Sizes based on ketene dimers

• US 4,614,546 A
• Filed: 05/29/1985
• Issued: 09/30/1986
• Est. Priority Date: 05/03/1982
• Status: Expired due to Fees

• Current Assignee: Bayer AG
• Original Assignee: Bayer AG
• Inventors: Beck, Ulrich, Schroer, Wolf-Dieter, Baumgen, Heinz, Mummenhoff, Peter
• Primary Examiner(s): Morris, Theodore
• Application Number:
  US06/738,640
• Time in Patent Office: 489 Days
• Field of Search: 162/164.6, 106/213, 106/210, 106/212, 524/102, 500/486, 500/466
• US Class Current: 106/209.1
• CPC Class Codes: D21H 17/17 Ketenes, e.g. ketene dimers

Abstract

New aqueous sizes, in particular paper sizes, are made available which contain

(a) ketene dimers of the formula ##STR1## in which R₁ and R₂ can be identical or different and represent hydrocarbon radicals having 6 to 30 carbon atoms,

(b) amine-modified starch,

(c) hydrophobic compound(s) which contain(s) one or more functional groups which are reactive towards OH groups within a pH range of 2 to 6, and

(d) if desired further auxiliaries.

Claims

1. Aqueous sizes based on ketene dimers, which contain

(a) ketene dimers of the formula ##STR3## in which R₁ and R₂ are identical or different and represent hydrocarbon radicals having 6 to 30 carbon atoms,

(b) amine-modified starch,

(c) hydrophobic compound (s) which contain (s) one or more functional groups which are reactive towards OH groups within a pH range of 2 to 6 in an amount of 0.2 to 0.7 mol of reactive functional group per 1000 parts by weight of ketene dimer said hydrophobic compound (s) being selected from the group consisting of acid halides which are derived from fatty acids having 12 to 30 carbon atoms or isocyanates, which contain hydrocarbon radicals having 14 to 36 carbon atoms.

2. Sizes according to claim 1, characterised in that 0.2 to 0.7 mol of reactive functional group is used per 1,000 parts by weight of ketene dimer of the formula (I).

3. Sizes according to claims 1 or 2, characterised in that the further auxiliaries are surface-active materials and/or solvents and/or thickeners and/or biocides and/or antifoams.

4. Sizes according to claims 1, 2, or 3, characterised in that the hydrophobic compound contains as the hydrophobic molecular part alkyl, alkenyl, cycloalkyl, aryl, aralkyl or alkylaryl groups and as reactive groups isocyanate groups.

5. Sizes according to claims 1, 2, 3 or 4, characterised in that the hydrophobic compound is colophony isocyanate, hexadecyl isocyanate, octadecyl isocyanate or a mixture thereof.

6. Sizes according to claims 1, 2, 3 or 4, characterised in that the hydrophobic compound is hexamethylene diisocyanate, toluylene-2,4-diisocyanate, toluylene-2,6-diisocyanate, bis-(4-isocyanatophenyl)-methane, 2,2-bis-(4-isocyanatophenyl)-propane or a mixture thereof.

7. Sizes according to claims 1, 2, 3, 4 or 5, characterised in that the hydrophobic compound is hexadecanoyl chloride, octadecanoyl chloride, oleoyl chloride, or a mixture thereof.

8. Process for preparing the sizes according to claim 1, characterised in that the hydrophobic compound is admixed to a melt of the ketene dimer of the formula (I), and the mixture, which can also contain further auxiliaries, is added to an aqueous solution of an amine-modified starch.