AU610944B2 - Treatment method for imparting antimicrobial and hydrophilic properties to aluminum surfaces - Google Patents

Description

THE COMMISSIONER or PATENTS.

Edwcl. Waters Sons, Melbourne. COMMONWFALTH OF AUSTRAL 6 1 09 4 4.10 PATENTS ACT 1952-69 COMPLETE SPECIFICATION.

(ORIGINAL)

Class Int. Class Application Number: Lodged: 24688/88 4. 11. 88 Complete Specification Lodged: Accepted: Published: 00J'iority.

0 00 0 00 00 0 0 00 0 tRelated Art 00.0 00 0 0 Name of Applicant: a 00 Address of Applicant: 0 00 0 0 0 Adoress for Service: NIHON PARKERIZING CO., LTD.

15-1, Nihonbashi, 1-chome, Chuo-ku, Tokyo 103, Japan RYORSUKE SAKO, AKIHIKO HASEBE, AKIRA NISHIHARA, HIROSHI OKITA and YASUNOBU MATSUSHIMA EDWD. WATERS SONS, 50 QUEEN STREET, MELBOURNE, AUSTRALIA, 3000.

Complete Specification for the invention entitled: TREATMENT METHOD FOR IMPARTING ANTIMICROBIAL AND HYDROPHILIC PROPERTIES TO ALUMINUM SURFACES The following statement is a full description of this invention, including the best method of performing it known to -US -day oVt. u u 11u u 1 1 W-,J.

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IHOPARKERIZING CO., LTD. I To: THz ComSSIONR op PAT sanag kbexecive Vice President T C O It7.

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PATENT

Docket M 4659 P A/NI o o 0 00 0 00 0 00 0 06 00 0 *0 a 0 00 0 0 o 00 0 000 0 0000 00 0 0 400 0 00 0 00 000 0 0 0 0 00 o 00 o oo o o 0 o o 00.000 o o 0 0a o TREATMENT METHOD FOR IMPARTING ANTIMICROBIAL AND HYDROPHILIC PROPERTIES TO ALUMINUM SURFACES Field of the Invention This invention relates to a surface treatment method for making the surfaces of metals, particularly aluminum and aluminum alloys (both being briefly denoted herein merely as "aluminum"), hydrophilic, resistant to growth of microbes, and corrosion resistant. More particularly, the present invention relates to a surface treatment method for aluminum materials for use in heat exchangers.

Statement of Related Art 10 There are many known surface treatments for aluminum heat exchangers and their components such as fins and the like with the objective of preventing white rust. Examples of these surface treatments are anodic oxidation coatings and resin coating treatments, including those which contain hexavalent chromium. These coated surfaces are almost entirely lacking an affinity for water; instead, they are water repellent. Chromate conversion coating treatments are also used, but such coatings have only a modest water affinity even on freshly formed coatings, and with the i 1 r t,

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o o o 00 0 Soo0 0000 0000 0 o 000 ad 0 00 So o oo o o o o a a passage of time, particularly under hot, dry conditions, chromate conversion coatings tend to become thoroughly hydrophobic surfaces.

The fin spacing in many heat exchangers has been made very small in order to pack as much cooling surface area as possible into a given volume and thereby improve the radiation or cooling effectiveness. When the cooling surfaces or fins are even moderately hydrophobic, having a water wetting angle substantially greater than zero, water droplets tend to form on the surfaces by condensation of water from the atmosphere. When the cooling surfaces are very closely spaced, such water droplets can easily bridge the spaces between adjacent surfaces, thereby impeding the smooth flow of air through the spaces between the cooling 15 surfaces and reducing the heat exchange efficiency.

Moreover, the water droplets accumulated in the fin gaps, because they are easily dispersed and scattered about by the heat exchanger's blower, are not effectively collected by any conventional droplet collector installed 20 at the bottom of a heat exchanger, so that the vicinity around the heat exchanger becomes wet.

Accordingly, in order to avoid the generation of the mesh-like obstruction by the water droplets remaining in the fin gaps, treatments have been proposed for the purpose 25 of imparting hydrophilicity to aluminum surfaces and improving their wettability by water.

In particular, the treatment of aluminum surfaces by silicates, for example, waterglass, etc., is widely employed as a hydrophilicizing treatment because of the 30 high water affinity and high heat resistance of the surfaces thus produced, as well as low cost. Proposed methods for this type of treatment include, for example, coating an aqueous silicate solution directly on conversion-treated aluminum or coating the silicate solution on the aluminum after the preliminary formation of an organic polymer film.

For example, Japanese Patent Application Laid Open 0 00 0 a 0 00 0 00 000 0 00) 0 400000 0 O O0 O a 0 a oou 0 0 00 0 0 0 0 00Q

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0 90 0 0 0 0 00 O 00 0 00 0 00 a oa 0 0 0 0000 0ooo 0000 o o 00 0 0 00 Number 50-38,645 proposes a method for the formation of a hydrophilic coating in which aluminum is first treated with a solution containing alkali metal carbonate and alkali metal chromate or alkali metal dichromate and is then treated with alkali metal silicate.

United States Patent 3,989,550 teaches a hydrophilicizing treatment method which consists of a first treatment with a solution containing fluorine, chromic acid, and phosphoric acid, in each case as ions. This is followed by treatment with an alkali metal silicate and then heating.

Japanese Patent Application Laid Open Number 54-57,264 teaches a heat exchanger that has surfaces with both corrosion resistance and hydrophilicity, as a result of the 15 formation of a conversion coating on the aluminum surfaces.

Here, after the surfaces of an aluminum plate-fin-type heat exchanger have been treated with an aqueous solution of a silicic acid compound, a treatment is then carried out with an aqueous alkaline solution which contains an alkaline 20 earth metal compound.

Japanese Patent Application Laid Open Number 57-82,467 teaches an improvement in physical properties by means of a post-treatment, and concerns not only the prevention of the discoloration of aluminum surfaces by hot water, but 25 also refers to an improvement in corrosion resistance. In this case, the aluminum surface is coated with an aqueous solution of an alkaline silicic acid material. After drying, an anticorrosion coating is then formed by neutralization with an acid such as nitric acid, etc.

30 Japanese Patent Application Laid Open Number 61-84,383 teaches a method for treating the surface of aluminum for heat-exchanger service whose characteristic feature is that the aluminum surface is first coated with an aqueous solution of an alkali metal silicate to which a borate has been added; after drying, an aqueous solution of an inorganic acid, organic acid, or acidic salt of an inorganic or organic acid is then applied. KBO 2 CaB40 7 0 00 0 00 0 00 0 00 000000 0 0 0 0 0 0 0 0 00 0 0 0 0 o0

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and Na2 B407 are taught as optimal examples of the borate, while phosphoric acid or dihydrogenphosphate, tannic acid, myoinositol hexaphosphate, polyacrylic acid, and their salts are given as optimal examples of the inorganic or organic acids and acidic salts thereof. Benefits taught for this method are an improvement in corrosion resistance and prevention of saponification of the lubricating oil applied in post-treatment of the treated aluminum.

Turning now to a consideration of the operation of automobile air conditioners and heating and/or cooling air conditioners in household service, one encounters the problem that an undesirable odor, which accompanies the fan draft during operation and particularly during start-up, often fills the interior of the conditioned room or o 0 15 passenger compartment. This odor tends to be stronger when o0o more time has elapsed from the installation or last 0 00 previous use of the air conditioner. The cause of the 0 oo worsening of the odor with increased time is believed to be 0000 00 proliferation of fungi and/or bacteria in the air 0.00 Co 0 20 conditioner, particularly on and between the fins of the 0 oo heat exchanger. With regard to preventive measures directed at this, discharging the air to the exterior using a bypass during the initial stage of operations and 00 sterilization using a sterilizing lamp have been proposed.

o03( 25 However, the most effective method involves the application to the heat exchanger itself of a coating which contains an antimicrobial agent.

o oThe following are examples of teachings of how to impart an affinity for water to the heat exchanger fin 30 surfaces while at the same time preventing the undesirable 0 0 OO0 odor, through the application of a coating which contains o an antimicrobial agent to the heat exchanger, filter, ducts, and the like, in air conditioning service: Japanese Patent Application Laid Open Numbers 58-10,051, 58-10,052, 58-101,717, 58-102,073, 59-124,428, 59-199,339, 60-50,397, and 61-168,675. However, in each case the antibacterial and antifungal agents in the preceding are organic j a .1 .1 :1 a t:ra 00 o o 0 00 0 00 0 00 0 oo 00 0000 00 0 0 6 0 0 0 compounds or their metal salts.

