A kind of preparation method of gas chromatography sample pad

A technology for gas chromatography and sampling pads, which is applied in the field of preparation of gas chromatography sampling pads, can solve the problems of increased cost, decreased air tightness, and inability to effectively reduce the loss of sampling pads, so as to achieve reduced loss, improved mechanical properties, The effect of increasing strength

Active Publication Date: 2022-02-15
浙江迪特西科技有限公司
View PDF5 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] The gas chromatography injection port septa prepared by the prior art fail to solve the problem of high temperature aging and degradation of the injection pad from the material point of view, resulting in the loss of the injection pad cannot be effectively reduced, and the number of times the injection pad is used Therefore, it is of great significance to develop a gas chromatography inlet septum with low loss at high temperature, no adhesion at the inlet, and good sealing performance after repeated use.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • A kind of preparation method of gas chromatography sample pad
  • A kind of preparation method of gas chromatography sample pad
  • A kind of preparation method of gas chromatography sample pad

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0036] Step 1, raw material pretreatment: 100g siloxane raw rubber, 35g hydrophobic modified white carbon black, 5g iron oxide, 0.5g iron trimethylsilanol at 130 o Mixing at C for 3h, then mixing in a mixture of 0.6g 2,4-dichlorodibenzoyl peroxide and 10g hydroxyl-terminated dimethyl silicone oil to obtain pretreated raw materials;

[0037] Step 2, vulcanization molding: add the pretreated raw materials into the injection pad mold of the flat vulcanizer, and o C, pre-vulcanized molding at 9Mpa for 30 minutes to obtain a pre-vulcanized injection pad;

[0038] Step 3, post-vulcanization: put the pre-vulcanized sampling pad in a blast oven at 250 o C under treatment for 24h, to obtain a vulcanized sampling pad;

[0039]Step 4, plasma treatment: place the vulcanized sample pad in the plasma source to treat the surface, the frequency of the plasma source is 2.45GHZ, the output power is 300W, the vacuum chamber pressure is 110Pa, and the processing time is 30min to obtain the gas ...

Embodiment 2

[0046] Step 1, raw material pretreatment: 100g siloxane raw rubber, 36.8g hydrophobically modified white carbon black, 6.3g titanium dioxide, 0.7g1,1'-bis(dimethylsilyl)ferrocene at 135.4 o Mixing at C for 2.6h, then mixed with a mixture of 0.7g tert-butyl peroxybenzoate and 10.6g hydroxy-terminated methylphenyl silicone oil, to obtain pretreated raw materials;

[0047] Step 2, vulcanization molding: add the pretreated raw materials into the injection pad mold of the flat vulcanizer, at 164 o C, pre-vulcanized molding at 10.4Mpa for 26.7min to obtain a pre-vulcanized injection pad;

[0048] Step 3, post-vulcanization: put the pre-vulcanized sampling pad in a blast oven at 245 o C under treatment for 26.4h, to obtain a vulcanized sampling pad;

[0049] Step 4, plasma treatment: place the vulcanized sampling pad in the plasma source to treat the surface, the frequency of the plasma source is 2.45GHZ, the output power is 336W, the pressure of the vacuum chamber is 117.8Pa, and ...

Embodiment 3

[0056] Step 1, raw material pretreatment: 100g siloxane raw rubber, 38.9g hydrophobic modified white carbon black, 7.6g chromium trioxide, 0.9g trimethylsilanol iron at 139 o Mixing at C for 2h, then mixed with a mixture of 0.8g di-tert-butyl peroxide and 11.7g hydroxyl-terminated diphenyl silicone oil, to obtain pretreated raw materials;

[0057] Step 2, vulcanization molding: add the pretreated raw materials into the injection pad mold of the flat vulcanizing machine, at 170.4 o C, pre-vulcanized molding at 10.9 Mpa for 25.2 minutes to obtain a pre-vulcanized injection pad;

[0058] Step 3, post-vulcanization: put the pre-vulcanized sample pad into the blast oven, o C under treatment for 33.1h, to obtain a vulcanized sampling pad;

[0059] Step 4, plasma treatment: place the vulcanized injection pad in the plasma source to treat the surface, the frequency of the plasma source is 2.45GHZ, the output power is 368W, the pressure in the vacuum chamber is 121.4Pa, and the treat...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

PropertyMeasurementUnit
specific surface areaaaaaaaaaaa
specific surface areaaaaaaaaaaa
specific surface areaaaaaaaaaaa
Login to view more

Abstract

The invention discloses a method for preparing a gas chromatography sample pad, which comprises the following steps: Step 1, raw material pretreatment: raw siloxane rubber, hydrophobic modified white carbon black, toner, and high-temperature-resistant additives are mixed at 130- 160 o Mixing at C for 1-3h, then mixed with the mixture of vulcanizing agent and silicone oil to obtain the pretreatment raw material; Step 2, vulcanization molding: adding the pretreatment raw material into the injection pad mold of the flat vulcanizer, at 160-200 o C, 9-14 Mpa pre-vulcanization molding 15-30min, to obtain a pre-vulcanized injection pad; step 3, post-vulcanization: put the pre-vulcanized injection pad into a blast oven, at 200-250 o C under treatment for 24-48h to obtain a vulcanized sampling pad; Step 4, plasma treatment: place the vulcanized sampling pad in a plasma source to treat the surface, the frequency of the plasma source is 2.45GHZ, the output power is 300-500W, and the vacuum The pressure in the chamber is 110-140Pa, and the processing time is 10-30min to obtain a gas chromatography sampling pad. The sample injection pad obtained by the invention has lower high temperature loss, higher strength and rebound sealing performance.

Description

technical field [0001] The invention relates to the field of polymer materials, in particular to a preparation method of a gas chromatography sample pad. Background technique [0002] Gas chromatography plays an important role in the convenience of sample composition analysis, and is an indispensable analysis method in the modern chemical and material industries. As a part of gas chromatography, the gas chromatography injection pad has a significant impact on the performance of the gas chromatography. The high-quality injection port septum will not introduce impurities during the gas chromatography analysis process, so that the obtained spectrum has no background noise. The influence greatly improves the accuracy of spectrum detection. [0003] However, most gas chromatographic septa degrade at high temperature during use, and the small molecules inside will diffuse into the gas chromatograph, causing background interference in the gas chromatograph, thus requiring updated ...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Patents(China)
IPC IPC(8): C08L83/08C08L83/04C08K9/06C08K7/26C08K5/14C08K5/56C08K3/22C08K13/06C08K3/30
CPCC08L83/08C08K2003/2265C08K2003/2241C08K2003/2251C08K2003/3027C08L2201/08C08L2205/02C08L2201/14C08L83/04C08K9/06C08K7/26C08K5/14C08K5/56C08K3/22C08K13/06C08K3/30
Inventor 傅强韩强俞慧萍付晓苗周游
Owner 浙江迪特西科技有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap