US2221420A - Article of manufacture - Google Patents

Article of manufacture Download PDF

Info

Publication number
US2221420A
US2221420A US175252A US17525237A US2221420A US 2221420 A US2221420 A US 2221420A US 175252 A US175252 A US 175252A US 17525237 A US17525237 A US 17525237A US 2221420 A US2221420 A US 2221420A
Authority
US
United States
Prior art keywords
sheet
olefin composition
composition
fibres
cement
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US175252A
Inventor
George W Clarvoe
Lester A H Baum
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Johns Manville Corp
Johns Manville
Original Assignee
Johns Manville
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Johns Manville filed Critical Johns Manville
Priority to US175252A priority Critical patent/US2221420A/en
Application granted granted Critical
Publication of US2221420A publication Critical patent/US2221420A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/02Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing hydraulic cements other than calcium sulfates
    • C04B28/04Portland cements
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/18Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing mixtures of the silica-lime type
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2111/00Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/20Resistance against chemical, physical or biological attack
    • C04B2111/27Water resistance, i.e. waterproof or water-repellent materials
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2111/00Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/20Resistance against chemical, physical or biological attack
    • C04B2111/28Fire resistance, i.e. materials resistant to accidental fires or high temperatures
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31652Of asbestos

Definitions

  • the invention relates to a sheet product, including an intimate mixture of fibres and a'calcareous cementing agent, and an olefin composition of kind to be described extending throughout the outer portions at least of the article.
  • Sheets made in accordance with the invention ,0 are useful for structural purposes. They-have advantages over impregnated asbestos-cement sheets previously known, especially for use at elevated temperatures such as would cause excessive warping of the sheets or burning out of the impregnating material in articles heretofore used at those temperatures.
  • FIGs. 1 and 2 show perspective views, partly broken away for clearness of illustration, of portions of sheets made in accordance with the invention.
  • sheet products including a cementing material I0, fibres ll distributed throughout the cement, and impregnating mate
  • impregnating material In the article shown in Fig. l the impregnating material extends throughout the entire sheet, from face to back, whereas in the article shown in Fig. 2 the material impregnates the outer portions only of the sheet. In either case, the impregnating material may extend over all edges of the sheet.
  • the base sheet is made by forming an intimate mixture of asbestos fibres, lime, finely dividedsilica,.and water, shaping, compressing, and then hardening the compressed material.
  • the asbestos fibres used may be Canadian chrysotile of about the fibre length commonly used in the manufacture of asbe shingles or siding units. For best results, however, the fibres are longer and more resilient, such as well dispersed amosite fibres, either alone or mixed with chrysotile fibres.
  • the proportion of fibres may be about to '70 parts by weight to 100 parts of the total dry weight of materials in the sheet.
  • silica used should be so finely ground that it reacts readily with the lime, under the influsheet into which stos-cement 8, 1937 Serial No. 175,252
  • the proportion of lime and silica may be varied somewhat, say, between to parts by weight or somewhat more of silica to 56 parts 10 of lime. There is used, preferably, approximately chemically equivalent amounts of the silica and lime. In any case, there should not be used such proportions that any substantial amount of free lime will appear in the finished product, when 15 the finished product during use is to be exposed to moisture.
  • the wet mixture is shaped into sheet form and strongly compressed, to remove some of the 25 water.
  • the mixture may be introduced into the bed of a hydraulic press provided with a filtering bottom and subjected there to high compression. It may be compressed, for example, at about 200 lac-1,300 pounds or more to 30 the square inch.
  • the ram used to apply the pressure should have a face, smooth or otherwise, to impart to a face of the sheet the desired facial planeness or configuration.
  • the apparatus described herein is not illus- 35 trated inasmuch as it is conventional.
  • the thus shaped and strongly compressed, wet sheet is subjected to: an elevated temperature, to cause reaction between the lime and the silica,
  • the steam-curing is effected preferably at a steam pressure of around 50 to 150 pounds to the square inch, a pressure of about pounds being preferred and the steam pressure being in- 45 creased very slowly to the selected maximum.
  • the p-riod of steaming to effect the reaction desired will vary with the temperature used and is longer the lower the maximum temperature. It is ordinarily sufficientto steam until the sheet 50 comes to have the selected maximum temperature practically throughout and then to continue the steaming for 2 or 3 hours longer.
  • the steam-cured sheet is then dried until its moisture content is so low as not to interfere 66 with subsequent impregnation with a water-repellent fluid.
  • the sheet may be dried at relatively low temperatures until it contains only a few per cent of water.