Boric acids, the oxyacids afforded by the hydration of B203, and their salts are known for antifungal and antibacterial applications.

Busan ll-Ml (sold by Buckman Laboratories, Inc., USA) is an anti-rust pigment which has barium metaborate as its principal component. It is marketed for paint and plastic applications as a pigment which also has antimicrobial properties, and it is registered with the EPA under No.

1448-17-AA. Its particle size is approximately 65% 2 micrometers, approximately 15% between 1 to 2 micrometers, and approximately 10% 1 micrometer.

Japanese Patent Application Laid Open Number 56-81,373 discloses an antifungal paint which contains zinc borate, 15 while Japanese Patent Application Laid Open Number 60-146,807 discloses the addition of a thickener, such as an acrylic acid polymer, etc., to an antifungal agent which contains hydrogen peroxide and boric acid. The latter refers to application as a coating on bathroom ceilings, 20 etc. Japanese Patent Application Laid Open Number 60-90,266 relates to a novel pigment which is obtained by a reaction in which a silicic acid compound is added to a phosphoric acid compound plus a boric acid compound plus Ca, Sn, Ba, Zn, Al, or their equivalents. This is 25 described as effective both as an antifungal as well as an anti-rust in paint applications.

As discussed above, a number of methods are known for the treatment of heat exchangers and aluminum used in their fins in order to impart hydrophilicity and antifungal 30 and/or antibacterial properties. Furthermore, treatment agents simultaneously manifesting both of these effects have also been proposed.

However, these known antifungal/antibacterial hydrophilicizing methods suffer from various disadvantages that are particularly notable in heat exchangers used for air conditioning. Surface-treatment agents with a high hydrophilicizing capacity are usually used to ameliorate 0 00 0 0 o oo 0 00 0 00 0 00 o eo 0 000000 0 0 0 0000 0I 0 0 0 0 0 0 0 0 0 0 0 06 i! 1 .1.

9r 00 00 0 0 RO 00 00 b o oo o o, 0*4 0 40 the problem of mesh-like obstruction by condensed water droplets. These agents are generally highly hydrophilic organic polymers or waterglass. These materials are water soluble, and water is generally used as the solvent in these hydrophilicizing treatment solutions, thus avoiding environmental problems and ignition hazards. When an antifungal is added to such an agent, a homogeneous mixed solution can be easily prepared if a water-soluble antifungal, for example, p-hydroxybenzoic acid, salicylic acid, sorbic acid, salts of the foregoing, borax, and the like, is used.

A problem with these water-soluble substances is their short term of effectiveness due to elution by condensed water during operation of the air conditioner. In a 15 specific response to this retention problem, a poorly water-soluble or water-insoluble organic antifungal can be used by emulsifying and dispersing it in water after dissolution in a suitable solvent, or an inorganic or organic antifungal can be suspended in water after 20 comminution, followed in either case by addition to the hydrophilicizing treatment solution. However, the hydrophilicizing treatment solutions afforded by these methods again suffer from several problems: in addition to stability problems with the solution itself due to 25 sedimentation and separation of the emulsified antifungal, it is difficult to obtain a uniform coating due to phase separation from the waterglass or hydrophilic polymer when the coating is dried.

Furthermore, due to the narrow fin spacing in heat 30 exchangers, as well as considerations of the heat conductivity and cost, it is advantageous for the coated hydrophilicizing film to form as thin a film as possible, less than 1 micrometer after drying. This places stringent requirements on comminution of particles to be suspended after grinding. Also, due to limitations in this regard, complete coverage cannot usually be obtained by a film produced using a hydrophilicizing treatment agent in which i t 0 4 0 0s O0 00 0 0 0 000.0 0 0 8 0o 0 0 0 4 00 11L_ I d w i.

antifungal particles are suspended; pinholes occur frequently and when they occur substantially reduce anticorrosion performance.

