[go: up one dir, main page]

CN1243854A - Process for preparing adhesive of urea-formaldehyde resin - Google Patents

Process for preparing adhesive of urea-formaldehyde resin Download PDF

Info

Publication number
CN1243854A
CN1243854A CN 98110988 CN98110988A CN1243854A CN 1243854 A CN1243854 A CN 1243854A CN 98110988 CN98110988 CN 98110988 CN 98110988 A CN98110988 A CN 98110988A CN 1243854 A CN1243854 A CN 1243854A
Authority
CN
China
Prior art keywords
urea
sodium hydroxide
reactor
reaction
value
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.)
Granted
Application number
CN 98110988
Other languages
Chinese (zh)
Other versions
CN1115369C (en
Inventor
陈剑慧
许志钢
管晨
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.)
YANGGUANG CULTURAL ARTICLES CO Ltd HANGZHOU CITY
Original Assignee
YANGGUANG CULTURAL ARTICLES CO Ltd HANGZHOU CITY
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by YANGGUANG CULTURAL ARTICLES CO Ltd HANGZHOU CITY filed Critical YANGGUANG CULTURAL ARTICLES CO Ltd HANGZHOU CITY
Priority to CN 98110988 priority Critical patent/CN1115369C/en
Publication of CN1243854A publication Critical patent/CN1243854A/en
Application granted granted Critical
Publication of CN1115369C publication Critical patent/CN1115369C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

  • Phenolic Resins Or Amino Resins (AREA)
  • Adhesives Or Adhesive Processes (AREA)

Abstract

A process for preparing a binder of urea-formaldehyde resin features that the mole ratio of urea to formaldehyde is controlled to 1 : (1.2-2.0); and the aqueous solution of sodium hydroxide, triethanolamine and hexamethinetetraamine is used as catalyst; the urea is added by several times by the fine-flowing dropping for the first time and the reaction takes place in weak acidity condition. Its advantages are high reaction speed, high binding characteristic and stability and better appearance of resultant resin, and excellent antiblocking performance.

