CA1045735A - Dispersions stables colophane - Google Patents

Dispersions stables colophane

Info

Publication number: CA1045735A
Authority: CA; Canada
Prior art keywords: rosin; fortified; fortified rosin; water; sizing
Prior art date: 1973-08-06
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

Application number

CA203,190A

Other languages

English (en)

Other versions

CA203190S (en

Inventor

Paul H. Aldrich

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.)

Hercules LLC

Original Assignee

Hercules LLC

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.)

1973-08-06

Filing date

1974-06-24

Publication date

1979-01-02

1974-06-24 Application filed by Hercules LLC filed Critical Hercules LLC

1979-01-02 Application granted granted Critical

1979-01-02 Publication of CA1045735A publication Critical patent/CA1045735A/fr

Status Expired legal-status Critical Current

Links

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KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical class OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
244000010375 Talinum crassifolium Species 0.000 description 1
235000015055 Talinum crassifolium Nutrition 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
LEHOTFFKMJEONL-UHFFFAOYSA-N Uric Acid Chemical compound N1C(=O)NC(=O)C2=C1NC(=O)N2 LEHOTFFKMJEONL-UHFFFAOYSA-N 0.000 description 1
TVWHNULVHGKJHS-UHFFFAOYSA-N Uric acid Natural products N1C(=O)NC(=O)C2NC(=O)NC21 TVWHNULVHGKJHS-UHFFFAOYSA-N 0.000 description 1
QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
239000012190 activator Substances 0.000 description 1
238000013019 agitation Methods 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
239000003513 alkali Substances 0.000 description 1
125000005250 alkyl acrylate group Chemical group 0.000 description 1
JZQOJFLIJNRDHK-CMDGGOBGSA-N alpha-irone Chemical compound CC1CC=C(C)C(\C=C\C(C)=O)C1(C)C JZQOJFLIJNRDHK-CMDGGOBGSA-N 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
229940107816 ammonium iodide Drugs 0.000 description 1
JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 1
229940073608 benzyl chloride Drugs 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
OTBHHUPVCYLGQO-UHFFFAOYSA-N bis(3-aminopropyl)amine Chemical compound NCCCNCCCN OTBHHUPVCYLGQO-UHFFFAOYSA-N 0.000 description 1
239000007844 bleaching agent Substances 0.000 description 1
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
150000007942 carboxylates Chemical class 0.000 description 1
125000002843 carboxylic acid group Chemical group 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
XENVCRGQTABGKY-ZHACJKMWSA-N chlorohydrin Chemical compound CC#CC#CC#CC#C\C=C\C(Cl)CO XENVCRGQTABGKY-ZHACJKMWSA-N 0.000 description 1
229910017052 cobalt Inorganic materials 0.000 description 1
239000010941 cobalt Substances 0.000 description 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
230000001143 conditioned effect Effects 0.000 description 1
239000000498 cooling water Substances 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
239000008120 corn starch Substances 0.000 description 1
IBAHLNWTOIHLKE-UHFFFAOYSA-N cyano cyanate Chemical compound N#COC#N IBAHLNWTOIHLKE-UHFFFAOYSA-N 0.000 description 1
JJCFRYNCJDLXIK-UHFFFAOYSA-N cyproheptadine Chemical compound C1CN(C)CCC1=C1C2=CC=CC=C2C=CC2=CC=CC=C21 JJCFRYNCJDLXIK-UHFFFAOYSA-N 0.000 description 1
230000007423 decrease Effects 0.000 description 1
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
GRWZHXKQBITJKP-UHFFFAOYSA-N dithionous acid Chemical class OS(=O)S(O)=O GRWZHXKQBITJKP-UHFFFAOYSA-N 0.000 description 1
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
GKIPXFAANLTWBM-UHFFFAOYSA-N epibromohydrin Chemical compound BrCC1CO1 GKIPXFAANLTWBM-UHFFFAOYSA-N 0.000 description 1
125000003700 epoxy group Chemical group 0.000 description 1
JOXWSDNHLSQKCC-UHFFFAOYSA-N ethenesulfonamide Chemical compound NS(=O)(=O)C=C JOXWSDNHLSQKCC-UHFFFAOYSA-N 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000012458 free base Substances 0.000 description 1
238000001879 gelation Methods 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
239000008233 hard water Substances 0.000 description 1
239000011121 hardwood Substances 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
XPXMKIXDFWLRAA-UHFFFAOYSA-N hydrazinide Chemical compound [NH-]N XPXMKIXDFWLRAA-UHFFFAOYSA-N 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
229920006270 hydrocarbon resin Polymers 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
150000002431 hydrogen Chemical class 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
239000003999 initiator Substances 0.000 description 1
HVTICUPFWKNHNG-UHFFFAOYSA-N iodoethane Chemical compound CCI HVTICUPFWKNHNG-UHFFFAOYSA-N 0.000 description 1
INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
239000007788 liquid Substances 0.000 description 1
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
229910052748 manganese Inorganic materials 0.000 description 1
239000011572 manganese Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
