[0001] The present invention relates to a method for applying a waterproof coating layer
to a roof, specifically suitable for a water-proofing of a flat roof.
[0002] Among typical coating materials for general roof water-proofing is a two-component
urethane resin. A conventional process of water-proofing using the two-component urethane
is generally described as follows:
[0003] Firstly, coating equipment such as cans containing, respectively, a prepolymer and
a hardener of the two-component urethane, a bucket, a portable mixer, and coating
tools, are carried up to a rooftop. The cans are opened to convey the prepolymer and
the hardener into the bucket in a predetermined mixing ratio, then the materials in
the bucket are mixed for three (3) to four (4) minutes by the portable mixer. The
mixture is carried to an area to be coated. The mixture is poured onto the area as
a plurality of stick-shaped materials arranged in parallel and spread to form a layer
of uniform thickness using coating tools.
[0004] After the coating work is finished, the empty cans and coating equipment are brought
down to the ground. The empty cans are usually abandoned as waste.
[0005] Accordingly, this kind of coating work inevitably entails manual processes by workers,
ranging from unloading of the equipment, preparation, and coating to arrangements
after the coating work, in which there exists a long need for saving labour. Another
problem also remains unsolved, i.e., disposal of the waste after the work such as
the emptied cans and the mixed urethane resin.
[0006] An alternative method proposed for the above smearing method is a rim spray method.
This method is typically implemented in work in common use corridors or on staircases
in condominiums.
[0007] The rim spray method, however, still has the following shortcomings. Firstly, a delivery
hose for the coating material must be preheated by electric wires wound therearound
upon application thereof. Secondly, since it may be very difficult to form a coated
layer with a thickness of over one (1) millimeter by spraying at one time, several
instances of spraying work may be required to obtain a coating layer with the necessary
thickness, for example three (3) to four (4) millimeters as a water-proofing film.
Furthermore, specifically in the case of application on rooftops, it has been almost
impossible to apply the rim spray method, since protection of existing structures
on the rooftop from the spray mist generated by spraying is difficult. Therefore,
implementation of the rim spraying method in rooftop works has been very difficult.
[0008] An object of the present invention is to provide a method for applying a waterproof
coating layer to a roof, which allows the prepolymer and the hardener of a two-component
urethane resin as coating material to be pumped up to a rooftop and, then, mixed and
discharged without preheating of the agents, throughout the year.
[0009] Another object of the present invention is to provide a method for applying a waterproof
coating layer to a roof, which can avoid work in loading, unloading and mixing of
the coating material, and work in protecting rooftop structures from the coating material
before coating, thus enabling improvements in coating work efficiency, easy arrangement
after the work, and saving labour.
[0010] Yet another object of the present invention is to provide a method for applying a
waterproof coating layer to a roof, enabling maximum reduction in the amount of waste
such as empty cans.
[0011] To accomplish these and other objects of the invention, according to one aspect of
the present invention, a method for applying a waterproof coating layer to a roof
to form a waterproof coating layer thereon by mixing and applying a two-component
urethane resin including a prepolymer and a hardener therein comprises the steps of
disposing means for transporting the prepolymer and the hardener, respectively, in
a predetermined ratio, the transporting means being placed on the ground, disposing
means for mixing the prepolymer and the hardener forwarded from the transporting means,
and means for discharging a mixture containing the prepolymer and the hardener in
the predetermined ratio to a surface to be coated, the mixing means being placed on
the rooftop and communicating with the transporting means, the discharging means being
integrally attached to the mixing means, and supplying the prepolymer and the hardener
by the transporting means to the mixing and discharging means so as to apply the mixture
of the prepolymer and the hardener to the surface to be coated on the rooftop, wherein
in spring, summer and autumn the viscosity of the prepolymer is set within the range
of 4000-7000 cps at 20°C, and the viscosity of the hardener is set within the range
of 3000-15000 cps at 20°C, and during winter the viscosity of the prepolymer is set
within the range of 1500-3500 cps at 20°C, and the viscosity of the hardener is set
within the range of 3000-7500 cps at 20°C.
