异丁烯残留量对丁基橡胶溴化的影响

溶液法制备丁基橡胶可以直接得到丁基橡胶胶液,为溴化节省工艺步骤。但由于丁基橡胶优异的气密性,使得胶液中未反应的异丁烯单体很难彻底脱除。采用顶空气相色谱建立了测定胶液中异丁烯质量浓度的方法,将含有不同质量浓度异丁烯的胶液溴化,探究了异丁烯残留量对丁基橡胶溴化的影响。结果表明,随着胶液中异丁烯质量浓度的增加,溴化丁基橡胶的含溴质量分数不断降低,且溴代仲位烯丙基结构与溴代伯位烯丙基结构的相对摩尔比值逐渐增大。     

高支纯亚麻嵌入式复合纱的工艺探讨

探究了利用嵌入式复合纺纱技术纺制高支纯亚麻纱.通过改造多功能纺纱小样机以实现嵌入式复合纺纱技术并对雨露沤麻过后的亚麻纤维进行化学脱胶和剪切处理,以70/30的比例和水溶性维纶短纤维混合制条做成粗纱后,在细纱机上纺制了嵌入式亚麻水溶性维纶复合纱,通过对成纱的强伸性、毛羽、条干均匀度的测试与比较进行了纺纱工艺的优化.结果表明,纺制20.7 tex亚麻水溶性维纶嵌入式复合纱的工艺最佳值为捻系数420、长丝预加张力7.5 cN、长丝与长丝间距8 mm、长丝与粗纱间距1.5 mm;经优化工艺试纺的20.7 tex亚麻水溶性维纶嵌入式复合纱,经退维处理后的纱线细度为8.9 tex;亚麻水溶性维纶嵌入式复合纱结构稳定、强力较高、条干均匀、毛羽少,为开发高档亚麻类面料提供了新的途径.     

Preparation and characterization of high strength and high modulus PVA fiber via dry-wet spinning with cross-linking of boric acid

To improve the mechanical properties of polyvinyl alcohol (PVA) fibers, a series of PVA fibers were prepared via dry-wet spinning with cross-linking of boric acid (BA) (PVA/BA fibers), and using the mixed solvent of dimethyl sulfoxide and water. Moreover, the final PVA/BA fibers were characterized by Fourier transform infrared spectra (FTIR), scanning electron microscopy (SEM), differential scanning calorimetery (DSC), thermogravimetric analyzer (TGA), powder X-ray diffraction (XRD) and yarn strength tester. Furthermore, with the increasing of BA content, FTIR analysis showed that the degree of crosslinking of BA with PVA increased. SEM images of final PVA/BA fibers presented smooth surfaces, and the diameters decreased firstly and then increased. DSC, TGA, and XRD analysis indicated that the melting temperatures, thermal properties and crystallinities first increased and then decreased with the increasing of BA content. In addition, mechanical properties measurements illustrated that the cross-linking existed at an optimal BA content of 0.3 wt%, and PVA/BA-0.3 fiber had the highest tensile strength and Young's modulus of 13.1 ± 0.4 and 360.2 ± 10.4 cN/dtex, respectively.     

Liquid crystal polyarylates containing 2,6-naphthalene dicarbonyl group (I): Effects of kinky monomers on thermal and anisotropic behaviors

A series of copolyarylates primarily based upon 2,6-naphthalene dicarboxylic acid, hydroxybenzoic acid and 4,4-biphenol were prepared by slurry-melt polymerization with Santotherm 66 as a heat exchange medium. The frequently used kinky monomer, resorcinol or isophthalic acid, was introduced into these copolyarylates to modify the chemical strcture. The relationship of the thermal behavior and the crystalline structures for these copolymers was studied by means of DSC and wide angle X-rays diffraction. The amount of mcorporated kinky modifier was found to produce a significant effect on the liquid crystalline phase and the melting temperature of the copolyarylates. All of these liquid crystal polymers exhibited nematic textures; shreaded and/or Schlieren type, depending upon the incorporated kinky monomer. The liquid crystal polymers modified by isophthalic acid (up to 40 mole % of 2,6-naphthalene dicarboxylic acid replaced by isophthalic acid) possessed shreaded texture however high the temperatures of the polymer melts were. The liquid crystal polymers modified by resorcinol (60 to 100 mole % of 4, 4-biphenol replaced by resorcinol), however, would have two types of nematic textures: the shreaded texture occurred when the temperature of the polymer melt was between the melting temperature and the anisotropic transition temperature; the Schlieren texture existed when the temperature of the polymer melt was high above the anisotropic transition temperature. The Schlieren texture formed only when a liquid crystal polymer revealed good flowability and lower rigidity. The polydomain concepts could be utilized to explain the observed textures of these copolyarylates clearly.     

A Synthetic Dynamic Polyvinyl Alcohol Photoresin for Fast Volumetric Bioprinting of Functional Ultrasoft Hydrogel Constructs

Tomographic volumetric bioprinting (VBP) enables fast photofabrication of cell-laden hydrogel constructs in one step, addressing the limitations of conventional layer-by-layer additive manufacturing. However, existing biomaterials that fulfill the physicochemical requirements of VBP are limited to gelatin-based photoresins of high polymer concentrations. The printed microenvironments are predominantly static and stiff, lacking sufficient capacity to support 3D cell growth. Here a dynamic resin based on thiol–ene photo-clickable polyvinyl alcohol (PVA) and thermo-sensitive sacrificial gelatin for fast VBP of functional ultrasoft cell-laden hydrogel constructs within 7–15 s is reported. Using gelatin allows VBP of permissive hydrogels with low PVA contents of 1.5%, providing a stress-relaxing environment for fast cell spreading, 3D osteogenic differentiation of embedded human mesenchymal stem cells and matrix mineralization. Additionally, site-specific immobilization of molecules-of-interest inside a PVA hydrogel is achieved by 3D tomographic thiol–ene photopatterning. This technique may enable spatiotemporal control of cell-material interactions and guides in vitro tissue formation using programmed cell-friendly light. Altogether, this study introduces a synthetic dynamic photoresin enabling fast VBP of functional ultrasoft hydrogel constructs with well-defined physicochemical properties and high efficiency.     

