CN105462006B - Antistatic butyronitrile gloves and preparation method thereof - Google Patents

Antistatic butyronitrile gloves and preparation method thereof Download PDF

Info

Publication number
CN105462006B
CN105462006B CN201510852327.6A CN201510852327A CN105462006B CN 105462006 B CN105462006 B CN 105462006B CN 201510852327 A CN201510852327 A CN 201510852327A CN 105462006 B CN105462006 B CN 105462006B
Authority
CN
China
Prior art keywords
antistatic
butyronitrile
butyronitrile gloves
gloves
clean
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.)
Active
Application number
CN201510852327.6A
Other languages
Chinese (zh)
Other versions
CN105462006A (en
Inventor
郭辉
林纯勇
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.)
Xinlun New Material Co.,Ltd.
Original Assignee
Shenzhen Selen Science & Technology 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
Application filed by Shenzhen Selen Science & Technology Co Ltd filed Critical Shenzhen Selen Science & Technology Co Ltd
Priority to CN201510852327.6A priority Critical patent/CN105462006B/en
Publication of CN105462006A publication Critical patent/CN105462006A/en
Application granted granted Critical
Publication of CN105462006B publication Critical patent/CN105462006B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K13/00Use of mixtures of ingredients not covered by one single of the preceding main groups, each of these compounds being essential
    • C08K13/02Organic and inorganic ingredients
    • AHUMAN NECESSITIES
    • A41WEARING APPAREL
    • A41DOUTERWEAR; PROTECTIVE GARMENTS; ACCESSORIES
    • A41D19/00Gloves
    • A41D19/0055Plastic or rubber gloves
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/24Crosslinking, e.g. vulcanising, of macromolecules
    • C08J3/26Crosslinking, e.g. vulcanising, of macromolecules of latex
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/02Elements
    • C08K3/06Sulfur
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/16Nitrogen-containing compounds
    • C08K5/34Heterocyclic compounds having nitrogen in the ring
    • C08K5/3442Heterocyclic compounds having nitrogen in the ring having two nitrogen atoms in the ring
    • C08K5/3445Five-membered rings
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/36Sulfur-, selenium-, or tellurium-containing compounds
    • C08K5/45Heterocyclic compounds having sulfur in the ring
    • C08K5/46Heterocyclic compounds having sulfur in the ring with oxygen or nitrogen in the ring
    • C08K5/47Thiazoles
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2309/00Characterised by the use of homopolymers or copolymers of conjugated diene hydrocarbons
    • C08J2309/02Copolymers with acrylonitrile
    • C08J2309/04Latex
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • C08K2003/2237Oxides; Hydroxides of metals of titanium
    • C08K2003/2241Titanium dioxide
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00Properties
    • C08L2201/04Antistatic

Abstract

The invention discloses a pair of antistatic butyronitrile gloves. The pair of butyronitrile gloves is mainly prepared from raw materials including butyronitrile latex, deionized water, potassium hydroxide, an accelerator, a vulcanizing agent, a catalyst, imidazolium salt type ionic liquid antistatic agents and the like. The problems that the domestic butyronitrile gloves for clean rooms have higher resistance and don't have an antistatic effect are solved; in the forming process of the gloves, the antistatic agents and butyronitrile latex have a cross-linking reaction, and the prepared butyronitrile gloves have the advantages of good antistatic effect and high cleanness and have the characteristics that the washability is good and the resistance value can be still maintained in the range from 106 omega to 108 omega after repeated ultra-clean washing. The invention further discloses a preparation method of the antistatic butyronitrile gloves. The butyronitrile gloves can be used in the environment of the clean rooms and plays a role in preventing static electricity and protecting operators and the environment of the clean rooms.

