Studies on chain extension of a novel bio-based engineering elastomer using 4,4-diphenyl methane diisocyanate as a chain extender

2014 ◽  
Vol 131 (18) ◽  
pp. n/a-n/a ◽  
Author(s):  
Lei Jiang ◽  
Hailan Kang ◽  
Zhao Wang ◽  
Liqun Zhang ◽  
Lixin Mao ◽  
...  
RSC Advances ◽  
2015 ◽  
Vol 5 (40) ◽  
pp. 31878-31885 ◽  
Author(s):  
Alvianto Wirasaputra ◽  
Jianqing Zhao ◽  
Yaming Zhu ◽  
Shumei Liu ◽  
Yanchao Yuan

Figure melt torque of PA6 mixed with different contents of chain extender BGPPO. The addition of small molecule diepoxide (BGPPO) greatly enhanced the melt torque, rheological and mechanical properties of polyamide-6 through chain extension reaction.


2019 ◽  
Vol 137 (10) ◽  
pp. 48453 ◽  
Author(s):  
Yanping Zheng ◽  
Puxin Zhu ◽  
Fei Cheng ◽  
Mi Zhou ◽  
Kang Zhang ◽  
...  

2019 ◽  
Vol 35 (3) ◽  
pp. 958-965 ◽  
Author(s):  
Jenjira Jirum ◽  
Yodthong Baimark

Biodegradable polymer blends based on stereocomplex polylactide (scPLA) and poly(butylene succinate) (PBS) were successfully formed by continuous two-step melt blending. An epoxy-based, multifunctional chain extender was chosen to enhance phase compatibility of the blends. Effects of PBS and chain extender on thermal, phase morphology, thermo-mechanical and tensile properties of the scPLA/PBS blends were determined. The PBS blending enhanced plasticizing effect and cold-crystallization of scPLA matrix in an amorphous region. The chain-extension reaction inhibited crystallization of PBS, PLA homo-crystallites and PLA stereocomplex-crystallites as well as reduced thermal stability of the scPLA/PBS blends because of formation of long-chain branched structures. It has been shown that the poor phase compatibility between continuous scPLA and dispersed PBS phases of the blends may be solved through melt blending with a chain extender. The chain extension of scPLA/PBS blends also improved thermo-mechanical properties and flexibility of the scPLA/PBS blend films.


Molecules ◽  
2019 ◽  
Vol 24 (23) ◽  
pp. 4317
Author(s):  
Wei Hu ◽  
Lei Wang ◽  
Quanyong Wang ◽  
Anbo Luan ◽  
Yuliang Mai ◽  
...  

The high crystallization at room temperature and high cost of polyoxytetramethylene glycol (PTMG) have become obstacles to its application. To overcome these problems, a segment of PTMG can be incorporated into a block copolymer. In this work, polypropylene (PPO) glycol-polyoxytetramethylene (PPO-PTMG) multiblock copolymers were designed and synthesized through a chain extension between hydroxyl (OH)-terminated PPO and PTMG oligomers. The chain extenders, feed ratios of the catalyst/chain extender/OH groups, reaction temperature, and time were optimized several times to obtain a PPO-PTMG with low crystallization and high molecular weight. Multiblock copolymers with low crystallization and high average molecular weight (Mn = 1.0–1.4 × 104 Dalton) were harvested using m-phthaloyl chloride as the chain extender. The OH-terminated PPO-PTMG multiblock copolymer with high Mn and a functionality near two was further siliconized by 3-isocyanatopropyltrimethoxysilane to synthesize a novel silyl-terminated polyether. This polyether has an appropriate vulcanizing property and potential applications in sealants/adhesive fields.


2014 ◽  
Vol 34 (7) ◽  
pp. 665-672 ◽  
Author(s):  
Yottha Srithep ◽  
Wuttipong Rungseesantivanon ◽  
Bongkot Hararak ◽  
Krisda Suchiva

Abstract Currently, use of poly(lactic acid) (PLA) is limited for commercial applications because it has a low heat resistance. In this research, an increase of over 40°C heat distortion temperature (HDT) of PLA alloy was obtained by blending PLA with polycarbonate (PC) and a chain extender (CE). Molecular weight, thermal, mechanical and morphological properties of PLA and PC blend with different CE contents were investigated. Gel permeation chromatography (GPC) results showed that some PLA-PC copolymers were produced and the compatibility of the PLA phase and in the PC phase was improved via the chain extension reaction. In addition, the reaction induced by CE also affected the crystallization behaviors of PLA, as observed from differential scanning calorimetry (DSC) results and the enthalpy of melting of PLA decreased with increasing CE content. The combined effects of the CE increasing molecular weight, improving compatibility and limiting the crystallization behavior of PLA/PC alloy greatly improved the HDT.