  • the sheet is then more completely dried at temperatures above the boiling point of water, say to the extent produced by being maintained at about 350 F. for 1 to 2 hours, with relatively free air circulation over the sheet.
  • the sheet is then impregnated.
  • the impregnating material is an olefin composition adapted to be resinified by heat, that is, to be made into a product that, after'cooling, is either hard or extremely viscous.
  • the composition separated by the fullers earth or clay, in the Gray tower process from products of the cracking of petroleum.
  • Particularly desirable is the product so separated from gasoline that has been made by cracking petroleumv in the vapor phase at high temperatures of the order of 1,000 to 1,200 F.
  • the preparation of this olefin composition is not a part of the present invention.
  • the olefin composition absorbed or separated from the gasoline fraction, in the tower process referred to may be recovered from the tower by any usual process.
  • gasoline and other solvents in vapor phase are passed over fullers earth, on which condensation of olefins takes place.
  • the condensed olefins are recovered by draining from the earth suitablycontinuously.
  • the tower may be warmed to an elevated temperature making the condensed olefin composition relatively mobile and adapted to flow readily from the tower. Excessive heating as well as baking at this point is avoided.
  • the olefin composition so recovered in the condition in which it is marketed and initially used by us, contains a substantial amount of volatile material.
  • the "resinifying to which we have referred is due largely or wholly to loss of volatile material or to polymerization or other chemical change that occurs on baking is immaterial to our invention. Without commitment to any theory of explanation, we include under resinifying" all thickening and/or hardening produced by baking.
  • a typical olefin composition so recovered has the following features:
  • the heat-resiniiying olefin composition is impregnated into the base sheet that has been made and dried as described above. For this purpose,
  • the said composition is first reduced in viscosity, as by being-heated to 300 to 400 F.
  • the sheet is then immersed in the warm composition and kept immersed therein until the impregnation has proceeded to the depth desired.
  • an impr'egnation of about A; to a; of an inch we immerse the dried sheet in the olefin composition for about 15 to 60 minutes, at 350 F.
  • the impregnated sheet is removed from the olefin composition, is allowed to drain'for a few minutes, and is then subjected to treatment to harden or resinify the said composition.
  • the impregnated sheet is baked for about onehalf hour to 6 hours at temperatures of approximately 275 to 400 F., the duration and temperature of the baking operation depending in part upon the viscosity or hardness desired in the impregnating composition in the finished article.
  • the duration and temperature of the baking operation depending in part upon the viscosity or hardness desired in the impregnating composition in the finished article.
  • we have found satisfactory period of time for drying, impregnation, and baking may be varied with the thickness of the sheets, being made. generally longer the thicker the sheets, and vice versa.
  • the method described is preferably modified slightly to produce the best results.
  • an admixed agent to prevent ashing of the olefin composition when the finished product is used at very high temperatures, as, for instance, at 450 to 500 F.
  • antioxidants for the olefin composition are used in very small proportion, as, for example, in proportion of the order of 1% of the weight of the olefin composition, such as to 2 or 3% or so.
  • the exact amount of antioxidant to be used depends in part upon the eflectiveness per unit of the agent selected and in part also upon the degree of protection required, the latter being determined by the conditions under which the finished article is to be used.
  • phthalic anhydride A very satisfactory agent to use with the olefin composition, for the purpose described, is phthalic anhydride. Besides decreasing the tendency to ashing, phthalic anhydride assists in the impregnation. It causes the olefin composition to penetrate more readily into the base sheet than is the case if the phthalic anhydride is omitted. Thus, the use of 1% of phthalic anhydride on the weight of the olefin practically doubles the rate of penetration of the olefin composition.
  • antioxidants may be mixed with the olefin composition, in place of the phthalic anhydride, as, for example, phenylcnediamine and gum guaiae.
  • Hydroquinone also possesses the property of reducing to some extent the ashing of the olefin composition at elevated temperatures.
  • the use of phthalic anhydride is especially advantageous.
  • the time required for impregnation may be shortened somewhat.
  • an antioxidant when used, the severity of baking conditions is increased, for a given hardness desired in the baked olefin composition. conducted for a half hour to three hours at temperatures within the range 325 to 450 F., ordinarily'the time being shortened as the temperature increases, within these ranges. For'insta'nce, very desirable conditions are one hour's baking at 400 F., or two hours at 350 F.
  • the resistance to ashing of products made as described may be illustrated by data for a specimen using phthalic anhydride as the antioxidant. With 1%. of phthalic anhydride on the weight of the olefin composition, a sheet made as described is substantially non-ashing when maintained in contact with air at a temperature of 500 F. for 5 to 6 hours. Any ashing produced is extremely slight and is confined to a very thin superficial layer. In fact, some specimens show practically no ashing under the conditions stated.
