Reaction of sodium perborate with a chlorinated cyclic hindered amine (TMP-Cl): I. Quantitative evaluation of active oxygen species in fabric bleaching

The reaction of N-chloro-4-hydroxy-2,2,6,6-tetramethylpiperidine (TMP-Cl) with sodium perborate (PB) was investigated with special reference to the generation of singlet oxygen and the possible application to a new oxidative bleaching process. Generation of the singlet oxygen (¹O₂), the hydroxyl radical (HO·) and superoxide anion radical (O₂·⁻) in the PB/TMP-Cl mixed solution was confirmed by the trapping reagent method. From the results of another experiment, in which the bleaching abilities of each active oxygen species were confirmed, the main active oxygen species contributing to the bleaching of purpurogallin, the skeleton of black tea pigment, in the PB/TMP-Cl system was concluded to be¹O₂.     

PB/TAED对织物氧漂洗涤的损伤研究

采用含有PB/TAED活化氧漂体系的洗衣粉对活性染料上染的棉织物进行洗涤.设计正交实验,在不同染料、洗涤剂、温度等条件下测试织物洗后的拉伸断裂强力、K/S值、色差,得出各因素对织物性能的影响.为更好地进行织物护理提供依据.     

Cold pad–batch bleaching of cotton fabrics with a TAED/H2O2 activating system

The cold pad–batch bleaching of cotton fabrics using a tetra acetyl ethylene diamine/hydrogen peroxide (TAED/H₂O₂) activating system is investigated in this study. The effects of key bleaching parameters (hydrogen peroxide dosage, sodium hydroxide dosage, TAED/H₂O₂ mol ratio and batch time) on the bleaching efficiency were investigated by single‐factor analysis and orthogonal experiment analysis. The performance of the activator TAED in the cold pad–batch process was examined and the activating mechanism is discussed. The optimised bleaching recipe and processing conditions are reported, and the optimal activated bleaching process is also compared with a conventional cold pad–batch bleaching process. The results show that the optimised TAED/H₂O₂ activated bleaching system could achieve high quality cotton bleaching with comparable fabric whiteness to the conventional system at much shorter batch times, and with significantly reduced fabric strength loss and decreased alkali consumption, which would be beneficial to sustained development of the textile wet‐processing industry.     

不同疏水缔合聚合物之间协同效应的研究

将丙烯酰胺(AM)/丙烯酸钠(Na AA)/十六烷基二甲基烯丙基氯化铵(C16DMAAC)共聚物(PA),与丙烯酰胺(AM)/丙烯酸钠(Na AA)/2-丙烯酰胺基十四烷基磺酸钠(Na AMC14S)共聚物(PB)混合得到混合溶液PA/PB。在5 000 mg/L Na Cl溶液中,固定聚合物质量浓度为2 000 mg/L的条件下,以黏度为依据确定了PA与PB的最佳质量比为3∶7,此时混合溶液PA/PB表观黏度为62.7 m Pa·s,高于单一聚合物溶液PA和PB的黏度。在最佳复合配比下,考察了Na Cl浓度、温度、剪切速率及聚合物浓度对混合溶液PA/PB黏度的影响,结果表明,混合溶液PA/PB具有比单一聚合物溶液PA和PB更好的耐温抗盐、抗剪切性能和增黏性能,证实PA与PB之间存在明显的协同效应。通过流变性测试获得特征松弛时间(TR)和平台区模量(G0)研究了两者的协同机理,表明混合溶液PA/PB网络结构交联点密度高于PA和PB,且强度强于PA和PB。     

黏胶纤维用落叶松溶解浆的清洁漂白

引言近年来,随着棉花价格的总体上涨和消费者对纺织材料舒适度的要求,给黏胶纤维带来了需求增长空间。作为黏胶纤维的原材料,国内目前的溶解浆产能难以满足客户需求。据统计,国内溶解浆存     

A Pilot-Scale Application of Ozone to Bleach Raw Cotton Fabric Using Various Additives

The influence of various additives on the efficiency of optimized ozone bleaching process at pilot scale has been discussed in this study. The results reveal that the best whiteness (63.79) and strength of bleached fabric is achieved with the addition of surfactant (2 g/L) at an ozone dose of 50 g/h, pH 5, and ozone treatment time of 45 min at room temperature. The dyeing quality of ozone-bleached and hydrogen peroxide-bleached fabric samples is almost identical. The analysis of variance of the experimental data validates that the process parameters have significantly affected the efficiency of ozone bleaching process.     