[0012] The equivalent ratio of NCO/NH
2+OH on mixing of the prepolymer and the hardener is preferably within the range of
from 1.25/1.00 to 1.05/1.00 in volume ratio.
[0013] The transporting means may comprise pressure feed equipment including a couple of
containers for storing, respectively, the prepolymer and the hardener of the two-component
urethane resin, a couple of pumps for transporting, respectively, the prepolymer and
the hardener from the containers in a predetermined ratio, and a couple of extension
hoses, each of one end of which is connected to the pumps, respectively.
[0014] The mixing means may be a static mixer. The static mixer is connected to each of
the other ends of the extension hoses.
[0015] The discharging means may comprise a discharge nozzle integrally provided with a
tip end portion of the static mixer.
[0016] Still other objects and advantages of the present invention will become readily apparent
to those skilled in this art from the following detailed description, wherein only
the preferred embodiment of the invention is shown and described, simply by way of
illustration of the best mode contemplated of carrying out the invention. As will
be realized, the invention is capable of other and different embodiments, and its
several details are capable of modifications in various obvious respects, all without
departing from the invention. Accordingly, the drawings and description are to be
regarded as illustrative in nature, and not as restrictive.
Fig. 1 shows a schematic flow diagram of one embodiment of the present invention;
and
Fig. 2 is an explanatory view of working process of one embodiment of the present
invention.
[0017] An apparatus employed in one embodiment of the present invention, generally comprises
a transportation vehicle 1, such as a truck, carrying pressure feed equipment constituting
a main portion of the apparatus, and manual operation type mixing and discharging
equipment 83 disposed on the rooftop of a building 2, which sequentially and automatically
mixes two-component urethane resin supplied from the pressure feed equipment and discharges
the mixture onto the surface to be coated. The two-component urethane resin is supplied
to the mixing and discharging equipment by the pressure feed equipment in separated
condition before mixing.
[0018] The pressure feed equipment includes such components disposed on a carrier 1a of
the vehicle 1 as a prepolymer tank 4, a hardener tank 5, a pneumatic pump 6, a pneumatic
pump 7 integrally equipped on a solvent can 7a as a solvent container, a nitrogen
gas bomb 8, a hose reel 9, and a compressed air source unit 10 for supplying compressed
air to the respective pumps.
[0019] It should be noted that, as shown in Fig. 2, the tanks 4, 5, the pumps 6, 7, the
gas bomb 8 and the hose reel 9 are installed on tables with casters 11, 12 and 14,
respectively to constitute a group of portable units independent from the carrier
1a. Though the mixing and discharging equipment 3 is shown with a certain exaggeration
in size in Fig. 2, the equipment 3 actually has reasonable dimensions so as to be
handled manually.
[0020] The compressed air source unit 10 comprises an air compressor 10a and a valve unit
10b. The compressor 10a is driven by an engine such as a Diesel engine.
[0021] The mixing and discharging equipment 3 includes a head block 18 and a static mixer
19. The head block 18 is connected to a discharging end of the pneumatic pump 6 and
to a tip end of an extension hose 17 for solvent transportation. The extension hose
17 is connected with the discharging ends of extension hoses 15 and 16 extended from
the hose reel 9 for conveying the prepolymer and the hardener, respectively, and with
the pneumatic pump 7. The static mixer 19 is integrally disposed on the tip portion
of the head block 18.
[0022] Drums 20 and 21 are containers of two hundred (200) liters for stock solution of
the prepolymer and the hardener of the waterproof urethane coating material. The prepolymer
and the hardener stored in the drums 20 and 21 are forwarded to the tanks 4 and 5,
respectively, by means of drum pumps 22 and 23 driven by the compressed air source
unit 10. The drums 20, 21 and the drum pumps 22, 23 may be placed at the predetermined
storage place after the material is conveyed into the tanks 4 and 5. Alternatively,
the drums 20, 21 may be usually carried on the vehicle 1 so that the prepolymer and
the hardener can be supplied to the tanks 4, 5 when necessary.
[0023] It is desirable that the prepolymer and the hardener are contained in bags such as
double wall polyethylene bags equipped in the drums 20, 21 so that the drums 20, 21
can be recycled after the materials stored in the drums are exhausted.
