CA1290091C - Process for the preparation of urea-formaldehyde resins - Google Patents
Process for the preparation of urea-formaldehyde resinsInfo
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- CA1290091C CA1290091C CA000542465A CA542465A CA1290091C CA 1290091 C CA1290091 C CA 1290091C CA 000542465 A CA000542465 A CA 000542465A CA 542465 A CA542465 A CA 542465A CA 1290091 C CA1290091 C CA 1290091C
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- Prior art keywords
- urea
- mixture
- formaldehyde
- process according
- molar ratio
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-
- 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
- C08G12/00—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
- C08G12/02—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
- C08G12/04—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds
- C08G12/10—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds with acyclic compounds having the moiety X=C(—N<)2 in which X is O, S or —N
- C08G12/12—Ureas; Thioureas
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L97/00—Compositions of lignin-containing materials
- C08L97/02—Lignocellulosic material, e.g. wood, straw or bagasse
Abstract
PROCESS FOR THE PREPARATION OF UREA-FORMALDEHYDE RESINS
ABSTRACT
Urea-formaldehyde resins which may be cured to give products having a low total extractable formaldehyde content are prepared by the following process:
(i) aqueous 30-50% formaldehyde and urea are mixed in a formaldehyde:urea molar ratio of 2-3:1 at pH 6-11, (ii) this mixture is heated to at least 50°C, preferably to at least 80°C, (iii) a mineral or organic acid is added to bring the mixture to pH 0.5-3.5, (iv) the mixture is heated at a temperature between 80°C and the reflux temperature, preferably for 15 minutes to 1 hour, (v) keeping the temperature at or above 80°C, a base is added to bring the mixture to pH 6.5-9 and (vi) urea is added until the formaldehyde:urea molar ratio is within the range 0.8-1.8:1.
In a modification of the process, solid particulate resins are obtained by reacting the mixture from step (v) with urea at a pH below 7 to increase the viscosity thereof, adding a base until the mixture reaches a pH of 6.5-9 and dehydrating the resulting mixture.
ABSTRACT
Urea-formaldehyde resins which may be cured to give products having a low total extractable formaldehyde content are prepared by the following process:
(i) aqueous 30-50% formaldehyde and urea are mixed in a formaldehyde:urea molar ratio of 2-3:1 at pH 6-11, (ii) this mixture is heated to at least 50°C, preferably to at least 80°C, (iii) a mineral or organic acid is added to bring the mixture to pH 0.5-3.5, (iv) the mixture is heated at a temperature between 80°C and the reflux temperature, preferably for 15 minutes to 1 hour, (v) keeping the temperature at or above 80°C, a base is added to bring the mixture to pH 6.5-9 and (vi) urea is added until the formaldehyde:urea molar ratio is within the range 0.8-1.8:1.
In a modification of the process, solid particulate resins are obtained by reacting the mixture from step (v) with urea at a pH below 7 to increase the viscosity thereof, adding a base until the mixture reaches a pH of 6.5-9 and dehydrating the resulting mixture.
Description
~:9()091 3-15971/~/ARL 372 PROCESS FOR THE PREPARATION OF UREA-FORMALDEHYDE RESINS
This invention relates to a new process for the preparation of urea-formaldehyde resins having a low extractable formaldehyde content.
Urea-formaldehyde resins are widely used in industry as binders for the production of wood-based materials, particularly chipboard, plywood, and various fibreboards. They are usually employed as colloidal aqueous solutions having a 60-70o solids content, the solids content being the percentage weight left when a 2 9 sample of the resin is heated at atmospheric pressure at 120C for 3 hours.
The resins themselves are complex mixtures of various condensation products, ranging from simple methylolated ureas to fairly high molecular weight materials, and the precise properties of any particular resin will depend upon its molar ratio (i.e. the ratio of formaldehyde to urea when used in its manufacture), the type and proportion of the various linkages within the resin structure, and the proportions of high and low molecular weight material. These last two factors are dependent upon the precise manufacturing method that is used.
Conventional commercial resins all liberate a certain amount of formaldehyde during hot curing and after cure has taken place. The latter liberation of formaldehyde can be a serious problem since it limits the use to which, for example, fibreboards and particle boards may be put. A board that liberates formaldehyde above a specified level cannot be used in unventilated areas.
The measurement of the total extractable formaldehyde is therefore an important test that is carried out on fibreboard and particle board samples, and is usually effected using the method of the Federation Europeenne des Syndicates des Fabricants des Panneaux de Particules (FESYP) and described in British Standard 1~11. In this test small rectangular blocks sawn from air-dried fibreboard or particle board are extracted with toluene, the toluene is washed with water, and the water measured iodometrically for formaldehyde.
A need exists for resins that have a very low content of extractable formaldehyde but which, in all their performance properties, behave like a conventional urea-formaldehyde resin.
The conventional method of manufacturing urea-formaldehyde resins comprises precondensing urea with formaldehyde in aqueous solution at the reflux at pH 7-9, and heating the mxiture at pH 5-6 until the desired degree of water insolubility or viscosity is reached. The product is neutralised and may then be evaporated and blended with a further quantity of urea if desired. Such conventional resins usually have a F:U molar ratio within the range 1.3-2.3:1.
Resins having a F:U molar ratio as low as 1:1 have been 9~
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described in British Patent Specification No. 1 420 017. These resins are said to be suitable for binding wood-based materials and are prepared by (i) condensing formaldehyde and urea at a F:U molar ratio of at least 3:1 and at pH 3 or less, (ii) adding urea to bring the molar ratio down to 2-2.75:1, and continuing to heat at pH 3 or less (iii) optionally, adding more urea su that the final molar ratio is within the range 1-2.75:1, (iv) adjusting the pH to 5-6.5 or to 8-10, and continuing the heating until the desired product is formed. This product may then be concentrated or dried, if desired. A serious drawback with this process is that, on an industrial scale, it is difficult to obtain a consistent product and there is a serious risk of the product forming an intractable gel during the process, such formation then requiring dismantling of the apparatus in order for it to be cleaned. Further, when the product has been made successfully, it has poor 'wash down' properties. This means that pipework, pumps etc. through which the resin has been passed are difficult to clean, due to the inherent stickiness of the resin.
Another process for preparing adhesive resins with low formaldehyde content is described in United States Patent No.
~ 85 4~ , In this process resins having a F:U molar ratio within g~
`~
the range 1.0 to 1.2:1 are prepared as follows:
(i) formaldehyde solution is acidiFied to pH 0.5-2.5, (ii) the acid solution is heated to 50-70C, (iii) urea is added slowly until the F:U molar ratio reaches 2.9 to 3.1:1 (iv) when the mixture reaches a given viscosity it is neutralised, and (v) urea is added to give a F:U molar ratio 1.0 to 1.2:1.
Like the previous process described, this process is difficult to control, especially on an industrial scale and unless careful control is maintained over the reaction the resin will gel during the condensation stage if the conditions that are described are strictly followed.
It has now been found that urea-formaldehyde resins having a low content of total extractable formaldehyde and which are suitable for bonding wood-based products, such as fibreboard or particleboard, may be prepared with a minimal risk of forming intractable gels if the urea is first methylolated under alkaline conditions at elevated temperature and in a F:U molar ratio within the range 2:1 to 3:1, this mixture is then acidified to a low pH
and condensation allowed to continue at elevated temperature. The mixture is neutralised and, in either order, it is concentrated if necessary and urea is added to adjust the F:U molar ratio to within the range 1.8 or less:1. This process facilitates formation of a resin which is water soluble and which, when freshly prepared, is completely transparent in appearance. This transparency is lost gradually on storing, the resin becoming slowly opalescent, so that examination of the turbidity of the resin gives an immediate indication oF its age or storage conditions.
Accordingly, this invention provides a process for the preparation oF urea-formaldehyde resins which comprises (i) mixing an aqueous formaldehyde solution containing 30-50O by weight of formaldehyde with urea at a formaldehyde:urea -molar ratio of 2 to 3:1 and at pH 6-11, (ii) heating the mixture to at least 50C, (iii) adding an acid until the mixture reaches a pH
within the range 0.5-3.5, (iv) heating the mixture at a temperature between 80C
and the reflux temperature, (v) with the mixture at a temperature of at least 80C, adding a base until the mixture reaches a pH within the range 6.5-9, and (vi) adding urea until the formaldehyde:urea molar ratio is within the range 0.8-1.8:1.