The present applicants have previously discovered that a hydrophilic film, which manifests an excellent corrosion resistance, excellent hydrophilicity, good initial odor characteristics, good film bonding, and good processing properties, can be obtained by coating and drying a waterglass hydrophilicizing treatment agent on aluminum surfaces followed by treatment with a solution containing a multivalent metal salt. This has been the subject of 5? c->\3i=4 22 c'c b- .23S Li Japanese Patent p -eaa-n--672-3r7-'2 3: No borate or other antimicrobial agent is used in the hydrophilicizing treatment according to these earlier 0o 15 inventions.

0 Description of the Invention Except in the operating examples or where otherwise 0 0 •0 expressly stated, all numbers in this description 000D o0 expressing quantities of materials or reaction conditions 0 20 are to be understood as modified by the word "about".

6 04 0 )D 00 0 .9 VI 0 '.4~l It has been discovered that an antimicrobial hydrophilicizing surface treatment, which will provide a high hydrophilicity, high corrosion resistance, and high antifungal performance, and which avoids difficulties with 25 lubricating oil coatability in post-treatment, and which results in low odor, both initial and long-term, can be obtained by first coating aluminum with a hydrophilicizing aqueous treatment solution containing an alkali metal and/or a quaternary ammonium silicate acid, along with 30 boric acid and/or its water-soluble salts, followed by heating and drying to form a homogeneous film, and by then carrying out treatment with a solution containing at least one species of multivalent metal salt or hydroxide.

While not wishing to be bound by theory, the applicants believe that the boric acid and/or water-soluble borate added to the waterglass hydrophilicizing treatment solution may be converted to a poorly ion-exchangeable p LI~

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0 a o 0 00 0 o or 00 e 0 00 0o o o 0 0 O0 multivalent metal salt by the subsequent aqueous multivalent metal salt solution. Elution by condensation water generated by operation of the heat exchanger is thus made more difficult. Furthermore, the multivalent metal ion may form a cross link between borate anions and the anionic silicate network characteristic of waterglasses by bonding to each kind of negatively charged entity. This would serve to strengthen the hydrophilic film.

The film formed in the present invention, besides preventing initial odor from heat exchangers that utilize it, also prevents the longer-term development of odor originating in the growth of bacteria and fungi.

The first treating solution used in this invention is an aqueous solution containing quaternary amine 15 silicate(s), for example, QAS 40 or QAS 25 from Nissan Chemical Industries, Limited, or alkali silicat(es), either of these types of silicates being alternatively referred to below as waterglass(es). Waterglasses do not have a fixed composition as do most salts, but can have greater or lesser amounts of silicon oxide for a given amount of cations. The solution for this invention preferably has a value of 0.5 to 8.5 for the (SiO 2 )/(monovalent cation) molar ratio, with Li, Na, and K preferred as monovalent cations. More preferably, the cations are Na or K and the 25 molar ratio is 1 to 2.

The preferred types of boric acids for the present invention are those with molecular formulas that can be matched by mixing B 2 0 3 with varying numbers of water molecules, for example, orthoboric acid (H 3 BO), metaboric 30 acid (HBO 2 and tetraboric acid (H 2

B

4 0 7 Waterglass, and particularly high SiO 2 waterglass, is prone to coagulation upon the addition of acidic substances. Thus instead of the free boric acids noted above, it is generally preferred to use neutral water-soluble salts, for example, sodium, potassium, or lithium borate. Furthermore, ammonium borate can also be admixed in part.

0 00 0o0 o 0 00 0 00 00 a o oo 0 0 0 0 0 0.)000 o o 0 0 o 0O a 0 I i F i- 00 t o o 00 t 0 a o o0000 oo 0 0 o0 Qn 1 It is often useful to add water soluble organic polymers to the solutions of silicates and borates described above. Suitable polymers include polyvinyl pyrrolidone, the water-soluble salts of polyacrylic acid or polymethacrylic acid, the polymers and copolymers of unsaturated acids such as maleic acid, or itaconic acid, the polymers and copolymers of acrylamide, methacrylamide, and their derivatives, the partial hydrolyzates of polyacrylamide and polymethacrylamide, polyvinyl alcohol, poly(2-hydroxyethyl acrylate), the alkali metal salts of polystyrenesulfonic acid, and pullulan.

