis of the AKD to the beta-keto acid and subsequent decarboxylation to the ketone -

Hydrolyse von Alkylketendimeren zu beta-Ketosäuren und Decarboxylierung zum Keton

follows the cracking of the stabilized AKD particles on the base paper mass, the melting of the solid AKD wax (at approx. 90 °C), the spreading of the liquid AKD wax by surface diffusion on the cellulose fibers and the formation of closed hydrophobic layers. The thickness of the hydrophobic layers depends on the AKD concentration in the dispersion.[24]

Ad 3. The hydrophobation of cellulose fibers with alkylated ketene dimers takes place most effectively in neutral or preferably weakly alkaline media (pH 7.5-9.0). The reaction temperature is generally 90-110 °C, with approximately 40% of the AKD used reacting with the cellulose.[23] After the reaction contact angles of >100° are measured, indicating the hydrophobic character of the AKD-modified model surfaces. The esterification of hydroxyl groups of cellulose fibers was also demonstrated by comparison reactions with 14C-labeled AKD.[23]

The sizing with AKD is suitable for the permanent hydrophobation of newspaper, printing and writing paper and cardboard used as a container for liquids (including foodstuffs such as milk), as well as for the improvement of shape stability and runnability.

Literature

  • Roberts, J.C. (1996), J.C. Roberts (ed.), Paper Chemistry, 2nd Edition, London: Chapman & Hall, ISBN 978-0-7514-0236-0
  • Johnson, D. (2009), I. Thorn, C.O. Au (ed.), Applications of Wet-End Paper Chemistry, 2nd Edition, Springer Netherlands, pp. 73–112, ISBN 978-1-4020-6037-3

References

  1. ^ http://www4.ncsu.edu/~hubbe/AKD.htm
  2. ^ Raimund Miller, Claudio Abaecherli, Adel Said, Barry Jackson "Ketenes" in Ullmann's Encyclopedia of Industrial Chemistry, 2001, Wiley-VCH, Weinheim. doi: 10.1002/14356007.a15_063
  3. ^ Werner J. Auhorn "Paper and Board, 3. Chemical Additives" in Ullmann's Encyclopedia of Industrial Chemistry Wiley-VCH, Weinheim. 2012. doi:10.1002/14356007.o18_o11
  4. ^ Gess, Jerome; Rend, Dominic (2005). "Alkenyl Succinic Anhydride (ASA)". Tappi Journal. 4: 25–30.
  5. ^ Wedekind, E. (1901), "Ueber die Gewinnung von Säurechloriden mit Hülfe von tertiären Aminen", Ber. Dtsch. Chem. Ges. (in German), 34 (2), pp. 2070–2077, doi:10.1002/cber.19013402122
  6. ^ Wedekind, E. (1902), "Ueber das Verhalten einiger Säurechloride bei der Chlorwasserstoffentziehung", Liebigs Ann. Chem. (in German), 323 (2), pp. 246–257, doi:10.1002/jlac.19023230206
  7. ^ a b Wedekind, E.; Weisswange, W. (1906), "Ueber die Synthese eines Diketons der Cyclobutanreihe", Ber. Dtsch. Chem. Ges. (in German), 39 (2), pp. 1631–1646, doi:10.1002/cber.19060390287
  8. ^ Wedekind, E.; Haeussermann, J. (1908), "Pyrononsynthesen mit Hilfe der Tertiärbasenreaktion I", Ber. Dtsch. Chem. Ges. (in German), 41 (2), pp. 2297–2302, doi:10.1002/cber.190804102135
  9. ^ Wedekind, E.; Häussermann, J.; Weisswange, W.; Müller, M. (1911), "Pyrononsynthesen mit Hilfe der Tertiärbasenreaktion II", Liebigs Ann. Chem. (in German), 378 (3), pp. 261–292, doi:10.1002/jlac.19113780302
  10. ^ Staudinger, H. (1905), "Ketene, eine neue Körperklasse", Ber. Dtsch. Chem. Ges. (in German), 38 (2), pp. 1735–1739, doi:10.1002/cber.19050380283
  11. ^ Staudinger, H.; Klever, H.W. (1907), "Über Ketene. 5. Mitteilung. Reaktionen des Dimethylketens", Ber. Dtsch. Chem. Ges. (in German), 40 (1), pp. 1149–1153, doi:10.1002/cber.190704001170
  12. ^ Wilsmore, N.T.M.; Stewart, A.W. (1908), "Keten. Bemerkungen zu der Abhandlung der HHrn. Staudinger und Klever", Ber. Dtsch. Chem. Ges. (in German), 41 (1), pp. 1025–1027, doi:10.1002/cber.190804101202
  13. ^ Huisgen, R.; Otto, P. (1968), "The mechanism of dimerization of dimethylketene", J. Am. Chem. Soc., 90 (19), pp. 5342–5343, doi:10.1021/ja.01021a090
  14. ^ "DIMETHYLKETENE β-LACTONE DIMER". Organic Syntheses. doi:10.15227/orgsyn.048.0072.
  15. ^ a b US 2369919, J.C. Sauer, "Ketoethenones and process therefor" 
  16. ^ Sauer, J.C. (1947), "Ketene dimers from acid chlorides", J. Am. Chem. Soc., 69 (10), pp. 2444–2448, doi:10.1021/ja.01202a058
  17. ^ Zhang, Z.; Li, G.; Hu, G.; Sun, Y. (2013), "Theoretical research on the mechanism of the dimerization reaction of alkyl ketenes", J. Chem., 2013, doi:10.1155/2013/481586
  18. ^ US 7960497, D.A. Gerstenhaber, "Preparation of alkyl ketene dimers" 
  19. ^ US 5344943, N. Brolund, "Long-chain ketene dimers" 
  20. ^ a b WO 03045936, R. Ettl, M. Winter, T. Freund, T. Kessler, G. Grimm, "Method for producing alkyl ketene dimers" 
  21. ^ US 2627477, W.F. Downey, "Higher alkyl ketene dimer emulsion" 
  22. ^ WO 2007141197, C. Hamers, A. Brockmeyer, M. Schmid, K. Lorenz, U. Riebeling, "Aqueous alkylketene dimer dispersions" 
  23. ^ a b c Lindström, T.; Larsson, T. (2005), STFI-Packfors (ed.), [Online A note on AKD-sizing: an investigation of real and apparent contradictions in literature regarding spreadin/diffusion of AKD on cellulose, Report no. 81] Check |url= value (help)
  24. ^ Lindfors, J.; Sahmi, J.; Laine, J.; Stenius, P. (2007), [PDF;938 KB "AKD and ASA model surfaces: preparation and characterization"] Check |url= value (help), BioResources, 2 (4), pp. 652–670