CN1133665C - High-molecular resin and its preparing process - Google Patents

High-molecular resin and its preparing process Download PDF

Info

Publication number
CN1133665C
CN1133665C CNB011381302A CN01138130A CN1133665C CN 1133665 C CN1133665 C CN 1133665C CN B011381302 A CNB011381302 A CN B011381302A CN 01138130 A CN01138130 A CN 01138130A CN 1133665 C CN1133665 C CN 1133665C
Authority
CN
China
Prior art keywords
parts
temperature
deionized water
food starch
stirring
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
Application number
CNB011381302A
Other languages
Chinese (zh)
Other versions
CN1359959A (en
Inventor
王建新
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.)
Wuxi Research Institute of Daily Chemical Products
Original Assignee
王建新
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 王建新 filed Critical 王建新
Priority to CNB011381302A priority Critical patent/CN1133665C/en
Publication of CN1359959A publication Critical patent/CN1359959A/en
Application granted granted Critical
Publication of CN1133665C publication Critical patent/CN1133665C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Landscapes

  • Compositions Of Macromolecular Compounds (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)

Abstract

The present invention discloses high-molecular resin and a preparing method thereof. The high-molecular resin is manufactured by using 70 to 80.5 parts of styrene, 15 to 22 parts of butyl acrylate, 0.5 to 1.0 parts of divinylbenzene, 2.5 to 3.8 parts of dibenzoyl peroxide, 0.5 to 1.5 parts of edible gelatin and 0.5 to 1.5 parts of edible starch through the steps of mixing, reaction, cleaning, dehydration, drying, sieving, etc. The high-molecular resin of the present invention has the advantages of nontoxicity, safety, low cost and no environmental pollution and can be used as the principal raw material of ink powder of a xerographic printer.