The weight ratios in the aqueous solution preferably is 5 to 100 parts, more preferably 20 to 60 parts, of borate for each 100 parts of waterglass, and 0 to 100 parts, more preferably 0 to 60 parts organic polymer for each 100 parts of the sum of the waterglass and borate.

Of course, in addition to the preceding, surfactants, leveling agents, non-boric acid antimicrobials, fragrances, colorants, defoamers, rust inhibitors, and the like can be 20 present. Also, in order to increase the hydrophilicity, hydrophilic metal oxide sols, for example, silica sols or alumina sols can also be added.

The hydrophilicizing treatment solution obtained as described above can be coated and then dried on a bare 25 aluminum surface, or it can be coated and dried after a conversion treatment or priming with an organic polymer has been used on the aluminum.

In the present context, aluminum also comprises aluminum alloys, and no specific restriction is placed on 30 the application methodology: coating can be carried out either on the sheet-form fin material or after installation in a heat exchanger. In other words, one may freely select from among brush application, immersion, spraying, roll coating, or flow coating, among others, according to the form of the substrate to be coated, quantity of application, and similar factors. Sheet-form fin material is typically roll coated, while the installed product is 0 00 0 0 0 0 00 0 00 0 0 0 o oo 0 00 0 0 0 0 0 0 000000 0 0 0 0 0 o 0 i- A 1 typically immersion coated.

After application of the hydrophilicizing treatment agent, the aluminum heat exchanger is dried by heating, without a water rinse, to form a hydrophilic coating film.

While the thickness of this film is not specifically restricted in the practice of this invention, thicknesses of approximately 0.02 to 2 microns are normally preferred and 0.05 to 1 micron will usually be most preferable.

Drying is typically conducted in a hot-air drying oven, but infrared heating or any other appropriate means can also be used. The usual hot-air drying oven has orifices through which hot air is ejected, and the aluminum heat exchanger or other object is dried by passage through the chamber while hot air is ejected from these holes.

While the drying conditions will vary substantially 0oc according to the part to be dried, 80 to 300 degrees 0 eCentigrade for 5 seconds to 30 minutes will usually be o* suitable, with the longer times at the lower temperatures, S and the shorter times at the higher temperatures.

0 0 20 The dried hydrophilic film is then treated with an o0 aqueous solution of the salt of a multivalent metal. Both flat fin sheet and assembled heat exchangers can be suitably treated by immersion, and flat fin sheet can also 00o 2 be treated by various other methods such as spraying, roll o 25 coating, and curtain coating, among others.

0 00 0 SUseable as the multivalent metal are magnesium, calcium, strontium, barium, aluminum, titanium, zirconium, 0 chromium, molybdenum, manganese, iron, cobalt, copper, zinc, tin, and any other cation with at least two charges 0 30 that forms a water soluble salt. Magnesium, calcium, o ooo 4 barium, and zinc are preferred. Water soluble solvents o osuch as alcohol can also be present in the treatment solutions. There is no limitation on the anion(s) present, so long as water solubility is obtained, the nitrates, nitrites, fluorides, carbonates, bicarbonates, and hydroxides are advantageous from the standpoint of corrosion resistance.

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~pcll--~ 4i-na~~: On the subject of the solution concentration, while practice of the invention will be possible as long as the cation's solubility is at least 0.01 mol/L-H 2 0, treatment is more effective at concentrations of at least 0.1 mol/L-H 20. With regard to the upper limit on the concentration, preferably no more than 3 moles of cations and particularly preferably no more than 2 mol metal ion/L-H2 0 is used from the standpoint of economics and because an excessive add-on in the absence of a water rinse can cause a deterioration in the heat-exchange performance. It is possible to use a slurry, for example, milk of lime, as long as some degree of solubility exists.

While no rigorous restriction applies to pH of the solution, one should avoid strongly acidic solutions 15 capable of decomposing the silicic acid salts of o o~ o0 multivalent metals, and the use of aqueous solutions with o0o a pH of 3 to 13 is preferred, while a pH of 4 to 12 is even o o more preferable.

