BCT-2无氨保存剂对浓缩天然胶乳保存效果及其性能的影响

研究了水溶性杀菌剂BCT-2保存浓缩天然胶乳的效果及对预硫化胶乳粘度、成膜特性、硫化胶膜干燥特性及力学性能的影响。结果表明,浓缩天然胶乳保存6个月以上的挥发性脂肪酸值最高为0. 048,要比GB/T 8289—2016的0. 06低,粘度和p H值也都符合应用的要求。预硫化胶乳的粘度在放置前6 d没有太大变化,不影响预硫化胶乳的基本性能,且成膜性能好;与传统高氨保存的硫化胶膜相比,BCT-2保存的硫化胶膜干燥时间短,干燥速率常数提高了5～6倍; BCT-2保存的硫化胶膜的拉伸强度变化不大,而撕裂强度为49. 31 k N/m。     

BCT-2无氨保存剂对浓缩天然胶乳保存效果及其性能的影响

研究了水溶性杀菌剂BCT-2保存浓缩天然胶乳的效果及对预硫化胶乳粘度、成膜特性、硫化胶膜干燥特性及力学性能的影响。结果表明,浓缩天然胶乳保存6个月以上的挥发性脂肪酸值最高为0. 048,要比GB/T 8289—2016的0. 06低,粘度和p H值也都符合应用的要求。预硫化胶乳的粘度在放置前6 d没有太大变化,不影响预硫化胶乳的基本性能,且成膜性能好;与传统高氨保存的硫化胶膜相比,BCT-2保存的硫化胶膜干燥时间短,干燥速率常数提高了5～6倍; BCT-2保存的硫化胶膜的拉伸强度变化不大,而撕裂强度为49. 31 k N/m。     

新型无氨保存剂HY对鲜天然胶乳及橡胶性能的影响

以不挥发水溶性广谱抗菌剂三嗪衍生物(HY)为鲜天然胶乳(NRL)的保存剂,研究保存剂HY对NRL保存效果及天然橡胶(NR)生胶和硫化胶性能的影响。结果表明:采用保存剂HY的NRL保存120h后,其粘度、pH值变化不大,且后期凝固用酸量显著减小,保存效果较好;NR生胶的各项指标均符合5#标准胶标准要求,且塑性保持率比氨保存生胶高10个单位值;NR硫化胶的物理性能明显优于氨保存剂硫化胶,尤其是拉伸强度提高了26%。     

天然橡胶和胶清橡胶的热氧降解特性研究

采用热重分析法(TGA)研究了胶清胶(NR-s)和天然橡胶(NR)在空气气氛中的热氧降解行为。结果表明:(1)NR-s和NR的TG图中均出现多个平台,对应的DTG图中均出现多个峰,因此其热氧降解均属于多步反应。(2)NR-s的T0.05(质量损失率为5%时的温度)为283℃,NR的T0.05为316℃,说明NR-s的热稳定性较NR有一定的下降。     

金属离子钝化剂添加工艺对胶清橡胶性能的影响

通过3种添加工艺将乙二胺四乙酸二钠(EDTA-2Na)、柠檬酸钠(Na CA)和三聚磷酸钠(STPP)3种金属离子钝化剂加入胶清橡胶,研究金属离子钝化剂对胶清橡胶硫化特性、物理性能和热氧老化性能的影响。结果表明:加入金属离子钝化剂对胶清橡胶硫化特性和物理性能影响较小,但能明显提高胶清橡胶的热氧老化性能;Na CA和EDTA-2Na在凝固前加入胶清对提高胶清橡胶热氧老化性能和热稳定性效果更好,STPP则在混炼过程中添加效果更好。     

纯化胶清橡胶的热氧降解研究

采用离心分离的方法制备了胶清橡胶,并测定了该胶清橡胶的蛋白质含量、水溶物含量、丙酮溶物含量、P0和PRI。为探讨水溶物和丙酮溶物对胶清橡胶的热稳定性的影响,采用热重分析法研究了胶清橡胶在空气气氛中的热氧降解行为。研究结果表明,胶清橡胶的蛋白质含量、水溶物含量和丙酮溶物含量较高,Po和PRI数值较低;胶清橡胶在空气中有3个降解过程,经过水和丙酮提纯后的胶清橡胶的热稳定性显著提高。     

