CN102608265B - 释放舱与被测试物接触的表面的处理方法 - Google Patents
释放舱与被测试物接触的表面的处理方法 Download PDFInfo
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- 239000002775 capsule Substances 0.000 title abstract 5
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- 239000010935 stainless steel Substances 0.000 claims abstract description 13
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- 229920001296 polysiloxane Polymers 0.000 claims description 24
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 16
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 9
- 239000003795 chemical substances by application Substances 0.000 claims description 9
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- 150000001875 compounds Chemical class 0.000 claims description 7
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- XLLIQLLCWZCATF-UHFFFAOYSA-N 2-methoxyethyl acetate Chemical compound COCCOC(C)=O XLLIQLLCWZCATF-UHFFFAOYSA-N 0.000 claims description 6
- 239000004593 Epoxy Substances 0.000 claims description 6
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 6
- 150000001412 amines Chemical class 0.000 claims description 6
- 150000004985 diamines Chemical class 0.000 claims description 6
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 102000004316 Oxidoreductases Human genes 0.000 claims description 4
- 108090000854 Oxidoreductases Proteins 0.000 claims description 4
- 239000004809 Teflon Substances 0.000 claims description 4
- 229920006362 Teflon® Polymers 0.000 claims description 4
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 claims description 4
- BCQZXOMGPXTTIC-UHFFFAOYSA-N halothane Chemical class FC(F)(F)C(Cl)Br BCQZXOMGPXTTIC-UHFFFAOYSA-N 0.000 claims description 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 4
- 239000000413 hydrolysate Substances 0.000 claims description 4
- 239000000463 material Substances 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 4
- 238000010422 painting Methods 0.000 claims description 4
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical class O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 claims description 4
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 claims description 4
- 235000012239 silicon dioxide Nutrition 0.000 claims description 4
