[0001] The present invention relates to a photosensitive recording material suitable for
use in electrophotography.
[0002] In electrophotography photoconductive materials are used to form a latent electrostatic
charge image that is developable with finely divided colouring material, called toner.
[0003] The developed image can then be permanently affixed to the photoconductive recording
material, e.g. photoconductive zinc oxide-binder layer, or transferred from the photoconductor
layer, e.g. selenium layer, onto a receptor material, e.g. plain paper and fixed thereon.
In electrophotographic copying and printing systems with toner transfer to a receptor
material the photoconductive recording material is reusable. In order to permit a
rapid multiple printing or copying a photoconductor layer has to be used that rapidly
looses its charge on photo-exposure and also rapidly regains its insulating state
after the exposure to receive again a sufficiently high electrostatic charge for a
next image formation. The failure of a material to return completely to its relatively
insulating state prior to succeeding charging/imaging steps is commonly known in the
art as "fatigue".
[0004] The fatigue phenomenon has been used as a guide in the selection of commercially
useful photoconductive materials, since the fatigue of the photoconductive layer limits
the copying rates achievable.
[0005] Another important property which determines whether a particular photosensitive recording
material is suitable for electrophotographic systems is its discharge-exposure relationship.
Conventional recording materials on the basis of an electrostatically charged photoconductive
layer exhibit a fairly gradual increase in discharge as a function of increasing exposure
to photoconductivity increasing electromagnetic radiation. The radiation dose, also
called exposure, required for 10 % and 90 % discharge differs normally by factors
of about 10 to 40 depending on the choice of photoconductive recording material.
[0006] Electrophotographic copying systems wherein such photoconductive recording materials
are used in the reproduction of halftone image originals, i.e. images composed of
equi-dense screen dots in which density variation is obtained only by varying dot
frequency or by varying dot size and dot frequency, yield images of degraded quality
(resolution) when compared with images obtained on lith-type silver halide emulsion
materials.
[0007] Electrophotographic printing systems operating with scanning light sources such as
analog-signal or digital-signal modulated laser beams or light emitting diodes with
such photoconductive recording materials likewise produce degraded prints due to the
enhancement of background and the blurring of the dots as a result of each dot having
a halo caused by the unsharp edge of the writing beam.
[0008] It is therefore desirable for high quality electrophotographic copying and printing
to have a photoconductive recording material with a sharp decrease in charge expressed
in voltage (V) (as a result of sharp increase in conductivity) within a narrow range
of photo-exposure dose (E) [E = photon-intensity (I) × time (t)]. More explicitly
it is desirable in order to avoid said image quality degradation to work with a photoconductive
recording material with which the exposures required for 10 % and 90 % discharge differ
by a factor of only 5 or less.
[0009] Another important property which determines whether or not a particular photoconductive
material is suited for electrophotographic copying is its photosensitivity that must
be high enough for use in copying apparatus operating with fairly low intensity light
reflected from the original.
[0010] Commercial usefulness further requires that the photoconductive layer has a chromatic
sensitivity that matches the wavelength(s) of the light of the light source, e.g.
a laser or has panchromatic sensitivity when white light is used e.g. to allow the
reproduction of all colours in balance.
[0011] Intensive efforts have been made to satisfy said requirements, e.g. the spectral
sensitivity of selenium has been extended to the longer wavelengths of the visible
spectrum by making alloys of selenium, tellurium and arsenic. In fact selenium-based
photoconductors remained for a long time the only really useful photoconductors although
many organic photoconductors were discovered.
[0012] The first generation of organic photoconductors consisted of single layers in which
a polymeric charge transport material such as poly(N-vinylcarbazole) (PVK) or charge
transport molecules such as the 1,2-dihydro-2,2,4-trimethylquinoline derivatives described
in US-P 3,830,647 and 3,832,171 dissolved in an inert polymeric binder such as a polycarbonate
were sensitized with dissolved dyes or dispersed pigment particles. Examples of the
latter are the so-called "photoemission active material" (PEAM) layers such as those
disclosed by Regensburger and Jakubowski in US-P 3,877,935 for novel xerographic plates
containing photoinjecting polynuclear quinone pigments including 4,10-dibromoanthanthrone
in concentrations of 0.1 to 5 percent by volume with 5 to 99 percent by volume of
photoconductor material. Hackett also described such layers in 1971 in the Journal
of Chemical Physics, Volume 55, page 3178 consisting of 25 wt% X-phthalocyanine dispersed
in poly(N-vinylcarbazole).
