CA1144013A - Method for waterproofing paper - Google Patents
Method for waterproofing paperInfo
- Publication number
- CA1144013A CA1144013A CA000346547A CA346547A CA1144013A CA 1144013 A CA1144013 A CA 1144013A CA 000346547 A CA000346547 A CA 000346547A CA 346547 A CA346547 A CA 346547A CA 1144013 A CA1144013 A CA 1144013A
- Authority
- CA
- Canada
- Prior art keywords
- alkyl
- web
- paper
- methyl
- water
- 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
Links
- 238000000034 method Methods 0.000 title claims description 26
- 238000004078 waterproofing Methods 0.000 title description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 60
- 239000003054 catalyst Substances 0.000 claims abstract description 29
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 22
- 239000002904 solvent Substances 0.000 claims abstract description 17
- 230000002940 repellent Effects 0.000 claims abstract description 16
- 239000005871 repellent Substances 0.000 claims abstract description 16
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 15
- 238000009833 condensation Methods 0.000 claims abstract description 6
- 230000005494 condensation Effects 0.000 claims abstract description 6
- 239000007921 spray Substances 0.000 claims description 13
- 239000002253 acid Substances 0.000 claims description 10
- 238000006243 chemical reaction Methods 0.000 claims description 9
- 238000006460 hydrolysis reaction Methods 0.000 claims description 8
- 150000002978 peroxides Chemical group 0.000 claims description 8
- 239000000047 product Substances 0.000 claims description 8
- 230000007062 hydrolysis Effects 0.000 claims description 7
- BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical group CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 claims description 5
- 229920005573 silicon-containing polymer Polymers 0.000 claims description 5
- 239000011248 coating agent Substances 0.000 claims description 4
- 239000008199 coating composition Substances 0.000 claims description 4
- 238000000576 coating method Methods 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- 239000007788 liquid Substances 0.000 claims description 4
- 150000004973 alkali metal peroxides Chemical class 0.000 claims description 3
- GAURFLBIDLSLQU-UHFFFAOYSA-N diethoxy(methyl)silicon Chemical group CCO[Si](C)OCC GAURFLBIDLSLQU-UHFFFAOYSA-N 0.000 claims description 3
- 239000007787 solid Substances 0.000 claims description 3
- CPUDPFPXCZDNGI-UHFFFAOYSA-N triethoxy(methyl)silane Chemical group CCO[Si](C)(OCC)OCC CPUDPFPXCZDNGI-UHFFFAOYSA-N 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 239000007795 chemical reaction product Substances 0.000 claims description 2
- 239000004615 ingredient Substances 0.000 claims description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 2
- 239000011707 mineral Substances 0.000 claims description 2
- 239000011148 porous material Substances 0.000 claims description 2
- SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 claims description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical group C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims 1
- PKTOVQRKCNPVKY-UHFFFAOYSA-N dimethoxy(methyl)silicon Chemical group CO[Si](C)OC PKTOVQRKCNPVKY-UHFFFAOYSA-N 0.000 claims 1
- 239000007789 gas Substances 0.000 claims 1
- 238000011282 treatment Methods 0.000 abstract description 10
- 125000003545 alkoxy group Chemical group 0.000 abstract description 3
- 238000004519 manufacturing process Methods 0.000 abstract 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 24
- 229910000077 silane Inorganic materials 0.000 description 24
- 239000000463 material Substances 0.000 description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 11
- 239000006227 byproduct Substances 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- 238000005507 spraying Methods 0.000 description 8
- -1 organo silicon halide Chemical class 0.000 description 7
- 229910052710 silicon Inorganic materials 0.000 description 7
- 239000010703 silicon Substances 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 6
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- RLJWTAURUFQFJP-UHFFFAOYSA-N propan-2-ol;titanium Chemical group [Ti].CC(C)O.CC(C)O.CC(C)O.CC(C)O RLJWTAURUFQFJP-UHFFFAOYSA-N 0.000 description 5
- VXUYXOFXAQZZMF-UHFFFAOYSA-N tetraisopropyl titanate Substances CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 5
- 150000001298 alcohols Chemical class 0.000 description 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 239000003921 oil Substances 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 125000002524 organometallic group Chemical group 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 2
- 229960000583 acetic acid Drugs 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 238000007865 diluting Methods 0.000 description 2
- YYLGKUPAFFKGRQ-UHFFFAOYSA-N dimethyldiethoxysilane Chemical compound CCO[Si](C)(C)OCC YYLGKUPAFFKGRQ-UHFFFAOYSA-N 0.000 description 2
- 231100000053 low toxicity Toxicity 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- XXQBEVHPUKOQEO-UHFFFAOYSA-N potassium superoxide Chemical compound [K+].[K+].[O-][O-] XXQBEVHPUKOQEO-UHFFFAOYSA-N 0.000 description 2
- 238000009877 rendering Methods 0.000 description 2
- PFUVRDFDKPNGAV-UHFFFAOYSA-N sodium peroxide Chemical compound [Na+].[Na+].[O-][O-] PFUVRDFDKPNGAV-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 2
- IJOOHPMOJXWVHK-UHFFFAOYSA-N trimethylsilyl-trifluoromethansulfonate Natural products C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 2
- 210000002268 wool Anatomy 0.000 description 2
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
- HRWFFDJQZODCGS-UHFFFAOYSA-N 2-methoxyethoxy(methyl)silane Chemical compound COCCO[SiH2]C HRWFFDJQZODCGS-UHFFFAOYSA-N 0.000 description 1
- VXEGSRKPIUDPQT-UHFFFAOYSA-N 4-[4-(4-methoxyphenyl)piperazin-1-yl]aniline Chemical compound C1=CC(OC)=CC=C1N1CCN(C=2C=CC(N)=CC=2)CC1 VXEGSRKPIUDPQT-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 239000005456 alcohol based solvent Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 210000000476 body water Anatomy 0.000 description 1
- FPCJKVGGYOAWIZ-UHFFFAOYSA-N butan-1-ol;titanium Chemical compound [Ti].CCCCO.CCCCO.CCCCO.CCCCO FPCJKVGGYOAWIZ-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000012159 carrier gas Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- JJQZDUKDJDQPMQ-UHFFFAOYSA-N dimethoxy(dimethyl)silane Chemical compound CO[Si](C)(C)OC JJQZDUKDJDQPMQ-UHFFFAOYSA-N 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 230000005661 hydrophobic surface Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- XQSFXFQDJCDXDT-UHFFFAOYSA-N hydroxysilicon Chemical compound [Si]O XQSFXFQDJCDXDT-UHFFFAOYSA-N 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- JLUFWMXJHAVVNN-UHFFFAOYSA-N methyltrichlorosilane Chemical compound C[Si](Cl)(Cl)Cl JLUFWMXJHAVVNN-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 230000009972 noncorrosive effect Effects 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 238000013031 physical testing Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 150000003377 silicon compounds Chemical class 0.000 description 1
- 239000005049 silicon tetrachloride Substances 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/50—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with organometallic compounds; with organic compounds containing boron, silicon, selenium or tellurium atoms
- D06M13/51—Compounds with at least one carbon-metal or carbon-boron, carbon-silicon, carbon-selenium, or carbon-tellurium bond
- D06M13/513—Compounds with at least one carbon-metal or carbon-boron, carbon-silicon, carbon-selenium, or carbon-tellurium bond with at least one carbon-silicon bond
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/03—Non-macromolecular organic compounds
- D21H17/05—Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
- D21H17/13—Silicon-containing compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Paper (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
ABSTRACT OF THE DISCLOSURE
An improved water repellent cellulosic web and a method of making the same which involves treating the web with an alkyl alkoxysiloxane containing at least one methyl group and at least two lower alkoxy groups in the presence of a condensa-tion catalyst and curing the resulting treated web for a time sufficient to increase the water repellency thereof. The treat-ment can be carried out in the presence of a solvent or in the absence of a solvent.