[0024] Typical examples of the prepolymer include addition compounds of known di-isocyanate
compounds or, occasionally, known polyisocyanate compounds and known compounds having
two or more -NCO radicals at the end of the molecule such as polyoxy-alkylene polyol
or polyester polyol. In other words, a typical substance employed as a prepolymer
for the present invention is an isocyanate prepolymer having two or more -NCO radicals
at the end thereof.
[0025] The hardener of the two-component urethane resin is a paste-like substance including
an aromatic diamine having active hydrogens reacting with the -NCO radicals in the
prepolymer and polyoxyalkylene polyol, a plasticizer, a catalyst, an inorganic filler,
a pigment, and other additives. The hardener should be selected so as to correspond
to the -NCO radicals in the prepolymer to be employed. Then, the composition of the
hardener may be set so that the equivalent ratio of the -NH
2 radical and -OH radical, i.e., NCO/NH
2+OH equivalent ratio expressed as the volume mixing ratio of the prepolymer and the
hardener, is between 1.25/1.0 and 1.05/1.0.
[0026] The viscosity of the prepolymer and the hardener should be adjusted to fall into
the following appropriate ranges in TABLE 1 at 20°C so that the prepolymer and the
hardener can be fed, mixed, and discharged by the pneumatic pumps at approximately
ten (10) to fifteen (15) kg/min without preheating, throughout the year.
TABLE 1
Viscosity ranges at 20°C |
Type of agent |
Viscosity (cps) |
Applicable seasons |
Prepolymer |
4000 to 7000 |
Spring/Summer/Autumn |
Hardener |
3000 to 15000 |
Prepolymer |
1500 to 3500 |
Winter |
Hardener |
3000 to 7500 |
[0027] The viscosity of the prepolymer is adjusted by adding a plasticizer, or a solvent,
or both, at the time of charging the raw materials or after termination of the reaction
in manufacturing thereof. The viscosity of the hardener can be adjusted by components
variable in amount in the liquid component of the agent, such as by a little variation
in the amount of plasticizer, variation in the amount of inorganic filler, and in
the compounding ratio of fillers with different particle sizes.
[0028] The prepolymer tank 4 is a simple sealed tank so as to prevent reaction of the agent
with water. Nitrogen gas is also supplied into the tank 4 from the nitrogen gas bomb
8 to maintain an inactive gas atmosphere therein.
[0029] Both of the prepolymer and the hardener are able to be transported under safe working
pressure throughout the year, while the discharging rate within the predetermined
range is secured.
[0030] The aforementioned appropriate viscosity ranges for the prepolymer and the hardener
are determined based on the following reasoning through experiments:
[0031] If the viscosity of the prepolymer for spring, summer and autumn use (to be employed
in spring, summer and autumn) is below 4000 cps at 20°C, the viscosity drops under
1000 cps where the air and material temperature is over 35°C at a job site specifically
in summer, to show a tendency to result in a mixing failure. On the other hand, if
the viscosity of the prepolymer for spring, summer and autumn use is set above 7000
cps at 20°C, the viscosity reaches 14000 to 18000 cps where air and material temperature
falls below 15°C in early spring or in late autumn, to increase the pump pressure
for measurement and transportation up to 150 to 160 kgf/cm
2. As a result, it is almost impossible to operate the apparatus continuously for safety
reasons and the discharging rate may also fall into an impractical range. With respect
to the hardener, the viscosity ranges have been determined in the same manner.
[0032] If the viscosity of the prepolymer for winter use (to be used during winter) is set
over 3500 cps at 20°C, the viscosity reaches above 15000 cps in midwinter to obstruct
safe and continuous operation of the pumps and decrease the discharging rate below
a practical value. A viscosity below 1500 cps at 20°C will tend to cause a mixing
failure at the relatively higher air temperature in early spring or in late autumn
since the viscosity falls below 1000 cps in that condition. The viscosity of the hardener
for winter use is determined in the same manner.
[0033] The pneumatic pump 6 for conveying the prepolymer and the hardener with the above
adjusted viscosity is of constant-volume type, and comprises a pneumatic motor 6a
connected to the compressed air source unit 10 and a pair of plunger pumps 6b, 6c
connected to the bottom portion of the pneumatic motor 6a. The suction ends of the
pumps 6b, 6c communicate with the tanks 4, 5, respectively.