[0013] D.R.Keams, G.Tollin and M.Calvin have reported in the Journal of Chemical Phycis
(Vol. 29, page 950 [1958] and Vol. 32, page 1020 [1960]) that at room temperature
the dark conductivity of pressed discs of phthalocyanine-o-chloranil mixtures increase
with increasing o-chloranil concentration from 10⁻⁹ Ω⁻¹-cm⁻¹ for pure phthalocyanine
to 10⁻²Ω⁻¹-cm⁻¹. This makes the attainment of an acceptable contrast potential of
about 500 V impossible using corona charging. Moreover, K.Nakatani, J.Hanna and H.Kokado
in their 1985 paper in the Japanese journal "Electrophotography", volume 24, page
2 showed that the dark conductivities of two layer organic photoconductors consisting
of a 15 µm transport layer consisting of 50% p-diethylaminobenzaldehydediphenylhydrazone
in polyester and a charge generating layer consisting of metal-free phthalocyanine
and an electron acceptor at a concentration of about 10% by weight increased with
the electron affinity (EA) of the electron acceptor with a 500-fold jump between EA's
of 1.37 and 1.55 eV (the EA of o-chloranil). On the basis of these observations a
photoconductor based on a mixture of metal-free phthalocyanine and o-chloranil would
seem unlikely to be able to attain an acceptable contrast potential using corona charging.
[0014] With 5 to 10 µm thick PEAM-layers consisting of about 40 % by weight of the p-type
charge transport material 2,4-bis(4-N,N-diethylaminophenyl)oxadiazole, 0.5 to 10%
by weight of N,N′-dimethylperylimide in a binder [ref. Chemiker Zeitung
106, 313 (1982)] Wiedemann observed photosensitivities expressed as half-value voltage
drop exposures (I
o.t
1/2) of 50 to 100 mJ/m2 for positive and negative charging.
[0015] Nakazawa, Muto and Tsutsumi in 1988 [Japan Hardcopy Proceedings May 16-18, 1988]
described a positively chargeable 18 µm PEAM-layer with metal-free phthalocyanine
and N,N′-bis(3,5-xylyl)perylimide as the sensitizing pigments and a charge carrier
transport material, which exhibited optimal photosensitivity (I
o.t
1/2) of 238 mJ/m2 at a metal-free phthalocyanine concentration of 0.3 % by weight, a
N,N′-bis(3,5-xylyl)perylimide concentration of 5.4 % by weight and a charge carrier
transport material concentration of 40.4 % by weight.
[0016] Such monolayer organic photoconductors were less interesting than selenium-photoconductors,
because of their poorer sensitivity, their very flat response to increasing exposure
dose and their rather large fatigue.
[0017] However, the discovery that 2,4,7-trinitro-9-fluorenone (TNF) in poly(N-vinylcarbazole)
(PVCz) formed a charge-transfer complex strongly improving the photosensitivity (ref.
US-P 3,484,237) opened the way for the use of organic photoconductors in copying machines
that could compete with the selenium-based machines.
[0018] TNF acts as an electron acceptor whereas PVCz serves as an electron donor. Films
consisting of said charge transfer complex with TNF:PVCz in 1:1 molar ratio are dark
brown, nearly black and exhibit high charge acceptance and low dark decay rates. However,
the exposures required for 10 % and 90 % discharges differed by more than a factor
of 10. Overall photosensitivity is comparable to that of amorphous selenium (ref.
Schaffert, R. M., IBM J. Res. Develop.,
15, 75 (1971).
[0019] Subsequently single layer photoconductive materials containing aggregates of photoconductors
which are both positively and negatively chargeable were developed, e.g. consisting
of ternary systems comprising a thio-pyrilium dye, a polycarbonate polymer and an
aromatic molecule such as bis(4-N,N-diethylamino-2-methyl-phenyl)-phenylmethane. In
1979 Mey et al [J.Appl.Phys.
50, 8090 (1979)] published surface potential-exposure characteristics for such photoconductive
recording materials with both negative and positive charging and for both emission-limited
discharge and high-intensity flash. In all cases the exposures required for 10 % and
90 % discharges differed by more than a factor of 10.
