WO1993010485A1 - Procede et solvants pour le fixage d'un toner a base de polystyrene sur un support de reproduction d'un appareil d'impression ou de copie - Google Patents
Procede et solvants pour le fixage d'un toner a base de polystyrene sur un support de reproduction d'un appareil d'impression ou de copie Download PDFInfo
- Publication number
- WO1993010485A1 WO1993010485A1 PCT/EP1992/002267 EP9202267W WO9310485A1 WO 1993010485 A1 WO1993010485 A1 WO 1993010485A1 EP 9202267 W EP9202267 W EP 9202267W WO 9310485 A1 WO9310485 A1 WO 9310485A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- solvent
- fixing
- toner
- polystyrene
- printing
- Prior art date
Links
- 239000002904 solvent Substances 0.000 title claims abstract description 29
- 238000000034 method Methods 0.000 title claims abstract description 14
- 238000007639 printing Methods 0.000 title claims abstract description 14
- 239000004793 Polystyrene Substances 0.000 title claims abstract description 13
- 229920002223 polystyrene Polymers 0.000 title claims abstract description 13
- 239000011159 matrix material Substances 0.000 claims abstract description 10
- 229920006037 cross link polymer Polymers 0.000 claims abstract description 5
- 239000000126 substance Substances 0.000 claims description 5
- 238000009835 boiling Methods 0.000 claims description 4
- 229920000642 polymer Polymers 0.000 claims description 4
- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical class F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 claims 2
- 239000003795 chemical substances by application Substances 0.000 description 12
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- 239000000203 mixture Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical class FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 4
- BOSAWIQFTJIYIS-UHFFFAOYSA-N 1,1,1-trichloro-2,2,2-trifluoroethane Chemical compound FC(F)(F)C(Cl)(Cl)Cl BOSAWIQFTJIYIS-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 230000002349 favourable effect Effects 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 2
- 238000003912 environmental pollution Methods 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000000834 fixative Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000004904 shortening Methods 0.000 description 2
- FRCHKSNAZZFGCA-UHFFFAOYSA-N 1,1-dichloro-1-fluoroethane Chemical compound CC(F)(Cl)Cl FRCHKSNAZZFGCA-UHFFFAOYSA-N 0.000 description 1
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 238000011982 device technology Methods 0.000 description 1
- 230000005686 electrostatic field Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000005294 ferromagnetic effect Effects 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 238000003384 imaging method Methods 0.000 description 1
- 230000005291 magnetic effect Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000010023 transfer printing Methods 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G11/00—Selection of substances for use as fixing agents
Definitions
- the invention relates to a method and a solvent for fixing a polystyrene-based toner on a recording medium of a printing or copying machine, the solvent being evaporated in a fixing device and acting on the toner in this state.
- the toner is dissolved in the vapor of a suitable solvent and intimate contact is achieved between the toner and the recording medium.
- An azeotropic mixture of trichlorotrifluoroethane (C 2 C1, F,) and acetone (C, HgO) is used as the solvent.
- the primary solvent here is acetone, while trichlorotrifluoroethane serves as a flame retardant.
- Trichlorotrifluoroethane (CFC R133) has a high ozone potential of 80% and a high greenhouse effect of 135%, which leads to environmental pollution if released.
- the object of the invention is therefore to provide a method for fixing a polystyrene-based toner to a recording medium of a printing or copying machine, which causes minimal environmental pollution with regard to ozone depletion potential and greenhouse effect and, on the other hand, also a constant, constant fixing quality differently constructed recording media guaranteed.
- Substances with the empirical formula C 2 HF. j Cl 2 are referred to as partially halogenated chlorofluorocarbons or hydrofluoroalkals. They are particularly environmentally friendly. From these compounds of the partially halogenated chlorofluorocarbons, the use of partially chlorinated fluorocarbons R123 and R141b has proven to be particularly favorable. Compared to toners with a non-crosslinked polymer matrix, the polymer matrix of which consists of polystyrene and metaacrylates, the partially chlorinated fluorocarbon HFCKW R123 has such a high dissolving effect that the R123 can be used as the sole fixing agent (without the addition of acetone).
- R123 as a fixing agent has the advantage, in addition to the low environmental impact, that it can be used in its pure form, so that a proportion of the mixture, like the known fixing agents, cannot become leaner during pressing. Since the fixing agent according to the invention consists of pure R123, underfixing can no longer occur. For this reason, different types of paper can be used as recording media. Furthermore, the fixative has a low dependence on air humidity In contrast to acetone, which is readily water-soluble, which is why regulation of the air humidity in the fixing device can be dispensed with, or the air moisture absorbed by the recording medium in the most varied amounts does not have a negative effect on the fixing process.
- the use of the fixing agent according to the invention enables a larger fixing window with regard to under- and over-fixing, ie a constant, constant fixing quality in the most varied of operating conditions without additional high control effort.
- FIG. 1 shows a basic illustration of an electrophotographic printing device.
- the heart of this device is a FT photoconductor drum.
