GB1571111A - Manufacture of resin bonded fibrous insulation - Google Patents

Manufacture of resin bonded fibrous insulation Download PDF

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Publication number
GB1571111A
GB1571111A GB4206476A GB4206476A GB1571111A GB 1571111 A GB1571111 A GB 1571111A GB 4206476 A GB4206476 A GB 4206476A GB 4206476 A GB4206476 A GB 4206476A GB 1571111 A GB1571111 A GB 1571111A
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United Kingdom
Prior art keywords
mat
binder
foam
impregnated
weight
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Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
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GB4206476A
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Newalls Insulation Co Ltd
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Newalls Insulation Co Ltd
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 Newalls Insulation Co Ltd filed Critical Newalls Insulation Co Ltd
Priority to GB4206476A priority Critical patent/GB1571111A/en
Priority to US05/840,238 priority patent/US4188355A/en
Priority to SE7711281A priority patent/SE425478B/en
Priority to IT51337/77A priority patent/IT1112098B/en
Priority to JP12084277A priority patent/JPS5349169A/en
Priority to FR7730195A priority patent/FR2367134A1/en
Priority to NL7711030A priority patent/NL7711030A/en
Priority to DE19772745529 priority patent/DE2745529A1/en
Publication of GB1571111A publication Critical patent/GB1571111A/en
Expired legal-status Critical Current

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Classifications

    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/42Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
    • D04H1/4209Inorganic fibres
    • D04H1/4218Glass fibres
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/58Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives
    • D04H1/64Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives the bonding agent being applied in wet state, e.g. chemical agents in dispersions or solutions
    • D04H1/68Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives the bonding agent being applied in wet state, e.g. chemical agents in dispersions or solutions the bonding agent being applied in the form of foam
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H3/00Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
    • D04H3/002Inorganic yarns or filaments
    • D04H3/004Glass yarns or filaments
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H3/00Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
    • D04H3/08Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating
    • D04H3/12Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating with filaments or yarns secured together by chemical or thermo-activatable bonding agents, e.g. adhesives, applied or incorporated in liquid or solid form

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Nonwoven Fabrics (AREA)
  • Reinforced Plastic Materials (AREA)