-i-
An improved water repellent cellulosic web and a method of making the same which involves treating the web with an alkyl alkoxysiloxane containing at least one methyl group and at least two lower alkoxy groups in the presence of a condensa-tion catalyst and curing the resulting treated web for a time sufficient to increase the water repellency thereof. The treat-ment can be carried out in the presence of a solvent or in the absence of a solvent.
-i-
Description
.
BACKGROUND OF T~IE INVENTION
FIELD OF THE INVENTION
The present invention is in the field of treating cellulosic webs such as paper webs for the purpose of rendering at least one surface thereof water repellent while retaining the inherent porosity and strength of the paper web.
DESCRIPTION OF THE P~IOR ART
There have been some disclosures in prior patents regarding the treatment of various materials with organic silicon compounds in order to render them water repellent.
For example, in U.S. Patent No. 2,306,222 to Patnode, there is a disclosure of treating various materials, including paper, with an organo-silicon halide such as methyl silicon chloride in vapor form to render the body water repellent. It was hypothesized that the organo-silicon halide vapors react with an adsorbed film of water to form the corresponding silicol which is strongly adsorbed and water repellent, or results in the formation of a water repellent silicone.
U.S. Patent No. 2,386,259 to Norton refers to the treatment of fabrics or paper to make them water repellent by treating such materials with the product obtained by the hydrolysis of a methyldihalogensilane.
Norton in U.S~ Patent No. 2,412,470 described a process for treating a solid body to render it water repellent which involved treating the same with a mixture containing about
BACKGROUND OF T~IE INVENTION
FIELD OF THE INVENTION
The present invention is in the field of treating cellulosic webs such as paper webs for the purpose of rendering at least one surface thereof water repellent while retaining the inherent porosity and strength of the paper web.
DESCRIPTION OF THE P~IOR ART
There have been some disclosures in prior patents regarding the treatment of various materials with organic silicon compounds in order to render them water repellent.
For example, in U.S. Patent No. 2,306,222 to Patnode, there is a disclosure of treating various materials, including paper, with an organo-silicon halide such as methyl silicon chloride in vapor form to render the body water repellent. It was hypothesized that the organo-silicon halide vapors react with an adsorbed film of water to form the corresponding silicol which is strongly adsorbed and water repellent, or results in the formation of a water repellent silicone.
U.S. Patent No. 2,386,259 to Norton refers to the treatment of fabrics or paper to make them water repellent by treating such materials with the product obtained by the hydrolysis of a methyldihalogensilane.
Norton in U.S~ Patent No. 2,412,470 described a process for treating a solid body to render it water repellent which involved treating the same with a mixture containing about
2.8 to 99.2% by ~eight of trimethyl silicon chloride and about 97.2 to 0.8% by weight of silicon tetrachloride.
U.S. Patent No. 2,961,338 to Robbart refers to a process of treating wool to render the same water repellent by reacting the same with an organo silicon halide in vapor -~
,~
form while the wool is at a relatively low moisture content.
Robbart in U.S. Patent No. 2,995,470 described a continuous process for treating material with vapors of a waterproofing substance such as an organo silicon halide wherein vapors of the treating reagent mixed with an inert carrier gas were introduced into an enclosed treating zone while a length of the material to be treated was passed continuously through the zone. Downstream from the reaction zone the spent vapors, including the by-products, were exhausted from the system.
The objective here was to remove the by-products as rapidly as possible so that they did not have an opportunity to build up appreciably in concentration.
Finally, in U.S. Patent No. 3,856,558 Robbart suggested rendering cellulosic materials water repellent by contacting the same while they have a water content between 2 and 7 weight percent with vapors of a lower alkyl silicon halide which reacts with water to form a siloxane and maintaining the cellulosic material and halide in contact between 0.1 and 8 seconds. The cond1tions are such that the cellulosic material being contacted is rendered water repellent and has a pH greater than 2.5. The objective of this technique was to eliminate the subsequent step of neutraIizing hydrogen chloride formed as a by-product of the alkyl silicon halide reaction with water.
While these disclosures appear in the prior art, the prior art has yet to come up with a method and composition for treating paper or other cellulosic products with silane solutions which is commercially acceptable. In those instances in which an alkyl silicon halide is used, the disposition of the resulting hydrogen chloride vapor has posed serious problems because of the corrosiveness of the hydrogen chloride, the contamination of the atmosphere, and the weakening of the paper 4~3
U.S. Patent No. 2,961,338 to Robbart refers to a process of treating wool to render the same water repellent by reacting the same with an organo silicon halide in vapor -~
,~
form while the wool is at a relatively low moisture content.