- a photoelectric layer is arranged on the surface of this photoconductor drum FT. This is initially evenly charged with the help of a corotron KO.
- the surface of the drum is partially illuminated. This can be done with the aid of a character generator, which can consist of a laser LA, a deflection cell AB and a polygon mirror PO.
- a character generator which has an arrangement of light-emitting diodes as the character-generating elements.
- the light emanating from the laser LA is split into partial beams in the deflection cell AB, for example an acousto-optical deflection cell, according to the characters to be printed, which are directed by the polygon mirror PO onto the surface of the photoconductor drum FT.
- the surface of the drum is partially discharged in accordance with the partial beams directed onto the photoconductor drum. If the electrophotographic printing device shown is used as a copying device, the image to be copied is imaged in a known manner on the photoconductor drum FT via appropriate optics.
- the charge images generated by the character generator or the imaging optics for a copy on the surface of the photoconductor drum FT are developed in a developer station ES, i.e. they are colored with a developer mixture.
- the developer station ES is constructed in a known manner, it can e.g. Magnetic brushes included.
- the charge images which have developed toner images on the photoconductor drum FT then reach a transfer printing station US.
- a corotron KOI is in turn arranged there. Due to the existing in the transfer station US electrostatic field, the toner images on a recording medium AT z. B. a paper web or single sheets pulled over. The toner images stick to the surface of the AT recording medium.
- the record carrier AT can be removed from a stack ST1 and fed to the transfer station US via feed beads VR.
- a roller RL is arranged behind the transfer station US, through which the recording medium is deflected and guided to a fixing device FR.
- the fixing device FR can consist of a housing GH through which the record carrier AT is passed.
- a solvent LM is formed, for example from one of the molecular formula C 2 HF, C1 2 designated connections, which generates the necessary steam for fixation.
- Such compounds are referred to as partially halogenated chlorofluorocarbons, which have the advantages described above.
- the partially chlorinated fluorocarbon HFCKW R123 has been found to be particularly advantageous.
- the solvent vapor produced in this way acts on the recording medium AT, in particular on the toner applied to the recording medium. It dissolves the toner particles so that they adhere permanently to the recording medium.
- a toner based on polystyrene is used as the toner. It has turned out to be favorable to have a toner with a non-crosslinked polymer matrix, the polymer matrix of which consists of polystyrene and metaacrylates. Compared to toner with a non-crosslinked polymer matrix whose polymer matrix consists of polystyrene and metaacrylates, the partially chlorinated fluorocarbon HFCKW R123 has such a high dissolving effect that the R123 can be used as the sole fixing agent, which has the advantages described above.
- Solvents with the empirical formula C 2 HF, C1 2 are partially halogenated chlorofluorocarbons. These partially halogenated chlorofluorocarbons are generally suitable as solvents for fixing devices in electrophotographic printing devices. Since - as described - a fixing steam is generated from the solvent, for example by evaporation on a baffle plate or heating plate, it is advantageous if the solvent has a low boiling point, so that, for example, no negative heat influences are exerted on the toner and the paper and the evaporation energy to be supplied is not too high. A boiling point of less than 35 * has proven to be favorable.
- Another partially halogenated fluorocarbon can also be used as the solvent, for example R141b with the formula CFC1 2 -CH 3 (1,1-dichloro-l-fluoroethane). It is known as a foaming agent for foamed plastics.
- the concentration of the fixing agent in the fixing chamber FR may be advantageous to raise somewhat compared to the known fixing agent.
- this can be achieved by mechanically shortening an ultrasonic measuring section serving as sensor S for the fixative concentration.
- This mechanical shortening of the ultrasonic measuring section shortens the length base for the measurement, which results in an automatic increase in the fixing agent concentration while maintaining the other control variables of a known control arrangement RA for regulating the fixing agent concentration in the fixing device .
- the known control arrangement RA controls a heating device HE which is connected to a voltage source SP and which is switched on and off with the aid of a switch SH.
- cold traps with seals DI are arranged at the entry and exit points of the award carrier.
- the recording medium AT arrives at further rollers RL1, RL2, via which the recording medium is transported to a recording stack ST2.
