NO301547B1 - Vannopplöselig fenolisk resol-urea-blanding og fremgangsmåte for fremstilling derav - Google Patents

Vannopplöselig fenolisk resol-urea-blanding og fremgangsmåte for fremstilling derav Download PDF

Info

Publication number: NO301547B1
Authority: NO; Norway
Prior art keywords: urea; formaldehyde; mixture; phenol; minutes
Prior art date: 1986-06-18

Application number

NO872540A

Other languages

English (en)

Norwegian (no)

Other versions

NO872540D0 (no

NO872540L (no

Inventor

Wayne R Walisser

Original Assignee

Borden Inc

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.)

1986-06-18

Filing date

1987-06-17

Publication date

1997-11-10

1987-06-17 Application filed by Borden Inc filed Critical Borden Inc

1987-06-17 Publication of NO872540D0 publication Critical patent/NO872540D0/no

1987-12-21 Publication of NO872540L publication Critical patent/NO872540L/no

1997-11-10 Publication of NO301547B1 publication Critical patent/NO301547B1/no

Links

239000004202 carbamide Substances 0.000 title claims abstract description 74
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 title claims abstract description 57
239000000203 mixture Substances 0.000 title claims abstract description 55
238000000034 method Methods 0.000 title claims description 38
230000008569 process Effects 0.000 title claims description 10
238000002360 preparation method Methods 0.000 title description 8
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims abstract description 145
239000011230 binding agent Substances 0.000 claims abstract description 76
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims abstract description 73
229920003987 resole Polymers 0.000 claims abstract description 67
238000006243 chemical reaction Methods 0.000 claims abstract description 66
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 51
238000003860 storage Methods 0.000 claims abstract description 39
239000002253 acid Substances 0.000 claims abstract description 22
230000007935 neutral effect Effects 0.000 claims abstract description 8
229920005989 resin Polymers 0.000 claims description 83
239000011347 resin Substances 0.000 claims description 83
229920001807 Urea-formaldehyde Polymers 0.000 claims description 48
239000000047 product Substances 0.000 claims description 47
230000002378 acidificating effect Effects 0.000 claims description 27
229920000642 polymer Polymers 0.000 claims description 23
239000000463 material Substances 0.000 claims description 20
DSKJXGYAJJHDOE-UHFFFAOYSA-N methylideneurea Chemical compound NC(=O)N=C DSKJXGYAJJHDOE-UHFFFAOYSA-N 0.000 claims description 18
239000007788 liquid Substances 0.000 claims description 17
ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 claims description 17
238000002425 crystallisation Methods 0.000 claims description 16
230000008025 crystallization Effects 0.000 claims description 16
238000004519 manufacturing process Methods 0.000 claims description 16
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239000007787 solid Substances 0.000 claims description 12
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238000006386 neutralization reaction Methods 0.000 claims description 9
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 8
238000007334 copolymerization reaction Methods 0.000 claims description 8
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238000004062 sedimentation Methods 0.000 claims description 7
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 claims description 6
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 claims description 4
235000019253 formic acid Nutrition 0.000 claims description 4
239000012263 liquid product Substances 0.000 claims description 3
LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 claims description 3
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239000000376 reactant Substances 0.000 claims 2
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239000013049 sediment Substances 0.000 abstract description 23
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239000000243 solution Substances 0.000 description 38
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238000010790 dilution Methods 0.000 description 10
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VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 4
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BVJSUAQZOZWCKN-UHFFFAOYSA-N p-hydroxybenzyl alcohol Chemical class OCC1=CC=C(O)C=C1 BVJSUAQZOZWCKN-UHFFFAOYSA-N 0.000 description 4
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GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 description 3
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QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
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239000004606 Fillers/Extenders Substances 0.000 description 2
WTDHULULXKLSOZ-UHFFFAOYSA-N Hydroxylamine hydrochloride Chemical compound Cl.ON WTDHULULXKLSOZ-UHFFFAOYSA-N 0.000 description 2
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
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QUBQYFYWUJJAAK-UHFFFAOYSA-N oxymethurea Chemical compound OCNC(=O)NCO QUBQYFYWUJJAAK-UHFFFAOYSA-N 0.000 description 2
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BAERPNBPLZWCES-UHFFFAOYSA-N (2-hydroxy-1-phosphonoethyl)phosphonic acid Chemical compound OCC(P(O)(O)=O)P(O)(O)=O BAERPNBPLZWCES-UHFFFAOYSA-N 0.000 description 1
LSHOSVDZPQVSRS-UHFFFAOYSA-N 1-aminoethenylphosphonic acid Chemical compound NC(=C)P(O)(O)=O LSHOSVDZPQVSRS-UHFFFAOYSA-N 0.000 description 1
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235000019738 Limestone Nutrition 0.000 description 1
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238000000975 co-precipitation Methods 0.000 description 1
238000012777 commercial manufacturing Methods 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
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238000006731 degradation reaction Methods 0.000 description 1
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QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 1
125000006840 diphenylmethane group Chemical class 0.000 description 1
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238000004817 gas chromatography Methods 0.000 description 1
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229910052757 nitrogen Inorganic materials 0.000 description 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
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150000003839 salts Chemical class 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000003352 sequestering agent Substances 0.000 description 1
229910000077 silane Inorganic materials 0.000 description 1
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238000011105 stabilization Methods 0.000 description 1
IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical compound NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
238000005979 thermal decomposition reaction Methods 0.000 description 1
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Classifications