2014 ◽  
pp. n/a-n/a ◽  
Author(s):  
Weihua Fan ◽  
Yue Zhao ◽  
Aijing Zhang ◽  
Yukun Liu ◽  
Yanxia Cao ◽  
...  

2016 ◽  
Vol 19 (4) ◽  
pp. 58-65
Author(s):  
Ha Thi Thai La

In this research, the PLA-diol were synthesized from lactic acid (LA) and 1.4 butanediols (BD) with a tin octoate Sn(Oct)2 catalyst at a temperature of 180 °C and the pressure 5 mmHg. The structure and properties of PLA-diol are analyzed by the following methods: GPC, 1H-NMR and DSC. As a result, with the change in the content of Sn (Oct)2 from 0.1 to 1.0%, the molecular weight Mn of PLA - diol increased gradually from 4.119,2 to 7.359,6 g / mol . In addition, the BD content increased from 2.0% to 5.0%, the average molecular weight of the product decreased gradually from 7.536,9 g / mol to 4.735 g / mol, respectively. This change will affect the ability to use PLA-diol in the next denaturation research to apply in the field of biodegradable polymer such as copolymer with polyurethane, copolymer with polyethylene glycol diacid, or chain extension with other polymer in a chain reaction,...


Author(s):  
Mohammad Mizanur Rahman ◽  
Md. Hasan Zahir ◽  
Han Do Kim

A series of waterborne polyurethane (WBPU)/modified lignin amine (MLA) adhesives was prepared using modified lignin amine (MLA) as a chain extender by a prepolymer mixing process. A successful Mannich reaction was achieved during the synthesis of MLA by reacting lignin with bis(3-aminopropyl)amine. Higher tensile strength, Young’s modulus and thermal stability were recorded for WBPU/MLA adhesives with higher MLA contents. The WBPU/MLA adhesive materials were used to coat PVC substrates. The adhesive strength increased with increasing MLA content. More importantly, the MLA also enhanced the WBPU/MLA coating in terms of adhesive strength at moderately high temperatures as well as under natural weather exposed conditions. The adhesive strength was essentially unaffected with 6.48 mole% MLA in the WBPU/MLA coating after exposure to natural weather conditions for 180 days.


1993 ◽  
Vol 28 (18) ◽  
pp. 4862-4867 ◽  
Author(s):  
Ming-Fung Lin ◽  
Yao-Chi Shu
Keyword(s):  
Nylon 6 ◽  

Author(s):  
Chang Dae Han

Thermoplastic polyurethane (TPU) has received considerable attention from both the scientific and industrial communities (Hepburn 1982; Oertel 1985; Saunders and Frish 1962). Applications for TPUs include automotive exterior body panels, medical implants such as the artificial heart, membranes, ski boots, and flexible tubing. Figure 10.1 gives a schematic that shows the architecture of TPU, consisting of hard and soft segments. Hard segments, which form a crystalline phase at service temperature, are composed of diisocyanate and short-chain diols as a chain extender, while soft segments, which control low-temperature properties, are composed of difunctional long-chain polydiols with molecular weights ranging from 500 to 5000. The soft segments form a flexible matrix between the hard domains. TPUs are synthesized by reacting difunctional long-chain diol with diisocyanate to form a prepolymer, which is then extended by a chain extender via one of two routes: (1) by a dihydric glycol chain extender or (2) by a diamine chain extender. The most commonly used diisocyanate is 4,4’-diphenylmethane diisocyanate (MDI), which reacts with a difunctional polyol forming soft segments, such as poly(tetramethylene adipate) (PTMA) or poly(oxytetramethylene) (POTM), to produce TPU, in which 1,4-butanediol (BDO) is used as a chain extender. There are two methods widely used to produce TPU: (1) one-shot reaction sequence and (2) two-stage reaction sequence. The reaction sequences for both methods are well documented in the literature (Hepburn 1982). It should be mentioned that MDI/BDO/PTMA produces ester-based TPU. One can also produce ether-based TPU when MDI reacts with POTM using BDO as a chain extender. TPUs are often referred to as “multiblock copolymers.” In order to have a better understanding of the rheological behavior of TPUs, one must first understand the relationships between the chemical structure and the morphology; thus, a complete characterization of the materials must be conducted. The rheological behavior of TPU depends, among many factors, on (1) the composition of the soft and hard segments, (2) the lengths of the soft and hard segments and the sequence length distribution, (3) anomalous linkages (branching, cross-linking), and (4) molecular weight.


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