[0020] A further search led to the discovery that if the sensitizing pigment in PEAM-layers
were cast in a thin layer adjacent to a thicker layer solely consisting of transport
molecules dissolved in an inert polymer binder or a polymeric charge transport material
sensitivity comparable with selenium-photoconductors together with a much steeper
response to increase in exposure dose and a much reduced fatigue were observed. Hackett
showed this in 1971 [J.Chem.Phys.
55, 3178 (1971)] for the system X-phthalocyanine and PVK. Hackett found that photoconductivity
was due to field dependent photogeneration of electron-hole pairs in the phthalocyanine
and hole injection into the PVCz. The transport of the positive charges, i.e. positive
hole-conduction proceeded easily in the PVCz layer. From that time on much research
has been devoted to developing improved photoconductive systems wherein charge generation
and charge transport materials are separate in two contiguous layers (see e.g. U.K.
Pat No. 1,577,859). However, such functionally separated double layer photoconductors
although generally exhibiting a steeper response to increasing exposure doses than
single layer photoconductors still exhibit exposure doses for 10 and 90 % discharge
differing by a factor of 10 or more as shown in comparative examples furtheron.
[0021] It is an object of the present invention to provide electrophotographic recording
materials with high photosensitivity which after being charged obtain a very sharp
decrease in voltage [ΔV] within a particular narrow range [ΔE] of photo-exposure doses,
viz. wherein the photo-exposure doses required for 10 % and 90 % discharge differ
by a factor of 5 or less.
[0022] Other objects and advantages of the present invention will appear from the further
description and examples.
[0023] In accordance with the present invention an electrophotographic recording material
is provided which comprises on an electrically conductive support a positively chargeable
photoconductive recording layer free from n-type charge transport material, which
layer contains in an electrically insulating organic polymeric binder material photoconductive
p-type pigment material mainly comprising a metal-free phthalocyanine in the χ-form,
wherein said layer has a thickness in the range of 4 to 40 µm and comprises 5 to 40
% by weight of said p-type pigment material in said electrically insulating organic
polymeric binder material that has a volume resistivity of at least 10¹⁴ Ohm-m, and
wherein said recording layer in electrostatically charged state requires for 10 %
and 90 % discharge respectively exposures to conductivity increasing electromagnetic
radiation that differ by a factor 5 or less.
[0024] p-Type pigment material optionally used in admixture with metal-free phthalocyanine
in χ-form may be inorganic or organic and may have any colour including white. The
p-type pigments is (are) dispersible in the organic polymeric binder of said photoconductive
recording layer.
[0025] Optionally the support of said photoconductive recording layer is pre-coated with
an adhesive and/or a blocking layer (rectifier layer) reducing or preventing positive
hole charge injection from the conductive support into the photoconductive recording
layer, and optionally the photoconductive recording layer is overcoated with an outermost
protective layer, more details about said layers being given furtheron.
[0026] In accordance with a preferred embodiment said photoconductive recording layer has
a thickness in the range of 5 to 35 µm and contains 6 to 30 % by weight of said p-type
pigment material.
[0027] By the term "p-type" material is understood a material having p-type conductance,
which means that the photocurrent (I
p) generated in said material when in contact with an illuminated transparent electrode
having positive polarity is larger than the photocurrent (I
n) generated when in contact with a negative illuminated electrode (I
p/I
n > 1), [ref. Hans Meier - Organic Semiconductors, Dark- and Photoconductivity of Organic
Solids - Verlag Chemie (1974), p. 410, point 3.]
[0028] By the term "n-type" material is understood a material having n-type conductance,
which means that the photocurrent (I
n) generated in said material when in contact with an illuminated transparent electrode
having negative electric polarity is larger than the photocurrent (I
p) generated when in contact with a positive illuminated electrode (I
n/I
p > 1)
[0029] The electrically insulating binder has preferably a volume resistivity which is not
higher than 10¹⁶ Ohm-m.
[0030] χ-metal-free phthalocyanines suitable for use according to the present invention
are described e.g. in US-P 3,594,163; US-P 3,816,118; US-P 3,894,868 and CA-P 899,870.