Robbart in U.S. Patent No. 2,995,470 described a continuous process for treating material with vapors of a waterproofing substance such as an organo silicon halide wherein vapors of the treating reagent mixed with an inert carrier gas were introduced into an enclosed treating zone while a length of the material to be treated was passed continuously through the zone. Downstream from the reaction zone the spent vapors, including the by-products, were exhausted from the system.
The objective here was to remove the by-products as rapidly as possible so that they did not have an opportunity to build up appreciably in concentration.
Finally, in U.S. Patent No. 3,856,558 Robbart suggested rendering cellulosic materials water repellent by contacting the same while they have a water content between 2 and 7 weight percent with vapors of a lower alkyl silicon halide which reacts with water to form a siloxane and maintaining the cellulosic material and halide in contact between 0.1 and 8 seconds. The cond1tions are such that the cellulosic material being contacted is rendered water repellent and has a pH greater than 2.5. The objective of this technique was to eliminate the subsequent step of neutraIizing hydrogen chloride formed as a by-product of the alkyl silicon halide reaction with water.
While these disclosures appear in the prior art, the prior art has yet to come up with a method and composition for treating paper or other cellulosic products with silane solutions which is commercially acceptable. In those instances in which an alkyl silicon halide is used, the disposition of the resulting hydrogen chloride vapor has posed serious problems because of the corrosiveness of the hydrogen chloride, the contamination of the atmosphere, and the weakening of the paper 4~3
- 3 -strength by its presence.
SUMMARY OF THE INVENTION
The present invention provides the method of improving the water repellency of a naturally porous paper web con-taining about 2 to 14% moisture by weight which comprises:
treating said web with a coating composition contain-ing as its active coating ingredient an alkyl alkoxysil-oxane having the formula:
~ CH3 ,~ , I
A- Si - B
B
/
; where A is H, CH3, or B and B is an OR group in which R is methyl or ethyl, said coating composition being in liquid form and being substantially devoid of solids, said treating being carried out in the presence of a '! condensation catalyst, and reacting said alkyl alkoxysilane with the water con-tained in said web to thereby prod~ce a water repellent paper wab in which the reaction product impregnates within the pores of the paper to render the paper water repellent while said paper retains substantially the porosity and strength characteristics of the untreated web.
, The process of the present invention can supplement l 25 or replace conventional wet end sizing systems. It is ap-- plied to the dry web by means of a spray giving maximum efficiency of use of the treating chemical. The reaction by-products, consisting of a lower alcohol, are non-cor-rosive and of low toxicity. The effect of the treatment on paper is to produce a strong resistance to water while retaining the same porosity and strength characteristics of ' the untreated sheet. The treatment of the present inven-tion can be applied to one or both sides of the sheet and the degree of water resistance can be controlled by con-.~ .
j~ ,f
SUMMARY OF THE INVENTION
The present invention provides the method of improving the water repellency of a naturally porous paper web con-taining about 2 to 14% moisture by weight which comprises:
treating said web with a coating composition contain-ing as its active coating ingredient an alkyl alkoxysil-oxane having the formula:
~ CH3 ,~ , I
A- Si - B
B
/
; where A is H, CH3, or B and B is an OR group in which R is methyl or ethyl, said coating composition being in liquid form and being substantially devoid of solids, said treating being carried out in the presence of a '! condensation catalyst, and reacting said alkyl alkoxysilane with the water con-tained in said web to thereby prod~ce a water repellent paper wab in which the reaction product impregnates within the pores of the paper to render the paper water repellent while said paper retains substantially the porosity and strength characteristics of the untreated web.
, The process of the present invention can supplement l 25 or replace conventional wet end sizing systems. It is ap-- plied to the dry web by means of a spray giving maximum efficiency of use of the treating chemical. The reaction by-products, consisting of a lower alcohol, are non-cor-rosive and of low toxicity. The effect of the treatment on paper is to produce a strong resistance to water while retaining the same porosity and strength characteristics of ' the untreated sheet. The treatment of the present inven-tion can be applied to one or both sides of the sheet and the degree of water resistance can be controlled by con-.~ .
j~ ,f
- 4 -trolling the severity of the treatment.
The alkyl alkoxysilane may be applied to the paper as such in the form of a spray, but is preferably introduced in the form of a solution in a suitable organic solvent such as a lower alcohol containing from 1 to 4 carbon ` atoms.
To cause the reaction between the alkoxysiloxane or its hydrolysis product to occur with the paper within reasonable ; t`imes, it is desirable to include a catalyst in the treating ` 10 mixture. Such catalyst may be a strong mineral acid, an alkali metal peroxide, or an organometallic catalyst dis-solved in a non-reactive organic solvent.
, After the spray application of the material to the web, the sprayed material can be cured by means of subjecting the `
same to a slightly elevated temperature of about 300F
(147C) or so for 15 to 60 seconds, or by leaving it at room temperature for at least 30 minutes.
BRIEF DESCRIPTION OF THE DRAWING
The single drawing in this application is a somewhat schematic view of a continuous system which can be used for applying the waterproofing material to a traveling paper web, and collecting and reusing the by-products.
,, .
DESCRIPTION OF THE PREFERRED E~BODIMENTS
In accordance with the present invention, a cellulosic paper web has its water repellency improved by treatment with a spray of an alkyl alkoxysiloxane or its hydrolysis product, the alkyl alkoxysiloxane having the following : formula:
A - Si - B
B
where A is H, CH3, or B and B is an OR group in which R is methyl or ethyl.
"':, j ~ ` f '~ --~
Examples of the alkoxysiloxanes coming under this generic expression are given below:
A. Methyl trimethoxysilane:
CH30 - Si - OCH3 B. Methyl triethoxysilane:
CH3CH20-- Si-- OCH2CH3 C. Dimethyl dimethoxysilane:
CH3 - Si - OCH3 : OCH3 D.. Dimethyl diethoxysilane:
CH3 - Si - OCH2CH3 ' E. Methyl aimethoxysilane:
H - Si - OCH3 ; ~5-~; F. Methyl diethoxysilane:
H - Si - OCH2CH3 G. Methyl methoxyethoxysilane:
H li - OCH2CH3 ~-~ OCH3 These alkoxysilanes react with water and cellulosic hydroxyl groups to produce a silicone polymer. The only by-product produced is a lower alcohol formed by hydrolysis of the alkoxy group. The alcohol by-product is relatively easy to dispose of, in contrast to hydrogen chloride, for example. Moreover, the surroundings can tolerate more of the alcohol than hydrogen chloride, as evidenced by the fact that the Environmental Protection Agency puts a limit of about 0.5 parts per million on hydrogen chloride in the atmosphere, ~ but the limit on methyl alcohol is on the order of 1,000 parts ; per million.