聚硼硅氧烷阻燃剂的合成工艺及其在聚碳酸酯中的应用

采用二步合成法制备了聚硼硅氧烷阻燃剂(PB),通过改变硼酸/硅烷比、缩合温度、水解时间优化了PB的合成工艺。同时研究了PB对聚碳酸酯(PC)阻燃性能和物理性能的影响。结果表明:严格控制硼酸/硅烷比和缩合温度是制备高效阻燃PB的关键,当硼酸/硅烷比(摩尔比)为1:1、缩合温度为100℃时所制备的PB的阻燃性能最好,在PC中添加5%(质量分数)该PB阻燃剂,PC的极限氧指数(LOI)从26%提高到39.4%。在热降解过程中,PB使PC的起始降解温度降低,但可使PC的热降解速率降低,高温残炭量增加,从而提高了PC的阻燃性能。添加PB可以基本保持PC优良的力学性能。另外,PB可保持PC原有的透明性,PC/PB阻燃材料仍旧呈透明状态。     

Synthesis of poly(tetrafluoroethylene)/poly(butadiene) core-shell particles and their graft copolymerization

This article describes how to convert the unreactive surface of poly(tetrafluoroethylene) (PTFE) into poly(styrene-co-acrylonitrile) (SAN). Composite particles with a crosslinked poly(butadiene) (PB) shell covered over a PTFE core were prepared by an emulsifier-free seeded emulsion polymerization of butadiene in the presence of PTFE latex. It was found that the increase in the PB crosslink density resulted in depressing the formation of PB secondary particles. Then, styrene and acrylonitrile were able to graft onto PB shell in high efficiency of 70%. SAN-modified PTFE/PB core-shell particles could eventually be dispersed homogeneously in a SAN matrix. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 68:185–190, 1998     

Influence of core–shell rubber particles synthesized with different initiation systems on the impact toughness of modified polystyrene

Core–shell poly(butadiene‐graft‐styrene) (PB‐g‐PS) rubber particles were synthesized with different initiation systems by emulsion grafting polymerization. These initiation systems included the redox initiators and an oil‐soluble initiator, 1,2‐azobisisobutyronitrile (AIBN). Then the PB‐g‐PS impact modifiers were blended with polystyrene (PS) to prepare the PS/PB‐g‐PS blends. In the condition of the same tensile yield strength on both samples, the Izod test showed that the notched impact strength of PS/PB‐g‐PS(AIBN) was 237.8 J/m, almost 7 times than that of the PS/PB‐g‐PS(redox) blend, 37.2 J/m. From transmission electron microscope (TEM) photographs, using the redox initiators, some microphase PS zones existed in the core of PB rubber particles, which is called “internal‐grafting.” This grafting way was inefficient on toughening. However, using AIBN as initiator, a great scale of PS subinclusion was seen within the PB particle core, and this microstructure increased the effective volume fraction of the rubber phase with a result of improving the toughness of modified polystyrene. The dynamic mechanical analysis (DMA) on both samples showed that the glass transition temperature (T_g) of rubber phase of PS/PB‐g‐PS(AIBN) was lower than that of PS/PB‐g‐PS(redox). As a result, the PB‐g‐PS(AIBN) had better toughening efficiency on modified polystyrene than the PB‐g‐PS(redox), which accorded with the Kerner approximate equation. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 738–744, 2007     

PB/ITO-PET柔性电致变色薄膜制备及性能研究

柔性电致变色器件具有体积小、重量轻、可弯曲等优点,在可穿戴设备、曲面显示器、节能及自适应伪装等领域具有潜在应用前景。本工作以铁氰化钾、氯化钾、无水氯化铁为原料,采用电沉积方法在ITO-PET柔性基底上沉积普鲁士蓝(PB)制得PB/ITO-PET电致变色薄膜,并利用扫描电子显微镜、紫外光谱仪、电化学工作站对PB/ITO-PET电致变色薄膜微观结构和电化学性能进行分析表征。结果表明,电沉积时间为200 s时得到的PB/ITO-PET电致变色薄膜在700 nm波长处光吸收率达到0.755,且PB/ITO-PET电致变色薄膜可在较低电压(0.6 V/-0.3 V)下实现着色和褪色。其光调制范围为68%,着色/褪色响应时间分别为9 s/8 s,着色效率为108 cm2/C。PB/ITO-PET电致变色薄膜经1000次着色-褪色循环后光调制范围为68%,着色效率为100.3 cm2/C。PB/ITO-PET电致变色薄膜500次弯曲,着色效率为105.5 cm2/C,并经1000次着色-褪色循环后着色效率为91 cm2/C,光调制范围为65%。利用ITO-PET为离子存储层(对电极)、凝胶电解质和PB/ITO-PET为工作电极组装得到柔性电致变色器件,其光调制范围为53%,着色/褪色响应时间分别为13 s/18 s。     