229960002523 mercuric chloride Drugs 0.000 description 1
229960003671 mercuric iodide Drugs 0.000 description 1
NGYIMTKLQULBOO-UHFFFAOYSA-L mercury dibromide Chemical compound Br[Hg]Br NGYIMTKLQULBOO-UHFFFAOYSA-L 0.000 description 1
LWJROJCJINYWOX-UHFFFAOYSA-L mercury dichloride Chemical compound Cl[Hg]Cl LWJROJCJINYWOX-UHFFFAOYSA-L 0.000 description 1
YFDLHELOZYVNJE-UHFFFAOYSA-L mercury diiodide Chemical compound I[Hg]I YFDLHELOZYVNJE-UHFFFAOYSA-L 0.000 description 1
HNEGQIOMVPPMNR-NSCUHMNNSA-N mesaconic acid Chemical compound OC(=O)C(/C)=C/C(O)=O HNEGQIOMVPPMNR-NSCUHMNNSA-N 0.000 description 1
150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
125000005395 methacrylic acid group Chemical group 0.000 description 1
229940102396 methyl bromide Drugs 0.000 description 1
XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
HNEGQIOMVPPMNR-UHFFFAOYSA-N methylfumaric acid Natural products OC(=O)C(C)=CC(O)=O HNEGQIOMVPPMNR-UHFFFAOYSA-N 0.000 description 1
239000004200 microcrystalline wax Substances 0.000 description 1
235000019808 microcrystalline wax Nutrition 0.000 description 1
HYSQEYLBJYFNMH-UHFFFAOYSA-N n'-(2-aminoethyl)-n'-methylethane-1,2-diamine Chemical compound NCCN(C)CCN HYSQEYLBJYFNMH-UHFFFAOYSA-N 0.000 description 1
DPXZYPCARKJGQV-UHFFFAOYSA-N n'-[2-[2-aminoethyl(methyl)amino]ethyl]-n'-methylethane-1,2-diamine Chemical compound NCCN(C)CCN(C)CCN DPXZYPCARKJGQV-UHFFFAOYSA-N 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000005608 naphthenic acid group Chemical group 0.000 description 1
230000003472 neutralizing effect Effects 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
238000010979 pH adjustment Methods 0.000 description 1
UCUUFSAXZMGPGH-UHFFFAOYSA-N penta-1,4-dien-3-one Chemical class C=CC(=O)C=C UCUUFSAXZMGPGH-UHFFFAOYSA-N 0.000 description 1
230000000737 periodic effect Effects 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
229920002401 polyacrylamide Polymers 0.000 description 1
229920006122 polyamide resin Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
239000001294 propane Substances 0.000 description 1
WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical group CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 1
AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
239000013055 pulp slurry Substances 0.000 description 1
239000000376 reactant Substances 0.000 description 1
230000036647 reaction Effects 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
238000010992 reflux Methods 0.000 description 1
238000004062 sedimentation Methods 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 1
235000009518 sodium iodide Nutrition 0.000 description 1
229940001584 sodium metabisulfite Drugs 0.000 description 1
235000010262 sodium metabisulphite Nutrition 0.000 description 1
239000011122 softwood Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
241000894007 species Species 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
235000011149 sulphuric acid Nutrition 0.000 description 1
150000003505 terpenes Chemical class 0.000 description 1
235000007586 terpenes Nutrition 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
150000004764 thiosulfuric acid derivatives Chemical class 0.000 description 1
229940116269 uric acid Drugs 0.000 description 1
239000008096 xylene Substances 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical class [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
- C08J3/03—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media
- C08J3/07—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media from polymer solutions
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/02—Polycondensates containing more than one epoxy group per molecule
- C08G59/10—Polycondensates containing more than one epoxy group per molecule of polyamines with epihalohydrins or precursors thereof
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L93/00—Compositions of natural resins; Compositions of derivatives thereof
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L93/00—Compositions of natural resins; Compositions of derivatives thereof
- C08L93/04—Rosin
- 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
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/46—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/54—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen
- D21H17/55—Polyamides; Polyaminoamides; Polyester-amides
- 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
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/46—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/54—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen
- D21H17/56—Polyamines; Polyimines; Polyester-imides
- 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
- D21H17/62—Rosin; Derivatives thereof
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2393/00—Characterised by the use of natural resins; Derivatives thereof

Landscapes

Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Dispersion Chemistry (AREA)
Paper (AREA)
Compositions Of Macromolecular Compounds (AREA)
Colloid Chemistry (AREA)