Description

A kind of Preparation of urea-formaldehyde resin adhesive method
The present invention relates to a kind of preparation method of aminoresin tackiness agent.
Urea formaldehyde resin adhesive is with low cost because of its raw material is easy to get at present, already is extensive use of at the bamboo lumber yard, has also obtained application simultaneously in granulated meal processing.The urea-formaldehyde resin adhesive production technique comprises the urea of certain mol proportion and formaldehyde under catalyst action, carries out addition reaction and polycondensation.The addition reaction of urea and formaldehyde is carried out under weak basic condition usually, and the polycondensation of urea and formaldehyde is carried out under solutions of weak acidity usually, discloses this technology as Chinese patent CN1038100C.But adopt this technology, speed of response is slow, and the bond properties of resin, outward appearance and stability can not be satisfactory.
The object of the present invention is to provide a kind of degree of adhesion height, have the Preparation of urea-formaldehyde resin adhesive method of good appearance and stable performance.
For achieving the above object, the present invention by the following technical solutions: the mol ratio of urea and formaldehyde is controlled at 1: between the 1.2-2.0, these two kinds of raw materials are in and carry out addition and polycondensation under the solutions of weak acidity, and comprise the steps:
A), formalin is added in the reactor, start stirring, and the adding basic catalyst is regulated pH value=5.5-7.0, described basic catalyst is the aqueous solution of sodium hydroxide, trolamine, hexamethylenetetramine, its weight proportion is a sodium hydroxide: three ethanol: six methynes, four ammonia: water=1-3: 0.5-20: 0.2-10: 100-200, and be warming up to 65-85 ℃;
B), the logical steam of the 55-85% of required urea total amount is melted, temperature is controlled at 75-85 ℃, and thread splashes into reactor in 20-40 minute;
C), drip urea after, between 90-100 ℃ insulation reaction 30-60 minute;
D), the usefulness 5-10% ammonia chloride aqueous solution is regulated pH value=4-5.5, and is added the surplus urea reaction to terminal;
E), with the pH value=6.5-7.5 of 10-15% aqueous sodium hydroxide solution conditioned reaction liquid, termination reaction;
F), use the chuck water quench to 30-45 ℃ of discharging barrelling reactor.
The present invention also can adopt following further technical scheme: add the polysiloxane surfactant of 0.1-1.0% at the reactant of discharging, carry out spraying drying then.
In general, being reflected under the solutions of weak acidity of urea and formaldehyde carried out, speed of response is very fast, Resin adhesive bond strength height, the outward appearance that generates and having good stability, though thermal discharge is big in its reaction process, in the production as control improper easy generation gelatin phenomenon, but owing to adopted technique scheme, splash into reactor after particularly the logical steam of urea being melted, and the selection by temperature of reaction, time, pH value, make that the speed of response of urea and formaldehyde is controlled effectively, broken through the forbidden zone that urea-formaldehyde resin in the past prepares under solutions of weak acidity; Can make the urea-formaldehyde resin prevented from caking owing in the reactant of discharging, add polysiloxane surfactant simultaneously, be in Powdered uniformly, easy to use.
The invention will be further described below in conjunction with embodiment.
Embodiment 1:
The mol ratio of urea and formaldehyde is 1: 1.6, and its reaction process step is as follows:
A), 37% formalin with 350kg adds in the reactor, and the adding basic catalyst is regulated pH value=6.5 under constantly stirring, described basic catalyst is the aqueous solution of sodium hydroxide, trolamine, hexamethylenetetramine, its weight proportion is a sodium hydroxide: trolamine: hexamethylenetetramine: water=1.2: 0.9: 0.7: 120, and be warming up to 68 ℃
B), with required urea total amount 78% promptly the logical steam of 125 kg melt, temperature is controlled at 80 ℃, and thread splashes into reactor in 25 minutes,
C), drip urea after, 92 ℃ of insulation reaction 35 minutes,
D), with 10% ammonia chloride aqueous solution conditioned reaction liquid pH value=4.8, and add remaining 35kg urea reaction to 20 ℃ of cloud points,
E), with pH value=7.0 of 15% aqueous sodium hydroxide solution conditioned reaction liquid, termination reaction,
F), with logical chuck cooling water temperature to the 35 ℃ discharging of reactor.
G), add the polysiloxane surfactant that accounts for reactant weight 0.25%, carry out spraying drying then and make powdery product at the reactant of discharging.
Embodiment 2:
The mol ratio of urea and formaldehyde is 1: 1.25, and its reaction process step is as follows:
A), 37% formalin with 380kg adds in the reactor, and the adding basic catalyst is regulated pH value=6.0 under constantly stirring, described basic catalyst is the aqueous solution of sodium hydroxide, trolamine, hexamethylenetetramine, its weight proportion is a sodium hydroxide: trolamine: hexamethylenetetramine: water=1.8: 2.1: 1.5: 150, and be warming up to 75 ℃
B), be that the logical steam of 160kg melts with 70% of required urea total amount, temperature is controlled at 80 ℃, and thread splashes into reactor in 35 minutes,
C), drip urea after, 95 ℃ of insulation reaction 52 minutes,
D), with 10% ammonia chloride aqueous solution conditioned reaction liquid pH value=5.3, and add remaining 70kg urea reaction to 20 ℃ of cloud points,
E), with pH value=7.0 of 15% aqueous sodium hydroxide solution conditioned reaction liquid, termination reaction,
F), with logical chuck cooling water temperature to the 30 ℃ discharging of reactor.
G), add the polysiloxane surfactant that accounts for reactant weight 0.55%, carry out spraying drying then and make powdery product at the reactant of discharging.
Embodiment 3:
The mol ratio of urea and formaldehyde is 1: 1.85, and its reaction process step is as follows:
A), 37% formalin with 420kg adds in the reactor, and the adding basic catalyst is regulated pH value=5.8 under constantly stirring, described basic catalyst is the aqueous solution of sodium hydroxide, trolamine, hexamethylenetetramine, its weight proportion is a sodium hydroxide: trolamine: hexamethylenetetramine: water=2.5: 6.0: 3.5: 180, and be warming up to 68 ℃
B), be that the logical steam of 111kg melts with 65% of required urea total amount, temperature is controlled at 82 ℃, and thread splashes into reactor in 28 minutes,
C), drip urea after, 98 ℃ of insulation reaction 45 minutes,
D), with 10% ammonia chloride aqueous solution conditioned reaction liquid pH value=4.5, and add remaining 60kg urea reaction to 20 ℃ of cloud points,
E), with pH value=7.0 of 15% aqueous sodium hydroxide solution conditioned reaction liquid, termination reaction,
F), with logical chuck cooling water temperature to the 30 ℃ discharging of reactor.
G), add the polysiloxane surfactant that accounts for reactant weight 0.85%, carry out spraying drying again and make powdery product at the reactant of discharging.

Claims (2)

1, a kind of Preparation of urea-formaldehyde resin adhesive method, the mol ratio of urea and formaldehyde is controlled at 1: between the 1.2-2.0, it is characterized in that these two kinds of raw materials are under the solutions of weak acidity reacts, and comprises the steps:
A), formalin is added in the reactor, start stirring, and the adding basic catalyst is regulated pH value=5.5-7.0, described basic catalyst is the aqueous solution of sodium hydroxide, trolamine, hexamethylenetetramine, its weight proportion is a sodium hydroxide: trolamine: six methynes, four ammonia: water=1-3: 0.5-20: 0.2-10: 100-200, and be warming up to 65-85 ℃;
B), the logical steam of the 55-85% of required urea total amount is melted, temperature is controlled at 75-85 ℃, and thread splashes into reactor in 20-40 minute;
C), drip urea after, between 90-100 ℃ insulation reaction 30-60 minute;
D), the usefulness 5-10% ammonia chloride aqueous solution is regulated pH value=4-5.5, and is added the surplus urea reaction to terminal;
E), with the pH value=6.5-7.5 of 10-15% aqueous sodium hydroxide solution conditioned reaction liquid, termination reaction;
F), reactor is led to the chuck cooling water temperature to 30-45 ℃ of discharging barrelling.
2, a kind of Preparation of urea-formaldehyde resin adhesive method as claimed in claim 1 is characterized in that the polysiloxane surfactant at the reactant adding 0.1-1.0% of discharging, then spraying drying.
CN 98110988 1998-07-31 1998-07-31 Process for preparing adhesive of urea-formaldehyde resin Expired - Fee Related CN1115369C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 98110988 CN1115369C (en) 1998-07-31 1998-07-31 Process for preparing adhesive of urea-formaldehyde resin