- 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
- C08G14/00—Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00
- C08G14/02—Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes
- C08G14/04—Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes with phenols
- C08G14/06—Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes with phenols and monomers containing hydrogen attached to nitrogen
- C08G14/08—Ureas; Thioureas
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
- C03C25/10—Coating
- C03C25/24—Coatings containing organic materials
- C03C25/26—Macromolecular compounds or prepolymers
- C03C25/32—Macromolecular compounds or prepolymers obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
- C03C25/34—Condensation polymers of aldehydes, e.g. with phenols, ureas, melamines, amides or amines
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
- C08L61/34—Condensation polymers of aldehydes or ketones with monomers covered by at least two of the groups C08L61/04, C08L61/18 and C08L61/20

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Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Life Sciences & Earth Sciences (AREA)
Geochemistry & Mineralogy (AREA)
Engineering & Computer Science (AREA)
General Chemical & Material Sciences (AREA)
General Life Sciences & Earth Sciences (AREA)
Materials Engineering (AREA)
Phenolic Resins Or Amino Resins (AREA)
Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Compositions Of Macromolecular Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Adhesives Or Adhesive Processes (AREA)
Paints Or Removers (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

NO872540A 1986-06-18 1987-06-17 Vannopplöselig fenolisk resol-urea-blanding og fremgangsmåte for fremstilling derav NO301547B1 (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US06/875,536 US4757108A (en)	1986-06-18	1986-06-18	Water soluble phenolic resole-urea composition

Publications (3)

Publication Number	Publication Date
NO872540D0 NO872540D0 (no)	1987-06-17
NO872540L NO872540L (no)	1987-12-21
NO301547B1 true NO301547B1 (no)	1997-11-10

Family

ID=25365972

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO872540A NO301547B1 (no)	1986-06-18	1987-06-17	Vannopplöselig fenolisk resol-urea-blanding og fremgangsmåte for fremstilling derav

Country Status (12)

Country	Link
US (1)	US4757108A (de)
EP (1)	EP0253488B1 (de)
JP (1)	JPH0788461B2 (de)
AT (1)	ATE92937T1 (de)
AU (1)	AU602695B2 (de)
BR (1)	BR8702940A (de)
CA (1)	CA1275537C (de)
DE (1)	DE3786960T2 (de)
ES (1)	ES2042565T3 (de)
MY (1)	MY102306A (de)
NO (1)	NO301547B1 (de)
PH (1)	PH23452A (de)