" The moisture content of the paper or other cellulosic base is not critical as long as it is within a reasonably dry range of about 2 to 14% by weight. The xeaction proceeds rapidly and to completion, particularly in the presence of a catalyst. The overall reaction is along the following lines:
:
l H 3 CH30-- Si-- OCH3 + 3H20 catalyst) ~,H
OCH3 ~IO-- Si-- OH + 3CH30H
OH
alkoxysilane hydroxysilane lCH3 1 r f fH3 1 HO-- Si -- OH + HO--- Si--- OHi~ ~ O--Si-- O-- Si O _ I I
OH OH _ OH OH _ x silicone polymer The silicone polymer sticks to the cellulose fibers forming a hydrophobic surface which provides a water repellency.
While the silane can be used as such, it is preferable to combine it with a diluting solvent so that it provides a solution of about 1 to 3% by volume of the silane. This pro- -vides the optimum coverage with the least waste. An average water repellent coating on paper can be produced with a solution containing 1.5 to 2~ by volume of the silane. The solvent used to dilute the silane can be nearly any volatile, anhydrous non-reactive organic liquid. ~he solvents which appear to work best for the solution are the lower alcohols containing 1 to 4 carbon atoms, such as ethanol or methanol.
Since the by-products are themselves alcohols, the use of alcohol solvents poses no additional disposal problem.
The speed and the extent of the polymerization is dependent on the type of catalyst used. There are three different categories of catalysts which are useful to polymerize the silanes: strong acids, peroxide condensation catalysts, and organometallic condensation catalys~s.
Concentrated strong acids lnclude materials such as sulfuric or nitric acid. Sulfuric acid appears to work best when added to the silane solution in the ratio of 1 ml of concentrated (95%) commercial acid to 250 ml silane solution. When the catalyst is added to the silane solution, a small amount of white precipitate may form due to water in the acid reacting with the silane. The paper is treated by spraying with the resulting solution and then curing. The curing can be accomplished by either heating at 300F (148C) for 15 to 60 seconds or allowing it to sit at room temperature for at least 30 minutes. Curing at room temperature is not very efficient because some silane loss will occur due to evaporation.
When treating the solution with a peroxide catalyst such as an alkali metal peroxide, the solvent can be the same as used in the case of a strong acid. In this technique, it is desirable that the silane be hydrolyzed before the peroxide catalyst is added. To accomplish this, a molar ratio of water equivalentto the number of alkoxy groups on the silane is added to the solution. An acid such as glacial acetic acid is added in a proportion of 1 ml acid to 400 ml solution to catalyze the hydrolysis. The solution should sit for at least one half hour to make sure that the silane is completely hydrolyzed. The hydrolysis reaction proceeds as follows:
CH30~ OCH3 ~ 3H20 HO--Si--OH + 3CH30H
A peroxide can be added to the hydrolysis product in the ratio of about 1 gram peroxide to 50') ml solution.
The best peroxide catalysts are sodium peroxide and potassium peroxide. This solution may be applied as a spray and the paper cured or 5 to 30 seconds at 300F (147C~ for 5 to 15 minutes at room temperature. These solutions are somewhat basic and therefore raise the pH of the paper. This dQes not necessarily damage the sheet although it is desirable to hold the paper as close to its original pH as possible.
In treating with an organometallic catalyst, the solvent for the silane must be anhydrous and cannot be an alcohol. This is because the catalyst will react with water and alcohols preventing catalyzation of the polymer. The sol~ent should be a non-reacti~e organic sol~ent such as benzene, pentane, trichloroethane, or trichloroethylene.
Trichloroethylene is the preferred solvent because it is non-flammable and has a low toxicity. A typical catalyst is tetra-iso-propyl titanate (TPT). This catalyst is added to the solution in the ratio of l ml TPT to 200 ml solution.
The solution is most advantageously applied by spraying.
The polymerization reaction is rapid and needs no curing or post-heating. Water repellency is imparted to the paper at the moment the spray contacts it. It has also been observed that during a period of several hours after the treatment there is a slight increase in the water repellency. This is due to short-chain silicone polymers joining to orm longer chains, thus giving a slight increase in hydrophobicity.
This solution does not affect the pH o the paper.
Organometallic tin compounds such as dibutyltin laurate, stannous oleate and tetrabutyl orthotitanate can also be used as catalysts. Tin compounds may be employed if the end use of the paper permits the presence of tin in the residual silicone.
_g_ A further description of the present invention will be made in conjunction with the attached drawiny which illustrates rather schematically a continuous system for treating paper with the improved process of the present invention.
In the accompanying Eigure, reference numeral 10 has been applied to a source of silane solution, usually in the form of a 1 to 3% by volume solution in a suitable organic solvent, but as will be hereinafter explained, the solvent need not always be present. The solution is withdrawn from the container 10 through a valve 11 where it is combined with a catalyst from a container 12. Metered amounts of the catalyst are provided from the container 12 through a valve 13 to be combined with the silane solution. The mixture of the two then passes through a conduit 14 into a pair of spray heads 15 and 16 which are arranged to treat opposite sides of a paper web 17. The paper web is guided over an upper guide roll 18, a lower guide roll 19, and a second upper guide roll 20 before it leaves the treating vessel generally indicated at reference numeral 21 in the drawings. Air for the spray heads 15 and 16 is supplied from a suitable source of compressed air ~not shown) through a valve 22 and is delivered to each of the spray heads.
The reaction between the catalyst-containing silane solution and the paper fibers is quite rapid. The only by-products of the reaction are the alcohol produced, the solvent used in the treating solution, and any unreacted silane. These products are directed by means of an effluent line 23 into a condenser 24. Here they are combined with additional amounts of alcohol which are recovered from the 4~
traveling web by means of vacuum boxes 25 and 26 positioned at the exit end of the chamber 21. The condensed materials, ; usually consisting mainly of alcohols, can then be recycled by means of a conduit 27 back into the silane solution con-tainer 10.