[0031] Examples of other p-type pigments dispersible in the binder of the negatively chargeable
recording layer of the electrophotographic recording material according to the present
invention are organic pigments from one of the following classes :
a) naphthalo- and phthalo-cyanines being not of the metal-free χ-form, e.g τ and η
7 metal-free phthalocyanines as described e.g. in US-P 4,749,637; metal, metal-oxy,
metal-halo and siloxy-silicon metal naphthalo- and phthalocyanines and siloxy-silicon
naphthalocyanines as described e.g. in EP-A 243 205; vanadyl phthalocyanines as described
e.g. in US-P 4,771,133; bromoindium phthalocyanines as described e.g. in US-P 4,666,802
and 4,727,139; and metal, metal-oxy and metal-halo naphthalocyanines as described
e.g. in EP 288 876.
b) quinoxaline pigments e.g.

c) dioxazine pigments with the general formula :

wherein
X is Cl, CONHC₆H₅, NHOCCH₃, NHC₆H₅, CONH₂;
Y is p-chlorophenyl, NHC₆H₅, NHOCCH₃, NH₂, OC₆H₅, H;
Z is H, alkoxy, e.g. OC₂H₅ or O-iso C₃H₇, Cl, NO₂ or COC₆H₅;
or Z and Y together form a substituted or unsubstituted heterocyclic ring, e.g.
Carbazole Dioxazine Violet (CI Pigment Violet 23, CI 51319) with the formula :

d) p-type polyazo pigments including bisazo-, trisazo- and tetrakisazo-pigments.
[0032] The resin binders are selected on the basis of optimal mechanical strength, adherence
to any adjacent layer(s) and favourable electrical properties and if the active layer
is at the same time the outermost layer also on the basis of reducing their surface
energy and frictional coefficient in order to improve the resistance of the surface
of the photosensitive recording material to toner smearing and abrasion and the ease
with which untransferred toner can be removed.
[0033] Suitable binder material for use in the recording material of the present invention
are organic resin materials, e.g. cellulose esters, acrylate and methacrylate resins,
e.g. cyanoacrylate resin, polyvinyl chloride, copolymers of vinyl chloride, e.g. copolyvinyl
chloride/acetate and copolyvinylchloride/maleic anhydride, polyester resins, e.g.
copolyesters of isophthalic acid and terephthalic acid with glycol, aromatic polycarbonate
resins and polyester carbonate resins.
[0034] The recording layer as outermost layer can be endowed with a low surface adhesion
and a low frictional coefficient by the incorporation therein of a resin comprising
a block copolyester or copolycarbonate having a fluorinated polyether block as described
in US-P 4,772,526.
[0035] A polyester resin particularly suited for use in combination with aromatic polycarbonate
binders is DYNAPOL L 206 (registered trade mark of Dynamit Nobel for a copolyester
of terephthalic acid and isophthalic acid with ethylene glycol and neopentyl glycol,
the molar ratio of tere- to isophthalic acid being 3/2). Said polyester resin improves
the adherence to aluminium that may form a conductive coating on the support of the
recording material.
[0036] Suitable aromatic polycarbonates can be prepared by methods such as those described
by D. Freitag, U. Grigo, P. R. Müller and W. Nouvertné in the Encyclopedia of Polymer
Science and Engineering, 2nd ed., Vol. II, pages 648-718, (1988) published by Wiley
and Sons Inc., and have one or more repeating units within the scope of the following
general formula :

wherein :
X represents

R¹, R², R³, R⁴, R⁷ and R⁸ each represents (same or different) hydrogen, halogen,
an alkyl group or an aryl group, and
R⁵ and R⁶ each represent (same or different) hydrogen, an alkyl group, an aryl group
or together represent the necessary atoms to close a cycloaliphatic ring, e.g. cyclohexane
ring.
[0037] Aromatic polycarbonates having a molecular weight in the range of 10,000 to 200,000
are preferred. Suitable polycarbonates having such a high molecular weight are sold
under the registered trade mark MAKROLON of Bayer AD, W-Germany.