Description

(54) IMPROVEMENTS IN AND RELATING TO THE MANUFACTURE OF RESIN BONDED FIBROUS INSULATION (71) We, NEWALLS INSULATION COMPANY LIMITED, a Company organised under the laws of Great Britain, of 20 St. Mary's Parsonage, Manchester M3 2NL (formerly of 77 Fountain Street, Manchester M2 2EA), do hereby declare the invention, for which we pray that a patent may be granted to us, and the method by which it is to be performed, to be particularly described in and by the following statement: The present invention relates to the manufacture of bonded non-woven fibrous mats, particularly comprised of glass fibres or mineral wool.
Such mats can be made by forming an airlaid mat, for example, by subjecting streams of molten glass or rock to the action of hot gases in the form of steam/air jets and to mechanical attenuation, prior to collection on a foraminous receptor surface in a forming hood. They can also be made from continuous filaments or strands, either as such or after chopping into staple fibre form prior to deposition on a receptor surface. A binder is sprayed onto the mat during or after formation and is thereafter cured in situ by the action of heat to form a bonded mat. Phenolic and polyester resins are commonly used in such processes, although other binders may also be used. Hot air and/or radiant heat are generally used to set the binder, for example by curing the resin.
The binder spraying step tends to be rather haphazard. It frequently results in excessive local concentrations of binder, losses of binder into the atmosphere and consequent pollution problems. Because of the high temperature of the newly-formed fibres and the presence of the hot gases used to attenuate them, the binder has to be sprayed at a high water content (for example, 80 - 90% water, 10 - 20% binder), although in practice most of this water is lost by evaporation together with a significant proportion of the binder.
The variations in the binder content throughout the mat may be considerable, for example, ~+5 /O relative to a target binder content in the finished product of 10% by weight, which means that in general the level of binder addition must be appreciably higher than would be necessary if the distribution were sensibly even.
It has been proposed to make bonded nonwoven fibrous mats by a process including the steps of forming a foam from a suspension/ solution of the binder and impregnating a non-woven fibrous mat with the foam. In such a process the impregnation step is carried out by applying the foam as a layer on one face of the mat, the foam being squeezed into the mat by. a roller, doctor blade or an endless belt, assisted by the application of suction at the opposite face of the mat. After impregnation, the binder may be caused to set in situ, for example, by heating, as mentioned above. However, the application of this prt cess to glass fibre and/or mineral wool mats has proved difficult due to the very high porosity of such mats and the tendency of the binder to migrate on drying/curing. Furthermore, the application of a foamed binder to a newly-formed mat of hot fibres on a production line can result in premature and/or uneven setting/curing of the binder, before proper impregnation of the mat has been accomplished.
According to the present invention, a bonded non-woven glass fibre or mineral wool mat is made by a process 'including the steps of forming a foam from an aqueous solution or suspension of a binder, impregnating a nonwoven mat with the foam and then selectively removing by the application of dielectric heating a major portion of the water from the mat prior to serting/curing the binder.
It is preferred that the amount of foamed binder applied to the mat is in excess of that required to give the desired binder solids content in the final dry product. The extent of the excess is preferably 50% or more by weight and the surplus is drawn through the impregnated mat prior to seKectiveli removing the water. Advantageously, the surplus is thereafter collected and re-circulated. Thermo settable resins are especially preferred as binders.
It has been found that the application of binder as an aqueous foam, particularly when applied in the excess just referred to gives significantly more uniform impregnation, typically of the order of +1% of the target value as opposed to the relatively high variability experienced with prior art processes.
This means that one can use less binder for a particular product density whilst maintaining substantially the same physical properties such as strength and rigidity. It also means that there can be a significant economy in binder consumption by virtue of the elimination of the conventional process step of spraying the binder into the forming hood mentioned earlier.
Losses due to evaporation/binder carry-over into the mat-forming hot gas streams through the foraminous receptor surface and the hot fibres are typically of the order of 1530% and these losses can be eliminated for all practical purposes. With more sufficient binder utilisation there may also be enhanced fire resistance due to the reduced total organic content of the final product. The water content of the foam is determined by a number of factors such as the temperature of the mat and the final target binder content in the product. Because the foam contains water it can safely be applied even to a hot mat on a production line, provided that the water content is high enough to cool the mat and at the same time prevent significant curing/ setting of the binder. However, it should be noted that even if the foam is applied to a hot mat, the water content of the impregnated mat (prior to selective removal of the major portion of the water) will be considerably higher than the water content of a similar bonded mat made by the traditional forming hood spraying process. For example, the latter process gives typical water contents of 4 6% (by weight), whereas the process of the present invention gives 10 - 30% water content. The use of a high water content and an excess of foam contributes not only to the uniformity of impregnation but also to maintaining that uniformity. The use of dielectric heating is particularly advantageous in this context since it enables the water to be removed from the whole thickness rather than from a single surface exposed to conventional heating. Effectively, high frequency heating dries the mat from the inside outwards to the surfaces. It also enables the mat to be dried to a controlled water content.