CA203,190A 1973-08-06 1974-06-24 Dispersions stables colophane Expired CA1045735A (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US38613573A	1973-08-06	1973-08-06

Publications (1)

Publication Number	Publication Date
CA1045735A true CA1045735A (fr)	1979-01-02

Family

ID=23524317

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA203,190A Expired CA1045735A (fr)	1973-08-06	1974-06-24	Dispersions stables colophane

Country Status (17)

Country	Link
JP (1)	JPS5834509B2 (fr)
AT (1)	AT337525B (fr)
BE (1)	BE818311A (fr)
BR (1)	BR7406444D0 (fr)
CA (1)	CA1045735A (fr)
CH (1)	CH606265A5 (fr)
DE (1)	DE2435614B2 (fr)
DK (1)	DK155219C (fr)
ES (1)	ES428964A1 (fr)
FI (1)	FI62126C (fr)
FR (1)	FR2240251B1 (fr)
GB (1)	GB1439116A (fr)
IT (1)	IT1017901B (fr)
NL (1)	NL7408707A (fr)
NO (1)	NO140992C (fr)
SE (1)	SE414951B (fr)
ZA (1)	ZA745014B (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5972094A (en) *	1996-05-24	1999-10-26	Hercules Incorporated	Sizing composition

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5025348U (fr) *	1973-06-29	1975-03-24
JPS5025346U (fr) *	1973-06-29	1975-03-24
JPS5025347U (fr) *	1973-06-29	1975-03-24
AU504229B2 (en)	1975-11-17	1979-10-04	A.C. Hatrick Chemicals Pty. Ltd.	Aqueous disperse of fortified rosin
NZ183271A (en) *	1976-03-08	1979-01-11	Hercules Inc	Sized paper and paper board;sizing composition
SE415679B (sv) *	1976-07-21	1980-10-20	Kenogard Ab	Forfarande for framstellning av en huvudsakligen stabil vattendispersion av kolofoniummaterial i nervaro av ett katjoniskt emulgermedel
JPS53115549A (en) *	1978-01-18	1978-10-09	Sharp Corp	Moisture exchanging element
JPS53115550A (en) *	1978-01-18	1978-10-09	Sharp Corp	Moisture exchanging element
US4263182A (en) *	1979-09-06	1981-04-21	Hercules Incorporated	Stable dispersions of fortified rosin
JPS57111355A (en) *	1980-12-27	1982-07-10	Harima Kasei Kogyo Kk	Preparation of aqueous reinforced rosin dispersion for paper making
JPS63191805U (fr) *	1987-05-27	1988-12-09
JP6180917B2 (ja) *	2013-12-19	2017-08-16	ハリマ化成株式会社	サイズ剤用分散剤、サイズ剤組成物および紙
JP6525397B2 (ja) *	2015-09-28	2019-06-05	荒川化学工業株式会社	ロジン系エマルジョンサイズ剤及び該サイズ剤を用いて得られる紙
JP6942754B2 (ja)	2019-06-11	2021-09-29	株式会社ミツバ	自動車のトランスミッションのクラッチ係合用電動オイルポンプ、自動車のトランスミッションのクラッチ係合用電動オイルポンプ制御方法、車両及び自動車のトランスミッションのクラッチ係合車両用電動オイルポンプ
JP7287218B2 (ja)	2019-09-26	2023-06-06	ニデックパワートレインシステムズ株式会社	電動オイルポンプの制御装置、電動オイルポンプ

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NL268563A (fr) *	1960-08-31
US3565755A (en) *	1969-03-27	1971-02-23	Hercules Inc	Rosin size and paper containing said size

1974
- 1974-06-24 CA CA203,190A patent/CA1045735A/fr not_active Expired
- 1974-06-27 NL NL7408707A patent/NL7408707A/xx not_active Application Discontinuation
- 1974-07-11 JP JP49079713A patent/JPS5834509B2/ja not_active Expired
- 1974-07-24 DE DE19742435614 patent/DE2435614B2/de not_active Ceased
- 1974-07-30 DK DK407274A patent/DK155219C/da not_active IP Right Cessation
- 1974-07-30 NO NO742757A patent/NO140992C/no unknown
- 1974-07-31 BE BE147131A patent/BE818311A/fr not_active IP Right Cessation
- 1974-07-31 FR FR7427208A patent/FR2240251B1/fr not_active Expired
- 1974-08-01 SE SE7409938A patent/SE414951B/xx unknown
- 1974-08-01 GB GB3408774A patent/GB1439116A/en not_active Expired
- 1974-08-02 FI FI2323/74A patent/FI62126C/fi active
- 1974-08-05 IT IT25980/74A patent/IT1017901B/it active
- 1974-08-05 AT AT638174A patent/AT337525B/de not_active IP Right Cessation
- 1974-08-05 CH CH1069274A patent/CH606265A5/xx not_active IP Right Cessation
- 1974-08-05 ES ES428964A patent/ES428964A1/es not_active Expired
- 1974-08-06 ZA ZA00745014A patent/ZA745014B/xx unknown
- 1974-08-06 BR BR6444/74A patent/BR7406444D0/pt unknown