The following specific examples illustrate the manner in which the invention is carried out, and the improved results achieved.
EXample I
A sample of 100 lb. bleached, unsized board was treated by spraying with a treating solution containing approximately 2% by volume methyl trimethoxysilane, with the balance methanol and a catalyst consisting of 1 ml of sulfuric acid per 250 ml of solution. The treated sample was then heated for 15 seconds in a 300F (147C~ oven. The sample became quite water resistant.
Example II
~ A sample of 100 lb. bleached, unsized board was treated as in Example I, using dimethyl diethoxysilane as the treating agent. Results substantially the same as those in Example I were obtained.
Example III
Samples of 100 lb. bleached, unsized board were treated by spraying with a solution containing approximately 2% by volume methyl tximethoxysilane, water in an amount of 3 moles of water for everv mole'of silane, acetic acid in an amount of 1 ml acid for 400 ml solution, in a lower alcohol solvent, using a catalyst of sodium peroxide in an amount of ^ `"~
1 gram per 500 ml solution. The samples were heated for varying periods of time in a 300F (147C) oven. All of the sheets developed similar water resistant properties.
'Exa~pl'e''IV
A sample of 325 lb. bleached blotter paper was treated with the same solution as in Example III and heated for 15 seconds in a 300F (147C) oven. The paper de~eloped excellent water resistant properties, and was resistant to continuous running water.
Example V
A sample of 325 lb. bleached blotter paper was treated by spraying with a solution containing approximately 2~ by volume methyl trimethoxysilane, dissolved in benzene, and containing TPT in an amount of 1 ml per 200 ml of solution.
No heating was done. The treated sheet was very water resistant, including resistance to running water.
Examp'le VI
The paper stock was treated as in Example V, but given only a very light spraying. The sheet was slightly water resistant to drops of water, but not to running water.
EXa p'le VII
The paper was treated with the same composition as in Example V, but with a very heavy spraying. The sheet which resulted was very resistant to water under any conditions.
E'x'ample VIII
This example utilized the same composition and procedure as in Examples V and VII, but the paper was treated 4~
on one side only. ~oth lightly treated and heavily treated papers were resistant on the treated side, with the greatest resistance in the heavily treated sheet. The untreated side of the heavily treated sheet showed a very slight water resistance.
EXample'IX
A sample of 100 lb. N.S.S.C., unbleached board was treated by spraying with the composition described in Example V. No heating was done. The treated sheet was water resistant, although only slightly resistant to running water.
Examp'le'X
The procedure here was the same as in Example IX, except the board was given only a li~ht treatment. The resulting product was very slightly water resistant.
''Exampl'e'XI
This procedure and composition was the same as used in Example IX, only a heavy treatment was applied. The resulting board was very water resistant, including resistance to running water.
'Exam~le XII
The composition and method were the same as in Examples IX and XI, except that the board was treated on one side'only. The normally treated side was slightly water resistant, and the untreated side had no water resistance~
When héavily treated, the'sheet was very water resistant on the treated side and slightly resistant on the untreated side.
:
!; Example' XIII
A sample of newsprint was treated with the solution set forth in Example V. An increased water resistance was ' developed in the sheet.
:;
Example XIV
The silane may be applied to a moving web without '~ the use of a diluting solvent. In this case, a catalyst such , as TPT should be present in amounts of from 10 to 15% by ~' volume of solution for maximum polymerization efficiency.
The application to the moving web must be in the form of a fine spray that atomizes but does not vaporize the silane.
, The treating chamber should be well ventila~ed to remove any vaporized silane and titania by-product from the reaction.
Th'e application of the silane solution is most easily ,, controlled by applying it as a spray or in the form of an,:, aerosol. The spray can be adjusted to give the degree of coating desired as well as an even application. The solvent remaining in the paper can be removed by means of a vacuum or by heating.
Physical testing was done on some of these samples produced according to the examples set forth above. In the following table, "MD" refers to testing in the machine direction, and "C~lD" refers to the cross machine direction.
'rhe Z-tensile strength tests were per~ormed by applying a double sided adhesive tapP to the paper and s~tretching the same in an Instron machine. The brightness figures were derived from a General ~lectric birghtness meter. The Unger -lA-oil test consisted in clamping a ring on the paper, pouring on oil under the ring, wiping off excess oil, and then weighing the sheet. The water absorption test was performed by applying about 0.1 ml of water to the paper, reflecting a light off it, and measuring the time elapsed until the reflection stops.
4L0~3 -_ J,~ ~ o N ~ ,n ~ ~ o co ~) N
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o a) ~ o o ~ 1` U L~
The alkyl alkoxysilane may be applied to the paper as such in the form of a spray, but is preferably introduced in the form of a solution in a suitable organic solvent such as a lower alcohol containing from 1 to 4 carbon ` atoms.
To cause the reaction between the alkoxysiloxane or its hydrolysis product to occur with the paper within reasonable ; t`imes, it is desirable to include a catalyst in the treating ` 10 mixture. Such catalyst may be a strong mineral acid, an alkali metal peroxide, or an organometallic catalyst dis-solved in a non-reactive organic solvent.
, After the spray application of the material to the web, the sprayed material can be cured by means of subjecting the `
same to a slightly elevated temperature of about 300F
(147C) or so for 15 to 60 seconds, or by leaving it at room temperature for at least 30 minutes.
BRIEF DESCRIPTION OF THE DRAWING
The single drawing in this application is a somewhat schematic view of a continuous system which can be used for applying the waterproofing material to a traveling paper web, and collecting and reusing the by-products.
,, .
DESCRIPTION OF THE PREFERRED E~BODIMENTS
In accordance with the present invention, a cellulosic paper web has its water repellency improved by treatment with a spray of an alkyl alkoxysiloxane or its hydrolysis product, the alkyl alkoxysiloxane having the following : formula:
A - Si - B
B
where A is H, CH3, or B and B is an OR group in which R is methyl or ethyl.
