专利摘要:
1348362 Record sheets NATIONAL CASH REGISTER CO 22 May 1972 [14 June 1971] 23874/72 Heading D2B Record sheets for use in pressure-sensitive copying processes comprise a supporting sheet carrying an oil-soluble metal salt of a phenolformaldehyde resin. The metal cation may be Al (III), Ba (II), Cd (II), Ce (III), Cs (I), Ca (II), Co (II), Cu (III), In (III), Mg (II), Mn (II), Mo (V), Ni (II), Pb (II), Na (I), Sr (II), Sn (II), Ti (IV), V (II), Zn (II) and Zr (IV). The metal resinate acts as a colourforming agent for base-reacting. colourless, chromogenic dye precursors. The latter may be carried on the same or a separate supporting sheet. The common solvent for the metal resinate and dye precusor may be encapsulated and isolated from one or both ¾f the reactants in a self-contained sheet. In a couplet system, the solvent may be carried on one of the sheets either on its own or together with one of the reactants, which is either dissolved in the solvent or isolated therefrom. Typical solvents include halogen - substituted and alkylated aromatic hydrocarbons and dialkyl phthalates.
公开号:SU1056889A3
申请号:SU721797541
申请日:1972-06-13
公开日:1983-11-23
发明作者:Вилфорд Брокет Брюс;Эрвин Миллер Роберт;Льюис Хайнкл Мери
申请人:Эплтон Пейперс Инк (Фирма);
IPC主号:
专利说明:

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The invention relates to copy papers intended for making copies with them in the process of typewriting. Copier paper, made of paper substrate and coating applied to it, is known (it is an acid-reactive dye of a phenolic type. The coating of such paper as an acid-reactive dye contains a mixture of phenol-formaldehyde resin and metal salt pj, but this paper is not sufficiently high resistance to punching due to low surface durability and puncture resistance. The aim of the invention is to increase the resistance of paper to punching. by increasing surface strength and puncture resistance. The goal is achieved by the fact that, in a copying paper made from a paper substrate and coated on it, including an acid-reactive coloring substance of a phenolic type, an acid-soluble phenol-formaldehyde resin contains an acid soluble salt , preferably salt, in an amount of 9-12% by weight of absolutely dry deposits / g. Both the metal part and the acid resin are part of the same oil The soluble molecule and both constituents are capable of reacting to color in an oil solution. This can be achieved by using certain oil-soluble metal salts of phenol-formaldehyde resins. Such salts are obtained by replacing a portion of the protons of the phenol of the phenol-formaldehyde resin with certain metal ions, which results in the so-called metal resinate. According to the invention, the dye precursor is applied either on the same substrate as said acid reaction substance or on a separate substrate. The common solvent dp of the reactants is placed in the crushing polymer material, better in the microcapsules, and separated from one or both of the reactants when they are on a single base. In a paired system containing two substrates, the solvent is retained on one of the substrates either alone or together with one of the reagents, which either dissolves in or dissolves in the solvent. The content (in wt.%) Of the metal ions in the metal resins used varies with the metal and resin chosen. Zinc, aluminum, barium, cadmium, calcium, cobalt, copper (w), indium, magnesium (i), manganese (I), molybdenum, nickel, lead, sodium, strontium, tin can be used as cations of this salt. , titanium, vanadium or zirconium (IJ /). The choice of metal for metal resins as developers that are resistant to discoloration of prints with a chromogenic substance does not have a great deal of importance because all metal resins are good in this respect. Cations such as zinc, cadmium and zirconium give metal-modified resins with the highest intensity of the fresh impression. The preparation of metal salts used in the proposed paper consists in the reaction of an oil-soluble phenol-aldehyde resin, better than a pair of substituted phenol-formaldehyde novolac resin with the desired one. metal hydroxide or oxide. A water-soluble intermediate metal resinate can also be obtained by treating pitch ;, with a strong base, such as aqueous sodium hydroxide, to produce an aqueous solution of sodium resins, followed by treating the sodium resins solution with an aqueous solution of the desired metal salt, zinc chloride, and precipitating the desired resins. metal in this case zinc rubber. According to a known method, a melt of an oil-soluble phenol-aldehyde novolak is reacted with the desired metal carboxylate or enoltome. This method is shown in Example 1, where the carpet is melted and treated with zinc oxybenzoate powder to produce zinc resin plus benzoic acid. If acetylacetonate is used instead of zinc oxybenzoate, then zinc rubber is formed along with free; m acetylacetone