Description

A kind of Polymer Resin And Its Preparation Method
Technical field
The present invention relates to a kind of main raw material---Polymer Resin And Its Preparation Method of making xerographic printer with ink powder
Background technology
Macromolecule resin is to produce the main raw material of xerographic printer with ink powder.At present, the synthetic binding resin of the solution method comparatively generally of usefulness.The macromolecule resin that adopts solution method to produce ,-Ma acid butyl ester terpolymer that its main raw material is a vinylbenzene--butyl acrylate--, solvent for use is a dimethylbenzene.Its preparation method is, adopts electrically heated, and two the reflection stills reactions in Fen Qiandao and road, back vacuumize curing at last.The macromolecule resin that adopts above-mentioned raw materials and method to produce, though can be as the raw material of xerographic printer ink powder, because employing dimethylbenzene is solvent, the resin of making has the residue of dimethylbenzene unavoidably.With this resin of dimethylbenzene residue and the ink powder that magnetic is made of having, still poisonous, harmful to HUMAN HEALTH.Because employing dimethylbenzene is solvent, make production cost higher again.Secondly, because this production method adopts electrically heated in reaction process, and Heating temperature higher (up to 250~280 ℃), careless slightly, dimethylbenzene gas will set off an explosion, and is very dangerous.Again secondly, behind the resin polymerization of producing in this way, need pulverize, not only can produce mechanicalness noise during pulverizing, and the dust that produces can pollute environment.
Summary of the invention
An object of the present invention is to provide a kind of macromolecule resin.This macromolecule resin is at the bottom of nontoxic, safety, the cost, do not pollute the environment.
Another object of the present invention provides a kind of method for preparing macromolecule resin.
Above-mentioned purpose of the present invention is realized by following technical solution:
Macromolecule resin of the present invention, make by the raw material of following parts by weight:
70~80.5 parts of vinylbenzene, 15~22 parts of butyl acrylates, 0.5~1.0 part of divinylbenzene, 2.5~3.8 parts of diphenyl peroxide potassium acetyls, edible Gelatinum oxhide 0.5~1.5, food starch 0.5~1.5.
Prepare the method for macromolecule resin of the present invention, may further comprise the steps:
(1) vinylbenzene, butyl acrylate, divinylbenzene and diphenyl peroxide potassium acetyl are put together, stirred 0.3~1.0 hour, mix, make compound, stand-by;
(2) according to edible Gelatinum oxhide: the ratio of hot water=1: 3.7, in edible Gelatinum oxhide, add temperature and be 85~95 ℃ hot water, through stirring, edible Gelatinum oxhide is fully dissolved, make the anti-stick solution A;
(3) according to food starch: the ratio of deionized water=1: 3.7, in food starch, add deionized water, through stirring, food starch is fully dissolved, make the anti-stick solution B;
(4) according to compound: the ratio of deionized water=1: 3, in reactor, add deionized water, and to its heating; When water temperature rises to 65~75 ℃, drop into anti-stick solution A and anti-stick solution B, when evenly stirring, continue its heating; When temperature rose to 80~90 ℃, constant temperature kept 3~5 hours;
(5) when continuing stirring, in 1.8~2.4 hours, above-mentioned compound is slowly splashed into;
(6) temperature is risen to 85~92 ℃, and constant temperature keeps allowing it naturally cool to 30~40 ℃ after 1~2 hour;
(7) material in the reactor is poured out, and elimination moisture wherein, the particulate state work in-process made;
(8) with whizzer the particulate state work in-process are cleaned, and slough wherein moisture;
(9) be that 50~60 ℃ baking oven was to the work in-process drying treatment of sloughing moisture 15~20 hours with temperature;
(10) with 30 purpose sieves, the work in-process that drying was handled sieve, and make macromolecule resin of the present invention.
Adopt such scheme, have the following advantages:
1. owing in the macromolecule resin raw material of the present invention, do not contain dimethylbenzene, nontoxic, harmless to HUMAN HEALTH;
Since macromolecule resin raw material of the present invention in do not contain dimethylbenzene, and with deionized water, edible Gelatinum oxhide and food starch as suspension, can reduce production costs greatly;
3. owing to do not contain dimethylbenzene in the macromolecule resin raw material of the present invention, the gas in the production process in the reactor is water vapor, can not set off an explosion, and is as safe as a house.
4. owing to adopt edible Gelatinum oxhide and food starch as binding agent in the macromolecule resin of the present invention, making the polymeric product is particle, needn't pulverize, and has avoided because of pulverizing the mechanicalness noise that produces and to the pollution of environment.
Embodiment
Below in conjunction with embodiment the present invention is described in further detail:
Embodiment one
Get 70 parts vinylbenzene, 19 parts butyl acrylate, 1.0 parts divinylbenzene, 2.5 parts diphenyl peroxide potassium acetyl, 0.5 part edible Gelatinum oxhide and 1.0 parts food starch.
Earlier vinylbenzene, butyl acrylate, divinylbenzene and diphenyl peroxide potassium acetyl are placed in the stirrer, stirred 0.3 hour, mix, obtain compound.
Secondly, according to edible Gelatinum oxhide: the ratio of hot water=1: 3.7, in edible Gelatinum oxhide, add temperature and be 85 ℃ hot water, through stirring, edible Gelatinum oxhide is fully dissolved, make the anti-stick solution A.
Simultaneously, according to food starch: the ratio of deionized water=1: 3.7, in food starch, add deionized water, through stirring, food starch is fully dissolved, make the anti-stick solution B.
Again secondly, according to compound: the ratio of deionized water=1: 3, in reactor, add deionized water, and to its heating.When water temperature rises to 75 ℃, drop into above-mentioned anti-stick solution A and anti-stick solution B, and when evenly stirring, continue its heating.When temperature rose to 80 ℃, constant temperature kept 3 hours.
Afterwards, when continuing stirring, in 1.8 hours, above-mentioned compound is slowly splashed into.
Afterwards, continue heating, temperature is risen to 90 ℃, after constant temperature under this temperature keeps 1 hour, allow it naturally cool to 35 ℃.
Afterwards, the material in the reactor is poured in the net cage, elimination moisture wherein obtains the particulate state work in-process.
Afterwards, the particulate state work in-process are cleaned, and slough wherein moisture with whizzer.
Then, be that 50 ℃ baking oven was to the particulate state work in-process baking of sloughing moisture 15 hours with temperature.
At last, with 30 purpose sieves, the particulate state work in-process that drying was handled sieve, and make macromolecule resin of the present invention.
Embodiment two
Get 75 parts vinylbenzene, 22 parts butyl acrylate, 0.5 part divinylbenzene, 3.2 parts diphenyl peroxide potassium acetyl, 1.0 parts edible Gelatinum oxhide and 1.5 parts food starch.
Earlier vinylbenzene, butyl acrylate, divinylbenzene and diphenyl peroxide potassium acetyl are placed in the stirrer, stirred 0.6 hour, mix, obtain compound.
Secondly, according to edible Gelatinum oxhide: the ratio of hot water=1: 3.7, in edible Gelatinum oxhide, add temperature and be 90 ℃ hot water, through stirring, edible Gelatinum oxhide is fully dissolved, make the anti-stick solution A.
Simultaneously, according to food starch: the ratio of deionized water=1: 3.7, in food starch, add deionized water, through stirring, food starch is fully dissolved, make the anti-stick solution B.
Again secondly, according to compound: the ratio of deionized water=1: 3, in reactor, add deionized water, and to its heating.When water temperature rises to 70 ℃, drop into above-mentioned anti-stick solution A and anti-stick solution B, and when evenly stirring, continue its heating.When temperature rose to 85 ℃, constant temperature kept 4 hours.
Afterwards, when continuing stirring, in 2.1 hours, above-mentioned compound is slowly splashed into.
Afterwards, continue heating, temperature is risen to 92 ℃, after constant temperature under this temperature keeps 1.5 hours, allow it naturally cool to 40 ℃.
Afterwards, the material in the reactor is poured in the net cage, elimination moisture wherein obtains the particulate state work in-process.
Afterwards, the particulate state work in-process are cleaned, and slough wherein moisture with whizzer.
Then, be that 55 ℃ baking oven was to the particulate state work in-process baking of sloughing moisture 18 hours with temperature.
At last, with 30 purpose sieves, the particulate state work in-process that drying was handled sieve, and make macromolecule resin of the present invention.
Embodiment three
Get 80 parts vinylbenzene, 16 parts butyl acrylate, 0.8 part divinylbenzene, 3.8 parts diphenyl peroxide potassium acetyl, 1.5 parts edible Gelatinum oxhide and 0.5 part food starch.
Earlier vinylbenzene, butyl acrylate, divinylbenzene and diphenyl peroxide potassium acetyl are placed in the stirrer, stirred 0.9 hour, mix, obtain compound.
Secondly, according to edible Gelatinum oxhide: the ratio of hot water=1: 3.7, in edible Gelatinum oxhide, add temperature and be 95 ℃ hot water, through stirring, edible Gelatinum oxhide is fully dissolved, make the anti-stick solution A.
Simultaneously, according to food starch: the ratio of deionized water=1: 3.7, in food starch, add deionized water, through stirring, food starch is fully dissolved, make the anti-stick solution B.
Again secondly, according to compound: the ratio of deionized water=1: 3, in reactor, add deionized water, and to its heating.When water temperature rises to 65 ℃, drop into above-mentioned anti-stick solution A and anti-stick solution B, and when evenly stirring, continue its heating.When temperature rose to 90 ℃, constant temperature kept 5 hours.
Afterwards, when continuing stirring, in 2.4 hours, above-mentioned compound is slowly splashed into.
Afterwards, continue heating, temperature is risen to 85 ℃, after constant temperature under this temperature keeps 2 hours, allow it naturally cool to 30 ℃.
Afterwards, the material in the reactor is poured in the net cage, elimination moisture wherein obtains the particulate state work in-process.
Afterwards, the particulate state work in-process are cleaned, and slough wherein moisture with whizzer.
Then, be that 60 ℃ baking oven was to the particulate state work in-process baking of sloughing moisture 20 hours with temperature.
At last, with 30 purpose sieves, the particulate state work in-process that drying was handled sieve, and make macromolecule resin of the present invention.

