CN1297641C - Detergent composition and detergent for liquid crystal cell - Google Patents
Detergent composition and detergent for liquid crystal cell Download PDFInfo
- Publication number
- CN1297641C CN1297641C CNB2004100956350A CN200410095635A CN1297641C CN 1297641 C CN1297641 C CN 1297641C CN B2004100956350 A CNB2004100956350 A CN B2004100956350A CN 200410095635 A CN200410095635 A CN 200410095635A CN 1297641 C CN1297641 C CN 1297641C
- Authority
- CN
- China
- Prior art keywords
- liquid crystal
- crystal cell
- alkyl
- weight
- poly suboxygen
- 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.)
- Expired - Fee Related
Links
- 239000004973 liquid crystal related substance Substances 0.000 title claims abstract description 70
- 210000002858 crystal cell Anatomy 0.000 title claims abstract description 37
- 239000000203 mixture Substances 0.000 title claims description 94
- 239000003599 detergent Substances 0.000 title abstract description 26
- -1 polyoxyethylene monostyrylphenyl ether Polymers 0.000 claims abstract description 25
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 21
- 238000005406 washing Methods 0.000 claims description 68
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 29
- 229910052799 carbon Inorganic materials 0.000 claims description 29
- BYLSIPUARIZAHZ-UHFFFAOYSA-N 2,4,6-tris(1-phenylethyl)phenol Chemical compound C=1C(C(C)C=2C=CC=CC=2)=C(O)C(C(C)C=2C=CC=CC=2)=CC=1C(C)C1=CC=CC=C1 BYLSIPUARIZAHZ-UHFFFAOYSA-N 0.000 claims description 20
- 125000000217 alkyl group Chemical group 0.000 claims description 20
- 239000004593 Epoxy Substances 0.000 claims description 16
- 150000001335 aliphatic alkanes Chemical class 0.000 claims description 16
- 229920000642 polymer Polymers 0.000 claims description 6
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 2
- 239000006185 dispersion Substances 0.000 abstract description 9
- 238000004140 cleaning Methods 0.000 abstract description 6
- 238000002156 mixing Methods 0.000 abstract description 3
- WIGIPJGWVLNDAF-UHFFFAOYSA-N 8-methyl-1-(8-methylnonoxy)nonane Chemical compound CC(C)CCCCCCCOCCCCCCCC(C)C WIGIPJGWVLNDAF-UHFFFAOYSA-N 0.000 abstract 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 abstract 1
- 239000011369 resultant mixture Substances 0.000 abstract 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 16
- 125000005504 styryl group Chemical group 0.000 description 16
- 230000000052 comparative effect Effects 0.000 description 11
- 239000000758 substrate Substances 0.000 description 10
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 9
- 150000002500 ions Chemical class 0.000 description 9
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 5
- 238000011156 evaluation Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 230000005012 migration Effects 0.000 description 5
- 238000013508 migration Methods 0.000 description 5
- PFTAWBLQPZVEMU-DZGCQCFKSA-N (+)-catechin Chemical compound C1([C@H]2OC3=CC(O)=CC(O)=C3C[C@@H]2O)=CC=C(O)C(O)=C1 PFTAWBLQPZVEMU-DZGCQCFKSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 229950001002 cianidanol Drugs 0.000 description 4
- RECVMTHOQWMYFX-UHFFFAOYSA-N oxygen(1+) dihydride Chemical group [OH2+] RECVMTHOQWMYFX-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 3
- NSOXQYCFHDMMGV-UHFFFAOYSA-N Tetrakis(2-hydroxypropyl)ethylenediamine Chemical compound CC(O)CN(CC(C)O)CCN(CC(C)O)CC(C)O NSOXQYCFHDMMGV-UHFFFAOYSA-N 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- 125000001118 alkylidene group Chemical group 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000000138 intercalating agent Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000005011 time of flight secondary ion mass spectroscopy Methods 0.000 description 3
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- CDMGNVWZXRKJNS-UHFFFAOYSA-N 2-benzylphenol Chemical compound OC1=CC=CC=C1CC1=CC=CC=C1 CDMGNVWZXRKJNS-UHFFFAOYSA-N 0.000 description 2
- GJYCVCVHRSWLNY-UHFFFAOYSA-N 2-butylphenol Chemical compound CCCCC1=CC=CC=C1O GJYCVCVHRSWLNY-UHFFFAOYSA-N 0.000 description 2
- DUIOKRXOKLLURE-UHFFFAOYSA-N 2-octylphenol Chemical compound CCCCCCCCC1=CC=CC=C1O DUIOKRXOKLLURE-UHFFFAOYSA-N 0.000 description 2
- PLLBRTOLHQQAQQ-UHFFFAOYSA-N 8-methylnonan-1-ol Chemical compound CC(C)CCCCCCCO PLLBRTOLHQQAQQ-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 238000005727 Friedel-Crafts reaction Methods 0.000 description 2