[0038] MAKROLON CD 2000 (registered trade mark) is a bisphenol A polycarbonate with molecular
weight in the range of 12,000 to 25,000 wherein

[0039] MAKROLON 5700 (registered trade mark) is a bisphenol A polycarbonate with molecular
weight in the range of 50,000 to 120,000 wherein

[0040] Further useful binder resins are silicone resins, polystyrene and copolymers of styrene
and maleic anhydride and copolymers of butadiene and styrene.
[0041] The photoconductive recording layer may contain further additives such as spectral
sensitizing agents known in the art, e.g. (poly)methine dyes, for enlarging the spectral
sensitivity of the applied photoconductive compounds, and compounds acting as stabilising
agents against deterioration by ultra-violet radiation, so-called UV-stabilizers,
e.g. benztriazoles.
[0042] For controlling the viscosity of the coating compositions and controlling their optical
clarity silicone oils may be used.
[0043] An adhesive layer and/or blocking layer being optionally present between the conductive
support and the photoconductive recording layer may contain or consist of one or more
of e.g. a polyester, a polyamide, nitrocellulose, hydrolysed silane, or aluminium
oxide. The total layer thickness of said layer(s) is preferably not more than 2 micron.
[0044] The photoconductive recording layer may be coated optionally with a thin protective
layer to endow its surface with improved abrasion resistance, a reduced frictional
coefficient, reduced tendency to toner smearing and more easy removal of untransferred
toner.
[0045] The thickness of a protective layer should be less than 5 µm thick and preferably
less than 2 µm thick to avoid a significant increase in residual potential.
[0046] Suitable resins for use in such protective layer are block copolyester or copolycarbonate
resins having a fluorinated polyether block as described e.g. in US-P 4,772,526, or
are copolymers of tetrafluoroethene or hexafluoropropene, optionally in combination
with resins compatible therewith, e.g. cellulose esters, acrylate and methacrylate
resins, e.g. cyanoacrylate resin, polyvinyl chloride, copolymers of vinyl chloride,
e.g. copolyvinyl chloride/acetate and copolyvinyl chloride/maleic anhydride, polyester
resins, aromatic polycarbonate resins or polyester-carbonate resins.
[0047] The conductive support may be made of any suitable conductive material. Typical conductors
include aluminum, steel, brass and paper and resin materials incorporating or coated
with conductivity enhancing substances, e.g. vacuum-deposited metal, dispersed carbon
black, graphite and conductive monomeric salts or a conductive polymer, e.g. a polymer
containing quaternized nitrogen atoms as in Calgon Conductive polymer 261 (trade mark
of Calgon Corporation, Inc., Pittsburgh, Pa., U.S.A.) described in US-P 3,832,171.
[0048] The support may be in the form of a foil, web or be part of a drum.
[0049] An electrophotographic recording process according to the present invention comprises
the steps of :
(1) overall positively electrostatically charging, e.g. with corona-device, the recording
material of the present invention,
(2) image-wise photo-exposing the recording material according to the present invention
thereby obtaining a latent electrostatic image.
[0050] The development of the latent electrostatic image commonly occurs preferably with
finely divided electrostatically attractable material, called toner particles that
are attracted by Coulomb force to the electrostatic charge pattern. The toner development
is a dry or liquid toner development known to those skilled in the art.
[0051] In positive-positive development toner particles deposit on those areas of the charge
carrying surface which are in positive-positive relation to the original image. In
reversal development, toner particles migrate and deposit on the recording surface
areas which are in negative-positive image value relation to the original. In the
latter case the areas discharged by photo-exposure obtain by induction through a properly
biased developing electrode a charge of opposite charge sign with respect to the charge
sign of the toner particles so that the toner becomes deposited in the photo-exposed
areas that were discharged in the imagewise exposure (ref. : R.M. Schaffert "Electrophotography"
- The Focal Press - London, New York, enlarged and revised edition 1975, p. 50-51
and T.P. Maclean "Electronic Imaging" Academic Press - London, 1979, p. 231).
[0052] According to a particular embodiment electrostatic charging, e.g. by corona, and
the imagewise photo-exposure proceed simultaneously.
[0053] Residual charge after toner development may be dissipated before starting a next
copying cycle by overall exposure and/or alternating current corona treatment.