复合保存剂BCT-2/NH_3对天然胶乳保存效果及天然橡胶性能的影响

将高效、绿色的水溶性广谱杀菌剂BCT-2与NH3复配保存鲜天然胶乳(NRL),研究了复合保存剂对NRL保存效果、天然橡胶(NR)的硫化特性和加工性能、NR硫化胶的物理机械性能的影响。结果表明,采用BCT-2/NH_3复合保存剂保存NRL效果良好,尤其是挥发脂肪酸值(VFA NO)在7天内始终维持在0.05以下;NR混炼胶的硫化速率和最大交联度比采用NH_3+TT/ZnO保存时更高;NR混炼胶的加工性能优良,网络结构较NH_3+TT/ZnO保存时更稳定;NR硫化胶的物理机械性能优于采用NH_3+TT/ZnO保存时硫化胶,拉伸强度达到26.23 MPa,撕裂强度达到30.71 k N/m。     

胶清凝固工艺的研究

研究了表面活性剂和氯化钙作为胶清的凝固体系,对胶清凝固效果和胶清橡胶性能的影响。结果表明,在胶清中加入十二烷基硫酸钠和氯化钙,可在36 h内使胶清完全凝固。当十二烷基硫酸钠为0.2%、氯化钙为3.0%时,胶清的凝固效果较好,胶清橡胶具有良好的综合性能。     

新型天然胶乳生物保存剂在标准胶制备中的应用研究

研究新型天然胶乳生物保存剂(简称生物保存剂)在标准胶制备中的应用,并与传统保存剂氨进行对比。结果表明:随着生物保存剂和氨质量分数的增大,天然胶乳的保存时间延长,当生物保存剂的质量分数大于0.010(按干胶计)时,天然胶乳的保存时间超过10 h;与采用氨保存的天然胶乳制备的标准胶相比,采用生物保存剂保存的天然胶乳制备的标准胶凝固用酸(甲酸)量大幅度减小,回收率较高,灰分含量、杂质含量、挥发分含量和塑性初值较大,塑性保持率和门尼粘度较低,胶料物理性能无明显差异,生产成本较低,生产环境改善。     

新型天然胶乳生物保存剂在标准胶生产中的应用研究

进行新型天然胶乳生物保存剂（简称生物保存剂）在标准胶制备中的应用研究,并与传统保存剂氨进行对比。结果表明：随着生物保存剂和氨质量分数的增大,天然胶乳的保存时间延长,当生物保存剂的质量分数大于0.010（按干胶计）时,天然胶乳的保存时间超过10 h;与采用氨保存的天然胶乳制备的标准胶相比,采用生物保存剂保存的天然胶乳制备的标准胶凝固用酸（甲酸）量大幅度减小,回收率较高,灰分含量、杂质含量、挥发分含量和塑性初值较大,塑性保持率和门尼粘度较低,胶料物理性能无明显差异,生产成本较低,生产环境改善。     

Characterization of enzyme‐deproteinized skim rubber

Skim natural rubber latex is a protein‐rich byproduct obtained during the centrifugal concentration of natural rubber latex. Skim latex has a very low dry rubber content (4–8%), and the rubber particles are smaller in size. It has a higher proportion of nonrubber solids, which are mostly proteinaceous in nature. It is difficult to coagulate, and it takes more processing time. The proteins in skim latex can be decomposed by proteolytic enzymes. This article discusses the use of stabilized liquid papain from the papaya plant (Carica papaya) for deproteinization followed by creaming for quick and easy coagulation of skim latex. The technological properties and aging characteristics of the deproteinized skim rubber are compared with those of conventionally prepared skim rubber and block rubber. The deproteinized skim rubber showed enhanced quality parameters. Particle size analysis revealed that deproteinization and creaming of the skim latex did not markedly change the particle size. Gel permeation chromatography showed a reduction in the quantity of fatty acids after deproteinization and creaming, which was reflected in the improvement of the aging characteristics in comparison with the control sample. Vulcanizates prepared with the deproteinized skim rubber had higher resilience, lower heat buildup, lower compression set, and good tensile strength and elongation at break in comparison with conventionally prepared skim rubber, and the properties were almost comparable to those of block rubber. The improvement in the mechanical properties and aging characteristics could be attributed to the reduction of the protein content, the partial removal of unsaturated fatty acids, and the removal of metal ions that were pro‐oxidants during the deproteinization and creaming process. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