[0034] The extension hoses 15, 16 are extended from the hose reel 9 and connected to the
discharging ends of the pumps 6b, 6c, respectively. Each of the hoses 15, 16 is approximately
100 m long to reach the 14th or 15th floor of a building. The discharging rate and
operation pressure of the pneumatic pump 6 is determined according to the length of
the hoses 15, 16.
[0035] In case that the mixing ratio of the prepolymer and the hardener is set at around
1/1 in volume ratio, the discharging rate is set at 3 to 16 kg/min based on the operating
conditions, and the normal pressure is set at 20 to 160 kg/cm
2 in consideration of economic operation of a constant-volume type pump. It is possible
to pump the prepolymer and the hardener up to the 14th or 15th floor and to mix and
discharge them without the need for preheating the agents, throughout the year, by
adjusting the viscosity of the prepolymer and the hardener.
[0036] The static mixer 19 of the discharging and mixing equipment 3 has a plurality of
helical stators for mixing therein. The prepolymer and the hardener introduced into
the mixer 19 are uniformly mixed by reaching the tip end portion thereof to be discharged
from the discharging nozzle 19a towards the surface to be coated in a stick-shaped
mixture. Therefore, the discharging operation and spreading work are alternately repeated
to constitute whole coating operation.
[0037] Discharging and stopping of the mixture of the prepolymer and the hardener is controlled
by opening and shutting a control valve 18a disposed upstream of the mixer 18. The
discharging rate of the mixture of the prepolymer and the hardener is set by adjustment
of such equipment as the pressure regulating valve equipped on the pneumatic pump
6.
[0038] During a pause in discharging, a solvent stored in the solvent can 7a is supplied
into the head block 18 by operating the pneumatic pump 7 for pressure feeding of the
solvent and opening a cock 18b connected to a solvent conveying extension hose 17.
The mixture of the prepolymer and the hardener remaining in the head block 18 and
the static mixer 19 is solved into the solvent to wash out the nozzle 19b from time
to time without disassembling the equipment. Thus, clogging by the cured resin mixture
can be prevented.
[0039] The waterproof coating process of the present invention using the above described
apparatus will be fully explained herebelow.
[0040] The transportation vehicle 1 is parked beside the building 2 where there is the working
site. After a wait on the ground, the extension hoses 15, 16 and 17 are extended from
the hose reel 9 towards the rooftop 2a. The mixing equipment 3 at the tip portion
of the hoses 15, 16 and 17 is hoisted up to the rooftop 2a to finish the unloading
work.
[0041] Then, the prepolymer and the hardener are forwarded up to the rooftop 2a by driving
the pumps 6, 7. At the rooftop 2a, the mixed resin is discharged through the discharging
nozzle 19a onto the surface to be coated and is spread out by the workers with application
tools. The coating work is thus performed.
[0042] In order to finish the work, the cock 18b of the head block 18 is opened to flow
solvent into the nozzle 19 and to wash out the mixed resin remaining in the nozzle
19 from time to time.
[0043] After the coating work is finished, the extension hoses 15, 16 and 17 are rolled
back onto the hose reel 9 and the mixing and discharging equipment 3 is carried down
to the ground. The residual prepolymer and the hardener are contained in the tanks
4, 5 in separated condition, and each residue may be brought back into the drums 20,
21, or stored for the next job after a conservation treatment.
[0044] The experimental examples of the present invention will be discussed herebelow according
to variation of the viscosity of the prepolymer and the hardener and the results therefrom.
Experimental example 1
[0045] The discharging test was conducted using the prepolymer and the hardener shown below.