For use as a binder for particle boards or fibreboards, the urea-formaldehyde resin should have a solids content of 40 to 75O. If it is necessary to evaporate the mixture in order to achieve such a solids content, the evaporation may be carried out, under ~;290~9 reduced pressure, either between stages (v) and (vi) or after stage ( Vl ) .
The initial mixing of formaldehyde solution, usually containing 35-40O by weight of formaldehyde, and urea usually takes place at a F:U molar ratio within the range 2.2 to Z.8:1, especially 2.3 to 2.5:1, and at pH 7-9. This mixture is then heated to at least 50C, usually to at least 80C and preferably to reflux. An acid is then added to bring the pH of the mixture to below 3.5, generally not above 3 and preferably within the range 1-2.5. The acid is preferably added while maintaining gentle reflux to keep the exothermic reaction under control. The type of acid used is not critical - inorganic or organic acids have both been found to be suitable. Typical acids that may be used include trichloroacetic, toluene-p-sulphonic, hydrochloric, sulphuric, sulphamic and phosphoric acids.
Heating of the acid mixture in step (iv) is preferably effected at reflux temperature; this heating is usually carried out for a period of from 1 minute to 2 hours, especially from 15 minutes to 1 hour. The temeprature of the reaction mxiture may be allowed to fall slightly, but this increases the risk of intractable gel formation, particularly when a formaldehyde:urea ratio up to 2.6:1 is used. In general, the temperature below which the reaction mixture should not be allowed to fall depends on the formaldehyde:urea ratio employed, lower ratios requiring higher temperatures to be maintained.
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When the Formaldehyde:urea ratio is up to 2.6:1, the reaction mixture is preferably maintained under reflux until the acid condensation stage (iv) has been terminated by the addition of the base in step (v). Heating of the reaction mixture in steps (ii), (iv) and (v) may be carried out under pressure, in which case the reflux temperature is, of course, higher and the respective heating time can generally be reduced.
For reasons of economy, the base which is used in step (v) is usually sodium hydroxide or potassium hydroxide, but any base that will raise the pH of the mixture to within the range 6.5 to 9 is satisfactory.
When the desired pH has been reached, the mixture is usually partially evaporated under reduced pressure to eliminate some of the water present, although this evaporation may take place after the further addition of urea. Evaporation is usually effected below 50C and preferably within the range 35-45C. The solids content of the product from this evaporation may be varied witnin fairly wide limits, depending upon the ultimate use of the final resin, but is usua71y within the range 50-65o by weight if the evaporation precedes urea addition, and 60-70o by weight if it follows urea addition. When the desired solids content has been reached, the mixture is usually cooled to a temperature below 50C~
preferably to within the range 25-45C~ before urea is added in step (vi). The mixture is usually stirred for 15 to 60 minutes ~?~ 9~
following addition of urea. Addition of urea gives the desired F:U molar ratio, preferably from 1.0 to 1.7:1, especially 1.2 to 1.5:1.
The process of the invention may be carried out batchwise or continuously. Resins made by this new process have their formaldehyde firmly bonded into the molecule, so that both the uncured and cured resins give low values for available formaldehyde.
This may be shown by measuring the total free formaldehyde from the uncured resin, the liberated formaldehyde from the hot curing of fibreboard or particle board, and the total extractable formaldehyde from cured fibreboard or particle board.
8y means of the process of the present invention, resins having remarkably good washdown properties can be prepared, so that apparatus which has been used for the uncured resin may be cleaned easily with a jet of cold water, as can any spillages. This is an important consideration in an industry where large quantities of resin are handled and, if the resin residues are allowed to remain and harden, an expensive strip-down of equipment is needed for cleaning.
The present invention also facilitates the production of resins having remarkable clarity when freshly prepared. ~esins having F:U
molar ratios of 1.8 or less have always been opalescent, or more usually thick white liquids. To make such resins as clear, transparent liquids allows an instant visible means of checking that the resin made by this process has been supplied and that contamination by other 1?~90~39~
_ 9 _ materials has not taken place.
These advantages can be achieved with no loss of strength in the resin. Products made using this resin, such as fibreboard and particleboard, generally have the strength which could be expected from products made with a conventional resin having the same solids content and F:U molar ratio.
Resins made by the process of this invention are particularly useful in the production of products known as medium density fibreboards, facilitating good processability and high production rates and showing good resistance to premature cure in blending operations.
These resins may be cured by any conventional means, usually by heating or by the addition of an acid hardener which cures the resins at ambient temperatures, such as formic, phosphoric, or hydrochloric acid, or using a heat-activated hardener such as an acid salt that liberates an acid when heated, preferably ammonium chloride.
Resins prepared by the process of the invention are useful in bonded lignocellulosic material, especially fibreboard or particleboard, the bonded materlal comprising the resin in cured form as a binder. A process for bonding two lignocellulosic surfaces together comprlses applying to at~least one of the surfaces a urea-formaldehyde resin prepared by the process of the invention, and holding the surfaces together while curing the resin. In a ~ - .
~9~
particular embodiment of this process, fibreboard or particle board is produced by mixing lignocellulosic fibres or particles~
preferably of wood, together with a binder comprising a urea-formaldehyde resin prepared by the process of the invention and, optionally, a heat-activated hardener therefor and heating the resulting mixture under pressure until the binder is cured. The optional heat-activated hardener can be any conventional heat-activated hardener for urea-formaldehyde resins, such as an acid salt which liberates an acid on heating, preferably ammonium chloride. In general, no hardener is used in the production of fibreboard, while the hardener is used in the manufacture of particleboard. The fibreboard or particleboard can be formed in a conventional press, using conventional curing conditions.
Conventional additives, such as a wax emulsion to improve moisture resistance of the product, can be included in the mixture of lignocellulosic material and binder.
The process of the invention as hereinbefore defined may be modified to produce resins in a solid particulate form. After step (v), instead of adding urea to give a resin having a formaldehyde:urea molar ratio of 0.8:1 to 1.8:1, the mixture from step (v), preferably after evaporation as hereinbefore described, is reacted with urea under acid conditions to give a higher molecular weight resin which is then neutralised and dehydrated to give a solid, particulate resin.
.
~29~39~
Accordingly, the invention also provides a modification of the process as hereinbefore described which comprises (a) carrying out steps (i) to (v) as hereinbefore described, (b) reacting the mixture from step (v) with urea at a pH
below 7 to increase the viscosity thereof, - -(c) adding a base until the mixture reaches a pH within the range 6.5-9, and (d) dehydrating the mixture to form a solid particulate resin.
The reaction of the mixture from step (v) with urea is usually carried out at a pH of 3 to 5 and a temperature of 30 to 60C, using urea in an amount sufficient to give the reaction mixture a formaldehyde:urea molar ratio of from 1~3:1 to 1.9:1, until the viscosity of the reaction mixture is 2 to 4 times the initial viscosity of the mixture. Preferably this reaction is carried out at a pH of 3.5 to 4.5 and a temperature of 35 to 50~C, using urea in an amount sufficient to give the reaction mixture a formaldehyde:urea molar ratio of 1.5:1 to 1.7:1, until the viscosity of the reaction mixture is 2.5 to 3.5 times the initial viscosity of the mixture. Preferably also, the mixture from step (v) is evaporated to a solids content of 40-65o~ preferably 50-60o~ by weight, for example by a method as hereinbefore described, before reaction with the urea.
Acids suitable for use in reducing the pH of the mixture .
from step (v) include those hereinbefore mentioned as suitable For use in step (iii). Any base that will raise the pH of the mixture to within the range 6.5 to 9 can be used in step (c); for reasons of economy, sodium hydroxide and potassium hydroxide are preferred.
