开发和验证一种改进的基于薄膜固相微萃取的标准气体产生瓶,用于可重复产生气体标准

ty10086 提交于 周三, 08/25/2021 - 16:38
文章英文标题
Development and validation of an improved, thin film solid phase microextraction based, standard gas generating vial for the repeatable generation of gaseous standards
正文
本文介绍了一种适用于GC-MS分析和质量控制的可重复生成气体标准的新型薄膜固相微萃取( TF-SPME )标准气体发生瓶的研制与验证。用纯聚二甲基硅氧烷( PDMS )、二乙烯基苯( DVB / PDMS )、亲水亲油平衡( HLB / PDMS )和Carboxen ( Car / PDMS )负载的碳网膜制备了小瓶,然后用改进的McReynolds标准加入苯、2 -戊酮、1 -硝基丙烷、吡啶、1 -戊醇、辛烷、十二烷和十六烷。吸附强度按照上述顺序确定,纯PDMS的吸附能力最弱,Car / PDMS的吸附能力最强。虽然更弱的纯PDMS气体产生瓶将McReynolds探针的仪器超负荷量转移到用于萃取的1.1   mm DVB / PDMS SPME箭头上,但使用Car / PDMS TF-SPME作为吸附剂制备的瓶未能提供比1 -硝基丙烷更易挥发性的分析物的持续可检测量。研究发现,DVB / PDMS和HLB / PDMS基小瓶能够保持对被测分析物的最佳吸附能力,提供足够强的吸附强度,在10次重复运行中不会出现任何耗尽,同时仍能提供一贯量的常规McReynolds组分。此外,所有分析物的活体内RSD均小于5 %,HLB和DVB瓶均具有良好的重复性。将瓶子有目的地提交200个加速耗尽萃取物( 1.1   mm DVB / PDMS箭头,55℃,3   min )后,DVB / PDMS制备的瓶子耗尽量分别为33 %、38 %、34 %、33 %、40 %和33 %,HLB / PDMS制备的瓶子耗尽量分别为苯、2 -戊酮、1 -硝基丙烷、吡啶、1 -戊醇和辛烷的21 %、16 %、12 %、31 %、16 %和0 %。采用用户典型萃取条件( 50 / 30 μm DVB / Car / PDMS固相微萃取纤维,35℃萃取1 min ),HLB / PDMS固相微萃取瓶未发现损耗,300次萃取/解吸循环后,相对标准偏差为1.1 ~ 3.0 %。最后,为了验证DVB / PDMS的真实世界适用性,利用DVB / PDMS小瓶对商用DVB / PDMS SPME箭头的纤维间重复性进行了评估,结果表明单个封装的箭头在统计上具有相似性( 95 %置信度下的方差分析)。
文章内容(英文)
This work presents the development and validation of novel thin film solid phase micro extraction (TF-SPME) based standard gas generating vials suitable for repeatable generation of gaseous standards for GC–MS analysis and quality control. The vials were developed using carbon mesh membranes loaded with pure polydimethylsiloxane (PDMS), divinylbenzene (DVB/PDMS), hydrophilic-lipophilic balance (HLB/PDMS), and carboxen (Car/PDMS) sorbents that were then spiked with modified McReynolds standards including benzene, 2-pentanone, 1-nitropropane, pyridine, 1-pentanol, octane, dodecane, and hexadecane. Sorbent strength was determined to follow the aforementioned order, with pure PDMS presenting the weakest sorption capabilities and Car/PDMS the strongest. While the weaker, pure PDMS based gas generating vials transferred an instrument-overloading amount of McReynolds probes to the 1.1 mm DVB/PDMS SPME arrows used for extraction, vials prepared using Car/PDMS TF-SPME as a sorbent failed to provide consistently detectable amounts of analytes less volatile than 1-nitropropane. The DVB/PDMS and HLB/PDMS based vials were found to maintain optimal sorption capabilities for the tested analytes, providing a sorption strength strong enough to not exhibit any depletion in 10 replicate runs, while still delivering a consistent amount of all the regular McReynolds components. Moreover, with intra-vial%RSDs of 5% or less for all analytes tested, these HLB and DVB vials were found to deliver very good repeatability. After purposely submitting vials to 200 accelerated depletion extractions (1.1 mm DVB/PDMS arrow at 55 °C for 3 min), vials prepared with DVB/PDMS were found to deplete by 33%, 38%, 34%, 33%, 40%, and 33% while vials prepared with HLB/PDMS were found to deplete by 21%, 16%, 12%, 31%, 16% and 0% for benzene, 2-pentanone, 1-nitropropane, pyridine, 1-pentanol, and octane, respectively. When user typical extractions conditions were used instead (50/30 μm DVB/Car/PDMS SPME fiber at 35 °C for 1 min), no depletion could be observed from the HLB/PDMS based vial while%RSDs ranged from 1.1–3.0% after the 300 extraction/desorption cycles. Finally, in efforts to demonstrate its real world applicability, the DVB/PDMS vial was used to evaluate the inter-fiber repeatability of commercial DVB/PDMS SPME arrows, with results demonstrating that arrows from a single package were statistically similar (ANOVA at 95% confidence).
来源出处
Journal|[J]Journal of Chromatography AVolume 1632, 2020. PP 461541-
DOI
https://doi.org/10.1016/j.chroma.2020.461541

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备注说明:

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