in a hot melt reaction. In one embodiment of this method, the metal salt can be added to the phenol-formaldehyde dehydrogenated mixture during resin production. When acid catalyzing condensation of monomeric phenols and aldehydes, water and acid are usually distilled off from the reaction mixture during the reaction. The addition of a water-soluble acidic metal salt, such as zinc chloride, to the condensation reaction is carried out in distilled hydrochloric acid, while leaving zinc resins as the product of the reaction. In this process, monomeric metal phenols are condensed (for example, zinc phenol) with aldehydes to form the desired metal resins. Example 1. A mixture of 2 kg of p-phenyl phenol formaldehyde resin is heated together with 400 g of zinc oxybenzoate with stirring for 1 h in an atmosphere of helium at elevated temperature. The temperature is gradually increased from room temperature to 200-220 ° C for about 45 minutes, then the cooler is given to for another 15 minutes. At the end of the reaction, the hot paraphenolformaldehyde zinc is poured from the reaction vessel, allowed to cool and solidify. The hardened resin is crushed under water in a mortar and is obtained finely; a spread powder suitable for applying a fine coating on a paper sheet. The zinc content of this resins (after rejecting a small amount of oil-insoluble inorganic sludge contained in the reaction products) is 5 wt.%. Suspension with 30 wt.% Solids for coating paper. Prepared by mixing the following ingredients in dry and wet matter, wt.%, Respectively: Zinc modified resin Kaolin clay Silica gel Calcium carbonate Styrene-butadiene latex Starch glue The paper is coated with an air knife and dried passing for 12 seconds through a high-speed air oven at an average temperature of about 87.8 s. A printed sheet with a primed coating containing an oil solution of lactone, a violet crystal, and benzoyl-leuco methylene blue is combined with the said sheets to obtain a receiving-receiving pair of sheets. Prouty 2. t on paper sheets that already have a coating of oil-containing microcapsules glued to the sheet with starch glue. The copying sheet produced in this way is mated with a second sheet of paper, previously soaked in a 2% solution of lactone in alcohol, and dried, leaving a residue of it on it at the coated side of the copying sheet facing the second sheet. When writing on the uncovered side of the copy paper with a pencil, the tokopi written appears on the second sheet as a result of the transfer of the metal-modified resin oil from the coated surface of the copy sheet to the contents of the lactone sheet. PRI me R 3. A solution of a metal-modified resin is obtained by dissolving in 50 parts of 1,2,4-trimethylbenzene 10 parts of paraphenol-formaldehyde resin and a solution of 14.5 parts of zinc naphthenate in 25 parts of a low-volatile hydrocarbon solvent, dispersing the oil solution in an aqueous solvent to obtain droplets with an average diameter of about 3.5 microns. The solution is encapsulated and the resulting capsules are applied as a coating on paper using polyvinyl alcohol as a binder for 10 parts of the capsule. Sheets coated with a cap of a metal-modified resin are matted with a sensitized sheet and a receiving-pair of sheets is obtained. When typing and handwriting with pressure, on the uncovered upper surface of the transfer sheet coated with capsules with resin, paired with a sensitized receiving sheet, get intense blue prints on the receiving sheet. EXAMPLE 4 A self-pressure sensitive sheet, a separate sheet containing all the color-producing elements, namely a metal-modified resin, a chromogenic dye precursor, an isolated solvent capable of dissolving both reagents, is obtained by applying a suspension of modified metal of the resin from the example on the primed coating of sheets of industrial paper or by applying a metal-modified resin containing the capsules of example 3 directly onto a sensitized sheet of same example. The proposed copier paper has significantly improved indicators of surface strength and puncture resistance. Thus, the strength of the surface of a known copying paper is 25 units. (wp) according to the IHT method, whereas the surface strength of the proposed 89 "paper is AO-50 units. These units characterize the viscosity of the ink used at a given temperature multiplied by the lowest speed of the printing rollers, at which a noticeable detachment of particles is observed. The puncture resistance of the proposed paper obtained in example I, is 61.9 units, according to the IHT method, while the known paper has a puncture resistance of 57.7 units. according to the IHT method. Improving these indicators prevents sticking and clogging of the surface of the printing device and, therefore, increases the resistance of the paper to penetration - one of the important performance properties of carbon paper.