- The dehydration step (d) can be carried out in a conventional spray drier to Form the particulate resin. By means of the process oF the invention, particulate resins having low values for available formaldehyde, both in the uncured and cured state, can be obtained, these resins having excellent tack properties and - :
being particularly suitable For use in binders for particle board, waFer board and plywood.
For use as a binder, the particulate resin may be mixed with a solid hardener therefor and optionally with additives, e.g.
flllers such as wood flour and china clay, to give a storage-stable composition known as a "one-shot" composition which can be activated by the addition of water. Suitable solid hardeners for use in such "one-shot" compositions are well-known; aluminium sulphate is the most generally used material. Alternatively, the particulate resin may be dissolved or dispersed in water to reform, in effect, a liquid resin which can be mixed with a hardener therefor and optlonally with additives For use as a binder. Conventional hardeners such as the acid and salt hardeners hereinbefore mentioned, can be used.
The invention is illustrated by reference to the following ~ ~2~
Examples in which all parts and percentages are by weight unless otherwise indicated. "w/v" indicates weight by volume. The solids contents are determined by heating a 2 9 sample at 120C for 3 hours under atmospheric pressure.
::
.
.
; :
~L~d90(~1 -Aqueous formaldehyde solution (23.93 kg; 38.56o HCHO) is treated with sodium hydroxide solution t76.4 ml; 10,o w/v NaOH), and urea (7.69 kg). The mixture, which is of pH 9 and has a f:U
molar ratio of 2.40:1~ is stirred and heated to reflux. It is allowed to cool slightly, to 98C, and an aqueous solution of sulphamic acid (343.6 ml; 20~o NH2503H) is added. The resultant mixture is of pH 2.0 ~ and this is heated under reflux for 30 minutes.
Whilst maintaining the reflux, sodium hydroxide solution (509.8 ml; 10o w/v NaOH) is added to give a neutral solution (pH 7).
This is allowed to cool to about 40C ~ at which temperature a vacuum is applied and water is distilled from the mixture, a total of 11. 3 kg water being collected. The solids content of the mixture is 59~o. Finally a further quantity of urea is added (5.40 kg), giving a F:U molar ratio of 1.41:1.
This resin is a water-soluble, colourless transparent liquid having the following properties:
Solids content 65,a Viscosity at 25C- 0.27 Pa s Free formaldehyde 0.3O
, ' 1~9 Aqueous formaldehyde solution (75.68 9; 38.56o HOHO) is treated with sodium hydroxide solution (0.24 ml; 10o w/v NaOH) followed by urea (24.32 9). The mixture, which is of pH 9 and has a F:U molar ratio of 2.40:1, is stirred and heated to reflux. Phosphoric acid solution (5.0 ml; 20o H3P04) is added, to bring the mixture to pH 2.0, and it is then heated under reflux for 30 minutes. Neutralisation with sodium hydroxide solution (20o) follows and the mixture is evaporated at about 40C to a solids content of 60o. The mixture i5 cooled and urea (17.08 9) is added, giving a F:U molar ratio of 1.~1:1.
This resin is a water-soluble, colourless transparent liquid having the following properties:
Solids content 71o Vlscosity at 25C 1.72 Pa s Softwood core chips (1540 9), dried to a moisture content of 2o, are blended with a mixture comprising the resin described in Example 1 (173.8 9), ammonium chloride solution (12.0 9;
10o NH4Cl), a commercial wax emulsion (12.0 9; 65o wax), and water (65.0 gj. Part of the resultant blend (1650 9) is placed within a wooden frame 355mm square, and consolidated at room temperature under a pressure of 791 kPa. The resultant consolidated 9~
sheet is removed from the Frame and compressed at 145C for 8 minutes under a pressure of 2.77 MPa. The resultant chipboard has a thickness of 19mm. The board is tested, with the following results:
F:U molar ratio 1.41:1 Resin content of board (O solids) _, _ . . . _ . .
Density ~kg/m3) 667 .
Modulus of rupture (mPa) 21.57 Transverse tensile 9O
strength (mPa) ' _ _ . _ _ . _ _ .
Total extractable 0.013 formaldehyde (Uo) _ It may therefore be seen that the total extractable formaldehyde, measured in accordance with BS 1811, in the board is extremely low.
~ ~:?~
_ Aqueous formaldehyde solution (75.68 9; 38.56o HCHO) is treated with sodium hydroxide solution (0.24 ml, 10o w/v NaOH) and urea (24.32 g). This mixture, which is of pH 9 and has a F:U ratio of 2.40:1~ is heated to reflux and sulphamic acid (1.2 ml; 15o NH2503H) is added, giving the mixture a pH of 2Ø The mixture is then heated under reflux for 30 minutes after which, while the reflux is maintained, aqueous NaOH is added to pH 7. After cooling to 25C~ urea (17.08 9) is added, and the product evaporated in vacuo below 40C to a final weight of 81.12 9.
The product is a colourless, transparent resin having an F:U molar ratio of 1.41 :1 ~ a solids content of 68.5o~ and a viscosity at 25C of 0. 58 Pa s.
Aqueous formaldehyde solution (748.3 9; 38.68o HCHO) is treated with sodium hydroxide solution (1.2 ml; 20o w/v NaOH) and urea (251.7 9). The mixture which is of pH 9 and has a F:U molar ratio of 2.30:1~ is stirred and heated to reflux. Aqueous sulphuric acid (20 ml; 15o H2S04) is addedg to bring the mixture to pH 2.0~
and it is then heated under reflux for 30 minutes. Aqueous sodium hydroxide (14 ml; 20o w/v NaOH) is added while maintaining the reflux to bring the mixture to pH 7.4. The mixture is then evaporated in vacuo at about 40C to a solids content of 59O. Urea (46.2 9) is added to part of the evpaorated resin (190. 3 9) to give a resin having a F:U molar ratio of 1.30:1. This resin is a water-soluble, colourless transparent liquid having a solids content of 66o and a viscosity at 25C of 0. 55 Pa s.
Example 1 is repeated to the stage at which water is distilled From the mixture, to a solids content of 57o. To 100 parts by weight of the resulting mixture, 25.55 parts by weight of urea is added to give a resin having a F:U molar ratio oF 1.25:1. This resin is a water-soluble colourless transparent liquid having a solids content of 66o and a viscosity at 25UC of 0. 32 Pa s.
Softwood core chips (1540 9)7 dried to a moisture content of 2o~ are blended with a mixture comprising the resin described in Example 6 (172 g), ammonium chloride solution (12 9; 10o NH4Cl), a commercial wax emulsion (12 g: 65o wax), and water (65 g). Part of the resultant blend (1650 g) is placed within a wooden frame 355 mm square, and consolidated at room temperature under a pressure of 791 kPa. The resultant consolidated sheet is removed From the frame and compressed at 145~C for 8 minutes under a pressure of 2.77 MPa. The resultant chipboard (particle board) has a thickness of 19mm. The board is tested, with the following results:
: :
F:U molar ratio 1.25:1 . .
Resin content of board (O solids) Density (kg/m ) 643 - - .
: Modulus of rupture (mPa) 14.01 - - - .
Transverse tensile strength (mPa) 0'54 .. . . ~ .
Total extractable formaldehyde-(n) 0.012 __ . . . : . . . .
: It can be seen that the total extractable formaldehyde, measured in accordance with BS 1811, in the board is extremely low.
:
9~9~
Example 5 is repeated to the stage where the mixture is evaporated, the evaporation being carried out to give a solids content of 50o instead of 59o. The evaporated mixture has a ; viscosity at 25C of 0.08 Pa s. Urea (30 parts) is added to the evaporated mixture (200 parts) and the resulting mixture is : stirred until the urea is dissolved, giving a mixture with a viscosity at 25C of 0.07 Pa s. The F:U molar ratio of the mixture is 1.57:1. The temperature of the mixture is adjusted, if necessary, to 34-40C and aqueous sulphuric acid (1 part; 15o H2504) is added ~ to bring the mixture to pH 3.9. The mixture is stirred for 3D
: ~ ~ : mlnutes, the temperature rising to 50C ~ ~samples being taken at ; regular intervals for viscosity determlnation, until the viscosity . ~ of the mixture is increased to 0.22 Pa s. Aqueous sodium hydroxide ` ~ (D.4 part; 20o NaOH) is added to bring the mixture to pH 7. The ~mixture is then dehydrated in a spray-drier to give a resin powder having a softening point of 133C~ a F:U molar ratio of 1.56:1 and ~: a free formaldehyde content of 0.27o.
