Bicharge photoconductive zinc oxides containing iodine

Abstract

Bicharge photoconductive zinc oxides useful in the production of photoprint papers providing good quality photoprints in both positive charge and reversal modes are prepared by heating photoconductive zinc oxide in air to a temperature of from about 100.degree.C. to about 500.degree.C. in the presence of iodine or an inorganic or organic iodide.

Description

This invention relates to bicharge photoconductive zinc oxides and methods of making them. Unlike ordinary photoconductive zinc oxides which perform well in negative charge photocopying, a bicharge zinc oxide can accept and discharge both negative and positive charges in a controlled manner which affords the production of either negative or positive photocopy. This dual capability adds much flexibility to the practical use of photocopy papers coated with the photoconductive zinc oxide. The bicharge capability is particularly useful and desirable in the microfilm copying art.

Commercially available bicharge zinc oxides are off-colored and produce low quality, speckled photoprints. The poor quality reproduction occurs in the positive charge mode (positive corona surface charge, subsequently developed with a negatively charged toner) and in reversal photocopying. The reversal process is particularly useful in copying microfilm where the negative microfilm is enlarged and reproduced as a positive print. This is accomplished by placing the photoimage, by light reflection, onto a negatively charged photoconductive surface. Subsequent development with a negatively charged toner yields the desired and conventional positive print.

I have discovered a simple, direct process for converting ordinary photoconductive zinc oxide into a white (i.e., colorless) bicharge photoconductive material which, when coated on photoprint paper, provides good quality photoprints in both positive charge and reversal modes. In this process elemental iodine, or organic or inorganic iodides, are mixed with the zinc oxide. The mixture, containing 0.005 to 0.1 weight percent of iodine (or its equivalent in iodide form), is heated in air at 100-500.degree.C. The residence time is selected to distribute the iodine or iodide uniformly throughout the mass of zinc oxide. In a preferred embodiment zinc oxide mixed with 0.02-0.05 weight percent of iodine, or the equivalent in iodide form, is heated in static air at 200-400.degree.C. for about 10-30 minutes. The resulting bicharge product is somewhat whiter than the starting zinc oxide, and is free flowing and odorless. A similar product is obtained by heating zinc oxide in an atmosphere of gently moving air containing an equivalent quantity of iodine or of a volatile iodide from an upstream source.

An effective alternative for adding the iodine is to dissolve it in a solvent such as water or carbon tetrachloride in which the zinc oxide is suspended. The resulting slurry is filtered, dried, and then heated in air to yield a bicharge photoconductive zinc oxide.

As mentioned above, the iodine may be provided as the element, or as an organic or inorganic iodide, including hydrogen iodide. Practically all of the iodine is retained when elemental iodine or inorganic iodides are used. Some iodine loss occurs when volatile organic iodides such as methyl and ethyl iodide are employed.

High quality positive charge and reversal photoprints require high positive charge acceptance (i.e., high positive charge saturation voltage) and decreased rate of dark decay of the acquired positive charge. The data in Table I show that the best bicharge photoproperties occur in the 0.01-0.03 weight percent iodine range where the positive saturation voltage is considerably higher than that of the untreated zinc oxide, and the rate of positive dark charge decay is considerably lower. This combination produces the contrast necessary to provide good quality positive charge and reversal photoprints. Table I also shows the relationship between bicharge photoprint quality and rate of dark decay of the positive charge in volts per second. The quality of the photoprints was scaled, by visual inspection, as follows: 6 = very poor; 5 = poor; 4 = fair; 3 = acceptable; 2 = moderately good; 1 = good. The scaling was based on print brightness, cleanliness, contrast, and speckling. For commercial practice, the print quality numerical ratings should be less than 4.

TABLE I__________________________________________________________________________Bicharge Photoproperties and Print Quality ofPapers Coated with Iodine-Treated PC Zinc Oxide.Effects of Iodine Concentration. All SamplesHeated in Air at 400.degree.C for 20 Minutes.__________________________________________________________________________ Dark Photoprint Quality Decay Reversal Positive Saturation Rate (-charge) (+charge)Sample Wt.% Iodine Charge Voltage V/Sec (-toner) (-toner)__________________________________________________________________________1 -- - 875 14.5 6 -- + 760 19.0 62 0.003 - 850 12.5 5 + 785 17.5 53 0.01 - 870 14.5 2 + 740 12.5 24 0.03 - 910 15.5 1 + 810 12.0 15 0.06 - 885 20.5 3 + 800 14.0 36 0.12 - 920 20.0 4 + 835 17.0 47 0.30 - 935 22.5 4 + 850 17.0 4__________________________________________________________________________

The data in Table II show that whereas bicharge print quality, in comparison with the untreated zinc oxide, is noticeably improved by heating the iodine-zinc oxide admixture over a wire temperature range of 100-500.degree.C., the preferred heating range is 100-400.degree.C.