  • the improved sheets made in accordance with this invention may be used directly without any such prewarping and subsequent planing.
  • a typical sheet made by us showed a warpage of only 0.007 inch in 24 inches when baked at 300 F. for 4 hours.
  • the product is satisfactorily resistant to abrasion, either before or after beingheated to the temperature used in testing warpage.
  • the product is water-resistant, on the one hand, and, on the other, sufficiently porous to permit satisfactorily uniform drying of wet core plates supported thereupon and heated in the usual core drying or baking ovens, at tem- 20 peratures ranging up to about 500 F.
  • Another type of base sheet may be substituted for the lime-silica-fibre sheet described above for impregnation by the olefin composition.
  • a fibre-reenforced cement 5 composition the cement being either Portland or a cement of high calcium alumihate content (cement fondu or Lumnite cement).
  • Portland cement' is used, thene is preferably admixed with it finely divided silica in amount 30 adequate theoretically to convert all of the basic ingredients of the Portland cement to monosilicates.
  • the cement composition with the admixed silica is cured by steaming, say, at' a pressure of saturated steam of 75 to 35 150 pounds to the square inch, maintained i contact with the sheet for several hours.
  • the fibre-reenforced cement sheet is dried and the heat-resinifyins olefin composition is impregnated and baked, in the manner described 40 above.
  • An antioxidant is used in case the-finished article is to be subjected during-use to temperatures that would cause ashing-in the absence of the antioxidant.
  • asbestos-cement sheets 45 made in regular manner, with plane face and without any sanding, if impregnated with the olefin composition described and then baked for several hours at about 300 F., do not warp badly during the said baking or during use as supports for foundry cores in the core drying or baking ovens.
  • the Portland cement, calcium aluminate cement, and calcium silicate formed by steam curing a mixture of lime and finely divided silica 55 are examples of a calcareous cementing material. While asbestos is preferred for the fibrous material of our improved sheets, other fibres may be used when the finished product is to be used at low or ordinary temperatures. In such so a case, there'may be used wood fibres, iute,hemp,
  • asbestos there may be used, besides asbestos, other mineral fibres, as for example, mineral wool, when the particularly desirable properties of asbestos are not necessary.
  • a dense, substantially non-warping, water resistant board comprising a calcareous cementing material, fibres distributed therethroughout, and a resinous polymerized olefin composition 5 impregnated into the article.
  • a dense, substantially non-warping, water resistant board comprising a calcareous cementing material, reenforcing fibres distributed therethroughout, and a resinous polymerized olefin 10 composition impregnating the outer; portions only of the article.
  • a dense, substantially non-warping, water resistant board comprising a sheet, including fibres and a binder therefor consisting of the product of a chemically reacted mixture of lime and finely divided silica, and a resinified olefin composition in resinous condition extendingthroughout the outer portions of the sheet.
  • a dense, substantially non-warping, water resistant board comprising a sheet, including fibres and a binder therefor consisting of the, product of a chemically reacted mixture of lime and finely divided silica, and a. resinified olefin composition in resinous condition extending throughout the outer portions ofthe sheet, the olefin composition including an antioxidant for the said composition. 5.
  • a dense, substantially non-warping, water resistant board comprising a sheet, including fibres and a binder therefor consisting of the product of a chemically reacted mixture of lime and finely divided silica, and a resinified olefin composition in resinous condition extending throughout the outer portions of the sheet, the said olefin composition including a small proportion of phthalic anhydride.
  • a dense, substantially non-warping, water resistant board comprising a sheet, including asbestos fibres and a binder therefor consisting of the reacted product of lime and finely divided silica, and'a resinous polymerized olefin composi-. tion extending throughout the outer portions of the sheet.
  • a dense, substantially non-warping, water resistant board comprising a sheet, including an intimate mixture of asbestos fibres and Portland cement in hardened condition, and a resinous polymerized olefin composition extending throughout the outer portions of the sheet.
  • a dense, substantially non-warping, water resistant board for use as a supporting plate for hot objects, comprising an intimate mixture of asbestos fibres and wheat-resistant calcareous cement in shaped and hardened condition and a polymerized resinous olefin composition impregnating the outer portions of the sheet.
  • a dense, substantially non-warping, water resistant board for use as a supporting plate for hot objects, comprising an intimate mixture of asbestos fibres and a heat-resistant calcareous cement in shaped and hardened condition and a polymerized resinous olefin composition impregnating the outer portions of the sheet, the olefin, composition including a very small proportion on the order of about 1% of admixed antioxidant for the said composition.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Laminated Bodies (AREA)