影响苯乙烯丙烯腈在聚丁二烯乳胶粒上接枝共聚反应的因素

采用种子乳液聚合技术在聚丁二烯 ( PB)乳胶粒上接枝共聚苯乙烯 ( St)和丙烯腈 ( AN) ,合成了一系列 PB-g-SAN共聚物 ( ABS)。将这些共聚物用丙酮溶解并在超速离心机上将 PB-g-SAN和未接枝在 PB上的游离 SAN分离 ,计算出 SAN在 PB上的接枝率和接枝效率。通过改变共聚单体的组成和加料时间 ,研究了接枝率和接枝效率的变化。结果表明 SAN的接枝率随着 PB含量的增加而降低 ,在共聚单体中增加引发剂 ( CHP)和分子量调节剂 ( TD-DM)的含量 ,SAN在 PB上的接枝率和接枝效率表现出了下降的趋势 ,而共聚单体的配比 St/ AN和加料时间对接枝率和接枝效率的影响不大。     

Magnetite/graphene oxide/Prussian blue composite with robust effectiveness for electromagnetic interference shielding

Considering the promising efficiency of composites, in the current study, a graphene oxide (GO)-magnetite-Prussian blue (PB) composite material was prepared. The composite exhibited electrical conductivity, magnetic permeability, and permittivity nature, and was evaluated using electromagnetic interference (EMI) shielding studies. GO was developed by the Hummer's method, ferrite (Fe₃O₄) was incorporated by the sol-gel method, and PB was introduced in the mixture by an in-situ process. The fabricated samples were studied by X-ray diffraction, Raman Spectroscopy, Fourier-transform infrared spectroscopy along with EMI shielding efficiency (SE) evaluation. The SE of ?71.66 dB of reflection losses was measured at a frequency of 1.5 MHz. The GO/Fe₃O₄/PB composite provided the best results for the detection in the 1–18 MHz frequency range because of its excellent electric and magnetic properties. The obtained results demonstrated that the GO/Fe₃O₄/PB composite has promising potential applications in EMI shielding.     

Effect of styrene‐butadiene triblock copolymer structure on its compatibilization efficiency in PS/PB and PS/PP blends

Two styrene‐butadiene triblock copolymers differing in the length of their styrene blocks (40S‐60B‐40S and 10S‐60B‐10S) were used as compatibilizers for PS/PB (4/1) and PS/PP (4/1) blends. The supramolecular structure of the copolymers determined by small‐angle X‐ray scattering (SAXS), morphology of the blends using transmission electron microscopy (TEM), and their tensile impact strength were chosen as criteria of the compatibilization efficiency of the copolymers used. Different mechanisms of compatibilization for “symmetrical” system (PS/PB/SBS) and “asymmetrical” system (PS/PP/SBS) were proved. While for the PS/PB blend, the 40S‐60B‐40S copolymer proved to be a good compatibilizer, for the PS/PP blend, surprisingly, the 10S‐60B‐10S copolymer is more efficient.     

A modus operandi toward interfacial enhancement of ethylene propylene diene monomer rubber/ polybenzoxazine blends using EPDM-grafted-vinyltrimethoxysilane copolymer

Compatibilization of polymer blends is performed to obtain synergistic effects in physical and mechanical properties. The present work demonstrates the ability of vinyltrimethoxysilane-grafted-ethylene propylene diene monomer rubber (VTMS-g-EPDM) to improve the compatibility between EPDM and polybenzoxazine (PB). EPDM reacted with 5 phr of VTMS showed the highest grafting efficiency as well as a relatively low gel content, and was added to EPDM/PB blends. The addition of 8 phr of compatibilizer to 70/30 (w/w) EPDM/PB reduced the dispersed PB droplet size from 3.1 μm to 800 nm. Effects of various blend compositions at constant dosage of compatibilizer (8 phr) on the swelling behavior and tensile properties of the samples were also studied. The tensile strength increased from 12 to 14.5 MPa upon adding the compatibilizer at 50/50 blend ratio of EPDM/PB; however, the increase in the PB content had no significant impact on the tensile strength in both compatibilized and non-compatibilized samples.     

Mg(OH)2引入方式对纸浆过氧化氢漂白工艺的影响

引言制浆造纸工业是废水和污染物排放的重要源头之一。传统含氯漂白会产生多种难降解、对环境具有高危害的含氯有机化合物,因此它们正在被过氧化氢漂白等无氯漂白工艺所取代。纸浆中的过渡金属离子可催化过氧化氢无效分解并形成对纤维素破化性强的自由基,因此常采用漂前酸洗、螯合及漂白保护剂等来消除和抑制过渡金属离子的影响。而如何使保护剂的功效得到更好的发挥,是     