- 239000004440 Isodecyl alcohol Substances 0.000 description 2
- 241001417527 Pempheridae Species 0.000 description 2
- MKYQPGPNVYRMHI-UHFFFAOYSA-N Triphenylethylene Chemical group C=1C=CC=CC=1C=C(C=1C=CC=CC=1)C1=CC=CC=C1 MKYQPGPNVYRMHI-UHFFFAOYSA-N 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 238000007259 addition reaction Methods 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 150000001555 benzenes Chemical class 0.000 description 2
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- MJEMIOXXNCZZFK-UHFFFAOYSA-N ethylone Chemical compound CCNC(C)C(=O)C1=CC=C2OCOC2=C1 MJEMIOXXNCZZFK-UHFFFAOYSA-N 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- 125000005702 oxyalkylene group Chemical group 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 238000010189 synthetic method Methods 0.000 description 2
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- PJANXHGTPQOBST-VAWYXSNFSA-N trans-stilbene Chemical group C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 2
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- XFRVVPUIAFSTFO-UHFFFAOYSA-N 1-Tridecanol Chemical compound CCCCCCCCCCCCCO XFRVVPUIAFSTFO-UHFFFAOYSA-N 0.000 description 1
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 1
- PRTFGFRBLXSBKF-UHFFFAOYSA-N 2-phenoxybut-1-enylbenzene Chemical compound C=1C=CC=CC=1C=C(CC)OC1=CC=CC=C1 PRTFGFRBLXSBKF-UHFFFAOYSA-N 0.000 description 1
- KJWMCPYEODZESQ-UHFFFAOYSA-N 4-Dodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=C(O)C=C1 KJWMCPYEODZESQ-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- 125000005233 alkylalcohol group Chemical group 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000002173 cutting fluid Substances 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000009878 intermolecular interaction Effects 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- 239000012454 non-polar solvent Substances 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 230000010287 polarization Effects 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000009991 scouring Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 229940087291 tridecyl alcohol Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/825—Mixtures of compounds all of which are non-ionic
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers of polyoxyalkylene glycols
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
- Liquid Crystal (AREA)
- Cleaning By Liquid Or Steam (AREA)
Abstract
The invention obtains a detergent for a liquid crystal cell which exhibits excellent performances in cleaning/removing liquid crystals deposited to the liquid crystal cell, costs low and is highly safe. The detergent for the liquid crystal cell comprises an aqueous dispersion prepared by mixing a component (a) comprising a polyoxyethylene monostyrylphenyl ether with a component (b) comprising a polyoxyethylene isodecyl ether in a weight ratio of 1:2 and adding ion-exchanged water to the resultant mixture to adjust its concentration to 0.5 wt% in the water. The detergent for the liquid crystal cell is a nonionic detergent that exhibits excellent performances in cleaning/removing remaining liquid crystals deposited to electrode portions of the liquid crystal cell and is low corrosive.
Description
Technical field
The present invention relates to a kind of washing composition, relate in particular in a kind of manufacturing process that is adapted at liquid crystal cell, the washing composition that liquid crystal cell etc. is washed.
Background technology
Liquid crystal cell usually a pair of glass substrate gummed by being formed with electrode and oriented film, inject liquid crystal, seal after scouring, remove liquid crystal, stick deflector plate and make attached to the slit of glass substrate with sealing agent.By this washing procedure to remove liquid crystal be in order to prevent because the residue of liquid crystal plays a part that remover causes that deflector plate comes off in its subsequent handling, the driving mechanism terminal connects not good, driving mechanism bottom filling interface discomfort, in the substrate slimming technology used can disengaging type coating shedding etc. the generation of all faults.