It has also been observed that dielectric heating causes a significant increase in the bulk of the mat, i.e. an increase in the thickness of the mat on selective removal of the water. The increase can be as much as three or four times the wet thickness of the mat immediately after impregnation. Although conventional drying methods do produce an increase in bulk, it has been observed that the increase caused by dielectric heating is usually greater. One result of this is that relatively low final dry densities of the order of 16Kg/m3 are possible. However, it is also possible to produce final densities of the order of 320 or more Kg/m3 by compacting the dry mat prior to curing/setting the binder.
The process of the present invention therefore exhibits a considerable degree of flexibility and enables the production of products over a wide range of final, dry density.
The process of the present invention is especially applicable to the production of mats of fibrous thermal insulation made from glass fibres, mineral wool or rockwool, where the binder is used to impart a degree of resilience and cohesion to the product without significantly reducing its porosity. The invention includes such products when made by a process according to the invention.
However, dielectric heating was previously thought impracticable in glass fibre/mineral wool manufacture because conventional binder application processes produce clots of binder in the mat and these react adversely to dielectric heating.
Using the process of the invention, it is also possible to impregnate a mat off the production line, which in some circumstances adds fiexi- bility to the overall manufacturing process.
In this particular case, the water content of the binder need not be as high as would be necessary for on-line application, because the mat would not normally need cooling. The binder and the water may be individually metered to give the mixture which is foamed.
This is preferred because it makes for maxi mum control of the binder solids present in the final dry product and makes changes in binder solids very easy to effect.
Whilst the dielectric heating is preferably applied only for as long as is necessary to selectively remove a major portion of the water, conventional heating being then used to set/cure the resin, it is also possible to use dielectric heating to set/cure the binder, before, during or after conferring a desired configuration on the mat. For example, a 6 to 12 second treatment can substantially dry a typical foam impregnated mat without significant effect on the binder. Where the binder is a thermosettable resin, a 20 second treatment would at least initiate curing of the resin. However, at production line speeds, such a long treatment time may be impracticable, or unduly expensive, or both.
Hitherto, the application of binder after mat formation has been difficult, if not entirely impracticable because of the desired bulky foraminous nature of the product.
Uniform impregnation is not achieved by spraying binder onto the faces of an alreadyformed mat and the use of a liquid binder tends to destroy the desired bulk. For these reasons, shaped products such as lengths of tubular pipe insulation have always been made from mat impregnated with a settable/curable binder during production. Because it is no longer necessary to impregnate with binder during mat formation, it is now possible to make and store completely unimpregnated mat for future use, without having to worry about binder shelf life and/or variations in binder properties from batch to batch. This unimpregnated mat can be subsequently impregnated, dried and shaped into such products as lengths of tubular pipe insulation, prior to setting/curing the binder in the usual way. The invention includes products made in this way from unimpregnated mat.
The present invention thus enables impregnation to be carried out at the most convenient time or location, thereby giving an essentially two-stage process in which mat formation and binder impregnation can be separated by any desired interval, with or without the optional step of also forming a shaped product from the impregnated mat.
A further advantage of dielectric heating lies in the fact that selective removal of water can be accomplished without producing significant binder fames. The output airstream from the dielectric heater may even be vented to atmosphere without the usual effluent problems.
Advantageously, the aqueous binder solution/suspension contains a minor amount of a surfactant to facilitate foaming; the exact level of surfactant addition and the solids content (dilution) of a particular binder being a matter for experiment in order to arrive at a desired binder content in the final product.
A further advantage of the process of the invention is that excess foamed binder and any fibres therein can be re-circulated because the binder does not have to be sprayed and because it is still neither set nor cured.
The invention also includes apparatus for carrying out the process of the invention, said apparatus including a foam generator, means for spreading an aqueous foam made thereby onto one face of a non-woven mat, means operable to urge the foam into the mat together with heating means operable to selectively remove a major portion of the water from the impregnated mat. The heating means is preferably a radio frequency heater.
Preferably the apparatus further includes means for collecting and recirculating excess foam from the mat during and/or after impregnation thereof.
The means for urging the foam into the mat preferably includes both a suction device operative on the opposite face of the mat to that onto which the foam is spread and means for pressing the foam into the mat towards said suction device. Because glass/mineral wool mats are very porous, the means for pressing the foam into the mat should preferably seal against at least that face of the mat to which the foam is applied. Otherwise, the suction device may simply draw air through any relatively thin or more permeably parts of the mat without thoroughly impregnating them with the foam. Particularly preferred apparatus for this purpose comprises a foraminous roller containing at least one suction head and an impermeable endless flexible belt, one run of which presses against the mat as it passes over the roller.