- 229920002545 silicone oil Polymers 0.000 claims description 4
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 claims description 3
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical group COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 claims description 3
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 claims description 3
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 claims description 3
- KSMVBYPXNKCPAJ-UHFFFAOYSA-N 4-Methylcyclohexylamine Chemical compound CC1CCC(N)CC1 KSMVBYPXNKCPAJ-UHFFFAOYSA-N 0.000 claims description 3
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- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 claims description 3
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims description 3
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 claims description 3
- 239000004952 Polyamide Substances 0.000 claims description 3
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 3
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- IMUDHTPIFIBORV-UHFFFAOYSA-N aminoethylpiperazine Chemical compound NCCN1CCNCC1 IMUDHTPIFIBORV-UHFFFAOYSA-N 0.000 claims description 3
- 238000001354 calcination Methods 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 239000006229 carbon black Substances 0.000 claims description 3
- 230000007797 corrosion Effects 0.000 claims description 3
- 238000005260 corrosion Methods 0.000 claims description 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 3
- 230000008021 deposition Effects 0.000 claims description 3
- 239000000539 dimer Substances 0.000 claims description 3
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
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- 125000000524 functional group Chemical group 0.000 claims description 3
- 229910002804 graphite Inorganic materials 0.000 claims description 3
- 239000010439 graphite Substances 0.000 claims description 3
- 125000000623 heterocyclic group Chemical group 0.000 claims description 3
- 125000001841 imino group Chemical group [H]N=* 0.000 claims description 3
- ZETYUTMSJWMKNQ-UHFFFAOYSA-N n,n',n'-trimethylhexane-1,6-diamine Chemical compound CNCCCCCCN(C)C ZETYUTMSJWMKNQ-UHFFFAOYSA-N 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- 229920002647 polyamide Polymers 0.000 claims description 3