Known liquid crystal molecule as polarized compounds is strong owing to intermolecular interaction, shows strong-hydrophobicity, so generally be difficult to disperse or dissolve to water system.Therefore, in order to wash, to remove, use the washing composition that has added ionic promoting agent, ionic washing assistant, ionic emulsifier etc. to be considered to the method for main flow attached to the liquid crystal on the liquid crystal cell.As such washing composition, the washing composition (patent documentation 1) that contains intercalating agent and alkaline matter, the washing composition (patent documentation 2) that contains the salt of being made up of ammonium cation and phosphoric acid ester negatively charged ion etc. are for example arranged.Again, also can use the intercalating agent be made up of the catechuic acid concentrated solution and combination, the quadrol of tensio-active agent is combination of intercalating agent and tensio-active agent and sulfonate etc.
[patent documentation 1] Japanese kokai publication hei 03-070800 communique
[patent documentation 2] TOHKEMY 2000-313899 communique
Yet, in the past for washing, remove the washing composition that uses attached to the liquid crystal on the liquid crystal cell and contain ionic substance, again, hygroscopic matter also is one of its ingredient.Therefore, the problem of existence is, if the part of these washing composition remains in the terminal part of liquid crystal cell, just tends to owing to ion moves electronic migration when causing liquid crystal drive with planar water.
Again, people are considering the nonpolar or polar solvent replacement ionic substance with parts such as halogen series solvent, tetrahydrofuran (THF) or acetone., these solvents are in burning-point, security, environmental problem or take the aspects such as necessity of explosion-proof method to have problems, and use very difficult in reality.
The content of invention
The present invention is in order to solve so far to washing, to remove the liquid crystal cell that uses attached to the liquid crystal on the liquid crystal cell and make with existing above-mentioned technical problem in the washing composition.
That is, the object of the present invention is to provide a kind of detergency height, nonionic that corrodibility is low is detergent composition.
Another object of the present invention is to provide a kind of washing, remove the liquid crystal cell washing composition that ability is strong, cost is low and safe attached to the liquid crystal on the liquid crystal cell again.
For achieving the above object, detergent composition of the present invention is characterised in that, contains: (a) the poly suboxygen alkyl alkyl oxide of the poly suboxygen alkyl styryl phenyl ether of 20 weight %~60 weight %, (b) 40 weight %~80 weight % ((a) and total (b) are 100 weight %).
Detergent composition of the present invention with this formation is because to the solvability height of liquid crystal, be again nonionic, so the problem that electronic migration brought when moving the liquid crystal drive that causes with planar water by ion is eliminated.
Preferably (a) poly suboxygen alkyl styryl phenyl ether accounts for 30 weight %~50 weight % to the weight ratio of 2 kinds of compositions that detergent composition of the present invention is contained, (b) poly suboxygen alkyl alkyl oxide accounts for 50 weight %~70 weight %.
Here, if composition (a) poly suboxygen alkyl styryl phenyl ether is characterised in that it is the polyalkylene oxides affixture of styrenated phenol, then can easily obtain with known synthetic method.Particularly, it is desirable to (a) poly suboxygen alkyl styryl phenyl ether is the addition polymer of the epoxy alkane of styrenated phenol and carbon number 2~4.At this moment, it is desirable to (a) polyoxy alkylidene styryl phenyl ether and be the addition polymer of epoxy alkane of the carbon number 2~4 of 1 mole of styrenated phenol and 4 moles~5 moles.Like this, be about 4 moles~5 moles by the resultant that adds that makes epoxy alkane, the molecular polarity of poly suboxygen alkyl styryl phenyl ether is died down, on the other hand, can improve solvability to liquid crystal.
Again, usually styrenated phenol exists with a single vinylbenzene thing, toluylene thing, triphenylethylene thing, if it is characterized in that, the purity of the single styrenated phenol in the styrenated phenol then can reduce the influence of the electronic migration when coming free ion to move the liquid crystal drive that causes with planar water significantly more than 85%.Especially it is desirable to (a) poly suboxygen alkyl styryl phenyl ether is the addition polymer of 1 mole of single styrenated phenol and 5 mol of alkylene oxide hydrocarbon.
Again, composition (b) poly suboxygen alkyl alkyl oxide is if is characterized in that having the straight or branched alkyl of carbon number 4~carbon number 18, then can improve the solvability of detergent composition of the present invention in water by leaps and bounds, thus can be modulated into can aqueous dispersions the aqueous cleaning that uses of form.
Here, (b) the poly suboxygen alkyl alkyl oxide it is desirable to, and the addition mole number of the alkylene oxide of carbon number 2~carbon number 4 is 1~10, especially it is desirable to, and the addition mole number of carbon number 2 or 3 alkylene oxide is 6.Better is that (b) poly suboxygen alkyl alkyl oxide has isodecyl.
But the present invention also can be understood as be have following feature the liquid crystal cell washing composition: the mixture and (c) water that contain the poly suboxygen alkyl alkyl oxide ((a) and total (b) are 100 weight %) of the poly suboxygen alkyl styryl phenyl ether that comprises (a) 20 weight %~60 weight %, (b) 40 weight %~80 weight %, with respect to mixture 1g with above-mentioned ratio of components, the content of water is 100g~1000g, and it washs, removes the excellent property attached to the liquid crystal on the liquid crystal cell.
It is desirable to (c) water here, is ion exchanged water.
Liquid crystal cell washing composition of the present invention does not contain ionic composition, in addition, by using under the form of the low concentration of water dispersion liquid of about 0.1 weight %, has per 1 premium on currency solution and makes the consoluet premium properties of 5g liquid crystal.Also have, the liquid crystal from liquid crystal cell washs, removes can not keep stable dispersion state again attached on the liquid crystal cell in the solution of washing composition, can remove fully by washing.
According to the present invention, it is washing composition that a kind of detergency height, nonionic that corrodibility is low are provided.
Embodiment
Below be described in detail with regard to best example of the present invention (below, be called the working of an invention form).
Employed in the detergent composition of this example (a) poly suboxygen alkyl styryl phenyl ether obtains as the polyalkylene oxides affixture of styrenated phenol.
Here, the synthetic method of styrenated phenol does not limit especially, can adopt known method.For example, can make by the Friedel-Crafts reaction of phenol and styrenic.As phenol, for example be phenol, alkylphenol, aryl phenol, aralkyl phenol etc.As alkylphenol, for example be cresylol, butylphenol, octyl phenol etc.As aryl phenol, for example be phenylphenol, xenyl phenol, naphthyl phenol etc.As aralkyl phenol, for example be benzylphenol, styroyl phenol etc.Wherein it would be desirable phenol, cresylol, phenylphenol.
As styrenic, for example be vinylbenzene, alpha-methyl styrene, Vinyl toluene again.Wherein it would be desirable vinylbenzene.
The reaction conditions of Friedel-Crafts reaction does not limit especially, for example, and can be in the presence of catalyzer, phenol and styrenic are reacted 110~140 ℃ temperature.
In addition, styrenated phenol, as adduction on the benzene nucleus of phenol the compound of styrenic, exist with a vinylbenzene thing, toluylene thing, triphenylethylene thing usually.Wherein, the one vinylbenzene thing of I mole styrenic that it would be desirable on the benzene nucleus of phenol adduction.Again, the concentration of the styrenated phenol in the styrenated phenol normally more than 85%, it is desirable to more than 90%, and better is more than 98%.
The polyalkylene oxides affixture of styrenated phenol can make by the addition reaction of styrenated phenol and epoxy alkane.The carbon number that it is desirable to epoxy alkane is 2~4.In the epoxy alkane, it is desirable to carbon number and be 2 oxyethane and carbon number and be 3 propylene oxide, it would be desirable oxyethane.The addition mole number of epoxy alkane is considered from the deliquescent angle to liquid crystal, normally 1 mole~10 moles, it is desirable to 2 moles~6 moles, and better is 4 moles~5 moles.Wherein, it would be desirable the affixture of 1 mole of one styrenated phenol and 5 moles of ethylene oxide.Condition to addition reaction is not particularly limited, but for example can carry out under 100 ℃~190 ℃ temperature.
The preferable form of employed in the detergent composition as this example (a) poly suboxygen alkyl styryl phenyl ether for example is the material with structure of following general formula (1) expression.
Here, in the formula (1), R
1Be the straight or branched alkylidene group of carbon number 2~carbon number 4, n is the addition mole number (1~3) of styryl, and m is the addition mole number (1~10) of oxyalkylene.
Then, be suitable for the affixture of the epoxy alkane that employed (b) poly suboxygen alkyl alkyl oxide in the detergent composition of this example can higher alcohols and obtain.As higher alcohols, for example be the straight or branched alkyl alcohol that contains carbon number 4~carbon number 18.Specifically, for example be 2-Ethylhexyl Alcohol, octanol, decyl alcohol, dodecanol, isodecyl alcohol, tridecyl alcohol, tetradecanol, stearyl alcohol, oleyl alcohol, octyl phenol, nonylphenol, 4-dodecylphenol etc.Wherein, it is desirable to isodecyl alcohol.