TABLE II______________________________________Photoprint Quality of Bicharge Paapers Coatedwith Iodine-Treated PC Zinc Oxide. Effect ofHeating Temperature of Iodine-Zinc Oxide Mix-tures at 0.03 wt. % Iodine.______________________________________ Photoprint Quality Temp. .degree.C of Reversal Positive Heat Treatment (-charge) (+charge)Sample. 20 Minutes (-toner) (-toner)______________________________________ 8 Room temp. (28.degree.C) 4 5 9 100 2 110 200 1 111 300 2 212 400 3 313 500 4 414 600 5 5______________________________________

Iodine and the iodides are uniquely effective for conferring bicharge photoproperties on normal photoconductive (PC) zinc oxide. As shown in Table III, of the four halogens, iodine alone provides good quality bicharge photoprints. Those prepared from bromine, chlorine or fluorine-treated photoconductive zinc oxide give photoprints of unacceptable quality.

TABLE III__________________________________________________________________________Bicharge Photoproperties and Print Quality ofPapers Coated with Halogen-Treated PC Zinc Oxide.Halogens Added at 0.013 Mole % Level (Equivalentto 0.04 wt. % Iodine). Samples Heated in Airat 420.degree.C.__________________________________________________________________________ Dark Photoprint Quality Charge to Decay Reversal Positive Halogen Coated Saturation Rate (-charge) (+charge)Sample Added Paper Voltage V/Sec (-toner) (-toner)__________________________________________________________________________15 Iodine - 950 22.0 1 + 905 16.5 116 Bromine - 930 14.0 5 + 805 22.5 517 Chlorine - 960 13.0 6 + 855 21.0 618 Fluorine - 940 17.0 4 + 790 24.5 4__________________________________________________________________________

The data in Table IV show that the iodine can be applied by suspending the zinc oxide in a water or carbon tetrachloride solution of the iodine. The samples were filtered, then air-dried at 110.degree.C. The water slurry process alone, without iodine, produces some improvement in bicharge print properties. However, the addition of iodine is required to obtain acceptably good quality bicharge photoprints.

TABLE IV__________________________________________________________________________Bicharge Photoproperties and Print Quality of PapersCoated with Iodine-Treated PC Zinc Oxide. SamplesSlurried in Solvent, Then Filtered and Air-Driedat 110.degree.C.__________________________________________________________________________ Dark Photoprint Quality Decay Reversal Positive Saturation Rate (-charge) (+chargeSample Wt. % Iodine Solvent Charge Voltage V/Sec (-toner) (-toner__________________________________________________________________________19 -- Water - 700 12.5 4 + 605 24.0 420 0.02 Water - 805 18.0 3 + 680 17.5 121 0.02 Carbon - 820 21.0 2 Tetrachloride + 765 15.5 2__________________________________________________________________________

The improvements obtained with a number of organic iodides are given in Table V. In particular, iodoform and ethyl iodide are as effective as iodine in this method.

TABLE V__________________________________________________________________________Bicharge Photoproperties and Print Quality of PapersCoated with PC Zinc Oxides Treated with OrganicHalides. Samples Heated in Air at 400.degree.C.__________________________________________________________________________ Dark Photoprint Quality Wt. % as Decay Reversal Positive Iodine or Saturation Rate (-charge) (+chargeSample Additive Equivalent Charge Voltage V/Sec (-toner) (-toner__________________________________________________________________________22 Iodine 0.04 - 930 20.0 1 + 885 17.5 323 Methyl Iodide 0.04 - 945 21.5 2 + 865 16.5 424 Ethyl Iodide 0.04 - 985 22.5 1 + 890 16.0 225 Iodobenzene 0.08 - 970 22.0 2 + 910 14.0 326 p-Diiodobenzene 0.04 - 985 23.5 2 + 870 18.0 427 Iodoform 0.04 - 910 22.0 1 + 845 15.5 128 Iodoform 0.08 - 985 29.0 2 + 895 15.0 1__________________________________________________________________________

The data in Table VI show that inorganic iodides, such as those of potassium, zinc, aluminum, and tin, produce beneficial bicharge effects. The samples were heated in air at 400.degree.C.