[Material combination 1]
Prepolymer
[0046]
- PPG-TDI prepolymer
- 97.5 weight parts
- Adipic acid-di-2-ethylhexyl
- 2.5 weight parts
- Total
- 100.0 weight parts
- NCO content
- 3.70%
- Specific gravity
- 1.05
- Viscosity
- 5300 cps/20°C
Hardener
[0047]
- Specific gravity
- 1.49
- Viscosity
- 5600 cps/20°C
[Test condition]
[0048]
- Outside air temperature
- 31°C
- Coating surface temperature
- 46°C
- Material temperature
- 29°C
- Extension hose length
- 100 m
- Working site
- Rooftop of the 3rd floor
[Result]
[0049] The air compressor was actuated to drive the respective drum pumps for the prepolymer
and the hardener and to forward the agents into the hopper. Then, the valve of the
pneumatic motor was opened and the valve of the regulator was gradually opened. When
the pressure was at 2.0 kgf/cm
2, the pressure gauges of the prepolymer and the hardener indicated 90-105 kgf/cm
2 and 60-70 kgf/cm
2, respectively. The constant-volume pump reciprocated thirty (30) times a minute.
The discharging ratio of the prepolymer and the hardener measured at the tip end portion
of the hose placed at the rooftop immediately before the head block 18 was 100/142.1
in weight ratio. According to the measured discharging ratio, the quantity of the
hardener was more than the planned value by 0.2%. However, this result was sufficiently
within allowable tolerances of design. The discharging rate from the static mixer
while the hoses were connected to the head block 18 was 15.3 kg/min. The discharged
mixture was spread flat in two (2) millimeters thickness with a scratching trowel
and the coated surface showed a uniform colour, which indicated that the prepolymer
and the hardener were sufficiently mixed.
Experimental example 2
[0050] The discharging test was conducted using the prepolymer and the hardener shown as
material combination 2.
[Material combination 2]
Prepolymer
[0051]
- PPG-TDI prepolymer
- 95.0 weight parts
- Adipic acid-di-2-ethylhexyl
- 2.5 weight parts
- Xylene
- 2.5 weight parts
- Total
- 100.0 weight parts
- NCO content
- 3.64%
- Specific gravity
- 1.048
- Viscosity
- 4000 cps/20°C
Hardener
[0052]
- Specific gravity
- 1.47
- Viscosity
- 3200 cps/20°C
[Test condition]
[0053]
- Outside air temperature
- 33°C
- Coating surface temperature
- 49°C
- Material temperature
- 30°C
- Extension hose length
- 100 m
- Working site
- Rooftop of the 3rd floor
[Result]
[0054] The discharging test was conducted according to the procedure in Example 1. The pumps
for the prepolymer and the hardener reciprocated thirty (30) times a minute at 1.3
kgf/cm
2 regulator pressure. The pressures for transportation of the prepolymer and the hardener
were 40-45 kgf/cm
2 and 35-40 kgf/cm
2, respectively. The discharged mixture was spread flat with a scratching trowel to
show a uniform gray colour, which indicated a good mixing condition. The measured
discharging rate from the mixer was 15.8 kg/min.
Experimental example 3
[0055] The discharging test was conducted using the prepolymer and the hardener shown as
combination 3 under the test conditions below.
[Material combination 3]
Prepolymer
[0056]
- PPG-TDI prepolymer
- 94.0 weight parts
- Adipic acid-di-2-ethylhexyl
- 3.0 weight parts
- Xylene
- 3.0 weight parts
- Total
- 100.0 weight parts
- NCO content
- 3.57%
- Specific gravity
- 1.046
- Viscosity
- 3600 cps/20°C
Hardener
[0057]
- Specific gravity
- 1.504
- Viscosity
- 2800 cps/20°C
[Test condition]
[0058]
- Outside air temperature
- 16°C
- Coating surface temperature
- 28°C
- Material temperature
- 15°C
- Extension hose length
- 100 m
- Working site
- Rooftop of the 3rd floor
[Result]
[0059] The discharging test was conducted according to the same procedure as in Example
2. The constant-volume pumps reciprocated thirty (30) times a minute at 1.0 kgf/cm
2 regulator pressure. The pressures for transportation of the prepolymer and the hardener
were 30-40 kgf/cm
2 and 25-33 kgf/cm
2, respectively. The measured discharging rate was 16.4 kg/min. The discharged mixture
was spread flat with a scratching trowel, and transparent line portions gradually
appeared. The coated surface was examined once cured on the next day, and a series
of air bubbles caused by small-scale blowing were observed along the line portions,
which were mixing failure portions of the prepolymer. It was also observed that the
colour at several portions in the coating layer had changed brown. It was presumed
that the quantity of hardener mixed with the prepolymer had been significantly larger
than appropriate. Furthermore, the hardener stored in the storage drum had separated
into a supernatant portion and a lower portion.