As epoxy alkane, it is desirable to carbon number 2~carbon number 4.In epoxy alkane, it is desirable to carbon number and be 2 oxyethane and carbon number and be 3 propylene oxide, it would be desirable oxyethane.Also can use the material of block structure with oxyethane and propylene oxide again.The addition mole number of epoxy alkane is considered the deliquescent angle of liquid crystal from water-soluble reaching, normally 1 mole~10 moles, it is desirable to 5 moles~7 moles, and better is 6 moles.
The ideal form of employed in the detergent composition as this example (b) poly suboxygen alkyl alkyl oxide for example is the material with structure of following general formula (2) expression.
R
2-O-(R
3O)
lH general formula (2)
Here, in the formula (2), R
2Be the straight or branched alkyl of carbon number 4~carbon number 18, R
3Be the straight or branched alkylidene group of carbon number 2~carbon number 4, l is the addition mole number (1~10) of oxyalkylene.
In (b) poly suboxygen alkyl alkyl oxide with general formula (2) expression, the addition amount of better is oxyethane is 6 moles a poly suboxygen ethyl isodecyl ether.
In the detergent composition of this example, composition (a) poly suboxygen alkyl styryl phenyl ether accounts for 20 weight %~60 weight %, it is desirable to account for 30 weight %~50 weight %, composition (b) poly suboxygen alkyl alkyl oxide accounts for 40 weight %~80 weight %'s, it is desirable to account for 50 weight %~70 weight % ((a) and total (b) are 100 weight %).Blending means to composition (a) and composition (b) does not limit especially, can use common blending means.
The detergent composition of this example can be directly uses with the form of the mixture of composition (a) and composition (b), also can be modulated into aqueous dispersions and use according to desirable.The occasion of under the form of aqueous dispersions, using, ratio of components to each composition in the aqueous dispersions does not limit especially, mixture 1g with respect to composition (a) poly suboxygen alkyl styryl phenyl ether and composition (b) poly suboxygen alkyl alkyl oxide contains composition (c) water 100g~1000g but usually.Here, it is desirable to, composition (c) water is ion exchanged water.
Be modulated into the detergent composition of form of the aqueous dispersions of such lower concentration, especially can be used as the liquid crystal cell that has excellent washing, removes and use with washing composition attached to the performance of the liquid crystal on the liquid crystal cell.To with such liquid crystal cell with detergent washing, remove attached to the method for the liquid crystal on the liquid crystal cell and do not limit especially, can suitably select.For example, can use dipping washing, shake washing, utilize in the washing, agitator treating, gas of the rotation of turner and so on or known means such as jet cleaning and ultrasonic washing in the liquid.Washing means as above can be implemented separately, also can several combinations implement.Again, liquid crystal cell can one group one group washing in once washing operation, also can organize washing more.Again, one of the quantity of the rinse bath of using during washing several can.Though the temperature of the detergent composition during washing does not limit especially, security in 20 ℃~60 ℃ scopes, good operability.
In addition, the detergent composition of this example as required, can mix other nonionic surface active agent.As nonionic surface active agent, for example be in polyalkylene polyamine polyalkylene oxides affixture, polyhydric alcohol fatty acid ester, polyhydric alcohol fatty acid ester polyalkylene oxides affixture and the benzyl phenol polyalkylene oxides affixture more than one etc.
[embodiment]
Embodiment below is shown, more specifically describes this example.This example is not limited to following embodiment but only otherwise exceed its essence.
(embodiment 1~embodiment 4, comparative example 1, comparative example 2)
JIS comb electrodes 2 type battery lead plates as washings, evenly are coated in liquid crystal (fluorine-containing is liquid crystal, " TM9701LA " that Merck company produces) on this battery lead plate, as the evaluation substrate.Then, the washing composition ((1)~(4)) that modulation has composition shown in the table 1 and concentration is in the aqueous solution of these washing composition, under 40 ℃, the evaluation that is coated with the apposition liquid crystal is flooded, stirred 2 minutes, afterwards with substrate, with flowing water washing 1 minute, drying was 30 minutes in cleaning baker (80 ℃).
Then, give the sine wave of the logical upper frequency 100Hz of exsiccant electrode, will measure as the dielectric loss amount, remain in the influence of evaluation with the detergent composition on the substrate thereby estimate owing to the phase differential that the interchange alternating electric field produces.Zone below frequency 100Hz is because because of dielectric loss appears in the surface polarization of planar water, free-water, ion becomes removable ion, becomes the major cause that migration is quickened.The numerical value of dielectric loss amount is more little, and it is more little with the influence of the detergent composition on the substrate then to remain in evaluation, and is just good more with washing composition as liquid crystal cell.
Again, for relatively, to quadrol be washing composition (detergent A: " LGL " that horizontal creek oil prodution industry Co., Ltd. produces) and catechuic acid be that washing composition (cleaning " NATURAL SWEEPER " that drug B: Yi Teng Garden (strain) produces) has also been measured the dielectric loss amount under similarity condition.The result is illustrated in the table 1.
Table 1
Embodiment | Comparative example | |||||
1 | 2 | 3 | 4 | 1 | 2 | |
Washing composition | (1) | (2) | (3) | (4) | A(*5) | B(*6) |
Composition (a) | MSP(*1) | MSP | DSP(*2) | DSP | - | - |
Composition (b) | SD(*3) | SDX(*4) | SDX | SD | - | - |
Weight ratio (a): (b) | 1∶2 | 1∶2 | 1∶2 | 1∶2 | - | - |
Solvent | Ion exchanged water | Ion exchanged water | Ion exchanged water | Ion exchanged water | - | Ion exchanged water |
Concentration (weight %) | 0.5 | 0.5 | 0.5 | 0.5 | 50 | 50 |
Dielectric loss (tan θ) drying | 0.0035 | 0.0051 | 0.0051 | 0.0065 | 0.0025 | 0.0075 |
Dissipation loss (tan θ) moistening (* 7) | 0.0055 | 0.0065 | 0.0075 | 0.0131 | 0.0055 | 0.0585 |
(* 1) poly suboxygen ethyl one styryl phenyl ether (oxyethane addition amount: 5 moles)
(* 2) poly suboxygen ethyl diphenylethyllene phenyl ether (oxyethane addition amount: 5 moles)
(* 3) poly suboxygen ethyl isodecyl ether (oxyethane addition amount: 6 moles)
(* 4) poly suboxygen alkyl isodecyl ether (epoxy alkane addition amount: 8 moles)
(* 5) ethylene glycol is washing composition (" LGL " that horizontal creek oil prodution industry (strain) is produced)
(* 6) catechuic acid is " the Natural Sweeper " that washing composition (Yi Teng Garden Co., Ltd. produces)
(* 7) room temperature, humidity 95%
From the result shown in the table 1 as can be seen: with poly suboxygen alkyl styryl phenyl ether (composition (a)) and poly suboxygen alkyl isodecyl ether (composition (b)) with weight ratio (a): (b)=mix, be modulated into the washing composition that concentration is the aqueous dispersions of 0.5 weight % (embodiment 1~embodiment 4) at 1: 2, the measured value of its dielectric loss (tan θ) is all little under drying regime and moisture state, illustrates that it has as the premium properties of low-cost, safe liquid crystal cell with washing composition.
Wherein, as can be seen, the measured value of the dielectric loss (tan θ) of the washing composition (1) (embodiment 1) that is mixed with so that poly suboxygen ethyl one styryl phenyl ether (oxyethane addition amount: 5 moles) is mixed with weight ratio with poly suboxygen ethyl isodecyl ether (oxyethane addition amount: 6 moles) at 1: 2 is little, illustrates being formed on evaluation especially little with the influence of the electrode on the substrate.
On the other hand, as can be seen, quadrol be washing composition (detergent A: comparative example 1), though little to estimating with the influence of the electrode of substrate, remove attached to the liquid crystal on the electrode, must under the state of high density, use, as washing composition, its cost is high.It can also be seen that catechuic acid is that (clean drug B: the measured value of dielectric loss comparative example 2) (tan θ) is big, and especially migration is quickened under moisture state, illustrates that the influence of counter electrode is big for washing composition.
(embodiment 5, comparative example 3, comparative example 4)
The washing composition (1) that utilization is used in embodiment 1 under condition similarly to Example 1, washs, removes attached to estimating with the liquid crystal on the substrate, measures the fragmention that is produced by the liquid crystal residue that remains on the electrode with TOF-SIMS.Also have, for relatively, to employed washing composition A in comparative example 1 and in comparative example 2 employed washing composition B, also carry out operation similarly to Example 1 after, measure the fragmention that produces by the liquid crystal residue that remains on the electrode with TOF-SIMS.The result is illustrated in table 2.
Table 2
From the result shown in the table 2, as can be seen: poly suboxygen ethyl-styryl phenyl ether (oxyethane addition amount: 5 moles) mixed with weight ratio with poly suboxygen ethyl isodecyl ether (oxyethane addition amount: 6 moles) at 1: 2 and the washing composition (1) (embodiment 5) that is mixed with, it is few with the fragmention amount that TOF-SIMS records, illustrate that the liquid crystal residue that remains on the electrode is few, strong as liquid crystal cell with the washability of washing composition.
On the other hand, as can be seen, when using washing composition A (comparative example 3) and washing composition B (comparative example 4), the liquid crystal residue that remains on the electrode is many, washing composition B especially, and residual liquid crystal residue approximately is 5 times of washing composition (1).
As applying flexibly example, washing composition of the present invention can be used to wash attached to dirts such as various oil such as the cutting fluid on the precision component, press oil, drawing oil, wax, lubricating grease.
Claims (7)
1, a kind of liquid crystal cell washing composition, it is characterized in that, the mixture and (c) ion exchanged water that comprise (b) poly suboxygen alkyl alkyl oxide of (a) poly suboxygen alkyl one styryl phenyl ether of 20 weight %~60 weight % and 40 weight %~80 weight %, wherein (a) and total (b) are 100 weight %, with respect to the described mixture of 1g, (c) ion exchanged water is 100g~1000g, wherein
Described (a) poly suboxygen alkyl one styryl phenyl ether is the addition polymer of the epoxy alkane of a styrenated phenol and carbon number 2~4,
Described (b) poly suboxygen alkyl alkyl oxide has the straight or branched alkyl of carbon number 4~carbon number 18, and in described (b) poly suboxygen alkyl alkyl oxide, the addition mole number of the epoxy alkane of carbon number 2~carbon number 4 is 1~10, and
Described washing composition does not contain ion component.
2, liquid crystal cell washing composition as claimed in claim 1 is characterized in that, described (a) poly suboxygen alkyl one styryl phenyl ether is the addition polymer of the epoxy alkane of 1 mole of one styrenated phenol and 4 moles~5 moles of carbon numbers 2~4.
3, liquid crystal cell washing composition as claimed in claim 1 is characterized in that, described (a) poly suboxygen alkyl one styryl phenyl ether is the addition polymer of 1 mole of one styrenated phenol and 5 moles of ethylene oxide.
4, liquid crystal cell washing composition as claimed in claim 1 is characterized in that, described (b) poly suboxygen alkyl alkyl oxide has isodecyl.
5, liquid crystal cell washing composition as claimed in claim 1 is characterized in that, in described (b) poly suboxygen alkyl alkyl oxide, the addition mole number of carbon number 2 or 3 epoxy alkane is 6.
6, liquid crystal cell washing composition as claimed in claim 1 is characterized in that, described (a) poly suboxygen alkyl one styryl phenyl ether accounts for 30 weight %~50 weight %, and described (b) poly suboxygen alkyl alkyl oxide accounts for 50 weight %~70 weight %.
7, liquid crystal cell washing composition as claimed in claim 1 is characterized in that, the concentration of a described styrenated phenol in styrenated phenol is not less than 85%.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
TW093134329A TW200530329A (en) | 2003-11-28 | 2004-11-10 | Detergent composition and detergent for liquid crystal cell |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2003400334 | 2003-11-28 | ||
JP2003400334A JP2005162780A (en) | 2003-11-28 | 2003-11-28 | Detergent composition and detergent for liquid crystal cell |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1637129A CN1637129A (en) | 2005-07-13 |
CN1297641C true CN1297641C (en) | 2007-01-31 |
Family
ID=34616652
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB2004100956350A Expired - Fee Related CN1297641C (en) | 2003-11-28 | 2004-11-26 | Detergent composition and detergent for liquid crystal cell |
Country Status (5)
Country | Link |
---|---|
US (1) | US20050119147A1 (en) |
JP (1) | JP2005162780A (en) |
CN (1) | CN1297641C (en) |
HK (1) | HK1077839B (en) |
TW (1) | TW200530329A (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5467741B2 (en) * | 2008-08-05 | 2014-04-09 | 花王株式会社 | Method for producing nonionic surfactant composition |
JP5216483B2 (en) * | 2008-08-26 | 2013-06-19 | 花王株式会社 | Cleaning composition for plastic lens mold |