The roller is preferably in the form of a drum with peripheral, radially-extending flanges because the use of a drum and particularly one with sidewalls has been found to give a better seal between the flexible belt and the drum, thereby utilising the suction more efficiently. Typically, radio frequency heaters operate at a frequency of approximately 27 mHz. In order that the invention be better understood, preferred embodiments of it will now be described by way of example with reference to the drawings accompanying the provisional specification in which: Figure 1 is a partly schematic side view showing one apparatus for carrying out a process according to the invention, and Figure 2 is a partly schematic side view showing part of the apparatus of Figure 1 in greater detail.
Where practicable, common reference numerals are used in both figures.
Referring briefly to Figure 1, this figure illustrates the application of the process and apparatus according to the invention to a glass mat production line.
In Figure 1, a forming hood assembly 31 comprises a large chamber 32 into which two glass fibre streams 33 are projected from centrifugal spinning heads 34 supplied by a glass furnace (not shown). The glass fibres are received on a foraminous belt 35, the formation of a mat 3 being aided by suction heads 36 underneath the top run of the belt.
The mat is compacted by a roller 37 and forwarded along an auxiliary conveyor 38, under a compacting roller 39 and fed into a foam impregnation apparatus 40 which will be described in detail later, with reference to Figure 2.
This is followed immediately by a second Figure 2 apparatus, designated 41, (but not fitted with a foam generator and delivery pipe, as will be discussed later). From the apparatus 41, the mat passes into a dielectric heating chamber 42 and thence into a curing oven 43, the initial portion only of which is shown. The apparatus 41 in this case serves only to remove surplus foam/liquid from the impregnated mat. The dielectric heating chamber 42 prepares the impregnated mat for the curing oven by selectively removing at least a major portion of the water from it and thereby drying the mat to a very ap preciable and controlled extent, the latter depending of course on the size of the chamber, the power level applied and the speed of the conveyor, i.e. the production speed which determines the duration of the treatment applied by a particular heater.
It will be appreciated that Figure 1 is purely illustrative and that much of the ancillary hardware has been omitted. However, for present purposes, it illustrates how conventional mat production apparatus can be combined with foam impregnation apparatus and a high frequency heater.
The detailed construction of the apparatus 40 and 41 will now be explained with the aid of Figure 2.
In Figure 2, an endless belt 1 is mounted for recirculation around a pair of drive/ support rollers 2. The direction of travel of the upper and lower runs of the belt are indicated by arrows and the upper run carries a glass fibre mat 3. A thermosettable resin solution tank 4 is located under the belt and resin is drawn from the tank by a pump 5 and fed to a foam generator 6, to which compressed air is also supplied by a pipe 7.
The foam generator is conventional and comprises a column containing glass beads. The action of the generator is to form an intimate mixture of resin and air by constraining both to follow common, restricted paths through the medium inside the column. On leaving the column, the mixture expands into a foam. The foam outlet 8 from the column feeds a delivery pipe 9 which serves two purposes.
Firstly it delivers foam 12 to a slit nozzle 10 extending widthwise of the mat 3 and secondly it provides for the collection of unfoamed liquid in a recovery tube 11. Any liquid collected is returned to the tank for re-use, via a pump 13 and pipe 14.
The mat covered by a layer of foam 12, is carried by the belt 1 under a doctor blade 24, towards and over a perforated drum 15, from which it passes along an auxiliary conveyor 16 to the dielectric heater of Figure 1.
The amount of foam applied is in excess of that required to give the desired binder solids content in the final, dry product, as discussed earlier. The extent of the excess is controlled by the depth of the layer of foam, 12, and this can be adjusted by, for example, changing the rate of foam production, or the speed of the belt 1, or the disposition of the doctor blade 24.
The perforated drum contains three stationary suction heads 17, respective axial outlet pipes 18a, 18b, 18c, each being connected to a vacuum source via a liquid resin trap (none of which is shown, in the interests of simplicity). Any liquid recovered by the traps is returned to the tank through the pipes schematically illustrated at 19. The drum has radially-extending side-walls of depth at least equal to the thickness of the mat to be impregnated, as indicated by dashed line 15a.
On the opposite side of the mat to the perforated drum an endless, impermeable flexible belt 20 is mounted for circulation around three support rollers 21, 22 and 23.
The belt 20 is deliberately arranged to be somewhat slack so that its lower run can be progressively displaced under the influence of the suction applied to the underside of the mat. The result is that the belt 20 augments the suction and gradually presses the foam progressively into the mat until impregnation is completed. The belt and drum sidewalls co-operate to seal the mat against the drum surface.
It will be appreciated that the apparatus will normally be fitted with ancillary dispensing equipment for feeding liquid thermosettable resin solution and surfactant to the tank 4, although in the interests of simplicity this too has been omitted from the figure.
It should also be noted that whilst the apparatus may form part of a complete production line including mat formation, resin curing and roll packaging operations, it may also be used to treat already-formed mats as a separate operation, as discussed earlier.