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CN103122053A (zh) *	2012-09-07	2013-05-29	谢再锋	一种尿素改性酚醛树脂的制备方法
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CN106336493B (zh) *	2016-08-31	2018-06-12	山东圣泉新材料股份有限公司	一种具有长储存期特性的高分子预聚体在炮泥中的应用
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1986
- 1986-06-18 US US06/875,536 patent/US4757108A/en not_active Expired - Fee Related
- 1986-08-28 CA CA000517101A patent/CA1275537C/en not_active Expired - Lifetime
1987
- 1987-06-02 PH PH35332A patent/PH23452A/en unknown
- 1987-06-05 AU AU73869/87A patent/AU602695B2/en not_active Ceased
- 1987-06-08 DE DE87305040T patent/DE3786960T2/de not_active Expired - Fee Related
- 1987-06-08 AT AT87305040T patent/ATE92937T1/de not_active IP Right Cessation
- 1987-06-08 ES ES87305040T patent/ES2042565T3/es not_active Expired - Lifetime
- 1987-06-08 EP EP87305040A patent/EP0253488B1/de not_active Expired - Lifetime
- 1987-06-10 BR BR8702940A patent/BR8702940A/pt unknown
- 1987-06-15 MY MYPI87000812A patent/MY102306A/en unknown
- 1987-06-17 NO NO872540A patent/NO301547B1/no unknown
- 1987-06-17 JP JP62149308A patent/JPH0788461B2/ja not_active Expired - Lifetime

Also Published As

Publication number	Publication date
PH23452A (en)	1989-08-07
AU602695B2 (en)	1990-10-25
JPS6361043A (ja)	1988-03-17
JPH0788461B2 (ja)	1995-09-27
EP0253488B1 (de)	1993-08-11
ES2042565T3 (es)	1993-12-16
CA1275537C (en)	1990-10-23
NO872540D0 (no)	1987-06-17
DE3786960D1 (de)	1993-09-16
ATE92937T1 (de)	1993-08-15
DE3786960T2 (de)	1993-12-23
AU7386987A (en)	1987-12-24
US4757108A (en)	1988-07-12
NO872540L (no)	1987-12-21
EP0253488A3 (en)	1990-06-13
BR8702940A (pt)	1988-03-08
MY102306A (en)	1992-05-28
EP0253488A2 (de)	1988-01-20

Publication	Publication Date	Title
NO301547B1 (no)	1997-11-10	Vannopplöselig fenolisk resol-urea-blanding og fremgangsmåte for fremstilling derav
AU737807B2 (en)	2001-08-30	Water soluble and storage stable resole-melamine resin
US5371140A (en)	1994-12-06	Emulsifiable phenolic resole resin
US4176105A (en)	1979-11-27	High temperature mineral fiber binder
CA2634327C (en)	2011-04-26	Low emission formaldehyde resin and binder for mineral fiber insulation
EP1446434B1 (de)	2008-10-22	Harz/bindemittel-system zur herstellung von geruchsarmen glasfaserprodukten
US6342271B1 (en)	2002-01-29	Phenolic resin for glue sizing composition, preparation method and glue sizing composition containing same
US5708121A (en)	1998-01-13	Storage stable melamine-modified phenolic resole resins using an alkaline condensation and polyhydroxyl compound stabilization
US4960826A (en)	1990-10-02	Melamine-containing resole resitol and resite compositions
AU612443B2 (en)	1991-07-11	New process for the preparation of aminoplastic resins having very low formaldehyde emission rates
NO115074B (de)	1968-07-15
US3932334A (en)	1976-01-13	Calcia catalyzed resins
US3432453A (en)	1969-03-11	De-ionizing treatment for phenolic resins using a soluble ammonium salt
AU604930B2 (en)	1991-01-03	Process for the preparation of urea-formaldehyde resins
NO302708B1 (no)	1998-04-14	Lim for isolasjonsglassfibre samt anvendelse derav
US4095010A (en)	1978-06-13	Glass fiber wool binder
US4235950A (en)	1980-11-25	High temperature mineral fiber binder
JPH0586805B2 (de)	1993-12-14
JP2003003329A (ja)	2003-01-08	フェノール樹脂繊維及びその製造方法
US20010029291A1 (en)	2001-10-11	High catalyst phenolic resin binder system
JPH06220149A (ja)	1994-08-09	アセトン・ホルムアルデヒド縮合物の製造方法
NO145594B (no)	1982-01-11	Elektroakustisk svinger for bruk i vann.
NO314407B1 (no)	2003-03-17	Fremgangsmåte for fremstilling av vandige aminoplastharpikser, de således oppnådde harpikser, deres anvendelse og trematerialer oppnådd vedanvendelsen
JPS59117516A (ja)	1984-07-06	フエノ−ル樹脂の製造法
HK1020743A (en)	2000-05-19	Water soluble and storage stable resole-melamine resin