Description

A kind of antistatic butyronitrile gloves and preparation method thereof
Technical field
The present invention relates to a kind of glove and preparation method thereof, more particularly to a kind of antistatic gloves and preparation method thereof.
Background technology
With the required precision more and more higher of high-tech product, more and more many products are required in the dustless of cleaning relatively Production, packaging and test in room, operator need to put on special clothing system to protect clean room environment.Glove are used as this The important component part for planting clothing system is largely used in dust free room, can not only protect product and producing region to avoid personnel Pollution, while also protecting personnel to avoid the injury of harmful components in production technology.
Natural rubber has elasticity good, durable, and the features such as with good acid resistance, can make various sizes specification Product, early stage has been used as toilet's protective gloves, but it easily causes human allergy, existing because allergy causes abroad Dead case occurs, and due to the price continuous rise of natural emulsion, causes cost constantly to rise, these problem days of one's doom The popularization of natural emulsion glove is made.Nitrile rubber is polymerized by acrylonitrile and butadiene, and dustless butyronitrile gloves are mainly Made by impregnating the techniques such as NBR latex, molding, sulfuration, surface treatment, dustless cleaning, with superior puncture resistance, resisted Chemical, friction resistant and power is persistently dressed, seldom produce allergy, safer protection can be provided for user, it is adaptable to no The clean room environment of same level, is widely used in medical treatment, electronics and food service industry.But without the butyronitrile of antistatic process Glove surface resistance is 1011More than Ω, does not possess electrostatic-proof function, and electrostatic is produced in use, easily injury skin and Destruction product, and potential safety hazard is brought in some occasions, accordingly, it would be desirable to carry out antistatic process to it.
Chinese patent CN103932432A discloses a kind of antistatic high-cleanness butyronitrile gloves, and the program can be to a certain degree It is upper to solve the problems, such as antistatic performance, but the antistatic butyronitrile gloves are the addition antistatic additive in clean cleaning process, and this resists Electrostatic agent is attached to glove surface, easily comes off in later stage cleaning and using process, and antistatic property is difficult to persistently;Chinese patent CN104621800A discloses a kind of antistatic butyronitrile gloves production program, simply adds common anti-static liquid, antistatic effect Bad, antistatic additive is easily separated out, and loses electrostatic-proof function.Therefore need to develop that a kind of antistatic effect is good and antistatic property Lasting butyronitrile gloves, playing prevents electrostatic, protects the purpose of product, operator and clean room environment.
The content of the invention
Not good with antistatic butyronitrile gloves anti-static effect for domestic market toilet, antistatic performance is difficult to hold Long, the present invention provide that a kind of cleanliness factor is high, washability is good, after ultra-clean cleaning sheet resistance still 106~108Between Ω The good butyronitrile gloves of static electricity resistance, while providing a kind of manufacture method of the antistatic butyronitrile gloves.
The technical scheme that the present invention is provided is that a kind of antistatic butyronitrile gloves are mainly made including following raw material:Fourth 20~40 parts of nitrile latex, 55~80 parts of deionized water, 0.3~0.5 part of potassium hydroxide, 0.1~0.3 part of accelerator, vulcanizing agent 0.2 ~0.4 part, 0.3~0.5 part of catalyst, 0~0.8 part of titanium dioxide, 0.5~1.5 part of antistatic additive, the antistatic additive includes Imidazole salt ionic liquid.
The imidazole salt ionic liquid is the compound containing the logical formula (I) of subordinate,
In formula (I), X-Including Cl-Or Br-, saturated straight chains or branched hydrocarbyl of the R including 1~18 carbon atom.
The accelerator includes N tert butyl benzothiazole 2 sulfenamide, 2-mercaptobenzothiazole, hexamethylenetetramine Or tetraethylthiuram disulfide, preferred N tert butyl benzothiazole 2 sulfenamide.
The vulcanizing agent includes sulfur.
The catalyst includes Zinc Oxide or magnesium oxide.
The present invention also provides a kind of manufacture method of antistatic butyronitrile gloves, comprises the steps:
(1) get the raw materials ready, prepare antistatic additive, prepare coagulant solution and chlorine water, it is standby;
(2) fingerprint is cleaned, fingerprint is first cleaned in the acid solution that pH value is 2~3, then in the alkali that pH value is 11~14 Property solution in clean, then rinsed clean is dried in 45 DEG C of baking ovens;
(3) impregnation, by butyronitrile latex, deionized water, potassium hydroxide, accelerator, vulcanizing agent, catalyst and step (1) system Standby antistatic additive is added in mixer, is stirred and is prepared into antistatic butyronitrile latex liquid;