"':, j ~ ` f '~ --~
Examples of the alkoxysiloxanes coming under this generic expression are given below:
A. Methyl trimethoxysilane:
CH30 - Si - OCH3 B. Methyl triethoxysilane:
CH3CH20-- Si-- OCH2CH3 C. Dimethyl dimethoxysilane:
CH3 - Si - OCH3 : OCH3 D.. Dimethyl diethoxysilane:
CH3 - Si - OCH2CH3 ' E. Methyl aimethoxysilane:
H - Si - OCH3 ; ~5-~; F. Methyl diethoxysilane:
H - Si - OCH2CH3 G. Methyl methoxyethoxysilane:
H li - OCH2CH3 ~-~ OCH3 These alkoxysilanes react with water and cellulosic hydroxyl groups to produce a silicone polymer. The only by-product produced is a lower alcohol formed by hydrolysis of the alkoxy group. The alcohol by-product is relatively easy to dispose of, in contrast to hydrogen chloride, for example. Moreover, the surroundings can tolerate more of the alcohol than hydrogen chloride, as evidenced by the fact that the Environmental Protection Agency puts a limit of about 0.5 parts per million on hydrogen chloride in the atmosphere, ~ but the limit on methyl alcohol is on the order of 1,000 parts ; per million.
" The moisture content of the paper or other cellulosic base is not critical as long as it is within a reasonably dry range of about 2 to 14% by weight. The xeaction proceeds rapidly and to completion, particularly in the presence of a catalyst. The overall reaction is along the following lines:
:
l H 3 CH30-- Si-- OCH3 + 3H20 catalyst) ~,H
OCH3 ~IO-- Si-- OH + 3CH30H
OH
alkoxysilane hydroxysilane lCH3 1 r f fH3 1 HO-- Si -- OH + HO--- Si--- OHi~ ~ O--Si-- O-- Si O _ I I
OH OH _ OH OH _ x silicone polymer The silicone polymer sticks to the cellulose fibers forming a hydrophobic surface which provides a water repellency.
While the silane can be used as such, it is preferable to combine it with a diluting solvent so that it provides a solution of about 1 to 3% by volume of the silane. This pro- -vides the optimum coverage with the least waste. An average water repellent coating on paper can be produced with a solution containing 1.5 to 2~ by volume of the silane. The solvent used to dilute the silane can be nearly any volatile, anhydrous non-reactive organic liquid. ~he solvents which appear to work best for the solution are the lower alcohols containing 1 to 4 carbon atoms, such as ethanol or methanol.
Since the by-products are themselves alcohols, the use of alcohol solvents poses no additional disposal problem.
The speed and the extent of the polymerization is dependent on the type of catalyst used. There are three different categories of catalysts which are useful to polymerize the silanes: strong acids, peroxide condensation catalysts, and organometallic condensation catalys~s.
Concentrated strong acids lnclude materials such as sulfuric or nitric acid. Sulfuric acid appears to work best when added to the silane solution in the ratio of 1 ml of concentrated (95%) commercial acid to 250 ml silane solution. When the catalyst is added to the silane solution, a small amount of white precipitate may form due to water in the acid reacting with the silane. The paper is treated by spraying with the resulting solution and then curing. The curing can be accomplished by either heating at 300F (148C) for 15 to 60 seconds or allowing it to sit at room temperature for at least 30 minutes. Curing at room temperature is not very efficient because some silane loss will occur due to evaporation.
When treating the solution with a peroxide catalyst such as an alkali metal peroxide, the solvent can be the same as used in the case of a strong acid. In this technique, it is desirable that the silane be hydrolyzed before the peroxide catalyst is added. To accomplish this, a molar ratio of water equivalentto the number of alkoxy groups on the silane is added to the solution. An acid such as glacial acetic acid is added in a proportion of 1 ml acid to 400 ml solution to catalyze the hydrolysis. The solution should sit for at least one half hour to make sure that the silane is completely hydrolyzed. The hydrolysis reaction proceeds as follows:
CH30~ OCH3 ~ 3H20 HO--Si--OH + 3CH30H
A peroxide can be added to the hydrolysis product in the ratio of about 1 gram peroxide to 50') ml solution.
The best peroxide catalysts are sodium peroxide and potassium peroxide. This solution may be applied as a spray and the paper cured or 5 to 30 seconds at 300F (147C~ for 5 to 15 minutes at room temperature. These solutions are somewhat basic and therefore raise the pH of the paper. This dQes not necessarily damage the sheet although it is desirable to hold the paper as close to its original pH as possible.
In treating with an organometallic catalyst, the solvent for the silane must be anhydrous and cannot be an alcohol. This is because the catalyst will react with water and alcohols preventing catalyzation of the polymer. The sol~ent should be a non-reacti~e organic sol~ent such as benzene, pentane, trichloroethane, or trichloroethylene.
Trichloroethylene is the preferred solvent because it is non-flammable and has a low toxicity. A typical catalyst is tetra-iso-propyl titanate (TPT). This catalyst is added to the solution in the ratio of l ml TPT to 200 ml solution.
The solution is most advantageously applied by spraying.
The polymerization reaction is rapid and needs no curing or post-heating. Water repellency is imparted to the paper at the moment the spray contacts it. It has also been observed that during a period of several hours after the treatment there is a slight increase in the water repellency. This is due to short-chain silicone polymers joining to orm longer chains, thus giving a slight increase in hydrophobicity.
This solution does not affect the pH o the paper.
Organometallic tin compounds such as dibutyltin laurate, stannous oleate and tetrabutyl orthotitanate can also be used as catalysts. Tin compounds may be employed if the end use of the paper permits the presence of tin in the residual silicone.
_g_ A further description of the present invention will be made in conjunction with the attached drawiny which illustrates rather schematically a continuous system for treating paper with the improved process of the present invention.
In the accompanying Eigure, reference numeral 10 has been applied to a source of silane solution, usually in the form of a 1 to 3% by volume solution in a suitable organic solvent, but as will be hereinafter explained, the solvent need not always be present. The solution is withdrawn from the container 10 through a valve 11 where it is combined with a catalyst from a container 12. Metered amounts of the catalyst are provided from the container 12 through a valve 13 to be combined with the silane solution. The mixture of the two then passes through a conduit 14 into a pair of spray heads 15 and 16 which are arranged to treat opposite sides of a paper web 17. The paper web is guided over an upper guide roll 18, a lower guide roll 19, and a second upper guide roll 20 before it leaves the treating vessel generally indicated at reference numeral 21 in the drawings. Air for the spray heads 15 and 16 is supplied from a suitable source of compressed air ~not shown) through a valve 22 and is delivered to each of the spray heads.