Claims (2)

1. macromolecule resin is characterized in that being made up of the raw material of following parts by weight:
70~80.5 parts of vinylbenzene, 15~22 parts of butyl acrylates, 0.5~1.0 part of divinylbenzene, 2.5~3.8 parts of diphenyl peroxide potassium acetyls, edible Gelatinum oxhide 0.5~1.5, food starch 0.5~1.5.
2. the method for preparing the described macromolecule resin of claim 1 is characterized in that may further comprise the steps successively:
(1) vinylbenzene, butyl acrylate, divinylbenzene and diphenyl peroxide potassium acetyl are put together, stirred 0.3~1.0 hour, mix, make compound, stand-by;
(2) according to edible Gelatinum oxhide: the ratio of hot water=1: 3.7, in edible Gelatinum oxhide, add temperature and be 85~95 ℃ hot water, through stirring, edible Gelatinum oxhide is fully dissolved, make the anti-stick solution A;
(3) according to food starch: the ratio of deionized water=1: 3.7, in food starch, add deionized water, through stirring, food starch is fully dissolved, make the anti-stick solution B;
(4) according to compound: the ratio of deionized water=1: 3, in reactor, add deionized water, and to its heating; When water temperature rises to 65~75 ℃, drop into anti-stick solution A and anti-stick solution B, when evenly stirring, continue its heating; When temperature rose to 80~90 ℃, constant temperature kept 3~5 hours;
(5) when continuing stirring, in 1.8~2.4 hours, above-mentioned compound is slowly splashed into;
(6) temperature is risen to 85~92 ℃, and constant temperature keeps allowing it naturally cool to 30~40 ℃ after 1~2 hour;
(7) material in the reactor is poured out, and elimination moisture wherein, the particulate state work in-process made;
(8) with whizzer the particulate state work in-process are cleaned, and slough wherein moisture;
(9) be that 50~60 ℃ baking oven was to the work in-process drying treatment of sloughing moisture 15~20 hours with temperature;
(10) with 30 purpose sieves, the work in-process that drying was handled sieve, and make macromolecule resin of the present invention.
CNB011381302A 2001-12-30 2001-12-30 High-molecular resin and its preparing process Expired - Fee Related CN1133665C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB011381302A CN1133665C (en) 2001-12-30 2001-12-30 High-molecular resin and its preparing process