(4) impregnate, by the fingerprint after cleaning impregnate 30 DEG C of coagulant solutions about 1 minute, drop of hanging down, drying for the first time, first 30 DEG C of antistatic butyronitrile latex liquid of secondary dipping about 20 seconds, drop of hanging down, second drying, second 30 DEG C of dipping are prevented under rotary state Electrostatic butyronitrile latex liquid about 20 seconds, drop of hanging down, dry for the third time under rotary state;
(5) sizing, leaching, by the product crimping after third time drying, are placed in 120~150 DEG C of curing cage, are rotating Add heat cure, then leaching under state;
(6) clean, successively by the chlorine water and clean water prepared in step (1) of the glued membrane after leaching, then dry, take off Mould, reverse osmosis water continuous wash 3 times, 20~30 minutes every time, then continuously washed 2 times, every time 45~60 points with EDI deionized waters Clock, automatic spin-drying, then the infrared drying at 45 DEG C, obtain antistatic butyronitrile gloves.
The imidazole salt ionic liquid is the compound containing the logical formula (I) of subordinate,
In formula (I), X-Including Cl-Or Br-, saturated straight chains or branched hydrocarbyl of the R including 1~18 carbon atom.
The accelerator includes N tert butyl benzothiazole 2 sulfenamide, 2-mercaptobenzothiazole, hexamethylenetetramine Or tetraethylthiuram disulfide, preferred N tert butyl benzothiazole 2 sulfenamide.
The vulcanizing agent includes sulfur.
The catalyst includes Zinc Oxide or magnesium oxide.
The coagulant solution is mainly including the component of following weight portion:80~90 parts of deionized water, calcium nitrate 8~15 Part, 0.1~0.2 part of propylene glycol alginate, 1~2 part of antitack agent.
The chlorine water is configured to the chlorine water that concentration is 0.01mol/L.
The full ionic structure of imidazole salt ionic liquid imparts its excellent electric conductivity in the present invention, in butyronitrile gloves , there is vulcanization crosslinking reaction between butyronitrile latex, in butyronitrile in formative stage, the carbon-carbon double bond fracture of imidazole salt ionic liquid Scattered cross-linked structure mutually is formed in latex, due to the presence of cross-bond, the migration of antistatic additive is prevented, butyronitrile is made Glove possess permanent antistatic effect, and Jing after many ultra-clean cleanings, sheet resistance can still maintain 106~108Between Ω.This The glyoxaline ion liquid antistatic additive of invention not only can improve the antistatic property of butyronitrile gloves, can also improve accelerator Activation capacity, the interface cohesion for promoting catalyst and butyronitrile latex acts on, and accelerates butyronitrile latex and butyronitrile latex and antistatic The vulcanization crosslinking speed of agent, improves curing efficiency and crosslink density, and not only antistatic property is good for made butyronitrile gloves, resists quiet Electric effect is lasting, and tensile strength is big.
Specific embodiment
The present invention is expanded on further with reference to specific embodiment, but the present invention is not limited only to this.
Test in the embodiment of the present invention includes:
(1) antistatic performance test:Antistatic butyronitrile gloves are taken out from vacuum packaging, in 23 DEG C, 52% humidity bar Balance under part 24 hours, then test pad of finger to the resistance value of wrist.
(2) cleanliness factor test:Test liquid powder amount (LPC) and IC ions, an antistatic butyronitrile gloves are put into In 300mL ultra-pure waters, shake 5 minutes, tweezers take out glove, leave liquid as test fluid, LPC liquid phases are then used respectively Grain calculating instrument and ion chromatograph test LPC and IC elemental release amounts.
(3) tensile strength and elongation at break are tested:With reference to GB7543-2006《Single use antiseptic rubber surgery handss Set》.
Heretofore described imidazole salt method for synthesizing ionic liquid reacts as follows formula (I), X-Including Cl-Or Br-, R Including the saturated straight chain or branched hydrocarbyl of 1~18 carbon atom.
Embodiment 1:20 parts of butyronitrile latex liquid, 77.7 parts of deionized water, 0.5 part of potassium hydroxide, 2-mercaptobenzothiazole 0.3 Part, 0.2 part of sulfur, 0.3 part of magnesium oxide, 0.5 part of 1- vinyl -3- methylimidazole villaumites, 0.5 part of titanium dioxide.
The manufacture method of the present embodiment antistatic butyronitrile gloves is comprised the following steps:
(1) get the raw materials ready, prepare 1- vinyl -3- methylimidazole villaumite antistatic additive;By 83.9 parts of deionized water, calcium nitrate 15 Part, 0.1 part of propylene glycol alginate, 1 part of antitack agent are added in mixer and prepare coagulant solution, are stirred;Prepare The chlorine water of 0.01mol/L, it is standby;
(2) fingerprint is cleaned, fingerprint is first cleaned in the acid solution that pH value is 2, then in the alkaline solution that pH value is 14 Middle cleaning, then rinsed clean, dries in 45 DEG C of baking ovens;
(3) impregnation, by butyronitrile latex, deionized water, potassium hydroxide, 2-mercaptobenzothiazole, sulfur, magnesium oxide, dioxy Change titanium and 1- vinyl -3- methylimidazole villaumites to add in mixer by above-mentioned formula, stir and be prepared into antistatic butyronitrile Latex;
(4) impregnate, by the fingerprint after cleaning impregnate 30 DEG C of coagulant solutions about 1 minute, drop of hanging down, drying for the first time, first 30 DEG C of antistatic butyronitrile latex liquid of secondary dipping about 20 seconds, drop of hanging down, second drying, second 30 DEG C of dipping are prevented under rotary state Electrostatic butyronitrile latex liquid about 20 seconds, drop of hanging down, dry for the third time under rotary state;