Aqueous formaldehyde solution (757.1 9; 38.50o HCHO) is : treated wlth sodium hydroxide solution (2.4 ml; 10o NaOH) and urea ~ (242.9 ~9). The mixture, whlch is of pH 9 and has a F:U molar ratio : ~ ~ :of 2.4:1, is stirred and heated to 80C, at which temperature it ~290(~91 is maintained for 15 minutes. Aqueous sulphuric acid (13.2 ml;
15o H2504) is added, to bring the mixture to pH below 3.5. The mixture is cooled to 80C and heated at this temperature for 30 minutes. Aqueous sodium hydroxide (10o NaOH) is then added to bring the mixture to pH 7. The mixture is then evaporated in vacuo at about 40C to a solids content of 59O. Urea (201 9) is added to the evaporated resin (695 9) to give a resin having a F:U molar ratio of 1. 3: 1. This resin is a water-soluble, colourless transparent liquid having a solids content of 65o and a viscosity at 25C of O.S Pa s.
Aqueous formaldehyde solution (784.6 9; 38.5o HCHO) is treated with sodium hydroxide solution (2. 4 ml; 10o NaOH), and urea (215.6 9). The mixture, which is of pH 9 and has a F:U molar ratio of 2.8:1 ~ is stirred and heated to reflux temperature, where it is maintained for 15 minutes. An aqueous solution of sulphuric acid (6.6 ml; 15o H2S04) is added. The resulting mixture, which is of pH 2.7~ is heated under reflux for 30 minutes.
Whilst maintaining the reflux, aqueous sodium hydroxide solution (10o NaOH) is added to give a neutral solution (pH 7).
This solution is evaporated in vacuo at 40C to a solids content of 59O~ urea is added to give a F:U molar ratio of 1.25:1 ~ and the mixture is stirred for 60 minutes.
This resin is a water-soluble, colourless transparent liquid having a solids content of 65o and a viscosity at 25C of 0.1 Pa s.
This invention relates to a new process for the preparation of urea-formaldehyde resins having a low extractable formaldehyde content.
Urea-formaldehyde resins are widely used in industry as binders for the production of wood-based materials, particularly chipboard, plywood, and various fibreboards. They are usually employed as colloidal aqueous solutions having a 60-70o solids content, the solids content being the percentage weight left when a 2 9 sample of the resin is heated at atmospheric pressure at 120C for 3 hours.
The resins themselves are complex mixtures of various condensation products, ranging from simple methylolated ureas to fairly high molecular weight materials, and the precise properties of any particular resin will depend upon its molar ratio (i.e. the ratio of formaldehyde to urea when used in its manufacture), the type and proportion of the various linkages within the resin structure, and the proportions of high and low molecular weight material. These last two factors are dependent upon the precise manufacturing method that is used.
Conventional commercial resins all liberate a certain amount of formaldehyde during hot curing and after cure has taken place. The latter liberation of formaldehyde can be a serious problem since it limits the use to which, for example, fibreboards and particle boards may be put. A board that liberates formaldehyde above a specified level cannot be used in unventilated areas.
The measurement of the total extractable formaldehyde is therefore an important test that is carried out on fibreboard and particle board samples, and is usually effected using the method of the Federation Europeenne des Syndicates des Fabricants des Panneaux de Particules (FESYP) and described in British Standard 1~11. In this test small rectangular blocks sawn from air-dried fibreboard or particle board are extracted with toluene, the toluene is washed with water, and the water measured iodometrically for formaldehyde.
A need exists for resins that have a very low content of extractable formaldehyde but which, in all their performance properties, behave like a conventional urea-formaldehyde resin.
The conventional method of manufacturing urea-formaldehyde resins comprises precondensing urea with formaldehyde in aqueous solution at the reflux at pH 7-9, and heating the mxiture at pH 5-6 until the desired degree of water insolubility or viscosity is reached. The product is neutralised and may then be evaporated and blended with a further quantity of urea if desired. Such conventional resins usually have a F:U molar ratio within the range 1.3-2.3:1.
Resins having a F:U molar ratio as low as 1:1 have been 9~
,,~
described in British Patent Specification No. 1 420 017. These resins are said to be suitable for binding wood-based materials and are prepared by (i) condensing formaldehyde and urea at a F:U molar ratio of at least 3:1 and at pH 3 or less, (ii) adding urea to bring the molar ratio down to 2-2.75:1, and continuing to heat at pH 3 or less (iii) optionally, adding more urea su that the final molar ratio is within the range 1-2.75:1, (iv) adjusting the pH to 5-6.5 or to 8-10, and continuing the heating until the desired product is formed. This product may then be concentrated or dried, if desired. A serious drawback with this process is that, on an industrial scale, it is difficult to obtain a consistent product and there is a serious risk of the product forming an intractable gel during the process, such formation then requiring dismantling of the apparatus in order for it to be cleaned. Further, when the product has been made successfully, it has poor 'wash down' properties. This means that pipework, pumps etc. through which the resin has been passed are difficult to clean, due to the inherent stickiness of the resin.
Another process for preparing adhesive resins with low formaldehyde content is described in United States Patent No.
~ 85 4~ , In this process resins having a F:U molar ratio within g~
`~
the range 1.0 to 1.2:1 are prepared as follows:
(i) formaldehyde solution is acidiFied to pH 0.5-2.5, (ii) the acid solution is heated to 50-70C, (iii) urea is added slowly until the F:U molar ratio reaches 2.9 to 3.1:1 (iv) when the mixture reaches a given viscosity it is neutralised, and (v) urea is added to give a F:U molar ratio 1.0 to 1.2:1.
Like the previous process described, this process is difficult to control, especially on an industrial scale and unless careful control is maintained over the reaction the resin will gel during the condensation stage if the conditions that are described are strictly followed.
It has now been found that urea-formaldehyde resins having a low content of total extractable formaldehyde and which are suitable for bonding wood-based products, such as fibreboard or particleboard, may be prepared with a minimal risk of forming intractable gels if the urea is first methylolated under alkaline conditions at elevated temperature and in a F:U molar ratio within the range 2:1 to 3:1, this mixture is then acidified to a low pH
and condensation allowed to continue at elevated temperature. The mixture is neutralised and, in either order, it is concentrated if necessary and urea is added to adjust the F:U molar ratio to within the range 1.8 or less:1. This process facilitates formation of a resin which is water soluble and which, when freshly prepared, is completely transparent in appearance. This transparency is lost gradually on storing, the resin becoming slowly opalescent, so that examination of the turbidity of the resin gives an immediate indication oF its age or storage conditions.
Accordingly, this invention provides a process for the preparation oF urea-formaldehyde resins which comprises (i) mixing an aqueous formaldehyde solution containing 30-50O by weight of formaldehyde with urea at a formaldehyde:urea -molar ratio of 2 to 3:1 and at pH 6-11, (ii) heating the mixture to at least 50C, (iii) adding an acid until the mixture reaches a pH
within the range 0.5-3.5, (iv) heating the mixture at a temperature between 80C
and the reflux temperature, (v) with the mixture at a temperature of at least 80C, adding a base until the mixture reaches a pH within the range 6.5-9, and (vi) adding urea until the formaldehyde:urea molar ratio is within the range 0.8-1.8:1.
For use as a binder for particle boards or fibreboards, the urea-formaldehyde resin should have a solids content of 40 to 75O. If it is necessary to evaporate the mixture in order to achieve such a solids content, the evaporation may be carried out, under ~;290~9 reduced pressure, either between stages (v) and (vi) or after stage ( Vl ) .
