Claims
- 1. An electrophotographic dry toner comprising toner particles having externally added fine particles of an inorganic compound adhered to a surface of the toner particles, the externally added fine particles having an average primary particle diameter of from 1 to 40 nm and having been surface treated with at least an amphoteric surface active agent selected from the group consisting of .alpha.-trimethylamino fatty acid, N-alkyl-.beta.-iminopropionic acid salt, N-alkyloxymethyl-N,N-diethylbetaine, N-alkyl-N,N-diamino ethylglycine hydrochloride, 2-alkylimidazoline, aminoethylimidazoline organic acid salt, N-alkylsulfobetaine, N-alkyltaurine salt, ##STR3## wherein R is an alkyl group having 8 to 18 carbon atoms; R.sup.1 is an alkyl group having 7 to 17 carbon atoms;
- R.sup.2 is an alkyl group having 12 to 18 carbon atoms;
- R.sup.3 is an alkyl group having 9 to 17 carbon atoms;
- R.sup.4 is an alkyl group having 1 to 2 carbon atoms;
- R.sup.5 is an alkyl group having 9 to 17 carbon atoms; and n is a positive integer.
- 2. An electrophotographic dry toner as claimed in claim 1, wherein said fine particles of an inoraganic compound are particles having been previously rendered hydrophobic.
- 3. An electrophotographic dry toner as claimed in claim 1, wherein said fine particles of an inoraganic compound are silica fine particles.
- 4. An electrophotographic dry toner as claimed in claim 1, wherein said amphoteric surface active agent is present in an amount of from 0.01 to 100 parts by weight per 100 parts by weight of the fine particles of an inorganic compound.
- 5. An electrophotographic dry toner as claimed in claim 1, wherein said fine particles of an inoraganic compound have been rendered hydrophobic by treating with an agent selected from the group consisting of alkylchlorosilanes, alkylalkoxysilanes, hexamethyldisilane and silicone oil.
- 6. An electrophotographic dry toner as claimed in claim 5, wherein said hydrophpbic agent is selected from the group consisting of methyltrichlorosilane, octyltrichlorosilane, dimethyl dichlorosilane, dimethyldidethoxysilane and octyltrimethoxy-silane.
- 7. An electrophotographic dry toner as claimed in claim 1, wherein said amphoteric surface active agent is selected from the group consisting of N-alkylnitrilotriacetic acid, N-alkyldimethylbetaine, .alpha.-trimethylamino fatty acid, N-alkyl-.beta.-aminopropionic acid salt, N-alkyl-.beta.-iminopropionic acid salt, N-alkyloxymethyl-N,N-diethylbetaine, N-alkyl-N,N-diamino ethylglycine hydrochloride, 2-alkylimidazoline, aminoethylimidazoline organic acid salt, N-alkylsulfobetaine and N-alkyltaurine salt.
- 8. An electrophotographic dry toner as claimed in claim 1, wherein said amphoteric surface active agent is selected from the group consisting of: ##STR4## wherein R is an alkyl group having 8 to 18 carbon atoms; R.sup.1 is an alkyl group having 7 to 17 carbon atoms;
- R.sup.2 is an alkyl group having 12 to 18 carbon atoms;
- R.sup.3 is an alkyl group having 9 to 17 carbon atoms;
- R.sup.4 is an alkyl group having 1 to 2 carbon atoms;
- R.sup.5 is an alkyl group having 9 to 17 carbon atoms;
- and n is a positive integer.
- 9. An clectrophotographic dry toner as claimed in claim 1, wherein said amphoteric surface active agent is ##STR5##
- 10. An electrophotographic dry toner as claimed in claim 1, wherein said amphoteric surface active agent is
- (4)-1
- C.sub.8 H.sub.17 NHCH.sub.2 CH.sub.2 COONa,
- (4)-2
- C.sub.14 H.sub.29 NHCH.sub.2 CH.sub.2 COONa, or
- (4)-3
- C.sub.18 H.sub.37 NHCH.sub.2 CH.sub.2 COONa.