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5972094A (en) *	1996-05-24	1999-10-26	Hercules Incorporated	Sizing composition
US6074468A (en) *	1996-05-24	2000-06-13	Hercules Incorporated	Sizing composition
US6165320A (en) *	1996-05-24	2000-12-26	Hercules Incorporated	Method of sizing

Also Published As

Publication number	Publication date
DE2435614B2 (de)	1977-12-08
DK155219C (da)	1989-07-24
FI232374A7 (fr)	1975-02-07
GB1439116A (en)	1976-06-09
FI62126B (fi)	1982-07-30
DK407274A (fr)	1975-04-01
SE7409938L (fr)	1975-02-07
JPS5834509B2 (ja)	1983-07-27
FI62126C (fi)	1982-11-10
FR2240251B1 (fr)	1979-09-21
NO140992B (no)	1979-09-10
BR7406444D0 (pt)	1975-05-27
NO140992C (no)	1979-12-19
ATA638174A (de)	1976-10-15
DE2435614A1 (de)	1975-02-27
SE414951B (sv)	1980-08-25
AU7196674A (en)	1976-02-05
FR2240251A1 (fr)	1975-03-07
CH606265A5 (fr)	1978-10-31
DK155219B (da)	1989-03-06
IT1017901B (it)	1977-08-10
NL7408707A (nl)	1975-02-10
JPS5036703A (fr)	1975-04-07
ZA745014B (en)	1975-08-27
BE818311A (fr)	1974-11-18
ES428964A1 (es)	1976-11-16
AT337525B (de)	1977-07-11
NO742757L (fr)	1975-03-03

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US4144123A (en)	1979-03-13	Incorporating a crosslinked polyamidoamine condensation product into paper-making pulp
US3049469A (en)	1962-08-14	Application of coating or impregnating materials to fibrous material
US4279794A (en)	1981-07-21	Sizing method and sizing composition for use therein
US4147586A (en)	1979-04-03	Cellulosic paper containing the reaction product of a dihaloalkane alkylene diamine adduct and epihalohydrin
US10633798B2 (en)	2020-04-28	Blends of polymers as wet strengthening agents for paper
EP2635634B1 (fr)	2017-03-22	Procédé d'utilisation de polymères à fonctionnalité aldéhyde pour augmenter les performances d'une machine à papier et améliorer le collage
US4263182A (en)	1981-04-21	Stable dispersions of fortified rosin
US4295931A (en)	1981-10-20	Sizing method and sizing composition for use therein
WO2000011046A1 (fr)	2000-03-02	Polyacrylamides anioniques et amphoteres modifies par dialdehyde utiles pour ameliorer la resistance du papier
US3899389A (en)	1975-08-12	Cellulosic materials internally sized with copolymers of alpha beta-ethylenically unsaturated hydrophobic monomers and ammoniated carboxylic acid comonomers
US4017431A (en)	1977-04-12	Aqueous dispersions of wax blends and a water-soluble cationic resin and paper sized therewith
JPH0244960B2 (fr)	1990-10-05
US10190261B2 (en)	2019-01-29	Strengthening resins for paper products
US4478682A (en)	1984-10-23	Sizing method and sizing composition for use therein
DE69210794T2 (de)	1996-10-17	Neue kationische Polyaminen als Hilfsmittel für Entwässerung und als Stabilizatore für Kolophonum enthaltende Leimungsmittel
US2767089A (en)	1956-10-16	Paper containing polyamide resins and process of producing same
US4407994A (en)	1983-10-04	Aqueous sizing composition comprising ketene dimer and epihalohydrin/polyamino polyamide/bis(hexamethylene)triamine reaction product
US3957574A (en)	1976-05-18	Sizing method and composition for use therein
US4109053A (en)	1978-08-22	Sizing paper with stable dispersions of hydrocarbon resins
AU654847B2 (en)	1994-11-24	Epihalohydrin/polyamine polymers containing low levels of dihalopropanols, process for making the same and paper sizes made therefrom
JPH09511551A (ja)	1997-11-18	湿潤紙力増強用樹脂組成物およびその製造方法
US3962159A (en)	1976-06-08	Graft copolymers of a polyamideamine substrate and starch, and method of making same
US3728215A (en)	1973-04-17	Aminopalyamide{13 acrylamide{13 polyaldehyde resins employing an alpha, beta-unsaturated monobasic carboxylic acid or ester to make the aminopolyamide and their utility as wet and dry strengthening agents in papermaking