CN1739867A - Repairing method and repairing agent for surface of inorganic plate - Google Patents

Repairing method and repairing agent for surface of inorganic plate Download PDF

Info

Publication number
CN1739867A
CN1739867A CN 200410056942 CN200410056942A CN1739867A CN 1739867 A CN1739867 A CN 1739867A CN 200410056942 CN200410056942 CN 200410056942 CN 200410056942 A CN200410056942 A CN 200410056942A CN 1739867 A CN1739867 A CN 1739867A
Authority
CN
China
Prior art keywords
inorganic
plating bath
control group
inorganic plate
experimental group
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN 200410056942
Other languages
Chinese (zh)
Other versions
CN100377796C (en
Inventor
龙清勇
叶杰
王德宗
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Yunxin Enterprise Co., Ltd.
Original Assignee
GUANJI SCI-TECH 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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=36092479&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CN1739867(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by GUANJI SCI-TECH Co Ltd filed Critical GUANJI SCI-TECH Co Ltd
Priority to CNB2004100569428A priority Critical patent/CN100377796C/en
Publication of CN1739867A publication Critical patent/CN1739867A/en
Application granted granted Critical
Publication of CN100377796C publication Critical patent/CN100377796C/en
Ceased legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Landscapes

  • Detergent Compositions (AREA)

Abstract

The present invention is repairing method and repairing agent for surface of inorganic plate. After inorganic plating liquid is applied to the surface of glass, ceramic tile, quartz tile, marble, granite, etc. with great amount of pores, the surface is polished and ground physically so as to disperse and fill the plating liquid homogeneously. The process can make the surface level, bright, hydrophilic, antifouling, weather resistant and chemical erosion resistant. Meanwhile, antiseptic material may be added to raise the antiseptic function. Especially, the raised surface hydrophilicity can reduce surface tension to form water drops to erode the base material.

Description

Inorganic plate surface repairing method and renovation agent thereof
Technical field
The present invention is about a kind of inorganic plate surface repairing method and renovation agent thereof, especially refer to that a kind of surface reparation plating bath can effectively be used in glass, ceramic tile, polishing quartz brick, marble, granite and artificial stone etc., a large amount of pores with its surface distributed, in physics rubbing down mode, plating bath is evenly disperseed and fill up, and then reach, characteristic such as suface-brightening, hydrophilic, anti-soil, weather-proof and anti-chemistry than high-flatness, the scope of using on the raising industry also can be added antibiotic material and be strengthened its antibacterial effect.
Background technology
Usually, substrate surface Chang Youkong such as general glass, ceramic tile, polishing quartz brick, marble, granite and artificial stone carefully shelter evil people and countenance evil practices easily, and in the pore can because of than wisp as material intrusion that dust, greasy dirt, floating material or penetration are stronger, make accumulation nutrient in its pore, the hole, hole, breed bacteria and mould, except that surface filth is influenced the outward appearance, also can quicken its oxidation and aging.
Present commercially available protective agent is emphasized its hydrophobicity and pollution resistance based on the constituent of fluororesin and organosilicon alkanes; Wherein:
Fluorine type resin is as: polytetrafluoroethylene (PTFE) or poly-inferior ethene, acrylic acid-fluororesin, epoxy-fluororesin, amido Ethyl formate-fluororesin, fluorinated olefins and the carbon-to-carbon unsaturated compound fluoridized;
Silane ketone is as alkoxy silane, the organic group alkoxy silane, polysiloxanes, colloidal silica, acrylic acid-silicones, epoxy-silicones, amido Ethyl formate-silicones, alkoxy silane hydrolysis product etc., independent or multiple mixture, its solvent generally has: toluene or dimethylbenzene etc. are aromatic hydrocarbon based, ethanol, alcohols such as n-butanol, ethylene glycol, many glycols such as the third two propyl alcohol, the ethylene glycol derivative class, hexane, heptane, aliphatic hydrocarbons such as cyclohexane, ester class, ketone, ethers, the vinegar amine, amine, chloroform, methyl-sulfoxide, organic solvents such as nitrobenzene;
Because of causing greasy dirt easily, its hydrophobicity adheres to; with the organic solvent is solvent; in process, pollute easily; and when temperature is higher than 50 ℃ when using; organic solvent can disengage very hard iron of the unhealthful and environment of poisonous carcinogenic substance; because of it is the organic resin class, weatherability and durability all remain to be discussed again, and real difficulty reaches the function of protection substrate surface.
Substrate surface if impose generally revolve cross, soak cross, mode such as coating, pore can stop plating bath to enter in the pore because of capillarity (as Fig. 1), after the dry tack free film forming, hole still can exist, and can't improve substrate surface and protection.
Summary of the invention
The present invention is except that abandoning habitual in the past organic protection agent; change with inorganic plating bath and use; and obtain even overlay film in physics rubbing down mode; can take to plating bath in the aperture smoothly in physics rubbing down mode; with its planing Hou Calipering can be protected, characteristics such as blast, hydrophilic, anti-soil, weather-proof and anti-chemistry, the scope of using on the raising industry.
The present invention also can add antimicrobial components such as one of silver (Ag), gold (Au), platinum (Pt) ion or its combination, to strengthen its antibacterial effect.
Simultaneously, the present invention also provides a kind of inorganic plate surface restoration agent that repair on above-mentioned inorganic plate surface that is used for, and described renovation agent is the inorganic plating bath of gained after the hydrolysis of organic metal alcohols.For example, silicates one or the mixed liquors more than two kinds such as silica, potassium silicate, lithium metasilicate, sodium metasilicate, alumina silicate, magnesium silicate.
Understand in order to allow the auditor that the present invention is had further, it is as follows now to be described with reference to the accompanying drawings the present invention.
Description of drawings
Fig. 1: the schematic diagram of substrate surface pore phenomenon.
Fig. 2: calcspar of the present invention.
Fig. 3: the calcspar of the embodiment of the invention.
The specific embodiment
See also shown in Figure 2, base material 1 of the present invention is glass, ceramic tile, polishing quartz brick, marble, granite and artificial stone etc., this base material 1 surface is crossed inorganic plating bath 2, is coated with, is soaked and mode plated film 10 such as cross to revolve, capable again rubbing down (polishing is ground) 20, inorganic plating bath 2 is evenly disperseed and fill up, near and reach lining base material 30 than high-flatness, it is surperficial thereby have characteristics such as blast, hydrophilic, anti-soil, weather-proof and anti-chemistry.
