Toners and/or toner mixtures

Details Toners and/or toner mixtures Toners and/or toner mixtures

1999-12-16

2001-03-06

Goodrow, John (Department: 1753)

Radiation imagery chemistry: process, composition, or product th

Electric or magnetic imagery, e.g., xerography,...

Post imaging process, finishing, or perfecting composition...

C430S111400, C430S137170

Reexamination Certificate

active

06197469

ABSTRACT:

BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to toners and/or toner mixtures.
2. Discussion of the Background
U.S. Pat. No. 5,424,258 discloses powdered silicon-aluminum mixed oxides of amorphous structure, synthesized by flame hydrolysis. The oxide compositions contain 65 to 72.1 wt. % Al
2
O
3
and 27.9 to 35 wt. % SiO
2
and have a BET surface ranging from 20 to 200 m
2
/g.
SUMMARY OF THE INVENTION
One object of the present invention is to provide a toner and/or toner mixture which contains pyrogenically synthesized alumina-silica mixed oxide which improves the properties of the toner and/or toner mixture.
Briefly, this object and other objects of the present invention as hereinafter will become more readily apparent can be attained by a toner and/or toner mixture which contains a pyrogenically synthesized silica-alumina mixed oxide as a component in addition to other components which complete a toner formulation.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
The discovery of the present invention is that the presence of a pyrogenically synthesized silica-alumina mixed oxide as an additive to a toner imparts improved properties to the toner. The amount of the pyrogenically synthesized silica-alumina incorporated in the toner normally ranges from 0.1 to 5.0% by weight based on the weight of toner. Other toner components include a pigment such as Fe
2
O
3
, a binder such as polyester resin and a charge controlling agent in the amounts these ingredients are normally used to prepare a toner.
The pyrogenically synthesized alumina-silica mixed oxide of the invention is per se known and can be prepared as described in U.S. Pat. No. 5,424,258 which is hereby incorporated by reference into the application.
In an embodiment of the invention, the Al
2
O
3
/SiO
2
mixed oxide may have a ratio of Al
2
O
3
to SiO
2
comprising 65±5 wt. % Al
2
O
3
and 35±5 wt. % SiO
2
.
In another embodiment of the invention, the pyrogenically synthesized Al
2
O
3
/SiO
2
mixed oxide can be surface-modified. The surface modification of the mixed alumina-silica oxide material can be achieved by the technique described in European Patent EP 0 722 922, hereby incorporated by reference. Suitable surface treatment compounds include:
(a) Organosilanes of the type (RO)
3
Si(C
n
H
2n+1
)
R=alkyl, such as e.g., methyl-, ethyl-, n-propyl-, i-propyl-, butyl- ,
n=1-20
(b) Organosilanes of the type R′
x
(RO)
y
Si(C
n
H
2+1
)
R=alkyl, such as e.g. methyl-, ethyl-, n-propyl-, i-propyl-, butyl- ,
R′=alkyl such as e.g. methyl-, ethyl-, n-propyl-, i-propyl-, butyl- ,
n=1-20
x+=3
x=1,2
y=1,2
(c) Organosilanes of the type (RO)
3
Si(CH
2
)
m
—R′
R=alkyl, such as methyl-, ethyl-, propyl- ,
m=0, 1-20
R′=methyl-, aryl (e.g., —C
6
H
5
, substituted phenyl groups)
—C
4
F
9
, —OCF
2
—CHF—CF
3
, —C
6
F
13
, —O—CF
2
—CHF
2
—NH
2
, —N
3
, —SCN, —CH═CH
2
,
—OOC(CH
3
)C═CH
2
—OCH
2
—CH(O)CH
2
—S
x
—(CH
2
)
3
Si(OR)
3
(d) Organosilanes of the type (R″)
x
(RO
y
Si(CH
2
)
m
—R′
R″=alkyl x+y=2
x=1, 2
y=1,2
m=0,1 to 20
R′=methyl-, aryl (e.g. —C
6
H
5
, substituted phenyl groups)
—C
4
F
9
, —OCF
2
—CHF—CF
3
, —C
6
F
13
, —O—CF
2
—CHF
2
—NH
2
—N
3
, —SCN, —CH═CH
2
,
—OOC(CH
3
)C═CH
2
—OCH
2
—CH(O)CH
2
—NH—COO—CH
3
, —NH—COO—CH
2
—CH
3
, —NH—(CH
2
)
3
Si(OR)
3
—S
x
—(CH
2
)
3
Si(OR)
3
(e) Halogenorganosilanes of the type X
3
Si(C
n
H
2n+1
)
X=Cl,Br
n=1-20
(f) Halogenorganosilanes of the type X
2
(R′)Si(C
n
H
2n+1
)
X=Cl, Br