- 11. An electrophotographic dry toner as claimed in claim 1, wherein said amphoteric surface active agent is
- (5)-1
- C.sub.10 H.sub.21 N(CH.sub.2 CH.sub.2 COONa).sub.2,
- (5)-2
- C.sub.13 H.sub.27 N(CH.sub.2 CH.sub.2 COONa).sub.2, or
- (5)-3
- C.sub.15 H.sub.31 N(CH.sub.2 CH.sub.2 COONa).sub.2.
- 12. An electrophotographic dry toner as claimed in claim 1, wherein said amphoteric surface active agent is
- (6)-1
- C.sub.12 H.sub.25 OCH.sub.2 N.sup.+ (C.sub.2 H.sub.5).sub.2 CH.sub.2 COO.sup.-,
- (6)-2
- C.sub.15 H.sub.31 OCH.sub.2 N.sup.+ (C.sub.2 H.sub.5).sub.2 CH.sub.2 COO.sup.-, or
- (6)-3
- C.sub.18 H.sub.37 OCH.sub.2 N.sup.+ (C.sub.2 H.sub.5).sub.2 CH.sub.2 COO.sup.-.
- 13. An electrophotographic dry toner as claimed in claim 1, wherein said amphoteric surface active agent is
- (7)-1
- C.sub.12 H.sub.25 NH(C.sub.2 H.sub.4 NH).sub.2 CH.sub.2 COOH.HC1, or
- (7)-2
- C.sub.16 H.sub.33 NH(C.sub.2 H.sub.4 NH).sub.2 CH.sub.2 CCOOH.HC1.
- 14. An electrophotographic dry toner as claimed in claim 1, wherein said amphoteric surface active agent is ##STR6##
- 15. An electrophotographic dry toner as claimed in claim 1, wherein said amphoteric surface active agent is
- (13)-1
- C.sub.12 H.sub.25 NHC.sub.2 H.sub.4 SO.sub.3 Na , or (13)-2
- C.sub.16 H.sub.33 NHC.sub.2 H.sub.4 SO.sub.3 Na.
- 16. An electrophotographic dry toner as claimed in claim 1, additionally comprising a carrier.
- 17. An electrophotographic dry toner as claimed in claim 1, wherein the inorganic compound of the externally added fine particles is selected from the group consisting of silica, alumina and titania.
- 18. An electrophotographic dry toner comprising toner particles having externally added fine particles of an inorganic compound having been surface treated with at least an amphoteric surface active agent, wherein said amphoteric surface active agent is ##STR7##
- 19. An electrophotographic dry toner comprising dry toner particles having externally added fine particles of an inorganic compound having been surface treated with at least one amphoteric surface active agent selected from the group consisting of ##STR8##
- 20. A process for preparing an electrophotographic dry toner comprising treating fine particles of an inorganic compound with an amphoteric surface active agent selected from the group consisting of ##STR9## and adding the fine particles to toner particles.
- 21. A process as claimed in claim 20, comprising dissolving or dispersing the amphoteric surface active agent in a solvent, adding the solution or dispersion to the fine particles of an inoraganic compound to coat the surface thereof and drying the particles to remove the solvent.
- 22. A process as claimed in claim 20, wherein said treating step is effected by use of a kneader coater, a spray dryer, a thermo processor or a fluidized bed apparatus.
- 23. A process according to claim 20, wherein the amount of amphoteric surface active agent is from 0.01 to 100% by weight based on the weight of the fine particles of an inoraganic compound.
Priority Claims (1)
Number |
Date |
Country |
Kind |
4-270732 |
Sep 1992 |
JPX |
|
Parent Case Info
This is a Continuation of application Ser. No. 08/498,498 filed Jul. 5, 1995, now abandoned, which in turn is a continuation of application Ser. No. 08/119,591 filed Sep. 13, 1993, now abandoned.
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Continuations (2)
|
Number |
Date |
Country |
Parent |
498498 |
Jul 1995 |
|
Parent |
119591 |
Sep 1993 |
|