0a10 As long as the effect of treatment according to the 20 application under consideration is not hindered, the 00 0 C a aqueous multivalent metal salt solution may contain various additives. For example, in addition to surfactants, defoamers, antimicrobials, fragrances, colorants, and the 0 like, when treating a surface bearing a chromic 25 acid/chromate conversion treatment, one may find it So Cr6+ o O effective to add a Cr reductant, for example, hydrazine salts, to reduce chromium elution. Furthermore, when the 000000 o aqueous multivalent metal salt solution is to be roll o0 00 coated on flat aluminum sheet, the addition of a thickener, 30 leveling agent, surfactant, or the like may be useful.

000000 When a slurry or aqueous solution of calcium hydroxide is 'o 6 used, a hydroxyl group-containing organic compound can also usefully be added in order to increase the solubility.

The time and temperature of treatment may be varied within wide limits. Short times at high temperatures may be used, but generally treatment at ambient temperature is preferred because of its lower cost.

11 _1 water and at least 0.01 mole per liter of a soluble salt or hydroxide of a cation with a charge of at Ip II I U jil

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O 15 0 I2 0003 o 20 0 00C a a 0 3 0o 0 0 0 o 35 The present invention is explained further in the following illustrative but not limiting examples, in which the following measurement methods were used: Contact angle (hydrophilicity). The contact angle for small (1 to 2 mm diameter) water droplets placed on the solid surface was measured using a FACE contact angle instrument (model CA-P from Kyowa Kaimen Kagaku). The contact angle was measured shortly after treatment of the samples according to this invention (designated in the Table below as "initial") and after five cycles of immersion for eight hours in running water at room temperature followed by drying for 16 hours at 80° C (designated in the following Table as "after water wash").

Corrosion resistance. This was based on the salt-spray test method of JIS Z-2371. The reported value is the spray test period until the white rust surface area reached Antimicrobial activity. The treated aluminum to be tested was cut into a 30 mm x 30 mm square and after immersion in running water for 1 week, was heat sterilized. This was fixed in the center of agar culture medium in a 90 mm petri dish. One mL of a microbial suspension, previously obtained by culturing the isolate from the adhered material on the surface of a heat exchanger, was uniformly spread on the test specimen and the culture medium surface. Scoring was performed, after incubation for 3 weeks at 28° C, according to the following table: score growth 0 no growth 1 very little growth 2 small amount of growth 3 moderate growth 4 heavy growth Initial Odor. This odor, which is believed due to volatilization of chemicals used in treatment, was 12 IC1 -I II 2 o 9 o tr o a r o *r o 4 f 004 o a 0 evaluated on a 5 point-scale by ten individuals who smelled humid air directed onto the treated sheet. A maximum score of 5 was allowed for the minimal amount of odor produced by a completely untreated aluminum sheet, while a minimum score of 1 was assigned to the unpleasant odor produced with a sheet subjected to a chromate treatment, then waterglass treatment (without any boron containing chemical mixed with the waterglass), then nitric acid treatment.

Bonding. Cellophane adhesive tape was adhered on the hydrophilic film and then quickly stripped off, and the external appearance was then evaluated.

Lubricating oil coatability (processability).

The status of the oil coating was visually evaluated 15 after immersion in Panting Oil AF-8F (from Idemitsu Sekiyu Kabushiki Kaisha) and standing for 1 minute.

Example 1 An aqueous mixed solution nonvolatiles) of 100 parts (based on solids) potassium waterglass (Sio 2

/K

2 0 20 molar ratio 3) and 35 parts potassium borate was coated, in a quantity affording a dry film thickness of 0.4 micrometers, on the surface of A-1100 aluminum sheet (0.1 mm thick). This was dried for 3 minutes in a 200 degrees Centigrade oven.

25 This sheet was then dipped for 30 seconds in a 3 aqueous solution of calcium nitrate, rinsed, and finally dried for 2 minutes in a 200 degrees Centigrade oven.

Example 2 This was the same as Example 1, except that before 30 beginning the treatments described in Example 1, the aluminum surface was treated with chromic acid/chromate and then coated with a water-soluble polyurethane (Elastron A-42 from Daiichi Kogyo Seiyaku Company, Limited). Drying for 3 minutes at 200 degrees Centigrade gave a film thickness of approximately 0.3 microns. This then received the same hydrophilicizing treatment solution as in Example 1, followed again by the same calcium nitrate solution dip 0 00 0 00 o0 0 0 00

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0 a 040004 0 0 040004 0 0o o0 0 00 o oG r 0 .4 as above.