R′=alkyl, such as e.g. as e.g. methyl-, ethyl-, n-propyl-, i-propyl-, butyl- ,
n=1-20
(hh) Halogenorganosilanes of the type X
3
Si(CH
2
)
m
-R′
X=Cl,Br
m=0, 1-20
R′=methyl-, aryl (e.g. —C
6
H
5
, substituted phenyl groups)
—C
4
F
9
, —OCF
2
—CHF—CF
3
, —C
6
F
13
, —O—CF
2
—CHF
2
—NH
2
, —N
3
, —SCN, —CH═CH
2
,
—OOC(CH
3
)C═CH
2
—OCH
2
—CH(O)CH
2
—S
x
—(CH
2
)
3
Si(OR)
3
(i) Halogenorganosilanes of the type (R)X
2
Si(CH
2
)
m
—R′
X=Cl,Br
R=alkyl, such as methyl-, ethyl-, propyl- ,
m=0, 1-20
R′=methyl-, aryl (e.g. —C
6
H
5
, substituted phenyl groups)
—C
4
F
9
, —OCF
2
—CHF—CF
3
, —C
6
F
13
, —O—CF
2
—CHF
2
—NH
2
, —N
3
, —SCN, —CH═CH
2
,
—OOC(CH
3
)C═CH
2
—OCH
2
—CH(O)CH
2
in which R can be ═methyl-, ethyl-, propyl-, butyl
—S
x
—(CH
2
)
3
Si(OR)
3
in which R can be ═methyl-, ethyl-, propyl-, butyl- ,
(j) Halogenorganosilanes of the type (R)
2
X Si (CH
2
)
m
—R′
X=Cl, Br
R=alkyl
m=0, 1-20
R′=methyl-, aryl (e.g. —C
6
H
5
, substituted phenyl groups)
—C
4
F
9
, —OCF
2
—CHF—CF
3
, —C
6
F
13
, —O—CF
2
—CHF
2
—NH
2
, —N
3
, —SCN, —CH═CH
2
,
—OOC(CH
3
)C═CH
2
—OCH
2
—CH(O)CH
2
—S
x
—(CH
2
)
3
Si(OR)
3
R=alkyl
R′=alkyl, vinyl
(l) A preferred silazane in hexamethyldisilazane (HMDS). Cyclic polysiloxanes of the type D 3, D 4, D 5 in which D 3, D 4 and D 5 signify cyclic polysiloxanes with 3, 4 or 5 units of the type —O—Si(CH
3
)
2
—, e.g., octamethylcyclotetrasiloxane=D 4
(m) polysiloxanes or silicone oils of the type
m=0, 1, 2, 3 . . . ∞
n=0, 1, 2, 3 . . . ∞
u=0, 1, 2, 3 . . . ∞
Y=CH
3
, H, C
n
H
2n+1
n=1-20
Y=Si(CH
3
)
3
, Si(CH
3
)
2
H
Si(CH
3
)
2
OH, Si(CH
3
)
2
(OCH
3
)
Si(CH
3
)
2
(CnH
2n+1
) n=1-20
R=alkyl such as C
n
H
2n+1
in which n=1 to 20, aryl such as phenyl- and substituted phenyl groups (CH
2
)n—NH
2
, H
R′=alkyl such as C
n
H
2n+1
in which n=1 to 20, aryl such as phenyl- and substituted phenyl groups (CH
2
)n—NH
2
, H
R″=alkyl such as C
n
H
2n+1
in which n=1 to 20, aryl such as phenyl- and substituted phenyl groups (CH
2
)n—NH
2
, H
″′=alkyl such as C
n
H
2n+1
in which n=1 to 20, aryl such as phenyl- and substituted phenyl groups (CH
2
)n—NH
2
, H
The pyrogenically produced alumina-silica mixed oxide is placed in a suitable mixing container. The mixed oxides are sprayed under intensive mixing optionally with water at first and then with the surface-modifying reagent or a mixture of several surface-modifying reagents. The material is mixed again for 15 to 30 minutes and subsequently tempered at a temperature of 100 to 400° C. for a period of 1 to 6 hours.
The water used can be acidified with an acid, e.g., hydrochloric acid, having a pH of 7 to 1. The surface-modifying reagent used can be dissolved in a suitable solvent such as, e.g., ethanol. The mixing and/or tempering can be carried out in an atmosphere of a protective gas such as, for example, nitrogen.
As a result of the incorporation of the pyrogenically synthesized, mixed alumina-silica oxide material of the invention, or the oxide material which is surface modified as mentioned above, into a toner formulation and/or toner formulation mixtures, the toner product of the invention has the following advantages:
(i) Better flowability of the toner powder;
(ii) More stable charging behavior of the toner as characterized by faster chargeability, a higher charge capacity and permitting constant charging over time.
Having now generally described this invention, a further understanding can be obtained by reference to certain specific examples which are provided herein for purposes of illustration only and are not intended to be limiting unless otherwise specified.


REFERENCES:
patent: 5296324 (1994-03-01), Akagi et al.
patent: 5424258 (1995-06-01), Mangold et al.
patent: 37 07 226 (1988-09-01), None
patent: 42 02 694 (1993-07-01), None
patent: 0 722 922 (2000-03-01), None
patent: 2 296 915 (1996-07-01), None

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