Consult shown in Figure 3ly, antibiotic material 3 also can be added to strengthen its antibacterial effect in base material 1 surface, and this antibiotic material 3 can be elected silver ion.
The formation of above-mentioned inorganic plating bath 2 can use the inorganic metal salt as inorganic plating bath, and for example the organic metal ester-type hydrolysis becomes the organic metal alcohols, and Calipering gets the inorganic metal salt plating bath after heating again, for example silester (Si (OC 2H 5) 4), tetraethyl titanate (Ti (OC 2H 5) 4) or the like.
In addition, the formation of inorganic silicic acid plating bath can be adopted allotments such as commercially available sodium metasilicate (waterglass), potassium silicate, lithium metasilicate, also can utilize organo-silicon ester hydrolysis, heating to generate inorganic silicate, its generation method: to use silester Si (OC 2H 5) 4(TEOS), hydrolysis forms silanol Si (OH) 4Generate amorphous silicas (SiO2) or before hydrolysis, add alkali metal in 80 ℃ of heating as potassium hydroxide, sodium, lithium, magnesium etc., and form metal metasilicate salt such as potassium silicate, sodium, lithium, magnesium, aluminium etc., and other inorganic metal salt also can use this method to form, as with tetraethyl titanate Ti (OC 2H 5) 4Deng.
Moreover, consult table 1 laboratory report of the present invention, be described as follows:
Table 1
Stone material Brightness Blast (%) Antifouling Water imbibition The grinding stone floor tile Brightness Blast (%) Antifouling Water imbibition The polishing quartz brick Brightness Blast (%) Antifouling Water imbibition
Experimental group 88 ◎ ● Experimental group 89 ◎ ● Experimental group 90 ◎ ●
Control group 60 46.7 △ × Control group 33 169.7 × × Control group 65 38.5 × ●
A Experimental group 76 ◎ ×-● Experimental group 78 ◎ ×-● Experimental group 80 ◎ ●
Control group 62 22.6 △ × Control group 43 81.4 × × Control group 63 27 × ●
B Experimental group 79 ◎ ×-● Experimental group 77 ◎ ×-● Experimental group 78 ◎ ●
Control group 46 71.7 △ × Control group 45 71.1 × × Control group 60 30 × ●
C Experimental group 82 ◎ ×-● Experimental group 78 ◎ ×-● Experimental group 78 ◎ ●
Control group 68 20.5 △ × Control group 43 81.4 × × Control group 62 25.8 × ●
A+B Experimental group 91 ◎ ● Experimental group 89 ◎ ● Experimental group 88 ◎ ●
Control group 68 33.8 △ × Control group 50 78 × × Control group 72 22.2 × ●
A+C Experimental group 89 ◎ ● Experimental group 90 ◎ ● Experimental group 89 ◎ ●
Control group 70 27.1 △ × Control group 50 80 × × Control group 76 17.1 × ●
B+C Experimental group 92 ◎ ● Experimental group 88 ◎ ● Experimental group 89 ◎ ●
Control group 69 33.3 △ × Control group 53 66 × × Control group 66 34.8 × ●
A+B +C Experimental group 92 ◎ ● Experimental group 86 ◎ ● Experimental group 92 ◎ ●
Control group 49 87.7 △ × Control group 56 53.6 × × Control group 56 64.3 × ●
D Experimental group 76 ◎ ×-● Experimental group 74 ◎ ×-● Experimental group 72 ◎ ●
Control group 53 43.4 △ × Control group 35 111 × × Control group 56 28.6 × ●
E Experimental group 76 ◎ ×-● Experimental group 80 ◎ ×-● Experimental group 79 ◎ ●
Control group 53 43.4 △ × Control group 65 23 × × Control group 60 31.7 × ●
F Experimental group 79 ◎ ×-● Experimental group 80 ◎ ×-● Experimental group 81 ◎ ●
Control group 51 55 △ × Control group 55 45.5 × × Control group 60 35 × ●
D+E Experimental group 89 ◎ ● Experimental group 88 ◎ ● Experimental group 92 ◎ ●
Control group 61 45.9 △ × Control group 53 66 × × Control group 63 46 × ●
D+F Experimental group 87 ◎ ● Experimental group 88 ◎ ● Experimental group 90 ◎ ●
Control group 61 42.6 △ × Control group 43 104.7 × × Control group 65 38.5 × ●
E+F Experimental group 88 ◎ ● Experimental group 88 ◎ ● Experimental group 90 ◎ ●
Control group 68 29.4 △ × Control group 54 63 × × Control group 68 32.4 × ●
D+E +F Experimental group 89 ◎ ● Experimental group 86 ◎ ● Experimental group 90 ◎ ●
Control group 60 48.3 △ × Control group 44 95.5 × × Control group 68 32.4 × ●
Brightness measuring: around base material to be measured, reach middle 5 records of averaging with the HORIBA photometer; Blast %:(experimental group-control group) ÷ control group * %
Antifouling ability: almost indifference *, still mark △, complete wiping ◎
Water absorbing force: obviously suction *, not obvious suction ●
Embodiment 1:
1, in the ethanol 700ml of stirring solvent, adds
2, silester 100ml+36% hydrochloric acid 15ml stirred after 30 minutes, added
3, pure water 85ml+5ml lithium hydroxide+5ml NaOH+5ml potassium hydroxide stirred after 30 minutes, added again
4, after pure water 100ml stirs 30 minutes again, be warming up to 80 ℃ and be cooled to normal temperature after totally 60 minutes.
The above-mentioned plating bath that makes is a plating bath 1, respectively at: 623# white granite (Fujian China product); Grinding stone floor tile (big water chestnut industrial corporation produce); Apply in polishing quartz brick (champion company products), function such as branch blast, waterproof, antifouling, hydrophily also is recorded in table 1.
Obviously find that in table 1 glossiness obviously increases by 15%～150%, antifouling ability is from wiping antifouling fully and hydrophily also has clear improvement.
Embodiment 2:
1, in the ethanol 200ml solvent that stirs, adds
2, silester 30ml+36% hydrochloric acid 5ml stirred after 30 minutes, added
3, pure water 30ml+5ml lithium hydroxide and stir 30 minutes after, add again
4, after pure water 30ml stirs 30 minutes again, be warming up to 80 ℃ and be cooled to normal temperature after totally 60 minutes; As mixing the A agent.
1, in the ethanol 200ml solvent that stirs, adds
2, silester 30ml+36% hydrochloric acid 5ml stirred after 30 minutes, added
3, pure water 30ml+5ml NaOH and stir 30 minutes after, add again
4, after pure water 30ml stirs 30 minutes again, be warming up to 80 ℃ and be cooled to normal temperature after totally 60 minutes; As mixing the B agent.
1, in the ethanol 200ml solvent that stirs, adds
2, silester 30ml+36% hydrochloric acid 5ml stirred after 30 minutes, added
3, pure water 30ml+5ml potassium hydroxide and stir 30 minutes after, add again
4, after pure water 30ml stirs 30 minutes again, be warming up to 80 ℃ and be cooled to normal temperature after totally 60 minutes; As the mixed C agent.
Above-mentioned A agent used separately be plating bath A
The B agent is used separately and is plating bath B
The C agent is used separately and is plating bath C
The A+B agent mixes to be used at 1: 1, as plating bath AB
The A+C agent mixes to be used at 1: 1, as plating bath AC
The B+C agent mixes to be used at 1: 1, as plating bath BC
The A+B+C agent mixes to be used at 1: 1: 1, as plating bath ABC
Method as 1 cloud of embodiment applies and is embedded in table 1
Embodiment 3:
In commercially available silicates product, get potassium silicate, sodium metasilicate and lithium metasilicate (the dish company of opening up obtains) respectively with
Potassium silicate is the D agent
Sodium metasilicate is the E agent
Lithium metasilicate is the F agent
Above-mentioned D agent used separately be plating bath D
The E agent is used separately and is plating bath E
The F agent is used separately and is plating bath F
The D+E agent mixes to be used at 1: 1, as plating bath DE
The D+F agent mixes to be used at 1: 1, as plating bath DF
The E+F agent mixes to be used at 1: 1, as plating bath EF
The D+E+F agent mixes to be used at 1: 1: 1, as plating bath DEF
Method as 1 cloud of embodiment applies and is embedded in table 1
Making and purpose of experiment base material:
Prepare one of 623# white granite 20cm * 20cm; One of grinding stone floor tile 20cm * 20cm; One of polishing quartz brick 20cm * 20cm; Wherein, on every kind of testing substrates, at 10cm * 20cm place, paste its area with adhesive tape (earth board) and organize in contrast, coat in the remaining experimental group with the above-mentioned inorganic plating bath 2ml that makes, with the 500/min waxing machine, pressure 15～20kg, rubbing down 1 minute totally three times
1, record examination control group and experimental group brightness with the HORIBA photometer, by formula: (experimental group-control group) ÷ control group * 100%, in the hope of brightening effect (%);
2, with black oiliness Mike pen (Sambalion board) in its experimental group and draw the A word in the group respectively to making, treat that through 3 minutes its dry back is to bedew the toilet paper wiping of (water), in the hope of antifouling ability, divide almost indifference *, still mark △, three kinds of wiping ◎ etc. fully;
3, with one of facial tissue (Shu Jie board), doubling doubling again becomes 10cm * 10cm approximately, the 3ml pure water is watered, and is placed in the middle of experiment and the control group, estimating its suction situation, divide obviously suction *, not obvious suction ● wait two kinds.
In table one, obviously find the single use of its silicate or mix use, all can effectively improve lining antifouling hydrophily of substrate surface and bright flatness.
In sum, the present invention repairs on the surface plating bath can effectively be used in glass, ceramic tile, polishing quartz brick, marble, granite and artificial stone etc., a large amount of pores with its surface distributed, in physics rubbing down mode, plating bath is evenly disperseed and fill up, and then reach than high-flatness, characteristics such as suface-brightening, hydrophilic, anti-soil, weather-proof and anti-chemistry, the scope of using on the raising industry, also can add antibiotic material and strengthen its antibacterial effect, because of utilizing on the industry, meet the legal key element of Patent Law invention, patent application is proposed then in accordance with the law.