[0054] Recording materials according to the present invention depending on the spectral
sensitivity of the photoconductive recording layer may be used in combination with
all kinds of photon-radiation, e.g. light of the visible spectrum, infra-red light,
near ultra-violet light and likewise X-rays when electron-positive hole pairs can
be formed by said radiation in the recording layer. Thus, they can be used in combination
with incandescent lamps, fluorescent lamps, laser light sources or light emitting
diodes by proper choice of the spectral sensitivity of the charge generating substance
or mixtures thereof.
[0055] The toner image obtained may be fixed onto the recording material or may be transferred
to a receptor material to form thereon after fixing the final visible image.
[0056] A recording material according to the present invention showing a particularly low
fatigue effect can be used in recording apparatus operating with rapidly following
copying cycles including the sequential steps of overall charging, imagewise exposing,
toner development and toner transfer to a receptor element.
[0057] The evaluations of electrophotographic properties determined on the recording materials
of the following examples relate to the performance of the recording materials in
an electrophotographic process with a reusable photoreceptor. The measurements of
the performance characteristics were carried out as follows :
[0058] Two procedures were used for evaluating the discharge as a function of exposure :
a routine sensitometric measurement in which the discharge was obtained for 8 different
exposures including zero exposure and a more refined measurement in which the discharge
was obtained for 360 different exposures in a single drum rotation.
[0059] In the routine sensitometric measurement the photoconductive recording sheet material
was mounted with its conductive backing on an aluminium drum which was earthed and
to which the conductive backing had been connected. The drum was rotated at a circumferential
speed of 5 cm/s and the recording material sequentially charged with a positive corona
at a voltage of +4,6 kV operating with a corona current of about 1 µA per cm of corona
wire, exposed (simulating image-wise exposure) with monochromatic light obtained from
a monochromator positioned at the circumference of the drum at an angle of 45° with
respect to the corona source for 400 ms, the voltage measured with an electrometer
probe positioned at an angle of 180° with respect to the corona source and finally
post-exposed with a halogen lamp producing 54,000 mJ/m2 positioned at an angle of
270° with respect to the corona source before starting a new copying cycle.
[0060] Each measurement consisted of 40 copying cycles with the exposure being changed every
5 copying cycles by using a constant light intensity (I
o) initially using no light attenuating filter, and thereupon sequentially a filter
with an optical density of 0.5, a filter with an optical density of 1.0, filters with
a total optical density of 1.5, a filter with an optical density of 2.0, filters with
a total optical density of 2.5, filters with a total optical density of 3.0 and finally
a shutter to shut off the exposing light. This gives the discharges for 8 predetermined
exposures.
[0061] In the refined sensitometric measurement the photoconductive recording sheet material
is mounted on an aluminium drum as described above. The drum was rotated at a circumferential
speed of 2 cm/s and the recording material sequentially charged with a positive corona
at a voltage of +4.3 kV operating with a corona current of about 0.5 µA per cm of
corona wire, exposed (simulating image-wise exposure) with monochromatic light obtained
from a monochromator positioned at the circumference of the drum at an angle of 40°
with respect to the corona source for 500 ms, the voltage measured with an electrometer
probe positioned at an angle of 90° with respect to the corona source and finally
post-exposed with a halogen lamp producing 2,000 mJ/m2 positioned at an angle of 300°
with respect to the corona source before starting a new copying cycle. Each measurement
consisted of a single copying cycle in which a density disc with continuously varying
optical density from an optical density of 0 to an optical density of 2.1 over a sector
of 210° was rotated in front of the monochromator synchronously with the rotation
of the drum with the surface potential being measured every degree of rotation. This
gives the discharges for 360 predetermined exposures and hence a complete sensitometric
curve, whereas the routine measurement only gives 8 points on that curve.
[0062] The recording material fatigue was determined using the same configuration as for
the routine sensitometric measurement, but in this case at a specific exposure. 100
Copying cycles were carried out in which 10 cycles without monochromatic light exposure
were alternated with 5 cycles with monochromatic light exposure. The charging level
(CL) was taken as the average charging level over the 90th to 100th cycle.
[0063] The % discharge is defined as :

wherein RP is the average residual potential over the 85th to 90th cycle. The fatigue
F can be calculated as the difference in residual potential in volts between said
RP and the average residual potential over the 10th to 15th cycle.