It should be noted in this latter context that whilst the resin will normally be cured on the production line, by means of hot air, and/ or radiant heat, or by further dielectric heating, it is not essential to cure at this stage and, of course, it is not even necessary toimpregnate and dry on the mat production line. The process of the invention can be applied to untreated mat at any time after production, thereby avoiding or minimizing processing problems resulting from the limited storage life of the thermosettable resins commonly used. In the particular context of a process involving a glass furnace, the ability to defer impregnation by any desired interval of time provides an at least partial solution to the problem of interruptions in production caused by the need to re-build the furnace when the refractory lining reaches the end of its useful life. Unimpregnated mat can be stored for use during such re-building.
The process may also be used to reimpregnate a mat, either with the same or a different resin, in the event that the initial impregnation was not satisfactory or a higher binder content is required.
The invention is also illustrated by the following examples.
Example 1 An unimpregnated glass fibre mat was made by a centrifugal spinning process as described in relation to Figure 1; the mat was one metre wide, 100mm thick and weighed 700 gm/m2.
An aqueous solution of a modified phenolformaldeheyde resin was made containing about 20% by weight of resin solids and 1% by weight (based on the resin solids) of a surfactant. This solution was foamed and applied to one face of the mat as a layer 30mum deep, using an apparatus as shown in Figure 2. The suction applied was 500mm of mercury and the linear speed of the mat was 6m/minute.
The impregnated, wet mat exhibited a total average pick-up of 18.2% by weight, of which 12.6% was water.
The wet mat was then exposed to radio frequency drying for 6 seconds by passing it through a radio frequency heater. The 6 second dwell time in the heater was sufficient to dry the mat to a 2% residual water content, without having any significant effect on the cure state of the resin. The dried, impregnated mat was passed through a hot air curing oven between two endless belts set 23rum apart to give a 25mm thick board product of density 32 kg/m3. The average cured resin solids content of the board was 5.4% by weight.
The range of solids content measured was 4.8 to 5.7% by weight.
Example 2 A similar unimpregnated mat to that of Example 1 was made and a foamed resin binder applied to it in exactly the same way, the only difference being that the initial solids content of the resin solution was 40% by weight instead of 20%.
The average pick-up of the wet mat was 45.2% by weight, of which 30.1% was water.
The radio frequency drying treatment was applied in this case for 13 seconds, which was sufficient to give virtually zero residual water content.
The dried, impregnated product was cut to size and pressed in a heated platen press into liner panels of asymmetrical thickness for automotive use, the thickness of each panel varying from 12mm at one end to 2mm at the other.
The temperature and duration of the pressing operation was sufficient to cure the resin, giving an average cured resin solids content of 14.6% by weight, the lower and upper departures from this average being 13.8 and 15.2% respectively. The density of the product was 68 kg/m3 (at the 12mm thickness) and 408 kg/m3 (at the 2mm thickness).
Example 3 The procedure of Example 1 was followed, but with a mat of weight 350gm/m2 and thickness 50mm. To this was applied the same foamed resin solution as in Example 1, but the linear speed of the mat was 12m/ minute and the suction was reduced to 250mm of mercury.
The average pick-up of the wet, impregnated mat was in the range 23.1 to 25.3% by weight, with a water content of 16.1 to 16.9%.
This mat was then dried to 2% residual water content, an 8 second radio frequency heating treatment being required for this.
Successive 1.5 metre lengths of the dried, impregnated mat were then formed into lengths of tubular pipe insulation prior to oven curing the resin with hot air. The final products were 915mm long (one yard nominal length) and had a wall thickness of 23mum at a bore size of 100mm; they had a density of 55.4k/m3 at an average cured resin solids content of 7.4%, the maximum lower and upper departures from this being 6.6 and 7.9%, respectively.
All of the foregoing Examples illustrate the application of the process of the invention to the manufacture of insulation products from already-prepared and unimpregnated mat, since no attempt was made to integrate the mat production and impregnation processes, the mat being made and stored in the un impregnated state until it was convenient to subject it to impregnation. In fact, the storage period could have been of indefinite duration, because until the resin solution is applied to the mat there is no problem as to the shelf life of the mat.
Whilst all the Examples given above were carried out using a laboratory-type radio frequency heater rated at ij KW (at a fre quency of 27 mHz), the actual power needed for a particular drying operation will naturally vary acocrding to the desired throughput and the water content ofthe mat. The choice of an appropriate size of heater for any particular conditions will be within the capabilities of those skilled in the art.
WHAT WE CLAIM IS:- 1. A process for the production of a bonded non-woven glass fibre or mineral wool mat wherein a non-woven mat is impregnated with a foam of an aqueous solution or suspension of a binder which is thereafter caused to set or cure in situ, and wherein a major portion of the water is removed by the application of dielectric heating.
2. A process according to Claim 1 wherein the binder foam is applied to the mat in excess of the amount required to give a desired binder solids content in the final dry product.
3. A process according to Claim 2, wherein the excess is 50% or more by weight.
4. A process according to Claim 2 or Claim 3, wherein the excess binder foam is drawn through and removed from the mat prior to removing the water.
5. A process according to Claim 4, wherein the excess binder foam removed from the mat is collected and re-circulated.
6. A process for the production of a bonded non-woven glass fibre or mineral wool mat comprising the steps of: 1. forming a non-woven mat of glass fibre or mineral wool by a melt spinning process,
**WARNING** end of DESC field may overlap start of CLMS **.