Description

0 2 2 2 L AW T E 0mm .VM. M N 1Q .mm 1 rm G Nov. 12, 19 40.
zzzvroRs.
ATTORNEY INV GEORGE W. CLAE LESTER A, H 5/! Patented Nov. 12, .1940
UNITED STATES V PATENT OFFICE Baum, Plainfield, N.
J.-, assignors to Johns- Manville Corporation, New York, N. Y., a corporation of New York Application November 1 9 Claims.
This invention facture.
More particularly, the invention relates to a sheet product, including an intimate mixture of fibres and a'calcareous cementing agent, and an olefin composition of kind to be described extending throughout the outer portions at least of the article.
Sheets made in accordance with the invention ,0 are useful for structural purposes. They-have advantages over impregnated asbestos-cement sheets previously known, especially for use at elevated temperatures such as would cause excessive warping of the sheets or burning out of the impregnating material in articles heretofore used at those temperatures.
The invention is illustrated in the attached drawing and will be exemplified by description in connection therewith.
Figs. 1 and 2 show perspective views, partly broken away for clearness of illustration, of portions of sheets made in accordance with the invention.
There are shown sheet products including a cementing material I0, fibres ll distributed throughout the cement, and impregnating materelates to an article oi manurial l2, In the article shown in Fig. l the impregnating material extends throughout the entire sheet, from face to back, whereas in the article shown in Fig. 2 the material impregnates the outer portions only of the sheet. In either case, the impregnating material may extend over all edges of the sheet.
The invention will be illustrated specifically by the following detailed example.
There is first made the base the impregnating material is later to be introduced. i
In one embodiment of the invention, the base sheet is made by forming an intimate mixture of asbestos fibres, lime, finely dividedsilica,.and water, shaping, compressing, and then hardening the compressed material.
The asbestos fibres used may be Canadian chrysotile of about the fibre length commonly used in the manufacture of asbe shingles or siding units. For best results, however, the fibres are longer and more resilient, such as well dispersed amosite fibres, either alone or mixed with chrysotile fibres. The proportion of fibres may be about to '70 parts by weight to 100 parts of the total dry weight of materials in the sheet.
The silica used should be so finely ground that it reacts readily with the lime, under the influsheet into which stos-cement 8, 1937 Serial No. 175,252
ence of steam at superatmospheric pressure, as, for instance, on curing for several hours at a pressure of saturated steam of 100 to 150 pounds to the square inch. We have used to advantage comminuted diatomaceous earth of about the l fineness that obtains in diatomaceous earth for use as filter aid in sugar refining.
The proportion of lime and silica may be varied somewhat, say, between to parts by weight or somewhat more of silica to 56 parts 10 of lime. There is used, preferably, approximately chemically equivalent amounts of the silica and lime. In any case, there should not be used such proportions that any substantial amount of free lime will appear in the finished product, when 15 the finished product during use is to be exposed to moisture. I
The selected ingredientsfibres, lime, and silica-are mixed thoroughly with each other and with water, the proportion of water used 20 being such as to render the mixture fluent and susceptible to ready and satisfactory shaping and consolidation.
The wet mixture is shaped into sheet form and strongly compressed, to remove some of the 25 water. Thus, the mixture may be introduced into the bed of a hydraulic press provided with a filtering bottom and subjected there to high compression. It may be compressed, for example, at about 200 lac-1,300 pounds or more to 30 the square inch. The ram used to apply the pressure should have a face, smooth or otherwise, to impart to a face of the sheet the desired facial planeness or configuration.
The apparatus described herein is not illus- 35 trated inasmuch as it is conventional.
The thus shaped and strongly compressed, wet sheet is subjected to: an elevated temperature, to cause reaction between the lime and the silica,