3D成型SiO_2/PVA水凝胶支架的摩擦行为

利用3D成型技术,通过先成型后冷冻交联2步法制备不同孔隙率的SiO_2/聚乙烯醇(PVA)水凝胶支架,研究了SiO_2/PVA水凝胶支架的重复摩擦行为,分析了SiO_2/PVA水凝胶支架的摩擦原理。结果表明:SiO_2/PVA水凝胶支架能够保持三维贯通的立体结构,最大孔隙率可达42.3%。低摩擦速率(10-6~10-3 m/s)下,SiO_2/PVA水凝胶支架摩擦力稍高于块体SiO_2/PVA水凝胶,且随孔隙率的提高而稍有降低;而高摩擦速率(10-2~1m/s)下,SiO_2/PVA水凝胶支架和块体SiO_2/PVA水凝胶的摩擦力相近,孔隙率对支架摩擦力影响不明显。低正压力载荷(0.3kPa)下,SiO_2/PVA水凝胶支架重复摩擦性优于块体SiO_2/PVA水凝胶,这与支架结构能保持稳定的水润滑层相关。     

碳酸钙填充对PVC增塑糊黏度的影响

文章研究了碳酸钙(CaCO_3)未填充和填充情况下,3种不同生产方法、相近聚合度的聚氯乙烯(PVC)糊树脂在对苯二甲酸二辛脂(DOTP)和乙酰柠檬酸三正丁酯(ATBC)2种增塑体系中的黏度性能,以及黏度性能与增塑糊中粒子颗粒形态关系。结果表明,无论CaCO_3填充与否,增塑糊黏度在DOTP体系下均比ATBC的大,主要与增塑剂分子结构有关;未填充CaCO_3时,增塑糊黏度性能主要受PVC糊树脂和增塑剂间相容性的影响,3种糊树脂与DOTP的相容性均比ATBC的好;填充CaCO_3后,几种增塑糊黏度均增大,黏度性能主要受相容性和树脂与CaCO_3粒子颗粒形貌的共同影响。     

Electrochemical deposition of polypyrrole–carbon nanotube films using steroid dispersants

Polypyrrole (PPR)–carbon nanotube (CNT) films were prepared by an electrodeposition method, combining PPR electropolymerization and anaphoresis of CNT. PPR polymerization experiments showed advantages of a dopant from the catechol family for the deposition of PPR films at reduced electrode potentials. The method allowed the formation of adherent films on stainless steel substrates. The amphiphilic molecules with steroid-like structures, such as carbenoxolone disodium salt, glycyrrhizic acid, ammonium salt, and sodium taurodeoxycholate, were used for dispersion and charging of CNT. The new dispersing agents showed outstanding dispersion ability. In addition to dispersing properties, electrodeposition experiments revealed film-forming properties of carbenoxolone and ability to form pure carbenoxolone or carbenoxolone–CNT films. The PPR–CNT films formed using carbenoxolone disodium salt, glycyrrhizic acid ammonium salt, and sodium taurodeoxycholate showed diverse microstructural features. The dispersion and deposition mechanisms were discussed.     

碳中和目标背景下包装行业发展的对策

目的 为了应对日益恶化的全球气候变化,并实现碳中和的目标,研究低碳化技术在包装行业的应用成为当下至关重要的任务。为了推动包装行业在碳中和背景下的低碳化转型,有必要对现有的低碳化技术进行分类和梳理。方法 从碳减排和碳移除两方面对包装行业已有的低碳化技术进行了研究。综述当前可降解生物塑料和聚合物单体化学循环技术在包装中的应用,介绍了几种清洁能源以及碳捕捉、碳利用和碳储存技术的发展现状。结论 对包装行业而言,实现碳中和的目标还面临着很多挑战。包装行业在推进碳中和目标时要选取与发展适合的低碳能源和碳中和技术。     

Single‐layered retardation films with negative wavelength dispersion birefringence made from liquid‐crystalline monomers

Organic light‐emitting diode displays have a cathode composed of a layer of highly reflective metal. Reflection of external light from this layer can be suppressed with a broadband quarter‐wave plate. Although various types of quarter‐wave plate retardation films have been prepared by copolymerizing, mixing, or laminating multiple polymers, ideal wavelength dispersion has not been achieved with thin retardation films because of their relatively low birefringence and the complexity of the procedure required manufacturing them. In this study, we developed (i) new liquid‐crystalline monomers with negative wavelength dispersion birefringence that we used to obtain thin, single‐layered retardation films suitable for coating and (ii) retardation films with different molecular alignments. We found that the monomers showed high solubility and high regularity of molecular alignment, with less damage to the substrate and alignment films. We also investigated the wavelength dispersion and thermal stability of the films. We succeeded in developing retardation films that had a homeotropic alignment or a hybrid alignment with negative wavelength dispersion. These alignments can be used to obtain antireflection films with an improved viewing angle for organic light‐emitting diode displays or next‐generation thin displays.