The reaction between the catalyst-containing silane solution and the paper fibers is quite rapid. The only by-products of the reaction are the alcohol produced, the solvent used in the treating solution, and any unreacted silane. These products are directed by means of an effluent line 23 into a condenser 24. Here they are combined with additional amounts of alcohol which are recovered from the 4~
traveling web by means of vacuum boxes 25 and 26 positioned at the exit end of the chamber 21. The condensed materials, ; usually consisting mainly of alcohols, can then be recycled by means of a conduit 27 back into the silane solution con-tainer 10.
The following specific examples illustrate the manner in which the invention is carried out, and the improved results achieved.
EXample I
A sample of 100 lb. bleached, unsized board was treated by spraying with a treating solution containing approximately 2% by volume methyl trimethoxysilane, with the balance methanol and a catalyst consisting of 1 ml of sulfuric acid per 250 ml of solution. The treated sample was then heated for 15 seconds in a 300F (147C~ oven. The sample became quite water resistant.
Example II
~ A sample of 100 lb. bleached, unsized board was treated as in Example I, using dimethyl diethoxysilane as the treating agent. Results substantially the same as those in Example I were obtained.
Example III
Samples of 100 lb. bleached, unsized board were treated by spraying with a solution containing approximately 2% by volume methyl tximethoxysilane, water in an amount of 3 moles of water for everv mole'of silane, acetic acid in an amount of 1 ml acid for 400 ml solution, in a lower alcohol solvent, using a catalyst of sodium peroxide in an amount of ^ `"~
1 gram per 500 ml solution. The samples were heated for varying periods of time in a 300F (147C) oven. All of the sheets developed similar water resistant properties.
'Exa~pl'e''IV
A sample of 325 lb. bleached blotter paper was treated with the same solution as in Example III and heated for 15 seconds in a 300F (147C) oven. The paper de~eloped excellent water resistant properties, and was resistant to continuous running water.
Example V
A sample of 325 lb. bleached blotter paper was treated by spraying with a solution containing approximately 2~ by volume methyl trimethoxysilane, dissolved in benzene, and containing TPT in an amount of 1 ml per 200 ml of solution.
No heating was done. The treated sheet was very water resistant, including resistance to running water.
Examp'le VI
The paper stock was treated as in Example V, but given only a very light spraying. The sheet was slightly water resistant to drops of water, but not to running water.
EXa p'le VII
The paper was treated with the same composition as in Example V, but with a very heavy spraying. The sheet which resulted was very resistant to water under any conditions.
E'x'ample VIII
This example utilized the same composition and procedure as in Examples V and VII, but the paper was treated 4~
on one side only. ~oth lightly treated and heavily treated papers were resistant on the treated side, with the greatest resistance in the heavily treated sheet. The untreated side of the heavily treated sheet showed a very slight water resistance.
EXample'IX
A sample of 100 lb. N.S.S.C., unbleached board was treated by spraying with the composition described in Example V. No heating was done. The treated sheet was water resistant, although only slightly resistant to running water.
Examp'le'X
The procedure here was the same as in Example IX, except the board was given only a li~ht treatment. The resulting product was very slightly water resistant.
''Exampl'e'XI
This procedure and composition was the same as used in Example IX, only a heavy treatment was applied. The resulting board was very water resistant, including resistance to running water.
'Exam~le XII
The composition and method were the same as in Examples IX and XI, except that the board was treated on one side'only. The normally treated side was slightly water resistant, and the untreated side had no water resistance~
When héavily treated, the'sheet was very water resistant on the treated side and slightly resistant on the untreated side.
:
!; Example' XIII
A sample of newsprint was treated with the solution set forth in Example V. An increased water resistance was ' developed in the sheet.
:;
Example XIV
The silane may be applied to a moving web without '~ the use of a diluting solvent. In this case, a catalyst such , as TPT should be present in amounts of from 10 to 15% by ~' volume of solution for maximum polymerization efficiency.
The application to the moving web must be in the form of a fine spray that atomizes but does not vaporize the silane.
, The treating chamber should be well ventila~ed to remove any vaporized silane and titania by-product from the reaction.
Th'e application of the silane solution is most easily ,, controlled by applying it as a spray or in the form of an,:, aerosol. The spray can be adjusted to give the degree of coating desired as well as an even application. The solvent remaining in the paper can be removed by means of a vacuum or by heating.
Physical testing was done on some of these samples produced according to the examples set forth above. In the following table, "MD" refers to testing in the machine direction, and "C~lD" refers to the cross machine direction.
'rhe Z-tensile strength tests were per~ormed by applying a double sided adhesive tapP to the paper and s~tretching the same in an Instron machine. The brightness figures were derived from a General ~lectric birghtness meter. The Unger -lA-oil test consisted in clamping a ring on the paper, pouring on oil under the ring, wiping off excess oil, and then weighing the sheet. The water absorption test was performed by applying about 0.1 ml of water to the paper, reflecting a light off it, and measuring the time elapsed until the reflection stops.
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O ~ ~ ~ ' ~ O 0 ~ u~ ~ CO
o a) ~ o o ~ 1` U L~
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o~
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, : ~ ~ ~ g - ~4~ L3 It should be evident that various modifications can be made to the described embodiments without departing from the scope of the present invention.
.~
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O O O L~ ~ O O U~ O O
~1 ~ ~I t~er~1 ~ CO CO CO ~ ~1 Ln ~1 'I ~ ~ ~ ~ ~ I I ,i O ~ ~ ~ ~ I` ~ CO ~ 00 O~ t~
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, : ~ ~ ~ g - ~4~ L3 It should be evident that various modifications can be made to the described embodiments without departing from the scope of the present invention.
.~
, .