Optimized Catalytic Bleaching Sequences for Eucalyptus Kraft Pulp

Contemporary multi-stage bleaching processes partially remove residual lignin and hexenuronic acid from cellulosic pulps. The reactions in the steps could be faster and consume smaller amounts of chemicals. Catalytic bleaching (H_cat), utilizing hypochlorite (H), triethylenediamine (DABCO) and its derivative N-carboxymethyl triethylenediamine (CM-DABCO), is a new discovery that has the potential to improve the chemical and energetic efficiency of bleaching processes in chemical pulp mills, e.g. through reducing the reaction time of the bleaching processes. The objective of this study was to clarify if new kraft pulp bleaching sequences with initial stage of chlorine dioxide (ClO₂; D) and an intermediate stage of H_cat could provide fully bleached pulps. The bleaching sequences of the studied eucalyptus pulps include D₀E_(OP)H_cat(Q)P and H_catZ/DP, which attained a final brightness of 88 and 89% ISO, respectively. H_catZ/DP showed to be the best sequence for the catalytic bleaching of eucalyptus kraft pulps. This study may open new doors to future bleaching of cellulose pulps with fewer towers and decreased use of chemicals.     

Studies on the Mineralization and Separation Efficiencies of a Magnetic Photocatalyst

A bench‐scale system was used to demonstrate the application of a recently developed magnetic titanium dioxide photocatalyst for the degradation of organics in aqueous systems. The integrated water treatment system included a photoreactor and magnetic separator for the recovery of the magnetic photocatalyst particles. Methylene blue (MB) was used as a test pollutant. The mineralization and bleaching efficiencies of methylene blue using the magnetic photocatalyst were found to be comparable to those of Degussa P25. The magnetic photocatalyst also demonstrated high magnetic separation efficiency. The recycled photocatalyst particles were found to have the same separation efficiency as the fresh catalyst, although the mineralization and bleaching efficiencies were lower.     

Preparation of modified polybutene‐1 by oxidation and limonene radical grafting using an Nd2O3‐assisted radical initiator system and its characterization

Free radical graft polymerization has been used as a modification method to incorporate functional groups into polyolefins using a melt‐mixing process. In this work, modification of polybutene‐1 (PB) was performed by limonene radical graft polymerization using the Nd₂O₃/dicumyl peroxide (DCP) radical initiator system with various mixing ratios in air. The effects of the modification on the crystallization and tensile behavior were studied in detail. The modified PB samples had ketone and limonene groups. The contents of both the ketone and the limonene groups were highest in the modified PB prepared using Nd₂O₃/DCP (2/0.2 wt%/PB), and a conjugated diene group was found to be produced by a side‐reaction. Excess Nd₂O₃ lowered the limonene graft content in the modified PB. The rate of crystal phase transition (II → I) decreased with an increase of limonene content. The presence of a small amount of the ketone group increased the rate, and the modified PB having a small ketone content exhibited more ductility due to its higher crystal phase transition rate. It was found that there was an optimum mixing ratio of the Nd₂O₃/DCP initiator system for the modification. The ketone and the limonene groups affected the rate of the crystal phase transition and the tensile properties of the modified PB. Copyright © 2010 Society of Chemical Industry     

Enhanced PAA bleaching of cotton by incorporating a cationic bleach activator

Peracetic acid is a well-known alternative to hydrogen peroxide as a bleaching agent for cotton. In this study, a novel cationic bleach activator, N -[4-(triethylammoniomethyl)benzoyl]butyrolactam chloride, was used in combination with peracetic acid to investigate the enhancement of cotton bleaching efficiency. The effects of temperature, pH and concentrations of activator and peracetic acid on the bleaching performance were studied using a statistical design of experiment. Adding activator to a peracetic acid bleaching bath improved the resultant whiteness of the substrate and at optimal conditions produced less fibre damage than when peracetic acid was used alone. In addition, the bleaching performance of both peracetic acid and hydrogen peroxide in the presence of activator was compared. In the absence of activator, the peracetic acid performance was considerably superior to a conventional hydrogen peroxide bleach system in which no bleach activator is present. However, addition of activator to the hydrogen peroxide bath increased the whiteness to a level comparable to peracetic acid.     

PC/ABS/聚硼硅氧烷阻燃合金的性能

采用X射线能谱分析(EDX)研究了PC/ABS/聚硼硅氧烷阻燃合金的燃烧行为,同时考察了阻燃PC/ABS合金的力学性能和加工性能。结果表明,聚硼硅氧烷(PB)中的Si元素会随着燃烧过程的进行逐渐在合金表面进行富集,形成富含Si的绝缘炭层覆盖在基体表面,阻止合金继续燃烧,从而有效提高了PC/ABS合金的阻燃性能。聚硼硅氧烷使PC/ABS合金体系的力学性能有所下降,但拉伸强度下降较少,PB对PC/ABS合金的冲击强度影响较大。在阻燃PC/ABS合金体系中加入相容剂马来酸酐接枝ABS,可使合金体系的力学性能得到明显提高。适量的PB可以改善PC/ABS合金的加工性能。