溶聚丁苯橡胶与不同结构顺丁橡胶并用的SiO2/SSBR/BR复合材料性能研究

传统的镍系顺丁橡胶BR9000和四种稀土顺丁橡胶以低并用比（25phr）与SSBR并用时,BR9000与SSBR并用的硫化胶性能与稀土顺丁橡胶并无明显差距,有些性能还要比一些稀土顺丁橡胶更加优良。稀土顺丁橡胶CB24在物理机械性能方面表现出较好的综合性能。具有长链支化结构的稀土顺丁橡胶Nd24EZ具有最高的直角撕裂强度和最低的裂纹扩展速率。具有长链支化结构和高门尼粘度的稀土顺丁橡胶Nd22EZ则具有最佳的滚动阻力和抗湿滑性能。CB24虽然在抗湿滑性能方面表现优良,但其滚动阻力性能在五种顺丁橡胶中是最差的。Nd22EZ与Nd24EZ与白炭黑的相互作用力最强,白炭黑分散最好,表现出最低的佩恩效应。CB24和SKD-NDII则与白炭黑相互作用力较弱,白炭黑分散较差,佩恩效应最强。     

Mechanical properties of thermoplastic elastomeric blends of chitosan and natural rubber latex

Thermoplastic chitosan/natural rubber blends (Cs/NR) were prepared from natural rubber latex and chitosan by solution casting technique. The blends were characterized by mechanical analysis (stress–strain) and the mechanical properties were found to vary with chitosan/natural rubber ratios. Experimental values were compared with different theoretical models. Effect of thermal aging on mechanical properties was also investigated. Dicumyl peroxide was used as the crosslinking agent. The effect of crosslinking on mechanical properties of Cs/NR has also been studied. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

三氯溴甲烷改性天然胶乳的研究

用三氯溴甲烷改性天然胶乳，研究了反应时间、反应温度、三氯溴甲烷的用量等对改性胶乳的硫化胶膜物理机械性能的影响，利用DSC对产物进行了分析。结果表明，反应时间为10h，反应温度在35℃时，所得胶膜物理机械性能较好；随着三氯溴甲烷用量的增加，改性天然胶乳的硫化胶膜物理机械性能下降：三氯溴甲烷改性天然胶乳的玻璃化温度高于未改性天然胶乳。     

Preparation and graft‐copolymerization of hydrogenated natural rubber in latex stage

Preparation and graft‐copolymerization of hydrogenated natural rubber are performed in latex stage after removal of proteins from the rubber with urea and surfactant. Hydrogenation of deproteinized natural rubber (DPNR) latex is carried out with palladium catalyst under hydrogen atmosphere. The hydrogenated DPNR (HDPNR) is crosslinked with a peroxide followed by graft‐copolymerization of styrene (Sty) and acrylonitrile (AN) in latex stage in order to prepare a graft‐copolymer of crosslinked HDPNR with poly(Sty‐co‐AN) (HDPNR‐graft‐PSAN). Characterization of the products is performed by nuclear magnetic resonance spectroscopy. The conversion of hydrogenation is investigated with respect to the catalyst feed, acidity (pH), and dry rubber content. In the resulting HDPNR‐graft‐PSAN, mole fraction of AN and Sty is 1.4 and 5.8 mol %, respectively. The graft‐copolymer is used to improve properties of PSAN as an impact modifier. The Charpy impact strength of crosslinked HDPNR‐graft‐PSAN/PSAN is about eight times as high as that of PSAN. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42435.     

水泥改性用丁苯胶乳的合成

采用种子乳液聚合法制备了丁苯共聚物/水泥复合材料专用丁苯胶乳,考察了复合乳化剂体系、种子胶乳用量、极性单体种类、聚合温度及加料方式等对乳胶粒尺寸及其分布和胶乳稳定性等的影响。结果表明,在小粒径种子体存在下,分批加乳化剂的加料方式是合成水泥专用丁苯胶乳的有效途径之一,平均粒径小且粒径分布窄的丁苯胶乳具有较好的稳定性。采用复合乳化剂体系、添加少量带极性的第三单体等可以较好地提高丁苯胶乳的化学和机械稳定性。     