Claims (15)

**WARNING** start of CLMS field may overlap end of DESC **. by weight (based on the resin solids) of a surfactant. This solution was foamed and applied to one face of the mat as a layer 30mum deep, using an apparatus as shown in Figure 2. The suction applied was 500mm of mercury and the linear speed of the mat was 6m/minute. The impregnated, wet mat exhibited a total average pick-up of 18.2% by weight, of which 12.6% was water. The wet mat was then exposed to radio frequency drying for 6 seconds by passing it through a radio frequency heater. The 6 second dwell time in the heater was sufficient to dry the mat to a 2% residual water content, without having any significant effect on the cure state of the resin. The dried, impregnated mat was passed through a hot air curing oven between two endless belts set 23rum apart to give a 25mm thick board product of density 32 kg/m3. The average cured resin solids content of the board was 5.4% by weight. The range of solids content measured was 4.8 to 5.7% by weight. Example 2 A similar unimpregnated mat to that of Example 1 was made and a foamed resin binder applied to it in exactly the same way, the only difference being that the initial solids content of the resin solution was 40% by weight instead of 20%. The average pick-up of the wet mat was 45.2% by weight, of which 30.1% was water. The radio frequency drying treatment was applied in this case for 13 seconds, which was sufficient to give virtually zero residual water content. The dried, impregnated product was cut to size and pressed in a heated platen press into liner panels of asymmetrical thickness for automotive use, the thickness of each panel varying from 12mm at one end to 2mm at the other. The temperature and duration of the pressing operation was sufficient to cure the resin, giving an average cured resin solids content of 14.6% by weight, the lower and upper departures from this average being 13.8 and 15.2% respectively. The density of the product was 68 kg/m3 (at the 12mm thickness) and 408 kg/m3 (at the 2mm thickness). Example 3 The procedure of Example 1 was followed, but with a mat of weight 350gm/m2 and thickness 50mm. To this was applied the same foamed resin solution as in Example 1, but the linear speed of the mat was 12m/ minute and the suction was reduced to 250mm of mercury. The average pick-up of the wet, impregnated mat was in the range 23.1 to 25.3% by weight, with a water content of 16.1 to 16.9%. This mat was then dried to 2% residual water content, an 8 second radio frequency heating treatment being required for this. Successive 1.5 metre lengths of the dried, impregnated mat were then formed into lengths of tubular pipe insulation prior to oven curing the resin with hot air. The final products were 915mm long (one yard nominal length) and had a wall thickness of 23mum at a bore size of 100mm; they had a density of 55.4k/m3 at an average cured resin solids content of 7.4%, the maximum lower and upper departures from this being 6.6 and 7.9%, respectively. All of the foregoing Examples illustrate the application of the process of the invention to the manufacture of insulation products from already-prepared and unimpregnated mat, since no attempt was made to integrate the mat production and impregnation processes, the mat being made and stored in the un impregnated state until it was convenient to subject it to impregnation. In fact, the storage period could have been of indefinite duration, because until the resin solution is applied to the mat there is no problem as to the shelf life of the mat. Whilst all the Examples given above were carried out using a laboratory-type radio frequency heater rated at ij KW (at a fre quency of 27 mHz), the actual power needed for a particular drying operation will naturally vary acocrding to the desired throughput and the water content ofthe mat. The choice of an appropriate size of heater for any particular conditions will be within the capabilities of those skilled in the art. WHAT WE CLAIM IS:-
1. A process for the production of a bonded non-woven glass fibre or mineral wool mat wherein a non-woven mat is impregnated with a foam of an aqueous solution or suspension of a binder which is thereafter caused to set or cure in situ, and wherein a major portion of the water is removed by the application of dielectric heating.
2. A process according to Claim 1 wherein the binder foam is applied to the mat in excess of the amount required to give a desired binder solids content in the final dry product.
3. A process according to Claim 2, wherein the excess is 50% or more by weight.
4. A process according to Claim 2 or Claim 3, wherein the excess binder foam is drawn through and removed from the mat prior to removing the water.
5. A process according to Claim 4, wherein the excess binder foam removed from the mat is collected and re-circulated.
6. A process for the production of a bonded non-woven glass fibre or mineral wool mat comprising the steps of:
1. forming a non-woven mat of glass fibre or mineral wool by a melt spinning process,
2. forming a foam from an aqueous solution or suspension of a settable or curable binder,
3. cooling said newly-formed mat by the application thereto of said foam so as to impregnate the mat therewith,
4. selectively removing by the application of dielectric heating a major portion of the water from the mat, and thereafter
5. causing the binder to set or cure in situ in the mat.
7. A process according to Claim 6, wherein the foamed binder is applied in excess of the amount required to give a desired binder solids content in the final, dry product and including the further step of drawing said excess through the mat and removing it therefrom prior to the step of removing the water.
8. A process according to any preceding claim wherein dielectric hearing is used to set or cure the binder.
9. Apparatus for the production of a bonded non-woven glass fibre or mineral wool mat, said apparatus including means for making a foam from an aqueous solution or suspension of a binder and means for applying the foam to the mat so as to impregnate it therewith, and dielectric heating means operable to selectively remove by evaporation a major portion of the water from the impregnated mat, together with means operable to remove and collect excess foamed binder from the impregnated mat prior to removing the water.
10. Apparatus according to Claim 11 including means for re-circulating the excess binder.
11. Apparatus according to any of Claims 9-11 including means for pressing the foam into the mat whilst maintaining a seal against at least that face of the mat to which the foam was applied.
12. Apparatus according to Claim 12, wherein the means for pressing the foam into the mat comprises an endless, flexible impermeable belt and a co-operating foraminuous drum containing a suction head and having radially-extending sidewalls.
13. A process for the production of a bonded non-woven glass fibre or mineral wool mat substantially as hereinbefore described with reference to and as illustrated by the drawings accompanying the Provisional Specification.
14. Apparatus for the production of a bonded non-woven glass fibre or mineral wool mat substantially as hereinbefore described with reference to and as illustrated by the drawings accompanying the Provisional Specification.
15. Bonded non-woven glass fibre or mineral wool mat products made by a process according to any of Claims 1-8 or Claim 13, or by the use of an apparatus according to any of Claims 9-12 or Claim 14.
GB4206476A 1976-10-09 1976-10-09 Manufacture of resin bonded fibrous insulation Expired GB1571111A (en)