- 229920000768 polyamine Polymers 0.000 claims description 3
- 229920000570 polyether Polymers 0.000 claims description 3
- 238000006116 polymerization reaction Methods 0.000 claims description 3
- 229920001451 polypropylene glycol Polymers 0.000 claims description 3
- LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 claims description 3
- 238000007788 roughening Methods 0.000 claims description 3
- 229910000077 silane Inorganic materials 0.000 claims description 3
- 239000000741 silica gel Substances 0.000 claims description 3
- 229910002027 silica gel Inorganic materials 0.000 claims description 3
- 239000000377 silicon dioxide Substances 0.000 claims description 3
- 229920005573 silicon-containing polymer Polymers 0.000 claims description 3
- 239000011780 sodium chloride Substances 0.000 claims description 3
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 claims description 3
- 229960001124 trientine Drugs 0.000 claims description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 3
- 229920002554 vinyl polymer Polymers 0.000 claims description 3
- 238000001514 detection method Methods 0.000 abstract description 7
- 230000000274 adsorptive effect Effects 0.000 abstract 1
- 238000003754 machining Methods 0.000 abstract 1
- 230000001590 oxidative effect Effects 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 43
- 150000002894 organic compounds Chemical class 0.000 description 6
- 238000009434 installation Methods 0.000 description 4
- 239000005416 organic matter Substances 0.000 description 4
- 230000008569 process Effects 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000009835 boiling Methods 0.000 description 2
- 239000011229 interlayer Substances 0.000 description 2
- 239000004973 liquid crystal related substance Substances 0.000 description 2
- 239000002841 Lewis acid Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
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Abstract
本发明公开了一种释放舱与被测试物接触的表面的处理方法,该方法包括以下步骤:(一)、所述各部件由不锈钢或玻璃加工而成,部件为不锈钢构件时,先用酸氧化,再用有机溶剂及水清洗,或者氧化后进行电解,再用有机溶剂及水清洗;部件为玻璃构件时,采用HCL或HF腐蚀,或采用物理方法使部件表面粗糙化;(二)、在经过步骤(一)清洗后的部件的表面加工去活层,或者先在经过步骤(一)清洗后的部件的表面加工中间层,然后在中间层的表面加工去活层。降低了表面吸附力,能大大减少被测试物吸附在舱体内壁及各部件与被测试物接触的表面上,使得从采样管的所取得的样品中得到的检测值更接近于舱体内被测试物的实际值,能有效提高释放舱的检测精度。