[0064] For a given corona voltage, corona current, separating distance of the corona wires
to recording surface and drum circumferential speed the charging level CL is only
dependent upon the thickness of the charge transport layer and its specific resistivity.
In practice CL expressed in volts should be preferably ≧ 30 d, where d is the total
thickness in µm of the combined photosensitive and protective layers.
[0065] In the accompanying Figure 1 a sensitometric curve is given with in the abscissa
logarithmic values of exposure dose at 650 nm [log E = log I.t] expressed in mJ/m²
and in the ordinate voltage values [V] measured on the charged recording layer during
the exposure using increasing exposure doses at constant exposure times.
EXAMPLE 1
[0066] In the production of the photosensitive recording materials a 100 µm thick polyester
film precoated with a vacuum-deposited conductive layer of aluminium was doctor-blade
coated with a dispersion of 15 wt % of the χ-form of metal-free phthalocyanine, 76.5
wt % of the aromatic polycarbonate MAKROLON CD 2000 (registered trade mark) and 8.5
wt % of a polyester adhesion-promoting additive DYNAPOL L206 (registered trademark)
to a thickness of 12 µm.
[0067] Said dispersion was prepared by first predispersing the χ-metal-free phthalocyanine
with 5% by weight of the aromatic polycarbonate MAKROLON CD 2000 (registered trade
mark) in the final formulation in dichloromethane for 20 minutes in a pearl mill.
The balance of the aromatic polycarbonate, the required quantity of a polyester adhesion-promoting
additive DYNAPOL L206 (registered trade mark) and the balance of dichloromethane were
then added and the resulting mixture mixed for a further 5 minutes in a pearl mill.
The dispersion was cast without further dilution with dichloromethane and the resulting
layer dried for 15 hours at 50°C.
[0068] The characteristics of the thus obtained photosensitive recording materials were
determined as described above. The sensitivity to monochromatic 650 nm light exposure
is expressed as the % discharge at an exposure (I₆₅₀t) of 83.5 mJ/m2 and the steepness
of the discharge-exposure dependence is expressed as the Δ% discharge observed between
exposures (I₆₅₀t) of 26.4 mJ/m2 and 83.5 mJ/m2, a factor of 3.16 difference in exposure.
The results are summarized below :
CL = +927 V
% discharge at I₆₅₀t of 83.5 mJ/m² = 97.1.
Δ% discharge between I₆₅₀t's of 26.4 and 83.5 mJ/m² = 91.4.
[0069] The sensitometric curve for this photosensitive recording material, determined using
the refined technique, is shown in Figure 1.
EXAMPLES 2 and 3 and COMPARATIVE EXAMPLE 1
[0070] The photosensitive recording materials of Examples 2 and 3 and Comparative Example
1 were prepared as described for Example 1 and their compositions are given in Table
1.
[0071] The characteristics of the thus obtained photosensitive recording materials were
determined as described above. The sensitivity to monochromatic 650 nm light exposure
is expressed as the % discharge at an exposure (I₆₅₀t) of 83.5 mJ/m² and the steepness
of the discharge-exposure dependencies is expressed as the Δ % discharge observed
between exposures (I₆₅₀t) of 26.4 mJ/m² and 83.5 mJ/m² or between exposures (I₆₅₀t)
of 83.5 mJ/m² and 264 mJ/m². The results are given in Table 1, wherein [P1] stands
for MAKROLON CD 2000 (registered trade mark) and [P2] stands for DYNAPOL L206 (registered
trade mark).
TABLE 1
Example No. |
χ-metal-free phthalocyanine |
P1 conc. |
P2 conc. |
layer thickness |
CL |
% discharge for I₆₅₀t = 83.5 mJ/m² |
Δ% discharge between I₆₅₀t's of 26.4 mJ/m² and 83.5 mJ/m² |
Δ% discharge between I₆₅₀t's of 83.5 mJ/m² and 264 mJ/m² |
|
[wt %] |
[wt %] |
[wt %] |
[µm] |
[V] |
|
|
|
2 |
7.5 |
83.25 |
9.25 |
12 |
+854 |
88.2 |
82.9 |
3.6 |
3 |
5.0 |
85.5 |
9.5 |
13 |
+1055 |
15.7 |
9.6 |
66.7 |
Compar. Example No. |
|
|
|
|
|
|
|
|
1 |
2.5 |
87.75 |
9.75 |
13 |
+1267 |
7.2 |
3.9 |
8.2 |
EXAMPLE 4
[0072] The photosensitive recording material of Example 4 was produced by first doctor blade
coating a 100 µm thick polyester film precoated with a vacuum-deposited conductive
layer of aluminium with a 1 % solution of γ-aminopropyl-triethoxy silane in aqueous
methanol. After evaporating the solvent and curing the resulting adhesion/blocking
layer at 100 °C for 30 minutes, the adhesion/blocking layer was overcoated with a
dispersion of the χ-form of metal-free phthalocyanine to a thickness of l4 µm.