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 98110988 CN1115369C (en) 1998-07-31 1998-07-31 Process for preparing adhesive of urea-formaldehyde resin

Publications (2)

Publication Number Publication Date
CN1243854A true CN1243854A (en) 2000-02-09
CN1115369C CN1115369C (en) 2003-07-23

Family

ID=5221000

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 98110988 Expired - Fee Related CN1115369C (en) 1998-07-31 1998-07-31 Process for preparing adhesive of urea-formaldehyde resin

Country Status (1)

Country Link
CN (1) CN1115369C (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102250572A (en) * 2011-06-17 2011-11-23 江苏赛奥生化有限公司 Preparation method of oxidized pueraria starch adhesive
CN103834338A (en) * 2014-03-20 2014-06-04 浙江红高梁木业有限公司 Adhesive for artificial board and preparation method thereof
CN103936524A (en) * 2014-05-08 2014-07-23 河南力浮科技有限公司 Method for producing urea formaldehyde controlled-release compound fertilizer
WO2014169749A1 (en) * 2013-04-19 2014-10-23 Ju Changlin Plant fibre composite fireproof plate and manufacturing method thereof

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100384899C (en) * 2006-03-15 2008-04-30 北京林业大学 Urea-formaldehyde resin and preparation method thereof

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102250572A (en) * 2011-06-17 2011-11-23 江苏赛奥生化有限公司 Preparation method of oxidized pueraria starch adhesive
WO2014169749A1 (en) * 2013-04-19 2014-10-23 Ju Changlin Plant fibre composite fireproof plate and manufacturing method thereof
CN103834338A (en) * 2014-03-20 2014-06-04 浙江红高梁木业有限公司 Adhesive for artificial board and preparation method thereof
CN103936524A (en) * 2014-05-08 2014-07-23 河南力浮科技有限公司 Method for producing urea formaldehyde controlled-release compound fertilizer

Also Published As

Publication number Publication date
CN1115369C (en) 2003-07-23

Similar Documents

Publication Publication Date Title
CA2433404C (en) Stable liquid melamine urea formaldehyde resins
CN1139645C (en) Powdered adhesive for wood material
CN1145059A (en) The controlled release matrix-type fertilizer and the process of preparation therefor
US4814422A (en) Pulverulent aminoplast adhesive resin for wood-base materials having a low formaldehyde emission, its preparation, and a formulated pulverulent aminoplast adhesive resin
CN1115369C (en) Process for preparing adhesive of urea-formaldehyde resin
CA2042927A1 (en) Lignosulfonate conditioning agent for urea particles
US3112343A (en) Free-flowing, storage stable granular or pelletized urea
US4789391A (en) Controlled release formulation for fertilizers
CN101538355B (en) Industrialized production method of urea-formaldehyde resin
CN101643480A (en) Preparation method of cobalt boracylate
CN1616510A (en) Production of modified dimeric cyanamide urea formadehyde copolymer resin and its use for producing dipped paper
US4756738A (en) Controlled release formulation for fertilizers
CN102250572B (en) Preparation method of oxidized pueraria starch adhesive
CN102190998A (en) Method for producing melamine formaldehyde resin adhesives
CN1342628A (en) Anti-blocking loosening agent for preparing loose composite fertilizer with long storage period
CN106046785A (en) High-temperature-resistant synthetic resin and preparation method thereof
US6335386B1 (en) Bonding materials
CN1264691A (en) Process for preparing urine-base compound fertilizer by fusing urea (urine) and spray granulating
US4957999A (en) Process for curing aminoplast resins
CN1219506A (en) Anticaking agent for ammonium nitrate
CN102277114B (en) Preparation method of bacterial protein urea formaldehyde adhesive
WO1992001018A2 (en) Formaldehyde resin curing agents
CN1182207C (en) High molecular polymer calking and productive method thereof
CN1042542C (en) High performance formol polymerization retarder and preparing process thereof
CN1827710A (en) Free formaldehyde scavenger and production method thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C19 Lapse of patent right due to non-payment of the annual fee
CF01 Termination of patent right due to non-payment of annual fee