The initial mixing of formaldehyde solution, usually containing 35-40O by weight of formaldehyde, and urea usually takes place at a F:U molar ratio within the range 2.2 to Z.8:1, especially 2.3 to 2.5:1, and at pH 7-9. This mixture is then heated to at least 50C, usually to at least 80C and preferably to reflux. An acid is then added to bring the pH of the mixture to below 3.5, generally not above 3 and preferably within the range 1-2.5. The acid is preferably added while maintaining gentle reflux to keep the exothermic reaction under control. The type of acid used is not critical - inorganic or organic acids have both been found to be suitable. Typical acids that may be used include trichloroacetic, toluene-p-sulphonic, hydrochloric, sulphuric, sulphamic and phosphoric acids.
Heating of the acid mixture in step (iv) is preferably effected at reflux temperature; this heating is usually carried out for a period of from 1 minute to 2 hours, especially from 15 minutes to 1 hour. The temeprature of the reaction mxiture may be allowed to fall slightly, but this increases the risk of intractable gel formation, particularly when a formaldehyde:urea ratio up to 2.6:1 is used. In general, the temperature below which the reaction mixture should not be allowed to fall depends on the formaldehyde:urea ratio employed, lower ratios requiring higher temperatures to be maintained.
~2~
When the Formaldehyde:urea ratio is up to 2.6:1, the reaction mixture is preferably maintained under reflux until the acid condensation stage (iv) has been terminated by the addition of the base in step (v). Heating of the reaction mixture in steps (ii), (iv) and (v) may be carried out under pressure, in which case the reflux temperature is, of course, higher and the respective heating time can generally be reduced.
For reasons of economy, the base which is used in step (v) is usually sodium hydroxide or potassium hydroxide, but any base that will raise the pH of the mixture to within the range 6.5 to 9 is satisfactory.
When the desired pH has been reached, the mixture is usually partially evaporated under reduced pressure to eliminate some of the water present, although this evaporation may take place after the further addition of urea. Evaporation is usually effected below 50C and preferably within the range 35-45C. The solids content of the product from this evaporation may be varied witnin fairly wide limits, depending upon the ultimate use of the final resin, but is usua71y within the range 50-65o by weight if the evaporation precedes urea addition, and 60-70o by weight if it follows urea addition. When the desired solids content has been reached, the mixture is usually cooled to a temperature below 50C~
preferably to within the range 25-45C~ before urea is added in step (vi). The mixture is usually stirred for 15 to 60 minutes ~?~ 9~
following addition of urea. Addition of urea gives the desired F:U molar ratio, preferably from 1.0 to 1.7:1, especially 1.2 to 1.5:1.
The process of the invention may be carried out batchwise or continuously. Resins made by this new process have their formaldehyde firmly bonded into the molecule, so that both the uncured and cured resins give low values for available formaldehyde.
This may be shown by measuring the total free formaldehyde from the uncured resin, the liberated formaldehyde from the hot curing of fibreboard or particle board, and the total extractable formaldehyde from cured fibreboard or particle board.
8y means of the process of the present invention, resins having remarkably good washdown properties can be prepared, so that apparatus which has been used for the uncured resin may be cleaned easily with a jet of cold water, as can any spillages. This is an important consideration in an industry where large quantities of resin are handled and, if the resin residues are allowed to remain and harden, an expensive strip-down of equipment is needed for cleaning.
The present invention also facilitates the production of resins having remarkable clarity when freshly prepared. ~esins having F:U
molar ratios of 1.8 or less have always been opalescent, or more usually thick white liquids. To make such resins as clear, transparent liquids allows an instant visible means of checking that the resin made by this process has been supplied and that contamination by other 1?~90~39~
_ 9 _ materials has not taken place.
These advantages can be achieved with no loss of strength in the resin. Products made using this resin, such as fibreboard and particleboard, generally have the strength which could be expected from products made with a conventional resin having the same solids content and F:U molar ratio.
Resins made by the process of this invention are particularly useful in the production of products known as medium density fibreboards, facilitating good processability and high production rates and showing good resistance to premature cure in blending operations.
These resins may be cured by any conventional means, usually by heating or by the addition of an acid hardener which cures the resins at ambient temperatures, such as formic, phosphoric, or hydrochloric acid, or using a heat-activated hardener such as an acid salt that liberates an acid when heated, preferably ammonium chloride.
Resins prepared by the process of the invention are useful in bonded lignocellulosic material, especially fibreboard or particleboard, the bonded materlal comprising the resin in cured form as a binder. A process for bonding two lignocellulosic surfaces together comprlses applying to at~least one of the surfaces a urea-formaldehyde resin prepared by the process of the invention, and holding the surfaces together while curing the resin. In a ~ - .
~9~
particular embodiment of this process, fibreboard or particle board is produced by mixing lignocellulosic fibres or particles~
preferably of wood, together with a binder comprising a urea-formaldehyde resin prepared by the process of the invention and, optionally, a heat-activated hardener therefor and heating the resulting mixture under pressure until the binder is cured. The optional heat-activated hardener can be any conventional heat-activated hardener for urea-formaldehyde resins, such as an acid salt which liberates an acid on heating, preferably ammonium chloride. In general, no hardener is used in the production of fibreboard, while the hardener is used in the manufacture of particleboard. The fibreboard or particleboard can be formed in a conventional press, using conventional curing conditions.
Conventional additives, such as a wax emulsion to improve moisture resistance of the product, can be included in the mixture of lignocellulosic material and binder.
The process of the invention as hereinbefore defined may be modified to produce resins in a solid particulate form. After step (v), instead of adding urea to give a resin having a formaldehyde:urea molar ratio of 0.8:1 to 1.8:1, the mixture from step (v), preferably after evaporation as hereinbefore described, is reacted with urea under acid conditions to give a higher molecular weight resin which is then neutralised and dehydrated to give a solid, particulate resin.
.
~29~39~
Accordingly, the invention also provides a modification of the process as hereinbefore described which comprises (a) carrying out steps (i) to (v) as hereinbefore described, (b) reacting the mixture from step (v) with urea at a pH
below 7 to increase the viscosity thereof, - -(c) adding a base until the mixture reaches a pH within the range 6.5-9, and (d) dehydrating the mixture to form a solid particulate resin.
The reaction of the mixture from step (v) with urea is usually carried out at a pH of 3 to 5 and a temperature of 30 to 60C, using urea in an amount sufficient to give the reaction mixture a formaldehyde:urea molar ratio of from 1~3:1 to 1.9:1, until the viscosity of the reaction mixture is 2 to 4 times the initial viscosity of the mixture. Preferably this reaction is carried out at a pH of 3.5 to 4.5 and a temperature of 35 to 50~C, using urea in an amount sufficient to give the reaction mixture a formaldehyde:urea molar ratio of 1.5:1 to 1.7:1, until the viscosity of the reaction mixture is 2.5 to 3.5 times the initial viscosity of the mixture. Preferably also, the mixture from step (v) is evaporated to a solids content of 40-65o~ preferably 50-60o~ by weight, for example by a method as hereinbefore described, before reaction with the urea.
Acids suitable for use in reducing the pH of the mixture .
from step (v) include those hereinbefore mentioned as suitable For use in step (iii). Any base that will raise the pH of the mixture to within the range 6.5 to 9 can be used in step (c); for reasons of economy, sodium hydroxide and potassium hydroxide are preferred.
- The dehydration step (d) can be carried out in a conventional spray drier to Form the particulate resin. By means of the process oF the invention, particulate resins having low values for available formaldehyde, both in the uncured and cured state, can be obtained, these resins having excellent tack properties and - :
being particularly suitable For use in binders for particle board, waFer board and plywood.
For use as a binder, the particulate resin may be mixed with a solid hardener therefor and optionally with additives, e.g.
flllers such as wood flour and china clay, to give a storage-stable composition known as a "one-shot" composition which can be activated by the addition of water. Suitable solid hardeners for use in such "one-shot" compositions are well-known; aluminium sulphate is the most generally used material. Alternatively, the particulate resin may be dissolved or dispersed in water to reform, in effect, a liquid resin which can be mixed with a hardener therefor and optlonally with additives For use as a binder. Conventional hardeners such as the acid and salt hardeners hereinbefore mentioned, can be used.
The invention is illustrated by reference to the following ~ ~2~
Examples in which all parts and percentages are by weight unless otherwise indicated. "w/v" indicates weight by volume. The solids contents are determined by heating a 2 9 sample at 120C for 3 hours under atmospheric pressure.
