Replication of liner collapse phenomenon observed in hyperbaric type IV hydrogen storage vessel by explosive decompression experiments

An experimental design based on representative sample is described in order to reproduce the detachment and deformation of the inner polymer layer (called liner) of hyperbaric hydrogen storage vessels during the emptying step. It is the first step of a better understanding of the mechanisms involved in the creation of a liner collapse. Results showed that a hydraulic testing machine fitted with a pressure hydrogen chamber enables to create a liner collapse on small samples by explosive decompression experiments. Tomographic observations have revealed that the collapse appears at the polymer liner/composite interface in areas that are not sufficiently bonded, nor consistently. Determination of liner collapse amplitudes, assessed by tomography, has underlined that, under some specific conditions, the deformation of the liner is permanent even when hydrogen has completely desorbed from the sample. In addition to liner collapses, composite cracks were also highlighted.     

锦纶莱卡包覆纱拉伸性能与包覆度的关系

用一定规格的锦纶丝、莱卡长丝在空心锭纺纱机上纺制了一系列不同包覆度的锦纶莱卡包覆纱,并对其成纱性能进行了拉伸试验分析,得到了包覆纱断裂强力、断裂伸长率与包覆度之间的相应规律.     

尼龙织物圆网印花的常见疵病与防止

尼龙织物圆网印花的绝大部分疵病是在印花机上直接产生的。本文简要分析常用生产工艺条件下印花疵病的产生原因并提出解决措施。     

尼龙织物圆网印花技术

从制版、配浆、印花、汽蒸和水洗固色后处理等方面，详细介绍尼龙织物圆网印花生产的工艺配方和操作技术特点，并对生产中常见的疵点进行分析，提出相应的解决措施。     

聚苯醚／聚酰胺合金的进展

介绍了聚苯醚／聚酰胺合金的开发现状,主要性能、应用领域及技术进展。     

Toxicity and Biodegradability Behavior of Xenobiotic Chemicals Before and After Ozonation: A Case Study with Commercial Textile Tannins

Ozonation of a natural tannin (NT; COD_o?=?1195 mg/L; TOC_o?=?342 mg/L; BOD_5,o?=?86 mg/L) and a synthetic tannin ST; COD_o?=?465 mg/L; TOC_o?=?55 mg/L; BOD_5,o?=?6 mg/L) being frequently applied in the polyamide dyeing process was investigated. Synthetic wastewater samples containing these tannins individually were prepared and subjected to ozonation at varying ozone doses (625– 1250 mgO₃/L wastewater), at pH?=?3.5 (the application pH of tannins) and pH?=?7.0 at an ozone dose of 1125 mgO₃/L wastewater. The collective environmental parameters COD, TOC, BOD₅, UV₂₅₄ and UV₂₈₀ (UV absorbance at 254 nm and 280 nm, representing aromatic and unsaturated moieties, respectively) were followed during ozonation. Changes in the biodegradability of the tannins were evaluated in terms of BOD₅ measurements conducted before and after ozonation. In addition, activated sludge inhibition tests employing heterotrophic biomass were run to elucidate the inhibitory effect of raw and ozonated textile tannins towards activated sludge biomass. Partial oxidation (45% COD removal at an ozone dose of 750 mg O₃/L wastewater and pH?=?3.5) of ST was sufficient to achieve elimination of its inhibitory effect towards heterotrophic biomass and acceptable biodegradability improvement, whereas the inhibitory effect and biodegradability of NT could not be reduced via ozonation under the same reaction conditions.     

用聚丙烯酸酯乳液提高轮胎帘线储存稳定性

研究了一种自交联型五元共聚聚丙烯酸酯乳液的单体种类和配比、加料顺序、表面活性剂的种类和用量、引发剂用量等合成工艺因素与乳液稳定性及其增粘和防紫外线、臭氧老化的关系。用这种乳液改性的ＲＦＬ浸渍液处理锦纶６６轮胎帘线，可以显著改善帘线的储存稳定性。     

Thermally reversible cross-linked polyamides and thermo-responsive gels by means of Diels-Alder reaction

Cross-linked polyamides and polyamide gels were prepared from maleimide-containing polyamides and a tri-functional furan compound and showed thermal reversibility in cross-linking behavior and in gel formation through Diels-Alder (DA) and retro-DA reactions. The rate constant k of the DA cross-linking reaction were 1.25-4.83×10⁻⁵ dm³ mol⁻¹ s⁻¹ in the temperature range of 20-60 °C with an activation energy of 32.1 kJ mol⁻¹. The cross-linking densities, thermal properties, and thermal reversibility of the polyamides/furan polymers were adjustable with the contents of maleimide groups in polyamides.     

Structure characterization of heat set and drawn polyamide 66 fibers by FTIR spectroscopy

Structural changes that occur during thermally induced and strain induced crystallization of polyamide 66 fibers were studied by infrared spectroscopy, density measurement and optical microscopy. Two bands at 924 and 1136 cm^–1 were shown to arise from the amorphous phase and assignment of the bands at 936 and 1200 cm^–1 to the crystalline phase were confirmed. We demonstrated that two different infrared spectroscopic methods could be used to determine the total crystallinity of polyamide 66 fibers. One is a calibration method in which the band ratio of 1200 and 1630 cm^–1 is plotted against the crystallinity measured by density measurements. The other one is an independent infrared method. Crystallinity obtained by the independent infrared spectroscopic method showed good agreement with crystallinity observed by density measurement. Infrared dichroism was used to obtain the crystalline orientation using the band at 936 cm^–1. The transition moment angle of 48° was found for the band at 936 cm^–1 with respect to chain axis. Amorphous orientation was obtained using Stein’s equation. Received: 18 September 2000 / Reviewed and accepted: 20 September 2000