Experimental example 4
[0060] The discharging test was conducted using the prepolymer and the hardener shown as
combination 4 under the test conditions below.
[Material combination 4]
Prepolymer
[0061]
- PPG-TDI prepolymer
- 97 weight parts
- Adipic acid-di-2-ethylhexyl
- 1 weight parts
- Xylene
- 2 weight parts
- Total
- 100 weight parts
- NCO content
- 3.73%
- Specific gravity
- 1.05
- Viscosity
- 6800 cps/20°C
Hardener
[0062]
- Specific gravity
- 1.51
- Viscosity
- 14000 cps/20°C
[Test condition]
[0063]
- Outside air temperature
- 16°C
- Coating surface temperature
- 28°C
- Material temperature
- 14°C
- Extension hose length
- 100 m
- Working site
- Rooftop of the 10th floor
[Result]
[0064] The discharging test was conducted according to the same procedure as in Example
1. The constant-volume pumps reciprocated twenty seven (27) times a minute at 4.8
kgf/cm
2 regulator pressure. The pressures for transportation of the prepolymer and the hardener
were 140-150 kgf/cm
2 and 145-155 kgf/cm
2, respectively. The measured discharging rate was 13 kg/min. The coated surface spread
with a scratching trowel showed a uniform colour tone and the mixing condition was
good.
Experimental example 5
[0065] The discharging test was conducted using the prepolymer and the hardener shown as
combination 5 under the test conditions below. The test was performed subsequent to
Example 4.
[Material combination 5]
Prepolymer
[0066]
- PPG-TDI prepolymer
- 98 weight parts
- Xylene
- 2 weight parts
- Total
- 100 weight parts
- NCO content
- 3.72%
- Specific gravity
- 1.051
- Viscosity
- 7800 cps/20°C
Hardener
[0067]
- Specific gravity
- 1.54
- Viscosity
- 16000 cps/20°C
[Test condition]
[0068]
- Outside air temperature
- 15°C
- Coating surface temperature
- 25°C
- Material temperature
- 14°C
- Extension hose length
- 100 m
- Working site
- Rooftop of the 10th floor
[Result]
[0069] The discharging test was conducted according to the same procedure as in Example
1. The constant-volume pumps reciprocated twelve (12) times a minute at 5.9 kgf/cm
2 regulator pressure. The pressures for transportation of the prepolymer and the hardener
were 160-170 kgf/cm
2 and 150-160 kgf/cm
2, respectively. In this condition, the test was halted since it seemed impossible
to operate the pumps continuously, for safety reasons, and the discharging rate became
very small. However, the condition of the discharged mixture was good.
Experimental example 6
[0070] The discharging test was conducted using the prepolymer and the hardener shown as
combination 6 under the test conditions below.
[Material combination 6]
Prepolymer
[0071]
- PPG-MDI prepolymer
- 92 weight parts
- Adipic acid-di-2-ethylhexyl
- 4 weight parts
- Xylene
- 4 weight parts
- Total
- 100 weight parts
- NCO content
- 4.72%
- Specific gravity
- 1.038
- Viscosity
- 1550 cps/20°C
Hardener
[0072]
- Specific gravity
- 1.414
- Viscosity
- 3100 cps/20°C
[Test condition]
[0073]
- Outside air temperature
- 6°C
- Coating surface temperature
- 13°C
- Material temperature
- 7°C
- Extension hose length
- 100 m
- Working site
- Rooftop of the 10th floor
[Result]
[0074] The discharging test was conducted according to the same procedure as in Example
1. The constant-volume pumps reciprocated thirty (30) times a minute at 3.2 kgf/cm
2 regulator pressure. The pressures for transportation of the prepolymer and the hardener
were 80-90 kgf/cm
2 and 70-80 kgf/cm
2, respectively. The measured discharging rate was 14.8 kg/min. The coated surface
of the discharged mixture spread with a scratching trowel generally showed a uniform
colour tone and the mixing condition was good.