权利要求:
Claims (1)
[1]
COPYING PAPER, consisting of a paper substrate and a coating deposited on it, including an phenol-type acid-reactive colorant, characterized in that, in order to increase the paper penetration resistance by increasing the surface strength and puncture resistance, the coating as an acid-reactive substance contains oil-soluble a salt of phenol-formaldehyde resin, preferably a zinc salt, in an amount of 9-12% of the total weight of the absolutely dry coating.
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类似技术:
公开号 | 公开日 | 专利标题
SU1056889A3|1983-11-23|Copying paper
US3540909A|1970-11-17|Pressure sensitive recording sheets employing 3,3-bis| phthalide
US3723156A|1973-03-27|Record material
US3663256A|1972-05-16|Mark-forming record material
US3509173A|1970-04-28|3,3-bis-| phthalides
US4197346A|1980-04-08|Self-contained pressure-sensitive record material and process of preparation
US3772052A|1973-11-13|Recording sheet and color developer therefor
US4165103A|1979-08-21|Method of preparing zinc-modified phenol-aldehyde novolak resins and use as a color-developing agent
US4173684A|1979-11-06|Production of novel metal modified novolak resins and their use in pressure sensitive papers
US4165102A|1979-08-21|Method of preparing zinc-modified phenol-aldehyde novolak resins and use as a color-developer
US4234212A|1980-11-18|Recording sheet
US4226962A|1980-10-07|Production of novel metal modified novolak resins and their use in pressure sensitive papers
US3952132A|1976-04-20|Recording sheet
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US3703397A|1972-11-21|Mark-forming record materials and process for their use
DE2826754C3|1980-12-11|Copy receiving sheet for pressure sensitive copier systems
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US4567496A|1986-01-28|Pressure-sensitive recording sheets
US5017546A|1991-05-21|Alkyl salicylate developer resin for carbonless copy paper and imaging use
US3732141A|1973-05-08|Pressure-sensitive record material
GB2030588A|1980-04-10|Recording sheet
US3834929A|1974-09-10|Color developer sheet for pressure sensitive recording paper
GB2100311A|1982-12-22|Microcapsule sheet for pressure-sensitive recording paper
同族专利:
公开号 | 公开日
DK134311B|1976-10-18|
JPS5525998B1|1980-07-10|
NO137533C|1978-03-15|
ES402993A1|1975-12-16|
AT315210B|1974-05-10|
DE2228431B2|1973-11-22|
BR7202681D0|1973-06-12|
IT947925B|1973-05-30|
CA981988A|1976-01-20|
BE784786A|1972-10-02|
US3732120A|1973-05-08|
DE2228431A1|1972-12-21|
GB1348362A|1974-03-13|
FR2141855A1|1973-01-26|
CH563247A5|1975-06-30|
SE373784B|1975-02-17|
DK134311C|1977-03-14|
FR2141855B1|1980-04-25|
AR200714A1|1974-12-13|
NL151663B|1976-12-15|
NL7207992A|1972-12-18|
DE2228431C3|1974-06-20|
NO137533B|1977-12-05|
ZA72742B|1972-10-25|
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法律状态:
优先权:
申请号 | 申请日 | 专利标题
US15283071A| true| 1971-06-14|1971-06-14|
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