::
.
.
; :
~L~d90(~1 -Aqueous formaldehyde solution (23.93 kg; 38.56o HCHO) is treated with sodium hydroxide solution t76.4 ml; 10,o w/v NaOH), and urea (7.69 kg). The mixture, which is of pH 9 and has a f:U
molar ratio of 2.40:1~ is stirred and heated to reflux. It is allowed to cool slightly, to 98C, and an aqueous solution of sulphamic acid (343.6 ml; 20~o NH2503H) is added. The resultant mixture is of pH 2.0 ~ and this is heated under reflux for 30 minutes.
Whilst maintaining the reflux, sodium hydroxide solution (509.8 ml; 10o w/v NaOH) is added to give a neutral solution (pH 7).
This is allowed to cool to about 40C ~ at which temperature a vacuum is applied and water is distilled from the mixture, a total of 11. 3 kg water being collected. The solids content of the mixture is 59~o. Finally a further quantity of urea is added (5.40 kg), giving a F:U molar ratio of 1.41:1.
This resin is a water-soluble, colourless transparent liquid having the following properties:
Solids content 65,a Viscosity at 25C- 0.27 Pa s Free formaldehyde 0.3O
, ' 1~9 Aqueous formaldehyde solution (75.68 9; 38.56o HOHO) is treated with sodium hydroxide solution (0.24 ml; 10o w/v NaOH) followed by urea (24.32 9). The mixture, which is of pH 9 and has a F:U molar ratio of 2.40:1, is stirred and heated to reflux. Phosphoric acid solution (5.0 ml; 20o H3P04) is added, to bring the mixture to pH 2.0, and it is then heated under reflux for 30 minutes. Neutralisation with sodium hydroxide solution (20o) follows and the mixture is evaporated at about 40C to a solids content of 60o. The mixture i5 cooled and urea (17.08 9) is added, giving a F:U molar ratio of 1.~1:1.
This resin is a water-soluble, colourless transparent liquid having the following properties:
Solids content 71o Vlscosity at 25C 1.72 Pa s Softwood core chips (1540 9), dried to a moisture content of 2o, are blended with a mixture comprising the resin described in Example 1 (173.8 9), ammonium chloride solution (12.0 9;
10o NH4Cl), a commercial wax emulsion (12.0 9; 65o wax), and water (65.0 gj. Part of the resultant blend (1650 9) is placed within a wooden frame 355mm square, and consolidated at room temperature under a pressure of 791 kPa. The resultant consolidated 9~
sheet is removed from the Frame and compressed at 145C for 8 minutes under a pressure of 2.77 MPa. The resultant chipboard has a thickness of 19mm. The board is tested, with the following results:
F:U molar ratio 1.41:1 Resin content of board (O solids) _, _ . . . _ . .
Density ~kg/m3) 667 .
Modulus of rupture (mPa) 21.57 Transverse tensile 9O
strength (mPa) ' _ _ . _ _ . _ _ .
Total extractable 0.013 formaldehyde (Uo) _ It may therefore be seen that the total extractable formaldehyde, measured in accordance with BS 1811, in the board is extremely low.
~ ~:?~
_ Aqueous formaldehyde solution (75.68 9; 38.56o HCHO) is treated with sodium hydroxide solution (0.24 ml, 10o w/v NaOH) and urea (24.32 g). This mixture, which is of pH 9 and has a F:U ratio of 2.40:1~ is heated to reflux and sulphamic acid (1.2 ml; 15o NH2503H) is added, giving the mixture a pH of 2Ø The mixture is then heated under reflux for 30 minutes after which, while the reflux is maintained, aqueous NaOH is added to pH 7. After cooling to 25C~ urea (17.08 9) is added, and the product evaporated in vacuo below 40C to a final weight of 81.12 9.
The product is a colourless, transparent resin having an F:U molar ratio of 1.41 :1 ~ a solids content of 68.5o~ and a viscosity at 25C of 0. 58 Pa s.
Aqueous formaldehyde solution (748.3 9; 38.68o HCHO) is treated with sodium hydroxide solution (1.2 ml; 20o w/v NaOH) and urea (251.7 9). The mixture which is of pH 9 and has a F:U molar ratio of 2.30:1~ is stirred and heated to reflux. Aqueous sulphuric acid (20 ml; 15o H2S04) is addedg to bring the mixture to pH 2.0~
and it is then heated under reflux for 30 minutes. Aqueous sodium hydroxide (14 ml; 20o w/v NaOH) is added while maintaining the reflux to bring the mixture to pH 7.4. The mixture is then evaporated in vacuo at about 40C to a solids content of 59O. Urea (46.2 9) is added to part of the evpaorated resin (190. 3 9) to give a resin having a F:U molar ratio of 1.30:1. This resin is a water-soluble, colourless transparent liquid having a solids content of 66o and a viscosity at 25C of 0. 55 Pa s.
Example 1 is repeated to the stage at which water is distilled From the mixture, to a solids content of 57o. To 100 parts by weight of the resulting mixture, 25.55 parts by weight of urea is added to give a resin having a F:U molar ratio oF 1.25:1. This resin is a water-soluble colourless transparent liquid having a solids content of 66o and a viscosity at 25UC of 0. 32 Pa s.
Softwood core chips (1540 9)7 dried to a moisture content of 2o~ are blended with a mixture comprising the resin described in Example 6 (172 g), ammonium chloride solution (12 9; 10o NH4Cl), a commercial wax emulsion (12 g: 65o wax), and water (65 g). Part of the resultant blend (1650 g) is placed within a wooden frame 355 mm square, and consolidated at room temperature under a pressure of 791 kPa. The resultant consolidated sheet is removed From the frame and compressed at 145~C for 8 minutes under a pressure of 2.77 MPa. The resultant chipboard (particle board) has a thickness of 19mm. The board is tested, with the following results:
: :
F:U molar ratio 1.25:1 . .
Resin content of board (O solids) Density (kg/m ) 643 - - .
: Modulus of rupture (mPa) 14.01 - - - .
Transverse tensile strength (mPa) 0'54 .. . . ~ .
Total extractable formaldehyde-(n) 0.012 __ . . . : . . . .
: It can be seen that the total extractable formaldehyde, measured in accordance with BS 1811, in the board is extremely low.
:
9~9~
Example 5 is repeated to the stage where the mixture is evaporated, the evaporation being carried out to give a solids content of 50o instead of 59o. The evaporated mixture has a ; viscosity at 25C of 0.08 Pa s. Urea (30 parts) is added to the evaporated mixture (200 parts) and the resulting mixture is : stirred until the urea is dissolved, giving a mixture with a viscosity at 25C of 0.07 Pa s. The F:U molar ratio of the mixture is 1.57:1. The temperature of the mixture is adjusted, if necessary, to 34-40C and aqueous sulphuric acid (1 part; 15o H2504) is added ~ to bring the mixture to pH 3.9. The mixture is stirred for 3D
: ~ ~ : mlnutes, the temperature rising to 50C ~ ~samples being taken at ; regular intervals for viscosity determlnation, until the viscosity . ~ of the mixture is increased to 0.22 Pa s. Aqueous sodium hydroxide ` ~ (D.4 part; 20o NaOH) is added to bring the mixture to pH 7. The ~mixture is then dehydrated in a spray-drier to give a resin powder having a softening point of 133C~ a F:U molar ratio of 1.56:1 and ~: a free formaldehyde content of 0.27o.
Aqueous formaldehyde solution (757.1 9; 38.50o HCHO) is : treated wlth sodium hydroxide solution (2.4 ml; 10o NaOH) and urea ~ (242.9 ~9). The mixture, whlch is of pH 9 and has a F:U molar ratio : ~ ~ :of 2.4:1, is stirred and heated to 80C, at which temperature it ~290(~91 is maintained for 15 minutes. Aqueous sulphuric acid (13.2 ml;
15o H2504) is added, to bring the mixture to pH below 3.5. The mixture is cooled to 80C and heated at this temperature for 30 minutes. Aqueous sodium hydroxide (10o NaOH) is then added to bring the mixture to pH 7. The mixture is then evaporated in vacuo at about 40C to a solids content of 59O. Urea (201 9) is added to the evaporated resin (695 9) to give a resin having a F:U molar ratio of 1. 3: 1. This resin is a water-soluble, colourless transparent liquid having a solids content of 65o and a viscosity at 25C of O.S Pa s.