Priority Applications (8)

Application Number Priority Date Filing Date Title
GB4206476A GB1571111A (en) 1976-10-09 1976-10-09 Manufacture of resin bonded fibrous insulation
US05/840,238 US4188355A (en) 1976-10-09 1977-10-07 Manufacture of fibrous webs
SE7711281A SE425478B (en) 1976-10-09 1977-10-07 KIT AND DEVICE FOR MANUFACTURING A BONDED NON-WOVEN GLASS FIBER OR MINERAL WOOL CARPET
IT51337/77A IT1112098B (en) 1976-10-09 1977-10-07 PROCESS AND APPARATUS FOR THE PRODUCTION OF GLASS OR ROCK OR SLIC FIBER MAT
JP12084277A JPS5349169A (en) 1976-10-09 1977-10-07 Manufacture of bonded unwoven fabric mat
FR7730195A FR2367134A1 (en) 1976-10-09 1977-10-07 MANUFACTURE OF BONDED MINERAL FIBER MATTRESSES, NOT WOVEN, BY IMPREGNATION WITH A BINDER FOAM IN SUSPENSION OR AQUEOUS SOLUTION
NL7711030A NL7711030A (en) 1976-10-09 1977-10-07 PROCESS FOR MANUFACTURING WITH GLASS FIBERS E.D. REINFORCED MATS.
DE19772745529 DE2745529A1 (en) 1976-10-09 1977-10-10 METHOD OF MANUFACTURING A BONDED GLASS FIBER OR MINERAL WOOL FLEECE MAT

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB4206476A GB1571111A (en) 1976-10-09 1976-10-09 Manufacture of resin bonded fibrous insulation

Publications (1)

Publication Number Publication Date
GB1571111A true GB1571111A (en) 1980-07-09

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Family Applications (1)

Application Number Title Priority Date Filing Date
GB4206476A Expired GB1571111A (en) 1976-10-09 1976-10-09 Manufacture of resin bonded fibrous insulation

Country Status (1)

Country Link
GB (1) GB1571111A (en)

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PCNP Patent ceased through non-payment of renewal fee