Description
技术领域
本发明涉及一种气体挥发性有机物(VOC)、半挥发性有机物(SVOC)及高沸点有机物检测用测试装置内部与被测试物接触的表面的处理方法。
技术背景
传统气体挥发性有机物(VOC)、半挥发性有机物(SVOC)及高沸点有机物检测用测试装置,其舱体内壁及各部件与被测试物接触的表面,由于存在一些吸附被测试物的化学键或者较强的表面张力,使得被测试物吸附在舱体内壁及各部件与被测试物接触的表面上,很难吹扫下来。对于极性化合物,由于舱体内壁及各部件与被测试物接触的表面某些化学键的影响,吸附力更强。因此舱体内壁及各部件与被测试物接触的表面必须进行处理,使得测试装置内表面化学键,如氢键、硅醇基、路易氏酸活化点点被覆盖,被测试物容易吸附在舱体内壁及各部件与被测试物接触的表面上,而取样分析被测试物的含量时,是用从测试装置的采样管的所取得的样品进行检测,由于舱体内壁及各部件与被测试物接触的表面吸咐了大量的被测试物,导致从样品中得到的检测值低于舱体内被测试物的实际值,检测误差大,不能有效满足高精度的检测需要。
发明内容
本发明的目的在于克服现有技术中上述缺陷:提供一种释放舱与被测试物接触的表面的处理方法,能大大减少被测试物吸附在舱体内壁及各部件与被测试物接触的表面上,有效提高释放舱的检测精度。
为实现上述目的,本发明提供的技术方案如下:构造一种释放舱与被测试物接触的表面的处理方法,该释放舱包括以下部件:舱体,与舱体连接的舱门、进气管、排气管、采样管,装设在舱体内的搅拌风机,风道板,该方法用于对所述舱体、舱门、进气管、排气管、采样管、搅拌风机及风道板中至少一部件与被测试物接触的表面的进行处理,包括以下步骤:
(一)、所述各部件由不锈钢或玻璃加工而成,部件为不锈钢构件时,先用酸氧化,再用有机溶剂及水清洗,或者氧化后进行电解,再用有机溶剂及水清洗;部件为玻璃构件时,采用HCL或HF腐蚀,或采用物理方法使部件表面粗糙化;
(二)、在经过步骤(一)清洗后的部件的表面加工去活层,或者先在经过步骤(一)清洗后的部件的表面加工中间层,然后在中间层的表面加工去活层。
部件为不锈钢构件时,所述中间层的加工是将经过步骤(一)清洗后的部件采用通入单硅烷在500℃以上的高温条件下煅烧而成SiO2层;或者是在经过步骤(一)清洗后的部件的表面涂有机硅胶后在500℃以上的高温条件下煅烧而成SiO2层;或者涂聚硅氧烷类和环糊精衍生物,高温500度以上煅烧而成SiO2层.所述聚硅氧烷类是聚二甲基硅氧烷、含苯基聚硅氧烷、含氰基聚硅氧烷、含氟聚硅氧烷、加入乙烯基的聚硅氧烷、端烃基聚硅氧烷或者在分子链与官能团间引入间隔基的聚硅氧烷,环糊精衍生物;所述中间层或者是采用在制孔剂中加入不含来源于芳香族的碳原子及杂环的环氧化合物和胺化合物在60-200℃下发生聚合反应,形成凝胶物,然后涂在经过步骤(一)清洗后的部件表面,用溶剂清洗制孔剂,留下骨架相后干燥处理而成三维网状或孔状骨架相,所述制孔剂为甲基溶纤剂、乙基溶纤剂,乙二醇-甲醚乙酸酯、丙二醇-甲醚乙酸酯等酯类,聚乙二醇或者聚丙二醇,所述环氧化合物为2,2,2-三-(2,3-环氧丙基)-异氰尿酸酯,所述胺化合物为乙二胺、二亚乙基三胺、三亚乙基四胺、三缩四乙二胺、亚氨基双丙胺/双(六亚甲基)三胺、1,3,6-三氨基甲基己烷、聚亚甲基二胺、三甲基六亚甲基二胺、聚醚二胺、异佛尔酮二胺、薄荷烷二胺、N-氨基乙基哌嗪、3,9-双(3-氨丙基)2,4,8,10-四氧螺环、双(4-氨基环己基)甲烷或者由聚胺类与二聚酸构成的脂肪族聚酰胺类;部件为玻璃构件时,采用在部件表面沉积二氧化硅、氯化钠或者石墨碳黑来生成中间层。
所述去活层的加工是采用低表面张力的含氢硅油或者聚乙二醇涂或浸在中间层或者部件表面上并在300℃以上的高温条件下烘烤而成;所述去活层的加工或者是将经过步骤(一)清洗后的部件表面或者中间层表面涂或者浸SiO2溶胶后在300℃以上的高温条件下烘烤,用溶剂去除多余物质而成,SiO2溶胶成分为甲基三氧基硅烷和四乙氧基硅烷水解物;所述去活层的加工或者是将经过步骤(一)清洗后的部件表面或者中间层表面涂或者浸聚苯并咪唑吡咯酮(PY)、聚四氟乙烯、聚氟烷类、正硅酸脂或者正硅酸乙脂类后300℃以上的高温条件下烘烤而成。
本发明所述释放舱与被测试物接触的表面的处理方法的有益效果是:通过采用该方法在经过步骤(一)清洗后的部件的表面加工去活层,或者先在经过步骤(一)清洗后的部件的表面加工中间层,然后在中间层的表面加工去活层。降低了舱体内壁及各部件与被测试物接触的表面的表面张力,能大大减少被测试物吸附在舱体内壁及各部件与被测试物接触的表面上,使得从采样管的所取得的样品中得到的检测值更接近于舱体内被测试物的实际值,从而有效提高释放舱的检测精度。
下面结合附图和实施例对本发明所述的释放舱与被测试物接触的表面的处理方法作进一步说明:
附图说明
图1是本发明释放舱与被测试物接触的表面的处理方法所述的释放舱涂有中间层及去活层的结构示意图;
图2是图1的A-A剖视放大图;