Examples 3 through 6 These were treated in the same general way as Examples 1 and 2, but with the variations in materials used as shown in Table 1.

Example 7 A chromic acid/chromate-treated aluminum heat exchanger was dipped into an aqueous mixed solution having total non volatiles, the non volatiles consisting of 100 parts waterglass no. 3, 40 parts sodium metaborate, and parts sodium polyacrylate. A good solution uptake was found upon withdrawal. The treated heat exchanger was then dried for 5 minutes at 200 degrees Centigrade, immersed for 1 minute in a 3% solution of calcium nitrate, withdrawn, 15 and finally dried for 2 minutes in a 200 degrees Centigrade oven.

O 09 0 oo 0 00 0 o 0 00 0 00 00o o *o o 0 0 0 0 0 00 20 Comoarison Examoles 1 and 2 o o 0 00 o oo 25 o 00 0 o o o Treatment followed the procedure of Example 1 or 2, respectively, but with the omission of the potassium borate.

Comparison Example 3 Treatment followed the procedure of Example 1, but with the omission of treatment with the aqueous calcium nitrate solution.

Comparison Example 4 Treatment followed the procedure of Example 3, but using phosphoric acid in place of the magnesium nitrate.

Comparison Example Treatment followed the procedure of Example 4, with the exceptions that the addition of potassium borate was omitted and a nitric acid rinse was executed in place of the aqueous barium nitrate rinse.

Comparison Example 6 0 0 30 00 0 0 00 0 a0 Treatment followed the procedure of Example 4, with the exceptions that the aqueous barium nitrate rinse was omitted and an aqueous slurry of barium metaborate was used in place of the potassium borate of Example 1.

14 I i i 'U r I ri i i Comparison Example 7 Treatminent followed the procedure of Example 7 with the exceptions that the addition of sodium metaborate was omitted and a phosphoric acid rinse was executed in place of the aqueous calcium nitrate rinse.

The heat exchangers used in Example 7 and the present comparison example were respectively installed in air conditioners, each then received 2 mL of the microbial suspension described above for the antimicrobial test, and each was then sprayed with approximately 10 mL of warm culture solution (100 mL water, 4 g glucose, 1 g peptone, and 0.5 g agar). After standing for 24 hours, each was then run through 10 cycles where 1 cycle comprised 1 hour of air cooling, 6 hours standing at room temperature, 1 0Oo 0 o 15 hour of air cooling, and 16 hours standing at room o° temperature. The odor at the start of air-conditioner o °operation was then evaluated by 10 people, on a scale o running from 1 point for a highly objectionable odor to a maximum of 5 points for minimal odor, similar to that used for scoring initial odor as described above. The average odor score for Comparison Example 7 was 2.3 points, against an average of 3.8 for Example 7 according to the invention.

0 00 o oO o o0 25 oaos o a 000000 0 30 30 00 0 0 a 0 goa Some results for Examples 1 through 7 and Comparison Examples 1 through 7 are collectively reported in the second part of Table 1. As a comparison of Examples 1 through 7 with Comparison Examples 1 through 7 makes clear, the invention of the present application not only affords an excellent hydrophilicity, corrosion resistance, initial odor resistance, bonding, and lubricating oil coatability, but also has longer lasting hydrophilicity and an excellent antimicrobial performance.

What is claimed is: II IIL _ll i ii i Table 1.