Aqueous formaldehyde solution (784.6 9; 38.5o HCHO) is treated with sodium hydroxide solution (2. 4 ml; 10o NaOH), and urea (215.6 9). The mixture, which is of pH 9 and has a F:U molar ratio of 2.8:1 ~ is stirred and heated to reflux temperature, where it is maintained for 15 minutes. An aqueous solution of sulphuric acid (6.6 ml; 15o H2S04) is added. The resulting mixture, which is of pH 2.7~ is heated under reflux for 30 minutes.
Whilst maintaining the reflux, aqueous sodium hydroxide solution (10o NaOH) is added to give a neutral solution (pH 7).
This solution is evaporated in vacuo at 40C to a solids content of 59O~ urea is added to give a F:U molar ratio of 1.25:1 ~ and the mixture is stirred for 60 minutes.
This resin is a water-soluble, colourless transparent liquid having a solids content of 65o and a viscosity at 25C of 0.1 Pa s.
Claims (20)
1. A process for the preparation of urea-formaldehyde resins which comprises (i) mixing an aqueous formaldehyde solution containing 30-50% by weight of formaldehyde with urea at a formaldehyde: urea molar ratio of 2 to 3:1 and at pH 5-11, (ii) heating the mixture to at least 50°C, (iii)adding an acid until the mixture reaches a pH within the range 0.5-3.5, (iv) heating the mixture at a temperature between 80°C and the reflux temperature, (v) with the mixture at a temperature of at least 80°C, adding a base until the mixture reaches a pH within the range 6.5-9, and (vi) adding urea until the formaldehyde: urea molar ratio is within the range 0.8-1.8:1.
2. A process according to claim 1, in which the initial formaldehyde: urea molar ratio is within the range 2.2 to 2.8:1.
3. A process according to claim 2, in which the initial formaldehyde: urea molar ratio is within the range 2.3 to 2.5:1.
4. A process according to claim 1, 2 or 3, in which the heating stage (ii) is effected to a temperature of at least 80°C.
5. A process according to claim 1, 2 or 3, in which acidification in stage (iii) is effected to pH 1-2.5.
6. A process according to claim 1, 2 or 3, in which the heating stage (iv) is effected at reflux temperature.
7. A process according to claim 1, 2 or 3, in which the heating stage (iv) is effected for a period of from 15 minutes to 1 hour.
8. A process according to claim 1, 2 or 3, in which the mixture is evaporated under reduced pressure, either between stages (v) and (vi) or after stage (vi), until the solids content is within the range 40-75% by weight.
9. A process according to Claim 8, in which the evaporation precedes the urea addition stage (vi) and is effected to give a solids content within the range 50-65% by weight.
10. A process according to claim 8, in which the evaporation follows the urea addition stage (vi) and is effected to give a solids content within the range 60-70% by weight.
11. A process according to claim 1, 2 or 3, in which addition or urea in stage (vi) gives a product having a formaldehyde: urea molar ratio within the range 1.0 to 1.7:1.
-23a- 28146-1
-23a- 28146-1
12. A process according to claim 11, in which the urea addition gives a product having a formaldehyde: urea molar ratio of 1.2 to 1.5:1.
13. A modification of the process according to claim 1 which comprises (a) carrying out steps (i) to (v) as defined in claim 1 , (b) reacting the mixture from step (v) with urea at a pH below 7 to increase the viscosity thereof, (c) adding a base until the mixture reaches a pH within the range 6.5-9, and (d) dehydrating the mixture to form a solid particulate resin.
14. A process according to claim 13, in which step (b) is carried out at a pH of 3 to 5 and a temperature of 30 to 60°C, using urea in an amount sufficient to give the reaction mixture a formaldehyde:urea molar ratio of from 1.3:1 to 1.9:1 until the viscosity of the reaction mixture is 2 to 4 times the initial viscosity thereof.
15. A process according to claim 14, in which step (b) is carried out at a pH of 3.5 to 4.5 and a temeprature of 35 to 50°C, using urea in an amount sufficient to give the reaction mixture a formaldehyde:urea molar ratio of from 1.5:1 to 1.7:1, until the viscosity of the reaction mixture is 2.5 to 3.5 times the initial viscosity thereof.
16. A process according to claim 13, 14 or 15, in which the mixture reacted with urea has a solids content of from 40 to 65%
by weight.
by weight.
17. A binder comprising a solid particulate resin obtained by a process according to claim 13, 14 or 15 and a solid hardener therefor.
18. A bonded lignocellulosic material comprising as binder a resin obtained by a process according to claim 1, 2, 3, 13, 14 or 15, said resin being in cured form.
19. A process for bonding two lignocellulosic surfaces together which comprises applying to at least one of the surfaces a resin prepared by a process according to claim 1, 2, 3, 13, 14 or 15 and holding the surfaces together while curing the resin.
20. A process for bonding two lignocellulosic surfaces together which comprises applying to at least one of the surfaces a resin prepared by a process according to claim 1, 2, 3, 13, 14 or 15 and holding the surfaces together while curing the resin, in which fibreboard or particle board is produced by mixing lignocellulosic fibres or particles together with a binder comprising a resin prepared by a process according to claim 1, 2, 3, 13, 14 or 15 and, optionally, a heat-activated hardener therefor and heating the resulting mixture under pressure until the binder is cured.
Priority Applications (11)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8615805A GB2192005B (en) | 1986-06-27 | 1986-06-27 | Process for the preparation of urea-formaldehyde resins |
| US07/275,036 US4968772A (en) | 1986-06-27 | 1987-07-18 | Process for the preparation of urea-formaldehyde resins |
| AT0905487A AT397965B (en) | 1986-06-27 | 1987-07-18 | METHOD FOR PRODUCING UREA FORMALDEHYDE RESINS, METHOD FOR PRODUCING A BINDING AGENT, METHOD FOR PRODUCING A BONDED LIGNOCELLULOSE MATERIAL, AND USES |
| JP62504528A JPH02500031A (en) | 1986-06-27 | 1987-07-18 | Method for producing urea-formaldehyde resin |
| NL8720365A NL8720365A (en) | 1986-06-27 | 1987-07-18 | PROCESS FOR THE PREPARATION OF UREA-FORMALDEHYD RESINS. |
| AU77808/87A AU605504B2 (en) | 1986-06-27 | 1987-07-18 | Process for the preparation of urea-formaldehyde resins |
| PCT/EP1987/000392 WO1989000587A1 (en) | 1986-06-27 | 1987-07-18 | Process for the preparation of urea-formaldehyde resins |
| CA000542465A CA1290091C (en) | 1986-06-27 | 1987-07-20 | Process for the preparation of urea-formaldehyde resins |
| BE8700827A BE1000759A4 (en) | 1986-06-27 | 1987-07-27 | PROCESSES FOR THE PREPARATION OF UREEFORMALDEHYDE RESINS, BINDER AND BINDED LIGNOCELLULOSIC MATERIAL COMPRISING A RESIN THUS PREPARED AND METHOD USING SUCH A RESIN TO BIND TWO LIGNOCELLULOSIC SURFACES. |