图3是图1的B-B剖视放大图;
图4是本发明释放舱与被测试物接触的表面的处理方法所述的释放舱涂有覆盖层的结构示意图;
图5是图4的C-C剖视放大图;
图6是图4的D-D剖视放大图。
具体实施方式
以下本发明所述释放舱与被测试物接触的表面的处理方法的最佳实施例,并不因此限定本发明的保护范围。
实施例一,参照图1、图2、图3,提供一种释放舱与被测试物接触的表面的处理方法,该释放舱包括以下部件:舱体1,与舱体1连接的舱门2、进气管4、排气管5、采样管6,装设在舱体1内的搅拌风机7,风道板8,该方法用于对所述舱体1、舱门2、进气管4、排气管5、采样管6、搅拌风机7及风道板8中至少一部件与被测试物接触的表面的进行处理,包括以下步骤:
(一)、所述各部件由不锈钢或玻璃加工而成,部件为不锈钢构件时,先用酸氧化,再用有机溶剂及水清洗,或者氧化后进行电解,再用有机溶剂及水清洗;部件为玻璃构件时,采用HCL或HF腐蚀,或采用物理方法使部件表面粗糙化;
(二)、先在经过步骤(一)清洗后的部件的表面加工中间层9,然后在中间层9的表面加工去活层10。
所述中间层9为SiO2层,或者为三维网状或孔状骨架相,厚度为亚微米到微米厚度。
所述去活层10的厚度为亚微米到微米厚度,为液晶膜结构。
部件为不锈钢构件时,所述中间层9的加工是将经过步骤(一)清洗后的部件采用通入单硅烷在500℃以上的高温条件下煅烧而成SiO2层;或者是在经过步骤(一)清洗后的部件的表面涂或浸有机硅胶后在500℃以上的高温条件下煅烧而成SiO2层;或者涂或浸聚硅氧烷类和环糊精衍生物,高温500度以上煅烧而成SiO2层.所述聚硅氧烷类是聚二甲基硅氧烷、含苯基聚硅氧烷、含氰基聚硅氧烷、含氟聚硅氧烷、加入乙烯基的聚硅氧烷、端烃基聚硅氧烷或者在分子链与官能团间引入间隔基的聚硅氧烷;所述中间层9或者是采用在制孔剂中加入不含来源于芳香族的碳原子及杂环的环氧化合物和胺化合物在60-200℃下发生聚合反应,形成凝胶物,然后涂浸在经过步骤(一)清洗后的部件表面,用溶剂清洗制孔剂,留下骨架相后干燥处理而成三维网状或孔状骨架相,所述制孔剂为甲基溶纤剂、乙基溶纤剂,乙二醇-甲醚乙酸酯、丙二醇-甲醚乙酸酯等酯类,聚乙二醇或者聚丙二醇,所述环氧化合物为2,2,2-三-(2,3-环氧丙基)-异氰尿酸酯,所述胺化合物为乙二胺、二亚乙基三胺、三亚乙基四胺、三缩四乙二胺、亚氨基双丙胺/双(六亚甲基)三胺、1,3,6-三氨基甲基己烷、聚亚甲基二胺、三甲基六亚甲基二胺、聚醚二胺、异佛尔酮二胺、薄荷烷二胺、N-氨基乙基哌嗪、3,9-双(3-氨丙基)2,4,8,10-四氧螺环、双(4-氨基环己基)甲烷或者由聚胺类与二聚酸构成的脂肪族聚酰胺类;部件为玻璃构件时,采用在部件表面沉积二氧化硅、氯化钠或者石墨碳黑来生成中间层9。
所述去活层10的加工是采用低表面张力的有机化合物涂或浸在中间层9表面上并在300℃以上的高温条件下烘烤而成;所述去活层10的加工或者是将中间层9表面涂或者浸SiO2溶胶后在300℃以上的高温条件下烘烤,用溶剂去除多余物质而成,所述SiO2溶胶成分为甲基三氧基硅烷和四乙氧基硅烷水解物;所述去活层10的加工或者是将中间层9表面涂或者浸聚苯并咪唑吡咯酮(PY)、聚四氟乙烯、聚氟烷类、正硅酸脂或者正硅酸乙脂类后300℃以上的高温条件下烘烤而成。
所述低表面张力的有机化合物为含氢硅油或者聚乙二醇。
实施例二,参照图4、图5、图6,提供一种释放舱与被测试物接触的表面的处理方法,该释放舱包括以下部件:舱体1,与舱体1连接的舱门2、进气管4、排气管5、采样管6,装设在舱体1内的搅拌风机7,风道板8,该方法用于对所述舱体1、舱门2、进气管4、排气管5、采样管6、搅拌风机7及风道板8中至少一部件与被测试物接触的表面的进行处理,包括以下步骤:
(一)、所述各部件由不锈钢或玻璃加工而成,部件为不锈钢构件时,先用酸氧化,再用有机溶剂及水清洗,或者氧化后进行电解,再用有机溶剂及水清洗;部件为玻璃构件时,用有机溶剂及水清洗;
(二)直接在经过步骤(一)清洗后的部件的表面加工去活层10。
所述去活层10的厚度为亚微米到微米厚度,为液晶膜结构。
所述去活层10的加工是采用低表面张力的有机化合物涂或浸在部件表面上并在300℃以上的高温条件下烘烤而成;所述去活层10的加工或者是将经过步骤(一)清洗后的部件表面涂或者浸SiO2溶胶后在300℃以上的高温条件下烘烤,用溶剂去除多余物质而成,所述SiO2溶胶成分为甲基三氧基硅烷和四乙氧基硅烷水解物;所述去活层10的加工或者是将经过步骤(一)清洗后的部件表面涂或者浸聚苯并咪唑吡咯酮(PY、聚四氟乙烯、聚氟烷类、正硅酸脂或者正硅酸乙脂类后300℃以上的高温条件下烘烤而成。
所述低表面张力的有机化合物为含氢硅油或者聚乙二醇。
上述实施例为本发明较佳的实施方式,但本发明的实施方式并不受上述实施例的限制,其他的任何未背离本发明的精神实质与原理下所作的改变、修饰、替代、组合、简化,均应为等效的置换方式,都包含在本发明的保护范围之内。
Claims (3)
1.一种释放舱与被测试物接触的表面的处理方法,该释放舱包括以下部件:舱体(1),与舱体(1)连接的舱门(2)、进气管(4)、排气管(5)、采样管(6),装设在舱体(1)内的搅拌风机(7),风道板(8),该方法用于对所述舱体(1)、舱门(2)、进气管(4)、排气管(5)、采样管(6)、搅拌风机(7)及风道板(8)中至少一部件与被测试物接触的表面的进行处理,其特征在于,包括以下步骤:
(一)、所述各部件由不锈钢或玻璃加工而成,部件为不锈钢构件时,先用酸氧化,再用有机溶剂及水清洗,或者氧化后进行电解,再用有机溶剂及水清洗;部件为玻璃构件时,采用HCL或HF腐蚀,或采用物理方法使部件表面粗糙化;
(二)、在经过步骤(一)清洗后的部件的表面加工去活层(10),或者先在经过步骤(一)清洗后的部件的表面加工中间层(9),然后在中间层(9)的表面加工去活层(10);
所述去活层(10)的加工是采用低表面张力的含氢硅油或者聚乙二醇涂或浸在中间层(9)或者部件表面上并在300℃以上的高温条件下烘烤而成;所述去活层(10)的加工或者是将经过步骤(一)清洗后的部件表面或者中间层(9)表面涂或者浸SiO2溶胶后在300℃以上的高温条件下烘烤,用溶剂去除多余物质而成,SiO2溶胶成分为甲基三氧基硅烷和四乙氧基硅烷水解物;所述去活层(10)的加工或者是将经过步骤(一)清洗后的部件表面或者中间层(9)表面涂或者浸聚苯并咪唑吡咯酮(PY)、聚四氟乙烯、聚氟烷类、正硅酸脂或者正硅酸乙脂类后300℃以上的高温条件下烘烤而成。
2.根据权利要求1所述的释放舱与被测试物接触的表面的处理方法,其特征在于,所述中间层(9)为SiO2层,或者为三维网状或孔状骨架相,厚度为亚微米到微米厚度。
3.根据权利要求2所述的释放舱与被测试物接触的表面的处理方法,其特征在于,部件为不锈钢构件时,所述中间层(9)的加工是将经过步骤(一)清洗后的部件采用通入单硅烷在500℃以上的高温条件下煅烧而成SiO2层;或者是在经过步骤(一)清洗后的部件的表面涂或浸有机硅胶后在500℃以上的高温条件下煅烧而成SiO2层;或者涂或浸聚硅氧烷类和环糊精衍生物,高温500度以上煅烧而成SiO2层,所述聚硅氧烷类是聚二甲基硅氧烷、含苯基聚硅氧烷、含氰基聚硅氧烷、含氟聚硅氧烷、加入乙烯基的聚硅氧烷、端烃基聚硅氧烷或者在分子链与官能团间引入间隔基的聚硅氧烷;所述中间层(9)或者是采用在制孔剂中加入不含来源于芳香族的碳原子及杂环的环氧化合物和胺化合物在60-200℃下发生聚合反应,形成凝胶物,然后涂浸在经过步骤(一)清洗后的部件表面,用溶剂清洗制孔剂,留下骨架相后干燥处理而成三维网状或孔状骨架相,所述制孔剂为甲基溶纤剂、乙基溶纤剂,乙二醇-甲醚乙酸酯、丙二醇-甲醚乙酸酯等酯类,聚乙二醇或者聚丙二醇,所述环氧化合物为2,2,2-三-(2,3-环氧丙基)-异氰尿酸酯,所述胺化合物为乙二胺、二亚乙基三胺、三亚乙基四胺、三缩四乙二胺、亚氨基双丙胺/双(六亚甲基)三胺、1,3,6-三氨基甲基己烷、聚亚甲基二胺、三甲基六亚甲基二胺、聚醚二胺、异佛尔酮二胺、薄荷烷二胺、N-氨基乙基哌嗪、3,9-双(3-氨丙基)2,4,8,10-四氧螺环、双(4-氨基环己基)甲烷或者由聚胺类与二聚酸构成的脂肪族聚酰胺类;部件为玻璃构件时,采用在部件表面沉积二氧化硅、氯化钠或者石墨碳黑来生成中间层(9)。
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| US (1) | US20160122234A1 (zh) |
| EP (1) | EP2821784B1 (zh) |
| JP (1) | JP5938485B2 (zh) |
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| CN102590458A (zh) * | 2012-02-27 | 2012-07-18 | 东莞市升微机电设备科技有限公司 | 具有循环风道的释放舱 |
| CN103575923B (zh) * | 2013-10-16 | 2015-10-28 | 东莞市升微机电设备科技有限公司 | 多单元挥发性有机物测试系统 |
| CN104914901B (zh) * | 2015-05-20 | 2018-01-30 | 东莞市升微机电设备科技有限公司 | 可对各支路的温、湿度及流量进行均衡调节的微型挥发性有机物释放舱系统 |
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Also Published As
| Publication number | Publication date |
|---|---|
| CN102608265A (zh) | 2012-07-25 |
| EP2821784A1 (en) | 2015-01-07 |
| JP5938485B2 (ja) | 2016-06-22 |
| US20160122234A1 (en) | 2016-05-05 |
| EP2821784A4 (en) | 2015-11-04 |
| WO2013127149A1 (zh) | 2013-09-06 |
| EP2821784B1 (en) | 2019-11-13 |
| JP2015508505A (ja) | 2015-03-19 |
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