CN109135419A - A kind of mark pen ink - Google Patents

A kind of mark pen ink Download PDF

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Publication number
CN109135419A
CN109135419A CN201811148637.XA CN201811148637A CN109135419A CN 109135419 A CN109135419 A CN 109135419A CN 201811148637 A CN201811148637 A CN 201811148637A CN 109135419 A CN109135419 A CN 109135419A
Authority
CN
China
Prior art keywords
parts
pen ink
mark pen
trialkyl phosphates
mark
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.)
Withdrawn
Application number
CN201811148637.XA
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Chinese (zh)
Inventor
龙承菊
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.)
Beicang Road Primary School In Guang'an City Guang'an District School
Original Assignee
Beicang Road Primary School In Guang'an City Guang'an District School
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Beicang Road Primary School In Guang'an City Guang'an District School filed Critical Beicang Road Primary School In Guang'an City Guang'an District School
Priority to CN201811148637.XA priority Critical patent/CN109135419A/en
Publication of CN109135419A publication Critical patent/CN109135419A/en
Withdrawn legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D11/00Inks
    • C09D11/16Writing inks

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)

Abstract

The invention discloses a kind of mark pen ink, which includes following composition by weight: 10 ~ 17 parts of ethyl acetate, 22 ~ 29 parts of dimethyl carbonate, 19 ~ 26 parts of diethylene-triamine pentaacetic acid, 27 ~ 33 parts of trialkyl phosphates, 10 ~ 14 parts of pigment.The invention proposes a kind of mark pen inks to improve tradition containing the biggish ester of toxicity, ketone, benzene class organic solvent, develop a kind of nontoxic mark pen ink, and develop to aqueous solvent direction is improved, the use environment of marking pen is substantially improved, keeps its application more universal.

Description

A kind of mark pen ink
Technical field
The present invention relates to inks fields, more particularly to a kind of mark pen ink.
Background technique
Marking pen is that one kind can submit a written statement to a higher authority writing note in paper, timber, metal, plastics, one or more materials such as ward off ceramics Number or mark pen.Marking pen is divided into permanent pen and aqueous marking pen.Aqueous marking pen can be in smooth body surface Or write on blank, it can be wiped with rag, what permanent pen was write is just not easy to wipe.
In view of chalk as teaching aid, there is serious pollution to environment, totally unfavorable to human health, chalk starts It updates: moist writing being become from stemness writing, i.e. development erasability blackboard ink.Then marking pen and its ink conduct The substitute products of chalk come into being.Marking pen belong to it is wet write xerotripsis class pen, be mark pen ink in the whiteboard surface for being covered with glaze layer On write in a manner of watercolor pencil, formed in plate face one layer thin because cellulose or trialkyl phosphate esters compound, writing is added Film can be wiped easily with dry cloth or blackboard eraser.The teaching aid is succeeded in developing already, but can not be promoted due to there are many defects.Such as: plate Face has coating easily to scratch, and reflecting rate is high, is not suitable for teaching in classroom;Ink uses organic solvent, at high cost, volatile, danger Evil health, pollution environment, writing amount is small, penetration is strong, and pollution plate face shading, the plate face service life is short etc..Mark pen ink is big Mostly it is black, is made by adding dyestuff, clipboard uses blank, since blank is easily reflective, so being difficult to promote in middle and primary schools. As the reach of science and marking pen are applied universal, the performance of mark pen ink is also being continuously improved and perfect, especially its The middle solvent as important component.Consider that more stringent requirements are proposed to it, and the selection of solvent is more from protection human health angle Add strictly, the invention proposes a kind of mark pen inks to change tradition containing the biggish ester of toxicity, ketone, benzene class organic solvent Into developing a kind of nontoxic mark pen ink, and develop to aqueous solvent direction is improved, substantially improve making for marking pen With environment, keep its application more universal.
Summary of the invention
Present invention mainly solves the technical issues of conventional white board ink be more toxic a kind of nontoxic marking pen be provided Ink, a kind of mark pen ink, which is characterized in that the mark pen ink includes following composition by weight: ethyl acetate 10~17 parts, 22~29 parts of dimethyl carbonate, 19~26 parts of diethylene-triamine pentaacetic acid, 27~33 parts of trialkyl phosphates, 10~14 parts of pigment.
Dimethyl carbonate has many advantages, such as that small toxicity, safety, pollution is small and transport is easy, and activity is good, in this hair It can cooperate with other components in bright.
Further, the composition by weight is 14 parts of ethyl acetate, 26 parts of dimethyl carbonate, diethylenetriamines 22 parts of pentaacetic acid.
Further, the pigment is phthalocyanine blue.
Further, the phthalocyanine blue is 12 parts.
Further, the trialkyl phosphates are organosilicon trialkyl phosphates.
Further, the organosilicon trialkyl phosphates are 30 parts.
Further, the ethyl acetate is that analysis is pure.
Further, the organosilicon trialkyl phosphates preparation method the following steps are included:
Specific embodiment
The present invention is described in further detail below with reference to embodiment, embodiments of the present invention are not limited thereto, Without departing from the idea case in the present invention described above, according to ordinary skill knowledge and customary means, various replace is made It changes and changes, should all be included within the scope of the invention.
Embodiment 1
The preparation of organosilicon trialkyl phosphates:
(1) 40 parts of vinyltrimethoxysilane are accurately weighed with SQP type electronic balance, polyethylene glycol monoacrylate 31 Part, it 17 parts of ethyl methacrylate, 13 parts of butyl acrylate, is transferred in beaker after mixing, then weigh peroxide diethyl 1.7 parts of hecanoic acid t-butyl ester are added in above-mentioned beaker, and it is spare to then move to annular safety funnel after mixing evenly with glass bar.
(2) it is weighed with SQP type electronic balance 7:3 in mass ratio and prepares dimethylbenzene: 80 parts of n-butanol mixed solvent, will mixed Bonding solvent is transferred in four-hole boiling flask, is placed in heating mantle and installs reaction unit, is opened heating mantle and is opened simultaneously condensed water Dropping funel is loaded onto when temperature is raised to 115 DEG C and starts mixture in agitation and dropping step (1), is added dropwise to complete in 4~5h, Then 1~2h of heat preservation adds 0.3 part of peroxide diethyl hecanoic acid t-butyl ester, and cooling obtains faint yellow sticky shape after keeping the temperature 4~5h Solution, be transferred in preprepared polypropylene vial save to get.
Embodiment 2
(1) 14 parts of ethyl acetate are weighed, 26 parts of dimethyl carbonate, organosilicon trialkyl phosphates are 30 parts, stir 70min It is uniformly mixed, forms mixture;
(2) weighing phthalocyanine blue is 12 parts, 22 parts of diethylene-triamine pentaacetic acid, at room temperature, is stirred 30min, will Mixture in step (1) is added, and continuess to mix 45min to get plate board pen ink of the present invention.
Embodiment 3
(1) 10 parts of ethyl acetate are weighed, 29 parts of dimethyl carbonate, organosilicon trialkyl phosphates are 27 parts, stir 70min It is uniformly mixed, forms mixture;
(2) weighing phthalocyanine blue is 10 parts, 26 parts of diethylene-triamine pentaacetic acid, at room temperature, is stirred 30min, will Mixture in step (1) is added, and continuess to mix 45min to get plate board pen ink of the present invention.
Embodiment 4
(1) 17 parts of ethyl acetate are weighed, 22 parts of dimethyl carbonate, organosilicon trialkyl phosphates are 33 parts, stir 70min It is uniformly mixed, forms mixture;
(2) weighing phthalocyanine blue is 14 parts, 19 parts of diethylene-triamine pentaacetic acid, at room temperature, is stirred 30min, will Mixture in step (1) is added, and continuess to mix 45min to get plate board pen ink of the present invention.
Embodiment 5
(1) 17.5 parts of ethyl acetate are weighed, 21.5 parts of dimethyl carbonate, organosilicon trialkyl phosphates are 33 parts, stirring 70min is uniformly mixed, and forms mixture;
(2) weighing phthalocyanine blue is 14.5 parts, 18.5 parts of diethylene-triamine pentaacetic acid, at room temperature, is stirred Mixture in step (1) is added, continuess to mix 45min to get plate board pen ink of the present invention by 30min.
Embodiment 6
(1) 16.5 parts of ethyl acetate are weighed, 21.5 parts of dimethyl carbonate, organosilicon trialkyl phosphates are 33 parts, stirring 70min is uniformly mixed, and forms mixture;
(2) weighing phthalocyanine blue is 14.5 parts, 17.5 parts of diethylene-triamine pentaacetic acid, at room temperature, is stirred Mixture in step (1) is added, continuess to mix 45min to get plate board pen ink of the present invention by 30min.
Embodiment 7
(1) 16.8 parts of ethyl acetate are weighed, 21.5 parts of dimethyl carbonate, organosilicon trialkyl phosphates are 33 parts, stirring 70min is uniformly mixed, and forms mixture;
(2) weighing phthalocyanine blue is 14.7 parts, 17.1 parts of diethylene-triamine pentaacetic acid, at room temperature, is stirred Mixture in step (1) is added, continuess to mix 45min to get plate board pen ink of the present invention by 30min.
Embodiment 8
(1) 17.9 parts of ethyl acetate are weighed, 22.1 parts of dimethyl carbonate, organosilicon trialkyl phosphates are 33 parts, stirring 70min is uniformly mixed, and forms mixture;
(2) weighing phthalocyanine blue is 14.3 parts, 19 parts of diethylene-triamine pentaacetic acid, at room temperature, is stirred 30min, Mixture in step (1) is added, continuess to mix 45min to get plate board pen ink of the present invention.
Embodiment 9
(1) 17.3 parts of ethyl acetate are weighed, 22.1 parts of dimethyl carbonate, organosilicon trialkyl phosphates are 33 parts, stirring 70min is uniformly mixed, and forms mixture;
(2) weighing phthalocyanine blue is 14.3 parts, 19.2 parts of diethylene-triamine pentaacetic acid, at room temperature, is stirred Mixture in step (1) is added, continuess to mix 45min to get plate board pen ink of the present invention by 30min.
Embodiment 10
Sample abbreviation sample 1~9 prepared by embodiment 2~9 carries out handwriting test, and experimental result is as follows:
The above description is only an embodiment of the present invention, is not intended to limit the scope of the invention, all to utilize this hair Equivalent structure or equivalent flow shift made by bright description is applied directly or indirectly in other relevant technology necks Domain is included within the scope of the present invention.

Claims (7)

1. a kind of mark pen ink, which is characterized in that the mark pen ink includes following composition by weight: ethyl acetate 10 ~ 17 parts, 22 ~ 29 parts of dimethyl carbonate, 19 ~ 26 parts of diethylene-triamine pentaacetic acid, 27 ~ 33 parts of trialkyl phosphates, pigment 10 ~ 14 parts.
2. a kind of mark pen ink according to claim 1, which is characterized in that the composition by weight is acetic acid 14 parts of ethyl ester, 26 parts of dimethyl carbonate, 22 parts of diethylene-triamine pentaacetic acid.
3. a kind of mark pen ink according to claim 1, which is characterized in that the pigment is phthalocyanine blue.
4. a kind of mark pen ink according to claim 1, which is characterized in that the phthalocyanine blue is calculated as 12 by weight Part.
5. a kind of mark pen ink according to claim 1, which is characterized in that the trialkyl phosphates are organosilicon three Alkyl phosphate.
6. a kind of mark pen ink according to claim 1, which is characterized in that the organosilicon trialkyl phosphates are by weight Amount part is calculated as 30 parts.
7. a kind of mark pen ink according to claim 1, which is characterized in that the ethyl acetate is that analysis is pure.
CN201811148637.XA 2018-09-29 2018-09-29 A kind of mark pen ink Withdrawn CN109135419A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201811148637.XA CN109135419A (en) 2018-09-29 2018-09-29 A kind of mark pen ink

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201811148637.XA CN109135419A (en) 2018-09-29 2018-09-29 A kind of mark pen ink

Publications (1)

Publication Number Publication Date
CN109135419A true CN109135419A (en) 2019-01-04

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
CN201811148637.XA Withdrawn CN109135419A (en) 2018-09-29 2018-09-29 A kind of mark pen ink

Country Status (1)

Country Link
CN (1) CN109135419A (en)

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WW01 Invention patent application withdrawn after publication
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Application publication date: 20190104