[0073] Said dispersion was prepared by mixing 1 g of the χ-form of metal-free phthalocyanine,
0.6 g of aromatic polycarbonate MAKROLON CD 2000 (registered trade mark) and 12.65
g of dichloromethane for 15 minutes in a pearl mill. 3.4 g of MAKROLON CD 2000 (registered
trade mark) and 12.56 g of dichloromethane were then added and the resulting mixture
mixed for a further 5 minutes to produce the composition with the desired viscosity
for coating.
[0074] The photosensitive layer was then dried for 16 hours at 50 °C.
[0075] The characteristics of the thus obtained photosensitive recording material were determined
as described above. The sensitivity to monochromatic 650 nm light exposure is expressed
as the % discharge at an exposure (I₆₅₀t) of 26.4 mJ/m² and the steepness of the discharge-exposure
dependence is expressed as the Δ% discharge observed between exposures (I₆₅₀t) of
8.35 mJ/m² and 26.4 mJ/m², a factor of 3.16 difference in exposure.
[0076] The results are summarized below :
CL = +957 V
% discharge at I₆₅₀t of 26.4 mJ/m² = 97.4.
Δ% discharge between I₆₅₀t's of 8.35 and 26.4 mJ/m² = 94.1.
EXAMPLE 5
[0077] The photosensitive recording material of Example 5 was produced as described for
Example 4 except that the dispersion was prepared by mixing 1 g of the χ-form of metal-free
phthalocyanine, 0.6 g of aromatic polycarbonate MAKROLON 3208 (registered trade mark)
and 14.4 g of dichloromethane for 48 hours in a ball mill. 3.2 g of MAKROLON 3208
(registered trade mark) and 16.35 g of dichloromethane were then added and the resulting
mixture mixed for a further 5 minutes to the composition with desired viscosity for
casting.
[0078] The photosensitive layer was then dried for 16 hours at 80 °C.
[0079] The characteristics of the thus obtained photosensitive recording material were determined
as described above. The sensitivity to monochromatic 780 nm light exposure is expressed
as the % discharge at an exposure (I₇₈₀t) of 6.56 mJ/m² and the steepness of the discharge-exposure
dependence is expressed as the % discharge observed between exposures (I₇₈₀t) of 2.07
mJ/m² and 6.56 mJ/m², a factor of 3.16 difference in exposure.
[0080] The results are summarized below :
CL = +1017 V
% discharge at I₇₈₀t of 6.56 mJ/m² = 95.3.
Δ% discharge between I₇₈₀t's of 2.07 and 6.56 mJ/m² = 97.9.
[0081] The higher value of the Δ% discharge than the % discharge at I 780t being effected
with 6.56 mJ/m² was due to slight photoconductor fatigue
EXAMPLE 6
[0082] The photosensitive recording material of Example 6 was prepared as described for
Example 1 but having in its composition 15 wt % of the χ-form of metal-free phthalocyanine,
5 wt % of the β-form of copper phthalocyanine (C.I. Pigment Blue 15:3), 72 wt % of
the aromatic polycarbonate MAKROLON CD2000 (registered trade mark) and 8 wt % of a
polyester adhesion-promoting additive DYNAPOL L206 (registered trade mark).
[0083] The characteristics of the thus obtained photosensitive recording material were determined
as described above and are summarized below :
CL = +865 V
% discharge at I₆₅₀t at 83.5 mJ/m² = 93.9.
Δ% discharge between I₆₅₀t's of 26.4 and 83.5 mJ/m² = 81.8.