(5) sizing, leaching, by the product crimping after third time drying, are placed in 120 DEG C of curing cage, in rotary state Down plus heat cure, then leaching;
(6) clean, successively by the glued membrane after the leaching chlorine water and clean water of 0.01mol/L, then drying, the demoulding, Reverse osmosis water continuous wash 3 times, 20 minutes every time, then with continuously washing 2 times of EDI deionized waters, 60 minutes every time, get rid of automatically It is dry, then the infrared drying at 45 DEG C, obtain antistatic butyronitrile gloves.
Embodiment 2:20 parts of butyronitrile latex liquid, 78.2 parts of deionized water, 0.5 part of potassium hydroxide, hexamethylenetetramine 0.3 Part, 0.2 part of sulfur, 0.3 part of magnesium oxide, 0.5 part of 1- vinyl -3- 1-Butyl-1H-imidazoles villaumite.
With embodiment 1, formula is changed to above-mentioned formula to the manufacture method of this embodiment antistatic butyronitrile gloves, in this embodiment It is not added with titanium dioxide.
Comparative example 2:20 parts of butyronitrile latex liquid, 78.7 parts of deionized water, 0.5 part of potassium hydroxide, hexamethylenetetramine 0.3 Part, 0.2 part of sulfur, 0.3 part of magnesium oxide.
With embodiment 2, formula is changed to above-mentioned formula to the manufacture method of this comparative example antistatic butyronitrile gloves.
Embodiment 3:30 parts of butyronitrile latex liquid, 67.4 parts of deionized water, 0.4 part of potassium hydroxide, hexamethylenetetramine 0.2 Part, 0.3 part of sulfur, 0.4 part of Zinc Oxide, 0.8 part of 1- vinyl -3- hexyl imidazoliums villaumite, 0.5 part of titanium dioxide.
The manufacture method of the present embodiment antistatic butyronitrile gloves is comprised the following steps:
(1) get the raw materials ready, prepare 1- vinyl -3- hexyl imidazolium villaumite antistatic additive;By 86.35 parts of deionized water, calcium nitrate 12 parts, 0.15 part of propylene glycol alginate, 1.5 parts of antitack agent add in mixers and prepare coagulant solution, stir; The chlorine water of 0.01mol/L is prepared, it is standby;
(2) fingerprint is cleaned, fingerprint is first cleaned in the acid solution that pH value is 3, then in the alkaline solution that pH value is 12 Middle cleaning, then rinsed clean, dries in 45 DEG C of baking ovens;
(3) impregnation, by butyronitrile latex, deionized water, potassium hydroxide, hexamethylenetetramine, sulfur, Zinc Oxide, 1- ethylene Base -3- hexyl imidazolium villaumites, titanium dioxide are added in mixer, are stirred and are prepared into antistatic butyronitrile latex liquid;
(4) impregnate, by the fingerprint after cleaning impregnate 30 DEG C of coagulant solutions about 1 minute, drop of hanging down, drying for the first time, first 30 DEG C of antistatic butyronitrile latex liquid of secondary dipping about 20 seconds, drop of hanging down, second drying, second 30 DEG C of dipping are prevented under rotary state Electrostatic butyronitrile latex liquid about 20 seconds, drop of hanging down, dry for the third time under rotary state;
(5) sizing, leaching, by the product crimping after third time drying, are placed in 140 DEG C of curing cage, in rotary state Down plus heat cure, then leaching;
(6) clean, successively by the chlorine water and clean water prepared in step (1) of the glued membrane after leaching, then dry, take off Mould, reverse osmosis water continuous wash 3 times, 30 minutes every time, then with continuously washing 2 times of EDI deionized waters, 45 minutes every time, automatically Dry, then the infrared drying at 45 DEG C, obtain antistatic butyronitrile gloves.
Embodiment 4:30 parts of butyronitrile latex liquid, 67.14 parts of deionized water, 0.4 part of potassium hydroxide, the N- tert-butyl group -2- benzos 0.2 part of thiazolesulfenamide, 0.33 part of sulfur, 0.42 part of Zinc Oxide, 0.84 part of 1- vinyl -3- n-octyl imidazoles villaumite, two 0.67 part of titanium oxide.
With embodiment 3, formula is changed to above-mentioned formula to the manufacture method of this embodiment antistatic butyronitrile gloves.
Comparative example 4:30 parts of butyronitrile latex liquid, 67.98 parts of deionized water, 0.4 part of potassium hydroxide, the N- tert-butyl group -2- benzos 0.2 part of thiazolesulfenamide, 0.33 part of sulfur, 0.42 part of Zinc Oxide, 0.67 part of titanium dioxide.
With embodiment 4, formula is changed to above-mentioned formula to the manufacture method of this comparative example antistatic butyronitrile gloves.
Comparative example 4 ':30 parts of butyronitrile latex liquid, 67.14 parts of deionized water, 0.4 part of potassium hydroxide, the N- tert-butyl group -2- benzos 0.2 part of thiazolesulfenamide, 0.33 part of sulfur, 0.42 part of Zinc Oxide, 0.84 part of anti-static liquid, 0.67 part of titanium dioxide.
With embodiment 4, formula is changed to above-mentioned formula to the manufacture method of this comparative example antistatic butyronitrile gloves.
Embodiment 5:40 parts of butyronitrile latex liquid, 56.4 parts of deionized water, 0.3 part of potassium hydroxide, tetraethyl base Flos Cymbidii Ensifolii 0.1 part of nurse, 0.4 part of sulfur, 0.5 part of Zinc Oxide, 1.5 parts of 1- vinyl -3- dodecyl imidazoles bromide, 0.8 part of titanium dioxide.
The manufacture method of the present embodiment antistatic butyronitrile gloves is comprised the following steps:
(1) get the raw materials ready, prepare 1- vinyl -3- dodecyl imidazole bromide antistatic additive;By 89.8 parts of deionized water, nitric acid 8 parts of calcium, 0.2 part of propylene glycol alginate, 2 parts of antitack agent are added in mixer and prepare coagulant solution, are stirred;Match somebody with somebody The chlorine water of 0.01mol/L processed, it is standby;
(2) fingerprint is cleaned, fingerprint is first cleaned in the acid solution that pH value is 3, then in the alkaline solution that pH value is 11 Middle cleaning, then rinsed clean, dries in 45 DEG C of baking ovens;
(3) impregnation, by butyronitrile latex, deionized water, potassium hydroxide, tetraethylthiuram disulfide, sulfur, Zinc Oxide, 1- vinyl -3- dodecyl imidazole bromides, titanium dioxide are added in mixer, are stirred and are prepared into antistatic butyronitrile latex Liquid;
(4) impregnate, by the fingerprint after cleaning impregnate 30 DEG C of coagulant solutions about 1 minute, drop of hanging down, drying for the first time, first 30 DEG C of antistatic butyronitrile latex liquid of secondary dipping about 20 seconds, drop of hanging down, second drying, second 30 DEG C of dipping are prevented under rotary state Electrostatic butyronitrile latex liquid about 20 seconds, drop of hanging down, dry for the third time under rotary state;
(5) sizing, leaching, by the product crimping after third time drying, are placed in 150 DEG C of curing cage, in rotary state Down plus heat cure, then leaching;
(6) clean, successively by the chlorine water and clean water prepared in step (1) of the glued membrane after leaching, then dry, take off Mould, reverse osmosis water continuous wash 3 times, 30 minutes every time, then with continuously washing 2 times of EDI deionized waters, 45 minutes every time, automatically Dry, then the infrared drying at 45 DEG C, obtain antistatic butyronitrile gloves.
Embodiment 6:40 parts of butyronitrile latex liquid, 57.2 parts of deionized water, 0.3 part of potassium hydroxide, tetraethyl base Flos Cymbidii Ensifolii 0.1 part of nurse, 0.4 part of sulfur, 0.5 part of Zinc Oxide, 1.5 parts of 1- vinyl -3- octadecyl imidazoles bromide.
With embodiment 5, formula is changed to above-mentioned formula to the manufacture method of this embodiment antistatic butyronitrile gloves, in this embodiment It is not added with titanium dioxide.
When above-described embodiment tests resistance, cleanliness factor, tensile strength, elongation at break and the sulfuration of antistatic butyronitrile gloves Between, test result is as shown in table 1 below.
The test of the resistance of butyronitrile gloves, cleanliness factor, tensile strength, elongation at break and cure time in the embodiment of table 1 Value
As shown in Table 1, do not add the butyronitrile gloves resistance value of antistatic additive very big, such as comparative example 2 and comparative example 4, antistatic Poor performance;And select common anti-static liquid as antistatic additive, such as comparative example 4 ', Jing after 5 ultra-clean cleanings, resistance still compared with Greatly, antistatic effect is poor;The antistatic butyronitrile gloves of present invention resistance Jing after 5 ultra-clean washings is less, is still maintained at 106~ 108Between Ω, its antistatic property is illustrated preferably, and washing fastness is good, this is because the imidazole salt ion that the present invention is selected , in butyronitrile gloves formative stage, there is vulcanization crosslinking between butyronitrile latex and react the network structure to form crosslinking in antistatic additive, These network structures can eliminate passage as electric charge, so as to reduce resistance;And the cross-bond for being formed is prevented from antistatic Agent is migrated, it is ensured that antistatic additive stable dispersion in butyronitrile gloves, makes butyronitrile gloves possess permanent antistatic effect, and Jing is more After secondary ultra-clean washing, resistance value is still relatively low.
Can also be learnt by data in table, in the butyronitrile latex using same concentrations, the liquid of butyronitrile gloves of the present invention is sent out Dust quantity and ion concentration are relatively low, illustrate that butyronitrile gloves cleanliness factor of the present invention is higher, this is because the antistatic butyronitrile handss of the present invention Set surface is difficult stored charge, is difficult to adsorb dust, at the same in inventive formulation each COMPONENTS COMPATIBILITY preferably, the grit for coming off compared with It is few.Titanium dioxide is added in the present invention, can play a part of to brighten, be alternatively arranged as carrier, be effectively facilitated vulcanizing agent, promote Enter the dispersibility and stability of agent and catalyst in butyronitrile latex, further improve the cleanliness factor of butyronitrile gloves.In addition, this Antistatic additive in bright improves curing efficiency, reduces cure time, enhances tensile strength, this is because the miaow of the present invention Azole ionic liquid antistatic additive can improve the activation capacity of accelerator, promote catalyst to make with the interface cohesion of butyronitrile latex With, the vulcanization crosslinking speed of butyronitrile latex and butyronitrile latex and antistatic additive is accelerated, curing efficiency and crosslink density are improve, Made butyronitrile gloves antistatic property is good, and persistently, tensile strength is big for antistatic effect.