Experimental example 7
[0075] The discharging test was conducted using the prepolymer and the hardener shown as
combination 7 under the test conditions below.
[Material combination 7]
Prepolymer
[0076]
- PPG-MDI prepolymer
- 94 weight parts
- Adipic acid-di-2-ethylhexyl
- 3 weight parts
- Xylene
- 3 weight parts
- Total
- 100 weight parts
- NCO content
- 4.80%
- Specific gravity
- 1.040
- Viscosity
- 3500 cps/20°C
Hardener
[0077]
- Specific gravity
- 1.423
- Viscosity
- 7450 cps/20°C
[Test condition]
[0078]
- Outside air temperature
- 5°C
- Coating surface temperature
- 15°C
- Material temperature
- 6°C
- Extension hose length
- 100 m
- Working site
- Rooftop of the 10th floor
[Result]
[0079] The discharging test was conducted according to the same procedure as in Example
1. The constant-volume pumps reciprocated twenty seven (27) times a minute at 5.5
kgf/cm
2 regulator pressure. The pressures for transportation of the prepolymer and the hardener
were 150-160 kgf/cm
2 and 120-130 kgf/cm
2, respectively. The measured discharging rate was 11.6 kg/min. The coated surface
spread with a scratching trowel showed a uniform colour tone and a good mixing condition.
Experimental example 8
[0080] The discharging test was conducted using the prepolymer and the hardener shown as
combination 8 under the test conditions below.
[Material combination 8]
Prepolymer
[0081]
- PPG-MDI prepolymer
- 92 weight parts
- Adipic acid-di-2-ethylhexyl
- 4 weight parts
- Xylene
- 4 weight parts
- Total
- 100 weight parts
- NCO content
- 4.70%
- Specific gravity
- 1.036
- Viscosity
- 1380 cps/20°C
Hardener
[0082]
- Specific gravity
- 1.410
- Viscosity
- 2800 cps/20°C
[Test condition]
[0083]
- Outside air temperature
- 22°C
- Coating surface temperature
- 34°C
- Material temperature
- 21°C
- Extension hose length
- 100 m
- Working site
- Rooftop of the 3rd floor
[Result]
[0084] The discharging test was conducted according to the same procedure as in Example
1. The constant-volume pumps reciprocated thirty (30) times a minute at 1.1 kgf/cm
2 regulator pressure. The pressures for transportation of the prepolymer and the hardener
were 20-30 kgf/cm
2 and 40-50 kgf/cm
2, respectively. The measured discharging rate was 16.2 kg/min. The discharged mixture
was spread flat with a scratching trowel, and transparent stripes appeared. The coated
surface was examined once cured and air bubbles were observed in the transparent portions.
Those portions were confirmed to include an unmixed prepolymer component. It was determined
that the mixing failure occurred because the prepolymer viscosity was too low.
Experimental example 9
[0085] The discharging test was conducted using the prepolymer and the hardener shown as
combination 9 under the test conditions below.
[Material combination 9]
Prepolymer
[0086]
- PPG-MDI prepolymer
- 94 weight parts
- Adipic acid-di-2-ethylhexyl
- 3 weight parts
- Xylene
- 3 weight parts
- Total
- 100 weight parts
- NCO content
- 4.81%
- Specific gravity
- 1.041
- Viscosity
- 3660 cps/20°C
Hardener
[0087]
- Specific gravity
- 1.425
- Viscosity
- 7700 cps/20°C
[Test condition]
[0088]
- Outside air temperature
- 5°C
- Coating surface temperature
- 9°C
- Material temperature
- 4°C
- Extension hose length
- 100 m
- Working site
- Rooftop of the 10th floor
[Result]
[0089] The discharging test was conducted according to the same procedure as in Example
1. The constant-volume pumps reciprocated ten (10) times a minute at 5.8 kgf/cm
2 regulator pressure. The pressures for transportation of the prepolymer and the hardener
were 160-170 kgf/cm
2 and 150-160 kgf/cm
2, respectively. The discharging rate was 4.1 kg/min. The pressure of the prepolymer
and hardener was too high to continue operation of the pumps.