TABLE VI__________________________________________________________________________ Dark Photoprint Quality Wt. % as Decay Reversal Positive Iodine or Saturation Rate (-charge) (+charge)Sample Additive Equivalent Charge Voltage V/Sec (-toner) (-toner)__________________________________________________________________________29 Stannic Iodide 0.04 - 915 21.0 3 + 855 14.5 330 Potassium Iodide 0.04 - 890 20.0 1 + 790 14.0 531 Zinc Iodide 0.04 - 878 16.0 1 + 790 12.0 332 Aluminum Iodide 0.04 - 860 11.0 3 + 850 17.0 3__________________________________________________________________________

The following are illustrative examples of the conversion of zinc oxide to bicharge zinc oxide:

Example 1

To a 120 g. sample of conventional photoconductive zinc oxide (French process zinc oxide prepared by the combustion in air of purified zinc vapor), having an average particle size of 0.22 .mu., were added 36 mg. (0.03 wt.%) of pulverized iodine. The mixture was shaken and tumbled periodically for several minutes, then heated in a covered pyrex dish at 400.degree.C for about 20 minutes. The relatively high vapor pressure of iodine ensures a uniform distribution of iodine throughout the mass of zinc oxide. Analysis of the white product showed essentially quantitative retention of the iodine.

EXAMPLE 2

To a slurry of 160 g. of conventional photoconductive zinc oxide in 350 ml. carbon tetrachloride were added 32 mg. (0.02 wt.%) iodine dissolved in 50 ml. of carbon tetrachloride. After stirring for 15 minutes, the slurry was filtered, and the cake was dried in air at 110.degree.C for one hour, then pulverized. The product was white.

EXAMPLE 3

To a slurry of 160 g. of conventional photoconductive zinc oxide in 300 ml. water were added 32 mg. (0.02 wt.%) of iodine dissolved in 200 ml. water. After stirring for 15 minutes, the slurry was filtered, and the cake was dried in air at 100 .degree.C for 2 hours, then pulverized. The product was white.

EXAMPLE 4

To 160 g. of conventional photoconductive zinc oxide were added 66 mg. of pulverized iodoform (CHI.sub.3). The mixture, after tumbling, was heated in a covered glass dish at 400.degree.C for about 20 minutes. The product was white.

EXAMPLE 5

To 200 g. of conventional photoconductive zinc oxide were added 135 mg. methyliodide (liquid, equivalent to 0.06 wt.% iodine). The mixture was tumbled for several minutes, then heated in a covered glass dish at 200.degree.C for about 20 minutes. The white product contained 0.037 weight percent of iodine.

EXAMPLE 6

To 160 g. of conventional photoconductive zinc oxide were added 84 mg. pulverized potassium iodide (equivalent to 0.04 wt.% iodine). The mixture, after tumbling, was heated in a covered glass dish at 400.degree.C for about 20 minutes. The product was white.

For testing the bicharge photoconductive zinc oxides were applied to a conductive base paper (Weyerhaeuser Base M) at a coating weight of 20 pounds per 3000 square feet. The coating mixture was composed of:

Zinc oxide 140 g.Modified Acrylic resin (DeSoto E-041,45% non-volatile solids) 44 g.Toluene 110 g.Dye Sensitizer; solution of 7.5 mg.Bromophenol Blue and 7.5 mg. Uraninein 6 ml. methanol

The coated papers were dark-adapted overnight. Electrical measurements on small samples of the coated papers were made on an M/K Stati Tester. The corona was charged to 6000 volts with a current flow of 25 microamperes in both negative and positive mode. Exposure to the corona charge was for about one second, after which the sample was retained in a dark chamber for 10 seconds to measure the rate of charge decay.

The photoprints were made and developed in an SCM Copier, Model 33 in which 6000 volts at 25 microamperes were applied to the corona unit. The papers were charged for 11/2 seconds, then imaged by exposure to 40 footcandles of light reflected from the master print for 11/2 seconds. The reversal prints were made by charging with a negative corona, then developing with a negatively charged toner (Clopay RSX-117). The positive prints were made by charging with a positive corona, then developing with the negatively charged toner.

The iodine compounds, other than elemental iodine, which are effective in the method of the invention include both organic and inorganic iodides such as metal iodides, hydrogen iodide, alkyl and aryl mono and polyiodides.

Claims

1. A method of producing bicharge photoconductive zinc oxide which comprises heating photoconductive zinc oxide in air to a temperature of from about 100.degree.C to about 500.degree.C. in the presence of iodine in an amount of from about 0.005 to about 0.1 percent by weight of the zinc oxide or an inorganic or organic iodide containing an equivalent amount of iodine for a time sufficient to distribute uniformly said iodine or iodide throughout the mass of said zinc oxide.

2. A method as defined in claim 1 wherein the time of heating is from about 10 to about 30 minutes.

3. A method as defined in claim 1 wherein iodine or inorganic or organic iodide is contacted with the zinc oxide admixed in a stream of air.

4. A method as defined in claim 1 wherein the zinc oxide is admixed with a solution or suspension of iodine or inorganic or organic iodide is mixed with the zinc oxide before heating in the presence of air.

5. Bicharge photoconductive zinc oxide produced by the process of claim 1.