to give calcium silicate as the heat-resistant o calcareous cementing agent in the finished product. The steam-curing is effected preferably at a steam pressure of around 50 to 150 pounds to the square inch, a pressure of about pounds being preferred and the steam pressure being in- 45 creased very slowly to the selected maximum. The p-riod of steaming to effect the reaction desired will vary with the temperature used and is longer the lower the maximum temperature. It is ordinarily sufficientto steam until the sheet 50 comes to have the selected maximum temperature practically throughout and then to continue the steaming for 2 or 3 hours longer.
The steam-cured sheet is then dried until its moisture content is so low as not to interfere 66 with subsequent impregnation with a water-repellent fluid. Thus, the sheet may be dried at relatively low temperatures until it contains only a few per cent of water. The sheet is then more completely dried at temperatures above the boiling point of water, say to the extent produced by being maintained at about 350 F. for 1 to 2 hours, with relatively free air circulation over the sheet.
The sheet is then impregnated. The impregnating material is an olefin composition adapted to be resinified by heat, that is, to be made into a product that, after'cooling, is either hard or extremely viscous. Thus, there may be used the composition separated by the fullers earth or clay, in the Gray tower process, from products of the cracking of petroleum. Particularly desirable is the product so separated from gasoline that has been made by cracking petroleumv in the vapor phase at high temperatures of the order of 1,000 to 1,200 F. The preparation of this olefin composition is not a part of the present invention. Also, the olefin composition absorbed or separated from the gasoline fraction, in the tower process referred to, may be recovered from the tower by any usual process. Thus gasoline and other solvents in vapor phase are passed over fullers earth, on which condensation of olefins takes place. The condensed olefins are recovered by draining from the earth suitablycontinuously. The tower may be warmed to an elevated temperature making the condensed olefin composition relatively mobile and adapted to flow readily from the tower. Excessive heating as well as baking at this point is avoided.
, The olefin composition so recovered, in the condition in which it is marketed and initially used by us, contains a substantial amount of volatile material. Whether the "resinifying to which we have referred is due largely or wholly to loss of volatile material or to polymerization or other chemical change that occurs on baking is immaterial to our invention. Without commitment to any theory of explanation, we include under resinifying" all thickening and/or hardening produced by baking.
A typical olefin composition so recovered has the following features:
Content of volatile material About 15% The heat-resiniiying olefin composition is impregnated into the base sheet that has been made and dried as described above. For this purpose,
the said composition is first reduced in viscosity, as by being-heated to 300 to 400 F. The sheet is then immersed in the warm composition and kept immersed therein until the impregnation has proceeded to the depth desired. For an impr'egnation of about A; to a; of an inch, we immerse the dried sheet in the olefin composition for about 15 to 60 minutes, at 350 F.
The impregnated sheet is removed from the olefin composition, is allowed to drain'for a few minutes, and is then subjected to treatment to harden or resinify the said composition. Thus, the impregnated sheet is baked for about onehalf hour to 6 hours at temperatures of approximately 275 to 400 F., the duration and temperature of the baking operation depending in part upon the viscosity or hardness desired in the impregnating composition in the finished article. For most purposes, we have found satisfactory period of time for drying, impregnation, and baking may be varied with the thickness of the sheets, being made. generally longer the thicker the sheets, and vice versa.
The method described is preferably modified slightly to produce the best results. In this modification there is' used an admixed agent to prevent ashing of the olefin composition, when the finished product is used at very high temperatures, as, for instance, at 450 to 500 F. For this purpose, we have found antioxidants for the olefin composition to be desirable. They are used in very small proportion, as, for example, in proportion of the order of 1% of the weight of the olefin composition, such as to 2 or 3% or so. The exact amount of antioxidant to be used depends in part upon the eflectiveness per unit of the agent selected and in part also upon the degree of protection required, the latter being determined by the conditions under which the finished article is to be used.
A very satisfactory agent to use with the olefin composition, for the purpose described, is phthalic anhydride. Besides decreasing the tendency to ashing, phthalic anhydride assists in the impregnation. It causes the olefin composition to penetrate more readily into the base sheet than is the case if the phthalic anhydride is omitted. Thus, the use of 1% of phthalic anhydride on the weight of the olefin practically doubles the rate of penetration of the olefin composition.
For some purposes, other antioxidants may be mixed with the olefin composition, in place of the phthalic anhydride, as, for example, phenylcnediamine and gum guaiae. Hydroquinone also possesses the property of reducing to some extent the ashing of the olefin composition at elevated temperatures. However, the use of phthalic anhydride is especially advantageous.
When there is used a penetrating agent, the time required for impregnation may be shortened somewhat. Also, when an antioxidant is used, the severity of baking conditions is increased, for a given hardness desired in the baked olefin composition. conducted for a half hour to three hours at temperatures within the range 325 to 450 F., ordinarily'the time being shortened as the temperature increases, within these ranges. For'insta'nce, very desirable conditions are one hour's baking at 400 F., or two hours at 350 F.
The resistance to ashing of products made as described may be illustrated by data for a specimen using phthalic anhydride as the antioxidant. With 1%. of phthalic anhydride on the weight of the olefin composition, a sheet made as described is substantially non-ashing when maintained in contact with air at a temperature of 500 F. for 5 to 6 hours. Any ashing produced is extremely slight and is confined to a very thin superficial layer. In fact, some specimens show practically no ashing under the conditions stated.
Products made as described have other interesting properties also.
They show very little warping at moderately elevated temperatures, as, for instance, when used as a support for cores or other objects to be dried or baked in foundry practice, as described in U. S. Patent 2,035,970, issued to Mac- Thus, the baking may be.
Ildowie on March 31, 1936. Whereas the impregnated sheets described by MacIldowie warp badly at foundry temperatures, unless the sheets are previously repeatedly baked to establish the permanent warpage therein and then planed, as
by sanding, the improved sheets made in accordance with this invention may be used directly without any such prewarping and subsequent planing. Thus, a typical sheet made by us showed a warpage of only 0.007 inch in 24 inches when baked at 300 F. for 4 hours.
Also, the product is satisfactorily resistant to abrasion, either before or after beingheated to the temperature used in testing warpage.
5 Finally, the product is water-resistant, on the one hand, and, on the other, sufficiently porous to permit satisfactorily uniform drying of wet core plates supported thereupon and heated in the usual core drying or baking ovens, at tem- 20 peratures ranging up to about 500 F.
Another type of base sheet may be substituted for the lime-silica-fibre sheet described above for impregnation by the olefin composition. Thus, there may be used a fibre-reenforced cement 5 composition, the cement being either Portland or a cement of high calcium alumihate content (cement fondu or Lumnite cement). When Portland cement' is used, thene is preferably admixed with it finely divided silica in amount 30 adequate theoretically to convert all of the basic ingredients of the Portland cement to monosilicates. In such case, the cement composition with the admixed silica is cured by steaming, say, at' a pressure of saturated steam of 75 to 35 150 pounds to the square inch, maintained i contact with the sheet for several hours.
The fibre-reenforced cement sheet, is dried and the heat-resinifyins olefin composition is impregnated and baked, in the manner described 40 above. An antioxidant is used in case the-finished article is to be subjected during-use to temperatures that would cause ashing-in the absence of the antioxidant.