Claims (18)
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. The method of improving the water repellency of a natur-ally porous paper web containing about 2 to 14% moisture by weight which comprises:
treating said web with a coating composition containing as its active coating ingredient an alkyl alkoxysiloxane having the formula:
where A is H, CH3, or B and s is an OR group in which R is methyl or ethyl, said coating composition being in liquid form and being substantially devoid of solids, said treating being carried out in the presence of a condensation catalyst, and reacting said alkyl alkoxysilane with water contained in said web to thereby produce a water repellent paper web in which the reaction product impregnates within the pores of the paper to render the paper water repellent while said paper retains substantially the porosity and strength characteristics of the untreated web.
treating said web with a coating composition containing as its active coating ingredient an alkyl alkoxysiloxane having the formula:
where A is H, CH3, or B and s is an OR group in which R is methyl or ethyl, said coating composition being in liquid form and being substantially devoid of solids, said treating being carried out in the presence of a condensation catalyst, and reacting said alkyl alkoxysilane with water contained in said web to thereby produce a water repellent paper web in which the reaction product impregnates within the pores of the paper to render the paper water repellent while said paper retains substantially the porosity and strength characteristics of the untreated web.
2. A method according to claim 1 in which said alkyl al-koxysilane is methyl trimethoxysilane.
3. A method according to claim 1 in which said alkyl al-koxysilane is methyl dimethoxysilane.
4. A method according to claim 1 in which said alkyl al-koxysilane is methyl triethoxysilane.
5. A method according to claim 1 in which said alkyl al-koxysilane is methyl diethoxysilane.
6. A method according to claim 1 in which said alkyl al-koxysiloxane is dissolved in a volatile liquid solvent which is non-reactive toward said alkyl alkoxysiloxane.
7. A method according to claim 6 in which said solvent is an aliphatic alcohol containing from 1 to 4 carbon atoms per molecule.
8. A method according to claim 6 in which said alkyl alkoxy-siloxane is dissolved in said solvent in an amount of from 1 to 3% by volume.
9. A method according to claim 1 in which said catalyst is a strong mineral acid.
10. A method according to claim 1 in which said catalyst is a peroxide condensation catalyst.
11. A method according to claim 10 in which said peroxide is an alkali metal peroxide.
12. A method according to claim 1 in which said alkyl al-koxysilane is applied to the web as a finely atomized spray in the absence of an added solvent.
13. A method according to claim 1 in which alkyl alkoxysi-lane is pre-hydrolyzed prior to application to said web.
14. A paper web having improved water repellency on at least one surface thereof while retaining substantially all of its natural porosity toward gases, said surface comprising a silicone polymer produced by reaction of water in said web with a hydroxysilane which itself is the hydrolysis product of an alkyl alkoxysiloxane having the formula:
where A is H, CH3 or B and B is an OR group in which R is methyl or ethyl.
where A is H, CH3 or B and B is an OR group in which R is methyl or ethyl.
15. A paper web according to claim 14 in which said alkyl alkoxysiloxane is methyl trimethoxysilane.
16. A paper web according to claim 14 in which said alkyl alkoxysiloxane is methyl dimathoxysilane.
17. A paper web according to claim 14 in which said alkyl alkoxysiloxane is methyl triethoxysilane.
18. A paper web according to claim 14 in which said alkyl alkoxysiloxane is methyl diethoxysilane.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US2824279A | 1979-04-09 | 1979-04-09 | |
| US28,242 | 1979-04-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1144013A true CA1144013A (en) | 1983-04-05 |
Family
ID=21842347
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000346547A Expired CA1144013A (en) | 1979-04-09 | 1980-02-27 | Method for waterproofing paper |
Country Status (8)
| Country | Link |
|---|---|
| JP (1) | JPS55137295A (en) |
| KR (1) | KR830002851B1 (en) |
| CA (1) | CA1144013A (en) |
| ES (1) | ES8100385A1 (en) |
| GB (1) | GB2045823B (en) |
| IN (1) | IN152598B (en) |
| IT (1) | IT1147350B (en) |
| PH (1) | PH15380A (en) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4664735A (en) * | 1982-09-30 | 1987-05-12 | Pernicano Vincent S | Heat transfer sheeting having release agent coat |
| CA1249903A (en) * | 1984-05-10 | 1989-02-14 | Christopher C. Mollett | Composition and method of deinking of recycled cellulosic material |
| FR2735705B1 (en) * | 1995-06-21 | 1997-09-12 | Croquelois Jean Pierre | METHOD FOR PROVIDING HYDROPHOBIC PROPERTIES TO A CELLULOSIC SUPPORT |
| JP4914546B2 (en) * | 2001-09-20 | 2012-04-11 | 株式会社キャステム | Paper manufacturing method |
| CN103154165A (en) * | 2010-10-07 | 2013-06-12 | 道康宁公司 | Biodegradable hydrophobic cellulosic substrates and methods for their production using reactive silanes |
| WO2019083056A1 (en) * | 2017-10-24 | 2019-05-02 | 한국생산기술연구원 | Water-and-oil repellent copolymer for coating paper through covalent bonding, preparation method therefor, and use thereof |
| DE102018124255A1 (en) * | 2018-10-01 | 2020-04-02 | Technische Universität Darmstadt | Nonwoven fabrics with asymmetrical silica impregnation and process for producing the nonwovens and their uses |
-
1980
- 1980-02-27 CA CA000346547A patent/CA1144013A/en not_active Expired
- 1980-02-27 GB GB8006594A patent/GB2045823B/en not_active Expired
- 1980-03-13 ES ES489494A patent/ES8100385A1/en not_active Expired
- 1980-03-17 JP JP3281180A patent/JPS55137295A/en active Pending
- 1980-03-25 PH PH23811A patent/PH15380A/en unknown
- 1980-04-03 IN IN388/CAL/80A patent/IN152598B/en unknown
- 1980-04-08 KR KR1019800001456A patent/KR830002851B1/en not_active Expired
- 1980-04-09 IT IT21267/80A patent/IT1147350B/en active
Also Published As
| Publication number | Publication date |
|---|---|
| KR830002956A (en) | 1983-05-31 |
| ES489494A0 (en) | 1980-11-01 |
| IT1147350B (en) | 1986-11-19 |
| ES8100385A1 (en) | 1980-11-01 |
| JPS55137295A (en) | 1980-10-25 |
| GB2045823B (en) | 1983-04-20 |
| IT8021267A0 (en) | 1980-04-09 |
| KR830002851B1 (en) | 1983-12-27 |
| IN152598B (en) | 1984-02-18 |
| PH15380A (en) | 1982-12-17 |
| GB2045823A (en) | 1980-11-05 |
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