| FR878710797A FR2618789B1 (en) | 1986-06-27 | 1987-07-30 | PROCESSES FOR THE PREPARATION OF UREA-FORMALDEHYDE RESINS, BINDER AND BINDED LIGNOCELLULOSIC MATERIAL COMPRISING A RESIN THUS PREPARED AND METHOD USING SUCH A RESIN TO BIND TWO LIGNOCELLULOSIC SURFACES |
| SE8803744A SE462392B (en) | 1986-06-27 | 1988-10-19 | PROCEDURES FOR PREPARING CARBAMIDE FORMAL HEARTS AND THEIR USE AS A BINDING AGENT |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8615805A GB2192005B (en) | 1986-06-27 | 1986-06-27 | Process for the preparation of urea-formaldehyde resins |
| AT0905487A AT397965B (en) | 1986-06-27 | 1987-07-18 | METHOD FOR PRODUCING UREA FORMALDEHYDE RESINS, METHOD FOR PRODUCING A BINDING AGENT, METHOD FOR PRODUCING A BONDED LIGNOCELLULOSE MATERIAL, AND USES |
| CA000542465A CA1290091C (en) | 1986-06-27 | 1987-07-20 | Process for the preparation of urea-formaldehyde resins |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1290091C true CA1290091C (en) | 1991-10-01 |
Family
ID=27151072
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000542465A Expired - Lifetime CA1290091C (en) | 1986-06-27 | 1987-07-20 | Process for the preparation of urea-formaldehyde resins |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US4968772A (en) |
| JP (1) | JPH02500031A (en) |
| AT (1) | AT397965B (en) |
| AU (1) | AU605504B2 (en) |
| BE (1) | BE1000759A4 (en) |
| CA (1) | CA1290091C (en) |
| FR (1) | FR2618789B1 (en) |
| GB (1) | GB2192005B (en) |
| NL (1) | NL8720365A (en) |
| SE (1) | SE462392B (en) |
| WO (1) | WO1989000587A1 (en) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8715305D0 (en) * | 1987-06-30 | 1987-08-05 | Ciba Geigy Ag | Process |
| FR2625204B1 (en) * | 1987-12-23 | 1991-12-06 | Charbonnages Ste Chimique | NEW PROCESS FOR THE MANUFACTURE OF UREE-FORMOL RESINS |
| GB9014985D0 (en) * | 1990-07-06 | 1990-08-29 | Dyno Industrier As | Formaldehyde resin curing agents |
| US5243015A (en) * | 1992-06-25 | 1993-09-07 | Georgia-Pacific Resins, Inc. | Latent catalyzed phenolic resole resin composition |
| WO1995022133A1 (en) * | 1994-02-08 | 1995-08-17 | Nauchno-Tekhnologicheskoe Predpriyatie 'ligand' | Method of obtaining a carbamide-formaldehyde resin and a condensate for the manufacture of the same |
| US5854309A (en) * | 1996-09-30 | 1998-12-29 | Blount; David H. | Flame retardant compositions utilizing amino condensation compounds |
| US6495655B2 (en) * | 1996-09-30 | 2002-12-17 | David H. Blount | Production of amino-aldehyde-phosphate resins and copolymers |
| US6051086A (en) * | 1998-06-08 | 2000-04-18 | Orica Explosives Technology Pty Ltd. | Buffered emulsion blasting agent |
| DE19849380A1 (en) * | 1998-10-27 | 2000-05-04 | Basf Ag | Low-water formroxane formaldehyde solutions |
| CN100344720C (en) * | 2006-03-30 | 2007-10-24 | 浙江林学院 | Environment protection, low cost urea resin gel |
| US20090163656A1 (en) * | 2007-12-21 | 2009-06-25 | Envont Llc | Hybrid vehicle systems |
| JP6040773B2 (en) * | 2010-11-15 | 2016-12-07 | 日産化学工業株式会社 | Thermosetting resin softening particles |
| CN103242201B (en) * | 2013-04-26 | 2015-06-10 | 中科院广州化学有限公司 | Preparation method of urea formaldehyde intermediate dimethylol urea |
| CN107344992B (en) * | 2017-06-01 | 2020-01-14 | 东莞市贝辉装饰材料有限公司 | Low-formaldehyde urea-formaldehyde resin and preparation method and application thereof |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT951962B (en) * | 1971-12-27 | 1973-07-10 | Sir Soc Italiana Resine Spa | PROCEDURE FOR THE PREPARATION OF RESINS FROM UREA AND FORMALDEHYDE |
| IT951964B (en) * | 1971-12-27 | 1973-07-10 | Sir Soc Italiana Resine Spa | PERFECTED PROCESS FOR THE PREPARATION OF RESINS FROM UREA AND FORMALDEHYDE |
| AU4804472A (en) * | 1972-01-27 | 1974-04-26 | Borden Inc | Urea-formaldehyde condensates |
| BE795631A (en) * | 1972-02-19 | 1973-08-20 | Basf Ag | AMINOPLAST BINDERS FOR WOOD-BASED MATERIALS |
| US3962166A (en) * | 1972-06-05 | 1976-06-08 | United Merchants And Manufacturers, Inc. | Stable urea-formaldehyde compositions |
| JPS5098953A (en) * | 1974-01-02 | 1975-08-06 | ||
| DE2448472C3 (en) * | 1974-10-11 | 1979-08-30 | Th. Goldschmidt Ag, 4300 Essen | Process for the production of solutions of urea-formaldehyde impregnating resins |
| US4032515A (en) * | 1974-11-04 | 1977-06-28 | Koppers Company, Inc. | Curable resorcinol terminated urea-formaldehyde resins |
| GB1480787A (en) * | 1975-09-11 | 1977-07-27 | Ciba Geigy Ag | Ureaformaldehyde resins |
| GB1570339A (en) * | 1976-06-23 | 1980-06-25 | Ici Ltd | Process for producing aqueous-formaldehyde resin solutions |
| DE2825590C2 (en) * | 1978-06-10 | 1983-05-05 | Th. Goldschmidt Ag, 4300 Essen | Process for the production of thermosetting urea-formaldehyde resins and their use |
| IT1209203B (en) * | 1980-04-10 | 1989-07-16 | Montedison Spa | UREIC NECKLACE WITH LOW DEVELOPMENT OF FORMALDEHYDE AND HIGH TACK VALUE. |
| US4381368A (en) * | 1982-02-16 | 1983-04-26 | Spurlock Harold N | Process for the preparation of urea-formaldehyde resins |
| US4410685A (en) * | 1982-09-10 | 1983-10-18 | Borden, Inc. | Hydrolytically stable urea-formaldehyde resins and process for manufacturing them |
| GB2150939B (en) * | 1983-12-09 | 1987-02-04 | Enigma Nv | A process for preparing urea-formaldehyde resins |
-
1986
- 1986-06-27 GB GB8615805A patent/GB2192005B/en not_active Expired
-
1987
- 1987-07-18 JP JP62504528A patent/JPH02500031A/en active Pending
- 1987-07-18 US US07/275,036 patent/US4968772A/en not_active Expired - Fee Related
- 1987-07-18 NL NL8720365A patent/NL8720365A/en not_active Application Discontinuation
- 1987-07-18 AT AT0905487A patent/AT397965B/en not_active IP Right Cessation
- 1987-07-18 AU AU77808/87A patent/AU605504B2/en not_active Ceased
- 1987-07-18 WO PCT/EP1987/000392 patent/WO1989000587A1/en active Application Filing
- 1987-07-20 CA CA000542465A patent/CA1290091C/en not_active Expired - Lifetime
- 1987-07-27 BE BE8700827A patent/BE1000759A4/en not_active IP Right Cessation
- 1987-07-30 FR FR878710797A patent/FR2618789B1/en not_active Expired - Lifetime
-
1988
- 1988-10-19 SE SE8803744A patent/SE462392B/en not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| NL8720365A (en) | 1989-05-01 |
| AT397965B (en) | 1994-08-25 |
| GB2192005B (en) | 1989-12-13 |
| FR2618789B1 (en) | 1990-10-12 |
| GB2192005A (en) | 1987-12-31 |
| JPH02500031A (en) | 1990-01-11 |
| SE8803744D0 (en) | 1988-10-19 |
| US4968772A (en) | 1990-11-06 |
| BE1000759A4 (en) | 1989-03-28 |
| AU7780887A (en) | 1989-02-13 |
| AU605504B2 (en) | 1991-01-17 |
| ATA905487A (en) | 1993-12-15 |
| WO1989000587A1 (en) | 1989-01-26 |
| SE8803744L (en) | 1989-01-19 |
| SE462392B (en) | 1990-06-18 |
| FR2618789A1 (en) | 1989-02-03 |
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| Date | Code | Title | Description |
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| MKLA | Lapsed |