Oil resistance and physical properties of in situ epoxidized natural rubber from high ammonia concentrated latex

Epoxidized natural rubber (ENR) was prepared via in situ epoxidation from high ammonia concentrated natural rubber latex with formic acid and hydrogen peroxide in the presence of a surfactant at 50°C for 4, 8, and 12 h. The obtained ENRs containing 20, 45, and 65 mol % of expoxide groups were denoted ENR20, ENR45, and ENR65, respectively. The differential scanning calorimetric study revealed that they exhibited higher glass transition temperatures than that of natural rubber (?62.4°C), at ?38.2°C for ENR20, ?27.8°C for ENR45, and ?19.7°C for ENR 65. It was clearly seen that their glass transition temperatures increased as the amount of epoxide groups increased. The prepared ENRs were compounded and vulcanized to prepare test specimens for determination of oil resistance and various physical properties. It was found that the swelling of ENRs in oils was substantially less than that of natural rubber. The oil resistance of ENR65 was comparable to that of nitrile rubber, commonly used as oil resistant rubber. ENR65 also showed higher hardness than other ENRs. Contrarily, ENR20 possessed superior tensile strength and compression set when compared with other ENRs. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 3948–3955, 2006     

Creaming of skim natural rubber latex with chitosan derivatives

To recover residual rubber from skim natural rubber (SNR) latex, a novel method was developed on the basis of the use of water‐soluble chitosan derivatives. An anionic chitosan derivative, N,O‐carboxymethyl chitosan (CMCh), and a cationic chitosan derivative, N‐(2‐hydroxy)propyl‐3‐trimethylammonium chitosan chloride (HTACh), were prepared. It was found that the creaming process could be achieved with both chitosan derivatives. By the addition of 7.34–10.3‐g/L CMCh, SNR latex was almost completely creamed, and no coagulation of SNR particles in the cream phase occurred. In the case of HTACh, the creaming process was achieved with a lower concentration (<3.70 g/L) than in the case of CMCh, but the size of SNR particles in the cream phase was larger. Solid‐state ¹³C‐NMR, thermogravimetric analysis, and ζ potential measurement results provided evidence that the creaming of SNR latex with CMCh and HTACh was controlled by the depletion flocculation and adsorption mechanisms, respectively. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Effect of zinc oxide nanoparticles as cure activator on the properties of natural rubber and nitrile rubber

Zinc oxide (ZnO) nanoparticles were synthesized by homogeneous precipitation and calcination method and were then characterized by transmission electron microscopy and X‐ray diffraction analysis. Synthesized ZnO was found to have no impurity and had a dimension ranging from 30–70 nm with an average of 50 nm. The effect of these ZnO nanoparticles as cure activator was studied for the first time in natural rubber (NR) and nitrile rubber (NBR) and compared with conventional rubber grade ZnO with special reference to mechanical and dynamic mechanical properties. From the rheograph, the maximum torque value was found to increase for both NR and NBR compounds containing ZnO nanoparticles. ZnO nanoparticles were found to be more uniformly dispersed in the rubber matrix in comparison with the conventional rubber grade ZnO as evident from scanning electron microscopy/X‐ray dot mapping analysis. The tensile strength was observed to improve by 80% for NR when ZnO nanoparticles were used as cure activator instead of conventional rubber grade ZnO. An improvement of 70% was observed in the case of NBR. The glass transition temperature (T_g) showed a positive shift by 6°C for both NR and NBR nanocomposites, which indicated an increase in crosslinking density. The swelling ratio was found to decrease in the case of both NR and NBR, and volume fraction of rubber in swollen gel was observed to increase, which supported the improvement in mechanical and dynamic mechanical properties. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007     

ACM/FKM并用胶的性能研究

研究了不同并用比的氟橡胶（FKM）和丙烯酸酯橡胶（ACM）并用胶的硫变特性、物理机械性能、耐老化性、热稳定性和压缩永久变形性能。实验结果表明：ACM与FKM可以很好地混合并且各自交联,从而制备综合性能优异的并用胶;并用比为30/70的ACM/FKM并用胶综合性能较佳,二段硫化后其物理机械性能和压缩永久变形性能明显改善,且耐热空气老化性能优异;热重分析结果表明,并用胶有很好的热稳定性。