Claims (7)

1. a kind of antistatic butyronitrile gloves, it is characterised in that be mainly made including following raw material:Butyronitrile latex 20~40 Part, 55~80 parts of deionized water, 0.3~0.5 part of potassium hydroxide, 0.1~0.3 part of accelerator, 0.2~0.4 part of vulcanizing agent, catalysis 0.3~0.5 part of agent, 0~0.8 part of titanium dioxide, 0.5~1.5 part of antistatic additive, the antistatic additive includes imidazole salt ion Liquid, described imidazole salt ionic liquid is the compound containing following logical formula (I)s,
In formula (I), X-Including Cl-Or Br-, saturated straight chains or branched hydrocarbyl of the R including 1~18 carbon atom.
2. antistatic butyronitrile gloves according to claim 1, it is characterised in that described accelerator include the N- tert-butyl groups- 2-[4-morpholinodithio sulfenamide, 2-mercaptobenzothiazole, hexamethylenetetramine or tetraethylthiuram disulfide.
3. antistatic butyronitrile gloves according to claim 1, it is characterised in that described accelerator include the N- tert-butyl groups- 2-[4-morpholinodithio sulfenamide.
4. antistatic butyronitrile gloves according to claim 1, it is characterised in that described vulcanizing agent includes sulfur.
5. antistatic butyronitrile gloves according to claim 1, it is characterised in that described catalyst includes Zinc Oxide or oxygen Change magnesium.
6. the manufacture method of the antistatic butyronitrile gloves described in claim 1, it is characterised in that comprise the steps:
(1) get the raw materials ready, prepare antistatic additive, prepare coagulant solution and chlorine water, it is standby;
(2) clean fingerprint, fingerprint first cleaned in the acid solution that pH value is 2~3, then pH value be 11~14 it is alkaline molten Clean in liquid, then rinsed clean, dry in 45 DEG C of baking ovens;
(3) impregnation, prepared by butyronitrile latex, deionized water, potassium hydroxide, accelerator, vulcanizing agent, catalyst and step (1) Antistatic additive is added in mixer, is stirred and is prepared into antistatic butyronitrile latex liquid;
(4) impregnate, fingerprint 30 DEG C of the dipping coagulant solution 1 minute after cleaning, drop of hanging down, for the first time drying, first time are impregnated 30 DEG C of antistatic butyronitrile latex liquid 20 seconds, drop of hanging down, under rotary state second drying, impregnate 30 DEG C of antistatic butyronitrile second Latex 20 seconds, drop of hanging down, dry for the third time under rotary state;
(5) sizing, leaching, by the product crimping after third time drying, are placed in 120~150 DEG C of curing cage, in rotary state Down plus heat cure, then leaching;
(6) clean, successively by the chlorine water and clean water prepared in step (1) of the glued membrane after leaching, then drying, the demoulding, Reverse osmosis water continuous wash 3 times, 20~30 minutes every time, then with continuously washing 2 times of EDI deionized waters, 45~60 minutes every time, Automatic spin-drying, then the infrared drying at 45 DEG C, obtain antistatic butyronitrile gloves.
7. the manufacture method of antistatic butyronitrile gloves according to claim 6, it is characterised in that described coagulant solution Mainly including the component of following weight portion:80~90 parts of deionized water, 8~15 parts of calcium nitrate, propylene glycol alginate 0.1~ 0.2 part, 1~2 part of antitack agent.
CN201510852327.6A 2015-11-30 2015-11-30 Antistatic butyronitrile gloves and preparation method thereof Active CN105462006B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201510852327.6A CN105462006B (en) 2015-11-30 2015-11-30 Antistatic butyronitrile gloves and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510852327.6A CN105462006B (en) 2015-11-30 2015-11-30 Antistatic butyronitrile gloves and preparation method thereof