No. aluminum substrate for borate post-treatment hydrophilicizing additive rinse treatment Example 1 no pretreatment sheet potassium borate calcium nitrate Example 2 chromic acid/chromate sheet potassium borate calcium nitrate primer Example 3 phosphoric acid/chromate sheet potassium borate magnesium nitrate Example 4 chromic acid/chromate sheet potassium borate barium nitrate Example 5 chromic acid/chromate sheet potassium borate calcium hydroxide Example 6 chromic acid/chromate sheet potassium borate zinc acetate Example 7 chromic acid/chromate heat sodium metaborate calcium nitrate exchanger 0 00 O O o 00 o 0o 0 o 0 00 0 0 0 0000 0000 0 0000 00 Q 0 o 0 0 00 Comparison Examples 1 2 no pretreatment chromic acid/chromate primer sheet sheet calcium nitrate calcium nitrate 0 00 0 0 a 0 00 00 0 0 400 0 0.0000 0 0 0 o0 o 0o 0 o 00 no pretreatment sheet phosphoric acid/chromate sheet chromic acid/chromate sheet chromic acid/chromate sheet chromic acid/chromate heat exchanger potassium borate potassium borate barium metaborate phosphoric acid nitric acid phosphoric acid (continued on the next page) i p Table 1. (continued from previous page) No. hydrophilicity corrosion initial antimicrobial bond- lubricating (contact angle) resistance odor performance ability oil coatability initial after water (hours) I wash Examplel1 50 10' -15' 192 4-5 1 Example 2 50 50 10' 480 5 1 Example 3 50 50 -10' 384 3-4 1 Examnple 4 50 100o-150 480 4-5 1 Example 5 50 50 -100 480 5 1 Example 6 50 100 -150 480 4 0-1 0Example 7 50 50 100 480 4 0 aC 0 0 0 0 0 00 0 0: 09 0 00 C~ 00 0 00 0 C 000 0 0 0 00 000 000106 0 0 Examples 1 2 3 4 5 6 7 100 150 <C 5' -15' 150 -200 100 -150 150 -200 150 -200 100 -150 168 480 120 360 *>480 480 480 3-4 4 3 2 1 3 2-3 3-4 3-4 2-3 4 3-4 2

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0 0 (note) o,,!0 *The evaluation method consisted of evaluation by odor and thus differed from the other examples and comparison examples.

Claims (1)

1. 2. 1 11. A process according to claim 6, wherein the salt 2 of step has sodium or potassium cations and a silica to 3 cation molar ratio of ab;"e 1 to -44t 2. 1 12. A process according to claim 5, wherein the salt 2 of step has sodium or potassium cations and a silica to o .oo 3 cation molar ratio of .a4ut 1 to-about 2. o°0 1 13. A process according to claim 4, wherein the salt o 2 of step has sodium or potassium cations and a silica to 3 cation mclar ratio of abAaet 1 to aea-t 2. 1 14. A process according to claim 3, wherein the salt Q 0 a 2 of step has sodium or potassium cations and a silica to 3 cation molar ratio of -abCut 1 to about 2. 1 15. A process according to claim 2, wherein the salt 0 00 2 of step has sodium or potassium cations and a silica to 0 0 0 a 3 cation molar ratio of about 1 to abou 2. o 1 16. A process according to claim 1, wherein the salt 0 2 of step has sodium or potassium cations and a silica to O".V00 0 3 cation molar ratio of abet 1 to about 2. 1 17. A process according to claim 16, comprising the S2 following additional treatments of the aluminum substrate 0 3 before step o 4 treatment with a conventional chromic acid and chromate ion containing treatment solution; and 6 coating the surface produced by the 7 treatment of part with a film about 0.3 microns 8 thick of a polyurethane elastomer. 19 1 18. A process according to claim 12, comprising the 2 following additional treatments of the aluminum substrate 3 before step 4 treatment with a conventional chromic acid and chromate ion containing treatment solution; and 6 coating the surface produced by the 7 treatment of part with a film about 0.3 microns 8 thick of a polyurethane elastomer. 1 19. A process according to claim 11, comprising the 2 following additional treatments of the aluminum substrate 3 before step 4 treatment with a conventional chromic acid and chromate ion containing treatment solution; and 6 coating the surface produced by the 7 treatment of part with a film about 0.3 microns S' 8 thick of a polyurethane elastomer. Sr 1 20. A process according to claim 9, comprising the 2 following additional treatments of the aluminum substrate 3 before step S 4 treatment with a conventional chromic acid and chromate ion containing treatment solution; and 6 coating the surface produced by the a 7 treatment of part with a film about 0.3 microns S 8 thick of a polyurethane elastomer. DATED this 4th day of November 1988. NIHON PARKERIZING CO., LTD. EDWD. WATERS SONS 04 oPATENT ATTORNEYS 50 QUEEN STREET MELBOURNE. VIC. 3000. a IO P tif i i"l tS-S Ih ptPg a da",g ou~V pages Ulm I A true and exact copy of the spacifofiwion oyigs ianu odgdo