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB011381302A CN1133665C (en) 2001-12-30 2001-12-30 High-molecular resin and its preparing process

Publications (2)

Publication Number Publication Date
CN1359959A CN1359959A (en) 2002-07-24
CN1133665C true CN1133665C (en) 2004-01-07

Family

ID=4674409

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB011381302A Expired - Fee Related CN1133665C (en) 2001-12-30 2001-12-30 High-molecular resin and its preparing process

Country Status (1)

Country Link
CN (1) CN1133665C (en)

Also Published As

Publication number Publication date
CN1359959A (en) 2002-07-24

Similar Documents

Publication Publication Date Title
CN1101355A (en) Method for production of acrylate and acrylate containing polymer
CN1865306A (en) Low content nitrile cross-linked powdery acrylonitrile butadiene preparation method
CN1693202A (en) Process for prepareing SAPO-34 molecular siever
CN1173018C (en) Coal briquette having superior strength and briquetting method thereof
CN1039003A (en) Titanium oxide method for making and titanium oxide goods
CN109111672B (en) Acrylate graft modified zeolite high-temperature-resistant composite material and preparation method thereof
CN1046878A (en) Finely powdery magnesium hydroxide and preparation method thereof
CN1133665C (en) High-molecular resin and its preparing process
CN1008099B (en) Process for preparation of thermoplastic mass
CN113003563B (en) Modified lignin carbon dots and preparation method and application thereof
CN1070383A (en) A kind of method for preparation of potassium type L zeolite
CN1197902C (en) Polyimide material filled with nano zinc oxide
CN1218452A (en) Synthesis of solid, powdery rare earth carboxylates by precipitation method
CN1280332C (en) Manufacturing method of biodegradable high polymer material-polylactic acid
CN1052987C (en) Method for preparing modified styrene butadiene rubber powder used as toughness-increased agent for poly vinyl chloride
CN1618827A (en) C9 maleic anhydride copolymer and its preparation method
CN1272352C (en) Method for preparing partially crosslinked hydroexpansivity acrylate-acrylic acid copolymer
CN1078237C (en) Method for making industrial briquette
CN1243055C (en) High water absorbing and retaining composite containing calcined kaolin and method for preparing the same
CN1240767C (en) High water absorbing and retaining composite containing sericite and method for preparing the same
CN1240768C (en) polyacrylic ester/inorganics I/inorganics II ternary compound particle and process for producing the same
CN100344659C (en) Preparation of water phase suspended swelling graft polypropylene
CN1216972C (en) Mesoporous rare earth doped titanium dioxide electrorheological liquid
CN1974618A (en) High molecular resin and its prepn
CN1197886C (en) High-molecular resin and process for preparing the same

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
ASS Succession or assignment of patent right

Owner name: WUXI XISHEN DAILY CHEMICAL PRODUCTS CO., LTD.

Free format text: FORMER OWNER: WANG JIANXIN

Effective date: 20100715

C41 Transfer of patent application or patent right or utility model
TR01 Transfer of patent right

Effective date of registration: 20100715

Address after: East Town Xishan District Wuxi City, Jiangsu Province, the 214101 East Road No. 22

Patentee after: Wuxi Research Institute of Daily Chemical Products

Address before: East Town Xishan District Wuxi City, Jiangsu Province, the 214101 East Road No. 22

Patentee before: Wang Jianxin

CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20040107

Termination date: 20141230

EXPY Termination of patent right or utility model