Claims (5)

1. an inorganic plate surface repairing method is characterized in that, earlier inorganic plating bath is crossed to revolve, is coated with, soaks and the mode plated film such as cross in substrate surface, goes rubbing down again, inorganic plating bath is evenly disperseed and fills up, and forms the higher lining base material of flatness.
2. inorganic plate surface repairing method as claimed in claim 1 is characterized in that: the base material plated film can add antimicrobial component simultaneously, to increase antibacterial effect.
3. inorganic plate surface repairing method as claimed in claim 2 is characterized in that: antimicrobial component contains one of silver (Ag), gold (Au), platinum (Pt) ion or its combination.
4. one kind is used for the inorganic plate surface restoration agent that repair on the described inorganic plate of claim 1 surface, and it is characterized in that: described renovation agent is the inorganic plating bath of gained after the hydrolysis of organic metal alcohols.
5. inorganic plate surface restoration agent as claimed in claim 4 is characterized in that: inorganic plating bath is silicates one or the mixed liquors more than two kinds such as silica, potassium silicate, lithium metasilicate, sodium metasilicate, alumina silicate, magnesium silicate.
CNB2004100569428A 2004-08-23 2004-08-23 Repairing method and repairing agent for surface of inorganic plate Ceased CN100377796C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB2004100569428A CN100377796C (en) 2004-08-23 2004-08-23 Repairing method and repairing agent for surface of inorganic plate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB2004100569428A CN100377796C (en) 2004-08-23 2004-08-23 Repairing method and repairing agent for surface of inorganic plate

Publications (2)

Publication Number Publication Date
CN1739867A true CN1739867A (en) 2006-03-01
CN100377796C CN100377796C (en) 2008-04-02

Family

ID=36092479

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB2004100569428A Ceased CN100377796C (en) 2004-08-23 2004-08-23 Repairing method and repairing agent for surface of inorganic plate

Country Status (1)

Country Link
CN (1) CN100377796C (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101069982B (en) * 2006-05-12 2011-07-06 环球石材（东莞）有限公司 Pure-white marble glue-mending method
CN102336587A (en) * 2010-07-23 2012-02-01 福建溪石股份有限公司 Method of filling on residual holes after slate material processing
CN102351437A (en) * 2011-08-01 2012-02-15 程道远 Novel glass after-mildew restoration agent
CN105945707A (en) * 2016-06-30 2016-09-21 禹州市远大塑料电器有限责任公司 Quartzite polishing and coating production device

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5681575A (en) * 1992-05-19 1997-10-28 Westaim Technologies Inc. Anti-microbial coating for medical devices