It has been found that asbestos-cement sheets 45 made in regular manner, with plane face and without any sanding, if impregnated with the olefin composition described and then baked for several hours at about 300 F., do not warp badly during the said baking or during use as supports for foundry cores in the core drying or baking ovens.
The Portland cement, calcium aluminate cement, and calcium silicate formed by steam curing a mixture of lime and finely divided silica 55 are examples of a calcareous cementing material. While asbestos is preferred for the fibrous material of our improved sheets, other fibres may be used when the finished product is to be used at low or ordinary temperatures. In such so a case, there'may be used wood fibres, iute,hemp,
or the like. Also, there may be used, besides asbestos, other mineral fibres, as for example, mineral wool, when the particularly desirable properties of asbestos are not necessary.
55 The details given are for the purpose of illustration, not restriction, and variations within the spirit of the invention are intended to be included in the scope of the appended claims.
What we claim is:
1. A dense, substantially non-warping, water resistant board comprising a calcareous cementing material, fibres distributed therethroughout, and a resinous polymerized olefin composition 5 impregnated into the article.
2. A dense, substantially non-warping, water resistant board comprising a calcareous cementing material, reenforcing fibres distributed therethroughout, and a resinous polymerized olefin 10 composition impregnating the outer; portions only of the article.
3. A dense, substantially non-warping, water resistant board comprising a sheet, including fibres and a binder therefor consisting of the product of a chemically reacted mixture of lime and finely divided silica, and a resinified olefin composition in resinous condition extendingthroughout the outer portions of the sheet.
4. A dense, substantially non-warping, water resistant board comprising a sheet, including fibres and a binder therefor consisting of the, product of a chemically reacted mixture of lime and finely divided silica, and a. resinified olefin composition in resinous condition extending throughout the outer portions ofthe sheet, the olefin composition including an antioxidant for the said composition. 5. A dense, substantially non-warping, water resistant board comprising a sheet, including fibres and a binder therefor consisting of the product of a chemically reacted mixture of lime and finely divided silica, and a resinified olefin composition in resinous condition extending throughout the outer portions of the sheet, the said olefin composition including a small proportion of phthalic anhydride.
6. A dense, substantially non-warping, water resistant board comprising a sheet, including asbestos fibres and a binder therefor consisting of the reacted product of lime and finely divided silica, and'a resinous polymerized olefin composi-. tion extending throughout the outer portions of the sheet.
7. A dense, substantially non-warping, water resistant boardcomprising a sheet, including an intimate mixture of asbestos fibres and Portland cement in hardened condition, and a resinous polymerized olefin composition extending throughout the outer portions of the sheet.
8. A dense, substantially non-warping, water resistant board, for use as a supporting plate for hot objects, comprising an intimate mixture of asbestos fibres and wheat-resistant calcareous cement in shaped and hardened condition and a polymerized resinous olefin composition impregnating the outer portions of the sheet.
9. ,A dense, substantially non-warping, water resistant board, for use as a supporting plate for hot objects, comprising an intimate mixture of asbestos fibres and a heat-resistant calcareous cement in shaped and hardened condition and a polymerized resinous olefin composition impregnating the outer portions of the sheet, the olefin, composition including a very small proportion on the order of about 1% of admixed antioxidant for the said composition.
' GEORGE W. CLARVOE.
LESTER A. H. BAUM.
US175252A 1937-11-18 1937-11-18 Article of manufacture Expired - Lifetime US2221420A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US175252A US2221420A (en) 1937-11-18 1937-11-18 Article of manufacture

