With the growing concern of the international community about the negative spillover effects of SOEs on trade, reaching a consensus among different stakeholders has become increasingly urgent. This paper argues that strengthening a redefined competition policy is a feasible alternative, or at least a complementary option to the existing trade framework. The reasons are as follows: (a) surrounding SOEs is not only trade-related, but also competition-related; (b) the existing SOE disciplines have defects when it comes to dealing with competition distortion effects; and (c) characteristics of competition policy make it easier to reach a “maximum common divisor” among all parties. Accordingly, competition policy needs to be redefined and pursued from an international and domestic level. It is necessary to strengthen the fundamental position of competition policy in China by integrating it into SOE reform measures, advancing the implementation of the Fair Competition Review System, and promoting the construction of the competitive neutrality system.

Until the year 2000, there was no specific statute enacted in Jordan that regulates unfair competition. In the year 2000, the Jordanian Unfair Competition Law No. 15 of 2000 was enacted. The Law deals with the issue of unfair competition in a very generic way. In addition to the Jordanian Unfair Competition Law, the principal statutory source of protection is implemented through the general rules and principles of civil law, particularly, tort law and injurious acts. Although the Jordanian Unfair Competition Law purports to implement a general legal regime on unfair competition, it includes very little in terms of substantive or procedural protection of unfair competition. Presently, the Jordanian legal system provides only very limited protection which is not adequate to accommodate unfair competition cases. Therefore, statutory changes are needed.

본 연구는 제올라이트 Y (Si/Al = 1.56)에서 Cs+ 이온 교환에 Ca2+ 이온의 경쟁 양이온 효과를 연구하기 위해 수행되었다. 완전히 탈수되고 부분적으로 Cs+ 이온으로 교환된 3개의 제올라이트 Y(Si/Al = 1.56)의 단결정은 혼합이온교환 용액을 사용하여 흐름법으로 제조되었으며, 전체 농도가 0.05 M인 이온교환용액의 CsNO3 : Ca(NO3)2 몰비는 1 : 1 (Crystal 1), 1 : 100 (Crystal 2) 및 1 : 250 (Crystal 3)이다. 이온교환된 단결정을 723 K에서 2일 동안 1 × 10-4 Pa로 진공 탈수시켰으며, 결정구조는 100(1) K에서 입방공간군 Fd3̅m을 사용하여 단결정 싱크트론 X선 회절법으로 해석하고 구조를 정밀화하였다. Crystal 1, 2 및 3의 단위세포당 화학식은 |Cs21Ca27|[Si117Al75O384]-FAU, |Cs2Ca36.5|[Si117Al75O384]-FAU 및 |Cs1Ca37|[Si117Al75O384]-FAU이다. 3개의 결정 모두에서, Ca2+ 이온은 D6Rs 내의 site I을 우선적으로 점유하고 있으며 나머지는 site I’, II’ 및 II를 점유하고 있다. 한편 주어진 이온교환용액의 초기 Cs+ 이온의 농도에 따라 Cs+ 이온의 분포에 중요한 차이가 관찰되었다. Crystal 1에서는 Cs+ 이온이 site II’, II, III와 III’에 위치하고 있으며, Crystal 2에서는 site II, IIIa, IIIb에 위치하고 있다. Crystal 3에서는 Cs+ 이온은 site IIIa 및 IIIb에만 위치하고 있다. 초기 Ca2+ 이온의 농도가 증가하고 Cs+ 이온의 농도가 감소에 따라 Cs+ 이온의 교환정도는 28.0에서 2.7과 1.3 %로 급격히 감소하였다.