Publications (2)

Publication Number Publication Date
CN105462006A CN105462006A (en) 2016-04-06
CN105462006B true CN105462006B (en) 2017-04-19

Family

ID=55600199

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201510852327.6A Active CN105462006B (en) 2015-11-30 2015-11-30 Antistatic butyronitrile gloves and preparation method thereof

Country Status (1)

Country Link
CN (1) CN105462006B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2021234651A1 (en) * 2020-05-22 2021-11-25 P.T. Medisafe Technologies Synthetic rubber latex compositions with ionic liquid for elastomeric gloves

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106397894B (en) * 2016-08-31 2018-05-29 苏州鸿博斯特超净科技股份有限公司 A kind of preparation method of butyronitrile gloves
JP6871383B2 (en) * 2016-12-15 2021-05-12 シントマー スンディリアン ブルハド Curable Polymer Latex Composition for Rubber Products Manufacturing
CN106835721A (en) * 2017-01-17 2017-06-13 南通强生安全防护科技股份有限公司 The preparation method of Graphene NBR latex frosted gloves
CN106835720A (en) * 2017-01-17 2017-06-13 南通强生安全防护科技股份有限公司 A kind of preparation method of NBR latex frosted gloves
CN107048542B (en) * 2017-05-23 2019-01-22 石家庄鸿欣橡胶制品有限公司 The disposably low halogen gloves of dustless butyronitrile and its preparation process
KR102164253B1 (en) * 2017-10-18 2020-10-12 주식회사 엘지화학 Method for preparing graft copolymer complex, graft copolymer complex and thermoplastic resin composition comprising the graft copolymer complex
CN107791544A (en) * 2017-11-27 2018-03-13 东莞久林吉良净化用品有限公司 A kind of method for reducing butyronitrile gloves grit and zwitterion content
CN108384078B (en) * 2018-02-24 2021-03-05 山东星宇手套有限公司 Preparation method of conductive protective colloid gloves
CN108822371A (en) * 2018-06-29 2018-11-16 镇江华扬乳胶制品有限公司 A kind of preparation method of high-cleanness Antistatic type emgloves
CN109354731A (en) * 2018-09-23 2019-02-19 南通嘉得利安全用品有限公司 A kind of antistatic protective gloves and preparation method thereof
CN110394930B (en) * 2019-07-29 2021-04-06 南通成德乳胶制品有限公司 Production method of disposable antistatic rubber surgical gloves
CN112720975A (en) * 2020-12-21 2021-04-30 山东巨辉石油科技有限公司 Hydrophobic wear-resistant labor protection gloves and manufacturing process thereof
CN115008660A (en) * 2022-05-16 2022-09-06 河北鸿泽塑胶科技有限公司 Preparation process of soft light and thin butyronitrile gloves