JP5800533B2 (en) * | 2011-03-08 | 2015-10-28 | 日華化学株式会社 | Washing soap |
JP7166819B2 (en) * | 2018-07-13 | 2022-11-08 | Cmcマテリアルズ株式会社 | Chemical mechanical polishing composition, rinse composition, chemical mechanical polishing method and rinse method |
WO2022224960A1 (en) * | 2021-04-19 | 2022-10-27 | デンカ株式会社 | Reagent composition and kit |
CN113122398B (en) * | 2021-04-23 | 2022-07-08 | 广州亦盛环保科技有限公司 | Water-based liquid crystal cleaning agent and preparation method and application thereof |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1384179A (en) * | 2001-05-07 | 2002-12-11 | 株式会社新药 | Industrial detergent composition and its production process |
US6494941B2 (en) * | 2000-10-02 | 2002-12-17 | Bayer Aktiengesellschaft | Active-compound-containing emulsions |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3233279B2 (en) * | 1998-10-06 | 2001-11-26 | 日本アイ・ビー・エム株式会社 | Cleaning composition and cleaning method |
DE10353603B4 (en) * | 2003-11-17 | 2006-01-19 | Clariant Gmbh | Use of ether carboxylic acids based on alkoxylated mono-, di- and / or tri (1-phenylethyl) phenols in cooling lubricants |
-
2003
- 2003-11-28 JP JP2003400334A patent/JP2005162780A/en active Pending
-
2004
- 2004-11-10 TW TW093134329A patent/TW200530329A/en unknown
- 2004-11-23 US US10/996,304 patent/US20050119147A1/en not_active Abandoned
- 2004-11-26 CN CNB2004100956350A patent/CN1297641C/en not_active Expired - Fee Related
-
2006
- 2006-01-06 HK HK06100296.5A patent/HK1077839B/en not_active IP Right Cessation
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6494941B2 (en) * | 2000-10-02 | 2002-12-17 | Bayer Aktiengesellschaft | Active-compound-containing emulsions |
CN1384179A (en) * | 2001-05-07 | 2002-12-11 | 株式会社新药 | Industrial detergent composition and its production process |
Also Published As
Publication number | Publication date |
---|---|
HK1077839B (en) | 2007-04-04 |
US20050119147A1 (en) | 2005-06-02 |
CN1637129A (en) | 2005-07-13 |
TW200530329A (en) | 2005-09-16 |
JP2005162780A (en) | 2005-06-23 |
HK1077839A1 (en) | 2006-02-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN1046527C (en) | Silane with hydrophilic group and preparation and application of same | |
CN1042353C (en) | Washing method using washing agent | |
CN1297641C (en) | Detergent composition and detergent for liquid crystal cell | |
JP3636817B2 (en) | Polysiloxane-polyoxyethylene-polyoxypropylene-triblock copolymer and antifoam compound containing the copolymer | |
CN1100826C (en) | Low viscosity mixtures of amphiphilic nonionic graft copolymers and viscosity-reducing additives | |
CN1177977A (en) | Bleaning process and composition | |
CN1564860A (en) | Cleaning composition | |
CN1891806A (en) | Alkaline detergent for an automatic analysing apparatus, process for cleaning an automatic analysing apparatus, and an automatic analysing apparatus | |
CN1721052A (en) | Waterpower liquid | |
JP5244278B2 (en) | Defoaming composition for water-based paint | |
WO1998032726A1 (en) | Novel ethylenically unsaturated amine salts of sulfonic, phosphoric and carboxylic acids | |
KR20140117888A (en) | Cleaning solution composition for sapphire wafer | |
JP6773569B2 (en) | Antistatic silicone resin composition | |
CN112877112B (en) | Efficient lubricating oil demulsifier and production method thereof | |
AU2892797A (en) | Floor treating composition | |
CN1226393C (en) | Oil production additive formulations | |
CN1020636C (en) | Detergent composition for washing rough feathers | |
US10982046B2 (en) | Reaction products and use of same in defoamer compositions and methods for defoaming | |
CN103666805B (en) | Liquid detergent | |
CN104399433A (en) | Composite material of phenolic pollutants in refinery waste water | |
JP6889649B2 (en) | Antistatic silicone resin composition | |
CN1880424A (en) | Cleaning agent composition and cleaning method | |
KR100381729B1 (en) | Detergent Composition of Water-Soluble System for Liquid Crystal Display Panel | |
CN115960597B (en) | Compound crude oil pour point depressant and preparation method thereof | |
CN108911187A (en) | A kind of efficient prefilming agent and preparation method thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
REG | Reference to a national code |
Ref country code: HK Ref legal event code: DE Ref document number: 1077839 Country of ref document: HK |
|
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
C17 | Cessation of patent right | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20070131 Termination date: 20091228 |