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US175252A US2221420A (en) 1937-11-18 1937-11-18 Article of manufacture

Publications (1)

Publication Number Publication Date
US2221420A true US2221420A (en) 1940-11-12

Family

ID=22639564

Family Applications (1)

Application Number Title Priority Date Filing Date
US175252A Expired - Lifetime US2221420A (en) 1937-11-18 1937-11-18 Article of manufacture

Country Status (1)

Country Link
US (1) US2221420A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2442519A (en) * 1943-08-06 1948-06-01 United States Gypsum Co Insulating material and method of making same
US2633433A (en) * 1946-05-02 1953-03-31 Baldwin Hill Company Insulating material
US3027278A (en) * 1957-04-22 1962-03-27 Diversified Technology Inc Carbon coating
US3413140A (en) * 1965-01-04 1968-11-26 Nat Gypsum Co Coating of autoclaved asbestoscement products

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2442519A (en) * 1943-08-06 1948-06-01 United States Gypsum Co Insulating material and method of making same
US2633433A (en) * 1946-05-02 1953-03-31 Baldwin Hill Company Insulating material
US3027278A (en) * 1957-04-22 1962-03-27 Diversified Technology Inc Carbon coating
US3413140A (en) * 1965-01-04 1968-11-26 Nat Gypsum Co Coating of autoclaved asbestoscement products

Similar Documents

Publication Publication Date Title
US2944291A (en) Process for steam treating magnesium cement fibrous panels
US2307629A (en) Cementitious article of manufacture
NO158939B (en) PROCEDURE FOR THE MANUFACTURING OF BUILDINGS OR BUILDINGS.
US2221420A (en) Article of manufacture
US2247355A (en) Method of making a compressed and densified product
US2208511A (en) Method of making dense wall panels
US3090699A (en) Sag-resistant fiberboard and method of making same
US1358394A (en) Manufacture of phenolic condensation products
US2044213A (en) Process of manufacturing hard board
US2035970A (en) Moisture and heat resistant article and method of making the same
US1976684A (en) Structural material
GB2244995A (en) Bamboo fiber-reinforced inorganic molded product
US2170434A (en) Article of manufacture and method of making the same
US2623828A (en) Cementitious material and method of making
US1916333A (en) Impregnated product and process of manufacture
US2326517A (en) Method of manufacturing fibrous insulation
US1804740A (en) Waterproof and dielectric asbestos lumber
US1995412A (en) Cold molding and rolling fiber plastic
US1548146A (en) Abrasive form and process of making the same
DE3315357C2 (en) Process for the production of lightweight insulating and structural elements from amorphous silica, which is obtained during ferrosilicon production
JP3361351B2 (en) Manufacturing method of calcium silicate plate
US769087A (en) Process of manufacturing or producing asbestos millboards, slates, plates, or tiles.
US2196135A (en) Abradant
US2168445A (en) Article of manufacture
US1610211A (en) Building material and method for producing same