[0090] While the present invention has been discussed in terms of the preferred embodiments,
the present invention should be implemented in various fashions with incorporating
modifications of the disclosed embodiments in addition, omission or modification of
the detailed construction, without departing from the principle of the invention.
Therefore, the present invention should be understood to include all embodiments encompassed
within the spirit of the invention set out in the appended claims.
1. A method for applying a waterproof coating layer to a roof to form a waterproof coating
layer thereon by mixing and applying a two-component urethane resin including a prepolymer
and a hardener therein, comprising the steps of:
disposing means (1) for transporting said prepolymer and said hardener, respectively,
in a predetermined ratio, said transporting means being placed on the ground;
disposing means (19) for mixing said prepolymer and said hardener forwarded from said
transporting means, and means (19a) for discharging a mixture containing said prepolymer
and said hardener in said predetermined ratio to a surface to be coated, said mixing
means being placed on the rooftop (2a) and communicating with said transporting means,
said discharging means being integrally attached to said mixing means; and
supplying said prepolymer and said hardener by said transporting means to said mixing
and discharging means so as to apply said mixture of the prepolymer and the hardener
to the surface to be coated on the rooftop,
wherein in spring, summer and autumn, the viscosity of said prepolymer is set within
the range of 4000-7000 cps at 20°C, and the viscosity of said hardener is set within
the range of 3000-15000 cps at 20°C, and during winter the viscosity of said prepolymer
is set within the range of 1500-3500 cps at 20°C, and the viscosity of said hardener
is set within the range of 3000-7500 cps at 20°C.
2. A method as claimed in claim 1, wherein the equivalent ratio of NCO/NH2+OH on mixing of said prepolymer and said hardener is within the range of from 1.25/1.00
to 1.05/1.00 in volume ratio.
3. A method as claimed in claim 1 or claim 2, wherein said transporting means comprises
pressure feed equipment including a couple of containers (4,5) for storing, respectively,
said prepolymer and said hardener of said two-component urethane resin, a couple of
pumps (6,7) for transporting, respectively, said prepolymer and said hardener from
said containers in a predetermined ratio, and a couple of extension hoses (15,16),
each of one end of which is connected to said pumps, respectively.
4. A method as claimed in claim 3, wherein said mixing means comprises a static mixer
(19), said static mixer being connected to each of the other ends of said extension
hoses.
5. A method as claimed in claim 4, wherein said discharging means comprises a discharge
nozzle (19a) integrally provided with a tip end portion of said static mixer.
6. A method for applying a waterproof coating layer to a roof to form a waterproof coating
layer thereon by mixing and applying a two-component urethane resin including a prepolymer
and a hardener therein, comprising the following steps of:
disposing pressure feed equipment on the ground, comprising a couple of containers
(4,5) for storing said two-component urethane resin of said prepolymer and said hardener,
respectively, a couple of pumps (6,7) for transporting said prepolymer and said hardener
from said containers in a predetermined ratio, respectively, and a couple of extension
hoses (15,16), each of one end of which is connected to said pumps, respectively;
disposing mixing and discharging equipment (3) on the roof (2a), said mixing and discharging
equipment being connected to each of the other ends of said extension hoses and comprising
a static mixer (19) for mixing said prepolymer and said hardener, and a discharge
nozzle (19a) integrally provided with a tip end portion of said static mixer for discharging
the mixed resin towards a surface to be coated; and
supplying said prepolymer and said hardener by said pressure feed equipment to said
mixing and discharging equipment to apply the mixture onto the roof,
wherein in spring, summer and autumn the viscosity of said prepolymer is set within
the range of 4000-7000 cps at 20°C, and the viscosity of said hardener is set within
the range of 3000-15000 cps at 20°C, and during winter the viscosity of said prepolymer
is set within the range of 1500-3500 cps at 20°C, and the viscosity of said hardener
is set within the range of 3000-7500 cps at 20°C.
7. A method as claimed in claim 6, wherein the equivalent ratio of NCO/NH2+OH on mixing of said prepolymer and said hardener is within the range of from 1.25/1.00
to 1.05/1.00 in volume ratio.