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Fixing For Electrophotography (AREA)
Abstract
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP92919887A EP0613572B1 (fr) | 1991-11-21 | 1992-09-30 | Procede et solvants pour le fixage d'un toner a base de polystyrene sur un support de reproduction d'un appareil d'impression ou de copie |
DE59202470T DE59202470D1 (de) | 1991-11-21 | 1992-09-30 | Verfahren und lösungsmittel zum fixieren eines auf polystyrolbasis aufgebauten toners auf einem aufzeichnungsträger eines druck- oder kopiergerätes. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP91119850.5 | 1991-11-21 | ||
EP91119850 | 1991-11-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1993010485A1 true WO1993010485A1 (fr) | 1993-05-27 |
Family
ID=8207359
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP1992/002267 WO1993010485A1 (fr) | 1991-11-21 | 1992-09-30 | Procede et solvants pour le fixage d'un toner a base de polystyrene sur un support de reproduction d'un appareil d'impression ou de copie |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP0613572B1 (fr) |
DE (1) | DE59202470D1 (fr) |
WO (1) | WO1993010485A1 (fr) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0605128A1 (fr) * | 1992-12-14 | 1994-07-06 | Interscience Computer Corporation | Un agent de fusion |
EP0700988A2 (fr) | 1994-07-15 | 1996-03-13 | Solvay Fluor und Derivate GmbH | Composition contenant difluorométhoxy-2,2,2-trifluoroéthane et utilisation |
WO1997007432A1 (fr) * | 1995-08-11 | 1997-02-27 | Interscience Computer Corporation | Procedes de fixation par vapeur de solvent et toners de couleur utilises dans ces procedes |
EP0784238A1 (fr) | 1996-01-15 | 1997-07-16 | SOLVAY (Société Anonyme) | Fixage d'un toner par des compositions d'hydrofluorocarbones gazeuses et ces compositions |
DE19914514A1 (de) * | 1999-03-30 | 2000-11-02 | Oce Printing Systems Gmbh | Einrichtung und Verfahren zum Drucken oder Kopieren, wobei das Tonerbild einem Lösungsmittel in Gasphase ausgesetzt wird |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10037464A1 (de) | 2000-08-01 | 2002-03-07 | Oce Printing Systems Gmbh | Vorrichtung und Verfahren zum Fixieren eines Tonerbildes unter Verwendung eines gerichteten Stroms aus Lösemitteldampf |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2029325A (en) * | 1978-08-11 | 1980-03-19 | Siemens Ag | Method of operating a non-mechanical printer or copier |
EP0465037A1 (fr) * | 1990-06-29 | 1992-01-08 | Minnesota Mining And Manufacturing Company | Composition de solvant |
-
1992
- 1992-09-30 WO PCT/EP1992/002267 patent/WO1993010485A1/fr active IP Right Grant
- 1992-09-30 EP EP92919887A patent/EP0613572B1/fr not_active Expired - Lifetime
- 1992-09-30 DE DE59202470T patent/DE59202470D1/de not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2029325A (en) * | 1978-08-11 | 1980-03-19 | Siemens Ag | Method of operating a non-mechanical printer or copier |
EP0465037A1 (fr) * | 1990-06-29 | 1992-01-08 | Minnesota Mining And Manufacturing Company | Composition de solvant |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0605128A1 (fr) * | 1992-12-14 | 1994-07-06 | Interscience Computer Corporation | Un agent de fusion |
EP0700988A2 (fr) | 1994-07-15 | 1996-03-13 | Solvay Fluor und Derivate GmbH | Composition contenant difluorométhoxy-2,2,2-trifluoroéthane et utilisation |
US5674825A (en) * | 1994-07-15 | 1997-10-07 | Solvay Fluor Und Derivate Gmbh | Difluoromethoxy-2,2,2-trifluoroethane compositions and methods of use |
US5888688A (en) * | 1994-07-15 | 1999-03-30 | Solvay Fluor Und Derivate Gmbh | Difluoromethoxy-2, 2, 2-trifluoroethane compositions and methods of use |
WO1997007432A1 (fr) * | 1995-08-11 | 1997-02-27 | Interscience Computer Corporation | Procedes de fixation par vapeur de solvent et toners de couleur utilises dans ces procedes |
GB2318421A (en) * | 1995-08-11 | 1998-04-22 | Interscience Computer Corp | Solvent vapor fixing methods and process color toners for use in same |
EP0784238A1 (fr) | 1996-01-15 | 1997-07-16 | SOLVAY (Société Anonyme) | Fixage d'un toner par des compositions d'hydrofluorocarbones gazeuses et ces compositions |
BE1009964A3 (fr) * | 1996-01-15 | 1997-11-04 | Solvay | Procede de fixage d'un toner dans un appareil d'impression ou de reproduction de documents et compositions utilisables dans ce procede. |
US5714298A (en) * | 1996-01-15 | 1998-02-03 | Solvay (Societe Anonyme) | Method for fixing a toner in a copier and compositions used in this method |
DE19914514A1 (de) * | 1999-03-30 | 2000-11-02 | Oce Printing Systems Gmbh | Einrichtung und Verfahren zum Drucken oder Kopieren, wobei das Tonerbild einem Lösungsmittel in Gasphase ausgesetzt wird |
DE19914514B4 (de) * | 1999-03-30 | 2007-10-18 | OCé PRINTING SYSTEMS GMBH | Einrichtung und Verfahren zum Drucken oder Kopieren, wobei das Tonerbild einem Lösungsmittel in Gasphase ausgesetzt wird |
Also Published As
Publication number | Publication date |
---|---|
DE59202470D1 (de) | 1995-07-13 |
EP0613572A1 (fr) | 1994-09-07 |
EP0613572B1 (fr) | 1995-06-07 |
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