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008044546A1 (en) * 2006-10-06 2008-04-17 Kuraray Co., Ltd. Polymer solid electrolyte, electrochemical device, and actuator element
JP5737512B2 (en) * 2011-06-30 2015-06-17 大日本印刷株式会社 Adhesive composition, adhesive sheet, and laminate
CN104621800A (en) * 2013-11-11 2015-05-20 江苏东菱塑胶有限公司 Butyronitrile glove preventing static and production method thereof
CN103932432B (en) * 2014-05-04 2016-03-23 河北鸿森塑胶科技有限公司 Disposable antistatic high-cleanness butyronitrile gloves preparation and treatment process
CN104212106B (en) * 2014-08-15 2016-08-24 深圳市新纶科技股份有限公司 Antistatic agent composition, anti-static thermoplastic compound resin composition and products formed

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2021234651A1 (en) * 2020-05-22 2021-11-25 P.T. Medisafe Technologies Synthetic rubber latex compositions with ionic liquid for elastomeric gloves

Also Published As

Publication number Publication date
CN105462006A (en) 2016-04-06

Similar Documents

Publication Publication Date Title
CN105462006B (en) Antistatic butyronitrile gloves and preparation method thereof
CN106397894B (en) A kind of preparation method of butyronitrile gloves
CN1137186C (en) Gloves constructed from neoprene copolymers and method of making same
CN109796640A (en) A kind of wear-resisting antiskid emgloves and preparation method thereof
KR102658786B1 (en) Water-Based Hydrogel Blend Coatings and Methods of Application to Elastomeric Articles
CN106213629A (en) A kind of preparation method of double-layer rubber glove
CN109354731A (en) A kind of antistatic protective gloves and preparation method thereof
CN103980562A (en) Rubber glove with antimicrobial and skin care functions
EP2020427A1 (en) Glove and process for manufacturing the same
CN110317380A (en) A kind of butyronitrile gloves and preparation method thereof
CN111333928A (en) Novel antistatic butyronitrile gloves and preparation method thereof
CN107841069A (en) A kind of PVC based composition and use thereof in packaging, foaming PVC gloves and preparation method thereof
CN1200132A (en) Improved methods for reducing allergenicity of natural rubber latex articles
CN104341570A (en) Antibacterial PU shoe material and preparation method thereof
JPS58186677A (en) Foamable silicone composition for treating fiber product
CN110951130A (en) Chemical protective gloves and preparation method thereof
US20040031086A1 (en) Low protein natural latex articles
US2526431A (en) Method of making rubber coated fabric articles
CN112778589B (en) Anti-aging butyronitrile material and application thereof
CN106702749A (en) Textile fabric surface modification treatment agent and preparation method thereof
CN103980563A (en) Allergy-free operating glove
CN103613802B (en) A kind of medical rubber glove and preparation method thereof
CN108623858A (en) A kind of acid cure polymerizing preparation method of medical gloves
CN109943078A (en) It is a kind of can selfreparing silica-gel gloves preparation method
KR100899678B1 (en) Down and processing method of down

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant
CP03 Change of name, title or address

Address after: 518000 32 / F, Haibin Huanqing building, 24 Futian Road, Weizhen community, Futian street, Shenzhen, Guangdong

Patentee after: Xinlun New Material Co.,Ltd.

Address before: 518000 room 314-315, Nanshan knowledge service building, No. 1 Qilin Road, Nanshan District, Shenzhen, Guangdong Province

Patentee before: SHENZHEN SELEN SCIENCE & TECHNOLOGY Co.,Ltd.

CP03 Change of name, title or address