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101069982B (en) * 2006-05-12 2011-07-06 环球石材（东莞）有限公司 Pure-white marble glue-mending method
CN102336587A (en) * 2010-07-23 2012-02-01 福建溪石股份有限公司 Method of filling on residual holes after slate material processing
CN102336587B (en) * 2010-07-23 2013-01-30 福建溪石股份有限公司 Method of filling on residual holes after slate material processing
CN102351437A (en) * 2011-08-01 2012-02-15 程道远 Novel glass after-mildew restoration agent
CN105945707A (en) * 2016-06-30 2016-09-21 禹州市远大塑料电器有限责任公司 Quartzite polishing and coating production device

Also Published As

Publication number Publication date
CN100377796C (en) 2008-04-02

Similar Documents

Publication Publication Date Title
JP5471441B2 (en) Hand-paintable sol-gel coating solution
CN1269924C (en) Composition for forming transparent polysiloxane coating and solidification thereof
Facio et al. Simple strategy for producing superhydrophobic nanocomposite coatings in situ on a building substrate
CN1171961C (en) Method of forming hydrophilic inorganic coating film and inorganic coating composition
CN1486354A (en) Non-aqueous coating compositions formed from silanes and metal alcoholates
WO2003102091A1 (en) Photocatalytic coating material, photocatalytic composite material and process for producing the same, self-cleaning water-based coating compositions, and self-cleaning member
CN1926194A (en) Rtv silicone composition offering rapid bond strength
CN1860196A (en) Water repellent coating film having low refractive index
CN101525504A (en) Photocatalytic self-cleaning film coating agent with self-layered isolation effect and preparation method thereof
JP2008247699A (en) Water-repellent, oil-repellent contamination preventive antireflection film and method for manufacturing the same, lens, glass sheet and glass formed with the film, and optical equipment, device using solar energy and display using them
JP2008015167A (en) Water-shedding, oil-shedding and antifouling light reflecting plate, method for manufacturing the same, and tunnel, road sign, display plate, vehicle and building using the same
CN101555385B (en) Water-reducible silicone coating and preparation method thereof
CN104231918B (en) The quick-dry type oiliness infiltration nano combined protective agent of film-forming type and preparation method and application
CN1784434A (en) VOC free latex coalescent systems
KR101892898B1 (en) Penetrating Ceramic Coating Agents Having Excellent Chemical Resistance and Method for Waterproof and Coating Thereof
CN105111870A (en) Organic and inorganic compound finish for outer walls
CN1739867A (en) Repairing method and repairing agent for surface of inorganic plate
JP5743281B2 (en) Building board
JP2006008902A (en) Photocatalytic coating composition
JP2014234398A (en) Gel-like composition and water absorption inhibitor
CN1884208A (en) Method for forming antisoil coating on substrate surface and products therefrom
JP5501076B2 (en) Aqueous solution type water repellent with oil stain removal function
CN113185897A (en) Super-hydrophobic self-cleaning crack sealer and preparation method thereof
JP2004000853A (en) Photocatalyst composition and photocatalyst film
KR20200050629A (en) Coating Composition and method thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C56 Change in the name or address of the patentee
CP03 Change of name, title or address

Address after: 2 floor, 687 Minsheng Road, Taoyuan County, Taiwan, China

Patentee after: Yunxin Enterprise Co., Ltd.

Address before: Taiwan, China

Patentee before: Guanji Sci-Tech Co., Ltd.

C56 Change in the name or address of the patentee

Owner name: YUNXINFANG ENTERPRISE CO., LTD.

Free format text: FORMER NAME: GUANJI TECHNOLOGY CO., LTD.

C35 Partial or whole invalidation of patent or utility model
IW01 Full invalidation of patent right

Decision date of declaring invalidation: 20100507

Decision number of declaring invalidation: 14787

Granted publication date: 20080402